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Surveillance of Vaccination Coverage Among Adult Populations — United States, 2014

Surveillance Summaries / February 5, 2016 / 65(1);1–36


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Walter W. Williams, MD1; Peng-Jun Lu, MD, PhD1; Alissa O’Halloran, MSPH1; David K. Kim, MD1; Lisa A. Grohskopf, MD2; Tamara Pilishvili, MPH3; Tami H. Skoff, MS3; Noele P. Nelson, MD, PhD4; Rafael Harpaz, MD5; Lauri E. Markowitz, MD6; Alfonso Rodriguez-Lainz, PhD, DVM7; Carolyn B. Bridges, MD1 (View author affiliations)

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Abstract

Problem/Condition: Overall, the prevalence of illness attributable to vaccine-preventable diseases is greater among adults than among children. Adults are recommended to receive vaccinations based on their age, underlying medical conditions, lifestyle, prior vaccinations, and other considerations. Updated vaccination recommendations from CDC are published annually in the U.S. Adult Immunization Schedule. Despite longstanding recommendations for use of many vaccines, vaccination coverage among U.S. adults is low.

Reporting Period: August 2013–June 2014 (for influenza vaccination) and January–December 2014 (for pneumococcal, tetanus and diphtheria [Td] and tetanus and diphtheria with acellular pertussis [Tdap], hepatitis A, hepatitis B, herpes zoster, and human papillomavirus [HPV] vaccination).

Description of System: The National Health Interview Survey (NHIS) is a continuous, cross-sectional national household survey of the noninstitutionalized U.S. civilian population. In-person interviews are conducted throughout the year in a probability sample of households, and NHIS data are compiled and released annually. The survey objective is to monitor the health of the U.S. population and provide estimates of health indicators, health care use and access, and health-related behaviors.

Results: Compared with data from the 2013 NHIS, increases in vaccination coverage occurred for Tdap vaccine among adults aged ≥19 years (a 2.9 percentage point increase to 20.1%) and herpes zoster vaccine among adults aged ≥60 years (a 3.6 percentage point increase to 27.9%). Aside from these modest improvements, vaccination coverage among adults in 2014 was similar to estimates from 2013 (for influenza coverage, similar to the 2012–13 season). Influenza vaccination coverage among adults aged ≥19 years was 43.2%. Pneumococcal vaccination coverage among high-risk persons aged 19–64 years was 20.3% and among adults aged ≥65 years was 61.3%. Td vaccination coverage among adults aged ≥19 years was 62.2%. Hepatitis A vaccination coverage among adults aged ≥19 years was 9.0%. Hepatitis B vaccination coverage among adults aged ≥19 years was 24.5%. HPV vaccination coverage among adults aged 19–26 years was 40.2% for females and 8.2% for males. Racial/ethnic differences in coverage persisted for all seven vaccines, with higher coverage generally for whites compared with most other groups. Adults without health insurance were significantly less likely than those with health insurance to report receipt of influenza vaccine (aged ≥19 years), pneumococcal vaccine (aged 19–64 years with high-risk conditions and aged ≥65 years), Td vaccine (aged ≥19 years), Tdap vaccine (aged ≥19 years and 19–64 years), hepatitis A vaccine (aged ≥19 years overall and among travelers), hepatitis B vaccine (aged ≥19 years, 19–49 years, and 19–59 years with diabetes), herpes zoster vaccine (aged ≥60 years and 60–64 years), and HPV vaccine (females aged 19–26 years and males aged 19–26 years). Adults who reported having a usual place for health care generally were more likely to receive recommended vaccinations than those who did not have a usual place for health care, regardless of whether they had health insurance. Vaccination coverage was significantly higher among those reporting one or more physician contacts in the past year compared with those who had not visited a physician in the past year, regardless of whether they had health insurance. Even among adults who had health insurance and ≥10 physician contacts within the past year, 23.8%–88.8% reported not having received vaccinations that were recommended either for all persons or for those with some specific indication. Overall, vaccination coverage among U.S.-born respondents was significantly higher than that of foreign-born respondents with few exceptions (influenza vaccination [adults aged 19–49 years], hepatitis A vaccination [adults aged ≥19 years], hepatitis B vaccination [adults with diabetes aged ≥60 years], and HPV vaccination [males aged 19–26 years]).

Interpretation: Overall, increases in adult vaccination coverage are needed. Although modest gains occurred in Tdap vaccination coverage among adults aged ≥19 years and herpes zoster vaccination coverage among adults aged ≥60 years, coverage for other vaccines and risk groups did not improve, and racial/ethnic disparities persisted for routinely recommended adult vaccines. Coverage for all vaccines for adults remained low, and missed opportunities to vaccinate adults continued. Although having health insurance coverage and a usual place for health care are associated with higher vaccination coverage, these factors alone do not assure optimal adult vaccination coverage.

Public Health Actions: Assessing associations with vaccination is important for understanding factors that contribute to low coverage rates and to disparities in vaccination, and for implementing strategies to improve vaccination coverage. Practices that have been demonstrated to improve vaccination coverage should be used. These practices include assessment of patients’ vaccination indications by health care providers and routine recommendation and offer of needed vaccines to adults, implementation of reminder-recall systems, use of standing-order programs for vaccination, and assessment of practice-level vaccination rates with feedback to staff members. For vaccination to be improved among those least likely to be up-to-date on recommended adult vaccines, efforts also are needed to identify adults who do not have a regular provider or insurance and who report fewer health care visits.

Introduction

Overall, the prevalence of illness attributable to vaccine-preventable diseases is greater among adults aged ≥19 years than among children aged ≤12 years (1–4). The prevalence of illness among older persons is especially high. For example, in recent years, an estimated 50%–70% of the average 226,000 annual influenza-related hospitalizations, 80%–90% of the 3,000–49,000 influenza-related deaths (data available at http://www.cdc.gov/flu/about/disease/65over.htm), and approximately half of the 13,500 cases of invasive pneumococcal disease (IPD) in the United States occurred among persons aged ≥65 years (1–3). The lifetime risk for herpes zoster (also known as shingles) is approximately 30%, with the risk increasing with age (4). Vaccinations are recommended throughout a person’s lifetime to prevent vaccine-preventable diseases and their sequelae. However, adult vaccination coverage remains low for most routinely recommended vaccines (5) and below Healthy People 2020 targets (https://www.healthypeople.gov/2020/topics-objectives/topic/immunization-and-infectious-diseases/objectives).

Many factors contribute to low adult vaccination rates, including limited public awareness about adult vaccinations, misinformation about vaccines, lack of vaccine requirements for adults, gaps in incorporation of routine vaccine needs assessment and recommendations for adults during health care visits, the cost of stocking vaccines and providing vaccination services, inadequate and/or inconsistent payment for vaccines and vaccine administration, complexities in how adult vaccinations are paid for by private as well as public insurers, lack of health insurance and limited funding for programs to vaccinate uninsured adults, and acute medical care taking precedence over preventive services (6–14). In October 2015, the Advisory Committee on Immunization Practices (ACIP) approved the adult immunization schedule for 2016 (15). With the exception of influenza vaccination, which is recommended for all adults each year, other adult vaccinations are recommended for specific populations based on a person’s age, health conditions, behavioral risk factors (e.g., injection drug use), occupation, travel, and other indications (15).

This report represents the first comprehensive release of adult vaccination coverage data to include assessment of associations with expanded data on demographic characteristics of respondents including access to health care. These findings can be used by public health practitioners, adult vaccination providers, and the general public to better understand factors that contribute to low vaccination and modify strategies and interventions to improve vaccination coverage.

Methods

To assess vaccination coverage among adults aged ≥19 years for selected vaccines and factors associated with vaccination, CDC analyzed data from the 2014 National Health Interview Survey (NHIS); for influenza coverage, data from the 2013 NHIS (August–December) also were used. This report highlights results of that analysis for influenza, pneumococcal, tetanus toxoid-containing (tetanus and diphtheria vaccine [Td] or tetanus and diphtheria with acellular pertussis vaccine [Tdap]), hepatitis A, hepatitis B, herpes zoster (shingles), and human papillomavirus (HPV) vaccines by selected demographic and access-to-care characteristics (e.g., age, race/ethnicity, vaccination indication, health insurance status, contacts with physicians, nativity and citizenship). Estimates of influenza vaccination coverage using 2014–15 season data from other sources have been published (16–18). The attributes, strengths, and limitations of each of these data sources have been described (19). Proportions were estimated of adults aged ≥19 years who received selected vaccinations during 2010–2014. Additional information on NHIS methods is available at http://www.cdc.gov/nchs/nhis/methods.htm.

Data Source and Collection

NHIS collects information about the health and health care of the noninstitutionalized U.S. civilian population using nationally representative samples. Face-to-face interviews are conducted by the U.S. Census Bureau for CDC’s National Center for Health Statistics. Questions about receipt of vaccinations recommended for adults are asked of one randomly selected adult within each family in the household. Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months and if so, in which month and year. Respondents were asked if they had ever had a pneumonia shot. The proportion of pneumococcal vaccination by type of vaccine (23-valent pneumococcal polysaccharide vaccine or 13-valent pneumococcal conjugate vaccine) was not measured. The presence of selected high-risk conditions as defined by ACIP for pneumococcal disease ( Box) (15) was determined by responses to questions in NHIS. Respondents were asked if they had received a tetanus shot in the past 10 years. Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was received in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Respondents were asked if they had ever received the hepatitis A vaccine, and if yes, how many doses were received. Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, whether they had received ≥3 doses or <3 doses. For hepatitis A and hepatitis B vaccination, data were collected on selected respondent characteristics that increase the risk for infection (travel to countries in which hepatitis A infections are endemic and having chronic liver disease, having diabetes, travel to countries in which hepatitis B infections are endemic, and having chronic liver disease, respectively). Respondents were asked if they had ever received a shingles vaccine and if they had ever received an HPV shot or cervical cancer vaccine, and if yes, age at the first dose.

Vaccination outcomes and demographic and other characteristics (e.g., health conditions, insurance status, and usual source and frequency of health care) are self-reported. Race/ethnicity was categorized as Hispanic or Latino, black, white, Asian, and “other.” Persons identified as Hispanic or Latino might be of any race. Persons identified as black, white, Asian, or other race are non-Hispanic. “Other” includes American Indian/Alaska Native and multiple race. The five racial/ethnic categories are mutually exclusive. Adults were classified as health care personnel (HCP) if they reported that they currently volunteer or work in a hospital, medical clinic, doctor’s office, dentist’s office, nursing home, or some other health care facility including part-time and unpaid work in a health care facility as well as professional nursing care provided in the home. Adults were considered insured if they reported having public health insurance coverage (Medicare, Medicaid, military health care [TRICARE/VA/CHAMP-VA], Indian Health Service, state-sponsored health plan, or other government program insurance) or private health insurance coverage. Respondents were asked if there is a place to which they usually go when sick or need advice on their health. Respondents answering yes were defined as having a usual place for health care.

Analysis

For the noninfluenza adult vaccination coverage estimates, the weighted proportion of respondents who reported receiving selected vaccinations was calculated. To better assess influenza vaccination coverage for the 2013–14 influenza season, CDC restricted reported coverage to persons who were interviewed during August 2013–June 2014 and vaccinated during July 2013–May 2014, using the Kaplan-Meier survival analysis procedure; 2013 NHIS data for August–December 2013 were used. Differences were measured as the simple difference between the 2012–13 and 2013–14 influenza seasons. Data for missing month and year (3.1%) were imputed.

To assess adjusted vaccination coverage and adjusted prevalence ratios for each vaccine, CDC used logistic regression and predicted marginal modeling for selected comparisons (health insurance status). Estimates were adjusted for age, sex, race/ethnicity, marital status, education, employment status, poverty level, number of physician contacts in the past year, usual source of health care, self-reported health status, nativity, and region of residence. Income-to-poverty ratio variables are included in the NHIS public use data file (http://www.cdc.gov/nchs/nhis/nhis_2014_data_release.htm). Poverty thresholds were defined according to family size using weighted average Census poverty thresholds from 2012, the average Consumer Price Index from 2012, actual Consumer Price Index values for January-July 2013, and projected Consumer Price Index values for August–December 2013 (ftp://ftp.cdc.gov/pub/Health_Statistics/NCHS/Dataset_Documentation/NHIS/2014/srvydesc.pd).

Weighted data were used to produce national vaccination coverage estimates. Point estimates and 95% confidence intervals (CIs) were calculated by using statistical software to account for the complex sample design. T tests were used for comparisons by race/ethnicity (with non-Hispanic white as the reference), for comparisons between 2014 and 2013, and comparisons of covariates to the reference group within each level of each characteristic (e.g., age group, health care personnel status, patient care status, access-to-care factors, nativity, years of residence in the United States, and citizenship status). For influenza vaccination, tests for linear trend were performed using a weighted linear regression on the season-specific estimates, using season number as the independent variable and weights as the inverse of the estimated variance of the estimated vaccination coverage. For vaccination with the other vaccines, tests for linear trend were performed in SUDAAN using the RATIO procedure. Statistical significance was defined as p<0.05. Coverage estimates are not reported for small sample size (n<30) or relative standard error (standard error/estimates) >0.3.

Results

The final sample adult component response rate for the 2014 NHIS was 58.9%. The total adult sample was 36,324 persons aged ≥19 years. The final sample adult component response rates for estimating influenza vaccination coverage for the 2013–14 influenza season were 61.2% for 2013 and 58.9% for 2014, respectively. The total adult sample for influenza coverage estimation was 32,296 persons aged ≥19 years.

Influenza Vaccination Coverage

Influenza vaccination coverage for the 2013–14 season among adults aged ≥19 years was 43.2%, similar to the NHIS estimate from the 2012–13 season (Table 1). Coverage among whites aged ≥19 years was higher (46.7%) than that for blacks (36.5%), Hispanics (33.2%) and those reporting other race (38.6%). Influenza coverage was 31.5% among adults aged 19–49 years and 47.7% among adults aged 50–64 years. Coverage among adults aged ≥65 years (71.5%) was higher compared with younger age groups. Among HCP aged ≥19 years, influenza vaccination coverage overall was 65.4%, similar to the estimate for 2013 (Table 2). Among HCP aged ≥19 years with and without direct patient care responsibilities, influenza vaccination coverage was 65.1% and 66.0%, respectively, similar to 2013 estimates (Table 3). Coverage was 74.8% for Hispanic HCP aged ≥19 years with direct patient care responsibilities, a 20.8 percentage point increase compared with the 2013 estimate. However, influenza vaccination coverage among HCP with direct patient care responsibilities was similar across all racial/ethnic groups (Table 3). During the 2009–10 through the 2013–14 influenza seasons, fewer than half of adults aged ≥19 years were vaccinated (range: 37.2%–43.2%) (Figures 1 and 2); 56.6%–67.3% of HCP reported influenza vaccination (Figure 2).

Pneumococcal Vaccination Coverage

Reported pneumococcal vaccination coverage (23-valent pneumococcal polysaccharide vaccine [PPSV23] and 13-valent pneumococcal conjugate vaccine [PCV13]) among adults aged 19–64 years at high risk was 20.3% overall, similar to the estimate from 2013 (Table 1). Coverage among whites aged 19–64 years at high risk was higher (21.1%) compared with Hispanics (16.4%) and Asians (14.6%) but was not significantly different for blacks (20.2%) and persons reporting other race (25.3%) compared with whites. Among adults aged ≥65 years, coverage was 61.3% overall, similar to the estimate for 2013. Coverage among whites aged ≥65 years (64.7%) was higher compared with blacks (49.8%), Hispanics (45.2%), and Asians (47.7%) (Table 1). During 2010–2014, pneumococcal vaccination coverage among adults aged 19–64 years at high risk and adults aged ≥65 years ranged from 18.5%–21.2% to 59.7%–62.3%, respectively (Figures 1 and 2).

Tetanus Vaccination Coverage

In 2014, the proportion of adults reporting having received any tetanus toxoid-containing vaccination during the past 10 years was 62.2% overall for adults aged ≥19 years, 62.6% for adults aged 19–49 years, 64.7% for adults aged 50–64 years, and 57.7% for adults aged ≥65 years (Table 1). The proportion of adults receiving tetanus vaccination during the past 10 years across all age groups did not change compared with 2013. Whites had higher coverage across all age groups compared with blacks, Hispanics, and Asians. During 2010–2014, tetanus vaccination among adults aged ≥19 years was unchanged at approximately 62% (Figures 1 and 3).

Among adults aged ≥19 years for whom Tdap vaccination specifically could be assessed, overall reported coverage in the past 9 years was 20.1%, a 2.9 percentage point increase compared with 2013 (Table 1). Tdap coverage for black (11.6%), Hispanic (12.4%), and Asian (15.5%) adults aged ≥19 years was lower compared with whites (23.8%). Coverage among adults aged ≥19 years who reported living with an infant aged <1 year* was 32.0%, higher than the 19.6% coverage among adults aged ≥19 years without household contact with an infant aged <1 year. During 2010–2014, Tdap vaccination coverage increased from 8.2% to 21.5% among adults aged 19–64 years, and during 2012–2014 increased from 8.0% to 14.0% among adults aged ≥65 years (Figures 1 and 3).

Among 16,823 respondents who reported receiving a tetanus vaccination during 2005–2014, more than half (51.3%) reported that they were not informed of the vaccination type, and 11.3% could not recall what type of tetanus vaccination they had received (Table 4). Of the remaining 37.4% of respondents who reported that they knew what type of tetanus vaccine they received, 70.1% reported receiving Tdap.

Overall Tdap vaccination of HCP aged ≥19 years reported in 2014 was 42.1%, similar to the estimate from 2013 (Table 2). White HCP had higher Tdap coverage (46.4%) compared with black HCP (24.8%) and Hispanic HCP (35.8%). Among HCP aged ≥19 years with direct patient care responsibilities, Tdap vaccination coverage was 47.5%, similar to the 2013 estimate (Table 3). Black HCP with direct patient care responsibilities had lower Tdap coverage (28.9%) compared with white HCP (52.4%), but coverage for HCP in the other racial/ethnic groups was similar to that for white HCP (Table 3). Tdap vaccination among HCP aged 19–64 years increased from 22.0% in 2010 to 43.0% in 2014. Tdap vaccination among HCP aged ≥65 years reported during 2012–2014 ranged from 16.9% to 30.7% (Figure 3). Among adults aged ≥19 years who received a tetanus vaccination and reported that they knew what type of tetanus vaccine they received, HCP were more likely to report receipt of Tdap (80.6%) than were non-HCP (68.0%) (Table 4).

Hepatitis A Vaccination Coverage

In 2014, reported hepatitis A vaccination coverage (≥2 doses) was 9.0% for adults aged ≥19 years, 12.1% among adults aged 19–49 years, and 5.5% among adults aged ≥50 years, similar to the estimates for 2013 (Table 1). Among adults aged 19–49 years, coverage for Hispanics (9.6%) was lower than that for whites (12.7%). Vaccination coverage was higher among adults aged ≥19 years who had traveled outside the United States since 1995 to a country in which hepatitis A is of high or intermediate endemicity (countries other than the countries of Europe, Japan, Australia, New Zealand, or Canada) than among respondents who did not travel outside the United States or had traveled only to countries in which the disease is of low endemicity (16.0% versus 5.5%, respectively). Vaccination coverage among adult travelers to countries with high or intermediate endemicity was similar to the estimate for 2013 (Table 1). Overall coverage among adults aged ≥19 years with chronic liver conditions was 13.8%, similar to the 2013 estimate. During 2010–2014 among adults aged ≥19 years, hepatitis A vaccination among travelers to countries with high or intermediate endemicity, among nontravelers, and among persons with chronic liver conditions remained stable (range: 14.6%–16.2%, 5.1%–5.7%, and 13.1%–14.9%, respectively) (Figure 4).

Hepatitis B Vaccination Coverage

Reported hepatitis B vaccination coverage (≥3 doses) among adults was 24.5% for adults aged ≥19 years, 32.2% among adults aged 19–49 years, and 15.7% among adults aged ≥50 years. Overall vaccination coverage among adults aged ≥19 years was similar to the 2013 estimate (Table 1). Vaccination coverage was higher among adults aged ≥19 years who had traveled outside the United States since 1995 to a country in which hepatitis B is of high or intermediate endemicity (countries other than the countries of Europe, Japan, Australia, New Zealand, or Canada) than among respondents who did not travel outside the United States or had traveled only to countries in which hepatitis B is of low endemicity (30.5% versus 21.4%, respectively). Among adults aged 19–49 years, vaccination coverage was lower for blacks (29.9%) and Hispanics (20.2%) compared with whites (36.3%). Overall coverage among adults aged ≥19 years with chronic liver conditions was 29.8%, similar to the 2013 estimate. Vaccination coverage for persons with diabetes was 23.5% for those aged 19–59 years and 13.5% for those aged ≥60 years, similar to estimates for 2013. Overall, hepatitis B vaccination coverage among HCP aged ≥19 years was 60.7%, similar to the estimate for 2013. Black (51.4%) and Hispanic HCP (51.1%) had lower coverage compared with white HCP (63.0%) (Table 2). Among HCP aged ≥19 years with direct patient care responsibilities, hepatitis B vaccination coverage was 67.7%, similar to the 2013 estimate (Table 3). Coverage for black HCP aged ≥19 years with direct patient care responsibilities was lower (56.6%) than that for white HCP with direct patient care responsibilities (70.9%) (Table 3). During 2010–2014, among adults aged ≥19 years, hepatitis B vaccination coverage among travelers to areas of high or intermediate endemicity, nontravelers, persons with chronic liver disease, and HCP varied (range: 30.5%–35.0%, 20.9%–23.2%, 29.8%–38.5%, and 60.7%–65.0%, respectively (Figure 4).

Herpes Zoster Vaccination Coverage

In 2014, among adults aged ≥60 years, 27.9% reported receiving herpes zoster vaccination to prevent shingles, an increase from the 24.2% reported in 2013 (Table 1). Whites aged ≥60 years had higher herpes zoster vaccination coverage (32.0%) compared with blacks (11.6%), Hispanics (14.6%), Asians (16.5%), and those reporting other race (16.2%). Among adults aged 60–64 years, 20.4% reported receiving herpes zoster vaccination, with blacks (8.1%) and Hispanics (11.2%) reporting lower coverage compared with that for whites (24.3%) (Table 1). Estimates were similar to those for 2013. Among adults aged ≥65 years, 31.1% reported herpes zoster vaccination, a 4.3 percentage point increase compared with 2013. Whites aged ≥65 years had higher herpes zoster vaccination coverage (35.0%) compared with blacks (13.5%), Hispanics (16.3%), Asians (20.7%), and those reporting other race (19.6%) (Table 1). Herpes zoster vaccination among adults aged ≥60 years increased from 14.4% in 2010 to 27.9% in 2014 (Figures 1 and 5).

HPV Vaccination Coverage

In 2014, among women aged 19–26 years, 40.2% reported receipt of ≥1 dose of HPV vaccine, similar to the estimate reported for 2013 (Table 1). Coverage was 44.8% among women aged 19–21 years, similar to the 2013 estimate. Coverage was 37.6% among those aged 22–26 years, a 5.3 percentage point increase compared with the 2013 estimate. Among women aged 19–26 years, Hispanics (28.1%) and Asians (22.8%) had lower coverage compared with whites (46.3%), but coverage for blacks (37.4%) and adults who indicated other race (47.3%) was similar to that for whites. Receipt of ≥1 dose of HPV vaccine among males aged 19–26 years was 8.2%, similar to the 2013 estimate. Coverage was 13.3% for males aged 19–21 years, a 5.6 percentage point increase compared with the estimate from 2013. Coverage was 5.4% for those aged 22–26 years, similar to the 2013 estimate.

Among women aged 19–26 years, 2.1% reported receiving the first dose of HPV vaccine at age 8–10 years, 7.4% at age 11–12 years, 58.1% at age 13–17 years, 12.5% at age 18 years, and 19.9% at age 19–26 years (Table 5). Among males aged 19–26 years, 13.0% reported receiving the first dose of HPV vaccine at age 8–10 years, 3.5% at age 11–12 years, 33.1% at age 13–17 years, 24.4% at age 18 years, and 25.9% at age 19–26 years. Among respondents aged 19–26 years, the difference between the age reported at the time of the interview and the age at which respondents indicated that the first dose of HPV vaccine was received was ≥10 years for 7.1% of women and for 13.8% of males. This would imply receipt of vaccination in 2004 or earlier, before HPV vaccine was licensed for use in 2006. Among females and males aged 19–26 years who had not received HPV prior to age 19 years, 11.8% and 2.3% reported receiving the first dose of HPV vaccine at age 19–26 years, respectively (Table 1). Fewer Hispanic females aged 19–26 years (7.4%) reported receiving the first dose of HPV vaccine at age 19–26 years compared with white females aged 19–26 years (13.9%) (Table 1). HPV vaccination increased from 20.7% in 2010 to 40.2% in 2014 for females aged 19–26 years, and from 2.1% in 2011 to 8.2% in 2014 among males aged 19–26 years (Figures 1 and 5).

Trends in Adult Vaccination Coverage

Estimated proportions of adults aged ≥19 years who received selected vaccinations during the period 2010–2014 are shown (Figures 1, 2, 3, 4, and 5). Although the point estimates for each year vary by only a few percentage points, linear trend tests indicated that influenza vaccination coverage significantly increased overall among persons aged ≥19 years from the 2009–10 influenza season to the 2013–14 season (test for trend: p = 0.01) (Figures 1 and 2). Influenza vaccination coverage did not increase significantly among HCP during this period (test for trend: p = 0.17) (Figure 2). During 2010–2014, pneumococcal vaccination coverage increased significantly only among high-risk persons aged 19–64 years (test for trend: p = 0.01) (Figures 1 and 2). During 2010–2014, significant increases also occurred for Tdap vaccination overall among persons aged ≥19 years (test for trend: p< 0.01) and among HCP aged 19–64 years and those aged ≥65 years (tests for trend: p< 0.01 and 0.03, respectively), herpes zoster vaccination of persons aged ≥60 years (test for trend, p< 0.01), and HPV vaccination of females and males aged 19–26 years (test for trend, p< 0.01) (Figures 1, 3, and 5). There was a significant downward trend for hepatitis B vaccination among travelers to countries with high or intermediate endemicity and for nontravelers (test for trend: p< 0.01) (Figure 4). Coverage did not show statistically significant changes during 2010–2014 for the other vaccines routinely recommended for adult populations (pneumococcal vaccination [persons aged ≥65 years] and overall tetanus vaccination [persons aged ≥19 years]) (tests for trend: p>0.05) (Figure 1).

Association of Health Insurance Status with Vaccination Coverage Among Adult Populations

Most study respondents (86.7%) indicated having some type of health insurance. Overall, vaccination coverage was lower among adults without health insurance compared with those with health insurance, except for overall hepatitis B vaccination among those aged ≥19 years with chronic liver conditions or diabetes (Table 6). For influenza, pneumococcal, Tdap, herpes zoster, and HPV vaccination, coverage was two to five times higher among those with health insurance compared with those without insurance (Table 6).

Adult vaccination coverage differed by the type of health insurance. Vaccination coverage was higher among adults with private health insurance compared with those reporting public health insurance for pneumococcal vaccination among adults aged ≥65 years, tetanus and Tdap vaccination (all ages), overall hepatitis A vaccination among adults aged ≥19 years, hepatitis B vaccination among adults aged ≥19 years overall and those with diabetes aged ≥19 years and ≥60 years, and herpes zoster vaccination among adults aged ≥60 years (Table 6). Vaccination coverage was significantly lower among adults with private insurance compared with those with public insurance for overall influenza vaccination among adults aged ≥19 years and for pneumococcal vaccination among adults aged 19–64 years with high-risk conditions (Table 6).

Association of Health Insurance Status and Having a Usual Place for Health Care with Vaccination Coverage

Generally, adults with a usual place for health care were more likely to report having received recommended vaccinations than those who did not have a usual place for health care, regardless of whether they had health insurance. Among adults with health insurance, coverage was significantly higher among those who reported having a usual place for health care compared with those who did not have a usual place for health care except for hepatitis A vaccination and hepatitis B vaccination (Table 7). Among adults without health insurance, coverage was significantly higher among adults who had a usual place for health care compared with those who did not for influenza vaccination, pneumococcal vaccination among adults aged 19–64 years with high-risk conditions, and overall tetanus vaccination among adults aged ≥19 years (Table 7).

Adult Vaccination Coverage by Health Insurance Status and Physician Contacts

With a few exceptions (overall hepatitis A vaccination among adults aged ≥19 years and HPV vaccination among women aged 19–26 years), vaccination coverage was significantly higher among those reporting having had one or more physician contacts in the past year compared with those who had not visited a physician in the past year, regardless of whether they had health insurance (Table 8). In addition, vaccination coverage generally increased as the number of physician contacts increased (Table 8).

Among adults who had health insurance and reported having had ≥10 physician contacts within the past year, 23.8%–88.8% reported not receiving vaccinations that either are recommended for all persons or are recommended for those with some specific indication (not receiving influenza vaccination, 39.4% [aged ≥19 years], 51.4% [aged 19–49 years], 38.3% [aged 50–64 years], 23.8% [aged ≥65 years]; not receiving pneumococcal vaccination, 61.4% [high-risk, aged 19–64 years], 29.3% [aged ≥65 years]; not receiving Td, 30.1% [aged ≥19 years]; not receiving Tdap, 68.7% [aged 19–64 years], 83.9% [aged ≥65 years]; hepatitis A, 82.4% [travelers aged ≥19 years], 82.0% [persons aged ≥19 years with chronic liver conditions]; hepatitis B, 62.9% [travelers aged ≥19 years], 67.1% [persons aged ≥19 years with chronic liver conditions], 64.7% [adults aged 19–59 with diabetes], 88.8% [adults aged ≥60 years with diabetes]; herpes zoster, 67.7%; and HPV, 51.6% [women aged 19–26 years]) (Table 8).

Association of Respondent Age with Adult Vaccination Coverage

Influenza and pneumococcal vaccination coverage among adults aged ≥65 years was higher compared with coverage among adults aged 19–64 years; however, Td and Tdap coverage among adults aged ≥65 years was lower compared with coverage among adults aged <65 years. Hepatitis B vaccination coverage among adults with diabetes aged ≥60 years was lower compared with coverage among adults aged 19–59 years with diabetes (Tables 6, 7, and 8). Herpes zoster coverage among adults aged ≥65 years was higher compared with coverage among adults aged 60–64 years (Table 6).

Adult Vaccination Coverage Adjusted for Selected Demographic and Access to Care Characteristics

Adults without health insurance were significantly less likely than those with health insurance to be vaccinated after adjusting for confounders for influenza (aged ≥19 years); pneumococcal (aged 19–64 years with high-risk conditions); hepatitis B (aged ≥19 years and 19–49 years); herpes zoster (aged ≥60 years), and HPV (females aged 19–26 years) vaccination (Table 9). The difference in adjusted vaccination coverage between respondents with and without health insurance for those for whom the difference was statistically significant ranged from 2.9% (hepatitis B vaccination among adults aged ≥19 years) to 13.3% (influenza vaccination among adults aged ≥19 years) (Table 9).

Adult Vaccination Coverage by Nativity, Years Living in the United States, and Citizenship

Overall, vaccination coverage among U.S.-born respondents was significantly higher than that of foreign-born respondents with few exceptions (Table 10). Exceptions were noted for influenza vaccination (adults aged 19–49 years), overall hepatitis A vaccination (adults aged ≥19 years), hepatitis B vaccination among adults with diabetes aged ≥19 years and those aged ≥60 years, and HPV vaccination of males aged 19–26 years. Vaccination coverage was higher for foreign-born persons living in the United States ≥10 years compared with those in the United States <10 years for influenza vaccination (overall for persons aged ≥19 years and adults aged ≥65 years). Vaccination coverage was significantly lower for foreign-born persons living in the United States ≥10 years compared with those living in the United States <10 years for hepatitis A vaccination (adults aged ≥19 years overall), and hepatitis B vaccination (among adults ≥19 years overall and those aged ≥19 years with diabetes). Except for pneumococcal vaccination of adults aged ≥65 years, Td vaccination of adults aged ≥65 years, hepatitis A vaccination, hepatitis B vaccination among adults with diabetes aged ≥19 years, and HPV vaccination among females aged 19–26 years, coverage among foreign-born adults who were U.S. citizens was higher than that for foreign-born respondents who were not U.S. citizens (Table 10).

Discussion

In 2014, adult vaccination coverage in the United States did not improve from 2013, except for modest increases in Tdap vaccination for adults aged ≥19 years and herpes zoster vaccination among adults ≥60 years. Vaccination coverage estimates for the four vaccines in this report that are included in Healthy People 2020 (influenza, pneumococcal, herpes zoster, and hepatitis B [for HCP] vaccines) are below the respective target levels, including among insured adults and adults with multiple health care visits in the past year. Racial/ethnic gaps in coverage persisted for all seven vaccines in this report and widened for Tdap and herpes zoster vaccination, with higher coverage generally for whites compared with most other groups. These data indicate multiple missed opportunities for vaccination and the need to increase routine assessment of adult vaccination needs, and vaccination with needed vaccines.

Influenza Vaccination

Since 2010, ACIP has recommended that all persons aged ≥6 months be vaccinated annually against influenza to prevent illness and related complications (20). Fewer than half of adults aged ≥19 years were vaccinated during the influenza seasons spanning the 2009–10 through 2013–14 seasons. Higher vaccination rates could have resulted in prevention of a substantial greater number of influenza cases and hospitalizations. For example, using a model published in 2013 (21), CDC estimated the amount of influenza-associated outcomes during the 2012–13 influenza season, a moderately severe season, that might have been prevented by influenza vaccination (22). For the 2013–14 influenza season, using updated estimates of vaccination coverage, vaccine effectiveness, and influenza hospitalizations, CDC estimates that influenza vaccination prevented approximately 7.2 million illnesses, 3.1 million medically attended illnesses, and 90,000 hospitalizations associated with influenza (23). If influenza vaccination levels had reached the Healthy People 2020 target of 70%, an estimated additional 5.9 million illnesses, 2.3 million medically attended illnesses, and 42,000 hospitalizations associated with influenza might have been averted. For the U.S. population to benefit more fully from influenza vaccines, more effort is needed to reach the Healthy People 2020 target. Ensuring that all persons who visit a health care provider during the influenza season receive a vaccination recommendation and offer from their provider and use of vaccination information systems could increase influenza vaccination rates and reduce the incidence of illness (24,25).

HCP are recommended for routine annual influenza vaccination (20,26). Preventing influenza among HCP who might serve as sources of influenza virus transmission provides additional protection to patients at risk for influenza complications. Although annual vaccination has long been recommended for HCP and is a high priority for reducing morbidity associated with influenza in health care settings (27–29), influenza vaccination coverage level among HCP aged ≥19 years during the 2013–14 season was 65.4% overall and 65.1% among those with direct patient care responsibilities. Higher HCP influenza vaccination coverage has been associated with employer requirements for vaccination and access to vaccination at the workplace at no cost for >1 day (17,30). Although less effective than workplace on-site vaccination, active employer promotion of influenza vaccine through such methods as incentives and personal reminders also has been associated with higher coverage compared with HCP whose employers did not implement any policies or activities related to influenza vaccination (17). These results indicate that a comprehensive strategy that includes easy access to vaccination at no cost on multiple days along with promotion of vaccination might increase HCP vaccination coverage. Employers and health care administrators can make use of the Guide to Community Preventive Services (24), which provides guidance on effective interventions to increase uptake of influenza vaccination among HCP.

Pneumococcal Vaccination

In August 2014, ACIP recommended routine use of PCV13 among adults aged ≥65 years (31). PCV13 should be administered in series with PPSV23, the vaccine recommended for adults aged ≥65 years since 1983. PPSV23 contains 12 serotypes in common with PCV13 and 11 additional serotypes. PCV13 vaccine reduces the risk for pneumococcal pneumonia and both PCV13 and PPSV23 have been demonstrated to reduce the risk for invasive pneumococcal infections (31,32). Because of the high proportion of invasive pneumococcal disease caused by serotypes unique to PPSV23, broader protection is expected to be provided through use of both PCV13 and PPSV23 in series. Adults who have already received PPSV23 and are recommended to receive PCV13 should receive PCV13 at least 1 year after PPSV23 vaccine. The survey data from 2014 NHIS could not be used to estimate the proportion of pneumococcal vaccinations by type (PCV13 versus PPSV23). The overall pneumococcal vaccination estimates in this report include respondents who might have received PCV13 and/or PPSV23. Pneumococcal vaccination of persons aged 19–64 years at high risk increased during the 5 years covered in this report but was unchanged among those aged ≥65 years, and both were well below Healthy People 2020 targets of 60% for persons aged 18–64 years at high risk and 90% for adults aged ≥65 years. Among persons aged ≥65 years, using PCV13 in series with PPSV23 could prevent an estimated 230 cases of invasive pneumococcal disease and approximately 12,000 cases of community-acquired pneumonia over the lifetime of a single cohort of persons aged 65 years (31). Achieving higher pneumococcal vaccination levels could improve these benefits.

Tetanus Toxoid-Containing Vaccination

In 2012, ACIP updated the adult Tdap vaccination recommendation to include all adults aged ≥19 years who have not yet received a dose of Tdap, including those aged ≥65 years (33). Tdap, when indicated, should be administered regardless of interval since the most recent Td. A single dose of Tdap is particularly important for adults who have or who anticipate having close contact with an infant aged <1 year (e.g., parents, grandparents, child care providers, and health care personnel) to reduce the risk for transmitting pertussis to infants too young to be vaccinated who are at greatest risk for severe pertussis, including hospitalization and death. Although there were modest increases in Tdap vaccination of adults from 2010 to 2014, coverage has remained low for all age groups and among adults living with an infant aged <1 year.

In hospital settings, transmission of pertussis has occurred from hospital visitors to patients, from HCP to patients, and from patients to HCP (34–37). Vaccinating HCP with Tdap will help protect them against pertussis and might reduce transmission to patients, other HCP, household members, and persons in the community (26,38). Health care providers should not miss an opportunity to vaccinate adults aged ≥19 years who have not received Tdap previously.

Hepatitis A Vaccination

Hepatitis A vaccination is recommended for any person seeking protection from hepatitis A virus infection, if some risk factor is present (e.g., on the basis of lifestyle, occupation, medical, or other indication), and for persons traveling to or working in countries that have high or intermediate endemicity of hepatitis A (15). Comprehensive information on all risk and occupation indications for hepatitis A vaccination were not collected in the 2014 NHIS. Information was available only for those with foreign travel to areas of high or intermediate endemicity and those with chronic liver disease. Although hepatitis A vaccination of persons who had traveled outside the United States to a country in which hepatitis A is of high or intermediate endemicity was higher in 2014 and preceding years than among respondents who did not travel outside the United States or had traveled only to countries in which the disease is of low endemicity, overall hepatitis A vaccination among travelers and persons with chronic liver disease has remained low. Health care providers are encouraged to assess the needs of their clients for this vaccine and offer it whenever appropriate.

Hepatitis B Vaccination

In December 2011, ACIP recommended that all previously unvaccinated adults aged 19–59 years with diabetes mellitus (type 1 and type 2) be vaccinated against hepatitis B as soon as possible after receiving a diagnosis of diabetes and that unvaccinated adults aged ≥60 years with diabetes may be vaccinated at the discretion of the treating clinician after assessing their risk and the likelihood of an adequate immune response to vaccination (39). Hepatitis B vaccination coverage in 2014 among persons with diabetes showed no improvement over estimates obtained before this recommendation, which underscores the need to improve awareness of increased risk for contracting acute hepatitis B among persons with diabetes and to increase hepatitis B vaccination in this population.

During 1982, when hepatitis B vaccine was first recommended for HCP, an estimated 10,000 infections occurred among persons employed in a medical or dental field. By 2004, the number of hepatitis B virus (HBV) infections among HCP had decreased to an estimated 304 infections, largely resulting from the implementation of routine pre-exposure vaccination and improved infection-control precautions (40–42). The risk for acquiring HBV infection from occupational exposures is dependent on the frequency of percutaneous and mucosal exposures to blood or body fluids (e.g., semen, and wound exudates) containing HBV, particularly fluids containing hepatitis B e antigen, a marker for high HBV replication and viral load (26). The risk is higher during the professional training period and can vary throughout a person’s career (43). All unvaccinated persons whose work- and training-related activities involve reasonably anticipated risk for exposure to blood or other infectious body fluids (e.g., HCP, long-term–care facility staff, and public safety workers) should be vaccinated with the complete, ≥3-dose hepatitis B vaccine series and undergo postvaccination serological testing to demonstrate protective antibody levels (44). During 2010–2014, estimates of hepatitis vaccination among HCP have not improved, ranging from 61%–65%, well below the Healthy People 2020 target of 90%. The Hospital Infection Control Practices Advisory Committee (HICPAC) has encouraged all facilities or organizations that provide direct patient care to formulate a comprehensive vaccination policy for all HCP (45). Implementation of HICPAC and CDC recommendations can assist hospital administrators, infection-control practitioners, employee health clinicians, and HCP in optimizing infection prevention and control programs.

Herpes Zoster Vaccination

ACIP recommends herpes zoster vaccination for adults aged ≥60 years (46). Although herpes zoster vaccination coverage increased in 2014 compared with 2013, it was 2.1 percentage points below the Healthy People 2020 target of 30%. Shortages of herpes zoster vaccine and a resulting lack of vaccine promotion likely contributed to low uptake during the first years after licensure. These shortages now appear to be resolved; however, other barriers persist, particularly the high cost for providers to purchase a supply, challenges to stocking the vaccine (which requires freezer storage), coverage for the vaccine under Medicare Part D, which results in billing challenges for medical providers (except pharmacist vaccine providers), and out-of-pocket payments for some Medicare Part D beneficiaries depending on their specific plan (47,48). Providers often refer patients to pharmacies for herpes zoster vaccination because reimbursement for Medicare Part D benefits is less complex. For adults aged ≥60 years with nongrandfathered private health insurance plans, herpes zoster vaccine is available with no out-of-pocket costs because of provisions of the Affordable Care Act (14,47,48).

HPV Vaccination

Although HPV vaccination increased significantly among age-eligible females during 2010–2014 (5,49,50), coverage has remained low. Since 2006, ACIP has recommended routine vaccination of adolescent girls and boys at ages 11 or 12 years and vaccination for females aged 13–26 years who have not been vaccinated previously (51). Since 2011, ACIP has recommended vaccination for males aged 13–21 years who have not been vaccinated previously or who have not completed the 3-dose series; males aged 22–26 years may be vaccinated. Approximately 12% of females and 2% of males aged 19–26 years not vaccinated at age ≤18 years reported receiving the first dose of HPV vaccine as catch-up at age 19–26 years. As more adolescents are vaccinated at the target age group and age into the group monitored in NHIS, vaccine coverage estimates are expected to increase.

Data on age at first dose of HPV vaccination of adults was collected for the first time in 2013. Most female and male respondents in the 2014 NHIS reported receiving the first dose of HPV vaccine at age ≥13 years, consistent with the fact that female respondents aged ≥21 years and all male respondents would have been aged >13 years at the time HPV vaccination was first recommended. Some respondents also indicated the first HPV vaccination dose was received before HPV vaccine was licensed for use in 2006, suggesting inaccurate recall.

In 2014, white women reported higher HPV coverage than Hispanic or Asian women. Black women and women reporting other race had coverage similar to that for whites. The findings for black, Hispanic, and Asian women contrast with data on HPV vaccination of adolescent girls aged 13–17 years reported in the 2014 National Immunization Survey–Teen (NIS-Teen) (52), which indicated that, among females, ≥1, ≥2, and ≥3 HPV dose coverage was higher among Hispanic adolescents and similar for Asian adolescents compared with white adolescents. Among black adolescents, ≥1 and ≥2 HPV dose coverage was also higher compared with estimates for white adolescents. HPV vaccination coverage for each HPV dose was higher for females living below poverty level compared with those at or above the poverty level. The higher coverage in NIS-Teen among black and Hispanic females and those living below the poverty level might be attributable in part to the continued effectiveness of the Vaccines for Children program, which provides recommended vaccines at no cost to eligible children through age 18 years (53). NIS-Teen estimates also are based on provider reports from medical records whereas NHIS vaccination data are self-reported. Young adults might not be able to recall accurately which vaccines they received as adolescents.

Although vaccination coverage has increased since a licensed HPV vaccine has been available and recommended by ACIP, many adolescent and young adult females remain unvaccinated and vulnerable to develop cancers that safe, effective HPV vaccines can prevent (51). Studies on the prevalence of genital HPV infection among women in the United States (54) and the seroprevalence of the nine HPV types in the 9-valent vaccine (55) indicated that many adult women have not been infected with high-risk HPV types, supporting implementation of ACIP-recommended catch-up vaccination. Until HPV vaccination increases among adolescents, a high proportion of unprotected young women eligible for HPV vaccination will be expected. Results from modeling and studies of the cost-effectiveness of HPV vaccination of young women have suggested that catch-up vaccination could reduce the amount of time needed to achieve population level impacts of vaccination (56,57). Findings from initial studies of vaccine impact in settings in which catch-up vaccination programs were successful in achieving high coverage rates among young women are consistent with these models (56,57). Continued efforts are needed to improve coverage among members of the primary target group for HPV vaccine, girls and boys aged 11–12 years, and among all racial and ethnic groups. Efforts also are needed to improve catch-up vaccination among those who have not started or completed their vaccination.

Health Insurance Status and Usual Place for Health Care

The findings in this report are consistent with a previous report (12) indicating that having health insurance was generally associated with a greater likelihood of having received recommended vaccinations. Even after demographic and access-to-care variables are controlled for, persons with health insurance were more likely to be vaccinated than those without insurance for several vaccines. The type of health insurance indicated by respondents had a significant association with vaccination coverage. Vaccination coverage was higher among adults with private health insurance compared with those reporting public health insurance for many of the vaccines, but this finding was not consistent for all vaccines and age groups. The factors contributing to vaccination levels by type of health insurance are not well understood. In one study (58), the percentage of persons with private health insurance declined during 1999–2011, ranging from 67% to 74% during 1999–2008, and was 64% during 2009–2011. This downward shift in private insurance coverage might have had an impact on adult vaccination coverage. The Affordable Care Act also might have had an impact on vaccination coverage (48). A better understanding of factors influencing vaccination by type of health insurance is needed.

Health insurance coverage, although beneficial in improving access to health care services, might not be sufficient in itself to achieve optimal adult vaccination. In this report, even among those with health insurance and ≥10 contacts with physicians during the preceding year and no contraindications, vaccination was still not routine. Up to 88.8% of adults reported not receiving one or more recommended vaccines. Provider attitudes toward adult vaccination, practice patterns that do not routinely incorporate assessments for vaccines for adults, and other barriers to vaccination might determine whether patients are offered and receive vaccines (6,8–10,12,14,59).

In general, persons with a usual place for health care were more likely to report having received recommended vaccinations than those who did not have a usual place for health care, regardless of whether they had health insurance, and vaccination coverage generally increased as the number of physician contacts increased. This observation suggests that an increased number of physician contacts might have facilitated opportunities to be reminded of the need for vaccinations, discussions about indicated vaccinations, and a recommendation and decision to vaccinate. These findings are also consistent with previous reports indicating that persons who have a usual place for health care or medical home and who seek medical care one or more times during the year are more likely to be vaccinated and receive other preventive services than those without a usual place for health care (59,60). Having a usual place for health care and routine physician contact can provide important opportunities for providers to educate their patients about vaccine-preventable diseases and recommend and offer vaccination (61–65).

Nativity

Overall, vaccination coverage was generally lower among the foreign-born compared with U.S.-born persons. Vaccination coverage for the foreign born differed by time lived in the United States. In a previous report (65), vaccination also was associated with language used for interview, race/ethnicity, and birth country/region. Among foreign born, vaccination coverage was generally lower among those who were not U.S. citizens, those interviewed in a language other than English, and non-Hispanic blacks or Hispanics compared with U.S. citizens, those interviewed in English, and non-Hispanic whites. The Hispanic foreign born had the lowest coverage for several vaccines. This finding is notable because foreign-born persons from Latin America account for more than half of all foreign-born adults in the United States (66–68). Vaccination coverage among the foreign born in the United States depends on the vaccinations they received as children or adults premigration, during migration, postmigration, or during return visits to their country of origin. Vaccination coverage and immunization schedules are different in many countries compared with the United States and vary by country and even by regions within countries (65,69–71). Although immigrant visa applicants and refugees destined for permanent resettlement in the United States are subject to ACIP-recommended vaccination requirements, the differences between the United States and other countries in the schedules of routine vaccinations among adults might contribute to differences in the coverage levels of the vaccines studied. In most countries, vaccination programs have focused historically on children (72–74). Depending on their origin, age at arrival, and year of arrival, foreign-born adults arriving in the United States might have differences in vaccination coverage compared with U.S.-born populations (75,76). After arrival in the United States, many foreign-born adults experience socioeconomic, cultural, linguistic, and other barriers to accessing health care and preventive services, including vaccination (66,67,77). The percentage of uninsured persons also is higher among non-U.S. citizens, recent immigrants, and those with poor/fair English proficiency (68,78). These populations might also be less aware of U.S. adult immunization recommendations (79). As the size and race/ethnic diversity of the foreign born population in the United States continues to increase, the findings of this and previous studies indicate that this population will be increasingly important to elimination of national adult vaccination disparities (80). Public policy makers, vaccination programs, and healthcare providers should consider foreign-born populations in their public health assessment, evaluation, and outreach programs that target disadvantaged groups (80).

Improving Adult Vaccination Coverage

Racial/ethnic gaps in coverage persisted for all seven vaccines in this report with higher coverage generally for whites compared with most other groups. Previous research has indicated a variety of factors that contribute to racial/ethnic differences in adult vaccination rates, including patient, provider, and system factors (81–84). Standardized offering of vaccines reduces these differences (85,86). Using an intensive combination of patient tracking, vaccination reminders for providers and patients, and patient outreach and assistance also reduces racial/ethnic vaccination differences (87). Incorporating standards for adult vaccination practices, which include routinely assessing vaccination needs during clinical encounters, providing a strong recommendation for vaccination to patients with indications, and then offering vaccination at the visit, can have a substantial impact on reducing vaccination disparities (25).

Many factors contribute to low adult vaccination rates, including limited awareness among the public about adult vaccinations, vaccine needs assessment often not routinely included in adult patient care, lack of vaccine requirements for adults, complexities in how adult vaccinations are paid for by private and public insurers, the financial risks for providers to stock vaccines and provide vaccination services, limited funding for programs to vaccinate uninsured adults, and acute medical care taking precedence over preventive services (6–14).

The most successful strategies to improve adult immunizations involve organizational change, such as initiating standing orders or protocols to ensure immunization assessment is routinely done and needed vaccines administered when indicated. The Community Preventive Services Task Force has evaluated vaccination interventions and identified effective, evidence-based strategies to improve vaccine use which can be applied to the adult population, including systems interventions, such as the use of standing orders or protocols for vaccinations, provider reminders, and reminders for patients for vaccines that are due (6,24). Provider recommendation remains an important factor associated with receipt of vaccine (18). In addition, ensuring convenient access to vaccination also is important for adults (88,89). The expanded availability of vaccine services in pharmacies and other retail settings provides an opportunity for patients to receive vaccines not stocked by their medical provider and to obtain vaccines outside of typical office hours (88,89).

Challenges posed by increasing access to vaccines for adults among a range of providers include vaccine record keeping and ensuring good communication among providers about a patient’s vaccination history. Both are essential to ensuring patients receive needed vaccines at recommended intervals and do not receive unnecessary vaccinations. State-based immunization information systems (also known as vaccine registries) are available for entry of adult vaccinations in 47 states (http://www.cdc.gov/vaccines/programs/iis/about.html) and can serve as a central point of access for providers to check for vaccinations received by adult patients and to document vaccinations they provide (90). Providers should check with their health department to identify those immunization information systems that have the capacity to enroll adult providers as some systems might be limited in their capacity to substantially expand access to immunization information systems beyond pediatric vaccine providers. Information about and contact information regarding use of IIS is available at http://www.cdc.gov/vaccines/programs/iis/contacts-registry-staff.html.

The use of clinical decision support systems in electronic medical records systems also can facilitate improved vaccination rates. For example, use of prompts in electronic medical records systems for adult vaccines by the Indian Health Service has resulted in substantially higher coverage rates compared to national estimates from the NHIS (6).

On the basis of the importance of the provider recommendation, evidence-based strategies for improving vaccine uptake in adults, the recognition that not all medical providers stock all ACIP-recommended vaccines for adults, the need for improved communication among the different health care providers that adults might have and other factors, the National Vaccine Advisory Committee published updated standards for adult immunization practice in 2014 with the intent of improving adult vaccination coverage of ACIP recommended vaccines. This guidance calls on health care providers, including those who do not stock vaccines, to 1) assess the vaccination status of patients at every clinical encounter; 2) recommend needed vaccines for patients; 3) offer recommended vaccines or, for providers who do not stock a needed vaccine, refer patients to a vaccine provider; and 4) document vaccines administered, including in IIS when available for use among adult patients (25). Resources to assist providers with implementation of the standards for adult immunization practice are available at http://www.cdc.gov/vaccines/hcp/patient-ed/adults/for-practice/standards/index.html. Additional resources are also available through the National Adult and Influenza Summit (NAIIS) (http://www.izsummitpartners.org) website resource library. NAIIS is a national coalition representing more than 130 public and private organizations interested in improving the use of ACIP-recommended vaccines for adults and influenza vaccine for persons of all ages.

Limitations

The findings in this report are subject to at least seven limitations. First, the NHIS sample excludes persons in the military and those residing in institutions, which might result in underestimation or overestimation of vaccination coverage levels. Second, the response rate was 58.9%. Nonresponse bias can result if respondents and nonrespondents differ in their vaccination rates. Third, the determination of vaccination status and identification of high-risk conditions in NHIS were not validated by medical records. Fourth, self-report of vaccination might be subject to recall bias. Young adults particularly might not be able to recall accurately vaccines received as infants or adolescents. However, adult self-reported vaccination status is sensitive for all seven vaccines in this report and specific for all except tetanus vaccination (91). Fifth, demographic and other characteristics (e.g., insurance status, usual source, and frequency of health care) were self-reported and were not validated. Sixth, the Tdap estimate is subject to considerable uncertainty. Respondents who reported a tetanus vaccination but were unable to say whether Td or Tdap was used during 2005–2014 were excluded from estimations of Tdap coverage, creating a potential for bias. Sensitivity calculations were conducted to assess the magnitude of potential bias. Depending on what proportion of excluded respondents actually received Tdap, actual Tdap coverage could fall within the range of 14.5%–46.9% for adults aged 19–64 years and 9.5%–41.6% for adults aged ≥65 years. Comparisons of Tdap coverage across years within subgroups might be affected by bias resulting from excluding persons who did not report the type of tetanus vaccine they received. Finally, the prevalence of selected behavioral characteristics in populations, including the use of preventive health services, vaccine safety concerns, state laws and vaccination intervention programs, cultural, religious, and other factors might affect vaccination coverage. Although NHIS collects information on use of other preventive health services, this information was not included in this analysis. NHIS did not collect information on these other factors.

Conclusion

Vaccination coverage levels among U.S. adults are low. Improvement in adult vaccination is needed to reduce the health consequences of vaccine-preventable diseases among adults. Awareness of the need for vaccines for adults is low among the general population and adult patients rely on provider recommendations for vaccination (6–9,11). Successful vaccination programs combine 1) education of potential vaccine recipients and publicity to promote vaccination; 2) increased access to vaccination services in health care settings; and 3) use of practices that improve vaccination coverage, including reminder-recall systems, efforts to remove administrative and financial barriers to vaccination, use of standing order programs for vaccination, and assessment of practice-level vaccination rates with feedback to staff members (24,25,92). Health care provider recommendations for vaccination are strongly associated with a patient’s receipt of vaccines (10,62–64). Incorporation of routine assessment of adult patient vaccination needs, recommendation, and offer of needed vaccinations for adults into routine clinical care of adults can help improve vaccination rates and narrow widening racial and ethnic disparities in vaccination coverage (24,25). The adult immunization schedule (15), updated annually, provides current recommendations for vaccinating adults and a ready resource for persons who provide health care services for adults in various settings. Assessing associations with vaccination is important for understanding factors that contribute to low coverage rates and to disparities in vaccination, and for implementing strategies to improve vaccination coverage.

Corresponding author: Walter W. Williams, Immunization Services Division, National Center for Immunization and Respiratory Diseases, CDC. Telephone: 404-718-8734; E-mail: www1@cdc.gov.

1Immunization Services Division, National Center for Immunization and Respiratory Diseases, CDC; 2Influenza Division, National Center for Immunization and Respiratory Diseases, CDC; 3Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, CDC; 4Division of Viral Hepatitis, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, CDC; 5Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, CDC; 6Division of Sexually Transmitted Disease Prevention, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, CDC; 7Division of Global Migration and Quarantine, National Center for Emerging and Zoonotic Infectious Diseases, CDC

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* In 2006, a single dose of Tdap was recommended for adults who have or who anticipate having close contact with an infant aged <1 year (e.g., parents, grandparents, child care providers, and health care personnel) to reduce the risk for transmitting pertussis.

Return to your place in the textBOX. Selected high-risk conditions for pneumococcal disease as defined by the Advisory Committee on Immunization Practices

Adults were considered at high risk for pneumococcal disease or its complications if they

  • had ever been told by a doctor or other health professional that they had diabetes, emphysema, chronic obstructive pulmonary disease, coronary heart disease, angina, heart attack, or other heart condition;

  • had a diagnosis of cancer during the previous 12 months (excluding nonmelanoma skin cancer);

  • had ever been told by a doctor or other health professional that they had lymphoma, leukemia, or blood cancer;

  • had been told by a doctor or other health professional that they had chronic bronchitis or weak or failing kidneys during the preceding 12 months;

  • had an asthma episode or attack during the preceding 12 months; or

  • were current smokers.

Source: CDC. Advisory Committee on Immunization Practices recommended immunization schedule for adults aged 19 years and older—United States, 2016. MMWR Morb Mortal Wkly Rep 2016. In press.

Return to your place in the textTABLE 1. Estimated proportion of adults aged ≥19 years who received selected vaccinations, by age group, high-risk status,* and race/ethnicity† — National Health Interview Survey, United States, 2014
Vaccination, age group, high-risk status, and race/ethnicity Sample size % (95% CI) Simple difference from 2013
Influenza vaccination, 2013–14 season§
≥19 yrs
Total 32,296 43.2 (42.1–44.4) 0.5
White 19,836 46.7 (45.3–48.2) 0.2
Black 4,424 36.5 (34.2–39.0) 2.7
Hispanic or Latino 5,341 33.2 (30.8–35.7) 2.4
Asian 1,847 44.6 (40.4–49.0) -3.8
Other 848 38.6 (32.6–45.3) -2.9
19–49 yrs
Total 16,454 31.5 (30.1–32.9) 1.1
White 8,954 32.8 (30.8–34.8) 1.0
Black 2,249 29.8 (26.7–33.0) 3.0
Hispanic or Latino 3,619 27.0 (24.2–30.0) 2.7
Asian 1,145 36.0 (31.6–40.8) -5.6
Other 487 32.4 (24.5–42.0) -1.7
50–64 yrs
Total 8,401 47.7 (45.7–49.7) -0.3
White 5,522 49.8 (47.4–52.3) -0.8
Black 1,304 39.9 (35.5–44.5) 3.0
Hispanic or Latino 1,014 40.7 (36.2–45.6) 1.5
Asian 347 51.6 (42.3–61.6) 0.3
Other 214 43.9 (31.6–58.5) -8.3
≥65 yrs
Total 7,441 71.5 (69.6–73.3) -0.2
White 5,360 73.4 (71.2–75.5) -0.2
Black 871 60.5 (54.3–66.9) 1.3
Hispanic or Latino 708 64.0 (58.2–69.7) -0.3
Asian 355 72.5 (63.2–81.1) -3.1
Other 147 63.6 (50.7–76.4) 1.2
Pneumococcal vaccination, ever**
19–64 yrs, high risk
Total 9,478 20.3 (19.0–21.6) -0.9
White 5,976 21.1 (19.5–22.8) -1.2
Black 1,450 20.2 (17.6–23.2) -1.0
Hispanic or Latino 1,403 16.4 (14.1–18.9) -1.5
Asian 300 14.6 (9.9–20.9) 3.6
Other 349 25.3 (18.5–33.6) 5.5
≥65 yrs
Total 8,281 61.3 (59.9–62.7) 1.6
White 6,054 64.7 (63.1–66.3) 1.1
Black 955 49.8 (45.4–54.1) 1.1
Hispanic or Latino 739 45.2 (40.8–49.7) 6.1
Asian 372 47.7 (41.3–54.2) 2.4
Other 161 69.4 (57.7–79.1) 14.8
Tetanus vaccination (received in past 10 years)††
≥19 yrs
Total 34,347 62.2 (61.4–63.1) 0.3
White 21,443 67.3 (66.3–68.2) 0.8
Black 4,591 50.7 (48.7–52.7) -1.6
Hispanic or Latino 5,601 52.1 (50.5–53.8) -0.2
Asian 1,839 50.5 (47.2–53.7) -1.1
Other 873 71.4 (66.6–75.8) 3.8
19–49 yrs
Total 17,231 62.6 (61.5–63.7) -0.3
White 9,526 69.0 (67.7–70.3) 0
Black 2,319 52.8 (50.1–55.6) -1.3
Hispanic or Latino 3,769 51.9 (49.9–53.9) -0.6
Asian 1,110 51.8 (47.5–56.1) -0.9
Other 507 72.0 (66.0–77.3) 6.0
50–64 yrs
Total 9,024 64.7 (63.1–66.1) 0.7
White 6,012 69.5 (67.7–71.2) 2.1
Black 1,325 49.9 (46.1–53.6) -4.5
Hispanic or Latino 1,104 54.6 (51.3–57.8) -0.4
Asian 373 49.1 (41.8–56.4) -4.3
Other 210 74.9 (66.1–82.1) 5.1
≥65 yrs
Total 8,092 57.7 (56.3–59.2) 1.4
White 5,905 60.6 (58.9–62.3) 1.1
Black 947 43.1 (39.4–47.0) 2.8
Hispanic or Latino 728 49.1 (44.7–53.6) 3.9
Asian 356 46.6 (40.2–53.1) 3.8
Other 156 63.1 (51.9–73.0) -9.3
Tetanus vaccination including pertussis vaccine (received in past 9 yrs)§§
≥19 yrs
Total 22,867 20.1 (19.3–20.8) 2.9¶¶
White 13,743 23.8 (22.8–24.8) 4.1¶¶
Black 3,212 11.6 (10.1–13.3) -1.0
Hispanic or Latino 3,945 12.4 (11.2–13.8) 2.3¶¶
Asian 1,366 15.5 (13.2–18.2) 0.1
Other 601 27.4 (22.2–33.3) 5.0
Living with an infant aged <1 yr 707 32.0 (27.7–36.6) 2.6
Not living with an infant aged <1 yr 22,160 19.6 (18.8–20.4) 2.9¶¶
19–64 yrs
Total 17,503 21.5 (20.6–22.3) 3.1¶¶
White 9,957 26.1 (25.0–27.3) 4.5¶¶
Black 2,542 12.7 (10.9–14.6) -1.0
Hispanic or Latino 3,422 13.0 (11.6–14.6) 2.6¶¶
Asian 1,094 15.6 (13.2–18.3) -0.6
Other 488 28.6 (23.0–35.0) 5.8
Living with an infant aged <1 yr 692 32.5 (28.1–37.1) 2.9
Not living with an infant aged <1 yr 16,811 20.9 (20.1–21.8) 3.1¶¶
≥65 yrs
Total 5,364 14.0 (12.7–15.5) 2.2
White 3,786 15.7 (14.1–17.6) 2.8¶¶
Black 670 5.0 (3.6–7.0) -1.5
Hispanic or Latino 523 6.6 (4.5–9.5) -0.8
Asian 272 15.2 (10.2–22.1) 4.1
Other 113 20.1 (11.6–32.5) 1.8
Living with an infant aged <1 yr 15 —*** — —
Not living with an infant aged <1 yr 5,349 14.0 (12.7–15.5) 2.2
Hepatitis A vaccination (at least 2 doses), ever†††
≥19 yrs
Total 31,392 9.0 (8.5–9.5) -0.1
Traveler§§§ 9,781 16.0 (14.9–17.0) 0.1
Nontraveler¶¶¶ 21,570 5.5 (5.0–6.0)**** -0.2
With chronic liver conditions, overall 422 13.8 (10.0–18.8) 0.5
19–49 yrs
Total 15,069 12.1 (11.3–12.9) -0.2
White 8,292 12.7 (11.7–13.9) 0.2
Black 2,063 11.1 (9.5–13.0) 0.1
Hispanic or Latino 3,323 9.6 (8.1–11.2) -1.1
Asian 957 15.2 (12.4–18.4) -0.9
Other 434 14.7 (10.5–20.2) -0.5
Traveler 5,487 18.8 (17.4–20.4) 0.1
Nontraveler 9,564 8.1 (7.4–8.9)**** -0.5
With chronic liver conditions, overall 100 18.2 (10.3–30.0) 3.7
≥50 yrs
Total 16,323 5.5 (5.1–6.0) 0.2
Traveler 4,294 11.9 (10.8–13.2) 0.2
Nontraveler 12,006 2.9 (2.5–3.4)**** 0.1
With chronic liver conditions, overall 322 12.3 (8.3–17.9) -0.4
Hepatitis B vaccination (at least 3 doses), ever††††
≥19 yrs
Total 32,571 24.5 (23.8–25.3) -0.5
Traveler 10,442 30.5 (29.2–31.8) -2.6¶¶
Nontraveler 22,088 21.4 (20.5–22.3)**** 0.5
With chronic liver conditions, overall 448 29.8 (23.9–36.5) -4.2
19–49 yrs
Total 15,987 32.2 (31.2–33.3) -0.4
White 8,839 36.3 (34.9–37.8) 1.1
Black 2,160 29.9 (27.4–32.5) -0.6
Hispanic or Latino 3,495 20.2 (18.2–22.3) -3.5¶¶
Asian 1,025 35.6 (32.1–39.2) -3.7
Other 468 33.5 (27.9–39.7) -1.3
Traveler 5,963 36.9 (35.2–38.7) -2.8¶¶
Nontraveler 10,007 29.4 (28.1–30.7)**** 1.0
With chronic liver conditions, overall 116 41.6 (30.3–53.8) 2.1
≥50 yrs
Total 16,584 15.7 (14.9–16.4) -0.4
Traveler 4,479 21.2 (19.7–22.7) -2.1
Nontraveler 12,081 13.3 (12.4–14.2)**** 0.2
With chronic liver conditions, overall 332 25.1 (18.9–32.6) -6.2
With diabetes, overall
19–59 yrs 1,367 23.5 (20.7–26.7) -2.8
≥60 yrs 2,097 13.5 (11.4–16.0) -0.3
Herpes zoster (shingles) vaccination, ever§§§§
≥60 yrs
Total 11,263 27.9 (26.6–29.1) 3.6¶¶
White 8,153 32.0 (30.5–33.5) 4.6¶¶
Black 1,352 11.6 (9.6–13.8) 0.9
Hispanic or Latino 1,037 14.6 (12.2–17.5) 5.2¶¶
Asian 492 16.5 (12.9–20.8) -6.1
Other 229 16.2 (9.9–25.3) -8.3
60–64 yrs
Total 2,912 20.4 (18.4–22.5) 2.2
White 2,038 24.3 (21.9–26.9) 3.4
Black 394 8.1 (5.1–12.5) 0.3
Hispanic or Latino 294 11.2 (7.6–16.3) 3.7
Asian 118 — — —
Other 68 — — —
≥65 yrs
Total 8,351 31.1 (29.6–32.6) 4.3¶¶
White 6,115 35.0 (33.3–36.9) 5.1¶¶
Black 958 13.5 (11.0–16.4) 1.3
Hispanic or Latino 743 16.3 (13.2–20.1) 5.9¶¶
Asian 374 20.7 (16.3–26.1) -4.2
Other 161 19.6 (11.2–32.0) -6.3
HPV vaccination among females (at least 1 dose), ever¶¶¶¶
19–21 yrs
Total 613 44.8 (37.3–52.6) 0.2
22–26 yrs
Total 1,427 37.6 (34.2–41.2) 5.3¶¶
19–26 yrs
Total 2,040 40.2 (36.6–44.0) 3.4
White 1,137 46.3 (40.9–51.7) 4.5
Black 279 37.4 (30.6–44.6) 6.8
Hispanic or Latino 408 28.1 (22.6–34.3) -2.3
Asian 137 22.8 (15.4–32.2) 2.9
Other 79 47.3 (31.3–63.9) 4.2
HPV vaccination among males (at least 1 dose), ever¶¶¶¶
19–26 yrs
Total 1,895 8.2 (6.6–10.3) 2.3
19–21 yrs
Total 596 13.3 (9.7–18.0) 5.6¶¶
22–26 yrs
Total 1,299 5.4 (4.0–7.2) 0.4
HPV vaccination among females (at least 1 dose), ever¶¶¶¶ who reported first HPV dose at age 19–26 yrs*****
Total 1,420 11.8 (9.8–14.3) -2.1
White 734 13.9 (10.8–17.7) -2.1
Black 208 14.1 (9.2–21.1) 1.8
Hispanic or Latino 314 7.4 (4.6–11.6) -2.8
Asian 113 — — —
Other 51 — — —
HPV vaccination among males (at least 1 dose), ever¶¶¶¶ who reported first HPV dose at age 19–26 yrs*****
Total 1,781 2.3 (1.5–3.5) 0.6
White 999 2.0 (1.1–3.4) 0.1
Black 215 — — —
Hispanic or Latino 372 — — —
Asian 124 — — —
Other 71 — — —

Abbreviations: CI = confidence interval; HPV = human papillomavirus; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.* Adults were considered at high risk for pneumococcal disease if they had ever been told by a doctor or other health professional that they had diabetes, emphysema, chronic obstructive pulmonary disease, coronary heart disease, angina, heart attack, or other heart condition; had a diagnosis of cancer during the previous 12 months (excluding nonmelanoma skin cancer); had ever been told by a doctor or other health professional that they had lymphoma, leukemia, or blood cancer; had been told by a doctor or other health professional that they had chronic bronchitis or weak or failing kidneys during the preceding 12 months; had an asthma episode or attack during the preceding 12 months; or were current smokers. For hepatitis A and hepatitis B vaccination, data were collected on selected respondent characteristics that increase the risk for infection (travel to countries where hepatitis A infections are endemic and having chronic liver disease; having diabetes, travel to countries where hepatitis B infections are endemic, and having chronic liver disease, respectively).
† Race/ethnicity was categorized as follows: Hispanic, black, white, Asian and “other.” In this report, persons identified as Hispanic might be of any race. Persons identified as black, white, Asian, or other race are non-Hispanic. “Other” includes American Indian/Alaska Native and multiple race. The five racial/ethnic categories are mutually exclusive.
§ Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months and if so, in which month and year. Missing month and year were imputed (3.1%) and interviews conducted during August 2013–June 2014 were used to estimate vaccination coverage during July 2013–May 2014 using Kaplan–Meier survival analysis. Differences were measured as the simple difference between the 2012–13 and 2013–14 influenza seasons.
p<0.05 by T test for comparisons with non-Hispanic white as the reference.
** Respondents were asked if they had ever had a pneumonia shot.
†† Respondents were asked if they had received a tetanus shot in the past 10 years. Vaccinated respondents included adults who received Td during the past 10 years or Tdap during 2005–2014.
§§ Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was given in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Among 36,324 respondents aged ≥19 yrs, those without a yes or “no classification for tetanus vaccination status within the preceding 10 years (n = 1,977 [5.4%]), for tetanus vaccination status during 2005–2014 (n = 1,098 [3.0%]), or those who reported tetanus vaccination during 2005–2014, but were not told vaccine type by the provider (n = 8,612 [23.7%]), did not know vaccine type (Td or Tdap) (n = 1,765 [4.9%]), or refused to answer or for whom data were not obtained (n=5 [0.01%]) were excluded, yielding a sample of 22,867 respondents aged ≥19 years for whom Tdap vaccination status could be assessed. In February 2012, ACIP recommended Tdap vaccination for all adults aged ≥19 years, including adults aged ≥65 years.
¶¶ p<0.05 by T test for comparisons between 2014 and 2013 within each level of each characteristic.
*** Estimate is not reliable due to small sample size (n<30) or relative standard error (standard error/estimates) >0.3.
††† Respondents were asked if they had ever received the hepatitis A vaccine, and if yes, were asked how many doses were received.
§§§Had traveled outside the United States to countries other than countries in Europe, Japan, Australia, New Zealand, or Canada since 1995.
¶¶¶Had not traveled outside the United States to countries other than countries in Europe, Japan, Australia, New Zealand, or Canada since 1995.
**** p<0.05 by T test for comparisons between persons who had traveled outside the United States to countries other than countries in Europe, Japan, Australia, New Zealand, or Canada since 1995 and persons who had not traveled outside the United States to these areas since 1995.
†††† Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, if they had received at least 3 doses or less than 3 doses.
§§§§ Respondents were asked if they had ever received a shingles vaccine.
¶¶¶¶ Respondents were asked if they had ever received the HPV shot or cervical cancer vaccine, and if yes, age at the first dose.
***** The denominator includes persons aged 19–26 years without HPV vaccination prior to age 19 years, and the numerator includes those in the denominator who reported first HPV dose at age 19–26 years.

Return to your place in the textTABLE 2. Estimated proportion of health care personnel* who received selected vaccinations, by race/ethnicity† — National Health Interview Survey, United States, 2014
Vaccination and race/ethnicity Sample size % (95% CI) Simple difference from 2013
Influenza vaccination, 2013–14 season§
≥19 yrs
Total 2,636 65.4 (61.0–69.9) -1.9
White 1,729 67.6 (61.7–73.4) -2.7
Black 406 50.3 (42.9–58.2) -1.8
Hispanic or Latino 288 65.6 (53.3–77.7) 6.1
Asian 157 77.7 (63.9–89.0) -2.6
Other 56 60.3 (37.1–84.1) -0.4
19–49 yrs
Total 1,590 61.7 (55.3–68.1) -1.5
White 947 63.4 (54.6–72.2) 0.3
Black 268 48.0 (38.8–58.1) -7.4
Hispanic or Latino 222 67.3 (50.8–82.9) 12.7
Asian 109 75.3 (62.6–86.4) -8.7
Other 44 61.0 (36.6–85.7) -8.0
50–64 yrs
Total 770 71.1 (65.8–76.3) -2.7
White 556 72.1 (66.0–77.9) -8.9**
Black 117 58.5 (43.6–74.0) 19.5
Hispanic or Latino 53 77.9 (60.0–91.7) 8.1
Asian 37 78.8 (48.4–97.4) 22.3
Other 7 —†† — —
≥65 yrs
Total 276 75.2 (66.6–83.0) -3.2
White 226 79.6 (70.8–87.2) 1.7
Black 21 — — —
Hispanic or Latino 13 — — —
Asian 11 — — —
Other 5 — — —
Tetanus vaccination including pertussis vaccine, past 9 years§§
≥19 yrs
Total 2,062 42.1 (39.1–45.0) 4.7
White 1,353 46.4 (42.7–50.2) 6.5**
Black 315 24.8 (18.8–31.9) -7.4
Hispanic or Latino 218 35.8 (27.8–44.7) 6.3
Asian 120 41.2 (29.9–53.5) 8.5
Other 56 39.5 (24.3–57.1) -7.3
19–64 yrs
Total 1,863 43.0 (40.0–46.1) 5.1
White 1,194 47.9 (44.0–51.8) 7.1**
Black 299 25.0 (18.9–32.3) -8.3
Hispanic or Latino 208 36.4 (28.2–45.4) 7.8
Asian 109 42.0 (30.3–54.7) 8.2
Other 53 39.6 (24.0–57.7) -9.2
≥65 yrs
Total 199 28.7 (21.2–37.6) -2.0
White 159 29.6 (20.9–40.0) -2.8
Black 16 — — —
Hispanic or Latino 10 — — —
Asian 11 — — —
Other 3 — — —
Hepatitis B vaccination (at least 3 doses), ever¶¶
≥19 yrs
Total 2,757 60.7 (58.1–63.2) -1.0
White 1,822 63.0 (59.7–66.3) 0.1
Black 420 51.4 (45.6–57.1) -7.5
Hispanic or Latino 295 51.1 (43.2–59.0) -2.9
Asian 154 68.2 (58.7–76.5) -0.7
Other 66 60.8 (44.7–74.8) 4.8

Abbreviations: CI = confidence interval; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.* Adults were classified as health care personnel if they reported they currently volunteer or work in a hospital, medical clinic, doctor’s office, dentist’s office, nursing home or some other health care facility including part-time and unpaid work in a health care facility as well as professional nursing care provided in the home.
† Race/ethnicity was categorized as follows: Hispanic, black, white, Asian and “other.” In this report, persons identified as Hispanic might be of any race. Persons identified as black, white, Asian, or other race are non-Hispanic. “Other” includes American Indian/Alaska Native and multiple race. The five racial/ethnic categories are mutually exclusive.
§ Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months and if so, in which month and year. Missing month and year were imputed (3.1%), and interviews conducted during August 2013–June 2014 were used to estimate vaccination coverage during July 2013–May 2014 using Kaplan-Meier survival analysis. Differences were measured as the simple difference between the 2012–13 and 2013–14 influenza seasons.
p<0.05 by T test for comparisons with non-Hispanic white as the reference.
** p<0.05 by T test for comparisons between 2014 and 2013 within each level of each characteristic.
†† Estimate is not reliable due to small sample size (n<30) or relative standard error (standard error/estimates) >0.3.
§§ Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was given in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Among 2,933 health care personnel aged ≥19 years, those without a yes or “no classification for tetanus vaccination status within the preceding 10 years (n = 68 [2.3%], for tetanus vaccination status during 2005–2014 (n = 75 [2.6%], or those who reported tetanus vaccination during 2005–2014, but were not told vaccine type by the provider (n = 608 [20.7%] or did not know vaccine type (Td or Tdap) (n = 120 [4.1%] were excluded, yielding a sample of 2,062 respondents aged ≥19 years for whom Tdap vaccination status could be assessed. In February 2012, ACIP recommended Tdap vaccination for all adults aged ≥19 years, including adults aged ≥65 years.
¶¶ Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, if they had received at least 3 doses or less than 3 doses.

Return to your place in the textTABLE 3. Estimated proportion of health care personnel* with direct patient care responsibilities who received selected vaccinations, by race/ethnicity — National Health Interview Survey, United States, 2014
Vaccination, direct patient care responsibilities,† and race/ethnicity§ Sample size % (95% CI) Simple difference from 2013
Influenza vaccination, 2013–14 season
≥19 yrs, with direct patient care responsibilities
Total 1,620 65.1 (58.6–71.6) -2.9
White 1,037 65.6 (56.7–74.3) -6.4
Black 268 52.9 (43.8–62.5) 4.3
Hispanic or Latino 175 74.8 (57.8–89.0) 20.8**
Asian 105 79.8 (62.9–92.5) -6.2
Other 35 60.7 (32.0–89.5) -4.4
≥19 yrs, without direct patient care responsibilities
Total 1,016 66.0 (59.9–72.1) -0.1
White 692 70.7 (63.3–77.8) 3.0
Black 138 43.9 (33.8–55.4)†† -11.9
Hispanic or Latino 113 52.6 (35.8–71.6) -16.9
Asian 52 72.3 (50.6–90.3) 0.1
Other 21 —§§ — —
Tetanus vaccination including pertussis vaccine, past 9 years¶¶
≥19 yrs, with direct patient care responsibilities
Total 1,355 47.5 (43.9–51.2) 5.6
White 880 52.4 (47.9–56.8) 7.6**
Black 220 28.9 (21.8–37.2)†† -7.7
Hispanic or Latino 139 43.5 (33.0–54.7) 8.5
Asian 82 45.1 (30.6–60.5) 10.7
Other 34 46.4 (25.7–68.3) -7.0
≥19 yrs, without direct patient care responsibilities
Total 707 31.6 (26.9–36.8)*** 2.0
White 473 35.5 (29.2–42.4)*** 3.4
Black 95 — — —
Hispanic or Latino 79 22.8 (12.5–38.1)*** 3.5
Asian 38 33.6 (18.2–53.7) 4.3
Other 22 — — —
Hepatitis B vaccination (at least 3 doses), ever†††
≥19 yrs, with direct patient care responsibilities
Total 1,754 67.7 (63.8–71.4) -5.0
White 1,140 70.9 (65.6–75.8) -3.8
Black 287 56.6 (49.6–63.3)†† -11.2**
Hispanic or Latino 178 59.4 (48.1–69.7) -5.6
Asian 107 69.2 (56.8–79.3) -4.1
Other 42 70.2 (52.4–83.5) -7.8
≥19 yrs, without direct patient care responsibilities
Total 1,003 47.6 (43.6–51.7)*** 2.5
White 682 49.1 (43.7–54.4)*** 4.0
Black 133 38.4 (29.4–48.3)*** -7.8
Hispanic or Latino 117 38.7 (29.0–49.4)*** 2.7
Asian 47 66.2 (48.3–80.4) 3.7
Other 24 — — —§§

Abbreviations: CI = confidence interval; HCP = health care personnel; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.* Adults were classified as HCP if they reported that they currently volunteer or work in a hospital, medical clinic, doctor’s office, dentist’s office, nursing home or some other health care facility including part-time and unpaid work in a health care facility as well as professional nursing care provided in the home.
† HCP were classified as having direct patient care responsibilities if they reported providing direct patient care (physical or hands-on contact with patients) as part of their routine work.
§ Race/ethnicity was categorized as follows: Hispanic, black, white, Asian and “other.” In this report, persons identified as Hispanic might be of any race. Persons identified as black, white, Asian, or other race are non-Hispanic. “Other” includes American Indian/Alaska Native and multiple race. The five racial/ethnic categories are mutually exclusive.
Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months and if so, in which month and year. Missing month and year were imputed (3.1%), and interviews conducted during August 2013–June 2014 were used to estimate vaccination coverage during July 2013–May 2014 using Kaplan-Meier survival analysis. Differences were measured as the simple difference between the 2012–13 and 2013–14 influenza seasons.
** p<0.05 by T test for comparisons between 2014 and 2013 within each level of each characteristic.
†† p<0.05 by T test for comparisons with non-Hispanic white as the reference.
§§ Estimate is not reliable due to small sample size (n<30) or relative standard error (standard error/estimates) >0.3.
¶¶ Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was given in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Among 2,933 HCP aged ≥19 years, those without a yes or “no classification for tetanus vaccination status within the preceding 10 years (n = 68 [2.3%], for tetanus vaccination status during 2005–2014 (n = 75 [2.6%], or those who reported tetanus vaccination during 2005–2014, but were not told vaccine type by the provider (n = 608 [20.7%] or did not know vaccine type (Td or Tdap) (n = 120 [4.1%] were excluded, yielding a sample of 2,062 respondents aged ≥19 years for whom Tdap vaccination status could be assessed. In February 2012, ACIP recommended Tdap vaccination for all adults aged ≥19 years, including adults aged ≥65 years.
*** p<0.05 by T test for comparisons between HCP with direct patient care responsibilities and HCP without direct patient care responsibilities.
††† Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, if they had received at least 3 doses or less than 3 doses.

Return to your place in the textFIGURE 1. Estimated proportion of adults aged =19 years who received selected vaccinations, by age group and high risk status — National Health Interview Survey, United States, 2010–2014
The figure shows the estimated percentage of U.S. adults aged ≥19 years who received selected vaccines. Data are from the National Health Interview Survey conducted during 2010–2014. Vaccines include tetanus-toxoid, pneumococcal, influenza, hepatitis A, hepatitis B, herpes zoster, and human papillomavirus vaccine. Vaccination coverage among U.S. adults remains low and shows little change from year to year.
Return to your place in the textFIGURE 2. Estimated proportion of adults aged =19 years who received influenza and pneumococcal vaccination, by age group and high risk status — National Health Interview Survey, United States, 2010–2014

The figure shows the estimated percentage of U.S. adults aged ≥19 years who received influenza and pneumococcal vaccines. Data are from the National Health Interview Survey conducted during 2010–2014.

Return to your place in the textFIGURE 3. Estimated proportion of adults aged =19 years who received tetanus and Tdap vaccination, by age group — National Health Interview Survey, United States, 2010–2014
The figure shows the estimated percentage of U.S. adults aged ≥19 years who received a tetanus toxoid-containing vaccine (either tetanus-diphtheria toxoid [Td] or tetanus, diphtheria, and acellular pertussis vaccine [Tdap]) and the proportion of those who received Tdap vaccine. Data are from the National Health Interview Survey conducted during 2010–2014. Tdap vaccination coverage data among adults aged ≥65 years are available beginning in 2012.
Return to your place in the textTABLE 4. Type of tetanus vaccine received, and proportion that were tetanus, diphtheria, acellular pertussis (Tdap) vaccine, among adults aged ≥19 years, by selected characteristics — National Health Interview Survey, United States, 2014
Characteristic Type of tetanus toxoid-containing vaccine received during 2005–2014 Proportion that was Tdap of the total tetanus toxoid-containing vaccine received during 2005–2014*
No. in sample Received Tdap Received other tetanus vaccine Doctor did not inform patient Could not recall vaccine type
% (95% CI) % (95% CI) % (95% CI) % (95% CI) No. in sample % (95% CI)
Age group (yrs)
≥19
Total 16,823 26.2 (25.2–27.3) 11.2 (10.4–12.0) 51.3 (49.9–52.8) 11.3 (10.3–12.3) 6,437 70.1 (68.2–72.0)
HCP† 1,800 46.6 (43.3–50.0) 11.2 (9.2–13.6) 35.1 (30.7–39.7) 7.1 (5.4–9.3) 1,072 80.6§ (77.2–83.6)
Non-HCP 15,009 23.8 (22.7–24.9) 11.2 (10.4–12.1) 53.3 (51.8–54.7) 11.7 (10.8–12.8) 5,363 68.0 (65.9–70.1)
19–64
Total 13,364 27.4 (26.3–28.6) 11.4 (10.5–12.3) 50.0 (48.5–51.5) 11.2 (10.2–12.3) 5,358 70.7 (68.6–72.7)
HCP 1,614 48.3 (44.7–51.9) 11.3 (9.2–13.7) 33.5 (28.9–38.3) 7.0 (5.2–9.2) 996 81.1§ (77.8–84.1)
Non-HCP 11,738 24.6 (23.4–25.8) 11.4 (10.4–12.4) 52.2 (50.7–53.8) 11.8 (10.8–12.9) 4,360 68.4 (66.0–70.7)
≥65
Total 3,459 20.5 (18.6–22.6) 10.3 (8.9–11.9) 57.7 (55.2–60.2) 11.4 (10.0–13.1) 1,079 66.5 (62.3–70.5)
HCP 186 27.2 (19.8–36.0) 10.6 (6.1–17.7) 53.3 (44.2–62.2) 8.9 (4.1–18.2) 76 71.9 (57.1–83.1)
Non-HCP 3,271 20.2 (18.2–22.3) 10.3 (8.9–11.9) 58.0 (55.5–60.5) 11.5 (10.0–13.2) 1,003 66.2 (61.8–70.3)

Abbreviations: CI = confidence interval; HCP = health care personnel; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.* Calculated by dividing the number of respondents who reported receiving Tdap by the sum of those who reported receiving Tdap and those who reported receiving other tetanus vaccination; respondents who reported that the doctor did not inform them of the vaccine type they received and those who could not recall the vaccine type were excluded.
† Adults were classified as HCP if they reported they currently volunteer or work in a hospital, medical clinic, doctor’s office, dentist’s office, nursing home or some other health care facility including part-time and unpaid work in a health care facility as well as professional nursing care provided in the home.
§ p<0.05 by T test for comparisons between HCP and non-HCP.

Return to your place in the textFIGURE 4. Estimated proportion of adults aged =19 years who received hepatitis A and hepatitis B vaccination, by age group and high risk status — National Health Interview Survey, United States, 2010–2014

The figure shows the estimated percentage of U.S. adults aged ≥19 years who received hepatitis A and hepatitis B vaccines. Data are from the National Health Interview Survey conducted during 2010–2014.

Return to your place in the textFIGURE 5. Estimated proportion of adults aged =19 years who received herpes zoster and HPV vaccination, by age group — National Health Interview Survey, United States, 2010–2014

The figure shows the estimated percentage of U.S. adults aged ≥19 years who received herpes zoster and human papillomavirus vaccines. Data are from the National Health Interview Survey conducted during 2010–2014.

Return to your place in the textTABLE 5. Age at first dose of human papillomavirus vaccination* and difference between age at interview† among adults aged 19–26 years — National Health Interview Survey, 2014, United States
Characteristic Female (N = 811) Male (N = 159)
No. Weighted % No. Weighted %
Age at first dose (yrs)
8–10 21 2.1 18 13.0
8 7 0.8 8 6.4
9 6 0.5 2 0.1
10 8 0.8 8 6.5
11–12 37 7.4 9 3.5
11 5 0.6 2 0.6
12 32 6.8 7 2.9
13–17 443 58.1 45 33.1
13 55 6.4 8 3.2
14 65 7.1 4 1.2
15 86 11.7 7 5.1
16 147 22.6 12 10.0
17 90 10.4 14 13.5
18 119 12.5 42 24.4
19–26 191 19.9 45 25.9
19 49 6.5 9 7.3
20 49 4.3 12 8.4
21 28 2.8 4 2.8
22 18 1.4 8 3.0
23 20 2.3 7 1.9
24 19 1.9 2 0.8
25 6 0.5 2 0.3
26 2 0.2 1 1.5
Difference between age at interview and age at first dose (yrs)
0 14 2.0 10 3.2
1 32 3.7 19 10.8
2 55 5.4 23 21.5
3 72 11.9 13 10.4
4 90 11.2 25 16.2
5 97 11.1 10 6.5
6 111 11.7 13 5.7
7 130 15.5 15 7.8
8 86 14.4 4 1.9
9 52 5.9 3 2.2
10 31 3.8 1 0
11 15 1.2 4 5.2
12 10 0.9 7 2.4
13 8 0.5 7 4.3
14 6 0.6 2 1.0
15 1 0.1 0 0
16 1 0 1 0.6
17 0 0 1 0
18 0 0 1 0.3

Abbreviation: HPV = human papillomavirus.* Respondents were asked, How old were you when you received your first HPV shot?† The simple difference between age reported at time of interview and age the respondent indicated the first dose of the HPV vaccine was received. A difference of zero indicates that a respondent’s reported age at first dose was the same as their age at interview.

Return to your place in the textTABLE 6. Estimated proportion of adults aged =19 years who received selected vaccinations, by age group, high-risk status,* and health insurance status† — National Health Interview Survey, United States, 2014
Vaccination, age group, high-risk status With health insurance Without health insurance
Overall Public Private % (95% CI)
% (95% CI) % (95% CI) % (95% CI)
Influenza vaccination (2013–-14 season)§
=19 yrs 48.0 (46.8–49.2) 54.3 (52.3–56.3)¶,** 45.7 (44.2–47.2) 15.9 (14.2–17.9)
19–49 yrs 35.9 (34.3–37.6) 37.0 (33.2–41.0) 35.7 (33.9–37.6) 14.3 (12.4–16.5)
50–64 yrs 51.3 (49.1–53.5)¶,†† 54.2 (50.3–58.2)¶,†† 50.5 (47.9–53.2)¶,†† 20.4 (16.6–24.8)††
=65 yrs 72.0 (70.1–73.8)¶,†† 70.2 (67.5–72.8)¶,†† 73.7 (71.0–76.4)¶,†† 35.1 (22.3–52.5)††
Pneumococcal vaccination, ever§§
19–64 yrs, high risk 22.5 (21.1–23.9) 29.2 (26.8–31.8)¶,** 19.5 (17.8–21.2) 11.0 (9.3–13.1)
=65 yrs 61.7 (60.2–63.1)¶,†† 58.3 (56.4–60.3)¶,**,†† 64.9 (62.8–66.8)¶,†† 24.3 (14.1–38.7)††
Tetanus vaccination, past 10 years¶¶
=19 yrs 63.9 (63.0–64.7) 58.2 (56.7–59.8)¶,** 65.8 (64.8–66.8) 52.0 (50.0–54.0)
19–49 yrs 65.0 (63.7–66.1) 61.7 (59.0–64.3)¶,** 65.7 (64.4–67.0) 52.5 (50.2–54.8)
50–64 yrs 66.5 (64.9–68.1) 60.7 (57.7–63.7)¶,** 68.0 (66.1–69.8)¶,†† 50.7 (46.8–54.6)
=65 yrs 57.9 (56.5–59.4)¶,†† 53.8 (51.7–55.8)¶,**,†† 61.9 (59.9–63.9)¶,†† 37.1 (24.8–51.4)††
Tetanus vaccination including pertussis vaccine, past 9 years***
=19 yrs 21.5 (20.7–22.3) 17.1 (15.7–18.6)¶,** 23.1 (22.1–24.1) 11.5 (10.0–13.2)
19–64 yrs 23.5 (22.6–24.5) 20.6 (18.5–22.8)¶,** 24.3 (23.2–25.3) 11.5 (10.0–13.2)
=65 yrs 14.1 (12.8–15.5)†† 12.3 (10.5–14.2)**,†† 16.0 (14.0–18.2)†† —††† —
Hepatitis A vaccination (at least 2 doses), ever§§§
=19 yrs, all adults 9.2 (8.7–9.8) 7.6 (6.8–8.5)** 9.8 (9.1–10.4) 7.6 (6.6–8.7)
=19 yrs, traveler¶¶¶ 16.7 (15.6–17.8) 15.7 (13.2–18.6) 16.9 (15.7–18.1) 11.0 (8.5–14.1)
Hepatitis B vaccination (at least 3 doses), ever****
=19 yrs, all adults 25.2 (24.4–26.0) 19.5 (18.2–20.9)** 27.2 (26.3–28.2) 20.2 (18.4–22.1)
19–49 yrs 34.6 (33.4–35.8) 32.5 (29.7–35.4) 35.1 (33.8–36.4) 22.8 (20.7–25.1)
=19 yrs, traveler 31.5 (30.1–32.8) 26.7 (24.0–29.6)** 32.5 (31.0–34.0) 23.2 (20.1–26.6)
=19 yrs, with chronic liver conditions 29.1 (23.0–36.1) 20.6 (14.0–29.1)** 36.4 (27.5–46.5) 37.0 (21.3–56.0)
=19 yrs, with diabetes 18.2 (16.4–20.3) 14.3 (12.2–16.6)** 21.4 (18.6–24.5) 14.1 (9.3–20.8)
19–59 yrs, with diabetes 25.1 (22.0–28.6) 22.0 (17.5–27.3) 26.8 (22.7–31.4) 12.9 (7.8–20.6)
=60 yrs, with diabetes 13.5 (11.3–15.9)†† 10.6 (8.4–13.3)**,†† 16.4 (13.1–20.4)†† — —
Herpes zoster (shingles) vaccination, ever††††
=60 yrs 28.7 (27.4–30.0) 25.6 (23.9–27.4)¶,** 30.9 (29.2–32.6) 5.6 (3.2–9.4)
60–64 yrs 22.0 (19.9–24.2) 15.5 (12.2–19.4)¶,** 23.9 (21.5–26.5) 6.0 (3.4–10.5)
=65 yrs 31.3 (29.8–32.8)†† 27.5 (25.6–29.4)**,†† 34.9 (32.9–37.1)†† — —
Human papillomavirus (HPV) vaccination among females (at least 1 dose), ever§§§§
19–26 yrs 44.5 (40.4–48.7) 39.4 (32.8–46.5) 46.6 (41.4–51.8) 21.3 (16.1–27.6)
HPV vaccination among males (at least 1 dose), ever§§§§
19–26 yrs 9.5 (7.4–12.0) 15.6 (9.5–24.5) 8.0 (6.2–10.4) 4.4 (2.6–7.2)
Human papillomavirus (HPV) vaccination among females (at least 1 dose), ever§§§§ who reported first HPV dose at age 19–26 years¶¶¶¶
19–26 yrs 13.8 (11.3–16.8) 12.1 (8.5–17.0) 14.5 (11.3–18.4) 5.5 (3.2–9.3)
HPV vaccination among males (at least 1 dose), ever†††† who reported first HPV dose at age 19–26 years§§§§
19–26 yrs 2.9 (1.9–4.5) — — 2.7 (1.7–4.3) — —

Abbreviations: CI = confidence interval; HPV = human papillomavirus; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.
* Adults were considered at high risk for pneumococcal disease if they had ever been told by a doctor or other health professional that they had diabetes, emphysema, chronic obstructive pulmonary disease, coronary heart disease, angina, heart attack, or other heart condition; had a diagnosis of cancer during the previous 12 months (excluding nonmelanoma skin cancer); had ever been told by a doctor or other health professional that they had lymphoma, leukemia, or blood cancer; had been told by a doctor or other health professional that they had chronic bronchitis or weak or failing kidneys during the preceding 12 months; had an asthma episode or attack during the preceding 12 months; or were current smokers. For hepatitis A and hepatitis B vaccination, data were collected on selected respondent characteristics that increase the risk for infection (travel to countries where hepatitis A infections are endemic and having chronic liver disease; having diabetes, travel to countries where hepatitis B infections are endemic, and having chronic liver disease, respectively).
† Adults were considered insured if they reported having public health insurance coverage (Medicare, Medicaid, military health care (TRICARE/VA/CHAMP-VA), Indian Health Service, state-sponsored health plan, or other government program insurance) or private health insurance coverage.
§ Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months and if so, in which month and year. Missing month and year were imputed (3.1%), and interviews conducted during August 2013–June 2014 were used to estimate vaccination coverage during July 2013–May 2014 using Kaplan-Meier survival analysis.
p<0.05 by T test for comparisons with without health insurance as the reference group.
** p<0.05 by T test for comparisons between private and public health insurance within each level of each characteristic.
†† p<0.05 by T test comparing persons aged 50–64 years and aged =65 years with persons aged 19–49 years for influenza; persons aged 19–64 years with high-risk conditions with persons aged =65 years for pneumococcal; persons aged 50–64 years and =65 years with persons aged 19–49 years for tetanus; persons aged 19–64 years with persons aged =65 years for Tdap; persons aged 19–59 years with diabetes with persons aged =60 years with diabetes for hepatitis B; and persons aged 60–64 years with persons aged =65 years for shingles.
§§ Respondents were asked if they had ever had a pneumonia shot.
¶¶Respondents were asked if they had received a tetanus shot in the past 10 years. Vaccinated respondents included adults who received Td during the past 10 years or Tdap during 2005–2014.
*** Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was given in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Among 36,324 respondents aged =19 years, those without a yes or “no classification for tetanus vaccination status within the preceding 10 years (n = 1,977 [5.4%]), for tetanus vaccination status during 2005–2014 (n = 1,098 [3.0%]), or those who reported tetanus vaccination during 2005–2014, but were not told vaccine type by the provider (n = 8,612 [23.7%]), did not know vaccine type (Td or Tdap) (n = 1,765 [4.9%]), or refused to answer or for whom data were not obtained (n=5 [0.01%]) were excluded, yielding a sample of 22,867 respondents aged =19 years for whom Tdap vaccination status could be assessed. In February 2012, ACIP recommended Tdap vaccination for all adults aged =19 years, including adults aged =65 years.
††† Estimate is not reliable due to small sample size (n<30) or relative standard error (standard error/estimates) >0.3.
§§§ Respondents were asked if they had ever received the hepatitis A vaccine, and if yes, were asked how many doses were received.
¶¶¶ Had traveled outside the United States to countries other than countries in Europe, Japan, Australia, New Zealand, or Canada since 1995.
**** Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, if they had received at least 3 doses or less than 3 doses.
†††† Respondents were asked if they had ever received a shingles vaccine.
§§§§ Respondents were asked if they had ever received the HPV shot or cervical cancer vaccine, and if yes, age at the first dose.
¶¶¶¶ The denominator includes persons aged 19–26 years without HPV vaccination prior to age 19 years, and the numerator includes those in the denominator who reported first HPV dose at age 19–26 years.

Return to your place in the textTABLE 7. Estimated proportion of adults aged ≥19 years who received selected vaccinations, by age group, high-risk status,* health insurance status, † and having a usual place for health care — National Health Interview Survey, United States, 2014
Vaccination, age group, high-risk status With health insurance Without health insurance
Have a usual place for health care§ Do not have a usual place for health care Have a usual place for health care Do not have a usual place for health care
% (95% CI) % (95% CI) % (95% CI) % (95% CI)
Influenza vaccination (2013–14 season)
≥19 yrs 50.1 (48.9–51.4) 24.2 (20.8–28.2)** 21.7 (19.0–24.7) 9.7 (7.8–12.1)**
19–49 yrs 37.7 (35.9–39.5) 23.9 (20.3–28.0)** 19.7 (16.7–23.2) 9.3 (7.3–11.8)**
50–64 yrs 52.8 (50.8–54.9)†† 24.1 (16.2–35.0)** 26.1 (20.9–32.2) 10.4 (6.0–17.6)**
≥65 yrs 73.1 (71.2–74.9)†† 30.0 (19.6–44.2)** 40.6 (23.2–64.2)†† —§§ —
Pneumococcal vaccination, ever¶¶
19–64 yrs, HR 24.0 (22.5–25.5) 7.9 (5.8–10.6)** 13.9 (11.5–16.7) 7.8 (5.5–10.9)**
≥65 yrs 62.6 (61.2–64.0)†† 24.2 (17.8–32.0)**,†† 34.0 (17.5–55.5)†† — —
Tetanus vaccination, past 10 years***
≥19 yrs 64.7 (63.8–65.6) 54.4 (51.5–57.3)** 54.5 (51.7–57.2) 49.3 (46.2–52.4)**
19–49 yrs 66.1 (64.7–67.4) 57.1 (54.2–60.0)** 54.9 (51.6–58.3) 50.3 (46.7–53.8)
50–64 yrs 67.3 (65.8–68.9) 51.3 (41.8–60.8)** 53.5 (48.5–58.5) 46.1 (39.8–52.6)
≥65 yrs 58.6 (57.1–60.1)†† 30.3 (22.5–39.4)**,†† 48.6 (30.8–66.7) — —
Tetanus vaccination including pertussis vaccine, past 9 years†††
≥19 yrs 22.0 (21.1–22.9) 16.3 (13.9–18.9)** 13.0 (11.0–15.3) 10.0 (7.9–12.5)
19–64 yrs 24.3 (23.3–25.3) 17.2 (14.7–20.1)** 13.0 (11.0–15.3) 10.0 (8.0–12.6)
≥65 yrs 14.4 (13.0–15.9)†† — — — — — —
Hepatitis A vaccination (at least 2 doses), ever§§§
≥19 yrs 9.0 (8.5–9.6) 11.4 (9.6–13.4)** 7.7 (6.3–9.3) 7.5 (5.8–9.6)
≥19 yrs, traveler¶¶¶ 16.3 (15.2–17.5) 20.5 (17.3–24.0)** 8.8 (6.7–11.5) 13.1 (8.9–18.9)
Hepatitis B vaccination (at least 3 doses), ever****
≥19 yrs 25.0 (24.2–25.8) 27.7 (25.0–30.5) 21.2 (18.9–23.8) 19.1 (16.5–22.0)
19–49 yrs 34.8 (33.6–36.1) 32.8 (29.8–35.8) 23.8 (21.1–26.8) 21.9 (18.8–25.3)
≥19 yrs, traveler 31.1 (29.7–32.5) 35.6 (31.8–39.7)** 24.2 (20.2–28.6) 22.2 (17.3–28.1)
≥19 yrs, with chronic liver conditions 29.1 (22.9–36.2) — — — — — —
≥19 yrs, with diabetes 18.4 (16.5–20.4) — — 13.6 (8.3–21.4) —
19–59 yrs, with diabetes 25.5 (22.3–29.0) — — — — — —
≥60 yrs, with diabetes 13.5 (11.3–16.0)†† — — — — — —
Herpes zoster (shingles) vaccination, ever††††
≥60 yrs 29.2 (28.0–30.6) 9.9 (6.2–15.5)** — — — —
HPV vaccination among females (at least 1 dose), ever§§§§
19–26 yrs 45.9 (41.5–50.3) 33.8 (26.7–41.8)** 24.7 (17.3–33.9) 17.4 (11.3–25.8)
HPV vaccination among males (at least 1 dose), ever§§§§
19–26 yrs 10.5 (8.0–13.5) — — — — — —
HPV) vaccination among females (at least 1 dose), ever§§§§ who reported first HPV dose at age 19–26 years¶¶¶¶
19–26 yrs 14.4 (11.6–17.7) 9.7 (5.9–15.5) — — — —
HPV vaccination among males (at least 1 dose), ever§§§§ who reported first HPV dose at age 19–26 years¶¶¶¶
19–26 yrs 3.0 (1.9–4.9) — — 0 ***** — —

Abbreviations: CI = confidence interval; HPV = human papillomavirus; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.* Adults were considered at high risk for pneumococcal disease if they had ever been told by a doctor or other health professional that they had diabetes, emphysema, chronic obstructive pulmonary disease, coronary heart disease, angina, heart attack, or other heart condition; had a diagnosis of cancer during the previous 12 months (excluding nonmelanoma skin cancer); had ever been told by a doctor or other health professional that they had lymphoma, leukemia, or blood cancer; had been told by a doctor or other health professional that they had chronic bronchitis or weak or failing kidneys during the preceding 12 months; had an asthma episode or attack during the preceding 12 months; or were current smokers. For hepatitis A and hepatitis B vaccination, data were collected on selected respondent characteristics that increase the risk for infection (travel to countries where hepatitis A infections are endemic and having chronic liver disease; having diabetes, travel to countries where hepatitis B infections are endemic, and having chronic liver disease, respectively).† Adults were considered insured if they reported having public health insurance coverage (Medicare, Medicaid, military health care (TRICARE/VA/CHAMP-VA), Indian Health Service, state-sponsored health plan, or other government program insurance) or private health insurance coverage.
§ Respondents were asked if there is a place they usually go when sick or need advice on their health. Respondents answering yes are defined as having a usual place for health care.
Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months and if so, in which month and year. Missing month and year were imputed (3.1%), and interviews conducted during August 2013–June 2014 were used to estimate vaccination coverage during July 2013–May 2014 using Kaplan-Meier survival analysis.
** p<0.05 by T test for comparisons with have a usual place for healthcare as the reference group.
†† p<0.05 by T test comparing persons aged 50–64 years and ≥65 years with persons aged 19–49 years for influenza; persons aged 19–64 years with high-risk conditions with persons aged ≥65 years for pneumococcal; persons aged 50–64 years and aged ≥65 years with persons aged 19–49 years for tetanus; persons aged 19–64 years with persons aged ≥65 years for Tdap; and persons aged 19–59 years with diabetes with persons aged ≥60 years with diabetes for hepatitis B.
§§ Estimate is not reliable due to small sample size (n<30) or relative standard error (standard error/estimates) >0.3.
¶¶ Respondents were asked if they had ever had a pneumonia shot.
*** Respondents were asked if they had received a tetanus shot in the past 10 years. Vaccinated respondents included adults who received Td during the past 10 years or Tdap during 2005–2014.
††† Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was given in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Among 36,324 respondents aged ≥19 years, those without a yes or “no classification for tetanus vaccination status within the preceding 10 years (n = 1,977 [5.4%]), for tetanus vaccination status during 2005–2014 (n = 1,098 [3.0%]), or those who reported tetanus vaccination during 2005–2014, but were not told vaccine type by the provider (n = 8,612 [23.7%]), did not know vaccine type (Td or Tdap) (n = 1,765 [4.9%]), or refused to answer or for whom data were not obtained (n=5 [0.01%]) were excluded, yielding a sample of 22,867 respondents aged ≥19 years for whom Tdap vaccination status could be assessed. In February 2012, ACIP recommended Tdap vaccination for all adults aged ≥19 years, including adults aged ≥65 years.
§§§ Respondents were asked if they had ever received the hepatitis A vaccine, and if yes, were asked how many doses were received.
¶¶¶ Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, if they had received at least 3 doses or less than 3 doses.
**** Respondents were asked if they had ever received a shingles vaccine.
†††† Respondents were asked if they had ever received the HPV shot or cervical cancer vaccine, and if yes, age at the first dose.
§§§§ The denominator includes persons aged 19–26 years without HPV vaccination prior to age 19 years, and the numerator includes those in the denominator who reported first HPV dose at age 19–26 years.¶¶¶¶ The confidence interval has not been generated because the estimate is zero.

Return to your place in the textTABLE 8. Estimated proportion of adults aged =19 years who received selected vaccinations, by age group, high-risk status,* health insurance status,† and physician contacts§ — National Health Interview Survey, United States, 2014
Vaccination, age group, high-risk status With health insurance Without health insurance
No. of physician contacts in the past 12 months No. of physician contacts in the past 12 months
None 1–3 4–9 =10 None 1–3 4–9 =10
% (95% CI) % (95% CI) % (95% CI) % (95% CI) % (95% CI) % (95% CI) % (95% CI) % (95% CI)
Influenza vaccination (2013–14 season)
=19 yrs 21.8 (19.3–24.6) 44.9 (43.3–46.6)** 60.1 (57.8–62.5)** 60.6 (57.9–63.2)** 9.0 (7.2–11.2) 19.7 (16.6–23.4)** 28.4 (21.6–36.8)** 27.6 (20.1–37.1)**
19–49 yrs 18.6 (15.9–21.7) 36.1 (33.8–38.5)** 44.5 (40.8–48.4)** 48.6 (43.9–53.5)** 7.9 (6.1–10.3) 19.0 (15.5–23.1)** 26.1 (17.9–37.0)** 25.1 (16.4–37.1)**
50–64 yrs 25.3 (19.7–32.1) 47.9 (45.1–50.7)**,†† 61.4 (57.6–65.2)**,†† 61.7 (57.2–66.3)**,†† 13.5 (8.7–20.6) 22.0 (15.7–30.4) 29.8 (20.6–41.7)** 26.9 (16.0–43.1)
=65 yrs 37.4 (30.4–45.5)†† 68.6 (65.8–71.4)**,†† 78.1 (75.1–81.0)**,†† 76.2 (72.0–80.3)**,†† —§§ — — — — — — —
Pneumococcal vaccination, ever¶¶
19–64 yrs, HR 7.1 (5.4–9.4) 16.6 (15.0–18.4)** 26.3 (23.8–29.0)** 38.6 (34.9–42.4)** 7.8 (5.4–11.1) 11.2 (8.3–14.8) 19.3 (13.4–26.9)** 18.3 (10.7–29.5)**
=65 yrs 32.6 (27.1–38.5)†† 57.2 (54.9–59.5)**,†† 66.4 (64.0–68.7)**,†† 70.7 (67.4–73.8)**,†† — — — — — — — —
Tetanus vaccination, past 10 years***
=19 yrs 51.0 (48.6–53.3) 64.2 (62.9–65.5)** 66.9 (65.4–68.5)** 69.9 (67.9–71.7)** 47.7 (44.8–50.6) 54.2 (50.9–57.5)** 59.1 (52.8–65.0)** 63.9 (55.4–71.7)**
19–49 yrs 52.6 (49.9–55.3) 65.9 (64.3–67.5)** 70.2 (67.4–72.8)** 71.9 (68.5–75.0)** 48.4 (45.1–51.8) 55.9 (51.9–59.8)** 59.6 (51.6–67.1)** 58.1 (48.3–67.4)
50–64 yrs 52.5 (46.8–58.2) 65.2 (63.0–67.3)** 70.2 (67.5–72.7)** 74.6 (71.2–77.7)** 45.7 (39.7–51.7) 50.2 (44.0–56.3) 57.7 (47.5–67.3)** 78.0 (63.5–87.8)**,††
=65 yrs 35.6 (29.6–42.1)†† 57.3 (55.0–59.6)**,†† 59.9 (57.5–62.3)**,†† 62.2 (58.9–65.5)**,†† — — — — — — — —
Tetanus vaccination including pertussis vaccine, past 9 years†††
=19 yrs 12.0 (10.4–13.8) 22.0 (20.8–23.2)** 23.7 (22.0–25.5)** 26.8 (24.6–29.0)** 9.0 (7.3–11.2) 12.4 (10.1–15.3)** 17.4 (12.3–24.1)** 19.8 (12.9–29.1)**
19–64 yrs 12.7 (10.9–14.7) 23.7 (22.4–25.1)** 27.7 (25.6–29.9)** 31.3 (28.6–34.2)** 9.1 (7.3–11.2) 12.6 (10.2–15.5)** 17.3 (12.2–24.0)** 19.0 (12.2–28.3)**
=65 yrs 6.0 (3.7–9.7)†† 13.7 (11.7–16.0)**,†† 15.2 (13.2–17.6)**,†† 16.1 (13.0–19.7)**,†† — — — — — — — —
Hepatitis A vaccination (at least 2 doses), ever§§§
=19 yrs 7.1 (6.1–8.3) 9.4 (8.7–10.1)** 9.1 (8.2–10.1)** 11.1 (9.7–12.7)** 6.1 (4.8–7.6) 8.9 (6.7–11.6) 8.4 (5.7–12.1) 10.5 (6.5–16.6)
=19 yrs, traveler¶¶¶ 12.8 (10.5–15.6) 16.5 (15.0–18.1)** 18.4 (16.2–20.9)** 17.6 (14.7–20.8)** 7.7 (5.4–11.0) 14.4 (9.5–21.3)** 11.6 (6.8–19.0) — —
=19 yrs, with chronic liver conditions — — 13.3 (7.2–23.1) — — 18.0 (11.1–27.9) — — — — — — — —
Hepatitis B vaccination (at least 3 doses), ever****
=19 yrs 20.4 (18.6–22.3) 25.6 (24.5–26.8)** 25.5 (23.9–27.2)** 28.2 (26.1–30.4)** 17.1 (14.8–19.6) 22.6 (19.5–25.9)** 22.2 (17.6–27.6) 30.6 (22.9–39.5)**
19–49 yrs 24.4 (22.2–26.9) 33.9 (32.3–35.5)** 40.5 (37.5–43.6)** 44.0 (40.5–47.6)** 18.9 (16.3–21.9) 26.2 (22.6–30.2)** 27.5 (21.2–35.0)** 30.9 (21.7–42.1)**
=19 yrs, traveler 24.9 (21.8–28.3) 31.9 (29.9–33.9)** 30.9 (28.3–33.6)** 37.1 (33.3–41.1)** 16.3 (12.4–21.1) 28.7 (23.3–34.8)** 26.4 (18.1–36.9) 39.8 (23.8–58.3)**
=19 yrs, with chronic liver conditions — — 30.1 (19.5–43.4) 26.6 (17.8–37.9) 32.9 (22.4–45.4) — — — — — — — —
19–59 yrs, with diabetes — — 22.6 (17.7–28.3) 22.6 (17.7–28.4) 35.3 (28.5–42.8) — — — — — — — —
=60 yrs, with diabetes — — 11.3 (8.3–15.2)†† 16.0 (12.4–20.4)†† 11.2 (8.1–15.4)†† — — — — — — — —
Herpes zoster (shingles) vaccination, ever††††
=60 yrs 10.2 (7.8–13.2) 28.0 (26.0–30.1)** 31.0 (29.0–33.0)** 32.3 (29.3–35.3)** — — — — — — — —
HPV vaccination among females (at least 1 dose), ever§§§§
19–26 yrs 24.9 (18.3–33.0) 41.5 (36.9–46.3)** 57.1 (46.7–66.9)** 48.4 (39.9–56.9)** 20.0 (12.3–30.8) 19.5 (12.6–29.0) — — — —
HPV vaccination among males (at least 1 dose), ever§§§§
19–26 yrs 5.7 (3.6–9.0) 9.1 (6.6–12.4) 19.1 (10.4–32.6)** — — — — — — — — — —
HPV vaccination among females (at least 1 dose), ever§§§§ who reported first HPV dose at age 19–26 years¶¶¶¶
19–26 yrs — — 13.5 (10.4–17.4) 20.3 (13.9–28.6) 12.5 (7.6–19.9) — — — — — — — —
HPV vaccination among males (at least 1 dose), ever§§§§ who reported first HPV dose at age 19–26 years¶¶¶¶
19–26 yrs — — — — — — — — 0 ***** — — — — — —

Abbreviations: CI = confidence interval; HPV = human papillomavirus; HR = high risk; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.
* Adults were considered at high risk for pneumococcal disease if they had ever been told by a doctor or other health professional that they had diabetes, emphysema, chronic obstructive pulmonary disease, coronary heart disease, angina, heart attack, or other heart condition; had a diagnosis of cancer during the previous 12 months (excluding nonmelanoma skin cancer); had ever been told by a doctor or other health professional that they had lymphoma, leukemia, or blood cancer; had been told by a doctor or other health professional that they had chronic bronchitis or weak or failing kidneys during the preceding 12 months; had an asthma episode or attack during the preceding 12 months; or were current smokers. For hepatitis A and hepatitis B vaccination, data were collected on selected respondent characteristics that increase the risk for infection (travel to countries where hepatitis A infections are endemic and having chronic liver disease; having diabetes, travel to countries where hepatitis B infections are endemic, and having chronic liver disease, respectively).
† Adults were considered insured if they reported having public health insurance coverage (Medicare, Medicaid, military health care [TRICARE/VA/CHAMP-VA], Indian Health Service, state-sponsored health plan, or other government program insurance) or private health insurance coverage.
§ Respondents were asked the number of times in the past 12 months that they saw a doctor other health care professional about their own health.
Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months and if so, in which month and year. Missing month and year were imputed (3.1%), and interviews conducted during August 2013–June 2014 were used to estimate vaccination coverage during July 2013–May 2014 using Kaplan-Meier survival analysis.
** p<0.05 by T test for comparisons with no physician contacts in the past 12 months as the reference group.
†† p<0.05 by T test comparing persons aged 50–64 years and aged =65 years with persons aged 19–49 years for influenza; persons aged 19–64 years with high-risk conditions with persons aged =65 years for pneumococcal; persons aged 50–64 years and aged =65 years with persons aged 19–49 years for tetanus; persons aged 19–64 years with persons aged =65 years for Tdap; and persons aged 19–59 years with diabetes with persons aged =60 years with diabetes for hepatitis B.
§§ Estimate is not reliable due to small sample size (n<30) or relative standard error (standard error/estimates) >0.3.
¶¶ Respondents were asked if they had ever had a pneumonia shot.
*** Respondents were asked if they had received a tetanus shot in the past 10 years. Vaccinated respondents included adults who received Td during the past 10 years or Tdap during 2005–2014.
††† Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was given in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Among 36,324 respondents aged =19 years, those without a yes or “no classification for tetanus vaccination status within the preceding 10 years (n = 1,977 [5.4%]), for tetanus vaccination status during 2005–2014 (n = 1,098 [3.0%]), or those who reported tetanus vaccination during 2005–2014, but were not told vaccine type by the provider (n = 8,612 [23.7%]), did not know vaccine type (Td or Tdap) (n = 1,765 [4.9%]), or refused to answer or for whom data were not obtained (n=5 [0.01%]) were excluded, yielding a sample of 22,867 respondents aged =19 years for whom Tdap vaccination status could be assessed. In February 2012, ACIP recommended Tdap vaccination for all adults aged =19 years, including adults aged =65 years.
§§§ Respondents were asked if they had ever received the hepatitis A vaccine, and if yes, were asked how many doses were received.
¶¶¶ Had traveled outside the United States to countries other than countries in Europe, Japan, Australia, New Zealand, or Canada since 1995.
**** Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, if they had received at least 3 doses or less than 3 doses.
†††† Respondents were asked if they had ever received a shingles vaccine.
§§§§ Respondents were asked if they had ever received the HPV shot or cervical cancer vaccine, and if yes, age at the first dose.
¶¶¶¶ The denominator includes persons aged 19–26 years without HPV vaccination prior to age 19 years, and the numerator includes those in the denominator who reported first HPV dose at age 19–26 years.
***** The confidence interval has not been generated because the estimate is zero.

Return to your place in the textTABLE 9. Adjusted vaccination coverage among adults aged =19 years, by age group, high-risk status,* and health insurance status†— National Health Interview Survey, United States, 2014
Vaccination, age group, high-risk status With health insurance Without health insurance Adjusted prevalence ratio (95% CI) Adjusted prevalence difference**
Adjusted§ vaccination coverage (95% CI) Adjusted vaccination coverage (95% CI)
Influenza vaccination (2013–14 season)††
=19 yrs 43.1 (42.2–44.1) 29.9 (27.6–32.2) 0.7 (0.6–0.7)§§ 13.3
Pneumococcal vaccination, ever¶¶              
19–64 yrs, HR 20.8 (19.4–22.2) 17.7 (15.0–20.8) 0.9 (0.7–1.0)§§ 3.1
=65 yrs 61.6 (60.2–63.1) 55.1 (36.1–72.7) 0.9 (0.6–1.3) 6.6
Tetanus vaccination, past 10 years***
=19 yrs 62.8 (61.9–63.8) 61.8 (59.7–63.9) 1.0 (0.9–1.0) 1.0
Tetanus vaccination including pertussis vaccine, past 9 years†††
=19 yrs 20.8 (20.0–21.7) 18.4 (16.0–21.0) 0.9 (0.8–1.0) 2.5
Hepatitis A vaccination (at least 2 doses), ever§§§
=19 yrs 9.3 (8.8–9.8) 8.4 (7.2–9.9) 0.9 (0.8–1.1) 0.8
=19 yrs, traveler¶¶¶ 16.6 (15.5–17.7) 13.4 (10.1–17.5) 0.8 (0.6–1.1) 3.2
Hepatitis B vaccination (at least 3 doses), ever****
=19 yrs 25.2 (24.5–26.0) 22.4 (20.4–24.4) 0.9 (0.8–1.0)§§ 2.9
19–49 yrs 33.0 (31.9–34.1) 29.8 (27.2–32.6) 0.9 (0.8–1.0)§§ 3.2
=19 yrs, with diabetes 17.9 (16.0–20.0) 15.2 (9.8–22.9) 0.9 (0.6–1.3) 2.7
Herpes zoster (shingles) vaccination, ever††††
=60 yrs 28.1 (26.8–29.4) 17.7 (10.8–27.5) 0.6 (0.4–1.0)§§ 10.4
HPV vaccination among females (at least 1 dose), ever§§§§
19–26 yrs 41.7 (38.0–45.5) 29.3 (22.1–37.7) 0.7 (0.5–0.9)§§ 12.4
HPV vaccination among males (at least 1 dose), ever§§§§
19–26 yrs —¶¶¶¶ — — — — — —
HPV vaccination among females (at least 1 dose), ever§§§§who reported first HPV dose at age 19–26 years*****
19–26 yrs 12.5 (10.2–15.3) 7.7 (4.6–12.8) 0.6 (0.4–1.1)§§ 4.8
HPV vaccination among males (at least 1 dose), ever§§§§who reported first HPV dose at age 19–26 years*****
19–26 yrs — — — — — — —

Abbreviations: CI = confidence interval; HPV = human papillomavirus; HR = high risk; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.
* Adults were considered at high risk for pneumococcal disease if they had ever been told by a doctor or other health professional that they had diabetes, emphysema, chronic obstructive pulmonary disease, coronary heart disease, angina, heart attack, or other heart condition; had a diagnosis of cancer during the previous 12 months (excluding nonmelanoma skin cancer); had ever been told by a doctor or other health professional that they had lymphoma, leukemia, or blood cancer; had been told by a doctor or other health professional that they had chronic bronchitis or weak or failing kidneys during the preceding 12 months; had an asthma episode or attack during the preceding 12 months; or were current smokers. For hepatitis A and hepatitis B vaccination, data were collected on selected respondent characteristics that increase the risk for infection (travel to countries where hepatitis A infections are endemic and having chronic liver disease; having diabetes, travel to countries where hepatitis B infections are endemic, and having chronic liver disease, respectively).
† Adults were considered insured if they reported having public health insurance coverage (Medicare, Medicaid, military health care [TRICARE/VA/CHAMP-VA], Indian Health Service, state-sponsored health plan, or other government program insurance) or private health insurance coverage.
§ Adjusted coverage estimates are based on predicted marginals from a multivariable logistic regression model. Estimates were adjusted for age, gender, race/ethnicity, marital status, education, employment status, poverty level, number of physician contacts in the past year, usual source of care, self-reported health status, nativity, and region of U.S. residence.
With health insurance is the reference group. The adjusted prevalence ratio is calculated by dividing adjusted vaccination coverage among those without health insurance by adjusted coverage among those with health insurance.
** Adjusted coverage among those with health insurance minus adjusted coverage among those without health insurance.
†† Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months. Influenza vaccination estimates are based on interviews conducted during August 2013–June 2014 and vaccination received during the past 12 months.
§§ p<0.05 by T test comparing adjusted coverage among those with health insurance to adjusted coverage among those without health insurance.
¶¶ Respondents were asked if they had ever had a pneumonia shot.
*** Respondents were asked if they had received a tetanus shot in the past 10 years. Vaccinated respondents included adults who received Td during the past 10 years or Tdap during 2005–2014.
††† Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was given in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Among 36,324 respondents aged =19 years, those without a yes or “no classification for tetanus vaccination status within the preceding 10 years (n = 1,977 [5.4%]), for tetanus vaccination status during 2005–2014 (n = 1,098 [3.0%]), or those who reported tetanus vaccination during 2005–2014, but were not told vaccine type by the provider (n = 8,612 [23.7%]), did not know vaccine type (Td or Tdap) (n = 1,765 [4.9%]), or refused to answer or for whom data were not obtained (n=5 [0.01%]) were excluded, yielding a sample of 22,867 respondents aged =19 years for whom Tdap vaccination status could be assessed. In February 2012, ACIP recommended Tdap vaccination for all adults aged =19 years, including adults aged =65 years.
§§§ Respondents were asked if they had ever received the hepatitis A vaccine, and if yes, were asked how many doses were received.
¶¶¶ Had traveled outside the United States to countries other than countries in Europe, Japan, Australia, New Zealand, or Canada since 1995.
**** Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, if they had received at least 3 doses or less than 3 doses.
†††† Respondents were asked if they had ever received a shingles vaccine.
§§§§ Respondents were asked if they had ever received the HPV shot or cervical cancer vaccine, and if yes, age at the first dose.
¶¶¶¶Sample size too small to run adjusted models.
***** The denominator includes persons aged 19–26 years without HPV vaccination prior to age 19 years, and the numerator includes those in the denominator who reported first HPV dose at age 19–26 years.

Return to your place in the textTABLE 10. Estimated proportion of adults aged ≥19 years who received selected vaccinations, by age group, high-risk status,* nativity, number of years living in the United States, and citizenship — National Health Interview Survey, United States, 2014
Vaccination, age group, high-risk status U.S.-born Foreign-born Foreign-born
Living in U.S. <10 yrs Living in U.S. ≥10 yrs U.S. citizen Non-U.S. citizen
% (95% CI) % (95% CI) % (95% CI) % (95% CI) % (95% CI) % (95% CI)
Influenza vaccination (2013–14 season)†
≥19 yrs 44.4 (43.1–45.6) 38.2 (35.9–40.6)§ 32.1 (26.9–38.0) 39.8 (37.4–42.3) 44.7 (41.9–47.5) 30.9 (27.8–34.3)**
19–49 yrs 31.7 (30.2–33.3) 30.4 (27.5–33.6) 31.3 (25.7–37.7) 30.3 (27.1–33.8) 33.8 (29.7–38.2) 28.1 (24.6–31.9)**
50–64 yrs 48.6 (46.5–50.7)†† 43.0 (38.6–47.7)§,†† 36.0 (20.0–59.0) 43.3 (38.8–48.1)†† 46.4 (40.9–52.2)†† 36.0 (29.0–44.0)**
≥65 yrs 72.7 (70.6–74.7)†† 63.8 (59.0–68.6)§,†† 38.9 (23.9–58.9) 66.7 (61.9–71.6)¶†† 67.5 (61.9–73.1)†† 51.3 (41.3–62.2)**,††
Pneumococcal vaccination, ever§§
19–64 yrs, HR 21.1 (19.7–22.5) 14.9 (12.7–17.5)§ 13.6 (8.2–21.8) 15.1 (12.7–17.8) 17.6 (14.1–21.7) 12.2 (9.1–16.0)**
≥65 yrs 64.7 (63.3–66.2)†† 40.8 (37.4–44.3)§,†† 31.8 (19.7–47.0)†† 41.8 (38.3–45.5)†† 42.2 (38.4–46.1)†† 35.2 (27.6–43.6)††
Tetanus vaccination, past 10 years¶¶
≥19 yrs 65.3 (64.4–66.2) 48.8 (47.1–50.4)§ 47.3 (43.7–50.9) 49.3 (47.4–51.2) 50.9 (48.7–53.2) 46.5 (44.1–48.9)**
19–49 yrs 66.3 (65.1–67.5) 48.7 (46.6–50.9)§ 47.3 (43.5–51.2) 49.5 (46.9–52.1) 52.3 (48.7–56.0) 46.4 (43.5–49.2)**
50–64 yrs 67.2 (65.6–68.8) 51.5 (48.3–54.6)§ 49.5 (37.7–61.4) 51.7 (48.3–55.1) 54.0 (49.8–58.2) 46.8 (41.3–52.3)**
≥65 yrs 59.9 (58.3–61.4)†† 44.5 (40.7–48.3)§ 42.0 (26.8–58.9) 45.0 (41.2–49.0) 43.8 (39.6–48.1)†† 47.8 (39.6–56.1)
Tetanus vaccination including pertussis vaccine, past 9 years***
≥19 yrs 22.4 (21.6–23.3) 10.7 (9.5–12.0)§ 11.2 (8.9–14.0) 10.6 (9.2–12.1) 12.1 (10.3–14.0) 9.2 (7.8–10.8)**
19–64 yrs 24.2 (23.2–25.2) 11.2 (9.8–12.7)§ 11.3 (9.0–14.2) 11.1 (9.5–12.9) 13.2 (11.2–15.6) 9.3 (7.9–11.1)**
≥65 yrs 15.2 (13.7–16.8)†† 7.8 (5.7–10.7)§,†† —††† — 7.8 (5.6–10.8)†† 8.1 (5.7–11.5)†† — —
Hepatitis A vaccination (at least 2 doses), ever§§§
≥19 yrs 9.1 (8.6–9.6) 8.3 (7.4–9.4) 11.7 (9.5–14.3) 7.5 (6.5–8.7) 8.7 (7.4–10.2) 8.0 (6.7–9.4)
≥19 yrs, traveler¶¶¶ 17.9 (16.7–19.2) 11.2 (9.7–12.9)§ 13.5 (10.7–17.0) 10.7 (9.1–12.5) 11.8 (9.9–14.1) 10.5 (8.5–12.9)
Hepatitis B vaccination (at least 3 doses), ever****
≥19 yrs 25.6 (24.8–26.4) 19.7 (18.4–21.2)§ 24.8 (21.8–28.0) 18.7 (17.2–20.2) 21.6 (19.7–23.7) 17.7 (16.0–19.6)**
19–49 yrs 34.6 (33.4–35.8) 23.3 (21.5–25.2)§ 25.3 (22.1–28.7) 22.7 (20.7–24.8) 28.7 (25.9–31.6) 19.6 (17.6–21.7)**
≥19 yrs, with diabetes 18.5 (16.5–20.8) 14.9 (11.6–18.9) 39.1 (19.8–62.4) 13.5 (10.3–17.4) 16.2 (12.2–21.2) 12.8 (7.8–20.4)
19–59 yrs, with diabetes 26.5 (23.1–30.2) 11.6 (7.5–17.6)§ — — 12.5 (8.0–18.8) 14.5 (8.5–23.7) — —
≥60 yrs, with diabetes 12.7 (10.4–15.4)†† 18.0 (12.8–24.6) — — 14.4 (9.8–20.8) 17.3 (11.6–25.1) — —
Herpes zoster (shingles) vaccination, ever††††
≥60 yrs 30.0 (28.6–31.4) 15.2 (13.1–17.6)§ — — 15.5 (13.3–18.0) 17.1 (14.5–19.9) 8.5 (5.5–13.0)**
HPV vaccination among females (at least 1 dose), ever§§§§
19–26 yrs 43.2 (39.0–47.4) 18.6 (13.9–24.4)§ 15.7 (9.4–25.0) 21.8 (14.7–31.2) 25.2 (16.1–37.3) 15.2 (9.6–23.3)
HPV vaccination among males (at least 1 dose), ever§§§§
19–26 yrs 8.5 (6.7–10.8) 6.8 (3.8–11.8) — — — — — — — —
HPV vaccination among females (at least 1 dose), ever§§§§ who reported first HPV dose at age 19–26 years¶¶¶¶
19–26 yrs 13.0 (10.6–15.9) 5.2 (3.0–9.0)§ — — — — — — — —
HPV vaccination among males (at least 1 dose), ever§§§§ who reported first HPV dose at age 19–26 years¶¶¶¶
19–26 yrs 2.4 (1.5–3.7) — — — — — — — — — —

Abbreviations: CI = confidence interval; HPV = human papillomavirus; HR = high risk; Td = tetanus-diphtheria toxoid; Tdap = tetanus, diphtheria, and acellular pertussis vaccine.* Adults were considered at high risk for pneumococcal disease if they had ever been told by a doctor or other health professional that they had diabetes, emphysema, chronic obstructive pulmonary disease, coronary heart disease, angina, heart attack, or other heart condition; had a diagnosis of cancer during the previous 12 months (excluding nonmelanoma skin cancer); had ever been told by a doctor or other health professional that they had lymphoma, leukemia, or blood cancer; had been told by a doctor or other health professional that they had chronic bronchitis or weak or failing kidneys during the preceding 12 months; had an asthma episode or attack during the preceding 12 months; or were current smokers. For hepatitis A and hepatitis B vaccination, data were collected on selected respondent characteristics that increase the risk for infection (travel to countries where hepatitis A infections are endemic and having chronic liver disease; having diabetes, travel to countries where hepatitis B infections are endemic, and having chronic liver disease, respectively).
† Respondents were asked if they had received an influenza shot or nasal spray in the past 12 months and if so, in which month and year. Missing month and year were imputed (3.1%), and interviews from August 2013–June 2014 were used to estimate vaccination coverage during July 2013–May 2014 using Kaplan-Meier survival analysis.
§ p<0.05 by T test for comparisons between U.S. born and foreign born.
p<0.05 by T test for comparisons between those living in the U.S. <10 years and those living in the United States ≥10 years.
** p<0.05 by T test comparing U.S. citizens and non-U.S. citizens.
†† p<0.05 by T test comparing persons aged 50–64 years and aged ≥65 years with persons 19–49 years for influenza; persons aged 19–64 years with high–risk conditions with persons aged ≥65 years for pneumococcal; persons aged 50–64 years and aged ≥65 years with persons aged 19–49 years for tetanus; persons aged 19–64 years with persons aged ≥65 years for Tdap; and persons aged 19–59 years with diabetes with persons aged ≥60 years with diabetes for hepatitis B.
§§ Respondents were asked if they had ever had a pneumonia shot.
¶¶ Respondents were asked if they had received a tetanus shot in the past 10 years. Vaccinated respondents included adults who received Td during the past 10 years or Tdap during 2005–2014.
*** Respondents who had received a tetanus shot in the past 10 years were asked if their most recent shot was given in 2005 or later. Respondents who had received a tetanus shot since 2005 were asked if they were told that their most recent tetanus shot included the pertussis or whooping cough vaccine. Among 36,324 respondents aged ≥19 years, those without a yes or “no classification for tetanus vaccination status within the preceding 10 years (n = 1,977 [5.4%]), for tetanus vaccination status during 2005–2014 (n = 1,098 [3.0%]), or those who reported tetanus vaccination during 2005–2014, but were not told vaccine type by the provider (n = 8,612 [23.7%]), did not know vaccine type (Td or Tdap) (n = 1,765 [4.9%]), or refused to answer or for whom data were not obtained (n=5 [0.01%]) were excluded, yielding a sample of 22,867 respondents aged ≥19 years for whom Tdap vaccination status could be assessed. In February 2012, ACIP recommended Tdap vaccination for all adults aged ≥19 years, including adults aged ≥65 years.
††† Estimate is not reliable due to small sample size (n<30) or relative standard error (standard error/estimates)>0.3.
§§§ Respondents were asked if they had ever received the hepatitis A vaccine, and if yes, were asked how many doses were received.
¶¶¶ Had traveled outside the United States to countries other than countries in Europe, Japan, Australia, New Zealand, or Canada since 1995.
**** Respondents were asked if they had ever received the hepatitis B vaccine, and if yes, if they had received at least 3 doses or less than 3 doses.
†††† Respondents were asked if they had ever received a shingles vaccine.
§§§§ Respondents were asked if they had ever received the HPV shot or cervical cancer vaccine, and if yes, age at the first dose.
¶¶¶¶ The denominator includes persons aged 19–26 years without HPV vaccination prior to age 19 years, and the numerator includes those in the denominator who reported first HPV dose at age 19–26 years.

Suggested citation for this article: Williams WW, Lu P, O’Halloran A, et al. Surveillance of Vaccination Coverage Among Adult Populations — United States, 2014. MMWR Surveill Summ 2016;65(No. SS-1)(No. SS-1):1–36. DOI: http://dx.doi.org/10.15585/mmwr.ss6501a1.

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