Published influenza vaccination coverage in health care workers (HCW) are calculated using two sources: self-report and vaccination records. The objective of this study was to determine whether self-report is a good proxy for recorded vaccination in HCW, as the degree of the relationship is not known, and whether vaccine behaviour influences self-reporting.
A cross-sectional study was conducted using a self-administered survey during September 2010. Considering the vaccination record as the gold standard of vaccination, the properties of self-report as a proxy of the record (sensitivity, specificity, positive predictive value, negative predictive value) were calculated. Concordance between the vaccination campaigns studied (2007–2010) was made using the Kappa index, and discordance was analyzed using McNemar’s test.
248 HCW responded. The 95% confidence intervals of coverage according to the vaccination record and to self-report overlapped, except for 2007, and the Kappa index showed a substantial concordance, except for 2007. McNemar’s test suggested that differences between discordant cases were not due to chance and it was found that the proportion of unvaccinated discordant cases was higher than that of vaccinated discordant cases.
In our study population, self-reported influenza vaccination coverage in HCW in the previous two years is a good proxy of the vaccination record. However, vaccination behaviour influences the self-report and explains a trend to overestimate coverage in self-reporting compared to the vaccination record. The sources of coverage should be taken into account whenever comparisons are made.
Citation: Llupià A, García-Basteiro AL, Mena G, Ríos J, Puig J, et al. (2012) Vaccination Behaviour Influences Self-Report of Influenza Vaccination Status: A Cross-Sectional Study among Health Care Workers. PLoS ONE 7(7): e39496. doi:10.1371/journal.pone.0039496
Editor: Joan A. Caylà, Public Health Agency of Barcelona, Spain
Received: February 17, 2012; Accepted: May 22, 2012; Published: July 11, 2012
Copyright: © 2012 Llupià et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was funded by the Solvay-Abbott Influenza Research Grant 2010. J Puig is funded by MTM2009-06973.The investigators were contracted by their institutions.The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: JMB has received fees for lectures, advice and participation in working groups funded by the pharmaceutical industry. He has participated as principal investigator in clinical trials of vaccines (influenza vaccines, and others) promoted by GlaxoSmithKline and Sanofi Pasteur MSD. All other authors declare they have no competing interests. This does not alter the authors’ adherence to all the PLoS ONE policies on sharing data and materials.
Influenza vaccination in health care workers (HCW) is recommended to protect patients and workers alike. Measurement of the coverage achieved allows estimates of the protection obtained in all HCW, monitoring of trends between seasons and measurement of the impact of the intervention. Russell et al  stress the importance of using the same target population for spatiotemporal comparisons between coverage. When making comparisons, reported coverage numerators are acquired from two sources: a) self-reported surveys of HCW – and, b) vaccination records –.
The relationship between these two forms of calculating coverage has been studied in at-risk populations in whom self-reported coverage seems a good proxy of coverage according to the vaccination record . However, it is not known whether the same relationship exists in HCW. There are several arguments for considering self-reporting a good proxy for registered vaccination status, for example that HCW have no major reasons to confuse or forget vaccinations. HCW are otherwise healthy people and therefore undergo few diagnostic or therapeutic procedures which they are easily able to recall. However, self-report might not be a good proxy because influenza vaccination is recommended by most institutions in the world – and widely extended to health centres, therefore HCW might tend to declare they had been vaccinated. In addition, annual vaccination might induce errors if HCW do not get the vaccine every season.
Assessing the degree of association between self-report and vaccination records in HCW could help to improve the reporting of coverage and provide criteria to compare different centers and time periods. The main objective of this study was to determine whether self-report was a good proxy for recorded vaccination in HCW. To our knowledge, is the first time that this question is considered amongst HCW. Secondary objectives were to determine whether there was any recall bias according to HCW vaccination behavior, whether the time between vaccination and the report had an influence and which factors were related to concordance/discordance between the self-report and the vaccination record.
During the study enrollment period, 480 on-duty HCW were randomly selected (Figure 1). Of the 300 HCW located, 13 declined to participate (participation rate amongst located HCW: 95.7%). Finally, 248 HCW met the study inclusion criteria. The characteristics of the study sample are shown in Table 1. The sample population was mostly female (68.5%) and with a permanent contract (82.7%). Refusal to participate was similar in all professional categories.
Figure 1. Flow chart for randomized HCW, participants, and subjects included in the study.doi:10.1371/journal.pone.0039496.g001
Table 1. Characteristics of health care workers included in the study.doi:10.1371/journal.pone.0039496.t001
Self-reported Coverage as a Proxy for Coverage According to the Vaccination Record and Analysis of Discordance
Table 2 shows that, except for the 2007 season, self-reported coverage had a good concordance (95% confidence intervals (95%CI) and Kappa index) with coverage according to the Occupational Health (OH) vaccination record. In 2008, 2009 seasonal influenza (2009s) and A(H1N1)pdm09 influenza (2009A), self-reported coverage was a good proxy for coverage according to the OH vaccination record, although there was a trend to overestimate the coverage obtained through the OH vaccination record.
Table 2. Validity of self-reported influenza vaccination in HCW compared to occupational health medical records (2007–2009).doi:10.1371/journal.pone.0039496.t002
Analysis of the characteristics of self-reporting for the four campaigns (table 2) shows that, considering the OH vaccination record as the gold standard, negative predictive values (NPV) were higher than positive predictive values (PPV). McNemar’s test showed that differences between discordant pairs did not appear to be due to chance. The direction of this difference between discordant pairs is shown in table 2, which calculates the proportion of discordant subjects for each vaccination status divided by the total number of discordant subjects. Except for the 2008 season, more discordant subjects reported being vaccinated when they were not than subjects who reported not being vaccinated when they were. In addition, the proportion of unvaccinated subjects who reported they were vaccinated was greater than the proportion of vaccinated subjects who reported they were not vaccinated. The 137 discordant subjects from all four campaigns studied were analyzed using the generalized estimating equations (GEE) model. No profile of vaccinated discordant subjects compared with unvaccinated discordant subjects was established according to sex, professional category, age, seniority in years and type of contract. Neither were differences found between unvaccinated discordant or concordant subjects and their self-report according to the same demographic variables.
The present study shows that self-reported influenza vaccination coverage in HCW is a good proxy for recorded vaccination coverage in the two previous years. The concordance, evaluated using the Kappa index and the CI of the coverage, supports this assertion. Self-reported coverage was consistently higher than coverage obtained through OH records in this study.
The finding that the proportion of unvaccinated discordant subjects was greater than the proportion of vaccinated discordant subjects may explain the tendency of self-reporting to overestimate coverage. Comparing these two groups in the different campaigns studied, in 2007, when the results show that self-reported vaccination was not a good proxy, the differences were even greater. This might suggest that either people remember better what they do than what they do not do or that, in case of doubt, people tend to be eager-to-please and thus state they are vaccinated. However, the underlying reason explaining these results needs to be further explored. With respect to the 2008 season, several factors may have influenced the fact that the coverage was not overestimated and that there was no disparity between discordant subjects. In 2008, a new model of vaccination campaign was introduced in our hospital , which may have better internalized by HCW, although there is not sufficient information to state that this occurred. In 2009, there were again a greater proportion of unvaccinated discordant subjects than vaccinated discordant subjects.
With respect to discordance in the self-report, taking the results of the 2009A campaign as an example, 20% of participants who self-reported being vaccinated were not, while 1.4% who had been vaccinated self-reported they had not. If it is assumed that the lack of memory is the same in vaccinated and unvaccinated subjects, the difference between these two percentages could be ascribed to being eager-to-please subjects who think they should have been vaccinated or that it is better to state they have been vaccinated because they recognize that vaccination is recommended by the hospital and the health authorities. Better characterization of these subjects could provide clues to approach groups who could potentially be convinced to be vaccinated, but the small sample of discordant subjects did not allow any pattern to be established. In the case of the 2009A campaign, contrary to what was expected given the low coverage achieved , no rejection effect was observed after A(H1N1)pdm09 influenza vaccination, when we expected to see vaccinated subjects who reported being unvaccinated. We also observed the eager-to-please effect, suggesting that HCW took no pride in not being vaccinated.
Comparison with other Studies and Implications
The literature review found eight studies comparing self-report with vaccination record , –. These studies were conducted in high-risk patients in whom influenza vaccination was indicated and their results (Table 3) are aligned with the findings of this study which: self-reported coverage is a good proxy but tends to overestimate the coverage calculated from the vaccination record. McNemar’s test was calculated for all these studies and showed that discordance did not appear to be due to chance and that, of the total number of discordant subjects, the proportion of unvaccinated discordant subjects was greater than that of vaccinated discordant subjects. In addition, NPV were higher than PPV. Two studies ,  retrospectively studied two vaccination seasons and found that self-report was a good proxy during these two seasons. High-risk patients exhibited the same behavior as our HCW, suggesting the presence of a social norm. In-depth studies of the qualitative aspects of the reasons leading HCW to be eager-to-please in order to define patterns would be of interest.
Table 3. Data of published studies comparing self-reported influenza vaccination in high-risk population.doi:10.1371/journal.pone.0039496.t003
Strengths and Limitations
One strength of this study is that the sample kept the proportions of professional category and vaccination coverage of the overall population in order to avoid participation bias due to unvaccinated subjects , . The sample characteristics were consistent with those of the whole population of hospital workers (Table 1). In addition, the coverage of the sample calculated using the OH vaccination record matched the coverage of the total number of HCW recorded in the hospital, indicating that the sample was representative and consistent, given that the CI overlapped and collected the time trend well. Other strengths were that four vaccination campaigns were analyzed together and that the number of subjects who declined to participate was very low.
Studies ,  have assessed the validity of vaccination records, which are also to some degree a proxy for real vaccination. It is difficult to confirm that a HCW is not vaccinated. However, we believe that our records are reliable. Most HCW can be presumed to be healthy and have few reasons for being vaccinated outside the workplace. In our hospital, the mobile unit covers all wards and is in contact with the majority of workers and also records the very-few HCW who report being vaccinated outside the hospital. A further limitation is that the Human Resources Department (HR) does not have a completely up-to-date record of the shift and location of each HCW, which would explain the number of workers not located or not known by their fellow-workers.
In our study population, self-reported influenza vaccination coverage in HCW is a good proxy for recorded vaccination coverage in the two previous years. In the different campaigns studied in the present paper and in the previous studies, the results show that, of the total number of discordant subjects, the proportion of unvaccinated discordant subjects was greater than that of vaccinated ones, suggesting that vaccination behavior influences the self-report. This explains the tendency to overestimate coverage using self-report compared with vaccination records. The sources of vaccination coverage should be taken into account when comparisons are made.
Study Design and Population
A cross-sectional study was conducted in HCW of the Hospital Clínic of Barcelona (HCB), a 700-bed public teaching hospital, during a two-week period in mid-September 2010, as part of the PIVAC (Professionals and Influenza VACcination) project. In the framework of the PIVAC project, a survey was conducted before and after an influenza vaccination promotion campaign. This survey addressed various aspects related to influenza vaccination in HCW such as the determinants of influenza vaccination, motivations, risk perception of influenza for themselves, patients and relatives, the impact and acceptation of different strategies and the validity of self-declaration. A total of 480 HCW were sequentially sought during the recruitment period following a randomly sorted list of the HCW of the hospital. We aimed to recruit 420 HCW out of a population of 5258, stratified by professional category (5 groups) and vaccination behaviour in the previous season. Recruitment tables were updated daily by the four interviewers.
Data Sources, Participants and Variables
We used three data sources: 1- PIVAC self-administered survey, 2- Vaccination history from OH medical records 3- HR datalist.
1- The items of the PIVAC survey used asked whether HCW had received influenza vaccination in the four previous campaigns (2007, 2008, 2009s and 2009A). 2- The OH medical record includes the act of vaccination and its date for each season. HCW in active work at the HCB in each season not registered in the OH vaccination record were considered as unvaccinated. Active HCW were considered as those working in the HCB for more than three, two and one years in the seasons 2007, 2008 and 2009, respectively. For each season, HCW surveyed who were not actively working in the HCB during this period were excluded.3- Demographic variables (sex, date of birth, years of work at HCB, contract type and professional category) were obtained from the HR datalist. The variable concordance was created by cross-matching the self-report with the OH vaccination record, with four categories: concordant vaccinated, concordant unvaccinated, discordant vaccinated and discordant unvaccinated.
Before 2008, influenza vaccination campaigns included educational-advertising material based on posters placed in strategic sites and institutional support at the onset by means of an e-mail to all HCW. HCW accessed free-of-charge voluntary influenza vaccination either by attending the Occupational Health Clinic, open from 8 a.m. to 17 p.m., five days a week, or by on-site contact with a mobile unit team staffed by one nurse per shift, including week-ends, who covered the whole hospital without previous forewarning of the route. Starting in 2008, a new model of campaign was implemented using incentives like prizes and the use of new technologies such as weekly emails and a hospital intranet website to post photos of vaccinated HCW .
The self-report was cross-matched with the OH vaccination records of the seasons included and with the demographic variables obtained. A descriptive analysis was made of the study population. For qualitative variables, the absolute frequency and percentage were determined. For quantitative variables, the central trend, position and dispersion were estimated by mean and standard deviation (SD). Taking the vaccination record as the gold standard for vaccination act, the basic properties of the self-report as a proxy of the vaccination record (sensitivity, specificity, positive predictive value, and negative predictive value) were calculated and their 95% Confidence Intervals (95%CI) was estimated. Concordance according to the vaccination campaign was analyzed using the Kappa index and their 95% CI  and discordance was analyzed using the McNemar test. The profile of discordant subjects was analyzed by means of a generalized estimating equations methodology using an unstructured matrix to account for within-subject variability. All analyses used a bilateral type I error of 5%. The analysis was performed using the SPSS v.15 and R v.2.12 statistical packages.
All study materials stated that the study was approved by the HCB Clinical Research Ethics Committee and that participation was voluntary. All personal data of HCW were dissociated and treated as confidential at all times.
We thank all Hospital Clínic of Barcelona workers who participated in this study. We thank the interviewers (Xavier L. Llauradó, Consol Llupià, Maya Ninova and Elisa Salas) and the project support staff (María Isabel Gómez) for their professionalism.
Conceived and designed the experiments: AL JP. Performed the experiments: AL AT GM JMB. Analyzed the data: AL AGB JR GM JP. Wrote the paper: AL.
- 1. Russell ML, Henderson EA (2003) The measurement of influenza vaccine coverage among health care workers. Am J Infect Control 31: 457–461.
- 2. Bryant KA, Stover B, Cain L, Levine GL, Siegel J, et al. (2004) Improving influenza immunization rates among healthcare workers caring for high-risk pediatric patients. Infect Contr Hosp Epidemiol 912–917.
- 3. Blank PR, Schwenkglenks M, Szucs TD (2009) Disparities in influenza vaccination coverage rates by target group in five European countries: trends over seven consecutive seasons. Infection 37: 390–400.
- 4. Walker FJ, Singleton JA, Pengjun LU, Wooten KG, Strikas RA (2006) Influenza vaccination of healthcare workers in the United States, 1989–2002. Infect Contr Hosp Epidemiol 27: 257–265.
- 5. de JuanesJR, García de Codes A, Arrazola MP, Jaen F, Sanz MI, et al. (2007) Influenza vaccination coverage among hospital personnel over three consecutive vaccination campaigns (2001–2002 to 2003–2004). Vaccine 25: 201–204.
- 6. Babcock HM, Gemeinhart N, Jones M, Dunagan WC, Woeltje KF (2010) Mandatory influenza vaccination of health care workers: translating policy to practice. Clin Infect Dis 50: 459.
- 7. Sartor C, Tissot-Dupont H, Zandotti C, Martin F, Roques P, et al. (2004) Use of a mobile cart influenza program for vaccination of hospital employees. Infect Contr Hosp Epidemiol 25: 918–922.
- 8. Bertin M, Scarpelli M, Proctor AW, Sharp J, Robitson, et al (2007) Novel use of the intranet to document health care personnel participation in a mandatory influenza vaccination reporting program. Am J Infect Control 35: 33–37.
- 9. Skull SA, Andrews RM, Byrnes GB, Kelly HA, Nolan TM, et al. (2007) Validity of self-reported influenza and pneumococcal vaccination status among a cohort of hospitalized elderly inpatients. Vaccine 25: 4775–4783.
- 10. Fiore A, Uyeki T, Broder K, Finelli L, Euler G, et al. (2010) Prevention and control of influenza with vaccines: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2010. MMWR. Recommendations and reports: Morbidity and mortality weekly report. Recommendations and reports/Centers for Disease Control, 59, 1.
- 11. National Health and Medical Research Council (Australia) (1997) The Australian immunisation handbook. National Health and Medical Research Council. 396 p.
- 12. Salisbury D, Ramsay M, Noakes K (2006) Immunisation against infectious disease. Department of Health. The Stationery Office/Tso. 518 p.
- 13. Llupià A, García-Basteiro AL, Olivé V, Costas L, Ríos J, et al. (2010) New interventions to increase influenza vaccination rates in health care workers. Am J Infect Control 38: 476–481.
- 14. Vírseda S, Restrepo MA, Arranz E, Magán-Tapia P, Fernández-Ruiz M, et al. (2010) Seasonal and Pandemic A (H1N1) 2009 influenza vaccination coverage and attitudes among health-care workers in a Spanish University Hospital. Vaccine 28: 4751–4757.
- 15. Hutchison BG (1989) Measurement of influenza vaccination status of the elderly by mailed questionnaire: response rate, validity and cost. Can J Public Health 80: 271–275.
- 16. Nichol KL, Korn JE, Baum P (1991) Estimation of outpatient risk characteristics and influenza vaccination status: validation of a self-administered questionnaire. Am J Prev Med7: 199–203.
- 17. Mac Donald R, Baken L, Nelson A, Nichol KL (1999) Validation of self-report of influenza and pneumococcal vaccination status in elderly outpatients. Am J Prev Med 16: 173–77.
- 18. Zimmerman RK, Raymund M, Janosky JE, Nowalk MP, Fine MJ (2003) Sensitivity and specificity of patient self-report of influenza and pneumococcal polysaccharide vaccinations among elderly outpatients in diverse patient care strata. Vaccine 21: 1486–1491.
- 19. Andrews RM (2005) Assessment of vaccine coverage following the introduction of a publicly funded pneumococcal vaccine program for the elderly in Victoria, Australia. Vaccine 23: 2756–2761.
- 20. Mangtani P, Shah A, Roberts JA (2007) Validation of influenza and pneumococcal vaccine status in adults based on self-report. Epidemiol Infect 135: 139–143.
- 21. Irving SA, Donahue JG, Shay DK, Ellis-Coyle TL, Belongia EA (2009) Evaluation of self-reported and registry-based influenza vaccination status in a Wisconsin cohort. Vaccine 27: 6546–6549.
- 22. Sy LS, Liu ILA, Solano Z, Cheetham TC, Lugg MM, et al. (2010) Accuracy of influenza vaccination status in a computer-based immunization tracking system of a managed care organization. Vaccine 28: 5254–5259.
- 23. Greene SK, Shi P, Dutta-Linn MM, Shoup JA, Hinrichsen VL, et al. (2009) Accuracy of data on influenza vaccination status at four Vaccine Safety Datalink sites. Am J Prev Med 37: 552–555.
- 24. Landis JR, Koch GG (1977) The measurement of observer agreement for categorical data. Biometrics 33: 159–174.