The effect of giving influenza vaccination to general practitioners: a controlled trial [NCT00221676]
- Michiels Barbara1Email author,
- Philips Hilde†1,
- Coenen Samuel†1, 2,
- Yane Fernande†3,
- Steinhauser Toon†1,
- Stuyck Sofie†1,
- Denekens Joke†1 and
- Van Royen Paul†1
© Barbara et al; licensee BioMed Central Ltd. 2006
Received: 01 February 2006
Accepted: 10 July 2006
Published: 10 July 2006
No efficacy studies of influenza vaccination given to GPs have yet been published. Therefore, our purpose was to assess the effect of an inactivated influenza vaccine given to GPs on the rate of clinical respiratory tract infections (RTIs) and proven influenza cases (influenza positive nose and throat swabs and a 4-fold titre rise), while adjusting for important covariates.
In a controlled trial during two consecutive winter periods (2002–2003 and 2003–2004) we compared (77 and 100) vaccinated with (45 and 40) unvaccinated GPs working in Flanders, Belgium. Influenza antibodies were measured immediately prior to and 3–5 weeks after vaccination, as well as after the influenza epidemic. During the influenza epidemic, GPs had to record their contact with influenza cases and their own RTI symptoms every day. If they became ill, the GPs had to take nose and throat swabs during the first 4 days. We performed a multivariate regression analysis for covariates using Generalized Estimating Equations.
One half of the GPs (vaccinated or not) developed an RTI during the 2 influenza epidemics. During the two influenza periods, 8.6% of the vaccinated and 14.7% of the unvaccinated GPs had positive swabs for influenza (RR: 0.59; 95%CI: 0.28 – 1.24). Multivariate analysis revealed that influenza vaccination prevented RTIs and swab-positive influenza only among young GPs (ORadj: 0.35; 95%CI: 0.13 – 0.96 and 0.1; 0.01 – 0.75 respectively for 30-year-old GPs). Independent of vaccination, a low basic antibody titre against influenza (ORadj 0.57; 95%CI: 0.37 – 0.89) and the presence of influenza cases in the family (ORadj 9.24; 95%CI: 2.91 – 29) were highly predictive of an episode of swab-positive influenza.
Influenza vaccination was shown to protect against proven influenza among young GPs. GPs, vaccinated or not, who are very vulnerable to influenza are those who have a low basic immunity against influenza and, in particular, those who have family members who develop influenza.
There are two important issues when considering influenza vaccination of general practitioners (GPs) as advocated by many guidelines. [1, 2] Firstly, an influenza vaccine must give personal protection to the GP. To a certain extent, this issue has been addressed by efficacy studies among healthy adults.  Secondly, vaccination might be useful for preventing transmission of influenza between GPs and their patients. For example, in long-term care hospitals, influenza vaccination of healthcare workers reduced mortality among the elderly. [4, 5]However, owing to the low basic immunity against influenza among healthy adults and healthcare workers working in long-term care facilities, the results of these studies are not fully applicable to general practice.
Since GPs have frequent close contact with many influenza cases, they build up a high basic immunity and probably only suffer from minor symptoms. [6, 7]Whether the vaccine adds substantial benefit to this naturally acquired immunity is unknown. Inactivated vaccines are not very useful in preventing cross-infection and the shedding of viruses from the nose and throat; [8, 9]they are only known to diminish the severity of the influenza symptoms and to prevent complications, especially when compared to intra-nasally administered influenza vaccines (inactivated whole virus, with adjuvants, or live cold-adapted) that elicit a better local immune response (mucosal IgA) in the nose, throat and airways. Unfortunately, these new vaccines are not yet commercially available in Europe.
Until now, no efficacy studies of influenza vaccination among GPs have been published. Therefore, our purpose was to assess the effect of an inactivated influenza vaccine given to GPs on clinical respiratory tract infections (RTIs) and, more particularly, against influenza cases with influenza-positive nose and throat swabs (diagnosed by reverse transcriptase polymerase chain reaction RT-PCR), in addition to serologically-defined influenza cases. We also adjusted for relevant covariates.
1. Design of the study
A controlled trial during two consecutive winter periods (2002–2003 and 2003–2004) was performed, comparing vaccinated and unvaccinated GPs working in Flanders recruited on a voluntary basis in July and August 2002 and 2003. First-year participants were asked to re-enter the study during the second winter period. Subjects were enrolled after giving their written informed consent. The study was approved by the Medical Ethics Committee of the University Clinic of Antwerp. Participating GPs had to fill in a questionnaire relating to their general characteristics and previous influenza vaccinations. Owing to ethical considerations, the GPs were free to choose whether or not to receive an influenza vaccination during the study period. Those who wanted to be vaccinated were instructed to have the 0.5-ml vaccine administered into the deltoid muscle, at the end of October of each study year. GlaxoSmithKline n.v. provided Alfarix®, a commercially available non-adjuvant trivalent inactivated split-influenza vaccine, to each participating GP personally for this study. In 2002 – 2003 and 2003 – 2004 the vaccine contained the same strains: 15 μg hemagglutinin from A/New Caledonia/20/99 (H1N1), A/Moscow/10/99 (= A/Panama/2007/99) (H3N2) and B/Hong Kong/330/2001.
2. Blood collection and serology
Blood specimens for the antibody studies were taken immediately prior to and 3–5 weeks after vaccination. Unvaccinated GPs only gave 1 blood specimen in November before the influenza epidemic, assuming this would give the same antibody titres as blood samples taken one month earlier (= pre-epidemic).
Three weeks after the influenza epidemic, both groups gave another blood specimen (= post-epidemic). The blood samples were collected by local medical laboratories for serum extraction and preservation (-20°C). After the last blood sample was taken, the serum tubes were transported to Viroclinics in Rotterdam.
Viroclinics did a hemagglutination-inhibition (HAI) test using standard methods to measure the influenza antibody titre against the circulating influenza strains. In 2002–2003, antibody titres were determined against A/H1N1 (IVR-116), A/H3N2 (ResVir-17) and B/Shangdong/7/'97. In 2003–2004, only one strain was circulating and therefore only the titre against A/H3N2 (Fujian-like) was measured. Each test was performed twice and the average titre was taken as the outcome. Laboratory personnel were blinded to the identity and study group of the serum samples. We considered a 4-fold or greater titre rise detected in the paired samples collected at any time between pre- and post-epidemic periods as indicative of an immune reaction following an influenza virus infection.
3. Daily diary recording
For 60 consecutive days (weekends and holidays included), the GPs were asked to complete diaries.
The GPs were asked to record the number of contacts with patients in general and with those diagnosed as influenza cases (patients, family and other contacts) in particular. The GPsalso had to report the number of influenza patients whomthey hadseenfor another reason within a week prior to having diagnosedthe patients with influenza. An influenza case was defined as any person for whom the GP established a clinical diagnosis of influenza on the basis of the following symptoms and signs: sudden onset, high fever (above 38°C), cough and myalgia.
GPs suffering from the slightest symptom of an RTI had to mention this in their diaries and record their oral body temperature, and also to record the severity of their own signs and symptoms. Furthermore, affected GPs had to indicate their diagnosis, their medication, and any sick leave taken.
After the recording periods ended, the diaries were sent by post (2002–2003) or collected personally (2003–2004).
4. Influenza virus detection
GPs were asked to brush their nose with two cotton swabs and their throat with 1 cotton swab from the first to the fourth day during each RTI that they developed during the recording period. The swabs were immersed in a transport medium (Earle's minimal essential medium (EMEM) with addition of antibiotics and antimycotic products) and were stored by the local medical laboratory where the samples were collected by a courier of the Scientific Institute of Public Health (IPH). After the influenza epidemic, the transport media were analysed with a nested RT-PCR test first to distinguish between A and B strains, and then to subtype the A strains as H3 or H1. Uncertain results were retested. Laboratory personnel were blinded to the identity and study group of the swabs.
A preliminary sample size estimation was performed using Epi-info. If we assumed a clinically significant vaccine efficacy of 70% in preventing influenza and an incidence of serologically-defined influenza in the unvaccinated group of 23%, or an incidence as defined by virus detection (RT-PCR) of 8.5% (result of a pilot study), then we needed 124 and 368 vaccinated GPs and 62 and 184 unvaccinated GPs respectively (a 2:1 ratio) for a power of 80% and a two-sided significance level of 0.05.
Differences in proportions were assessed by Pearson χ2 tests and odds ratios (95%CI); continuous variables were analysed by Student's t-tests after converting serum titres to the natural logarithm using SPSS version 12.0.
We performed a multivariate regression analysis for relevant covariates using Generalized Estimating Equations (GEE) (GENMOD in SAS statistics version 8.02) following the Hierarchical Backward Elimination Approach of Kleinbaum to determine which factors other than vaccination influence the three dichotomous outcomes defined as RTIs in general, RTIs with influenza-positive nose and throat swabs, and RTIs with influenza-positive nose and throat swabs and/or a 4-fold titre rise. Confounding variables of interest included: study year; age in years; basic immunity (lnT1); mean number of patient contacts/day; mean number of influenza patients/day; family members with influenza; colleagues with influenza; having young children (<7 years); and working in a Child and Family preventive medicine facility (Table 3). In addition, significant interaction terms between vaccination and these confounding variables were introduced in the model.
1. General characteristics
In 2003, we had to consider 47 (46 vaccinated) second serum samples to be missing because these were taken during the influenza epidemic that started as early as November 22, 2003. Thirteen sick GPs in 2002 and 11 sick GPs in 2003 did not take nose and throat swabs as requested.
General characteristics of participating GPs: figures are numbers (percentage) unless stated otherwise.
Mean (SE) of age
Influenza vaccine 1 and 2 years before
3/43 (7.0) ‡
3/38 (7.9) ‡
Influenza vaccine 1 year before
3/44 (6.8) ‡
3/39 (7.7) ‡
Influenza vaccine 1, 2, and 3 years before
3/38 (7.9) ‡
Influenza vaccine 2 years before
8/43 (18.6) ‡
3/38 (7.9) ‡
Influenza vaccine 3 years before
6/42 (14.3) ‡
4/38 (10.5) ‡
Influenza disease 1 year before
Working in Child and Family preventive medicine facility
Having young children < 7 years of age
Seroprotection at baseline1 against A:/H3N2
15/36 (41.7) †
GMT12 A:/H3N2 (SE)
77.26 (1.19) †
22.34 (1.23) ‡
Information from the diaries
GPs with family members with influenza
GPs with colleagues with influenza
Mean (SE) number of patient contacts/day
17.9 (1.3) †
16.6 (1.2) †
Mean (SE) number of patients with influenza/day
2. Efficacy and effectiveness of influenza vaccination
Efficacy and effectiveness of influenza vaccination according to different outcomes: crude results
Number of GPs with a respiratory tract infection
0.66 – 1.32
0.72 – 1.54
0.76 – 1.27
Number of GPs with a respiratory tract infection and positive nose and throat swabs
0.13 – 4.94
0.23 – 1.13
0.28 – 1.24
Number of GPs with a respiratory tract infection and a 4-fold hemagglutination-inhibition antibody titre rise
0.05 – 1.45
0.10 – 1.13
0.10 – 0.75
Number of GPs with a respiratory tract infection and positive swab or 4-fold hemagglutination-inhibition antibody titre rise
0.13 – 1.55
0.24 – 1.19
0.22 – 0.88
Effect of influenza vaccination on respiratory tract infections (RTIs) in general, with influenza positive swabs and/or 4-fold titre rise: multivariate regression analysis for correlated data (GEE)
RTI in general (n = 202)
RTI with positive swabs for influenza (n = 202)
RTI with pos swabs and/or 4-fold titre rise for influenza (n = 150)
Vaccine†2 when GP is 30 years old
Vaccine† when GP is 50 years old
Basic immunity (natural logarithm of titre1)‡4
Mean number of patient contacts/day‡5
Mean number of contacts with influenza patients/day‡6
Family members with influenza†
Colleagues with influenza†
Having young children < 7 years of age†
Working in Child and family preventive medicine facility†
† dichotomous yes(1), no(0)
2 Crude OR vaccine =
3 OR for difference of 20 years
4 OR for a difference of 1 in natural logarithm of titre1
5 OR for a difference of 20 patients
6 OR for a difference of 2 influenza patients
The mean of the highest body temperature of every RTI episode was 37.4°C in the influenza infections (positive swabs); this was statistically significantly higher than during the other RTIs (p = 0.005). In general, the influenza infections lasted 2 days longer (p = 0.03). Of the GPs with positive swabs, 20% took sick leave, compared to 12% of GPs suffering from other RTIs (p = 0.3).
3. Multivariate analysis
Multivariate analysis revealed that influenza vaccination prevented both respiratory tract infections in general and proven influenza during an influenza epidemic, especially among young general practitioners. Independently of vaccination, a low basic antibody titre against influenza and the presence of influenza cases in the family were highly predictive of an episode of influenza with positive swabs and/or a 4-fold titre rise.
During the recording periods in both years, half the GPs had some form of RTI. That 50% of GPs were affected by RTIs seems rather high, but could be explained by the fact that even mild symptoms were recorded and reflects the occurrence of mild infections through which natural immunity is constantly updated. The general RTI definition used in this study was too imprecise to allow a significant vaccination effect to be shown.
Our study was slightly underpowered for demonstrating statistically significant efficacy of an influenza vaccination in preventing RTIs with RT-PCR-positive nose and throat swabs. There was a large difference in efficacy between the two years: 22% in 2002 and 49% in 2003. Furthermore, in the unvaccinated group, the incidence of positive influenza cases rose from 5% in 2002 to 23% in 2003. During the first study period (2002), there was a high basic immunity against influenza A as the cumulative result of the previous 2 years in which the circulating influenza virus A strains did not change much. According to the IPH, the peak incidence of influenza-like illnesses in the community was 5% in week 9 in the first study year and 10% in week 50 of the following influenza season (2003–2004) (Figure 1). During 2003/2004, a slightly different influenza A virus was circulating. Although this new A/Fujian-like A/H3N2 virus was different from the A strains contained in the vaccine, the vaccine elicited a good immune response. [15, 16]An epidemiological study performed among GPs during the Asian influenza epidemic of 1957 concluded that, in many parts of Britain, doctors were exposed to a risk of influenza at least double that of the general population in their practices. 
The RT-PCR test is more sensitive than a virus culture, [4, 18]since it also detects dead virus particles and is not quantitative. Therefore, no conclusions can be drawn about the degree of infectivity of the GPs with positive nose and throat swabs. No significant difference was seen between the GPs with infectious influenza and the other GPs with RTIs with respect to comparing the number of patients diagnosed with influenza and seen by the GP 1 week before for another reason, and 14 days before and after the GP became ill.
This study confirmed the efficacy of influenza vaccination on serologically-defined influenza; the efficacy of influenza vaccination was 72% for the 2 years combined, which is comparable with an efficacy of 88% (95%CI: 47–97%) in preventing a 4-fold titre rise against A/H3N2 reported by Wilde et al. Since no studies of the efficacy of influenza vaccination among GPs have previously been published, we can only compare our results with trials performed among other healthcare professionals working in hospitals. A Cochrane review dealing with vaccines given to prevent influenza in healthy adults included the results of trials involving healthcare workers. None of these studies demonstrated significant efficacy of influenza vaccination on influenza cases (clinically defined and sometimes serologically confirmed), and none of the studies presented results that evaluated the ability of vaccination to interrupt the spread of the disease (see [additional file 1]: existing literature concerning our study results.)
Multivariate analysis revealed that the effect of influenza vaccine decreased with age. Young GPs have a higher incidence of influenza, and they have families with young children. Although these findings need to be confirmed by larger studies, they suggest that young GPs should be the first to be vaccinated against influenza. Medical students and postgraduate trainees would also benefit from being among the first to be vaccinated.
However, the question arises as to whether influenza vaccination can be stopped at a certain age. It is likely that GPs who have been working for more than 20 years in full-time practice and who have enough yearly contact with influenza patients do not need to be vaccinated. Healthcare workers with fewer patient contacts need influenza vaccination throughout their entire career. These considerations are only applicable in the inter-pandemic period. When a new virus emerges, such as an adapted avian influenza virus, and then when an appropriate vaccine is available, all healthcare workers, without exception, would be a priority group for vaccination.
The level of anti-hemagglutinin antibody titres before vaccination is another independent protective variable that has been known for quite some time. It was relatively high in our GP population and reflects the cumulative effect of previous vaccinations and natural infections. In our study, age was not related to the antibody titre levels before the influenza epidemic. In addition to serological immunity, other immune factors, such as cellular and local mucosal immunity, which were not measured in this study, may play an important role. 
Another underestimated factor is the infectiousness of family members with influenza. Independently of age or vaccination status, sick family members, especially children, were found to be very contagious. This result is not new, [24, 25]but the consequences have been minimized. Among GPs during the 1957 Asian influenza epidemic, it was noted that 9 of 19 GPs with a typical influenza attack had a family member who had influenza. The authors concluded that GPs were liable to be infected with influenza at home, even after avoiding infection for several weeks during repeated daily contact with patients who have influenza. Neuraminidase-inhibitors could be taken preventively by healthcare workers who have a family member who most probably has influenza during an influenza epidemic. Treating GPs only when they already have influenza is not useful, as the signs and symptoms will most likely be mild and non-specific, making the diagnosis of influenza difficult. However, the use of neuraminidase-inhibitors has already resulted in resistant virus strains; thus, prevention using a better-designed vaccine is preferable.
Further research is needed, focusing particularly on assessing the efficacy of new vaccines for use among healthcare workers in preveningt influenza virus growth in the nose and throat.
Some limitations of this study need to be considered. It was underpowered for detecting a significant effect of influenza vaccination on influenza cases with positive nose and throat swabs; to detect an efficacy of 70% with a measured incidence of proven influenza of 14.7% in the unvaccinated group, at least 208 vaccinated and 104 unvaccinated GPs would have been needed. However, it remains to be determined whether the efficacy in healthcare workers need not be higher to prevent possible infectious cases of influenza and protect against transmission to patients. If we assume an efficacy of 90% as clinically relevant, we only needed 108 vaccinated and 54 unvaccinated GPs to participate in our study.
Unfortunately, the influenza epidemic started very early in the second study year (November 22, 2003). Therefore, 47 serum samples taken after vaccination (T2) during this epidemic were classified as missing. Titres measured in these samples were significantly higher than those taken before November 22, 2003. There were no differences between the GPs with missing serum samples and those used in the analysis, except that fewer GPs with missing serology had allergies; however, since allergy was not related to the incidence of RTIs or influenza, this did not affect the results. The only problem that remains is an underestimation of influenza cases that were defined as a 4-fold titre rise after the epidemic. However, this definition of an influenza case remains questionable, especially in a study group with high antibody titres before the influenza epidemic. Since the unvaccinated group started with a lower antibody titre, a greater number of 4-fold titre rise cases could be expected in this group. Other authors [7, 19, 28, 29]have already mentioned this disproportion and have noted that it is of no clinical importance.
In this article we did not focus on the immunogenetic properties of the vaccine, because knowing the efficacy of the vaccine on clinical outcomes after an epidemic challenge is far more appropriate for policy development. Although the GPs in our study were not chosen at random, we believe the results are representative. In fact, the average age of the participants did not differ from national averages. In 2003, slightly more women than average participated in our study, but this was taken into account in the multivariate analysis.
It is possible that a selection bias was introduced by having the GPs themselves choose whether to be vaccinated. Indeed, the most important difference between vaccinated and unvaccinated GPs was the number of influenza vaccinations in previous years and their effect on basic immunity. However, this too was taken into account in the multivariate analysis.
Among general practitioners, the efficacy of an influenza vaccination against proven influenza (virological and/or serological defined) was rather moderate in this clinical trial performed during two consecutive winter periods (2002–2003); however, the efficacy was substantially higher among younger GPs. Thus, younger GPs should be the first to be vaccinated. Family members with influenza, rather than the daily burden of influenza patients, make every GP, vaccinated or not, very vulnerable to infectious influenza. Every GP should be aware of this route of infection and should take adequate precautions.
This study would not have been possible without the cooperation of the 190 Flemish general practitioners who participated in the study and provided their own data and blood samples. Advice concerning the design of the study, given by Prof. Dr. Pierre Van Damme from the WHO collaborating Centre for the Evaluation of Vaccination at the University of Antwerp, was greatly appreciated.
We thank Eurogenerics nv for their funding (mostly to pay the HAI analyses by Viroclinics Rotterdam) and logistic support, and GlaxoSmithKline nv for providing Alfarix®. The department of Family Medicine of the University of Antwerp provided the additional financial and logistic support. The sponsors of the study played no role in study design, data collection, data analysis, data interpretation or writing of the report. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication.
- Harper SA, Fukuda K, Uyeki TM, Cox NJ, Bridges CB: Prevention and Control of influenza: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2005, 54: 1-40.PubMedGoogle Scholar
- Poland GA, Tosh P, Jacobson RM: Requiring influenza vaccination for health care workers: seven truths we must accept. Vaccine. 2005, 23: 2251-2255. 10.1016/j.vaccine.2005.01.043.View ArticlePubMedGoogle Scholar
- Demicheli V, Rivetti D, Deeks JJ, Jefferson TO: Vaccines for preventing influenza in healthy adults (Cochrane review). Cochrane Database Syst Rev. 2005, 2.Google Scholar
- Carman WF, Elder AG, Wallace LA, McAulay K, Walker A, Murray GD, Stott DJ: Effects of influenza vaccination of health-care workers on mortality of elderly people in long-term care: a randomised controlled trial. Lancet. 2000, 355: 93-97. 10.1016/S0140-6736(99)05190-9.View ArticlePubMedGoogle Scholar
- Potter J, Stott DJ, Roberts MA: Influenza Vaccination of Health Care Workers in Long-Term- Care Hospitals Reduces the Mortality of Elderly Patients. J Infect Diseases. 1997, 175: 1-6.View ArticleGoogle Scholar
- Michiels B, Coenen S, Avonts D, Van Royen P, Denekens J: Who benefits from an influenza vaccination of GPs?. Vaccine. 2001, 20: 1-2. 10.1016/S0264-410X(01)00255-9.View ArticlePubMedGoogle Scholar
- Elder AG, O'Donnell B, McCruden EAB, Symington IS, Carman WF: Incidence and recall of influenza in a cohort of Glasgow healthcare workers during the 1993–1994 epidemic: results of serum testing and questionnaire. BMJ. 1996, 313: 1241-1242.View ArticlePubMedPubMed CentralGoogle Scholar
- Betts RF, Treanor JJ: Approaches to improved influenza vaccination. Vaccine. 2000, 18: 1690-1695. 10.1016/S0264-410X(99)00508-3.View ArticlePubMedGoogle Scholar
- Clements ML, Betts RF, Murphy BR: Advantage of live attenuated cold-adapted influenza A virus over inactivated vaccine for A/Washington/80 (H3N2) wild-type virus infection. Lancet. 1984, 1: 705-708. 10.1016/S0140-6736(84)92222-0.View ArticlePubMedGoogle Scholar
- Greenbaum E, Engelhard D, Levy R, Schlezinger M, Morag A, Zakay-Rones Z: Mucosal (SIgA) and serum (IgG) immunologic responses in young adults following intranasal administration of one or two doses of inactivated, trivalent anti-influenza vaccine. Vaccine. 2004, 22: 2566-2577. 10.1016/j.vaccine.2003.12.018.View ArticlePubMedGoogle Scholar
- Halperin SA, Smith B, Clarke K, Treanor J, Mabrouk T, Germain M: Phase I, randomized, controlled trial to study the reactogenicity and immunogenicity of a nasal, inactivated trivalent influenza virus vaccine in healthy adults. Human Vaccines. 2005, 1: 37-42.View ArticlePubMedGoogle Scholar
- Kleinbaum DG, Klein M: Logistic Regression. 2002, New York: Springer-VerlagGoogle Scholar
- European Influenza Surveillance Scheme: Annual report: 2002–2003 influenza season. 2004, NIVEL, Utrecht, the NetherlandsGoogle Scholar
- Yane F, Libotte ML, Brochier B: Surveillance van griep in België. Seizoen 2003–2004. 2004, Scientific Institute of Public Health, National Influenza Centre, Brussels, BelgiëGoogle Scholar
- Russell KL, Ryan MAK, Hawksworth A, Freed NE, Irvine M, Daum LT: Effectiveness of the 2003–2004 influenza vaccine among US military basic trainees: a year of suboptimal match between vaccine and circulating strain. Vaccine. 2005, 23: 1981-1985. 10.1016/j.vaccine.2004.10.023.View ArticlePubMedGoogle Scholar
- Michiels B, Philips H, Coenen S, Denekens J, Van Royen P: Serum antibodies against circulating influenza strains among vaccinated and unvaccinated general practitioners during two consecutive years (2002–2003). Vaccine. 2006, 24: 3145-3152. 10.1016/j.vaccine.2006.01.040.View ArticlePubMedGoogle Scholar
- Epidemic Observation Unit: Retrospective survey of the 1957 epidemic of Asian influenza. Part II. J Coll Gen Pract. 1958, 1: 258-260.Google Scholar
- Ellis JS, Fleming DM, Zambon MC: Multiplex reverse transcription-PCR for surveillance of influenza A and B viruses in England and Wales in 1995 and 1996. J Clin Microbiol. 1997, 35: 2076-2082.PubMedPubMed CentralGoogle Scholar
- Wilde JA, McMillan JA, Serwint J, Butta J, O'Riordan MA, Steinhoff MC: Effectiveness of influenza vaccine in health care professionals. A randomized trial. JAMA. 1999, 281: 908-913. 10.1001/jama.281.10.908.View ArticlePubMedGoogle Scholar
- Monto AS, Ross HW: Acute respiratory illness in the community: effect of family composition, smoking and chronic symptoms. Br J Prev Soc Med. 1977, 31: 101-108.PubMedPubMed CentralGoogle Scholar
- Harbarth S, Siegrist CA, Schira JC, Wunderli W, Pittet D: Influenza immunization: improving compliance of health care workers. Inf Control Hosp Epidemiol. 1998, 19.Google Scholar
- Palache AM, Beyer WEP, Lüchters G, Völker R, Sprenger MJW, Masurel N: Influenza vaccines: the effect of vaccine dose on antibody response in primed populations during the ongoing interpandemic period. A review of the literature. Vaccine. 1993, 11: 892-908. 10.1016/0264-410X(93)90375-8.View ArticlePubMedGoogle Scholar
- Stevenson PG, Doherty PC: Cell-mediated immune response to influenza virus. Textbook of influenza. Edited by: KG N. 1998, Oxford: Blackwell Science Ltd, 278-287.Google Scholar
- Fox JP, Cooney MK, Hall CE, Foy Hm: Influenza virus infections in Seattle families, 1975–1979. Am J Epidemiol. 1982, 116: 228-242.PubMedGoogle Scholar
- Nguyen-Van-Tam JS: Epidemiology of Influenza. Textbook of Influenza. Edited by: Nicholson KG. 1998, Oxford: Blackwell Science Ltd, 181-206.Google Scholar
- Jefferson T, Demicheli V, Deeks J, Rivetti D: Neuraminidase inhibitors for preventing and treating influenza in healthy adults [Systematic Review]. Cochrane Database of Systematic Reviews. 2005, 3.Google Scholar
- Kiso M, Mitamura K, Sakai-Tagawa Y, Shiraishi K, Kawakami C, Kimura K, Hayden F, Sugaya N, Kawaoka Y: Resistant influenza A viruses in children treated with oseltamivir: descriptive study. Lancet. 2004, 364: 759-765. 10.1016/S0140-6736(04)16934-1.View ArticlePubMedGoogle Scholar
- Edwards KM, Dupont WD, Westrich MK, Plummer WD, Palmer PS, Wright PF: A randomized controlled trial of cold-adapted and inactivated vaccines for prevention of influenza A disease. J Infect Dis. 1994, 169: 68-76.View ArticlePubMedGoogle Scholar
- Keitel WA, Cate TR, Couch RB, Huggins LL, Hess KR: Efficacy of repeated annual immunization with inactivated influenza virus vaccines over a five year period. Vaccine. 1997, 15: 1114-1122. 10.1016/S0264-410X(97)00003-0.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1741-7015/4/17/prepub