Review: Vaccination reduces the incidence of serologically confirmed influenza in healthy adultsPDF
ACP J Club. 2005 May-Jun;142:70. doi:10.7326/ACPJC-2005-142-3-070
Clinical Impact Ratings
Demicheli V, Rivetti D, Deeks JJ, Jefferson TO. Vaccines for preventing influenza in healthy adults. Cochrane Database Syst Rev. 2004;(3):CD001269. [PubMed ID: 15266445]
Is vaccination effective for reducing the incidence and severity of influenza in healthy persons 14 to 60 years of age?
Data sources: Cochrane Central Register of Controlled Trials (Issue 1, 2004), MEDLINE (1966 to 2003), EMBASE/Excerpta Medica (1990 to 2003), bibliographies of relevant articles, and manufacturers and researchers.
Study selection and assessment: Quasirandomized or randomized controlled trials (RCTs) (published in any language) that evaluated the effectiveness of influenza vaccines for protection from exposure to naturally occurring influenza in healthy persons 14 to 60 years age.
Outcomes: Incidence of clinically defined influenza (CDI) (unspecified or specified on the basis of specific symptoms or signs), serologically confirmed influenza (SCI), adverse effects, and working days lost.
25 RCTs (n = 59 566) (47 comparisons) met the selection criteria. For influenza vaccine (inactivated parenteral vaccine [IP], live aerosol vaccine [LA], or inactivated aerosol vaccine [IA]) vs placebo: Rates of CDI and SCI were lower in the IP group than in the placebo group (Table). Rates of specified CDI and SCI were also lower in the LA group than in the placebo group (Table). The rate of unspecified CDI was lower in the IA group than in the placebo group (Table). IPs were associated with increased rates of local tenderness and soreness (overall relative risk increase [RRI] for local effects 256%, 95% CI 214 to 303), whereas LAs were associated with increased rates of sore throats and coryza (overall RRI 56%, CI 31 to 87). For at least 1 vaccine recommended for that year vs placebo or other vaccines: The rate of CDI was lower in the vaccine group (IP, LA, and IA groups combined) than in the placebo groups (relative risk reduction [RRR] 22%, CI 14 to 30) (27 comparisons). The rate of SCI was lower in the combined IP and LA group than in the control group (placebo or noninfluenza vaccine) (RRR 68%, CI 57 to 76) (21 comparisons). The number of working days lost was lower in the IP group than in the control group (weighted mean difference 0.16, CI 0.04 to 0.29) (7 comparisons). For vaccines matching circulating strains vs placebo or other vaccines: The rate of CDI was lower in the vaccine group (IP, LA, and IA groups combined) than in the placebo group (RRR 33%, CI 20 to 44) (16 comparisons). Overall, the rate of SCI was lower in the combined vaccine group than in the control group (RRR 75%, CI 62 to 84) (13 comparisons).
In healthy persons 14 to 60 years of age, vaccines reduce the incidence of serologically confirmed influenza.
Source of funding: Ministry of Defense UK.
For correspondence: Dr. V. Demicheli, Servizo Sovrazonale di Epidemiologia, Piemonte, Italy. E-mail firstname.lastname@example.org.
Table. Influenza vaccines (inactivated parenteral vaccine [IP], live aerosol vaccine [LA], or inactivated aerosol vaccine [IA]) vs placebo for preventing influenza in healthy persons 14 to 60 years of age at mean 87 days*
|Outcomes||Number of comparisons (n)||Comparisons||Weighted event rates||RRR (95% CI)†||NNT (CI)|
|CDI unspecified||8 (6566)||IP vs placebo||17% vs 21%||31% (5 to 51)||25 (13 to ∞)|
|2 (438)||IA vs placebo||7% vs 20%||65% (32 to 82)||8 (4 to 50)|
|CDI specified||10 (4271)||IP vs placebo||36% vs 44%||22% (9 to 33)||12 (7 to 34)|
|2 (4591)||LA vs placebo||20% vs 23%||15% (5 to 24)||34 (17 to 100)|
|2 (1069)||IA vs placebo||20% vs 28%||27% (0 to 47)||17 (7 to ∞)|
|SCI||9 (2411)||IP vs placebo||2% vs 8%||67% (51 to 78)||17 (13 to 34)|
|2 (427)||LA vs placebo||0.5% vs 8.5%||79% (44 to 92)||13 (6 to ∞)|
*CDI = clinically defined influenza; SCI = serologically confirmed influenza. Other
abbreviations defined in Glossary; weighted event rates, NNT, and CI calculated from data in article using a random-effects
†RRR is referred to as vaccine efficacy in the Cochrane review.
Influenza is a complicated public health problem. Both the antigenic makeup of the virus and the number of new cases can vary greatly from year to year, and the demand for the vaccine is also unpredictable. In a bad year, influenza can cause thousands of excess deaths in susceptible patients. The 2004 to 2005 season has been particularly complicated because a major manufacturer failed to meet safety standards, greatly reducing the availability of vaccine early in the season, and the recommendations have been expanded (1).
The Cochrane review by Demicheli and colleagues confirms the effectiveness of both the widely used IP vaccine and the recently approved LA vaccine for reducing the incidence of SCI in healthy persons 14 to 60 years of age. However, vaccination is not currently recommended for most of this population (only those > 50 y of age, or those who live with or care for persons at high risk) (1). The LA vaccine is only approved for those between 5 and 49 years of age and is not recommended for health care workers who are continually exposed to high-risk patients because of concerns about transmission of the live vaccine virus (1).
So, what does this review add? It confirms that vaccination can have direct benefit with little toxicity in all age groups, and supports recent suggestions that vaccine policy should be broadened to include the entire community (2). Thus, physicians who struggle to keep up with the changing recommendations should feel comfortable erring on the side of commission, rather than omission: If you offer vaccination to everyone who comes through your doors, you will do little if any harm, and you may save lives.
Henry S. Sacks, PhD, MD
Mount Sinai School of Medicine
New York, New York, USA
1. Harper SA, Fukuda K, Uyeki TM, et al. Prevention and control of influenza: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep. 2004;53(RR-6):1-40. [PubMed ID: 15163927]
2. Griffiths PD. Should vaccines and antiviral therapy for influenza now be deployed strategically? [Editorial]. Rev Med Virol. 2004;14:137-9. [PubMed ID: 15124230]