Impact of the pneumococcal conjugate vaccine on
otitis media
BRUCE FIREMAN, MA; STEVEN B. BLACK, MD; HENRY R. SHINEFIELD, MD; JANELLE LEE,
DRPH; EDWIN LEWIS, MPH; PAULA RAY, MPH
Context.
The heptavalent pneumococcal conjugate vaccine (PCV)
is recommended for infants to protect against invasive disease, but its impact
on otitis might also have public health importance.
Objective.
To examine the impact of PCV on the incidence of
otitis media, frequent otitis media and tympanostomy tube procedures and to
assess whether the effectiveness of the vaccine wanes after age 24 months and
varies by race, sex or season.
Design, setting and patients..
From 1995 to 1998, 37 868 children at Kaiser
Permanente in Northern California were randomized to receive PCV or a control
vaccine in a double blind trial and were followed through April 1999.
Interventions.
Children received a primary series at 2, 4 and 6
months of age and a booster at 12 to 15 months.
Main outcome measures.
Visits for otitis, frequent visits for otitis and
tympanostomy tube procedures. Otitis was ascertained from diagnosis checklists
routinely marked by physicians.
Results.
Control children averaged 1.8 otitis visits per
year. Children given PCV had fewer otitis visits than control children in
every age group, sex, race and season examined. Intention-to-treat analysis
permitted rejection of the null hypothesis that PCV is ineffective against
otitis media (P< 0.0001).
In children who completed the primary series per protocol, PCV reduced otitis
visits by 7.8% [95% confidence interval (CI), 5.4 to 10.2%] and antibiotic
prescriptions by 5.7% (CI 4.2 to 7.2%). Frequent otitis was reduced by amounts
that increased with otitis frequency, from a 10% reduction in the risk of 3
visits to a 26% reduction in the risk of 10 visits within a 6-month period.
Tube placements were reduced by 24% (CI 12 to 35%).
Conclusion.
In children followed up to 3.5 years, PCV provided
a moderate amount of protection against ear infections while reducing frequent
otitis media and tube procedures by greater amounts.
From the Kaiser Permanente Division of
Research and the Kaiser Permanente Vaccine Studies Center, Oakland, CA.
Accepted for publication Sept. 24, 2002.
Address for reprints: Bruce Fireman, Division
of Research, Kaiser Permanente, 2000 Broadway, Oakland, CA 94612. Fax
510-891-3508; E-mail bruce.fireman@kp.org.
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