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Question clinique
Does spacing out the influenza vaccine from other childhood vaccinations lessen the risk of fever in children 12 months to 16 months of age?
L’Essentiel
One approach to vaccine hesitancy has been to space out vaccine administration to avoid "overloading the immune system." Adding inactivated quadrivalent influenza vaccine (IIV4) to 13-valent pneumococcal conjugate vaccine (PCV13) and diphtheria-tetanus-acellular pertussis (DTaP) vaccine (usually along with one other additional childhood vaccine) did not increase the risk of fever as compared with giving the flu jab a week later. Antipyretic use immediately after the vaccine visit was higher in the group getting all the vaccines at once despite no increase in fever, which may represent anticipatory worry. 1b-
Référence
Plan de l'etude: Randomized controlled trial (nonblinded)
Financement: Government
Cadre: Outpatient (primary care)
Sommaire
These researchers evaluated 206 children aged 12 to 16 months (median age = 14.6 months) to this open (nonmasked) study. The children were randomized, using concealed allocation, into a simultaneous or sequential group. The simultaneous group received PCV13, DTaP, and IIV4 at visit 1 and no vaccines at visit 2. The sequential group received PCV13 and DTaP at visit 1 and IIV4 at visit 2. At the first visit, most children (89%) received at least one other vaccine in addition to those studied, including Hib conjugate vaccine (78%), measles, mumps, rubella, and varicella (34%), and hepatitis A (40%). By my count, this means the typical child received as few as 18 antigens and as many as 27 antigens at one time. Participants were monitored for fever (38°C) and antipyretic use during the 8 days after the visits. The addition of the influenza vaccine to the mélange of antigens did not increase the likelihood of fever (8.1% in the simultaneous group and 9.3% in the sequential group). Even though few children (8% in each group) had a fever in the first 2 days after visit 1, more children in the simultaneous group received an antipyretic dose for any reason (37.4% vs 22.4%; P = .02). This may be due to increased fussiness or be a testament to anticipatory anxiety or the power of suggestion. That the study took 1.5 years to enroll this many patients at 2 different sites tells me the authors had a hard time getting clinicians or parents to participate, thereby skewing the study participants to those whose clinicians and parents were not unduly concerned about vaccine safety.
Reviewer
Allen F. Shaughnessy, PharmD, MMedEd
Professor of Family Medicine
Tufts University
Boston, MA