Combined Effects of Antenatal Receipt of Influenza Vaccine by Mothers and Pneumococcal Conjugate Vaccine Receipt by Infants: Results from a Randomized, Blinded, Controlled Trial
被引:17
作者:
Omer, Saad B.
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Emory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
Emory Univ, Sch Med, Atlanta, GA 30322 USA
Kaiser Permanente Georgia, Ctr Hlth Res Southeast, Atlanta, GA USAEmory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
Omer, Saad B.
[1
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Zaman, Khalequ
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ICDDRB, Dhaka, BangladeshEmory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
Zaman, Khalequ
[6
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Roy, Eliza
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ICDDRB, Dhaka, BangladeshEmory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
Roy, Eliza
[6
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Arifeen, Shams E.
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机构:
ICDDRB, Dhaka, BangladeshEmory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
Arifeen, Shams E.
[6
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Raqib, Rubhana
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ICDDRB, Dhaka, BangladeshEmory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
Raqib, Rubhana
[6
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Noory, Laila
[1
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Seib, Katherine
[1
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Breiman, Robert F.
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机构:
US Ctr Dis Control & Prevent, Nairobi, KenyaEmory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
Breiman, Robert F.
[7
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Steinhoff, Mark C.
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Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Baltimore, MD USA
Cincinnati Childrens Hosp, Global Hlth Ctr, Cincinnati, OH USAEmory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
Steinhoff, Mark C.
[4
,5
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机构:
[1] Emory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Atlanta, GA 30322 USA
[3] Kaiser Permanente Georgia, Ctr Hlth Res Southeast, Atlanta, GA USA
A 2 x 2 factorial trial was performed to determine the efficacy of antennal influenza vaccination of mothers plus pneumococcal conjugate vaccination of their infants against respiratory illness during early infancy. The efficacy of trivalent inactivated influenza vaccine (TIV; delivered to mothers) plus 7-valent pneumococcal vaccine (PCV7; delivered to infants) was higher than the efficacy of TIV alone or PCV7 alone. During the period of the study in which influenza was circulating, the efficacy of TIV plus PCV7 was 72.4% (95% confidence interval, 30.2%-89.1%) against febrile respiratory illness and 66.4% (95% CI, 14.3%-86.9%) against medically attended acute respiratory illness. Clinical Trials registration NCT00142389.