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The Effect of a Second Dose of Measles Vaccine at 18 Months of Age on Nonaccidental Deaths and Hospital Admissions in Guinea-Bissau: Interim Analysis of a Randomized Controlled Trial.
Berendsen, Mike L T; Silva, Isaquel; Balé, Carlitos; Nielsen, Sebastian; Hvidt, Sophus; Martins, Cesario L; Benn, Christine S; Aaby, Peter.
  • Berendsen MLT; Bandim Health Project, Department of Clinical Research, University of Southern Denmark and Odense University Hospital, Odense, Denmark.
  • Silva I; Bandim Health Project, Indepth Network, Bissau, Guinea-Bissau.
  • Balé C; Department of Internal Medicine, Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Nielsen S; Bandim Health Project, Indepth Network, Bissau, Guinea-Bissau.
  • Hvidt S; Bandim Health Project, Indepth Network, Bissau, Guinea-Bissau.
  • Martins CL; Bandim Health Project, Department of Clinical Research, University of Southern Denmark and Odense University Hospital, Odense, Denmark.
  • Benn CS; Bandim Health Project, Indepth Network, Bissau, Guinea-Bissau.
  • Aaby P; Bandim Health Project, Indepth Network, Bissau, Guinea-Bissau.
Clin Infect Dis ; 75(8): 1370-1378, 2022 10 12.
Article en En | MEDLINE | ID: mdl-35218356
ABSTRACT

BACKGROUND:

The world is set on the eradication of measles. Continuation of the measles vaccine (MV) after eradication could still reduce morbidity because the MV has so-called beneficial nonspecific effects. We evaluated the effect of a "booster" dose of the MV on overall severe morbidity.

METHODS:

We conducted a randomized controlled trial among children aged 17.5 to 48 months in Guinea-Bissau, where the MV is recommended only at 9 months of age. At the time of this interim analysis, 3164 children had been allocated 11 to a second dose of measles vaccine (MV2) at 18 months of age or to no vaccine. Severe morbidity (a composite outcome of nonaccidental deaths and hospital admissions) rate ratios (SMRRs) were calculated by Cox regression analysis censored for national oral polio vaccine (OPV) campaigns.

RESULTS:

There were no measles cases during the trial period. There were 43 nonaccidental deaths or hospital admissions during follow-up. Severe morbidity was 2.6 per 100 person-years in the MV2 group and 3.6 per 100 person-years among controls; hence, the estimated effect of MV2 on severe morbidity was 28% (SMRR, 0.72; 95% confidence interval [CI], .38-1.38). At 12 months of follow-up, the number needed to treat to prevent 1 severe morbidity event was 137 children. After OPV campaigns, the estimated effect of MV2 was reduced to 9% (SMRR, 0.91; 95% CI, .46-1.81).

CONCLUSIONS:

MV2 may reduce nonmeasles severe morbidity by 28% (-38% to 62%), although this did not achieve statistical significance in this study. If significant in higher powered studies, this has major implications for child health, even after measles eradication. CLINICAL TRIALS REGISTRATION NCT02943681.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacuna Antisarampión / Sarampión Tipo de estudio: Clinical_trials Límite: Child / Humans / Infant País como asunto: Africa Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacuna Antisarampión / Sarampión Tipo de estudio: Clinical_trials Límite: Child / Humans / Infant País como asunto: Africa Idioma: En Año: 2022 Tipo del documento: Article