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The Lancet
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#1Arghavan Salles (Stanford University)H-Index: 8
#2Esther K. Choo (OHSU: Oregon Health & Science University)H-Index: 9
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#1Jonathon R. Campbell (McGill University)H-Index: 1
#2Mayara L Bastos (McGill University)
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#1Leonardo Martinez (Stanford University)H-Index: 7
#2Olivia Cords (Stanford University)H-Index: 3
Last. Sanjay BasuH-Index: 59
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Summary Background Tens of millions of children are exposed to Mycobacterium tuberculosis globally every year; however, there are no contemporary estimates of the risk of developing tuberculosis in exposed children. The effectiveness of contact investigations and preventive therapy remains poorly understood. Methods In this systematic review and meta-analysis, we investigated the development of tuberculosis in children closely exposed to a tuberculosis case and followed for incident disease. We ...
1 CitationsSource
#1Nolwenn Boujan (Heidelberg University)
#2Cyrill Géraud (Heidelberg University)H-Index: 13
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#1Ilina Singh (University of Oxford)H-Index: 24
#2Huseyin Naci (LSE: London School of Economics and Political Science)H-Index: 24
Last. Andrea Cipriani (University of Oxford)H-Index: 45
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#1Huseyin Naci (LSE: London School of Economics and Political Science)H-Index: 24
#1Andrea CiprianiH-Index: 45
Last. T. Scott Stroup (Columbia University)H-Index: 24
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Certain limitations of evidence available on drugs and devices at the time of market approval often persist in the post-marketing period. Often, post-marketing research landscape is fragmented. When regulatory agencies require pharmaceutical and device manufacturers to conduct studies in the post-marketing period, these studies might remain incomplete many years after approval. Even when completed, many post-marketing studies lack meaningful active comparators, have observational designs, and mi...
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