id | Study | Lib. in paper | Exposition period | Study type |
Control type |
Tags | OR 95%CI | x1/n1 x0/n0 | no cases | no exposed | ROB | Ref. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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S5304 R13750 |
Jourdain a, 2018 | Neonatal adverse event of grade 3 or 4 or serious adverse event (< 1 year) | 3rd trimester | randomized controlled trial | unexposed, sick | Adjustment: Randomisation Control group: Unexposed, sick Exposed group: TDF (only) Indication: CHB | 1.17 [0.71;1.94] C | 43/161 38/160 | 81 | 161 |
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ref | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
S5282 R13646 |
Chi, 2007 | Neonatal serious adverse event (within 2 weeks pp). | late pregnancy | randomized controlled trial | unexposed, sick | Adjustment: Randomisation Control group: Unexposed, sick Exposed group: TDF/emtracitabine Indication: HIV | 0.86 [0.46;1.62] C | 20/198 23/199 | 43 | 198 |
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ref | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Total | 2 studies | 1.04 [0.70;1.54] | 124 | 359 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
x1: number of endpoints among exposed, n1: number of exposed; x0: number of endpoints among non exposed, n0: number of non exposed; C: calculated odds ratio from numbers of events and effectives |
Funnel plot not drawn. Less than 3 points.
Asymetry test p-value = NaN (by Egger's regression)
not enought points
Funnel plot not drawn. Less than 3 points.
excluded