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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S5153 R13439 |
Pintye, 2017 | Pregnancy loss (< 20 weeks) | at least 1st trimester | prospective cohort | exposed to other treatment, sick | Adjustment: Yes Control group: zidovudine/lamivudine-based Exposed group: TDF/lamivudine-based Indication: PrEP | 1.11 [0.25;4.88] | 13/- 6/- | 19 | - |
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ref | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
S5265 R13632 |
Mugo, 2014 | Pregnancy losses <20 weeks’ gestation | early pregnancy | randomized controlled trial | unexposed, sick | Adjustment: Randomisation Control group: Unexposed, sick Exposed group: TDF (only) Indication: PrEP | 0.86 [0.50;1.49] C | 49/174 30/96 | 79 | 174 |
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ref | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
S5122 R13298 |
Gibb, 2012 | Miscarriages/terminations (< 22 weeks) | throughout pregnancy | prospective cohort | exposed to other treatment, sick | Adjustment: No Control group: zidovudine/lamivudine-based Exposed group: TDF/zidovudine/lamivudine Indication: HIV | 1.13 [0.71;1.81] C | 90/251 38/115 | 128 | 251 |
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ref | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Total | 3 studies | 1.01 [0.72;1.43] | 226 | 425 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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