Download het volledig rapport (302 p.) - KCE
Download het volledig rapport (302 p.) - KCE
Download het volledig rapport (302 p.) - KCE
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<strong>KCE</strong> reports vol. 6A Prenatale zorg 138<br />
Study Ref Population Intervention Outcomes Results Comments Study<br />
type<br />
EL<br />
al., 2002<br />
pregnancy vs. placebo Very preterm births (n OR 0.86 (95% CI 0.57 to the trials (p = 0.37)<br />
Cochrane review<br />
or micronutrient = 1578, 2 RCTs) 1.31)<br />
supplementation All preterm births (n = OR 0.88 (95% CI 0.68 to ** There were only 3<br />
Most recent update 2002<br />
1577, 2 RCTs) 1.13)<br />
maternal deaths<br />
Low birth weight (n = OR 0.71 (95% CI 0.40 to<br />
1486, 2 RCTs) 1.28)<br />
Very low birth weight OR 0.71 (95% CI 0.40 to<br />
(n = 1483, 2 RCTs) 1.28)<br />
Postpartum CD4 levels<br />
(n = 727, 1 RCT)<br />
Weighted mean<br />
difference 4.0, 95% CI<br />
51.06 to 43.06<br />
Maternal death (n = OR 0.49 (95% CI 0.04 to<br />
728, 1 RCT)** 5.40)<br />
Ricci and 4 436 women between 34 to 38 Caesarean section Adverse effects of Higher rates of fever in Analysis by actual mode RCT 1b<br />
Parazzini, [418] weeks pregnancy with delivery vs. vaginal delivery in HIV1 women who gave births of delivery<br />
2000<br />
confirmed HIV-1 diagnosis delivery<br />
infected women (i.e., by Caesarean section, but<br />
without indication (or<br />
fever, wound infection, no significant differences<br />
contraindication) for<br />
anaest<strong>het</strong>ic, anaemia, in complication rates<br />
caesarean section delivery in<br />
other)<br />
between women treated<br />
various European countries,<br />
with zidovudine in<br />
including the UK<br />
pregnancy and those not<br />
treated<br />
Cunningham 4 242 from original PACTG Emergence of Detection of resistance Detection of resistance International,<br />
OB 3<br />
et al., 2002 [419] (only US and French sites nevirapine resistance mutations prior to mutations prior to multicentre substudy of<br />
included) study with 25 mutations at 6 weeks receipt of study drug receipt of study drug: PACTG 316<br />
excluded from final analysis postpartum in women<br />
5/217 women (2.3%)<br />
receiving standard Detection of resistance<br />
Risk for development of<br />
(RCT substudy)<br />
antiretroviral treatment mutations at 6 weeks Detection of resistance resistant mutations not<br />
postpartum among mutations at 6 weeks correlated with CD4<br />
women who received postpartum among cell counts or HIV-1<br />
the study drug (single women who received the RNA viral load at<br />
dose oral 200 mg to study drug: 14/95 (15%, delivery or with type of<br />
mother and 2 mg/kg to 95% CI 8 to 23%) antiretroviral therapy