WHO/HIV/2013.74 © World Health Organization 2013
This work was commissioned by the World Health Organization and carried out by The University of California, San Francisco (UCSF), Cochrane Review Group on HIV/AIDS
1 GRADE table: Should integrated HIV and maternal and child health services versus referral to HIV services be used for providing HIV care to pregnant women living with HIV and their infants?
Author(s): Alicen B. Spaulding, Deborah Bain-Brickley, Hana Azman Date: 2012-10-30
Question: Should integrated HIV and maternal and child health services versus referral to HIV services be used for providing HIV care to pregnant women living with HIV and their infants?
Settings: Rwanda, Kenya and Zambia
Bibliography: Killam 2010, Ong'ech 2012, SHAIP study 2012, Tsague 2010
Quality assessment No. of patients Effect
Quality Importance No. of
studies Design Risk of
bias Inconsistency Indirectness Imprecision Other considerations
Integrated HIV and maternal and
child health services
Referral to HIV services
Relative
(95% CI) Absolute
Maternal mortality (follow-up 12 months)
1 observational studies
no serious risk of bias
no serious inconsistency
no serious indirectness
serious1 none 9/569
(1.6%)
8/603 (1.3%)
RR 1.19 (0.46 to 3.07)
3 more per 1000 (from 7
fewer to 27 more)
⊕ΟΟΟ VERY LOW
CRITICAL
Morbidity (follow-up 12 months)
12 observational studies
no serious risk of bias
no serious inconsistency
no serious indirectness
serious1 none 22/121
(18.2%)
21/121 (17.4%)
RR 1.05 (0.61 to 1.8)
9 more per 1000 (from 68
fewer to 139 more)
⊕ΟΟΟ VERY LOW
CRITICAL
Immune response (follow-up 12 months)
33 observational studies4
no serious risk of bias
no serious inconsistency
no serious indirectness
no serious imprecision
none 982/3921
(25%)
752/2881 (26.1%)
RR 0.92 (0.67 to 1.27)
21 fewer per 1000 (from 86
fewer to 70 more)
⊕⊕ΟΟ LOW
CRITICAL
WHO/HIV/2013.74 © World Health Organization 2013
This work was commissioned by the World Health Organization and carried out by The University of California, San Francisco (UCSF), Cochrane Review Group on HIV/AIDS
2
Retention (follow-up 12 and 24 months)
25 observational studies4
no serious risk of bias
no serious inconsistency
no serious indirectness
no serious imprecision
none 356/457
(77.9%)
183/287 (63.8%)
RR 1.11 (0.76 to 1.62)
70 more per 1000 (from 153
fewer to 395 more)
⊕⊕ΟΟ LOW
CRITICAL
ART initiation (follow-up 12 months)
36 observational studies4
no serious risk of bias
no serious inconsistency
no serious indirectness
no serious imprecision
none 486/1204
(40.4%)
168/966 (17.4%)
RR 1.71 (0.79 to 3.72)
123 more per 1000 (from 37 fewer to 473
more)
⊕⊕ΟΟ LOW
IMPORTANT
Adherence to ART during pregnancy
1 observational studies
no serious risk of bias
no serious inconsistency
no serious indirectness
serious1 none 455/569
(80%)
398/603 (66%)
RR 1.21 (1.13 to 1.3)
139 more per 1000 (from 86 more to 198
more)
⊕ΟΟΟ VERY LOW
IMPORTANT
Uptake of infant HIV testing at six months of life
1 observational studies
no serious risk of bias
no serious inconsistency
no serious indirectness
serious1 none 82/214
(38.3%)
93/232 (40.1%)
RR 0.96 (0.76 to 1.21)
16 fewer per 1000 (from 96
fewer to 84 more)
⊕ΟΟΟ VERY LOW
IMPORTANT
Enrolment in care (follow-up 12 months)
2 observational studies4
No serious risk of bias
no serious inconsistency
no serious indirectness
no serious imprecision
none 875/1309
(66.8%)
256/778 (32.9%)
RR 2.03 (1.82 to 2.26)
339 more per 1000 (from 270
more to 415 more)
⊕⊕ΟΟ LOW
IMPORTANT
Satisfaction with care among women living with HIV (cross-sectional)
1 observational studies
no serious risk of bias
no serious inconsistency
no serious indirectness
serious1 none 23/29
(79.3%)
14/26 (53.8%)
RR 1.47 (0.99 to 2.2)
253 more per 1000 (from 5 fewer to 646
more)
⊕ΟΟΟ VERY LOW
IMPORTANT
WHO/HIV/2013.74 © World Health Organization 2013
This work was commissioned by the World Health Organization and carried out by The University of California, San Francisco (UCSF), Cochrane Review Group on HIV/AIDS
3
1 Small number of events.
2 Defined as those who developed WHO stage 3 or 4 disease.
3 Defined in one study as CD4 <250 cells/mm3, one study as CD4 <350 and the final study as CD4 <200.
4 Three prospective observational cohort studies and one stepped-wedge evaluation study.
5 Defined in one study as 90-day retention among those who initiated ART and in the other study as still enrolled at 12 months.
6 Defined in one study as initiation of ART within 60 days before delivery or estimated due date, in another study as ART initiation among women with CD4 cell counts <350 cells/mm3 and in the final study as those initiating ART within one year of follow-up.