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WHO recommendations on antenatal care for a positive pregnancy experience

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E.3: Group <strong>antenatal</strong> <strong>care</strong><br />

RECOMMENDATION E.3: Group <strong>antenatal</strong> <strong>care</strong> provided by qualified health-<strong>care</strong> professi<strong>on</strong>als<br />

may be offered as an alternative to individual <strong>antenatal</strong> <strong>care</strong> <strong>for</strong> pregnant women in the c<strong>on</strong>text<br />

of rigorous research, depending <strong>on</strong> a woman’s preferences and provided that the infrastructure<br />

and resources <strong>for</strong> delivery of group <strong>antenatal</strong> <strong>care</strong> are available. (C<strong>on</strong>text-specific recommendati<strong>on</strong><br />

– research)<br />

Remarks<br />

• With the group ANC model, the first visit <strong>for</strong> all pregnant women is an individual visit. Then at subsequent<br />

visits, the usual individual <strong>pregnancy</strong> health assessment, held in a private examinati<strong>on</strong> area, is integrated<br />

into a group ANC sessi<strong>on</strong>, with facilitated educati<strong>on</strong>al activities and peer support.<br />

• Health-<strong>care</strong> facilities need to be seeing sufficient numbers of pregnant women, as allocati<strong>on</strong> to groups is<br />

ideally per<strong>for</strong>med according to gestati<strong>on</strong>al age.<br />

• Health-<strong>care</strong> providers need to have appropriate facilities to deal with group sessi<strong>on</strong>s, including access<br />

to large, well ventilated rooms or sheltered spaces with adequate seating. A private space should be<br />

available <strong>for</strong> examinati<strong>on</strong>s, and opportunities should be given <strong>for</strong> private c<strong>on</strong>versati<strong>on</strong>s.<br />

• Group ANC may take l<strong>on</strong>ger than individual ANC, and this may pose practical problems <strong>for</strong> some women<br />

in terms of work and child<strong>care</strong>. Health-<strong>care</strong> providers should be able to offer a variety of time slots <strong>for</strong><br />

group sessi<strong>on</strong>s (morning, afterno<strong>on</strong>, evening) and should c<strong>on</strong>sider making individual <strong>care</strong> available as<br />

well.<br />

• The GDG noted that group ANC may have acceptability and feasibility issues in settings where perceived<br />

differences keep people apart, e.g. women from different castes in India may not wish to be in a group<br />

together.<br />

• Group ANC studies are under way in Nepal, Uganda and five other low-income countries, and the GDG<br />

was in<strong>for</strong>med by a GDG member that some of these studies are due to report so<strong>on</strong>. Core outcomes of<br />

studies of group ANC should include maternal and perinatal health outcomes, coverage, and women's<br />

and providers' <strong>experience</strong>s.<br />

Summary of evidence and c<strong>on</strong>siderati<strong>on</strong>s<br />

Effects of group ANC compared with individual<br />

ANC (EB Table E.3)<br />

The evidence <strong>on</strong> the effects of group ANC was<br />

derived from a Cochrane review that included<br />

four trials involving 2350 women (174). Two trials<br />

from the USA used a group ANC model known as<br />

CenteringPregnancy®, in which group ANC was<br />

c<strong>on</strong>ducted in circles of 8–12 women of similar<br />

gestati<strong>on</strong>al age, meeting <strong>for</strong> 8–10 sessi<strong>on</strong>s during<br />

<strong>pregnancy</strong>, with each sessi<strong>on</strong> lasting 90–120 minutes.<br />

ssi<strong>on</strong>s included self-assessment activities (blood<br />

pressure measurement), facilitated educati<strong>on</strong>al<br />

discussi<strong>on</strong>s and time to socialize, with individual<br />

examinati<strong>on</strong>s per<strong>for</strong>med in a private/screenedoff<br />

area. One trial c<strong>on</strong>ducted in Sweden used a<br />

group model similar to the USA model but mainly<br />

assessed provider outcomes and c<strong>on</strong>tributed little<br />

data to the review. The fourth trial, c<strong>on</strong>ducted in the<br />

Islamic Republic of Iran, was a cluster-RCT in which<br />

group ANC was described as being similar to the<br />

CenteringPregnancy® approach.<br />

Maternal outcomes<br />

Moderate-certainty evidence indicates that group<br />

ANC probably does not have an important effect <strong>on</strong><br />

vaginal birth rates compared with individual ANC<br />

(1 trial, 322 women; RR: 0.96, 95% CI: 0.80–1.15).<br />

But low-certainty evidence suggests that it may lead<br />

to higher women’s satisfacti<strong>on</strong> scores (1 trial, 993<br />

women; MD: 4.9, 95% CI: 3.10–6.70).<br />

Fetal and ne<strong>on</strong>atal outcomes<br />

Moderate-certainty evidence indicates that group<br />

ANC probably has little or no effect <strong>on</strong> low birth<br />

weight (3 trials, 1935 ne<strong>on</strong>ates; RR: 0.92, 95% CI:<br />

0.68–1.23) and low-certainty evidence suggests that<br />

it may have little or no effect <strong>on</strong> perinatal mortality<br />

(3 trials, 1943 ne<strong>on</strong>ates; RR: 0.63, 95% CI: 0.32–1.25).<br />

However, low-certainty evidence also suggests that<br />

group ANC may reduce preterm birth (3 trials, 1888<br />

women; RR: 0.75, 95% CI: 0.57–1.00); this evidence<br />

includes the possibility of no effect. Evidence <strong>on</strong><br />

the risk of having an SGA ne<strong>on</strong>ate is of a very low<br />

certainty.<br />

Chapter 3. Evidence and <str<strong>on</strong>g>recommendati<strong>on</strong>s</str<strong>on</strong>g> 91

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