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WHO guidelines for the management of postpartum haemorrhage ...

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<strong>WHO</strong> <strong>guidelines</strong> <strong>for</strong> <strong>the</strong> <strong>management</strong> <strong>of</strong> <strong>postpartum</strong> <strong>haemorrhage</strong> and retained placenta<br />

B. Management <strong>of</strong> atonic PPH<br />

Table B1. Adjunct use <strong>of</strong> misoprostol in women who received prophylactic oxytocin in <strong>the</strong> third stage <strong>of</strong> labour (34)<br />

No. <strong>of</strong><br />

studies<br />

Quality assessment<br />

Design Limitations Inconsistency Indirectness Imprecision<br />

Additional blood loss ≥500 ml<br />

4<br />

Randomized<br />

trial<br />

No serious<br />

limitations<br />

Additional blood loss ≥1000 ml<br />

3<br />

Randomized<br />

trial<br />

Blood transfusion<br />

4<br />

Hysterectomy<br />

3<br />

Randomized<br />

trial<br />

Randomized<br />

trial<br />

Additional uterotonics<br />

3<br />

Shivering<br />

4<br />

Randomized<br />

trial<br />

Randomized<br />

trial<br />

No serious<br />

limitations<br />

No serious<br />

limitations<br />

No serious<br />

limitations<br />

No serious<br />

limitations<br />

No serious<br />

limitations<br />

No serious<br />

inconsistency<br />

No serious<br />

inconsistency<br />

No serious<br />

inconsistency<br />

No serious<br />

inconsistency<br />

No serious<br />

inconsistency<br />

No serious<br />

inconsistency<br />

No serious<br />

indirectness<br />

No serious<br />

indirectness<br />

No serious<br />

indirectness<br />

No serious<br />

indirectness<br />

No serious<br />

indirectness<br />

No serious<br />

indirectness<br />

No serious<br />

imprecision<br />

O<strong>the</strong>r<br />

considerations<br />

None<br />

Serious 1 None<br />

No serious<br />

imprecision<br />

None<br />

Very serious 1 None<br />

No serious<br />

imprecision<br />

None<br />

Serious 1 None<br />

Summary <strong>of</strong> findings<br />

No. <strong>of</strong> patients Effect<br />

Primary<br />

outcomes<br />

170/929<br />

(18.3%)<br />

20/899<br />

(2.2%)<br />

138/927<br />

(14.9%)<br />

5/900<br />

(0.6%)<br />

253/894<br />

(28.3%)<br />

556/928<br />

(59.9%)<br />

Controls<br />

200/950<br />

(21.1%)<br />

27/915<br />

(3.1%)<br />

147/949<br />

(14.5%)<br />

5/919<br />

(0.4%)<br />

271/910<br />

(28.3%)<br />

270/948<br />

(17.7%)<br />

Relative<br />

(95% CI)<br />

RR 0.83<br />

(0.64–<br />

1.07)<br />

RR 0.76<br />

(0.43–<br />

1.34)<br />

RR 0.96<br />

(0.77–<br />

1.19)<br />

RR 0.93<br />

(0.16–<br />

5.41)<br />

RR 0.96<br />

(0.84–1.1)<br />

RR 2.24<br />

(1.72–<br />

2.91)<br />

Absolute<br />

Quality<br />

29 fewer<br />

per 1000 High<br />

7 fewer<br />

per 1000 Moderate<br />

6 fewer<br />

per 1000 High<br />

0 fewer<br />

per 1000 Low<br />

11 fewer<br />

per 1000 High<br />

219 more<br />

per 1000 Moderate<br />

1<br />

Wide confidence interval.<br />

Importance<br />

Critical<br />

Critical<br />

Critical<br />

Critical<br />

Critical<br />

Important<br />

28

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