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Download het volledig rapport (302 p.) - KCE

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<strong>KCE</strong> reports vol. 6A Prenatale zorg 184<br />

Study Ref Population Intervention Outcomes Results<br />

to 3.17<br />

Comment<br />

s<br />

Goldenberg<br />

et al., 1996<br />

4 [545] 2929 women from 10<br />

centres in the USA<br />

from 1992 to 1994<br />

Measurement of fetal fibronectin in the<br />

cervix and vagina every two weeks from<br />

22 to 24 weeks of gestation to 30<br />

weeks of gestation as a screening test<br />

for preterm birth<br />

Sensitivity and specificity<br />

(positive test defined as<br />

fetal fibronectin greater<br />

than or equal to 50<br />

ng/mL)<br />

at 19 weeks or more, 9.7%<br />

vs. 3.7%, RR 2.63, 95% CI<br />

1.75 to 3.94<br />

Sensitivity and specificity for<br />

birth at 34 weeks or earlier<br />

for fetal fibronection<br />

measurement at:<br />

24 weeks, 23% (95%<br />

CI 16 to 31) and 97%<br />

26 weeks, 22% (95%<br />

CI 14 to 32) and 97%<br />

28 weeks, 20% (95%<br />

CI 11 to 30) and 97%<br />

30 weeks, 29% (95%<br />

CI 18 to 41) and 96%<br />

Sensitivity of fibronectin at<br />

22 to 24 weeks for preterm<br />

birth occurring at:<br />

24 to 27 weeks, 63%<br />

(95% CI 38 to 84)<br />

24 to 29 weeks, 54%<br />

(95% CI 28 to 66)<br />

24 to 31 weeks, 38%<br />

(95% CI 25 to 53)<br />

Study<br />

type<br />

EL<br />

CH 2a

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