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Download het volledig rapport (302 p.) - KCE

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<strong>KCE</strong> reports vol. 6A Prenatale zorg 71<br />

Study Ref Population Intervention Outcomes Results Comments<br />

0.41%<br />

Study<br />

type<br />

Carriers for a 350 carriers for a<br />

haemoglobin haemoglobin<br />

variant variant (1.5%)<br />

What are the adverse maternal and perinatal outcomes associated with haemoglobinopathies?<br />

Study Ref Population Intervention Outcomes Results Comments Study<br />

Davies<br />

et al.,<br />

2000<br />

4 [275] 751 pregnant women with<br />

sickle trait or disease and<br />

265 pregnant women with<br />

beta-thalassaemia trait or<br />

disease from 1986 to 1995<br />

Women attended counselling (n = 623/751<br />

(83%) in sickle cases; n = 246/265 (93%) in<br />

beta-thalassaemia cases), partners tested (n<br />

= 481/623 (77%) in sickle cases; n = 234/246<br />

(88%) in beta-thalassaemia cases), postnatal<br />

diagnosis offered<br />

Pregnancies at<br />

risk<br />

Outcomes of<br />

pregnancies at<br />

risk<br />

Estimates of<br />

prevalence among<br />

all live births in<br />

England<br />

Sickle cell pregnancies<br />

at risk: 113/481 (23%)<br />

Beta-thalassaemia<br />

pregnancies at risk:<br />

22/234 (9.4%)<br />

Outcomes of at risk<br />

pregnancies:<br />

Sickle cell:<br />

16 of 108 women<br />

who returned for<br />

follow-up accepted<br />

prenatal diagnosis<br />

(15%)<br />

3 terminations<br />

from 4 affected<br />

pregnancies<br />

22 affected births<br />

from 92 of 108<br />

women who did<br />

The prevalence<br />

estimates allow<br />

for terminations<br />

type<br />

HTA<br />

RW<br />

CSS<br />

EL<br />

EL<br />

3

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