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Download het volledig rapport (302 p.) - KCE

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<strong>KCE</strong> reports vol. 6A Prenatale zorg 73<br />

Study Ref Population Intervention Outcomes Results<br />

unaffected<br />

pregnancies<br />

Comments Study<br />

type<br />

Prevalence estimates:<br />

17 infants born<br />

each year with<br />

beta-thalassaemia<br />

(0.03/1000 live<br />

births)<br />

160 infants born<br />

each year with<br />

sickle cell disorder<br />

(0.25/1000 live<br />

births)<br />

Does recording of racial background in the notes of pregnant women help in selective screening for haemoglobinopathies?<br />

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

Aspinall<br />

et al.,<br />

2003<br />

Modell et<br />

al., 2000<br />

4 [281] N/A Assessing effectiveness of<br />

questions about ethnic origin<br />

4 [276] 400 pregnancies in<br />

138 women in the<br />

UK from 1990 to<br />

1994<br />

Audit to evaluate the quality of<br />

antenatal screening for<br />

haemoglobinopathy and<br />

genetic counselling<br />

Quality of data<br />

collected<br />

Haemoglobinopath<br />

y affected<br />

Screening offered<br />

Risk group misclassification as high as<br />

20%<br />

June quarter 2000 data from Hospital<br />

Episode Statistics indicate ethnic<br />

group data missing from 43% of<br />

records in London and 37% in<br />

England<br />

138/400 (35%) pregnancies with<br />

haemoglobinopathy<br />

68/138 (49%) of affected pregnancies<br />

had been offered screening at first<br />

This study assumes<br />

that antenatal<br />

screening for Hb<br />

disorders is standard<br />

practice in the UK<br />

EL<br />

EL<br />

type<br />

RW 3<br />

CSS 3

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