A model for preconceptional prediction of recurrent early-onset preeclampsia: derivation and internal validation.

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Publication year
2011Source
Reproductive Sciences, 18, 11, (2011), pp. 1154-1159ISSN
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1 november 2011
Publication type
Article / Letter to editor

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Organization
Gynaecology
Journal title
Reproductive Sciences
Volume
vol. 18
Issue
iss. 11
Page start
p. 1154
Page end
p. 1159
Subject
NCEBP 14: Cardiovascular diseasesAbstract
OBJECTIVE: To develop a model to identify women at very low risk of recurrent early-onset preeclampsia. METHODS: We enrolled 407 women who had experienced early-onset preeclampsia in their first pregnancy, resulting in a delivery before 34 weeks' gestation. Preeclampsia was defined as hypertension (systolic blood pressure >/=140 mm Hg and/or diastolic blood pressure >/=90 mm Hg) after 20 weeks' gestation with de novo proteinuria (>/=300 mg urinary protein excretion/day). Based on the previous published evidence and expert opinion, 5 predictors (gestational age at previous birth, prior small-for-gestational-age newborn, fasting blood glucose, body mass index, and hypertension) were entered in a logistic regression model. Discrimination and calibration were evaluated after adjusting for overfitting by bootstrapping techniques. RESULTS: Early-onset disease recurred in 28 (6.9%) of 407 women. The area under the receiver operating characteristic (ROC) curve of the model was 0.65 (95% CI: 0.56-0.74). Calibration was good, indicated by a nonsignificant Hosmer-Lemeshow test (P = .11). Using a predicted absolute risk threshold of, for example, 4.6% (ie, women identified with an estimated risk either above or below 4.6%), the sensitivity was 100%, with a specificity of 26%. In such a strategy, no women who developed preeclampsia were missed, while 98 of the 407 women would be regarded as low risk of recurrent early-onset preeclampsia, not necessarily requiring intensified antenatal care. CONCLUSION: Our model may be helpful in the identification of women at very low risk of recurrent early-onset preeclampsia. Before widespread application, our model should be validated in other populations.
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- Electronic publications [100861]
- Faculty of Medical Sciences [80017]
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