Single deepest vertical pocket or amniotic fluid index as evaluation test for predicting adverse pregnancy outcome (SAFE trial): a multicenter, open-label, randomized controlled trial

Author:

Kehl S.12,Schelkle A.2,Thomas A.3,Puhl A.4,Meqdad K.3,Tuschy B.2,Berlit S.2,Weiss C.5,Bayer C.1,Heimrich J.1,Dammer U.1,Raabe E.1,Winkler M.1,Faschingbauer F.1,Beckmann M. W.1,Sütterlin M.2

Affiliation:

1. Department of Obstetrics and Gynaecology; Erlangen University Hospital; Erlangen Germany

2. Department of Obstetrics and Gynaecology; University Medical Centre Mannheim, Heidelberg University; Heidelberg Germany

3. Department of Obstetrics; Charité Virchow-Klinikum; Berlin Germany

4. Department of Obstetrics and Gynaecology; University Medical Centre Mainz; Mainz Germany

5. Department of Medical Statistics and Biomathematics; University Medical Centre Mannheim, Heidelberg University; Heidelberg Germany

Publisher

Wiley

Subject

Obstetrics and Gynaecology,Radiology Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Reference17 articles.

1. Amniotic fluid volume assessment with the four-quadrant technique at 36-42 weeks' gestation;Phelan;J Reprod Med,1987

2. Ultrasound evaluation of amniotic fluid volume. I. The relationship of marginal and decreased amniotic fluid volumes to perinatal outcome;Chamberlain;Am J Obstet Gynecol,1984

3. Fetal biophysical profile scoring: a prospective study in 1,184 high-risk patients;Manning;Am J Obstet Gynecol,1981

4. Nonstress testing with acoustic stimulation and amniotic fluid volume assessment: 5973 tests without unexpected fetal death;Clark;Am J Obstet Gynecol,1989

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