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Article type: Research Article
Authors: Bar, J.; | Rabinerson, D. | Padoa, A. | Nitzan, Z. | Neri, A. | Fisch, B. | Hod, M.
Affiliations: Department of Obstetrics and Gynecology, Rabin Medical Center, Beilinson Campus, Petah Tiqva, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
Note: [] Correspondence: Jacob Bar, MD, Department of Obstetrics and Gynecology, Beilinson Medical Center, Petah Tiqva 49 100, Israel. Tel.: 972 3 937 7408; Fax: 972 3 921 1660.
Abstract: We evaluated the known metabolic effects of aspirin in pregnant hypertensive patients. Eighty-seven pregnant women (12th–24th gestational week) were randomly allocated to low-dose aspirin or placebo treatment. Between the 24th–28th gestational week the following tests were performed: oral glucose tolerance test, venous blood pH and base excess, coagulation profile, platelet count, morning (8 a.m.) cortisol, creatinine clearance and serum uric acid. A significantly higher serum uric acid level was detected in the low-dose aspirin group (5.6±2.2 mg/dl) compared with the placebo group (4.7±1.2 mg/dl, p=0.048). No other significant difference was found for any of the other parameters tested. We conclude that low-dose aspirin treatment during the second half of pregnancy in hypertensive patients seems safe in terms of its effect on various maternal metabolic effects.
Keywords: Aspirin, low-dose, adverse effects, pregnancy, hypertension
DOI: 10.3233/JRS-1997-10404
Journal: International Journal of Risk and Safety in Medicine, vol. 10, no. 4, pp. 249-254, 1997
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