Literature DB >> 16483184

Teratogenicity with angiotensin II receptor antagonists in pregnancy.

E Boix1, P Zapater, A Picó, O Moreno.   

Abstract

Angiotensin converting enzyme (ACE) inhibitors and angiotensin II (AT-II)-receptor-antagonists have been demonstrated to cause fetotoxicity when administered to women during the second and third trimester of pregnancy. Although use of ACE inhibitors during the first trimester of pregnancy seems to be safe, with no associated teratogenicity, there is not sufficient information regarding the safety of first-trimester exposure to AT-II-receptor-antagonists. We report a case of exencephaly and unilateral renal agenesia in a fetus of a diabetic woman who became pregnant while taking irbesartan.

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Year:  2005        PMID: 16483184     DOI: 10.1007/BF03345344

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  20 in total

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2.  Angiotensin-II-receptor inhibitors in pregnancy.

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3.  Defective embryogenesis with angiotensin II receptor antagonists in pregnancy.

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5.  Overview of randomised trials of diuretics in pregnancy.

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6.  Losartan and fetal toxic effects.

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7.  Evaluation of the reproductive and developmental toxicity of the AT1-selective angiotensin II receptor antagonist losartan in rats.

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8.  Angiotensin II-receptor-antagonists: further evidence of fetotoxicity but not teratogenicity.

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Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2003-08

Review 9.  ACE inhibitor fetopathy and hypocalvaria: the kidney-skull connection.

Authors:  M Barr; M M Cohen
Journal:  Teratology       Date:  1991-11

Review 10.  Teratogen update: angiotensin-converting enzyme inhibitors.

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  7 in total

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6.  Through the Lens of Chronic Kidney Disease: A Qualitative Study of the Experiences of Young Women Living With CKD.

Authors:  Heather Beanlands; Elizabeth McCay; Sheryll Pahati; Michelle A Hladunewich
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7.  Large-Conductance Calcium-Activated Potassium Channel Opener, NS1619, Protects Against Mesenteric Artery Remodeling Induced by Agonistic Autoantibodies Against the Angiotensin II Type 1 Receptor.

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  7 in total

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