Literature DB >> 3326631

Hypertension in pregnancy: whom and how to treat.

W F Lubbe1.   

Abstract

1. Elucidation of some of the mechanisms responsible for blood pressure elevation in pregnancy has permitted therapy to be based on more rational principles. The decreased arterial reactivity encountered in normotensive pregnancy is most likely mediated by prostaglandins; preventive therapy using low dose aspirin is an option to prevent development of proteinuria in pre-existing hypertension and provide prophylaxis against pregnancy-induced hypertension. 2. Antihypertensive therapy utilizing sympathetic inhibition with either methyldopa or alpha- and beta-adrenoceptor blockade yields the most promising results. Vasodilation with hydralazine, calcium entry blockers (nifedipine), intravenous labetalol or diazoxide is primarily used in severely hypertensive patients. The use of orally administered nifedipine in severely hypertensive women is associated with encouraging results. 3. It is clear that women with blood pressure levels greater than 170/110 mm Hg need antihypertensive therapy for maternal safety; it remains to be proven to what extent foetal growth and welfare can be improved in women with diastolic pressure levels 85-110 mm Hg when adrenoceptor blocking agents are used for blood pressure control. Initial studies are suggestive of improved foetal growth, prevention of proteinuria and the respiratory distress syndrome but more long-term controlled studies are required. 4. In a recent study, at our institution, of foetal growth during long term antihypertensive therapy, treatment with pindolol yielded better foetal growth than therapy with atenolol. It is as yet unclear whether the ISA or beta 2-mediated vasodilation associated with pindolol was responsible for the improved foetal growth. Further controlled studies are indicated in hypertension in pregnancy to confirm the suggested benefits of beta-adrenoceptor blocker therapy.

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Year:  1987        PMID: 3326631      PMCID: PMC1386203          DOI: 10.1111/j.1365-2125.1987.tb03263.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  10 in total

1.  Preeclampsia: an imbalance in placental prostacyclin and thromboxane production.

Authors:  S W Walsh
Journal:  Am J Obstet Gynecol       Date:  1985-06-01       Impact factor: 8.661

2.  Prevention of pre-eclampsia by early antiplatelet therapy.

Authors:  M Beaufils; S Uzan; R Donsimoni; J C Colau
Journal:  Lancet       Date:  1985-04-13       Impact factor: 79.321

Review 3.  Antihypertensive drugs in pregnancy.

Authors:  R P Naden; C W Redman
Journal:  Clin Perinatol       Date:  1985-10       Impact factor: 3.430

4.  A prospective study of blood pressure in pregnancy: prediction of preeclampsia.

Authors:  J M Moutquin; C Rainville; L Giroux; P Raynauld; G Amyot; R Bilodeau; N Pelland
Journal:  Am J Obstet Gynecol       Date:  1985-01-15       Impact factor: 8.661

Review 5.  Hypertension in pregnancy. Pathophysiology and management.

Authors:  W F Lubbe
Journal:  Drugs       Date:  1984-08       Impact factor: 9.546

6.  Labetalol for the treatment of hypertension in pregnancy. Pharmacokinetics and effects on the uteroplacental blood flow.

Authors:  L Nylund; N O Lunell; R Lewander; B Sarby; S Thornström
Journal:  Acta Obstet Gynecol Scand Suppl       Date:  1984

Review 7.  Hypertension in pregnancy: definitions, familial factor, and remote prognosis.

Authors:  L C Chesley
Journal:  Kidney Int       Date:  1980-08       Impact factor: 10.612

8.  Placebo-controlled trial of atenolol in treatment of pregnancy-associated hypertension.

Authors:  P C Rubin; L Butters; D M Clark; B Reynolds; D J Sumner; D Steedman; R A Low; J L Reid
Journal:  Lancet       Date:  1983-02-26       Impact factor: 79.321

9.  Platelet activation in preeclampsia.

Authors:  M L Socol; C P Weiner; G Louis; K Rehnberg; E C Rossi
Journal:  Am J Obstet Gynecol       Date:  1985-02-15       Impact factor: 8.661

10.  Comparison of the alpha and beta blocking drug, labetalol, and methyl dopa in the treatment of moderate and severe pregnancy-induced hypertension.

Authors:  G D Lamming; F Broughton Pipkin; E M Symonds
Journal:  Clin Exp Hypertens       Date:  1980       Impact factor: 1.749

  10 in total

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