verapamil successfully controls severe postpartum hypertension

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Verapamil Successfully Controls Severe Postpartum Hypertension According to a preliminary study Gestational protein uric hypertension can lead to increased risks of cerebrovascular accidents, cardiac and respiratory failure, renal and hepatic decompensation and blood-related abnormalities for the mother. Current management of postpartum hypertension involves the use of potent and toxic drugs and there are limited treatment options. Therefore, a preliminary open study was conducted to determine the efficacy of verapamil in the treatment of 10 women with severe postpartum gestational proteinuric hypertension (diastolic BP of 105mm Hg). All patients received IV verapamil infused initially at a rate of 40 mg/hour and titrated thereafter to achieve a diastolic BP of 80-100mm Hg. Once goal BP was achieved, patients changed to oral prazosin therapy. 30 min after beginning verapamil infusion, mean BP decreased from 192/123 to 133/85 (p < O.01/p < 0.02). The greatest decrease in BP was evident within the first 5 min of infusion and diastolic BP fell to < 100mm Hg in all patients within 15 min. HR did not change significantly over the infusion period. Two patients experienced facial flushing and 1 a worsened headache. The authors concluded that ' ... the use of Intravenously titrated verapamll Is a safe, rapidly effective and well·tolerated method of treating severe postpartum prote/nuric hypertension'. Belfort MA. Moore PJ South Af"can Medical Journal 74 265·267, 17 Sep 1988 1761 0156-2703/88/100HJ007/0$01.00/0 CI AD/s Press INPHAlWA" 1 Oct 1988 7

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Page 1: Verapamil Successfully Controls Severe Postpartum Hypertension

Verapamil Successfully Controls Severe Postpartum Hypertension According to a preliminary study

Gestational protein uric hypertension can lead to increased risks of cerebrovascular accidents, cardiac and respiratory failure, renal and hepatic decompensation and blood-related abnormalities for the mother. Current management of postpartum hypertension involves the use of potent and toxic drugs and there are limited treatment options. Therefore, a preliminary open study was conducted to determine the efficacy of verapamil in the treatment of 10 women with severe postpartum gestational proteinuric hypertension (diastolic BP of ~ 105mm Hg). All patients received IV verapamil infused initially at a rate of 40 mg/hour and titrated thereafter to achieve a diastolic BP of 80-100mm Hg. Once goal BP was achieved, patients changed to oral prazosin therapy.

30 min after beginning verapamil infusion, mean BP decreased from 192/123 to 133/85 (p < O.01/p < 0.02). The greatest decrease in BP was evident within the first 5 min of infusion and diastolic BP fell to < 100mm Hg in all patients within 15 min. HR did not change significantly over the infusion period. Two patients experienced facial flushing and 1 a worsened headache.

The authors concluded that ' ... the use of Intravenously titrated verapamll Is a safe, rapidly effective and well·tolerated method of treating severe postpartum prote/nuric hypertension'. Belfort MA. Moore PJ South Af"can Medical Journal 74 265·267, 17 Sep 1988 1761

0156-2703/88/100HJ007/0$01.00/0 CI AD/s Press INPHAlWA" 1 Oct 1988 7