速尿与螺内酯固定剂量联合应用治疗非数字化充血性心力衰竭。

Pharmatherapeutica Pub Date : 1986-01-01
J Yasky, G A Ledesma, A Tutera, L F Collia
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引用次数: 0

摘要

17例非数字化的充血性心力衰竭患者仅使用固定剂量的20mg呋塞米和50mg螺内酯或20mg呋塞米和100mg螺内酯,每日剂量1或2粒,持续4周。所选患者的严重程度等级在III级和IV级之间。其中10例患者有严重程度的呼吸困难。根据心力衰竭评分的降低、水肿的减轻程度和呼吸困难的缓解程度进行评估。测量的安全变量包括实验室、超声心动图和副作用监测。在为期4周的研究期结束时,心脏评分显著降低(46%至51%),呼吸困难完全缓解,对安全变量无不良影响。这些结果表明,在不同时使用洋地黄的情况下,用固定剂量联合产品安全治疗充血性心力衰竭患者是可能的。
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The treatment of non-digitalized congestive heart failure patients with a fixed-dose combination of furosemide and spironolactone.

Seventeen non-digitalized congestive heart failure patients were treated with only the fixed-dose combinations of 20 mg furosemide and 50 mg spironolactone or 20 mg furosemide and 100 mg spironolactone, in a daily dose of 1 or 2 capsules, over a 4-week period. The selected patients had a severity rating ranging between Grades III and IV. Ten of these patients had a severe grade of dyspnoea. Assessments were made on the basis of the reduction in cardiac failure score, extent of reduction in oedema, and relief of dyspnoea. Safety variables measured included laboratory, echocardiographic and side-effect monitoring. By the end of the 4-week study period, significant reduction (46% to 51%) in cardiac score and complete relief of dyspnoea with no adverse effects on safety variables were recorded. These results indicate that it is possible to treat patients with congestive heart failure safely with the fixed-dose combination product without the concurrent use of digitalis.

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