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高血压患者服用卡托普利(开博通)治疗的观察(为期一年)。

Observations with captopril (Tensiomin) treatment in hypertensive patients (one-year period).

作者信息

Bányai T, Gyimesi A, Pocsay G, Iványi J

出版信息

Ther Hung. 1989;37(3):144-50.

PMID:2686089
Abstract

In the treatment of patients suffering from therapy-resistant hypertension the angiotensin converting enzyme inhibitor captopril seems to be one of the most promising drugs of the past decade. The authors examined and followed the effect of captopril (Tensiomin) for one year in 13 severe therapy-resistant hypertensive patients. The average arterial blood pressure of 12 patients suffering from essential hypertension and 1 patient with renal hypertension was, before the introduction of captopril therapy, 215/120 mmHg (SD +/- 23/18). At the end of the one-year examination period the average blood pressure was 186/111 mmHg (SD +/- 25/19). The acute effect of captopril was found to be very favourable, and the required blood pressure fall could be obtained during its long-term use even in cases of renal failure. Except for one case multiple combination therapy had to be applied in all patients for the moderation of blood pressure (in 5 cases 4, in 2 cases 5, in 1 case 6 drugs). The long-term use of the drug did not influence notably the serum potassium-carbamide-creatinine and SGOT values or the white blood cell count. On the basis of their results the authors emphasize that the therapeutic effectivity of captopril monotherapy is not sufficient in severe therapy-resistant hypertension cases, its adjuvant action may be expected in drug combinations. With daily doses lower than 200 mg demonstrable side-effects did not occur.

摘要

在治疗顽固性高血压患者时,血管紧张素转换酶抑制剂卡托普利似乎是过去十年中最有前景的药物之一。作者对13例重度顽固性高血压患者使用卡托普利(开博通)进行了为期一年的检查和跟踪。12例原发性高血压患者和1例肾性高血压患者在开始卡托普利治疗前的平均动脉血压为215/120 mmHg(标准差±23/18)。在为期一年的检查期结束时,平均血压为186/111 mmHg(标准差±25/19)。发现卡托普利的急性效果非常好,即使在肾衰竭病例中,长期使用该药物也能使血压下降至所需水平。除1例患者外,所有患者都必须采用多种联合治疗来控制血压(5例使用4种药物,2例使用5种药物,1例使用6种药物)。长期使用该药物对血清钾、尿素、肌酐、谷草转氨酶值或白细胞计数没有显著影响。基于他们的研究结果,作者强调,在重度顽固性高血压病例中,卡托普利单一疗法的治疗效果并不充分,在联合用药中可能期望其起到辅助作用。每日剂量低于200 mg时未出现明显的副作用。

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