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西拉普利对高血压患者心脏收缩和舒张功能的影响。

The effect of cilazapril on systolic and diastolic cardiac function in hypertensive patients.

作者信息

Schneeweiss A, Green T, Krakuer J, Goldhamer E, Szucs T, Marmor A

机构信息

Geriatric Cardiology Research Foundation, Tel-Aviv, Israel.

出版信息

J Hum Hypertens. 1989 Aug;3(4):251-4.

PMID:2529375
Abstract

Diastolic function may be impaired in hypertensives even before alterations occur in systolic function. We studied the effect of a single dose of cilazapril, 5 mg orally, on systolic and diastolic cardiac function in 20 hypertensive patients using a double-blind crossover placebo controlled design. All patients had mild to moderate concentric left ventricular hypertrophy, preserved systolic function and long standing hypertension (for a period of 11.9 +/- 9.0 years). Radionuclide scintigraphy was performed with cilazapril and placebo, given one week apart. A two-week washout period of all cardioactive drugs preceded the study. Within one hour of oral administration of cilazapril blood pressure was significantly lowered. The absolute time to peak filling rate of the left ventricle, as well as the time to peak filling rate expressed as a percentage of diastole, were reduced from 176 +/- 34 to 158 +/- 33 msec (P less than 0.01) and from 46 +/- 10% to 37 +/- 8% (P less than 0.02) (reduction by 9% and 18.4%, respectively). Heart rate, left and right ventricular ejection fraction and peak filling rate was not significantly altered. Placebo had no significant effect. The effect of cilazapril is most probably related to afterload reduction. In conclusion; cilazapril seems to improve diastolic cardiac function in hypertensive patients. Long-term therapy may result in improvement of other, less sensitive indices of diastolic dysfunction.

摘要

高血压患者即使在收缩功能出现改变之前,舒张功能也可能已受损。我们采用双盲交叉安慰剂对照设计,研究了口服单剂量5毫克西拉普利对20例高血压患者心脏收缩和舒张功能的影响。所有患者均有轻度至中度向心性左心室肥厚、收缩功能保留且患有长期高血压(病程为11.9±9.0年)。分别在服用西拉普利和安慰剂一周后进行放射性核素闪烁扫描。在研究前,所有心血管活性药物均有两周的洗脱期。口服西拉普利后一小时内血压显著降低。左心室峰值充盈率的绝对时间以及以舒张期百分比表示的峰值充盈率时间,分别从176±34毫秒降至158±33毫秒(P<0.01),从46±10%降至37±8%(P<0.02)(分别降低9%和18.4%)。心率、左心室和右心室射血分数以及峰值充盈率均无显著改变。安慰剂无显著作用。西拉普利的作用很可能与降低后负荷有关。总之,西拉普利似乎可改善高血压患者的心脏舒张功能。长期治疗可能会使舒张功能障碍的其他不太敏感指标得到改善。

相似文献

1
The effect of cilazapril on systolic and diastolic cardiac function in hypertensive patients.西拉普利对高血压患者心脏收缩和舒张功能的影响。
J Hum Hypertens. 1989 Aug;3(4):251-4.
2
A single dose of cilazapril improves diastolic function in hypertensive patients.单次服用西拉普利可改善高血压患者的舒张功能。
Am J Med. 1989 Dec 26;87(6B):61S-63S. doi: 10.1016/0002-9343(89)90095-8.
3
The acute and chronic effects of cilazapril on cardiac function in hypertensive patients.西拉普利对高血压患者心脏功能的急慢性影响。
Kardiol Pol. 1990;33(8):13-6.
4
Comparative evaluation of the effect of afterload- and preload-reducing drugs on diastolic cardiac function in hypertensive patients.后负荷降低药物和前负荷降低药物对高血压患者舒张期心脏功能影响的比较评估
Cardiology. 1991;78(1):39-44. doi: 10.1159/000174763.
5
Comparative evaluation of the acute and chronic effects of cilazapril and hydrochlorothiazide on diastolic cardiac function in hypertensive patients.西拉普利和氢氯噻嗪对高血压患者舒张期心功能急性和慢性影响的比较评价
J Hum Hypertens. 1990 Oct;4(5):535-9.
6
Long-term evaluation of cilazapril in severe hypertension. Assessment of left ventricular and renal function.西拉普利治疗重度高血压的长期评估。左心室和肾功能评估。
Am J Med. 1989 Dec 26;87(6B):56S-60S.
7
[Effect of cilazapril therapy on diastolic filling and left ventricular hypertrophy in patients with arterial hypertension].[西拉普利治疗对动脉高血压患者舒张期充盈及左心室肥厚的影响]
Minerva Cardioangiol. 1993 May;41(5):205-9.
8
The 24 h blood pressure responses of hypertensives to a once-a-day cilazapril regimen.
Can J Cardiol. 1990 Mar;6(2):53-8.
9
Antihypertensive duration of action of cilazapril in patients with mild to moderate essential hypertension.
Drugs. 1991;41 Suppl 1:31-6. doi: 10.2165/00003495-199100411-00007.
10
Comparative effects of captopril and nifedipine on diastolic and systolic cardiac function in elderly hypertensive patients.卡托普利与硝苯地平对老年高血压患者舒张和收缩心脏功能的比较效应
J Hypertens Suppl. 1988 Nov;6(1):S101-3.

引用本文的文献

1
Cilazapril. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in cardiovascular disease.
Drugs. 1991 May;41(5):799-820. doi: 10.2165/00003495-199141050-00008.