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用于治疗高血压的固定剂量复方药物:一项批判性综述。

Fixed-dose combination medications for the treatment of hypertension: a critical review.

作者信息

Oster J R, Epstein M

机构信息

Nephrology Section, VA Medical Center, Miami, FL 33125.

出版信息

J Clin Hypertens. 1987 Sep;3(3):278-93.

PMID:2889806
Abstract

Aside from the retrospective analysis of Clark and Troop (1), no large-scale controlled study has been designed specifically to assess the advantages and disadvantages of fixed-dose antihypertensive combinations. The use of fixed-dose antihypertensive combinations is no longer the anathema of the academician. The principal advantages of fixed-ratio combinations are simplicity of use, potentiation of blood-pressure-lowering efficacy, and potential counterbalancing of certain side effects. An additional advantage might be improvement in broad-based cost effectiveness, that is, a potential reduction in the need for frequent laboratory surveillance and in the frequency of office visits. The principal disadvantage is the relative inflexibility of dosage adjustment. Antihypertensive therapy should be initiated with a single drug preparation, with subsequent substitution of a combination product when appropriate. Tables 4 and 5 summarize, respectively, some of the important factors to consider and the theoretical requirements when contemplating the use of fixed-dose antihypertensive combinations. Diuretic/beta-blocker combinations are particularly attractive because of the enormous long-term experience with each component, their proven efficacy and additional salutary effects, their generally acceptable and sometimes offsetting side effects, and their potential for once-a-day dosing. It seems likely that CEI/diuretic and perhaps calcium-channel blocker/diuretic combinations also have great merit.

摘要

除了克拉克和特鲁普的回顾性分析(1)外,尚未专门设计大规模对照研究来评估固定剂量抗高血压联合用药的优缺点。固定剂量抗高血压联合用药已不再是学者们所忌讳的。固定比例联合用药的主要优点是使用简便、增强降压效果以及可能抵消某些副作用。另一个优点可能是提高总体成本效益,即有可能减少频繁进行实验室监测的需求以及门诊就诊的频率。主要缺点是剂量调整相对缺乏灵活性。抗高血压治疗应从单一药物制剂开始,随后在适当的时候改用联合产品。表4和表5分别总结了在考虑使用固定剂量抗高血压联合用药时需要考虑的一些重要因素和理论要求。利尿剂/β受体阻滞剂联合用药特别有吸引力,因为对每种成分都有丰富的长期经验,其已证实的疗效和额外的有益作用,其普遍可接受且有时相互抵消的副作用,以及每日一次给药的可能性。血管紧张素转换酶抑制剂/利尿剂以及或许钙通道阻滞剂/利尿剂联合用药似乎也有很大的优点。

相似文献

1
Fixed-dose combination medications for the treatment of hypertension: a critical review.用于治疗高血压的固定剂量复方药物:一项批判性综述。
J Clin Hypertens. 1987 Sep;3(3):278-93.
2
Combination antihypertensive drugs: recommendations for use.联合降压药物:使用建议
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3
[Fixed-dosage combinations in the treatment of hypertension].[固定剂量复方制剂治疗高血压]
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4
The effects of antihypertensive combination therapy on lipid and glucose metabolism: hydrochlorothiazide plus sotalol vs. hydrochlorothiazide plus captopril.降压联合治疗对脂质和葡萄糖代谢的影响:氢氯噻嗪加索他洛尔与氢氯噻嗪加卡托普利的对比
Int J Clin Pharmacol Ther. 1997 Jun;35(6):231-4.
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Fixed dose combinations of ACE inhibitors.血管紧张素转换酶抑制剂的固定剂量复方制剂
Br J Clin Pract. 1996 Dec;50(8):454-65.
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The choice of an initial antihypertensive agent.
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Shifting trends in the pharmacologic treatment of hypertension in a Nigerian tertiary hospital: a real-world evaluation of the efficacy, safety, rationality and pharmaco-economics of old and newer antihypertensive drugs.尼日利亚一家三级医院高血压药物治疗的趋势变化:对新旧抗高血压药物的疗效、安全性、合理性和药物经济学的真实世界评估
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Effects of a fixed-dose ACE inhibitor-diuretic combination on ambulatory blood pressure and arterial properties in isolated systolic hypertension.固定剂量血管紧张素转换酶抑制剂-利尿剂联合用药对单纯收缩期高血压患者动态血压及动脉特性的影响
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引用本文的文献

1
Low-dose combination therapy as first-line hypertension treatment for blacks and nonblacks.低剂量联合疗法作为黑人和非黑人高血压的一线治疗方法。
J Natl Med Assoc. 1999 Jan;91(1):40-8.
2
[Reserpine-diuretic combinations in therapy of arterial hypertension. Current considerations].[利血平-利尿剂联合用药治疗动脉高血压。当前的考量]
Med Klin (Munich). 1998 Dec 15;93(12):733-7. doi: 10.1007/BF03044812.
3
Fixed-dose combination antihypertensive drugs. Do they have a role in rational therapy?固定剂量复方抗高血压药物。它们在合理治疗中起作用吗?
Drugs. 1994 Jul;48(1):16-24. doi: 10.2165/00003495-199448010-00003.
4
Chronic antihypertensive treatment with captopril plus hydrochlorothiazide improves aortic distensibility in the spontaneously hypertensive rat.卡托普利联合氢氯噻嗪的慢性抗高血压治疗可改善自发性高血压大鼠的主动脉扩张性。
Br J Pharmacol. 1992 Nov;107(3):710-4. doi: 10.1111/j.1476-5381.1992.tb14511.x.