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血管迷走性晕厥:普萘洛尔、纳多洛尔和安慰剂对晕厥复发及患者健康影响的前瞻性、随机、交叉评估

Vasovagal syncope: a prospective, randomized, crossover evaluation of the effect of propranolol, nadolol and placebo on syncope recurrence and patients' well-being.

作者信息

Flevari Panagiota, Livanis Efthimios G, Theodorakis George N, Zarvalis Elias, Mesiskli Theoni, Kremastinos Dimitrios Th

机构信息

Second Department of Cardiology, Onassis Cardiac Surgery Center, Athens, Greece.

出版信息

J Am Coll Cardiol. 2002 Aug 7;40(3):499-504. doi: 10.1016/s0735-1097(02)01974-5.

Abstract

OBJECTIVES

We sought to assess the relative therapeutic efficacy of propranolol, nadolol and placebo in recurrent vasovagal syncope (VVS).

BACKGROUND

Central and peripheral mechanisms have been implicated in the pathogenesis of VVS. Propranolol, nadolol and placebo have different sites of action on central and/or peripheral mechanisms. It has not yet been clarified whether one of the aforementioned treatments is more efficient than the others in reducing clinical episodes and exerting a beneficial effect on patients' well-being.

METHODS

We studied 30 consecutive patients with recurrent VVS and a positive head-up tilt test. All were serially and randomly assigned to propranolol, nadolol or placebo. Therapy with each drug lasted three months. On the day of drug crossover, patients reported the total number of syncopal and presyncopal attacks during the previous period. They also gave a general assessment of their quality of life, taking into account: 1) symptom recurrence; 2) drug side effects; and 3) their personal well-being during therapy (scale 0 to 4: 0 = very bad/discontinuation; 1 = bad; 2 = good; 3 = very good; 4 = excellent). At the end of the nine-month follow-up period, they reported whether they preferred a specific treatment over the others.

RESULTS

Spontaneous syncopal and presyncopal episode recurrence during each three-month follow-up period was reduced by all drugs tested (analysis of variance [ANOVA]: chi-square = 67.4, p < 0.0001 for syncopal attacks; chi-square = 60.1, p < 0.0001 for presyncopal attacks) No differences were observed in the recurrence of syncope and presyncope among the three drugs. All drugs improved the patients' well-being (ANOVA: chi-square = 61.9, p < 0.0001).

CONCLUSIONS

Propranolol, nadolol and placebo are equally effective treatments in VVS, as demonstrated by a reduction in the recurrence of syncope and presyncope, as well as an improvement in the patients' well-being.

摘要

目的

我们旨在评估普萘洛尔、纳多洛尔和安慰剂在复发性血管迷走性晕厥(VVS)中的相对治疗效果。

背景

中枢和外周机制与VVS的发病机制有关。普萘洛尔、纳多洛尔和安慰剂在中枢和/或外周机制上有不同的作用位点。上述治疗方法中是否有一种在减少临床发作和对患者健康产生有益影响方面比其他方法更有效,目前尚未明确。

方法

我们研究了30例连续的复发性VVS且直立倾斜试验阳性的患者。所有患者均被连续随机分配接受普萘洛尔、纳多洛尔或安慰剂治疗。每种药物的治疗持续三个月。在药物交叉当天,患者报告前一时期晕厥和晕厥前发作的总数。他们还对自己的生活质量进行了总体评估,考虑因素包括:1)症状复发;2)药物副作用;3)治疗期间的个人健康状况(0至4分:0 = 非常差/停药;1 = 差;2 = 好;3 = 非常好;4 = 优秀)。在九个月的随访期结束时,他们报告是否更喜欢某一种特定治疗方法。

结果

所有测试药物均使每三个月随访期内的自发性晕厥和晕厥前发作复发率降低(方差分析[ANOVA]:晕厥发作的卡方值 = 67.4,p < 0.0001;晕厥前发作的卡方值 = 60.1,p < 0.0001)。三种药物在晕厥和晕厥前发作的复发率方面未观察到差异。所有药物均改善了患者的健康状况(ANOVA:卡方值 = 61.9,p < 0.0001)。

结论

普萘洛尔、纳多洛尔和安慰剂在VVS中是同样有效的治疗方法,这体现在晕厥和晕厥前发作复发率降低以及患者健康状况改善方面。

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