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β受体阻滞剂对蛛网膜下腔出血后的患者有益。

Beta-blockade benefits patients following a subarachnoid haemorrhage.

作者信息

Neil-Dwyer G, Walter P, Cruickshank J M

出版信息

Eur J Clin Pharmacol. 1985;28 Suppl:25-9. doi: 10.1007/BF00543706.

DOI:10.1007/BF00543706
PMID:2865145
Abstract

Previous studies have shown that ECG changes following a subarachnoid haemorrhage are associated with increased catecholamine levels, necrotic myocardial lesions, and a poor prognosis. Furthermore, beta-blockade using propranolol reverses some of the ECG changes and prevents necrotic myocardial lesions. This study was established to assess the affects of adrenergic blockade on morbidity and mortality following subarachnoid haemorrhage. Patients were admitted to the randomized double-blind between-patients study if they presented at the neurosurgical unit within 48 hours of a subarachnoid haemorrhage confirmed by lumbar puncture. Of 224 patients, the first 118 received an alpha-blocker, phentolamine 20 mg three-hourly, and either the beta-blocker propranolol 80 mg eight-hourly, or placebo. The last 106 patients received either propranolol or placebo. Treatment was continued for three weeks. Assessment at four weeks revealed significant improvements in the treated group for neurological deficit (p = 0.003) and death (p = 0.02). More treated patients underwent operation and those that did had a better outcome (p = 0.01). Assessment at one year showed that although patients had improved in both groups, patients in the treated group had significantly fewer neurological deficits (p = 0.003). There were fewer deaths in the treated group but this difference was not significant (p = 0.09). Possible mechanisms for this protective effect of propranolol may include a reduction in plasma renin activity, a reduction in pulmonary oedema, prevention of myocardial infarcts, and a reduction in cerebral oxygen requirements. It is concluded that early beta-blockade benefits patients with subarachnoid haemorrhage, in terms of fewer neurological deficits, for up to one year.

摘要

既往研究表明,蛛网膜下腔出血后的心电图改变与儿茶酚胺水平升高、坏死性心肌损害及预后不良有关。此外,使用普萘洛尔进行β受体阻滞可逆转部分心电图改变,并预防坏死性心肌损害。本研究旨在评估肾上腺素能阻滞对蛛网膜下腔出血后发病率和死亡率的影响。若患者在经腰椎穿刺证实蛛网膜下腔出血后48小时内就诊于神经外科病房,则纳入随机双盲患者间研究。224例患者中,前118例接受α受体阻滞剂酚妥拉明,每3小时20mg,以及β受体阻滞剂普萘洛尔每8小时80mg或安慰剂。最后106例患者接受普萘洛尔或安慰剂。治疗持续3周。4周时评估显示,治疗组在神经功能缺损(p = 0.003)和死亡(p = 0.02)方面有显著改善。更多接受治疗的患者接受了手术,且手术患者预后更好(p = 0.01)。1年时评估显示,尽管两组患者均有改善,但治疗组患者的神经功能缺损显著减少(p = 0.003)。治疗组死亡人数较少,但差异不显著(p = 0.09)。普萘洛尔这种保护作用的可能机制可能包括血浆肾素活性降低、肺水肿减轻、心肌梗死预防及脑氧需求减少。结论是,早期β受体阻滞对蛛网膜下腔出血患者有益,可减少神经功能缺损,长达1年。

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