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哌唑嗪与普萘洛尔在嗜铬细胞瘤术前管理中的应用

Prazosin and propranolol in preoperative management of pheochromocytoma.

作者信息

Cubeddu L X, Zarate N A, Rosales C B, Zschaeck D W

出版信息

Clin Pharmacol Ther. 1982 Aug;32(2):156-60. doi: 10.1038/clpt.1982.141.

DOI:10.1038/clpt.1982.141
PMID:7094503
Abstract

Combined use of prazosin and propranolol was effective in preoperative management of three patients with norepinephrine(NE)-secreting pheochromocytoma (PHEO). On admission, all were symptomatic and had moderate to severe hypertension despite treatment with diuretics, propranolol, and sympatholytics. Optimal symptomatic and blood pressure (BP) control was achieved with 6 to 10 mg/day prazosin and 120 to 480 mg/day propranolol every 6 hr in equally divided doses. With this therapy, BP and hematocrit were reduced to levels similar to those found in the postoperative period. The daily urinary excretion of catecholamines and their metabolites was not modified during therapy with prazosin and propranolol. There was a drop in supine systolic (40 to 64 mm Hg) and diastolic (32 to 52 mm Hg) BP in all patients 1 to 2 hr after the first dose of prazosin (1-mg tablet); in two subjects this was accompanied by a larger orthostatic fall (74 and 92 mm Hg systolic; 65 and 78 mm Hg diastolic BP). The high incidence of first-dose effect suggests that a single oral dose of 1 mg of prazosin could aid in the diagnosis of PHEO. The effectiveness of prazosin in controlling the hypertension induced by NE-secreting PHEO suggests that, in man, pressure responses to augmented levels of NE are mediated solely through alpha 1-receptors.

摘要

哌唑嗪与普萘洛尔联合使用对3例分泌去甲肾上腺素(NE)的嗜铬细胞瘤(PHEO)患者的术前管理有效。入院时,尽管使用了利尿剂、普萘洛尔和抗交感神经药,但所有患者均有症状且患有中度至重度高血压。通过每6小时给予6至10毫克/天的哌唑嗪和120至480毫克/天的普萘洛尔,分等量剂量服用,实现了最佳的症状控制和血压(BP)控制。采用这种治疗方法,血压和血细胞比容降至与术后时期相似的水平。在使用哌唑嗪和普萘洛尔治疗期间,儿茶酚胺及其代谢产物的每日尿排泄量未发生改变。所有患者在服用第一剂哌唑嗪(1毫克片剂)后1至2小时,仰卧位收缩压(40至64毫米汞柱)和舒张压(32至52毫米汞柱)均下降;在两名受试者中,这伴随着更大的直立性下降(收缩压分别为74和92毫米汞柱;舒张压分别为65和78毫米汞柱)。首剂效应的高发生率表明,单次口服1毫克哌唑嗪可能有助于PHEO的诊断。哌唑嗪在控制由分泌NE的PHEO引起的高血压方面的有效性表明,在人类中,对NE水平升高的压力反应仅通过α1受体介导。

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