CHOLINESTERASE DEFICIENCY AND THE CHURG-STRAUSS-SYNDROME

被引：6
|
作者：
TAYLOR, BL
WHITTAKER, M
VANHEERDEN, V
BRITTEN, J
机构：
[1] ROYAL CHILDRENS HOSP,PARKVILLE,VIC 3052,AUSTRALIA
[2] ROYAL DEVON & EXETER HOSP,ANAESTHET,EXETER EX2 5DW,DEVON,ENGLAND
[3] UNIV EXETER,DEPT CHEM,EXETER EX4 4DQ,ENGLAND
[4] HAMMERSMITH HOSP,CHOLINESTERASE RES UNIT,LONDON W12 0HS,ENGLAND
来源：
ANAESTHESIA | 1990年 / 45卷 / 08期
关键词：
Complications; Churg‐Strauss syndrome; Enzymes; cholinesterase;
D O I：
10.1111/j.1365-2044.1990.tb14390.x
中图分类号：
R614 [麻醉学];
学科分类号：
100217 ;
摘要：
We report two patients with the Churg–Strauss syndrome who were found to have decreased cholinesterase activity despite normal phenotypes. Suspicion of abnormal sensitivity to suxamethonium in the first case was raised after prolonged paralysis under anaesthesia. The findings in the second were incidental during the course of intensive care treatment. Both patients received immunosuppressive therapy. Differentiation between the effects of this and the disease process itself cannot be established. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
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页码：649 / 652
页数：4
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