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青霉素对全科医疗中链球菌性咽炎临床病程的影响。

Effect of penicillin on the clinical course of streptococcal pharyngitis in general practice.

作者信息

De Meyere M, Mervielde Y, Verschraegen G, Bogaert M

机构信息

Department of General Practice, University Gent, Belgium.

出版信息

Eur J Clin Pharmacol. 1992;43(6):581-5. doi: 10.1007/BF02284954.

Abstract

The aim of the study was to explore whether penicillin was superior to placebo in altering the clinical course of proven streptococcal pharyngitis. A randomised, parallel, double blind placebo controlled trial of 10 days duration was undertaken in 42 general practices in the Gent region (Flemish part of Belgium). Phenoxymethylpenicillin (adults 250 mg t.i.d. and children 125 mg t.i.d.) or placebo were administrated to 173 patients, aged 5 to 50 y, with acute sore throat and a positive culture for Group A beta-haemolytic streptococci. Penicillin and placebo tablets were identical. Patient compliance was monitored by assay of penicillin in urine (Sarcina lutea method). The primary outcome variable was sore throat as recorded by the physician on Day 3. The experiences of the patients themselves over the 10 day period were also assessed. Secondary outcome variables were other local and general symptoms and signs of streptococcal throat infection. In the penicillin group on Day 3, 23.2% of the patients still complained of sore throat versus 65.9% in the placebo group: difference 42.7% (C.I. 29.4%, 56.1%). This finding was confirmed by survival analysis of the symptom 'sore throat', as recorded by the patients. The physicians recorded on Day 3 a significant positive effect on another symptom (malaise: P < 0.04) and certain clinical signs (abnormal throat: P < 0.07; and redness of throat: P < 0.003). Penicillin had more adverse effects than placebo (P < 0.007). It also inhibited the rise in ASLO (P < 0.001). In this study in general practice, penicillin had a slight but definitive positive effect on the clinical evolution of streptococcal pharyngitis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

该研究的目的是探究青霉素在改变已确诊的链球菌性咽炎临床病程方面是否优于安慰剂。在比利时弗拉芒地区根特市的42家全科诊所进行了一项为期10天的随机、平行、双盲安慰剂对照试验。173名年龄在5至50岁、患有急性咽痛且A组β溶血性链球菌培养呈阳性的患者,被给予苯氧甲基青霉素(成人250毫克每日三次,儿童125毫克每日三次)或安慰剂。青霉素和安慰剂片剂外观相同。通过尿液中青霉素检测(藤黄八叠球菌法)监测患者的依从性。主要结局变量是医生在第3天记录的咽痛情况。同时也评估了患者在10天期间自身的体验。次要结局变量是链球菌性咽喉感染的其他局部和全身症状及体征。在第3天,青霉素组中23.2%的患者仍诉说有咽痛,而安慰剂组为65.9%:差异为42.7%(置信区间29.4%,56.1%)。患者记录的“咽痛”症状的生存分析证实了这一发现。医生在第3天记录到对另一症状(不适:P<0.04)和某些临床体征(咽喉异常:P<0.07;咽喉发红:P<0.003)有显著的积极影响。青霉素的不良反应比安慰剂更多(P<0.007)。它还抑制了抗链球菌溶血素O(ASLO)的升高(P<0.001)。在这项全科诊所研究中,青霉素对链球菌性咽炎的临床进展有轻微但明确的积极作用。(摘要截选至250词)

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