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弥漫性外耳道炎:一项关于新型耳用溶液的多中心研究过程中的临床和微生物学发现

Diffuse otitis externa: clinical and microbiologic findings in the course of a multicenter study on a new otic solution.

作者信息

Cassisi N, Cohn A, Davidson T, Witten B R

出版信息

Ann Otol Rhinol Laryngol Suppl. 1977 May-Jun;86(3 Pt 3 Suppl 39):1-16. doi: 10.1177/00034894770863s201.

Abstract

This report reviews the literature on the epidemiology, pathogenesis and bacteriology of diffuse otitis externa. Four departments of otolaryngology undertook identical studies of these factors, as well as the efficacy and safety of two similar antibiotic-corticosteroid formulations; one a suspension and the other a clear solution. A total of 239 patients, or 283 ears, were studied, utilizing objective clinical as well as correlative bacteriologic criteria. A high degree of clinical and bacteriologic efficacy was demonstrated by the medications irrespective of the formulation, infecting organism, patient's age, length of disease history, severity, or geographic location. There was no statistical difference between either formulation, both achieving a clinical efficacy rate of 97% and a bacteriologic efficacy rate of 83%. Drug related side effects occurred in 1.9% of the patients given the solution and in 1.1% of those given the suspension.

摘要

本报告回顾了有关弥漫性外耳道炎的流行病学、发病机制和细菌学的文献。四个耳鼻喉科对这些因素以及两种相似的抗生素 - 皮质类固醇制剂(一种为混悬液,另一种为澄清溶液)的疗效和安全性进行了相同的研究。共对239例患者(或283只耳朵)进行了研究,采用了客观的临床标准以及相关的细菌学标准。无论制剂、感染微生物、患者年龄、病史长短、严重程度或地理位置如何,这些药物均显示出高度的临床和细菌学疗效。两种制剂之间无统计学差异,临床有效率均达到97%,细菌学有效率均为83%。接受溶液制剂的患者中1.9%出现与药物相关的副作用,接受混悬液制剂的患者中1.1%出现相关副作用。

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