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阿奇霉素三日疗程治疗中度重症社区获得性肺炎的疗效

Efficacy of a three day course of azithromycin in moderately severe community-acquired pneumonia.

作者信息

Rizzato G, Montemurro L, Fraioli P, Montanari G, Fanti D, Pozzoli R, Magliano E

机构信息

Ente Ospedale Niguarda, Centro Thorax Divisione Medica Vergani e Servizio di Microbiologia, Milan, Italy.

出版信息

Eur Respir J. 1995 Mar;8(3):398-402. doi: 10.1183/09031936.95.08030398.

Abstract

This study was designed to evaluate the efficacy of a 3 day course of azithromycin in low to moderately severe community-acquired pneumonia. Forty patients with low to moderately severe community-acquired pneumonia (29 males, 11 females, mean age 46 +/- 17 yrs; 20 pretreated with betalactams for 2-10 days with no results before admission to hospital; 18 with evidence of co-morbidity) were enrolled in an open, randomized study with azithromycin, 500 mg q.d. oral therapy for 3 days, versus clarithromycin, 250 mg b.i.d. oral therapy for 10 +/- 2 days. The aetiology of pneumonia was identified in 18 patients by serology (nine Mycoplasma pneumoniae, four Chlamydia pneumoniae, five Legionella pneumophila; one patient with chlamydial infection also had Klebsiella pneumoniae bacteraemia). A presumptive aetiological diagnosis was obtained with sputum culture in three other patients (one Haemophilus influenzae, two Haemophilus parainfluenzae), all strains were sole isolates with 10(8) Colony forming units (CFU), and with Gram stain in one patient with Streptococcus pneumoniae. All patients in the azithromycin group (one after a second 3 day course), and all but two (of those available for evaluation) of the clarithromycin group were cured. Defervescence occurred after 2.6 +/- 1.6 days, and chest roentgenogram cleared after 8.9 +/- 3.3 days, with no difference between the two groups. Tolerance was good, and there were no withdrawals from therapy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在评估阿奇霉素3日疗程治疗轻至中度社区获得性肺炎的疗效。40例轻至中度社区获得性肺炎患者(男29例,女11例,平均年龄46±17岁;20例入院前接受β-内酰胺类药物治疗2 - 10天无效;18例有合并症)被纳入一项开放性随机研究,比较阿奇霉素500mg每日1次口服治疗3天与克拉霉素250mg每日2次口服治疗10±2天的疗效。18例患者通过血清学确定肺炎病因(9例肺炎支原体、4例肺炎衣原体、5例嗜肺军团菌;1例衣原体感染患者同时有肺炎克雷伯菌菌血症)。另外3例患者通过痰培养获得推测性病因诊断(1例流感嗜血杆菌、2例副流感嗜血杆菌),所有菌株均为单一分离株,菌落形成单位为10⁸CFU,1例肺炎链球菌患者通过革兰氏染色确诊。阿奇霉素组所有患者(1例接受第二个3日疗程后)以及克拉霉素组除2例(可供评估者)外的所有患者均治愈。退热发生于2.6±1.6天,胸部X线片在8.9±3.3天恢复正常,两组之间无差异。耐受性良好,无治疗中断情况。(摘要截选至250字)

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