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慢性阻塞性肺疾病急性加重期肺炎支原体感染的血清学证据。

Serological evidence of Mycoplasma pneumoniae infection in acute exacerbation of COPD.

作者信息

Lieberman David, Lieberman Devora, Ben-Yaakov M, Shmarkov O, Gelfer Y, Varshavsky R, Ohana B, Lazarovich Z, Boldur I

机构信息

Pulmonary Unit, Soroka Medical Center and the Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

出版信息

Diagn Microbiol Infect Dis. 2002 Sep;44(1):1-6. doi: 10.1016/s0732-8893(02)00421-2.

Abstract

A prospective study was conducted to identify and characterize hospitalizations for acute exacerbation of chronic obstructive pulmonary disease (AECOPD) with serologic evidence of infection with Mycoplasma pneumoniae (Mp). Two hundred forty hospitalizations for AECOPD were included in a 17-month prospective study. Paired sera were obtained for each of the hospitalizations and were tested serologically for Mp using a commercial enzyme immunoassay (EIA) kit. Only significant changes, according to the formula in the manufacturer's instructions, in antibody titers for IgM and/or IgG and/or IgA were considered diagnostic for Mp infection. In 34 hospitalizations (14.2%) the serologic tests for Mp were positive (MpH). In 29 of these hospitalizations (85%) a significant change in IgA was found. In 11 of these hospitalizations (32%) the only change identified was in IgA. In 24 MpH (71%) there was serologic evidence for infection with at least one other respiratory pathogen. In comparison to the 206 hospitalizations without serologic evidence of infection with Mp, MpH had higher rates of inhaled steroid therapy (41% vs. 24%, p = 0.033) and a longer time interval between the appearance of dyspnea and hospitalization (6.6 +/- 3.8 days vs. 5.0 +/- 3.5 days, p = 0.012). There were no significant differences between these two groups in a broad spectrum of patient- and exacerbation-related clinical variables. Specific antibiotic therapy for Mp in the MpH group did not shorten the hospital stay. Serologic evidence of Mp infection is common in patients hospitalized for AECOPD, and is usually based on changes in specific IgA antibody titers. In most MpH another respiratory pathogen can be identified. The vast majority of clinical characteristics are the same in patients with and without serologic evidence of infection with Mp. The practical implications of these findings should be clarified in further studies.

摘要

进行了一项前瞻性研究,以识别和描述伴有肺炎支原体(Mp)感染血清学证据的慢性阻塞性肺疾病急性加重(AECOPD)的住院情况。在一项为期17个月的前瞻性研究中纳入了240例AECOPD住院病例。为每例住院患者采集配对血清,并使用商用酶免疫测定(EIA)试剂盒进行Mp血清学检测。根据制造商说明书中的公式,仅IgM和/或IgG和/或IgA抗体滴度的显著变化被视为Mp感染的诊断依据。在34例住院病例(14.2%)中,Mp血清学检测呈阳性(MpH)。在其中29例住院病例(85%)中发现IgA有显著变化。在其中11例住院病例(32%)中,唯一确定的变化是IgA。在24例MpH(71%)中,有至少一种其他呼吸道病原体感染的血清学证据。与206例无Mp感染血清学证据的住院病例相比,MpH吸入类固醇治疗的比例更高(41%对24%,p = 0.033),且出现呼吸困难至住院的时间间隔更长(6.6±3.8天对5.0±3.5天,p = 0.012)。在广泛的患者及加重相关临床变量方面,这两组之间没有显著差异。MpH组针对Mp的特异性抗生素治疗并未缩短住院时间。Mp感染的血清学证据在因AECOPD住院的患者中很常见,且通常基于特异性IgA抗体滴度的变化。在大多数MpH病例中可识别出另一种呼吸道病原体。有和无Mp感染血清学证据的患者的绝大多数临床特征相同。这些发现的实际意义应在进一步研究中阐明。

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