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非住院患者中产超广谱β-内酰胺酶细菌产生的危险因素。

Risk factors for the development of extended-spectrum beta-lactamase-producing bacteria in nonhospitalized patients.

作者信息

Colodner R, Rock W, Chazan B, Keller N, Guy N, Sakran W, Raz R

机构信息

Clinical Microbiology Laboratory, Ha'Emek Medical Center, 18101 Afula, Israel.

出版信息

Eur J Clin Microbiol Infect Dis. 2004 Mar;23(3):163-7. doi: 10.1007/s10096-003-1084-2. Epub 2004 Feb 19.

Abstract

Although the risk factors for acquiring infection by extended-spectrum beta-lactamase (ESBL)-producing bacteria have been investigated in hospitalized patients, such risk factors have not been defined in the community setting. In this study, clinical data from a total of 311 nonhospitalized patients with community-acquired urinary tract infection (128 with ESBL-positive strains and 183 with ESBL-negative strains) were obtained. According to a multivariate analysis, the following were identified as independent risk factors: previous hospitalization in the past 3 months (OR=8.95, 95%CI, 3.77-21.25), antibiotic treatment in the past 3 months (OR=3.23, 95%CI, 1.76-5.91), age over 60 years (OR=2.65, 95%CI, 1.45-4.83), diabetes (OR=2.57, 95%CI, 1.20-5.51), male gender (OR=2.47, 95%CI, 1.22-5.01), Klebsiella pneumoniae infection (OR=2.31, 95%CI, 1.17-4.54), previous use of third-generation cephalosporins (P=0.014, OR=15.8, 95%CI, 1.7-143), previous use of second-generation cephalosporins (P<0.0001, OR=10.1, 95%CI, 4.2-24), previous use of quinolones (P=0.001, OR=4.1, 95%CI, 1.8-9.0), and previous use of penicillin (P=0.003, OR=4.0, 95%CI, 1.6-9.0).

摘要

尽管已对住院患者感染产超广谱β-内酰胺酶(ESBL)细菌的风险因素进行了研究,但在社区环境中尚未明确此类风险因素。在本研究中,获取了总共311例社区获得性尿路感染的非住院患者的临床数据(128例为ESBL阳性菌株感染,183例为ESBL阴性菌株感染)。根据多变量分析,确定以下为独立风险因素:过去3个月内曾住院(OR = 8.95,95%CI,3.77 - 21.25)、过去3个月内接受抗生素治疗(OR = 3.23,95%CI,1.76 - 5.91)、年龄超过60岁(OR = 2.65,95%CI,1.45 - 4.83)、糖尿病(OR = 2.57,95%CI,1.20 - 5.51)、男性(OR = 2.47,95%CI,1.22 - 5.01)、肺炎克雷伯菌感染(OR = 2.31,95%CI,1.17 - 4.54)、既往使用第三代头孢菌素(P = 0.014,OR = 15.8,95%CI,1.7 - 143)、既往使用第二代头孢菌素(P < 0.0001,OR = 10.1,95%CI,4.2 - 24)、既往使用喹诺酮类药物(P = 0.001,OR = 4.1,95%CI,1.8 - 9.0)以及既往使用青霉素(P = 0.003,OR = 4.0,95%CI,1.6 - 9.0)。

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