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囊性纤维化患者中嗜麦芽窄食单胞菌出现的危险因素。

Risk factors for emergence of Stenotrophomonas maltophilia in cystic fibrosis.

作者信息

Talmaciu I, Varlotta L, Mortensen J, Schidlow D V

机构信息

Cystic Fibrosis Center, St. Christopher's Hospital for Children, Department of Pediatrics, Medical College of Pennsylvania, Hahnemann University School of Medicine, Philadelphia, Pennsylvania.

出版信息

Pediatr Pulmonol. 2000 Jul;30(1):10-5. doi: 10.1002/1099-0496(200007)30:1<10::aid-ppul3>3.0.co;2-q.

Abstract

The number of patients with cystic fibrosis (CF) whose sputum culture has yielded Stenotrophomonas maltophilia has increased in the last 5 years at St. Christopher's Hospital for Children. We conducted a case-control study to determine risk factors for recovery of S. maltophilia in respiratory secretions from patients with CF. We reviewed the outpatient and inpatient records of patients colonized with S. maltophilia between 1993 and 1997, and of age-matched (at time of initial recovery of S. maltophilia) control patients with CF who had never had a positive sputum culture for S. maltophilia. Variables included age at time of CF diagnosis, gender, severity of CF (based on Shwachman-Kulczycki (S-K) scores and spirometry), frequency of hospitalizations, use of oral, intravenous, or inhaled antibiotics, and use of oral or inhaled corticosteroids in the 2 years prior to the first isolation of S. maltophilia from respiratory secretions. Statistical methods included stepwise logistic regression to determine risk factors for acquisition of S. maltophilia. During the study period, 58 patients with CF had a positive sputum or deep throat culture for S. maltophilia. The distribution of S. maltophilia acquisition by year increased from 7 patients in 1993 (incidence, 2.8%) to 16 in 1997 (incidence, 6.2%). Patients positive for S. maltophilia were found to have significantly worse growth parameters, S-K score, and spirometric values than S. maltophilia-negative CF controls (P < 0.05). Stepwise logistic regression demonstrated that treatment with long-term antibiotics (P = 0.0016) and number of days of intravenous antibiotic therapy (P = 0.035) were significant risk factors for S. maltophilia colonization in our group of CF patients. We conclude that patients with CF whose respiratory secretions yield S. maltophilia have an overall worse clinical status at the time of initial S. maltophilia isolation than noncolonized patients, and that preceding treatment with antibiotics may have predisposed them to the acquisition of this bacterium in their respiratory secretions.

摘要

在过去5年里,圣克里斯托弗儿童医院痰液培养出嗜麦芽窄食单胞菌的囊性纤维化(CF)患者数量有所增加。我们进行了一项病例对照研究,以确定CF患者呼吸道分泌物中嗜麦芽窄食单胞菌检出的危险因素。我们查阅了1993年至1997年间嗜麦芽窄食单胞菌定植患者以及年龄匹配(在首次检出嗜麦芽窄食单胞菌时)的从未有过嗜麦芽窄食单胞菌痰培养阳性的CF对照患者的门诊和住院记录。变量包括CF诊断时的年龄、性别、CF严重程度(基于施瓦克曼 - 库尔奇茨基(S - K)评分和肺功能测定)、住院频率、在首次从呼吸道分泌物中分离出嗜麦芽窄食单胞菌前2年使用口服、静脉或吸入抗生素的情况以及使用口服或吸入皮质类固醇的情况。统计方法包括逐步逻辑回归以确定嗜麦芽窄食单胞菌感染的危险因素。在研究期间,58例CF患者痰或咽拭子培养出嗜麦芽窄食单胞菌阳性。嗜麦芽窄食单胞菌感染的年度分布从1993年的7例(发病率2.8%)增加到1997年的16例(发病率6.2%)。发现嗜麦芽窄食单胞菌阳性患者的生长参数、S - K评分和肺功能测定值明显比嗜麦芽窄食单胞菌阴性的CF对照患者差(P < 0.05)。逐步逻辑回归表明,长期使用抗生素治疗(P = 0.0016)和静脉抗生素治疗天数(P = 0.035)是我们这组CF患者嗜麦芽窄食单胞菌定植的重要危险因素。我们得出结论,呼吸道分泌物中检出嗜麦芽窄食单胞菌的CF患者在首次检出嗜麦芽窄食单胞菌时的总体临床状况比未定植患者差,并且先前使用抗生素治疗可能使他们易在呼吸道分泌物中感染这种细菌。

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