Endimiani Andrea, Luzzaro Francesco, Brigante Gioconda, Perilli Mariagrazia, Lombardi Gianluigi, Amicosante Gianfranco, Rossolini Gian Maria, Toniolo Antonio
Laboratorio di Microbiologia, Ospedale di Circolo e Università dell'Insubria, Viale Borri 57, 21100 Varese, Italy.
Antimicrob Agents Chemother. 2005 Jul;49(7):2598-605. doi: 10.1128/AAC.49.7.2598-2605.2005.
Bloodstream infection (BSI) due to Proteus mirabilis strains is a relatively uncommon clinical entity, and its significance has received little attention. This study was initiated to evaluate risk factors and treatment outcome of BSI episodes due to P. mirabilis producing extended-spectrum beta-lactamases (ESBLs). Twenty-five BSI episodes caused by P. mirabilis occurred at our hospital (Ospedale di Circolo e Fondazione Macchi, Varese, Italy) over a 7.5-year period. Phenotypic and molecular methods were used to assess ESBL production. Clinical records of BSI patients were examined retrospectively. Demographic data, underlying diseases (according to McCabe and Jackson classification and Charlson weighted index), risk factors, and treatment outcome were investigated by comparing cases due to ESBL-positive strains to cases due to ESBL-negative strains. Eleven isolates were found to express ESBLs (TEM-52 or TEM-92). The remaining 14 isolates were ESBL negative and were uniformly susceptible to extended-spectrum cephalosporins and monobactams. Comparison of the two groups showed that previous hospitalization in a nursing home (P = 0.04) and use of bladder catheter (P = 0.01) were significant risk factors for infections due to ESBL-positive strains. In addition, cases due to ESBL-positive strains showed a significantly higher mortality attributable to BSI (P = 0.04). BSI cases due to ESBL-negative isolates uniformly responded to therapy, whereas 5/11 cases due to ESBL-positive isolates failed to respond (P < 0.01). Use of carbapenems was associated with complete response independently of ESBL production. Therapeutic failure and mortality may occur in BSI episodes caused by ESBL-positive P. mirabilis isolates. Thus, recognition of ESBL-positive strains appears to be critical for the clinical management of patients with systemic P. mirabilis infections.
奇异变形杆菌引起的血流感染(BSI)是一种相对不常见的临床病症,其重要性很少受到关注。本研究旨在评估产超广谱β-内酰胺酶(ESBLs)的奇异变形杆菌所致BSI发作的危险因素和治疗结果。在7.5年期间,我院(意大利瓦雷泽Circolo医院和Macchi基金会)发生了25例由奇异变形杆菌引起的BSI发作。采用表型和分子方法评估ESBL的产生。对BSI患者的临床记录进行回顾性检查。通过比较ESBL阳性菌株病例与ESBL阴性菌株病例,调查人口统计学数据、基础疾病(根据McCabe和Jackson分类以及Charlson加权指数)、危险因素和治疗结果。发现11株分离株表达ESBLs(TEM-52或TEM-92)。其余14株分离株为ESBL阴性,对超广谱头孢菌素和单环β-内酰胺类药物均敏感。两组比较显示,先前在疗养院住院(P = 0.04)和使用膀胱导管(P = 0.01)是ESBL阳性菌株感染的重要危险因素。此外,ESBL阳性菌株所致病例因BSI导致的死亡率显著更高(P = 0.04)。ESBL阴性分离株所致的BSI病例对治疗均有反应,而ESBL阳性分离株所致的11例病例中有5例无反应(P < 0.01)。碳青霉烯类药物的使用与完全反应相关,与ESBL产生无关。ESBL阳性奇异变形杆菌分离株引起的BSI发作可能会出现治疗失败和死亡。因此,识别ESBL阳性菌株对于全身性奇异变形杆菌感染患者的临床管理似乎至关重要。