Marini Bernard L, Hough Shannon M, Gregg Kevin S, Abu-Seir Haya, Nagel Jerod L
Department of Pharmacy Services and Clinical Sciences, University of Michigan Health System and College of Pharmacy, 1111 E. Catherine St., Rm 300, Ann Arbor, MI, 48109, USA.
Support Care Cancer. 2015 Aug;23(8):2287-95. doi: 10.1007/s00520-014-2582-8. Epub 2015 Jan 10.
Febrile neutropenia (FN) is a life-threatening complication of cancer therapy, and initial ineffective therapy is associated with poor outcomes. Piperacillin/tazobactam (PTZ) is a commonly used empiric antibiotic for the treatment of FN, but resistance among Gram-negative pathogens is well described. We conducted a retrospective case-control study to identify risk factors for PTZ-resistant (PTZ-R) Gram-negative isolates.
Hematology/oncology patients with FN from November 2007 to November 2013 with a positive culture for Gram-negative bacilli were divided into two groups: PTZ-sensitive (PTZ-S) and PTZ-R. A multivariable model using logistic regression was constructed to identify risk factors for PTZ-R.
A total of 171 patients were included (25 PTZ-R, 146 PTZ-S), yielding a 14.6 % resistance rate. Thirty-day all-cause mortality was significantly higher in the PTZ-R group (29 vs 11 %, P = 0.024). Multivariable analysis yielded intensive care unit (ICU) status (odds ratio (OR) 20.18; 95 % confidence interval (CI) 1.03-397.35; P = 0.048), antibiotics for > 14 days in the previous 90 days (OR 6.02; CI 1.17-30.93; P = 0.032), and respiratory source (OR 13.65; CI 1.14-163.57; P = 0.039) as significant risk factors for PTZ-R, and the receiver operating characteristic area under the curve of the model was 0.894. Among PTZ-R isolates, 88 % were sensitive to meropenem and 100 % were sensitive to amikacin.
Given the high mortality rates in the PTZ-R group, a risk-factor-guided approach driven by this multivariable model may help identify patients that could benefit from amikacin combination therapy to help optimize empiric therapy in this setting.
发热性中性粒细胞减少症(FN)是癌症治疗中一种危及生命的并发症,初始治疗无效与不良预后相关。哌拉西林/他唑巴坦(PTZ)是治疗FN常用的经验性抗生素,但革兰氏阴性病原体的耐药情况已有详细描述。我们进行了一项回顾性病例对照研究,以确定耐PTZ(PTZ-R)革兰氏阴性菌分离株的危险因素。
2007年11月至2013年11月期间患有FN且革兰氏阴性杆菌培养阳性的血液学/肿瘤学患者分为两组:PTZ敏感(PTZ-S)组和PTZ-R组。构建了一个使用逻辑回归的多变量模型来确定PTZ-R的危险因素。
共纳入171例患者(25例PTZ-R,146例PTZ-S),耐药率为14.6%。PTZ-R组的30天全因死亡率显著更高(29%对11%,P = 0.024)。多变量分析得出重症监护病房(ICU)状态(比值比(OR)20.18;95%置信区间(CI)1.03 - 397.35;P = 0.048)、前90天内使用抗生素超过14天(OR 6.02;CI 1.17 - 30.93;P = 0.032)以及呼吸道感染源(OR 13.65;CI 1.14 - 163.57;P = 0.039)是PTZ-R的显著危险因素,该模型的曲线下受试者工作特征面积为0.894。在PTZ-R分离株中,88%对美罗培南敏感,100%对阿米卡星敏感。
鉴于PTZ-R组的高死亡率,由该多变量模型驱动的危险因素导向方法可能有助于识别可从阿米卡星联合治疗中获益的患者,以帮助优化这种情况下的经验性治疗。