Scappaticci Gianni B, Perissinotti Anthony J, Nagel Jerod L, Bixby Dale L, Marini Bernard L
Department of Pharmacy Services and Clinical Sciences, University of Michigan Health System and College of Pharmacy, Ann Arbor, MI, USA.
Department of Internal Medicine, Division of Haematology and Oncology, University of Michigan, Ann Arbor, MI, USA.
J Antimicrob Chemother. 2017 May 1;72(5):1488-1495. doi: 10.1093/jac/dkx005.
The incidence of Clostridium difficile infection (CDI) in adults with malignancy is 7%-14% compared with 1%-2% in the general hospitalized population. Despite the increased incidence of CDI in this population, a major concern is the propensity of CDI to recur, leading to delays in therapy impacting outcomes. We conducted a retrospective case-control study to identify risk factors for recurrent CDI (rCDI) and to determine the impact of rCDI on adult patients with a haematological malignancy.
Adult haematology patients with CDI from June 2010 to December 2014 were divided into two groups: rCDI and non-rCDI. Multivariable models using logistic regression were constructed to identify risk factors for rCDI.
A total of 100 patients in our study yielded a 41% recurrence rate. CDI impacted chemotherapy significantly more in the rCDI group (53.7% versus 11.9%, P <0.001), primarily due to interruptions in established treatment plans (46.3% versus 10.3%, P <0.001). Risk factors for rCDI identified at index included salvage lymphoma chemotherapy (OR 9.64, 95% CI 1.02-91.15, P = 0.048) and severe CDI (OR 4.82, 95% CI 1.31-17.66, P = 0.018). Longitudinal risk factors included exposure to fluoroquinolones (OR 3.96, 95% CI 1.04-15.15, P = 0.044), ceftriaxone (OR 18.93, 95% CI 1.27-281.95, P = 0.033) and piperacillin/tazobactam (OR 10.4, 95% CI 1.81-59.64, P = 0.009).
Haematology patients exhibit a higher rate of rCDI than general hospitalized patients. Utilization of this multivariable model to guide index CDI therapy at index may help to decrease the rCDI and prevent delays or interruptions in chemotherapy.
恶性肿瘤成年患者艰难梭菌感染(CDI)的发生率为7%-14%,而普通住院患者的发生率为1%-2%。尽管该人群中CDI的发生率有所增加,但一个主要担忧是CDI容易复发,导致治疗延迟,影响治疗结果。我们进行了一项回顾性病例对照研究,以确定复发性CDI(rCDI)的危险因素,并确定rCDI对血液系统恶性肿瘤成年患者的影响。
将2010年6月至2014年12月期间患有CDI的成年血液科患者分为两组:rCDI组和非rCDI组。使用逻辑回归构建多变量模型,以确定rCDI的危险因素。
我们研究中的100名患者复发率为41%。rCDI组中CDI对化疗的影响明显更大(53.7%对11.9%,P<0.001),主要是由于既定治疗计划的中断(46.3%对10.3%,P<0.001)。初次感染时确定的rCDI危险因素包括挽救性淋巴瘤化疗(比值比9.64,95%置信区间1.02-91.15,P=0.048)和严重CDI(比值比4.82,95%置信区间1.31-17.66,P=0.018)。纵向危险因素包括使用氟喹诺酮类药物(比值比3.96,95%置信区间1.04-15.15,P=0.044)、头孢曲松(比值比18.93,95%置信区间1.27-281.95,P=0.033)和哌拉西林/他唑巴坦(比值比10.4,95%置信区间1.81-59.64,P=0.009)。
血液科患者的rCDI发生率高于普通住院患者。在初次感染时使用该多变量模型指导CDI治疗,可能有助于降低rCDI的发生率,并防止化疗延迟或中断。