Working Committee for Hospital Epidemiology and Infection Control, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Rua Dr Eneas de Carvalho Aguiar, 255, São Paulo, SP, 05403-900, Brazil,
Infection. 2015 Jun;43(3):315-23. doi: 10.1007/s15010-015-0743-4. Epub 2015 Feb 18.
Solid organ transplant recipients are especially susceptible to healthcare-associated infections with Klebsiella pneumoniae carbapenemase-producing K. pneumoniae (KPC-Kp-HAIs). The aim of the study was to evaluate risk factors and outcome of these infections in kidney transplant recipients.
This was a retrospective cohort of kidney transplant (KTx) recipients between January 2009 and December 2013. Cases were defined as patients who developed KPC-Kp-HAI, confirmed by PCR for bla( KPC) gene after KTx during the study period. We analysed variables related to recipient; induction immunosuppressant therapy; delayed graft function; use of invasive devices; SOFA score on the first day of infection; type of therapy; time from positive culture to appropriate antimicrobial therapy; bacteraemia; and concomitant infection. Outcome measures were the occurrence of KPC-Kp-HAI and 30-day mortality after KPC-Kp-HAI.
A total of 1,101 were submitted to KTx in the period, 21 patients were classified as infected with KPC-Kp. Another ten patients had KPC-Kp-HAI in the period and were transplanted before 2009. Of those 31 patients, 48.4 % showed evidence of prior colonization and 38.7 % had bacteraemia. The most common site of infection was the surgical wound. Risk factors for KPC-Kp-HAI were multi-organ transplantation and the use of a ureteral stent. Eight of the infected patients experienced recurrence of the infection. The 30-day mortality rate was 41.9 %. Survival was significantly lower among the patients with KPC-Kp-HAI (72 vs. 89.1 %; P = 0.002). The only risk factor independently associated with 30-day mortality was an elevated SOFA score on the first day of infection.
In KTx recipients, the occurrence of KPC-Kp-HAI was related to invasive devices and type of transplant; these infections had a high rate of recurrence and reduced survival after KTx.
实体器官移植受者尤其容易发生与产碳青霉烯酶肺炎克雷伯菌(KPC-Kp)相关的医源性感染。本研究旨在评估肾移植受者中这些感染的危险因素和结局。
这是一项回顾性队列研究,纳入 2009 年 1 月至 2013 年 12 月期间接受肾移植(KTx)的患者。病例定义为在研究期间发生 KPC-Kp-HAI 的患者,经 PCR 检测 bla(KPC)基因阳性。我们分析了与受者相关的变量;诱导免疫抑制剂治疗;延迟移植物功能;使用有创设备;感染第一天的 SOFA 评分;治疗类型;从阳性培养到适当抗菌治疗的时间;菌血症;和合并感染。观察指标为发生 KPC-Kp-HAI 和 KPC-Kp-HAI 后 30 天死亡率。
该期间共进行了 1101 例 KTx,21 例患者被诊断为感染 KPC-Kp。该期间另有 10 例患者在 2009 年前接受 KTx 时发生了 KPC-Kp-HAI。在这 31 例患者中,48.4%有定植的证据,38.7%有菌血症。最常见的感染部位是手术切口。KPC-Kp-HAI 的危险因素是多器官移植和使用输尿管支架。8 例感染患者发生感染复发。30 天死亡率为 41.9%。KPC-Kp-HAI 患者的生存率明显降低(72%对 89.1%;P=0.002)。感染后 30 天死亡的唯一独立危险因素是感染第一天的 SOFA 评分升高。
在肾移植受者中,KPC-Kp-HAI 的发生与有创设备和移植类型有关;这些感染的复发率高,移植后生存率降低。