Unit of Infectious Diseases, Hospital Universitario "12 de Octubre" (Centro de Actividades Ambulatorias, 2ª planta, bloque D, Avda. de Córdoba, s/n, 28041), Instituto de Investigación Hospital "12 de Octubre" (i+12), School of Medicine, Universidad Complutense, Madrid, Spain,
Infection. 2015 Aug;43(4):413-22. doi: 10.1007/s15010-015-0737-2. Epub 2015 Feb 13.
To identify reversible risk factors for Clostridium difficile infection (CDI) after kidney transplantation (KT) that could lead to a reduction in its incidence and associated complications.
We performed a single-center case-control study in which 41 patients undergoing KT between February 2009 and July 2013 who developed a first episode of post-transplant CDI were included as cases. Patients transplanted at the same calendar day (± 2 weeks) as each case with no evidence of CDI and comparable risk exposure period were chosen as controls (2:1 ratio). Serum immunoglobulin and complement levels were systematically measured at baseline and months 1 and 6 after transplantation.
Multivariate regression analysis identified age-adjusted Charlson comorbidity index (odds ratio [OR] per unitary increment 1.31; P value = 0.043), delayed graft function (OR 2.76; P value = 0.039), prior cytomegalovirus (CMV) disease (OR 6.85; P value = 0.011) and prior acute graft rejection (OR 5.92; P value = 0.008) as risk factors for post-transplant CDI. Cases with their first episode of CDI occurring beyond the first month were more likely to have IgG hypogammaglobulinemia (HGG) at month 1 (P value = 0.002), whereas cases with CDI beyond the sixth month were more likely to have HGG of any class at month 6 (P value = 0.003). Poor outcome (graft loss and/or all-cause mortality) was more common among cases (adjusted hazard ratio 5.69; P value = 0.001).
The occurrence of CDI exerts a detrimental effect on graft and patient outcome. Post-transplant HGG was a potentially modifiable risk factor for CDI in KT recipients.
确定肾移植(KT)后导致艰难梭菌感染(CDI)发生率及其相关并发症降低的可逆危险因素。
我们进行了一项单中心病例对照研究,纳入了 2009 年 2 月至 2013 年 7 月期间接受首次肾移植且发生移植后 CDI 的 41 例患者作为病例。选择在同一日历日(±2 周)接受移植且无 CDI 证据和可比风险暴露期的患者作为对照(2:1 比例)。在移植前、移植后 1 个月和 6 个月时系统测量血清免疫球蛋白和补体水平。
多变量回归分析确定年龄调整Charlson 合并症指数(每单位增量的比值比 [OR] 为 1.31;P 值 = 0.043)、延迟移植物功能(OR 2.76;P 值 = 0.039)、巨细胞病毒(CMV)病史(OR 6.85;P 值 = 0.011)和急性移植物排斥(OR 5.92;P 值 = 0.008)是移植后 CDI 的危险因素。首次 CDI 发作发生在第 1 个月之后的病例在第 1 个月时更有可能发生 IgG 低丙种球蛋白血症(HGG)(P 值 = 0.002),而在第 6 个月以后发生 CDI 的病例在第 6 个月时更有可能发生任何类别 HGG(P 值 = 0.003)。不良结局(移植物丢失和/或全因死亡率)在病例中更为常见(调整后的危险比为 5.69;P 值 = 0.001)。
CDI 的发生对移植物和患者的结局产生不利影响。移植后 HGG 是 KT 受者 CDI 的潜在可改变危险因素。