1 University of Wisconsin Hospital and Clinics, Madison WI, USA.
2 University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, USA.
Ann Pharmacother. 2019 Oct;53(10):1020-1025. doi: 10.1177/1060028019845003. Epub 2019 Apr 21.
Modifiable risk-factors associated with (CDI) in renal-transplant (RTX) have not been clearly established and peri-transplant risk has not been described.
Evaluate epidemiology, risk-factors and outcomes after CDI occurring in the first 90 days after RTX (CDI-90). Observational cohort study/survival analysis of adult RTX recipients from 1/1/2012-12/31/2015. Primary outcome was CDI-90 incidence/risk-factors. Secondary outcome was evaluation of post-90 day transplant outcomes.
982 patients met inclusion criteria; 46 with CDI-90 and 936 without (comparator). CDI incidence in the total population was 4.7% at 90 days, 6.3% at 1 year, and 6.4% at 3 years. Incidence of CDI-90 was 5%; time to diagnosis was 19.4±25 days (median 7). Risk-factors for CDI-90 were alemtuzumab induction (Hazard ratio [HR] 1.5, 95% CI(1.1-2.0), = 0.005) and age at transplant (HR 1.007/year, 95% CI (1.002-1.012), = 0.007). However, risk-factors for CDI at any time were different; donation-after-circulatory-death (DCD) donor (HR 2.5 95% CI (1.3-4.9), = 0.008) and female gender (HR 1.6 95% CI (1.0-2.7), = 0.049). On Kaplan-Meier, CDI-90 appeared to have an impact on patient/graft survival, however when analyzed in a multivariable stepwise Cox proportional hazards model, only age was significantly associated with survival ( = 0.002).
Incidence of CDI-90 is low, mostly occurring in the first post-operative month. Risk-factors vary temporally based on time from transplant. In the early post-op period induction agent and age at transplant are significant, but not after. Associations between CDI and negative graft outcomes appear to be largely driven by age. Future studies validating these risk-factors as well as targeted prophylaxis strategies and their effect on long term graft outcomes and the host microbiome are needed.
与肾移植(RTX)相关的可改变的风险因素尚未明确,且移植前的风险尚未描述。
评估在 RTX 后 90 天内发生的(CDI)的流行病学、风险因素和结果(CDI-90)。对 2012 年 1 月 1 日至 2015 年 12 月 31 日期间接受 RTX 的成人患者进行了队列研究/生存分析。主要结局是 CDI-90 的发生率/风险因素。次要结局是评估 90 天后移植结局。
982 名患者符合纳入标准;46 名患者发生 CDI-90,936 名患者未发生(对照组)。在总人群中,90 天的 CDI 发生率为 4.7%,1 年时为 6.3%,3 年时为 6.4%。CDI-90 的发生率为 5%;诊断时间为 19.4±25 天(中位数 7)。CDI-90 的风险因素为 alemtuzumab 诱导(风险比[HR]1.5,95%置信区间(1.1-2.0),=0.005)和移植时的年龄(HR 1.007/年,95%置信区间(1.002-1.012),=0.007)。然而,任何时候 CDI 的风险因素都不同;供体死后循环死亡(DCD)供体(HR 2.5,95%置信区间(1.3-4.9),=0.008)和女性(HR 1.6,95%置信区间(1.0-2.7),=0.049)。在 Kaplan-Meier 分析中,CDI-90 似乎对患者/移植物的生存有影响,但在多变量逐步 Cox 比例风险模型中分析时,只有年龄与生存显著相关(=0.002)。
CDI-90 的发生率较低,主要发生在术后第一个月。风险因素根据移植时间而变化。在术后早期,诱导剂和移植时的年龄是显著的,但不是在术后。CDI 与负面移植物结局之间的关联似乎主要是由年龄驱动的。需要进一步的研究来验证这些风险因素,以及靶向预防策略及其对长期移植物结局和宿主微生物组的影响。