Gaynor Jeffrey J, Guerra Giselle, Vianna Rodrigo, Tabbara Marina M, Graell Enric Lledo, Ciancio Gaetano
Department of Surgery, Miami Transplant Institute, University of Miami Miller School of Medicine; Miami, Florida, USA.
Department of Medicine, Miami Transplant Institute, University of Miami Miller School of Medicine; Miami, Florida, USA.
Kidney Int Rep. 2024 Feb 1;9(6):1580-1589. doi: 10.1016/j.ekir.2024.01.050. eCollection 2024 Jun.
Modern competing risks analysis has 2 primary goals in clinical epidemiology as follows: (i) to maximize the clinician's knowledge of etiologic associations existing between potential predictor variables and various cause-specific outcomes via cause-specific hazard models, and (ii) to maximize the clinician's knowledge of noteworthy differences existing in cause-specific patient risk via cause-specific subdistribution hazard models (cumulative incidence functions [CIFs]). A perfect application exists in analyzing the following 4 distinct outcomes after listing for a deceased donor kidney transplant (DDKT): (i) receiving a DDKT, (ii) receiving a living donor kidney transplant (LDKT), (iii) waitlist removal due to patient mortality or a deteriorating medical condition, and (iv) waitlist removal due to other reasons. It is important to realize that obtaining a complete understanding of subdistribution hazard ratios (HRs) is simply not possible without first having knowledge of the multivariable relationships existing between the potential predictor variables and the cause-specific hazards (perspective #1), because the cause-specific hazards form the "building blocks" of CIFs. In addition, though we believe that a worthy and practical alternative to estimating the median waiting-time-to DDKT is to ask, "what is the conditional probability of the patient receiving a DDKT, given that he or she would not previously experience one of the competing events (known as the cause-specific conditional failure probability)," only an appropriate estimator of this conditional type of cumulative incidence should be used (perspective #2). One suggested estimator, the well-known "one minus Kaplan-Meier" approach (censoring competing events), simply does not represent any probability in the presence of competing risks and will almost always produce biased estimates (thus, it should never be used).
(i)通过特定病因风险模型,最大化临床医生对潜在预测变量与各种特定病因结局之间存在的病因关联的了解;(ii)通过特定病因的亚分布风险模型(累积发病率函数[CIFs]),最大化临床医生对特定病因患者风险中存在的显著差异的了解。在分析 deceased donor kidney transplant(DDKT, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney 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transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant, deceased donor kidney transplant(此处原文重复,疑有误)后列出的以下4种不同结局时存在完美应用:(i)接受 deceased donor kidney transplant(DDKT),(ii)接受活体供肾移植(LDKT),(iii)因患者死亡或病情恶化而从等待名单中移除,以及(iv)因其他原因从等待名单中移除。必须认识到,如果没有首先了解潜在预测变量与特定病因风险之间存在的多变量关系(观点#1),就根本不可能完全理解亚分布风险比(HRs),因为特定病因风险构成了CIFs的“基石”。此外,尽管我们认为,估计等待 deceased donor kidney transplant(DDKT)的中位时间的一个有价值且实用的替代方法是询问“在患者先前未经历任何竞争事件的情况下,其接受 deceased donor kidney transplant(DDKT)的条件概率是多少(称为特定病因条件失败概率)”,但应仅使用这种条件类型累积发病率的适当估计器(观点#2)。一种建议估计器,即著名的“1减去Kaplan-Meier”方法(对竞争事件进行删失),在存在竞争风险的情况下根本不代表任何概率,并且几乎总是会产生有偏差的估计(因此,绝不应该使用)。