Sabanayagam Dharshana, Lopez Pedro, Boroumand Farzaneh, Chau Katrina, Au Eric H, Gately Ryan, Bakar K Shuvo, Zhu Lin, Teixeira-Pinto Armando, Lim Wai H, Wong Germaine
Sydney School of Public Health, University of Sydney, Sydney; Centre for Kidney Research, Children's Hospital at Westmead, Sydney; Department of Renal and Transplantation Medicine, Westmead Hospital, Westmead.
Pleural Medicine Unit, Institute for Respiratory Health, Perth; Grupo de Pesquisa em Exercício para Populações Clínicas, Universidade de Caxias do Sul, Caxias do Sul, Brazil; Programa de Pós-Graduação em Ciências da Saúde, Universidade de Caxias do Sul, Caxias do Sul, Brazil.
Am J Kidney Dis. 2025 Oct;86(4):475-486.e1. doi: 10.1053/j.ajkd.2025.05.009. Epub 2025 Jul 8.
RATIONALE & OBJECTIVE: Little is known about the association between sex and specific causes of peritoneal dialysis (PD) discontinuation. This study assessed the association of sex with all-cause and cause-specific PD discontinuation and explored the factors mediating these relationships.
Retrospective cohort study.
SETTING & PARTICIPANTS: All patients with kidney failure who started PD between 2005 and 2019 in Australia.
Sex.
All-cause (transfer to hemodialysis for≥30 days or death) PD discontinuation, PD discontinuation related to inadequate dialysis, and PD discontinuation related to infection.
Adjusted cause-specific proportional hazards regression models were used to assess the association of sex with all-cause and cause-specific PD discontinuation. Counterfactual mediation analysis was conducted to explore potential mediators (sociodemographic status, geographical remoteness, cardiovascular disease, diabetes, history of peritonitis, late referral, smoking status, and body mass index) of these associations. Sensitivity analyses using the Fine and Gray method were implemented to address the competing risks of death, kidney transplantation, and other causes of PD discontinuation.
Of 9,748 incident patients, 6,001 experienced PD discontinuation from any cause (2,098 died, 793 were inadequate dialysis related, 1,442 were infection related, and 1,668 were other cause), with a median follow-up of 1.47 years (IQR, 0.67-2.73). Men were more likely to experience PD discontinuation from any cause (HR, 1.09 [95% CI, 1.03-1.14], P=0.002) or for inadequate dialysis (HR, 1.71[95% CI, 1.47-1.99], P<0.001) but not for infection (HR, 0.95[95% CI, 0.85-1.05], P=0.3). The mediation analyses found that 76.9% of the total effect of sex on all-cause PD discontinuation was explained by mediators, including cardiovascular disease, smoking status, and diabetes, whereas less than 10% of the total effect of sex on PD discontinuation from inadequate dialysis was explained by mediators.
Residual and unmeasured confounders, such as biological differences, behavioral patterns, hospitalizations, frailty, and severity of comorbidities.
Men were more likely than women to experience PD discontinuation from any cause and from inadequate dialysis. This relationship was mediated by multiple morbidities for PD discontinuation from any cause but not for PD discontinuation for inadequate dialysis. These findings may inform future studies evaluating biological and sociodemographic factors that may contribute to these observed sex differences.
PLAIN-LANGUAGE SUMMARY: Sex and gender differences can influence kidney disease risk, progression, access to care, and outcomes. However, their role in peritoneal dialysis (PD) discontinuation is not well understood. We studied the association between sex and PD discontinuation in Australian patients with kidney failure from 2005 to 2019, and whether sociodemographic factors and comorbidities influenced this relationship. We found that men were more likely to discontinue PD overall and because of inadequate dialysis but not because of infectious complications. Cardiovascular disease, smoking, and diabetes explained most of the differences between men and women for all-cause PD discontinuation but not for discontinuation due to inadequate dialysis. These findings may inform future studies evaluating biological and sociodemographic factors that may contribute to these observed sex differences.
关于性别与腹膜透析(PD)终止的具体原因之间的关联,目前知之甚少。本研究评估了性别与全因及特定原因导致的PD终止之间的关联,并探讨了介导这些关系的因素。
回顾性队列研究。
2005年至2019年期间在澳大利亚开始进行PD的所有肾衰竭患者。
性别。
全因(转为血液透析≥30天或死亡)导致的PD终止、与透析不充分相关的PD终止以及与感染相关的PD终止。
使用调整后的特定原因比例风险回归模型来评估性别与全因及特定原因导致的PD终止之间的关联。进行反事实中介分析以探索这些关联的潜在中介因素(社会人口统计学状况、地理偏远程度、心血管疾病、糖尿病、腹膜炎病史、延迟转诊、吸烟状况和体重指数)。采用Fine和Gray方法进行敏感性分析,以处理死亡、肾移植及其他导致PD终止的原因所带来的竞争风险。
在9748例新发病例患者中,6001例因任何原因终止了PD(2098例死亡,793例与透析不充分相关,1442例与感染相关,1668例为其他原因),中位随访时间为1.47年(四分位间距,0.67 - 2.73)。男性因任何原因终止PD的可能性更高(风险比[HR],1.09[95%置信区间,1.03 - 1.14],P = 0.002),因透析不充分而终止PD的可能性也更高(HR,1.71[95%置信区间,1.47 - 1.99],P < 0.001),但因感染而终止PD的可能性并非如此(HR,0.95[95%置信区间,0.85 - 1.05],P = 0.3)。中介分析发现,性别对全因PD终止的总效应中有76.9%可由中介因素解释,包括心血管疾病、吸烟状况和糖尿病,而性别对因透析不充分导致的PD终止的总效应中只有不到10%可由中介因素解释。
存在残余和未测量的混杂因素,如生物学差异、行为模式、住院情况、虚弱程度和合并症的严重程度。
男性因任何原因以及因透析不充分而终止PD的可能性均高于女性。这种关系在因任何原因导致的PD终止中由多种合并症介导,但在因透析不充分导致的PD终止中并非如此。这些发现可能为未来评估可能导致这些观察到的性别差异的生物学和社会人口统计学因素的研究提供参考。
性别差异可影响肾脏疾病的风险、进展、获得治疗的机会及结局。然而,它们在腹膜透析(PD)终止中的作用尚不清楚。我们研究了2005年至2019年澳大利亚肾衰竭患者中性别与PD终止之间的关联,以及社会人口统计学因素和合并症是否影响这种关系。我们发现,男性总体上更有可能终止PD,且是由于透析不充分而非感染并发症。心血管疾病、吸烟和糖尿病解释了男性和女性在全因PD终止方面的大部分差异,但在因透析不充分导致的终止方面并非如此。这些发现可能为未来评估可能导致这些观察到的性别差异的生物学和社会人口统计学因素的研究提供参考。