Peritoneal dialysis versus haemodialysis for people commencing dialysis

Isabelle Éthier(Centre Hospitalier de l’Université de Montréal), Ashik Hayat(Princess Alexandra Hospital), Juan Pei(First Affiliated Hospital of Xiamen University), Carmel M. Hawley(Translational Research Institute), Ross S. Francis(The University of Queensland), Germaine Wong(The University of Sydney), Jonathan C. Craig(Flinders University), Andrea K. Viecelli(Princess Alexandra Hospital), Htay Htay(Singapore General Hospital), Samantha Ng(Princess Alexandra Hospital), Saskia Leibowitz(Logan Hospital), David W. Johnson(Princess Alexandra Hospital), Yeoungjee Cho(Translational Research Institute)
Cochrane Database of Systematic Reviews
June 20, 2024
Cited by 16Open Access
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Abstract

BACKGROUND: Peritoneal dialysis (PD) and haemodialysis (HD) are two possible modalities for people with kidney failure commencing dialysis. Only a few randomised controlled trials (RCTs) have evaluated PD versus HD. The benefits and harms of the two modalities remain uncertain. This review includes both RCTs and non-randomised studies of interventions (NRSIs). OBJECTIVES: To evaluate the benefits and harms of PD, compared to HD, in people with kidney failure initiating dialysis. SEARCH METHODS: We searched the Cochrane Kidney and Transplant Register of Studies from 2000 to June 2024 using search terms relevant to this review. Studies in the Register were identified through searches of CENTRAL, MEDLINE, and EMBASE, conference proceedings, the International Clinical Trials Registry Platform (ICTRP) Search Portal, and ClinicalTrials.gov. MEDLINE and EMBASE were searched for NRSIs from 2000 until 28 March 2023. SELECTION CRITERIA: RCTs and NRSIs evaluating PD compared to HD in people initiating dialysis were eligible. DATA COLLECTION AND ANALYSIS: Two investigators independently assessed if the studies were eligible and then extracted data. Risk of bias was assessed using standard Cochrane methods, and relevant outcomes were extracted for each report. The primary outcome was residual kidney function (RKF). Secondary outcomes included all-cause, cardiovascular and infection-related death, infection, cardiovascular disease, hospitalisation, technique survival, life participation and fatigue. MAIN RESULTS: = 97%; very low certainty). AUTHORS' CONCLUSIONS: The comparative effectiveness of PD and HD on the preservation of RKF, all-cause and cause-specific death risk, the incidence of bacteraemia, other vascular complications (e.g. stroke, cardiovascular events) and patient-reported outcomes (e.g. life participation and fatigue) are uncertain, based on data obtained mostly from NRSIs, as only two RCTs were included.


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