Hicham I Cheikh Hassan, Karumathil Murali, Jenny H C Chen, Judy Mullan
{"title":"血管通路类型对腹膜透析患者过渡到血液透析临床结果的影响:一项ANZDATA研究。","authors":"Hicham I Cheikh Hassan, Karumathil Murali, Jenny H C Chen, Judy Mullan","doi":"10.1093/ckj/sfaf025","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Type of vascular access used for haemodialysis is associated with long-term outcomes. However, the effect of access on haemodialysis transfer for peritoneal dialysis (PD) patients has not been fully explored.</p><p><strong>Methods: </strong>A retrospective cohort study was performed in incident adult PD patients from the Australian and New Zealand Dialysis and Transplant (ANZDATA) Registry who transferred to haemodialysis between 2004 and 2022. Associations between vascular access on transfer [central venous catheter (CVC) or arterio-venous access (AVA)] and clinical outcomes (all-cause mortality, cause-specific mortality, kidney transplantation and return to PD) were compared using Cox proportional hazards analysis and competing risk models.</p><p><strong>Results: </strong>Of 6824 patients, 65% used a CVC on transfer and 35% an AVA. Variability of access type at transfer between centres was high (range 13%-98% for CVC). AVA transfer was associated with a longer PD vintage (1.6 versus 1.2 years, <i>P </i>< .001) and inadequate PD as a cause of transfer (29% versus 15%, <i>P </i>< .001). All-cause mortality was lower for AVA transfer compared with a CVC [hazard ratio (HR) 0.71, 95% confidence interval (CI) 0.66-0.77]. The risk was lowest for infection-related mortality (HR 0.59, 95% CI 0.45-0.77) Kidney transplantation was more likely in AVA transfer compared with a CVC (HR 1.18, 95% CI 1.05-1.33), but return to PD was less likely (HR 0.67, 95% CI 0.59-0.71). Results remained consistent in the competing risk analysis.</p><p><strong>Conclusions: </strong>Patients who transferred with an AVA, compared with a CVC, showed better survival and kidney transplantation rates, but were less likely to return to PD.</p>","PeriodicalId":10435,"journal":{"name":"Clinical Kidney Journal","volume":"18 3","pages":"sfaf025"},"PeriodicalIF":3.9000,"publicationDate":"2025-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11883222/pdf/","citationCount":"0","resultStr":"{\"title\":\"Impact of type of vascular access on clinical outcomes in peritoneal dialysis patients transitioning to haemodialysis: an ANZDATA study.\",\"authors\":\"Hicham I Cheikh Hassan, Karumathil Murali, Jenny H C Chen, Judy Mullan\",\"doi\":\"10.1093/ckj/sfaf025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Type of vascular access used for haemodialysis is associated with long-term outcomes. However, the effect of access on haemodialysis transfer for peritoneal dialysis (PD) patients has not been fully explored.</p><p><strong>Methods: </strong>A retrospective cohort study was performed in incident adult PD patients from the Australian and New Zealand Dialysis and Transplant (ANZDATA) Registry who transferred to haemodialysis between 2004 and 2022. Associations between vascular access on transfer [central venous catheter (CVC) or arterio-venous access (AVA)] and clinical outcomes (all-cause mortality, cause-specific mortality, kidney transplantation and return to PD) were compared using Cox proportional hazards analysis and competing risk models.</p><p><strong>Results: </strong>Of 6824 patients, 65% used a CVC on transfer and 35% an AVA. Variability of access type at transfer between centres was high (range 13%-98% for CVC). AVA transfer was associated with a longer PD vintage (1.6 versus 1.2 years, <i>P </i>< .001) and inadequate PD as a cause of transfer (29% versus 15%, <i>P </i>< .001). All-cause mortality was lower for AVA transfer compared with a CVC [hazard ratio (HR) 0.71, 95% confidence interval (CI) 0.66-0.77]. The risk was lowest for infection-related mortality (HR 0.59, 95% CI 0.45-0.77) Kidney transplantation was more likely in AVA transfer compared with a CVC (HR 1.18, 95% CI 1.05-1.33), but return to PD was less likely (HR 0.67, 95% CI 0.59-0.71). Results remained consistent in the competing risk analysis.</p><p><strong>Conclusions: </strong>Patients who transferred with an AVA, compared with a CVC, showed better survival and kidney transplantation rates, but were less likely to return to PD.</p>\",\"PeriodicalId\":10435,\"journal\":{\"name\":\"Clinical Kidney Journal\",\"volume\":\"18 3\",\"pages\":\"sfaf025\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-01-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11883222/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Kidney Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/ckj/sfaf025\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Kidney Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/ckj/sfaf025","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Impact of type of vascular access on clinical outcomes in peritoneal dialysis patients transitioning to haemodialysis: an ANZDATA study.
Background: Type of vascular access used for haemodialysis is associated with long-term outcomes. However, the effect of access on haemodialysis transfer for peritoneal dialysis (PD) patients has not been fully explored.
Methods: A retrospective cohort study was performed in incident adult PD patients from the Australian and New Zealand Dialysis and Transplant (ANZDATA) Registry who transferred to haemodialysis between 2004 and 2022. Associations between vascular access on transfer [central venous catheter (CVC) or arterio-venous access (AVA)] and clinical outcomes (all-cause mortality, cause-specific mortality, kidney transplantation and return to PD) were compared using Cox proportional hazards analysis and competing risk models.
Results: Of 6824 patients, 65% used a CVC on transfer and 35% an AVA. Variability of access type at transfer between centres was high (range 13%-98% for CVC). AVA transfer was associated with a longer PD vintage (1.6 versus 1.2 years, P < .001) and inadequate PD as a cause of transfer (29% versus 15%, P < .001). All-cause mortality was lower for AVA transfer compared with a CVC [hazard ratio (HR) 0.71, 95% confidence interval (CI) 0.66-0.77]. The risk was lowest for infection-related mortality (HR 0.59, 95% CI 0.45-0.77) Kidney transplantation was more likely in AVA transfer compared with a CVC (HR 1.18, 95% CI 1.05-1.33), but return to PD was less likely (HR 0.67, 95% CI 0.59-0.71). Results remained consistent in the competing risk analysis.
Conclusions: Patients who transferred with an AVA, compared with a CVC, showed better survival and kidney transplantation rates, but were less likely to return to PD.
期刊介绍:
About the Journal
Clinical Kidney Journal: Clinical and Translational Nephrology (ckj), an official journal of the ERA-EDTA (European Renal Association-European Dialysis and Transplant Association), is a fully open access, online only journal publishing bimonthly. The journal is an essential educational and training resource integrating clinical, translational and educational research into clinical practice. ckj aims to contribute to a translational research culture among nephrologists and kidney pathologists that helps close the gap between basic researchers and practicing clinicians and promote sorely needed innovation in the Nephrology field. All research articles in this journal have undergone peer review.