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Dose of hemodialysis and survival: A marginal structural model analysis

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dc.contributor.author Lertdumrongluk P.
dc.contributor.author Streja E.
dc.contributor.author Rhee C.M.
dc.contributor.author Park J.
dc.contributor.author Arah O.A.
dc.contributor.author Brunelli S.M.
dc.contributor.author Nissenson A.R.
dc.contributor.author Gillen D.
dc.contributor.author Kalantar-Zadeh K.
dc.date.accessioned 2021-04-05T03:32:40Z
dc.date.available 2021-04-05T03:32:40Z
dc.date.issued 2014
dc.identifier.issn 2508095
dc.identifier.other 2-s2.0-84899615517
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/13919
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-84899615517&doi=10.1159%2f000362285&partnerID=40&md5=2c5eddfd053a835ed40176ca98d8993c
dc.description.abstract Background: Observational studies have consistently demonstrated the survival benefits of a greater dialysis dose in maintenance hemodialysis (MHD) patients, whereas randomized controlled trials have shown conflicting results. The possible causal impact of dialysis dose on mortality needs to be investigated using rich cohort data analyzed with novel statistical methods such as marginal structural models (MSMs) that account for time-varying confounding and exposure. Methods: We quantified the effect of delivered dose of hemodialysis (HD) [single-pool Kt/V (spKt/V)] on mortality risk in a contemporary cohort of 68,110 patients undergoing HD 3 times weekly (7/2001-9/2005). We compared conventional Cox proportional hazard and MSM survival analyses, accounting for time-varying confounding by applying longitudinally modeled inverse-probability-of-dialysis-dose weights to each observation. Results: In conventional Cox models, baseline spKt/V showed a weak negative association with mortality, while higher time-averaged spKt/V was strongly associated with lower mortality risk. In MSM analyses, compared to a spKt/V range of 1.2-<1.4, a spKt/V range of <1.2 was associated with a higher risk of mortality [HR (95% CI) 1.67 (1.54-1.80)], whereas mortality risks were significantly lower with higher spKt/V [HRs (95% CI): 0.74 (0.70-0.78), 0.63 (0.59-0.66), 0.56 (0.52-0.60), and 0.56 (0.52-0.61) for spKt/V ranges of 1.4-<1.6, 1.6-<1.8, 1.8-<2.0, and ≥2.0, respectively]. Thus, MSM analyses showed that the greatest survival advantage of a higher dialysis dose was observed for a spKt/V range of 1.8-<2.0, and the dialysis dose-mortality relationship was robust in almost all subgroups of patients. Conclusions: Higher HD doses were robustly associated with greater survival in MSM analyses that more fully and appropriately accounted for time-varying confounding. © 2014 S. Karger AG, Basel.
dc.subject albumin
dc.subject creatinine
dc.subject phosphorus
dc.subject adult
dc.subject aged
dc.subject albumin blood level
dc.subject article
dc.subject body mass
dc.subject body size
dc.subject cohort analysis
dc.subject creatinine blood level
dc.subject diabetes mellitus
dc.subject female
dc.subject follow up
dc.subject hemodialysis
dc.subject human
dc.subject major clinical study
dc.subject male
dc.subject marginal structural model
dc.subject mortality
dc.subject outcome assessment
dc.subject priority journal
dc.subject proportional hazards model
dc.subject sensitivity analysis
dc.subject statistical analysis
dc.subject survival
dc.subject treatment duration
dc.subject Article
dc.subject correlation analysis
dc.subject middle aged
dc.subject mortality
dc.subject risk reduction
dc.subject statistical model
dc.subject Kidney Failure, Chronic
dc.subject procedures
dc.subject renal replacement therapy
dc.subject retrospective study
dc.subject survival
dc.subject Adult
dc.subject Aged
dc.subject Female
dc.subject Humans
dc.subject Kidney Failure, Chronic
dc.subject Male
dc.subject Middle Aged
dc.subject Models, Statistical
dc.subject Proportional Hazards Models
dc.subject Renal Dialysis
dc.subject Retrospective Studies
dc.subject Survival Analysis
dc.title Dose of hemodialysis and survival: A marginal structural model analysis
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation American Journal of Nephrology. Vol 39, No.5 (2014), p.383-391
dc.identifier.doi 10.1159/000362285


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