GFR at Initiation of Dialysis and Mortality in CKD: A Meta-analysis

Background The proportion of patients with advanced chronic kidney disease (CKD) initiating dialysis therapy at a higher glomerular filtration rate (GFR) has increased during the past decade. Recent data suggest that higher GFR may be associated with increased mortality. Study Design A meta-analysis...

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Veröffentlicht in:American journal of kidney diseases 2012-06, Vol.59 (6), p.829-840
Hauptverfasser: Susantitaphong, Paweena, MD, Altamimi, Sarah, MBBS, Ashkar, Motaz, MBBS, Balk, Ethan M., MD, MPH, Stel, Vianda S., PhD, Wright, Seth, MD, Jaber, Bertrand L., MD, MS
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container_end_page 840
container_issue 6
container_start_page 829
container_title American journal of kidney diseases
container_volume 59
creator Susantitaphong, Paweena, MD
Altamimi, Sarah, MBBS
Ashkar, Motaz, MBBS
Balk, Ethan M., MD, MPH
Stel, Vianda S., PhD
Wright, Seth, MD
Jaber, Bertrand L., MD, MS
description Background The proportion of patients with advanced chronic kidney disease (CKD) initiating dialysis therapy at a higher glomerular filtration rate (GFR) has increased during the past decade. Recent data suggest that higher GFR may be associated with increased mortality. Study Design A meta-analysis of cohort studies and trials. Setting & Population Patients with advanced CKD. Selection Criteria for Studies We performed a systematic literature search in MEDLINE, Cochrane Central Register of Controlled Trials, ClinicalTrials.gov , American Society of Nephrology abstracts, and bibliographies of retrieved articles to identify studies reporting on GFR at dialysis therapy initiation and mortality. Predictor Estimated or calculated GFR at dialysis therapy initiation. Outcome Pooled adjusted hazard ratio (HR) of continuous GFR for all-cause mortality. Results 16 cohort studies and 1 randomized controlled trial were identified (n = 1,081,116). By meta-analysis restricted to 15 cohorts (n = 1,079,917), higher GFR at dialysis therapy initiation was associated with a higher pooled adjusted HR for all-cause mortality (1.04; 95% CI, 1.03-1.05; P < 0.001). However, there was significant heterogeneity ( I2 = 97%; P < 0.001). The association persisted among the 9 cohorts that adjusted analytically for nutritional covariates (HR, 1.03; 95% CI, 1.02-1.04; P < 0.001; residual I2 = 97%). The highest mortality risk was observed in hemodialysis cohorts (HR, 1.05; 95% CI, 1.02-1.08; P < 0.001), whereas there was no association between GFR and mortality in peritoneal dialysis cohorts (HR, 1.04; 95% CI, 0.99-1.08, P = 0.1; residual I2 = 98%). Finally, higher GFR was associated with a lower mortality risk in cohorts that calculated GFR (HR, 0.80; 95% CI, 0.71-0.91; P = 0.003), contrasting with a higher mortality risk in cohorts that estimated GFR (HR, 1.04; 95% CI, 1.03-1.05; P < 0.001; residual I2 = 97%). Limitations Paucity of randomized controlled trials, different methods for determining GFR, and substantial heterogeneity. Conclusions Higher estimated rather than calculated GFR at dialysis therapy initiation is associated with a higher mortality risk in patients with advanced CKD, independent of nutritional status. Although there was substantial heterogeneity of effect size estimates across studies, this observation requires further study.
doi_str_mv 10.1053/j.ajkd.2012.01.015
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Recent data suggest that higher GFR may be associated with increased mortality. Study Design A meta-analysis of cohort studies and trials. Setting & Population Patients with advanced CKD. Selection Criteria for Studies We performed a systematic literature search in MEDLINE, Cochrane Central Register of Controlled Trials, ClinicalTrials.gov , American Society of Nephrology abstracts, and bibliographies of retrieved articles to identify studies reporting on GFR at dialysis therapy initiation and mortality. Predictor Estimated or calculated GFR at dialysis therapy initiation. Outcome Pooled adjusted hazard ratio (HR) of continuous GFR for all-cause mortality. Results 16 cohort studies and 1 randomized controlled trial were identified (n = 1,081,116). By meta-analysis restricted to 15 cohorts (n = 1,079,917), higher GFR at dialysis therapy initiation was associated with a higher pooled adjusted HR for all-cause mortality (1.04; 95% CI, 1.03-1.05; P < 0.001). However, there was significant heterogeneity ( I2 = 97%; P < 0.001). The association persisted among the 9 cohorts that adjusted analytically for nutritional covariates (HR, 1.03; 95% CI, 1.02-1.04; P < 0.001; residual I2 = 97%). The highest mortality risk was observed in hemodialysis cohorts (HR, 1.05; 95% CI, 1.02-1.08; P < 0.001), whereas there was no association between GFR and mortality in peritoneal dialysis cohorts (HR, 1.04; 95% CI, 0.99-1.08, P = 0.1; residual I2 = 98%). Finally, higher GFR was associated with a lower mortality risk in cohorts that calculated GFR (HR, 0.80; 95% CI, 0.71-0.91; P = 0.003), contrasting with a higher mortality risk in cohorts that estimated GFR (HR, 1.04; 95% CI, 1.03-1.05; P < 0.001; residual I2 = 97%). Limitations Paucity of randomized controlled trials, different methods for determining GFR, and substantial heterogeneity. Conclusions Higher estimated rather than calculated GFR at dialysis therapy initiation is associated with a higher mortality risk in patients with advanced CKD, independent of nutritional status. Although there was substantial heterogeneity of effect size estimates across studies, this observation requires further study.]]></description><identifier>ISSN: 0272-6386</identifier><identifier>EISSN: 1523-6838</identifier><identifier>DOI: 10.1053/j.ajkd.2012.01.015</identifier><identifier>PMID: 22465328</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Cause of Death ; chronic kidney disease (CKD) ; Cohort Studies ; early initiation ; Emergency and intensive care: renal failure. Dialysis management ; End-stage renal disease (ESRD) ; Female ; glomerular filtration rate (GFR) ; Glomerular Filtration Rate - physiology ; hemodialysis ; Humans ; Intensive care medicine ; Kidney Failure, Chronic - diagnosis ; Kidney Failure, Chronic - mortality ; Kidney Failure, Chronic - therapy ; Kidneys ; late initiation ; Male ; Medical sciences ; mortality ; Nephrology ; Nephrology. Urinary tract diseases ; peritoneal dialysis ; Peritoneal Dialysis - methods ; Peritoneal Dialysis - mortality ; Prognosis ; Randomized Controlled Trials as Topic ; Renal Dialysis - methods ; Renal Dialysis - mortality ; Renal Insufficiency, Chronic - diagnosis ; Renal Insufficiency, Chronic - mortality ; Renal Insufficiency, Chronic - therapy ; Risk Assessment ; Severity of Illness Index ; Survival Analysis ; United States ; Urinary system involvement in other diseases. Miscellaneous</subject><ispartof>American journal of kidney diseases, 2012-06, Vol.59 (6), p.829-840</ispartof><rights>National Kidney Foundation, Inc.</rights><rights>2012 National Kidney Foundation, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.</rights><rights>2012 The National Kidney Foundation, Inc. Published by Elsevier Inc. 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Recent data suggest that higher GFR may be associated with increased mortality. Study Design A meta-analysis of cohort studies and trials. Setting & Population Patients with advanced CKD. Selection Criteria for Studies We performed a systematic literature search in MEDLINE, Cochrane Central Register of Controlled Trials, ClinicalTrials.gov , American Society of Nephrology abstracts, and bibliographies of retrieved articles to identify studies reporting on GFR at dialysis therapy initiation and mortality. Predictor Estimated or calculated GFR at dialysis therapy initiation. Outcome Pooled adjusted hazard ratio (HR) of continuous GFR for all-cause mortality. Results 16 cohort studies and 1 randomized controlled trial were identified (n = 1,081,116). By meta-analysis restricted to 15 cohorts (n = 1,079,917), higher GFR at dialysis therapy initiation was associated with a higher pooled adjusted HR for all-cause mortality (1.04; 95% CI, 1.03-1.05; P < 0.001). However, there was significant heterogeneity ( I2 = 97%; P < 0.001). The association persisted among the 9 cohorts that adjusted analytically for nutritional covariates (HR, 1.03; 95% CI, 1.02-1.04; P < 0.001; residual I2 = 97%). The highest mortality risk was observed in hemodialysis cohorts (HR, 1.05; 95% CI, 1.02-1.08; P < 0.001), whereas there was no association between GFR and mortality in peritoneal dialysis cohorts (HR, 1.04; 95% CI, 0.99-1.08, P = 0.1; residual I2 = 98%). Finally, higher GFR was associated with a lower mortality risk in cohorts that calculated GFR (HR, 0.80; 95% CI, 0.71-0.91; P = 0.003), contrasting with a higher mortality risk in cohorts that estimated GFR (HR, 1.04; 95% CI, 1.03-1.05; P < 0.001; residual I2 = 97%). Limitations Paucity of randomized controlled trials, different methods for determining GFR, and substantial heterogeneity. Conclusions Higher estimated rather than calculated GFR at dialysis therapy initiation is associated with a higher mortality risk in patients with advanced CKD, independent of nutritional status. Although there was substantial heterogeneity of effect size estimates across studies, this observation requires further study.]]></description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Cause of Death</subject><subject>chronic kidney disease (CKD)</subject><subject>Cohort Studies</subject><subject>early initiation</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>End-stage renal disease (ESRD)</subject><subject>Female</subject><subject>glomerular filtration rate (GFR)</subject><subject>Glomerular Filtration Rate - physiology</subject><subject>hemodialysis</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Kidney Failure, Chronic - diagnosis</subject><subject>Kidney Failure, Chronic - mortality</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Kidneys</subject><subject>late initiation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>mortality</subject><subject>Nephrology</subject><subject>Nephrology. Urinary tract diseases</subject><subject>peritoneal dialysis</subject><subject>Peritoneal Dialysis - methods</subject><subject>Peritoneal Dialysis - mortality</subject><subject>Prognosis</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Renal Dialysis - methods</subject><subject>Renal Dialysis - mortality</subject><subject>Renal Insufficiency, Chronic - diagnosis</subject><subject>Renal Insufficiency, Chronic - mortality</subject><subject>Renal Insufficiency, Chronic - therapy</subject><subject>Risk Assessment</subject><subject>Severity of Illness Index</subject><subject>Survival Analysis</subject><subject>United States</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><issn>0272-6386</issn><issn>1523-6838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kl1rFDEUhoModq3-AS8kN4I3s54kk8yMSKFsbS22CH5ch7OZjGY6m9QkW9h_b4Zd68eFcCAXed5z3rw5hDxnsGQgxetxieNNv-TA-BJYKfmALJjkolKtaB-SBfCGV0q06og8SWkEgE4o9ZgccV4rKXi7IKuL808UM730LjvMLngaBnrmcNollyj6nl6HmHFyeUedp6sPZ2_oKb22GSv0e-opeTTglOyzw3lMvp6_-7J6X119vLhcnV5VRoHKFW8syq7FGqzAoRF90ytsjaqVamsu162sB-QgkHM7dFKxum-h67lsQMLacHFMTvZ9b7frje2N9TnipG-j22Dc6YBO_33j3Xf9LdxpITrJeVMavDo0iOHH1qasNy4ZO03obdgmzUqEtRKdqgvK96iJIaVoh_sxDPScvh71nL6e09fASskievGnwXvJr7gL8PIAYDI4DRG9cek3JzspmYDCvd1ztsR552zUyTjrje1dtCbrPrj_-zj5R24m512ZeGN3No1hG8vXlffqVDT687wn85owDlCcduIndmW1tw</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Susantitaphong, Paweena, MD</creator><creator>Altamimi, Sarah, MBBS</creator><creator>Ashkar, Motaz, MBBS</creator><creator>Balk, Ethan M., MD, MPH</creator><creator>Stel, Vianda S., PhD</creator><creator>Wright, Seth, MD</creator><creator>Jaber, Bertrand L., MD, MS</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120601</creationdate><title>GFR at Initiation of Dialysis and Mortality in CKD: A Meta-analysis</title><author>Susantitaphong, Paweena, MD ; Altamimi, Sarah, MBBS ; Ashkar, Motaz, MBBS ; Balk, Ethan M., MD, MPH ; Stel, Vianda S., PhD ; Wright, Seth, MD ; Jaber, Bertrand L., MD, MS</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c606t-27ea598a40e3af73d7d6a8c64668425b854fa203a22ef95614d809d257050bc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Cause of Death</topic><topic>chronic kidney disease (CKD)</topic><topic>Cohort Studies</topic><topic>early initiation</topic><topic>Emergency and intensive care: renal failure. Dialysis management</topic><topic>End-stage renal disease (ESRD)</topic><topic>Female</topic><topic>glomerular filtration rate (GFR)</topic><topic>Glomerular Filtration Rate - physiology</topic><topic>hemodialysis</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Kidney Failure, Chronic - diagnosis</topic><topic>Kidney Failure, Chronic - mortality</topic><topic>Kidney Failure, Chronic - therapy</topic><topic>Kidneys</topic><topic>late initiation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>mortality</topic><topic>Nephrology</topic><topic>Nephrology. Urinary tract diseases</topic><topic>peritoneal dialysis</topic><topic>Peritoneal Dialysis - methods</topic><topic>Peritoneal Dialysis - mortality</topic><topic>Prognosis</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Renal Dialysis - methods</topic><topic>Renal Dialysis - mortality</topic><topic>Renal Insufficiency, Chronic - diagnosis</topic><topic>Renal Insufficiency, Chronic - mortality</topic><topic>Renal Insufficiency, Chronic - therapy</topic><topic>Risk Assessment</topic><topic>Severity of Illness Index</topic><topic>Survival Analysis</topic><topic>United States</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Susantitaphong, Paweena, MD</creatorcontrib><creatorcontrib>Altamimi, Sarah, MBBS</creatorcontrib><creatorcontrib>Ashkar, Motaz, MBBS</creatorcontrib><creatorcontrib>Balk, Ethan M., MD, MPH</creatorcontrib><creatorcontrib>Stel, Vianda S., PhD</creatorcontrib><creatorcontrib>Wright, Seth, MD</creatorcontrib><creatorcontrib>Jaber, Bertrand L., MD, MS</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of kidney diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Susantitaphong, Paweena, MD</au><au>Altamimi, Sarah, MBBS</au><au>Ashkar, Motaz, MBBS</au><au>Balk, Ethan M., MD, MPH</au><au>Stel, Vianda S., PhD</au><au>Wright, Seth, MD</au><au>Jaber, Bertrand L., MD, MS</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GFR at Initiation of Dialysis and Mortality in CKD: A Meta-analysis</atitle><jtitle>American journal of kidney diseases</jtitle><addtitle>Am J Kidney Dis</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>59</volume><issue>6</issue><spage>829</spage><epage>840</epage><pages>829-840</pages><issn>0272-6386</issn><eissn>1523-6838</eissn><abstract><![CDATA[Background The proportion of patients with advanced chronic kidney disease (CKD) initiating dialysis therapy at a higher glomerular filtration rate (GFR) has increased during the past decade. Recent data suggest that higher GFR may be associated with increased mortality. Study Design A meta-analysis of cohort studies and trials. Setting & Population Patients with advanced CKD. Selection Criteria for Studies We performed a systematic literature search in MEDLINE, Cochrane Central Register of Controlled Trials, ClinicalTrials.gov , American Society of Nephrology abstracts, and bibliographies of retrieved articles to identify studies reporting on GFR at dialysis therapy initiation and mortality. Predictor Estimated or calculated GFR at dialysis therapy initiation. Outcome Pooled adjusted hazard ratio (HR) of continuous GFR for all-cause mortality. Results 16 cohort studies and 1 randomized controlled trial were identified (n = 1,081,116). By meta-analysis restricted to 15 cohorts (n = 1,079,917), higher GFR at dialysis therapy initiation was associated with a higher pooled adjusted HR for all-cause mortality (1.04; 95% CI, 1.03-1.05; P < 0.001). However, there was significant heterogeneity ( I2 = 97%; P < 0.001). The association persisted among the 9 cohorts that adjusted analytically for nutritional covariates (HR, 1.03; 95% CI, 1.02-1.04; P < 0.001; residual I2 = 97%). The highest mortality risk was observed in hemodialysis cohorts (HR, 1.05; 95% CI, 1.02-1.08; P < 0.001), whereas there was no association between GFR and mortality in peritoneal dialysis cohorts (HR, 1.04; 95% CI, 0.99-1.08, P = 0.1; residual I2 = 98%). Finally, higher GFR was associated with a lower mortality risk in cohorts that calculated GFR (HR, 0.80; 95% CI, 0.71-0.91; P = 0.003), contrasting with a higher mortality risk in cohorts that estimated GFR (HR, 1.04; 95% CI, 1.03-1.05; P < 0.001; residual I2 = 97%). Limitations Paucity of randomized controlled trials, different methods for determining GFR, and substantial heterogeneity. Conclusions Higher estimated rather than calculated GFR at dialysis therapy initiation is associated with a higher mortality risk in patients with advanced CKD, independent of nutritional status. Although there was substantial heterogeneity of effect size estimates across studies, this observation requires further study.]]></abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>22465328</pmid><doi>10.1053/j.ajkd.2012.01.015</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Cause of Death
chronic kidney disease (CKD)
Cohort Studies
early initiation
Emergency and intensive care: renal failure. Dialysis management
End-stage renal disease (ESRD)
Female
glomerular filtration rate (GFR)
Glomerular Filtration Rate - physiology
hemodialysis
Humans
Intensive care medicine
Kidney Failure, Chronic - diagnosis
Kidney Failure, Chronic - mortality
Kidney Failure, Chronic - therapy
Kidneys
late initiation
Male
Medical sciences
mortality
Nephrology
Nephrology. Urinary tract diseases
peritoneal dialysis
Peritoneal Dialysis - methods
Peritoneal Dialysis - mortality
Prognosis
Randomized Controlled Trials as Topic
Renal Dialysis - methods
Renal Dialysis - mortality
Renal Insufficiency, Chronic - diagnosis
Renal Insufficiency, Chronic - mortality
Renal Insufficiency, Chronic - therapy
Risk Assessment
Severity of Illness Index
Survival Analysis
United States
Urinary system involvement in other diseases. Miscellaneous
title GFR at Initiation of Dialysis and Mortality in CKD: A Meta-analysis
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