Evidence map›Paper›PMID 22465328›Full record

SynthesisAmerican journal of kidney diseases : the official journal of the National Kidney Foundation2012

GFR at initiation of dialysis and mortality in CKD: a meta-analysis.

Paweena Susantitaphong, Sarah Altamimi, Motaz Ashkar, Ethan M Balk, Vianda S Stel, Seth Wright, Bertrand L Jaber

Registry-linked trialAbstract readComparative StudyMeta-AnalysisReview
In one paragraph

Synthesis in American journal of kidney diseases : the official journal of the National Kidney Foundation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03385902 (Impact on Mortality of Timing of Dialysis Initiation in Patients With End-stage Renal Disease by a Novel Assessment Based on Fuzzy Mathematics), which is not on this map. Cited by 53 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 5 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03385902 nacompletednot on this mapstarted 2018, after this paper: background citation

Impact on Mortality of Timing of Dialysis Initiation in Patients With End-stage Renal Disease by a Novel Assessment Based on Fuzzy Mathematics

TypeinterventionalSponsorThe First Affiliated Hospital of Dalian Medical UniversityRan2018 to 2024Enrolled388ConditionsChronic Kidney DiseaseArmsoptimal start time, late start time
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
  3. Guideline
  4. Canadian Society of Nephrology 2014 clinical practice guideline for timing the initiation of chronic dialysis.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2014
    Guideline
  5. Pooled it
  6. Trial
  7. Trial
  8. Comparative effectiveness of early versus conventional timing of dialysis initiation in advanced CKD.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2014
    Trial
  9. Association between GFR estimated by multiple methods at dialysis commencement and patient survival.Clinical journal of the American Society of Nephrology : CJASN · 2014
    Trial
  10. Article
  11. Observational
  12. Article
  13. Article
  14. Article
  15. Observational
  16. Article
  17. Article
  18. Article
  19. Article
  20. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Paweena SusantitaphongDepartment of Medicine, Division of Nephrology, Kidney and Dialysis Research Laboratory, St. Elizabeth's Medical Center, Boston, MA 02135, USA.
Sarah Altamimi
Motaz Ashkar
Ethan M Balk
Vianda S Stel
Seth Wright
Bertrand L Jaber

Funding

TUFTS CLINICAL AND TRANSLATION SCIENCE INSTITUTE (UL1): BPCAUL1RR025752 · NCRR · TUFTS UNIVERSITY BOSTON · PI SELKER, HARRY P. · 2008 to 2011
$17.6M
NCRR NIH HHS UL1 RR025752
6 · The paper itself

Abstract

backgroundThe 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

designA 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.

results16 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 (I(2) = 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 I(2) = 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 I(2) = 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 I(2) = 97%). LIMITATIONS: Paucity of randomized controlled trials, different methods for determining GFR, and substantial heterogeneity.

conclusionsHigher 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.

Indexed as

Cause of DeathCohort StudiesFemaleGlomerular Filtration RateHumansKidney Failure, ChronicMalePeritoneal DialysisPrognosisRandomized Controlled Trials as TopicRenal DialysisRenal Insufficiency, ChronicRisk AssessmentSeverity of Illness IndexSurvival AnalysisUnited States

Identifiers

PMID22465328
PMCPMC3395227

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.