Evidence map›Paper›PMID 31135821›Full record

Trial reportJAMA internal medicine2019

Association Between the Publication of the Initiating Dialysis Early and Late Trial and the Timing of Dialysis Initiation in Canada.

Thomas W Ferguson, Amit X Garg, Manish M Sood, Claudio Rigatto, Elaine Chau, Paul Komenda, David Naimark, Gihad E Nesrallah, Steven D Soroka, Monica Beaulieu and 5 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in JAMA internal medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02183987 (Knowledge Translation Interventions to Prevent the Early Initiation of Dialysis), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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.

NCT02183987 nacompletednot on this map

Knowledge Translation Interventions to Prevent the Early Initiation of Dialysis: A Cluster Randomized Trial

TypeinterventionalSponsorUniversity of ManitobaRan2014 to 2016Enrolled55ConditionsChronic Kidney DiseaseArmsActive Knowledge Translation Intervention
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
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  8. Review
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

15 authors.

Thomas W FergusonDepartment of Internal Medicine, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Amit X GargDepartment of Epidemiology and Biostatistics, Western University, London, Ontario, Canada.
Manish M SoodThe Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Claudio RigattoDepartment of Internal Medicine, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Elaine ChauDepartment of Internal Medicine, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Paul KomendaDepartment of Internal Medicine, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
David NaimarkInstitute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
Gihad E NesrallahInstitute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.
Steven D SorokaDepartment of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
Monica BeaulieuDepartment of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Ahsan AlamDepartment of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.
S Joseph KimInstitute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
Stephanie DixonDepartment of Epidemiology and Biostatistics, Western University, London, Ontario, Canada.
Braden MannsO'Brien Institute for Public Health, University of Calgary, Calgary, Alberta, Canada.
Navdeep TangriDepartment of Internal Medicine, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Funding

CIHR
6 · The paper itself

Abstract

Importance: Published in 2010, the Initiating Dialysis Early and Late (IDEAL) randomized clinical trial, which randomized patients with an estimated glomerular filtration rate (GFR) between 10 and 15 mL/min/1.73 m2 to planned initiation of dialysis with an estimated GFR between 10 and 14 mL/min/1.73 m2 (early start) or an estimated GFR between 5 and 7 mL/min/1.73 m2 (late start), concluded that early initiation was not associated with improved survival or clinical outcomes. Objective: To assess the association between the IDEAL trial results and the proportion of early dialysis starts over time. Design, Setting, and Participants: This interrupted time series analysis used data from the Canadian Organ Replacement Register to study adult (≥18 years of age) patients with incident chronic dialysis between January 1, 2006, and December 31, 2015, in Canada, which has a universal health care system. Patients from the province of Quebec were excluded because its privacy laws preclude submission of deidentified data without first-person consent. The patients included in the study (n = 28 468) had at least 90 days of nephrologist care before starting dialysis and a recorded estimated GFR at dialysis initiation. Data analyses were performed from November 2016 to January 2019. Main Outcomes and Measures: The primary outcome was the proportion of early dialysis starts (estimated GFR >10.5 mL/min/1.73 m2), and the secondary outcomes included the proportions of acute inpatient dialysis starts, patients who started dialysis using a home modality, and patients receiving hemodialysis who started with an arteriovenous access. Measures included the trend prior to the IDEAL trial publication, the change in this trend after publication, and the immediate consequence of publication. Results: The final cohort comprised 28 468 patients, of whom 17 342 (60.9%) were male and the mean (SD) age was 64.8 (14.6) years. Before the IDEAL trial, a statistically significant increasing trend was observed in the monthly proportion of early dialysis starts (adjusted rate ratio, 1.002; 95% CI, 1.001-1.004; P = .004). After the IDEAL trial, an immediate decrease was observed in the proportion of early dialysis starts (rate ratio, 0.874; 95% CI, 0.818-0.933; P < .001), along with a statistically significant change in trend between the pretrial and posttrial periods (rate ratio, 0.994; 95% CI, 0.992-0.996; P < .001). No statistically significant differences were found in acute inpatient dialysis initiations, the proportion of patients receiving home dialysis as the initial modality, or the proportion of arteriovenous access creation at hemodialysis initiation after the IDEAL trial publication. Conclusions and Relevance: The publication of the IDEAL trial appeared to be associated with an immediate and meaningful change in the timing of dialysis initiation in Canada.

Indexed as

Renal DialysisAgedCanadaFemaleHome Care ServicesHumansKidney Failure, ChronicMaleMiddle AgedTime Factors

Identifiers

PMID31135821
PMCPMC6547160

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.