Evidence map›Paper›PMID 32953126›Full record

ArticleCanadian journal of kidney health and disease2020

A Provincial Survey of the Contemporary Management of Autosomal Dominant Polycystic Kidney Disease.

Tae Won Yi, Adeera Levin, Micheli Bevilacqua, Mark Canney

Open access · goldAbstract read
In one paragraph

Article in Canadian journal of kidney health and disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 32% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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

4 authors at 1 institution in 1 country.

Tae Won YiDivision of Nephrology, The University of British Columbia, Vancouver, Canada.ORCID https://orcid.org/0000-0003-3350-1170
Adeera LevinDivision of Nephrology, The University of British Columbia, Vancouver, Canada.
Micheli BevilacquaDivision of Nephrology, The University of British Columbia, Vancouver, Canada.
Mark CanneyDivision of Nephrology, The University of British Columbia, Vancouver, Canada.
University of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent years have witnessed an encouraging expansion of knowledge and management tools in the care of patients with autosomal dominant polycystic kidney disease (ADPKD), including measurement of total kidney volume as a biomarker of disease progression, stringent blood pressure targets to slow cyst growth, and targeted treatments such as tolvaptan.

objectivesWe sought to evaluate clinicians' familiarity with, and usage of, novel evidence-based management tools for ADPKD.

designOn-line survey.

settingBritish Columbia, Canada.

participantsNephrologists in academic and community practice (excluding clinicians who practice exclusively in transplantation). MEASUREMENTS: Participants answered multiple-choice questions in 6 domains: sources of information, self-identified needs for optimal care delivery, prognostication, imaging tests, blood pressure targets, and use of tolvaptan.

methodsAn online survey was developed and disseminated via email to 65 nephrologists engaged in current clinical practice in British Columbia.

resultsA total of 29 nephrologists (45%) completed the questionnaire. The most popular source of information was the primary literature (83% of respondents). While 86% of respondents reported assessing the risk of disease progression before the onset of kidney function decline, most were using traditional metrics such as blood pressure and proteinuria rather than validated prediction tools such as the Mayo Classification. Although 90% of respondents obtained additional imaging after diagnosis in some or all of their ADPKD patients, only 1 in 5 reported being confident in their ability to interpret kidney size. The recommended blood pressure (BP) target of <110/75 mmHg was sought by 17% of respondents. All respondents reported being familiar with the literature regarding tolvaptan; however, only half were confident in their ability to identify suitable patients for treatment. The top 3 needs identified by clinicians were better access to medications (69%), clear management protocols (66%), and easier access to imaging tests (59%). LIMITATIONS: Funding mechanisms for tolvaptan can vary; therefore, clinicians' experience with the drug may not be generalizable. Although the response rate was acceptable, the survey is nonetheless subject to responder bias.

conclusionThis survey indicates that there is substantial variability in the usage of, and familiarity with, evidence-based ADPKD management tools among contemporary nephrologists, contributing to incomplete translation of evidence into clinical practice. Providing greater access to tolvaptan or imaging tests is unlikely to improve patient care without enhancing knowledge translation and education.

trial registrationNot applicable as this was a survey.

Indexed as

autosomal dominant polycystic kidney diseaseevidence-based medicineknowledge translationsurveytolvaptan

Identifiers

PMID32953126
PMCPMC7476332
OpenAlexW3082087942

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.