Evidence map›Paper›PMID 25716610›Full record

ArticleJIMD reports2015

Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in Canada.

Monica F Lamoureux, Kylie Tingley, Jonathan B Kronick, Beth K Potter, Alicia K J Chan, Doug Coyle, Linda Dodds, Sarah Dyack, Annette Feigenbaum, Michael Geraghty and 21 more

Abstract read
In one paragraph

Article in JIMD reports, 2015. 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
–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.

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.

  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

31 authors.

Monica F LamoureuxChildren's Hospital of Eastern Ontario, Ottawa, ON, Canada, K1H 8L1.
Kylie Tingley
Jonathan B Kronick
Beth K Potter
Alicia K J Chan
Doug Coyle
Linda Dodds
Sarah Dyack
Annette Feigenbaum
Michael Geraghty
Jane Gillis
Cheryl Rockman-Greenberg
Aneal Khan
Julian Little
Jennifer MacKenzie
Bruno Maranda
Aizeddin Mhanni
John J Mitchell
Grant Mitchell
Anne-Marie Laberge
Murray Potter
Chitra Prasad
Komudi Siriwardena
Kathy N Speechley
Sylvia Stockler
Yannis Trakadis
Lesley Turner
Clara Van Karnebeek
Kumanan Wilson
Pranesh Chakraborty
Canadian Inherited Metabolic Diseases Research Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNearly all children in Canada with an inherited metabolic disease (IMD) are treated at one of the country's Hereditary Metabolic Disease Treatment Centres. We sought to understand the system of care for paediatric IMD patients in Canada in order to identify sources of variation and inform future research priorities.

methodsTreatment centres were contacted by email and invited to complete a web-based survey. The questionnaire addressed, for each centre, the population size served and scope of practice, available human resources and clinic services and research capacity. Survey responses were analyzed descriptively.

resultsWe received responses from 13 of the 14 treatment centres invited to participate. These centres represent at least 85% of the Canadian population, with over half of the centres located in southern Ontario and Quebec. All centres reported paediatric patients with IMDs as their main patient population. A variety of dedicated staff was identified; every centre reported having at least one physician and one dietician. The most common ancillary services available included telehealth (11/12 respondents) and biochemical genetic laboratory testing (10/12), with a high variability of access to on-site laboratory tests. A majority of centres indicated access to additional off-site services, but barriers to these were reported. All but one centre indicated previous experience with research.

conclusionsThe variation we identified in the organization of care highlights the need to investigate the association between practice differences and health outcomes for paediatric IMD patients to inform policies that establish equitable access to services that are beneficial.

Identifiers

PMID25716610
PMCPMC4470950

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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.