Evidence map›Paper›PMID 33596965›Full record

ArticleOrphanet journal of rare diseases2021

Belgian rare diseases plan in clinical pathology: identification of key biochemical diagnostic tests and establishment of reference laboratories and financing conditions.

Nathalie M Vandevelde, Pieter Vermeersch, Katrien M J Devreese, Marie-Françoise Vincent, Béatrice Gulbis, François Eyskens, François Boemer, André Gothot, Viviane O Van Hoof, Carolien Bonroy and 11 more

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

21 authors at 8 institutions in 1 country.

Nathalie M VandeveldeDepartment of Quality of Laboratories, Sciensano, Rue Juliette Wytsmanstraat 14, 1050, Brussels, Belgium. nathalie.vandevelde@sciensano.be.ORCID 0000-0003-0157-7963
Pieter VermeerschRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Katrien M J DevreeseRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Marie-Françoise VincentRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Béatrice GulbisRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
François EyskensCenter of Inherited Metabolic Diseases, Antwerp University Hospital, Edegem, Belgium.
François BoemerRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
André GothotRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Viviane O Van HoofRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Carolien BonroyRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Hedwig StepmanRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Geert A MartensRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Xavier BossuytRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Laurence RoosensRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Julie SmetClinical Pathology, LHUB-ULB, Université Libre de Bruxelles, Brussels, Belgium.
Hilde LaeremansLaboratory of Pediatric Research, Free University of Brussels, Brussels, Belgium.
Ilse WeetsRare Diseases Working Group, Belgian National Commission on Clinical Pathology, Brussels, Belgium.
Jean-Marc MinonLaboratory and Department of Blood Transfusion, CHR de la Citadelle, Liège, Belgium.
Kris VernelenDepartment of Quality of Laboratories, Sciensano, Rue Juliette Wytsmanstraat 14, 1050, Brussels, Belgium.
Wim CouckeDepartment of Quality of Laboratories, Sciensano, Rue Juliette Wytsmanstraat 14, 1050, Brussels, Belgium.
Advisory Board of the Action 1 of the Belgian National Plan for Rare Diseases
Sciensano (Belgium) · BEGhent University Hospital · BEUniversité Libre de Bruxelles · BEAntwerp University Hospital · BEUniversitair Ziekenhuis Leuven · BEUniversity of Liège · BECliniques Universitaires Saint-Luc · BEVrije Universiteit Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOne objective of the Belgian Rare Diseases plan is to improve patients' management using phenotypic tests and, more specifically, the access to those tests by identifying the biochemical analyses used for rare diseases, developing new financing conditions and establishing reference laboratories.

methodsA feasibility study was performed from May 2015 until August 2016 in order to select the financeable biochemical analyses, and, among them, those that should be performed by reference laboratories. This selection was based on an inventory of analyses used for rare diseases and a survey addressed to the Belgian laboratories of clinical pathology (investigating the annual analytical costs, volumes, turnaround times and the tests unavailable in Belgium and outsourced abroad). A proposal of financeable analyses, financing modalities, reference laboratories' scope and budget estimation was developed and submitted to the Belgian healthcare authorities. After its approval in December 2016, the implementation phase took place from January 2017 until December 2019.

resultsIn 2019, new reimbursement conditions have been published for 46 analyses and eighteen reference laboratories have been recognized. Collaborations have also been developed with 5 foreign laboratories in order to organize the outsourcing and financing of 9 analyses unavailable in Belgium.

conclusionsIn the context of clinical pathology and rare diseases, this initiative enabled to identify unreimbursed analyses and to meet the most crucial financial needs. It also contributed to improve patients' management by establishing Belgian reference laboratories and foreign referral laboratories for highly-specific analyses and a permanent surveillance, quality and financing framework for those tests.

Indexed as

Diagnostic Tests, RoutineRare DiseasesBelgiumBudgetsHumansLaboratoriesClinical pathologyExpertiseFinancingRare diseasesReference laboratoriesReimbursement codes

Identifiers

PMID33596965
PMCPMC7890854
OpenAlexW3112477162

What OpenQuestion holds

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LicenceCC BY
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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.