Evidence map›Paper›PMID 37349725›Full record

ArticleOrphanet journal of rare diseases2023

Estimated costs for Duchenne muscular dystrophy care in Brazil.

Nayê Balzan Schneider, Erica Caetano Roos, Ana Lúcia Portella Staub, Isabela Possebon Bevilacqua, Ana Carolina de Almeida, Tamiê de Camargo Martins, Natalia Bergamelli Ramos, Priscilla Loze, Jonas Alex Morales Saute, Ana Paula Beck da Silva Etges and 1 more

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 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.

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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
  4. Article
  5. 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

11 authors.

Nayê Balzan SchneiderNational Institute of Science and Technology for Health Technology Assessment (IATS)- CNPq/Brazil (project: 465518/2014-1), Porto Alegre, Brazil.
Erica Caetano RoosPrograma de Pós-Graduação em Engenharia de Produção, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Ana Lúcia Portella StaubCentro de Pesquisa Clínica, Hospital de Clínicas de Porto Alegre, Neurogenética, Porto Alegre, Brazil.
Isabela Possebon BevilacquaCentro de Pesquisa Clínica, Hospital de Clínicas de Porto Alegre, Neurogenética, Porto Alegre, Brazil.
Ana Carolina de AlmeidaProdutos Roche Químicos e Farmacêuticos S/A, São Paulo, SP, Brazil.
Tamiê de Camargo MartinsProdutos Roche Químicos e Farmacêuticos S/A, São Paulo, SP, Brazil.
Natalia Bergamelli RamosProdutos Roche Químicos e Farmacêuticos S/A, São Paulo, SP, Brazil.
Priscilla LozeProdutos Roche Químicos e Farmacêuticos S/A, São Paulo, SP, Brazil.
Jonas Alex Morales SauteCentro de Pesquisa Clínica, Hospital de Clínicas de Porto Alegre, Neurogenética, Porto Alegre, Brazil.
Ana Paula Beck da Silva EtgesNational Institute of Science and Technology for Health Technology Assessment (IATS)- CNPq/Brazil (project: 465518/2014-1), Porto Alegre, Brazil. anabsetges@gmail.com.
Carisi Anne PolanczykNational Institute of Science and Technology for Health Technology Assessment (IATS)- CNPq/Brazil (project: 465518/2014-1), Porto Alegre, Brazil.

Funding

Produtos Roche Químicos e Farmacêuticos S/A do Brasil Produtos Roche Químicos e Farmacêuticos S/A do Brasil
6 · The paper itself

Abstract

backgroundThe economic burden of rare diseases on health systems is still not widely measured, with the generation of accurate information about the costs with medical care for subjects with rare diseases being crucial when defining health policies. Duchenne Muscular Dystrophy (DMD) is the most common form of muscular dystrophy, with new technologies recently being studied for its management. Information about the costs related to the disease in Latin America is scarce, and the objective of this study is to evaluate the annual hospital, home care and transportation costs per patient with DMD treatment in Brazil.

resultsData from 27 patients were included, the median annual cost per patient was R$ 17,121 (IQR R$ 6,786; 25,621). Home care expenditures accounted for 92% of the total costs, followed by hospital costs (6%) and transportation costs (2%). Medications and loss of family, and patient's productivity are among the most representative consumption items. When disease worsening due to loss of the ability to walk was incorporated to the analysis, it was shown that wheelchair users account for an incremental cost of 23% compared with non-wheelchair users.

conclusionsThis is an original study in Latin America to measure DMD costs using the micro-costing technique. Generating accurate information about costs is crucial to provide health managers with information that could help establish more sustainable policies when deciding upon rare diseases in emerging countries.

Indexed as

Cost of IllnessMuscular Dystrophy, DuchenneBrazilHealth Care CostsHumansRare DiseasesCost of illnessMuscular dystrophy, DuchenneNeuromuscular diseasesRare diseases

Identifiers

PMID37349725
PMCPMC10288739

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Registered trials

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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.