Evidence map›Paper›PMID 38730191›Full record

ArticleJournal of community genetics2024

The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysis.

Luiza M Neves, Márcia Pinto, Olivia A Zin, Daniela P Cunha, Bruna N S Agonigi, Fabiana L Motta, Leonardo H F Gomes, Dafne D G Horovitz, Daltro C Almeida, Jocieli Malacarne and 8 more

Abstract read
In one paragraph

Article in Journal of community genetics, 2024. 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. Observational
  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

18 authors.

Luiza M NevesInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Márcia PintoInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil. mftpinto@gmail.com.
Olivia A ZinDepartment of Ophthalmology, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil.
Daniela P CunhaInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Bruna N S AgonigiInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Fabiana L Motta5Instituto de Genética Ocular, São Paulo, 04552-050, Brazil.
Leonardo H F GomesInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Dafne D G HorovitzInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Daltro C AlmeidaInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Jocieli MalacarneInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Leticia GuidaInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Andressa BragaInstituto Nacional de Cardiologia, Rio de Janeiro, 22240-006, Brazil.
Adriana Bastos CarvalhoInstituto Nacional de Cardiologia, Rio de Janeiro, 22240-006, Brazil.
Eduardo PereiraINSEAD, Fontainebleau, France.
Ana Paula S RodriguesDepartment of Ophthalmology, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil.
Juliana M F SallumDepartment of Ophthalmology, Universidade Federal de São Paulo, São Paulo, 04039-032, Brazil.
Andrea A ZinInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.
Zilton F M VasconcelosInstituto Fernandes Figueira-Fundação Oswaldo Cruz, Rio de Janeiro, 22250-020, Brazil.

Funding

Brazilian National Program of Support to the Health Assistance of the Person with Deficiency (PRONAS/PCD) 25000.193451/2019-21Foundation for the scientific and technological development in health IFF-002-FEX-22
6 · The paper itself

Abstract

Up to 25% of pediatric cataract cases are inherited. There is sparse information in the literature regarding the cost of whole-exome sequencing (WES) for suspected hereditary pediatric cataracts. Molecular diagnosis of suspected hereditary pediatric cataracts is important for comprehensive genetic counseling. We performed a partial economic evaluation with a mixed costing analysis, using reimbursement data and microcosting approach with a bottom-up technique to estimate the cost of using WES for genetic diagnosis of suspected hereditary pediatric cataracts from the perspective of the Brazilian governmental health care system. One hundred and ten participants from twenty-nine families in Rio de Janeiro (RJ) were included. Costs of consumables, staff and equipment were calculated. Two scenarios were created: (1) The reference scenario included patients from RJ with suspected hereditary pediatric cataracts plus two family members. (2) The alternative scenario considered other genetic diseases, resulting in 5,280 exams per month. Sensitivity analysis was also performed. In the reference scenario, the total cost per exam was 700.09 United States dollars (USD), and in the alternative scenario, the total cost was 559.23 USD. The cost of WES alone was 527.85 USD in the reference scenario and 386.98 USD in the alternative scenario. Sensitivity analysis revealed that the largest costs were associated with consumables in both scenarios. Economic evaluations can help inform policy decisions, especially in middle-income countries such as Brazil.

Indexed as

Congenital cataractsHereditary cataractsMicrocostingMixed costing health economicsPediatric cataractsWhole-exome sequencing

Identifiers

PMID38730191
PMCPMC11217199

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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.