Evidence map›Paper›PMID 38409492›Full record

ArticleThe European journal of health economics : HEPAC : health economics in prevention and care2024

Assessment of health state utilities associated with adult and pediatric acid sphingomyelinase deficiency (ASMD).

Louis S Matza, Katie D Stewart, Marie Fournier, Donna Rowen, Robin Lachmann, Maurizio Scarpa, Eugen Mengel, Travis Obermeyer, Evren Ayik, Fernando Laredo and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The European journal of health economics : HEPAC : health economics in prevention and care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 at 9 institutions in 5 countries.

Louis S MatzaPatient-Centered Research, Evidera, 7101 Wisconsin Avenue, Suite 1400, Bethesda, MD, 20814, USA. louis.matza@evidera.com.ORCID http://orcid.org/0000-0001-6374-5948
Katie D StewartPatient-Centered Research, Evidera, 7101 Wisconsin Avenue, Suite 1400, Bethesda, MD, 20814, USA.
Marie FournierSanofi, Chilly-Mazarin, France.
Donna RowenSchool of Health and Related Research, University of Sheffield, Sheffield, UK.
Robin LachmannUniversity College London Hospitals, London, UK.
Maurizio ScarpaCentro Coordinamento Regionale Malattie Rare, Azienda Sanitaria Universitaria del Friuli Centrale, Udine, Italy.
Eugen MengelSphinCS-Institute of Clinical Science for Lysosomal Storage Diseases, Hochheim, Germany.
Travis ObermeyerNNPDF, Charlotte, NC, USA.
Evren Ayik, Fresno, CA, USA.
Fernando LaredoSanofi, São Paulo, Brazil.
Ruth Pulikottil-JacobSanofi, Thames Valley Park, Reading, UK.
Azienda Unità Sanitaria Locale di Ferrara · ITFresno City College · USGramercy Research Group (United States) · USIthaka Harbors · USRoyal London Hospital · GBSanofi (Brazil) · BRSanofi (France) · FRSanofi (United Kingdom) · GBUniversity of Sheffield · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAcid sphingomyelinase deficiency (ASMD) type B is a rare genetic disorder leading to enlargement of the spleen and liver, pulmonary dysfunction, and other symptoms. Cost-utility analyses are often conducted to quantify the value of new treatments, and these analyses require health state utilities. Therefore, the purpose of this study was to estimate utilities associated with varying levels of severity of adult and pediatric ASMD type B.

methodsSeven adult and seven child health state vignettes describing ASMD were developed based on published literature, clinical trial results, and interviews with clinicians, patients with ASMD, and parents of children with ASMD. The health states were valued in time trade-off interviews with adult general population respondents in the UK.

resultsInterviews were completed with 202 participants (50.0% female; mean age = 41.3 years). The health state representing ASMD without impairment had the highest mean utility for both the adult and child health states (0.92/0.94), and severe ASMD had the lowest mean utility (0.33/0.45). Every child health state had a significantly greater utility than the corresponding adult health state. Differences between adult/child paired states ranged from 0.02 to 0.13. Subgroup analyses explored the impact of parenting status on valuation of child health states. DISCUSSION: Greater severity of ASMD was associated with lower mean utility. Results have implications for valuation of pediatric health states. The resulting utilities may be useful in cost-utility modeling estimating the value of treatment for ASMD.

Indexed as

Cost-Benefit AnalysisHealth StatusNiemann-Pick Disease, Type BAdolescentAdultChildChild, PreschoolFemaleHumansInterviews as TopicMaleMiddle AgedQuality-Adjusted Life YearsQuality of LifeSeverity of Illness IndexUnited KingdomAcid sphingomyelinase deficiencyPediatric utilityRare diseaseTime trade-offTTOUtility

Identifiers

PMID38409492
PMCPMC11442559
OpenAlexW4392194523

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LicenceCC BY
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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.