Evidence map›Paper›PMID 34236542›Full record

ArticleThe European journal of health economics : HEPAC : health economics in prevention and care2022

Costs and management of patients with hemophilia A in France: the Hemraude study.

C Laurendeau, J Goudemand, M Trossaert, B Polack, R Varin, C Godard, F Hadim, B Detournay

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In one paragraph

Article in The European journal of health economics : HEPAC : health economics in prevention and care, 2022. 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
1.2field-weighted citation impact, top 21% 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, 11 citations in OpenAlex.

  1. Haemophilia in France: Modelisation of the Clinical Pathway for Patients.International journal of environmental research and public health · 2022
    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

8 authors at 6 institutions in 1 country.

C LaurendeauCemka, 43, Boulevard Maréchal Joffre, 92340, Bourg-la-Reine, France.
J GoudemandDepartment of Hemostasis and Transfusion, Lille University Hospital, Lille, France.
M TrossaertHematology Department, University Hospital, Nantes, France.
B PolackLaboratory TIMC-IMAG, UMRS 5525, Hematology Department, University Hospital, CNRS University Grenoble-Alpes, Grenoble, France.
R VarinClinical Pharmacy Department, University Hospital, Rouen, France.
C GodardRoche, Boulogne, France.
F HadimRoche, Boulogne, France.
B DetournayCemka, 43, Boulevard Maréchal Joffre, 92340, Bourg-la-Reine, France. bruno.detournay@cemka.fr.ORCID http://orcid.org/0000-0001-7843-4608
Cemka-Eval (France) · FRRoche (France) · FRCentre Hospitalier Universitaire de Nantes · FRCentre National de la Recherche Scientifique · FRUniversité de Lille · FRUniversité de Rouen Normandie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe Hemraude study was conducted to describe the profile of patients with HA, disease management, and economic burden in a collective perspective.

methodsThis retrospective study was conducted using the French administrative healthcare claims database SNIIRAM/SNDS. Male patients treated for hemophilia A with a long-term illness (ALD) status or invalidity were included in the study between January 1, 2016 and December 31, 2017. Patients were classified in six treatment groups: no treatment, on-demand FVIII, prophylactic FVIII, FVIII in immune tolerance induction (ITI) protocol, on-demand bypassing agents, and prophylactic bypassing agents. Patients treated with FVIII in ITI protocol and those treated with bypassing agents are deemed to have developed inhibitors. HA patients were compared to a control population without coagulation disorder and matched (ratio 1:3) on age and sex.

resultsA total of 4172 patients were included in the analysis, aged on average 35.2 years, 5.3% had HIV infection, and 8.8% had hepatitis B or C. In 2017, half of the patients received no treatment for HA, 46.7% were treated with FVIII (25% on demand, 20.6% with prophylaxis, and 1.1% ITI), 1.5% with bypassing agents. Patients treated with prophylactic treatments, either inhibitor or non-inhibitor, were less likely to be hospitalized for severe bleeding compared to patients receiving on-demand treatments. The average annual costs for HA management per patient were 72,209.60 €. The highest costs were observed in patients treated with FVIII in ITI protocol and those receiving prophylactic bypassing agents.

conclusionDirect costs of HA treatments for HA may be very high especially in the small percentage of patients developing inhibitors or treated with ITI protocol.

Indexed as

Hemophilia AHIV InfectionsAgedFactor VIIIHemorrhageHumansMaleRetrospective StudiesFactor VIIIBypassing agentDirect costsEconomic burdenFactor VIIIHemophilia AInhibitors

Identifiers

PMID34236542
OpenAlexW3181762364

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.