Evidence map›Paper›PMID 26124687›Full record

ArticleJournal of blood medicine2015

Issues in assessing products for the treatment of hemophilia - the intersection between efficacy, economics, and ethics.

Albert Farrugia, Declan Noone, Uwe Schlenkrich, Steffen Schlenkrich, Brian O'Mahony, Josephine Cassar

Abstract read
In one paragraph

Article in Journal of blood medicine, 2015. 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. Hemostats in the clinic.Bioengineering & translational medicine · 2024
    Review
  2. 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

6 authors.

Albert FarrugiaSchool of Surgery, QEII Medical Centre, The University of Western Australia (M509), Crawley, WA, Australia ; College of Medicine, Medicine and Environment, Australian National University, Canberra, WA, Australia.
Declan NooneIrish Haemophilia Society, Dublin, Ireland.
Uwe SchlenkrichDeutsche Hämophiliegesellschaft (DHG), Hamburg, Germany.
Steffen SchlenkrichAm Holzbiel, Erfurt-Töttleben, Germany.
Brian O'MahonyIrish Haemophilia Society, Dublin, Ireland.
Josephine CassarFaculty of Health, University of Canberra, Canberra, WA, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Following the obviation of the pathogen safety threats posed by previous generations of clotting factor concentrates for the treatment of hemophilia, the principal issue facing the patient community is timely access to adequate supplies of continuously improving therapies. The application of evidence-based medicine has enhanced the basis of hemophilia therapy, while resulting in some challenges to patient care. Increasingly, the criteria used for the approval and payment of treatment products by regulatory and reimbursement agencies, respectively, are becoming inflexible and unrealistic. This is occurring particularly in the requirements for demonstrating product efficacy. Concurrently, emerging evidence of the interpatient variability in the clinical response to therapy has led to the proposed personalization of therapeutic regimens. Possible impediments to optimal care include competitive tensions among suppliers who seek to gain label claims for reimbursement purposes, which result in clinical trial designs of, arguably, unethical design, carried out in poor countries. We synthesize these converging developments to suggest some changes to the current hemophilia treatment paradigm, which should make it more patient-centric and enable speedier access to new therapies.

Indexed as

clinical trialshemophiliareimbursementstandardstreatment products

Identifiers

PMID26124687
PMCPMC4476485

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.