Evidence map›Paper›PMID 27734213›Full record

ArticleHealth care analysis : HCA : journal of health philosophy and policy2017

The (Ir)relevance of Group Size in Health Care Priority Setting: A Reply to Juth.

Lars Sandman, Erik Gustavsson

Abstract read
In one paragraph

Article in Health care analysis : HCA : journal of health philosophy and policy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Should Severity Assessments in Healthcare Priority Setting be Risk- and Time-Sensitive?Health care analysis : HCA : journal of health philosophy and policy · 2023
    Article
  5. Article
  6. Review
  7. Why We Don't Need "Unmet Needs"! On the Concepts of Unmet Need and Severity in Health-Care Priority Setting.Health care analysis : HCA : journal of health philosophy and policy · 2019
    Article
  8. Article
  9. Prioritising, Ranking and Resource Implementation - A Normative Analysis.International journal of health policy and management · 2018
    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

2 authors.

Lars SandmanNational Centre for Priority Setting in Health-Care, Linköping University, 581 83, Linköping, Sweden. lars.sandman@liu.se.ORCID http://orcid.org/0000-0003-0987-7653
Erik GustavssonNational Centre for Priority Setting in Health-Care, Linköping University, 581 83, Linköping, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

How to handle orphan drugs for rare diseases is a pressing problem in current health-care. Due to the group size of patients affecting the cost of treatment, they risk being disadvantaged in relation to existing cost-effectiveness thresholds. In an article by Niklas Juth it has been argued that it is irrelevant to take indirectly operative factors like group size into account since such a compensation would risk discounting the use of cost, a relevant factor, altogether. In this article we analyze Juth's argument and observe that we already do compensate for indirectly operative factors, both outside and within cost-effectiveness evaluations, for formal equality reasons. Based on this we argue that we have reason to set cost-effectiveness thresholds to integrate equity concerns also including formal equality considerations. We find no reason not to compensate for group size to the extent we already compensate for other factors. Moreover, groups size implying a systematic disadvantage also on a global scale, i.e. taking different aspects of the health condition of patients suffering from rare diseases into account, will provide strong reason for why group size is indeed relevant to compensate for (if anything).

Indexed as

Health PrioritiesCost-Benefit AnalysisHumansVulnerable PopulationsCost-effectivenessEqualityFormal equalityJusticeOrphan drugsPriority settingRare diseases

Identifiers

PMID27734213
PMCPMC5313590

What OpenQuestion holds

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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.