Literature DB >> 23921536

Criteria for fairly allocating scarce health-care resources to genetic tests: which matter most?

Wolf H Rogowski1, Scott D Grosse2, Jörg Schmidtke3, Georg Marckmann4.   

Abstract

The use of genetic tests is expanding rapidly. Given limited health-care budgets throughout Europe and few national coverage decisions specifically for genetic tests, decisions about allocating scarce resources to genetic tests are frequently ad hoc and left to lower-level decision makers. This study assesses substantive ethical and economic criteria to prioritize genetic services in a reasonable and fair manner. Principles for allocating health-care resources can be classified into four categories: need-based allocation; maximizing total benefits; treating people equally; and promoting and rewarding social usefulness. In the face of scarcity, the degree of an individual's need for medical intervention is an important criterion. Also, different economic concepts of efficiency are of relevance in the theory and practice of prioritizing genetic tests. Equity concerns are most likely to be relevant in terms of avoiding undesirable inequities, which may also set boundaries to the use of efficiency as a prioritization criterion. The aim of promoting and rewarding social usefulness is unlikely to be relevant to the question of what priority a genetic test should have in clinical practice. Further work is needed to select an appropriate set of criteria; operationalize them; and assign weights before some kind of standardized priority information can be added to information sources for genetic services. Besides the substantive criteria, formal considerations like those pointed out in the framework of accountability for reasonableness need to be considered in decision making.

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Year:  2013        PMID: 23921536      PMCID: PMC3865392          DOI: 10.1038/ejhg.2013.172

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  45 in total

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Authors:  R Cookson; P Dolan
Journal:  J Med Ethics       Date:  2000-10       Impact factor: 2.903

2.  Explaining income-related inequalities in doctor utilisation in Europe.

Authors:  Eddy van Doorslaer; Xander Koolman; Andrew M Jones
Journal:  Health Econ       Date:  2004-07       Impact factor: 3.046

3.  Points to consider in assessing and appraising predictive genetic tests.

Authors:  Wolf H Rogowski; Scott D Grosse; Jürgen John; Helena Kääriäinen; Alastair Kent; Ulf Kristofferson; Jörg Schmidtke
Journal:  J Community Genet       Date:  2010-10-16

Review 4.  Challenges of translating genetic tests into clinical and public health practice.

Authors:  Wolf H Rogowski; Scott D Grosse; Muin J Khoury
Journal:  Nat Rev Genet       Date:  2009-07       Impact factor: 53.242

5.  Principles for allocation of scarce medical interventions.

Authors:  Govind Persad; Alan Wertheimer; Ezekiel J Emanuel
Journal:  Lancet       Date:  2009-01-31       Impact factor: 79.321

Review 6.  Economic methods for valuing the outcomes of genetic testing: beyond cost-effectiveness analysis.

Authors:  Scott D Grosse; Sarah Wordsworth; Katherine Payne
Journal:  Genet Med       Date:  2008-09       Impact factor: 8.822

7.  [National and regional prioritisation in Swedish health care: experiences from cardiology].

Authors:  Jörg Carlsson
Journal:  Z Evid Fortbild Qual Gesundhwes       Date:  2012-06-27

8.  Ethical issues in prenatal diagnosis.

Authors:  S R Johnson; T E Elkins
Journal:  Clin Obstet Gynecol       Date:  1988-06       Impact factor: 2.190

9.  Technology assessment and resource allocation for predictive genetic testing: a study of the perspectives of Canadian genetic health care providers.

Authors:  Alethea Adair; Robyn Hyde-Lay; Edna Einsiedel; Timothy Caulfield
Journal:  BMC Med Ethics       Date:  2009-06-18       Impact factor: 2.652

10.  Clearing up the hazy road from bench to bedside: a framework for integrating the fourth hurdle into translational medicine.

Authors:  Wolf H Rogowski; Susanne C Hartz; Jürgen H John
Journal:  BMC Health Serv Res       Date:  2008-09-24       Impact factor: 2.655

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  14 in total

1.  Fair allocation of health-care resources: finding a model that does not disenfranchise users of genetic services. A commentary on Rogowski et al....

Authors:  Heather Skirton
Journal:  Eur J Hum Genet       Date:  2013-08-07       Impact factor: 4.246

2.  A theory-informed systematic review of clinicians' genetic testing practices.

Authors:  Jean L Paul; Hanna Leslie; Alison H Trainer; Clara Gaff
Journal:  Eur J Hum Genet       Date:  2018-06-11       Impact factor: 4.246

3.  Barriers to clinical adoption of next-generation sequencing: a policy Delphi panel's solutions.

Authors:  Donna A Messner; Pei Koay; Jennifer Al Naber; Robert Cook-Deegan; Mary Majumder; Gail Javitt; Rachel Dvoskin; Juli Bollinger; Margaret Curnutte; Amy L McGuire
Journal:  Per Med       Date:  2017-06-23       Impact factor: 2.512

Review 4.  Conceptualising 'Benefits Beyond Health' in the Context of the Quality-Adjusted Life-Year: A Critical Interpretive Synthesis.

Authors:  Lidia Engel; Stirling Bryan; David G T Whitehurst
Journal:  Pharmacoeconomics       Date:  2021-08-23       Impact factor: 4.981

5.  Parental Attitudes Toward Clinical Genomic Sequencing in Children With Critical Cardiac Disease.

Authors:  Dana B Gal; Natalie Deuitch; Sandra Soo Jin Lee; Rosalie Tang Simon; Danton S Char
Journal:  Pediatr Crit Care Med       Date:  2021-08-01       Impact factor: 3.971

Review 6.  Funding decisions for newborn screening: a comparative review of 22 decision processes in Europe.

Authors:  Katharina Elisabeth Fischer; Wolf Henning Rogowski
Journal:  Int J Environ Res Public Health       Date:  2014-05-19       Impact factor: 3.390

7.  Patient and interest organizations' views on personalized medicine: a qualitative study.

Authors:  Isabelle Budin-Ljøsne; Jennifer R Harris
Journal:  BMC Med Ethics       Date:  2016-05-13       Impact factor: 2.652

8.  Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape.

Authors:  Kim C A Holtkamp; Evelien M Vos; Tessel Rigter; Phillis Lakeman; Lidewij Henneman; Martina C Cornel
Journal:  BMC Health Serv Res       Date:  2017-02-16       Impact factor: 2.655

9.  Ethical issues in preconception genetic carrier screening.

Authors:  Ulrik Kihlbom
Journal:  Ups J Med Sci       Date:  2016-07-08       Impact factor: 2.384

10.  Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.

Authors:  Franziska Severin; Pascal Borry; Martina C Cornel; Norman Daniels; Florence Fellmann; Shirley Victoria Hodgson; Heidi C Howard; Jürgen John; Helena Kääriäinen; Hülya Kayserili; Alastair Kent; Florian Koerber; Ulf Kristoffersson; Mark Kroese; Celine Lewis; Georg Marckmann; Peter Meyer; Arne Pfeufer; Jörg Schmidtke; Heather Skirton; Lisbeth Tranebjærg; Wolf H Rogowski
Journal:  Eur J Hum Genet       Date:  2014-09-24       Impact factor: 4.246

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