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Ethical Questions Linked to Rare Diseases and Orphan Drugs – A Systematic Review

BACKGROUND: Rare or orphan diseases have become an important target of healthcare activities all over the world. The study aims to identify ethical questions linked to rare diseases and orphan drugs and ethical principles or approaches applied to solve them. METHODS: Relevant peer-reviewed articles...

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Autores principales: Kacetl, Jaroslav, Marešová, Petra, Maskuriy, Raihan, Selamat, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568613/
https://www.ncbi.nlm.nih.gov/pubmed/33116992
http://dx.doi.org/10.2147/RMHP.S260641
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author Kacetl, Jaroslav
Marešová, Petra
Maskuriy, Raihan
Selamat, Ali
author_facet Kacetl, Jaroslav
Marešová, Petra
Maskuriy, Raihan
Selamat, Ali
author_sort Kacetl, Jaroslav
collection PubMed
description BACKGROUND: Rare or orphan diseases have become an important target of healthcare activities all over the world. The study aims to identify ethical questions linked to rare diseases and orphan drugs and ethical principles or approaches applied to solve them. METHODS: Relevant peer-reviewed articles were identified by means of a systematic review. The literature was searched from 20 May 2020 to 20 June 2020. The search included the databases PubMed, Scopus and Web of Science (2010 – April 2020). A total of 4,139 papers related to rare diseases were identified; with 1,205 papers obtained from Scopus; 2,476 papers from PubMed; and 458 from Web of Science with keyword search “ethics” AND “rare” AND “disease”, “ethical” AND “orphan”, “ethical” AND “orphan” AND “drug”, and “ethical” AND “rare“ AND “disease”. Finally, XX studies were chosen for further analysis. RESULTS: The main findings reveal five main ethical issues. The most essential one shows that funding research and development in the field of orphan drugs poses an almost impossible dilemma. Other issues include the significance of non-economic values like compassion and beneficence in decision-making related to orphan drugs and rare diseases; the identification of limits to labelling diseases as rare; barriers to global, supranational and international cooperation; and last but not least, determining and establishing panels of decision-makers. CONCLUSIONS: A strictly global approach would be the most appropriate way to deal with rare diseases. Nonetheless, international, let alone global, cooperation seems to be completely beyond the reach of the current international community, although the EU, for instance, has a centralized procedure for labelling orphan drugs. This deficit in international cooperation can be partly explained by the fact that the current technologically globalized world still lacks globally accepted ethical values and rules. This is further aggravated by unresolved international and intercultural conflicts. In addition, the sub-interests of various parties as well as the lack of desire to deal with other people’s problems need to be taken into account. The aforementioned problems are difficult to avoid. Nevertheless, let us be cautiously optimistic. At least, there are people who raise ethical questions about rare diseases and orphan drugs.
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spelling pubmed-75686132020-10-27 Ethical Questions Linked to Rare Diseases and Orphan Drugs – A Systematic Review Kacetl, Jaroslav Marešová, Petra Maskuriy, Raihan Selamat, Ali Risk Manag Healthc Policy Original Research BACKGROUND: Rare or orphan diseases have become an important target of healthcare activities all over the world. The study aims to identify ethical questions linked to rare diseases and orphan drugs and ethical principles or approaches applied to solve them. METHODS: Relevant peer-reviewed articles were identified by means of a systematic review. The literature was searched from 20 May 2020 to 20 June 2020. The search included the databases PubMed, Scopus and Web of Science (2010 – April 2020). A total of 4,139 papers related to rare diseases were identified; with 1,205 papers obtained from Scopus; 2,476 papers from PubMed; and 458 from Web of Science with keyword search “ethics” AND “rare” AND “disease”, “ethical” AND “orphan”, “ethical” AND “orphan” AND “drug”, and “ethical” AND “rare“ AND “disease”. Finally, XX studies were chosen for further analysis. RESULTS: The main findings reveal five main ethical issues. The most essential one shows that funding research and development in the field of orphan drugs poses an almost impossible dilemma. Other issues include the significance of non-economic values like compassion and beneficence in decision-making related to orphan drugs and rare diseases; the identification of limits to labelling diseases as rare; barriers to global, supranational and international cooperation; and last but not least, determining and establishing panels of decision-makers. CONCLUSIONS: A strictly global approach would be the most appropriate way to deal with rare diseases. Nonetheless, international, let alone global, cooperation seems to be completely beyond the reach of the current international community, although the EU, for instance, has a centralized procedure for labelling orphan drugs. This deficit in international cooperation can be partly explained by the fact that the current technologically globalized world still lacks globally accepted ethical values and rules. This is further aggravated by unresolved international and intercultural conflicts. In addition, the sub-interests of various parties as well as the lack of desire to deal with other people’s problems need to be taken into account. The aforementioned problems are difficult to avoid. Nevertheless, let us be cautiously optimistic. At least, there are people who raise ethical questions about rare diseases and orphan drugs. Dove 2020-10-13 /pmc/articles/PMC7568613/ /pubmed/33116992 http://dx.doi.org/10.2147/RMHP.S260641 Text en © 2020 Kacetl et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Kacetl, Jaroslav
Marešová, Petra
Maskuriy, Raihan
Selamat, Ali
Ethical Questions Linked to Rare Diseases and Orphan Drugs – A Systematic Review
title Ethical Questions Linked to Rare Diseases and Orphan Drugs – A Systematic Review
title_full Ethical Questions Linked to Rare Diseases and Orphan Drugs – A Systematic Review
title_fullStr Ethical Questions Linked to Rare Diseases and Orphan Drugs – A Systematic Review
title_full_unstemmed Ethical Questions Linked to Rare Diseases and Orphan Drugs – A Systematic Review
title_short Ethical Questions Linked to Rare Diseases and Orphan Drugs – A Systematic Review
title_sort ethical questions linked to rare diseases and orphan drugs – a systematic review
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568613/
https://www.ncbi.nlm.nih.gov/pubmed/33116992
http://dx.doi.org/10.2147/RMHP.S260641
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