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The Development of Practice Recommendations for Drug-Disease Interactions by Literature Review and Expert Opinion
BACKGROUND: Drug-disease interactions negatively affect the benefit/risk ratio of drugs for specific populations. In these conditions drugs should be avoided, adjusted, or accompanied by extra monitoring. The motivation for many drug-disease interactions in the Summary of Product Characteristics (Sm...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243438/ https://www.ncbi.nlm.nih.gov/pubmed/32499701 http://dx.doi.org/10.3389/fphar.2020.00707 |
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author | van Tongeren, Justine M. Z. Harkes-Idzinga, S. Froukje van der Sijs, Heleen Atiqi, Roya van den Bemt, Bart J. F. Draijer, L. Willem Hiel, Deline Kerremans, Adrian Kremers, Bart de Leeuw, Marc Olthoff, Marleen V. Pham, T. Kim-Loan Valentijn-Robertz, Ricky Tsoi, Kayan Wichers, Iris de Wit, Maaike Borgsteede, Sander D. |
author_facet | van Tongeren, Justine M. Z. Harkes-Idzinga, S. Froukje van der Sijs, Heleen Atiqi, Roya van den Bemt, Bart J. F. Draijer, L. Willem Hiel, Deline Kerremans, Adrian Kremers, Bart de Leeuw, Marc Olthoff, Marleen V. Pham, T. Kim-Loan Valentijn-Robertz, Ricky Tsoi, Kayan Wichers, Iris de Wit, Maaike Borgsteede, Sander D. |
author_sort | van Tongeren, Justine M. Z. |
collection | PubMed |
description | BACKGROUND: Drug-disease interactions negatively affect the benefit/risk ratio of drugs for specific populations. In these conditions drugs should be avoided, adjusted, or accompanied by extra monitoring. The motivation for many drug-disease interactions in the Summary of Product Characteristics (SmPC) is sometimes insufficiently supported by (accessible) evidence. As a consequence the translation of SmPC to clinical practice may lead to non-specific recommendations. For the translation of this information to the real world, it is necessary to evaluate the available knowledge about drug-disease interactions, and to formulate specific recommendations for prescribers and pharmacists. The aim of this paper is to describe a standardized method how to develop practice recommendations for drug-disease interactions by literature review and expert opinion. METHODS: The development of recommendations for drug-disease interactions will follow a six-step plan involving a multidisciplinary expert panel (1). The scope of the drug-disease interaction will be specified by defining the disease and by describing relevant effects of this drug-disease interaction. Drugs possibly involved in this drug-disease interaction are selected by checking the official product information, literature, and expert opinion (2). Evidence will be collected from the official product information, guidelines, handbooks, and primary literature (3). Study characteristics and outcomes will be evaluated and presented in standardized reports, including preliminary conclusions on the clinical relevance and practice recommendations (4). The multidisciplinary expert panel will discuss the reports and will either adopt or adjust the conclusions (5). Practice recommendations will be integrated in clinical decision support systems and published (6). The results of the evaluated drug-disease interactions will remain up-to-date by screening new risk information, periodic literature review, and (re)assessments initiated by health care providers. ACTIONABLE RECOMMENDATIONS: The practice recommendations will result in advices for specific DDSI. The content and considerations of these DDSIs will be published and implemented in all Clinical Decision Support Systems in the Netherlands. DISCUSSION: The recommendations result in professional guidance in the context of individual patient care. The professional will be supported in the decision making in concerning pharmacotherapy for the treatment of a medical problem, and the clinical risks of the proposed medication in combination with specific diseases. |
format | Online Article Text |
id | pubmed-7243438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72434382020-06-03 The Development of Practice Recommendations for Drug-Disease Interactions by Literature Review and Expert Opinion van Tongeren, Justine M. Z. Harkes-Idzinga, S. Froukje van der Sijs, Heleen Atiqi, Roya van den Bemt, Bart J. F. Draijer, L. Willem Hiel, Deline Kerremans, Adrian Kremers, Bart de Leeuw, Marc Olthoff, Marleen V. Pham, T. Kim-Loan Valentijn-Robertz, Ricky Tsoi, Kayan Wichers, Iris de Wit, Maaike Borgsteede, Sander D. Front Pharmacol Pharmacology BACKGROUND: Drug-disease interactions negatively affect the benefit/risk ratio of drugs for specific populations. In these conditions drugs should be avoided, adjusted, or accompanied by extra monitoring. The motivation for many drug-disease interactions in the Summary of Product Characteristics (SmPC) is sometimes insufficiently supported by (accessible) evidence. As a consequence the translation of SmPC to clinical practice may lead to non-specific recommendations. For the translation of this information to the real world, it is necessary to evaluate the available knowledge about drug-disease interactions, and to formulate specific recommendations for prescribers and pharmacists. The aim of this paper is to describe a standardized method how to develop practice recommendations for drug-disease interactions by literature review and expert opinion. METHODS: The development of recommendations for drug-disease interactions will follow a six-step plan involving a multidisciplinary expert panel (1). The scope of the drug-disease interaction will be specified by defining the disease and by describing relevant effects of this drug-disease interaction. Drugs possibly involved in this drug-disease interaction are selected by checking the official product information, literature, and expert opinion (2). Evidence will be collected from the official product information, guidelines, handbooks, and primary literature (3). Study characteristics and outcomes will be evaluated and presented in standardized reports, including preliminary conclusions on the clinical relevance and practice recommendations (4). The multidisciplinary expert panel will discuss the reports and will either adopt or adjust the conclusions (5). Practice recommendations will be integrated in clinical decision support systems and published (6). The results of the evaluated drug-disease interactions will remain up-to-date by screening new risk information, periodic literature review, and (re)assessments initiated by health care providers. ACTIONABLE RECOMMENDATIONS: The practice recommendations will result in advices for specific DDSI. The content and considerations of these DDSIs will be published and implemented in all Clinical Decision Support Systems in the Netherlands. DISCUSSION: The recommendations result in professional guidance in the context of individual patient care. The professional will be supported in the decision making in concerning pharmacotherapy for the treatment of a medical problem, and the clinical risks of the proposed medication in combination with specific diseases. Frontiers Media S.A. 2020-05-15 /pmc/articles/PMC7243438/ /pubmed/32499701 http://dx.doi.org/10.3389/fphar.2020.00707 Text en Copyright © 2020 van Tongeren, Harkes-Idzinga, van der Sijs, Atiqi, van den Bemt, Draijer, Hiel, Kerremans, Kremers, de Leeuw, Olthoff, Pham, Valentijn-Robertz, Tsoi, Wichers, de Wit and Borgsteede http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology van Tongeren, Justine M. Z. Harkes-Idzinga, S. Froukje van der Sijs, Heleen Atiqi, Roya van den Bemt, Bart J. F. Draijer, L. Willem Hiel, Deline Kerremans, Adrian Kremers, Bart de Leeuw, Marc Olthoff, Marleen V. Pham, T. Kim-Loan Valentijn-Robertz, Ricky Tsoi, Kayan Wichers, Iris de Wit, Maaike Borgsteede, Sander D. The Development of Practice Recommendations for Drug-Disease Interactions by Literature Review and Expert Opinion |
title | The Development of Practice Recommendations for Drug-Disease Interactions by Literature Review and Expert Opinion |
title_full | The Development of Practice Recommendations for Drug-Disease Interactions by Literature Review and Expert Opinion |
title_fullStr | The Development of Practice Recommendations for Drug-Disease Interactions by Literature Review and Expert Opinion |
title_full_unstemmed | The Development of Practice Recommendations for Drug-Disease Interactions by Literature Review and Expert Opinion |
title_short | The Development of Practice Recommendations for Drug-Disease Interactions by Literature Review and Expert Opinion |
title_sort | development of practice recommendations for drug-disease interactions by literature review and expert opinion |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243438/ https://www.ncbi.nlm.nih.gov/pubmed/32499701 http://dx.doi.org/10.3389/fphar.2020.00707 |
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