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Disease monitoring strategies in inflammatory bowel diseases: What do we mean by “tight control”?
In recent years, there has been a critical change in treatment paradigms in inflammatory bowel diseases (IBD) triggered by the arrival of new effective treatments aiming to prevent disease progression, bowel damage and disability. The insufficiency of symptomatic disease control and the well-known d...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848014/ https://www.ncbi.nlm.nih.gov/pubmed/31749591 http://dx.doi.org/10.3748/wjg.v25.i41.6172 |
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author | Gonczi, Lorant Bessissow, Talat Lakatos, Peter Laszlo |
author_facet | Gonczi, Lorant Bessissow, Talat Lakatos, Peter Laszlo |
author_sort | Gonczi, Lorant |
collection | PubMed |
description | In recent years, there has been a critical change in treatment paradigms in inflammatory bowel diseases (IBD) triggered by the arrival of new effective treatments aiming to prevent disease progression, bowel damage and disability. The insufficiency of symptomatic disease control and the well-known discordance between symptoms and objective measures of disease activity lead to the need of reviewing conventional treatment algorithms and developing new concepts of optimal therapeutic strategy. The treat-to-target strategies, defined by the selecting therapeutic targets in inflammatory bowel disease consensus recommendation, move away from only symptomatic disease control and support targeting composite therapeutic endpoints (clinical and endoscopical remission) and timely assessment. Emerging data suggest that early therapy using a treat-to-target approach and an algorithmic therapy escalation using regular disease monitoring by clinical and biochemical markers (fecal calprotectin and C-reactive protein) leads to improved outcomes. This review aims to present the emerging strategies and supporting evidence in the current therapeutic paradigm of IBD including the concepts of “early intervention”, “treat-to-target” and “tight control” strategies. We also discuss the real-word experience and applicability of these new strategies and give an overview on the future perspectives and areas in need of further research and potential improvement regarding treatment targets and (“tight”) disease monitoring strategies. |
format | Online Article Text |
id | pubmed-6848014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-68480142019-11-20 Disease monitoring strategies in inflammatory bowel diseases: What do we mean by “tight control”? Gonczi, Lorant Bessissow, Talat Lakatos, Peter Laszlo World J Gastroenterol Review In recent years, there has been a critical change in treatment paradigms in inflammatory bowel diseases (IBD) triggered by the arrival of new effective treatments aiming to prevent disease progression, bowel damage and disability. The insufficiency of symptomatic disease control and the well-known discordance between symptoms and objective measures of disease activity lead to the need of reviewing conventional treatment algorithms and developing new concepts of optimal therapeutic strategy. The treat-to-target strategies, defined by the selecting therapeutic targets in inflammatory bowel disease consensus recommendation, move away from only symptomatic disease control and support targeting composite therapeutic endpoints (clinical and endoscopical remission) and timely assessment. Emerging data suggest that early therapy using a treat-to-target approach and an algorithmic therapy escalation using regular disease monitoring by clinical and biochemical markers (fecal calprotectin and C-reactive protein) leads to improved outcomes. This review aims to present the emerging strategies and supporting evidence in the current therapeutic paradigm of IBD including the concepts of “early intervention”, “treat-to-target” and “tight control” strategies. We also discuss the real-word experience and applicability of these new strategies and give an overview on the future perspectives and areas in need of further research and potential improvement regarding treatment targets and (“tight”) disease monitoring strategies. Baishideng Publishing Group Inc 2019-11-07 2019-11-07 /pmc/articles/PMC6848014/ /pubmed/31749591 http://dx.doi.org/10.3748/wjg.v25.i41.6172 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Review Gonczi, Lorant Bessissow, Talat Lakatos, Peter Laszlo Disease monitoring strategies in inflammatory bowel diseases: What do we mean by “tight control”? |
title | Disease monitoring strategies in inflammatory bowel diseases: What do we mean by “tight control”? |
title_full | Disease monitoring strategies in inflammatory bowel diseases: What do we mean by “tight control”? |
title_fullStr | Disease monitoring strategies in inflammatory bowel diseases: What do we mean by “tight control”? |
title_full_unstemmed | Disease monitoring strategies in inflammatory bowel diseases: What do we mean by “tight control”? |
title_short | Disease monitoring strategies in inflammatory bowel diseases: What do we mean by “tight control”? |
title_sort | disease monitoring strategies in inflammatory bowel diseases: what do we mean by “tight control”? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848014/ https://www.ncbi.nlm.nih.gov/pubmed/31749591 http://dx.doi.org/10.3748/wjg.v25.i41.6172 |
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