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Fluid hydration to prevent post-ERCP pancreatitis in average- to high-risk patients receiving prophylactic rectal NSAIDs (FLUYT trial): study protocol for a randomized controlled trial
BACKGROUND: Post-endoscopic retrograde cholangiopancreatography (ERCP) pancreatitis (PEP) is the most common complication of ERCP and may run a severe course. Evidence suggests that vigorous periprocedural hydration can prevent PEP, but studies to date have significant methodological drawbacks. Impo...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879873/ https://www.ncbi.nlm.nih.gov/pubmed/29606135 http://dx.doi.org/10.1186/s13063-018-2583-x |
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author | Smeets, Xavier J. N. M. da Costa, David W. Fockens, Paul Mulder, Chris J. J. Timmer, Robin Kievit, Wietske Zegers, Marieke Bruno, Marco J. Besselink, Marc G. H. Vleggaar, Frank P. van der Hulst, Rene W. M. Poen, Alexander C. Heine, Gerbrand D. N. Venneman, Niels G. Kolkman, Jeroen J. Baak, Lubbertus C. Römkens, Tessa E. H. van Dijk, Sven M. Hallensleben, Nora D. L. van de Vrie, Wim Seerden, Tom C. J. Tan, Adriaan C. I. T. L. Voorburg, Annet M. C. J. Poley, Jan-Werner Witteman, Ben J. Bhalla, Abha Hadithi, Muhammed Thijs, Willem J. Schwartz, Matthijs P. Vrolijk, Jan Maarten Verdonk, Robert C. van Delft, Foke Keulemans, Yolande van Goor, Harry Drenth, Joost P. H. van Geenen, Erwin J. M. |
author_facet | Smeets, Xavier J. N. M. da Costa, David W. Fockens, Paul Mulder, Chris J. J. Timmer, Robin Kievit, Wietske Zegers, Marieke Bruno, Marco J. Besselink, Marc G. H. Vleggaar, Frank P. van der Hulst, Rene W. M. Poen, Alexander C. Heine, Gerbrand D. N. Venneman, Niels G. Kolkman, Jeroen J. Baak, Lubbertus C. Römkens, Tessa E. H. van Dijk, Sven M. Hallensleben, Nora D. L. van de Vrie, Wim Seerden, Tom C. J. Tan, Adriaan C. I. T. L. Voorburg, Annet M. C. J. Poley, Jan-Werner Witteman, Ben J. Bhalla, Abha Hadithi, Muhammed Thijs, Willem J. Schwartz, Matthijs P. Vrolijk, Jan Maarten Verdonk, Robert C. van Delft, Foke Keulemans, Yolande van Goor, Harry Drenth, Joost P. H. van Geenen, Erwin J. M. |
author_sort | Smeets, Xavier J. N. M. |
collection | PubMed |
description | BACKGROUND: Post-endoscopic retrograde cholangiopancreatography (ERCP) pancreatitis (PEP) is the most common complication of ERCP and may run a severe course. Evidence suggests that vigorous periprocedural hydration can prevent PEP, but studies to date have significant methodological drawbacks. Importantly, evidence for its added value in patients already receiving prophylactic rectal non-steroidal anti-inflammatory drugs (NSAIDs) is lacking and the cost-effectiveness of the approach has not been investigated. We hypothesize that combination therapy of rectal NSAIDs and periprocedural hydration would significantly lower the incidence of post-ERCP pancreatitis compared to rectal NSAIDs alone in moderate- to high-risk patients undergoing ERCP. METHODS: The FLUYT trial is a multicenter, parallel group, open label, superiority randomized controlled trial. A total of 826 moderate- to high-risk patients undergoing ERCP that receive prophylactic rectal NSAIDs will be randomized to a control group (no fluids or normal saline with a maximum of 1.5 mL/kg/h and 3 L/24 h) or intervention group (lactated Ringer’s solution with 20 mL/kg over 60 min at start of ERCP, followed by 3 mL/kg/h for 8 h thereafter). The primary endpoint is the incidence of post-ERCP pancreatitis. Secondary endpoints include PEP severity, hydration-related complications, and cost-effectiveness. DISCUSSION: The FLUYT trial design, including hydration schedule, fluid type, and sample size, maximize its power of identifying a potential difference in post-ERCP pancreatitis incidence in patients receiving prophylactic rectal NSAIDs. TRIAL REGISTRATION: EudraCT: 2015-000829-37. Registered on 18 February 2015. ISRCTN: 13659155. Registered on 18 May 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-2583-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5879873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58798732018-04-04 Fluid hydration to prevent post-ERCP pancreatitis in average- to high-risk patients receiving prophylactic rectal NSAIDs (FLUYT trial): study protocol for a randomized controlled trial Smeets, Xavier J. N. M. da Costa, David W. Fockens, Paul Mulder, Chris J. J. Timmer, Robin Kievit, Wietske Zegers, Marieke Bruno, Marco J. Besselink, Marc G. H. Vleggaar, Frank P. van der Hulst, Rene W. M. Poen, Alexander C. Heine, Gerbrand D. N. Venneman, Niels G. Kolkman, Jeroen J. Baak, Lubbertus C. Römkens, Tessa E. H. van Dijk, Sven M. Hallensleben, Nora D. L. van de Vrie, Wim Seerden, Tom C. J. Tan, Adriaan C. I. T. L. Voorburg, Annet M. C. J. Poley, Jan-Werner Witteman, Ben J. Bhalla, Abha Hadithi, Muhammed Thijs, Willem J. Schwartz, Matthijs P. Vrolijk, Jan Maarten Verdonk, Robert C. van Delft, Foke Keulemans, Yolande van Goor, Harry Drenth, Joost P. H. van Geenen, Erwin J. M. Trials Study Protocol BACKGROUND: Post-endoscopic retrograde cholangiopancreatography (ERCP) pancreatitis (PEP) is the most common complication of ERCP and may run a severe course. Evidence suggests that vigorous periprocedural hydration can prevent PEP, but studies to date have significant methodological drawbacks. Importantly, evidence for its added value in patients already receiving prophylactic rectal non-steroidal anti-inflammatory drugs (NSAIDs) is lacking and the cost-effectiveness of the approach has not been investigated. We hypothesize that combination therapy of rectal NSAIDs and periprocedural hydration would significantly lower the incidence of post-ERCP pancreatitis compared to rectal NSAIDs alone in moderate- to high-risk patients undergoing ERCP. METHODS: The FLUYT trial is a multicenter, parallel group, open label, superiority randomized controlled trial. A total of 826 moderate- to high-risk patients undergoing ERCP that receive prophylactic rectal NSAIDs will be randomized to a control group (no fluids or normal saline with a maximum of 1.5 mL/kg/h and 3 L/24 h) or intervention group (lactated Ringer’s solution with 20 mL/kg over 60 min at start of ERCP, followed by 3 mL/kg/h for 8 h thereafter). The primary endpoint is the incidence of post-ERCP pancreatitis. Secondary endpoints include PEP severity, hydration-related complications, and cost-effectiveness. DISCUSSION: The FLUYT trial design, including hydration schedule, fluid type, and sample size, maximize its power of identifying a potential difference in post-ERCP pancreatitis incidence in patients receiving prophylactic rectal NSAIDs. TRIAL REGISTRATION: EudraCT: 2015-000829-37. Registered on 18 February 2015. ISRCTN: 13659155. Registered on 18 May 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-2583-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-02 /pmc/articles/PMC5879873/ /pubmed/29606135 http://dx.doi.org/10.1186/s13063-018-2583-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Smeets, Xavier J. N. M. da Costa, David W. Fockens, Paul Mulder, Chris J. J. Timmer, Robin Kievit, Wietske Zegers, Marieke Bruno, Marco J. Besselink, Marc G. H. Vleggaar, Frank P. van der Hulst, Rene W. M. Poen, Alexander C. Heine, Gerbrand D. N. Venneman, Niels G. Kolkman, Jeroen J. Baak, Lubbertus C. Römkens, Tessa E. H. van Dijk, Sven M. Hallensleben, Nora D. L. van de Vrie, Wim Seerden, Tom C. J. Tan, Adriaan C. I. T. L. Voorburg, Annet M. C. J. Poley, Jan-Werner Witteman, Ben J. Bhalla, Abha Hadithi, Muhammed Thijs, Willem J. Schwartz, Matthijs P. Vrolijk, Jan Maarten Verdonk, Robert C. van Delft, Foke Keulemans, Yolande van Goor, Harry Drenth, Joost P. H. van Geenen, Erwin J. M. Fluid hydration to prevent post-ERCP pancreatitis in average- to high-risk patients receiving prophylactic rectal NSAIDs (FLUYT trial): study protocol for a randomized controlled trial |
title | Fluid hydration to prevent post-ERCP pancreatitis in average- to high-risk patients receiving prophylactic rectal NSAIDs (FLUYT trial): study protocol for a randomized controlled trial |
title_full | Fluid hydration to prevent post-ERCP pancreatitis in average- to high-risk patients receiving prophylactic rectal NSAIDs (FLUYT trial): study protocol for a randomized controlled trial |
title_fullStr | Fluid hydration to prevent post-ERCP pancreatitis in average- to high-risk patients receiving prophylactic rectal NSAIDs (FLUYT trial): study protocol for a randomized controlled trial |
title_full_unstemmed | Fluid hydration to prevent post-ERCP pancreatitis in average- to high-risk patients receiving prophylactic rectal NSAIDs (FLUYT trial): study protocol for a randomized controlled trial |
title_short | Fluid hydration to prevent post-ERCP pancreatitis in average- to high-risk patients receiving prophylactic rectal NSAIDs (FLUYT trial): study protocol for a randomized controlled trial |
title_sort | fluid hydration to prevent post-ercp pancreatitis in average- to high-risk patients receiving prophylactic rectal nsaids (fluyt trial): study protocol for a randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5879873/ https://www.ncbi.nlm.nih.gov/pubmed/29606135 http://dx.doi.org/10.1186/s13063-018-2583-x |
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