Preferences on the Use of Prokinetic Agents in Adult Intensive Care Unit Patients-An International Survey
- PMID: 40275492
- PMCID: PMC12022387
- DOI: 10.1111/aas.70045
Preferences on the Use of Prokinetic Agents in Adult Intensive Care Unit Patients-An International Survey
Abstract
Introduction: Feeding intolerance complicates enteral nutrition in intensive care unit (ICU) patients but is poorly defined. Prokinetic agents are administered to facilitate the uptake of enteral nutrition, but preferences for their use among clinicians in ICUs are unknown.
Methods: We conducted an international electronic survey targeting ICU doctors. The survey included 76 questions that focused on symptoms considered when assessing feeding intolerance, preferences for using prokinetic agents, and willingness to participate in a future randomised trial on prokinetic agents.
Results: We received 830 responses from 17 countries, with an overall response rate of 29%. Most respondents were specialists working in mixed ICUs. Feeding intolerance was assessed by 90% of respondents in their clinical work, though only 36% considered it well defined. Gastric residual volume and vomiting were symptoms most frequently used for defining feeding intolerance. Metoclopramide was the preferred prokinetic agent (54% of respondents), followed by erythromycin (42%). Four out of five considered using combination therapy, primarily a combination of metoclopramide and erythromycin (89%). Concerns about side effects were reported for all agents, with extrapyramidal symptoms and QT prolongation being the most common across agents. The majority (91%) of respondents supported a future randomised trial comparing prokinetic agents to placebo.
Conclusion: This international survey found practice variations in the symptoms reportedly used to assess feeding intolerance. Metoclopramide was the preferred prokinetic agent, followed by erythromycin. Most respondents supported a future randomised trial.
Keywords: feeding intolerance; intensive care; prokinetic agents; survey.
© 2025 The Author(s). Acta Anaesthesiologica Scandinavica published by John Wiley & Sons Ltd on behalf of Acta Anaesthesiologica Scandinavica Foundation.
Conflict of interest statement
The Department of Intensive Care at Rigshospitalet‐Copenhagen University Hospital (MHM) has received funding from the Novo Nordisk Foundation and Sygeforsikringen ‘Denmark’ outside the submitted work. A.R.B. has received speaker or consultancy fees from Nutricia and VIPUN Medical and is holding a grant from the Estonian Research Council (PRG1255) outside the submitted work. The Department of Intensive Care, University Hospital, Inselspital, reports grants from Orion Pharma, Abbott Nutrition International, B. Braun Medical AG, CSEM AG, Edwards Lifesciences Services GmbH, Kenta Biotech Ltd., Maquet Critical Care AB, Omnicare Clinical Research AG, Nestle, Pierre Fabre Pharma AG, Pfizer, Bard Medica S.A., Abbott AG, Anandic Medical Systems, Pan Gas AG Healthcare, Bracco, Hamilton Medical AG, Fresenius Kabi, Getinge Group Maquet AG, Dräger AG, Teleflex Medical GmbH, GlaxoSmithKline, Merck Sharp and Dohme AG, Eli Lilly and Company, Baxter, Astellas, AstraZeneca, CSL Behring, Novartis, Covidien, Phagenesis, Cytel and Nycomed outside the project. The money was paid into departmental funds; no personal financial gain applied. Finally, this research was conducted during the tenure of a Health Research Council of New Zealand Clinical Practioner Research Fellowship held by Paul Young. The Medical Research Institute of New Zealand is supported by Independent Research Organisation Funding from the Health Research Council of New Zealand.
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References
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- Blaser A. R., Starkopf J., Kirsimägi Ü., and Deane A. M., “Definition, Prevalence, and Outcome of Feeding Intolerance in Intensive Care: A Systematic Review and Meta‐Analysis,” Acta Anaesthesiologica Scandinavica 58 (2014): 914–922. - PubMed
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