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  5. A randomized clinical trial of methylnaltrexone for the treatment of opioid induced constipation & gastrointestinal stasis in intensive care patients; results from the MOTION trial
 
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A randomized clinical trial of methylnaltrexone for the treatment of opioid induced constipation & gastrointestinal stasis in intensive care patients; results from the MOTION trial
File(s)
Patel et al MOTION accepted 060120.pdf (464.5 KB)
Accepted version
Author(s)
Patel, Parind B
Brett, Stephen
O'Callaghan, David
Anjum, Aisha
Cross, Mary
more
Type
Journal Article
Abstract
PurposeConstipation can be a significant problem in critically unwell patients, associated with detrimental outcomes. Opioids are thought to contribute to the mechanism of bowel dysfunction. We tested if methylnaltrexone, a pure peripheral mu-opioid receptor antagonist, could reverse opioid induced constipationMethodsThe MOTION trial is a multi-centre, double blind, randomised placebo controlled trial to investigate whether methylnaltrexone alleviatesopioid induced constipation (OIC) in critical care patients. Eligibility criteria included adult ICU patients who were mechanically ventilated, receiving opioids and were constipated (had not opened bowels for a minimum 48 hours) despite prior administration of regular laxatives as per local bowel management protocol. The primary outcome was time to significant rescue-free laxation. Secondary outcomes included gastric residual volume, tolerance of enteral feeds, requirement for rescue laxatives, requirement for prokinetics, average number of bowel movements per day,escalation of opioid dose due to antagonism/reversal of analgesia, incidence of ventilator-associated pneumonia, incidence of diarrhoea and Clostridium difficileinfection and finally 28 day, ICU and hospital mortality.ResultsA total of 84 patients were enrolled and randomized (41 to methylnaltrexone and 43 to placebo). The baseline demographic characteristics of the two groups were generally well balanced. There was no significant differencein time to rescue-free laxation between the groups (Hazard ratio 1.42, 95%CI 0.82-2.46, p=0.22). There were no significant differencesin the majority of secondary outcomes, particularly days 1-3. However, during days 4-28, there were fewer median number of bowel movements per day in the methylnaltrexone group, (p=0.01) and a greater incidence of diarrhoea in the placebo group (p=0.02). There was a marked difference in mortality between the groups, with ten deaths in the methylnaltrexone group and two in the placebo group during days 4-28. (p=0.007).ConclusionWe found no evidence to support the addition of methylnaltrexone to regular laxatives for the treatment of opioidinduced constipation in critically ill patients, however the confidence interval was wide and a clinically important difference cannot be excluded.
Date Issued
2020-02-03
Date Acceptance
2019-12-23
Citation
Intensive Care Medicine, 2020, 46, pp.747-755
URI
http://hdl.handle.net/10044/1/76582
URL
https://link.springer.com/article/10.1007%2Fs00134-019-05913-6
DOI
https://www.dx.doi.org/10.1007/s00134-019-05913-6
ISSN
0342-4642
Publisher
Springer (part of Springer Nature)
Start Page
747
End Page
755
Journal / Book Title
Intensive Care Medicine
Volume
46
Copyright Statement
© 2020 Springer-Verlag. The final publication is available at Springer via https://doi.org/10.1007/s00134-019-05913-6
Sponsor
National Institute for Health Research
Identifier
https://link.springer.com/article/10.1007%2Fs00134-019-05913-6
Grant Number
RDA24 79560 and 79660
Subjects
Science & Technology
Life Sciences & Biomedicine
Critical Care Medicine
General & Internal Medicine
Methylnaltrexone
Constipation
Laxatives
Critical care
REFLUX
Constipation
Critical care
Laxatives
Methylnaltrexone
1103 Clinical Sciences
1117 Public Health and Health Services
Emergency & Critical Care Medicine
Publication Status
Published
Date Publish Online
2020-02-03
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