Skip to main content
Top
Published in: Digestive Diseases and Sciences 8/2022

14-08-2021 | Hepatic Encephalopathy | Original Article

Reversal of Feed Intolerance by Prokinetics Improves Survival in Critically Ill Cirrhosis Patients

Authors: Rajan Vijayaraghavan, Rakhi Maiwall, Vinod Arora, Ashok Choudhary, Jaya Benjamin, Prashant Aggarwal, Kapil Dev Jamwal, Guresh Kumar, Y. K. Joshi, Shiv K. Sarin

Published in: Digestive Diseases and Sciences | Issue 8/2022

Login to get access

Abstract

Background and Aims

Feed intolerance (FI) is common in cirrhosis patients in intensive care units (ICU). Prokinetics are the first line treatment for FI but their efficacy and safety in critically ill patient with cirrhosis is unknown. We evaluated the role of prokinetics in reversal of FI and clinical outcomes.

Methods

Consecutive patients admitted in ICU developing new-onset FI, were randomized to receive either intravenous metoclopramide (Gr.A, n = 28), erythromycin (Gr.B, n = 27) or placebo (Gr.C, n = 28). FI was defined with the presence of 3 of 5 variables- absence of bowel sounds, gastric residual volume ≥ 500 ml, vomiting, diarrhoea and bowel distension. Primary end-point was complete resolution of FI (≥ 3 variables resolved) within 24-h and secondary end-points included resolution within 72-h and survival at 7-days.

Results

Of the 1030 ICU patients, 201 (19.5%) developed FI and 83 patients were randomized. Baseline parameters between the groups were comparable. Complete resolution at 24-h was higher in Gr.A (7.14%) and B (22.2%) than C (0%, p = 0.017). Overall, 58 (69.9%) patients achieved resolution within 72 h, more with metoclopramide (n = 24, 85.7%) and erythromycin (n = 25, 92.6%) than with placebo (n = 9, 32.1%, p < 0.001). The 7-day survival was better in patients who achieved resolution within 72-h (65.5 vs. 36%, p = 0.011) than non-responders. High lactate (OR-3.32, CI-1.45–7.70, p = 0.005), shock at baseline (OR-6.34, CI-1.67–24.1, p = 0.007) and resolution of FI within 72 h (OR-0.11, CI, 0.03–0.51, p = 0.04) predicted 7-day mortality.

Conclusions

FI is common in critically-ill cirrhosis patients and non-resolution carries high mortality. Early recognition and treatment with prokinetics is recommended to improve short-term survival.
Literature
1.
go back to reference Reintam A, Parm P, Kitus R et al. Gastrointestinal symptoms in intensive care patients. Acta Anaesthesiol Scand. 2009;53:318–324.CrossRef Reintam A, Parm P, Kitus R et al. Gastrointestinal symptoms in intensive care patients. Acta Anaesthesiol Scand. 2009;53:318–324.CrossRef
2.
go back to reference Deane AM, Chapman MJ, Reintam Blaser A et al. Pathophysiology and treatment of gastrointestinal motility disorders in the acutely ill. Nutr Clin Pract. 2009;34:23–26.CrossRef Deane AM, Chapman MJ, Reintam Blaser A et al. Pathophysiology and treatment of gastrointestinal motility disorders in the acutely ill. Nutr Clin Pract. 2009;34:23–26.CrossRef
3.
go back to reference Verne GN, Soldevia-Pico C, Robinson ME et al. Autonomic dysfunction and gastroparesis in cirrhosis. J Clin Gastroenterol. 2004;38:72–76.CrossRef Verne GN, Soldevia-Pico C, Robinson ME et al. Autonomic dysfunction and gastroparesis in cirrhosis. J Clin Gastroenterol. 2004;38:72–76.CrossRef
4.
go back to reference Kalaitzakis E, Sadik R, Holst JJ et al. Gut transit is associated with gastrointestinal symptoms and gut hormone profile in patients with cirrhosis. Clin Gastroenterol Hepatol. 2009;7:346–352.CrossRef Kalaitzakis E, Sadik R, Holst JJ et al. Gut transit is associated with gastrointestinal symptoms and gut hormone profile in patients with cirrhosis. Clin Gastroenterol Hepatol. 2009;7:346–352.CrossRef
5.
go back to reference Carvalho L, Parise ER. Evaluation of nutritional status of nonhospitalized patients with liver cirrhosis. Arg Gastroenterol. 2006;43:269–274.CrossRef Carvalho L, Parise ER. Evaluation of nutritional status of nonhospitalized patients with liver cirrhosis. Arg Gastroenterol. 2006;43:269–274.CrossRef
6.
go back to reference Gungabissoon U, Hacquoil K, Bains C et al. Prevalence, risk factors, clinical consequences, and treatment of enteral feed intolerance during critical illness. JPEN J Parenter Enteral Nutr. 2015;39:441–448.CrossRef Gungabissoon U, Hacquoil K, Bains C et al. Prevalence, risk factors, clinical consequences, and treatment of enteral feed intolerance during critical illness. JPEN J Parenter Enteral Nutr. 2015;39:441–448.CrossRef
7.
go back to reference Reintam Blaser A, Starkopf L, Deane AM et al. Comparison of different definitions of feeding intolerance: a retrospective observational study. Clin Nutr. 2015;34:956–961.CrossRef Reintam Blaser A, Starkopf L, Deane AM et al. Comparison of different definitions of feeding intolerance: a retrospective observational study. Clin Nutr. 2015;34:956–961.CrossRef
8.
go back to reference Reignier J, Mercier E, Le Gouge A et al. Effect of not monitoring residual gastric volumes on risk of ventilator-associated pneumonia in adults receiving mechanical ventilation and early enteral feeding: a randomized controlled trial. JAMA. 2013;309:249–256.CrossRef Reignier J, Mercier E, Le Gouge A et al. Effect of not monitoring residual gastric volumes on risk of ventilator-associated pneumonia in adults receiving mechanical ventilation and early enteral feeding: a randomized controlled trial. JAMA. 2013;309:249–256.CrossRef
9.
go back to reference Rhodes A, Evans LE, Alhazzani W et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock: 2016. Intensive Care Med. 2017;43:304–377.CrossRef Rhodes A, Evans LE, Alhazzani W et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock: 2016. Intensive Care Med. 2017;43:304–377.CrossRef
10.
go back to reference Singer P, Blaser AR, Berger MM et al. ESPEN guidelines on clinical nutrition in the intensive care unit. Clin Nutr. 2019;38:48–79.CrossRef Singer P, Blaser AR, Berger MM et al. ESPEN guidelines on clinical nutrition in the intensive care unit. Clin Nutr. 2019;38:48–79.CrossRef
11.
go back to reference Reignier J, Boisrame-Helms J, Brisard L et al. NUTRIREA-2 Trial Investigators; Clinical Research in Intensive Care and Sepsis (CRICS) group. Enteral versus parenteral early nutrition in ventilated adults with shock: a randomized, controlled, multicenter, open-label, parallel-group study (NUTRIREA-2). Lancet. 2018;391:133–143.CrossRef Reignier J, Boisrame-Helms J, Brisard L et al. NUTRIREA-2 Trial Investigators; Clinical Research in Intensive Care and Sepsis (CRICS) group. Enteral versus parenteral early nutrition in ventilated adults with shock: a randomized, controlled, multicenter, open-label, parallel-group study (NUTRIREA-2). Lancet. 2018;391:133–143.CrossRef
12.
go back to reference Nguyen NQ, Chapman MJ, Fraser RJ et al. Erythromycin is more effective than metoclopramide in the treatment of feed intolerance in critical illness. Crit Care Med. 2007;35:483–489.CrossRef Nguyen NQ, Chapman MJ, Fraser RJ et al. Erythromycin is more effective than metoclopramide in the treatment of feed intolerance in critical illness. Crit Care Med. 2007;35:483–489.CrossRef
13.
go back to reference Hersch M, Krasilnikov V, Helviz Y et al. Prokinetic drugs for gastric emptying in critically ill ventilated patients: Analysis through breath testing. J Crit Care. 2015;30:e7-13. Hersch M, Krasilnikov V, Helviz Y et al. Prokinetic drugs for gastric emptying in critically ill ventilated patients: Analysis through breath testing. J Crit Care. 2015;30:e7-13.
14.
go back to reference Lewis K, Algahtani Z, Mcintyre L et al. The efficacy and safety of prokinetic agents in critically ill patients receiving enteral nutrition: a systematic review and meta-analysis of randomized trials. Crit Care. 2016;20:259.CrossRef Lewis K, Algahtani Z, Mcintyre L et al. The efficacy and safety of prokinetic agents in critically ill patients receiving enteral nutrition: a systematic review and meta-analysis of randomized trials. Crit Care. 2016;20:259.CrossRef
15.
go back to reference Ritz MA, Chapman MJ, Fraser RJ et al. Erythromycin dose of 70mg accelerates gastric emptying as effectively as 200mg in the critically ill. Intensive Care Med. 2005;31:949–954.CrossRef Ritz MA, Chapman MJ, Fraser RJ et al. Erythromycin dose of 70mg accelerates gastric emptying as effectively as 200mg in the critically ill. Intensive Care Med. 2005;31:949–954.CrossRef
16.
go back to reference Sarin SK, Kedarisetty CK, Abbas Z et al. Acute-on-chronic liver failure: consensus recommendations of the Asia Pacific Association for the Study of Liver (APASL) 2014. Hepatol Int. 2014;8:453–471.CrossRef Sarin SK, Kedarisetty CK, Abbas Z et al. Acute-on-chronic liver failure: consensus recommendations of the Asia Pacific Association for the Study of Liver (APASL) 2014. Hepatol Int. 2014;8:453–471.CrossRef
17.
go back to reference Montejo JC, Minambres E, Bordeje L et al. Gastric residual volume during enteral nutrition in ICU patients. Intensive care Med. 2010;36:1386–1393.CrossRef Montejo JC, Minambres E, Bordeje L et al. Gastric residual volume during enteral nutrition in ICU patients. Intensive care Med. 2010;36:1386–1393.CrossRef
18.
go back to reference Reintam Blaser A, Starkopf J, Kirsimagi U et al. definition, Prevalence, and Outcomes of Feeding Intolerance in Intensive Care: A Systematic Review and Meta-Analysis. Acta Anaesthesiol Scand. 2014;58:914–922.CrossRef Reintam Blaser A, Starkopf J, Kirsimagi U et al. definition, Prevalence, and Outcomes of Feeding Intolerance in Intensive Care: A Systematic Review and Meta-Analysis. Acta Anaesthesiol Scand. 2014;58:914–922.CrossRef
19.
go back to reference Harvey SE, Parrott F, Harrison DA et al. Trial of the Route of Early Nutritional Support in Critically Ill Adults. N Engl J Med. 2014;371:1673–1684.CrossRef Harvey SE, Parrott F, Harrison DA et al. Trial of the Route of Early Nutritional Support in Critically Ill Adults. N Engl J Med. 2014;371:1673–1684.CrossRef
20.
go back to reference Weist R, lawson M, Geuking M. Pathological Bacterial Translocation in Liver Cirrhosis. J Hepatol. 2014;60:197–209.CrossRef Weist R, lawson M, Geuking M. Pathological Bacterial Translocation in Liver Cirrhosis. J Hepatol. 2014;60:197–209.CrossRef
21.
go back to reference Alukal J, Thulavath P. Gastrointestinal Failure in Critically Ill Patients with Cirrhosis. Am J Gastroenterol 2019;114:1231–1237.CrossRef Alukal J, Thulavath P. Gastrointestinal Failure in Critically Ill Patients with Cirrhosis. Am J Gastroenterol 2019;114:1231–1237.CrossRef
22.
go back to reference Bajaj JS, Vargas HE, Reddy KR et al. association between intestinal microbiota collected at hospital admission and outcomes of patients with cirrhosis. Clin Gastroenterol Hepatol. 2019;17:756–765.CrossRef Bajaj JS, Vargas HE, Reddy KR et al. association between intestinal microbiota collected at hospital admission and outcomes of patients with cirrhosis. Clin Gastroenterol Hepatol. 2019;17:756–765.CrossRef
23.
go back to reference Chen Y, Guo J, Qian G et al. Gut dysbiosis in acute-on-chronic liver failure and its predictive value for mortality. J Gastroenterol Hepatol. 2015;30:1429–1437.CrossRef Chen Y, Guo J, Qian G et al. Gut dysbiosis in acute-on-chronic liver failure and its predictive value for mortality. J Gastroenterol Hepatol. 2015;30:1429–1437.CrossRef
Metadata
Title
Reversal of Feed Intolerance by Prokinetics Improves Survival in Critically Ill Cirrhosis Patients
Authors
Rajan Vijayaraghavan
Rakhi Maiwall
Vinod Arora
Ashok Choudhary
Jaya Benjamin
Prashant Aggarwal
Kapil Dev Jamwal
Guresh Kumar
Y. K. Joshi
Shiv K. Sarin
Publication date
14-08-2021
Publisher
Springer US
Published in
Digestive Diseases and Sciences / Issue 8/2022
Print ISSN: 0163-2116
Electronic ISSN: 1573-2568
DOI
https://doi.org/10.1007/s10620-021-07185-x

Other articles of this Issue 8/2022

Digestive Diseases and Sciences 8/2022 Go to the issue