Continuous terlipressin infusion is associated with improved diet intake and muscle strength in patients awaiting liver transplant.
Malnutrition
cirrhosis
hepatorenal syndrome
liver transplantation
sarcopenia
Journal
JHEP reports : innovation in hepatology
ISSN: 2589-5559
Titre abrégé: JHEP Rep
Pays: Netherlands
ID NLM: 101761237
Informations de publication
Date de publication:
Aug 2019
Aug 2019
Historique:
received:
01
02
2019
revised:
30
04
2019
accepted:
08
05
2019
entrez:
11
2
2020
pubmed:
11
2
2020
medline:
11
2
2020
Statut:
epublish
Résumé
Portal hypertension contributes to the pathogenesis of malnutrition and sarcopenia in cirrhosis via multiple mechanisms. Terlipressin is a vasopressin analogue that we administer via continuous outpatient infusion, as a bridge to transplantation in patients with hepatorenal syndrome or refractory ascites. We describe, for the first time, the impact of outpatient terlipressin on nutritional and muscle parameters. Nutrition (subjective global assessment), handgrip strength, dietary intake (energy, protein), frequency of paracentesis and severity of liver disease (model for end-stage liver disease score) were prospectively recorded at terlipressin commencement and follow-up (transplantation, cessation or census date). Nineteen patients were included (89% male, median age 59.6 years, median model for end-stage liver disease score 24), of whom 12 had hepatorenal syndrome and 7 had refractory ascites. All patients were malnourished at baseline, 63% (n = 12) had sarcopenic-range grip strength, and mean paracentesis frequency was 2.86 ± 1.62/month. Median duration of terlipressin was 51 days (interquartile range 29-222). Fourteen patients (74%) were transplanted, 2 delisted (10%) and 3 (16%) continued terlipressin. Energy and protein intake improved significantly following terlipressin, from 17.94 ± 5.43 kcal/kg to 27.70 ± 7.48 kcal/kg, and 0.74 ± 0.28 g/kg to 1.16 ± 0.31 g/kg, respectively (both Continuous terlipressin infusion reduces the complications of portal hypertension and is associated with an improvement in nutritional and muscle parameters in patients on the liver transplant waiting list, in whom such characteristics usually demonstrate progressive decline. This validates both the aetiological role of portal hypertension in malnutrition and represents a promising new anabolic therapy. Malnutrition and poor muscle strength are common in liver disease and often get worse while patients await liver transplant. Terlipressin is a medication used to treat portal hypertension in patients with hepatorenal syndrome. It is usually given for a few days or weeks in patients confined to hospital. Our centre provides outpatient terlipressin for weeks to months as a bridge to liver transplant. In patients treated with terlipressin at our hospital, we observed a substantial increase in their dietary intake and muscle strength, which may improve their quality of life and outcomes after liver transplant.
Sections du résumé
BACKGROUND & AIMS
OBJECTIVE
Portal hypertension contributes to the pathogenesis of malnutrition and sarcopenia in cirrhosis via multiple mechanisms. Terlipressin is a vasopressin analogue that we administer via continuous outpatient infusion, as a bridge to transplantation in patients with hepatorenal syndrome or refractory ascites. We describe, for the first time, the impact of outpatient terlipressin on nutritional and muscle parameters.
METHODS
METHODS
Nutrition (subjective global assessment), handgrip strength, dietary intake (energy, protein), frequency of paracentesis and severity of liver disease (model for end-stage liver disease score) were prospectively recorded at terlipressin commencement and follow-up (transplantation, cessation or census date).
RESULTS
RESULTS
Nineteen patients were included (89% male, median age 59.6 years, median model for end-stage liver disease score 24), of whom 12 had hepatorenal syndrome and 7 had refractory ascites. All patients were malnourished at baseline, 63% (n = 12) had sarcopenic-range grip strength, and mean paracentesis frequency was 2.86 ± 1.62/month. Median duration of terlipressin was 51 days (interquartile range 29-222). Fourteen patients (74%) were transplanted, 2 delisted (10%) and 3 (16%) continued terlipressin. Energy and protein intake improved significantly following terlipressin, from 17.94 ± 5.43 kcal/kg to 27.70 ± 7.48 kcal/kg, and 0.74 ± 0.28 g/kg to 1.16 ± 0.31 g/kg, respectively (both
CONCLUSION
CONCLUSIONS
Continuous terlipressin infusion reduces the complications of portal hypertension and is associated with an improvement in nutritional and muscle parameters in patients on the liver transplant waiting list, in whom such characteristics usually demonstrate progressive decline. This validates both the aetiological role of portal hypertension in malnutrition and represents a promising new anabolic therapy.
LAY SUMMARY
BACKGROUND
Malnutrition and poor muscle strength are common in liver disease and often get worse while patients await liver transplant. Terlipressin is a medication used to treat portal hypertension in patients with hepatorenal syndrome. It is usually given for a few days or weeks in patients confined to hospital. Our centre provides outpatient terlipressin for weeks to months as a bridge to liver transplant. In patients treated with terlipressin at our hospital, we observed a substantial increase in their dietary intake and muscle strength, which may improve their quality of life and outcomes after liver transplant.
Identifiants
pubmed: 32039358
doi: 10.1016/j.jhepr.2019.05.002
pii: S2589-5559(19)30035-7
pmc: PMC7001556
doi:
Types de publication
Journal Article
Langues
eng
Pagination
107-113Informations de copyright
© 2019 The Author(s).
Références
Hepatology. 2016 Feb;63(2):574-80
pubmed: 26517301
JPEN J Parenter Enteral Nutr. 2001 May-Jun;25(3):120-31
pubmed: 11334061
Indian J Gastroenterol. 2017 Jul;36(4):275-281
pubmed: 28856568
J Hepatol. 2017 Nov;67(5):940-949
pubmed: 28645737
J Hepatol. 2018 Aug;69(2):406-460
pubmed: 29653741
Am J Transplant. 2018 Aug;18(8):1986-1994
pubmed: 29380529
Clin Nutr. 2006 Apr;25(2):285-94
pubmed: 16707194
Hepatology. 2017 Mar;65(3):1044-1057
pubmed: 28027577
Liver Transpl. 2018 Jan;24(1):122-139
pubmed: 29024353
Transplantation. 2016 Nov;100(11):2416-2423
pubmed: 27495765
JPEN J Parenter Enteral Nutr. 1987 Jan-Feb;11(1):8-13
pubmed: 3820522
Hepatology. 2018 Mar;67(3):1014-1026
pubmed: 29059469
Am J Transplant. 2016 Aug;16(8):2277-92
pubmed: 26813115
Nutrition. 2013 Oct;29(10):1252-8
pubmed: 24012087
Nutrition. 2018 Mar;47:21-26
pubmed: 29429530
Sci Rep. 2018 May 29;8(1):8210
pubmed: 29844325
Age Ageing. 2010 Jul;39(4):412-23
pubmed: 20392703
J Hepatol. 2004 Feb;40(2):228-33
pubmed: 14739092
J Hepatol. 2015 Apr;62(4):968-74
pubmed: 25638527
J Clin Exp Hepatol. 2015 Mar;5(Suppl 1):S29-36
pubmed: 26041954
Am J Gastroenterol. 2001 Aug;96(8):2442-7
pubmed: 11513188
J Hepatol. 2013 Sep;59(3):482-9
pubmed: 23665185
Curr Treat Options Gastroenterol. 2016 Jun;14(2):257-73
pubmed: 27023701
Dig Dis Sci. 1996 Mar;41(3):557-61
pubmed: 8617136
Eur J Gastroenterol Hepatol. 2013 Jan;25(1):85-93
pubmed: 23011041