Noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center study

Kamesh Gupta,1 Pooja Rani,1 Anurag Rohatgi,1 Mukesh Verma,1 Shivani Handa,2 Keemi Dalal,1 Anand Jain1 1Department of Internal Medicine, Lady Hardinge Medical College, New Delhi, India; 2Department of Gastroenterology, Liver Associates of Texas, Houston, TX, USA Objective: To evaluate the effectivene...

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Main Authors: Gupta K, Rani P, Rohatgi A, Verma M, Handa S, Dalal K, Jain A
Format: Article
Language:English
Published: Dove Medical Press 2018-09-01
Series:Clinical and Experimental Gastroenterology
Subjects:
Online Access:https://www.dovepress.com/noradrenaline-for-reverting-hepatorenal-syndrome-a-prospective-observa-peer-reviewed-article-CEG
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spelling doaj-99d4d4f8e5b94a54a13d6d047a161bd22020-11-25T02:27:50ZengDove Medical PressClinical and Experimental Gastroenterology1178-70232018-09-01Volume 1131732440694Noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center studyGupta KRani PRohatgi AVerma MHanda SDalal KJain AKamesh Gupta,1 Pooja Rani,1 Anurag Rohatgi,1 Mukesh Verma,1 Shivani Handa,2 Keemi Dalal,1 Anand Jain1 1Department of Internal Medicine, Lady Hardinge Medical College, New Delhi, India; 2Department of Gastroenterology, Liver Associates of Texas, Houston, TX, USA Objective: To evaluate the effectiveness of noradrenaline for the treatment of hepatorenal syndrome (HRS).Background: HRS represents the development of renal failure in cirrhotic patients. The standard treatment for HRS is terlipressin, which, as opposed to noradrenaline, is more expensive and less accessible in most tertiary care centers.Patients and methods: Thirty consecutive patients with HRS type 1 received noradrenaline (1–4.0 mg/hour) and albumin for 14 days. The parameters recorded were: serum creatinine levels, creatinine clearance, mean arterial pressure (MAP), urine output, and serum sodium levels evaluated at baseline and on treatment days 1, 3, 7, and 14.Results: Most patients achieved serum creatinine levels <1.5 mg/dL and were considered responders (22/30, 73%), whereas eight patients (27%) were nonresponders. At baseline, responders and nonresponders differed only regarding initial bilirubin levels and international normalized ratio values. Treatment duration was 7.5±3.2 days. Responders experienced a significant (p<0.05) decrease in serum creatinine levels (from 3.26±0.48 to 1.28±0.14 mg/dL), as well as a significant increase (p<0.05) in creatinine clearance (from 21±4.1 to 67.7±12.1 mL/min), urine output (from 583±41.1 to 1163±105 mL/day), MAP (from 79.2±2.94 to 93.9±2.34 mmHg), and serum sodium levels (from 125±2.01 to 132.3±1.39 mEq/L). In nonresponders, the MAP increased, but serum creatinine levels also increased, reflecting a decrease in creatinine clearance and urine output, with no significant change in serum sodium levels over the duration of the treatment.Conclusion: In most patients, noradrenaline treatment induced systemic vasoconstriction resulting in HRS reversal, with acceptable safety, in agreement with previously reported outcomes of terlipressin treatment. Keywords: hepatorenal syndrome, vasoconstrictor drug, noradrenaline, CKD, hypovolemiahttps://www.dovepress.com/noradrenaline-for-reverting-hepatorenal-syndrome-a-prospective-observa-peer-reviewed-article-CEGhepatorenal syndromevasoconstrictor drugnoradrenaline
collection DOAJ
language English
format Article
sources DOAJ
author Gupta K
Rani P
Rohatgi A
Verma M
Handa S
Dalal K
Jain A
spellingShingle Gupta K
Rani P
Rohatgi A
Verma M
Handa S
Dalal K
Jain A
Noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center study
Clinical and Experimental Gastroenterology
hepatorenal syndrome
vasoconstrictor drug
noradrenaline
author_facet Gupta K
Rani P
Rohatgi A
Verma M
Handa S
Dalal K
Jain A
author_sort Gupta K
title Noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center study
title_short Noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center study
title_full Noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center study
title_fullStr Noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center study
title_full_unstemmed Noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center study
title_sort noradrenaline for reverting hepatorenal syndrome: a prospective, observational, single-center study
publisher Dove Medical Press
series Clinical and Experimental Gastroenterology
issn 1178-7023
publishDate 2018-09-01
description Kamesh Gupta,1 Pooja Rani,1 Anurag Rohatgi,1 Mukesh Verma,1 Shivani Handa,2 Keemi Dalal,1 Anand Jain1 1Department of Internal Medicine, Lady Hardinge Medical College, New Delhi, India; 2Department of Gastroenterology, Liver Associates of Texas, Houston, TX, USA Objective: To evaluate the effectiveness of noradrenaline for the treatment of hepatorenal syndrome (HRS).Background: HRS represents the development of renal failure in cirrhotic patients. The standard treatment for HRS is terlipressin, which, as opposed to noradrenaline, is more expensive and less accessible in most tertiary care centers.Patients and methods: Thirty consecutive patients with HRS type 1 received noradrenaline (1–4.0 mg/hour) and albumin for 14 days. The parameters recorded were: serum creatinine levels, creatinine clearance, mean arterial pressure (MAP), urine output, and serum sodium levels evaluated at baseline and on treatment days 1, 3, 7, and 14.Results: Most patients achieved serum creatinine levels <1.5 mg/dL and were considered responders (22/30, 73%), whereas eight patients (27%) were nonresponders. At baseline, responders and nonresponders differed only regarding initial bilirubin levels and international normalized ratio values. Treatment duration was 7.5±3.2 days. Responders experienced a significant (p<0.05) decrease in serum creatinine levels (from 3.26±0.48 to 1.28±0.14 mg/dL), as well as a significant increase (p<0.05) in creatinine clearance (from 21±4.1 to 67.7±12.1 mL/min), urine output (from 583±41.1 to 1163±105 mL/day), MAP (from 79.2±2.94 to 93.9±2.34 mmHg), and serum sodium levels (from 125±2.01 to 132.3±1.39 mEq/L). In nonresponders, the MAP increased, but serum creatinine levels also increased, reflecting a decrease in creatinine clearance and urine output, with no significant change in serum sodium levels over the duration of the treatment.Conclusion: In most patients, noradrenaline treatment induced systemic vasoconstriction resulting in HRS reversal, with acceptable safety, in agreement with previously reported outcomes of terlipressin treatment. Keywords: hepatorenal syndrome, vasoconstrictor drug, noradrenaline, CKD, hypovolemia
topic hepatorenal syndrome
vasoconstrictor drug
noradrenaline
url https://www.dovepress.com/noradrenaline-for-reverting-hepatorenal-syndrome-a-prospective-observa-peer-reviewed-article-CEG
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