eISSN: 2449-8238
ISSN: 2392-1099
Clinical and Experimental Hepatology
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SCImago Journal & Country Rank
2/2020
vol. 6
 
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abstract:
Original paper

Left ventricular diastolic dysfunction in liver transplantation: a stronger association with non-alcoholic steatohepatitis

Hemnishil K. Marella
1
,
Faisal Kamal
2
,
Rahul Peravali
3
,
Jake Jacob
4
,
Satheesh P. Nair
5

  1. Department of Medicine, University of Tennessee Health Science Center, Memphis TN, USA
  2. Division of Gastroenterology and Hepatology, University of Tennessee Health Science Center, Memphis, TN, USA
  3. College of Medicine, University of Tennessee Health Science Center, Memphis, TN, USA
  4. Department of Medicine, Baylor College of Medicine, Houston, TX, USA
  5. Division of Transplant Surgery, Department of Surgery, Methodist University Hospital Transplant Institute, University of Tennessee Health Science Center, Memphis, TN, USA
Clin Exp HEPATOL 2020; 6, 2: 158–162
Online publish date: 2020/06/01
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Aim of the study
Cardiovascular death is an important cause of mortality in end stage liver disease (ESLD) patients undergoing orthotopic liver transplant (OLT). Left ventricular diastolic dysfunction (LVDD) is often the early manifestation and only measurable manifestation of cirrhotic cardiomyopathy. Therefore, it is important to understand the risk factors for LVDD in ESLD patients undergoing OLT and its immediate impact post-operatively.

Material and methods
Electronic medical records (EMR) of 100 consecutive patients who underwent OLT were reviewed at the University of Tennessee/Methodist University Hospital in Memphis, Tennessee, USA. Transthoracic echocardiogram (TTE) reports were accessed to evaluate for LVDD based on the latest 2016 American Society of Echocardiography and European Association of Cardiovascular Imaging guidelines. The clinical and demographic variables were obtained and variable quality measures, incidence of cardiac arrhythmias, and 30-day all-cause mortality were compared.

Results
Patients with LVDD were older (62.7 ±6.3 years vs. 55.9 ±12.3 years, p = 0.017) and were more often female (57% vs. 31%, p = 0.026). In addition, patients with non-alcoholic steatohepatitis (NASH) were more likely to have LVDD (48% vs. 12%, p = 0.001). In contrast, patients with alcoholic liver disease were less likely to have LVDD (10% vs. 33%, p = 0.032). In a multivariate logistic regression analysis, NASH (OR = 4.4 [95% CI: 1.33-14.5], p = 0.015) and female gender (OR = 3.31 [95% CI: 1.09-9.99], p = 0.033) were independent predictors of LVDD.

Conclusions
In our cohort of patients, the presence of NASH was associated with a higher risk of LVDD. However, presence of LVDD did not influence immediate post-transplant outcome or 30-day all-cause mortality.

keywords:

non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), left ventricular diastolic dysfunction (LVDD)

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