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Journal of Clinical Diagnosis and Treatment

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Kusztal Maciej*
 
Editorial Office, Journal of Clinical Diagnosis and Treatment, United Kingdom, Email: clindiagtreat@emedicinejournals.com
 
*Correspondence: Kusztal Maciej, Editorial Office, Journal of Clinical Diagnosis and Treatment, United Kingdom, Email: clindiagtreat@emedicinejournals.com

Received: 02-Jan-2022, Manuscript No. PULJCDT-22-3939; Editor assigned: 15-Jan-2022, Pre QC No. PULJCDT-22-3939(PQ); Reviewed: 31-Jan-2022 QC No. PULJCDT-22-3939; Revised: 02-Feb-2022, Manuscript No. PULJCDT-22-3939(R); Published: 12-Feb-2022, DOI: 10.37532/puljcdt.22.4(1).04

This open-access article is distributed under the terms of the Creative Commons Attribution Non-Commercial License (CC BY-NC) (http://creativecommons.org/licenses/by-nc/4.0/), which permits reuse, distribution and reproduction of the article, provided that the original work is properly cited and the reuse is restricted to noncommercial purposes. For commercial reuse, contact reprints@pulsus.com

Abstract

Cirrhotic Cardiomyopathy (CCM) is a condition concerning heart muscle dysfunction, occurring among patients with cirrhosis. Cirrhosis leads to the development of a hyperdynamic syndrome, which is manifested by high cardiac output, increased heart rate and effective arterial blood volume, accompanied by reduced total systemic vascular resistance.

Purpose

The aim of the study is to screen patients with cirrhosis, which may lead to earlier diagnosing CCM and hyperdynamic syndrome with its consequences among them.

Methods

Basic group characteristic differs between aetiologies of liver diseases. Median NTproBNP level was highest in ALD group (253 pg/ml) and viral group (177.5 pg/ul) compared to autoimmune group (51 pg/ul) and other (114 pg/ml). Median QTc interval was more prolonged in patients with viral aetiology (456 ms) and ALD aetiology (441 ms) than autoimmune aetiology (422 ms) and other aetiology (431 ms). Highest median CO were observed in viral group (6 L/min) and ALD group (5.7 L/min) and lower in autoimmune group (5.35 L/min) and other (5.2 L/min). Median SVRI was lowest in viral aetiology (1700 dyn- s/cm-5/m2 ) and ALD aetiology (1888dyn- s/cm-5 /m2 ) and higher in autoimmune aetiology (2067dyn- s/cm-5/m2 ) and other aetiology (2432dyn-s/cm-5/m2 ). There was no statistical difference in distance median value between aetiological groups (407 m in ALD patients’ group, 412.5 m in autoimmune patients’ group, 384 m in viral patients’ group and 400 m for other aetiology patients’ group; p=NS). The haemodynamic parameters (CO, SV, SVRI) were not correlated with MELD score and Child Pugh score (p=NS). DBP was positively correlated with MELD score (r= -0.25; p=0,009) and ChildPugh score (r= -0.31; p=0.003). The distance was negatively correlated with severity of the liver disease based on MELD score (r=-0.34; p=0.0048) score and Child-Pugh score (r= -0.321; p=0,0072). Preliminary results show statistically significant correlations between distance in 6MWT and eGFR (r=0.78; p=0,0082), Systemic Vascular Resistance (SVR) at the end of 6MWT (r=0.197 ;p=0.0011), Diastolic Blood Pressure (DBP) at the end of 6MWT (r=0.45;p=0.014) and NTproBNP (r=0.28; p=0.0008) level, patient’s weight (r=0.286; p=0.044) and height (r=0.37; p=0.008).

Conclusion

Preliminary results show that we can detect subclinical alterations in patients’ circulatory parameters by non-invasive haemodynamic monitoring. In our study patients with viral and ALD etiology presented more advanced liver cirrhosis stages and more pronounced manifestations of hyperdynamic syndrome which may later progress to CCM. Positive correlation of liver cirrhosis stage and NTproBNP, QTc and 6MWT distance may suggest heart function impairment in course of liver disease.

 
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