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Relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients

BACKGROUND: There is evidence that in cirrhotic patients, certain hemodynamic parameters, such as blood pressure and heart rate, are related to the severity of liver disease. This study investigated whether non-invasive 24-hour ambulatory blood pressure and heart rate are more closely associated wit...

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Autores principales: Tzamouranis, Dimitris G, Alexopoulou, Alexandra, Dourakis, Spyros P, Stergiou, George S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013079/
https://www.ncbi.nlm.nih.gov/pubmed/21143998
http://dx.doi.org/10.1186/1471-230X-10-143
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author Tzamouranis, Dimitris G
Alexopoulou, Alexandra
Dourakis, Spyros P
Stergiou, George S
author_facet Tzamouranis, Dimitris G
Alexopoulou, Alexandra
Dourakis, Spyros P
Stergiou, George S
author_sort Tzamouranis, Dimitris G
collection PubMed
description BACKGROUND: There is evidence that in cirrhotic patients, certain hemodynamic parameters, such as blood pressure and heart rate, are related to the severity of liver disease. This study investigated whether non-invasive 24-hour ambulatory blood pressure and heart rate are more closely associated with markers of liver disease severity than conventional office measurements. METHODS: Ambulatory patients with cirrhosis underwent office blood pressure and heart rate measurements, 24-hour ambulatory blood pressure monitoring and blood laboratory tests. RESULTS: Fifty-one patients (32 men, mean age 57.4 ± 11.3 years) completed the study. Twenty six patients had compensated liver cirrhosis (group A) and 25 patients had more advanced liver disease (group B). Group A and B patients differed significantly both in ambulatory asleep diastolic blood pressure (p < 0.05) and office diastolic blood pressure (p < 0.01), which were lower in more advanced liver disease. Office blood pressure and heart rate correlations were similar to or even stronger than ambulatory ones. Ambulatory blood pressure and heart rate awake-asleep variation (dipping) showed a relatively flat pattern as markers of liver dysfunction were deteriorating. The strongest correlations were found with both ambulatory and office heart rate, which increased as indicators of severity of liver disease were worsening. CONCLUSIONS: Heart rate seems to be a more reliable marker of ongoing liver dysfunction than blood pressure. Evaluation of blood pressure and heart rate with 24-hour ambulatory measurement does not seem to offer more information than conventional office measurements.
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spelling pubmed-30130792011-01-01 Relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients Tzamouranis, Dimitris G Alexopoulou, Alexandra Dourakis, Spyros P Stergiou, George S BMC Gastroenterol Research Article BACKGROUND: There is evidence that in cirrhotic patients, certain hemodynamic parameters, such as blood pressure and heart rate, are related to the severity of liver disease. This study investigated whether non-invasive 24-hour ambulatory blood pressure and heart rate are more closely associated with markers of liver disease severity than conventional office measurements. METHODS: Ambulatory patients with cirrhosis underwent office blood pressure and heart rate measurements, 24-hour ambulatory blood pressure monitoring and blood laboratory tests. RESULTS: Fifty-one patients (32 men, mean age 57.4 ± 11.3 years) completed the study. Twenty six patients had compensated liver cirrhosis (group A) and 25 patients had more advanced liver disease (group B). Group A and B patients differed significantly both in ambulatory asleep diastolic blood pressure (p < 0.05) and office diastolic blood pressure (p < 0.01), which were lower in more advanced liver disease. Office blood pressure and heart rate correlations were similar to or even stronger than ambulatory ones. Ambulatory blood pressure and heart rate awake-asleep variation (dipping) showed a relatively flat pattern as markers of liver dysfunction were deteriorating. The strongest correlations were found with both ambulatory and office heart rate, which increased as indicators of severity of liver disease were worsening. CONCLUSIONS: Heart rate seems to be a more reliable marker of ongoing liver dysfunction than blood pressure. Evaluation of blood pressure and heart rate with 24-hour ambulatory measurement does not seem to offer more information than conventional office measurements. BioMed Central 2010-12-12 /pmc/articles/PMC3013079/ /pubmed/21143998 http://dx.doi.org/10.1186/1471-230X-10-143 Text en Copyright ©2010 Tzamouranis et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tzamouranis, Dimitris G
Alexopoulou, Alexandra
Dourakis, Spyros P
Stergiou, George S
Relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients
title Relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients
title_full Relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients
title_fullStr Relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients
title_full_unstemmed Relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients
title_short Relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients
title_sort relationship of 24-hour ambulatory blood pressure and heart rate with markers of hepatic function in cirrhotic patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3013079/
https://www.ncbi.nlm.nih.gov/pubmed/21143998
http://dx.doi.org/10.1186/1471-230X-10-143
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