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Hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry
BACKGROUND: Hepatopulmonary syndrome (HPS) is a rare complication of liver diseases of different etiologies and may indicate a poor prognosis. Therefore, a simple non-invasive screening method to detect HPS would be highly desirable. In this study pulse oximetry was evaluated to identify patients wi...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1508152/ https://www.ncbi.nlm.nih.gov/pubmed/16638132 http://dx.doi.org/10.1186/1471-230X-6-15 |
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author | Deibert, Peter Allgaier, Hans-Peter Loesch, Stefanie Müller, Claudia Olschewski, Manfred Hamm, Hinrich Maier, Klaus-Peter Blum, Hubert Erich |
author_facet | Deibert, Peter Allgaier, Hans-Peter Loesch, Stefanie Müller, Claudia Olschewski, Manfred Hamm, Hinrich Maier, Klaus-Peter Blum, Hubert Erich |
author_sort | Deibert, Peter |
collection | PubMed |
description | BACKGROUND: Hepatopulmonary syndrome (HPS) is a rare complication of liver diseases of different etiologies and may indicate a poor prognosis. Therefore, a simple non-invasive screening method to detect HPS would be highly desirable. In this study pulse oximetry was evaluated to identify patients with HPS. METHODS: In 316 consecutive patients with liver cirrhosis (n = 245), chronic hepatitis (n = 69) or non-cirrhotic portal hypertension (n = 2) arterial oxygen saturation (SaO(2)) was determined using a pulse oximeter. In patients with SaO(2 )≤92% in supine position and/or a decrease of ≥4% after change from supine to upright position further diagnostic procedures were performed, including contrast-enhanced echocardiography and perfusion lung scan. RESULTS: Seventeen patients (5.4%) had a pathological SaO(2). Four patients (1.3%) had HPS. HPS patients had a significant lower mean SaO(2 )in supine (89.7%, SD 5.4 vs. 96.0%, SD 2.3; p = 0.003) and upright position (84.3%, SD 5.0 vs. 96.0%, SD 2.4; p = 0.001) and had a lower mean PaO(2 )(56.2 mm Hg, SD 15.2 vs. 71.2 mm Hg, SD 20.2; p = 0.02) as compared to patients without HPS. The mean ΔSaO(2 )(difference between supine and upright position) was 5.50 (SD 7) in HPS patients compared to non-HPS patients who showed no change (p = 0.001). There was a strong correlation between shunt volume and the SaO(2 )values (R = -0.94). CONCLUSION: Arterial SaO(2 )determination in supine and upright position is a useful non-invasive screening test for HPS and correlates well with the intrapulmonary shunt volume. |
format | Text |
id | pubmed-1508152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15081522006-07-15 Hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry Deibert, Peter Allgaier, Hans-Peter Loesch, Stefanie Müller, Claudia Olschewski, Manfred Hamm, Hinrich Maier, Klaus-Peter Blum, Hubert Erich BMC Gastroenterol Research Article BACKGROUND: Hepatopulmonary syndrome (HPS) is a rare complication of liver diseases of different etiologies and may indicate a poor prognosis. Therefore, a simple non-invasive screening method to detect HPS would be highly desirable. In this study pulse oximetry was evaluated to identify patients with HPS. METHODS: In 316 consecutive patients with liver cirrhosis (n = 245), chronic hepatitis (n = 69) or non-cirrhotic portal hypertension (n = 2) arterial oxygen saturation (SaO(2)) was determined using a pulse oximeter. In patients with SaO(2 )≤92% in supine position and/or a decrease of ≥4% after change from supine to upright position further diagnostic procedures were performed, including contrast-enhanced echocardiography and perfusion lung scan. RESULTS: Seventeen patients (5.4%) had a pathological SaO(2). Four patients (1.3%) had HPS. HPS patients had a significant lower mean SaO(2 )in supine (89.7%, SD 5.4 vs. 96.0%, SD 2.3; p = 0.003) and upright position (84.3%, SD 5.0 vs. 96.0%, SD 2.4; p = 0.001) and had a lower mean PaO(2 )(56.2 mm Hg, SD 15.2 vs. 71.2 mm Hg, SD 20.2; p = 0.02) as compared to patients without HPS. The mean ΔSaO(2 )(difference between supine and upright position) was 5.50 (SD 7) in HPS patients compared to non-HPS patients who showed no change (p = 0.001). There was a strong correlation between shunt volume and the SaO(2 )values (R = -0.94). CONCLUSION: Arterial SaO(2 )determination in supine and upright position is a useful non-invasive screening test for HPS and correlates well with the intrapulmonary shunt volume. BioMed Central 2006-04-25 /pmc/articles/PMC1508152/ /pubmed/16638132 http://dx.doi.org/10.1186/1471-230X-6-15 Text en Copyright © 2006 Deibert et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Deibert, Peter Allgaier, Hans-Peter Loesch, Stefanie Müller, Claudia Olschewski, Manfred Hamm, Hinrich Maier, Klaus-Peter Blum, Hubert Erich Hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry |
title | Hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry |
title_full | Hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry |
title_fullStr | Hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry |
title_full_unstemmed | Hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry |
title_short | Hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry |
title_sort | hepatopulmonary syndrome in patients with chronic liver disease: role of pulse oximetry |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1508152/ https://www.ncbi.nlm.nih.gov/pubmed/16638132 http://dx.doi.org/10.1186/1471-230X-6-15 |
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