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Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension

AIMS: Portopulmonary hypertension (PoPH) is a subtype of pulmonary arterial hypertension related to portal hypertension. The definitive diagnosis of PoPH is made by invasive right heart catheterization. Alternatively, pulmonary arterial hypertension may be recognized noninvasively from the tricuspid...

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Autores principales: Yamashita, Koji, Kurosaki, Masayuki, Nakanishi, Hiroyuki, Tanaka, Yuki, Ishido, Shun, Inada, Kento, Kirino, Sakura, Hayakawa, Yuka, Matsumoto, Hiroaki, Nobusawa, Tsubasa, Kakegawa, Tatsuya, Higuchi, Mayu, Takaura, Kenta, Tanaka, Shohei, Maeyashiki, Chiaki, Kaneko, Shun, Tamaki, Nobuharu, Yasui, Yutaka, Tsuchiya, Kaoru, Takahashi, Yuka, Miyazaki, Ryoichi, Ashikaga, Takashi, Enomoto, Nobuyuki, Izumi, Namiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667407/
https://www.ncbi.nlm.nih.gov/pubmed/36406650
http://dx.doi.org/10.1002/jgh3.12821
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author Yamashita, Koji
Kurosaki, Masayuki
Nakanishi, Hiroyuki
Tanaka, Yuki
Ishido, Shun
Inada, Kento
Kirino, Sakura
Hayakawa, Yuka
Matsumoto, Hiroaki
Nobusawa, Tsubasa
Kakegawa, Tatsuya
Higuchi, Mayu
Takaura, Kenta
Tanaka, Shohei
Maeyashiki, Chiaki
Kaneko, Shun
Tamaki, Nobuharu
Yasui, Yutaka
Tsuchiya, Kaoru
Takahashi, Yuka
Miyazaki, Ryoichi
Ashikaga, Takashi
Enomoto, Nobuyuki
Izumi, Namiki
author_facet Yamashita, Koji
Kurosaki, Masayuki
Nakanishi, Hiroyuki
Tanaka, Yuki
Ishido, Shun
Inada, Kento
Kirino, Sakura
Hayakawa, Yuka
Matsumoto, Hiroaki
Nobusawa, Tsubasa
Kakegawa, Tatsuya
Higuchi, Mayu
Takaura, Kenta
Tanaka, Shohei
Maeyashiki, Chiaki
Kaneko, Shun
Tamaki, Nobuharu
Yasui, Yutaka
Tsuchiya, Kaoru
Takahashi, Yuka
Miyazaki, Ryoichi
Ashikaga, Takashi
Enomoto, Nobuyuki
Izumi, Namiki
author_sort Yamashita, Koji
collection PubMed
description AIMS: Portopulmonary hypertension (PoPH) is a subtype of pulmonary arterial hypertension related to portal hypertension. The definitive diagnosis of PoPH is made by invasive right heart catheterization. Alternatively, pulmonary arterial hypertension may be recognized noninvasively from the tricuspid regurgitant pressure gradient (TRPG), measured by echocardiography. In this study, we aimed to establish a simple algorithm to identify chronic liver disease patients with a high TRPG value in order to narrow down the candidates to receive echocardiography. METHODS AND RESULTS: TRPG was measured by echocardiography in 152 patients with chronic liver disease. Factors predictive of TRPG >30 mmHg were investigated. There were 28 (18%) cases with TRPG >30 mmHg. Independent factors associated with a high TRPG were the presence of shortness of breath, high serum brain natriuretic peptide (BNP), and low serum albumin. Child–Pugh class or the presence of ascites, varices, or encephalopathy was not associated with TRPG. There was a correlation between the serum BNP and TRPG, and the optimal cutoff value of BNP by the Youden index was 122 pg/mL, and by 100% sensitivity was 50 pg/mL. A combination of these factors identified patients with a high probability of TRPG >30 mmHg (n = 12, positive predictive value [PPV] of 83%), no probability (n = 80, PPV 0%), and intermediate probability (n = 60, PPV 25–34%). This algorithm has reduced the number of patients needing echocardiography by 53%. CONCLUSIONS: A simple algorithm using the presence of shortness of breath, serum BNP, and albumin levels can narrow down the candidates to receive echocardiography.
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spelling pubmed-96674072022-11-17 Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension Yamashita, Koji Kurosaki, Masayuki Nakanishi, Hiroyuki Tanaka, Yuki Ishido, Shun Inada, Kento Kirino, Sakura Hayakawa, Yuka Matsumoto, Hiroaki Nobusawa, Tsubasa Kakegawa, Tatsuya Higuchi, Mayu Takaura, Kenta Tanaka, Shohei Maeyashiki, Chiaki Kaneko, Shun Tamaki, Nobuharu Yasui, Yutaka Tsuchiya, Kaoru Takahashi, Yuka Miyazaki, Ryoichi Ashikaga, Takashi Enomoto, Nobuyuki Izumi, Namiki JGH Open Original Articles AIMS: Portopulmonary hypertension (PoPH) is a subtype of pulmonary arterial hypertension related to portal hypertension. The definitive diagnosis of PoPH is made by invasive right heart catheterization. Alternatively, pulmonary arterial hypertension may be recognized noninvasively from the tricuspid regurgitant pressure gradient (TRPG), measured by echocardiography. In this study, we aimed to establish a simple algorithm to identify chronic liver disease patients with a high TRPG value in order to narrow down the candidates to receive echocardiography. METHODS AND RESULTS: TRPG was measured by echocardiography in 152 patients with chronic liver disease. Factors predictive of TRPG >30 mmHg were investigated. There were 28 (18%) cases with TRPG >30 mmHg. Independent factors associated with a high TRPG were the presence of shortness of breath, high serum brain natriuretic peptide (BNP), and low serum albumin. Child–Pugh class or the presence of ascites, varices, or encephalopathy was not associated with TRPG. There was a correlation between the serum BNP and TRPG, and the optimal cutoff value of BNP by the Youden index was 122 pg/mL, and by 100% sensitivity was 50 pg/mL. A combination of these factors identified patients with a high probability of TRPG >30 mmHg (n = 12, positive predictive value [PPV] of 83%), no probability (n = 80, PPV 0%), and intermediate probability (n = 60, PPV 25–34%). This algorithm has reduced the number of patients needing echocardiography by 53%. CONCLUSIONS: A simple algorithm using the presence of shortness of breath, serum BNP, and albumin levels can narrow down the candidates to receive echocardiography. Wiley Publishing Asia Pty Ltd 2022-09-16 /pmc/articles/PMC9667407/ /pubmed/36406650 http://dx.doi.org/10.1002/jgh3.12821 Text en © 2022 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Yamashita, Koji
Kurosaki, Masayuki
Nakanishi, Hiroyuki
Tanaka, Yuki
Ishido, Shun
Inada, Kento
Kirino, Sakura
Hayakawa, Yuka
Matsumoto, Hiroaki
Nobusawa, Tsubasa
Kakegawa, Tatsuya
Higuchi, Mayu
Takaura, Kenta
Tanaka, Shohei
Maeyashiki, Chiaki
Kaneko, Shun
Tamaki, Nobuharu
Yasui, Yutaka
Tsuchiya, Kaoru
Takahashi, Yuka
Miyazaki, Ryoichi
Ashikaga, Takashi
Enomoto, Nobuyuki
Izumi, Namiki
Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension
title Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension
title_full Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension
title_fullStr Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension
title_full_unstemmed Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension
title_short Simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension
title_sort simple algorithm to narrow down the candidates to receive echocardiography in patients with chronic liver disease for suspected pulmonary hypertension
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667407/
https://www.ncbi.nlm.nih.gov/pubmed/36406650
http://dx.doi.org/10.1002/jgh3.12821
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