Diagnosis of Hepatopulmonary Syndrome in a Large Integrated Health System.


Journal

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775

Informations de publication

Date de publication:
11 2021
Historique:
received: 24 06 2020
revised: 26 08 2020
accepted: 20 09 2020
pubmed: 3 10 2020
medline: 11 11 2021
entrez: 2 10 2020
Statut: ppublish

Résumé

Data on the accuracy of the diagnosis of hepatopulmonary syndrome (HPS) in cirrhosis is limited. We evaluated the clinical characteristics of patients with International Classification of Diseases (ICD) codes for hepatopulmonary syndrome (HPS) in a large integrated health system. A retrospective review of encounters was performed of all patients with ICD-9-CM and/or ICD-10-CM diagnosis of cirrhosis and HPS from 2014-2019 in a multi-state health system. Demographics and cardiopulmonary testing closest to the time of HPS diagnosis were recorded. HPS was defined using standard criteria. A total of 42,749 unique individuals with cirrhosis were identified. An ICD diagnosis of HPS was found in 194 patients (0.45%), of which 182 had clinically confirmed cirrhosis. 143 (78.5%) underwent contrast-enhanced transthoracic echocardiography, and 98 (54%) had delayed shunting. Among them, 61 patients had a documented arterial blood gas, with 53 showing abnormal oxygenation (A-a gradient of >15 mm Hg). 12 were excluded due to significant pulmonary function test abnormalities and abnormal oxygenation from other cardiopulmonary diseases. Ultimately, 41 (22.5%) fulfilled the criteria for HPS. When stratifying those with an ICD code diagnosis of HPS into HPS, no HPS and indeterminate HPS groups, based on standard diagnostic criteria for HPS, we found that the confirmed HPS patients had similar complications except for less portopulmonary hypertension, worse gas exchange, less cardiopulmonary disease and were more often diagnosed in transplant centers. The diagnosis of HPS by ICD code is made in an extremely small subset of a sizeable cirrhotic cohort. When made, only a minority of these patients meet diagnostic criteria. Our findings highlight the need for improved education and more effective screening algorithms.

Sections du résumé

BACKGROUND & AIMS
Data on the accuracy of the diagnosis of hepatopulmonary syndrome (HPS) in cirrhosis is limited. We evaluated the clinical characteristics of patients with International Classification of Diseases (ICD) codes for hepatopulmonary syndrome (HPS) in a large integrated health system.
METHODS
A retrospective review of encounters was performed of all patients with ICD-9-CM and/or ICD-10-CM diagnosis of cirrhosis and HPS from 2014-2019 in a multi-state health system. Demographics and cardiopulmonary testing closest to the time of HPS diagnosis were recorded. HPS was defined using standard criteria.
RESULTS
A total of 42,749 unique individuals with cirrhosis were identified. An ICD diagnosis of HPS was found in 194 patients (0.45%), of which 182 had clinically confirmed cirrhosis. 143 (78.5%) underwent contrast-enhanced transthoracic echocardiography, and 98 (54%) had delayed shunting. Among them, 61 patients had a documented arterial blood gas, with 53 showing abnormal oxygenation (A-a gradient of >15 mm Hg). 12 were excluded due to significant pulmonary function test abnormalities and abnormal oxygenation from other cardiopulmonary diseases. Ultimately, 41 (22.5%) fulfilled the criteria for HPS. When stratifying those with an ICD code diagnosis of HPS into HPS, no HPS and indeterminate HPS groups, based on standard diagnostic criteria for HPS, we found that the confirmed HPS patients had similar complications except for less portopulmonary hypertension, worse gas exchange, less cardiopulmonary disease and were more often diagnosed in transplant centers.
CONCLUSIONS
The diagnosis of HPS by ICD code is made in an extremely small subset of a sizeable cirrhotic cohort. When made, only a minority of these patients meet diagnostic criteria. Our findings highlight the need for improved education and more effective screening algorithms.

Identifiants

pubmed: 33007510
pii: S1542-3565(20)31380-X
doi: 10.1016/j.cgh.2020.09.050
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2370-2378

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Shoma Bommena (S)

Department of Medicine, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona; Department of Internal Medicine, Banner University Medical Center-Phoenix, Phoenix, Arizona. Electronic address: shoma@email.arizona.edu.

Richard D Gerkin (RD)

Department of Medicine, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona; Department of Internal Medicine, Banner University Medical Center-Phoenix, Phoenix, Arizona.

Sumit Agarwal (S)

Department of Medicine, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona; Department of Internal Medicine, Banner University Medical Center-Phoenix, Phoenix, Arizona.

Sarah Raevens (S)

Department of Internal Medicine, Ghent University, Ghent, Belgium.

Marilyn K Glassberg (MK)

Department of Medicine, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona; Department of Internal Medicine, Banner University Medical Center-Phoenix, Phoenix, Arizona.

Michael B Fallon (MB)

Department of Medicine, University of Arizona College of Medicine-Phoenix, Phoenix, Arizona; Department of Internal Medicine, Banner University Medical Center-Phoenix, Phoenix, Arizona.

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