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Healthcare status of adults with pulmonary hypertension due to congenital heart disease

BACKGROUND: In the long-term course of treated and untreated congenital heart defects (CHD), pulmonary hypertension (PH) is one of the most relevant complications. Since PH carries a high risk for mortality and morbidity, it is important to improve the status of healthcare and medical knowledge rega...

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Autores principales: Busse, Amely J., Freilinger, Sebastian, Eicken, Andreas, Ewert, Peter, Freiberger, Annika, Huntgeburth, Michael, Nagdyman, Nicole, von Scheidt, Fabian, Kaemmerer, Harald, Weyand, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808107/
https://www.ncbi.nlm.nih.gov/pubmed/36605078
http://dx.doi.org/10.21037/cdt-22-281
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author Busse, Amely J.
Freilinger, Sebastian
Eicken, Andreas
Ewert, Peter
Freiberger, Annika
Huntgeburth, Michael
Nagdyman, Nicole
von Scheidt, Fabian
Kaemmerer, Harald
Weyand, Michael
author_facet Busse, Amely J.
Freilinger, Sebastian
Eicken, Andreas
Ewert, Peter
Freiberger, Annika
Huntgeburth, Michael
Nagdyman, Nicole
von Scheidt, Fabian
Kaemmerer, Harald
Weyand, Michael
author_sort Busse, Amely J.
collection PubMed
description BACKGROUND: In the long-term course of treated and untreated congenital heart defects (CHD), pulmonary hypertension (PH) is one of the most relevant complications. Since PH carries a high risk for mortality and morbidity, it is important to improve the status of healthcare and medical knowledge regarding the affected patients. Therefore, this study aimed to determine the current medical care status, health-related knowledge, and specific counseling needs of adults with various forms of CHD (ACHD) who are at increased risk of developing PH, as well as those with manifest PH. METHODS: In this retrospective cross-sectional study, a representative sample of 803 ACHD were analyzed. Patients were split into three groups based on CHD: low risk for PH, at risk for pre- or post-capillary PH, and manifest PH. Data collection took place between September 2017 until February 2018 in a tertiary care center for ACHD. Healthcare status and specific needs for information or advice were analyzed using a questionnaire designed by our group. The state of knowledge of the patients was assessed by comparing this questionnaire and the corresponding medical records. RESULTS: Both patients with manifest PH (n=51) and patients at risk to develop PH (n=629) were insufficiently informed about their health status, specific care structures available to them, and patient organizations. About 50% of the patients had specific counseling needs, especially regarding physical capability and sports, daily stress, rehabilitation measures, and pregnancy. Only 47.8% of patients with manifest PH were aware of suffering from PH (P<0.001). In particular, the patients had large knowledge deficits regarding comorbidities related to their health condition. CONCLUSIONS: PH is a quantitatively and qualitatively underestimated residuum or sequela of CHD that significantly affects outcome and prognosis in ACHD. Multidisciplinary, structured, and specific counseling of affected individuals with corresponding risk constellations is urgently needed. A prerequisite for this is closer collaboration between primary care physicians (PCPs), such as general practitioners, family physicians, internists, or general cardiologists, and ACHD specialists. Targeted patient counseling and care could have a positive impact on the level of awareness of those affected and favorably influence their prognosis.
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spelling pubmed-98081072023-01-04 Healthcare status of adults with pulmonary hypertension due to congenital heart disease Busse, Amely J. Freilinger, Sebastian Eicken, Andreas Ewert, Peter Freiberger, Annika Huntgeburth, Michael Nagdyman, Nicole von Scheidt, Fabian Kaemmerer, Harald Weyand, Michael Cardiovasc Diagn Ther Original Article BACKGROUND: In the long-term course of treated and untreated congenital heart defects (CHD), pulmonary hypertension (PH) is one of the most relevant complications. Since PH carries a high risk for mortality and morbidity, it is important to improve the status of healthcare and medical knowledge regarding the affected patients. Therefore, this study aimed to determine the current medical care status, health-related knowledge, and specific counseling needs of adults with various forms of CHD (ACHD) who are at increased risk of developing PH, as well as those with manifest PH. METHODS: In this retrospective cross-sectional study, a representative sample of 803 ACHD were analyzed. Patients were split into three groups based on CHD: low risk for PH, at risk for pre- or post-capillary PH, and manifest PH. Data collection took place between September 2017 until February 2018 in a tertiary care center for ACHD. Healthcare status and specific needs for information or advice were analyzed using a questionnaire designed by our group. The state of knowledge of the patients was assessed by comparing this questionnaire and the corresponding medical records. RESULTS: Both patients with manifest PH (n=51) and patients at risk to develop PH (n=629) were insufficiently informed about their health status, specific care structures available to them, and patient organizations. About 50% of the patients had specific counseling needs, especially regarding physical capability and sports, daily stress, rehabilitation measures, and pregnancy. Only 47.8% of patients with manifest PH were aware of suffering from PH (P<0.001). In particular, the patients had large knowledge deficits regarding comorbidities related to their health condition. CONCLUSIONS: PH is a quantitatively and qualitatively underestimated residuum or sequela of CHD that significantly affects outcome and prognosis in ACHD. Multidisciplinary, structured, and specific counseling of affected individuals with corresponding risk constellations is urgently needed. A prerequisite for this is closer collaboration between primary care physicians (PCPs), such as general practitioners, family physicians, internists, or general cardiologists, and ACHD specialists. Targeted patient counseling and care could have a positive impact on the level of awareness of those affected and favorably influence their prognosis. AME Publishing Company 2022-12 /pmc/articles/PMC9808107/ /pubmed/36605078 http://dx.doi.org/10.21037/cdt-22-281 Text en 2022 Cardiovascular Diagnosis and Therapy. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Busse, Amely J.
Freilinger, Sebastian
Eicken, Andreas
Ewert, Peter
Freiberger, Annika
Huntgeburth, Michael
Nagdyman, Nicole
von Scheidt, Fabian
Kaemmerer, Harald
Weyand, Michael
Healthcare status of adults with pulmonary hypertension due to congenital heart disease
title Healthcare status of adults with pulmonary hypertension due to congenital heart disease
title_full Healthcare status of adults with pulmonary hypertension due to congenital heart disease
title_fullStr Healthcare status of adults with pulmonary hypertension due to congenital heart disease
title_full_unstemmed Healthcare status of adults with pulmonary hypertension due to congenital heart disease
title_short Healthcare status of adults with pulmonary hypertension due to congenital heart disease
title_sort healthcare status of adults with pulmonary hypertension due to congenital heart disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808107/
https://www.ncbi.nlm.nih.gov/pubmed/36605078
http://dx.doi.org/10.21037/cdt-22-281
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