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author Chivers, Sian
Cleary, Aoife
Knowles, Rachel
Babu-Narayan, Sonya V
Simpson, John M
Nashat, Heba
Dimopoulos, Konstantinos
Gatzoulis, Michael A
Wilson, Dirk
Prica, Milos
Anthony, James
Clift, Paul F
Jowett, Victoria
Jenkins, Petra
Khodaghalian, Bernadette
Jones, Caroline B
Hardiman, Antonia
Head, Catherine
Miller, Owen
Chung, Natali AY
Mahmood, Umar
Bu'Lock, Frances A
Ramcharan, Tristan KW
Chikermane, Ashish
Shortland, Jennifer
Tometzki, Andrew
Crossland, David S
Reinhardt, Zdenka
Lewis, Clive
Rittey, Leila
Hares, Dominic
Panagiotopoulou, Olga
Smith, Benjamin
Najih L, Muhammad
Bharucha, Tara
Daubeney, Piers EF
author_facet Chivers, Sian
Cleary, Aoife
Knowles, Rachel
Babu-Narayan, Sonya V
Simpson, John M
Nashat, Heba
Dimopoulos, Konstantinos
Gatzoulis, Michael A
Wilson, Dirk
Prica, Milos
Anthony, James
Clift, Paul F
Jowett, Victoria
Jenkins, Petra
Khodaghalian, Bernadette
Jones, Caroline B
Hardiman, Antonia
Head, Catherine
Miller, Owen
Chung, Natali AY
Mahmood, Umar
Bu'Lock, Frances A
Ramcharan, Tristan KW
Chikermane, Ashish
Shortland, Jennifer
Tometzki, Andrew
Crossland, David S
Reinhardt, Zdenka
Lewis, Clive
Rittey, Leila
Hares, Dominic
Panagiotopoulou, Olga
Smith, Benjamin
Najih L, Muhammad
Bharucha, Tara
Daubeney, Piers EF
author_sort Chivers, Sian
collection PubMed
description BACKGROUND: COVID-19 has caused significant worldwide morbidity and mortality. Congenital heart disease (CHD) is likely to increase vulnerability and understanding the predictors of adverse outcomes is key to optimising care. OBJECTIVE: Ascertain the impact of COVID-19 on people with CHD and define risk factors for adverse outcomes. METHODS: Multicentre UK study undertaken 1 March 2020–30 June 2021 during the COVID-19 pandemic. Data were collected on CHD diagnoses, clinical presentation and outcomes. Multivariable logistic regression with multiple imputation was performed to explore predictors of death and hospitalisation. RESULTS: There were 405 reported cases (127 paediatric/278 adult). In children (age <16 years), there were 5 (3.9%) deaths. Adjusted ORs (AORs) for hospitalisation in children were significantly lower with each ascending year of age (OR 0.85, 95% CI 0.75 to 0.96 (p<0.01)). In adults, there were 24 (8.6%) deaths (19 with comorbidities) and 74 (26.6%) hospital admissions. AORs for death in adults were significantly increased with each year of age (OR 1.05, 95% CI 1.01 to 1.10 (p<0.01)) and with pulmonary arterial hypertension (PAH; OR 5.99, 95% CI 1.34 to 26.91 (p=0.02)). AORs for hospitalisation in adults were significantly higher with each additional year of age (OR 1.03, 95% CI 1.00 to 1.05 (p=0.04)), additional comorbidities (OR 3.23, 95% CI 1.31 to 7.97 (p=0.01)) and genetic disease (OR 2.87, 95% CI 1.04 to 7.94 (p=0.04)). CONCLUSIONS: Children were at low risk of death and hospitalisation secondary to COVID-19 even with severe CHD, but hospital admission rates were higher in younger children, independent of comorbidity. In adults, higher likelihood of death was associated with increasing age and PAH, and of hospitalisation with age, comorbidities and genetic disease. An individualised approach, based on age and comorbidities, should be taken to COVID-19 management in patients with CHD.
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spelling pubmed-103572972023-07-21 COVID-19 in congenital heart disease (COaCHeD) study Chivers, Sian Cleary, Aoife Knowles, Rachel Babu-Narayan, Sonya V Simpson, John M Nashat, Heba Dimopoulos, Konstantinos Gatzoulis, Michael A Wilson, Dirk Prica, Milos Anthony, James Clift, Paul F Jowett, Victoria Jenkins, Petra Khodaghalian, Bernadette Jones, Caroline B Hardiman, Antonia Head, Catherine Miller, Owen Chung, Natali AY Mahmood, Umar Bu'Lock, Frances A Ramcharan, Tristan KW Chikermane, Ashish Shortland, Jennifer Tometzki, Andrew Crossland, David S Reinhardt, Zdenka Lewis, Clive Rittey, Leila Hares, Dominic Panagiotopoulou, Olga Smith, Benjamin Najih L, Muhammad Bharucha, Tara Daubeney, Piers EF Open Heart Congenital Heart Disease BACKGROUND: COVID-19 has caused significant worldwide morbidity and mortality. Congenital heart disease (CHD) is likely to increase vulnerability and understanding the predictors of adverse outcomes is key to optimising care. OBJECTIVE: Ascertain the impact of COVID-19 on people with CHD and define risk factors for adverse outcomes. METHODS: Multicentre UK study undertaken 1 March 2020–30 June 2021 during the COVID-19 pandemic. Data were collected on CHD diagnoses, clinical presentation and outcomes. Multivariable logistic regression with multiple imputation was performed to explore predictors of death and hospitalisation. RESULTS: There were 405 reported cases (127 paediatric/278 adult). In children (age <16 years), there were 5 (3.9%) deaths. Adjusted ORs (AORs) for hospitalisation in children were significantly lower with each ascending year of age (OR 0.85, 95% CI 0.75 to 0.96 (p<0.01)). In adults, there were 24 (8.6%) deaths (19 with comorbidities) and 74 (26.6%) hospital admissions. AORs for death in adults were significantly increased with each year of age (OR 1.05, 95% CI 1.01 to 1.10 (p<0.01)) and with pulmonary arterial hypertension (PAH; OR 5.99, 95% CI 1.34 to 26.91 (p=0.02)). AORs for hospitalisation in adults were significantly higher with each additional year of age (OR 1.03, 95% CI 1.00 to 1.05 (p=0.04)), additional comorbidities (OR 3.23, 95% CI 1.31 to 7.97 (p=0.01)) and genetic disease (OR 2.87, 95% CI 1.04 to 7.94 (p=0.04)). CONCLUSIONS: Children were at low risk of death and hospitalisation secondary to COVID-19 even with severe CHD, but hospital admission rates were higher in younger children, independent of comorbidity. In adults, higher likelihood of death was associated with increasing age and PAH, and of hospitalisation with age, comorbidities and genetic disease. An individualised approach, based on age and comorbidities, should be taken to COVID-19 management in patients with CHD. BMJ Publishing Group 2023-07-17 /pmc/articles/PMC10357297/ /pubmed/37460271 http://dx.doi.org/10.1136/openhrt-2023-002356 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Congenital Heart Disease
Chivers, Sian
Cleary, Aoife
Knowles, Rachel
Babu-Narayan, Sonya V
Simpson, John M
Nashat, Heba
Dimopoulos, Konstantinos
Gatzoulis, Michael A
Wilson, Dirk
Prica, Milos
Anthony, James
Clift, Paul F
Jowett, Victoria
Jenkins, Petra
Khodaghalian, Bernadette
Jones, Caroline B
Hardiman, Antonia
Head, Catherine
Miller, Owen
Chung, Natali AY
Mahmood, Umar
Bu'Lock, Frances A
Ramcharan, Tristan KW
Chikermane, Ashish
Shortland, Jennifer
Tometzki, Andrew
Crossland, David S
Reinhardt, Zdenka
Lewis, Clive
Rittey, Leila
Hares, Dominic
Panagiotopoulou, Olga
Smith, Benjamin
Najih L, Muhammad
Bharucha, Tara
Daubeney, Piers EF
COVID-19 in congenital heart disease (COaCHeD) study
title COVID-19 in congenital heart disease (COaCHeD) study
title_full COVID-19 in congenital heart disease (COaCHeD) study
title_fullStr COVID-19 in congenital heart disease (COaCHeD) study
title_full_unstemmed COVID-19 in congenital heart disease (COaCHeD) study
title_short COVID-19 in congenital heart disease (COaCHeD) study
title_sort covid-19 in congenital heart disease (coached) study
topic Congenital Heart Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357297/
https://www.ncbi.nlm.nih.gov/pubmed/37460271
http://dx.doi.org/10.1136/openhrt-2023-002356
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