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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.
Afiliação
  • Chivers S; Department of Congenital Cardiology, Royal Brompton & Harefield NHS Foundation Trust, London, UK.
  • Cleary A; Department of Congenital Cardiology, Evelina London Children's Hospital, London, UK.
  • Knowles R; Department of Congenital Cardiology, Evelina London Children's Hospital, London, UK.
  • Babu-Narayan SV; Department of Congenital Cardiology, Great Ormond Street Hospital for Children, London, UK.
  • Simpson JM; Department of Public Health Medicine, Great Ormond Street Hospital for Children, London, UK.
  • Nashat H; UCL Great Ormond Street Institute of Child Health Population Policy and Practice, London, UK.
  • Dimopoulos K; Department of Congenital Cardiology, Royal Brompton & Harefield NHS Foundation Trust, London, UK.
  • Gatzoulis MA; Imperial College London, London, UK.
  • Wilson D; Department of Congenital Cardiology, Evelina London Children's Hospital, London, UK.
  • Prica M; Department of Adult Congenital heart disease, Royal Brompton & Harefield NHS Foundation Trust, London, UK.
  • Anthony J; Department of Adult Congenital heart disease, Royal Brompton & Harefield NHS Foundation Trust, London, UK.
  • Clift PF; Department of Adult Congenital heart disease, Royal Brompton & Harefield NHS Foundation Trust, London, UK.
  • Jowett V; Department of Congenital Cardiology, University Hospital of Wales Healthcare NHS Trust, Cardiff, UK.
  • Jenkins P; Department of Adult Congenital heart disease, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Khodaghalian B; Department of Adult Congenital heart disease, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Jones CB; Department of Adult Congenital heart disease, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Hardiman A; Department of Congenital Cardiology, Great Ormond Street Hospital for Children, London, UK.
  • Head C; Department of Adult Congenital heart disease, Liverpool Heart and Chest Hospital NHS Foundation Trust, Liverpool, UK.
  • Miller O; Department of Congenital Cardiology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
  • Chung NA; Department of Congenital Cardiology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
  • Mahmood U; Department of Adult Congenital heart disease, Norfolk and Norwich University Hospital NHS Trust, Norwich, UK.
  • Bu'Lock FA; Department of Adult Congenital heart disease, Norfolk and Norwich University Hospital NHS Trust, Norwich, UK.
  • Ramcharan TK; Department of Congenital Cardiology, Evelina London Children's Hospital, London, UK.
  • Chikermane A; Department of Adult Congenital heart disease, St Thomas' Hospital, London, UK.
  • Shortland J; Department of Congenital Cardiology, Glenfield Hospital East Midlands Congenital Heart Centre, Leicester, UK.
  • Tometzki A; Department of Congenital Cardiology, Glenfield Hospital East Midlands Congenital Heart Centre, Leicester, UK.
  • Crossland DS; Department of Congenital Cardiology, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
  • Reinhardt Z; Department of Congenital Cardiology, Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
  • Lewis C; Department of Congenital Cardiology, Bristol Royal Hospital for Children, Bristol, UK.
  • Rittey L; Department of Congenital Cardiology, Bristol Royal Hospital for Children, Bristol, UK.
  • Hares D; Department of Congenital Cardiology, Freeman Hospital Cardiothoracic Centre, Newcastle upon Tyne, UK.
  • Panagiotopoulou O; Department of Congenital Cardiology, Freeman Hospital Cardiothoracic Centre, Newcastle upon Tyne, UK.
  • Smith B; Department of Adult Congenital heart disease, Papworth Hospital, Cambridge, UK.
  • Najih L M; Department of Congenital Cardiology, Leeds Children's Hospital, Leeds, UK.
  • Bharucha T; Department of Congenital Cardiology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Daubeney PE; Department of Congenital Cardiology, Royal Hospital for Sick Children Yorkhill, Glasgow, UK.
Open Heart ; 10(2)2023 07.
Article em En | MEDLINE | ID: mdl-37460271
ABSTRACT

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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipertensão Arterial Pulmonar / COVID-19 / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Humans Idioma: En Revista: Open Heart Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipertensão Arterial Pulmonar / COVID-19 / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Humans Idioma: En Revista: Open Heart Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido