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A systematic review of clinical study evidence for pulmonary vasodilator therapy following surgery with cardiopulmonary bypass in children with CHD.
Foote, Henry P; Hornik, Christoph P; Hill, Kevin D; Rotta, Alexandre T; Kumar, Karan R; Thompson, Elizabeth J.
Afiliação
  • Foote HP; Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
  • Hornik CP; Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
  • Hill KD; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
  • Rotta AT; Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
  • Kumar KR; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
  • Thompson EJ; Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.
Cardiol Young ; : 1-18, 2022 Jul 20.
Article em En | MEDLINE | ID: mdl-35856267
ABSTRACT

OBJECTIVES:

Complications from pulmonary hypertension are one of the leading contributors to morbidity and mortality post-cardiopulmonary bypass surgery in children with CHD. Pulmonary vasodilator therapies are commonly used post-operatively, but the optimal target patient population, therapy choice, timing of therapy initiation, and duration of therapy are not well defined.

METHODS:

We used PubMed and EMBASE to identify studies from 2000 to 2020 investigating the use of pulmonary vasodilator therapy post-cardiopulmonary bypass in children aged 0-18 years. To ensure eligibility criteria, studies were systematically reviewed by two independent reviewers.

RESULTS:

We identified 26 studies of 42,971 children across four medication classes; 23 were single centre, 14 were prospective, and 11 involved randomisation (four of which employed a placebo-control arm). A disproportionate number of children were from a single retrospective study of 41,872 patients. Definitions varied, but change in pulmonary haemodynamics was the most common primary outcome, used in 14 studies. Six studies had clinical endpoints, with mortality the primary endpoint for two studies. Treatment with inhaled nitric oxide, iloprost, and sildenafil all resulted in improved haemodynamics in specific cohorts of children with post-operative pulmonary hypertension, although improved outcomes were not consistently demonstrated across all treated children. Iloprost may be a cheaper alternative to inhaled nitric oxide with similar haemodynamic response.

CONCLUSION:

Studies were predominantly single-centre, a control arm was rarely used in randomised studies, and haemodynamic endpoints varied significantly. Further research is needed to reduce post-operative morbidity and mortality from pulmonary hypertension in children with CHD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article