Literature DB >> 27683607

Clinical classification in pediatric pulmonary arterial hypertension associated with congenital heart disease.

Willemijn M H Zijlstra1, Johannes M Douwes1, Mark-Jan Ploegstra1, Usha Krishnan2, Marcus T R Roofthooft1, Hans L Hillege3, D Dunbar Ivy4, Erika B Rosenzweig2, Rolf M F Berger1.   

Abstract

Congenital heart disease (CHD) is a frequent cause of pediatric pulmonary arterial hypertension (PAH), with diverse etiology and outcome. We aimed to describe phenotypic heterogeneity in pediatric PAH associated with CHD (PAH-CHD), assess the applicability of the Nice CHD classification, and explore whether this classification accurately reflects patient/disease characteristics and survival. All children with CHD from a contemporary cohort of consecutive pediatric PAH patients followed in three major referral centers (Denver, New York, the Netherlands) were characterized and classified on the basis of the latest proposed clinical classification for PAH-CHD (World Symposium on Pulmonary Hypertension, Nice, 2013). According to this classification, 24% of 134 children were classified into group 1, 14% into group 2, 19% into group 3, and 30% into group 4; 11% could not be classified. Types of CHD and hemodynamic profile differed between groups, with the highest right atrial pressure in group 4 (P < 0.040). Group 3 children had Down syndrome less frequently (P = 0.011) but other (un)defined syndromes most frequently (P = 0.063) and received most intense PAH-targeted therapy (P = 0.003). With 15 deaths and one lung transplant (12%; median follow-up: 4.3 years), survival differences could not be demonstrated between the groups in the Nice CHD classification. Pediatric PAH-CHD is a heterogeneous condition frequently associated with extracardiac, developmental factors that are believed to affect disease development. The Nice CHD classification identifies groups with specific patient/disease characteristics. However, a substantial proportion of children could not be classified. Group 3 forms a distinct disease entity. Its prognostic value could not be determined because of the low number of events. The Nice CHD classification supports clinical characterization of PAH-CHD; however, further refinement is needed to classify all children with PAH-CHD.

Entities:  

Keywords:  Nice congenital heart disease classification; congenital heart disease; pediatrics; pulmonary hypertension; survival

Year:  2016        PMID: 27683607      PMCID: PMC5019083          DOI: 10.1086/687764

Source DB:  PubMed          Journal:  Pulm Circ        ISSN: 2045-8932            Impact factor:   3.017


  29 in total

1.  Four- and seven-year outcomes of patients with congenital heart disease-associated pulmonary arterial hypertension (from the REVEAL Registry).

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Journal:  Am J Cardiol       Date:  2013-10-04       Impact factor: 2.778

2.  Pediatric pulmonary hypertension in the Netherlands: epidemiology and characterization during the period 1991 to 2005.

Authors:  Rosa Laura E van Loon; Marcus T R Roofthooft; Hans L Hillege; Arend D J ten Harkel; Magdalena van Osch-Gevers; Tammo Delhaas; Livia Kapusta; Jan L M Strengers; Lukas Rammeloo; Sally-Ann B Clur; Barbara J M Mulder; Rolf M F Berger
Journal:  Circulation       Date:  2011-09-26       Impact factor: 29.690

3.  Clinical features of paediatric pulmonary hypertension: a registry study.

Authors:  Rolf M F Berger; Maurice Beghetti; Tilman Humpl; Gary E Raskob; D Dunbar Ivy; Zhi-Cheng Jing; Damien Bonnet; Ingram Schulze-Neick; Robyn J Barst
Journal:  Lancet       Date:  2012-01-11       Impact factor: 79.321

4.  Natural history and prognosis of atrial septal defect.

Authors:  R J Craig; A Selzer
Journal:  Circulation       Date:  1968-05       Impact factor: 29.690

5.  Assumed oxygen consumption based on calculation from dye dilution cardiac output: an improved formula.

Authors:  A Bergstra; R B van Dijk; H L Hillege; K I Lie; G A Mook
Journal:  Eur Heart J       Date:  1995-05       Impact factor: 29.983

6.  Acute pulmonary vasodilator response in paediatric and adult pulmonary arterial hypertension: occurrence and prognostic value when comparing three response criteria.

Authors:  Johannes M Douwes; Rosa L E van Loon; Elke S Hoendermis; Anton Vonk-Noordegraaf; Marcus T R Roofthooft; Melle D Talsma; Hans L Hillege; Rolf M F Berger
Journal:  Eur Heart J       Date:  2011-09-04       Impact factor: 29.983

7.  Treatment and survival in children with pulmonary arterial hypertension: the UK Pulmonary Hypertension Service for Children 2001-2006.

Authors:  S G Haworth; A A Hislop
Journal:  Heart       Date:  2008-10-24       Impact factor: 5.994

Review 8.  Pulmonary arterial hypertension in congenital cardiac disease--the need for refinement of the Evian-Venice classification.

Authors:  Mirjam E van Albada; Rolf M F Berger
Journal:  Cardiol Young       Date:  2008-01-21       Impact factor: 1.093

9.  Vascular structure in lung tissue obtained at biopsy correlated with pulmonary hemodynamic findings after repair of congenital heart defects.

Authors:  M Rabinovitch; J F Keane; W I Norwood; A R Castaneda; L Reid
Journal:  Circulation       Date:  1984-04       Impact factor: 29.690

10.  A consensus approach to the classification of pediatric pulmonary hypertensive vascular disease: Report from the PVRI Pediatric Taskforce, Panama 2011.

Authors:  Maria Jesus Del Cerro; Steven Abman; Gabriel Diaz; Alexandra Heath Freudenthal; Franz Freudenthal; S Harikrishnan; Sheila G Haworth; Dunbar Ivy; Antonio A Lopes; J Usha Raj; Julio Sandoval; Kurt Stenmark; Ian Adatia
Journal:  Pulm Circ       Date:  2011       Impact factor: 3.017

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  8 in total

Review 1.  Management of Pulmonary Arterial Hypertension in the Pediatric Patient.

Authors:  Jordan E Ezekian; Kevin D Hill
Journal:  Curr Cardiol Rep       Date:  2019-11-28       Impact factor: 2.931

2.  Pulmonary arterial hypertension in the USA: an epidemiological study in a large insured pediatric population.

Authors:  Lin Li; Susan Jick; Stefanie Breitenstein; Gemzel Hernandez; Alexander Michel; David Vizcaya
Journal:  Pulm Circ       Date:  2017-02-01       Impact factor: 3.017

Review 3.  Diagnosis, Evaluation and Treatment of Pulmonary Arterial Hypertension in Children.

Authors:  Benjamin S Frank; D Dunbar Ivy
Journal:  Children (Basel)       Date:  2018-03-23

4.  Residual Pulmonary Hypertension more than 20 Years after Repair of Shunt Lesions.

Authors:  Dovilė Jančauskaitė; Virginija Rudienė; Gabrielius Jakutis; Laurie W Geenen; Jolien W Roos-Hesselink; Lina Gumbienė
Journal:  Medicina (Kaunas)       Date:  2020-06-16       Impact factor: 2.430

5.  Paediatric pulmonary arterial hypertension: updates on definition, classification, diagnostics and management.

Authors:  Erika B Rosenzweig; Steven H Abman; Ian Adatia; Maurice Beghetti; Damien Bonnet; Sheila Haworth; D Dunbar Ivy; Rolf M F Berger
Journal:  Eur Respir J       Date:  2019-01-24       Impact factor: 16.671

Review 6.  Treatment of pediatric pulmonary arterial hypertension: A focus on the NO-sGC-cGMP pathway.

Authors:  Maurice Beghetti; Matthias Gorenflo; D Dunbar Ivy; Shahin Moledina; Damien Bonnet
Journal:  Pediatr Pulmonol       Date:  2019-07-16

7.  Maternal and fetal outcomes of pregnant women with pulmonary arterial hypertension associated with congenital heart disease in Beijing, China: A retrospective study.

Authors:  Yang Liu; Yanna Li; Jun Zhang; Dawei Zhang; Jiachen Li; Yichen Zhao; Kemin Liu; Xiaolong Ma; Chen Bai; Hong Gu; Xiangming Fan; Jiangang Wang
Journal:  Pulm Circ       Date:  2022-04-22       Impact factor: 2.886

8.  Potts anastomosis in children with severe pulmonary arterial hypertension and atrial septal defect.

Authors:  Alice Capel; Marilyne Lévy; Isabelle Szezepanski; Sophie Malekzadeh-Milani; Pascal Vouhé; Damien Bonnet
Journal:  ESC Heart Fail       Date:  2020-11-20
  8 in total

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