Your browser doesn't support javascript.
loading
Repair of congenital heart disease with associated pulmonaryhypertension in children: what are the minimal investigativeprocedures? Consensus statement from the Congenital HeartDisease and Pediatric Task Forces, Pulmonary VascularResearch Institute (PVRI)
Lopes, Antonio Augusto; Barst, Robyn J; Haworth, Sheila Glennis; Rabinovitch, Marlene; Al Dabbagh, Maha; del Cerro, Maria Jesus; Ivy, Dunbar; Kashour, Tarek; Kumar, Krishna; Harikrishnan, S; D’Alto, Michele; Thomaz, Ana Maria; Zorzanelli, Leına; Aiello, Vera D; Mocumbi, Ana Olga; Santana, Maria Virginia T; Galal, Ahmed Nasser; Banjar, Hanaa; Tamimi, Omar; Heath, Alexandra; Flores, Patricia C; Diaz, Gabriel; Sandoval, Julio; Shyam Kothari; Shahin Moledina; Goncalves, Rilvani C; Barreto, Alessandra C; Binotto, Maria Angelica; Maia, Margarida; Al Habshan, Fahad; Adatia, Ian.
Afiliação
  • Lopes, Antonio Augusto; Instituto do Coração. São Paulo. BR
  • Barst, Robyn J; Columbia University College of Physicians and Surgeons. Nova Iorque. US
  • Haworth, Sheila Glennis; University College. Londres. GB
  • Rabinovitch, Marlene; Stanford University School of Medicine. Stanford. US
  • Al Dabbagh, Maha; King Fahd Armed Forces Hospital. Jeddah. SA
  • del Cerro, Maria Jesus; La Paz Children’s Hospital. Madri. ES
  • Ivy, Dunbar; Children’s Hospital Colorado. Aurora. US
  • Kashour, Tarek; King Saud University. Riyadh. SA
  • Kumar, Krishna; Amrita Institute of Medical Sciences. Kerala. IN
  • Harikrishnan, S; Sree Chitra Tirunal Institute for Medical Sciences and Technology. Trivandrum. IN
  • D’Alto, Michele; Second University of Naples. Napole. IT
  • Thomaz, Ana Maria; Instituto do Coração. São Paulo. BR
  • Zorzanelli, Leına; Instituto do Coração. São Paulo. BR
  • Aiello, Vera D; Instituto do Coração. São Paulo. BR
  • Mocumbi, Ana Olga; National Institute of Health. Maputo. MZ
  • Santana, Maria Virginia T; Instituto Dante Pazzanese de Cardiologia. São Paulo. BR
  • Galal, Ahmed Nasser; King Fahd Armed Forces Hospital. Jeddah. SA
  • Banjar, Hanaa; King Faisal Specialist Hospital and Research Center. Riyadh. SA
  • Tamimi, Omar; King Abdulaziz Cardiac Center. Riyadh. SA
  • Heath, Alexandra; Kardiozentrum. La Paz. BO
  • Flores, Patricia C; Hospital Patronato Municipal San Jose Sur. Quito. EC
  • Diaz, Gabriel; Universidad Nacional de Colombia. Bogota. CO
  • Sandoval, Julio; National Institute of Cardiology. Cidade do Mexico. MX
  • Shyam Kothari; All India Institute of Medical Sciences. Nova Delhi. IN
  • Shahin Moledina; Great Ormond Street Hospital. Londres. GB
  • Goncalves, Rilvani C; Instituto do Coração. São Paulo. BR
  • Barreto, Alessandra C; Instituto do Coração. São Paulo. BR
  • Binotto, Maria Angelica; Instituto do Coração. São Paulo. BR
  • Maia, Margarida; Universidade Federal de Minas Gerais. Belo Horizonte. BR
  • Al Habshan, Fahad; King Abdulaziz Cardiac Center. Riyadh. SA
  • Adatia, Ian; Stollery Children’s Hospital. Alberta. CA
Pulm Circ ; 4(2): 330-341, 2014. ilus
Article em En | SES-SP, SESSP-IDPCPROD, SES-SP | ID: biblio-1065804
Biblioteca responsável: BR79.1
Localização: BR79.1
ABSTRACT
Standardization of the diagnostic routine for children with congenital heart disease associatedwith pulmonary arterial hypertension (PAH-CHD) is crucial, in particular since inappropriate assignmentto repair of the cardiac lesions (e.g., surgical repair in patients with elevated pulmonary vascular resistance)may be detrimental and associated with poor outcomes. Thus, members of the Congenital HeartDisease and Pediatric Task Forces of the Pulmonary Vascular Research Institute decided to conduct asurvey aimed at collecting expert opinion from different institutions in several countries, covering manyaspects of the management of PAH-CHD, from clinical recognition to noninvasive and invasive diagnosticprocedures and immediate postoperative support. In privileged communities, the vast majority of childrenwith congenital cardiac shunts are now treated early in life, on the basis of noninvasive diagnostic evaluation,and have an uneventful postoperative course, with no residual PAH. However, a small percentageof patients (older at presentation, with extracardiac syndromes or absence of clinical features of increasedpulmonary blood flow, thus suggesting elevated pulmonary vascular resistance) remain at a higher risk ofcomplications and unfavorable outcomes. These patients need a more sophisticated diagnostic approach,including invasive procedures. The authors emphasize that decision making regarding operability is basednot only on cardiac catheterization data but also on the complete diagnostic picture, which includes theclinical history, physical examination, and all aspects of noninvasive evaluation.
Assuntos
Buscar no Google
Coleções: 06-national / BR Base de dados: SES-SP / SESSP-IDPCPROD Assunto principal: Cirurgia Torácica / Cateterismo / Cardiopatias Congênitas / Hipertensão Pulmonar Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Pulm Circ Ano de publicação: 2014 Tipo de documento: Article
Buscar no Google
Coleções: 06-national / BR Base de dados: SES-SP / SESSP-IDPCPROD Assunto principal: Cirurgia Torácica / Cateterismo / Cardiopatias Congênitas / Hipertensão Pulmonar Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Pulm Circ Ano de publicação: 2014 Tipo de documento: Article