Literature DB >> 6697454

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

M Rabinovitch, J F Keane, W I Norwood, A R Castaneda, L Reid.   

Abstract

At the time of surgical repair, a lung biopsy was performed on patients with congenital heart defects who either had pulmonary hypertension or in whom it would be likely to develop if the lesion were not corrected. Pulmonary vascular changes, assessed morphometrically and also according to the classification of Heath and Edwards (Circulation 18: 533, 1958), were correlated with the postoperative pulmonary hemodynamic findings: mean pulmonary arterial pressure the day after correction and mean pulmonary arterial pressure and pulmonary vascular resistance measured 1 year later. On the first postoperative day, increased mean pulmonary arterial pressure was uncommon in patients with morphometric grade A or B (mild) biopsy findings and Heath-Edwards grade N (normal), and if it was present it was of a mild degree. Mean pulmonary arterial pressure was commonly elevated in those with grade B (severe) or C (mild or severe) and Heath-Edwards grade I biopsy results and was more frequently elevated in those with grade II findings. Moderate-to-severe elevation of mean pulmonary arterial pressure was invariable in patients with Heath-Edwards grade III changes regardless of the morphometric grade. One year after repair, mean pulmonary arterial pressure and/or pulmonary vascular resistance were normal in all patients whose conditions were corrected surgically before 9 months of age regardless of the severity of the pulmonary vascular changes. Values were normal in patients whose conditions were repaired surgically at 9 months of age or later who had grade A or B (mild) morphometric findings with any Heath-Edwards grade or grade B (severe) morphometric findings with Heath-Edwards grade I but were increased in half of the patients with grade B (severe) morphometric findings and Heath-Edwards grade II or with grade C (mild or severe) and Heath-Edwards grade I or II changes. Pulmonary arterial pressure and pulmonary vascular resistance were increased in all patients whose conditions were repaired after 2 years of age with grade C morphometric findings and to a severe degree if associated with Heath-Edwards grade III. Thus, although the Heath-Edwards grade can usually be used to identify patients at risk for pulmonary hypertension in the early postoperative period, both the morphometric and the Heath-Edwards grades as well as the age of the patient at the time of repair can be used to determine whether pulmonary arterial pressure and resistance eventually return to normal or remain elevated.

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Year:  1984        PMID: 6697454     DOI: 10.1161/01.cir.69.4.655

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  45 in total

1.  Unidirectional valved patch closure of ventricular septal defects with severe pulmonary arterial hypertension.

Authors:  Sachin Talwar; Shiv Kumar Choudhary; Sanket Garg; Anita Saxena; Sivasubramanian Ramakrishnan; Shyam Sunder Kothari; Rajnish Juneja; Balram Airan
Journal:  Interact Cardiovasc Thorac Surg       Date:  2012-03-08

2.  Pulmonary function in children after surgical and percutaneous closure of atrial septal defect.

Authors:  Mahmoud Zaqout; Frans De Baets; Petra Schelstraete; Bert Suys; Joseph Panzer; Katrien Francois; Thierry Bove; Ilse Coomans; Daniel De Wolf
Journal:  Pediatr Cardiol       Date:  2010-08-20       Impact factor: 1.655

3.  Closure of symptomatic ventricular septal defects: how early is too early?

Authors:  B Kogon; H Butler; P Kirshbom; K Kanter; M McConnell
Journal:  Pediatr Cardiol       Date:  2007-08-04       Impact factor: 1.655

Review 4.  Pulmonary hypertension complicating congenital heart disease.

Authors:  J Eduardo Rame
Journal:  Curr Cardiol Rep       Date:  2009-07       Impact factor: 2.931

5.  Pulmonary function in children with atrial septal defect before and after heart surgery.

Authors:  J Sulc; V Andrle; J Hruda; B Hucín; M Samánek; A Zapletal
Journal:  Heart       Date:  1998-11       Impact factor: 5.994

6.  EXPRESS: Parameters associated with outcome in pediatric patients with congenital heart disease and pulmonary hypertension subjected to combined vasodilator and surgical treatments.

Authors:  Ana Maria Thomaz; Luiz Junya Kajita; Vera D Aiello; Leína Zorzanelli; Filomena Rbg Galas; Cleide G Machado; Miguel Barbero-Marcial; Marcelo B Jatene; Marlene Rabinovitch; Antonio Augusto Lopes
Journal:  Pulm Circ       Date:  2019-02-26       Impact factor: 3.017

7.  Management of pulmonary hypertension in Down syndrome.

Authors:  Amy Hawkins; Simon Langton-Hewer; John Henderson; Robert Michael Tulloh
Journal:  Eur J Pediatr       Date:  2011-01-04       Impact factor: 3.183

8.  Implication of in vivo circulating fibrocytes ablation in experimental pulmonary hypertension murine model.

Authors:  Vandana S Nikam; Sandeep Nikam; Akyl Sydykov; Katrin Ahlbrecht; Rory E Morty; Werner Seeger; Robert Voswinckel
Journal:  Br J Pharmacol       Date:  2020-04-12       Impact factor: 8.739

Review 9.  Pulmonary Hypertension.

Authors:  Peter Oishi; Jeffrey R Fineman
Journal:  Pediatr Crit Care Med       Date:  2016-08       Impact factor: 3.624

10.  Effect of nicardipine on pulmonary hypertension after repair of congenital heart defects in early postoperative period.

Authors:  K Maruyama; J Maruyama; H Utsunomiya; K Furuhashi; M Kurobuchi; Y Katayama; I Yada; M Muneyuki
Journal:  J Anesth       Date:  1993-01       Impact factor: 2.078

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