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191
Case Report
6. Granton JT, Rabinovitch M. Pulmonary ar- terial hypertension in congenital heart dis- ease. Cardiol Clin. 2002;20:441-457. PMID: 12371012
7. Goetschmann S, Dibernardo S, Steinmann H, Pavlovic M, Sekarski N, Pfammatter, P. Frequency of severe pulmonary hy- pertension complicating “isolated” atri- al septal defect in infancy. Am J Cardiol. 2008;102:340-342. DOI: 10.1016/j.amj- card.2008.03.061
8. Davidson A, Chandrasekaran K, Guida L, Holsclaw DS Jr. Enhancement of hypox- emia by atrial shunting in cystic brosis. Chest. 1990;98:543-545. PMID: 2394134
9. Espiritu JD, Kleinhenz ME. Patent foramen ovale is the most prevalent echocardio- graphic abnormality in adult cystic brosis.
Am J Resp Crit Care Med. 2000;161:A71. 10. Warnes CA, Williams RG, Bashore TM, Child JS, Connolly HM, Dearani JA, et al. ACC/ AHA 2008 guidelines for the manage- ment of adults with congenital heart dis- ease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writ- ing Committee to Develop Guidelines on the Management of Adults With Con- genital Heart Disease). Developed in Col- laboration With the American Society of Echocardiography, Heart Rhythm Society, International Society for Adult Congenital Heart Disease, Society for Cardiovascular Angiography and Interventions, and So- ciety of Thoracic Surgeons. J Am Coll Car- diol. 2008;52:e143-e263. DOI: 10.1016/j.
jacc.2008.10.001
11. Belton M, Gyi KM. Improvement in pulmo- nary function following closure of a patent foramen ovale in a man with cystic bro- sis. J R Soc Med. 2009;102:S59-S62. DOI: 10.1258/jrsm.2009.s19013
Saidi A. et al.
ASD Closure in Patient with Cystic Fibrosis
Cite this article as: Saidi A, Carveth H, Tandar A. Improvement in Pulmonary Function After Closure of Atrial Septal Defect in a Patient With Cystic Fibrosis. Structural Heart Disease. 2017;3(6):187- 191. DOI: https://doi.org/10.12945/j. jshd.2017.022.17