Literature DB >> 17418647

Lung transplantation for cystic fibrosis: current concepts and one center's experience.

J E Spahr1, R B Love, M Francois, K Radford, K C Meyer.   

Abstract

BACKGROUND: Although new approaches to the treatment of patients with cystic fibrosis (CF) are significantly prolonging their lives, most patients will eventually develop respiratory failure due to progressive bronchiectasis caused by chronic lung infection and inflammation and die from to respiratory failure. We examined our center's (University of Wisconsin Hospital and Clinics) experience with lung transplantation for patients with CF and reviewed the literature to examine current and evolving approaches to transplantation for this indication.
METHODS: We reviewed all published literature pertaining to lung transplantation for CF through 2006, and we reviewed all aspects of transplantation for patients with CF at our institution from 1994 to 2005.
RESULTS: Major complications following lung transplantation include acute rejection, bacterial infection, and bronchiolitis obliterans. Five-year survival at UWHC (Kaplan-Meier) is 67%, and survival was not adversely affected by transplanting patients receiving mechanical ventilation. The major cause of death for transplant recipients was bronchiolitis obliterans syndrome (BOS).
CONCLUSIONS: Lung transplantation for CF is associated with acceptable survival rates and can improve quality of life. Lung transplant should be offered to all patients with advanced CF lung disease if they meet currently accepted inclusion and exclusion criteria.

Entities:  

Mesh:

Year:  2007        PMID: 17418647     DOI: 10.1016/j.jcf.2006.12.010

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  8 in total

1.  Extra corporeal membrane oxygenation (ECMO) therapy in a 3-year-old child with cystic fibrosis: a tale of hope.

Authors:  Patrick Stafler; Colin Wallis
Journal:  J R Soc Med       Date:  2009-07       Impact factor: 5.344

2.  Physical therapy management of a patient on portable extracorporeal membrane oxygenation as a bridge to lung transplantation: a case report.

Authors:  John D Lowman; Tamara K Kirk; Diane E Clark
Journal:  Cardiopulm Phys Ther J       Date:  2012-03

Review 3.  Lung transplantation for cystic fibrosis: results, indications, complications, and controversies.

Authors:  Joseph P Lynch; David M Sayah; John A Belperio; S Sam Weigt
Journal:  Semin Respir Crit Care Med       Date:  2015-03-31       Impact factor: 3.119

Review 4.  Immunosuppression Drug Therapy in Lung Transplantation for Cystic Fibrosis.

Authors:  Pamela Burcham; Lisa Sarzynski; Sabrina Khalfoun; Kimberly J Novak; Julie C Miller; Dmitry Tumin; Don Hayes
Journal:  Paediatr Drugs       Date:  2017-08       Impact factor: 3.022

5.  Inactivation of the rhlA gene in Pseudomonas aeruginosa prevents rhamnolipid production, disabling the protection against polymorphonuclear leukocytes.

Authors:  Maria Van Gennip; Louise Dahl Christensen; Morten Alhede; Richard Phipps; Peter Østrup Jensen; Lars Christophersen; Sünje Johanna Pamp; Claus Moser; Per Jensen Mikkelsen; Andrew Y Koh; Tim Tolker-Nielsen; Gerald B Pier; Niels Høiby; Michael Givskov; Thomas Bjarnsholt
Journal:  APMIS       Date:  2009-07       Impact factor: 3.205

Review 6.  Pulmonary hypertension survival effects and treatment options in cystic fibrosis.

Authors:  Adriano R Tonelli
Journal:  Curr Opin Pulm Med       Date:  2013-11       Impact factor: 3.155

Review 7.  What's new in cystic fibrosis? From treating symptoms to correction of the basic defect.

Authors:  Marijke Proesmans; François Vermeulen; Kris De Boeck
Journal:  Eur J Pediatr       Date:  2008-04-04       Impact factor: 3.183

8.  Longitudinal impact of demographic and clinical variables on health-related quality of life in cystic fibrosis.

Authors:  Janice Abbott; Alison M Morton; Margaret A Hurley; Steven P Conway
Journal:  BMJ Open       Date:  2015-05-19       Impact factor: 2.692

  8 in total

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