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Lung transplantation for cystic fibrosis. | LitMetric

AI Article Synopsis

  • * Recent debates have emerged in the U.S. regarding the survival benefits of lung transplants for CF patients, while research from the UK and Canada indicates a clear survival advantage for those who receive transplants.
  • * Experts from multiple countries convened to discuss advancements in lung transplantation techniques, outcomes measurement, and patient care, aiming to enhance the long-term success of transplants in CF patients.

Article Abstract

Lung transplantation is a complex, high-risk, potentially life-saving therapy for the end-stage lung disease of cystic fibrosis (CF). The decision to pursue transplantation involves comparing the likelihood of survival with and without transplantation as well as assessing the effect of wait-listing and transplantation on the patient's quality of life. Although recent population-based analyses of the US lung allocation system for the CF population have raised controversies about the survival benefits of transplantation, studies from the United Kingdom and Canada have suggested a definite survival advantage for those receiving transplants. In response to these and other controversies, leaders in transplantation and CF met together in Lansdowne, Virginia, to consider the state of the art in lung transplantation for CF in an international context, focusing on advances in surgical technique, measurement of outcomes, use of prognostic criteria, variations in local control over listing, and prioritization among the United States, Canada, the United Kingdom, and The Netherlands, patient adherence before and after transplantation and other issues in the broader context of lung transplantation. Finally, the conference members carefully considered how efforts to improve outcomes for lung transplantation for CF lung disease might best be studied. This Roundtable seeks to communicate the substance of our discussions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797068PMC
http://dx.doi.org/10.1513/pats.2009008-088TLDOI Listing

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