FAQsLiving With CFTransplants

Lung Transplant Facts

Lung transplantation is something a person with CF might consider late in the progression of the disease, when life expectancy is about 1-2 more years and quality of life is severely compromised.

Here are some numerical facts about lung transplants.

YEAR NUMBER OF REPORTED DOUBLE LUNG TRANSPLANTS
2003 1228
2004 1402
2005 1653
2006 1881
2007 2036
2008 2127
2009 2365
2010 2646
2011 2850
2012 2905
2013 3133
  • From the Cystic Fibrosis Foundation: In 2013, 245 people with CF received a lung transplant and the median age of the recipient was 31.
  • If one looks at the survival statistics for lung transplant, it is important to separate the patients who have CF from patients who receive a transplant for other reasons. The survival rates are more promising for CF patients than patients as a whole. According to the NIH, about 51 percent of overall patients survive 5 years after a lung transplant. In contrast, the publication Science Daily reported that “the five-year survival rate for Canadians with cystic fibrosis who have received a lung transplant is 67 percent and half of those who have had transplants live beyond 10 years…”
  • A recent study published in the Journal of Thoracic Cardiovascular Surgery showed that CFRD does not impact survival AFTER transplantation. “The presence of diabetes mellitus is associated with significantly increased riskĀ for death in patients with CF on the wait list before lung transplantation, but does not influence survival after transplantation.”
  • Research into donor height and gender is helping to improve survival rates. Specifically, using predicted total lung capacity rather than height of the donors and recipients may improve outcomes by preventing gender-related size mismatch.

For more information and experiences with lung transplants, visit the Transplant Forum of our site. Here are some threads you will find.

A member’s daughter underwent a lung transplant recently and she has some questions:
http://cysticfibrosis.com/forums/topic/13-days-post-dbl-lung-tx/

 

Read a blog about a member’s transplant experience where she examines how people with CF talk about transplants.
http://cysticfibrosis.com/forums/topic/changing-the-way-we-talk-about-transplant/

 

This is a thread about transplant centers and B. Cepacia:
http://cysticfibrosis.com/forums/topic/out-of-state-transplants-because-of-b-cepacia/

Lung image by Patrick J. Lynch, medical illustrator

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