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Berlin 2008
Monday, 06.10.2008
Lung and bone marrow transplantation: miscellaneous
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Patient reported quality of life in advanced cystic fibrosis (CF) lung disease assessed for lung transplantation
S. Doe, A. De Soyza, J. Lordan, A. Fisher, P. Corris (Newcastle-upon Tyne, United Kingdom)
Source:
Annual Congress 2008 - Lung and bone marrow transplantation: miscellaneous
Session:
Lung and bone marrow transplantation: miscellaneous
Session type:
E-Communication Session
Number:
1627
Abstract
Background
Advanced lung disease causes premature mortality in CF. Lung transplantation offers a 10-year survival of over 50% in experienced centres. A decision to list for transplant is based upon many factors though no objective measurement of patient reported quality of life (QOL) occurs.
Aim
To evaluate an objective measure of QOL in patients with advanced CF lung disease attending for lung transplant assessment.
Method
48 Patients attending for transplant assessment completed the Short Form 36 (SF36). The score was then correlated with disease severity and transplant assessment outcome.
Results
Median age: 25 yrs (16-51); median FEV1: 25% pred. (11-47); median Pa02: 8.9 kPa (6.7-14); mean six minute walk distance (6MWD): 470m (65-770). Median BMI: 18.8kg/m2 (14-24). A wide range of QOL scores was noted: Total SF36 ranged from 17-89; Physical health domain 5-83; Mental health domain 14-89. 26 patients were listed and had significantly worse FEV1 predicted 20% vs 29% ; p<0.01. Median Pa02 8.2kPa (6.7-14) vs 9.75kPa (8.3-12.9); p<0.01. There were no significant differences in 6MWD and BMI. QOL was poorer in the listed group: Median Total SF36 41 (17-81) vs 59 (23-89); p=0.043 with poorer scores in the mental health domain: Median score 43 (14-78) vs 61 (25-89); p=0.03. Physical health was not significantly poorer: Median 29.5 (5-73) vs 48.5 (10-83); p=0.06.
Conclusions
Wide variability in QOL was reported by the cohort. Those listed had worse lung function but similar exercise capacity. QOL is poorer in those listed particularly in the mental health domain. This may influence listing decisions. Future studies of CF specific QOL measures, SF-36 and survival may be useful.
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Citations should be made in the following way:
S. Doe, A. De Soyza, J. Lordan, A. Fisher, P. Corris (Newcastle-upon Tyne, United Kingdom). Patient reported quality of life in advanced cystic fibrosis (CF) lung disease assessed for lung transplantation. Eur Respir J 2008; 32: Suppl. 52, 1627
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