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Survival after single versus bilateral lung transplantation for COPD and pulmonary fibrosis. A. Demir, D. Van Raemdonck, G. Verleden, L. Dupont, W. Coosemans, H. Decaluwé, P. De Leyn, P. Nafteux, T. Lerut. University Hospital Gasthuisberg Leuven Belgium.
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Survival after single versus bilateral lung transplantation for COPD and pulmonary fibrosis A. Demir, D. Van Raemdonck, G. Verleden, L. Dupont, W. Coosemans, H. Decaluwé, P. De Leyn, P. Nafteux, T. Lerut University HospitalGasthuisberg Leuven Belgium
NUMBER OF LUNG TRANSPLANTS REPORTED BY YEAR AND PROCEDURE TYPE NOTE: This figure includes only the lung transplants that are reported to the ISHLT Transplant Registry. As such, this should not be construed as representing changes in the number of lung transplants performed worldwide. ISHLT 2009
ADULT LUNG TRANSPLANTATION: Indications(1/1995-6/2008) ISHLT 2009
ADULT LUNG TRANSPLANTATION: Distribution of Procedure Type for Major Indications(1992-2007) ISHLT 2009
ADULT LUNG TRANSPLANTATIONProcedure Type within Indication, by Year ISHLT 2009
ADULT LUNG TRANSPLANTATION: Indications for Single Lung Transplants (Transplants: January 1995 - June 2008) *Other includes: Sarcoidosis: 2.1% Bronchiectasis: 0.4% Congenital Heart Disease: 0.2% LAM: 0.8% OB (non-ReTx): 0.5% Miscellaneous: 6.3% ISHLT 2009
ADULT LUNG TRANSPLANTATION: Indications for Bilateral/Double Lung Transplants (Transplants: January 1995 - June 2008) *Other includes: Sarcoidosis: 2.9% Bronchiectasis: 4.5% Congenital Heart Disease: 1.1% LAM: 1.2% OB (non-ReTx): 1.1% Miscellaneous: 7.7% ISHLT 2009
ADULT LUNG TRANSPLANTATIONKaplan-Meier Survival (Transplants: January 1994 - June 2007) ISHLT 2009
Aim • Whether single lung transplantation (SLTx) or bilateral lung transplantation (BLTx) should be preferred for patients with end-stage pulmonary fibrosis and COPD remains unknown. • The objective of this retrospective study was to analyze factors recorded in a prospective database that are predictive for long-term survival in our lung transplant cohort
Patients and Methods • Between July 1991 and December 2009 • 329 LTx with COPD and Fibrotic patients, • 193 M and 136 F, Mean age:54.5 years [23-69] • COPD patients (n=226) • BLTx (65%) • SLTx (35%) • Fibrotic patients (n=103) • SLTx (56%) • BLTx (44%)
The overall 5 and 10-year survival rate was 65% and 51% for recipients with COPD and 57% and 41% recipients with pulmonary fibrosis (p=0.09).
ADULT LUNG TRANSPLANTATIONKaplan-Meier Survival By Diagnosis(Transplants: January 1990 – June 2007) Survival comparisons Alpha-1 vs. CF: p < 0.0001Alpha-1 vs. COPD: p < 0.0001 Alpha-1 vs. IPF: p < 0.0001Alpha-1 vs.Sarcoidosis: p = 0.0380 CF vs. COPD: p < 0.0001CF vs. IPF: p < 0.0001 CF vs. IPAH: p < 0.0001 CF vs. Sarcoidosis: p < 0.0001 IPAH vs. IPF: p = 0.0046 COPD vs. IPF: p < 0.0001 Note: Other comparisons are not statistically different. ISHLT 2009
ADULT LUNG TRANSPLANTATIONKaplan-Meier Survival By Diagnosis(Transplants: January 1990 – June 2007) Survival comparisons Alpha-1 vs. CF: p < 0.0001 Alpha-1 vs. COPD: p < 0.0001 Alpha-1 vs. IPF: p < 0.0001 Alpha-1 vs.Sarcoidosis: p = 0.0380 CF vs. COPD: p < 0.0001 CF vs. IPF: p < 0.0001 CF vs. IPAH: p < 0.0001 CF vs. Sarcoidosis: p < 0.0001 IPAH vs. IPF: p = 0.0046 COPD vs. IPF: p < 0.0001 ISHLT 2009
ADULT LUNG TRANSPLANTATIONKaplan-Meier Survival by Procedure Type (Transplants: January 1990 – June 2007) Diagnosis: Emphysema/COPD ISHLT 2009
Overall 5-year survival rate was higher after BLTX compared to SLTx in recipients with COPD (77% vs. 49%; p < 0.001)
ADULT LUNG TRANSPLANTATIONKaplan-Meier Survival by Procedure Type(Transplants: January 1990 – June 2007)Diagnosis: Idiopathic Pulmonary Fibrosis ISHLT 2009
Overall 5-year survival rate wasn’t after BLTX compared to SLTxin recipients with fibrosis (55% versus 56%; p=0.35)
Bilateral versus single lung transplantation was not a predictor of early (30 day) and late (60 day) mortality after LTx in recipients with COPD and pulmonary fibrosis (p>0.05). • The length of the ICU stay in the bilateral group was significantly longer after LTx in recipients with COPD (p=0.03).
Conclusion • Mortality, morbidity and long-term survival did not differ between BLTx vs SLTx in patients with pulmonary fibrosis.. However, BLTx leads to better long-term survival in recipients with COPD. SLTx may result in fatal complications in the remaining native emphysematous lung.
Potential advantages for SSLTx • No more native lung present • Specific native lung problems may be avoided • Acute hyperinflation • Chronic hyperinflation • Infectıon • Effect of aspergillus pneumonia native lung • Tumour of the natıve lung • Survival benefit (?) • Early postoperative • Late: BOS development • Better QOL and performance?
Potential disadvantages • Increasing waiting lists • Why using two lungs if one may be sufficient? • Increasing waiting list mortality