Sustained low diffusing capacity in hepatopulmonary syndrome after liver transplantation
Sustained low diffusing capacity in hepatopulmonary syndrome after liver transplantation作者机构:Serveis de Pneumologia Anestesiologia and Hepatologia. Institut d'Investigacions Biomèdiques August Pi i Sunyer Hospital Clínic Universitat de Barcelona Barcelona Spain Serveis de Pneumologia Anestesiologia and Hepatologia. Institut d’Investigacions Biomèdiques August Pi i Sunyer Hospital Clínic Universitat de Barcelona Barcelona Spain
出 版 物:《World Journal of Gastroenterology》 (世界胃肠病学杂志(英文版))
年 卷 期:2006年第12卷第36期
页 面:5878-5883页
核心收录:
基 金:Supported by Red Respira-ISCIII-RTIC-03/11 and Generalitat de Catalunya No. 2005SGR-00822
摘 要:AIM: To study the presence of sustained low diffusing capacity (DLCO) after liver transplantation (LT) in patients with hepatopulmonary syndrome (HPS).METHODS: Six patients with mild-to-severe HPS and 24 without HPS who underwent LT were prospectively followed before and after LT at mid-term (median, 15 mo). HPS patients were also assessed at long-tem (median, 86 mo).RESULTS: Before LT, HPS patients showed lower PaO2 (71 ± 8 mmHg), higher AaPO2 (43 ± 10 mmHg) and lower DLCO (54% ± 9% predicted), due to a combination of moderate-to-severe ventilation-perfusion (VA/Q) imbalance, mild shunt and diffusion limitation, than non-HPS patients (94 ± 4 mmHg and 19 ± 3 mmHg, and 85% ± 3% predicted, respectively) (P 0.05 each). Seven non-HPS patients had also reduced DLCO (70% ± 4% predicted).At mid- and long-term after LT, compared to pre-LT, HPS patients normalized PaO2 (91 ± 3 mmHg and 87 ± 5 mmHg), AaPO2 (14 ± 3 mmHg and 23 ± 5 mmHg) and all VA/Q descriptors (P 0.05 each) without changes in DLCO (53% ± 8% and 56% ± 7% predicted, respectively). Post-LT DLCO in non-HPS patients with pre-LT low DLCO was unchanged (75% ± 6% predicted).CONCLUSION: While complete VA/Q resolution in HPS indicates a reversible functional disturbance, sustained low DLCO after LT also present in some non-HPS patients, points to persistence of sub-clinical liver-induced pulmonary vascular changes.