作者
Lukas Stolz,Martin Orban,Nicole Karam,Edith Lubos,Mirjam G. Wild,Ludwig T. Weckbach,Thomas Stocker,Fabien Praz,Daniel Braun,Kornelia Löw,Sebastian Hausleiter,Konstantin Stark,Philipp M. Doldi,Noémie Tence,Martin Orban,Satoshi Higuchi,Magda Haum,Stephan Windecker,Christian Hagl,Julia Mayerle,Michael Näbauer,Daniel Kalbacher,Steffen Maßberg,Jörg Hausleiter
摘要
Aims The impact of the cardio‐hepatic syndrome (CHS) on outcomes in patients undergoing mitral valve transcatheter edge‐to‐edge repair (M‐TEER) for relevant mitral regurgitation (MR) is unknown. The objectives of this study were three‐fold: (i) to characterize the pattern of hepatic impairment, (ii) to investigate the prognostic value of CHS, and (iii) to evaluate the changes in hepatic function after M‐TEER. Methods and results Hepatic impairment was quantified by laboratory parameters of liver function. In accordance with existing literature, two types of CHS were distinguished: ischaemic type I CHS (elevation of both transaminases) and cholestatic type II CHS (elevation of two out of three parameters of hepatic cholestasis). The impact of CHS on 2‐year mortality was evaluated using a Cox model. The change in hepatic function after M‐TEER was assessed by laboratory testing at follow‐up. We analysed 1083 patients who underwent M‐TEER for relevant primary or secondary MR at four European centres between 2008 and 2019. Ischaemic type I and cholestatic type II CHS were observed in 11.1% and 23.0% of patients, respectively. Predictors for 2‐year all‐cause mortality differed by MR aetiology. While in primary MR cholestatic type II CHS was independently associated with 2‐year mortality, ischaemic CHS type I was an independent mortality predictor in secondary MR patients. At follow‐up, patients with MR reduction ≤2+ (obtained in 90.7% of patients) presented with improved parameters of hepatic function (median reduction of 0.2 mg/dl, 0.2 U/L and 21 U/L for bilirubin, alanine aminotransferase and gamma‐glutamyl transferase, respectively, p < 0.01). Conclusions The CHS is frequently observed in patients undergoing M‐TEER and significantly impairs 2‐year survival. Successful M‐TEER may have beneficial effects on CHS.