4.5 Article

Cerebral embolisation during transcatheter edge-to-edge repair of the mitral valve with the MitraClip system: a prospective, observational study

期刊

EUROINTERVENTION
卷 18, 期 2, 页码 E160-+

出版社

EUROPA EDITION
DOI: 10.4244/EIJ-D-21-00646

关键词

cerebral protection; mitral valve repair; stroke

资金

  1. German Heart Foundation/German Foundation of Heart Research
  2. Berlin Institute of Health
  3. DFG [EXC-2049 -390688087]
  4. BMBF
  5. EU
  6. Corona Foundation
  7. Fondation Leducq
  8. Charite -Universitatsmedizin Berlin
  9. DZNE
  10. DZHK

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This study aims to identify the procedural step(s) associated with an increased risk of cerebral embolisation during transcatheter edge-to-edge repair of the mitral valve (TEER-MV) and evaluate the risk of stroke and brain ischemia after the procedure. The results showed that there is a higher risk of cerebral embolisation during device interaction with the mitral valve, and larger infarct volume is associated with neurological deterioration.
Background: New ischaemic brain lesions on magnetic resonance imaging (MRI) are reported in up to 86% of patients after transcatheter edge-to-edge repair of the mitral valve (TEER-MV). Knowledge of the exact procedural step(s) that carry the highest risk for cerebral embolisation may help to further improve the procedure. Aims: The aim of this study was to identify the procedural step(s) that are associated with an increased risk of cerebral embolisation during TEER-MV with the MitraClip system. Furthermore, the risk of overt stroke and silent brain ischaemia after TEER-MV was assessed. Methods: In this prospective, pre-specified observational study, all patients underwent continuous transcranial Doppler examination during TEER-MV to detect microembolic signals (MES). MES were assigned to specific procedural steps: (1) transseptal puncture and placement of the guide, (2) advancing and adjustment of the clip in the left atrium, (3) device interaction with the MV, and (4) removal of the clip delivery system and the guide. Neurological examination using the National Institutes of Health Stroke Scale (NIHSS) and cerebral MRI were performed before and after TEER-MV. Results: Fifty-four patients were included. The number of MES differed significantly between the procedural steps with the highest numbers observed during device interaction with the MV. Mild neurological deterioration (NIHSS <= 3) occurred in 9/54 patients. New ischaemic lesions were detected in 21/24 patients who underwent MRI. Larger infarct volume was significantly associated with neurological deterioration. Conclusions: Cerebral embolisation is immanent to TEER-MV and predominantly occurs during device interaction with the MV. Improvements to the procedure may focus on this procedural step.

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