“…Late complications, (1 year or more postoperative) including implant or wire extrusion, dislocation of transducer/coupler assembly and loss of coupling (e.g., increase in in situ thresholds) need to be reported, as well as technical complications and device failures. If a revision surgery was necessary, it must be stated whether it was due to medical/ surgical (procedure) or device-related reasons [Ernst et al, 2016;Gavilan et al, 2015;Hobson et al, 2010;Lassaletta et al, 2016;Mohamad et al, 2016;Van Rompaey et al, 2011;Wazen et al, 2011;Zwartenkot et al, 2016].…”