Same case as mdrs# 2134265-2017-10914, 2134265-2017-10916, 2134265-2017-10917, 2134265-2017-10918, 2134265-2017-10920, 2134265-2017-10930, 2134265-2017-10932, 2134265-2017-10933, 2134265-2017-10934.It was reported that patient death occurred.The target lesion was located in the left main (lm) to mid left anterior descending artery (lad).The lm to mid lad were rotablated successfully using a 1.75 rotalink burr, a rotalink advancer, and a 300 cm rotawire per the directions for use (dfu).The lesion was dilated with a 3.0x20mm nc emerge® balloon.A 3.0x20mm synergy¿ stent was introduced but failed to cross the mid lad lesion.The lesion was dilated with a 3.5x20mm nc emerge® balloon and the same 3.0x20mm synergy¿ stent was successfully delivered.A 3.0x24mm synergy¿ stent was deployed in the proximal lad and a 4.0x20mm promus premier¿ stent was deployed in the proximal lad into the lm.A new 3.5x20mm nc emerge® balloon was used to post dilate the stents in the lad and a 4.0x15mm nc emerge® balloon was used to post dilate the promus premier¿ stent in the lm.While the 4.0x15mm nc emerge® balloon was being inflated briefly, the patient complained of chest pain.The physician did a final inflation at the very proximal end of the promus premier¿ stent.As the physician took a cine of the final result, the patient's blood pressure dropped and the patient became non responsive.A medical emergency was called but the patient died.
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