| Literature DB >> 29850412 |
Yukio Aikawa1, Yu Kataoka2, Tomoaki Kanaya3, Makoto Amaki2, Yoshio Tahara2, Yasuhide Asaumi2, Hideaki Kanzaki2, Teruo Noguchi2, Tomoyuki Fujita4, Junjiro Kobayashi4, Satoshi Yasuda2.
Abstract
A 73-year-old man with severe aortic valve stenosis successfully underwent transcatheter aortic valve replacement (TAVR) using CoreValveTM (29 mm, Medtronic Inc., Minneapolis, MN, USA). Four years after the TAVR, he was hospitalized due to anterior ST-segment elevation myocardial infarction. Despite the need for prompt restoration of coronary flow in the infarct-related artery, the implanted CoreValveTM profoundly restricted the manipulation of diagnostic catheters during the coronary angiography. In particular, (I) guidewire easily migrated into the space between CoreValveTM and aorta vessel wall; (II) the nickel-titanium frame of CoreValveTM limited the space to manipulate catheters, making difficult to advance Judkins left (JL) 4, Judkins right (JR) 4 and Amplatz left 1 into coronary cusps; and (III) selecting specific spot within frame was required for cannulation. Left and right coronary arteries were barely engaged by JL3.5 and modified JR4, respectively. Percutaneous coronary intervention (PCI) for culprit lesion in the left-anterior descending artery was successfully completed by 6-French JL3.5 (BritetipTM, Cordis, Milpitas, CA, USA) with drug-eluting stent implantation. Meticulous strategies and understanding of the prosthetic valve geometry are warranted to conduct PCI in patients who underwent TAVR.Entities:
Keywords: ST-segment myocardial infarction; primary percutaneous coronary intervention (primary PCI); transcatheter aortic valve replacement (TAVR)
Year: 2018 PMID: 29850412 PMCID: PMC5951996 DOI: 10.21037/cdt.2018.04.02
Source DB: PubMed Journal: Cardiovasc Diagn Ther ISSN: 2223-3652