|
Catalog Number UNK SJM TRIFECTA VALVE |
Device Problem
Perivalvular Leak (1457)
|
Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
|
Event Date 01/01/2013 |
Event Type
malfunction
|
Manufacturer Narrative
|
B3 - date of event is estimated.D4 - the udi number is not known as the part and lot numbers were not provided the additional patient effects reported in the article are captured under a separate medwatch report investigation is not yet complete.A follow-up report will be submitted with all additional relevant information.Na.
|
|
Event Description
|
The article, "minimally invasive surgical aortic valve replacement versus transfemoral transcatheter aortic valve implantation in low-risk octogenarians", was reviewed.The article presented a retrospective, single center study on low-risk (society of thoracic surgeons [sts] score<4%) octogenarians before and after transfemoral transcatheter aortic valve implantation (tf-tavi) and minimally invasive aortic valve replacement (mini-avr) performed between (b)(6) 2013 and (b)(6) 2019; follow-up was completed in (b)(6) 2022.Devices included in this study were sapien 3/xt, evolut r, portico, trifecta, enable, perceval, intuity, and other unknown.The article concluded that in the present study on low-risk octogenarians, transfemoral tavi and minimally invasive avr showed comparable short-term and mid-term results.Both procedures are deemed safe and effective.Larger randomized controlled trials will be required to determine which low risk patients will benefit most from tavi.[the primary and corresponding author was (b)(6) the time frame of the study was from (b)(6) 2013 to (b)(6) 2019.A total of (b)(6) patients were included in this study, of which 20 received an abbott device.The average age was 83.8 years and the average gender was female.Comorbidities included arterial hypertension, diabetes mellitus, coronary artery disease, prior myocardial infarction, peripheral vascular disease, syncope, atrial fibrillation, pulmonary hypertension, chronic pulmonary disease, prior stroke, prior transient ischemic attack, and tumor.
|
|
Manufacturer Narrative
|
B3 - date of event is estimated.D4 - the udi number is not known as the part and lot numbers were not provided the additional patient effects reported in the article are captured under a separate medwatch report summarized patient outcomes/complications of trifecta valve were reported in a research article in a subject population with multiple co-morbidities including arterial hypertension, diabetes mellitus, coronary artery disease, prior myocardial infarction, peripheral vascular disease, syncope, atrial fibrillation, pulmonary hypertension, chronic pulmonary disease, prior stroke, prior transient ischemic attack, and tumor.Some of the complications reported were acute kidney injury, new onset atrial fibrillation, permanent pacemaker implant, stroke, transient ischemic attack, bleeding, and paravalvular leak.A more comprehensive assessment could not be performed as the event was non-contemporaneously reported through a literature review and no device or individual patient information was received for analysis.
|
|
Search Alerts/Recalls
|
|
|