TY - JOUR
T1 - Association between Transcatheter Aortic Valve Replacement and Early Postprocedural Stroke
AU - Huded, Chetan P.
AU - Tuzcu, E. Murat
AU - Krishnaswamy, Amar
AU - Mick, Stephanie L.
AU - Kleiman, Neal S.
AU - Svensson, Lars G.
AU - Carroll, John
AU - Thourani, Vinod H.
AU - Kirtane, Ajay J.
AU - Manandhar, Pratik
AU - Kosinski, Andrzej S.
AU - Vemulapalli, Sreekanth
AU - Kapadia, Samir R.
N1 - Funding Information:
reports receiving funding for clinical trials and educational support from Medtronic. Dr Svensson reports receiving grants from the Cleveland Clinic during the conduct of the study and that he is an unpaid member of the executive committee of the PARTNER Trial and chairman of the PARTNER publications committee. Dr Carroll reports serving as a clinical trial investigator for Medtronic and Edwards Lifesciences. Dr Thourani reports receiving grants and personal fees from Edwards Lifesciences and grants from Medtronic during the conduct of the study. Dr Kirtane reports receiving institutional funding to Columbia University and/or Cardiovascular Research Foundation from Medtronic, Boston Scientific, Abbott Vascular, Abiomed, CSI, CathWorks, Siemens, Philips, and ReCor Medical. Dr Vemulapalli reports receiving grants from the American College of Cardiology, Society of Thoracic Surgeons, Abbott Vascular, and Patient Centered Outcomes Research Institute; grants and personal fees from Boston Scientific; personal fees from Janssen, and grants from Institutes outside the submitted work. No other disclosures were reported.
Publisher Copyright:
© 2019 American Medical Association. All rights reserved.
PY - 2019/6/18
Y1 - 2019/6/18
N2 - Importance: Reducing postprocedural stroke is important to improve the safety of transcatheter aortic valve replacement (TAVR). Objective: This study evaluated the trends of stroke occurring within 30 days after the procedure during the first 5 years TAVR was used in the United States, the association of stroke with 30-day mortality, and the association of medical therapy with 30-day stroke risk. Design, Setting, and Participants: Retrospective cohort study including 101430 patients who were treated with femoral and nonfemoral TAVR at 521 US hospitals in the Society of Thoracic Surgeons/American College of Cardiology Transcatheter Valve Therapies Registry from November 9, 2011, through May 31, 2017. Thirty-day follow-up ended June 30, 2017. Exposures: TAVR. Main Outcomes and Measures: The rates of 30-day transient ischemic attack and stroke were assessed. Association of stroke with 30-day mortality and association of antithrombotic medical therapies with postdischarge 30-day stroke were assessed with a Cox proportional hazards model and propensity-score matching, respectively. Results: Among 101430 patients included in the study (median age, 83 years [interquartile range {IQR}, 76-87 years]; 47797 women [47.1%]; and 85147 patients [83.9%] treated via femoral access), 30-day postprocedure follow-up data was assessed in all patients. At day 30, there were 2290 patients (2.3%) with a stroke of any kind (95% CI, 2.2%-2.4%), and 373 patients (0.4%) with transient ischemic attacks (95% CI, 0.3%-0.4%). During the study period, 30-day stroke rates were stable without an increasing or decreasing trend in all patients (P for trend =.22) and in the large femoral access subgroup (P trend =.47). Among cases of stroke within 30 days, 1119 strokes (48.9%) occurred within the first day and 1567 (68.4%) within 3 days following TAVR. The occurrence of stroke was associated with a significant increase in 30-day mortality: 383 patients (16.7%) of 2290 who had a stroke vs 3662 patients (3.7%) of 99140 who did not have a stroke died (P <.001; risk-adjusted hazard ratio [HR], 6.1 [95% CI, 5.4-6.8]; P <.001). After propensity-score matching, 30-day stroke risk was not associated with whether patients in the femoral cohort were (0.55%) or were not (0.52%) treated with dual antiplatelet therapy at hospital discharge (HR, 1.04; 95% CI, 0.74-1.46) nor was it associated with whether patients in the nonfemoral cohort were (0.71%) or were not (0.69%) treated with dual antiplatelet therapy (HR, 1.02; 95% CI, 0.54-1.95). Similarly, 30-day stroke risk was not associated with whether patients in the femoral cohort were (0.57%) or were not (0.55) treated with oral anticoagulant therapy at hospital discharge (HR, 1.03; 95% CI, 0.73-1.46) nor was it associated with whether patients in the nonfemoral cohort were (0.75%) or were not (0.82%) treated with an oral anticoagulant (HR, 0.93; 95% CI, 0.47-1.83). Conclusions and Relevance: Between 2011 and 2017, the rate of 30-day stroke following transcatheter aortic valve replacement in a US registry population remained stable..
AB - Importance: Reducing postprocedural stroke is important to improve the safety of transcatheter aortic valve replacement (TAVR). Objective: This study evaluated the trends of stroke occurring within 30 days after the procedure during the first 5 years TAVR was used in the United States, the association of stroke with 30-day mortality, and the association of medical therapy with 30-day stroke risk. Design, Setting, and Participants: Retrospective cohort study including 101430 patients who were treated with femoral and nonfemoral TAVR at 521 US hospitals in the Society of Thoracic Surgeons/American College of Cardiology Transcatheter Valve Therapies Registry from November 9, 2011, through May 31, 2017. Thirty-day follow-up ended June 30, 2017. Exposures: TAVR. Main Outcomes and Measures: The rates of 30-day transient ischemic attack and stroke were assessed. Association of stroke with 30-day mortality and association of antithrombotic medical therapies with postdischarge 30-day stroke were assessed with a Cox proportional hazards model and propensity-score matching, respectively. Results: Among 101430 patients included in the study (median age, 83 years [interquartile range {IQR}, 76-87 years]; 47797 women [47.1%]; and 85147 patients [83.9%] treated via femoral access), 30-day postprocedure follow-up data was assessed in all patients. At day 30, there were 2290 patients (2.3%) with a stroke of any kind (95% CI, 2.2%-2.4%), and 373 patients (0.4%) with transient ischemic attacks (95% CI, 0.3%-0.4%). During the study period, 30-day stroke rates were stable without an increasing or decreasing trend in all patients (P for trend =.22) and in the large femoral access subgroup (P trend =.47). Among cases of stroke within 30 days, 1119 strokes (48.9%) occurred within the first day and 1567 (68.4%) within 3 days following TAVR. The occurrence of stroke was associated with a significant increase in 30-day mortality: 383 patients (16.7%) of 2290 who had a stroke vs 3662 patients (3.7%) of 99140 who did not have a stroke died (P <.001; risk-adjusted hazard ratio [HR], 6.1 [95% CI, 5.4-6.8]; P <.001). After propensity-score matching, 30-day stroke risk was not associated with whether patients in the femoral cohort were (0.55%) or were not (0.52%) treated with dual antiplatelet therapy at hospital discharge (HR, 1.04; 95% CI, 0.74-1.46) nor was it associated with whether patients in the nonfemoral cohort were (0.71%) or were not (0.69%) treated with dual antiplatelet therapy (HR, 1.02; 95% CI, 0.54-1.95). Similarly, 30-day stroke risk was not associated with whether patients in the femoral cohort were (0.57%) or were not (0.55) treated with oral anticoagulant therapy at hospital discharge (HR, 1.03; 95% CI, 0.73-1.46) nor was it associated with whether patients in the nonfemoral cohort were (0.75%) or were not (0.82%) treated with an oral anticoagulant (HR, 0.93; 95% CI, 0.47-1.83). Conclusions and Relevance: Between 2011 and 2017, the rate of 30-day stroke following transcatheter aortic valve replacement in a US registry population remained stable..
KW - Aged
KW - Aged, 80 and over
KW - Aortic Valve/surgery
KW - Aortic Valve Stenosis/surgery
KW - Female
KW - Heart Valve Prosthesis
KW - Humans
KW - Male
KW - Prognosis
KW - Propensity Score
KW - Proportional Hazards Models
KW - Registries
KW - Retrospective Studies
KW - Stroke/epidemiology
KW - Transcatheter Aortic Valve Replacement/adverse effects
KW - United States/epidemiology
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U2 - 10.1001/jama.2019.7525
DO - 10.1001/jama.2019.7525
M3 - Article
C2 - 31211345
AN - SCOPUS:85067333448
SN - 0098-7484
VL - 321
SP - 2306
EP - 2315
JO - JAMA - Journal of the American Medical Association
JF - JAMA - Journal of the American Medical Association
IS - 23
ER -