TY - JOUR
T1 - Short- and long-term adverse events in patients on temporary circulatory support before durable ventricular assist device
T2 - An IMACS registry analysis
AU - Ton, Van Khue
AU - Xie, Rongbing
AU - Hernandez-Montfort, Jaime A.
AU - Meyns, Bart
AU - Nakatani, Takeshi
AU - Yanase, Masanobu
AU - Shaw, Steve
AU - Pettit, Stephen
AU - Netuka, Ivan
AU - Kirklin, James
AU - Goldstein, Daniel J.
AU - Cowger, Jennifer
N1 - Funding Information:
Dr Ton received research grant from Medtronic. Dr Hernandez-Montfort is a consultant for Abiomed. Dr Meyns received research grant from Abiomed. Dr Shaw received honoraria for educational presentations from Abbott. Dr Netuka received research grant from and is a consultant for Abbott, served as a principal investigator for Carmat, and as an advisory board member for LeviticusCardio Ltd and Evaheart Inc. Dr Kirklin received partial salary support paid to his institution as Director of INTERMACS MCS Registry Data Center, and a one-time $2,500 fee as the chair of DSMB for clinical trial of pediatric valved conduit from Xeltis. Dr Goldstein received surgical proctor and educator fees from Abbott, and personal fee from ISHLT (as International Society for Heart and Lung Transplantation Mechanical Circulatory Support Registry [IMACS] director). Dr Cowger is a consultant for Medtronic and Procyrion and a paid speaker for Abbott and Medtronic. Other authors have no disclosures.
Publisher Copyright:
© 2020 International Society for Heart and Lung Transplantation
PY - 2020/4
Y1 - 2020/4
N2 - BACKGROUND: Patients with cardiogenic shock (CS) needing temporary circulatory support (TCS) have poor survival rates after implantation of durable ventricular assist device (dVAD). We aimed to characterize post-dVAD adverse event burden and survival rates in patients requiring pre-operative TCS. METHOD: We analyzed 13,511 adults (Interagency Registry for Mechanically Assisted Circulatory Support [INTERMACS] Profiles 1–3) with continuous-flow dVADs in International Society for Heart and Lung Transplantation Registry for Mechanically Assisted Circulatory Support (2013–2017) according to the need for pre-operative TCS (n = 5,632) vs no TCS (n = 7,879). Of these, 726 (5.4%) had biventricular assist devices (BiVAD). Furthermore, we compared prevalent rates (events/100 patient-months) of bleeding, device-related infection, hemorrhagic and ischemic cerebrovascular accidents (hemorrhagic cerebral vascular accident [hCVA], and ischemic cerebral vascular accident [iCVA]) in early (<3 months) and late (≥3 months) post-operative periods. RESULTS: TCS included extracorporeal membrane oxygenation (ECMO) (n = 1,138), intra-aortic balloon pump (IABP) (n = 3,901), and other TCS (n = 593). Within 3 post-operative months, there were more major bleeding and cerebrovascular accidents (CVAs) in patients with pre-operative ECMO (events/100 patient-months rates: bleeding = 19, hCVA = 1.6, iCVA = 2.8) or IABP (bleeding = 17.3, hCVA = 1.5, iCVA = 1.5) vs no TCS (bleeding = 13.2, hCVA = 1.1, iCVA = 1.2, all p < 0.05). After 3 months, adverse events were lower and similar in all groups. Patients with ECMO had the worst short- and long-term survival rates. Patients with BiVAD had the worst survival rate regardless of need for pre-operative TCS. CVA and multiorgan failures were the common causes of death for patients with TCS and patients without TCS. CONCLUSIONS: Patients requiring TCS before dVAD had a sicker phenotype and higher rates of early post-operative adverse events than patients without TCS. ECMO was associated with very high early ischemic stroke, bleeding, and mortality. The extreme CS phenotype needing ECMO warrants a higher-level profile status, such as INTERMACS “0.”
AB - BACKGROUND: Patients with cardiogenic shock (CS) needing temporary circulatory support (TCS) have poor survival rates after implantation of durable ventricular assist device (dVAD). We aimed to characterize post-dVAD adverse event burden and survival rates in patients requiring pre-operative TCS. METHOD: We analyzed 13,511 adults (Interagency Registry for Mechanically Assisted Circulatory Support [INTERMACS] Profiles 1–3) with continuous-flow dVADs in International Society for Heart and Lung Transplantation Registry for Mechanically Assisted Circulatory Support (2013–2017) according to the need for pre-operative TCS (n = 5,632) vs no TCS (n = 7,879). Of these, 726 (5.4%) had biventricular assist devices (BiVAD). Furthermore, we compared prevalent rates (events/100 patient-months) of bleeding, device-related infection, hemorrhagic and ischemic cerebrovascular accidents (hemorrhagic cerebral vascular accident [hCVA], and ischemic cerebral vascular accident [iCVA]) in early (<3 months) and late (≥3 months) post-operative periods. RESULTS: TCS included extracorporeal membrane oxygenation (ECMO) (n = 1,138), intra-aortic balloon pump (IABP) (n = 3,901), and other TCS (n = 593). Within 3 post-operative months, there were more major bleeding and cerebrovascular accidents (CVAs) in patients with pre-operative ECMO (events/100 patient-months rates: bleeding = 19, hCVA = 1.6, iCVA = 2.8) or IABP (bleeding = 17.3, hCVA = 1.5, iCVA = 1.5) vs no TCS (bleeding = 13.2, hCVA = 1.1, iCVA = 1.2, all p < 0.05). After 3 months, adverse events were lower and similar in all groups. Patients with ECMO had the worst short- and long-term survival rates. Patients with BiVAD had the worst survival rate regardless of need for pre-operative TCS. CVA and multiorgan failures were the common causes of death for patients with TCS and patients without TCS. CONCLUSIONS: Patients requiring TCS before dVAD had a sicker phenotype and higher rates of early post-operative adverse events than patients without TCS. ECMO was associated with very high early ischemic stroke, bleeding, and mortality. The extreme CS phenotype needing ECMO warrants a higher-level profile status, such as INTERMACS “0.”
KW - adverse events
KW - bleeding stroke
KW - cardiogenic shock
KW - extracorporeal membrane oxygenation
KW - mortality
KW - temporary mechanical circulatory support
KW - ventricular assist device
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U2 - 10.1016/j.healun.2019.12.011
DO - 10.1016/j.healun.2019.12.011
M3 - Article
C2 - 32029401
AN - SCOPUS:85078793015
SN - 1053-2498
VL - 39
SP - 342
EP - 352
JO - Journal of Heart and Lung Transplantation
JF - Journal of Heart and Lung Transplantation
IS - 4
ER -