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Hemocompatibility-Related Outcomes in the MOMENTUM 3 Trial at 6 Months: A Randomized Controlled Study of a Fully Magnetically Levitated Pump in Advanced Heart Failure.
Uriel, Nir; Colombo, Paolo C; Cleveland, Joseph C; Long, James W; Salerno, Christopher; Goldstein, Daniel J; Patel, Chetan B; Ewald, Gregory A; Tatooles, Antone J; Silvestry, Scott C; John, Ranjit; Caldeira, Christiano; Jeevanandam, Valluvan; Boyle, Andrew J; Sundareswaran, Kartik S; Sood, Poornima; Mehra, Mandeep R.
Afiliação
  • Uriel N; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Colombo PC; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Cleveland JC; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Long JW; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Salerno C; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Goldstein DJ; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Patel CB; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Ewald GA; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Tatooles AJ; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Silvestry SC; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • John R; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Caldeira C; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Jeevanandam V; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Boyle AJ; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Sundareswaran KS; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Sood P; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
  • Mehra MR; From University of Chicago School of Medicine and Medical Center, IL (N.U., V.J.); Columbia University College of Physicians and Surgeons and New York Presbyterian Hospital, New York, NY (P.C.C.); University of Colorado School of Medicine, Denver (J.C.C.); Integris Baptist Medical Center, Oklahoma C
Circulation ; 135(21): 2003-2012, 2017 May 23.
Article em En | MEDLINE | ID: mdl-28385948
ABSTRACT

BACKGROUND:

The HeartMate 3 (HM3) Left Ventricular Assist System (LVAS) (Abbott) is a centrifugal, fully magnetically levitated, continuous-flow blood pump engineered to enhance hemocompatibility and reduce shear stress on blood components. The MOMENTUM 3 trial (Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy With HeartMate 3) compares the HM3 LVAS with the HeartMate II (HMII) LVAS (Abbott) in advanced heart failure refractory to medical management, irrespective of therapeutic intention (bridge to transplant versus destination therapy). This investigation reported its primary outcome in the short-term cohort (n=294; 6-month follow-up), demonstrating superiority of the HM3 for the trial primary end point (survival free of a disabling stroke or reoperation to replace the pump for malfunction), driven by a reduced need for reoperations. The aim of this analysis was to evaluate the aggregate of hemocompatibility-related clinical adverse events (HRAEs) between the 2 LVAS.

METHODS:

We conducted a secondary end point evaluation of HRAE (survival free of any nonsurgical bleeding, thromboembolic event, pump thrombosis, or neurological event) in the short-term cohort (as-treated cohort n=289) at 6 months. The net burden of HRAE was also assessed by using a previously described hemocompatibility score, which uses 4 escalating tiers of hierarchal severity to derive a total score for events encountered during the entire follow-up experience for each patient.

RESULTS:

In 289 patients in the as-treated group (151 the HM3 and 138 the HMII), survival free of any HRAE was achieved in 69% of the HM3 group and in 55% of the HMII group (hazard ratio, 0.62; confidence interval, 0.42-0.91; P=0.012). Using the hemocompatibility score, the HM3 group demonstrated less pump thrombosis requiring reoperation (0 versus 36 points, P<0.001) or medically managed pump thrombosis (0 versus 5 points, P=0.02), and fewer nondisabling strokes (6 versus 24 points, P=0.026) than the control HMII LVAS. The net hemocompatibility score in the HM3 in comparison with the HMII patients was 101 (0.67±1.50 points/patient) versus 137 (0.99±1.79 points/patient) (odds ratio, 0.64; confidence interval, 0.39-1.03; P=0.065).

CONCLUSIONS:

In this secondary analysis of the MOMENTUM 3 trial, the HM3 LVAS demonstrated greater freedom from HRAEs in comparison with the HMII LVAS at 6 months. CLINICAL TRIAL REGISTRATION URL http//clinicaltrials.gov. Unique identifier NCT02224755.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coração Auxiliar / Função Ventricular Esquerda / Imãs / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Circulation Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coração Auxiliar / Função Ventricular Esquerda / Imãs / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Circulation Ano de publicação: 2017 Tipo de documento: Article