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March 1, 1999The Annals of Thoracic Surgery366 citationsOpen Access

The REMATCH trial: rationale, design, and end points

EREric A. RoseAMAlan J. MoskowitzMPMilton Packer

Key Points

  • To evaluate the effectiveness of left ventricular assist devices compared to optimal medical management in patients with end-stage heart failure awaiting transplantation.
  • Multicenter randomized trial design comparing two treatment approaches.
  • Participants include patients with end-stage heart failure not qualifying for cardiac transplantation.
  • Assessment of long-term implantation outcomes and management strategies.
  • The trial aims to determine the benefits of left ventricular assist devices in managing heart failure symptoms.
  • Data from the trial will help shape future clinical procedures and expand device usage.
  • Expectations include improved quality of life and survival rates for patients.

Abstract

BACKGROUND: Because left ventricular assist devices have recently been approved by the Food and Drug Administration to support the circulation of patients with end-stage heart failure awaiting cardiac transplantation, these devices are increasingly being considered as a potential alternative to biologic cardiac replacement. The Randomized Evaluation of Mechanical Assistance for the Treatment of Congestive Heart Failure (REMATCH) trial is a multicenter study supported by the National Heart, Lung, and Blood Institute to compare long-term implantation of left ventricular assist devices with optimal medical management for patients with end-stage heart failure who require, but do not qualify to receive cardiac transplantation. METHODS: We discuss the rationale for conducting REMATCH, the obstacles to designing this and other randomized surgical trials, the lessons learned in conducting the multicenter pilot study, and the features of the REMATCH study design (objectives, target population, treatments, end points, analysis, and trial organization). CONCLUSIONS: We consider what will be learned from REMATCH, expectations for expanding the use of left ventricular assist devices, and future directions for assessing clinical procedures.

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Cite This Study

Rose et al. (1999) studied this question.

synapsesocial.com/papers/69ff959f2ff633f3657799b0https://doi.org/10.1016/s0003-4975(99)00042-9
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