スティーブンlangford cardiowest技術株式会社
The CardioWest TAH-t was presented by SynCardia's Vice President of Clinical Support, Steve Langford, at the 2007 Willem Kolff Symposium in Kampen, the Netherlands. Langford started with the artificial heart in 1983 when it was called the Jarvik 7 and worked with Dr. Kolff and Dr. Robert Jarvik. Since 1985, Langford has worked with Dr. Jack
Abstract. Background: The CardioWest temporary total artificial heart (TAH-t) replaces both native ventricles of the heart and is more beneficial for a select group of patients than most other typical ventricular assist devices (VADs). This review will expand on the current literature and highlight the chronology of this device.
The CardioWest Total Artificial Heart receives FDA approval, becoming the first TAH to do so. The official name given to the device through the FDA approval process is the SynCardia temporary CardioWest™ Total Artificial Heart. 2008.05 - 2008.07. CMS Reimbursement
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The CardioWest trial started in 1993 in six United States institutions under an investigational device exemption from the Food and Drug Administration. Four centers contributed 27 implant and 18 matched retrospective control patients. Results. Of the implant patients, 25 (93%) received a transplant, 24 (89% of the total, 96% of those
tained with the CardioWest TAR and other devices. Materials and Methods Since 1993, we have implanted 37 CardioWest TARs in 36 patients (Table 1). The cause of heart failure was ischemic in 14 patients (40%), idiopathic in 12 patients (32%), and other in 10 patients (28%). The indication for implantation was unresponsiveness to
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