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Echo IQ Signs Integration Agreement With Flagship US Hospital
ACCESS Newswire · Echo IQ

In This Article:

  • Integration follows successful trial of EchoSolv-AS by Beth Israel researchers on a historical cohort of 31,000 patients

  • Trial successfully validated the technology's key performance metrics, accuracy and potential to identify additional patients with Aortic Stenosis (AS)

  • Beth Israel Deaconess Medical Centre (BIDMC) is a world-renowned health facility of the Harvard Medical School

  • The organization undertakes 30,000 echoes annually

SYDNEY, AUSTRALIA / ACCESSWIRE / December 10, 2024 / AI and Medical Technology company Echo IQ Limited ("the Company") (ASX:EIQ) is pleased to advise that it has commenced integration of its EchoSolv-AS solution with Beth Israel Deaconess Medical Center (‘Beth Israel' or ‘BIDMC'), a leading Harvard Medical Teaching Hospital in Boston, Massachusetts. This marks Echo IQ's flagship deployment of EchoSolv-AS with a major hospital group in the USA, following the recent receipt of FDA clearance (refer ASX announcement: 8 October 2024).

Beth Israel is an academic medical center specializing in the latest technologies and teaching initiatives. It hosts 743 licensed beds, manages 37,606 inpatient discharges per annum and has nearly 50,000 emergency department visits and 803,000 outpatient visits annuallyi. The organization undertakes approximately 30,000 echocardiograms yearly, and the integration is expected to further validate the application of EchoSolv-AS in real life practice.

The integration follows the completion of a successful trial of EchoSolv-AS at Beth Israel in September 2024, in which BIDMC researchers validated the technology's key performance metrics.

During the trial, BIDMC tested EchoSolv-AS across routine echocardiographic reports from over 31,000 US Medicare beneficiaries at Beth Israel. EchoSolv-AS identified 98% of patients who met clinical guidelines for severe aortic stenosis (‘AS'), as well as more than 1,000 patients who likely had severe AS, but did not meet clinical guidelines. Non-guideline patients had the same risk of death as those with severe AS, but only 6.6% of them received life extending treatment, compared to 20.2% of patients who were diagnosed with severe AS. The findings of the clinical trial were published in medical research journal, JACC Advancesii.

To integrate the technology, BIDMC will utilise EchoSolv-AS on a no-cost basis while the Company pursues relevant reimbursement codes for users of the technology under insurance. Reimbursement codes are anticipated to be secured in the coming quarters, marking an important commercial milestone which when achieved will allow for first revenues to be recognized.