{"id":45689,"date":"2022-06-30T15:01:58","date_gmt":"2022-06-30T13:01:58","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/heartbeam-expands-patient-population-for-emergency-department-software-technology-solution\/"},"modified":"2022-06-30T15:01:58","modified_gmt":"2022-06-30T13:01:58","slug":"heartbeam-expands-patient-population-for-emergency-department-software-technology-solution","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/heartbeam-expands-patient-population-for-emergency-department-software-technology-solution\/","title":{"rendered":"HeartBeam Expands Patient Population for Emergency Department Software Technology Solution"},"content":{"rendered":"
\n

\nExpanded Scope of Clinical Validation Study Will Provide Access to a Broader Patient Population<\/i>\n<\/p>\n

\nCompany Expects to File 510K No Later Than August 15, 2022<\/i>\n<\/p>\n

SANTA CLARA, Calif.–(BUSINESS WIRE)–HeartBeam, Inc. (NASDAQ: BEAT), a developmental stage digital healthcare company with a proprietary ECG telemedicine technology for heart attack detection, announced today that HeartBeam is expanding the available patient population for the Company\u2019s Emergency Department software technology solution.\n<\/p>\n

<\/a><\/p>\n

\nIn evaluating the ECG database for the clinical validation of HeartBeam\u2019s platform technology, a significant portion of consecutive patients fell into the category of unstable angina, a serious cardiac condition. In light of the most recent 2021 AHA\/ACC\/ASE\/CHEST\/SAEM\/SCCT\/SCMR Guideline for the Evaluation and Diagnosis of Chest Pain and in consultation with its clinical advisors, HeartBeam elected to include the full data set for clinical validation studying in support of the 510K submission. The expanded scope of the clinical validation study will provide access to a broader patient population for HeartBeam\u2019s technology once cleared by the FDA.\n<\/p>\n

\nDue to the expanded available patient population, HeartBeam expects to file a 510K with the full data set for clinical validation no later than August 15, 2022 and does not affect the timeline for 510K submission of the Telehealth product.\n<\/p>\n

\n\u201cIt is important to include unstable angina as a diagnosis for analysis. Patients with unstable angina may have subtle electrical changes brought on by ischemia without definitive injury to the cardiac tissue,\u201d said Russell Jones, MD, Interventional Cardiologist, Chair of the Ischemia Performance Improvement Committee at Phoebe Putney Health System. \u201cGiven HeartBeam\u2019s advanced technology solution, there is potential to identify patients who cannot be diagnosed by traditional ECG capabilities but may require intervention.\u201d\n<\/p>\n

\nHeartBeam\u2019s platform technology is anticipated to assist physicians in identifying patients who present with chest pain to facilitate rapid detection of a heart attack and determine an appropriate treatment regimen. Chest pain is the second most common reason for an emergency department visit, with high costs associated with these visits. HeartBeam\u2019s software solution may offer more accurate heart attack detection to triage patients and expedite treatment. The HeartBeam technology platform has not yet been evaluated by the FDA and is not approved for clinical use in the USA or other global geographies.\n<\/p>\n

\n\u201cWe believe our commercialization path is on track,\u201d said Branislav Vajdic, PhD, CEO and founder. \u201cThe decision to include the broader patient population does not impact the scheduled submission for HeartBeam\u2019s core technology platform for our Telehealth solution, which remains on schedule to submit in Q4 2022.\u201d\n<\/p>\n

\nAbout HeartBeam, Inc.<\/b>\n<\/p>\n

\nHeartBeam, Inc. (NASDAQ: BEAT) is a development stage digital healthcare company with proprietary ECG telemedicine technology that will redefine the way high risk cardiovascular patients are diagnosed in an ambulatory setting at any time and any place. Its breakthrough solution employs a reusable, credit card sized, 3D vector ECG recording device and cloud-based software capable of assisting a physician in diagnosing a wide range of cardiovascular disease. HeartBeam is initially focusing on a huge unmet need of helping diagnose heart attacks in patients outside of a medical institution. No single lead ECG technology can offer this value to patients and their physicians. This underserved market is several times larger than the cardiac arrhythmia detection market based on the prevalence of patients with coronary artery disease at high risk of heart attack. For more information, visit www.heartbeam.com<\/a>.\n<\/p>\n

\nForward-Looking Statements<\/b>\n<\/p>\n

\nAll statements in this release that are not based on historical fact are \u201cforward-looking statements.\u201d While management has based any forward-looking statements included in this release on its current expectations, the information on which such expectations were based may change. Forward-looking statements involve inherent risks and uncertainties which could cause actual results to differ materially from those in the forward-looking statements, as a result of various factors including those risks and uncertainties described in the Risk Factors and in Management\u2019s Discussion and Analysis of Financial Condition and Results of Operations sections of our in our Forms 10-K, 10-Q and other reports filed with the SEC and available at www.sec.gov<\/a>. We urge you to consider those risks and uncertainties in evaluating our forward-looking statements. We caution readers not to place undue reliance upon any such forward-looking statements, which speak only as of the date made. Except as otherwise required by the federal securities laws, we disclaim any obligation or undertaking to publicly release any updates or revisions to any forward-looking statement contained herein (or elsewhere) to reflect any change in our expectations with regard thereto or any change in events, conditions or circumstances on which any such statement is based.\n<\/p>\n

Contacts<\/b> <\/p>\n

\nMedia and Investor Relations Contact:<\/b>
Chris Tyson<\/b>
Executive Vice President
\n
MZ North America
\n
Direct: 949-491-8235
\n
BEAT@mzgroup.us<\/a>
www.mzgroup.us<\/a>\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

Expanded Scope of Clinical Validation Study Will Provide Access to a Broader Patient Population Company Expects to File 510K No Later Than August 15, 2022 SANTA CLARA, Calif.–(BUSINESS WIRE)–HeartBeam, Inc. (NASDAQ: BEAT), a developmental stage digital healthcare company with a proprietary ECG telemedicine technology for heart attack detection, announced today that HeartBeam is expanding the … [Read more…]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-45689","6":"format-standard","7":"category-industry"},"yoast_head":"\nHeartBeam Expands Patient Population for Emergency Department Software Technology Solution - Pharma Trend<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/pharma-trend.com\/en\/heartbeam-expands-patient-population-for-emergency-department-software-technology-solution\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"HeartBeam Expands Patient Population for Emergency Department Software Technology Solution - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"Expanded Scope of Clinical Validation Study Will Provide Access to a Broader Patient Population Company Expects to File 510K No Later Than August 15, 2022 SANTA CLARA, Calif.–(BUSINESS WIRE)–HeartBeam, Inc. 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