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Myriad Genetics and Flatiron Health Partner to Make Genetic Testing More Accessible With Electronic Medical Record Integration

Myriad Genetics and Flatiron Health Partner to Make Genetic Testing More Accessible With Electronic Medical Record Integration

萬基遺傳和Flatiron Health合作,通過電子醫療記錄集成使基因檢測更容易獲得
GlobeNewswire ·  10/15 21:00

Myriad's MyRisk test is the first hereditary cancer test integrated into Flatiron's OncoEMR

Myriad的MyRisk測試是首個整合進Flatiron的OncoEMR的遺傳癌症測試。

SALT LAKE CITY, Oct. 15, 2024 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in genetic testing and precision medicine, today announced a collaboration with Flatiron Health, a leading health tech company dedicated to expanding the possibilities of point of care solutions in oncology. This collaboration allows physicians to order Myriad's MyRisk Hereditary Cancer Test and view the results of the test directly in Flatiron's cloud-based Electronic Medical Record (EMR) platform, OncoEMR. MyRisk is the first hereditary cancer test to be incorporated into Flatiron's OncoEMR.

2024年10月15日,鹽湖城(GLOBE NEWSWIRE)— 萬基遺傳公司納斯達克(NASDAQ:MYGN)的基因檢測和精準醫療領域領導者,宣佈與Flatiron Health合作。Flatiron Health是一家專注拓展腫瘤點對點解決方案可能性的領先健康科技公司。此次合作使醫生可以在Flatiron基於雲的電子病歷(EMR)平台OncoEMR中直接下訂單進行Myriad的MyRisk遺傳癌症測試,並查看測試結果。MyRisk是第一個被整合進Flatiron的OncoEMR的遺傳癌症測試。

The integration allows 4,200 providers at over 800 community-based cancer care locations across the U.S. in Flatiron's network to conveniently order, receive, and review MyRisk testing results directly through their daily OncoEMR system. By creating a streamlined, end-to-end workflow for germline testing in OncoEMR, clinicians have access to the results they need at point-of-care, facilitating personalized treatment decisions for patients while reducing administrative burdens and improving turnaround times for results.

這一整合使美國全國800多家社區癌症護理中心的4200名醫療服務提供者在Flatiron網絡中可以方便地通過他們的OncoEMR系統直接下訂單、接收和審閱MyRisk測試結果。通過在OncoEMR中爲生殖系檢測打造了簡化的端到端工作流程,臨床醫生可以在病人就診時獲取所需結果,促進對患者的個性化治療決策,同時減少行政負擔,提高結果的交付時間。

"Our collaboration with Flatiron integrates MyRisk testing with practicing clinicians' current workflows, potentially enhancing access to and usability of germline testing for more personalized patient care," said George Daneker Jr, MD, President and Chief Clinical Officer of Oncology, Myriad Genetics. "By making germline testing interoperable with OncoEMR, we aim to simplify the ordering experience for clinicians in Flatiron's extensive network and provide important health information that may help improve patient care and outcomes. We look forward to expanding the availability of our other genomic testing solutions onto the OncoEMR platform in the future, addressing the needs of even more patients."

「我們與Flatiron的合作將MyRisk測試整合到臨床醫生當前的工作流程中,可能增強更加個性化患者護理的可及性和可用性,」萬基遺傳腫瘤學總裁兼首席臨床官George Daneker Jr, MD表示。「通過與OncoEMR互操作的生殖系檢測,我們旨在簡化Flatiron廣泛網絡內臨床醫生的下訂單體驗,並提供可能有助於改善患者護理和結果的重要健康信息。我們期待未來將我們其他基因組檢測解決方案擴展至OncoEMR平台,以滿足更多患者的需求。」

"As we continue to advance personalized medicine, the importance of germline testing at the point of care is critical to improving patient outcomes," said Stephen Speicher, MD, Senior Medical Director, Head of Clinical Oncology and Patient Safety at Flatiron Health. "By giving physicians the ability to order Myriad's MyRisk Hereditary Cancer Test and to view the results directly within OncoEMR, we're offering clinicians a seamless way to access the information they need to practice precision medicine, facilitating better patient outcomes, more time with patients, and a better care experience for physicians and their patients."

「隨着我們繼續推動個性化醫療,原生系列檢測在護理點的重要性對提高患者預後至關重要,」Flatiron Health的醫學博士、臨床腫瘤學與患者安全主任Stephen Speicher表示。「通過讓醫生有能力訂購萬基遺傳的MyRisk遺傳癌症檢測,並直接在OncoEMR中查看結果,我們爲臨床醫生提供了無縫訪問所需信息的方式,促進更好的患者預後,更多與患者交流的時間,以及爲醫生及患者提供更好的護理體驗。」

The integration is available now to all OncoEMR users.

該集成現已提供給所有OncoEMR用戶。

About Myriad Genetics
Myriad Genetics is a leading genetic testing and precision medicine company dedicated to advancing health and well-being for all. Myriad develops and offers genetic tests that help assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where genetic insights can significantly improve patient care and lower healthcare costs. For more information, visit .

關於Myriad Genetics
萬基遺傳是一家領先的基因檢測和精準醫學公司,致力於推進所有人的健康和福祉。萬基遺傳開發並提供基因檢測,幫助評估發病風險或疾病進展,並指導治療決策,涉及醫療專業領域的基因洞察可以顯著改善患者護理,並降低醫療保健成本。欲了解更多信息,請訪問。

Safe Harbor Statement
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including statements relating to how the company's collaboration with Flatiron may facilitate personalized treatment decisions for patients while reducing administrative burdens and improving turnaround times for results and how by making germline testing interoperable with OncoEMR, the company aims to simplify the ordering experience for clinicians in Flatiron's extensive network and provide important health information that may help improve patient care and outcomes. These "forward-looking statements" are management's expectations of future events as of the date hereof and are subject to known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated. Such factors include those risks described in the company's filings with the U.S. Securities and Exchange Commission, including the company's Annual Report on Form 10-K filed on February 28, 2024, as well as any updates to those risk factors filed from time to time in the company's Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. Myriad is not under any obligation, and it expressly disclaims any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events or otherwise except as required by law.

免責聲明
本新聞稿包含根據1995年《私人證券訴訟改革法案》的「前瞻性聲明」,包括與Flatiron合作如何有助於爲患者提供個性化治療決策,同時減少行政負擔、提高結果的週轉時間,以及通過使生殖系檢測與OncoEMR可互操作,公司旨在簡化Flatiron廣泛網絡中臨床醫生的訂購體驗,並提供可能有助於改善患者護理和預後的重要健康信息。這些「前瞻性聲明」是管理層對未來事件的期望,截至本日期,可能受到已知和未知風險和不確定性的影響,這些風險和不確定性可能導致實際結果、狀況和事件與預期不符,併產生不利影響。此類因素包括公司提交給美國證券交易委員會的文件中描述的風險,包括公司於2024年2月28日提交的年度報告表格10-k,以及公司不時在季度報告表格10-Q或當前報告表格8-k中提交的任何風險因素的更新。萬基遺傳沒有義務,明確否認任何義務,要更新或修改任何前瞻性聲明,除非法律要求。

About Flatiron Health
Flatiron Health is a healthtech company expanding the possibilities for point of care solutions in oncology and using data for good to power smarter care for every person with cancer. Through machine learning and AI, real-world evidence, and breakthroughs in clinical trials, we continue to transform patients' real-life experiences into knowledge and create a more modern, connected oncology ecosystem. Flatiron Health is an independent affiliate of the Roche Group.

關於Flatiron Health
Flatiron Health是一家致力於擴大癌症治療點解決方案的健康科技公司,利用數據爲善,爲每個癌症患者提供更智能的護理。通過機器學習和人工智能、真實世界證據以及臨床試驗的突破,我們繼續將患者的真實生活經驗轉化爲知識,並打造更現代、更聯通的腫瘤生態系統。Flatiron Health是羅氏集團的獨立附屬公司。

Myriad Genetics Investor Contact
Matt Scalo
(801) 584-3532
IR@myriad.com

萬基遺傳投資者聯繫
Matt Scalo
(801) 584-3532
IR@myriad.com

Myriad Genetics Media Contact
Glenn Farrell
(385) 318-3718
PR@myriad.com

萬基遺傳媒體聯繫
格倫·法雷爾
(385) 318-3718
PR@myriad.com

Flatiron Health Media Contact
Nina Toor
press@flatiron.com

Flatiron Health媒體聯繫
Nina Toor
press@flatiron.com


譯文內容由第三人軟體翻譯。


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