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Speranza Therapeutics Offers Outcomes-based Care Program Using an Opioid Withdrawal Management Medical Device to Reduce AMA Rates


News provided by

Speranza Therapeutics

Dec 15, 2021, 09:05 ET

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BOCA RATON, Fla., Dec. 15, 2021 /PRNewswire/ -- Speranza Therapeutics announces the launch of an outcomes-based care program for providers treating patients experiencing opioid withdrawal. Opioid withdrawal symptoms commence when a patient using opioids either stops using or decreases their dose. Providers in Addiction Treatment facilities and Pain Management practices deal with patients suffering from withdrawal on a daily basis.

The number one reason patients abandon treatment prematurely is the fear of withdrawal symptoms. There is a high cost to providers when patients leave Against Medical Advice (AMA) since the greatest cost to the facility is the admission process. Keeping more patients in treatment helps providers and health plans to avoid costly readmissions.

"Through recent partnerships with leading inpatient facilities, Speranza has witnessed significant reductions in patients leaving AMA by using Speranza Therapeutics S.T. Genesis," says Todd Krasinsky, Speranza Therapeutics Co-Founder and Chief Strategy Officer. S.T. Genesis is a noninvasive, drug-free device that reduces the physical and emotional effects of opioid withdrawal. "When withdrawal symptoms are managed, the patient remains comfortable, engaged, and capable of staying in treatment longer," explains Mr. Krasinsky. As a result, Speranza decided to launch its outcomes-based program to support facilities in adopting S.T. Genesis by measuring the correlation between overall facility AMA rates and the device.

"We have seen an increase in patients afflicted with opioid use disorder abandoning treatment during the first few days of the withdrawal management process," says Jeffrey Thomas, MHS, LPC, CAADC, CEO of White Deer Run facility in Allenwood, PA. "These patients respond especially well to the device and as a result, have remained engaged in treatment."

Providers using the S.T. Genesis averaged a 50% reduction in AMA rates compared to opioid replacement induction protocols, and 90% of those patients went on to longer term treatment programs in Residential Treatment Centers or through Intensive Outpatient Programs.

S.T. Genesis is a 510(k) FDA-cleared percutaneous nerve stimulator that is applied to the patient's ear for a period of 5 days. Studies report a 93% reduction in patients' Clinical Opiate Withdrawal Scale (COWS) scores within the first hour. S.T. Genesis is an innovative solution with the ability to help patients across the country. Providers should contact [email protected] for more information.

About Speranza Therapeutics
Founded in 2019, Speranza Therapeutics is a medical technology company dedicated to providing better patient outcomes while decreasing the cost of care.

Media Contact:
Todd Krasinsky
[email protected]

SOURCE Speranza Therapeutics

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