Novel Device for Continuous Automatic Monitoring of Kidney Function of Hospitalized Patients Introduced

Sereno Medical's Sentinel(tm) Bedside Urine Output Monitor for Early Detection and Prevention of Acute Kidney Injury Reduces Patient Risk

Serenno Medical, a developer of medical devices for patient monitoring in a hospital setting, reveals SentinelTM, a novel, robust device for automatic monitoring and detection of kidney damage in hospitalized patients. The Sentinel device is a continuous urine output monitor that measures urine flow rate and volume in real-time.

Continuous automatic kidney function assessment allows the early detection of Acute Kidney Injury (AKI), a common condition in hospitalized patients that significantly increases the risk of mortality during and after hospitalization. Accurate measurement of urine output (UO) is clinically accepted as the best method for monitoring kidney function. However, UO is currently monitored intermittently and manually by ICU nurses, therefore acute changes in urine flow are difficult to detect. Thus, kidney injury is often detected relatively late, sometimes after it is impossible to prevent further progression.

Sentinel offers a simple and cost-effective solution for the precise, continuous measurement of urine flow rate in real-time. The system promotes early detection of kidney injury, while there is still time to intervene and prevent further damage. It aims to automatically and accurately detect small changes in kidney function, taking the workload off the nursing staff while delivering actionable data. The device works in synergy with existing hospital equipment (any catheter and bag) and requires a short and simple, non-invasive installation. It fits the complicated intensive care unit (ICU) and operating room environments and is fully functional in any patient condition or hospital environment.

Prof. Manu Malbrain, MD, PhD, ICU Director, University Hospital Brussels, Co-founder and Former-President WSACS and Co-founder and President of the International Fluid Academy, said, “Urine output measurement is a key parameter to assess kidney function. However, correct urine output determination is often difficult at the bedside and is usually only performed intermittently and manually. Moreover, the kidneys are often the first organ to stop functioning properly, therefore continuous urine output measurement would be a valuable tool in the management of critically ill, unstable patients.”

Serenno Medical recently completed its first multicenter clinical trial with the Sentinel system, showing high reliability and accuracy in a wide range of environments and patient conditions, including low and high urine flow rates, regardless of patient position, during surgical procedures, and including continuous monitoring of patients in a mobile hospital bed. The clinical trial, conducted at three ICU units in Sheba and Rabin Medical centers in Israel, included more than 40 patients and over 1,300 hours of monitoring. Results show over 96% accuracy and reliability.

“Serenno has developed a unique product that will bring tremendous value to patients hospitalized in ICU units along with a simple digital solution that will bring great economic value to hospitals,” stated Shimon Eckhouse, PhD, Chairman of Serenno Medical. “Serenno’s successful clinical trial is a great testament to the quality and performance of the Company’s product.”

“The successful results of our first clinical trial will allow the company to move forward to manufacturing the device for commercial usage and enable us to bring this best-in-class product to the global medical markets,” said Tomer Lark, Co-Founder and CEO of Serenno Medical. “We expect to receive FDA clearance for the system during 2020 and believe that our patent-pending device has the potential to become the standard-of-care in the OR and ICU, benefiting millions of patients around the world.”

 

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”