New York, NY - On October 2, 2013, PLC Systems announced that it RenalGuard forced diuresis system was used following a kidney transplant procedure performed in Brazil, potentially an additional use of the company’s technology. Kidney transplant cases represent a large potential market for RenalGuard. In 2012 there were almost 17,000 kidney transplants performed in the US alone.
RenalGuard was developed to prevent contrast induced nephropathy in patients who have been subjected to contrast-enhanced CT scans. There are approximately 8 million cardiac catheterizations and 80 million contrast-enhanced CT scans worldwide, annual imaging procedure volume that accounts for an estimated 8.8 million global (US + Western Europe) cases of CIN annually. cardiac catheterization cases represent the initial target market for RenalGuard.
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Company Description:
PLC Systems Inc. (PLCSF: OTC BB), a medical technology company headquartered in Milford, MA, has developed RenalGuard, a forced diuresis system for hydrating high-risk (with pre-existing renal failure) patients who are subjected to contrast-enhanced medical imaging procedures. Such patients are at risk for contrast-induced nephropathy (CIN), kidney damage stemming from exposure to intravenously administered contrast media. As standard hydration protocols do not adequately protect high-risk patients from CIN, RenalGuard potentially addresses an unmet need in millions of patients.
RenalGuard is an automated closed-loop fluid replacement controller. It promotes a high volume of urine output (diuresis) which it precisely monitors and measures. It intravenously replaces the exact amount of fluid that has been excreted, maintaining the proper fluid balance within the kidneys. By continuous fluid replacement and the use of a diuretic (which increase the formation of urine), RenalGuard aims to produce high urine flow rates, rapidly “flushing” potentially toxic contrast agents and minimizing damage to the kidneys.
RenalGuard is CE marked and is already on the market in Europe. A US Phase II/III clinical trial started in January 2012, setting the stage for US release after FDA approval.
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