Chlorhexidine impregnated sponge is 1B recommendation

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Intravenous product: Ethicon report “The CDC’s 2011 Guidelines for the Prevention of Intravascular Catheter-Related Infections defines a recommendation classified as Category 1B as “strongly recommended for implementation and supported by some experimental, clinical, or epidemiologic studies and a strong theoretical rationale.” BIOPATCH® Protective Disk with CHG, distributed by Ethicon, Inc., has been shown to reduce the risk of CLABSIs in controlled, randomized clinical trials involving more than 4,000 patients.

“The new guidelines reinforce the findings from multiple clinical studies that have shown that BIOPATCH® is proven safe and effective in reducing the risk of CRBSIs in patients with central venous or arterial catheters. No other CHG dressing product on the market has been clinically proven to reduce this risk, and we are very pleased that the Category 1B recommendation has been based on clinical evidence related only to BIOPATCH®, said Earl Adamy, director of BIOPATCH® sales and marketing at the Ethicon US Head quarters.

The guidelines indicate that patients should be treated with “a chlorhexidine-impregnated sponge dressing for temporary short-term catheters in patients older than 2 months of age, if the CLABSI rate is not decreasing despite adherence to basic prevention measures, including education and training, appropriate use of chlorhexidine for skin antisepsis, and MSB [maximal sterile barrier precautions]. Category IB. Guidelines also specify “no recommendation is made for other types of chlorhexidine dressings (Unresolved Issue).”

Our skin provides very effective protection against infection, but when the skin barrier is broken and a catheter is inserted into vascular tissue, the risk of bacteria migrating down the catheter itself or the catheter tract into the bloodstream increases significantly. BIOPATCH® has a unique proprietary design that allows for 360-degree contact with the skin and continuous delivery of CHG around the site of catheter insertion,” said William Jarvis, MD, former acting director of the CDC’s Hospital Infections Program and the former assistant chief of the National Nosocomial Infections Surveillance (NNIS) system.*

The safety and effectiveness of BIOPATCH® have not been established for children less than 16 years of age. The protective disk is not to be used on premature infants or on patients with a known sensitivity to CHG.

BIOPATCH® is marketed by Ethicon, Inc., a trusted, worldwide leader in surgical care. For over a century, Ethicon has continuously introduced innovations for wound closure, general surgery, wound management, women’s health and urology and aesthetic medicine that fulfill the Companys vision: restoration of body and of life.

BIOPATCH® Protective Disk with CHG is the only chlorhexidine gluconate-impregnated sponge dressing clinically proven to reduce central line-associated bloodstream infections (CLABSIs). BIOPATCH® is available to order direct from the UK dedicated sales team.”

For further product information
TEL: 0800 783 9189 EMAIL: biopatch@medgb.jnj.com

* Paid consultant to Ethicon, Inc.

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