Dr. Jacques, Thank you for your question.
NFPA 99 recommends that hyperbaric facilities utilize the NFPA risk assessment flowchart to assess dressings and items that have not been evaluated or deemed safe for use in the hyperbaric chamber. The risk assessment process is not always straightforward in providing a yes or no answer. Frequently, approval of a particular product is determined by mitigating measures. For example, can the dressing be removed before treatment and replaced after the treatment? If you would like, I can meet with you to discuss risk assessment and the Go No-Go tool in further detail.
I have also attached a study performed by Bernatchez et al., "Hyperbaric Oxygen Therapy and Oxygen Compatibility of Skin and Wound Care Products," that should provide additional insight into the factors to consider when determining the safety of a product.
Thanks again for reaching out to us. Jeff
Dr. Jacques, conducting a risk assessment is best practice, and recommended by NFPA 99, our regulatory resource. I am including links to topics in WoundReference that discuss prohibited items, risk assessment and the Burman scoring system.
https://woundreference.com/app/topic?id=prohibited-item-assessment
https://woundreference.com/app/topic?id=how-to-assess-prohibited-items-the-go-nogo-risk-assessment-tool-and-the-burmans
We should also coordinate time to meet and discuss in further datail. When you get a chance please email me your availability.
I look forward to talking with you soon.
Jeff
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