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Wound Management News
Vibrio cases, deaths in Florida doubled after Hurricane Ian
Vibrio cases and deaths in Florida spiked last year after Hurricane Ian, lending credence to concerns that larger, longer, warmer tropical storms may increase the risk for viral infections, according to a study.
Pain scores may indicate treatment response in patients with pyoderma gangrenosum
Pain as a patient-reported outcome measure during the treatment of pyoderma gangrenosum may indicate whether a patient is responding to treatment, according to a research letter published in JAMA Dermatology.
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Botanical drug may outperform standard of care for treatment of severe thermal burns
Results from DETECT, the phase 3 study that supported the FDA approval of NexoBrid for the treatment of severe thermal burns, was recently published in the Journal of Burn Care & Research, Vericel announced in a release.
CDC issues health advisory about recent reports of fatal Vibrio vulnificus
On Sept. 1, the CDC issued a health advisory concerning an increased rate of infections in the United States of a flesh-eating bacterium called Vibrio vulnificus.
VIDEO: New antimicrobial wound healing matrix highlighted at Maui Derm NP+PA
In this Healio video exclusive, George Martin, MD, discusses highlights from Maui Derm NP+PA, including a new wound healing matrix, which he said improves healing and reduces infection rates.
Diacerein 1% may benefit patients with severe epidermolysis bullosa simplex
Diacerein 1% ointment was comparable to vehicle in study endpoints but did outperform vehicle when stratified by disease severity in the treatment of patients with epidermolysis bullosa simplex, according to a study.
FDA approves Avita’s premarket approval supplement for Recell, shares rise 13%
The FDA has approved Avita Medical’s premarket approval supplement for the use of its Recell System for the treatment of full-thickness skin defects, according to a press release.
VeriCyn Wound Wash receives FDA 510(k) clearance
The VeriCyn Wound Wash medical device by Armis Biopharma has received 510(k) clearance from the FDA for use in cleansing wounds of debris, according to a company press release.
Understanding benefits, shortcomings of skin substitutes can help guide treatment
Considering the unique characteristics of different skin substitutes will provide improved wound care management that meets patient needs, according to a study.
FDA approves Vyjuvek for dystrophic epidermolysis bullosa
The FDA has approved Vyjuvek (beremagene geperpavec-svdt), an investigational non-invasive, topical, redosable gene therapy for the treatment of dystrophic epidermolysis bullosa, Krystal Biotech announced in a press release.
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Headline News
Rise in alcohol use during pandemic endures as 'an alarming public health issue'
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Headline News
Rise in alcohol use during pandemic endures as 'an alarming public health issue'
November 14, 20242 min read -
Headline News
AI identified patient messages sent by proxies, but also broke confidentiality
November 14, 20242 min read -
Headline News
Diabetes inequities persist worldwide, especially for low-, middle-income countries
November 14, 20243 min read