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Retrospective case studies evaluation: BETAplast® PRO-N dressing

10 July 2019

This document contains a series of case reports describing the use of BETAplast® PRO-N Dressing in patients with a range of chronic and acute wounds of varying aetiology and severity. 

Each case study was carried out for a period of 1 month, or longer, with regular assessments. A photographic record of the wound was also taken at each review to document progress.

All patients were assessed for:

■ Improvement or deterioration to the wound

■ Change in wound size

■ Condition of the wound bed and surrounding skin

■ Signs and symptoms of infection

■ Wound exudate levels

■ Pain


Wound pain was assessed between dressing changes and during dressing removal using a visual analogue scale (VAS) where 0 = no pain and 10 = unbearable pain.

The clinicians undertaking the study were asked to rate how satisfied they were with the use of BETAplast‰ PRO-N (from highly satisfied, satisfied, neutral or not satisfied), and to comment on its ease of use, conformability and adherent properties.

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