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Clinical Newsletter

Regular updates on our latest clinical studies.

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Our research and development teams operate at a global level and generate synergies from our collective expertise and by drawing on related disciplines. We are also constantly exchanging information at an international level with independent technical institutions, key opinion leaders and multipliers in order to be able to ensure cooperation and knowledge management of the highest order. As part of this process, we also conduct extensive research, the results of which we continually present in workshops, at conferences and symposiums - either in documentation or talks given by our cooperation partners - and also publish in renowned scientific journals. This database contains a large number of these evidence-based scientific articles, most of which have been evaluated by independent assessors:

  1. Poster

    Evaluation clinique d’un pansement à base de cellulose et de polyhexanide

    Poster presented at CPC 2009 18.01.2009 Paris, France
  2. Poster

    L'évaluation des antiseptiques utilisés pour les plaies dans les conditions de tests de provocation de résistance avec des souches internationales de SARM

    Poster presented at CPC 2009 18.01.2009 Paris, France
  3. Poster

    Capacité de fixation de collagène d’origines différentes pour PDGF-BB

    Poster presented at CPC 2009 18.01.2009 Paris, France
  4. Journal article

    The use of Flivasorb® in highly exuding wounds

    British journal of nursing (Mark Allen Publishing) 2009 18 (15)

    Exudate can be an excellent indicator of what is happening within a wound and, therefore, provides valuable information during patient assessment. The volume, consistency, and particularly odour and colour, of any exudate will inform the practitioner about bacterial contamination, infection and stage of healing (Hampton and Collins, 2003). However, in the chronic wound, exudate must be effectively managed if the optimal moist environment necessary for wound healing is to be created, the negative effects of chronic exudate on fibroblasts are to be avoided (Phillips et al, 1998), and the surrounding skin protected from the risks of maceration (White, 2006). It is, therefore, important to understand chronic exudate and its effects so that appropriate treatment for the wound and peri-wound area is provided. Flivasorb® (Activa Healthcare) dressings, which include superabsorber particles, can absorb the exudate and retain it firmly within the dressing, ensuring that the potentially damaging chronic wound exudate does not reflect back onto the wound, causing maceration. This article will describe the role of exudates in wound healing, the problems associated with chronic wound exudates and how Flivasorb dressings with superabsorbent particles can provide an optimum healing environment in highly exuding wounds.

    Products Vliwasorb
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  5. Journal article

    Flivasorb® and the management of exudate

    Wounds UK 2009 5 (2) 63 66

    Wound care provides many challenges but none moreso than the management of high levels of exudate. The challenge is not only to be cost-effective and prevent maceration, but to improve the quality of life for the patient. Chronic wound fluid can be damaging to the wound healing process giving an added problem. This article examines the properties of Flivasorb® (Activa Healthcare), a wound dressing containing super absorbent polymer particles which not only absorbs high levels of exudate, but can retain the damaging particles in exudate, locking them inside the dressing.

    Products Vliwasorb
  6. Journal article

    Treating venous ulceration

    Journal of Community Nursing 2009 23 (6) 34 37
  7. Journal article

    VIABILITY AND PROLIFERATION OF FIBROBLASTS, KERATINOCYTES AND HACAT-CELLS INFLUENCED BY POLLHEXANTDE

    Wound Rep Reg 2009 17 83
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  8. Journal article

    QUELLE COMPRESSION SUR DES PATIENT$ IMMOBILES: ALLONGEMENT COURT OU ALLONGEMENT LONG?

    LA REVUE FRANCOPHONE OE GERIATRIE ET OE GERONTOLOGIE 2009 155 (16) 278 283
  9. Journal article

    Development and Implementation of a Clinical Pathway To Improve Venous Leg Ulcer Treatment

    Wounds 2009 21 (5) 127 133
  10. Journal article

    Comparative in vitro study on cytotoxicity, antimicrobial activity, and binding capacity for pathophysiological factors in chronic wounds of alginate and silver-containing alginate

    Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society 2009 17 (4) 511 521

    Chronic wounds contain elevated levels of proteases, proinflammatory cytokines, and free radicals. The presence of bacteria further exaggerates the tissue-damaging processes. For successful treatment, the wound dressing needs to manage wound exudates, create a moist environment, inhibit infection, bind pathophysiological factors that are detrimental to wound healing, and provide thermal isolation. Furthermore, it has to relieve pain, be easy to use, show no allergic potency, and not release toxic residues. The present study suggests a comprehensive in vitro approach to enable the assessment of wound dressings to support optimal conditions for wound healing. Three alginate-based wound dressings: alginate alone, alginate containing ionic silver, and alginate with nanocrystalline silver, were tested for biocompatibility, antimicrobial activity, and influence on chronic wound parameters such as elastase, matrix metalloproteases-2, tumor necrosis factor-alpha, interleukin-8, and free radical formation. Alginate was found to bind considerable amounts of elastase, reduce the concentration of proinflammatory cytokines and inhibit the formation of free radicals. Furthermore, alginate showed antibacterial activity and high biocompatibility. Incorporation of silver into alginate fibers increased antimicrobial activity and improved the binding affinity for elastase, matrix metalloproteases-2, and the proinflammatory cytokines tested. Addition of silver also enhanced the antioxidant capacity. However, a distinct negative effect of silver-containing alginates on human HaCaT keratinocytes was noted in vitro.

    PMID 19614916