Page 1324 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
P. 1324

Wound management and infections of synovial structures                       1299



  VetBooks.ir  for additional features of haemostasis such as the  Repair
                                                         The repair phase is characterised by the presence
          fibrin mesh network and the chemoattraction of
          neutrophils. The haemostatic phase may last a few
                                                         tive tissue matrix (granulation tissue), and lead to
          minutes to a few hours.                        of fibroblasts, which produce collagen and connec-
                                                         wound contraction. The granulation tissue scaffold
          Inflammation                                   facilitates the migration of epithelial cells. During
          The inflammatory response is characterised mostly   second-intention or open wound healing, epitheliali-
          by the presence of neutrophils, which are bacteri-  sation and contraction are ultimately responsible for
          cidal and protect the body against invasion by for-  wound repair (Fig. 13.5). This is only possible if the
          eign organisms or substances. The release of local   wound is clear of debris, infection, tissue necrosis
          chemotactic factors serves as a migration signal for   and exuberant granulation tissue.  Epithelialisation
          the neutrophils, which begin a process of diapede-  can begin as soon as 12 hours post wounding in pri-
          sis and migration to the injury site. Other factors   mary healing or after 4 or 5 days in secondary wound
          released at a local level (e.g. serotonin, histamine,   healing.  Wound  contraction  is  most  important  in
          bradykinin) are responsible for a vasodilatory   secondary wound closure and stops with contact
          response and an increase in vascular permeability,   inhibition between cells, excessive tension, exuber-
          which further facilitates neutrophil migration. The   ant granulation tissue or if full-thickness grafts are
          acute inflammatory phase starts within minutes of   applied before the 5th day of healing.
          a wound occurring and lasts for a few hours to days
          depending on the severity of the injury and degree of
          contamination. The activation and death of neutro-  13.5
          phils is responsible for the release of enzymatic prod-
          ucts and inflammatory mediators. In the absence of
          infection, neutrophils are not necessary for wound
          healing. It is important to emphasise that the appro-
          priate balance between acute and chronic inflam-
          mation is necessary for a wound to heal optimally
          by second intention. While acute inflammation has
          been shown to have beneficial effects in wound heal-
          ing and should be encouraged, chronic inflammation
          promotes the production of exuberant granulation
          tissue and should be discouraged.

          Debridement
          The debridement phase begins within a few hours
          of the injury and its duration depends on the sever-
          ity of the injury. It starts with the enzymatic break-
          down of debris by substances released from the dead
          neutrophils. Monocytes are chemoattracted into
          the wound at the same time as neutrophils and are
          responsible for the elimination of debris, necrotic
          tissue, foreign substances and microorganisms.
          Unlike neutrophils, monocytes are necessary for
          wound healing to progress. They transform into   Fig. 13.5  A wound on the dorsal aspect of the upper
          macrophages once in the wound and remain there   cannon that is being treated by second-intention
          for days to weeks, regulating the progression of   healing. Note the healthy granulation-tissue bed and
          wound healing.                                 active epithelial edges.
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