Page 5 - OxyBand Research Background
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Journal of Burn Care & Research
         Volume 35, Number 3                                                                Lairet et al    217



         appearance, four patients’ OxyBand wounds were       The type of dressing used did not have an impact
         judged to have  better cosmetic  outcome, and five   on the final cosmetic outcome of the wound. There
         patients’ Xeroform wounds were deemed to have      was no pattern formation in the final OxyBand
         better cosmetic appearance.                        wounds at 30 to 45 days, and cosmetic appearance
           Nursing time was not measured in this study. Each   was judged to be similar to the control Xeroform
         patient visit required 30 to 45 minutes of hands-on   wounds by independent surgeons familiar with burn
         time by the research nurse, or up to 60 minutes if   wounds.
         photographs were taken. The time required to per-    A border of approximately 2 cm on all sides of
         form an OxyBand dressing change was on the order   the wound is required for the OxyBand dressing to
         of 2 minutes.                                      adhere, which must be taken into consideration. At
                                                            the time of this clinical study, only one size of the
         DISCUSSION                                         dressing was available. This, of course, is a limita-
                                                            tion in comparison with Xeroform, which can be
         The harvesting of donor sites during split-thickness   trimmed to fit or pieced together to fit virtually any
         skin-grafting procedures creates a new wound. Care   size wound. Although a variety of sizes and configu-
         of such wounds involves techniques to promote      rations of the OxyBand dressing could be manufac-
         rapid reepithelialization. The longer the wound    tured, it still likely will require some uninjured skin
         remains open, the higher the risk of infection. Dress-  around the margins to allow the dressing to adhere.
         ings that optimize the donor-site healing allow for   Xeroform dressing has been widely available for
         reharvesting of donor sites more rapidly, which can   many years and is inexpensive. The commercial cost
         be life-saving for patients with large burn surface area   of OxyBand dressings is not yet known, but will
         involvement. Dressings such as Xeroform have been   almost certainly cost more than Xeroform gauze.
         used for many years as donor-site dressings because   The decreased levels of pain reported by patients,
         of their availability, low cost, and relative ease of   and possibly the decreased requirements for pain
         application. This study prospectively compared a   medication as a result, may help offset the price of
         new product, OxyBand, with our control donor-site   the OxyBand dressing. It is also difficult to place a
         dressing, Xeroform. Healing time, as well as per-  price on the value of time to healing. For a patient
         ceived pain and cosmetic outcome, were assessed.   with a large percent body surface area full-thickness
           We found a statistically significant decrease in the   burn, speeding healing by a few days would allow
         healing time of donor-site wounds dressed with the   more  rapid  coverage  of  the  excised  wounds  with
         OxyBand dressing compared with the Xeroform-       autologous tissue. This may prevent an infection or
         dressed wounds. Not one of our subjects had a      reduce the amount of temporary closures (allograft,
         donor wound dressed with Xeroform heal faster than   Integra, or other  products) before final  closure is
         the study wound, although some subjects’ wounds    achieved.
         were found to be healed on the same day.             A limitation of the study involved being able to
           Our results also demonstrated that the OxyBand   determine the day of healing of each wound. This
         dressing was associated with less pain at each post-  issue was multifactorial. In a few instances, patients
         operative data-collection point. Subjects’ comments   were late for follow-up visits, so the true day of heal-
         about  the  dressings  were  recorded  at  their  final   ing may have been the day prior. Also, the OxyBand
         30- to 45-day visit, and every patient who made    dressing was not removed every day to inspect the
         a comment had a positive remark about the com-     wound. To maximize the benefit the wound would
         fort of OxyBand dressings. No such remarks were    receive from being in an oxygen-saturated environ-
         made about the comparison dressing. The OxyBand    ment, the decision was made to initially only remove
         dressing keeps the wound occluded and moist dur-   the dressing on postoperative days 4 and 8. The fre-
         ing the healing process. In contrast, Xeroform is left   quency of dressing changes was then increased to
         exposed to the air in order to dry. It eventually hard-  every 2 days in an attempt to more closely capture
         ens before it separates from the wound as it is reepi-  the day of healing, as our experience has been that
         thelialized. The nonadherent characteristic of the   most donor wounds are healed approximately 10 to
         OxyBand dressing (with regard to the wound) may    14 days after skin harvest. Perhaps if the dressing was
         explain the decreased pain reported at the wound   changed daily, we may have more accurately identi-
         site by subjects. Whether topical oxygen also modu-  fied the day of healing. This idea was rejected, how-
         lates the pain response is unknown. Further studies   ever, as patient compliance with the follow-up visit
         should be done to look more closely at the relation-  schedule may have been reduced. Another limitation
         ship between oxygen-diffusion dressings and pain.  is the unblinded nature of this study.
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