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CLINICAL PRACTICE

Practical Scar Care

BY Deepak Mistry he first consideration in scar treatment is Some individuals have prevention. Events that occur during the a genetically inherited T management of the open wound are influ - characterized by ential. Providing a healthy environment for the wound extreme and excess scar scar to heal is most important. pro duction. These scars are Once the wound is closed, treatment can begin to called keloid scars, and they are very different than prevent too much scarring. Over the past two decades, hypertrophic scars—although they do share some several new therapeutic approaches to scar manage - common features. Keloid scars tend to become much ment have been reported. These new approaches larger than the original wound. They usually persist promise to add substantially to existing therapeutic and reoccur after surgical excision. approaches. This article attempts to summarize most of these new concepts. Anti-inflammatory Agents Limiting is paramount to scar reduction. Scar Information Inhibition of inflammation using injec - Scars are produced as the result of tions is one of the oldest and most established wound . Instead of replac - approaches to scar management. The broad effects ing damaged with regener - include inhibition of protein synthesis, including colla - ated identical tissue, human and gen and other proteins. However, most animal wounds are healed the adverse side effects of repeated injections as well Normal scar by filling the wound with scar. In the - as the frequent occurrence of depigmentation are ory, this allows faster yet less perfect major drawbacks to this approach. Steroids are not . However, today most people would effective for treatment of older, asymptomatic scars rather their wounds heal without scarring, even if this that are less metabolically active. requires more time. Although non-steroidal anti-inflammatory drugs Scars can be limiting and disfiguring, (NSAIDs) have been used to prevent particularly when the is extensive. internal scarring in arthritis for decades, The amount of scar produced is a they have only recently been used for consequence of many factors, including hypertrophic and keloid scar manage - Deepak Mistry, BSc, is a graduate of the the extent of traumatized tissue around ment. Our experience suggests that the University of Chicago the wound, how long the wound remains newer type-2 cyclo-oxygenase inhibitors and is currently open, the anatomic location, and genetically are very effective in reducing symptoms involved in the determined healing factors. When more scar of pruritus. They also seem to induce scar research and forms than is desirable, the scar is considered hyper - maturation and involution. development of trophic. Initial rapid growth followed by gradual fading Salicylic acid and acetylsalicylic acid (aspirin) are new approaches to scar reduction at and shrinkage characterize hypertrophic scars over powerful anti-inflammatory medications that are Avocet Polymer several years. This often leads to widened, unattractive commonly used to treat skin inflammation-related Technologies Inc. skin defects. ail ments. Salicylates (two to five per cent) are com -

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©3M, 2004 0409-MS-20675B monly used to control skin inflammation and are rou - trol scar formation. Like elastic garments, the mechanism tinely used in treatment products. We have found of action is not known, but hypotheses reported in the topical salicylates to be among the most effective anti-scar literature include induction of scar hypoxia, increased agents. These agents should not be used on open hydration of the covering the scar and wounds. Topical aspirin should be used under a increased scar temperature. Several reports have shown physician’s guidance because some patients, particularly that hydrogel sheeting is equally effective as silicone asthmatics, may develop hypersensitivity. and has fewer adverse side effects. Hydrogel sheeting has Anti-histamines are commonly used to control symp - been approved by the U.S. Food and Drug Administration toms of scar pruritus. However, they have other important (FDA) as substantially equivalent to silicone for treatment anti-scar properties. Anti-histamines, particularly the H1 of hypertrophic scars. Hydrogels have the added advan - blockers, inhibit the inflammatory response, resulting in tages of use as a drug delivery vehicle as well as having reduced scar formation and increased comfort. Reducing a higher heat capacity for buffering scar temperature. patient itching and scratching reduces the inflammation and the scar growth rate. Finally, anti-histamines in high Surgical Removal doses are well known to inhibit synthesis. The most common indications for surgical removal of scars are the following: large scars that are unlikely to be Inhibitors of Gene Transcription substantially reduced using medical therapy within a The anti-cancer drugs mitomycin-c and 5-fluorouracil practical timeframe; scars that harbor infection; and scar inhibit population growth of cells by blocking DNA contractures that hamper movement function. Surgical replication. A single application in the first few days revision of hypertrophic or keloid scars is associated after wound closure seems to be effective in scar reduc - with a high recurrence rate. Gentle surgical technique tion under laboratory conditions. Further investigation is critically important because inflamed scar tissue will be needed to determine how this approach can be produces a tremendous scar response to trauma. used clinically. Adjunctive measures to reduce inflammation, skin tension and other factors are essential to reduce Acceleration of Scar Degradation recurrence. Use of lasers and other burning techniques for While steroids and NSAIDs act to limit scar production, scar removal is very controversial. other strategies act to induce or accelerate scar degrada - In order to reduce the scar recurrence rate after tion. This approach may be the best for management , effective scar control medications should be of older hypertrophic scars and older . The rate of initiated pre-operatively and continued post-operatively. tissue breakdown can be increased by both pharmaco - Our experience suggests that most patients with scars logic and physicochemical means. large enough to require surgical excision require both systemic COX-2 inhibitors and long-acting H1 anti-hista - Occlusive Dressings mines to induce scar degradation and reduce recurrence. After elastic pressure wrap dressings applied to healing Increasingly, our experience suggests that topical scars were observed to be effective in the reduction application of NSAIDs to healing wounds will be the most of scar formation, 20–24 mmHg pressure garments practical approach. Trans-epidermal delivery of these have become the mainstay of scar prevention. The agents is enhanced by the application of an occlusive mechanism of action of pressure dressings is unknown barrier such as hydrogel sheeting. because they remain effective even when they lose elasticity and pressure several weeks after daily use. Conclusion Measurements show a decrease in wound metabolism Hypertrophic and keloid scarring can be essentially with an increase in collagenase activity. Drawbacks to reduced to inflammation mediated dermal , their use are primarily related to their thermal insulation suggesting that there is much insight into effective man - and movement restriction. agement that can be gleaned from dermatological and Hydrogel and silicone sheeting have been used to con - rheumatologic conditions of similar pathophysiology.

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E E T T P P D D C E C E O O E A E A B D M B D M

SILVERCEL * Hydroalginate dressing with Silver combines the potent broad-spectrum antimicrobial action of silver with the enhanced exudate management properties of new hydroalginate technology. • Unique Hydroalginate technology provides superior absorbency for the management of moderate to hea - vily exuding wounds. • New X-Static® silver technology combines a sustained and balanced release of silver ions with a broad spectrum of anti-microbial activity. • High wet tensile strength allows for easy intact removal. • Dressing gelling properties minimize disruption to healing tissues.

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* Trademark of Johnson & Johnson - X-STATIC ® is a registered trademark of Noble Biomaterials, Inc Johnson & Johnson Wound Management is a Unit of Johnson & Johnson Medical Products, a Division of Johnson & Johnson Inc.