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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_612_Библиотеки_им_академика_М_И_Перельмана

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donor site produces a copious amount of serosanguinous fluid that can be a tremendous nuisance to the patient, nursing staff, and surgical team. To address these issues, one popular dressing regimen involves the use of alginate or absorbent foam dressings on the donor wound itself covered by a self-adherent, semiocclusive film, all wrapped with cotton gauze and an elastic bandage. The dressings are reinforced as needed for leakage and left in place for 1 to 2 weeks. Benefits include elimination of exposure to air, retention of pro-regeneration mitogens eluting from the wound, and adequate bulk to catch the inevitable serous fluid that spills out. In fact, recent literature strongly supports this dressing regimen compared to prior approaches such as application of petroleum impregnated gauze or plain cotton gauze dressings.
36
Modifications to Expand Indications
Although many “routine” wounds are grafted with split-thickness skin grafts meshed 1.5:1, larger and less ideal wounds may require more expanded grafts. Widely expanded meshing up to 9:1 may be employed in extreme situations,
6,37
though users need to be prepared for the special care and handling required by these widely spaced grafts. Variations of the Meek micrografting technique, using small, widely meshed pieces of skin, have seen a resurgence of use, most commonly in >30% total body surface area burns and poor quality wound beds.
6,38
These micrografts may be easier to handle
than widely meshed grafts and may reepithelialize more quickly,
6,39
but require labor-intensive surgical technique for harvest and preparation.38 The modified Meek technique has been associated with successful take and rapid healing.
8
Donor site modifications may also be useful, particularly in wounds of large surface areas. Donor site morbidity may be minimized by creative approaches such as harvest of a split-thickness skin graft and dermis-only graft from the same site. Depending on use of the epidermal layer, the donor site can be autografted for more natural healing or used in the wound to double the surface area treated by any given donor site.
6,40,41
Some authors recommend regrafting the donor site with leftover skin graft; however, some results have been inferior.
6,42
Mincing the leftover pieces of skin graft and reapplying
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can also potentially help the donor site.6 Split-thickness skin grafts allow repeated use of a donor site after reepithelialization,6 though authors demonstrate decreased functionality of repeatedly used skin.
43
OUTCOMES
There has not been substantial interest in clinical outcomes following skin grafting in the 21st century as most of these studies were performed in the second half of the 20th century. A review of decades-old literature would most likely miss the goal of this chapter. In lieu of that, we will provide a brief narrative explanation of the data.
In patients with no or minimal medical morbidities who undergo skin grafting in appropriately prepared wounds, skin graft take is consistently reliable. Clinical experience over decades supports the widespread utilization of this reconstructive modality. Much of that intergenerational knowledge comes from the era prior to negative­pressure wound therapy, so contemporary surgeons should feel confident offering autologous skin grafting to most patients in this population.
For patients with consequential patient-level morbidities, skin grafting can be less reliable. Common medical conditions known to predispose to poor graft take are included in Table 6.1, but this is by no means exhaustive.27 We strongly recommend that surgeons seek to optimize these conditions prior to definitive skin graft reconstruction, if possible.
TABLE 6.1. PREDISPOSING FACTORS TO POOR SKIN
GRAFT SUCCESS
Medications/Exposures Diseases/Conditions
Chemotherapy Congestive heart failure Radiation (prior or Severe diabetes mellitus
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planned) Glucocorticoids Obesity Smoking Peripheral artery disease especially
with venous stasis
Acquired immunodeficiency
syndrome (though not human immunodeficiency virus infection alone)
In terms of patient satisfaction, full-thickness grafts are preferred over split-thickness grafts because of the much less burdensome donor site of the full-thickness graft.35 In fact, in large studies of patients undergoing split-thickness grafting with 1-year follow-up, the overwhelming majority of patients listed the donor site as their primary concern.35 Other issues include poor esthetics in terms of color and texture match to surrounding tissue as well as consequences of graft contraction. However, when comparing skin grafting to secondary healing, patients preferred the significantly shortened duration of healing associated with skin grafting.35 These are important considerations when counseling patients as to the best course of treatment for wounds that may require skin grafting.
SKIN SUBSTITUTES
Skin substitutes exist in many forms. They may be used to address common goals of wound management to promote healing of the wound itself or to manage the wound and increase its readiness for other, more definitive reconstructions. A selected sample will be discussed.
Allografts and xenografts (eg, porcine, piscine) convey temporary benefits of wound coverage, including decreased risk of infection and fluid loss, and they may be applied at the bedside, decreasing financial and clinical costs. However, antigenicity is a concern and must be carefully factored into decision-making in transplant patients or those who may become such.6 Porcine allograft is readily
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available and makes biologic sense because of its similar histopathological characteristics to human skin; however, religious beliefs must be considered.6 Recent interest has occurred around the use of tilapia skin.
6
Acellular dermal matrices (ADMs) harvested from animal sources, such as human, bovine, and porcine, serve many functions, including support of soft-tissue reconstructions. They have experienced widespread use in various anatomic regions such as the abdomen for hernia repair and chest for breast reconstruction. There are many varieties, often produced with proprietary processing methodologies. Further discussion of the rich clinical complexity of ADMs is outside the scope of this chapter.
Combinations of synthetic and biologic constructs also serve as skin substitutes. Dermal matrices, such as Dermagraft and Apligraf (both from Organogenesis, Canton, MA), protect the wound bed and become vascularized over the course of weeks, converting wounds to candidacy for skin grafting and strengthening the durability of the skin graft.44 Vascularization of these types of products can occur from wound margins, becoming confluent over critical exposed structures without vascularity such as denuded bone, tendon, and cartilage.44 The vascularized matrix may then support a skin graft with the final reconstructed soft tissue demonstrating improved contour, thickness, strength, malleability, and elasticity when compared to skin graft alone.44 The first dermal replacement matrix, Integra (Integra LifeSciences, Princeton, NJ), is still popular today, consisting of bovine collagen and chondroitin-6-sulfate glycosaminoglycan as dermis and silicone sheeting as the epidermis.6 Following time for vascularization of the dermal analog, the silicone layer is replaced with skin grafting (Figure 6.3).4 Options also exist for dermal replacement matrices accepting of skin grafting in a single stage, such as MatriDerm.
6,45,46
Hyaluronic acid constructs such as Hyalomatrix have also been created as dermal substitutes, because hyaluronic acid is known to impact epidermal cell proliferation and migration, fibroblast differentiation to myofibroblasts, reepithelialization, and granulation.6 Overall, these
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technologies are so powerful that they have become standard tools for soft-tissue reconstruction.
FIGURE 6.3. Combined therapeutic approach with skin
substitute application and skin grafting. A. Patient with an open fracture of the left lateral ankle. B. Remaining wound with tenuous soft-tissue coverage of bone and hardware following open reduction and internal fixation. C. Integra (Integra LifeSciences, Princeton, NJ) applied to the wound. D. Vascularized neodermis filling the wound bed after negative-pressure wound therapy for several weeks. E. Split-thickness skin graft applied over vascularized neodermis. F. Healing several weeks postoperatively from the final operation.
Regarding autologous cells harvesting and processing, in addition to the previously discussed CEA, the RECELL (Avita Medical, Valencia, CA) method allows immediate spraying of noncultured autologous cells, expanding donor site to recipient site size rations to
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1:80. Small (on the order of 5-10 cm2) split-thickness grafts are harvested and processed to produce a solution with suspended, live autologous cellular elements. Very widely meshed split- thickness grafts (usually one to six meshing) is placed on a wound and the cellular solution then sprayed on. While this technique allows drastic increases in treatable surface area and demonstrates durable and esthetic results deemed similar to split-thickness skin grafts with reduced donor site size and pain, its time-consuming nature may limit its usefulness for the sickest patients susceptible to greater stress from longer surgeries.
6,47
QUESTIONS
1. An 82-year-old patient receives a skin graft to a chronic lower extremity wound. Initial nutrition to the graft is achieved via which process?
a. Derivation b. Inosculation
c. Revascularization
d. Imbibition
2. A 36-year-old patient returns to the clinic having removed the bolster dressing applied over a meshed split-thickness graft to a traumatic wound from a motor vehicle collision 24 hours after surgery. What factor is most likely responsible for graft failure?
a. Hematoma b. Seroma
c. Shear
d. Infection
3. A 72-year-old patient with multiple medical comorbidities sustains a full-thickness scalp injury with a 5 cm2 area of exposed skull without periosteum. What is the most appropriate definitive management?
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a. Wet to dry dressing changes until healing by secondary
intention is complete
b. Split-thickness skin grafting immediately following
adequate wound debridement
c. Early bilaminar dermal matrix application followed by
staged skin graft reconstruction
d. Latissimus muscle free tissue transfer with immediate
skin graft application
ANSWERS AND EXPLANATIONS
1. Answer: d.  Imbibition is the first step in skin graft survival.
Inosculation is classically taught as the second step; however, it has fallen by the wayside in favor of alternate theories of revascularization beginning with angiogenesis. Derivation is not a step in skin graft “take.”
2. Answer: c.  While all choices may detrimentally impact skin graft “take” or successful healing, meshed skin grafts are less likely to develop hematomas and seromas because of the interstices of the meshing. Infection would be unlikely to occur so rapidly at 24 hours following surgery. Sahear forces are common causes of skin graft failure, particularly with inadequate fixation of the graft to the wound bed as would occur with early discontinuation of the bolster dressing.
3. Answer: c.  With a relatively large area of exposed bone without periosteum, healing by secondary intention will likely fail because of the inability of the granulation tissue from the wound margins to progress over a large surface area, and at best, it will take a prolonged period of time. Split-thickness skin grafting alone in the setting of a sizable wound without underlying vascularized tissue will likely fail because of the need for a graft to receive nutrition and vascularity from the underlying wound bed. A latissimus muscle free flap with skin graft is an
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aggressive surgery with increased donor site morbidity and operative time and risk. Bilaminar dermal matrix application followed by staged skin grafting would allow vascularity to progress from the wound margins through the dermal matrix confluently across the wound, creating a hospitable environment for staged skin grafting.
REFERENCES
1. Mathes SJ, Nahai F. Clinical Applications for Muscle and Musculocutaneous Flaps. C.V. Mosby; 1982.
2. Mathes SJ, Nahai F. Reconstructive Surgery: Principles, Anatomy & Technique. Vol 2. Churchill Livingstone; 1997. St. Louis: Quality Medical.
3. Golieb LJ, Krieger LM. From the reconstructive ladder to the reconstructive elevator. Plast Reconstr Surg. 1994;93(7):1503-1504.
4. Pavri SN, Hsia HC. Concepts of skin graft and skin substitutes. In: Chung K., ed. Grabb and Smith’s Plastic Surgery. 8th ed. Wolters Kluwer; 2019:49-56.
5. Bogdanov SB, Gilevich IV, Melkonyan KI, Sotnichenko AS, Alekseenko SN, Porhanov VA. Total full-thickness skin grafting for treating patients with extensive facial burn injury: a 10-year experience. Burns. 2021;47(6):1389-1398.
6. Kohlhauser M, Luze H, Nischwi SP, Kamolz LP. Historical evolution of skin grafting: a journey through time. Medicina. 2021;57(4):348.
7. Tanner JC, Vandeput J, Olley JF. The mesh skin graft. Plast Reconstr Surg. 1964;34:287-292.
8. Singh M, Nuutila K, Collins KC, Huang A. Evolution of skin grafting for treatment of burns: Reverdin pinch grafting to Tanner mesh grafting and beyond. Burns. 2017;43(6):1149-1154.
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9. Matsumura H, Matsushima A, Ueyama M, Kumagai N. Application of the cultured epidermal autograft “JACE®” for treatment of severe burns: results of a 6-year multicenter surveillance in Japan. Burns. 2016;42(4):769-776.
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the microvasculature growing in the fibrin interface between a skin graft and the recipient site. Microvasc Res. 2008;75(1):119-129.
Vollmar B. A new model for studying the revascularization of skin grafts in vivo: the role of angiogenesis. Plast Reconstr Surg. 2008;122(6):1669-1680.
vessels of skin graft and host bed: a fortuitous encounter. Br J Plast Surg. 1975;28(4):274-282.
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Techniques of Plastic Surgery and Their Surgical Applications. 10th ed. Churchill Livingstone; 2000.
an artificial skin substitute. J Plast Reconstr Aesthet Surg. 2012;65(11):1544-1550.
grafts in head and neck surgery. Am J Surg. 1962;104:721-726.
craniofacial reconstruction. Surgeon. Published online May 4,
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2022:S1479.
Clin Microbiol. 2014;52(8):2753-2756.
PG. Outcome of split-thickness skin grafts after external beam radiotherapy. Ann Plast Surg. 2004;52(6):551-556; discussion 557.
Clay RP. Outcomes of skin graft reconstructions with the use of Vacuum Assisted Closure (VAC(R)) dressing for irradiated extremity sarcoma defects. World J Surg Oncol. 2007;5:138.
surgery in irradiated areas: analysis of 200 consecutive cases. Eur J Surg Oncol. 1997;23(1):48-53.
damage. Plast Reconstr Surg. 1982;70(2):179-185.
Skin graft survival after external beam irradiation. Plast Reconstr Surg. 1999;103(7):1902-1908.
thickness autogenous skin grafts and donor sites. Arch Surg. 1965;91(4):658-670.
thickness graft necrosis. Arch Dermatol. 1991;127(7):1012-1015.
factors for lower limb skin graft failure. Dermatol Res Pract. 2014;2014:582080.
systematic literature review. J Burn Care Res. 2020;41:S98-S99.
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