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Epidemiology ofSoft-Tissue Injuries oftheHead andNeck
2
One of the main causes of facial scarring is facial soft-tissue injury. It can appear either in combi­nation with fractures of the underlying facial bones or merely as injury to the soft tissues of the face.
Facial trauma (including blunt, penetrating injuries, and facial fractures) is common. It was seen in over one-third (34%) of all trauma patients reported in the Major Trauma Outcome Study (MTOS) from 1982 to 1987, which included 87,174 trauma patients from 139 North American hospitals (single largest trauma data­base in North America) (Sastry etal. 1995). The leading specic trauma diagnoses were open wound of nose, face, and mouth (42%), followed by contusion to the face and neck (15.4%) and supercial injury to the face and neck (13.4%). Facial fractures were seen in 25% of the patients (Sastry etal. 1995).
In another, more recent, study from the United Kingdom, facial injuries represented 4% of all admissions at 163 accident and emergency (A&E) departments (England, Scotland, Wales, and Northern Ireland). Over the study week from 09:00h on Friday 12 September 1997 to 08:59h on Friday 19 September 1997, there were 6114 patients with facial injuries out of a total of 152,692 A&E attendances (Hutchison et al.
1998).
Age is an important variant in facial/neck soft­tissue injuries. Shinya et al. (1993) retrospec­tively analyzed 108 patients with facial injuries
from falling. The latter injuries were common in little children. In those under 6years of age, they comprised 45.4% of injuries. The authors observed age-dependent characteristic injury sites. In patients under 2years, the forehead was mainly injured; in small children, the chin; in stu­dents, the lip; and in older persons, the cheek was the main location of the injury. The authors attrib­uted this disparity to the different mechanisms of injury. They also observed that the injury pattern depended on age, varying activities, and tissue strength. In children <6years of age, small lac­erations on the forehead or chin were most com­mon (Shinya et al. 1993). O’Neil et al. (2008) reviewed 39,850 escalator-related injuries. The head was the second most common injured body part (25%, 95% CI: 20.5–29.5%). The rate of head injuries and the rate of hospitalizations increased with age. Gassner et al. (2003) in a review of a large member of patients with cranio­maxillofacial trauma (9543 cases with 21,067 injuries) reported that older people were more prone to soft-tissue injuries with a rising risk of 2% per year of age, although no statistically sig­nicant differences were found between the sexes for soft-tissue trauma.
Various causes cause facial soft-tissue inju­ries. There are differences in the reported inci­dence per cause, depending on age and country of origin of the study. Li etal. (2006) in a retro­spective analysis of 3958 patients with facial injuries from China reported that the most
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 C. A. Ioannidis, Soft Tissue Injuries of the Head and Neck,
https://doi.org/10.1007/978-3-031-14915-3_2
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2 Epidemiology ofSoft-Tissue Injuries oftheHead andNeck
common cause of injury was trafc accident (30.6%), followed by falls (21.4%) and collision (15.8%). Gassner etal. (2004) in a study of cra­niomaxillofacial trauma in children from Austria (3385 cases with 6060 injuries) reported that the most common cause of injury was play (58.2%), followed by sports (31.8%), trafc accidents (5%), acts of violence (3.9%), and other causes (1.1%). The same authors in another study of 9543 cases with craniomaxillofacial trauma including all ages reported that the main cause was activity of daily life (38%), followed by sports (31%), violence (12%), trafc accidents (12%), work accidents (5%), and other causes (2%) (Gassner et al. 2003). Hutchison et al. (1998) in a study from the United Kingdom reported that 40% of the facial injuries were caused by falls. Twenty-four percent of the facial injuries were caused by assault. The commonest sites for assault were the street followed by pub­lic drinking establishments. More women than men were assaulted at home. The 15–25 age groups suffered the greatest number of facial injuries caused by assault. Fifty-ve percent of assaults were related to alcohol consumption. Eight percent of assaults were with bottles or glasses. Only 5% of the facial injuries occurred in road trafc accidents (RTAs). Fifteen percent of RTA victims had consumed alcohol. At least 27% of all the facial injuries in all age groups were related to alcohol consumption within 4h of the injury. In the over-15 age groups, alcohol con­sumption was associated with 90% of facial inju­ries occurring in bars, 45% on the street, and 25% in the home. Assault, RTA, and alcohol consump­tion conveyed an increased risk of serious facial injury (Hutchison etal. 1998). The probability of suffering soft-tissue injuries (p<0.05) was raised in trafc accidents by 58%, in sports by 12%, during assaults by 31%, and in activity of daily life/play accidents by 16% (Gassner etal. 2003).
As cell phones become part of everyday life, they tend to become more hazardous. Povolotskiy et al. (2020) retrospectively reviewed 2501 patients who presented with injuries of the head and neck related to cell phone use. The most commonly reported subsites of injuries in the head and neck area included the head (33.1%),
the face (eyelid, eye area, and nose) (32.7%), and neck (12.5%). The most common injury diagno­ses were laceration (26.3%), contusion/abrasion (24.5%), and internal organ injury (18.4%). Age group distributions showed that most injuries associated with cell phone user distraction occurred among individuals aged 13–29years. In addition, those younger than 13years were sig­nicantly more likely to sustain direct mechani­cal injury from a cell phone (82.1%) than to have a cell phone use-associated injury (17.9%).
There are various types of soft-tissue injuries: lacerations, abrasions (excoriations), contusions, and burns. Lacerations seem to be the most fre­quently occurring injuries. In the study by Gassner etal. (2003), they comprised 41.3% of all soft-tissue injuries (3205/7769). Excoriations comprised 23.9% and contusions 11.1% of all soft-tissue injuries. The mean age is ca 26years (Gassner etal. 2003); however, they can occur at all ages. Males seem to be involved more fre­quently than females. There was a 2.1:1 (Gassner et al. 2003) male-to-female ratio. According to another study, the ratio of male to female was
4.27:1 (Li et al. 2006). Both age and gender, however, vary greatly depending on the injury mechanism (Gassner etal. 2003). In a study of escalator-related injuries among older adults, the mean age of the study population was 80.1years and 73.3% of the patients were females (O’Neil etal. 2008). Similar ndings were reported more recently in a study of 426 individuals aged 60 years or older hospitalized due to fall. The main victims were women aged 80 or over. Occurrences were common in the daytime period and due to falls from self-height. Soft-tissue inju­ries in head and face were common, whereas facial fractures showed low frequency (Cavalcanti et al. 2020). Ninety-seven percent of children 5–18years of age having sustained cheer leading­related injuries in the United States were females (Shields and Smith 2006).
Facial soft-tissue injuries occur as solitary injuries in a large number of cases. The majority of facial injuries reported by Gassner (62.5%) were merely injuries to the soft tissues of the face. Other authors reported lower percentages. In a series of 2798 cases, Subhashraj etal. (2007)
2 Epidemiology ofSoft-Tissue Injuries oftheHead andNeck
7
reported that 42% of patients had soft-tissue inju­ries, and Li etal. (2006) reported that a total of 794/3598 patients (20.1%) showed only soft­tissue injuries. In the remaining patients, there were concomitant fractures of the underlying facial bones present.
Burns requiring medical attention rank fourth among all injuries (Peck 2011). Fortunately, the vast majority of burns are not fatal. However, in low-income and middle-income countries (e.g., East Mediterranean Region), burn injuries are one of the leading causes of mortality (Othman and Kendrick 2010). The global mortality rate is reported to be 4.8 per 100,000 per year (Othman and Kendrick 2010). Nonetheless, re-related burns are also among the leading causes of disability- adjusted life years lost in low- and middle-income countries (Peck 2011).
The WHO estimates indicate that globally there were more than 7.1 million re-related unintentional burns (ICD-10: X01-X09) in 2004 giving an overall incidence rate of 110 per 100,000 per year. The reported incidence varies between different countries. The incidence in the East Mediterranean region was 187 per 100,000 per year compared to the lowest incidence in the Americas which was 19 and the highest inci­dence in Southeast Asia which was 243 per 100,000 per year (WHO 2004).
Risk factors for burns include those related to socioeconomic status, race and ethnicity, age, and gender, as well as those factors pertaining to the region of residence, intent of injury, and comorbidity (Peck 2011). The etiology and nature of burn injuries vary signicantly by coun­try (Dissanaike and Rahimi 2009). Gender differ­ences play a signicant role in the risk of burn injuries, across a spectrum with a predominance of women injured in res from cooking and heat­ing fuels in the developing world and industrial accidents primarily affecting men in developed nations. Children are particularly vulnerable to burn injuries, accounting for almost 50% of all burn patients in some studies. A majority of pedi­atric burns are scald injuries usually affecting very young children below the age of 5 years. Finally, the elderly form a rapidly increasing pro­portion of the population in many countries and
are often burdened with comorbidities that are likely to pose signicant challenges in burn care (Dissanaike and Rahimi 2009).
The head and neck are often the most fre­quently affected body areas. In an adult population- based study from the Calgary Health Region, Canada, burns of the head and neck were the most prevalent (22.2%) (Burton etal. 2009). D’Souza et al. (2009) reviewed 2,054,563 patients < or = 20years of age who were treated in US emergency departments for burn-related injuries between 1990 and 2006. The body parts injured most frequently were the hand/nger (36.0%), followed by the head/face (21.1%). Chemicals and cleaners, compared with other products, were 5.6 times (95% CI: 5.3–5.9 times) more likely to burn the head and face than other body parts. A comparative study by Teo et al. (2012) illustrates the differences encountered in different countries. Pediatric burns presenting in the Royal Aberdeen Children’s Hospital (RACH), Scotland, and the Red Cross War Memorial Children’s Hospital (RXH), Cape Town, South Africa, in 2009 were reviewed. During 2009, the RACH received 192 children with burns (1% of total emergencies) and the RXH received 994 (11% of total emergencies). At the RACH, most burns involved the hands and were single site (79%), while at the RXH, most were multiple sites (76%) and involved the face. Scalds accounted for the majority of injuries in both hos­pitals (RACH 45%, RXH 77%). Several other studies indicated the face as the most common or the second most common (after the hands) burned body area (Kauvar etal. 2006; Foster etal. 2011). Fatusi et al. (2006) reviewed the outcome and associated factors in burn injuries with and with­out facial involvement. Fuel-related ames con­stituted the leading cause in both facial (71.1%) and non-facial involved burns (65.3%). There was no signicant difference in the incidence of inhalation injury between burns with facial involvement and burns without facial involve­ment; however, cases of facial involvement had signicantly lower incidences of wound infec­tions. No signicant difference was seen in the incidence of mortality between burns with facial involvement (31.6%) and burns without facial
8
2 Epidemiology ofSoft-Tissue Injuries oftheHead andNeck
involvement (30.7%). A study from Lille, France, showed that the total burn area was less than 10% in 63% of the cases. The average facial burned area was 4%. The cheek, the forehead, and the chin were most frequently involved (Capon­Degardin etal. 2001). On the other hand, accord­ing to a study on 222 consecutive patients with major burns, facial injury was one of the predic­tors of risk of death, as shown by the multivariate logistic regression analysis of factors predicting survival in patients with burn injury (Ganesamoni etal. 2010).
Like burns, the majority of abrasions and con­tusions are injuries of minor to moderate severity. A few patients suffer injuries of such severity that endanger the individual’s life. The different types of injuries and the special problems related to each location (facial units) will be analyzed in the following chapters.
References
Burton KR, Sharma VK, Harrop R, etal. A population-
based study of the epidemiology of acute adult burn
injuries in the Calgary Health Region and factors asso-
ciated with mortality and hospital length of stay from
1995 to 2004. Burns. 2009;35:572–9. Capon-Degardin N, Martinot-Duquennoy V, Lesage-
Maillard V, et al. [Facial burns in children. 197
patients]. Ann Chir Plast Esthet. 2001;46:190–5. Cavalcanti AF, Formiga S, de Arruda T, et al. Head and
face injuries in elderly patients victims of fall. A single
trauma center analysis. Stomatologija. 2020;22:39–43. D’Souza, Nelson NG, McKenzie LB.Pediatric burn inju-
ries treated in US emergency departments between
1990 and 2006. Pediatrics. 2009;124:1424–30. Dissanaike S, Rahimi M.Epidemiology of burn injuries:
highlighting cultural and socio-demographic aspects.
Int Rev Psychiatry. 2009;21:505–11. Fatusi OA, Fatusi AO, Olabanji, etal. Management out-
come and associated factors in burn injuries with and
without facial involvement in a Nigerian population. J
Burn Care Res. 2006;27:869–76. Foster MA, Moledina J, Jeffrey SL.Epidemiology of U.K.
military burns. J Burn Care Res. 2011;32:415–20.
Ganesamoni S, Kate V, Sadasivan J. Epidemiology of
hospitalized burn patients in a tertiary care hospital in South India. Burns. 2010;36:422–9.
Gassner R, Tuli T, Hächl O, et al. Craniomaxillofacial
trauma: a 10-year review of 9,543 cases with 21,067 injuries. J Craniomaxillofac Surg. 2003;31:51–61.
Gassner R, Tuli T, Hächl O, et al. Craniomaxillofacial
trauma in children: a review of 3,385 cases with 6,060 injuries in 10 years. J Oral Maxillofac Surg. 2004;62:399–407.
Hutchison IL, Magennis P, Shepherd JP, etal. The BAOMS
United Kingdom survey of facial injuries part 1: aeti­ology and the association with alcohol consump­tion. British Association of Oral and Maxillofacial Surgeons. Br J Oral Maxillofac Surg. 1998;36:3–13.
Kauvar DS, Cancio LC, Wolf SE, et al. Comparison of
combat and non-combat burns from ongoing U.S. mil­itary operations. J Surg Res. 2006;132:195–200.
Li YS, Tian WD, Li SW, etal. [Retrospective analysis of
3,958 patients with facial injuries]. Zhonghua Kou Qiang Yi Xue Za Zhi. 2006;41:385–7.
O’Neil J, Steele GK, Huisingh C, etal. Escalator-related
injuries among older adults in the United States, 1991–2005. Accid Anal Prev. 2008;40:527–33.
Othman N, Kendrick D.Epidemiology of burn injuries in
the East Mediterranean Region: a systematic review. BMC Public Health. 2010;10:83.
Peck MD. Epidemiology of burns throughout the
world. Part I: Distribution and risk factors. Burns. 2011;37:1087–100.
Povolotskiy R, Gupta N, Leverant AB, et al. Head and
neck injuries associated with cell phone use. JAMA Otolaryngol Head Neck Surg. 2020;146:122–7.
Sastry SM, Sastry CM, Paul BK, etal. Leading causes of
facial trauma in the major trauma outcome study. Plast Reconstr Surg. 1995;95:196–7.
Shields BJ, Smith GA.Cheer leading-related injuries to
children 5 to 18 years of age: United States, 1990-
2002. Pediatrics. 2006;117:122–9.
Shinya K, Taira T, Sawada M, etal. Facial injuries from
falling: age-dependent characteristics. Ann Plast Surg. 1993;30:417–23.
Subhashraj K, Nandockumar N, Revimbran C. Review
of maxillofacial injuries in Chennai, India: a study of 2,748 cases. Br J Oral Maxillofac Surg. 2007;45:637–9.
Teo AI, Van As AB, Cooper J.A comparison of the epi-
demiology of pediatric burns in Scotland and South Africa. Burns. 2012;38:802–6.
WHO. Annual incidence (000s) for selected causes, in
WHO Regions (a), estimates for 2004. Geneva: WHO;
2004. http://www.who.int/healthinfo/global burden
disease/estimatesregional/en/index.htm.
General Principles ofWound Management
3.1 Principles ofPatient
Management
The principles of facial soft-tissue injuries are similar for all age groups:
1. Restoration and preservation of function
2. Achievement of optimal cosmetic results with
a minimum of scar formation by placing all of the anatomic landmarks in their proper location
3
Soft-tissue injuries encompass a spectrum that includes ecchymoses, lacerations, contusions, abrasions, degloving injuries, avulsions, and burns (Figs.3.1, 3.2, 3.3, and 3.4). Minor soft­tissue injuries are the most common facial inju­ries. Most injuries may be repaired on an outpatient basis using local anesthesia. In chil­dren, however, sedation is often required. If the injuries are extensive or if there are underlying fractures, it is advisable to use general anesthesia for better control of the repair environment and in order to optimize the outcome. Facial wounds without additional injuries are repaired as soon as possible. In major trauma, while instituting the resuscitative measures, the wound may be dealt with after 4–6h.
Patients with facial injuries often suffer from associated trauma to other parts of the body (Fig. 3.5) that may require more urgent atten­tion. The prevalence of head and neck injuries in
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 C. A. Ioannidis, Soft Tissue Injuries of the Head and Neck,
https://doi.org/10.1007/978-3-031-14915-3_3
Fig. 3.1 Male victim of a road trafc accident (RTA) with facial ecchymoses, lacerations, contusions, and abrasions
major trauma patients is poorly documented in the literature (Mohamed etal. 2021). In a retro­spective review of 5364 patients from 26 hospi­tals in Ireland, the authors documented soft-tissue injuries in ca 23% of the patients (Mohamed et al. 2021). Head/facial injuries
9
10
Fig. 3.2 Female patient with facial ecchymoses, lacera­tions, and abrasions as a result of an RTA
Fig. 3.3 Male patient with traumatic ecchymosis and lac­erations of the left side of the face
(HF) were more lethal and presented with severe morbidity compared to other bodily injuries. Of the HF injured patients, 2817/4799 (59%) died during their presentation to the ED vs. 365/3048 (12%) of the other bodily injuries (Quenzer etal. 2021).
The priorities of emergency trauma care must always be airway maintenance (A), control of
3 General Principles ofWound Management
Fig. 3.4 Male patient with burns of the facial region
breathing (B), and circulation (C). Evaluation of cranial and maxillofacial soft-tissue injuries should begin while the patient is being stabilized.
Photographic documentation should be a part of the initial evaluation, especially if the patient is to be treated on an outpatient basis. Photographic documentation helps patients with future insurance claims and physicians to address medicolegal matters and serves as a safeguard against possible litigation involving the causative parties.
Through a comprehensive and accurate his­tory, insight may be gained into the nature of the soft-tissue injury and whether associated fractures are also present. If the presence of for­eign bodies (Fig.3.6) or associated maxillofa­cial fractures is suspected, imaging studies are indicated. Plain radiographs often provide sub­optimal results, and computer scans are then indicated (Fig.3.7). Severe craniomaxillofacial injuries warrant a CT scan of the brain, thus providing the opportunity to obtain a concur­rent maxillofacial CT scan for clear denition of bone injuries (Fig.3.8). After the history and physical examination are completed, thorough wound examination is vital. Optimal treatment of facial injuries depends on a thorough initial evaluation (what tissue constituents are lost and
3.1 Principles ofPatient Management
11
ab
cd
Fig. 3.5
(a–e) Concomitant injuries and burns of the torso and limbs in patients with H&N injuries
12
3 General Principles ofWound Management
e
Fig. 3.5 (continued)
a
b
Fig. 3.6 Piece of glass (foreign body) which was removed from the orbit of a patient with an orbital injury
c
de
Fig. 3.7 (a) Patient with bilateral eyelid ecchymoses and limited lacerations to the right eyebrow and upper eyelid. (b, c) CT scans of the same patient showing extensive
what tissues are exposed) and detailed descrip­tion of the injury in the medical records. Complications following acute facial injuries will be predictably minimized if the treatment is meticulously planned and executed. After
injury (fractures) to the fronto-orbito-basal skeleton. (d, e) Peroperative pictures showing the fractured area. Note the open frontal sinus
irrigation, initial assessment can be facilitated if the wound is inltrated with 2% xylocaine with epinephrine, 1:100,000. The edges can then be easier retracted, to explore the depth of the wound, which may contain embedded for-
3.2 Wound Preparation
13
Fig. 3.8 (a) Victim of an RTA with a depression of the nasofrontal area. (b, c) CT scans of the brain. (d) Clinical picture showing the nasofrontal fracture. (From Ioannides etal. 1993, with permission)
a
cd
eign bodies, hematomas, or bone fragments in cases of underlying fractures (Juncar et al.
2020). To prevent future deformities or an
unsightly scar, copious irrigation and meticu­lous removal of all foreign material are of an utmost importance. Loupe magnication is sometimes necessary to successfully complete the debridement.
Thorough examination of the wound provides information such as the condition of the sur­rounding tissue, the location of the injury, the angle of the defect in relation to relaxed skin ten­sion lines, and the involvement of signicant ana­tomical structures. Nerves, parotid ducts, lacrimal ducts, and other critical facial structures may be involved. These will be further analyzed in the following chapters.
Whenever there is a composite full-thickness loss of tissue, the requirement is lining, support, and cover (eyelids, nose, ear, cheek, etc.).
Occasionally, consultation of other medical specialists is necessary, e.g., ophthalmologists, in cases of severe eyelid trauma. The type of the injury, its location and extent, and the involve­ment of vital facial structures will aid the surgeon to decide on the type of anesthesia (local, local with sedation, general) and set up the treatment plan.
b
3.2 Wound Preparation
The lines of tension in the skin were rst noted by Dupuytren in 1832 (Place et al. 1997). (Langer
1861) also described the normal tension lines of
the skin, called “Langer’s lines” (Place et al.
1997).
Borges has written extensively on the subject
and lists 36 descriptive terms for skin lines (Borges 1973). He refers to the skin lines as “relaxed skin tension lines.” Wrinkle lines are generally the same as the relaxed tension lines and lie perpendicular to the long axis of the underlying muscles. Maximal contraction occurs when a scar crosses the lines of minimal tension at a right angle.
When a wound is already present as a result of
trauma, it is important to consider how and to what extent it transgresses the normal tension lines of the face and whether it can be modied to a more “favorable” orientation. It often proves impossible or undesirable to make if conforming as a primary maneuver, because of potential infection, poor blood supply of wound margins, skin damage, etc. (McGregor 1989). The aim should therefore be to prepare it for the time when, at a later date, it can be modied to con­form to the principles of placing a facial scar, if
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3 General Principles ofWound Management
the result of wound repair is not satisfactory. Langer’s lines do not seem to be a static feature but are dynamic with rotation of up to 90° with facial movement. It is possible that this rotation in the axis of mechanical tension will affect the appearance of the resulting scar (Bush et al.
2007).
It is axiomatic that a thorough debridement of
all dirt and foreign material should be the rst step the surgeon must take. The presence or absence of damaged tissue determines whether or not parts of a wound should be excised. In the face, the problem of excisional policy is more difcult than elsewhere in the body. Excision of damaged tissue converts a wound to an “atrau­matic” one, in an attempt to get a satisfactory nal result primarily. In more extensive wounds, however, tissue excision may result in closure under tension and a stretched or hypertrophic scar or even a deformity. A more conservative approach with removal of only necrotic tissue is advocated. In this way, the salvage of tissue is permitted, which might otherwise be excised, and which later may prove valuable. One, how­ever, is prepared for eventual secondary correc­tion of the resulting scar.
The secret in suturing an irregular wound is to
look for landmarks on either side to match. Time spent tting a “jigsaw” of tissue accurately at the time of original suture is never wasted (McGregor
1989).
An added difculty arises when there has been
actual loss of tissue. The governing principle is to replace surviving tissues in their correct anatomi­cal position, so that the defect can be properly displayed and assessed in terms of tissue lost. In some cases of extensive tissue loss, tissue replace­ment with regional or free tissue transfer is nec­essary. This can also be the case when there is a full-thickness defect with opening into the mouth, which cannot be closed without undue distortion.
In deciding on the extent of surgical debride-
ment, one must often know when a part of trau­matized tissue is viable or not. In other words, the surgeon has to check on the vascularity. Blanching on pressure and the presence of dermal bleeding are both evidences of an active circulation. In the
face and scalp, tissue vascularization is the rich­est of the whole body; therefore, tissue excision should not be carried out lightly. In case of doubt, it is advisable to be conservative and keep tissue instead of removing it, as there is a good chance that it will “pick up.” The state of tissue vascular­ity is assessed through the color of the overlying skin. For this reason, the antiseptic chosen for skin sterilization should be the one which does not stain the skin or tissues. Betadine® (povidone­iodine 10% in an alcoholic solution), suitable otherwise, should not be used; satisfactory agents are cetrimide and chlorhexidine.
The wound edges to be sutured ought to be vertical if the best scar result is to be achieved. When preparing the wound for suture, the sur­geon, with little tissue sacrice, should aim at rendering the wound edges vertical. In cases of an extensive, oblique wound or a degloving injury, the method of suturing is altered. Accurate suturing is also easier when the opposing sur­faces are equally thick. A slight undermining of both edges (for a few millimeters) allows slight wound eversion. Wider undermining is occasion­ally required, in order to achieve a wound closure without tension. When doing that, the surgeon should be careful not to endanger the vascularity of the aps. In the face, the appropriate level is deep to the dermis, so that the subdermal vascular plexus is kept unharmed, while leaving the branches of the facial nerve undisturbed. In the scalp, the plane is between the galea aponeuro­tica and the pericranium. The vascular anatomy of the scalp is such that extensive undermining can be carried out safely (McGregor 1989). Surgeons vary in the extent to which they make use of undermining in this way. It is important to recognize its limitations and dangers of using it in the presence of damaged tissue, particularly involving degloving. Undermining should be done by experienced surgeons, because other­wise the harm will be bigger than the benet. When more than minimal advancement is required to allow a wound to be closed, some authors advocate the use of skin grafts (McGregor
1989). The latter, however, may produce a poor
cosmetic result.