eMedicine Specialties > Emergency Medicine > Trauma & Orthopedics

Fracture, Face

Thomas Widell, MD, Vice Chairman, Assistant Professor, Department of Emergency Medicine, Rosalind Franklin School of Medicine/The Chicago Medical School, North Chicago, Illinois; Associate Residency Director, University of Chicago Emergency Medicine Program, Chicago, Illinois; Program Director Emergency Medical Education, Attending Physician, Mount Sinai Hospital Medical Center, Chicago, Illinois

Updated: Mar 6, 2008

Introduction

Background

In approximately 400 BC, Hippocrates provided the first description of a variety of facial injuries. Rene Le Fort used cadaver studies in 1900 to provide detailed descriptions of 3 basic types of facial fracture.

Endotracheal anesthesia and radiography developed during the First World War led to better understanding and treatment of facial fractures. During the Second World War, a multidisciplinary approach to treatment of facial fractures continued to improve the outcomes of severely injured soldiers. The more recent introduction of CT reconstruction, along with new surgical techniques, has improved cosmetic results immensely.

Pathophysiology

Maxillofacial fractures result from blunt or penetrating trauma. Blunt injuries are far more common, including vehicular accidents, altercations, sports-related trauma, occupational injuries, and falls. Penetrating injuries include gunshot wounds, stabbings, and explosions.

Mass, density, and shape of the striking object, as well as speed of impact, directly affect type and severity of facial injury. The force required to fracture various facial bones may be classified as high impact (greater than 50 times force of gravity [g]) or low impact (less than 50 g).

  • High impact
    • Supraorbital rim: 200 g
    • Symphysis mandible: 100 g
    • Frontal-glabellar: 100 g
    • Angle of mandible: 70 g
  • Low impact
    • Zygoma: 50 g
    • Nasal bone: 30 g

Simple nasal fractures are the most common of all facial fractures. They must be distinguished from the more serious nasoethmoidal (NOE) fractures. NOE fractures extend into the nose through the ethmoid bones. Fractures through the ethmoid are prone to cerebrospinal fluid (CSF) leaks from dural tears.

Zygomatic arch fractures tend to occur in 2-3 places along the arch. Often 3 breaks occur, 1 at each end of the arch and a third in the middle, forming a V-shaped fracture; this often impinges on the temporalis muscle below, causing trismus.

Zygomaticomaxillary (tripod) fractures result from a direct blow to the cheek. Fracture occurs at articulations of the zygoma with the frontal bone maxillae and zygomatic arch and often extends through the orbital floor. Because the infraorbital nerve passes through the orbital floor, hypesthesia often occurs in its sensory distribution.

Alveolar fractures occur just above the level of the teeth through the alveolar portion of the maxilla. Usually a group of teeth is loose, and blood is noted at the gingival line.

Le Fort fractures

Le Fort or midface fractures are classified into 3 types and occasionally are mixed from one side of the face to the other.

  • Le Fort I: Horizontal maxillary fracture separates the maxillary process (hard palate) from the rest of the maxilla. Fracture extends through the lower third of the septum and involves the maxillary sinus. This is below the level of the infraorbital nerve and thus does not cause hypesthesia.
  • Le Fort II: Pyramidal fracture starts at the nasal bone, extends through the lacrimal bone, and courses downward through the zygomaticomaxillary suture. It courses posteriorly through the maxilla and below the zygoma into the upper pterygoid plates. The inner canthus of the nasal bridge is widened. Because the fracture extends through the zygoma, near the exit of the infraorbital nerve, hypesthesia often is present. Bilateral subcutaneous hematomas often are present.
  • Le Fort III: Craniofacial dysjunction also starts at the nasal bridge. It extends posteriorly through the ethmoid bones and laterally through the orbits below the optic foramen, through the pterygomaxillary suture into the sphenopalatine fossa. This fracture separates facial bones from cranium, causing the face to appear long and flat (ie, dish face).

For more information, see Medscape's Trauma Resource Center.

Frequency

United States

Approximately 3 million facial injuries occur annually, but most do not involve maxillofacial fractures. One study placed the incidence of severe maxillofacial injury (fractures and lacerations) at 0.04-0.09% for motor vehicle collisions. Motor vehicle-related injuries are more common in rural areas, and altercation-related injuries are more frequent in inner cities.

Mortality/Morbidity

Incidence of other major injuries is as high as 50% in high-impact facial fractures, compared with 21% for low-impact fractures. Motor vehicle collision-related fractures are more likely to have associated injuries than violence-related fractures. The mortality rate is as high as 12% in high-impact fractures but is rarely due to maxillofacial injury. The incidence of associated cervical spine injuries has been reported in the 0.2-6% range.

Sex

Adult male-to-female ratio is 3:1. Suspect domestic violence or sexual assault in women as this may coexist in 30% of cases.

Age

Male predominance is reduced to 3:2 in children. Child abuse should be suspected, particularly in nonmotor vehicular injuries.

Clinical

History

  • First priority is to perform a primary survey and attend to ABCs, as maxillofacial fractures are caused by significant trauma. Initially, focus on assessment of airway patency, breathing, circulation, and gross neurologic function, as well as control of the cervical spine.
  • Once life-threatening issues are addressed, obtain a thorough history.
    • Allergies
    • Medications
    • Past medical history
    • Last meal
    • Events leading to injury
  • Ask specific questions regarding injury.
    • What was the mechanism of injury?
    • Did the patient lose consciousness?
    • Has the patient had any visual problems such as double or blurred vision?
    • Has the patient had any hearing problems, such as decreased hearing or tinnitus?
    • Do teeth come together normally (normal occlusion)?
    • Is patient able to bite down without pain?
    • Does the patient have areas of numbness or tingling on the face?
    • In women, ask if the injury was from a partner or if they feel threatened by anyone.
    • In children, ask questions to determine if child abuse is an issue.

Physical

  • Complete examination of the face is necessary, since multiple injuries easily occur. Portions of the examination specific for facial bones are marked with an asterisk (*).
    • Inspect face for asymmetry, which is often easiest to do looking down from the head of the bed.*
    • Inspect open wounds for foreign bodies and palpate for bony injury.*
    • Palpate the bony structures of the supraorbital ridge and frontal bone for step-off fractures.
    • Thoroughly examine eyes for injury, abnormality of ocular movements, and visual acuity.*
    • Inspect nares for telecanthus and widening of the nasal bridge, and palpate for tenderness and crepitus.*
    • Inspect nasal septum for septal hematoma and clear rhinorrhea, which may suggest a CSF leak.*
    • Palpate zygoma along its arch as well as its articulations with the frontal bone, temporal bone, and maxillae.*
    • Check facial stability by grasping teeth and hard palate and gently pushing back and forth, then up and down, feeling for movement or instability of midface.*
    • Inspect teeth for fracture and bleeding at the gum line (a sign of fracture through the alveolar bone), and test for stability.*
    • Check teeth for malocclusion and step-off.* Inspect for bleeding between teeth at the gum line (a sign of mandibular fracture).
    • Palpate mandible for tenderness, swelling, and step-off along its symphysis, body, angle, and condyle anterior to the ear canal.
    • Evaluate supraorbital, infraorbital*, inferior alveolar, and mental nerve distributions for hypesthesia or anesthesia.
  • Nasal bone fracture: This is diagnosed by a history of trauma with swelling, tenderness, and crepitus over the nasal bridge. The patient may have had epistaxis that has resolved, but no clear fluid (CSF) should be present.
  • NOE fracture: Suspect NOE if the patient has evidence of a nasal fracture with telecanthus, widening of the nasal bridge with detached medial canthus, and epistaxis or CSF rhinorrhea.
  • Zygoma fracture: Physical findings of a depressed malar eminence with tenderness suggest a zygoma or zygomatic arch fracture. Often edema is marked, which can obscure the depression. The patient may complain of pain in the cheek on movement of the jaw. The patient may have trismus or difficulty opening the mouth from impingement of the temporalis muscle as it passes under the zygoma.
  • Tripod fracture
    • Suspect tripod fracture after blunt force to the cheek with physical findings of marked periorbital edema and ecchymosis. Malar flattening may be seen early, but marked swelling of overlying tissues often obscures this finding. Lateral canthus may be depressed if the zygoma is displaced inferiorly. Hypesthesia of the infraorbital nerve often is present, because the fracture extends through the orbit into the zygomaticomaxillary area where the nerve exits.
    • Palpating the zygomaticomaxillary arch from inside the mouth may reveal a step-off fracture. A step-off may be noted at the zygomaticofrontal suture or on the zygomatic arch as well. Eye injuries may be associated with these fractures; thus, a thorough eye examination is important to document and act upon.
  • Le Fort fractures
    • Le Fort I fractures: Physical findings include facial edema and mobility of the hard palate. This is evaluated by grasping the incisors and hard palate and gently pushing in and out.
    • Le Fort II fractures: Findings include marked facial edema with telecanthus, bilateral subconjunctival hemorrhages, and mobility of the maxilla. Epistaxis or CSF rhinorrhea may be noted.
    • Le Fort III fractures: Findings include the appearance of facial elongation and flattening (ie, dishface deformity). Maxilla often is displaced posteriorly, causing an anterior open bite. Grasping the teeth and hard palate and gently moving them results in movement of all facial bones in relation to the cranium. CSF rhinorrhea is almost always present but may be obscured by epistaxis.

Differential Diagnoses

Corneal Abrasion
Globe Rupture
Corneal Laceration
Neck Trauma
Dislocations, Mandible
Pediatrics, Child Abuse
Domestic Violence
Retinal Detachment
Elder Abuse
Sexual Assault
Epidural Hematoma
Subdural Hematoma
Fractures, Frontal
Fractures, Mandible
Fractures, Orbital

Other Problems to Be Considered

Dentate, avulsed
Dentate, displaced
Dentate, fractures

Workup

Laboratory Studies

  • Base need for laboratory studies upon extent of concomitant nonfacial trauma.
  • If injuries are isolated to face and surgery is planned, order preoperative laboratory tests.

Imaging Studies

  • Nasal bone fractures
    • Nasal bone fractures can be diagnosed clinically by history and physical examination. Plain nasal films consisting of a lateral view coning down on the nose and a Waters view can confirm the diagnosis but are of little practical use. If edema has resolved and no deformity is noted, x-rays are unnecessary.
    • If deformity persists after resolution of edema, films may be obtained at follow-up to help plan the repair. Omission of ED films is cost-effective, since most nasal fractures do not need to be reduced.
  • Nasoethmoidal fracture
    • If nasal fracture is suspected and evidence suggests ethmoidal bone involvement, such as CSF rhinorrhea or widening of the nasal bridge with telecanthus, plain films are of little use.
    • Coronal CT scan of the facial bones is the best test to determine the extent of fracture. A 3-D reconstruction may help the consultant should surgery be required.
  • Zygoma fracture
    • Best film for evaluating zygomatic arch is an underexposed submental view, also known as bucket handle view, because arches appear as bucket handles.
    • Fracture also can be seen on a Waters view, and in some cases on a Towne view, of a facial series.
  • Tripod fracture
    • If tripod fracture is suspected, plain films should include Waters, Caldwell, and underexposed submental views.
    • Waters view is best to evaluate the inferior orbital rim, maxillary extension of the zygoma, and the maxillary sinus.
    • Caldwell view evaluates the frontal process of the zygoma and the zygomaticofrontal suture.
    • Underexposed submental view evaluates the zygomatic arch.
    • Coronal CT scan of facial bones often is used to better evaluate these fractures, especially with use of 3-D reconstruction to improve visualization of the fracture for reduction. If tripod fracture is suspected strongly, obtaining CT scan directly without plain films is probably most cost-effective.
  • Le Fort fractures
    • Coronal CT scan of facial bones has replaced plain films in evaluation of Le Fort fractures, especially with use of 3-D reconstruction. Since Le Fort fractures often are mixed from one side to the other, CT scan is superior to plain films and makes visualization of the fracture for repair much easier. If CT is not available, a facial series with lateral, Waters, and Caldwell views can be used to evaluate the fracture. Almost all Le Fort fractures cause blood to collect in the maxillary sinus.
    • Le Fort I fractures: Imaging demonstrates a fracture extending horizontally across the inferior maxilla, sometimes including a fracture of the lateral sinus wall, extending into the palatine bones and pterygoid plates.
    • Le Fort II fractures: Imaging demonstrates disruption of the inferior orbital rim lateral to the infraorbital canal and a fracture of the medial orbital wall and nasal bone. The fracture extends posteriorly into the pterygoid plates.
    • Le Fort III fractures: Imaging demonstrates fractures at the zygomaticofrontal suture, zygoma, medial orbital wall, and nasal bone extending posteriorly through the orbit at the pterygomaxillary suture into the sphenopalatine fossa.

Other Tests

  • Perform chest films if teeth are missing to rule out tooth aspiration.
  • Test clear rhinorrhea for glucose. Nasal secretions, unlike CSF, are normally low in glucose. If blood is present, this test is unreliable. Blood-tinged fluid can be placed on filter paper to look for a double ring sign of CSF around blood, but this is not a reliable test.

Procedures

  • When CSF rhinorrhea is suspected, fluorescein may be injected into the lumbar subarachnoid space. Observe with a Wood lamp 30 minutes later for fluorescence of nasal discharge; if present, this confirms CSF rhinorrhea. This procedure is not usually performed by emergency physicians.

Treatment

Prehospital Care

  • ABCs are first priority. If necessary, hold airway open by chin lift or jaw thrust. Avoid nasotracheal route of intubation because of the risk of intracranial tube placement.
  • Place patient on a backboard and collar if cervical spine injury is suspected.
  • Treat hypoventilation with intubation and bag ventilation.
  • Control actively bleeding wounds with direct pressure.

Emergency Department Care

  • ABCs take priority. Reassess airway frequently. Early intubation, before edema occurs, can make airway control much easier than waiting until a problem arises from obstruction. When intubation by oral route is impossible, perform cricothyroidotomy to secure airway.
  • Before using paralytics in an intubation, carefully evaluate the ability to manage the airway with a bag and mask or laryngeal airway. If unable to manage the airway, do not paralyze the patient. Fiber optic guides or bronchoscopic-guided intubation may be an option. If in doubt, prepare for a cricothyrotomy before attempting the airway with either sedation or paralytics.
  • Avoid the temptation to focus on the obvious facial deformity, thereby failing to perform a complete primary survey. Other life-threatening conditions need to be diagnosed rapidly and appropriate resuscitation undertaken. Follow this with a complete secondary survey.
  • Evaluation of facial fractures is part of the secondary survey.
  • Once the cervical spine has been cleared allow the patient to sit with suction available to facilitate maintenance of the airway.
  • Epistaxis may require anterior nasal packing to control bleeding. Posterior packing occasionally may be needed.
  • Drain septal hematomas to avoid necrosis of septal cartilage.

Consultations

  • Refer patients with facial fractures to an oral and maxillofacial surgeon, ear, nose, and throat (ENT) surgeon, or plastic surgeon who is experienced in care of these injuries.
  • Consult a neurosurgeon if a CSF leak is diagnosed or suspected.
  • Refer care of patients with multiple injuries to a surgeon with experience in trauma care. If a surgeon with trauma experience is not available, transfer patient to a higher-level trauma center.
  • The incidence of posttraumatic stress disorder is high in patients with facial injuries, and consultation with a psychiatrist should be considered.

Medication

When airway control is needed, rapid sequence induction often is the preferred method. Perform rapid sequence induction, using medications to induce unconsciousness and muscle paralysis to facilitate intubation. A cricothyroidotomy kit should be at bedside if oral intubation cannot be accomplished.

Provide adequate analgesia, including opioids, NSAIDs, or local anesthetics. Prophylactic antibiotics are controversial when a CSF leak is identified or when the fracture involves the sinuses. It is usually left to the discretion of the specialist assuming care of the patient. If the nares has been packed for epistaxis, prophylactic antibiotics should be used to prevent infection, including toxic shook syndrome. If the patient has an open wound, update tetanus immunization.

Nonsteroidal anti-inflammatory agents (NSAIDs)

These drugs are used most commonly for relief of mild to moderately severe pain. Effects of NSAIDs in treatment of pain tend to be patient specific, yet ibuprofen is usually DOC for initial therapy. Other options include flurbiprofen, ketoprofen, and naproxen.


Ibuprofen (Ibuprin, Advil, Motrin)

Usually DOC for treatment of mild to moderately severe pain, if no contraindications. Inhibits inflammatory reactions and pain, probably by decreasing activity of enzyme cyclooxygenase, which inhibits prostaglandin synthesis.

Dosing

Adult

200-400 mg PO q4-6h prn; not to exceed 3.2 g/d

Pediatric

<6 months: Not established
6 months to 12 years: 20-40 mg/kg/d PO divided tid/qid
>12 years: Administer as in adults

Interactions

Aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity; may decrease effects of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT in patients taking anticoagulants—monitor PT closely and instruct patients to watch for signs of bleeding; may increase risk of methotrexate toxicity; may increase phenytoin levels

Contraindications

Documented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; high risk of bleeding

Precautions

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in coagulation abnormalities or during anticoagulant therapy


Naproxen (Anaprox, Naprelan, Naprosyn)

For relief of mild to moderately severe pain. Inhibits inflammatory reactions and pain by decreasing activity of enzyme cyclooxygenase, which decreases prostaglandin synthesis.

Dosing

Adult

500 mg PO followed by 250 mg q6-8h; not to exceed 1.25 g/d

Pediatric

<2 years: Not established
>2 years: 2.5 mg/kg/dose PO; not to exceed 10 mg/kg/d

Interactions

Aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity; may decrease effects of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT in patients taking anticoagulants—monitor PT closely and instruct patients to watch for signs of bleeding; may increase risk of methotrexate toxicity; may increase phenytoin levels

Contraindications

Documented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency

Precautions

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Acute renal insufficiency, interstitial nephritis, hyperkalemia, hyponatremia, and renal papillary necrosis may occur; patients with preexisting renal disease or compromised renal perfusion risk acute renal failure; leukopenia occurs rarely, is transient, and usually returns to normal during therapy; persistent leukopenia, granulocytopenia, or thrombocytopenia warrants further evaluation and may require discontinuation of drug


Flurbiprofen (Ansaid)

Has analgesic, antipyretic, and anti-inflammatory effects. May inhibit cyclooxygenase enzyme, inhibiting prostaglandin biosynthesis.

Dosing

Adult

200-300 mg/d PO divided bid/qid

Pediatric

Not established

Interactions

Aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity; may decrease effects of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT in patients taking anticoagulants—monitor PT closely and instruct patients to watch for signs of bleeding; may increase risk of methotrexate toxicity; may increase phenytoin levels

Contraindications

Documented hypersensitivity

Precautions

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Acute renal insufficiency, interstitial nephritis, hyperkalemia, hyponatremia, and renal papillary necrosis may occur; patients with preexisting renal disease or compromised renal perfusion risk acute renal failure; leukopenia occurs rarely, is transient, and usually returns to normal during therapy; persistent leukopenia, granulocytopenia, or thrombocytopenia warrants further evaluation and may require discontinuation of drug


Ketoprofen (Oruvail, Orudis, Actron)

Used for relief of mild to moderately severe pain and inflammation. Administer small dosages initially to patients with small bodies, older persons, and those with renal or liver disease. Doses higher than 75 mg do not increase therapeutic effects. Administer high doses with caution and closely observe patients for response.

Dosing

Adult

25-50 mg PO q6-8h prn; not to exceed 300 mg/d

Pediatric

<3 months: Not established
3 months to 14 years: 0.1–1 mg/kg PO q6-8h
>12 years: Administer as in adults

Interactions

Aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity; may decrease effects of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT in patients taking anticoagulants—monitor PT closely and instruct patients to watch for signs of bleeding; may increase risk of methotrexate toxicity; may increase phenytoin levels

Contraindications

Documented hypersensitivity

Precautions

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in coagulation abnormalities or during anticoagulant therapy

Analgesics

Pain control is essential to quality patient care. It ensures patient comfort, promotes pulmonary toilet, and aids physical therapy regimens. Many analgesics have sedating properties that benefit patients who have sustained fractures.


Acetaminophen (Tylenol, Panadol, aspirin-free Anacin)

DOC for treatment of pain in patients with documented hypersensitivity to aspirin and NSAIDs, those with upper GI disease, or those taking oral anticoagulants.

Dosing

Adult

325-650 mg PO q4-6h or 1000 mg tid/qid; not to exceed 4 g/d

Pediatric

<12 years: 10-15 mg/kg/dose PO q4-6h prn; not to exceed 2.6 g/d
>12 years: 325-650 mg PO q4h; not to exceed 5 doses/d

Interactions

Rifampin can reduce analgesic effects; barbiturates, carbamazepine, hydantoins, and isoniazid may increase hepatotoxicity

Contraindications

Documented hypersensitivity; known G-6-P deficiency

Precautions

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Hepatotoxicity possible in chronic alcoholics following various dose levels; severe or recurrent pain or high or continued fever may indicate a serious illness; acetaminophen is contained in many OTC products, and combined use with these products may result in cumulative acetaminophen doses exceeding recommended maximum dose


Acetaminophen and codeine (Tylenol #3)

Drug combination indicated for treatment of mild to moderately severe pain.

Dosing

Adult

30-60 mg based on codeine content PO q4-6h or 1-2 tabs q4h; not to exceed 12 tabs/d

Pediatric

0.5-1 mg/kg/dose based on codeine content PO q4-6h; 10-15 mg/kg/dose based on acetaminophen content; not to exceed 2.6 g/d of acetaminophen

Interactions

CNS depressants or tricyclic antidepressants increase toxicity

Contraindications

Documented hypersensitivity

Precautions

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in patients dependent on opiates since this substitution may result in acute opiate-withdrawal symptoms; caution in severe renal or hepatic dysfunction


Hydrocodone bitartrate and acetaminophen (Vicodin ES)

Drug combination indicated for relief of moderately severe to severe pain.

Dosing

Adult

1-2 tab/cap PO q4-6h prn

Pediatric

<12 years: 10-15 mg/kg/dose acetaminophen PO q4-6h prn; not to exceed 2.6 g/d of acetaminophen
>12 years: 750 mg acetaminophen PO q4h; single dose not to exceed 10 mg of hydrocodone bitartrate; not to exceed 5 doses/d

Interactions

Phenothiazines may decrease analgesic effects; CNS depressants or tricyclic antidepressants increase toxicity

Contraindications

Documented hypersensitivity; high-altitude cerebral edema; elevated intracranial pressure

Precautions

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Tablets contain metabisulfite which may cause hypersensitivity; caution in patients dependent on opiates since this substitution may result in acute opiate-withdrawal symptoms; caution in severe renal or hepatic dysfunction


Oxycodone and acetaminophen (Percocet)

Drug combination indicated for relief of moderately severe to severe pain. DOC for aspirin-hypersensitive patients.

Dosing

Adult

1-2 tab/cap PO q4-6h prn

Pediatric

0.05-0.15 mg/kg/dose oxycodone PO q4-6h prn; not to exceed 5 mg/dose of oxycodone

Interactions

Phenothiazines may decrease analgesic effects; CNS depressants or tricyclic antidepressants increase toxicity

Contraindications

Documented hypersensitivity

Precautions

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Duration of action may increase in elderly persons; be aware of total daily dose of acetaminophen patient is receiving; do not exceed 4000 mg/24 h of acetaminophen; higher doses may cause liver toxicity


Oxycodone and aspirin (Percodan)

Drug combination indicated for relief of moderately severe to severe pain.

Dosing

Adult

1-2 tab/cap PO q4-6h prn

Pediatric

0.05-0.15 mg/kg/dose oxycodone PO q4-6h prn; not to exceed 5 mg/dose of oxycodone

Interactions

Phenothiazines may decrease analgesic effects; CNS depressants or tricyclic antidepressants increase toxicity; may potentiate anticoagulant effects of warfarin

Contraindications

Documented hypersensitivity; liver damage; hypoprothrombinemia; vitamin K deficiency; bleeding disorders; asthma
Because of association of aspirin with Reye syndrome, do not use in children (<16 y) who have flu

Precautions

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Duration of action may increase in elderly persons; caution in renal or liver impairment, peptic ulcer disease, and erosive gastritis


Morphine sulfate (Duramorph, Astramorph, MS Contin)

DOC for narcotic analgesia due to its reliable and predictable effects, safety, and ease of reversibility with naloxone. Morphine sulfate administered IV may be dosed in a number of ways and commonly is titrated until desired effect obtained.

Dosing

Adult

Starting dose: 0.1 mg/kg IV/IM/SC
Maintenance dose: 5-20 mg/70 kg IV/IM/SC q4h
Relatively hypovolemic patients: Start with 2 mg IV/IM/SC and reassess hemodynamic effects of dose

Pediatric

Neonates: 0.05-0.2 mg/kg IV prn
Children: 0.1-0.2 mg/kg IV q2-4h prn

Interactions

Phenothiazines may antagonize analgesic effects; tricyclic antidepressants, MAOIs, and other CNS depressants may potentiate adverse effects

Contraindications

Documented hypersensitivity; hypotension; potentially compromised airway in which establishing rapid airway control would be difficult

Precautions

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Avoid in hypotension, respiratory depression, nausea, emesis, constipation, and urinary retention; caution in atrial flutter and other supraventricular tachycardias; has vagolytic action and may increase ventricular response rate

Antibiotics

Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.


Cephalexin (Biocef, Keflex, Keftab)

First-generation cephalosporin that inhibits bacterial replication by inhibiting bacterial cell wall synthesis. Bactericidal and effective against rapidly growing organisms forming cell walls.
Resistance occurs by alteration of penicillin-binding proteins. Effective for treatment of infections caused by streptococcal or staphylococci, including penicillinase-producing staphylococci. May use to initiate therapy when streptococcal or staphylococcal infection is suspected.
Used orally when outpatient management is indicated.

Dosing

Adult

250-1000 mg PO q6h; not to exceed 4 g/d

Pediatric

25-50 mg/kg/d PO q6h; not to exceed 3 g/d

Interactions

Coadministration with aminoglycosides increases nephrotoxic potential

Contraindications

Documented hypersensitivity

Precautions

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in severe renal insufficiency (high doses may cause CNS toxicity); superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy


Sulfamethoxazole and trimethoprim (Bactrim, Bactrim DS, Septra, Septra DS)

Inhibits bacterial growth by inhibiting synthesis of dihydrofolic acid.

Dosing

Adult

160 mg (trimethoprim)/800 mg (sulfamethoxazole) PO q12h (ie, 1 double-strength [DS] tab q12h)

Pediatric

5-10 mg/kg/d (based on trimethoprim component) PO divided bid

Interactions

May increase PT when used with warfarin (perform coagulation tests and adjust dose accordingly); coadministration with dapsone may increase blood levels of both drugs; coadministration of diuretics increases incidence of thrombocytopenia purpura in elderly persons; phenytoin levels may increase with coadministration; may potentiate effects of methotrexate in bone marrow depression; hypoglycemic response to sulfonylureas may increase with coadministration; may increase levels of zidovudine

Contraindications

Documented hypersensitivity; megaloblastic anemia due to folate deficiency

Precautions

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Do not use during last trimester of pregnancy because of potential toxicity to newborn (eg, jaundice, hemolytic anemia, kernicterus)
Dosage adjustments (adult adjustments)
CrCl (mL/min) 80-50: Recommended IV dose q18h
CrCl 50-10: Recommended IV dose q24h
CrCl <10: Not recommended
HD: 4-5 mg/kg after HD
During peritoneal dialysis: 0.16-0.8 g q48h
Discontinue at first appearance of skin rash or sign of adverse reaction; obtain CBCs frequently; discontinue therapy if significant hematologic changes occur; goiter, diuresis, and hypoglycemia may occur with sulfonamides; prolonged IV infusions or high doses may cause bone marrow depression (if signs occur, give 5-15 mg/d leucovorin); caution in folate deficiency (eg, chronic alcoholics, elderly persons, those receiving anticonvulsant therapy, or those with malabsorption syndrome); hemolysis may occur in G-6-PD deficiency; patients with AIDS may not tolerate or respond to TMP-SMZ; caution in renal or hepatic impairment (perform urinalyses and renal function tests during therapy); give fluids to prevent crystalluria and stone formation


Amoxicillin and clavulanate (Augmentin, Augmentin XR)

Amoxicillin inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins. Addition of clavulanate inhibits beta-lactamase producing bacteria.
Good alternative antibiotic for patients allergic or intolerant to the macrolide class. Usually is well tolerated and provides good coverage to most infectious agents. Not effective against Mycoplasma and Legionella species. The half-life of oral dosage form is 1-1.3 h. Has good tissue penetration but does not enter cerebrospinal fluid.
For children > 3 months, base dosing protocol on amoxicillin content. Because of different amoxicillin/clavulanic acid ratios in 250-mg tab (250/125) vs 250-mg chewable tab (250/62.5), do not use 250-mg tab until child weighs >40 kg.

Dosing

Adult

875 mg PO bid for 7-10 d

Pediatric

<3 months: 125 mg/5 mL PO susp based on amoxicillin; 30 mg/kg/d divided bid for 7-10 d
>3 months: if using 200 mg/5 mL or 400 mg/5 mL susp, 45 mg/kg/d PO q12h; if using 125 mg/5 mL or 250 mg/5 mL susp, 40 mg/kg/d PO q8h for 7-10 d
>40 kg: Administer as in adults

Interactions

Coadministration with warfarin or heparin, increases risk of bleeding; may act synergistically against selected microorganisms when coadministered with aminoglycosides; coadministration with allopurinol may increase incidence of amoxicillin rash; may decrease efficacy of oral contraceptives when administered concomitantly

Contraindications

Documented hypersensitivity

Precautions

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Hepatic impairment may occur with prolonged treatment in elderly persons; diarrhea may occur; adjust dose in renal impairment; cross allergy may occur with other beta-lactams and cephalosporins

Anxiolytics

Patients with painful injuries usually experience significant anxiety. Anxiolytics allow a smaller analgesic dose to achieve the same effect.


Lorazepam (Ativan)

Sedative hypnotic in benzodiazepine class that has short onset of effect and relatively long half-life. By increasing action of GABA, a major inhibitory neurotransmitter, may depress all levels of CNS, including limbic and reticular formation. Excellent for sedating patients for longer than 24-h period. Monitor patient's BP after administering dose. Adjust as necessary.

Dosing

Adult

Initial dose: 2 mg total or 0.044 mg/kg IV, whichever is smaller

Pediatric

0.05-0.1 mg/kg IV slowly q2-5min; may repeat dose of 0.05 mg/kg IV slowly

Interactions

Alcohol, phenothiazines, barbiturates, and MAOIs increase toxicity

Contraindications

Documented hypersensitivity; preexisting CNS depression; hypotension; narrow-angle glaucoma

Precautions

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in renal or hepatic impairment, myasthenia gravis, organic brain syndrome, or Parkinson disease

Follow-up

Further Inpatient Care

  • Patients with NOE fractures generally require admission to monitor for a CSF leak and observe for signs of meningitis or brain abscess, which are known complications.
  • Patients with zygomatic arch fractures who have significant trismus or inability to open the mouth may require admission for observation because of potential problems with aspiration or airway obstruction from vomiting.
  • Patients with tripod fractures with eye involvement generally require admission to ophthalmology.
  • Patients with Le Fort fractures may require admission for further workup prior to open reduction and internal fixation. Patients also may need a short admission if arch wires are used, because of the risk of obstruction or aspiration should they vomit. During the hospital stay, teach patients how to remove the crossband so the mouth can be opened if they need to vomit.
  • Patients with multiple traumas should be admitted to a surgeon with trauma experience to coordinate care of all injuries.
  • The incidence of posttraumatic stress disorder is high in patients with facial injuries, and consultation with a psychiatrist should be considered.

Further Outpatient Care

  • Patients with simple nasal fractures can be discharged home with follow-up in 5-7 days when edema has decreased. Avoid delaying follow-up care, because fracture healing may begin prior to a necessary reduction. Give patients epistaxis instructions and instruct to return if clear fluid from nose is noted.
  • Patients with simple zygomatic arch fractures, without trismus or mouth opening problems, can be discharged home with proper follow-up care.
  • Patients with tripod fractures without eye involvement can be discharged home with appropriate follow-up care.

Inpatient & Outpatient Medications

  • Facial fractures tend to be very painful. Provide adequate analgesia, including oral opioids and NSAIDs. If nasal packing is used, antibiotics are generally used to prevent toxic shock.

Transfer

  • If appropriate specialists are not available, transfer the patient to a higher-level hospital. This is particularly important in patients with multiple injuries.

Deterrence/Prevention

  • Use of seatbelts and airbags can reduce incidence of facial injuries in motor vehicle accidents. Use of helmets with facial guards can reduce injury in motorcycle accidents and in accidents in such sports as skiing, snowboarding, hockey, and football.

Complications

  • Continued CSF leaks can occur, although most stop by 2-3 weeks after the injury.
  • Meningitis and abscesses are serious infections that can occur when a CSF leak is present. Observe patients closely for signs and symptoms.
  • Sepsis
  • Scars and facial deformity
  • Injury to infraorbital nerve in tripod and Le Fort II fractures that extends through the infraorbital foramen where the nerve exits
  • Posttraumatic stress disorder

Patient Education

  • If band arch wires are placed, teach patients how to release the crossband in an emergency.
  • Give instructions for epistaxis if this has occurred.
  • Discuss the risk of posttraumatic stress disorder.
  • For excellent patient education resources, visit eMedicine's Back, Ribs, Neck, and Head Center and Breaks, Fractures, and Dislocations Center. Also, see eMedicine's patient education articles Black Eye.

Miscellaneous

Medicolegal Pitfalls

  • Failure to diagnose fractures correctly or fully
  • Failure to diagnose associated intracranial, intrathoracic, intraabdominal, or cervical spine injuries. This occurs when the physician focuses on an obvious injury, missing a life-threatening injury because a complete workup in the secondary survey was never completed.
  • Failure to evaluate associated ocular injuries adequately

Special Concerns

  • Always consider loss of airway and cervical spine, intracranial, and intraabdominal injuries.
  • Evaluate possibility of eye injury.
  • Carefully evaluate eye and extraocular muscle function.

References

  1. Glynn SM, Asarnow JR, Asarnow R, et al. The development of acute post-traumatic stress disorder after orofacial injury: a prospective study in a large urban hospital. J Oral Maxillofac Surg. Jul 2003;61(7):785-92. [Medline].

  2. Hendler BH. Maxillofacial trauma. In: Rosen P, ed. Emergency Medicine Concepts and Clinical Practice. Mosby-Year Book; 1998:1093-1103.

  3. McGill J, Ling LJ, Taylor S. Facial trauma. In: Rosen P, ed. Diagnostic Radiology in Emergency Medicine. Mosby-Year Book; 1992:51-76.

  4. Smith RG. Maxillofacial injuries. In: Harwood-Nuss A, ed. The Clinical Practice of Emergency Medicine. Lippincott, Williams and Wilkins; 1991:337-343.

  5. Snell RS, Smith MS. The face, scalp, and mouth. In: Clinical Anatomy for Emergency Medicine. Mosby-Year Book; 1993:206-241.

  6. Spoor TC, Ramocki JM, Kwito GM. Ocular trauma. In: Wilson RF, Walt AJ, eds. Management of Trauma: Pitfalls and Practice. Lippincott, Williams & Wilkins; 1996:225-241.

  7. Sullivan WG. Trauma to the face. In: Wilson RF, Walt AJ, eds. Management of Trauma: Pitfalls and Practice. 2nd ed. Lippincott, Williams & Wilkins; 1996:242-269.

  8. Thomas, SH, Sheperd, SM. Maxillofacial injuries. In: Harwood- Nuss, ed. The Clinical Practice of Emergency Medicine. Lippincott, Williams & Wilkins; 1996:408-18.

  9. McCay MP. Facial trauma. In: Marx JA, Hockberger RS, Walls RM, et al, eds. Rosen's Emergency Medicine, Concepts and Clinical Practice. Vol 1. 6th ed. Philadelphia, PA: Mosby; 2006:39, 382-398.

  10. Hasan N, Colucciello SA. Maxillofacial trauma. In: Tintinalli JE, Gabor KD, Stapczynski SJ, eds. Emergency Medicine: A Comprehensive Study Guide. 6th ed. McGraw-Hill Co Inc; 2004:chap 257, p1583-159.

Keywords

face fracture, facial fracture, facial injury, alveolar fracture, Le Fort fracture, maxillofacial fracture, nasal fracture, zygoma fracture, simple nasal fracture, zygomatic arch fractures, zygomaticomaxillary fracture, tripod fractures, nasoethmoidal fractures, midface fracture  

Contributor Information and Disclosures

Author

Thomas Widell, MD, Vice Chairman, Assistant Professor, Department of Emergency Medicine, Rosalind Franklin School of Medicine/The Chicago Medical School, North Chicago, Illinois; Associate Residency Director, University of Chicago Emergency Medicine Program, Chicago, Illinois; Program Director Emergency Medical Education, Attending Physician, Mount Sinai Hospital Medical Center, Chicago, Illinois
Disclosure: Nothing to disclose.

Medical Editor

Francis Counselman, MD, Program Director, Chair, Professor, Department of Emergency Medicine, Eastern Virginia Medical School
Francis Counselman, MD is a member of the following medical societies: American College of Emergency Physicians and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Tom Scaletta, MD, Past-President, American Academy of Emergency Medicine; Chairperson, Department of Emergency Medicine, Edward Hospital; Assistant Professor of Emergency Medicine, Rush Medical College and Cook County Hospital
Tom Scaletta, MD is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

Steven C Dronen, MD, FAAEM, Director of Emergency Services, Director of Chest Pain Center, Department of Emergency Medicine, Ft Sanders Sevier Medical Center
Steven C Dronen, MD, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

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