eMedicine Specialties > Sports Medicine > Face and Head

Facial Fractures: Treatment & Medication

Author: Timothy J Rupp, MD, FACEP, Associate Medical Director, Physicians Emergency Care Associates, Methodist Health System, Dallas, Texas; Staff Physician, Innovative Emergency Medicine, Frisco, Texas; Staff Physician, Department of Emergency Medicine, Children's Medical Center of Dallas, Dallas, Texas
Coauthor(s): Steven Karageanes, DO, Director, Primary Care Sports Medicine Fellowship, Director, Sports Medicine Education, Center for Orthopedics and Neuroscience; Department of Medical Education, Oakwood Healthcare System
Contributor Information and Disclosures

Updated: Mar 14, 2008

Treatment

Acute Phase

Medical Issues/Complications

  • Frontal fracture: Repair of the anterior wall may be delayed, but posterior wall fractures require immediate neurosurgical evaluation. The decision regarding whether prophylaxis with antibiotics is needed should be left to the consulting surgeon.
  • Orbital fracture: The initial treatment is generally supportive, including head elevation, ice, and analgesics. The indications for surgical repair are controversial and may include diplopia that persists 2 weeks after the injury, large fractures, and enophthalmos. Orbital fractures that result in inferior rectus muscle entrapment, inferior orbital nerve entrapment, enophthalmus, or orbital dystopia may result in both cosmetic and functional impairment and should be referred to a specialist (ie, ophthalmologist, oral-maxillofacial surgeon, or plastic surgeon) within 24 hours to insure prompt resolution.10
  • Nasal fracture: An angulated nasal fracture can be reduced by exerting firm, quick pressure with the thumbs toward the midline or by inserting a soft probe in the nares to elevate the depressed or deviated septum into anatomic position.5 Ongoing management of these injuries consists of control of epistaxis and supportive care with analgesics. Operative repair is best performed early, within 1-2 hours following the injury, or in 10-14 days following the injury once the swelling and edema has receded. Any open wounds require antibiotics.
  • Zygomatic/zygomaticomaxillary fracture: Open reduction and internal fixation to restore the normal contour is the standard of care.
  • Maxillary (Le Fort) fracture: Open reduction with internal fixation is the standard. If CSF rhinorrhea is present, a neurosurgeon should be consulted. Prophylactic antibiotics are warranted if the fracture extends through the tooth-bearing region or through the nasal or sinus mucosa.
  • Mandibular fracture: Most cases require admission with fixation. These fractures often require antibiotics because of their location in the tooth-bearing region. Penicillin or clindamycin are acceptable choices.

Related Medscape topics:
Resource Center Sepsis
Resource Center Wound Management

Consultations

Once a fracture has been identified, an appropriate surgeon or specialist (ie, plastic surgeon; ophthalmologist; ear, nose, and throat specialist; oral-maxillofacial surgeon; or neurosurgeon) provides the definitive care.

Medication

The goals of pharmacotherapy are to reduce morbidity and prevent complications.

Analgesics

Pain control is essential to quality patient care. Analgesics ensure patient comfort and have sedating properties, which are beneficial for patients who have sustained injuries.

Related Medscape topics:
Resource Center Pain Management: Advanced Approaches to Chronic Pain Management
Resource Center Pain Management: Pharmacologic Approaches


Ibuprofen (Motrin, Ibuprin)

DOC for patients with mild to moderate pain. Inhibits inflammatory reactions and pain by decreasing prostaglandin synthesis.

Adult

400 mg PO q4h or 800 mg PO q8h; not to exceed 2400 mg qd

Pediatric

4-10 mg/kg PO q6-8h prn; not to exceed 50 mg/kg/d

Coadministration with aspirin increases the risk of inducing serious NSAID-related adverse effects; probenecid may increase the concentrations and, possibly, the toxicity of NSAIDs; may decrease the effect of hydralazine, captopril, and beta-blockers; may decrease the diuretic effects of furosemide and thiazides; may increase PT duration when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase the risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently

Documented hypersensitivity; aspirin/NSAID-induced asthma; third trimester of pregnancy

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 patients with congestive heart failure, nasal polyps, hypertension, and decreased renal and hepatic function, and in elderly patients; caution in the presence of coagulation abnormalities or during anticoagulant therapy


Acetaminophen (Feverall, Tylenol, Aspirin Free Anacin)

DOC for pain in patients with a documented hypersensitivity to aspirin or NSAIDs, with upper GI disease, or who are taking PO anticoagulants.

Adult

325-1000 mg PO/PR q4-6h; not to exceed 4 g/d

Pediatric

10-15 mg/kg PO/PR q6-8h prn; not to exceed (if >12 y) 4 g/d

Alcohol, barbiturates, carbamazepine, INH, and phenytoin increase the risk of hepatotoxicity; rifampin decreases acetaminophen efficacy; acetaminophen doses >2 g/d may potentiate the warfarin effect and increase INR

Documented hypersensitivity; known G6PD

Pregnancy

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

Precautions

Hepatotoxicity is possible in people with long-term alcoholism 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 that exceed the recommended maximum dose


Acetaminophen and hydrocodone (Lortab, Norcet, Vicodin, Lorcet HD)

Drug combination indicated for moderate to severe pain.

Adult

1-2 tab PO q4-6h prn; not to exceed 8 tab/d

Pediatric

500/7.5 per 15 mL, 0.6 mg/kg/d PO divided q6-8h; not to exceed 1.25 mg/dose if <2 y, 5 mg/dose if 2-12 y, 10 mg/dose if >12 y

Alcohol and INH increase the risk of hepatotoxicity; anticholinergics and antidiarrheals combination increase the risk of severe constipation; CNS depressants increase the risk of CNS depression; MAOIs increase the risk of severe hypertension; TCAs in combination increases the concentration of both drugs

Documented hypersensitivity; depressed respiratory function; increased ICP; acute abdominal pain; pseudomembranous colitis; toxin-related diarrhea; impaired liver function

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

The tablets contain metabisulfite, which may cause hypersensitivity; caution in patients who are dependent on opiates because this substitution may result in acute opiate withdrawal symptoms; caution in the presence of severe renal or hepatic dysfunction


Aspirin and oxycodone (Percodan, Roxiprin, Codoxy)

Drug combination indicated for the relief of moderate to severe pain.

Adult

1 tab or cap PO q6h

Pediatric

Not established

Phenothiazines may decrease the analgesic effects; conversely, toxicity increases when administered concurrently with CNS depressants or tricyclic antidepressants; may also potentiate the anticoagulant effects of warfarin

Documented hypersensitivity; liver damage; hypoprothrombinemia; vitamin K deficiency; bleeding disorders; asthma; use in children who have the flu and are <16 y (due to the association of aspirin with Reye syndrome)

Pregnancy

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

Precautions

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


Ketorolac (Toradol)

Inhibits prostaglandin synthesis by decreasing the activity of the enzyme cyclooxygenase, which results in decreased formation of prostaglandin precursors.

Adult

30 mg IV/IM q6h; not to exceed 120 mg/d

10 mg PO q4-6h; not to exceed 40 mg/d

Combined duration of PO/IV/IM not to exceed 5 d

Pediatric

Not established

Coadministration with aspirin increases the risk of inducing serious NSAID-related adverse effects; probenecid may increase the concentrations and, possibly, the toxicity of NSAIDs; may decrease the effect of hydralazine, captopril, and beta-blockers; may decrease the diuretic effects of furosemide and thiazides; may increase PT duration when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase the risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently

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

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, hyperkalemia, hyponatremia, interstitial nephritis, and renal papillary necrosis may occur; increases the risk of acute renal failure in patients with preexisting renal disease or compromised renal perfusion; low WBC counts (rare) usually return to normal during ongoing therapy; discontinue therapy if persistent leukopenia, granulocytopenia, or thrombocytopenia occurs


Morphine (Duramorph, Astramorph, MS Contin)

DOC for analgesia because of its reliable and predictable effects, safety profile, and ease of reversibility with naloxone.

Various IV doses are used; commonly titrated until desired effect is obtained.

Adult

10 mg IM/SC q4h prn

Alternatively, 10-30 mg PO q4h or 10-20 mg PR q4h

Pediatric

0.2-0.5 mg/kg PO/PR q4-6h
Alternatively, 0.1-0.2 mg/kg IV/IM/SC q2-4h; not to exceed 15 mg/dose

Anticholinergics increase the risk of severe constipation; buprenorphine blocks the effects of morphine; precipitates withdrawal; cimetidine increases the effects of morphine; CNS depressants increase the risk of CNS depression; MAOIs combination increases the risk of hypotension and respiratory depression; rifampin decreases morphine concentrations; morphine may increase the serum levels of zidovudine

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

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

Antiemetics

Antiemetics are useful in the treatment of symptomatic nausea.


Promethazine (Phenergan, Anergan, Prorex, Phenazine)

Anti-dopaminergic agent that is effective in treating emesis. Blocks postsynaptic mesolimbic dopaminergic receptors in the brain and reduces stimuli to the brainstem reticular system.

Adult

12.5-25 mg PO/IM q4-6h prn

Pediatric

<2 years: Contraindicated

0.25-1 mg/kg PO/IM/PR q4-6h prn; not to exceed 25 mg/dose

May have additive effects when used concurrently with other CNS depressants or anticonvulsants; coadministration with epinephrine may cause hypotension

Documented hypersensitivity; glaucoma, narrow-angle; lactation; children younger than 2 y (incidences of death due to respiratory depression)

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 the presence of impaired liver function, elderly patients, seizure disorder, and asthma


Ondansetron (Zofran)

Selective 5-HT3-receptor antagonist that blocks serotonin both peripherally and centrally. Prevents nausea and vomiting associated with emetogenic cancer chemotherapy (eg, high-dose cisplatin) and complete body radiotherapy.

Adult

4 mg/dose IV

Alternatively, 0.15 mg/kg/dose PO

Pediatric

Not established

Although cytochrome P-450 inducers (eg, barbiturates, rifampin, carbamazepine, phenytoin) can potentially change the half-life and clearance of ondansetron, a dosage adjustment is not usually required

Pregnancy

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

Precautions

Medication is to be administered for prevention of nausea and vomiting, not for rescue of nausea and vomiting

More on Facial Fractures

Overview: Facial Fractures
Differential Diagnoses & Workup: Facial Fractures
Treatment & Medication: Facial Fractures
Follow-up: Facial Fractures
Multimedia: Facial Fractures
References

References

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  2. Boden BP, Tacchetti R, Mueller FO. Catastrophic injuries in high school and college baseball players. Am J Sports Med. Jul-Aug 2004;32(5):1189-96. [Medline].

  3. Schulz RC. Facial Injuries. 2nd ed. Chicago, Ill: Yearbook Medical Publishers, Inc; 1977.

  4. Laskin DM. Protecting the faces of America. J Oral Maxillofac Surg. Apr 2000;58(4):363. [Medline].

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  6. Tanaka N, Hayashi S, Suzuki K, et al. [Clinical study of maxillofacial fractures sustained during sports and games] [Japanese]. Kokubyo Gakkai Zasshi. Sep 1992;59(3):571-7. [Medline].

  7. Iida S, Kogo M, Sugiura T, Mima T, Matsuya T. Retrospective analysis of 1502 patients with facial fractures. Int J Oral Maxillofac Surg. Aug 2001;30(4):286-90. [Medline].

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  9. Reyes Mendez D, Lapointe A. Nasal trauma and fractures in children. UpToDate [serial online]. May 2007;Accessed September 14, 2007. Available at www.UpToDate.com.

  10. Neuman MI, Bachur RG. Orbital fractures. UpToDate [serial online]. September 2006;Accessed September 14, 2007. Available at www.UpToDate.com.

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Further Reading

Keywords

maxillofacial fractures, tripod fractures, tetrapod fractures, blow-in fractures, blow-out fractures, blow out fractures, broken jaw, broken cheek, broken nose, Le Fort fracture, LeFort fracture, face fracture, nasal fracture, nasal bone fracture, orbital fracture, orbital floor fracture, orbital wall fracture

Contributor Information and Disclosures

Author

Timothy J Rupp, MD, FACEP, Associate Medical Director, Physicians Emergency Care Associates, Methodist Health System, Dallas, Texas; Staff Physician, Innovative Emergency Medicine, Frisco, Texas; Staff Physician, Department of Emergency Medicine, Children's Medical Center of Dallas, Dallas, Texas
Timothy J Rupp, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, Gay and Lesbian Medical Association, Society for Academic Emergency Medicine, and Texas Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

Steven Karageanes, DO, Director, Primary Care Sports Medicine Fellowship, Director, Sports Medicine Education, Center for Orthopedics and Neuroscience; Department of Medical Education, Oakwood Healthcare System
Steven Karageanes, DO is a member of the following medical societies: American Medical Association, American Osteopathic Association, and Michigan State Medical Society
Disclosure: Nothing to disclose.

Medical Editor

Gerard A Malanga, MD, Founder and Director, New Jersey Sports Medicine Institute; Director of Pain Management, Overlook Hospital; Director of Sports Medicine, Sports Medicine Fellowship Director, Mountainside Hospital; Clinical Chief, Rehabilitation Medicine and Electrodiagnosis, St Michael's Medical Center; Medical Director, Consultant, Horizon Healthcare Worker's Compensation Services, Blue Cross and Blue Shield Worker's Compensation
Gerard A Malanga, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Physical Medicine and Rehabilitation, American College of Sports Medicine, North American Spine Society, and Physiatric Association of Spine, Sports and Occupational Rehabilitation
Disclosure: Nothing to disclose.

Pharmacy Editor

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

Managing Editor

Henry T Goitz, MD, Chief, Sports Medicine, Associate Professor, Department of Orthopaedic Surgery, Medical College of Ohio
Henry T Goitz, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons and American Orthopaedic Society for Sports Medicine
Disclosure: Nothing to disclose.

CME Editor

Jon B Whitehurst, MD, Clinical Instructor of Surgery, University of Illinois College of Medicine; Partner and Executive Board Member, Rockford Orthopedic Associates; Orthopedic Chairman, Rockford Memorial Hospital
Jon B Whitehurst, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American Orthopaedic Society for Sports Medicine, and Arthroscopy Association of North America
Disclosure: Nothing to disclose.

Chief Editor

Craig C Young, MD, Professor, Departments of Orthopedic Surgery and Community and Family Medicine, Medical Director of Sports Medicine, Sports Medicine Fellowship Director, Medical College of Wisconsin
Craig C Young, MD is a member of the following medical societies: American Academy of Family Physicians, American College of Sports Medicine, American Medical Society for Sports Medicine, Phi Beta Kappa, and Wilderness Medical Society
Disclosure: Nothing to disclose.

 
 
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