eMedicine Specialties > Pediatrics: General Medicine > Dermatology

Frostbite: Treatment & Medication

Author: David Cheng, MD, Assistant Professor of Emergency Medicine, Associate Emergency Medicine Residency Director, Associate Medical Director of Emergency Services, University of Arkansas Medical Sciences
Coauthor(s): Tonya M Thompson, MD, MA, Assistant Professor, Departments of Pediatrics and Emergency Medicine; Associate Fellowship Director, Pediatric Emergency Medicine Fellowship; Associate Medical Director, The PULSE Simulation Center, Arkansas Children's Hospital, University of Arkansas for Medical Sciences College of Medicine; Ramy Yakobi, MD, MBA, Medical Director of Emergency Department, Beth Israel/Kings Highway Division; Lecturer, Physician Assistant School, Cornell School of Medicine; Lecturer, Pre-hospital Management of Patient, Cornell/New York Presbyterian Hospital; Director of Emergency Department, New York Community Hospital
Contributor Information and Disclosures

Updated: May 13, 2009

Treatment

Medical Care

  • Address ABCs and life threats before the frostbite.
  • Correct any systemic hypothermia to a core temperature of 34°C before treating the frostbite.
  • The goal of frostbite treatment is to salvage as much tissue as possible, to achieve maximal return of function, and to prevent complications.
  • Remove the patient from cold.
  • Replace wet and constrictive clothing with dry loose clothing.
  • Rewarm the frostbitten area if no danger of refreezing is observed. Walking on frozen frostbitten areas and risking tissue chipping and fracture is considered better than thawing and refreezing.
  • Avoid rubbing the area.
  • Rapid rewarming is the single most effective therapy for frostbite.3 Avoid inadvertent slow rewarming or overheating.
  • Rewarm in circulating water (ie, whirlpool bath) at 40-42°C.
  • Thawing takes about 20-40 minutes for superficial injuries and as long as 1 hour for deep injuries.
  • Treatment is complete when the distal area of the extremity is flushed, soft, and pliable.
  • Encourage active gentle motion of the frostbitten area during the rewarming.
  • Constantly monitor water temperature to ensure it does not exceed 43.3°C.
  • The most common error is premature termination of the rewarming process from noncompliance because of reperfusion pain.
  • Avoid dry heat because of unequal heating, inability to control the temperature, and the tendency to desiccate the tissue.
  • Avoid massaging the area during rewarming because it further traumatizes the injury.
  • Analgesics (eg, ibuprofen, morphine) for pain relief are indicated during and after rewarming.
  • Once the skin is thawed, protect the area from further injury and reexposure to cold. Elevate the area and splint. Change the sterile nonadherent dressing 2-4 times a day. Prevent infection. Aid circulation. Provide rehabilitation.
  • Provide local wound care with dressing changed 2-4 times a day.
  • Apply topical aloe vera cream to all frostbitten areas every 6 hours to inhibit arachidonic cascade, especially thromboxane synthesis. Other arachidonic cascade inhibitor agents currently being investigated include topical methimazole (thromboxane synthetase inhibitor) and topical methylprednisolone acetate (phospholipase A2 inhibitor).
  • Aspirate clear blisters to prevent thromboxane and prostaglandin-mediated tissue damage.
  • In order to avoid desiccation and infection of underlying deep layers, do not debride hemorrhagic blisters.
  • Manage fractures and dislocations conservatively until thawing is complete.
  • Providing medical sympathectomy with intravenous reserpine (alpha-blocking agent) at 0.5 mg into the affected terminal artery for adult patients achieves better pain relief and edema reduction than surgical sympathectomy. The reserpine effect begins in 3-24 hours and persists for 2-4 weeks. However, the intravenous form is no longer available in the United States and has not been used on pediatric patients.
  • Administer tetanus prophylaxis.
  • Antibacterial prophylaxis can be considered because the postthaw edema is predisposed to infection.
    • Frostbite infections tend to involve staphylococci, streptococci, enterococci, and Pseudomonas pathogens.
    • Avoid topical antibiotics because they interfere with the aloe vera cream.
    • Administer penicillin G intravenously every 6 hours for 48-72 hours.
  • Investigational therapy is available. Numerous ancillary modalities have been suggested, but efficacy is questionable because of lack of well-controlled human trials.
    • Thrombolysis using intra-arterial tissue plasminogen activator (t-PA) in deep frostbite to decrease tissue loss via 10% when administered within 24 hours of exposure
    • Limaprost (prostaglandin E1 analogue) as therapeutic vasodilator to increase peripheral blood flow
    • Alpha-blocker buflomedil to increase peripheral blood flow
    • Low molecular weight dextran as antisludging agent to decrease RBC clumping (may be effective if administered very early in the treatment process)
    • Arachidonic acid cascade inhibitors
    • Heparinization
    • Hyperbaric oxygen (anecdotal)
    • Subatmospheric pressure therapy (anecdotal)4
    • Pentoxifylline
    • Vitamin C

Surgical Care

  • The only indication for early surgical intervention is postthaw compartment syndrome warranting fasciotomy.
  • Because of extreme difficulty in differentiating viable tissue from nonviable tissue in the first few weeks after frostbite injury, amputation surgery is best avoided until a complete demarcation and separation of gangrenous tissue occurs. This process normally takes 6-8 weeks. Consider early amputation if liquefaction, moist gangrene, or infection develops in the frostbitten area.
  • Skin grafting may be required.
  • Escharotomy may be appropriate if the eschar is preventing circulation or limb motion.
  • Fasciotomy may be appropriate if elevated compartment pressure occurs.
  • Surgical sympathectomy may be appropriate.
    • Paradoxically, it increases tissue edema formation if performed too early after the frostbite injury.
    • If reserved for 24-48 hours after rewarming, sympathectomy increases peripheral blood flow to salvage tissues.
  • Long-term surgical management includes the following options:
    • Debridement of demarcated nonviable tissue: The demarcation process usually takes 1-3 months from the time of initial exposure.5
    • Skin grafting
    • Reconstruction of nose, ears, fingers, and toes
    • Referral to physical rehabilitation

Consultations

Frostbite treatment is a multidisciplinary process using the following specialists:

  • Pediatric emergency medicine physician to stabilize the patient
  • Pediatrician to provide inpatient medical treatment
  • Surgeon to provide the surgical care
  • Physical therapist to provide the rehabilitation
  • Psychiatrist to help the child and family cope with any permanent disability

Diet

  • No restriction on diet is required, but a high-protein, high-calorie diet is suggested to promote healing.

Activity

  • Rest the injured area initially.
  • Elevate injured area to reduce swelling.
  • Perform physical therapy to increase flexibility and dexterity once the injury begins to heal.

Medication

The goal of medical management is to rewarm the injury as quickly as possible, provide pain control during the rewarming, reduce reperfusion injury, prevent frostbite complications, and decrease long-term sequelae.

Analgesics

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


Ibuprofen (Advil, Motrin)

Blocks synthesis of thromboxane/prostaglandins to reduce reperfusion injury. Prevents platelet aggregation. Preferable to aspirin because not associated with Reye syndrome.

Adult

400 mg PO q4-6h, 600 mg q6h, or 800 mg q8h while symptoms persist; not to exceed 3.2 g/d

Pediatric

20-40 mg/kg/d PO divided tid/qid

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

Pregnancy

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

Precautions

Category D in third trimester of pregnancy; caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy


Morphine (Duramorph, MS Contin)

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

Adult

Starting dose: 0.1 mg/kg IV/IM/SC
Maintenance dose: 5-20 mg/70 kg IV/IM/SC q4h

Pediatric

Neonates: 0.05-0.2 mg/kg IV q4h prn
Infants and children: 0.1-0.2 mg/kg IV q4h prn

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

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

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

Herbal products

These agents are applied to debrided blisters and intact hemorrhagic blisters to minimize thromboxane synthesis.


Aloe vera

Inhibits arachidonic cascade, especially thromboxane synthesis.

Adult

Apply 70% concentration to affected area q6h

Pediatric

Administer as in adults

Applying topically with corticosteroids may enhance anti-inflammatory activity in the skin

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

For external use only

Antibiotics

Antibiotic prophylaxis must be comprehensive and should cover all likely pathogens in the context of the clinical setting.


Penicillin G (Pfizerpen, Wycillin, Permapen)

Interferes with synthesis of cell wall mucopeptide during active multiplication, resulting in bactericidal activity against susceptible microorganisms.

Adult

12-18 million U/d IV divided q4h

Pediatric

50,000 U/kg IV q6h for 48-72 h

Pregnancy

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

Precautions

Caution in impaired renal function

Immunizing agents

These agents are used to treat any person with a wound that might be contaminated with tetanus spores.


Tetanus immunoglobulin (Hyper-Tet)

Used for passive immunization in patients who have not been previously vaccinated for tetanus.

Adult

250-500 U IM in opposite extremity to tetanus toxoid

Pediatric

250 U IM in opposite extremity to tetanus toxoid

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

Antibodies in the globulin preparation may interfere with immune response to vaccination; persons with isolated IgA deficiency have potential for developing antibodies to IgA and could have anaphylactic reactions to subsequent administration of blood products that contain IgA; do not perform skin testing because intradermal injection of concentrated gamma globulin may cause localized area of inflammation and can be misinterpreted, causing the medication to be withheld from a patient not allergic to this material; true allergic responses to human gamma globulin administered in prescribed IM manner are extremely rare; do not admix with other medications because usually incompatible


Diphtheria-tetanus toxoid (DT, Td adsorbed)

Used to induce active immunity against tetanus in selected patients. Immunizing agent of choice for most adults and children >7 y are tetanus and diphtheria toxoids. Necessary to administer booster doses to maintain tetanus immunity throughout life.
Patients who are pregnant should receive only tetanus toxoid, not a product containing diphtheria antigen.
In children and adults, may administer into deltoid or midlateral thigh muscles. In infants, preferred site of administration is the mid thigh laterally.

Adult

Primary immunization: 0.5 mL IM, give 2 injections 4-8 wk apart and a third dose 6-12 mo after second injection
Booster dose: 0.5 mL IM q10y

Pediatric

<7 years: Administer TD
Primary immunization: 0.5 mL IM, administer 2 injections 4-8 wk apart and a third dose 6-12 mo after second injection
>7 years:
Administer as in adults
Booster dose: 0.5 mL (Td) IM q10y

Patients receiving immunosuppressants, including corticosteroids or radiation therapy, may remain susceptible despite immunization because of poor immune response; cimetidine may enhance or augment delayed hypersensitivity responses to skin test antigens; avoid concurrent use of medication with systemic chloramphenicol because it may impair amnestic response to tetanus toxoid; concurrent use of tetanus immunoglobulin may delay development of active immunity by several days (interaction is nevertheless clinically insignificant and does not preclude concurrent use)

Documented hypersensitivity; a history of any type of neurological symptoms or signs following administration of this product; outbreak of poliomyelitis (FDA recommends that elective tetanus immunization be deferred during any outbreak of poliomyelitis because tetanus toxoid injections are an important cause of provocative poliomyelitis)

Pregnancy
Precautions

Do not use to treat actual tetanus infections or for immediate prophylaxis of unimmunized individuals (use instead tetanus antitoxin, preferably human tetanus immunoglobulin); diminished antibody response to active immunization may be observed in patients receiving immunosuppressive therapy; better to defer primary diphtheria immunization until immunosuppressive therapy is discontinued; routine immunization of symptomatic and asymptomatic persons infected with HIV is recommended

More on Frostbite

Overview: Frostbite
Differential Diagnoses & Workup: Frostbite
Treatment & Medication: Frostbite
Follow-up: Frostbite
Multimedia: Frostbite
References
Further Reading

References

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Keywords

frostbite, freezing, high-altitude mountaineering frostbite, freezing injury, general frostbite, cutaneous vasodilation, frostbite injury, reperfusion injury, hypothermia, frostnip, exposure to extreme cold, perniosis, hypothermia, hypoxia, neurapraxia, reperfusion inflammatory injury, edema, cold insensitivity, paresthesia, muscle atrophy, hyperhidrosis, anhidrosis, blister, diabetes mellitus, thyroid disease, vascular disease, treatment, diagnosis

Contributor Information and Disclosures

Author

David Cheng, MD, Assistant Professor of Emergency Medicine, Associate Emergency Medicine Residency Director, Associate Medical Director of Emergency Services, University of Arkansas Medical Sciences
David Cheng, MD is a member of the following medical societies: American College of Emergency Physicians, American Heart Association, Council of Emergency Medicine Residency Directors, International Society for Mountain Medicine, National Association of EMS Physicians, Society for Academic Emergency Medicine, Society of Critical Care Medicine, and Wilderness Medical Society
Disclosure: Nothing to disclose.

Coauthor(s)

Tonya M Thompson, MD, MA, Assistant Professor, Departments of Pediatrics and Emergency Medicine; Associate Fellowship Director, Pediatric Emergency Medicine Fellowship; Associate Medical Director, The PULSE Simulation Center, Arkansas Children's Hospital, University of Arkansas for Medical Sciences College of Medicine
Tonya M Thompson, MD, MA is a member of the following medical societies: Ambulatory Pediatric Association, American Academy of Pediatrics, American College of Emergency Physicians, American Medical Women's Association, Phi Beta Kappa, and Southern Society for Pediatric Research
Disclosure: Nothing to disclose.

Ramy Yakobi, MD, MBA, Medical Director of Emergency Department, Beth Israel/Kings Highway Division; Lecturer, Physician Assistant School, Cornell School of Medicine; Lecturer, Pre-hospital Management of Patient, Cornell/New York Presbyterian Hospital; Director of Emergency Department, New York Community Hospital
Ramy Yakobi, MD, MBA is a member of the following medical societies: American Academy of Emergency Medicine and American College of Emergency Physicians
Disclosure: Nothing to disclose.

Medical Editor

Harold K Simon, MD, MBA, Professor of Pediatrics and Emergency Medicine, Associate Division Director of Pediatric Emergency Medicine, Director of Research, Division of Pediatric Emergency Medicine, Emory University School of Medicine, Children's Healthcare of Atlanta at Egleston
Harold K Simon, MD, MBA is a member of the following medical societies: Ambulatory Pediatric Association, American Academy of Pediatrics, American Pediatric Society, and Sigma Xi
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Wayne Wolfram, MD, MPH, Clinical Associate Professor, Departments of Pediatrics, Children's Hospital and University of Cincinnati
Wayne Wolfram, MD, MPH is a member of the following medical societies: American Academy of Emergency Medicine, American Academy of Pediatrics, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

CME Editor

Daniel Rauch, MD, FAAP, Director, Pediatric Hospitalist Program, Associate Professor, Department of Pediatrics, New York University School of Medicine
Daniel Rauch, MD, FAAP is a member of the following medical societies: Ambulatory Pediatric Association, American Academy of Pediatrics, and Society of Hospital Medicine
Disclosure: Baxter Honoraria Consulting

Chief Editor

Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center
Dirk M Elston, MD is a member of the following medical societies: American Academy of Dermatology
Disclosure: Nothing to disclose.

 
 
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