Moccasin Envenomation Follow-up

  • Author: Sean P Bush, MD, FACEP; Chief Editor: Rick Kulkarni, MD   more...
 
Updated: May 3, 2011
 

Further Inpatient Care

Patients believed to have dry bites, in which no venom effects develop, should be observed for at least 8 hours. Close follow-up and/or recheck examination is recommended.

Patients who have minimal snake envenomation may be admitted for overnight observation, or they may be discharged if signs of envenomation do not progress for at least 8 hours.

Patients whose envenomation is severe enough to require antivenom should be admitted.

Several reports in the literature have documented instances in which patients who were initially discharged with a mild envenomation returned in several hours with significant injury and required antivenom and admission. However, because the denominator (patients who go home with no progression) is not known, it is unclear whether the strategy of admitting all patients with mild envenomation is cost-effective.

Regardless of the period of observations, patients who are discharged should be instructed to return to the hospital if pain or swelling increase or if new symptoms develop. Because patients at home rarely elevate their envenomated limbs consistently, some increase in swelling is expected during the first 1-3 days after the patient goes home. If not accompanied by increasing pain or other signs/symptoms, this is not a concern.

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Further Outpatient Care

Discharge instructions should include the following:

  • Keep the envenomated extremity elevated.
  • Return immediately if swelling worsens or pain becomes severe.
  • Return immediately if any abnormal bleeding or bruising, dark tarry stools, or severe headache occurs.
  • Return for signs of wound infection, such as fever, worsening redness, or swelling immediately adjacent to the bite site, or drainage of pus. Because tenderness at the bite site, more generalized swelling, and lymphangitic streaking are common manifestations of the envenomation itself, these are less useful as signs of infection.
  • Return or follow up if a fever, itchy rash, joint pain, or swollen lymph nodes occur any time during the next few weeks.
  • Do not take nonsteroidal anti-inflammatory drugs (NSAIDs), such as aspirin, ibuprofen (Motrin, Advil), or naproxen (Naprosyn, Aleve) for 2 weeks after the snakebite. Acetaminophen (Tylenol) or a prescribed pain medication can be taken.
  • Do not participate in contact sports, undergo elective surgery, or have dental work for 2 weeks after the snakebite.
  • Drink plenty of liquids. Return if urine decreases in amount or becomes cola colored.
  • Referral to a physical therapist or surgeon may be indicated.
  • Patients who developed severe coagulopathy or thrombocytopenia should have these studies rechecked in 3 days, and as needed for signs of coagulation problems (eg, bleeding gums, easy bruising).
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Inpatient & Outpatient Medications

Administer antihistamines and steroids if serum sickness to antivenom develops.

Short courses of opioid pain medications are often required.

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Transfer

If indicated, patients may require transfer after stabilization to a facility where antivenom can be administered.

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Deterrence/Prevention

Never handle a venomous snake, even if it is believed to be dead.

Do not reach or step into places outdoors that are not visible.

At home, remove debris in which snakes might hide (eg, log piles). Remove items, such as bird feeders, that might attract snakes—seeds that fall from bird feeders attract rodents, which attract snakes.

Heavy clothing (such as hiking boots) may retard some strikes.

Young children should be closely supervised, and older children should be educated to avoid snakes.[6]

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Complications

Complications of envenomation may include the following:

  • Bleeding
  • Compartment syndrome
  • Skin and soft tissue necrosis
  • Infection
  • Death

Antivenom-associated complications may include the following:[19]

Immediate hypersensitivity reactions

Anaphylaxis is a type I (immediate) hypersensitivity reaction, which may be life threatening.

Anaphylactoid reactions are histamine release stimulated by rapid infusion of medications, such as antivenom, that do not involve immune system sensitization.

Both anaphylactic and anaphylactoid reactions may be characterized by urticaria, airway swelling, wheezing, and shock. Anaphylactoid reactions are related to the rate of infusion; anaphylactic reactions are not related to rate or dose.

Urticaria occurs in approximately 8% of patients treated with crotaline Fab antivenom; more severe reactions such as wheezing and hypotension occur in approximately 2%.

Immediate hypersensitivity is treated by halting the infusion and administering antihistamines, steroids, and epinephrine as needed. If continued antivenom therapy is necessary, it is often possible to complete the antivenom infusion, after appropriate therapy, at a slower rate.

Delayed hypersensitivity reactions

Urticaria has been reported in approximately 8% of patients treated with crotaline Fab antivenom; wheezing is reported in 2%, and serum sickness in less than 10%.

Serum sickness is a type III (delayed) hypersensitivity reaction.

Serum sickness is characterized by fever, urticaria or petechial rash, lymphadenopathy, and arthritis, that may occur 5 days to 3 weeks after antivenom administration. Although serum sickness is uncomfortable, it is usually benign and self-limited.

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Prognosis

Nearly all patients fully recover after moccasin envenomation.

Some patients have long-term problems with limb pain and/or swelling, particularly after physical exertion. The proportion of patients that develop these sequelae and the impact of antivenom therapy on this incidence are not known.

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Patient Education

Call professionals, such as animal control, to move snakes.

Never attempt to handle, possess, or kill venomous reptiles.

For excellent patient education resources, visit eMedicine's Bites and Stings Center. Also, see eMedicine's patient education article Snakebite.

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Contributor Information and Disclosures
Author

Sean P Bush, MD, FACEP  Professor of Emergency Medicine, Loma Linda University School of Medicine; Consulting Staff, Envenomation Specialist, Department of Emergency Medicine, Loma Linda University Medical Center

Sean P Bush, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians, International Society on Toxicology, Society for Academic Emergency Medicine, and Wilderness Medical Society

Disclosure: Protherics Consulting fee Consulting; Nycomed (formerly Fougera) Grant/research funds Speaking and teaching; Rare Disease Therapeutics Grant/research funds Research; Bioclon Grant/research funds Research

Coauthor(s)

Eric J Lavonas, MD, FACEP  Associate Director, Rocky Mountain Poison and Drug Center; Assistant Professor, University of Colorado School of Medicine

Eric J Lavonas, MD, FACEP is a member of the following medical societies: Alpha Omega Alpha, American Academy of Clinical Toxicology, American College of Emergency Physicians, American College of Medical Toxicology, Colorado Medical Society, Phi Beta Kappa, and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Specialty Editor Board

Robert L Norris, MD  Professor, Department of Surgery, Chief, Division of Emergency Medicine, Stanford University Medical Center

Robert L Norris, MD is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, California Medical Association, International Society of Toxinology, Society for Academic Emergency Medicine, and Wilderness Medical Society

Disclosure: Nothing to disclose.

John T VanDeVoort, PharmD  Regional Director of Pharmacy, Sacred Heart and St Joseph's Hospitals

John T VanDeVoort, PharmD is a member of the following medical societies: American Society of Health-System Pharmacists

Disclosure: Nothing to disclose.

David Eitel, MD, MBA  Associate Professor, Department of Emergency Medicine, York Hospital; Physician Advisor for Case Management, Wellspan Health System, York

David Eitel, MD, MBA is a member of the following medical societies: American College of Emergency Physicians, American Society of Pediatric Nephrology, Society for Academic Emergency Medicine, and Society of Critical Care Medicine

Disclosure: Nothing to disclose.

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

Rick Kulkarni, MD  Attending Physician, Department of Emergency Medicine, Cambridge Health Alliance, Division of Emergency Medicine, Harvard Medical School

Rick Kulkarni, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine

Disclosure: WebMD Salary Employment

References
  1. Wingert WA, Pattabhiraman TR, Cleland R, Meyer P, Pattabhiraman R, Russell FE. Distribution and pathology of copperhead (agkistrodon contortrix) venom. Toxicon. 1980;18(5-6):591-601. [Medline].

  2. Sullivan JB, Wingert WA, Norris RL Jr. North American venomous reptile bites. In: PS Auerbach, ed. Wilderness Medicine: Management of Wilderness and Environmental Emergencies. Vol 2. St. Louis: Mosby-Year Book; 1995:680-709.

  3. Thorson A, Lavonas EJ, Rouse AM, Kerns WP 2nd. Copperhead envenomations in the Carolinas. J Toxicol Clin Toxicol. 2003;41(1):29-35. [Medline].

  4. Bronstein AC, Spyker DA, Cantilena LR Jr, Green J, Rumack BH, Heard SE. 2006 Annual Report of the American Association of Poison Control Centers' National Poison Data System (NPDS). Clin Toxicol (Phila). Dec 2007;45(8):815-917. [Medline].

  5. Spiller HA, Bosse GM. Prospective study of morbidity associated with snakebite envenomation. J Toxicol Clin Toxicol. 2003;41(2):125-30. [Medline].

  6. Bush SP, Thomas TL, et al. Envenomations in children. Pediatr Emerg Med Rep. 1997;2:1-12.

  7. Scharman EJ, Noffsinger VD. Copperhead snakebites: clinical severity of local effects. Ann Emerg Med. Jul 2001;38(1):55-61. [Medline].

  8. Bush SP, Hegewald KG, Green SM, Cardwell MD, Hayes WK. Effects of a negative pressure venom extraction device (Extractor) on local tissue injury after artificial rattlesnake envenomation in a porcine model. Wilderness Environ Med. Fall 2000;11(3):180-8. [Medline].

  9. Bush SP. Snakebite suction devices don't remove venom: they just suck. Ann Emerg Med. Feb 2004;43(2):187-8. [Medline].

  10. Burch JM, Agarwal R, Mattox KL, Feliciano DV, Jordan GL Jr. The treatment of crotalid envenomation without antivenin. J Trauma. Jan 1988;28(1):35-43. [Medline].

  11. Whitley RE. Conservative treatment of copperhead snakebites without antivenin. J Trauma. Aug 1996;41(2):219-21. [Medline].

  12. Dart RC, McNally JT, Spaite DW, Gustafson R. The Sequelae of Pitviper Poisoning in the United States. In: Campbell JA, Brooks DE, editors. Biology of the Pitvipers: Tyler, TX: Selva; 2002:395-404.

  13. Gold BS, Wingert WA. Snake venom poisoning in the United States: a review of therapeutic practice. South Med J. Jun 1994;87(6):579-89. [Medline].

  14. Lavonas EJ, Ruha AM, Banner W, Bebarta V, Bernstein JN, Bush SP, et al. Unified treatment algorithm for the management of crotaline snakebite in the United States: results of an evidence-informed consensus workshop. BMC Emerg Med. Feb 3 2011;11:2. [Medline]. [Full Text].

  15. Dart RC, Seifert SA, Carroll L, Clark RF, Hall E, Boyer-Hassen LV, et al. Affinity-purified, mixed monospecific crotalid antivenom ovine Fab for the treatment of crotalid venom poisoning. Ann Emerg Med. Jul 1997;30(1):33-9. [Medline].

  16. Lawrence WT, Giannopoulos A, Hansen A. Pit viper bites: rational management in locales in which copperheads and cottonmouths predominate. Ann Plast Surg. Mar 1996;36(3):276-85. [Medline].

  17. Ruha AM, Curry SC, Beuhler M, Katz K, Brooks DE, Graeme KA, et al. Initial postmarketing experience with crotalidae polyvalent immune Fab for treatment of rattlesnake envenomation. Ann Emerg Med. Jun 2002;39(6):609-15. [Medline].

  18. Dart RC, Seifert SA, Boyer LV, Clark RF, Hall E, McKinney P, et al. A randomized multicenter trial of crotalinae polyvalent immune Fab (ovine) antivenom for the treatment for crotaline snakebite in the United States. Arch Intern Med. Sep 10 2001;161(16):2030-6. [Medline].

  19. Jurkovich GJ, Luterman A, McCullar K, et al. Complications of Crotalidae Antivenin Therapy. Journal of Trauma. 1998;28:1032-1037.

  20. Lavonas EJ, Gerardo CJ, O'Malley G, Arnold TC, Bush SP, Banner W Jr, et al. Initial experience with Crotalidae polyvalent immune Fab (ovine) antivenom in the treatment of copperhead snakebite. Ann Emerg Med. Feb 2004;43(2):200-6. [Medline].

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Snake envenomations, moccasins. Copperhead (Agkistrodon contortrix). Photo courtesy of Sean Bush, MD.
Snake envenomations, moccasins. Cottonmouth or water moccasin (Agkistrodon piscivorus). Photo courtesy of Sean Bush, MD.
Snake envenomations, moccasins. Copperhead (Agkistrodon contortrix). Photo courtesy of George Bush.
Wound measurement in snakebites. Courtesy of Carolinas Poison Center.
Crotaline treatment algorithm.
 
 
 
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