Lizard Envenomation

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Background

There are 2 extant species of lizards known to be venomous, the Gila monster (Heloderma suspectum, with 2 subspecies) and the Mexican beaded lizard (Heloderma horridum, with 4 subspecies). 

There is ongoing debate regarding possible venom production by some other lizard species such as the Komodo dragon (Varanus komodoensis), but there is no current evidence to support human envenomations by any other lizards,[1] and these will not be further discussed in this article.



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A Gila monster (Heloderma suspectum). Photo by Michael Cardwell.

The Gila monster is found in the desert regions of Arizona, western New Mexico, southeastern California,[2] the southern tip of Nevada, extreme southwestern Utah, and northwestern Mexico. The beaded lizard is found only in Mexico and Guatemala, south of the range of the Gila monster.

Both lizards have heavy bodies with large heads and powerful jaws. The beaded lizard is larger than the Gila monster, reaching almost a meter in length, whereas the Gila monster's maximal size is approximately 0.5 m.



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Close-up of the head of a Gila monster. Clearly evident is the bulging musculature of the jaws, which gives this animal a tenacious bite. Photo by Hol....

Pathophysiology

The venom apparatus is much less sophisticated than that of most venomous snakes. A pair of multilobed labial venom glands (modified submandibular glands) lie in the anterior portion of the lower jaw. Venom is conducted from each lobe through a single duct (H horridum) or a series of ducts (H suspectum) and is deposited into a labial mucosal pocket adjacent to the anterior teeth.[3]

The teeth (approximately 20 per jaw) are grooved and loosely attached to the jaws. Venom is conducted via capillary action along these grooves into the victim's tissues as the lizard bites and chews. The more irritated the lizard is when it bites, the more it salivates and the greater the venom yield. Effective envenomation in humans probably occurs in less than 70% of bites.



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The dentition of a Gila monster. The grooved surfaces of the teeth are evident. These grooves allow for venom movement from the venom glands into the ....

The venoms of these 2 lizards are remarkably similar and contain a number of components, including L-amino acid oxidase, hyaluronidase, phospholipase A, serotonin, and highly active kallikreins that release vasoactive kinins. The venom contains no neurotoxins or any enzymes that significantly affect coagulation. In laboratory animals, the venom is as potent as some rattlesnake venoms. Rare hypersensitivity to helodermatid venom has been reported.[4, 5]

Epidemiology

Frequency

United States

Bites are very infrequent and usually involve captive specimens. A significant number of bites probably go unreported because private keepers of these protected lizards may be reluctant to seek medical attention.

International

No data regarding current incidence of bites by venomous lizards in Mexico are available.

Race

No data are available to support any racial predilection to lizard bites.

Sex

Young males are more likely to intentionally interact with venomous wildlife, and are, therefore at greater risk for bites.

Age

While there are no large studies reporting the age distribution of venomous lizard bites, it is likely that those at greatest risk will be children, adolescents, and young adults. Young children may be at increased risk of bites if they come across a wild Heloderma specimen, as they may not comprehend the risk. Adolescents and young adults may be more prone to intentionally interact with or collect such lizards, despite knowing their venomous nature.

Prognosis

The prognosis is excellent for those with a lizard envenomation, although pain may be an issue for many days. No substantiated deaths caused solely by a Gila monster bite have occurred in the United States.19 It is believed that a prolonged bite received by a small individual, such as an infant or toddler, could result in death.

Severe pain following a helodermatid bite may last many hours and generalized weakness can persist for several days. Described rare complications include shock, myocardial infarction, allergic/anaphylactic reaction, and coagulopathy.[5, 6, 7]

Patient Education

Bitten victims should receive instructions regarding standard wound care, elevation of the bitten extremity, signs and symptoms of infection, and medications to be taken.

Patients should be educated to avoid close interactions with potentially dangerous wildlife in the future.

History

The vast majority of individuals who are bitten by Gila monsters or beaded lizards are intentionally interacting with the animals, and the history of the bite usually is clear.

To help estimate the severity of envenomation, it is important to estimate the length of time the lizard remained attached to the victim. While an effective envenomation can occur with a contact time of a few seconds, if the lizard manages to hang on for a period of minutes, the bite could be very serious, potentially lethal.

The victim may present with many signs and symptoms, including the following:

Physical Examination

Vital signs should be assessed and closely monitored.

Local signs are as follows:

Systemic signs are as follows:

Complications

Any of the attendant complications of shock may be encountered.

Myocardial infarction may occur.

Coagulopathy is a rare complication.

Wound infections may occur, especially in the setting of a retained tooth.

Necrosis is notably rare.

Allergic or anaphylactic reactions are also rare, but have been described.[5]

Laboratory Studies

The most common CBC count finding is an elevation in the WBC count. In rare severe cases, a drop in the platelet count may occur.

Measure serum electrolyte levels, particularly if there is a history of significant underlying disease.

Helodermatid venoms do not appear to have any anticoagulant fractions. However, very rarely, reports of abnormal coagulation studies with severe bites have been documented. These rare coagulopathies are likely secondary to hemostatic changes occurring as a result of severe endothelial cell damage.

It is reasonable to obtain a prothrombin time, an activated partial thromboplastin time, a fibrinogen level, and a measure of fibrin degradation products.

Perform a urinalysis and look for any evidence of blood or casts.

A cardiac panel, including a CK-MB, myoglobin, and troponin should be obtained if the victim has evidence of hemodynamic instability, chest pain, or an abnormal ECG result.

Imaging Studies

A chest radiograph should be obtained if the victim is experiencing chest pain, shortness of breath, or has significant comorbidities.

Soft tissue radiographs may be obtained to look for retained teeth, although the sensitivity is low. Occasionally, gas may be seen in the soft tissues and likely represents air introduced into the wound during the biting/chewing process.[8]   A bedside ultrasound might also reveal retained teeth.

Other Tests

Obtaining an ECG is prudent.  T-wave abnormalities, conduction disturbances, and 2 cases of acute myocardial infarction (one in a young patient without chest pain who had a possible history of cocaine use but no other cardiac risk factors) have been reported.[6, 7]

Prehospital Care

No evidence-based recommendations have been determined for field management of lizard envenomation.

If the lizard remains attached to the victim, it immediately should be removed by any of a number of methods, such as prying the jaws apart with a stick or metal object, holding a flame under the animal's chin, or submerging the lizard in cold water. Care should be exercised to prevent additional bites to the victim or rescuer as the lizard will be enraged.

If possible, the wound should be washed quickly with running water. Place a dressing on the wound to control any active bleeding, and apply a splint to limit movement of the extremity. The limb can be kept at approximately heart level during transport to medical care.

No evidence to recommend the use of constrictive bands, compressive dressings, or suction is available. Tourniquets should not be used.

Do not make any incisions into the already damaged tissues.

Although ice has been used to reduce pain, it can exacerbate local vasospasm.

Victims showing evidence of shock should be kept in a supine position with legs elevated. If oxygen and intravenous fluids are available, these should be administered during transport to the hospital.

Emergency Department Care

Closely monitor vital signs.

Immediately begin cardiac and pulse oximetry monitoring.[9]

Establish 2 IV lines with isotonic sodium chloride solution.

If hypotension occurs, begin brisk crystalloid resuscitation. If vital signs fail to improve with adequate saline infusion (eg, 20-40 mL/kg), albumin can be administered. Vasopressor agents rarely are necessary, but they may be beneficial in refractory cases.

Wound care

Clean the wounds with soap and water, and evaluate them for retained foreign bodies.

A local anesthetic, such as lidocaine (without epinephrine), can be injected at the bite site to aid in pain control and to assist in exploration of the wounds for retained teeth or damage to underlying structures.[10] Regional nerve blocks and judicious use of narcotics can be helpful in controlling pain.[11] A non–histamine-releasing narcotic, such as fentanyl, may be preferable.

The extremity should be splinted and kept at (or slightly above) the patient's heart level to reduce edema.

Because of the significant local tissue trauma, prophylactic broad-spectrum antibiotics may be administered for a few days, although this treatment is controversial and untested.

Tetanus immunization status should be updated as necessary.

Further Care

Inpatient

Admit patients with a significant systemic reaction or with abnormal lab studies and/or ECG findings, possibly to a monitored setting.

The bitten extremity should be placed in a well-padded splint and elevated to the patient's heart level or higher to reduce edema.

Institute standard daily wound care, including cleansing, topical antibiotic application, and dressing.

Physical therapy can help speed the return to full function.

Admission for pain control may be warranted.

Transfer

Transfer of victims with evidence of severe envenoming to a center with experience in dealing with these cases may be prudent. Consultation with an experienced provider is recommended (see Consultations).

Outpatient

All victims of helodermatid bites should be observed in the ED for at least 6 hours.

Reliable patients who are relatively asymptomatic, with normal vital signs and lab findings, can be discharged with instructions to return for any worsening symptoms. A responsible adult should be available to help the patient return if necessary.

Provide instructions for wound care (eg, wash the wounds twice per day with soap and water; apply a topical antibiotic ointment and dressing).

Signs and symptoms of wound infection should be discussed with the patient.

Arrange a follow-up appointment for a wound check in 24-48 hours.

Give a prescription for antibiotics (eg, cephalexin) to patients who are being prophylactically treated.

A prescription for a narcotic analgesic, such as hydrocodone, may be appropriate.

 

Consultations

Consult an expert in reptile envenomations to assist in management, as necessary. An excellent resource for assistance is the University of Arizona Poison and Drug Information Center (telephone: 520-626-6016).

Prevention

Avoid handling or otherwise disturbing venomous lizards.

Because these creatures spend approximately 99% of their lives underground, the opportunity to see one in the wild is a great privilege. The urge to pick up or capture it should be strongly suppressed. These animals are legally protected in all regions in which they occur.



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A Gila monster (Heloderma suspectum). Photo by Holly McNally.

Medication Summary

No specific agents are used to treat lizard envenomations. Although 2 experimental antivenoms have been produced for the Gila monster, neither has been made commercially available. Drug therapy is entirely symptomatic (eg, local anesthetics, analgesics, antiemetics). If antibiotics are administered, they should be broad-spectrum and they should provide coverage for gram-negative organisms. For the rare case of anaphylaxis/angioedema, therapy should be instituted with sympathomimetic agents, antihistamines, and/or steroids.

Epinephrine (Adrenalin, EpiPen)

Clinical Context:  Epinephrine is the drug of choice for the treatment of anaphylactoid reactions. Alpha-agonist effects increase peripheral vascular resistance and reverse peripheral vasodilatation and vascular permeability, thus helping to restore vascular tone and blood pressure. The beta-agonist effects increase heart rate and inotropism and cause bronchodilatation.

Class Summary

Cardiovascular agents possess alpha- and beta-adrenergic effects that are useful in reversing anaphylactic reactions (eg, angioedema, bronchospasm, hypotension).

Methylprednisolone (Solu-Medrol)

Clinical Context:  Methylprednisolone decreases inflammation by suppressing the migration of polymorphonuclear leukocytes and reversing increased capillary permeability.

Prednisone (Deltasone, Orasone, Meticorten)

Clinical Context:  Prednisone decreases inflammation by suppressing the migration of polymorphonuclear leukocytes and reversing increased capillary permeability.

Class Summary

Corticosteroids onset of action is approximately 4-6 hours, although some synergistic activity may be noted when simultaneously used with sympathomimetic agents. Steroids may be needed in the rare event of an allergic reaction to lizard venom. Corticosteroids have no role in the management of envenomation itself.

Diphenhydramine (Benadryl, Benylin, Bydramine)

Clinical Context:  Diphenhydramine is used for the symptomatic relief of allergic symptoms caused by histamine released in response to allergens.

Cimetidine (Tagamet)

Clinical Context:  Cimetidine is an H2 antagonist that, when combined with an H1 type, may be useful in treating itching and flushing in anaphylaxis, pruritus, urticaria, and contact dermatitis that do not respond to H1-receptor antagonists alone. Use it in addition to H1 antihistamines.

Class Summary

Antihistamines prevent the histamine response in sensory nerve endings and blood vessels. They are more effective in preventing a histamine response than in reversing it.

Lidocaine anesthetic

Clinical Context:  Lidocaine is an amide local anesthetic used in 1-2% concentration. It inhibits depolarization of type C sensory neurons by blocking sodium channels. Epinephrine should be avoided in venomous lizard bites to prevent causing additional local tissue ischemia.

Class Summary

Local anesthetics can be injected, either locally or regionally, to reduce pain and facilitate exploration of wounds (to rule out damage to underlying structures or retained teeth).

Fentanyl citrate (Sublimaze)

Clinical Context:  Fentanyl is a synthetic opioid that is 75-200 times more potent and has a much shorter half-life than morphine sulfate. It has less hypotensive effects and is safer in patients with hyperactive airway disease than morphine because of minimal-to-no associated histamine release. By itself, it causes little cardiovascular compromise, although the addition of benzodiazepines or other sedatives may result in decreased cardiac output and blood pressure. Fentanyl is highly lipophilic and protein-bound. Prolonged exposure leads to an accumulation in fat and delays the weaning process. Consider using a continuous infusion because of the short half-life of fentanyl. The parenteral form is the drug of choice for conscious sedation analgesia. It is ideal for analgesic action of short duration during anesthesia and the immediate postoperative period. It is an excellent choice for pain management and sedation of short duration (30-60 min), and it is easy to titrate. Its effects are easily and quickly reversed by naloxone.

After initial parenteral dose, subsequent parenteral doses should not be titrated more frequently than every 3 hours or every 6 hours thereafter. Transdermal form is used only for chronic pain conditions in opioid-tolerant patients. When using a transdermal dosage form, the majority of patients are controlled with 72-hour dosing intervals; however, some patients require dosing intervals of 48 hours.

Class Summary

Patients may require narcotic analgesics for pain control after venomous lizard bites. In choosing a narcotic analgesic, to prevent worsening venom effects, it is best to select a narcotic that has less tendency to induce histamine release, such as fentanyl.

Author

Robert L Norris, MD, Professor Emeritus, Department of Emergency Medicine, Stanford University Medical Center

Disclosure: Nothing to disclose.

Specialty Editors

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

Disclosure: Nothing to disclose.

Amin Antoine Kazzi, MD, Professor of Clinical Emergency Medicine, Department of Emergency Medicine, American University of Beirut, Lebanon

Disclosure: Nothing to disclose.

Chief Editor

Joe Alcock, MD, MS, Associate Professor, Department of Emergency Medicine, University of New Mexico Health Sciences Center

Disclosure: Nothing to disclose.

Additional Contributors

Mark S Slabinski, MD, FACEP, FAAEM, Vice President, USACS Central

Disclosure: Nothing to disclose.

References

  1. Fry BG, Wroe S, Teeuwisse W, et al. A central role for venom in predation by Varanus komodoensis (Komodo Dragon) and the extinct giant Varanus (Megalania) priscus. Proc Natl Acad Sci U S A. 2009 Jun 2. 106 (22):8969-74. [View Abstract]
  2. Beck DD. Biology of Gila Monsters and Beaded Lizards. Berkeley, CA: University of California Press; 2005. 1-211.
  3. Strimple PD, Tomassoni AJ, Otten EJ. Report on envenomation by a Gila monster (Heloderma suspectum) with a discussion of venom apparatus, clinical findings, and treatment. Wilderness Environ Med. 1997 May. 8(2):111-6. [View Abstract]
  4. Mebs D. Clinical toxicology of Helodermatidae lizard bites. In: Handbook of Clinical Toxicology of Animal Venoms and Poisons. 1995: 361-366.
  5. Piacentine J, Curry SC, Ryan PJ. Life-threatening anaphylaxis following gila monster bite. Ann Emer Med. 1986. 15:959-961. [View Abstract]
  6. Bou-Abboud CF, Kardassakis DG. Acute myocardial infarction following a Gila monster (Heloderma suspectum cinctum) bite. West J Med. 1988. 148(5):577-579. [View Abstract]
  7. Preston CA. Hypotension, myocardial infarction, and coagulopathy following gila monster bite. J Emerg Med. 1989 Jan-Feb. 7 (1):37-40. [View Abstract]
  8. French RN, Ash J, Brooks DE. Gila monster bite. Clin Toxicol (Phila). 2012 Feb. 50(2):151-2. [View Abstract]
  9. Torp KD, Simon LV. Pulse Oximetry. 2018 Jan. [View Abstract]
  10. Torp KD, Simon LV. Toxicity, Lidocaine. 2018 Jan. [View Abstract]
  11. Ramos-Matos CF, Lopez-Ojeda W. Fentanyl. 2018 Jan. [View Abstract]
  12. French R, Brooks D, Ruha AM, Shirazi F, Chase P, Boesen K, et al. Gila monster (Heloderma suspectum) envenomation: Descriptive analysis of calls to United States Poison Centers with focus on Arizona cases. Clin Toxicol (Phila). 2015 Jan. 53 (1):60-70. [View Abstract]
  13. Brown DE, Carmony NB. Gila Monster: Facts and Folklore of America's Aztec Lizard. 1991. 1-126.

A Gila monster (Heloderma suspectum). Photo by Michael Cardwell.

Close-up of the head of a Gila monster. Clearly evident is the bulging musculature of the jaws, which gives this animal a tenacious bite. Photo by Holly McNally.

The dentition of a Gila monster. The grooved surfaces of the teeth are evident. These grooves allow for venom movement from the venom glands into the victim's tissues. Photo by Michael Cardwell.

A Gila monster (Heloderma suspectum). Photo by Holly McNally.

A Gila monster (Heloderma suspectum). Photo by Holly McNally.

Close-up of the head of a Gila monster. Clearly evident is the bulging musculature of the jaws, which gives this animal a tenacious bite. Photo by Holly McNally.

The dentition of a Gila monster. The grooved surfaces of the teeth are evident. These grooves allow for venom movement from the venom glands into the victim's tissues. Photo by Michael Cardwell.

A Gila monster (Heloderma suspectum). Photo by Michael Cardwell.