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Scorpion Envenomation

Author: Sean P Bush, MD, FACEP, Professor of Emergency Medicine, Envenomation Specialist, Department of Emergency Medicine, Loma Linda University School of Medicine; Consulting Staff, Loma Linda University Medical Center
Coauthor(s): Charles J Gerardo, MD, FACEP, Assistant Professor, Department of Surgery, Division of Emergency Medicine, Duke University School of Medicine; Director of Clinical Affairs, Trauma Liaison, Division of Emergency Medicine, Duke University Medical Center
Contributor Information and Disclosures

Updated: Jul 24, 2008

Introduction

Background

Envenomation from most scorpions results in a simple, painful, local reaction that can be treated with analgesics, antihistamines, and symptomatic/supportive care. This article focuses on scorpions that generally are considered more dangerous to humans. All of the potentially lethal scorpions belong to the family Buthidae, with the exception of one genus, Hemiscorpius, which belongs to the family Scorpionidae (ie, Ischnuridae). A triangular sternal plate helps distinguish Buthidae from other scorpion families in which the sternal plate is more pentagonal (see Media file 3). Scorpions of medical significance include the following genera in the given distributions:

  • Centruroides - Southern United States, Mexico, Central America, and the Caribbean (Centruroides exilicauda is found in the Baja California peninsula of Mexico and Centruroides sculpturatus is found in the state of Sonora, Mexico and the southwestern United States, primarily Arizona and small parts of Utah, New Mexico, Nevada, and California.) The accepted taxonomy of the bark scorpion has changed over time. Either C exilicauda or C sculpturatus have been accepted at various times. However, recent evidence from biochemical, genetic, and physiologic characterization of their venom suggests that they are two different species as listed above.
  • Tityus - Central America, South America, and the Caribbean
  • Buthus - Across the Mediterranean area, from Spain to the Middle East
  • Mesobuthus - Throughout Asia
  • Parabuthus - Western and southern Africa
  • Buthotus (ie, Hottentotta) - Across southern Africa to southeast Asia
  • Leiurus - Across northern Africa and the Middle East
  • Androctonus - Northern Africa to southwest Asia

Note that scorpions may be found outside their natural range of distribution when inadvertently transported with items such as luggage.

Pathophysiology

Scorpions grasp prey with pincers, arch their tails over their bodies, and deliver venom with the stinger. They inject venom from glands located lateral to the tip of the stinger.

Scorpion venom may contain multiple toxins and other compounds. Venom composition is complex, and detailed discussion of its pharmacological effects is beyond the scope of this article. The most important clinical effects of envenomation are neuromuscular, neuroautonomic, or local tissue effects. The primary targets of scorpion venom are voltage-dependent ion channels, of which sodium channels are the best studied. Venom toxins alter these channels, leading to prolonged neuronal activity. Many end-organ effects are secondary to this excessive excitation. Autonomic excitation leads to cardiopulmonary effects observed after some scorpion envenomations. Somatic and cranial nerve hyperactivity results from neuromuscular overstimulation. Additionally, serotonin may be found in scorpion venom and is thought to contribute to the pain associated with scorpion envenomation.

Frequency

United States

In 2006, a total of 16,231 scorpion envenomations were reported to the American Association of Poison Control Centers. However, because of underreporting, this is probably an underestimation of the true number of stings.

International

Reliable statistics on scorpion envenomation are not available. Many potentially dangerous scorpions inhabit the underdeveloped or developing world. Consequently, numerous envenomations go unreported, and true incidence is unknown.

Mortality/Morbidity

Accurate worldwide data do not exist. The highest reported mortality rate is recorded in data from Mexico, with estimates as high as 1000 deaths in 1 year. In the United States, 4 deaths were reported in an 11-year period according to one source.1 However, no deaths were reported to the American Association of Poison Control Centers from 1983 to 1999. Only one death from the Arizona bark scorpion (C sculpturatus) has been reported since 1964.2 Ironically, the highest and lowest mortality estimates are associated with different species within the same genus of scorpion (Centruroides).

  • Children and elderly persons have an increased risk of mortality.
  • In terms of venom lethality, the venom of Androctonus australis and Leiurus quinquestriatus are the most toxic. C sculpturatus venom is low in toxicity compared with most scorpions of medical importance.

Clinical

History

  • Pain and paresthesias often are present.
  • Nausea and vomiting are common.
  • Specimen identification by an entomologist may be helpful (if the scorpion can be captured safely).

Physical

  • Local tissue effects vary among species.
    • Minimal local tissue effects are present with Centruroides envenomation.
    • Significant local tissue reaction rules out C exilicauda envenomation.
    • Tapping over the injury site (ie, tap test) may cause severe pain after a sting by C exilicauda.
  • Tachycardia and other dysrhythmias are caused by autonomic effects primarily, although direct myocardial toxicity with arrhythmogenic effects has been described.
  • Hypertension or hypotension may be present.
  • The patient may have hyperthermia.
  • Respiratory arrest and loss of protective airway reflexes are common causes of mortality.
  • Pulmonary edema has been described and may be secondary to cardiogenic causes and to increased capillary permeability.
  • Autonomic effects include the following:
    • Sympathetic overdrive symptoms predominate, causing tachycardia, hypertension, hyperthermia, and pulmonary edema.
    • Parasympathetic symptoms include hypotension, bradycardia, salivation, lacrimation, urination, defecation, and gastric emptying.
  • Cranial nerve effects include the following:
    • Classic roving or rotary eye movements, blurred vision, tongue fasciculations, and loss of pharyngeal muscle control may be observed.
    • Difficulty swallowing combined with excessive salivary secretions may lead to respiratory difficulty.
  • Somatic effects include the following:
    • Restlessness and involuntary muscle jerking that can be mistaken for seizures have been described.
    • Presence of true seizures in Centruroides envenomation is controversial and has not been proven to occur. Seizures are described in association with other scorpion envenomations.
    • Cerebral infarction, cerebral thrombosis, and acute hypertensive encephalopathy have been described with a variety of Buthidae scorpion envenomations.

Causes

  • The causes of scorpion envenomation are primarily accidental.

More on Scorpion Envenomation

Overview: Scorpion Envenomation
Differential Diagnoses & Workup: Scorpion Envenomation
Treatment & Medication: Scorpion Envenomation
Follow-up: Scorpion Envenomation
Multimedia: Scorpion Envenomation
References

References

  1. Langley RL, Morrow WE. Deaths resulting from animal attacks in the United States. Wilderness Environ Med. Feb 1997;8(1):8-16. [Medline].

  2. Boyer L, Heubner K, McNally J, Buchanan P. Death from Centruroides scorpion sting allergy [abstract]. J Toxicol Clin Toxicol. 2001;39:561-562.

  3. Al-Asmari AK, Al-Seif AA, Hassen MA, Abdulmaksood NA. Role of prazosin on cardiovascular manifestations and pulmonary edema following severe scorpion stings in Saudi Arabia. Saudi Med J. Feb 2008;29(2):299-302. [Medline].

  4. Amitai Y, Mines Y, Aker M, Goitein K. Scorpion sting in children. A review of 51 cases. Clin Pediatr (Phila). Mar 1985;24(3):136-40. [Medline].

  5. Bawaskar HS, Bawaskar PH. Utility of scorpion antivenin vs prazosin in the management of severe Mesobuthus tamulus (Indian red scorpion) envenoming at rural setting. J Assoc Physicians India. Jan 2007;55:14-21. [Medline].

  6. Biswal N, Bashir RA, Murmu UC, Mathai B, Balachander J, Srinivasan S. Outcome of scorpion sting envenomation after a protocol guided therapy. Indian J Pediatr. Jul 2006;73(7):577-82. [Medline].

  7. Biswal N, Mathai B, Bhatia BD. Scorpion sting envenomation: complications and management. Indian Pediatr. Aug 1993;30(8):1055-9. [Medline].

  8. Bond GR. Antivenin administration for Centruroides scorpion sting: risks and benefits. Ann Emerg Med. Jul 1992;21(7):788-91. [Medline].

  9. Boyer D. The American Zoo and Aquarium Association and the American Association of Poison Control Centers Antivenom Index. 1999;16-7.

  10. Bush SP. Envenomation by the scorpion (Centruroides limbatus) outside its natural range and recognition of medically important scorpions. Wilderness Environ Med. Autumn 1999;10(3):161-4. [Medline].

  11. Conner DA, Seldon BS. Scorpion envenomation. In: Auerbach PS, ed. Wilderness Medicine: Management of Wilderness and Environmental. Vol 3. Mosby-Year Book; 1995:831-42.

  12. Curry SC, Vance MV, Ryan PJ, et al. Envenomation by the scorpion Centruroides sculpturatus. J Toxicol Clin Toxicol. 1983-84;21(4-5):417-49. [Medline].

  13. Freire-Maia L, Campos JA, Amaral CF. Approaches to the treatment of scorpion envenoming. Toxicon. Sep 1994;32(9):1009-14. [Medline].

  14. Gateau T, Bloom M, Clark R. Response to specific Centruroides sculpturatus antivenom in 151 cases of scorpion stings. J Toxicol Clin Toxicol. 1994;32(2):165-71. [Medline].

  15. Gibly R, Williams M, Walter FG, McNally J, Conroy C, Berg RA. Continuous intravenous midazolam infusion for Centruroides exilicauda scorpion envenomation. Ann Emerg Med. Nov 1999;34(5):620-5. [Medline].

  16. Gueron M, Ilia R, Sofer S. The cardiovascular system after scorpion envenomation. A review. J Toxicol Clin Toxicol. 1992;30(2):245-58. [Medline].

  17. Ismail M. The scorpion envenoming syndrome. Toxicon. Jul 1995;33(7):825-58. [Medline].

  18. Ismail M. The treatment of the scorpion envenoming syndrome: the Saudi experience with serotherapy. Toxicon. Sep 1994;32(9):1019-26. [Medline].

  19. Keegan HL. Scorpions of Medical Importance. Vol 1. University Press of Mississippi: 1980:1-140.

  20. Likes K, Banner W Jr, Chavez M. Centruroides exilicauda envenomation in Arizona. West J Med. Nov 1984;141(5):634-7. [Medline].

  21. Natu VS, Murthy RK, Deodhar KP. Efficacy of species specific anti-scorpion venom serum (AScVS) against severe, serious scorpion stings (Mesobuthus tamulus concanesis Pocock)--an experience from rural hospital in western Maharashtra. J Assoc Physicians India. Apr 2006;54:283-7. [Medline].

  22. Nouira S, Boukef R, Nciri N, Haguiga H, Elatrous S, Besbes L, et al. A clinical score predicting the need for hospitalization in scorpion envenomation. Am J Emerg Med. May 2007;25(4):414-9. [Medline].

  23. Riley BD, LoVecchio F, Pizon AF. Lack of scorpion antivenom leads to increased pediatric ICU admissions. Ann Emerg Med. Apr 2006;47(4):398-9. [Medline].

  24. Rimsza ME, Zimmerman DR, Bergeson PS. Scorpion envenomation. Pediatrics. Aug 1980;66(2):298-302. [Medline].

  25. Simard JM, Watt DD. Venoms and toxins. In: The Biology of Scorpions. Polis GA, ed. Stanford University Press; 1990:414-44.

  26. Sofer S. Scorpion envenomation. Intensive Care Med. Aug 1995;21(8):626-8. [Medline].

  27. Suchard JR, Hilder R. Atropine use in Centruroides scorpion envenomation. J Toxicol Clin Toxicol. 2001;39(6):595-8; discussion 599. [Medline].

  28. Valdez-Cruz NA, Davila S, Licea A, Corona M, Zamudio FZ, García-Valdes J, et al. Biochemical, genetic and physiological characterization of venom components from two species of scorpions: Centruroides exilicauda Wood and Centruroides sculpturatus Ewing. Biochimie. Jun 2004;86(6):387-96. [Medline].

Further Reading

Keywords

scorpion sting, scorpion envenomation, scorpion venom, Buthidae, Scorpionidae, Ischnuridae, Centruroides, Centruroides exilicauda, Tityus, Buthus, Mesobuthus, Buthotus, Buthus tamulus, Hottentotta, Leiurus, Leiurus quinquestriatus, Leiurus quinquestriatus, Androctonus, Androctonus australis, Hemiscorpius, Hemiscorpius lepturus

Contributor Information and Disclosures

Author

Sean P Bush, MD, FACEP, Professor of Emergency Medicine, Envenomation Specialist, Department of Emergency Medicine, Loma Linda University School of Medicine; Consulting Staff, Loma Linda University Medical Center
Sean P Bush, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians, Society for Academic Emergency Medicine, and Wilderness Medical Society
Disclosure: Protherics Consulting fee Consulting; Fougera Grant/research funds Speaking and teaching; Rare Disease Therapeutics Grant/research funds Research; Bioclon Grant/research funds Research

Coauthor(s)

Charles J Gerardo, MD, FACEP, Assistant Professor, Department of Surgery, Division of Emergency Medicine, Duke University School of Medicine; Director of Clinical Affairs, Trauma Liaison, Division of Emergency Medicine, Duke University Medical Center
Charles J Gerardo, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians, Council of Emergency Medicine Residency Directors, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Medical Editor

Robert Norris, MD, Chief, Associate Professor, Department of Surgery, Division of Emergency Medicine, Stanford University Medical Center
Robert Norris, MD is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, California Medical Association, and Wilderness Medical Society
Disclosure: Nothing to disclose.

Pharmacy Editor

John T VanDeVoort, PharmD, ABAT, Director of Pharmacy, Sacred Heart Hospital
John T VanDeVoort, PharmD, ABAT is a member of the following medical societies: American Academy of Clinical Toxicology and American Society of Health-System Pharmacists
Disclosure: Nothing to disclose.

Managing Editor

James S Walker, DO, Program Coordinator, Associate Professor, Department of Emergency Medicine, University of Oklahoma Health Sciences Center
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

Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School
Jonathan Adler, MD is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
Disclosure: eMedicine.com, Inc. Consulting fee Consulting

 
 
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