eMedicine Specialties > Emergency Medicine > Environmental

Hymenoptera Stings: Treatment & Medication

Author: Hemant H Vankawala, MD, Attending Physician, 24 Hour Emergency Room, Houston and Dallas; Attending Physician, Baylor University Medical Center; Medical Director, Big Bend National Park; Medical Director, Terlingua Fire and EMS; Medical Director, MedCare Ambulance Company
Coauthor(s): Randy Park, MD, Chair, Associate Professor, Department of Emergency Medicine, Denton Regional Medical Center
Contributor Information and Disclosures

Updated: Apr 9, 2009

Treatment

Prehospital Care

  • Prehospital care must assess severity immediately and provide immediate appropriate treatment, because the most endangered patients die within 30 minutes of a sting.
  • Local reactions can be life threatening if swelling occludes the airway. Initiate invasive measures to secure the airway if this occurs. Otherwise, the following local care measures suffice:
  • Diphenhydramine limits the size of the local reaction.
  • Clean wound and remove stinger if present.
  • Apply ice or cool packs.
  • Elevate extremity to limit edema.
  • Manage generalized reactions similarly to anaphylaxis, even in the absence of shock. Check airway and ventilatory status. Treatment should include an initial intravenous (IV) bolus of 10-20 mL/kg isotonic crystalloids in addition to diphenhydramine and epinephrine.
  • If the patient has not removed the stinger, it should be removed as soon as possible by the first caregiver on the scene. Delay increases venom load, so the fastest removal technique is the best. Pinching and traction is an acceptable technique.

Emergency Department Care

  • Corticosteroids and cimetidine may be given IV; vasopressors such as dopamine can be used to provide vascular support.
  • Patients developing respiratory arrest require ventilatory support.
  • Blood products may be required in the event of disseminated intravascular coagulation (DIC).

Consultations

  • Refer all patients with generalized reactions to an allergist as soon as possible, because risk of fatal reaction is inversely related to length of time since the last sting.

Medication

Medications used to treat Hymenoptera stings include antihistamines (H1, H2), steroids, alpha- and beta-receptor agonists, and bronchodilators.

Antihistamines

These drugs directly block effects of some venom and effects of endogenously released histamine.


Diphenhydramine (Benadryl)

DOC for all stings, is an H1 and partial H2 receptor blocker used for symptomatic relief of allergic symptoms caused by histamine released in response to allergens.

Adult

50-75 mg PO/IM q4h; IV may be administered slowly in emergency situations

Pediatric

1-2 mg/kg PO/IM

Potentiates effect of CNS depressants; due to alcohol content, do not give syrup dosage form to patient taking medications that can cause disulfiramlike reactions

Documented hypersensitivity; MAOIs

Pregnancy

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

Precautions

May exacerbate angle-closure glaucoma, hyperthyroidism, peptic ulcer, and urinary tract obstruction


Cimetidine (Tagamet)

Indicated for systemic reaction that does not respond completely to diphenhydramine, or when severity indicates need for maximal treatment.

Adult

300-800 mg IV q6h

Pediatric

5 mg/kg IV q6h

Can increase blood levels of theophylline, warfarin, tricyclic antidepressants, triamterene, phenytoin, quinidine, propranolol, metronidazole, procainamide, and lidocaine

Pregnancy

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

Precautions

Older patients may experience confusional states; may cause impotence and gynecomastia in young males due to weak antiandrogen properties; may increase levels of many drugs; consider adjusting dosage or discontinuing treatment if renal function changes occur during therapy

Bronchodilators

Epinephrine causes vasoconstriction, bronchodilation, and increased cardiac output. The effects of albuterol and theophylline are more focused on bronchodilation.


Epinephrine (Epi-Pen)

DOC for systemic reactions, has alpha-agonist effects that increase peripheral vascular resistance and reverse peripheral vasodilation, systemic hypotension, and vascular permeability. Conversely, beta-agonist activity of epinephrine produces bronchodilation, chronotropic cardiac activity, and positive inotropic effects. Epinephrine may be self-administered through auto-injectors.

Adult

0.2-1 mg IV/SC

Pediatric

0.01-0.1 mg/kg IV/SC

Increases the toxicity of beta- and alpha-blocking agents and of halogenated inhalational anesthetics

Documented hypersensitivity; cardiac arrhythmias; angle-closure glaucoma; avoid coadministration with local anesthesia in areas such as fingers or toes because vasoconstriction may produce sloughing of the tissue; do not use during labor as it may delay the second stage of labor

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 older persons and in patients with diabetes mellitus, hyperthyroidism, prostatic hypertrophy, hypertension, cardiovascular disease, and cerebrovascular insufficiency; rapid IV infusions may cause death from cerebrovascular hemorrhage or cardiac arrhythmias


Albuterol (Proventil, Ventolin)

Adjunctive treatment for bronchospasm given by nebulization, it is a beta-agonist useful to treat bronchospasm refractory to epinephrine. Relaxes bronchial smooth muscle by action on beta2-receptors and has little effect on cardiac muscle contractility.

Adult

2.5 mg by nebulization in 3 cc saline
May be repeated q15min or administered continuously in severe cases

Pediatric

0.1 mg/kg by nebulization in 3 mL saline, not to exceed 2.5 mg
May be repeated q15min or administered continuously in severe cases

Beta-adrenergic blockers antagonize effects; inhaled ipratropium may increase duration of bronchodilatation by albuterol; cardiovascular effects may increase with MAOIs, inhaled anesthetics, tricyclic antidepressants, and sympathomimetic agents

Documented hypersensitivity; adrenergic amines, or related products; history of tachycardia

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 hyperthyroidism, diabetes mellitus, and cardiovascular disorders


Theophylline (Aminophylline)

Used to relieve bronchospasm in resistant cases, acts to decrease muscle tone in both small and large airways in lungs, thus increasing ventilation.
Efficacy managing bronchodilation may be due to its potentiation of exogenous catecholamines, stimulation of endogenous catecholamine release, and diaphragmatic muscular relaxation. Effects as a bronchodilator usually are seen at levels considered to be toxic (>20 mg/dL).

Adult

Loading dose: 5-6 mg/kg IV over 30 min, then 0.9 mg/h
Adjust rate as tolerated to achieve therapeutic levels of 10-20 mcg/mL

Pediatric

Administer as in adults

Aminoglutethimide, barbiturates, carbamazepine, ketoconazole, loop diuretics, charcoal, hydantoins, phenobarbital, phenytoin, rifampin, isoniazid, and sympathomimetics may decrease effects of theophylline; theophylline effects may increase with allopurinol, beta-blockers, ciprofloxacin, corticosteroids, disulfiram, quinolones, thyroid hormones, ephedrine, carbamazepine, cimetidine, erythromycin, macrolides, propranolol, and interferon

Documented hypersensitivity; uncontrolled arrhythmias, peptic ulcers, hyperthyroidism, uncontrolled seizure disorders

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 peptic ulcer, hypertension, tachyarrhythmias, hyperthyroidism, and compromised cardiac function; do not inject IV solution faster than 25 mg/min; patients diagnosed with pulmonary edema or liver dysfunction are at increased risk of toxicity because of reduced drug clearance

Corticosteroids

These drugs act to stabilize lymphocytes and to reduce release of endogenous vasoactive compounds.


Methylprednisolone (Solu-Medrol, Depo-Medrol)

Indicated in all cases of generalized reaction unless contraindications exist. Useful to treat inflammatory and allergic reactions. May decrease inflammation by reversing increased capillary permeability and suppressing PMN activity.

Adult

0.25-1 g IV over 30 min q6h

Pediatric

0.2-2 mg/kg IV over 30 min q6h

Coadministration with digoxin may increase digitalis toxicity secondary to hypokalemia; estrogens may increase levels of methylprednisolone; phenobarbital, phenytoin and rifampin may decrease levels of methylprednisolone (adjust dose); monitor patients for hypokalemia when taking medication concurrently with diuretics

Documented hypersensitivity; viral, fungal, or tubercular skin infections

Pregnancy

C - Safety for use during pregnancy has not been established.

Precautions

Hyperglycemia, edema, osteonecrosis, peptic ulcer disease, hypokalemia, osteoporosis, euphoria, psychosis, growth suppression, myopathy, and infections are possible complications of glucocorticoid use

More on Hymenoptera Stings

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

References

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Further Reading

Clinical guidelines

Stinging insect hypersensitivity: a practice parameter update. Moffitt JE, Golden DB, Reisman RE, Lee R, Nicklas R, Freeman T, deShazo R, Tracy J, Bernstein IL, Blessing-Moore J, Khan DA, Lang DM, Portnoy JM, Schuller DE, Spector SL, Tilles SA. Stinging insect hypersensitivity: a practice parameter update. J Allergy Clin Immunol 2004 Oct;114(4):869-86.

Keywords

bee stings, yellow jacket sting, hornet sting, ant stings, wasp stings, vespid stings, bee envenomations, Hymenoptera envenomations, ant envenomations, wasp envenomations, vespid envenomations, Apis species, wasps, ants, severe anaphylactoid reactions, angioedema, respiratoryarrest, fatal allergic reactions, urticaria, confluent red rash

syncope, anxiety, confusion, wheezing, tachypnea, hypotension, laryngoedema, lingular edema, uvular edema, delirium, shock, honeybee stings, Africanized honeybee, , isoamylacetate, pheromone, apiotherapy, fire ants, , fire ant venom, Harvester ants, species

Contributor Information and Disclosures

Author

Hemant H Vankawala, MD, Attending Physician, 24 Hour Emergency Room, Houston and Dallas; Attending Physician, Baylor University Medical Center; Medical Director, Big Bend National Park; Medical Director, Terlingua Fire and EMS; Medical Director, MedCare Ambulance Company
Hemant H Vankawala, MD is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, Emergency Medicine Residents Association, Society for Academic Emergency Medicine, and Texas Medical Association
Disclosure: Nothing to disclose.

Coauthor(s)

Randy Park, MD, Chair, Associate Professor, Department of Emergency Medicine, Denton Regional Medical Center
Disclosure: Nothing to disclose.

Medical Editor

Dan Danzl, MD, Chair, Department of Emergency Medicine, Professor, University of Louisville Hospital
Dan Danzl, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, Kentucky Medical Association, Society for Academic Emergency Medicine, and Wilderness Medical Society
Disclosure: Nothing to disclose.

Pharmacy Editor

John T VanDeVoort, PharmD, Regional Director of Pharmacy, Sacred Heart & 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.

Managing Editor

James Steven Walker, DO, MS, Clinical Professor of Surgery, Department of Surgery, University of Oklahoma Health Sciences Center
James Steven Walker, DO, MS is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, and American Osteopathic Association
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

Scott H Plantz, MD, FAAEM, Associate Clinical Professor of Emergency Medicine, Rosalind Franklin University of Medicine and Science, Chicago Medical School; Medical Director, WeCare Med, Inc
Scott H Plantz, MD, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine
Disclosure: Nothing to disclose.

 
 
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