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Wasp Stings: Treatment & Medication

Author: Carl A Mealie, MD, Assistant Professor, Department of Emergency Medicine, Albert Einstein College of Medicine; Medical Director of Emergency Care Institute, Chief of Clinical Operations, Department of Emergency Medicine, Long Island Jewish Medical Center
Coauthor(s): Alan S Multz, MD, Associate Professor of Clinical Medicine, Albert Einstein College of Medicine; Program Director, Internal Medicine Residency, Associate Chairman, Department of Medicine, Long Island Jewish Medical Center; Max Vernon Wisgerhof, MD, Fellowship Program Director, Department of Endocrinology and Metabolism, Henry Ford Hospital
Contributor Information and Disclosures

Updated: Jun 17, 2009

Treatment

Medical Care

Prehospital Care and Emergency Department Care

The "ABCs" of patient resuscitation and care take precedent. Airway patency and security is the prime concern, especially if there is any evidence of potential airway obstruction from angioedema manifested by stridor, hoarseness of voice, difficulty swallowing, or pooling of secretions. Breathing should be assessed for the rate, depth and adequacy of ventilation with pulse oximetry and auscultation of the chest to determine air movement, and the presence of wheezing from bronchial constriction and spasm. The patient's circulatory status should be evaluated for presence of distributive shock, assessing the blood pressure, nail bed capillary refill, and the patient's mental status.

Specific Considerations

  • Local wound care: Apply ice to keep the area comfortably cool and to reduce swelling. Unlike honeybee stings, members of the wasp family (including hornets and yellow jackets) generally do not lose their stinging apparatus in the wound. Consider a secondary bacterial infection at the site in patients who present several days after the sting with fever or continued redness, warmth, swelling, and tenderness over the site or progression of the redness—red streaks that progress proximally.
  • Urticaria: Antihistamines remain the mainstay of therapy. H1 blockers such as oral diphenhydramine (Benadryl) or hydroxyzine (Atarax) have proven useful in reducing the severity of the itching and rash. Oral steroids (eg, prednisone, methylprednisolone [Medrol]) can be added to the regimen if needed, depending on the extent and severity of the patient's symptoms. Epinephrine, 0.3-0.5 mL subcutaneously in a 1:1000 solution, can also be used. Although it reverses the extent and itching of the urticaria, its benefit-to-risk ratio must be considered. The alpha effect of epinephrine increases the systemic vascular resistance, while its beta effect has a positive inotropic and chronotropic effect on the heart. This produces an increase in the heart's work and increases the myocardial oxygen demand. This may have a deleterious effect in patients with preexisting heart disease or coronary artery disease.
  • Anaphylaxis: The patient may present with airway obstruction due to angioedema, respiratory compromise due to bronchospasm, or circulatory collapse or with a combination of these 3 conditions. Follow the ABCs of emergency medicine as expediently as possible. The airway must be secured. Intubate the patient with rapid sequence technique upon evidence of impending airway obstruction due to swelling or evidence of respiratory failure due to bronchospasm. Establish 2 large-bore intravenous lines to provide a route for medication administration and for fluid bolus in the event of circulatory collapse. Place the patient on both pulse oximetry and a cardiac monitor.
    • Angioedema: If intubation is impossible because of the degree of swelling, obtain a surgical airway through cricothyrotomy. Surgical cricothyrotomy is contraindicated in patients younger than 8 years. In these cases, perform needle cricothyrotomy using the largest-bore needle practical as a temporizing measure. Obtain an emergency consultation with an anesthesiologist and an otorhinolaryngologist (ENT) to prepare the child for the operating room for definitive angioedema/airway management if parenteral beta agonists, histamine 1 (H1) blockers, and glucocorticoids do not relieve the obstruction.
    • Bronchospasm
      • Treatment of bronchospasm without obstruction depends on the acuity of the patient's presentation. Treat mild-to-moderate distress with a combination of nebulized beta agonist (eg, albuterol 0.5 mL of 0.5% solution in 2.5 mL of normal saline nebulized q15min) and parenteral glucocorticoids (eg, methylprednisolone 125 mg IV). As the severity of the respiratory distress increases, weigh the benefit-to-risk ratio of using a parenteral beta agonist (eg, epinephrine). As bronchospasm worsens, a point of peaked expiratory flow and forced expiratory volume decrease occurs and the only area being ventilated with the nebulized beta agonist is the appropriately named dead space.
      • Epinephrine, 0.3-0.5 mL of a 1:1000 solution, may be administered intramuscularly. Its onset of action should be 3-5 minutes; however, impending circulatory collapse with peripheral vasoconstriction due to anaphylaxis may make this route ineffective. Intravenous epinephrine using 3-5 mL (0.3-0.5 mg) of the 1:10,000 solution (0.1 mg/mL) diluted in 10 mL of normal saline or distilled water should be administered slowly over a 1- to 2-minute period, depending on the patient's condition.3
      • As an alternative, 3-5 mL of 1:10,000 solution can also be administered via the endotracheal tube. Administer this solution via a catheter with the tip placed below the end of the endotracheal tube and then flushed through with several milliliters of saline or distilled water. Several positive ventilations follow to force the epinephrine into the terminal bronchioles and alveoli.
      • Vasopressin 40 IU has also been used for refractory hypotension.
    • Hypotension: The cause of hypotension is multifactorial. Histamine, prostaglandin, and leukotriene can reduce the systemic vascular resistance by vasodilating the peripheral vessels and increase the capillary endothelial permeability, allowing extravasation of fluid into the third space. The net effect of both of these processes increases the vascular bed and decreases the amount of fluid in the vascular compartment. Begin treatment with the establishment of 2 large-bore intravenous lines and crystalloid fluid boluses. Vasopressors then can be added, depending on the patient's clinical appearance. Epinephrine can be administered via continuous infusion by mixing 1 mg in 250 mL of normal saline and infusing at a rate of 0.5-1 mL/min. Norepinephrine (Levophed) can also be used. It has the advantage of having more of an alpha effect and less of a beta effect than epinephrine.

Surgical Care

Consider a surgical airway in any patient with evidence of upper airway edema or laryngeal spasm who is experiencing respiratory deterioration. The equipment and expertise to perform a cricothyrotomy should be readily available if orotracheal or nasotracheal intubation cannot be achieved.

Consultations

  • A consultation with an otorhinolaryngologist may be necessary to visualize the epiglottic and supraglottic regions with a flexible fiberoptic laryngoscope in patients who experience throat tightness or throat closing and who present with little or no objective signs of airway compromise.
  • In patients with symptoms of throat tightness or throat closing with mild-to-moderate signs of airway compromise or patients who have evidence of early airway obstruction on flexible fiberoptic laryngoscopy, consultation with an anesthesiologist may be necessary to assist in securing the airway.
    • Patients who have moderate-to-severe signs and symptoms of airway compromise, such as increasing dyspnea, hoarseness, dysphagia, inability to clear secretions, use of accessory muscles, or decreasing oxygen saturation on pulse oximetry, require emergent consultation with both an anesthesiologist and an otorhinolaryngologist to place a surgical airway if intubation is unsuccessful. Rapid sequence intubation in these patients should be used with caution. The airway may be maintained open only by the patient's laryngeal muscles. The use of paralytics may allow the airway to be completely occluded.

Activity

  • Advise patients who have experienced an allergic reaction to prior wasp stings or to any Hymenoptera stings to exercise caution while outdoors during mild-to-warm weather.
    • Advise these patients to avoid wearing any scented material (eg, perfume, hairspray, soaps, deodorants, sunscreen).
    • Brightly colored clothing, especially floral designs, should be avoided.
    • Tell patients who have experienced a severe reaction to a wasp sting to curtail solitary outdoor activities. Advise that the patient should be accompanied when outdoors and away from populated areas (eg, hiking, fishing) in case help is needed.
  • Because odors tend to attract wasps, tell patients and their families to examine the home environment to decrease risks of attracting insects.
    • Cover garbage pails.
    • Remove rotting fruit on the vine or tree or after having fallen to the ground.
  • Encourage patients to carry EpiPen auto-injectors when outdoors and to have one device in the home. Advise the patient that auto-injectors left in the car for prolonged periods during hot days may not be effective. They should periodically review the expiration date of the auto-injectors.

Medication

Medication use varies depending on the severity of the wasp sting. Antihistamines are used to treat mild urticarial symptoms. Catecholamines are needed in extreme cases (eg, anaphylaxis).

Antihistamines

H1-receptor antagonists block the effects of histamine. Diphenhydramine and hydroxyzine are two of the most widely used H1 blockers for oral and parenteral use in wasp stings.


Diphenhydramine (Benadryl)

For symptomatic relief of symptoms caused by release of histamine in allergic reactions.

Adult

25-50 mg PO/IV/IM q4-6h

Pediatric

2 mg/kg PO q4-6h
1-2 mg/kg IV/IM q4-6h

Potentiates effect of CNS depressants; because of alcohol content, do not administer syrup dosage form to patients who are taking medications that can cause disulfiramlike reactions

Documented hypersensitivity; MAOIs may prolong and intensify its effects

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

May exacerbate angle-closure glaucoma, hyperthyroidism, peptic ulcer, and urinary tract obstruction; drowsiness or visual disturbances may occur (advise patients against driving); MAOIs may prolong or intensify its effects


Hydroxyzine (Atarax, Vistaril)

Antagonizes H1 receptors in periphery. May suppress histamine activity in subcortical region of CNS.

Adult

Atarax: 25 mg PO q8h
Vistaril: 25-100 mg IM q6-8h

Pediatric

Atarax:
<6 years: 50 mg/d PO in divided doses
>6 years: 100 mg/d PO in divided doses
Vistaril: 2 mg/kg IM q6-8h

CNS depression may increase with alcohol or other CNS depressants

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

Associated with clinical exacerbations of porphyria (may not be safe for porphyric patients); ECG abnormalities (alterations in T waves) may occur; may cause drowsiness

Glucocorticoids

These agents modulate and decrease the inflammatory response to the sting. Onset of action is delayed for several hours; therefore, glucocorticoids have very little effect in the acute setting. Early administration continues to stabilize the patient.


Methylprednisolone (Solu-Medrol, Medrol)

Steroids ameliorate delayed effects of anaphylactoid reactions and may limit biphasic anaphylaxis. In severe cases of serum sickness, parenteral steroids may be beneficial to reduce inflammatory effects of this immune complex–mediated disease.

Adult

125 mg IV

Pediatric

30 mg/kg IV q4h

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 - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

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


Prednisone (Sterapred)

May decrease inflammation by reversing increased capillary permeability and suppressing PMN activity.

Adult

20-40 mg PO

Pediatric

Not established

Coadministration with estrogens may decrease prednisone clearance; concurrent use with digoxin may cause digitalis toxicity secondary to hypokalemia; phenobarbital, phenytoin, and rifampin may increase metabolism of glucocorticoids (consider increasing maintenance dose); monitor for hypokalemia with coadministration of diuretics

Documented hypersensitivity; viral infection; peptic ulcer disease; hepatic dysfunction; connective tissue infections; fungal or tubercular skin infections; GI disease

Pregnancy

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

Precautions

Abrupt discontinuation of glucocorticoids may cause adrenal crisis; hyperglycemia, edema, osteonecrosis, myopathy, peptic ulcer disease, hypokalemia, osteoporosis, euphoria, psychosis, myasthenia gravis, growth suppression, and infections may occur with glucocorticoid use

Sympathomimetics

Epinephrine and the inhaled beta agonist albuterol reverse the effect of histamine (rather than blocking the effect).


Epinephrine (Adrenalin, EpiPen)

DOC for treating anaphylactoid reactions. Has alpha-agonist effects that include increased peripheral vascular resistance, reversed peripheral vasodilatation, systemic hypotension, and vascular permeability. Beta-agonist effects of epinephrine include bronchodilatation, chronotropic cardiac activity, and positive inotropic effects.
Epinephrine can be administered SC for mild-to-moderate reactions and IV and via ET.

Adult

0.01 mg/kg to maximum dose of 0.5 mg IM of 1:1000 solution q5-15min

Pediatric

Not established

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

Documented hypersensitivity; cardiac arrhythmias; angle-closure glaucoma; local anesthesia in areas such as fingers or toes is contraindicated because vasoconstriction may produce sloughing of tissue; do not use during labor (may delay 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 elderly patients, prostatic hypertrophy, hypertension, cardiovascular disease, diabetes mellitus, hyperthyroidism, and cerebrovascular insufficiency; rapid IV infusions may cause death from cerebrovascular hemorrhage or cardiac arrhythmias


Albuterol (Proventil, Ventolin)

Beta agonist for bronchospasm refractory to epinephrine. Relaxes bronchial smooth muscle by action on beta2 receptors with little effect on cardiac muscle contractility.

Adult

Albuterol sulfate 0.5% inhalation solution: 2.5 mg of albuterol
To administer 2.5 mg of albuterol, dilute 0.5 mL of the 0.5% solution with 2.5 mL of sterile normal saline solution; adjust flow rate of nebulizer to administer solution over 5-15 min

Pediatric

<2 years: Not established
2-12 years: Base initial dose on body weight, 0.1-0.15 mg/kg; not to exceed 2.5 mg
>12 years: 2.5 mg of albuterol
To administer 2.5 mg of albuterol, dilute 0.5 mL of the 0.5% solution with 2.5 mL of sterile normal saline solution; adjust flow rate of nebulizer to administer solution over 5-15 min

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

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


Glucagon

DOC for severe anaphylaxis in patients who take beta-blockers (should be used in addition to epinephrine, not as a substitute).
Pancreatic alpha cells of the islets of Langerhans produce glucagon, a polypeptide hormone. Exerts opposite effects of insulin on blood glucose. Glucagon elevates blood glucose levels by inhibiting glycogen synthesis and enhancing formation of glucose from noncarbohydrate sources, such as proteins and fats (gluconeogenesis). Increases hydrolysis of glycogen to glucose (glycogenolysis) in liver in addition to accelerating hepatic glycogenolysis and lipolysis in adipose tissue. Glucagon also increases force of contraction in the heart and has a relaxant effect on GI tract.
Dose used for anaphylaxis is higher than the usual dose of 1 mg (1 U) IV/IM/SC used to treat hypoglycemia.

Adult

1-5 mg IV bolus, followed by infusion of 5-15 mcg/min titrated against BP

Pediatric

Hypoglycemia:
<20 kg: 0.5 mg (0.5 U) or a dose equivalent to 20-30 mcg/kg
>20 kg: 1 mg (1 U) IV/IM/SC
Anaphylaxis: May need higher doses

Effects of anticoagulants may be enhanced by glucagon (although onset may be delayed); monitor prothrombin activity and for signs of bleeding in patients receiving anticoagulants; adjust dose accordingly

Documented hypersensitivity; pheochromocytoma

Pregnancy

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

Precautions

Monitor blood glucose levels in hypoglycemic patients until they are asymptomatic; glucagon is effective in treating hypoglycemia only if sufficient liver glycogen is present; since liver glycogen availability is necessary to treat hypoglycemic patients, glucagon has virtually no effects on patients in states of starvation, adrenal insufficiency, or chronic hypoglycemia

Antihistamine, H2 Blocker

The combination of H1 and H2 antagonists may be useful in chronic idiopathic urticaria not responding to H1 antagonists alone. It may also be useful for itching and flushing in anaphylaxis, pruritus, urticaria, and contact dermatitis.


Famotidine (Pepcid)

H2 antagonist that, when combined with an H1 type, may be useful in treating allergic reactions that do not respond to H1 antagonists alone.

Adult

20 mg IV bid

Pediatric

Not established; suggested dose is 1-2 mg/kg/d IV divided q6h; not to exceed 40 mg/d

May decrease effects of ketoconazole and itraconazole

Pregnancy

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

Precautions

If changes in renal function occur during therapy, consider adjusting dose or discontinuing treatment; may increase risk of necrotizing enterocolitis in premature infants

More on Wasp Stings

Overview: Wasp Stings
Differential Diagnoses & Workup: Wasp Stings
Treatment & Medication: Wasp Stings
Follow-up: Wasp Stings
Multimedia: Wasp Stings
References

References

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Further Reading

Keywords

wasp stings, wasp, wasp insect, bee stings, insect stings, wasp venom, Hymenoptera stings, Hymenoptera bites, yellow jacket stings, wasp envenomation, Vespidae stings, urticaria, Hymenoptera, Vespidae, wasp bite

Contributor Information and Disclosures

Author

Carl A Mealie, MD, Assistant Professor, Department of Emergency Medicine, Albert Einstein College of Medicine; Medical Director of Emergency Care Institute, Chief of Clinical Operations, Department of Emergency Medicine, Long Island Jewish Medical Center
Carl A Mealie, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American College of Physicians, American Medical Association, New York Academy of Medicine, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Coauthor(s)

Alan S Multz, MD, Associate Professor of Clinical Medicine, Albert Einstein College of Medicine; Program Director, Internal Medicine Residency, Associate Chairman, Department of Medicine, Long Island Jewish Medical Center
Alan S Multz, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Chest Physicians, American College of Physicians, American Thoracic Society, and Society of Critical Care Medicine
Disclosure: Astellas Pharmaceutical Honoraria Consulting; Merck Pharmaceutical Honoraria Speaking and teaching; The Medicines Company Honoraria Consulting; Schering Plough Honoraria Speaking and teaching; Wyeth Pharmaceuticals Honoraria Speaking and teaching; Pfizer Honoraria Speaking and teaching

Max Vernon Wisgerhof, MD, Fellowship Program Director, Department of Endocrinology and Metabolism, Henry Ford Hospital
Max Vernon Wisgerhof, MD is a member of the following medical societies: American College of Physicians, American Diabetes Association, American Thyroid Association, and Endocrine Society
Disclosure: Nothing to disclose.

Medical Editor

Lisa Kirkland, MD, FACP, CNSP, MSHA, Assistant Professor, Department of Internal Medicine, Division of Hospital Medicine, Mayo Clinic; ANW Intensivists, Abbott Northwestern Hospital
Lisa Kirkland, MD, FACP, CNSP, MSHA is a member of the following medical societies: American College of Physicians, Society of Critical Care Medicine, and Society of Hospital Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

CME Editor

Timothy D Rice, MD, Associate Professor, Departments of Internal Medicine and Pediatrics and Adolescent Medicine, Saint Louis University School of Medicine
Timothy D Rice, MD is a member of the following medical societies: American Academy of Pediatrics and American College of Physicians
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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