You are in: eMedicine Specialties > Emergency Medicine > ENVIRONMENTAL Caterpillar EnvenomationArticle Last Updated: Feb 9, 2007AUTHOR AND EDITOR INFORMATIONAuthor: Robert Norris, MD, Chief, Associate Professor, Department of Surgery, Division of Emergency Medicine, Stanford University Medical Center Robert Norris is a member of the following medical societies: American College of Emergency Physicians, American Medical Association, California Medical Association, and Wilderness Medical Society Editors: Samuel M Keim, MD, Associate Professor, Department of Emergency Medicine, University of Arizona College of Medicine; John T VanDeVoort, PharmD, ABAT, Director of Pharmacy, Sacred Heart Hospital; Gino A Farina, MD, Program Director, Associate Professor of Clinical Emergency Medicine, Department of Emergency Medicine, Long Island Jewish Medical Center, Albert Einstein College of Medicine; 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; Scott H Plantz, MD, FAAEM, Associate Professor, Research Director, Department of Emergency Medicine, Mount Sinai School of Medicine Author and Editor Disclosure Synonyms and related keywords: caterpillar envenomations, Megalopyge opercularis, M opercularis, caterpillar dermatitis, erucism, dermatitis, lepidopterism, Lepidoptera, Arthropoda, Insecta, puss caterpillar, asp, caterpillar sting, Lonomia INTRODUCTIONBackgroundMore than 165,000 species of caterpillars in the order Lepidoptera (phylum Arthropoda, class Insecta) exist. About 150 are of medical importance. This importance lies in the ability of many species to induce an irritant or toxic dermatitis in humans and in the ability of some species to sting. Caterpillars are the larval forms of moths and butterflies. After hatching from their eggs, caterpillars pass through 4-5 instars (stages between molts) before they pupate in a cocoon. The adult moth or butterfly emerges from the cocoon to reproduce the next generation. More than 50 species in the United States alone are capable of inflicting a painful sting. Seasonal epidemics of dermatitis can occur when caterpillars are numerous. The most dangerous caterpillar in the United States is the puss caterpillar or asp (Megalopyge opercularis; see Image 1), the larval form of the flannel moth. It is found throughout the Southeast, from Maryland to Mexico. Stings from this species are common from June through September. PathophysiologyHuman disease from caterpillars or moths usually arises from direct contact, exposure to substances or animals that have been infested with caterpillars or their webs, or contact with airborne caterpillar debris. Diaz classifies the diseases caused by caterpillars into 5 groups: erucism, lepidopterism, dendrolimiasis, ophthalmia nodosa, and consumptive coagulopathy with secondary fibrinolysis. Erucism (caterpillar dermatitis) is characterized by a localized, pruritic, maculopapular contact dermatitis and urticaria that follows contact with toxic hairs, spines, or hemolymph, either directly or following aerosolization. Lepidopterism is a systemic illness that occurs following such contact, and it is typified by diffuse urticaria, upper airway inflammation, nausea, vomiting, headache, and bronchospasm. Dendrolimiasis is a more chronic illness that follows contact with the Asian Dendorlimus pini caterpillar. Patients with this disorder demonstrate a pruritic maculopapular rash and migratory polyarthritis/polychondritis, which can progress to chronic osteoarthritis. Occasionally, acute scleritis occurs as well. Ophthalmia nodosa presents with acute conjunctivitis, progressing to panophthalmitis, following penetration of the cornea by urticating hairs. Consumptive coagulopathy with secondary fibrinolysis occurs most commonly following stings by the South American Lonomia caterpillar whose venom activates factor X and prothrombin. Patients can demonstrate bleeding from almost any anatomic site and may develop acute renal failure. Caterpillar venoms are produced by glandular cells in the epithelium and are stored in and injected by urticating hairs and spines (setae). Many species produce toxic hemolymph, which can cause human disease. In some patients, immunoglobulin E (IgE) antibodies are produced following contact, resulting in a hypersensitive state and the production of generalized urticaria on subsequent re-contact. A few caterpillars lacking urticating hairs are capable of inducing a contact dermatitis (type IV hypersensitivity). Some caterpillars and moths release their toxic hairs into the environment, where the hairs can be inhaled. Pets or contaminated objects also can carry venomous hairs. In any of these situations, contact with the hairs can cause rhinitis or respiratory disease. Seasonal epidemics of respiratory disease have occurred in Latin America because of this phenomenon. The pathologic response leading to erucism or lepidopterism consists of acute inflammation and cellular infiltration around hairs that have penetrated the skin or conjunctiva or have been inhaled into the respiratory tract. In the skin, diffuse vascular dilatation occurs, with subsequent edema formation in the superficial dermis and ballooning of keratinocytes within the epidermis that can lead to vesiculation. In the eye, hairs have a remarkable penetrating capacity and may work their way into the cornea, anterior chamber, or lens, where an intense inflammatory response occurs secondary to the nature of the foreign material and direct toxic effects. Caterpillar venom-filled spines, found only in the larval forms (adult moths and butterflies do not sting), are hollow structures with a single basal poison cell that produces toxin. When pressed into the skin, the tip of the spine fractures, and the venom is injected under pressure. Toxicity declines significantly after the creature's death, but irritant or toxic hairs may retain the ability to cause dermatitis for years. Likewise, the toxic hemolymph of some caterpillars retains its potency for prolonged periods after the animal's death. Caterpillar venoms are poorly studied but may contain peptides, hyaluronidase, phospholipase A, and biogenic amines such as histamine or histamine-releasing substances. Some, such as the South American Lonomia species, contain fibrinolytic proteases and coagulation activators that can stimulate a consumptive coagulopathy and renal failure in victims. FrequencyUnited StatesAlthough no accurate information is available, epidemics of erucism and lepidopterism have been reported. These include school closings, outbreaks of dermatitis and rhinitis in the thousands, and symptoms in more than 500,000 people caused by airborne caterpillar hair dispersion. InternationalNo accurate information is available, though it appears that the incidence of human disease is increasing. Mortality/MorbidityOccasional case reports of death from erucism exist, but death is very rare following stings by most species. Death may be secondary to a hypersensitivity reaction or bleeding diathesis in cases involving caterpillars of the Saturniidae family. In this family, South American Lonomia caterpillars have a high fatality rate (approximately 1.7%) due to the toxicity of their venoms and the fact that many exposures lead to multiple stings due to the communal natura of these species. No deaths have been reported following M opercularis stings.
CLINICALHistory
Physical
DIFFERENTIALSAnaphylaxis Bites, Insects Catscratch Disease Centipede Envenomations Corneal Abrasion Corneal Laceration Corneal Ulceration and Ulcerative Keratitis Dermatitis, Atopic Dermatitis, Contact Disseminated Intravascular Coagulation Erysipelas Idiopathic Thrombocytopenic Purpura Impetigo Iritis and Uveitis Millipede Envenomations Molluscum Contagiosum Pediatrics, Henoch-Schönlein Purpura Pediculosis Pityriasis Rosea Plant Poisoning, Resins Plant Poisoning, Toxicodendron Scabies Scleritis Scorpion Envenomations Spider Envenomations, Brown Recluse Spider Envenomations, Funnel Web Spider Envenomations, Redback Spider Envenomations, Tarantula Spider Envenomations, Widow
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| Drug Name | Diphenhydramine (Benadryl, Benylin, Bydramine) |
|---|---|
| Description | Used for symptomatic relief of allergic symptoms caused by histamine released in response to allergens. |
| Adult Dose | 25-50 mg PO q6-8h prn; not to exceed 400 mg/d 10-50 mg IV/IM q6-8h prn; not to exceed 400 mg/d |
| Pediatric Dose | 12.5-25 mg PO tid/qid or 5 mg/kg/d or 150 mg/m2/d divided tid/qid; not to exceed 300 mg/d 5 mg/kg/d or 150 mg/m2/d IV/IM divided qid; not to exceed 300 mg/d |
| Contraindications | Documented hypersensitivity |
| Interactions | Potentiates effect of CNS depressants; due to alcohol content, do not give syrup dosage form to patients taking medications that can cause disulfiramlike reactions |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | May exacerbate angle-closure glaucoma, hyperthyroidism, peptic ulcer, and urinary tract obstruction |
| Drug Name | Chlorpheniramine maleate (Chlor-Trimeton) |
|---|---|
| Description | Competes with histamine for H1-receptor sites on effector cells in blood vessels and respiratory tract. |
| Adult Dose | 10-20 mg IV/IM/SC as a single dose; not to exceed 40 mg/d 4 mg PO q4-6h; not to exceed 24 mg/d Sustained release: 8-12 mg PO q8-12h; not to exceed 24 g/d |
| Pediatric Dose | 2-6 years: 1 mg q4-6h IV/IM/SC in equally divided doses; not to exceed 6 mg/d 6-12 years: 2 mg PO q4-6h; not to exceed 12 mg/d PO Sustained release: 8 mg PO hs |
| Contraindications | Documented hypersensitivity; acute asthma attacks; narrow-angle glaucoma; bladder neck obstruction; symptomatic prostate hypertrophy; stenosing peptic ulcer |
| Interactions | CNS toxicity increases with coadministration of other CNS depressants, TCAs, MAOIs, and phenothiazines |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | May cause significant confusional symptoms; not for administration to premature or full-term neonates |
| Drug Name | Cimetidine (Tagamet) |
|---|---|
| Description | 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 in addition to H1 antihistamines. |
| Adult Dose | Patients with persistent symptoms: 300 mg IV followed by PO administration as outpatient q6h for 2 d or for as long as clinically indicated |
| Pediatric Dose | 25-30 mg/kg/d IV in 6 divided doses |
| Contraindications | Documented hypersensitivity |
| Interactions | Can increase blood levels of theophylline, warfarin, TCAs, triamterene, phenytoin, quinidine, propranolol, metronidazole, procainamide, and lidocaine |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Elderly patients may experience confusional states; may cause impotence and gynecomastia in young males; may increase levels of many drugs; adjust dose or discontinue treatment if changes in renal function occur |
Onset of action is approximately 4-6 h, and they have limited benefit in the initial acute treatment of rapidly deteriorating anaphylactic patients. However, corticosteroids may benefit patients with persistent bronchospasm or hypotension.
Topical steroids can help reduce cutaneous inflammatory response in caterpillar-induced dermatitis.
| Drug Name | Methylprednisolone sodium succinate (Solu-Medrol) |
|---|---|
| Description | Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing increased capillary permeability. |
| Adult Dose | Loading dose: 125-250 mg IV, followed by 0.5-1 mg/kg/dose q6h for up to 5 d |
| Pediatric Dose | Loading dose: 2 mg/kg IV, followed by 0.5-1 mg/kg/dose q6h for up to 5 d |
| Contraindications | Documented hypersensitivity; viral, fungal, or tubercular skin infections |
| Interactions | Coadministration with digoxin may increase digitalis toxicity secondary to hypokalemia; estrogens may increase levels; phenobarbital, phenytoin, and rifampin may decrease levels (adjust dose); monitor patients for hypokalemia when taking medication concurrently with diuretics |
| 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 |
| Drug Name | Prednisone (Deltasone, Orasone, Meticorten) |
|---|---|
| Description | Decreases inflammation by suppressing migration of polymorphonuclear leukocytes and reversing increased capillary permeability. |
| Adult Dose | 1-2 mg/kg PO qd or divided bid until symptom resolution, followed by a 1-wk taper |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; viral, fungal, or tubercular infections |
| Interactions | 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 |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Abrupt discontinuation may cause adrenal crisis; hyperglycemia, edema, osteonecrosis, myopathy, peptic ulcer disease, hypokalemia, osteoporosis, euphoria, psychosis, myasthenia gravis, growth suppression, and infections may occur |
| Drug Name | Topical hydrocortisone (Westcort, Dermacort, Cortaid) |
|---|---|
| Description | DOC for reducing cutaneous inflammatory response in caterpillar-induced dermatitis. Adrenocorticosteroid derivative suitable for application to skin or external mucous membranes. Has mineralocorticoid and glucocorticoid effects resulting in anti-inflammatory activity. |
| Adult Dose | Apply sparingly to affected areas bid/qid |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; viral, fungal, and bacterial skin infections |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Prolonged use, applying over large surface areas, application of potent steroids, and occlusive dressings may increase systemic absorption of corticosteroids and may cause Cushing syndrome, reversible HPA axis suppression, hyperglycemia, and glycosuria |
Via combined alpha-adrenergic and beta-adrenergic agonist action, sympathomimetics are effective in reversing acute bronchospasm of allergic or irritant origin.
An additional option in the management of persistent bronchospasm is via anticholinergics. These agents block the action of acetylcholine at parasympathetic sites in bronchial smooth muscle, causing bronchodilation.
| Drug Name | Albuterol sulfate (Ventolin, Proventil) |
|---|---|
| Description | Beta agonist useful in treatment of bronchospasm refractory to epinephrine. Relaxes bronchial smooth muscle by acting on beta 2 receptors with little effect on heart rate. |
| Adult Dose | 2-4 mg/dose PO divided tid/qid; not to exceed 32 mg/d Inhalant: 1-2 inhalations q4-6h; not to exceed 12 inhalations/d Nebulizer: 0.5 mL (2.5 mg) of 0.5% inhalation solution diluted in 1-2.5 mL of normal saline q4-6h; higher frequency may be used for intensive care patients |
| Pediatric Dose | 2-6 years: 0.1-0.2 mg/kg/dose PO divided tid; not to exceed 12 mg/d 6-12 years: 2 mg/dose PO divided tid/qid; not to exceed 24 mg/d >12 years: Administer as in adults Inhalant dose: <12 years: Using a tube spacer, give 1-2 inhalations qid >12 years: Administer as in adults Nebulizer dose: <5 years: 0.25-0.5 mL (1.25-2.5 mg) of 0.5% inhalation solution diluted in 1-2.5 mL of normal saline q4-6h in equally divided doses >5 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Beta-adrenergic blockers antagonize effects; inhaled ipratropium may increase duration of bronchodilatation by albuterol; cardiovascular effects may increase with MAOIs, inhaled anesthetics, TCAs, and sympathomimetic agents |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in hyperthyroidism, diabetes mellitus, and cardiovascular disorders |
| Drug Name | Epinephrine (Adrenalin, EpiPen) |
|---|---|
| Description | Alpha-agonist effects increase peripheral vascular resistance and reverse peripheral vasodilatation, vascular permeability, and systemic hypotension. Conversely, beta-agonist effects produce bronchodilatation, cause positive inotropic and chronotropic cardiac activity, and result in an increased production of intracellular cAMP. |
| Adult Dose | Initial dose: 0.01 mL/kg IM/SC of 1:1000 solution, not to exceed 0.5 mL of 1:1000 solution (0.5 mg); if accessible, administer fraction of total dose (0.1-0.2 mL) at site of antigenic exposure Severe anaphylaxis (laryngeal edema, respiratory failure, shock): 10 mL of 1:100,000 dilution of aqueous epinephrine IV over 10 min; if no improvement is seen, establish continuous infusion in which 1 mcg/min of a 4-mcg/mL concentration is started and increased to 4 mcg/min prn |
| Pediatric Dose | Infuse 0.1 mcg/kg/min IV with increasing increments of 0.1 mcg/kg/min; not to exceed 1.5 mcg/kg/min |
| Contraindications | Documented hypersensitivity; cardiac arrhythmias or angle-closure glaucoma; local anesthesia in areas such as fingers or toes because vasoconstriction may produce sloughing of tissue; do not use during labor (may delay second stage of labor) |
| Interactions | Increases toxicity of beta-blocking and alpha-blocking agents and that of halogenated inhalational anesthetics |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| 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 |
| Drug Name | Ipratropium bromide (Atrovent) |
|---|---|
| Description | Synthetic quaternary anticholinergic ammonium compound chemically related to atropine; has antisecretory properties; when applied locally, inhibits secretions from serous and seromucous glands lining nasal mucosa. |
| Adult Dose | Nebulizer: 1 U dose vial (500 mcg) tid/qid with doses 6-8 h apart Metered dose inhaler: 2 inhalations q4-6h qid; not to exceed 12 inhalations in 24 h |
| Pediatric Dose | Nebulizer: 250 mcg tid Metered dose inhaler: 1-2 inhalations tid; not to exceed 6 inhalations in 24 h |
| Contraindications | Documented hypersensitivity |
| Interactions | Drugs with anticholinergic properties, such as dronabinol, may increase toxicity; albuterol increases effects |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Caution in narrow-angle glaucoma, prostatic hypertrophy, and bladder neck obstruction |
Pain control is essential to quality patient care. Most analgesics have sedating properties, which may be beneficial for patients who have sustained severe caterpillar stings.
| Drug Name | Aspirin (Anacin, Ascriptin, Bayer Aspirin, Bufferin) |
|---|---|
| Description | Used for treatment of mild to moderate pain and headache. |
| Adult Dose | 325-650 mg PO q4-6h; not to exceed 4 g/d |
| Pediatric Dose | 10-15 mg/kg/dose PO q4-6h; not to exceed 60-80 mg/kg/d |
| Contraindications | Documented hypersensitivity; liver damage; hypoprothrombinemia; vitamin K deficiency; bleeding disorders; asthma; due to association of aspirin with Reye syndrome, do not use in children ( <16 y) with flu |
| Interactions | Effects may decrease with antacids and urinary alkalinizers; corticosteroids decrease salicylate serum levels; additive hypoprothrombinemic effects and increased bleeding time may occur with coadministration of anticoagulants; may antagonize uricosuric effects of probenecid and increase toxicity of phenytoin and valproic acid; doses > 2 g/d may potentiate glucose-lowering effect of sulfonylurea drugs |
| Pregnancy | D - Unsafe in pregnancy |
| Precautions | May cause transient decrease in renal function and aggravate chronic kidney disease; extreme caution in patients with severe anemia, with history of blood coagulation defects, or who are taking anticoagulants |
| Drug Name | Morphine sulfate (Duramorph, Astramorph, MS Contin) |
|---|---|
| Description | Parenteral opiates may be necessary to manage extreme pain in patients with severe stings. |
| Adult Dose | 0.1 mg/kg in 2-4 mg increments IV; titrate to desired effect |
| Pediatric Dose | 0.1 mg/kg IV; titrate to desired effect |
| Contraindications | Documented hypersensitivity; hypotension; potentially compromised airway with uncertain rapid airway control; nausea; emesis; constipation; urinary retention |
| Interactions | TCAs, MAOIs, and other CNS depressants may potentiate adverse effects |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Avoid in hypotension, respiratory depression, nausea, emesis, constipation, and urinary retention; caution in atrial flutter and other supraventricular tachycardias; has vagolytic action and may increase ventricular response rate |
| Drug Name | Hydrocodone and acetaminophen (Vicodin) |
|---|---|
| Description | Drug combination indicated for relief of moderate to severe pain. |
| Adult Dose | 1-2 tab or cap PO q4-6h prn pain |
| Pediatric Dose | Single dose not to exceed 10 mg of hydrocodone bitartrate or 2.6 g/d of acetaminophen <12 years: Administer based on acetaminophen dose of 10-15 mg/kg/dose PO q4-6h prn >12 years: Administer based on acetaminophen dose of 750 mg PO q4h Not to exceed 5 doses in 24 h |
| Contraindications | Documented hypersensitivity; elevated ICP |
| Interactions | Coadministration with phenothiazines may decrease analgesic effects; toxicity increases with CNS depressants or TCAs |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Tablets contain metabisulfite, which may cause hypersensitivity; caution in patients dependent on opiates since this substitution may result in acute opiate-withdrawal symptoms upon discontinuation; caution in severe renal or hepatic dysfunction |
NSAIDs can be effective in reducing discomfort associated with caterpillar-induced dermatitis.
| Drug Name | Indomethacin (Indocin, Indochron ER) |
|---|---|
| Description | Commonly prescribed NSAID used for reducing inflammatory responses. Rapidly absorbed; metabolism occurs in liver by demethylation, deacetylation, and glucuronide conjugation; inhibits prostaglandin synthesis. |
| Adult Dose | 25-50 mg PO bid/tid 75 mg SR PO bid; not to exceed 200 mg/d |
| Pediatric Dose | 1-2 mg/kg/d divided PO bid/qid; not to exceed 4 mg/kg/d or 150-200 mg/d |
| Contraindications | Documented hypersensitivity; GI bleeding or renal insufficiency; coagulopathy |
| Interactions | Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Category D in third trimester of pregnancy; acute renal insufficiency, hyperkalemia, hyponatremia, interstitial nephritis, and renal papillary necrosis may occur; increases risk of acute renal failure in patients with preexisting renal disease or compromised renal perfusion; reversible leukopenia may occur (discontinue if persistent leukopenia, granulocytopenia, or thrombocytopenia) |
These agents may be used to support organ perfusion in hypotensive patients unresponsive to intravenous volume expansion.
| Drug Name | Dopamine (Intropin) |
|---|---|
| Description | May be required to support BP in the face of hypotension caused by anaphylactic/anaphylactoid reaction that is unresponsive to fluids and epinephrine. |
| Adult Dose | 5-20 mcg/kg/min IV; titrate to effect |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; patients diagnosed with pheochromocytoma or ventricular fibrillation |
| Interactions | Phenytoin, alpha-adrenergic and beta-adrenergic blockers, general anesthesia, and MAOIs increase and prolong effects |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Closely monitor urine flow, cardiac output, pulmonary wedge pressure, and BP during infusion; prior to infusion, correct hypovolemia with either whole blood or plasma, as indicated; monitoring central venous pressure or left ventricular filling pressure may be helpful in detecting and treating hypovolemia |
Used for tetanus immunization. A booster injection in previously immunized individuals is recommended to prevent this potentially lethal syndrome.
| Drug Name | Tetanus toxoid |
|---|---|
| Description | Used to induce active immunity against tetanus in selected patients. Immunizing agents of choice for most adults and children > 7 y are tetanus and diphtheria toxoids. Necessary to administer booster doses to maintain tetanus immunity throughout life. Pregnant patients should receive only tetanus toxoid, not a diphtheria antigen-containing product. In children and adults, may administer into deltoid or midlateral thigh muscles. In infants, preferred site of administration is mid thigh laterally. |
| Adult Dose | Primary immunization: 0.5 mL IM; give 2 injections 4-8 wk apart and a third dose 6-12 mo after second injection Booster dose: 0.5 mL q10y |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; a history of any type of neurologic symptoms or signs following administration of this product; FDA recommends that elective tetanus immunization be deferred during any outbreak of poliomyelitis because tetanus toxoid injections are an important cause of provocative poliomyelitis |
| Interactions | Patients receiving immunosuppressants, including corticosteroids or radiation therapy, may remain susceptible despite immunization due to poor immune response; cimetidine may enhance or augment delayed-hypersensitivity responses to skin-test antigens; avoid concurrent use with systemic chloramphenicol since it may impair amnestic response to tetanus toxoid; concurrent use of tetanus immune globulin may delay development of active immunity by several days (interaction is nevertheless clinically insignificant and does not preclude concurrent use) |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Do not use to treat actual tetanus infections or for immediate prophylaxis of unimmunized individuals (use instead tetanus antitoxin, preferably human tetanus immune globulin); diminished antibody response to active immunization may be seen in patients receiving immunosuppressive therapy; better to defer primary diphtheria immunization until immunosuppressive therapy discontinued; routine immunization of symptomatic and asymptomatic HIV-infected persons is recommended |
| Media file 1: Caterpillar envenomations. Puss caterpillar or asp. Photo courtesy of the Arizona Poison and Drug Information Center. | |
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Caterpillar Envenomation excerpt
Article Last Updated: Feb 9, 2007