You are in: eMedicine Specialties > Emergency Medicine > INFECTIOUS DISEASES ErysipelasArticle Last Updated: Jun 13, 2006AUTHOR AND EDITOR INFORMATIONAuthor: Geofrey Nochimson, MD, Consulting Staff, Department of Emergency Medicine, Sentara Careplex Hospital Geofrey Nochimson is a member of the following medical societies: American College of Emergency Physicians Editors: Francis Counselman, MD, Program Director, Chair, Professor, Department of Emergency Medicine, Eastern Virginia Medical School; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Eddy Lang, MDCM, CCFP (EM), CSPQ, Assistant Professor, Department of Family Medicine, McGill University; Consulting Staff, Department of Emergency Medicine, The Sir Mortimer B Davis-Jewish General Hospital; 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; Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School Author and Editor Disclosure Synonyms and related keywords: erysipelas, group A beta-hemolytic streptococci, hemolytic streptococcus, skin infection, painful rash, erythematous rash, edematous rash, abrasions, skin ulcers, insect bites, eczema, psoriatic lesions, lymphatic obstruction, lymphatic edema, saphenous vein grafting in lower extremities, postradical mastectomy, immunocompromised patients, INTRODUCTIONBackgroundErysipelas is a skin infection typically caused by group A beta-hemolytic streptococci, although other streptococcal groups are occasionally causative agents. Infection involves the dermis and lymphatics and is a more superficial subcutaneous infection of the skin than cellulitis. Erysipelas is characterized by intense erythema, induration, and a sharply demarcated border, which differentiates it from other skin infections. PathophysiologyThe skin is the primary organ system affected. FrequencyUnited StatesIncreasing incidence has been noted since the late 1980s. Mortality/MorbidityErysipelas generally is benign; however, it can be fatal when associated with bacteremia in very young, elderly, or immunocompromised patients. The mortality rate is less than 1% in treated cases. SexSlight female predominance is observed. AgeInfection occurs at extremes of age, but erysipelas is primarily a disease of adults. CLINICALHistory
Physical
Causes
DIFFERENTIALSAngioedema Cellulitis Dermatitis, Contact Herpes Zoster Necrotizing Fasciitis Systemic Lupus Erythematosus Urticaria
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| Drug Name | Penicillin G (Pfizerpen) |
|---|---|
| Description | Interferes with synthesis of cell wall mucopeptides during active multiplication, resulting in bactericidal activity against susceptible microorganisms, including streptococci. DOC as streptococcal resistance very rarely has been reported in those strains likely to cause erysipelas. Resistance not yet observed in group A strains. |
| Adult Dose | 600,000-2,000,000 U/kg IV divided q6h |
| Pediatric Dose | 50,000-250,000 U/kg IV divided q4h |
| Contraindications | Documented hypersensitivity |
| Interactions | Probenecid may increase penicillin effectiveness by decreasing its clearance; coadministration of tetracyclines may decrease penicillin effectiveness |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Caution with impaired renal function |
| Drug Name | Erythromycin (EES, E-Mycin, Ery-Tab) |
|---|---|
| Description | Inhibits RNA-dependent protein synthesis, possibly by stimulating the dissociation of peptidyl t-RNA from ribosomes; arrests bacterial growth. Indicated to treat infections caused by streptococci in penicillin-allergic patients. |
| Adult Dose | Mild cases: 250-500 mg PO qid Severe cases: 500 mg IV q4-6h |
| Pediatric Dose | Mild cases: 30-50 mg/kg/d PO qid Severe cases: 50 mg/kg/d IV q6h |
| Contraindications | Documented hypersensitivity; hepatic impairment |
| Interactions | Theophylline, digoxin, carbamazepine, and cyclosporine toxicity may increase when coadministered with erythromycin; also may potentiate the anticoagulant effects of warfarin; coadministration with lovastatin and simvastatin increases risk of rhabdomyolysis |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Use with caution in patients with liver disease; estolate preparation of erythromycin may cause cholestatic jaundice; GI adverse effects are common, thus doses should be given after meals; discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occur; consider clarithromycin or azithromycin for less GI upset, and for easier dosing |
| Drug Name | Penicillin VK (Veetids) |
|---|---|
| Description | Used in mild cases. It inhibits biosynthesis of cell wall mucopeptides and is effective during the stage of active multiplication. Inadequate concentrations may produce only bacteriostatic effects. |
| Adult Dose | 250-500 mg PO qid |
| Pediatric Dose | 25-50 mg/kg/d PO divided qid |
| Contraindications | Documented hypersensitivity |
| Interactions | Probenecid may increase penicillin effectiveness by decreasing its clearance; coadministration of tetracyclines may decrease the effect of penicillin |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution with impaired renal function |
| Drug Name | Cephalexin (Keflex, Biocef) |
|---|---|
| Description | First-generation cephalosporin that inhibits bacterial growth by inhibiting bacterial cell wall synthesis. Bactericidal and effective against rapidly growing organisms forming cell walls. Acceptable alternative to penicillin and may be useful in patients with minor penicillin allergies. |
| Adult Dose | 250-500 mg PO qid |
| Pediatric Dose | 25-50 mg/kg/d PO divided q6h |
| Contraindications | Documented hypersensitivity |
| Interactions | Aminoglycosides increase nephrotoxic potential of cephalexin |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Adjust dose in renal impairment |
Pain control is essential to quality patient care. These drugs ensure patient comfort, promote pulmonary toilet, and have sedating properties beneficial to patients who have sustained trauma or who experience pain.
| Drug Name | Acetaminophen (Tylenol, Panadol, Aspirin Free Anacin) |
|---|---|
| Description | DOC for treating pain in patients with documented hypersensitivity to aspirin or other NSAIDs, who are diagnosed with upper GI disease, or who take oral anticoagulants. |
| Adult Dose | 325-650 mg PO q4-6h or 1000 mg tid/qid; not to exceed 4 g/d |
| Pediatric Dose | <12 years: 10-15 mg/kg PO q4-6h prn; not to exceed 2.6 g/d >12 years: 325-650 mg PO q4h; not to exceed 5 doses q24h |
| Contraindications | Documented hypersensitivity; G-6-PD deficiency |
| Interactions | Rifampin may interact to reduce the analgesic effects of APAP; conversely, barbiturates, carbamazepine, hydantoins, and isoniazid may increase APAP hepatotoxicity |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Hepatotoxicity possible in persons with chronic alcoholism following various dose levels of acetaminophen |
| Drug Name | Acetaminophen and codeine (Tylenol 3) |
|---|---|
| Description | For treatment of mild to moderate pain. |
| Adult Dose | 30-60 mg (based on codeine content) PO q4-6h or 1-2 tab PO q4h; not to exceed 12 tab q24h |
| Pediatric Dose | Based on codeine: 0.5-1 mg/kg/dose PO q4-6h prn; not to exceed 5 doses q24h |
| Contraindications | Documented hypersensitivity |
| Interactions | Increased toxicity with coadministration of CNS depressants or tricyclic antidepressants |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Administer with caution in opiate-dependent patients because this substitution may result in acute opiate withdrawal symptoms; exercise caution when patients have severe renal or hepatic dysfunction |
| Drug Name | Hydrocodone bitartrate and acetaminophen (Vicodin ES) |
|---|---|
| Description | For relief of moderate to severe pain. |
| Adult Dose | 1-2 tab/cap PO q4-6h prn pain |
| Pediatric Dose | <12 years: 10-15 mg/kg/dose acetaminophen PO q4-6h prn; not to exceed 2.6 g/d acetaminophen or 5 mg of hydrocodone bitartrate/dose >12 years: 750 mg acetaminophen PO q4h; not to exceed 5 doses/d acetaminophen or 10 mg of hydrocodone bitartrate/dose |
| Contraindications | Documented hypersensitivity; elevated intracranial pressure |
| Interactions | Phenothiazines may decrease its analgesic effects; toxicity increases with coadministration of CNS depressants or tricyclic antidepressants |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Tablets contain metabisulfite, which may cause allergic reactions; administer with caution in opiate-dependent patients because this substitution may result in acute opiate withdrawal symptoms; exercise caution in severe renal or hepatic dysfunction |
| Drug Name | Oxycodone and acetaminophen (Percocet) |
|---|---|
| Description | For relief of moderate to severe pain. DOC for aspirin-hypersensitive patients. |
| Adult Dose | 1-2 tab or cap PO q4-6h prn pain |
| Pediatric Dose | 0.05-0.15 mg/kg PO oxycodone; not to exceed 5 mg of oxycodone q4-6h prn |
| Contraindications | Documented hypersensitivity |
| Interactions | Phenothiazines may decrease analgesic effects; toxicity increases with coadministration of either CNS depressants or tricyclic antidepressants |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Duration of action may increase in elderly patients; be aware of total daily dose of acetaminophen; the maximum dose of acetaminophen is 4000 mg/d; higher doses may cause liver toxicity |
| Drug Name | Aspirin (Anacin, Ascriptin, Bayer Aspirin) |
|---|---|
| Description | Blocks prostaglandin synthetase action, which in turn inhibits prostaglandin synthesis and prevents formation of platelet-aggregating thromboxane A2; acts on hypothalamic heat-regulating center to reduce fever. |
| Adult Dose | 325-650 mg PO q4-6h; not to exceed 4 g/d |
| Pediatric Dose | 10-15 mg/kg 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; avoid use in patients with severe anemia, with history of blood coagulation defects, or taking anticoagulants |
| Drug Name | Ibuprofen (Ibuprin, Advil, Motrin) |
|---|---|
| Description | Usually the DOC for treating mild to moderate pain, if no contraindications exist. One of the few NSAIDs indicated for reduction of fever. |
| Adult Dose | 200-400 mg PO q4-6h while symptoms persist; not to exceed 3.2 g/d |
| Pediatric Dose | 6 months to 12 years: 20-40 mg/kg/d PO divided tid/qid >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity; peptic ulcer disease, recent GI bleeding or perforation, renal insufficiency, high risk of bleeding |
| 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; monitor PT closely (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; caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy |
Article Last Updated: Jun 13, 2006