TABLE 36-4.
Antibiotic Treatment Guidelines for Selected Group A Streptococcus Infections
| Rationale | Medication | Evidence* | Dose | Comments |
|---|---|---|---|---|
| Group A Streptococcus pharyngitis | ||||
|
Oral phenoxymethylpenicillin (penicillin V) | 1 | 10 mg/kg up to 500 mg BD for 10 days | Treatment may be primarily for symptom alleviation unless the risk of sequelae is high |
| Oral amoxicillin | 1 | ≤30 kg: 750 mg daily for 10 days >30 kg: 1500 mg daily for 10 days |
Not proven to prevent acute rheumatic fever | |
| IM benzathine penicillin G | 1 | 3–6kg: 225 mg 6–10kg: 337.5 mg 10–15kg: 450 mg 15–20kg: 675 mg 20+ kg: 900 mg as a single dose |
Preferred where risk of rheumatic fever is high and adherence to oral therapy not assured | |
| Oral roxithromycin† | 1 | 20 mg/kg up to 500 mg daily for 3 days | If hypersensitive to penicillin | |
| Impetigo | ||||
|
Topical mupirocin 2% ointment | 1 | 8-hourly for 7 days | Preferred for mild disease, but not proven in high-endemic settings. Use saline, soap water or 0.1% potassium permanganate to remove crusts prior to applying. Strains of Staphylococcus aureus may be resistant or may acquire resistance to topical antibiotics |
| Oral di/flucloxacillin | 1 | 12.5 mg/kg up to 500 mg q 6-hourly for 10 days | First-line treatment if multiple lesions and S. aureus is likely | |
| IM benzathine penicillin G | 1 | 3–6kg: 225 mg 6–10kg: 337.5 mg 10–15kg: 450 mg 15–20kg: 675 mg 20+ kg: 900 mg as a single dose |
Preferred in endemic settings where risk of acute post-streptococcal glomerulonephritis is high and/or adherence to oral therapy not assured. Exclude S. aureus infection if refractory to treatment | |
| Oral erythromycin | 1 | 12.5 mg/kg up to 500 mg TDS for 10 days | If hypersensitive to penicillin | |
| Erysipelas and cellulitis mild/early | ||||
|
Oral di/flucloxacillin |
1 |
12.5 mg/kg up to 500 mg q 6-hourly for 7–10 days |
Switch to IV therapy if failure to respond and consider resistant pathogens, e.g. methicillin-resistant Staphylococcus aureus (MRSA) |
| Oral phenoxymethylpenicillin (penicillin V) |
2 | 10 mg/kg up to 500 mg BD for 10 days | If S. aureus is unlikely (e.g. early erysipelas or perianal cellulitis) or if Group A Streptococcus confirmed on culture. Exclude S. aureus infection if refractory to treatment | |
| Oral cephalexin | 1 | 12.5 mg/kg up to 500 mg q 8hourly for 7–10 days | If non-immediate type hypersensitivity to penicillins | |
| Oral clindamycin | 1 | 10 mg/kg up to 450 mg q 8-hourly for 7–10days | If immediate type hypersensitivity to penicillin or infection with clindamycin-sensitive MRSA likely | |
| Erysipelas and cellulitis moderate-to-severe | ||||
|
IV di/flucloxacillin | 1 | 50 mg/kg up to 2 g q 6-hourly | Preferred treatment unless MRSA is likely |
| IV cephalothin | 2 | 50 mg/kg up to 2 g q 6-hourly | If non-immediate type hypersensitivity to penicillin | |
| IV/Oral clindamycin | 1 | 10 mg/kg up to 450 mg q 8-hourly for 7–10 days | If immediate type hypersensitivity to penicillin or infection with clindamycin sensitive MRSA likely. Bioavailability of clindamycin is high so oral clindamycin can be considered except in infants | |
| IV vancomycin | 1 | 25 mg/kg (<12 yr use 30 mg/kg) up to 1g BD | If infection with clindamycin-resistant MRSA likely. Adjust dose on basis of trough blood levels | |
| Necrotizing fasciitis§ | ||||
|
IV meropenem | 5 | 25 mg/kg up to 1 g q 8-hourly | Broad-spectrum cover is recommended in addition to surgical debridement until Group A Streptococcus infection is confirmed, thereafter penicillin + clindamycin is recommended |
| IV benzylpenicillin | 2 | 45 mg/kg up to 1.8 g q 4-hourly | If Group A Streptococcus infection is confirmed. Use in addition to surgical debridement | |
| IV cephalothin | 5 | 50 mg/kg up to 2 g q 6-hourly | If GAS confirmed and non-immediate type hypersensitivity to penicillin. If there is a history of immediate-type hypersensitivity to ß-lactams, seek expert advice | |
| + IV clindamycin | 2 | 15 mg/kg up to 600 mg q 8-hourly | Use as an adjunct to meropenem or penicillin if Group A Streptococcus infection is suspected or confirmed | |
| Streptococcal toxic shock syndrome (STSS)§ | ||||
|
Intravenous immunoglobulin (IVIG) | 4 | 2 g/kg as an immediate infusion, repeated once in 48–72 h if necessary | Use as an adjunct to penicillin and clindamycin therapy +/− debridement as recommended above for necrotizing fasciitis |
| Acute rheumatic fever treatment | ||||
|
Aspirin | 1 | 80–100mg/kg/day (up to 4–8 g/day) in 4–5 divided doses | For the control of pain of acute rheumatic fever arthritis. Duration dependent on clinical response |
| IM benzathine penicillin G | 5 | ≤20 kg: 450 mg as a single dose >20 kg: 900 mg as a single dose |
Preferred where adherence to oral therapy not assured. Treatment should focus on pain relief with salicylates and management of cardiac failure | |
| Oral phenoxymethylpenicillin (penicillin V) | 5 | 250 mg BD for 10 days | An acceptable alternative to benzathine penicillin if adherence can be assured, e.g. in hospital | |
| Oral prednisolone | 5 | 1–2 mg/kg/day (up to 80 mg/day) | Not routinely recommended for carditis, but may be considered for severe carditis if surgery is not an option | |
| Carbamazepine | 3 | 7–10 mg/kg/day in 3 divided doses | Not routinely recommended for management of chorea, but may be considered in severe cases | |
| Acute rheumatic fever prophylaxis | ||||
|
IM benzathine penicillin G |
1 |
<20 kg: 450 mg >20 kg: 900 mg every 3–4 weeks |
Preferred regimen. Should be continued for at least 10 years and at least until patient is 21 years old. Patients with established valve disease may require longer duration. Four-weekly injections satisfactory if a good control programme is in place |
| Oral phenoxymethylpenicillin (penicillin V) | 1 | 250 mg BD | Associated with inferior adherence. Only where IM injections are refused or risk of progressive carditis very low | |
| Oral erythromycin | 5 | 250 mg BD | If hypersensitive to penicillin. Dose for erythromycin ethyl succinate is 400 mg BD | |
Level of evidence: 1=randomized controlled trial, 2=comparative clinical study > 20 patients, 3=comparative clinical study < 20 patients, 4=case series, 5=expert opinion on basis of in vitro data or animal studies.
Roxithromycin, semi-synthetic macrolide not commercially available in the USA.
Intravenous immune globulin (IVIG) 2 g/kg as a single infusion, repeated if necessary 24–48 hours later is also recommended for necrotizing fasciitis or other severe invasive Group A Streptococcus infections (e.g. impending STSS). If indicated, IVIG should be administered as early as possible.