Staphylococcus aureus infection medical therapy: Difference between revisions
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Revision as of 23:12, 7 August 2015
Staphylococcus aureus infection Main page |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Medical Therapy
Antimicrobial Regimen
- Staphylococcus aureus treatment
- 1. Infectious endocarditis[1]
- 1.1 In adults
- Preferred regimen (1): Vancomycin 15-20 mg/kg IV q8-12h
- Preferred regimen (2): Daptomycin 6mg/kg/dose IV qd
- 2. Intravascular catheter-related infections[2]
- 2.1 Methicillin susceptible Staphylococcus aureus (MSSA)
- Preferred regimen (1): Nafcillin 2 g IV q6h
- Preferred regimen (2): Oxacillin 2 g IV q6h
- Alternative regimen (1): Cefazolin 2 g IV q8h
- Alternative regimen (2): Vancomycin 15 mg/kg IV q12h
- 2.1.1 Pediatric dose of Nafcillin
- 2.1.1.1 Neonates (< 4 weeks)
- 2.1.1.2 Infants and children (> 4 weeks)
- Nafcillin 100–200 mg/kg/day q4–6h
- 2.1.2 Pediatric dose of Oxacillin
- 2.1.2.1 Neonates (< 4 weeks)
- For < 1200 g: Oxacillin 50 mg/kg/day q12h
- For Postnatal age < 7 days and 1200–2000 g: Oxacillin 50–100 mg/kg/day q12h
- For Postnatal age < 7 days and > 2000 g: Oxacillin 75–150 mg/kg/day q8h
- For Postnatal age ≥ 7 days and 1200–2000 g: Oxacillin 75–150 mg/kg/day q8h
- For Postnatal age ≥ 7 days and > 2000 g: Oxacillin 100–200 mg/kg/day q6h
- 2.1.2.2 Infants and children(> 4weeks)
- Oxacillin 150–200 mg/kg/day q4–6h
- 2.1.3 Pediatric dose of Cefazolin
- Postnatal age > 7 days and > 2000 g: Cefazolin 60 mg/kg/day q8h
- 2.1.3.2 Infants and children (> 4 weeks)
- Cefazolin 50 mg/kg/day q8h.
- 2.1.4 Pediatric dose of Vancomycin
- 2.1.4.1 Neonates (< 4 weeks)
- Postnatal age ≤ 7 days and < 1200 g: Vancomycin 15 mg/kg/day q24h.
- Postnatal age ≤ 7 days and 1200–2000 g: Vancomycin 10–15 mg/kg q12–18h.
- Postnatal age ≤ 7 days and > 2000 g: Vancomycin 10–15 mg/kg q8–12h.
- Postnatal age > 7 days and < 1200 g: Vancomycin 15 mg/kg/day q24h.
- Postnatal age > 7 days and 1200–2000 g: Vancomycin 10–15 mg/kg q8–12h.
- Postnatal age > 7 days and > 2000 g: Vancomycin 15–20 mg/kg q8h.
- 2.1.4.2 Infants and children (> 4 weeks)
- Vancomycin 40 mg/kg/day q6–8h.
- 2.2 Methicillin resistant Staphylococcus aureus (MRSA)
- Preferred regimen (1): Vancomycin 15 mg/kg IV q12h
- Preferred regimen (2): Daptomycin 6–8 mg/kg/day IV
- Preferred regimen (3): Linezolid 10 mg/kg IV/PO q12h
- Preferred regimen (4): Vancomycin 15 mg/kg IV q12h AND (Rifampicin IV or Gentamycin IV)
- Preferred regimen (5): Trimethoprim-Sulfamethoxazole 6–12 mg TMP/kg/day q12h alone (if susceptible)
- 2.2.1 Pediatric dose of Linezolid
- 2.2.1.1 Neonates (< 4 weeks)
- 2.2.1.2 Infants and children < 12 years (> 4 weeks)
- Linezolid 10 mg/kg q8h
- 2.2.1.3 Children ≥ 12 years and adolescents
- Linezolid 10 mg/kg q12h
- 2.2.2 Pediatric dose of Gentamycin
- 2.2.2.1 Neonates (< 4 weeks)
- Premature neonates and < 1000 g: Gentamycin 3.5 mg/kg q24h
- < 1200 g: Gentamycin 2.5 mg/kg q18-24h.
- Postnatal age ≤ 7 days: Gentamycin 2.5 mg/kg q12h.
- Postnatal age > 7 days and 1200–2000 g: Gentamycin 2.5 mg/kg q8-12h.
- Postnatal age > 7 days and > 1200 g: Gentamycin 2.5 mg/kg q8h.
- Premature neonates with normal renal function: Gentamycin 3.5–4 mg/kg q24h.
- Term neonates with normal renal function: Gentamycin 3.5–5 mg/kg q24h.
- 2.2.2.2 Infants and children < 5 years (> 4 weeks)
- Gentamycin 2.5 mg/kg q8h; qd dosing in patients with normal renal function, Gentamycin 5–7.5 mg/kg q24h.
- 2.2.2.3 Children ≥ 5 years
- Gentamycin 2–2.5 mg/kg q8h; qd with normal renal function, Gentamycin 5–7.5 mg/kg q24h.
- 2.2.3 Pediatric dose of Trimethoprim-Sulfamethoxazole
- 2.2.3.1 Infants > 2 months of age and children of mild-to-moderate infections
- Trimethoprim-Sulfamethoxazole 6–12 mg TMP/kg/day q12h; serious infection- Trimethoprim-Sulfamethoxazole 15–20 mg TMP/kg/day q6-8h.
- 3. Cellulitis[3]
- 3.1 Purulent cellulitis (defined as cellulitis associated with purulent drainage or exudate in the absence of a drainable abscess)
- 3.1.1 In adults
- Preferred regimen (1): Clindamycin 300–450 mg PO tid
- Preferred regimen (2): Trimethoprim-Sulfamethoxazole 1–2 DS (double strength) tab PO bid
- Preferred regimen (3): Doxycycline 100 mg PO bid
- Preferred regimen (4): Minocycline 200 mg as a single dose THEN 100 mg PO bid
- Preferred regimen (5): Linezolid 600 mg PO bid
- 3.1.2 In children
- Preferred regimen (1): Clindamycin 10–13 mg/kg PO q6–8h, not to exceed 40 mg/kg/day
- Preferred regimen (2): Trimethoprim 4–6 mg/kg, Sulfamethoxazole 20–30 mg/kg PO q12h
- Preferred regimen (3)
- 3.1 If patient body weight < 45kg then Doxycycline 2 mg/kg PO q12h
- 3.2 If patient body weight 45kg then Doxycycline adult dose
- Preferred regimen (4): Minocycline 4 mg/kg PO 200 mg as a single dose, THEN Minocycline 2 mg/kg PO q12h
- Preferred regimen (5): Linezolid 10 mg/kg PO q8h, (max: 600 mg)
- 3.2 Nonpurulent cellulitis (defined as cellulitis with no purulent drainage or exudate and no associated abscess)
- 3.2.1 In adults
- Preferred regimen (1): Beta-lactam (eg, Cephalexin and Dicloxacillin) 500 mg PO qid
- Preferred regimen (2): Clindamycin 300–450 mg PO tid
- Preferred regimen (3): Amoxicillin 500 PO mg tid
- Preferred regimen (4): Linezolid 600 mg PO bid
- Note (1): Empirical therapy for beta-hemolytic streptococci is recommended. Empirical coverage for CA-MRSA is recommended in patients who do not respond to beta-lactam therapy and may be considered in those with systemic toxicity.
- Note (2): Provide coverage for both beta-hemolytic streptococci and CA-MRSA beta-lactam (eg, Amoxicillin) with or without Trimethoprim-Sulfamethoxazole or a Tetracycline
- 3.2.2 In children
- Preferred regimen (1): Clindamycin 10–13 mg/kg PO q6–8h, not to exceed 40 mg/kg/day
- Preferred regimen (2): Trimethoprim 4–6 mg/kg, Sulfamethoxazole 20–30 mg/kg PO q12h
- Preferred regimen (3): Linezolid 10 mg/kg PO q8h, not to exceed 600 mg
- Note (1): Clindamycin causes Clostridium difficile–associated disease may occur more frequently, compared with other oral agents.
- Note (2): Trimethoprim-Sulfamethoxazole not recommended for women in the third trimester of pregnancy and for children ,2 months of age.
- Note (3): Tetracyclines are not recommended for children under 8 years of age and are pregnancy category D.
-
- 4.1 Methicillin-resistant Staphylococcus aureus (MRSA)
- 4.1.1 In adults
- Preferred regimen: Vancomycin 30–45 mg/kg/day IV q8–12h for 4–6 weeks
- Alternative regimen (1): Linezolid 600 mg PO/IV q12h for 4–6 weeks
- Alternative regimen (2): Trimethoprim-Sulfamethoxazole 5 mg/kg PO/IV q8–12h for 4–6 weeks
- 4.1.2 In children
- Preferred regimen (1): Vancomycin15 mg/kg/dose IV q6h
- Preferred regimen (2): Linezolid 10 mg/kg/dose PO/IV q8h
- Note: Consider the addition of Rifampin 600 mg qd OR 300–450 mg bid to Vancomycin.
- 4.2 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen (1): Nafcillin 2 g IV q4h
- Preferred regimen (2): Oxacillin 2 g IV q4h
- Alternative regimen: Vancomycin 30–45 mg/kg/day IV q8–12h
-
-
- 5.1 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Vancomycin 30–45 mg/kg/day IV q8–12h with or without Rifampin 600 mg IV or PO q24h
- Note: Shunt removal is recommended, and it should not be replaced until cerebrospinal fluid cultures are repeatedly negative.
- 5.2 Methicillin-susceptible Staphylococcus aureus (MSSA)
-
-
- 6.1 Penicillin-susceptible Staphylococcus aureus or Streptococcus
- Preferred regimen: Penicillin G 4 MU IV q4h for 2–4 weeks, THEN PO to complete 6–8 weeks
- 6.2 Methicillin-susceptible Staphylococcus aureus or Streptococcus
- Preferred regimen (1): Cefazolin 2 g IV q8h for 2–4 weeks, THEN PO to complete 6–8 weeks
- Preferred regimen (2): Nafcillin 2 g IV q4h for 2–4 weeks, THEN PO to complete 6–8 weeks
- Preferred regimen (3): Oxacillin 2 g IV q4h for 2–4 weeks, THEN PO to complete 6–8 weeks
- Alternative regimen: Clindamycin 600 mg IV q6h for 2–4 weeks, THEN PO to complete 6–8 weeks
- 6.3 Methicillin-resistant Staphylococcus aureus (MRSA)
- 6.3.1 In adults
- Preferred regimen: Vancomycin loading dose 25–30 mg/kg IV THEN Vancomycin 15–20 mg/kg IV q8–12h for 2–4 weeks, THEN PO to complete 6–8 weeks
- Alternative regimen (1): Linezolid 600 mg PO/IV q12h for 4–6 weeks
- Alternative regimen (2): Trimethoprim-Sulfamethoxazole 5 mg/kg PO/IV q8–12h for 4–6 weeks
- 6.3.2 Pediatric dose
- Preferred regimen (1): Vancomycin 15 mg/kg IV q6h
- Preferred regimen (2): Linezolid 10 mg/kg PO/IV q8h
-
- Note: Consider the addition of Rifampin 600 mg qd or 300–450 mg bid to Vancomycin in adult patients..
- 7. Bacterial meningitis
- 7.1 Methicillin susceptible Staphylococcus aureus (MSSA)
- Preferred regimen (1): Nafcillin 9–12 g/day IV q4h
- Preferred regimen (2): Oxacillin 9–12 g/day IV q4h
- Alternative regimen (1): Vancomycin 30–45 mg/kg/day IV q8–12h
- Alternative regimen (2): Meropenem 6 g/day IV q8h
- 7.2 Methicillin resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Vancomycin 30–45 mg/kg/day IV q8–12h
- Alternative regimen (1): Trimethoprim-Sulfamethoxazole 10–20 mg/kg/day q6–12h
- Alternative regimen (2): Linezolid 600 mg IV q12h
- Note: Consider the addition of Rifampin 600 mg qd or 300–450 mg bid to Vancomycin in adult patients.
- 8. Septic thrombosis of cavernous or dural venous sinus[13]
- 8.1 Methicillin-resistant Staphylococcus aureus (MRSA)
- 8.1.1 In adults
- Preferred regimen: Vancomycin 15–20 mg/kg IV q8–12h for 4–6 weeks
- Alternative regimen (1): Linezolid 600 mg PO/IV q12h for 4–6 weeks
- Alternative regimen (2): Trimethoprim-Sulfamethoxazole 5 mg/kg/dose PO/IV q8–12h for 4–6 weeks
- 8.1.2 Pediatric dose
- Preferred regimen (1): Vancomycin 15 mg/kg IV q6h
- Preferred regimen (2): Linezolid 10 mg/kg PO/IV q8h
- Note (1): Surgical evaluation for incision and drainage of contiguous sites of infection or abscess is recommended whenever possible.
- Note (2): Consider the addition of Rifampin 600 mg qd or 300–450 mg bid to Vancomycin.
- 9. Subdural empyema
- 9.1 Methicillin-resistant Staphylococcus aureus (MRSA)[14]
- 9.1.1 In adults
- Preferred regimen: Vancomycin 30–45 mg/kg/day IV q8–12h for 4–6 weeks
- Alternative regimen (1): Linezolid 600 mg PO/IV q12h for 4–6 weeks
- Alternative regimen (2): Trimethoprim-Sulfamethoxazole 5 mg/kg PO/IV q8–12h for 4–6 weeks
- 9.1.2 In children
- Preferred regimen (1): Vancomycin 15 mg/kg IV q6h
- Preferred regimen (2): Linezolid 10 mg/kg PO/IV q8h
- Note: Consider the addition of Rifampin 600 mg qd or 300–450 mg bid to Vancomycin.
- 10. Acute conjunctivitis[15]
- 10.1 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Vancomycin ointment 1% qid
- 11. Appendicitis
- 11.1 Health care–associated complicated intra-abdominal infection[16]
- 11.1.1 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Vancomycin 15–20 mg/kg IV q8–12h
- 12. Diverticulitis
- 12.1 Health care–associated complicated intra-abdominal infection[16]
- 12.1.1 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Vancomycin 15–20 mg/kg IV q8–12h.
- 13. Peritonitis secondary to bowel perforation, peritonitis secondary to ruptured appendix, peritonitis secondary to ruptured appendix, typhlitis
- 13.1 Health care–associated complicated intra-abdominal infection[16]
- 13.1.1 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Vancomycin 15–20 mg/kg IV q8–12h
- 14. Cystic fibrosis[17]
- 14.1 Adults
- 14.1.1 If methicillin sensitive staphylococcus aureus
- 14.1.2 If methicillin resistant staphylococcus aureus
- Preferred Regimen (1): Vancomycin 15-20 mg/kg IV q8-12h
- Preferred Regimen (2): Linezolid 600 mg PO/IV q12h
- 14.2 Pediatric
- 14.2.1 If methicillin sensitive staphylococcus aureus
- 14.2.2 If methicillin resistant staphylococcus aureus
- Preferred Regimen (1): Vancomycin 40 mg/kg q6-8h (Age >28 days)
- Preferred Regimen (2): Linezolid 10 mg/kg PO/IV q8h (up to age 12)
- 15. Bronchiectasis[18]
- 15.1 In adults
- 15.1.1 Recommended first-line treatment and length of treatment
- 15.1.1.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen: Flucloxacillin 500 mg PO qds for 14 days
- 15.1.1.2 Methicillin-resistant Staphylococcus aureus (MRSA)
- Patient's body weight is < 50 kg
- Preferred regimen: Rifampicin 450 mg PO qd AND Trimethoprim 200 mg PO bd for 14 days
- Patient's body weight is > 50 kg
- Preferred regimen: Rifampicin 600 mg PO qd AND Trimethoprim 200 mg PO bd for 14 days
- 15.1.1.3 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen (1): Vancomycin 1 g IV bd (monitor serum levels and adjust dose accordingly)
- Preferred regimen (2): Teicoplanin 400 mg qd for 14 days
- 15.1.2 Recommended second-line treatment and length of treatment
- 15.1.2.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen: Clarithromycin 500 mg PO bd 14 days
- 15.1.2.2 Methicillin-resistant Staphylococcus aureus (MRSA)
- Patient's body weight is < 50 kg
- Preferred regimen: Rifampicin 450 mg PO qd AND Doxycycline 200 mg PO qd for 14 days
- Patient's body weight is > 50 kg
- Preferred regimen: Rifampicin 600 mg PO qd AND Doxycycline 200 mg PO qd for 14 days
- Third-line: Linezolid 600 mg bd for 14 days
- 15.1.2.3 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Linezolid 600 mg IV bd for 14 days
- 15.2 In children
- 15.2.1 Recommended first-line treatment and length of treatment
- 15.2.1.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen: Flucloxacillin
- 15.2.1.2 Methicillin-resistant Staphylococcus aureus (MRSA)
- 15.2.1.2.1 Children (< 12 yr)
- Preferred regimen: Trimethoprim 4-6 mg/kg/day PO q12h
- 15.2.1.2.2 Children (> 12 yr)
- Preferred regimen (1): Trimethoprim 100-200 mg PO q12h
- Preferred regimen (2): Rifampicin 450 mg PO od (or Rifampicin 600 mg PO od)
- 15.2.1.3 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen (1): Vancomycin 45-60 mg/kg/day IV q8-12h
- Preferred regimen (2): Teicoplanin 400 mg qd for 14 days
- 15.2.2 Recommended second-line treatment and length of treatment
- 15.2.2.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen: Clarithromycin 15 mg/kg/day PO q12h
- 15.2.2.2 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen (1): Rifampicin AND Doxycycline 2-5 mg/kg/day PO/IV q12-24h (max dose: 200 mg/24 hr)
- Preferred regimen (2): Rifampicin AND Doxycycline 2-5 mg/kg/day PO/IV q12-24h (max dose: 200 mg/24 hr)
- Third-line: Linezolid 10 mg/kg PO/IV q12h
- 15.2.2.3 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Linezolid 10 mg/kg PO/IV q12h
- 15.3 Long-term oral antibiotic treatment
- 15.3.1 In adults
- 15.3.1.1 Recommended first-line treatment and length of treatment
- 15.3.1.1.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen: Flucloxacillin 500 mg PO bd
- 15.3.1.2 Recommended second-line treatment and length of treatment
- 15.3.1.2.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen: Clarithromycin 250 mg PO bd
- 16. Empyema[19]
- Preferred regimen (1): Nafcillin 2 gm IV q4h
- Preferred regimen (2): oxacillin 2 gm IV q4h (if MSSA)
- Alternative regimen (1): Vancomycin 1 gm IV q12h
- Alternative regimen (2): Linezolid 600 mg PO bid (if MRSA)
- 17. Community-acquired pneumonia[20]
- 17.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred Regimen (1): Nafcillin 1000-2000 mg q4h
- Preferred Regimen (2): Oxacillin 2 g IV q4h
- Preferred Regimen (3): Flucloxacillin 250 mg IM/IV q6h
- Alternative Regimen (1): Cefazolin 500 mg IV q12h
- Alternative Regimen (2): Clindamycin 150-450 mg PO q6-8h
- 17.2 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred Regimen (1): Vancomycin 45-60 mg/kg/day q8-12h (max: 2000 mg/dose) for 7-21 days
- Preferred Regimen (2): Linezolid 600 mg PO/IV q12h for 10-14 days
- Alternative Regimen: Trimethoprim-Sulfamethoxazole 1-2 double-strength tablets (800/160 mg) q12-24h
- 18. Olecranon bursitis or prepatellar bursitis
- 18.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen (1): Nafcillin 2 g IV q4h
- Preferred regimen (2): Oxacillin 2 g IV q4h
- Preferred regimen (3): Dicloxacillin 500 mg PO qid
- 18.2 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen (1): Vancomycin 1 g IV q12h
- Preferred regimen (2): Linezolid 600 mg PO qd
- Note: Initially aspirate q24h and treat for a minimum of 2–3 weeks.
- 19. Septic arthritis
- 19.1 In adults
- 19.1.1 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Vancomycin 15–20 mg/kg IV q8–12h
- Alternative regimen (1): Daptomycin 6 mg/kg IV q24h in adults
- Alternative regimen (2): Linezolid 600 mg PO/IV q12h
- Alternative regimen (3): Clindamycin 600 mg PO/IV q8h
- Alternative regimen (4): TMP-SMX 3.5–4.0 mg/kg PO/IV q8–12h
- 19.2.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen (1): Nafcillin 2 g IV q6h
- Preferred regimen (2): Clindamycin 900 mg IV q8h
- Alternative regimen (1): Cefazolin 0.25–1 g IV/IM q6–8h
- Alternative regimen (2): Vancomycin 500 mg IV q6h or 1 g IV q12h
- 19.2 In childern
- Preferred regimen (1): Vancomycin 15 mg/kg IV q6h
- Preferred regimen (2): Daptomycin 6–10 mg/kg IV q24h
- Preferred regimen (3): Linezolid 10 mg/kg PO/IV q8h
- Preferred regimen (4): Clindamycin 10–13 mg/kg PO/IV q6–8h
- 20. Septic arthritis, prosthetic joint infection (device-related osteoarticular infections)
- 20.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen (1): Nafcillin 2 g IV q4–6h
- Preferred regimen (2): Oxacillin 2 g IV q4–6h
- Alternative regimen (1): Cefazolin 1–2 g IV q8h
- Alternative regimen (2): Ceftriaxone 2 g IV q24h
- Alternative regimen (if allergic to penicillins) (3): Clindamycin 900 mg IV q8h
- Alternative regimen (if allergic to penicillins) (4): Vancomycin 15–20 mg/kg IV q8–12h, (max: 2 g per dose)
- 20.2 Methicillin-resistant Staphylococcus aureus (MRSA)
- Early-onset (2 months after surgery) or acute hematogenous prosthetic joint infections involving a stable implant with short duration (< 3 weeks) of symptoms and debridement (but device retention)
- Preferred regimen: Vancomycin AND Rifampin 600 mg PO qd or 300–450 mg PO bid for 2 weeks
- Alternative regimen (1): Daptomycin 6 mg/kg IV q24h AND Rifampin 600 mg PO qd or 300–450 mg PO bid for 2 weeks
- Alternative regimen (2): Linezolid 600 IV q8h AND Rifampin 600 mg PO qd or 300–450 mg PO bid for 2 weeks
- Note: The above regimen should be followed by Rifampin and a Fluoroquinolone, TMP/SMX, a Tetracycline or Clindamycin for 3-6 months for hips and knees, respectively.
- 21. Hematogenous osteomyelitis
- 21.1 Adult (> 21 yrs)
- 21.1.1 Methicillin-resistant Staphylococcus aureus (MRSA) possible
- Preferred regimen: Vancomycin 1 gm IV q12h (if over 100 kg, 1.5 gm IV q12h)
- 21.1.2 Methicillin-resistant Staphylococcus aureus (MRSA) unlikely
- 21.2 Children (> 4 months)-Adult
- 21.2.1 Methicillin-resistant Staphylococcus aureus (MRSA) possible
- Preferred regimen: Vancomycin 40 mg IV q6–8h
- 21.2.2 Methicillin-resistant Staphylococcus aureus (MRSA) unlikely
- Preferred regimen (1): Nafcillin
- Preferred regimen (2): Oxacillin q6h (max. 8–12 gm per day)
- Note: Add Ceftazidime 50 mg q8h or Cefepime 150 mg q8h if Gram negative bacilli on Gram stain
- 21.3 Newborn (< 4 months.)
- 21.3.1 Methicillin-resistant Staphylococcus aureus (MRSA) possible
- Preferred regimen (1): Vancomycin AND Ceftazidime 2 gm IV q8h
- Preferred regimen (2): Vancomycin AND Cefepime 2 gm IV q12h
- 21.3.2 Methicillin-resistant Staphylococcus aureus (MRSA) unlikely
- Preferred regimen (1): Nafcillin AND Ceftazidime
- Preferred regimen (2): Oxacillin AND Cefepime
- 21.4 Specific therapy
- 21.4.1 Methicillin-susceptible Staphylococcus aureus (MSSA)
- Preferred regimen (1): Nafcillin
- Preferred regimen (2): Oxacillin 2 gm IV q4h
- Preferred regimen (3): Cefazolin 2 gm IV q8h
- Alternative regimen: Vancomycin 1 gm IV q12h (if over 100 kg, 1.5 gm IV q12h)
- 21.4.2 Methicillin-resistant Staphylococcus aureus (MRSA)
- Preferred regimen: Vancomycin 1 gm IV q12h
- Alternative regimen: Linezolid 600 mg q12h PO/IV with or without Rifampin 300 mg PO/IV bid
- 22. Diabetic foot osteomyelitis
- High risk for MRSA
- Preferred regimen (1): Linezolid 600 mg IV or PO q12h
- Preferred regimen (2): Daptomycin 4 mg/kg IV q24h
- Preferred regimen (3): Vancomycin 15–20 mg/kg IV q8–12h (trough: 10–20 mg/L)
- 23. Necrotizing fasciitis[21]
- 23.1 In adult
- Preferred regimen (1): Nafcillin 1–2 g IV q4h (severe Pencillin allergy: Vancomycin, linezolid, quinupristin/dalfopristin, daptomycin)
- Preferred regimen (2): Oxacillin 1–2 g IV q4h
- Preferred regimen (3): Cefazolin 1 g IV q8h
- Preferred regimen (4): Vancomycin 15 mg/kg IV bid
- Preferred regimen (5): Clindamycin 600–900 mg IV q8h
- 23.2 In childern
- Preferred regimen (1): Nafcillin 50 mg/kg/dose IV q6h (severe Pencillin allergy: Vancomycin, linezolid, quinupristin/dalfopristin, daptomycin)
- Preferred regimen (2): Oxacillin 50 mg/kg/dose IV q6h
- Preferred regimen (3): Cefazolin 33 mg/kg/dose IV q8h
- Preferred regimen (4): Vancomycin 15 mg/kg/dose IV q6h
- Preferred regimen (5): Clindamycin 10–13 mg/kg/dose IV q8h (Bacteriostatic; potential cross-resistance and emergence of resistance in erythromycin-resistant strains; inducible resistance in methicillin resistent staphylococcus aureus)
- 24. Staphylococcal toxic shock syndrome[22]
- 24.1 Methicillin sensitive Staphylococcus aureus
- Preferred regimen (1): Cloxacillin 250-500 mg PO q6h (max dose: 4 g/24 hr)
- Preferred regimen (2): Nafcillin 4-12 g/24 hr IV q4-6hr (max dose: 12 g/24 hr)
- Preferred regimen (3): Cefazolin 0.5-2g IV/IM q8h (max dose: 12 g/24 hr) AND Clindamycin 150-600 mg IV, IM/PO q6-8h (max dose: 5 g/24 hr IV or IM or 2 g/24 hr PO)
- Alternative regimen (1): Clarithromycin 250-500 mg PO q12h (max dose: 1 g/24 hr) AND Clindamycin 150-600 mg IV, IM/PO q6-8h (max dose: 5 g/24 hr IV/IM or 2 g/24h PO)
- Alternative regimen (2): Rifampicin AND Linezolid 600 mg IV/PO q12h
- Alternative regimen (3): Daptomycin
- Alternative regimen (4): Tigecycline 100 mg loading dose THEN 50 mg IV q12h
- 24.2 Methicillin resistant Staphylococcus aureus
- Preferred regimen (1): Clindamycin 150-600 mg IV, IM/PO q6-8h (max dose: 5 g/24h IV/IM or 2 g/24h PO)
- Preferred regimen (2): Linezolid 600 mg IV/PO q12h AND Vancomycin 15-20 mg/kg IV q8-12h, (max: 2 g per dose)
- Preferred regimen (3): Teicoplanin
- Alternative regimen (1): Rifampicin AND Linezolid 600 mg IV/PO q12h
- Alternative regimen (2): Daptomycin
- Alternative regimen (3): Tigecycline 100 mg loading dose THEN 50 mg IV q12h
- 24.3 Glycopeptide resistant or intermediate Staphylococcus aureus
- Preferred regimen: Linezolid 600 mg IV/PO q12h AND Clindamycin 150-600 mg IV, IM/PO q6-8h (max dose: 5 g/24 hr IV/IM or 2 g/24h PO) (if sensitive)
- Alternative regimen (1): Daptomycin
- Alternative regimen (2): Tigecycline 100 mg loading dose THEN 50 mg IV q12h
References
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- ↑ Stevens DL, Bisno AL, Chambers HF, Dellinger EP, Goldstein EJ, Gorbach SL; et al. (2014). "Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America". Clin Infect Dis. 59 (2): e10–52. doi:10.1093/cid/ciu444. PMID 24973422.
- ↑ Bennett, John (2015). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Elsevier/Saunders. ISBN 978-1455748013.
- ↑ Bartlett, John (2012). Johns Hopkins ABX guide : diagnosis and treatment of infectious diseases. Burlington, MA: Jones and Bartlett Learning. ISBN 978-1449625580.
- ↑ Liu, Catherine; Bayer, Arnold; Cosgrove, Sara E.; Daum, Robert S.; Fridkin, Scott K.; Gorwitz, Rachel J.; Kaplan, Sheldon L.; Karchmer, Adolf W.; Levine, Donald P.; Murray, Barbara E.; J Rybak, Michael; Talan, David A.; Chambers, Henry F.; Infectious Diseases Society of America (2011-02-01). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children". Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America. 52 (3): –18-55. doi:10.1093/cid/ciq146. ISSN 1537-6591. PMID 21208910.
- ↑ Tunkel, Allan R.; Hartman, Barry J.; Kaplan, Sheldon L.; Kaufman, Bruce A.; Roos, Karen L.; Scheld, W. Michael; Whitley, Richard J. (2004-11-01). "Practice guidelines for the management of bacterial meningitis". Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America. 39 (9): 1267–1284. doi:10.1086/425368. ISSN 1537-6591. PMID 15494903.
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- ↑ Liu, Catherine; Bayer, Arnold; Cosgrove, Sara E.; Daum, Robert S.; Fridkin, Scott K.; Gorwitz, Rachel J.; Kaplan, Sheldon L.; Karchmer, Adolf W.; Levine, Donald P.; Murray, Barbara E.; J Rybak, Michael; Talan, David A.; Chambers, Henry F.; Infectious Diseases Society of America (2011-02-01). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children". Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America. 52 (3): –18-55. doi:10.1093/cid/ciq146. ISSN 1537-6591. PMID 21208910.
- ↑ Liu, Catherine; Bayer, Arnold; Cosgrove, Sara E.; Daum, Robert S.; Fridkin, Scott K.; Gorwitz, Rachel J.; Kaplan, Sheldon L.; Karchmer, Adolf W.; Levine, Donald P.; Murray, Barbara E.; J Rybak, Michael; Talan, David A.; Chambers, Henry F.; Infectious Diseases Society of America (2011-02-01). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children". Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America. 52 (3): –18-55. doi:10.1093/cid/ciq146. ISSN 1537-6591. PMID 21208910.
- ↑ Liu, Catherine; Bayer, Arnold; Cosgrove, Sara E.; Daum, Robert S.; Fridkin, Scott K.; Gorwitz, Rachel J.; Kaplan, Sheldon L.; Karchmer, Adolf W.; Levine, Donald P.; Murray, Barbara E.; J Rybak, Michael; Talan, David A.; Chambers, Henry F.; Infectious Diseases Society of America (2011-02-01). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children". Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America. 52 (3): –18-55. doi:10.1093/cid/ciq146. ISSN 1537-6591. PMID 21208910.
- ↑ Azari, Amir A.; Barney, Neal P. (2013-10-23). "Conjunctivitis: a systematic review of diagnosis and treatment". JAMA. 310 (16): 1721–1729. doi:10.1001/jama.2013.280318. ISSN 1538-3598. PMC 4049531. PMID 24150468.
- ↑ 16.0 16.1 16.2 Solomkin JS, Mazuski JE, Bradley JS, Rodvold KA, Goldstein EJ, Baron EJ; et al. (2010). "Diagnosis and management of complicated intra-abdominal infection in adults and children: guidelines by the Surgical Infection Society and the Infectious Diseases Society of America". Clin Infect Dis. 50 (2): 133–64. doi:10.1086/649554. PMID 20034345.
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- ↑ Pasteur MC, Bilton D, Hill AT, British Thoracic Society Bronchiectasis non-CF Guideline Group (2010). "British Thoracic Society guideline for non-CF bronchiectasis". Thorax. 65 Suppl 1: i1–58. doi:10.1136/thx.2010.136119. PMID 20627931.
- ↑ Gilbert, David (2015). The Sanford guide to antimicrobial therapy. Sperryville, Va: Antimicrobial Therapy. ISBN 978-1930808843.
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- ↑ Stevens DL, Bisno AL, Chambers HF, Dellinger EP, Goldstein EJ, Gorbach SL; et al. (2014). "Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the infectious diseases society of America". Clin Infect Dis. 59 (2): 147–59. doi:10.1093/cid/ciu296. PMID 24947530.
- ↑ Lappin E, Ferguson AJ (2009). "Gram-positive toxic shock syndromes". Lancet Infect Dis. 9 (5): 281–90. doi:10.1016/S1473-3099(09)70066-0. PMID 19393958.