Staphylococcus aureus bacteremia: Difference between revisions
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Staphylococcus aureus bacteremia
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===Etiology=== |
===Etiology=== |
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*[[Skin and soft tissue infection]], including infections of a [[decubitus ulcer]] in hospitalized patients |
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*IVDU |
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*[[Infective endocarditis]] |
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*[[Osteomyelitis]] |
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*[[Septic arthritis]] |
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*[[Septic thrombophlebitis]] |
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*[[Central line-associated bloodstream infection]] |
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*Injection drug use |
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*Poor dentition |
*Poor dentition |
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*Dental work |
*Dental work |
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*May have back pain unrelated to spinal osteomyelitis |
*May have back pain unrelated to spinal osteomyelitis |
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*May present with focus of metastatic disease |
*May present with focus of metastatic disease |
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===Prognosis=== |
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*Associated with about 30% mortality[[CiteRef::bai2022st]] |
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*Mortality halved by ID consult in observational studies |
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*Prognosis worse with |
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**Increased age |
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**Female sex |
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**[[Pneumonia]] or source unknown |
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**[[Dementia]] |
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**Increasing comorbidities |
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**[[Shock]] at time of presentation |
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**Institutionalized patient |
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==Investigations== |
==Investigations== |
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***Injection drug use |
***Injection drug use |
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***Persistent bacteremia beyond 72 hours |
***Persistent bacteremia beyond 72 hours |
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**Can also use [[ |
**Can also use [[VIRSTA score]] to decide if they need TEE[[CiteRef::tubiana2016th]] |
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***Highest sensitivity (~99%), though specificity only 35% |
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***The high sensitivity gives very high negative predictive value of ~99% |
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***Likely preferred to others like the [[PREDICT score]], which has lower sensitivity though higher specificity[[CiteRef::van der vaart2021pr]] |
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==Management== |
==Management== |
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*Infectious diseases consultation |
*Infectious diseases consultation |
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*Must rule out endocarditis! TTE, followed by TEE if suspicion remains high (see [[PREDICT score]]) |
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=== Echocardiography === |
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*Must rule out endocarditis! TTE, followed by TEE if suspicion remains high (see [[VIRSTA score]]) |
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**Low risk for endocarditis (no TEE) if all of the following: |
**Low risk for endocarditis (no TEE) if all of the following: |
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***No intracardiac device |
***No intracardiac device |
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***Sterile follow-up blood cultures within 4 days from the initial set |
***Sterile follow-up blood cultures within 4 days from the initial set |
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***No hemodialysis |
***No hemodialysis |
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***Nosocomial acquisition |
***Nosocomial acquisition |
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***Absence of secondary foci |
***Absence of secondary foci |
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***No clinical signs of endocarditis |
***No clinical signs of endocarditis |
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***No evidence of metastases |
***No evidence of metastases |
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***+/- identified source has been removed |
***+/- identified source has been removed |
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*Two-week course acceptable if uncomplicated, otherwise 4-6 weeks |
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=== Antimicrobial Therapy === |
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*Two-week course acceptable if uncomplicated, otherwise 4-6 weeks based on clinical course and underlying foci of infection |
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*MSSA: [[cloxacillin]] 2g IV q4h for 2 weeks ([[cefazolin]] as an alternative) |
*MSSA: [[cloxacillin]] 2g IV q4h for 2 weeks ([[cefazolin]] as an alternative) |
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*MRSA: [[vancomycin]] 1g IV q12h for 2 weeks |
*MRSA: [[vancomycin]] 1g IV q12h for 2 weeks |
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**Adjust based on serum trough before every fourth dose |
**Adjust based on serum trough before every fourth dose |
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**Target trough 15-20 |
**Target trough 15-20 |
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*Standard of care is still currently IV therapy for the duration, though there is emerging evidence for treating a number of deep-seated infections ([[osteomyelitis]], [[Infective endocarditis|endocarditis]]) with early oral antibiotics, including infections caused by [[Staphylococcus aureus]] |
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== |
=== Dosing === |
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==== Penicillin- or Methicillin-Susceptible Strains ==== |
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*Mortality 20-50% at 30 days, 60% at 1 year |
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{| class="wikitable" |
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*Mortality halved by ID consult |
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!Antibiotic |
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*Prognosis worse with |
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!Renal Function |
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**Increased age |
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!Standard Dose |
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**Female sex |
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!Critical Illness Dose† |
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**Pneumonia or source unknown |
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|- |
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**Dementia |
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| rowspan="4" |[[benzylpenicillin]] (pen G) |
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**Increasing comorbidities |
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| eGFR >50 |
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**Shock at time of presentation |
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| 1.8 g (3 MU) q4h |
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**Institutionalized patient |
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| 2.4 g (4 MU) q4h |
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|- |
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|eGFR 10-50 |
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|1.8 g (3 MU) q6h |
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|1.8 g (3 MU) q4h |
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|- |
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|eGFR <10 |
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|1.8 g (3 MU) load, then 1.2 g (2 MU) q8h |
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|2.4 g load, then 1.2 g (2 MU) q6h |
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|- |
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| CRRT |
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| 1.2 g (2 MU) q6h |
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|1.8 g (3 MU) q6h |
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|- |
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| rowspan="3" |[[flucloxacillin]] |
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|eGFR ≥10 |
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|2 g q6h |
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|2 g q4h |
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|- |
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|eGFR <10 |
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|1 g q6h |
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|1 g q4h |
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|- |
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|CRRT |
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|2 g q6h |
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|2 g q6h |
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|- |
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|[[cloxacillin]] |
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|any |
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|2 g q4h |
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|2 g q4h |
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|- |
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| rowspan="4" |[[cefazolin]] |
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|eGFR >40 |
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|2 g q8h |
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|2 g q6h |
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|- |
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|eGFR 20-40 |
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|2 g q12h |
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| 2 g q12h |
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|- |
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|eGFR <20 |
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|1 g q24h |
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|1 g q24h |
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|- |
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|CRRT |
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|2 g q12h |
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|2 g q12h |
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|}*† Critical illness dosing should be used for patients with septic shock, admitted to ICU, with endocarditis, or with CNS infection (excluding spinal epidural abscess) |
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**May be decreased to standard dosing once no longer requiring mechanical ventilation or vasopressors for at least 24 hours |
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===== Methicillin-Resistant Strains ===== |
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====== Vancomycin Dosing ====== |
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* [[Vancomycin]] dosing may follow local guidelines |
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*Includes loading dose of 25 mg/kg (max 3 g) if considered appropriate by the physician, then maintenance dosing at 15-20 mg/kg q12h, adjusted to target AUC 400-600 mg h/L or trough 10-20 mg/L |
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====== Daptomycin Dosing ====== |
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{| class="wikitable" |
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!Renal Function |
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!Suggested Dose |
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|- |
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|eGFR >50 |
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|8-10 mg/kg q24h |
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|- |
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|eGFR 11-50 |
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|6-8 mg/kg q24h |
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|- |
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|eGFR ≤10 |
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|8 mg/kg q48h |
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|- |
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|CRRT |
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|8 mg/kg q48h |
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|- |
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|HD |
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|8 mg/kg q48h, given after dialysis |
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|} |
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====== Adjunctive Cefazolin Dosing ====== |
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{| class="wikitable" |
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!Renal Function |
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!Suggested Dose |
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|- |
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| CrCl >40 |
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|2 g q8h |
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|- |
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|CrCl 20-40 |
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| 2 g q12h |
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|- |
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| CrCl <20 |
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|1 g q24h |
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|- |
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|CRRT |
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| 1 g q8h or 2 g q12h |
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|- |
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|HD |
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|2 g after each dialysis session |
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|} |
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==== Early Oral Switch ==== |
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{| class="wikitable" |
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!Silo |
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!IV Antibiotic |
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!Suggested First-Line |
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! Suggested Second-Line (ordered) |
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|- |
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| rowspan="2" | PSSA |
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|[[benzylpenicillin]] |
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|[[amoxicillin]] |
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|[[flucloxacillin]]/[[dicloxacillin]], [[cefalexin]]/[[cefadroxil]], [[linezolid]] |
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|- |
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|([[Flucloxacillin|flu]])[[cloxacillin]] |
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|[[flucloxacillin]]/[[dicloxacillin]] |
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|[[amoxicillin]], [[cefalexin]]/[[cefadroxil]], [[linezolid]] |
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|- |
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| rowspan="2" |MSSA |
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|([[Flucloxacillin|flu]])[[cloxacillin]] |
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|[[flucloxacillin]]/[[dicloxacillin]] |
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|[[cefalexin]]/[[cefadroxil]], [[linezolid]] |
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|- |
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|[[cefazolin]] |
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|[[cefalexin]]/[[cefadroxil]] |
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|[[flucloxacillin]]/[[dicloxacillin]], [[linezolid]] |
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|- |
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| rowspan="2" |MRSA |
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|[[vancomycin]]/[[daptomycin]] |
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|[[linezolid]] |
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|[[fluoroquinolone]]+[[rifampin]], [[TMP-SMX]], [[fusidic acid]]+[[rifampin]] |
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|- |
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|[[vancomycin]]/[[daptomycin]]+[[cefazolin]] |
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|[[linezolid]] |
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|[[fluoroquinolone]]+[[rifampin]], [[TMP-SMX]], [[fusidic acid]]+[[rifampin]] |
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|} |
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{| class="wikitable" |
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!Antibiotic |
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!Renal Function |
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!Suggested Dose |
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!Notes |
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|- |
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| rowspan="5" |[[amoxicillin]] |
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|normal |
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|1 g q6h ± [[probenecid]] |
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| |
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|- |
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|CrCl 10-30 |
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|1 g q8h |
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| |
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|- |
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|CrCl <10 |
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|1 g q12h |
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| |
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|- |
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|CRRT |
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|1 g q8h |
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| |
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|- |
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|HD/PD |
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|1 g q12h |
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| |
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|- |
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| rowspan="6" |[[cefadroxil]] |
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|normal |
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|1 g q12h |
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| |
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|- |
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|CrCl 10-50 |
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|1 g then 500 mg q12h |
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| |
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|- |
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|CrCl <10 |
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|1 g then 500 mg q36h |
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| |
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|- |
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|CRRT |
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|1 g then 500 mg q12h |
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| |
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|- |
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|HD |
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|1 g then 1 g post-HD |
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| |
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|- |
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|PD |
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|500 mg q24h |
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| |
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|- |
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| rowspan="4" |[[cefalexin]] |
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|normal |
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|1 g q6h ± [[probenecid]] |
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| |
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|- |
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|CrCl <10 |
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|1 g q12h |
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| |
|||
|- |
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|CRRT |
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|1 g q6h |
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| |
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|- |
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|HD/PD |
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|1 g q12h |
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| |
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|- |
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| rowspan="4" |[[ciprofloxacin]] |
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|normal |
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|750 mg q12h |
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| |
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|- |
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|CrCl <30 |
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|750 mg q24h |
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| |
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|- |
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|CRRT |
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|250-500 mg q12h |
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| |
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|- |
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|HD/PD |
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|750 mg q24h |
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| |
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|- |
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|[[clindamycin]] |
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|any |
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|450 mg q8h |
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| |
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|- |
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|[[cloxacillin]] |
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|any |
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|1 g q6h |
|||
| |
|||
|- |
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| rowspan="4" |[[dicloxacillin]] |
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|normal |
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|1 g q6h |
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| |
|||
|- |
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|CrCl <10 |
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|1 g q8h |
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| |
|||
|- |
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|CRRT |
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|1 g q6h |
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| |
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|- |
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|HD/PD |
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|1 g q8h |
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| |
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|- |
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|[[doxycycline]] |
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|any |
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|100 mg q12h |
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| |
|||
|- |
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| rowspan="4" |[[flucloxacillin]] |
|||
|normal |
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|1 g q6h |
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| |
|||
|- |
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|CrCl <10 |
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|1 g q8h |
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| |
|||
|- |
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|CRRT |
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|1 g q6h |
|||
| |
|||
|- |
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|HD/PD |
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|1 g q8h |
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| |
|||
|- |
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|[[fusidic acid]] |
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|any |
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|500 mg q24h |
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| |
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|- |
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| rowspan="5" |[[levofloxacin]] |
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|normal |
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|750 mg q24h |
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| |
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|- |
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|CrCl 20-49 |
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|750 mg q48h |
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| |
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|- |
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|CrCl <20 |
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|750 mg then 500 mg q48h |
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| |
|||
|- |
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|CRRT |
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|250 mg q24h |
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| |
|||
|- |
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|HD/PD |
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|750 mg then 500 mg q48h |
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| |
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|- |
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| rowspan="4" |[[linezolid]] |
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|normal |
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|600 mg q12h |
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| |
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|- |
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|CrCl <10 |
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|600 mg q24h |
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| |
|||
|- |
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|CRRT |
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|600 mg q12h |
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| |
|||
|- |
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|HD/PD |
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|600 mg q24h |
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| |
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|- |
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|[[moxifloxacin]] |
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|any |
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|400 mg daily |
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| |
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|- |
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| rowspan="3" |[[probenecid]] |
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|CrCl ≥60 |
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|500 mg with each dose of β-lactam |
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| |
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|- |
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|CrCl 30-60 |
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|250 mg with each dose of β-lactam |
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| |
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|- |
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|CrCl <30 |
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|avoid use |
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| |
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|- |
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| rowspan="2" |[[rifampin]] |
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|any (weight <60kg) |
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|600 mg daily |
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| |
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|- |
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|any (weight >60 kg) |
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|900 mg daily |
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| |
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|- |
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|[[tedizolid]] |
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|any |
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|200 mg q24h |
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| |
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|- |
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| rowspan="4" |[[TMP-SMX]] |
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|normal |
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|2 DS q12h or 1 DS q8h |
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| |
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|- |
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|CrCl 26-50 |
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|normal dose for 14 days then 1 DS q12h |
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| |
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|- |
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|CrCl 15-25 |
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|normal dose for 3 days then 2 DS q24h |
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| |
|||
|- |
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|CrCl <15 |
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|avoid use |
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| |
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|} |
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==== Adjunctive Clindamycin ==== |
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*[[Clindamycin]] 600 mg IV q8h for 5 days as adjunctive therapy regardless of clindamycin susceptibility |
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*Alternative is 450 mg p.o. q8h for 5 days, though preference for IV |
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==Further Reading== |
==Further Reading== |
||
{{DISPLAYTITLE:''Staphylococcus aureus'' bacteremia}} |
{{DISPLAYTITLE:''Staphylococcus aureus'' bacteremia}} |
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[[Category:Endovascular infections]] |
[[Category:Endovascular infections]] |
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[[Category:Bacteremias]] |
Latest revision as of 12:43, 27 September 2024
Background
Classification
- Community-onset: positive blood culture obtained within 48 hours of presentation
- Nosocomial: positive blood culture obtained after 48 hours of presentation
Etiology
- Skin and soft tissue infection, including infections of a decubitus ulcer in hospitalized patients
- Infective endocarditis
- Osteomyelitis
- Septic arthritis
- Septic thrombophlebitis
- Central line-associated bloodstream infection
- Injection drug use
- Poor dentition
- Dental work
Clinical Manifestations
- Often non-specific fevers and chills, diagnosed on blood cultures
- May have back pain unrelated to spinal osteomyelitis
- May present with focus of metastatic disease
Prognosis
- Associated with about 30% mortality1
- Mortality halved by ID consult in observational studies
- Prognosis worse with
Investigations
- Repeat blood cultures every 24 to 48 hours until negative
- Transthoracic echo (TTE) or transesophageal echo (TEE)
- A modern TTE that is good-quality and shows normal valves is quite good, though TEE is still better
- TEE is strongly suggested in certain cases:
- Cerebral or peripheral emboli
- Meningitis
- Implantable cardiac device or prosthetic heart valve
- Prior infective endocarditis
- Native valve disease
- Injection drug use
- Persistent bacteremia beyond 72 hours
- Can also use VIRSTA score to decide if they need TEE2
- Highest sensitivity (~99%), though specificity only 35%
- The high sensitivity gives very high negative predictive value of ~99%
- Likely preferred to others like the PREDICT score, which has lower sensitivity though higher specificity3
Management
- Infectious diseases consultation
Echocardiography
- Must rule out endocarditis! TTE, followed by TEE if suspicion remains high (see VIRSTA score)
- Low risk for endocarditis (no TEE) if all of the following:
- No intracardiac device
- Sterile follow-up blood cultures within 4 days from the initial set
- No hemodialysis
- Nosocomial acquisition
- Absence of secondary foci
- No clinical signs of endocarditis
- Uncomplicated if all of the following:
- Endocarditis is excluded
- No implanted prostheses
- Blood cultures clear by 2-4 days
- Defervesces within 72 hours
- No evidence of metastases
- +/- identified source has been removed
- Low risk for endocarditis (no TEE) if all of the following:
Antimicrobial Therapy
- Two-week course acceptable if uncomplicated, otherwise 4-6 weeks based on clinical course and underlying foci of infection
- MSSA: cloxacillin 2g IV q4h for 2 weeks (cefazolin as an alternative)
- MRSA: vancomycin 1g IV q12h for 2 weeks
- Adjust based on serum trough before every fourth dose
- Target trough 15-20
- Standard of care is still currently IV therapy for the duration, though there is emerging evidence for treating a number of deep-seated infections (osteomyelitis, endocarditis) with early oral antibiotics, including infections caused by Staphylococcus aureus
Dosing
Penicillin- or Methicillin-Susceptible Strains
Antibiotic | Renal Function | Standard Dose | Critical Illness Dose† |
---|---|---|---|
benzylpenicillin (pen G) | eGFR >50 | 1.8 g (3 MU) q4h | 2.4 g (4 MU) q4h |
eGFR 10-50 | 1.8 g (3 MU) q6h | 1.8 g (3 MU) q4h | |
eGFR <10 | 1.8 g (3 MU) load, then 1.2 g (2 MU) q8h | 2.4 g load, then 1.2 g (2 MU) q6h | |
CRRT | 1.2 g (2 MU) q6h | 1.8 g (3 MU) q6h | |
flucloxacillin | eGFR ≥10 | 2 g q6h | 2 g q4h |
eGFR <10 | 1 g q6h | 1 g q4h | |
CRRT | 2 g q6h | 2 g q6h | |
cloxacillin | any | 2 g q4h | 2 g q4h |
cefazolin | eGFR >40 | 2 g q8h | 2 g q6h |
eGFR 20-40 | 2 g q12h | 2 g q12h | |
eGFR <20 | 1 g q24h | 1 g q24h | |
CRRT | 2 g q12h | 2 g q12h |
*† Critical illness dosing should be used for patients with septic shock, admitted to ICU, with endocarditis, or with CNS infection (excluding spinal epidural abscess)
- May be decreased to standard dosing once no longer requiring mechanical ventilation or vasopressors for at least 24 hours
Methicillin-Resistant Strains
Vancomycin Dosing
- Vancomycin dosing may follow local guidelines
- Includes loading dose of 25 mg/kg (max 3 g) if considered appropriate by the physician, then maintenance dosing at 15-20 mg/kg q12h, adjusted to target AUC 400-600 mg h/L or trough 10-20 mg/L
Daptomycin Dosing
Renal Function | Suggested Dose |
---|---|
eGFR >50 | 8-10 mg/kg q24h |
eGFR 11-50 | 6-8 mg/kg q24h |
eGFR ≤10 | 8 mg/kg q48h |
CRRT | 8 mg/kg q48h |
HD | 8 mg/kg q48h, given after dialysis |
Adjunctive Cefazolin Dosing
Renal Function | Suggested Dose |
---|---|
CrCl >40 | 2 g q8h |
CrCl 20-40 | 2 g q12h |
CrCl <20 | 1 g q24h |
CRRT | 1 g q8h or 2 g q12h |
HD | 2 g after each dialysis session |
Early Oral Switch
Silo | IV Antibiotic | Suggested First-Line | Suggested Second-Line (ordered) |
---|---|---|---|
PSSA | benzylpenicillin | amoxicillin | flucloxacillin/dicloxacillin, cefalexin/cefadroxil, linezolid |
(flu)cloxacillin | flucloxacillin/dicloxacillin | amoxicillin, cefalexin/cefadroxil, linezolid | |
MSSA | (flu)cloxacillin | flucloxacillin/dicloxacillin | cefalexin/cefadroxil, linezolid |
cefazolin | cefalexin/cefadroxil | flucloxacillin/dicloxacillin, linezolid | |
MRSA | vancomycin/daptomycin | linezolid | fluoroquinolone+rifampin, TMP-SMX, fusidic acid+rifampin |
vancomycin/daptomycin+cefazolin | linezolid | fluoroquinolone+rifampin, TMP-SMX, fusidic acid+rifampin |
Antibiotic | Renal Function | Suggested Dose | Notes |
---|---|---|---|
amoxicillin | normal | 1 g q6h ± probenecid | |
CrCl 10-30 | 1 g q8h | ||
CrCl <10 | 1 g q12h | ||
CRRT | 1 g q8h | ||
HD/PD | 1 g q12h | ||
cefadroxil | normal | 1 g q12h | |
CrCl 10-50 | 1 g then 500 mg q12h | ||
CrCl <10 | 1 g then 500 mg q36h | ||
CRRT | 1 g then 500 mg q12h | ||
HD | 1 g then 1 g post-HD | ||
PD | 500 mg q24h | ||
cefalexin | normal | 1 g q6h ± probenecid | |
CrCl <10 | 1 g q12h | ||
CRRT | 1 g q6h | ||
HD/PD | 1 g q12h | ||
ciprofloxacin | normal | 750 mg q12h | |
CrCl <30 | 750 mg q24h | ||
CRRT | 250-500 mg q12h | ||
HD/PD | 750 mg q24h | ||
clindamycin | any | 450 mg q8h | |
cloxacillin | any | 1 g q6h | |
dicloxacillin | normal | 1 g q6h | |
CrCl <10 | 1 g q8h | ||
CRRT | 1 g q6h | ||
HD/PD | 1 g q8h | ||
doxycycline | any | 100 mg q12h | |
flucloxacillin | normal | 1 g q6h | |
CrCl <10 | 1 g q8h | ||
CRRT | 1 g q6h | ||
HD/PD | 1 g q8h | ||
fusidic acid | any | 500 mg q24h | |
levofloxacin | normal | 750 mg q24h | |
CrCl 20-49 | 750 mg q48h | ||
CrCl <20 | 750 mg then 500 mg q48h | ||
CRRT | 250 mg q24h | ||
HD/PD | 750 mg then 500 mg q48h | ||
linezolid | normal | 600 mg q12h | |
CrCl <10 | 600 mg q24h | ||
CRRT | 600 mg q12h | ||
HD/PD | 600 mg q24h | ||
moxifloxacin | any | 400 mg daily | |
probenecid | CrCl ≥60 | 500 mg with each dose of β-lactam | |
CrCl 30-60 | 250 mg with each dose of β-lactam | ||
CrCl <30 | avoid use | ||
rifampin | any (weight <60kg) | 600 mg daily | |
any (weight >60 kg) | 900 mg daily | ||
tedizolid | any | 200 mg q24h | |
TMP-SMX | normal | 2 DS q12h or 1 DS q8h | |
CrCl 26-50 | normal dose for 14 days then 1 DS q12h | ||
CrCl 15-25 | normal dose for 3 days then 2 DS q24h | ||
CrCl <15 | avoid use |
Adjunctive Clindamycin
- Clindamycin 600 mg IV q8h for 5 days as adjunctive therapy regardless of clindamycin susceptibility
- Alternative is 450 mg p.o. q8h for 5 days, though preference for IV
Further Reading
References
- ^ Anthony D. Bai, Carson KL. Lo, Adam S. Komorowski, Mallika Suresh, Kevin Guo, Akhil Garg, Pranav Tandon, Julien Senecal, Olivier Del Corpo, Isabella Stefanova, Clare Fogarty, Guillaume Butler-Laporte, Emily G. McDonald, Matthew P. Cheng, Andrew M. Morris, Mark Loeb, Todd C. Lee. Staphylococcus aureus bacteremia mortality: A systematic review and meta-analysis. Clinical Microbiology and Infection. 2022. doi:10.1016/j.cmi.2022.03.015.
- ^ Sarah Tubiana, Xavier Duval, François Alla, Christine Selton-Suty, Pierre Tattevin, François Delahaye, Lionel Piroth, Catherine Chirouze, Jean-Philippe Lavigne, Marie-Line Erpelding, Bruno Hoen, François Vandenesch, Bernard Iung, Vincent Le Moing. The VIRSTA score, a prediction score to estimate risk of infective endocarditis and determine priority for echocardiography in patients with Staphylococcus aureus bacteremia. Journal of Infection. 2016;72(5):544-553. doi:10.1016/j.jinf.2016.02.003.
- ^ Thomas W van der Vaart, Jan M Prins, Robin Soetekouw, Gitte van Twillert, Jan Veenstra, Bjorn L Herpers, Wouter Rozemeijer, Rogier R Jansen, Marc J M Bonten, Jan T M van der Meer. Prediction Rules for Ruling Out Endocarditis in Patients With Staphylococcus aureus Bacteremia. Clinical Infectious Diseases. 2021;74(8):1442-1449. doi:10.1093/cid/ciab632.