Staphylococcus aureus bacteremia: Difference between revisions
From IDWiki
Staphylococcus aureus bacteremia
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(ββ) Β |
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==Background== |
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= Classification = |
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===Classification=== |
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* |
*'''Community-onset:''' positive blood culture obtained within 48 hours of presentation |
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* |
*'''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 |
|||
* IVDU |
|||
*[[Infective endocarditis]] |
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* Poor dentition |
|||
*[[Osteomyelitis]] |
|||
* Dental work |
|||
*[[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=== |
|||
= Investigations = |
|||
*Associated with about 30% mortality[[CiteRef::bai2022st]] |
|||
= Management = |
|||
*Mortality halved by ID consult in observational studies |
|||
*Prognosis worse with |
|||
**Increased age |
|||
**Female sex |
|||
**[[Pneumonia]] or source unknown |
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**[[Dementia]] |
|||
**Increasing comorbidities |
|||
**[[Shock]] at time of presentation |
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**Institutionalized patient |
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==Investigations== |
|||
* Infectious diseases consultation |
|||
* Must rule out endocarditis! TTE, followed by TEE if suspicion remains high |
|||
* 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 of S. aureus |
|||
** Absence of secondary foci |
|||
** No clinical signs of endocarditis |
|||
* Uncomplicated if |
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** 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 |
|||
* Two-week course acceptable if uncomplicated, otherwise 4-6 weeks |
|||
* 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 |
|||
*Repeat blood cultures every 24 to 48 hours until negative |
|||
= Prognosis = |
|||
*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: |
|||
***[[Embolic stroke|Cerebral]] or peripheral emboli |
|||
***[[Meningitis]] |
|||
***[[Cardiovascular implantable electronic device infection|Implantable cardiac device]] or [[prosthetic heart valve]] |
|||
***Prior [[infective endocarditis]] |
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***Native valve disease |
|||
***Injection drug use |
|||
***Persistent bacteremia beyond 72 hours |
|||
**Can also use [[VIRSTA score]] to decide if they need TEE[[CiteRef::tubiana2016th]] |
|||
***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 specificity[[CiteRef::van der vaart2021pr]] |
|||
==Management== |
|||
* Mortality 20-50% at 30 days, 60% at 1 year |
|||
* Mortality halved by ID consult |
|||
* Prognosis worse with |
|||
** Increased age |
|||
** Female sex |
|||
** Pneumonia or source unknown |
|||
** Dementia |
|||
** Increasing comorbidities |
|||
** Shock at time of presentation |
|||
** Institutionalized patient |
|||
*Infectious diseases consultation |
|||
= Further Reading = |
|||
=== 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 |
|||
=== 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]], [[Infective endocarditis|endocarditis]]) with early oral antibiotics, including infections caused by [[Staphylococcus aureus]] |
|||
=== Dosing === |
|||
==== Penicillin- or Methicillin-Susceptible Strains ==== |
|||
{| class="wikitable" |
|||
!Antibiotic |
|||
!Renal Function |
|||
!Standard Dose |
|||
!Critical Illness Doseβ |
|||
|- |
|||
| rowspan="4" |[[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 |
|||
|- |
|||
| rowspan="3" |[[flucloxacillin]] |
|||
|eGFR β₯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 |
|||
|- |
|||
| rowspan="4" |[[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 |
|||
|}*β 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 ====== |
|||
{| class="wikitable" |
|||
!Renal Function |
|||
!Suggested Dose |
|||
|- |
|||
|eGFR >50 |
|||
|8-10 mg/kg q24h |
|||
|- |
|||
|eGFR 11-50 |
|||
|6-8 mg/kg q24h |
|||
|- |
|||
|eGFR β€10 |
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|8 mg/kg q48h |
|||
|- |
|||
|CRRT |
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|8 mg/kg q48h |
|||
|- |
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|HD |
|||
|8 mg/kg q48h, given after dialysis |
|||
|} |
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====== Adjunctive Cefazolin Dosing ====== |
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{| class="wikitable" |
|||
!Renal Function |
|||
!Suggested Dose |
|||
|- |
|||
| CrCl >40 |
|||
|2 g q8h |
|||
|- |
|||
|CrCl 20-40 |
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| 2 g q12h |
|||
|- |
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| CrCl <20 |
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|1 g q24h |
|||
|- |
|||
|CRRT |
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| 1 g q8h or 2 g q12h |
|||
|- |
|||
|HD |
|||
|2 g after each dialysis session |
|||
|} |
|||
==== Early Oral Switch ==== |
|||
{| class="wikitable" |
|||
!Silo |
|||
!IV Antibiotic |
|||
!Suggested First-Line |
|||
! Suggested Second-Line (ordered) |
|||
|- |
|||
| rowspan="2" | PSSA |
|||
|[[benzylpenicillin]] |
|||
|[[amoxicillin]] |
|||
|[[flucloxacillin]]/[[dicloxacillin]], [[cefalexin]]/[[cefadroxil]], [[linezolid]] |
|||
|- |
|||
|([[Flucloxacillin|flu]])[[cloxacillin]] |
|||
|[[flucloxacillin]]/[[dicloxacillin]] |
|||
|[[amoxicillin]], [[cefalexin]]/[[cefadroxil]], [[linezolid]] |
|||
|- |
|||
| rowspan="2" |MSSA |
|||
|([[Flucloxacillin|flu]])[[cloxacillin]] |
|||
|[[flucloxacillin]]/[[dicloxacillin]] |
|||
|[[cefalexin]]/[[cefadroxil]], [[linezolid]] |
|||
|- |
|||
|[[cefazolin]] |
|||
|[[cefalexin]]/[[cefadroxil]] |
|||
|[[flucloxacillin]]/[[dicloxacillin]], [[linezolid]] |
|||
|- |
|||
| rowspan="2" |MRSA |
|||
|[[vancomycin]]/[[daptomycin]] |
|||
|[[linezolid]] |
|||
|[[fluoroquinolone]]+[[rifampin]], [[TMP-SMX]], [[fusidic acid]]+[[rifampin]] |
|||
|- |
|||
|[[vancomycin]]/[[daptomycin]]+[[cefazolin]] |
|||
|[[linezolid]] |
|||
|[[fluoroquinolone]]+[[rifampin]], [[TMP-SMX]], [[fusidic acid]]+[[rifampin]] |
|||
|} |
|||
{| class="wikitable" |
|||
!Antibiotic |
|||
!Renal Function |
|||
!Suggested Dose |
|||
!Notes |
|||
|- |
|||
| rowspan="5" |[[amoxicillin]] |
|||
|normal |
|||
|1 g q6h Β± [[probenecid]] |
|||
| |
|||
|- |
|||
|CrCl 10-30 |
|||
|1 g q8h |
|||
| |
|||
|- |
|||
|CrCl <10 |
|||
|1 g q12h |
|||
| |
|||
|- |
|||
|CRRT |
|||
|1 g q8h |
|||
| |
|||
|- |
|||
|HD/PD |
|||
|1 g q12h |
|||
| |
|||
|- |
|||
| rowspan="6" |[[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 |
|||
| |
|||
|- |
|||
| rowspan="4" |[[cefalexin]] |
|||
|normal |
|||
|1 g q6h Β± [[probenecid]] |
|||
| |
|||
|- |
|||
|CrCl <10 |
|||
|1 g q12h |
|||
| |
|||
|- |
|||
|CRRT |
|||
|1 g q6h |
|||
| |
|||
|- |
|||
|HD/PD |
|||
|1 g q12h |
|||
| |
|||
|- |
|||
| rowspan="4" |[[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 |
|||
| |
|||
|- |
|||
| rowspan="4" |[[dicloxacillin]] |
|||
|normal |
|||
|1 g q6h |
|||
| |
|||
|- |
|||
|CrCl <10 |
|||
|1 g q8h |
|||
| |
|||
|- |
|||
|CRRT |
|||
|1 g q6h |
|||
| |
|||
|- |
|||
|HD/PD |
|||
|1 g q8h |
|||
| |
|||
|- |
|||
|[[doxycycline]] |
|||
|any |
|||
|100 mg q12h |
|||
| |
|||
|- |
|||
| rowspan="4" |[[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 |
|||
| |
|||
|- |
|||
| rowspan="5" |[[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 |
|||
| |
|||
|- |
|||
| rowspan="4" |[[linezolid]] |
|||
|normal |
|||
|600 mg q12h |
|||
| |
|||
|- |
|||
|CrCl <10 |
|||
|600 mg q24h |
|||
| |
|||
|- |
|||
|CRRT |
|||
|600 mg q12h |
|||
| |
|||
|- |
|||
|HD/PD |
|||
|600 mg q24h |
|||
| |
|||
|- |
|||
|[[moxifloxacin]] |
|||
|any |
|||
|400 mg daily |
|||
| |
|||
|- |
|||
| rowspan="3" |[[probenecid]] |
|||
|CrCl β₯60 |
|||
|500 mg with each dose of Ξ²-lactam |
|||
| |
|||
|- |
|||
|CrCl 30-60 |
|||
|250 mg with each dose of Ξ²-lactam |
|||
| |
|||
|- |
|||
|CrCl <30 |
|||
|avoid use |
|||
| |
|||
|- |
|||
| rowspan="2" |[[rifampin]] |
|||
|any (weight <60kg) |
|||
|600 mg daily |
|||
| |
|||
|- |
|||
|any (weight >60 kg) |
|||
|900 mg daily |
|||
| |
|||
|- |
|||
|[[tedizolid]] |
|||
|any |
|||
|200 mg q24h |
|||
| |
|||
|- |
|||
| rowspan="4" |[[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== |
|||
{{DISPLAYTITLE:''Staphylococcus aureus'' bacteremia}} |
{{DISPLAYTITLE:''Staphylococcus aureus'' bacteremia}} |
||
[[Category: |
[[Category:Endovascular infections]] |
||
[[Category: |
[[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 Doseβ |
---|---|---|---|
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 β₯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 |
*β 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 β€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 Β± 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 Β± 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 β₯60 | 500 mg with each dose of Ξ²-lactam | |
CrCl 30-60 | 250 mg with each dose of Ξ²-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.
- ^ Bharath Raj Palraj, Larry M. Baddour, Erik P. Hess, James M. Steckelberg, Walter R. Wilson, Brian D. Lahr, M. Rizwan Sohail. Predicting Risk of Endocarditis Using a Clinical Tool (PREDICT): Scoring System to Guide Use of Echocardiography in the Management of Staphylococcus aureus Bacteremia. Clinical Infectious Diseases. 2015;61(1):18-28. doi:10.1093/cid/civ235.
- ^ 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.