Sandbox:Reddy 2: Difference between revisions
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|Vancomycin | |Vancomycin | ||
|Vanc | |Vanc | ||
|If ''S. aureus'' is methicillin-susceptible then cefazolin 2 g IV q8h or nafcillin 2 g IV q4h are the antibiotics of choice. | | | ||
Obtain bone biopsy to determine microbiologic cause prior to initiation of antimicrobial therapy if blood cultures are negative and patient clinically stable. | * If ''S. aureus'' is methicillin-susceptible then cefazolin 2 g IV q8h or nafcillin 2 g IV q4h are the antibiotics of choice. | ||
* Obtain bone biopsy to determine microbiologic cause prior to initiation of antimicrobial therapy if blood cultures are negative and patient clinically stable. | |||
|- | |- | ||
|With vascular insufficiency or diabetes mellitus (e.g. severe diabetic foot ulcer) | |With vascular insufficiency or diabetes mellitus (e.g. severe diabetic foot ulcer) | ||
Line 47: | Line 49: | ||
'''Metronidazole'''500 mg IV q8h (if patient critically ill) | '''Metronidazole'''500 mg IV q8h (if patient critically ill) | ||
|Other organisms are possible, esp. with hardware microbiologic diagnosis and ID consultation recommended | | | ||
Obtain bone biopsy to determine microbiologic cause prior to initiation of antimicrobial therapy if patient clinically stable | * Other organisms are possible, esp. with hardware microbiologic diagnosis and ID consultation recommended | ||
* Obtain bone biopsy to determine microbiologic cause prior to initiation of antimicrobial therapy if patient clinically stable | |||
Once stable, switch to oral antibiotics based on susceptibility results. | * Once stable, switch to oral antibiotics based on susceptibility results. | ||
|- | |- | ||
|'''Septic Arthritis''' | |'''Septic Arthritis''' | ||
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|} | |} | ||
{| class="wikitable" | {| class="wikitable" | ||
|- | |- | ||
|'''Brain abscess''' | |'''Brain abscess''' | ||
Line 148: | Line 147: | ||
'''TMP/SMX''' (if ''Listeria'') 15 mg/kg/day (in divided doses) | '''TMP/SMX''' (if ''Listeria'') 15 mg/kg/day (in divided doses) | ||
|Therapy should be guided by Gram stain. | | | ||
If bacterial meningitis suspected'','' dexamethasone 10 mg PO/IV q6h x 4 days given before or with initial dose of antibiotics. | * Therapy should be guided by Gram stain. | ||
* If bacterial meningitis suspected'','' dexamethasone 10 mg PO/IV q6h x 4 days given before or with initial dose of antibiotics. | |||
* Coverage for ''Listeria'' with TMP/SMX or ampicillin should be added for patients who are <2 or >50 years of age or immunocompromised. | |||
|- | |- | ||
|'''Meningitis''' | |'''Meningitis''' | ||
Line 174: | Line 175: | ||
|} | |} | ||
{| class="wikitable" | {| class="wikitable" | ||
|- | |- | ||
|'''Native Valve''' | |'''Native Valve''' | ||
Line 201: | Line 197: | ||
'''Ciprofloxacin'''ID-R: VASF 400 mg IV q12h | '''Ciprofloxacin'''ID-R: VASF 400 mg IV q12h | ||
|Narrow coverage to microbiologically confirmed pathogens | | | ||
* Narrow coverage to microbiologically confirmed pathogens | |||
* Addition of Gram-negative coverage should be considered if the patient has a sub-acute presentation. | |||
|- | |- | ||
|'''Prosthetic Valve''' | |'''Prosthetic Valve''' | ||
Line 219: | Line 217: | ||
| | | | ||
|Rifampin has numerous clinically significant drug interactions. Medication lists should be reviewed for potential drug-drug interactions with rifampin. | |Rifampin has numerous clinically significant drug interactions. Medication lists should be reviewed for potential drug-drug interactions with rifampin. | ||
|} | |||
{| class="wikitable" | |||
|'''Spontaneous Bacterial Peritonitis (SBP)''' | |||
|''E. coli'' | |||
''Klebsiella spp.'' | |||
'<nowiki/>'''Streptococci. spp''.''''' | |||
|'''Ceftriaxone''' 1 g IV daily x 5 days | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS | |||
'''Aztreonam''' 2 g IV q8h | |||
| | |||
|- | |||
|'''Secondary Peritonitis''' | |||
'''Mild-Moderate''' intra-abdominal abscess | |||
|''E. coli'' | |||
''Klebsiella'' | |||
''B. fragilis'' | |||
''Streptococci spp'' | |||
''S. aureus'' | |||
|'''Ertapenem''' 1g IV daily | |||
OR | |||
'''Piperacillin/tazobactam''' 3.375 g IV q6h - 4.5g IV q6h | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS | |||
'''Aztreonam''' 2 g IV q8h | |||
PLUS | |||
'''Metronidazole'''500 mg IV q8h | |||
| | |||
|- | |||
|'''Secondary Peritonitis''' | |||
'''Severe''' (major peritoneal soilage, large or multiple abscesses, patient hemodynamically unstable) | |||
|''E. coli'' | |||
''Klebsiella'' | |||
''B. fragilis'' | |||
''P. aeruginosa'' | |||
''Enterococcus spp.'' | |||
''Streptococcus spp'' | |||
''S. aureus'' | |||
|'''Vancomycin''' | |||
PLUS | |||
'''Piperacillin/tazobactam''' 4.5 g IV q6h | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS | |||
'''Aztreonam''' 2 g IV q8h | |||
PLUS | |||
'''Metronidazole'''500 mg IV q8h | |||
|For hemodynamically unstable health-care associated infection, consider meropenem. | |||
|- | |||
|''Clostridium difficile''-associated diarrhea | |||
|''Clostridium difficile'' | |||
|Initial episode, mild to moderate disease | |||
(WBC ≤15K and SCr less than 1.5 times premorbid level) | |||
'''Vancomycin''' 125mg PO q6h x 10-14 days. If unable to obtain at discharge, can complete course with '''Metronidazole'''500mg po q8h | |||
Initial episode, severe disease | |||
(WBC >15k and/or 50% increase in SCr) | |||
'''Vancomycin''' 125mg PO q6h x 10-14 days. | |||
Initial episode, severe disease with complications | |||
(Severe disease with hypotension, shock, ilios, and/or megacolon) | |||
'''Vancomycin''' 500mg PO/NG q6h x 10-14 days | |||
PLUS | |||
'''Metronidazole''' 500 mg IV q8h x 10-14 days | |||
WITH OR WITHOUT | |||
'''Vancomycin''' PR Rectal vancomycin should be considered in patients with ileus. It is given as 500 mg in 100 mL of 0.9% NaCl and instilled q6h (retain each dose for 1h) | |||
* First recurrence | |||
Same therapy as initial episode, stratified by illness severity | |||
* First recurrence, special population (hematologic malignancy with >30 days expected neutropenia, recent HSCT, recent treatment for GVHD, solid organ transplant <3 months) | |||
'''Fidaxomicin'''ID-R: UCSF SFGH VASF 200mg PO BID x10 days | |||
* Second recurrence | |||
'''Vancomycin''' with tapered or pulsed regimen | |||
PLUS | |||
Consult ID, GI | |||
PLUS | |||
Evaluate for fecal microbiota transplant | |||
| | |||
* IV metronidazole alone is not indicated for treatment of ''C. difficile'' diarrhea. | |||
* IV metronidazole should only be used in combination with PO vancomycin in the ICU. | |||
* Recurrence in 5-30% of patients after first episode and 33-60% after second episode. | |||
* ID CONSULT recommended in patients with severe disease with complications or multiply recurrent disease, and for consideration of rectal vancomycin administration. | |||
| | |||
|} | |||
{| class="wikitable" | |||
|'<nowiki/>'''''Endometritis'''''' | |||
|''Bacteroides'' | |||
''Prevotella bivia'' | |||
Group B & Astreptococci | |||
Enterobacteriaceae | |||
''M. hominis'' | |||
|'''''1st line:''''' | |||
'''Cefoxitin''' 2 g IV q6h | |||
'''''2nd line:''''' | |||
'''Ertapenem''' 1 g IV daily | |||
'''''3rd line:''''' | |||
'''Ampicillin/sulbactam''' 3 g IV q6h | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS | |||
'''Gentamicin''' | |||
PLUS | |||
'''Metronidazole''' 500 mg IV q12h | |||
| | |||
* If test for chlamydia is positive add azithromycin or doxycycline. | |||
* Continue antibiotics until afebrile for 24-48 hours. | |||
* If still febrile > 48 hours and on cefoxitin or clindamycin/gentamicin postpartum, switch to ertapenem. | |||
* Wait 48 hours on an antibiotic regimen before considering regimen failed. | |||
|} | |||
{| class="wikitable" | |||
|'''Peritonsillar abscess,''' deep neck infections | |||
|Group A streptococci | |||
Anaerobes | |||
''S. aureus'' | |||
|'''Ampicillin/sulbactam''' 3 g IV q6h | |||
WITH OR WITHOUT* | |||
'''Vancomycin''' | |||
Alternatively: | |||
'''Ertapenem''' 1 g IV daily | |||
WITH OR WITHOUT* | |||
'''Vancomycin''' | |||
Alternatively: | |||
'''Metronidazole''' 500 mg IV/PO q8h | |||
PLUS | |||
'''Ceftriaxone'''1 g IV q24h | |||
WITH OR WITHOUT* | |||
'''Vancomycin''' | |||
|For severe PCN allergy: | |||
'''Clindamycin'''ID-R: VASF 600 – 900 mg IV q8h | |||
PLUS | |||
'''Ciprofloxacin'''ID-R: VASF 400 mg IV q12h | |||
OR | |||
'''Levofloxacin'''ID-R: VASF 500 mg IV daily | |||
|Often polymicrobial | |||
* Combinations of piperacillin/tazobactam, ampicillin/sulbactam, or ertapenem PLUS metronidazole should not be used. | |||
* Consider vancomycin use for patients at high risk for MRSA | |||
|} | |||
{| class="wikitable" | |||
|'''Line-related bacteremia''' | |||
|''S. epidermidis'' | |||
''S. aureus'' | |||
''Enterococci spp.'' | |||
Gram-negative rods* | |||
''Yeast**'' | |||
|'''Vancomycin''' | |||
WITH OR WITHOUT* one of: | |||
'''Piperacillin/tazobactam''' | |||
ID-R: SFGH | |||
4.5 g IV q6h | |||
OR | |||
'<nowiki/>''Cefepime'''I'<nowiki/>''''' 2 g IV q8h | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
WITH OR WITHOUT* one of: | |||
'''Aztreonam''' ID-R: SFGH 2 g q8h | |||
| | |||
* Remove the offending intravascular device immediately, if possible. | |||
* Consider Gram-negative coverage for immunocompromised patients or those with prolonged hospitalization, recent antibiotic exposure or sepsis. | |||
|} | |||
{| class="wikitable" | |||
| rowspan="2" |'''Community-Acquired Pneumonia''' | |||
|'''Immunocompetent patient''' – Medical Ward | |||
|''S. pneumoniae'' | |||
''Mycoplasma pneumoniae'' | |||
''Chlamydia pneumoniae'' | |||
''H. influenzae'' | |||
''Legionella pneumophilia'' | |||
''Klebsiella pneumoniae'' | |||
''(alcoholics)'' | |||
|No Recent antibiotic therapy:* | |||
'''Ceftriaxone''' 1 g IV daily | |||
PLUS | |||
'<nowiki/>'''''Doxycycline''''''100 mg PO/IV q12h | |||
|For severe PCN allergy: | |||
'''Levofloxacin''' 750 mg PO/IV daily | |||
OR | |||
'''Moxifloxacin'''ID-R: SFGH 400 mg PO/IV daily | |||
| | |||
* If patient has had recent antibiotic therapy, antibiotics from a different class should be selected (i.e. recent use of a fluoroquinolone should dictate selection of a non-fluoroquinolone regimen, and vice versa). | |||
* Consider influenza testing and treatment with oseltamivir. | |||
|- | |- | ||
|'''Community-Acquired Pneumonia''' | |||
'''Immunocompetent patient''' – ICU | |||
|''S. pneumoniae'' | |||
''Mycoplasma pneumoniae'' | |||
''Chlamydia pneumoniae'' | |||
''H. influenzae'' | |||
''Legionella pneumophilia'' | |||
''Klebsiella pneumoniae'' | |||
(alcoholics) | |||
''S. aureus'' | |||
|'''Ceftriaxone''' 1 g IV daily | |||
PLUS | |||
'''Azithromycin''' 500 mg IV daily | |||
WITH OR WITHOUT*: | |||
'''Vancomycin''' | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS one of: | |||
'''Levofloxacin''' 750 mg IV daily | |||
OR | |||
'''Moxifloxacin''' 400 mg IV daily | |||
| | |||
* MRSA risk factors: prior influenza, presence cavitary disease, empyema. | |||
* Consider influenza testing and treatment with oseltamivir. | |||
* If no microbiologic confirmation of MRSA then discontinue vancomycin. | |||
* See HCAP for risk factors for infection with ''Pseudomonas aeruginosa.'' | |||
|- | |||
|'''Healthcare –associated pneumonia (HCAP):''' | |||
acquired in long-term care facility where antimicrobials used or ''Pseudomonas'' risk factors (see Comments) | |||
|''S.aureus'' | |||
''S.pneumoniae'' | |||
''H.influenzae'' | |||
Antibiotic sensitive enteric gram negative bacilli: | |||
''E. coli'' | |||
''Enterobacter aerogenes'' | |||
''Klebsiella pneumoniae'' | |||
''Proteus mirabilis'' | |||
''Serratia marcesans'' | |||
''P. aeruginosa (''if risk factors present) | |||
|Hemodynamically stable & no ''Pseudomonas'' risk factors | |||
'''Vancomycin''' | |||
PLUS one of: | |||
'''Ertapenem''' 1 g IV daily | |||
WITH OR WITHOUT one of*: | |||
'''Doxycycline''' 100 mg IV/PO BID | |||
OR | |||
'''Levofloxacin''' 750 mg IV/PO daily | |||
Hemodynamically unstable or ''Pseudomonas'' risk factors | |||
'''Vancomycin''' | |||
PLUS one of: | |||
'''Piperacillin/tazobactam'''ID-R: SFGH 4.5 g IV q6h | |||
OR | |||
'''Cefepime'''ID-R: SFGH VASF 2 g IV q8h-q12h | |||
WITH OR WITHOUT*: | |||
'''Azithromycin''' 500 mg IV daily | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS one of: | |||
'''Aztreonam'''ID-R: SFGH 2 g IV q8h | |||
WITH OR WITHOUT one of*: | |||
'''Doxycycline''' 100 mg IV/PO BID | |||
OR | |||
'''Azithromycin''' 500 mg IV daily | |||
| | | | ||
| | | | ||
* ''Pseudomonas'' risk factors include: structural lung disease, repeated exacerbations of severe COPD leading to frequent steroid and/or antibiotic use, recent mechanical ventilation, recent prior exposure to broad-spectrum antibiotics | |||
* Avoid using levofloxacin if the patient has recently been treated with a fluoroquinolone. | |||
* For patients admitted from the community with HCAP and not treated with levofloxacin, consider adding atypical coverage with doxycycline (floor patients) or azithromycin (ICU patients). | |||
|- | |||
| rowspan="2" |'''Hospital-acquired pneumonia''' | |||
|'''EARLY ONSET''' | |||
including ventilator-associated or less than 5 days of hospitalization, no risk factors for drug-resistant organisms* | |||
|''S. aureus'' | |||
''S.pneumoniae'' | |||
''H.influenzae'' | |||
Antibiotic sensitive enteric gram negative bacilli: | |||
''E. coli'' | |||
''Enterobacter aerogenes'' | |||
''Klebsiella pneumoniae'' | |||
''Proteus mirabilis'' | |||
''Serratia marcesans'' | |||
|'''Vancomycin''' | |||
PLUS one of | |||
'''Levofloxacin''' 750 mg IV daily | |||
OR | |||
'''Ertapenem''' 1 g IV daily | |||
| | | | ||
| | | | ||
* Risk factors include recent antibiotic exposure (within 30 days). | |||
* Consider influenza testing and treatment with oseltamivir when influenza is known to be circulating. | |||
|- | |||
|'''LATE ONSET''' | |||
including ventilator-associated OR ≥ 5 days of hospitalization or risk factors for resistant organisms* | |||
|''E. coli'' | |||
''Enterobacter aerogenes'' | |||
''P. aeruginosa'' | |||
''Klebsiella pneumoniae'' | |||
'<nowiki/>'''S. aureus'''' | |||
|'''Vancomycin''' | |||
PLUS one of: | |||
'''Piperacillin/tazobactam''' 4.5 g IV q6h | |||
OR | |||
'''Cefepime''' 2 g IV q8-12h | |||
''Alternatively'': | |||
'''Vancomycin''' | |||
PLUS | |||
'''Meropenem''' 1-2 g IV q8h** | |||
|For severe PCN allergy: | |||
'''Vancomycin'''2 | |||
PLUS | |||
'''Aztreonam''' 2 g IV q8h | |||
WITH OR WITHOUT***: | |||
'''Tobramycin''' | |||
|**Consider use in patients with current or recent use (< 7 days) of piperacillin/tazobactam or cefepime and in patients with recent infection with multidrug resistant gram-negative bacteria. | |||
<nowiki>***</nowiki>Weigh risks and benefits of adding aminoglycoside for critical illness, immunocompromise, or history of infection or colonization with drug-resistant Gram-negative rods. | |||
|} | |||
{| class="wikitable" | |||
|'<nowiki/>'''''Septic Shock'''''' | |||
Community onest, no recent healthcare exposure | |||
|Enterobacteriaceae | |||
''S. aureus'' | |||
''Streptococci spp.'' | |||
|'''Vancomycin''' | |||
PLUS one of: | |||
'''Piperacillin/''' | |||
'''Tazobactam'''ID-R: SFGH 4.5 g IV q8h | |||
OR | |||
'<nowiki/>'''''Ertapenem'''''' 1 g IV daily | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS | |||
'''Metronidazole''' 500 mg IV/PO q8h | |||
PLUS one of | |||
'''Aztreonam'''ID-R: SFGH 2 g IV q8h | |||
OR | |||
'''Tobramycin''' | |||
| | | | ||
|- | |||
|'''Healthcare-associated and/or previous antibiotic therapy''' | |||
|Enterobacteriaceae | |||
''S. aureus'' | |||
''Streptococci spp.'' | |||
''P. aeruginosa'' | |||
|'''Vancomycin''' | |||
PLUS | |||
'''Piperacillin/''' | |||
'''Tazobactam''' 4.5 g IV q6h | |||
OR | |||
'''Cefepime''' 2 g IV q8h | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS | |||
'''Metronidazole''' 500 mg IV q8h | |||
AND | |||
'''Aztreonam''' 2 g IV q8h | |||
WITH OR WITHOUT: | |||
'''Tobramycin''' | |||
|''For patients with neutropenia, organ transplant, severe hepatic failure, or current/recent (<7 days) piperacillin/tazobactam or cefepime:'' | |||
'''Vancomycin''' | |||
''Plus'' | |||
'''Meropenem''' 1-2 g IV q8h | |||
|} | |||
{| class="wikitable" | |||
|'<nowiki/>'''''Abscess'''''' | |||
|'<nowiki/>'''S.aureus'''' | |||
|Vancomycin | |||
|Empirical Gram-negative and/or anaerobic coverage is not routinely indicated. | |||
Incision and drainage is primary therapy for abscesses. After incision and drainage and once patient is stable, switch to oral antibiotics based on culture and susceptibility results. | |||
|- | |||
|'<nowiki/>'''''Cellulitis'''''' | |||
|Group A streptococci | |||
Other beta-hemolytic streptococci | |||
''S.aureus'' | |||
|'''Vancomycin''' | |||
''Alternatively:'' | |||
'''Cefazolin''' 1 g IV q8h if patient is stable and cellulitis is not associated with an abscess or other purulent focus of infection | |||
|Empirical Gram-negative and/or anaerobic coverage is not routinely indicated. | |||
|- | |||
|'''Necrotizing fasciitis or suspected deep tissue extension''' | |||
|Group A streptococci | |||
''S. aureus'' | |||
Anaerobes | |||
Gram-negative rods | |||
|'''Vancomycin''' | |||
PLUS ONE OF: | |||
'''Piperacillin/tazobactam''' 4.5 g IV q6-8h | |||
OR | |||
'''Ertapenem''' 1 g IV daily | |||
ALL WITH: | |||
'''Clindamycin'''600 – 900 mg IV q8h | |||
Alternatively if infection is health-care associated: | |||
'''Vancomycin''' | |||
PLUS | |||
'''Meropenem'''1-2 g IV q8h | |||
PLUS | |||
'''Clindamycin'''600-900 mg IV q8h | |||
|For severe PCN allergy: | |||
'''Vancomycin''' | |||
PLUS | |||
'''Aztreonam'''ID-R: SFGH 2 g IV q8h | |||
PLUS | |||
'''Clindamycin''' ID-R: VASF 600-900 mg IV q8h | |||
Clindamycin added for anti-toxin properties. Limited data support use for infections caused by Group A streptococci and ''Clostridium perfringens.'' Discontinue clindamycin once adequate surgical debridement is achieved. | |||
|} | |||
{| class="wikitable" | |||
|'''Asymptomatic bacteriuria''' | |||
|Enterobacteriaceae | |||
''Enterococcus''species | |||
|No treatment required | |||
|Exceptions: pregnant women, patients having traumatic urologic procedures, recent kidney transplant . | |||
|- | |||
|'''Catheter-associated candiduria''' | |||
|'''''Candida'' species''' | |||
|No treatment required | |||
|Pyuria alone is not an indication for treatment. | |||
|- | |||
|'''Community-acquired Pyelonephritis''' | |||
|Enterobacteriaceae ''(E. coli)'' | |||
|'''Ceftriaxone''' | |||
1 g IV q24h | |||
OR | |||
'''Cefazolin''' 1g IV q8h (VASF only) | |||
OR | |||
'''Ertapenem''' 1g IV daily | |||
|For '''severe''' PCN allergy: | |||
'''Vancomycin''' | |||
PLUS ONE OF EITHER: | |||
'''Gentamicin''' | |||
OR | |||
'''Aztreonam''' ID-R: SFGH | |||
2 g IV q8h | |||
'''Duration of therapy 7-14 days based on clinical response.''' | |||
|- | |||
|'''Healthcare-associated UTI''' | |||
|Enterobacteriaceae ''(e.g. E. coli)'' | |||
''P. aeruginosa'' (less common) | |||
|'''Ceftriaxone''' | |||
1 g IV q24h | |||
OR | |||
'''Ertapenem''' 1g IV daily | |||
OR | |||
'''Piperacillin/tazobactam'''ID-R: SFGH 4.5g IV q8h | |||
|For '''severe''' PCN allergy: | |||
ONE OF:Criteria: signs and symptoms compatible with a UTI, no other identified source of infection, & ≥ 1000 cfu of ≥ 1 bacterial species on urine culture | |||
'''Gentamicin''' | |||
OR | |||
'''Aztreonam''' ID-R: SFGH | |||
2 g IV q8h | |||
BOTH WITH OR WITHOUT: | |||
'''Vancomycin''' | |||
* Pyuria alone is not an indication for treatment. | |||
* A negative urinalysis suggests an alternative source of infection. | |||
* Remove catheter if possible. | |||
* Switch to oral therapy when susceptibilities known and patient stable. | |||
* 7 days of therapy is recommend if patient has prompt resolution of symptoms | |||
|} | |} |
Latest revision as of 19:45, 29 June 2017
Hospitalized patients
Infection | Organisms | First DOC | Alternative | ||
---|---|---|---|---|---|
Osteomyelitis | Presumed hematogenous source or contiguous without vascular insufficiency | S. aureus | Vancomycin | Vanc |
|
With vascular insufficiency or diabetes mellitus (e.g. severe diabetic foot ulcer) | S. aureus
Enterobacteriaceae Anaerobes |
Vancomycin
PLUS ONE OF: Piperacillin/Tazobactam 4.5 g IV q6-8h OR Ertapenem 1 g IV daily |
For severe PCN allergy:
Vancomycin PLUS ONE OF: Ciprofloxacin400 mg IV q12h OR Levofloxacin 750 mg IV daily OR Aztreonam 2 g IV q8h ALL WITH OR WITHOUT: Metronidazole500 mg IV q8h (if patient critically ill) |
| |
Septic Arthritis | S. aureus
Streptococci spp. N. gonorrhoeae Enterobacteriaceae (rarely) |
Vancomycin
PLUS Ceftriaxone1 g IV daily |
For severe PCN allergy:
Vancomycin PLUS ONE OF: Ciprofloxacin 400 mg IV q12h OR Levofloxacin 500 mg IV daily OR Aztreonam g IV q8h if gonococcus is strongly suspected |
Gram stain recommended to guide therapy.
Narrow coverage to microbiologically confirmed pathogens. |
Brain abscess | Streptococci (anaerobic or aerobic)
Bacteroides spp Prevotella spp Enterobacteriacea |
Ceftriaxone
2 g IV q12h PLUS Metronidazole 500 mg PO/IV q8h WITH OR WITHOUT*: Vancomycin |
Aztreonam
2 g IV q8h PLUS Vancomycin PLUS Metronidazole 500 mg PO/IV q8h |
Consider expanded Gram-positive coverage if patient at risk for drug-resistant streptococci or MRSA |
Meningitis
Community-onset |
S. pneumoniae
Neisseria meningitidis Listeria (especially in immuno-compromised, elderly patients, and alcoholics) |
ceftriaxone
2 g IV q12h PLUS Vancomycin WITH OR WITHOUT* one of: TMP/SMX 15 mg/kg/day (in divided doses) OR 'Ampicillin' 2 g IV q4h |
For severe PCN allergy:
Vancomycin PLUS Aztreonam2 g IV q6h-q8h WITH OR WITHOUT*: TMP/SMX (if Listeria) 15 mg/kg/day (in divided doses) |
|
Meningitis
Post-neurosurgical or device associated |
S. aureus
Coagulase negative Staphylococci Gram negative rods |
Cefepime
PLUS 'Vancomycin' |
For severe PCN allergy:
Aztreonam 2 g IV q6h-q8h PLUS Vancomycin |
Native Valve | S. aureus
Streptococci spp. Enterococcus spp. Occasional gram negative rods HACEK < 5% |
Vancomycin
WITH or WITHOUT* Ceftriaxone 2 g IV daily |
For severe PCN allergy:
Vancomycin WITH or WITHOUT* CiprofloxacinID-R: VASF 400 mg IV q12h |
|
Prosthetic Valve | S. aureus
S. epidermidis |
Vancomycin
PLUS Rifampin300 mg PO q8h PLUS Gentamicin 1 mg/kg/dose IV q8h for initial two weeks only Single daily dose of gentamicin is not recommended |
Rifampin has numerous clinically significant drug interactions. Medication lists should be reviewed for potential drug-drug interactions with rifampin. |
Spontaneous Bacterial Peritonitis (SBP) | E. coli
Klebsiella spp. 'Streptococci. spp. |
Ceftriaxone 1 g IV daily x 5 days | For severe PCN allergy:
Vancomycin PLUS Aztreonam 2 g IV q8h |
|
Secondary Peritonitis
Mild-Moderate intra-abdominal abscess |
E. coli
Klebsiella B. fragilis Streptococci spp S. aureus |
Ertapenem 1g IV daily
OR Piperacillin/tazobactam 3.375 g IV q6h - 4.5g IV q6h |
For severe PCN allergy:
Vancomycin PLUS Aztreonam 2 g IV q8h PLUS Metronidazole500 mg IV q8h |
|
Secondary Peritonitis
Severe (major peritoneal soilage, large or multiple abscesses, patient hemodynamically unstable) |
E. coli
Klebsiella B. fragilis P. aeruginosa Enterococcus spp. Streptococcus spp S. aureus |
Vancomycin
PLUS Piperacillin/tazobactam 4.5 g IV q6h |
For severe PCN allergy:
Vancomycin PLUS Aztreonam 2 g IV q8h PLUS Metronidazole500 mg IV q8h |
For hemodynamically unstable health-care associated infection, consider meropenem. |
Clostridium difficile-associated diarrhea | Clostridium difficile | Initial episode, mild to moderate disease
(WBC ≤15K and SCr less than 1.5 times premorbid level) Vancomycin 125mg PO q6h x 10-14 days. If unable to obtain at discharge, can complete course with Metronidazole500mg po q8h Initial episode, severe disease (WBC >15k and/or 50% increase in SCr) Vancomycin 125mg PO q6h x 10-14 days. Initial episode, severe disease with complications (Severe disease with hypotension, shock, ilios, and/or megacolon) Vancomycin 500mg PO/NG q6h x 10-14 days PLUS Metronidazole 500 mg IV q8h x 10-14 days WITH OR WITHOUT Vancomycin PR Rectal vancomycin should be considered in patients with ileus. It is given as 500 mg in 100 mL of 0.9% NaCl and instilled q6h (retain each dose for 1h)
Same therapy as initial episode, stratified by illness severity
FidaxomicinID-R: UCSF SFGH VASF 200mg PO BID x10 days
Vancomycin with tapered or pulsed regimen PLUS Consult ID, GI PLUS Evaluate for fecal microbiota transplant |
|
'Endometritis' | Bacteroides
Prevotella bivia Group B & Astreptococci Enterobacteriaceae M. hominis |
1st line:
Cefoxitin 2 g IV q6h 2nd line: Ertapenem 1 g IV daily 3rd line: Ampicillin/sulbactam 3 g IV q6h |
For severe PCN allergy:
Vancomycin PLUS Gentamicin PLUS Metronidazole 500 mg IV q12h |
|
Peritonsillar abscess, deep neck infections | Group A streptococci
Anaerobes S. aureus |
Ampicillin/sulbactam 3 g IV q6h
WITH OR WITHOUT* Vancomycin Alternatively: Ertapenem 1 g IV daily WITH OR WITHOUT* Vancomycin Alternatively: Metronidazole 500 mg IV/PO q8h PLUS Ceftriaxone1 g IV q24h WITH OR WITHOUT* Vancomycin |
For severe PCN allergy:
ClindamycinID-R: VASF 600 – 900 mg IV q8h PLUS CiprofloxacinID-R: VASF 400 mg IV q12h OR LevofloxacinID-R: VASF 500 mg IV daily |
Often polymicrobial
|
Line-related bacteremia | S. epidermidis
S. aureus Enterococci spp. Gram-negative rods* Yeast** |
Vancomycin
WITH OR WITHOUT* one of: Piperacillin/tazobactam ID-R: SFGH 4.5 g IV q6h OR 'CefepimeI' 2 g IV q8h |
For severe PCN allergy:
Vancomycin WITH OR WITHOUT* one of: Aztreonam ID-R: SFGH 2 g q8h |
|
Community-Acquired Pneumonia | Immunocompetent patient – Medical Ward | S. pneumoniae
Mycoplasma pneumoniae Chlamydia pneumoniae H. influenzae Legionella pneumophilia Klebsiella pneumoniae (alcoholics) |
No Recent antibiotic therapy:*
Ceftriaxone 1 g IV daily PLUS 'Doxycycline'100 mg PO/IV q12h |
For severe PCN allergy:
Levofloxacin 750 mg PO/IV daily OR MoxifloxacinID-R: SFGH 400 mg PO/IV daily |
|
Community-Acquired Pneumonia
Immunocompetent patient – ICU |
S. pneumoniae
Mycoplasma pneumoniae Chlamydia pneumoniae H. influenzae Legionella pneumophilia Klebsiella pneumoniae (alcoholics) S. aureus |
Ceftriaxone 1 g IV daily
PLUS Azithromycin 500 mg IV daily WITH OR WITHOUT*: Vancomycin |
For severe PCN allergy:
Vancomycin PLUS one of: Levofloxacin 750 mg IV daily OR Moxifloxacin 400 mg IV daily |
| |
Healthcare –associated pneumonia (HCAP):
acquired in long-term care facility where antimicrobials used or Pseudomonas risk factors (see Comments) |
S.aureus
S.pneumoniae H.influenzae Antibiotic sensitive enteric gram negative bacilli: E. coli Enterobacter aerogenes Klebsiella pneumoniae Proteus mirabilis Serratia marcesans P. aeruginosa (if risk factors present) |
Hemodynamically stable & no Pseudomonas risk factors
Vancomycin PLUS one of: Ertapenem 1 g IV daily WITH OR WITHOUT one of*: Doxycycline 100 mg IV/PO BID OR Levofloxacin 750 mg IV/PO daily Hemodynamically unstable or Pseudomonas risk factors Vancomycin PLUS one of: Piperacillin/tazobactamID-R: SFGH 4.5 g IV q6h OR CefepimeID-R: SFGH VASF 2 g IV q8h-q12h WITH OR WITHOUT*: Azithromycin 500 mg IV daily |
For severe PCN allergy:
Vancomycin PLUS one of: AztreonamID-R: SFGH 2 g IV q8h WITH OR WITHOUT one of*: Doxycycline 100 mg IV/PO BID OR Azithromycin 500 mg IV daily |
| |
Hospital-acquired pneumonia | EARLY ONSET
including ventilator-associated or less than 5 days of hospitalization, no risk factors for drug-resistant organisms* |
S. aureus
S.pneumoniae H.influenzae Antibiotic sensitive enteric gram negative bacilli: E. coli Enterobacter aerogenes Klebsiella pneumoniae Proteus mirabilis Serratia marcesans |
Vancomycin
PLUS one of Levofloxacin 750 mg IV daily OR Ertapenem 1 g IV daily |
| |
LATE ONSET
including ventilator-associated OR ≥ 5 days of hospitalization or risk factors for resistant organisms* |
E. coli
Enterobacter aerogenes P. aeruginosa Klebsiella pneumoniae 'S. aureus' |
Vancomycin
PLUS one of: Piperacillin/tazobactam 4.5 g IV q6h OR Cefepime 2 g IV q8-12h Alternatively: Vancomycin PLUS Meropenem 1-2 g IV q8h** |
For severe PCN allergy:
Vancomycin2 PLUS Aztreonam 2 g IV q8h WITH OR WITHOUT***: Tobramycin |
**Consider use in patients with current or recent use (< 7 days) of piperacillin/tazobactam or cefepime and in patients with recent infection with multidrug resistant gram-negative bacteria.
***Weigh risks and benefits of adding aminoglycoside for critical illness, immunocompromise, or history of infection or colonization with drug-resistant Gram-negative rods. |
'Septic Shock'
Community onest, no recent healthcare exposure |
Enterobacteriaceae
S. aureus Streptococci spp. |
Vancomycin
PLUS one of: Piperacillin/ TazobactamID-R: SFGH 4.5 g IV q8h OR 'Ertapenem' 1 g IV daily |
For severe PCN allergy:
Vancomycin PLUS Metronidazole 500 mg IV/PO q8h PLUS one of AztreonamID-R: SFGH 2 g IV q8h OR Tobramycin |
|
Healthcare-associated and/or previous antibiotic therapy | Enterobacteriaceae
S. aureus Streptococci spp. P. aeruginosa |
Vancomycin
PLUS Piperacillin/ Tazobactam 4.5 g IV q6h OR Cefepime 2 g IV q8h |
For severe PCN allergy:
Vancomycin PLUS Metronidazole 500 mg IV q8h AND Aztreonam 2 g IV q8h WITH OR WITHOUT: Tobramycin |
For patients with neutropenia, organ transplant, severe hepatic failure, or current/recent (<7 days) piperacillin/tazobactam or cefepime:
Vancomycin Plus Meropenem 1-2 g IV q8h |
'Abscess' | 'S.aureus' | Vancomycin | Empirical Gram-negative and/or anaerobic coverage is not routinely indicated.
Incision and drainage is primary therapy for abscesses. After incision and drainage and once patient is stable, switch to oral antibiotics based on culture and susceptibility results. |
'Cellulitis' | Group A streptococci
Other beta-hemolytic streptococci S.aureus |
Vancomycin
Alternatively: Cefazolin 1 g IV q8h if patient is stable and cellulitis is not associated with an abscess or other purulent focus of infection |
Empirical Gram-negative and/or anaerobic coverage is not routinely indicated. |
Necrotizing fasciitis or suspected deep tissue extension | Group A streptococci
S. aureus Anaerobes Gram-negative rods |
Vancomycin
PLUS ONE OF: Piperacillin/tazobactam 4.5 g IV q6-8h OR Ertapenem 1 g IV daily ALL WITH: Clindamycin600 – 900 mg IV q8h Alternatively if infection is health-care associated: Vancomycin PLUS Meropenem1-2 g IV q8h PLUS Clindamycin600-900 mg IV q8h |
For severe PCN allergy:
Vancomycin PLUS AztreonamID-R: SFGH 2 g IV q8h PLUS Clindamycin ID-R: VASF 600-900 mg IV q8h Clindamycin added for anti-toxin properties. Limited data support use for infections caused by Group A streptococci and Clostridium perfringens. Discontinue clindamycin once adequate surgical debridement is achieved. |
Asymptomatic bacteriuria | Enterobacteriaceae
Enterococcusspecies |
No treatment required | Exceptions: pregnant women, patients having traumatic urologic procedures, recent kidney transplant . |
Catheter-associated candiduria | Candida species | No treatment required | Pyuria alone is not an indication for treatment. |
Community-acquired Pyelonephritis | Enterobacteriaceae (E. coli) | Ceftriaxone
1 g IV q24h OR Cefazolin 1g IV q8h (VASF only) OR Ertapenem 1g IV daily |
For severe PCN allergy:
Vancomycin PLUS ONE OF EITHER: Gentamicin OR Aztreonam ID-R: SFGH 2 g IV q8h Duration of therapy 7-14 days based on clinical response. |
Healthcare-associated UTI | Enterobacteriaceae (e.g. E. coli)
P. aeruginosa (less common) |
Ceftriaxone
1 g IV q24h OR Ertapenem 1g IV daily OR Piperacillin/tazobactamID-R: SFGH 4.5g IV q8h |
For severe PCN allergy:
ONE OF:Criteria: signs and symptoms compatible with a UTI, no other identified source of infection, & ≥ 1000 cfu of ≥ 1 bacterial species on urine culture Gentamicin OR Aztreonam ID-R: SFGH 2 g IV q8h BOTH WITH OR WITHOUT: Vancomycin
|