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Hospitalized patients
{| class="wikitable"
!Infection
!
!Organisms
!First DOC
!Alternative
!
|-
| rowspan="2" |'''Osteomyelitis'''
|Presumed hematogenous source or contiguous without vascular insufficiency
|''S. aureus''
|Vancomycin
|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.
|-
|With vascular insufficiency or diabetes mellitus (e.g. severe diabetic foot ulcer)
|''S. aureus'' 
Enterobacteriaceae


==Overview==
Anaerobes
{{Infobox_Disease |
|'''Vancomycin'''
  Name          = {{PAGENAME}} |
PLUS ONE OF:
  Image          = |
  Caption        = |
  DiseasesDB    = 5901 |
  ICD10          = {{ICD10|Q|43|1|q|38}} |
  ICD9          = {{ICD9|751.3}} |
  ICDO          = |
  OMIM          = 142623 |
  MedlinePlus    = 001140 |
  eMedicineSubj  = med |
  eMedicineTopic = 1016 |
  MeshID        = D006627 |
}}
{{SI}}
'''Hirschsprung's disease''', or '''congenital aganglionic megacolon''', involves an enlargement of the [[colon (anatomy)|colon]], caused by [[bowel obstruction]] resulting from an [[ganglion|aganglionic]] section of [[bowel]] (the normal [[Enteric nervous system|enteric nerves]] are absent) that starts at the anus and progresses upwards. The length of bowel that is affected varies but seldom stretches for more than a foot or so.


==History and Description==
'''Piperacillin/Tazobactam''' 4.5 g IV q6-8h
This disease is named for [[Harald Hirschsprung]], the [[Denmark|Danish]] [[physician]] who first described the disease in [[1886]], describing two infants who had died with swollen bellies. "The autopsies showed identical pictures with a pronounced dilatation and hypertrophy of the colon as the dominant features" (Madsen 17).  


Hirschsprung’s disease is a [[congenital]] disorder of the colon in which certain nerve cells, known as ganglion cells, are absent, causing chronic constipation (Worman and Ganiats 487). In some cases the child may have delayed toilet training. A [[barium enema]] is the mainstay of diagnosis of Hirschsprung’s, though a rectal [[biopsy]] showing the lack of ganglion cells is the only certain method of diagnosis.
OR


The usual treatment is "pull-through" surgery where the portion of the colon that does have nerve cells is pulled through and sewn over the part that lacks nerve cells (National Digestive Diseases Information Clearinghouse). For a long time, Hirschsprung’s was considered a multi-factorial disorder, where a combination of nature and nurture were considered to be the cause (Madsen 19). However, in August of [[1993]], two articles by independent groups in ''Nature Genetics'' said that Hirschsprung’s disease could be mapped to a stretch of [[chromosome 10 (human)|chromosome 10]] (Angrist 351). This research also suggested that a single gene was responsible for the disorder. However, the researchers were unable to isolate the single gene that they thought caused Hirschsprung’s.
'''Ertapenem''' 1 g IV daily
|For '''severe''' PCN allergy:
'''Vancomycin'''


==Genetic basis==
PLUS ONE OF:
In 2002, scientists thought they found the solution.  According to this new research, the interaction between two proteins [[genetic code|encoded]] by two variant genes caused Hirschsprung’s.  The [[RET proto-oncogene]] on [[chromosome 10]] was identified one of the [[gene]]s involved, and it was determined that [[mutation|dominant mutation]]s may occur within this [[gene]] leading to a loss of function for the protein it [[genetic code|encoded]] (Passarge 11).  The protein with which RET has to interact in order for Hirschsprung’s disease to develop is termed EDNRB, and is encoded by the [[gene]] ''EDNRB'' located on [[chromosome 13 (human)|chromosome 13]].  Six other genes were discovered to be associated with Hirschsprung’s.  According to the study, these genes are GDNF on [[chromosome 5 (human)|chromosome 5]], EDN3 on [[chromosome 20 (human)|chromosome 20]], SOX10 on [[chromosome 22 (human)|chromosome 22]], ECE1 on [[chromosome 1 (human)|chromosome 1]], NTN on [[chromosome 19 (human)|chromosome 19]], and SIP1 on [[chromosome 2 (human)|chromosome 2]].  These scientists concluded that the mode of inheritance for Hirschsprung’s is oligogenic inheritance (Passarge 11).  This means that two mutated genes interact to cause a disorder.  Variations in RET and EDNRB have to coexist in order for a child to get Hirschsprung’s.  However, although six other genes were shown to have an effect on Hirschsprung’s, the researchers were unable to determine how they interacted with RET and EDNRB.  Thus, the specifics of the origins of the disease are still not completely known. More recently, syndromic cases of Hischprung's disease (that is, associated with other defects of the [[autonomic nervous system]]) were shown to be caused by mutations in the homeobox gene [[PHOX2B]].


RET codes for proteins that help the neural crest cells (which become ganglion cells) move through the digestive tract during the development of the embryo (Sawin). EDNRB codes for proteins to actually connect these nerve cells to the digestive tract. This means that the absence of certain nerve fibers in the colon could be directly related to these two genes mutating so the wrong proteins are produced. Research published in June of 2004 suggests that there are actually ten genes associated with Hirschsprung’s disease (Puri and Shinkai). Also, new research suggests that mutations in genomic sequences involved in regulating EDNRB have a bigger impact on Hirschsprung’s disease than previously thought.
'''Ciprofloxacin'''400 mg IV q12h


Dr. Bob Sawin of Seattle’s Children's Hospital notes that it is generally accepted in the scientific community that the gene RET is the most important gene when looking for the genetic cause of Hirschsprung’s disease.  RET can mutate in many ways, and is associated with Down syndrome.  Since [[Down Syndrome]] is comorbid in two percent of Hirschsprung’s cases, there is a likelihood that RET is involved heavily in both Hirschprung's disease and Down Syndrome.  RET is also associated with [[thyroid cancer]] and [[neuroblastoma]] (Sawin).  Both of these disorders have also been observed in Hirschsprung’s patients with greater frequency than in the general population.  One function that RET controls is the travel of the [[neural crest cell]]s through the [[intestine]]s in the developing [[fetus]].  When RET mutations cause Hirschsprung’s disease, “the cells start traveling through the colon, only to be stopped once the mutation occurs” (Sawin).  The earlier the mutation of RET occurs in Hirschsprung’s disease, the more severe the disorder becomes (Sawin).
OR


While researchers remain uncertain of the exact genetic cause of Hirschsprung’s disease, Dr. Sawin notes that in familial cases, (in which families have multiple affected patients) Hirschsprung’s disease exhibits autosomal dominant transmission, with the gene RET being dominant. However, in sporadic cases, Sawin notes that there has been no inheritance pattern identified.
'''Levofloxacin''' 750 mg IV daily


Treating Hirschsprung’s is much easier than determining the genetic causes of this disorder. The only way to treat Hirschsprung’s disease is through surgery (National Digestive Diseases Information Clearinghouse). If Hirschsprung’s goes untreated, the patient can develop [[enterocolitis]], the inflammation of the small intestine and the colon (Sawin). This was the cause of death of the two boys that Harald Hirschsprung observed. Surgery is now used to remove the non-functioning portion of the bowel in order to restore bowel function (Sawin).
OR


Hirschsprung's disease, [[hypoganglionosis]], gut dysmotility, gut transit disorders and intussusception have been recorded with the dominantly inherited neurovisceral porphyrias (acute intermittent porphyria, hereditary coproporphyria, variegate porphyria).  Children may require enzyme or DNA testing for these disorders as they may not produce or excrete porphyrins prepuberty.
'''Aztreonam''' 2 g IV q8h


==Surgical treatment==
ALL WITH OR WITHOUT:
There used to be two steps typically used to achieve this goal.
* The first stage used to be a [[colostomy]]. When a colostomy is performed, the large intestine is cut and an opening is made through the abdomen. This allows bowel contents to be discharged into a bag.
* Later, when the child’s weight, age, and condition is right, a pull-through procedure is performed.


Orvar Swenson, the same man who discovered the cause of Hirschsprung’s, first performed it in [[1948]] (Swenson 839). The pull-through procedure repairs the colon by connecting the functioning portion of the bowel to the anus. The pull through procedure is the typical method for treating Hirschsprung’s in younger patients. Swenson devised the original procedure, but the pull-through surgery has been modified many times. Sawin, an expert in pull-through surgery, notes that, "Although there are about five different pull-through procedures, they are all more or less equally effective in treating the disorder."
'''Metronidazole'''500 mg IV q8h (if patient critically ill)
|
* Other organisms are possible, esp. with hardware microbiologic diagnosis and ID consultation recommended


The Swenson, Soave, Duhamel, and Boley procedures all vary slightly from each other with equivalent results (Sawin).
* Obtain bone biopsy to determine microbiologic cause prior to initiation of antimicrobial therapy if patient clinically stable
* The Swenson procedure leaves a small portion of the diseased bowel.
* The Soave procedure leaves the outer wall of the colon unaltered.
* The Boley procedure is just a small modification of the Soave procedure.
* The Duhamel procedure uses a surgical stapler to connect the good and bad bowel. The front of the bowel will end up with no cells, but the back will be healthy (Sawin).


Sawin notes that “Pull-through procedures used to require a colostomy, but with increased awareness among doctors and parents about the symptoms of Hirschsprung’s and with early diagnosis, doctors can keep the colon clean and perform the pull-through procedure without a colostomy”. In general, “85 percent of patients that have the pull-through surgery live normal lives afterwards. The other 15 percent have to take a laxative for the rest of their lives”.
* Once stable, switch to oral antibiotics based on susceptibility results.
|-
|'''Septic Arthritis'''
|
|''S. aureus''
''Streptococci spp.''


In rare cases, if the mother has Hirschsprung’s and passes it on to her child, the child is said to have “total Hirschsprung’s”, where there are no ganglion cells at all in the colon (Sawin). In this case, the Martin pull-through operation is conducted. The Martin operation is the most invasive of the operations, for it requires a colostomy no matter how early you diagnose total Hirschsprung’s.  
''N. gonorrhoeae''


Even rarer, notes Dr. Sawin, "there are times where the disease begins in the small intestine, making treatment even harder". When a child has total Hirschsprung's or small intestine Hirschsprung's, an [[ileostomy]] or jejunostomy is conducted along with the Martin operation, and the child is then treated for [[short bowel syndrome]]. On very rare occasions, pull-through surgery is not the preferred method when it comes to treating Hirschsprung’s disease.
''Enterobacteriaceae (rarely)''
|'''Vancomycin'''
PLUS


If the affected portion of the lower intestine is restricted to the lower portion of the rectum, other surgical procedures, such as the posterior rectal myectomy, can be performed.
'''Ceftriaxone'''1 g IV daily
|For '''severe''' PCN allergy:
'''Vancomycin'''


When suspicion of Hirschsprung's is high, and barium enema has been inconclusive, rectal [[biopsy]] can be used to definitively diagnose the disease.
PLUS ONE OF:


==See also==
'''Ciprofloxacin''' 400 mg IV q12h
*[[Intestinal Neuronal Dysplasia]]


==External links==
OR
*{{OMIM|164761}} (''RET'' gene, the "rearranged during transfection" protooncogene)
*{{OMIM|142623}} (OMIM page on Hirschsprung's disease)
* [http://www.hirschsprungs.info/ Hirschsprung Support: "The Hirschsprungs & Motility Disorders Support Network (HMDSN)"]
*[http://www.hopkinsmedicine.org/geneticmedicine/CR/Hirschsprung/HomeHirschsprung.html "John Hopkins Medicine- THE HIRSCHSPRUNG DISEASE STUDY WEBSITE"]


'''Levofloxacin''' 500 mg IV daily


{{Gastroenterology}}
OR
{{Congenital malformations and deformations of digestive system}}


[[Category:Gastroenterology]]
'''Aztreonam''' g IV q8h if gonococcus is strongly suspected
|Gram stain recommended to guide therapy.
Narrow coverage to microbiologically confirmed pathogens.
|}
{| class="wikitable"
|-
|'''Brain abscess'''
|Streptococci (anaerobic or aerobic)
''Bacteroides spp''


[[ca:malaltia de Hirschsprung]]
''Prevotella'' spp
[[de:Morbus Hirschsprung]]
[[es:Enfermedad de Hirschsprung]]
[[fr:Maladie de Hirschsprung]]
[[nl:Ziekte van Hirschsprung]]
[[pl:Choroba Hirschsprunga]]
[[fi:Hirschsprungin tauti]]


{{WH}}
Enterobacteriacea
{{WikiDoc Sources}}
|'''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
 
'<nowiki/>'''''Ampicillin'''''' 2 g IV q4h
|For '''severe''' PCN allergy:
'''Vancomycin'''
 
PLUS
 
'''Aztreonam'''2 g IV q6h-q8h
 
WITH OR WITHOUT*:
 
'''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. 
 
* Coverage for ''Listeria'' with TMP/SMX or ampicillin should be added for patients who are <2 or >50 years of age or immunocompromised.
|-
|'''Meningitis'''
Post-neurosurgical or device associated
|''S. aureus''
Coagulase negative
 
Staphylococci
 
Gram negative rods
|'''Cefepime'''
PLUS
 
'<nowiki/>'''''Vancomycin'''''' 
|For '''severe''' PCN allergy:
'''Aztreonam''' 2 g IV q6h-q8h
 
PLUS
 
'''Vancomycin'''
|
|}
{| class="wikitable"
|-
|'''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*
 
'''Ciprofloxacin'''ID-R: VASF 400 mg IV q12h
|
* Narrow coverage to microbiologically confirmed pathogens
 
* Addition of Gram-negative coverage should be considered if the patient has a sub-acute presentation.
|-
|'''Prosthetic Valve'''
|''S. aureus''
''S. epidermidis''
|'''Vancomycin'''
PLUS
 
'''Rifampin'''300 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.
|}
{| 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
  • 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) 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)

  • 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.
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)

  • 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

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

  • Narrow coverage to microbiologically confirmed pathogens
  • Addition of Gram-negative coverage should be considered if the patient has a sub-acute presentation.
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)

  • 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)

FidaxomicinID-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.
'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.
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
  • Combinations of piperacillin/tazobactam, ampicillin/sulbactam, or ertapenem PLUS metronidazole should not be used.
  • Consider vancomycin use for patients at high risk for MRSA
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

  • 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.
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

  • 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/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

  • 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).
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

'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

  • 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