Pyelonephritis medical therapy: Difference between revisions

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{{Pyelonephritis}}
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==Overview==
==Overview==
All patients with pyelonephritis should be treated empirically with antimicrobial therapy. Mild pyelonephritis may be managed with oral antimicrobial therapy, and an initial intravenous dose may be administered depending on local resistance patterns. Patients with [[dehydration]], [[nausea]], [[vomiting]], or signs of [[sepsis]] should be admitted and should receive parenteral therapy. Medical therapies for pyelonephritis include [[fluoroquinolone]]s, [[TMP-SMX]], [[β-lactam]]s, and [[aminoglycoside]]s.


Mild pyelonephritis may be managed with oral antimicrobial therapy, and an initial intravenous dose may be administered depending on local resistance patterns. Patients with [[dehydration]], [[nausea]], [[vomiting]], or signs of [[sepsis]] should be admitted and should receive parenteral therapy. [[Fluoroquinolone]]s, [[Aminoglycoside]]s, [[TMP/SMZ|Trimethoprim-Sulfamethoxazole]], [[Carbapenem]]s, and extended-spectrum [[Cephalosporin]]s and [[Penicillins]] are commonly used in the treatment of acute pyelonephritis.<ref name="Gupta-2011">{{Cite journal  | last1 = Gupta | first1 = K. | last2 = Hooton | first2 = TM. | last3 = Naber|first3 = KG. | last4 = Wullt | first4 = B. | last5 = Colgan | first5 = R. | last6 = Miller | first6 = LG. | last7 = Moran | first7 = GJ. | last8 = Nicolle | first8 = LE. | last9 = Raz | first9 = R. | title = International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. | journal = Clin Infect Dis | volume = 52 | issue = 5 | pages = e103-20 | month = Mar | year = 2011 | doi = 10.1093/cid/ciq257|PMID = 21292654 }}</ref> [[Fluoroquinolones]] and [[Aminoglycosides]] should be avoided in pregnant patients.
==Medical Therapy==
 
* All patients with pyelonephritis should be treated empirically with antimicrobial therapy.
==Principles of Therapy for Acute Pyelonephritis==
* Before initiating antimicrobial treatment for suspected pyelonephritis, a urine culture and susceptibility test should always be performed.
 
* Mild pyelonephritis may be managed with oral antimicrobial therapy, and an initial intravenous dose may be administered depending on local resistance patterns. Patients with [[dehydration]], [[nausea]], [[vomiting]], or signs of [[sepsis]] should be admitted and should receive parenteral therapy.<ref name="Gupta-2011">{{Cite journal  | last1 = Gupta | first1 = K. | last2 = Hooton | first2 = TM. | last3 = Naber|first3 = KG. | last4 = Wullt | first4 = B. | last5 = Colgan | first5 = R. | last6 = Miller | first6 = LG. | last7 = Moran | first7 = GJ. | last8 = Nicolle | first8 = LE. | last9 = Raz | first9 = R. | title = International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. | journal = Clin Infect Dis | volume = 52 | issue = 5 | pages = e103-20 | month = Mar | year = 2011 | doi = 10.1093/cid/ciq257|PMID = 21292654 }}</ref>
* Before initiating antimicrobial treatment for suspected pyelonephritis, a urine culture and susceptibility test should always be performed to help tailor empiric therapy.
* Optimal management depends on the severity of illness at presentation, regional resistance data, and host factors.
 
*When local resistance patterns are unknown, an initial intravenous (IV) dose of a long-acting, broad-spectrum antimicrobial agent may be considered.
* Optimal management depends on severity of illness at presentation, local resistance data, and host factors; when local resistance patterns are unknown, an initial intravenous dose of a long-acting, broad-spectrum antimicrobial agent may be considered.
* Oral [[beta-lactam]]s are less effective than either [[TMP/SMX|trimethoprim-sulfamethoxazole]], [[fluoroquinolone]]s, or [[aminoglycosides]] in eradicating uropathogens.
 
* Uncomplicated pyelonephritis due to [[MRSA]] is uncommon, and there is insufficient evidence to support empiric use of an [[MRSA]]-active agent.
* Oral [[beta-lactam]]s are less effective than [[TMP/SMZ|trimethoprim-sulfamethoxazole]], [[fluoroquinolone]]s, or [[aminoglycosides]] in eradicating uropathogens.
 
* Uncomplicated pyelonephritis due to [[MRSA]] is uncommon and there is insufficient evidence to support empiric use of an [[MRSA]]-active agent.
 
* [[Ampicillin]] should be limited to treating suspected ''[[Enterococcus]]'' infection and co-administered with an [[aminoglycoside]].
 
* [[Fluoroquinolone]]s and [[aminoglycoside]]s should be avoided in pregnant patients.
 
* Pregnant women, patients who failed to respond to oral therapy, and patients with [[nausea]], [[vomiting]], high [[fever]], marked [[leukocytosis]], or [[dehydration]] should be hospitalized and managed with parenteral antibiotics.<ref name="Warren-1999">{{Cite journal  | last1 = Warren | first1 = JW. | last2 = Abrutyn | first2 = E. | last3 = Hebel | first3 = JR. | last4 = Johnson |first4 = JR. | last5 = Schaeffer | first5 = AJ. | last6 = Stamm | first6 = WE. | title = Guidelines for antimicrobial treatment of uncomplicated acute bacterial cystitis and acute pyelonephritis in women. Infectious Diseases Society of America (IDSA). | journal = Clin Infect Dis | volume = 29 | issue = 4 | pages = 745-58 | month = Oct | year = 1999 | doi = 10.1086/520427 | PMID = 10589881 }}</ref>
* Pregnant women, patients who failed to respond to oral therapy, and patients with [[nausea]], [[vomiting]], high [[fever]], marked [[leukocytosis]], or [[dehydration]] should be hospitalized and managed with parenteral antibiotics.<ref name="Warren-1999">{{Cite journal  | last1 = Warren | first1 = JW. | last2 = Abrutyn | first2 = E. | last3 = Hebel | first3 = JR. | last4 = Johnson |first4 = JR. | last5 = Schaeffer | first5 = AJ. | last6 = Stamm | first6 = WE. | title = Guidelines for antimicrobial treatment of uncomplicated acute bacterial cystitis and acute pyelonephritis in women. Infectious Diseases Society of America (IDSA). | journal = Clin Infect Dis | volume = 29 | issue = 4 | pages = 745-58 | month = Oct | year = 1999 | doi = 10.1086/520427 | PMID = 10589881 }}</ref>


==Empiric Therapy for Acute Pyelonephritis (Outpatient & Inpatient) <SMALL><SMALL><SMALL><SMALL><SMALL>Adapted from ''Clin Infect Dis. 2011;52(5):e103-20.''<ref name="Gupta-2011"<ref>{{Cite journal | last1 = Gupta | first1 = K. | last2 = Hooton | first2 = TM. | last3 = Naber | first3 = KG. | last4 = Wullt | first4 = B. | last5 = Colgan | first5 = R. | last6 = Miller | first6 = LG. | last7 = Moran | first7 = GJ. | last8 = Nicolle | first8 = LE. | last9 = Raz | first9 = R. | title = International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. | journal = Clin Infect Dis | volume = 52 | issue = 5 | pages = e103-20 | month = Mar | year = 2011 | doi = 10.1093/cid/ciq257 | PMID = 21292654 }}</ref></SMALL></SMALL></SMALL></SMALL></SMALL>==
===Antimicrobial Therapy===
 
*'''Pyelonephritis empiric therapy'''
{|
:*'''Outpatient treatment'''
| valign=top |
::*Preferred regimen, regional fluoroquinolone resistance < 10%: [[Ciprofloxacin]] 500 mg PO q12h x 7 days '''±''' 400 mg IV in a single dose {{or}} [[Ciprofloxacin]] XR 1000 mg PO q24h for 7 days {{or}} [[Levofloxacin]] 750 mg PO q24h for 5 days
{| style="background: #FFFFFF;"
::*Preferred regimen, regional fluoroquinolone resistance > 10%: ([[Ciprofloxacin]] 500 mg PO q12h x 7 days '''±''' 400 mg IV in a single dose {{or}} [[Ciprofloxacin]] XR 1000 mg PO q24h for 7 days {{or}} [[Levofloxacin]] 750 mg PO q24h for 5 days) {{and}} ([[Ceftriaxone]] 1 g IV x 1 dose {{or}} [[Gentamicin]] 7 mg/kg IV x 1 dose {{or}} [[Tobramycin]] 7 mg/kg IV x 1 dose {{or}} [[Amikacin]] 20 mg/kg IV x 1 dose)
| valign=top |
::*Alternative regimen (1), regional fluoroquinolone resistance < 10%: [[TMP-SMX]] 160/800 mg PO q12h x 14 days
{| style="float: left; cellpadding=0; cellspacing= 0; width: 400px;"
::Alternative regimen (2), regional fluoroquinolone resistance > 10%: [[TMP-SMX]] 160/800 mg PO q12h x 14 days {{and}} ([[Ceftriaxone]] 1 g IV x 1 dose {{or}} [[Gentamicin]] 7 mg/kg IV x 1 dose {{or}} [[Tobramycin]] 7 mg/kg IV x 1 {{or}} [[Amikacin]] 20 mg/kg IV x 1 dose
! style="height: 30px; line-height: 30px; background: #4479BA; border: 0px; font-size: 100%; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5);" align=center | {{fontcolor|#FFF|Acute Pyelonephritis, Outpatient}}
::*Alternative regimen (3): ([[Amoxicillin-clavulanate potassium|Amoxicillin–Clavulanate]] 500/125 mg PO q12h x 14 days {{or}} [[Amoxicillin-clavulanate potassium|Amoxicillin–Clavulanate]] 250/125 mg PO q8h x 5–7 days {{or} [[Cefaclor]] 500 mg PO q8h x 7 days) {{and}} ([[Ceftriaxone]] 1 g IV in a single dose {{or}} [[Gentamicin]] 7 mg/kg IV in a single dose {{or}} [[Tobramycin]] 7 mg/kg IV in a single dose {{or}} [[Amikacin]] 20 mg/kg IV in a single dose )
|-
:*'''Inpatient treatment'''<ref name="pmid21292654">{{cite journal| author=Gupta K, Hooton TM, Naber KG, Wullt B, Colgan R, Miller LG et al.| title=International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 5 | pages= e103-20 | pmid=21292654 | doi=10.1093/cid/ciq257 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21292654  }} </ref>::*Preferred regimen: [[Ciprofloxacin]] 400 mg IV q12h for 10-14 days {{or}} [[Levofloxacin]] 750 mg IV q24h for 10-14 days
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Preferred Regimen
::*Alternative regimen (1): [[Gentamicin]] 7 mg/kg IV q24h for 10-14 days '''±''' [[Ampicillin]] 500 mg IV q6h for 10-14 days
|-
::*Alternative regimen (2): [[Tobramycin]] 7 mg/kg IV q24h for 10-14 days '''±''' [[Ampicillin]] 500 mg IV q6h for 10-14 days
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ciprofloxacin]] 500 mg PO q12h x 7 days''''' ± '''''400 mg IV x 1 dose''''' <BR> OR <BR> ▸ '''''[[Ciprofloxacin]] XR 1000 mg PO q24h for 7 days'''''<BR> OR <BR> ▸ '''''[[Levofloxacin]] 750 mg PO q24h for 5 days'''''
::*Alternative regimen (3): [[Amikacin]] 20 mg/kg IV q24h for 10-14 days '''±''' [[Ampicillin]] 500 mg IV q6h for 10-14 days
|-
::*Alternative regimen (4): [[Cefotaxime]] 1-2 g IV q8h for 10-14 days '''±''' ([[Gentamicin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Tobramycin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Amikacin]] 20 mg/kg IV q24h for 10-14 days)
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | PLUS <SMALL> '''''(if fluoroquinolone resistance >10%)''''' </SMALL>
::*Alternative regimen (5): [[Ceftriaxone]] 1 g IV q24h '''±''' ([[Gentamicin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Tobramycin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Amikacin]] 20 mg/kg IV q24h for 10-14 days)
|-
::*Alternative regimen (6): [[Ceftazidime]] 12 g IV q8h '''±''' ([[Gentamicin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Tobramycin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Amikacin]] 20 mg/kg IV q24h for 10-14 days)
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ceftriaxone]] 1 g IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Gentamicin]] 7 mg/kg IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Tobramycin]] 7 mg/kg IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Amikacin]] 20 mg/kg IV x 1 dose'''''
::*Alternative regimen (7): [[Ampicillin-Sulbactam]] 1.5 g IV q6h '''±''' ([[Gentamicin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Tobramycin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Amikacin]] 20 mg/kg IV q24h for 10-14 days)
|-
::*Alternative regimen (8): [[Piperacillin-Tazobactam]] 3.375 g IV q4-6h '''±''' ([[Gentamicin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Tobramycin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Amikacin]] 20 mg/kg IV q24h for 10-14 days)
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Alternative Regimen 1
::*Alternative regimen (9): [[Ticarcillin-Clavulanate]] 3.1 g IV q4-6h '''±''' ([[Gentamicin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Tobramycin]] 7 mg/kg IV q24h for 10-14 days {{or}} [[Amikacin]] 20 mg/kg IV q24h for 10-14 days)
|-
::*Alternative regimen (10): [[Meropenem]] 500 mg IV q8h for 10-14 days
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[TMP/SMZ]] 160/800 mg PO q12h x 14 days'''''
::*Alternative regimen (11): [[Ertapenem]] 1 g IV q24h for 10-14 days
|-
::*Alternative regimen (12): [[Doripenem]] 500 mg IV q8h for 10-14 days
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | PLUS <SMALL> '''''(if TMP/SMZ resistance unknown)'''''</SMALL>
::*Alternative regimen (13): [[Aztreonam]] 1 g IV q8-12h for 10-14 days
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ceftriaxone]] 1 g IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Gentamicin]] 7 mg/kg IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Tobramycin]] 7 mg/kg IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Amikacin]] 20 mg/kg IV x 1 dose'''''
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Alternative Regimen 2
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Amoxicillin-clavulanate potassium|Amoxicillin–Clavulanate]] 500/125 mg PO q12h x 14 days'''''<BR> OR <BR> ▸ '''''[[Amoxicillin-clavulanate potassium|Amoxicillin–Clavulanate]] 250/125 mg PO q8h x 5–7 days'''''<BR> OR <BR> ▸ '''''[[Cefaclor]] 500 mg PO q8h x 7 days'''''
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | PLUS
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ceftriaxone]] 1 g IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Gentamicin]] 7 mg/kg IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Tobramycin]] 7 mg/kg IV x 1 dose'''''<BR> OR <BR> ▸ '''''[[Amikacin]] 20 mg/kg IV x 1 dose'''''
|-
|}
|}
|}
*'''Pathogen-directed therapy'''<ref name="pmid21292654">{{cite journal| author=Gupta K, Hooton TM, Naber KG, Wullt B, Colgan R, Miller LG et al.| title=International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 5 | pages= e103-20 | pmid=21292654 | doi=10.1093/cid/ciq257 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21292654 }} </ref>
| valign=top |
:*'''''Enterococcus spp.'''''<ref name="pmid21292654">{{cite journal| author=Gupta K, Hooton TM, Naber KG, Wullt B, Colgan R, Miller LG et al.| title=International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 5 | pages= e103-20 | pmid=21292654 | doi=10.1093/cid/ciq257 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21292654  }} </ref>::*Preferred regimen: [[Ampicillin]] 2 g IV q6h for 10-14 days {{and}} [[Gentamicin]] 3-5 mg/kg/day IV q8h for 10-14 days
{| style="background: #FFFFFF;"
*'''Specific considerations'''
| valign=top |
:*'''Pregnancy'''<ref>{{Cite web  | last =  | first =  | title = http://www.uroweb.org/gls/pdf/18_Urological%20infections_LR.pdf | url =http://www.uroweb.org/gls/pdf/18_Urological%20infections_LR.pdf | publisher =  | date =  | accessdate = }}</ref>
{| style="float: left; cellpadding=0; cellspacing= 0; width: 450px;"
::*'''Pyelonephritis empiric therapy'''
! style="height: 30px; line-height: 30px; background: #4479BA; border: 0px; font-size: 100%; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5);" align=center | {{fontcolor|#FFF|Acute Pyelonephritis, Inpatient}}
:::*Preferred regimen (1): [[Ceftriaxone]] 1-2 g IV/IM q24h for 10-14 days
|-
:::*Preferred regimen (2): [[Aztreonam]] 1 g IV q8-12h for 10-14 days
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Preferred Regimen
:::*Preferred regimen (3): [[Piperacillin-Tazobactam]] 3.375-4.5 g IV q6h for 10-14 days
|-
:::*Preferred regimen (4): [[Imipenem-Cilastatin]] 500 mg IV q6h for 10-14 days
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ciprofloxacin]] 400 mg IV q12h'''''<BR> OR <BR> ▸ '''''[[Levofloxacin]] 750 mg IV q24h'''''
:::*Note: Fluoroquinolones and aminoglycosides should be avoided in pregnant patients
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Alternative Regimen 1
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Gentamicin]] 7 mg/kg IV q24h''''' ± '''''[[Ampicillin]] 500 mg IV q6h'''''<BR> OR <BR> ▸ '''''[[Tobramycin]] 7 mg/kg IV q24h''''' ± '''''[[Ampicillin]] 500 mg IV q6h'''''<BR> OR <BR> ▸ '''''[[Amikacin]] 20 mg/kg IV q24h''''' ± '''''[[Ampicillin]] 500 mg IV q6h'''''
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Alternative Regimen 2
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Cefotaxime]] 1–2 gm IV q8h'''''<BR> OR <BR> ▸ '''''[[Ceftriaxone]] 1 gm IV q24h'''''<BR> OR <BR> ▸ '''''[[Ceftazidime]] 2 gm IV q8h'''''<BR> OR <BR> ▸ '''''[[Ampicillin sulbactam|Ampicillin–Sulbactam]] 1.5 g IV q6h'''''<BR> OR <BR> ▸ '''''[[Piperacillin-Tazobactam|Piperacillin–Tazobactam]] 3.375 gm IV q4–6h'''''<BR> OR <BR> ▸ '''''[[Ticarcillin clavulanate|Ticarcillin–Clavulanate]] 3.1 gm IV q4–6h'''''
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | WITH OR WITHOUT
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Gentamicin]] 7 mg/kg IV q24h'''''<BR> OR <BR> ▸ '''''[[Tobramycin]] 7 mg/kg IV q24h'''''<BR> OR <BR> ▸ '''''[[Amikacin]] 20 mg/kg IV q24h'''''
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5;" align=center | '''''Alternative Regimen 3'''''
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Meropenem]] 500 mg IV q8h'''''<BR> OR <BR> ▸ '''''[[Ertapenem]] 1 g IV q24h'''''<BR> OR <BR> ▸ '''''[[Doripenem]] 500 mg IV q8h'''''<BR> OR <BR> ▸ '''''[[Aztreonam]] 1 g IV q8–12h'''''
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5;" align=left | <SMALL> '''Antibiotics should be administered for ≥10–14 days based on local resistance patterns.''' <BR> '''De-escalation to oral antibiotics may be considered 24–48 hours after defervescence.''' </SMALL>
|-
|}
|}
|}
 
==Empiric Therapy for Acute Pyelonephritis (Pregnancy) <SMALL><SMALL><SMALL><SMALL><SMALL>Adapted from ''European Association of Urology's Guidelines on Urological Infections.''<ref>{{Cite web  | last =  | first =  | title = http://www.uroweb.org/gls/pdf/18_Urological%20infections_LR.pdf | url =http://www.uroweb.org/gls/pdf/18_Urological%20infections_LR.pdf | publisher = | date | accessdate = }}</ref></SMALL></SMALL></SMALL></SMALL></SMALL>==
 
{| style="background: #FFFFFF;"
| valign=top |
{| style="float: left; cellpadding=0; cellspacing= 0; width: 400px;"
! style="height: 30px; line-height: 30px; background: #4479BA; border: 0px; font-size: 100%; text-shadow: 0 -1px 0 rgba(0, 0, 0, 0.5);" align=center |{{fontcolor|#FFF|Pyelonephritis, Pregnancy}}
|-
| style="padding: 0 5px; font-size: 90%; background: #F5F5F5; font-weight: bold; font-style: italic;" align=center | Preferred Regimen
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ceftriaxone]] 1–2 g IV/IM q24h'''''<BR> OR <BR> ▸ '''''[[Aztreonam]] 1 g IV q8–12h'''''<BR> OR <BR> ▸ '''''[[Piperacillin-Tazobactam|Piperacillin–Tazobactam]] 3.375–4.5 g IV q6h'''''<BR> OR <BR> ▸ '''''[[Cefepime]] 1 g IV q12h'''''<BR> OR <BR> ▸ '''''[[Imipenem-Cilastatin|Imipenem–Cilastatin]] 500 mg IV q6h'''''
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | OR
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Ampicillin]] 2 g IV q6h'''''
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | PLUS
|-
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC" align=left | ▸ '''''[[Gentamicin]] 3–5 mg/kg/day IV q8h'''''
|}
|}
 
==Antimicrobial regimen==
'''Pyelonephritis'''<ref name="pmid21292654">{{cite journal| author=Gupta K, Hooton TM, Naber KG, Wullt B, Colgan R, Miller LG et al.| title=International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 5 | pages= e103-20 | pmid=21292654 | doi=10.1093/cid/ciq257 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21292654  }} </ref>
:*  '''Condition 1: patients not requiring hospitalization where the prevalence of resistance of community uropathogens to fluoroquinolones is not known to exceed 10%'''
::* Preferred regimen: [[Ciprofloxacin]] PO 500 mg bid for 7 days {{withorwithout}} an initial [[Ciprofloxacin]] 400mg IV single dose
:::* Note (1): If an initial one-time intravenous agent is used, a long-acting antimicrobial, such as 1 g of [[Ceftriaxone]] or a consolidated 24-h dose of an [[Aminoglycoside]], could be used in lieu of an intravenous fluoroquinolone
:::* Note (2): If the prevalence of fluoroquinolone resistance is thought to exceed 10%, an initial one-time intravenous dose of a long-acting parenteral antimicrobial, such as 1 g of ceftriaxone or a consolidated 24-h dose of an aminoglycoside, is recommended.
::* Alternative regimen: A once-daily oral fluoroquinolone, [[Ciprofloxacin]] 1000 mg extended release PO qd for 7 days {{or}} [[Levofloxacin]] 750 mg PO qd for 5 days.
:::* Note: If the prevalence of fluoroquinolone resistance is thought to exceed 10%, an initial intravenous dose of a long-acting parenteral antimicrobial, such as [[Ceftriaxone]] 1 g IM/IV or a consolidated 24-h dose of an [[Aminoglycoside]], is recommended.
:*  '''Condition 2: When the uropathogen is known to be susceptible'''
::* Preferred regimen: [[Trimethoprim-sulfamethoxazole]] 160/800 mg (1 double-strength tablet) bid PO for 14 days.
:::* Note: If [[trimethoprim-sulfamethoxazole]] is used when the susceptibility is not known, an initial intravenous dose of a long-acting parenteral antimicrobial, such as 1 g of ceftriaxone {{or}} a consolidated 24-h dose of an aminoglycoside, is recommended.
:::* Note: Oral [[β-lactam]] agents are less effective than other available agents for treatment of pyelonephritis. If an oral β-lactam agent is used, an initial intravenous dose of a long-acting parenteral antimicrobial, such as 1 g of ceftriaxone {{or}} a consolidated 24-h dose of an aminoglycoside, is recommended.
:*  '''Condition 3: Patients require hospitalization (high fever, high white blood cell count, vomiting, dehydration, or evidence of sepsis)'''
::* Preferred regimen: intravenous antimicrobial regimen, such as a [[Fluoroquinolone]]; an [[Aminoglycoside]] {{withorwithout}} [[Ampicillin]]; an extended-spectrum [[Cephalosporin]] or extended-spectrum [[Penicillin]] {{withorwithout}} an [[Aminoglycoside]]; [[Carbapenem]]
:::* Note: The choice between these agents should be based on local resistance data, and the regimen should be tailored on the basis of susceptibility results.


==References==
==References==

Revision as of 14:31, 6 October 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

All patients with pyelonephritis should be treated empirically with antimicrobial therapy. Mild pyelonephritis may be managed with oral antimicrobial therapy, and an initial intravenous dose may be administered depending on local resistance patterns. Patients with dehydration, nausea, vomiting, or signs of sepsis should be admitted and should receive parenteral therapy. Medical therapies for pyelonephritis include fluoroquinolones, TMP-SMX, β-lactams, and aminoglycosides.

Medical Therapy

  • All patients with pyelonephritis should be treated empirically with antimicrobial therapy.
  • Before initiating antimicrobial treatment for suspected pyelonephritis, a urine culture and susceptibility test should always be performed.
  • Mild pyelonephritis may be managed with oral antimicrobial therapy, and an initial intravenous dose may be administered depending on local resistance patterns. Patients with dehydration, nausea, vomiting, or signs of sepsis should be admitted and should receive parenteral therapy.[1]
  • Optimal management depends on the severity of illness at presentation, regional resistance data, and host factors.
  • When local resistance patterns are unknown, an initial intravenous (IV) dose of a long-acting, broad-spectrum antimicrobial agent may be considered.
  • Oral beta-lactams are less effective than either trimethoprim-sulfamethoxazole, fluoroquinolones, or aminoglycosides in eradicating uropathogens.
  • Uncomplicated pyelonephritis due to MRSA is uncommon, and there is insufficient evidence to support empiric use of an MRSA-active agent.
  • Pregnant women, patients who failed to respond to oral therapy, and patients with nausea, vomiting, high fever, marked leukocytosis, or dehydration should be hospitalized and managed with parenteral antibiotics.[2]

Antimicrobial Therapy

  • Pyelonephritis empiric therapy
  • Outpatient treatment
  • Preferred regimen, regional fluoroquinolone resistance < 10%: Ciprofloxacin 500 mg PO q12h x 7 days ± 400 mg IV in a single dose OR Ciprofloxacin XR 1000 mg PO q24h for 7 days OR Levofloxacin 750 mg PO q24h for 5 days
  • Preferred regimen, regional fluoroquinolone resistance > 10%: (Ciprofloxacin 500 mg PO q12h x 7 days ± 400 mg IV in a single dose OR Ciprofloxacin XR 1000 mg PO q24h for 7 days OR Levofloxacin 750 mg PO q24h for 5 days) AND (Ceftriaxone 1 g IV x 1 dose OR Gentamicin 7 mg/kg IV x 1 dose OR Tobramycin 7 mg/kg IV x 1 dose OR Amikacin 20 mg/kg IV x 1 dose)
  • Alternative regimen (1), regional fluoroquinolone resistance < 10%: TMP-SMX 160/800 mg PO q12h x 14 days
Alternative regimen (2), regional fluoroquinolone resistance > 10%: TMP-SMX 160/800 mg PO q12h x 14 days AND (Ceftriaxone 1 g IV x 1 dose OR Gentamicin 7 mg/kg IV x 1 dose OR Tobramycin 7 mg/kg IV x 1 OR Amikacin 20 mg/kg IV x 1 dose
  • Alternative regimen (1): Gentamicin 7 mg/kg IV q24h for 10-14 days ± Ampicillin 500 mg IV q6h for 10-14 days
  • Alternative regimen (2): Tobramycin 7 mg/kg IV q24h for 10-14 days ± Ampicillin 500 mg IV q6h for 10-14 days
  • Alternative regimen (3): Amikacin 20 mg/kg IV q24h for 10-14 days ± Ampicillin 500 mg IV q6h for 10-14 days
::*Alternative regimen (4): Cefotaxime 1-2 g IV q8h for 10-14 days ± (Gentamicin 7 mg/kg IV q24h for 10-14 days OR Tobramycin 7 mg/kg IV q24h for 10-14 days OR Amikacin 20 mg/kg IV q24h for 10-14 days)

|}

  • Pathogen-directed therapy[3]
  • Enterococcus spp.[3]::*Preferred regimen: Ampicillin 2 g IV q6h for 10-14 days AND Gentamicin 3-5 mg/kg/day IV q8h for 10-14 days
  • Specific considerations
  • Pyelonephritis empiric therapy
  • Preferred regimen (1): Ceftriaxone 1-2 g IV/IM q24h for 10-14 days
  • Preferred regimen (2): Aztreonam 1 g IV q8-12h for 10-14 days
  • Preferred regimen (3): Piperacillin-Tazobactam 3.375-4.5 g IV q6h for 10-14 days
  • Preferred regimen (4): Imipenem-Cilastatin 500 mg IV q6h for 10-14 days
  • Note: Fluoroquinolones and aminoglycosides should be avoided in pregnant patients

References

  1. Gupta, K.; Hooton, TM.; Naber, KG.; Wullt, B.; Colgan, R.; Miller, LG.; Moran, GJ.; Nicolle, LE.; Raz, R. (2011). "International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases". Clin Infect Dis. 52 (5): e103–20. doi:10.1093/cid/ciq257. PMID 21292654. Unknown parameter |month= ignored (help)
  2. Warren, JW.; Abrutyn, E.; Hebel, JR.; Johnson, JR.; Schaeffer, AJ.; Stamm, WE. (1999). "Guidelines for antimicrobial treatment of uncomplicated acute bacterial cystitis and acute pyelonephritis in women. Infectious Diseases Society of America (IDSA)". Clin Infect Dis. 29 (4): 745–58. doi:10.1086/520427. PMID 10589881. Unknown parameter |month= ignored (help)
  3. 3.0 3.1 3.2 Gupta K, Hooton TM, Naber KG, Wullt B, Colgan R, Miller LG; et al. (2011). "International clinical practice guidelines for the treatment of acute uncomplicated cystitis and pyelonephritis in women: A 2010 update by the Infectious Diseases Society of America and the European Society for Microbiology and Infectious Diseases". Clin Infect Dis. 52 (5): e103–20. doi:10.1093/cid/ciq257. PMID 21292654.
  4. "http://www.uroweb.org/gls/pdf/18_Urological%20infections_LR.pdf" (PDF). External link in |title= (help)