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:::*Preferred regimen (3): [[Piperacillin-Tazobactam]] 3.375-4.5 g IV q6h 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
:::*Preferred regimen (4): [[Imipenem-Cilastatin]] 500 mg IV q6h for 10-14 days
:::*Note: Fluoroquinolones and aminoglycosides should be avoided in pregnant patients
:::*Note: [[Fluoroquinolones]] and [[aminoglycosides]] should be avoided in pregnant patients


==References==
==References==

Revision as of 16:57, 31 January 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Usama Talib, BSc, MD [2]

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. [1]

Medical Therapy

The medical therapy for pyelonephritis has a few important aspects to be kept in mind:[1]

  • 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.[2]
  • 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.[3]

Antimicrobial Therapy

As a broader rule, antibiotics are started only after the sample has been drawn for culture. Uncomplicated pyelonephritis is treated with specific and short duration (5 to 14 days) of antibiotics while complicated pyelonephritis is treated with broad spectrum and longer duration (at least 14-21 days) of antibiotics.[4]

  • Pyelonephritis empiric therapy
  • Outpatient treatment
  • Inpatient treatment[5]
  • Pathogen-directed therapy[5]
  • Enterococcus spp.[5]
  • 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
  • Pregnancy

In event of a pregnancy the treatment of pyelonephritis ha stop be done in an in patient setting due to higher and severe complications risks. Intravenous antibiotics should be given for the initial 1-2 days at least until the patient is not febrile and then continued on oral therapy.[6]

  • Pyelonephritis empiric therapy

References

  1. 1.0 1.1 Ramakrishnan K, Scheid DC (2005). "Diagnosis and management of acute pyelonephritis in adults". Am Fam Physician. 71 (5): 933–42. PMID 15768623.
  2. 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 up date 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); line feed character in |title= at position 132 (help)
  3. 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)
  4. Hooton TM (2012). "Clinical practice. Uncomplicated urinary tract infection". N Engl J Med. 366 (11): 1028–37. doi:10.1056/NEJMcp1104429. PMID 22417256.
  5. 5.0 5.1 5.2 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.
  6. "http://www.uroweb.org/gls/pdf/18_Urological%20infections_LR.pdf" (PDF). External link in |title= (help)