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Pyelonephritis
By :Khashayar Cyrus
 Definition
 Epidemiology and Risk Fctors
 Etiology
 Pathogenesis
 Clinical feature
 Lab diagnosis
 Treatment
Definition:
 inflammation of the parenchyma and
lining of renal pelvis of kidney
Epidemiology and Risk Fctors:
 Host factor:
 Female :Shorter urethra
 Male : uncircumcised infant  bacterial colonization
inside prepuce and urethra
 Catherization
◦ DIRECT: Bacteria carried directly into bladder during
insertion
◦ INDIRECT:Facilitation of bacterial access via
 lumen of catheter
 Tracking up between outside catheter and urethral
wall
Host factor:
• Normal urine flow disruption ( obstruction )
Incomplete bladder emptying  > 2-3ml residual
urine infection  ascent of infection  pyelonephritis
 Pregnancy
 Prostatic hypertrophy
 Renal calculi
 Tumor
 Stricture
 Loss of neurological control of bladder and sphincter(
spina bifida , paraplegia, multiple sclerosis)
 Vesicourethral reflux ( urine reflux from bladder to
ureter, renal pelvis and parenchyma)
 Diabetes Mellitus  diabetic neuropathy interfere
with bladder function
 Diabetes Mellitus  Impaired cytokine secretion
Host factor:
 genetic background of the host
 familial disposition to pyelonephritis
 women with recurrent UTI
 Have had their first UTI before the age of 15 years
 persistent vaginal colonization
 Mutations in host response genes(those coding forToll-
like receptors and the interleukin 8 receptor)
Host factor:
 Factors independently associated with pyelonephritis
in young healthy women include:
• Frequent sexual intercourse
 New sexual partner,
 UTI in the previous 1 2 months,
 Maternal history of UTI,
 Diabetes
 Incontinence.
 spermicide use
 And cystoceles ,incontinence and residual urine in
postmenopausal women,
Etiology:
 The uropathogens causing Pyelonephritis vary by clinical
syndrome but are usually enteric gram-negative rods
that have migrated to the urinary tract.The susceptibility
patterns of these organisms vary by clinical syndrome
and by geography.
 Gram negative organism
 E.coli (common)
 Proteus mirabilis, Citrobacter, klebsiella, enterobacter,
proteus pseudomonas aeruginosa
 Gram positive organism
 Staph.saprophyticus, Staph. Epidermidis enterococcus,
Corynebacteria and lactobacilli
Virus Parasite
 Rare
 Virus Human
polymaviruses , JC and
BK
 Cytomegalovirus and
rubella
 Korean hemorrhagic
fever virus
 Mumps and HIV
 Recovered in urine in
absence of UTI
 Fungi : candida spp
and histoplasma
capsulatum
 Protozoa :
trichomonas vaginalis
 Helminth:
schistosoma
haematobium
Pathogenesis:
 The urinary tract can be viewed as an anatomic unit united by a
continuous column of urine extending from the urethra to the
kidneys. Inthe majority of UTIs bacteria establish infection by
ascending from the urethra to the bladder. Continuing ascent up the
ureter to the kidney is the pathway for most renal parenchymal
infections.
Vaginal Ecology:
 Colonization of the vaginal introitus and periurethral
area with organisms from the intestinal flora (usually
E. coli)
 Sexual intercourse is associated with an increased
risk of vaginal colonization with E. coli
 Nonoxynol-9 in spermicide is toxic to the normal
vaginal microflora and thus is likewise associated with
an increased risk of E. coli vaginal colonization and
bacteriuria
AnatomicalAnd FunctionalAbnormalities
 urinary stasis or obstruction
 Foreign bodies:stones or urinary catheters
 vesicoureteral reflux
 ureteral obstruction secondary to prostatic
hypertrophy
 neurogenic bladder
 urinary diversion surgery
Microbial Fators:
 Uropathogenic E. Coli (UPEC)
◦ Pyelonephritis associated pili (PAP) adhesion
to urethral and bladder epithellium in
◦ K antigen that help E coli to be phagocytosis-
resistant
◦ Hemolysin ( membrane damaging toxin)
Clinical Feature
 Mild pyelonephritis:
 low-grade fever
 with or without lower-back or costovertebral-angle pain
 severe pyelonephritis:
 High fever “picket-fence” 72hr
 Nausea
 vomiting
 flank and/or loin pain
 Emphysematous pyelonephritis:
 exclusively in diabetic patients
 production of gas in renal and perinephric tissues
 bilateral papillary necrosis
 rise in the serum creatinine level
 Xanthogranulomatous pyelonephritis
 chronic urinary obstruction (often by staghorn calculi)
 chronic infection
 Suppurative destruction of renal tissue
 Pyelonephritis can also be complicated by
intraparenchymal abscess formation; this situation should
be suspected when a patient has continued fever and/or
bacteremia despite antibacterial therapy.
Laboratory Diagnosis:
 The Urine DipstickTest:
 Rapid diagnostic test
 Appearance ofWBC in urine
 test for nitrite & leukocyte esterase
 ( family Enterobacteriaceae, in detected in urine PMN )
 Negative outcome ,it s not sufficient for pregnancy women
 Urinalysis:
 WBC in Cast shape due to of pyelonephritis
 NoWBC ,No Infection
 Urine Culture:
 Method of Sampling:
 Clean Catch:
 Straight Catheterization:
 foley cathatere:
 Suprapubic Aspiration:
 Urine culture interpretation:
 It is positve with colony count equal or more than 10
power 2 In women with dysuria & pyuria
 It is positve with colony count > 10 power 3 In Men
Treatment:
 Fluoroquinolones the first- line therapy for acute
uncomplicated pyelonephritis
 A randomizedclinical trial demonstrated that a 7-day
course of therapy with oral ciprofloxacin (500 mg twice
daily with or without an initial IV 400-mg dose)Was highly
effective for the initial management of pyelonephritis in
the outpatient setting
 OralTMP-SMX (one double-strength tablet twice daily
for14 days) also is effective for treatment of acute
uncomplicated pyelonephritis if the uropathogen is known
to be susceptible.
 If the pathogen's susceptibility is not known andTMP SMX
 is used an initial IV l -g dose of ceftriaxone is
recommended
 Options for parenteral therapy for uncomplicated
pyelonephritis include fluoroquinolones an extended-
spectrum cephalosporin with or without
anaminoglycoside
 o r acarbapenem. Combinations of a ß-Iactam and a ß-
Iacta mase inhibitor (e.g .ampicillin-sulbactam,
ticarcillinc Lavulanate piperacillin-tazobactam) or
imipenem-cilastatin can be used in patients with more
complicated histories previous episodes of
pyelonephritis or recent urinary tract manipulations
Pyelonephritis
Pyelonephritis

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Pyelonephritis

  • 2.  Definition  Epidemiology and Risk Fctors  Etiology  Pathogenesis  Clinical feature  Lab diagnosis  Treatment
  • 3. Definition:  inflammation of the parenchyma and lining of renal pelvis of kidney
  • 4. Epidemiology and Risk Fctors:  Host factor:  Female :Shorter urethra  Male : uncircumcised infant  bacterial colonization inside prepuce and urethra  Catherization ◦ DIRECT: Bacteria carried directly into bladder during insertion ◦ INDIRECT:Facilitation of bacterial access via  lumen of catheter  Tracking up between outside catheter and urethral wall
  • 5. Host factor: • Normal urine flow disruption ( obstruction ) Incomplete bladder emptying  > 2-3ml residual urine infection  ascent of infection  pyelonephritis  Pregnancy  Prostatic hypertrophy  Renal calculi  Tumor  Stricture  Loss of neurological control of bladder and sphincter( spina bifida , paraplegia, multiple sclerosis)  Vesicourethral reflux ( urine reflux from bladder to ureter, renal pelvis and parenchyma)  Diabetes Mellitus  diabetic neuropathy interfere with bladder function  Diabetes Mellitus  Impaired cytokine secretion
  • 6. Host factor:  genetic background of the host  familial disposition to pyelonephritis  women with recurrent UTI  Have had their first UTI before the age of 15 years  persistent vaginal colonization  Mutations in host response genes(those coding forToll- like receptors and the interleukin 8 receptor)
  • 7. Host factor:  Factors independently associated with pyelonephritis in young healthy women include: • Frequent sexual intercourse  New sexual partner,  UTI in the previous 1 2 months,  Maternal history of UTI,  Diabetes  Incontinence.  spermicide use  And cystoceles ,incontinence and residual urine in postmenopausal women,
  • 8. Etiology:  The uropathogens causing Pyelonephritis vary by clinical syndrome but are usually enteric gram-negative rods that have migrated to the urinary tract.The susceptibility patterns of these organisms vary by clinical syndrome and by geography.  Gram negative organism  E.coli (common)  Proteus mirabilis, Citrobacter, klebsiella, enterobacter, proteus pseudomonas aeruginosa  Gram positive organism  Staph.saprophyticus, Staph. Epidermidis enterococcus, Corynebacteria and lactobacilli
  • 9. Virus Parasite  Rare  Virus Human polymaviruses , JC and BK  Cytomegalovirus and rubella  Korean hemorrhagic fever virus  Mumps and HIV  Recovered in urine in absence of UTI  Fungi : candida spp and histoplasma capsulatum  Protozoa : trichomonas vaginalis  Helminth: schistosoma haematobium
  • 10. Pathogenesis:  The urinary tract can be viewed as an anatomic unit united by a continuous column of urine extending from the urethra to the kidneys. Inthe majority of UTIs bacteria establish infection by ascending from the urethra to the bladder. Continuing ascent up the ureter to the kidney is the pathway for most renal parenchymal infections.
  • 11. Vaginal Ecology:  Colonization of the vaginal introitus and periurethral area with organisms from the intestinal flora (usually E. coli)  Sexual intercourse is associated with an increased risk of vaginal colonization with E. coli  Nonoxynol-9 in spermicide is toxic to the normal vaginal microflora and thus is likewise associated with an increased risk of E. coli vaginal colonization and bacteriuria
  • 12. AnatomicalAnd FunctionalAbnormalities  urinary stasis or obstruction  Foreign bodies:stones or urinary catheters  vesicoureteral reflux  ureteral obstruction secondary to prostatic hypertrophy  neurogenic bladder  urinary diversion surgery
  • 13. Microbial Fators:  Uropathogenic E. Coli (UPEC) ◦ Pyelonephritis associated pili (PAP) adhesion to urethral and bladder epithellium in ◦ K antigen that help E coli to be phagocytosis- resistant ◦ Hemolysin ( membrane damaging toxin)
  • 14. Clinical Feature  Mild pyelonephritis:  low-grade fever  with or without lower-back or costovertebral-angle pain  severe pyelonephritis:  High fever “picket-fence” 72hr  Nausea  vomiting  flank and/or loin pain
  • 15.  Emphysematous pyelonephritis:  exclusively in diabetic patients  production of gas in renal and perinephric tissues  bilateral papillary necrosis  rise in the serum creatinine level  Xanthogranulomatous pyelonephritis  chronic urinary obstruction (often by staghorn calculi)  chronic infection  Suppurative destruction of renal tissue  Pyelonephritis can also be complicated by intraparenchymal abscess formation; this situation should be suspected when a patient has continued fever and/or bacteremia despite antibacterial therapy.
  • 16. Laboratory Diagnosis:  The Urine DipstickTest:  Rapid diagnostic test  Appearance ofWBC in urine  test for nitrite & leukocyte esterase  ( family Enterobacteriaceae, in detected in urine PMN )  Negative outcome ,it s not sufficient for pregnancy women  Urinalysis:  WBC in Cast shape due to of pyelonephritis  NoWBC ,No Infection
  • 17.  Urine Culture:  Method of Sampling:  Clean Catch:  Straight Catheterization:  foley cathatere:  Suprapubic Aspiration:  Urine culture interpretation:  It is positve with colony count equal or more than 10 power 2 In women with dysuria & pyuria  It is positve with colony count > 10 power 3 In Men
  • 18. Treatment:  Fluoroquinolones the first- line therapy for acute uncomplicated pyelonephritis  A randomizedclinical trial demonstrated that a 7-day course of therapy with oral ciprofloxacin (500 mg twice daily with or without an initial IV 400-mg dose)Was highly effective for the initial management of pyelonephritis in the outpatient setting  OralTMP-SMX (one double-strength tablet twice daily for14 days) also is effective for treatment of acute uncomplicated pyelonephritis if the uropathogen is known to be susceptible.  If the pathogen's susceptibility is not known andTMP SMX  is used an initial IV l -g dose of ceftriaxone is recommended
  • 19.  Options for parenteral therapy for uncomplicated pyelonephritis include fluoroquinolones an extended- spectrum cephalosporin with or without anaminoglycoside  o r acarbapenem. Combinations of a ß-Iactam and a ß- Iacta mase inhibitor (e.g .ampicillin-sulbactam, ticarcillinc Lavulanate piperacillin-tazobactam) or imipenem-cilastatin can be used in patients with more complicated histories previous episodes of pyelonephritis or recent urinary tract manipulations