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Interstitial Cystitis (IC)
chronic inflammation of urinary bladder of unknown causes
aka painful bladder syndrome
F>M, 20-30 y/o
possibly autoimmune bc it is sometimes seen with systemic lupus erythematosus
Pathophysiology of interstitial cystitis
chronic inflammation → damaged bladder tissue → fibrosis
mast cell overactivity → increase histamine → bladder wall edema → obstruction / decrease volume
signs and symptoms of interstitial cystitis
urgency, frequency, small urine output
irritation of bladder wall → bleeding (hematuria) and pain (dysuria) during urination
chronic inflammation can cause:
fibrosis
hemorrhagic ulcers - Hunner’s ulcers
urinary frequency (up to 60x day/night)
testing for interstitial cystitis
frequency, urgency, dysuria without infection
UA: WNL + APF (anti-proliferative factor)
treatment for interstitial cystitis
no cure
current pharmacologic treatments are not very effective
elmiron, botulinum toxin (BTX-A), possible cystectomy
Urinary Tract Infection (UTI)
urethritis, cystitis ± pyelonephritis
MC nosocomial infection
common cause of confusion in elderly
causes of UTI
E.coli
many other bactera
increased risk of UTI
females, DM, urinary catheters
poor hygiene
dehydration
compromised immune system
signs and symptoms of urethritis and cystitis
dysuria, frequency, urgency
fever, n/v, hematuria
testing for UTI
urine analysis (UA)- best intital test
bacteria
nitrites
leukocyte
esterase
WBCs
urine culture and sensitivity
Xray, CT scan
leukocytes
costovertebral tenderness (murphy’s punch)
treatment for UTI
oral antibiotics if only urethritis and cystitis
IV antibiotics with fever and pyelonephritis
stress incontinence
MC in women < 60
incontinence with laughing, coughing, sneezing, lifting
decreased pelvic floor muscle strength
urge incontinence
MC in “older adults”
detrusor hyperreflexia (aka reflex bladder)
involuntary loss of urine
constant dripping, nocturia
neurological disorders → parkinson’s disease, MS, CNS, or peripheral nerve damage
overflow incontinence
blockage of the bladder outlet (BPH, prostate cancer, urethra narrowing)
bladder is always full, frequently leaks urine, urgency
signs and symptoms of urinary incontinence
urgency
frequency
dysuria
suprapubic pain
testing for urinary incontinence
clinical
pelvic U/S
R/O UTI
Nephrolithiasis
aka kidney stones or renal calculi
M 10% > F 7%
causes of nephrolithiasis
diet, dehydration, sedentary lifestyle, medication side effects
types of nephrolithiasis
calcium stones → MCC
struvite stones → kidney infections
uric acid stones → gouty arthritis
Calcium Stones (70-80%)
MC: calcium oxalate (80%)
calcium phosphate (15%)
risk factors: hypercalciuria, hyperoxaluria, alkaline urine
uric acid stones (7%)
gouty arthritis (Gout)
acidic urine
struvite stones (15%)
magnesium - ammonium - phosphate
f >M
staghorn caliculi (large)
risk factors
alkaline urine
infection with urease producing bacteria
proteus, klebsiella, pseudomonas
Where are Staghorn Calculi located and the size
large
fill the minor and major calyces
Where are Non-Staghorn Calculi located and the size
located in calyces, renal pelvis or in the ureter
If stone is <5mm
50% chance of spontaneous passgae
If stone >1cm
0% chance of spontaneous passage
Nephrolithiasis signs and symptoms
moderate to severe pain
renal colic
flank pain radiating to the groin
signs of renal pelvis obstruction or upper ureter obstruction
n/v, dysuria, hematuria
testing for nephrolithiasis
UA
CT
renal function tests
calcium, pth
Ureterscope
surgical treatment that is required for nephrolithiasis if it is in the ureter
Nephroscope
surgical treatment that is required for nephrolithiasis if it is in the kidney
shock wave lithotripsy
surgical treatment that is required for nephrolithiasis using sound waves to pulverize stones
Kidney Blood tests
BUN - Blood urea nitrogen
CR - Creatinine
GFR - glomerular filtration rate
sodium and potassium levels
vit D / Ca 2+
albumin/protein
RBCs
Kidney Urine Tests
urine output
albumin/protein
casts
Urine Casts
tubular casts
tubule shaped particles
Glomerulonephritis
group of conditions that injure the glomeruli (filtration) in the nephron
may be acute or chronic
causes of glomerulonephritis
berger’s disease, PIGN
SLE, AI, bacterial endocarditis, HTN, DM
signs and symptoms of glomerulonephritis
proteinuria, oliguria
hematuria
HTN, edema
testing for glomeruloephritis
BUN, creatinine, CT, biopsy
Azotemia
high BUN and/or Cr
Uremia
high BUN with symptoms
Oliguria
Urine Output <500ml/day
Anuria
no urine output
Acute Renal Failure (ARF) aka Acute Kidney Injury (AKI)
Acute renal insufficiency
Chronic Renal Failure (CRF)
Chronic Kidney Disease (CKD)
Glomerulonephritis
Anigen-Ab complex → Inflammation → decrease GFR
Post infectious Glomerulonephritis (PIGN)
immune complex deposition → inflammation and glomerular injury
age 5-15years
will present 1-2 weeks after a sore throat OR up to 6 weeks after impetigo
signs and symptoms of PIGN
fever + periorbital edema + flank pain
diagnosis of PIGN
anti-streptolysin O antibodies (ASO)
hematuria, proteinuria, RBC casts in urine, cola colored urine
azotemia (decreased GFR, increased BUN, increase Cr)
Periorbital edema (around the eyes)
IgA Nephropathy aka Berger’s Disease
IgA deposition in glomeruli
MCC of glomerulonephritis worldwide
M > F
20-30 yo
causes of Berger’s Disease
usually starts within a day or two after a non-specific respiratory tract infection or GI infection
signs and symptoms of Berger’s Disease
dark brown/bloody/rust color urine
25% of cases progress to CKD in 20-30 years
testing for Berger’s Disease
increase BUN, increase Cr, decrease GFR
U/A: proteinuria, hematuria
HTN, Edema, decreased urinary output
MAT: biopsy (IgA deposits)
treatment for Berger’s Disease
no cure but meds can slow progress
20% eventually need dialysis and transplantation (recurrence is possible even after kidney transplant)
Acute Kidney Injury
loss of kidney function (increase BUN and increase Cr, decrease GFR)
may be acute or chronic
causes of Acute Kidney Infection
prerenal azotemia (before the kidney)
intrarenal azotemia (in the kidney)
postrenal azotemia (after the kidney)
Prerenal Azotemia
BUN: Cr> 15:1
decrease blood flow into the kidney
hypotension, dehydration
Intrarenal Azotemia
BUN: Cr < 15:1
acute kidney injury
kidney damage → inflammation
Postrenal azotemia
urine outflow obstruction
BPH, bilateral nephrolithiasis, bladder tumor
BUN: Cr is variable
signs and symptoms of acute kidney injury
decrease urine output → edema
fatigue, confusion, dyspnea
AMS, seizures
testing for acute kidney injury
daily urine output <500mL
BUN and Cr , GFR
electrolytes
KUB ultrasound
abd/pelvic CT scan
Chronic Kidney Disease aka Chronic Renal Failure
decreased GFR
<60mL/min/1.73.m² for 3+ months
acute may become chronic
when a particular amount of nephrons are affected/destroyed, the remaining nephrons begin a process of irreversible sclerosis that leads to a progressive decline in the GFR
signs and symptoms of chronic kidney disease
headaches
decreased ability to concentrate urine
polyuria → oliguria
increase BUN and serum creatinine
edema
GFR
mild anemia
increase BP weakness and fatigue
tests for chronic kidney disease
increase BUN
increase Cr
decreased GFR
treatment for chronic kidney disease
dialysis or kidney transplant
Stages 1-3b of CKD
asymptomatic
Stages 4-5 of CKD
symptomatic
anemia
hyperkalemia
HTN, edema
decreased albumin
dyslipidemia
Stage 5 CKD
end stage renal disease
requires dialysis or kidney transplant