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8/14/2019 Renal_Urinary Tracvcnt Abnormalities.ppt
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Abnormalities of theUrinary Tract
Dr. K A W Karunasekera
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Vesico-Ureteric Reflux
Backflow of urine from bladder to ureters
Reflux - Iry- Most VUR are congenital
- IIry- trauma, neuropathic
bladder
Has a strong familial tendency
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Classification
International classification
I Reflux in to lower ureter
II VR in ureter/s + nodilatation
III With dilatation
IV With gross dilatation
V IRR (urine from renal pelvis
to papillae)
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Effect of VUR on kidney
Direct transmission of organisms
with pressure
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Prognosis
70-80% of all, but severe disappear
Recurrent UTI with VUR causesrenal scarring
Reflux nephropathy
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Management
Medical managementUninterrupted low dose prophylaxis
Regular frequent voidingDouble maturation at bedtime
Liberal fluid intakeRegular bowel habitsFollow up
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Management contd.
Surgical management
Indications:
Recurrent UTI on medicaltherapy
Grade IV & V
Ureteric re-implantation
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Urinary Tract Obstruction
From urethral meatus to calices
Causes:Congenital Trauma
Tumours Stones
Inflammation Post-surgery
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Clinical Presentation
For investigation of UTI and renalimpairment
FTT, diarrhoea, vomiting
Poor stream of urine, incontinence
and dribbling Acute retention
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Common Conditions in
Children
P-U junction obstruction
Posterior urethral valves
Functional obstruction - Neuropathicbladder
Other causes: megaureter,ectopicureter, ureterocele,diverticulum, urethralstricture
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Posterior Urethral Valves
Due to v shaped mucosal folds
in the prostatic urethra in males
Urinary obstruction and dilatation
of the bladder and post.urethra
VUR is associated in 2/3 of cases
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Presentation
Majority present in infancywith UTI, uremia, FTT, poor
stream, dribbling
Incontinence especially daytime
Neonates with palpable bladder
and poor stream Acute retention
Antenatal USS
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Diagnosis & Treatment
MCUG
Surgery- Referral- Iryablation of valves
or
- vesicotomy and latesurgery
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Presentations :
Palpable renal mass
Abdominal / flank or back painHaematuria with minor trauma
UTIRenal failure
Antenatal maternal USS
PUJ Obstruction
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Diagnosis & Treatment
IVU
Surgery
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Other Congenital Abnormalities
of UT Renal agenesis
B/L - incompatible with life
Potter syndrome
Unilateral - compatible with life
Renal dysplasia & hypoplasiaRare, end up in CRF
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Infantile Polycystic Kidney
Autosomal recessive
cysts due to dilated collecting ducts
Majority have liver involvement Presentation : B\L renal lumps
microscopic haematuria
HT& RF Diagnosed by IVU
Treatment: Supportive and renal
transplant
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Adult Polycystic Kidney
A.dominant
Symptoms in 3rd and 4th decades
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Abnormalities contd.
Duplication of renal pelvis & ureter varying degree can occur with or
without other abnormalities
Neuropathic or Neurogenic bladder
due to abnormal or faultyinnervations
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Bladder Neck Obstruction
Causes:
Often congenital
- Spina bifida, cerebral palsy,
sacral agenesis, spinal cord
lesions, sacrococcygeal
tumour
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Neurogenic Bladder
Deterioration of upper urinary tract
Urinary incontinence
Associated VUR present in 50% of
cases
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Types of Neurogenic Bladder
Low pressure bladder:
- Low back pressure
- Bladder is atonic- Sphincters paralyzed
High pressure bladder
- Due to incordination
(sphincter dys-synergia)
- High back pressure +VUR
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Treatment
To decrease back pressure
To decrease infection To achieve continence, if possible
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To reduce back pressure
- Intermittent catheterization
- Increased bladder volume- Sphincterotomy
Infection
- Antibiotic prophylaxis
- Treatment of acute infection
Treatment contd.
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To achieve continence
- repeated catheterization
- urinary diversion- artificial sphincter device
Prognosis :HT & RF are common
Treatment contd.
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Bladder Extrophy
(Ectopia vesicae)
Rare , Bladder protrudes, mucosa is
exposed
Treatment
cover the lesion with a silastic
shield and transfer to the surgical unit