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Approach to Renal Tract Abnormalities
In Neonates
Dr. Tarek Kotb
MBBCH CAIRO UNIVERSITY
MRCPCH UK
NICU –MCH- Buraydah Qassim
ANTENATALLY DIAGNOSED RENAL TRACT
ABNORMALITIES
Urine production is important antenatally for production of
amniotic fluid and the normal development of the urinary
and pulmonary systems.
Abnormalities of the urinary tract are among the most
common detected antenatally and account for a significant
(4%) part of perinatal mortality.
More common in males (60%) than females.
HYDRONEPHROSIS
Antenatal detection of hydronephrosis of
any degree should be investigated
postnatally
Unilateral hydronephrosis
Should be scanned at 1 week, then again at 2-3
months .
Following the first day check the parents should be
given appointments for both of these scans, and a
clinic appointment following the second. They should
be asked to come to SCBU immediately following the
first, for discussion of the result, which the radiologist
will write down and give to them.
Unilateral hydronephrosis
information needed in scan at 1 week
• AP diameter of the renal pelvis
• Presence or absence of dilated calyces
• Length of the kidneys
• Whether dilated ureters are seen
• Bladder wall thickness (if bladder distended)
• Cortical thickness
• Confirmation of the diagnosis
or detection of other structural anomalies.
During follow-up we may classify hydronephrosis
based on 3 criteria
1.The largest AP diameter of the pelvis antenatally or
neonatally.
2. Its function based on MAG3 (done at GOS)
3. The presence or absence of reflux into the renal pelvis
based on MCUG
(1).The largest AP diameter of the pelvis
antenatally or neonatally
ReferMAG 3
At 2 months
TrimethoprimdischargeAP DIAMETER
♣< 10 mm AFTER 2
MONTHS SCAN
♣10-15 mm
Normal calyces
♣♣10-15 mm
Dilated calyces
♣♣15-19 mm
♣♣♣> 20 mm
MCUG should be performed in any case
where:
• There is ureteric dilatation
• The bladder wall is thicker than 5mm
• US suggests renal scarring
• It appears that there may be a ureterocoele
or duplex system
• UTI occurs
• There is bilateral hydronephrosis (both > 15 mm).
If MAG3 or MCUG are not indicated, follow up
should be with USS at 6 months (and at one year,
if required).
Infants may be discharged once the AP diameter
is <10mm.
If follow-up is required beyond one year, this is
best provided by general paediatricians
(2). Its function based on MAG3
Poor function = < 20% )
Moderate = 20-39% ) of total renal
function
Good = >= 40% )
If function is <44%, the baby should be
referred to consultant pediatric surgeon,
otherwise USS should be repeated at six
months and again with repeat Mag3 at 1yr.
(3). The presence or absence of
reflux into the renal pelvis based
on MCUG
If an initial MCUG shows
significant reflux, the presence of
scarring should be investigated
with DMSA at 4 months, and
antibiotics continued.
Babies should then be referred to
consultant pediatric surgeon for
follow up at 1½ yrs (50% have
resolved by 2yrs).
Bilateral Hydronephrosis (>15 mm)
1. USS at 2-3 days, Mag-3 at 3/12.
2. Start Trimethoprim.
3. MCUG.
4. Urgent referral to consultant pediatric surgery.
NB USS at < 2 days can be misleading due to low
urine output.
MULTICYSTIC KIDNEYS
These are non-functional and
usually associated with an atretic
ureter and often with contra lateral
obstruction.
M>F R>L
65% are impalpable in the first three
months of life.
About 30% of multicystic kidneys
are initially incorrectly diagnosed as
hydronephrosis.
•The size of the kidney on USS is important
prognostically as 90% of those >6cm long at
any time tend to increase in size, while those
remaining <6cm tend to involute.
•There is no risk of UTI in an isolated MCDK as
there is no blood supply to the dysplastic
tissue and the cysts constitute a closed
system, however, 10-15% of MCDK have grade
2 vesico-ureteric reflux in the contra-lateral
kidney, and
Postnatal investigation of multicystic
kidneys
< 6cm>6 cmUSS
USS at 2 monthsreferAt 1 week
USS at 1 yearreferAt 2 months
Discharge with
yearly BP
referAt 1 year
Indications for MCUG and Prophylactic
Trimethoprim
1. Anomaly in contra-lateral kidney pre or
postnatally
2. Abnormal bladder
3. Dilated ureters(s)
4. UTI
Indications for Nephrectomy
1. Mass causing respiratory embarrassment or
feeding problems
2. Ipsilateral anomaly (usually ureterocoele)
3. Size > 6cm at 1½ yrs
BLADDER OUTFLOW
OBSTRUCTION (PUV)
These males are often born
preterm 30-36wks.
Present with:
1. Bilateral/unilateral
hydronephrosis
2. ± dilated ureter(s)
3. Distended bladder
4. Oligo-hydramnios
Management
• Urgent referral especially if distended bladder.
• Do not MCUG before referral as this makes endoscopic
diagnosis and treatment difficult.
• If bladder decompression is necessary before transfer,
this should be via a suprapubic catheter.
• Vesico-amniotic shunting in-utero is still controversial.
Babies with already impaired renal function as suggested
by oligo-hydramnios and abnormal U&E are unlikely to
benefit.
THANKS

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Renal tract anomalies

  • 1. Approach to Renal Tract Abnormalities In Neonates Dr. Tarek Kotb MBBCH CAIRO UNIVERSITY MRCPCH UK NICU –MCH- Buraydah Qassim
  • 2. ANTENATALLY DIAGNOSED RENAL TRACT ABNORMALITIES Urine production is important antenatally for production of amniotic fluid and the normal development of the urinary and pulmonary systems. Abnormalities of the urinary tract are among the most common detected antenatally and account for a significant (4%) part of perinatal mortality. More common in males (60%) than females.
  • 3. HYDRONEPHROSIS Antenatal detection of hydronephrosis of any degree should be investigated postnatally
  • 4. Unilateral hydronephrosis Should be scanned at 1 week, then again at 2-3 months . Following the first day check the parents should be given appointments for both of these scans, and a clinic appointment following the second. They should be asked to come to SCBU immediately following the first, for discussion of the result, which the radiologist will write down and give to them.
  • 5. Unilateral hydronephrosis information needed in scan at 1 week • AP diameter of the renal pelvis • Presence or absence of dilated calyces • Length of the kidneys • Whether dilated ureters are seen • Bladder wall thickness (if bladder distended) • Cortical thickness • Confirmation of the diagnosis or detection of other structural anomalies.
  • 6. During follow-up we may classify hydronephrosis based on 3 criteria 1.The largest AP diameter of the pelvis antenatally or neonatally. 2. Its function based on MAG3 (done at GOS) 3. The presence or absence of reflux into the renal pelvis based on MCUG
  • 7. (1).The largest AP diameter of the pelvis antenatally or neonatally ReferMAG 3 At 2 months TrimethoprimdischargeAP DIAMETER ♣< 10 mm AFTER 2 MONTHS SCAN ♣10-15 mm Normal calyces ♣♣10-15 mm Dilated calyces ♣♣15-19 mm ♣♣♣> 20 mm
  • 8. MCUG should be performed in any case where: • There is ureteric dilatation • The bladder wall is thicker than 5mm • US suggests renal scarring • It appears that there may be a ureterocoele or duplex system • UTI occurs • There is bilateral hydronephrosis (both > 15 mm).
  • 9. If MAG3 or MCUG are not indicated, follow up should be with USS at 6 months (and at one year, if required). Infants may be discharged once the AP diameter is <10mm. If follow-up is required beyond one year, this is best provided by general paediatricians
  • 10. (2). Its function based on MAG3 Poor function = < 20% ) Moderate = 20-39% ) of total renal function Good = >= 40% ) If function is <44%, the baby should be referred to consultant pediatric surgeon, otherwise USS should be repeated at six months and again with repeat Mag3 at 1yr.
  • 11. (3). The presence or absence of reflux into the renal pelvis based on MCUG If an initial MCUG shows significant reflux, the presence of scarring should be investigated with DMSA at 4 months, and antibiotics continued. Babies should then be referred to consultant pediatric surgeon for follow up at 1½ yrs (50% have resolved by 2yrs).
  • 12. Bilateral Hydronephrosis (>15 mm) 1. USS at 2-3 days, Mag-3 at 3/12. 2. Start Trimethoprim. 3. MCUG. 4. Urgent referral to consultant pediatric surgery. NB USS at < 2 days can be misleading due to low urine output.
  • 13. MULTICYSTIC KIDNEYS These are non-functional and usually associated with an atretic ureter and often with contra lateral obstruction. M>F R>L 65% are impalpable in the first three months of life. About 30% of multicystic kidneys are initially incorrectly diagnosed as hydronephrosis.
  • 14. •The size of the kidney on USS is important prognostically as 90% of those >6cm long at any time tend to increase in size, while those remaining <6cm tend to involute. •There is no risk of UTI in an isolated MCDK as there is no blood supply to the dysplastic tissue and the cysts constitute a closed system, however, 10-15% of MCDK have grade 2 vesico-ureteric reflux in the contra-lateral kidney, and
  • 15. Postnatal investigation of multicystic kidneys < 6cm>6 cmUSS USS at 2 monthsreferAt 1 week USS at 1 yearreferAt 2 months Discharge with yearly BP referAt 1 year
  • 16. Indications for MCUG and Prophylactic Trimethoprim 1. Anomaly in contra-lateral kidney pre or postnatally 2. Abnormal bladder 3. Dilated ureters(s) 4. UTI
  • 17. Indications for Nephrectomy 1. Mass causing respiratory embarrassment or feeding problems 2. Ipsilateral anomaly (usually ureterocoele) 3. Size > 6cm at 1½ yrs
  • 18. BLADDER OUTFLOW OBSTRUCTION (PUV) These males are often born preterm 30-36wks. Present with: 1. Bilateral/unilateral hydronephrosis 2. ± dilated ureter(s) 3. Distended bladder 4. Oligo-hydramnios
  • 19. Management • Urgent referral especially if distended bladder. • Do not MCUG before referral as this makes endoscopic diagnosis and treatment difficult. • If bladder decompression is necessary before transfer, this should be via a suprapubic catheter. • Vesico-amniotic shunting in-utero is still controversial. Babies with already impaired renal function as suggested by oligo-hydramnios and abnormal U&E are unlikely to benefit.
  • 20.