3. INTRODUCTION
Fetal hydronephrosis (dilatation of
the renal collecting system) is the
most common abnormality found
on prenatal ultrasound.
1-5 % of all pregnancy
Male : female 2:1
Bilateral in 20-40 %
The goal of postnatal management
is to identify those with significant
congenital anomalies of the kidney
and urinary tract while avoiding
unnecessary testing in patients
with physiologic or clinically
insignificant hydronephrosis.
4. DEFINITION OF ANTENATAL
HYDRONEPHROSIS(ANH)
Anteroposterior diameter (APD) of the renal pelvis in the
transverse plane is the most studied parameter for
assessing ANH in utero
Threshold APD value that separates normal from
abnormal does not exist
No consensus on the optimal APD threshold for need of
postnatal follow up
Factors affecting APD:
Gestational age
Hydration status of the mother
Degree of bladder distention
6. GRADING ANH BY APD
ANH grade APD second
trimester, mm
APD third
trimester, mm
Mild
≤ 7 ≤ 9
Moderate
7–10 9–15
Severe
> 10 > 15
APD greater than 15 mm represents severe or significant
hydronephrosis
A value of 4-5 mm is an appropriate threshold for considering the APD to
be abnormal.
8. Natural history of ANH
The vast majority of the cases of
hydronephrosis diagnosed during the
second trimester have been noted to
resolve during follow-up imaging in the
third trimester.
- Majority of SFU G1-2 resolve by 18months
- If increasing hydronephrosis occurs , it
does so early in life and often during the
first year.
- Multivariate analysis showed larger APD
and SFU grade 4 to be associated with a
lower likehood of resolution. Michelle et al J
Ped Urol 2011
Surgery
25%
Persistence
23%
Resolution
52%
9. POSTNATAL EVALUATION
PHYSICAL EXAMINATION
Abdominal mass :enlarged kidney due to obstructive
uropathy or multicystic dysplastic kidney (MCDK).
A palpable bladder in a male infant, especially after
voiding, may suggest posterior urethral valves.
A male infant with prune belly syndrome will have
deficient abdominal wall musculature and undescended
testes.
11. POSTNATAL IMAGING OF ANH
ULTRASOUND
The first postnatal scan must be delayed for a week to
avoid the false-negative results that may be produced by
US within the first 24-48 h when the baby is relatively
oliguric.
A second scan at 6 weeks is necessary because initial
scans may be normal and subsequent scans may show
postnatal hydronephrosis.
APD
Calyceal / ureteral dilation
Corticomedullary differentiation
Thinned cortex
Cortical cysts
Ureterocele
12. POSTNATAL IMAGING OF ANH
VCUG
○ Vesicoureteral reflux(VUR)
○ Posterior urethral valves(PUV)
○ Ureterocele
Antibiotics (Amoxicillin 10mg/kg/d or cephalexin
5mg/kg/d) until VCUG done
Controversy exists around whether children with SFU 0–
2 on postnatal US should get a VCUG.
13. POSTNATAL IMAGING OF ANH
DIURETIC RENOGRAPHY
RPD is > 10mm even in the presence of VUR
SFU G3 & G4
Timing and selection
4–6 weeks of age
Tc MAG3 is more accurate assessment of both
function and drainage than TcDTPA.
Clearance of half of the isotope (t ½) within 10-
15min ------------------- no obstruction.
T1/2 > 20 min ------------ significant obstruction,
while T1/2 15-20 min. is intermediate.
14. POSTNATAL IMAGING OF ANH
DIURETIC RENOGRAPHY
Type 1: normal uptake
with prompt washout
Type 2: a rising uptake
curve with no response to
diuretics, which suggests
obstruction
Type 3: an initially rising
curve that falls rapidly in
response to diuretics,
which suggests non
obstructive dilatation
15. SURGICAL INTERVENTION
Recommendation for surgical intervention
- Obstructive wash-out curve (T ½ exceeds 20 min.)
with Differential function < 40%
- Progressive decrease in differential function on
sequential nuclear renogram
Exception to split renal function – severe bilateral
hydronephrosis or obstruction, as the absence of a
normal contralateral kidney with which to compare the
hydronephrotic kidney
Renal unit that demonstrates the least function should
be repaired first.
16. POSTNATAL IMAGING OF ANH
MRU
Gadolinium-enhanced MRU
Advantages :
- Superior anatomical and functional information even if
poor function or bilateral disease, no radiation
- Contrast non toxic
Disadvantages :
- Expensive
- Complexity of the software protocol needed to process
the MRI information
- Requires sedation and monitoring
For solitary kidneys or bilateral renal involvement,
MRU is superior than DR as individual kidney
function (GFR) may be assessed.
17. POSTNATAL IMAGING OF ANH
IVU
At 6 weeks
Advantages : good anatomy if function is good
Disadvantages : inaccurate if poor function, nephrotoxic
contrast, radiation exposure.
DR and MRU may not be available and in such cases
intravenous urogram may be the only test used.
18. TRANSIENT HYDRONEPHROSIS
41 – 88%
Most children with a pelvic
dilation <6 mm diagnosed
during the 2nd trimester or
<8 mm diagnosed during
the 3rd trimester have
transient hydronephrosis
[Mallik et al Pediat Nephrol 2008].
Insufficient maturation of
the UPJ or the VUJ
Fetal ureteric fold
VUR
Antenatal postnatal
19. UPJ OBSTRUCTION
Antenately: hydronephrosis with
no ureteric dilatation , normal
bladder and amniotic fluid volume
10-30%
Likehood of UPJ obstruction is
more with antenatal APD > 15mm
(Rickood et al BJU 1991)
Only 19-25% of children with
prenatally diagnosed UPJ
obstruction require surgical
intervention .Diagnosis :1- Diuretic
renography
2- Differential renal
function
Management : Pyeloplasty if renal
function depressed to < 40% of the
total
20. VUR
10-20%
Degree of dilatation does not correlate with VUR
A normal postnatal US does not exclude reflux
Antibiotic prophylaxis
Up to 60% of refluxing units resolve within 2 yrs
including grade IV and V reflux .Most patients with VUR
and low-grade hydronephrosis can be followed without
surgical intervention
21. VUJ OBSTRUCTION / MEGAURETER
5-10%.
Megaureter : suspected when dilated ureter >7mm with no
reflux
Renography is used to differentiate obstructed from non
obstructed megaureter
The majority will spontaneously resolve during postnatal
follow up - Conservative with similar protocol like UPJ
obstruction
- Surgical excision , tapering of the distal end and
reimplantation --- high complication rate in neonates
- Open insertion of a JJ stent as a temporizing procedure
reported with excellent results
22. MCDK
4-6 %
Renal parenchyma is completely replaced
by non communicating cysts of variable
sizes and no discernible renal cortex
Not hereditary unlike PCKD
Occasionally confused with UPJ
obstruction
Diagnosis confirmed with US and DMSA
Nephrectomy for symptomatic masses of
if infection occurs.
Management of asymptomatic cases is
very controversial as the incidence of
short term complications is very low and
the MCDK resolves in a number of
patients by the age of 5 years
23. PUV
1: 8000 newborn
1) Prenatal hydronephrosis (often
bilateral)
2) Dilated, thick-walled bladder
that fails to empty
3) Dilated posterior urethra; and
4) Decreased amniotic fluid
suggests the presence of lower
urinary tract obstruction
Elevated fetal urinary Na, Cl & B
microglobulin are antenatal
predictors of poor outcome
24. PUV
- Postnataly: catheterization ----in all
suspected cases
US & VCUG to be done within 48 hrs
- Definite management : PUV ablation
1/3 of patients with PUV eventually develop
renal insufficiency
- Prognosis is worse if the diagnosis is
suspected antenately with severe obstruction,
hydroureteronephrosis and oligohydramnios
25. PUV
ANTINATAL INTERVENTION
Vesicoamniotic shunting
Aim :Decompression will restore amniotic
fluid---> prevent development of fetal
pulmonary hypoplasia .
Intervention is only warranted if the
ultrasound findings and fetal urinary
markers suggest salvageable renal
function
Complications : Shunt blockage or
migration, preterm labor, urinary ascitis,
chorioamnionitis, intrauterine death.
Outcome: Perinatal survival 47%
Post renal insufficiency 87.5%
Intrauterine fulguration of PUV has
been limited to very few centers at this
time
26. URETEROCELE
Cystic dilatation of
the intravesical ureter
1:5000
Commonly associated with
duplicated systems
10-20 % bilateral
Associated with ectopic
insertion of the ureter in 75 % of cases.
Postnataly diagnosed by US
VCUG is used to show whether reflux
is into a lower pole or ectopic ureter
MAG3 is needed to assess the function
Treatment :
Initially Endoscopic puncture
Definitive upper pole heminephro-
ureterectomy
27. SUMMARY
All ANH should be investigated with a post-natal US.
Antenatal hydronephrosis does not necessary imply
obstruction, nor give any indication of the function of an
affected kidney.
The role of prophylactic antibiotics initiated at birth is
controversial.
The need to further investigate mild postnatal
hydronephrosis (SFU 0–2) with a VCUG is controversial,
and depends on the physician’s attitude toward
diagnosing asymptomatic VUR.
28. SUMMARY
Persistent moderate or severe hydronephrosis (SFU3–4)
should be investigated with a VCUG, followed by diuretic
renography if the hydronephrosis cannot be explained by VUR.
Most diagnoses made based on a finding of prenatal
hydronephrosis can be handled conservatively.
Indications for surgical intervention include reduced
differential function (<40%), greater than 5% decrease in
baseline differential function, progressive increase in
hydronephrosis, febrile infection or poor parental
compliance
Prenatal intervention for hydronephrosis is indicated only
in very select instances and in specialized centers . Even when
well selected, intervention is highly controversial.