TY - JOUR
T1 - FETAL URINE ANALYSIS TO PREDICT POOR
POSTNATAL FUNCTION IN TWO CASES OF
CONGENITAL URINARY OBSTRUCTION
AU - Rossi, Cristina
AU - Dessì, M
AU - Masini, Lucia
AU - Manzoni, Carlo
AU - Caruso, Alessandro
AU - Zuppi, Cecilia
AU - Calla', Cinzia Anna Maria
PY - 2013
Y1 - 2013
N2 - Background: Untreated fetal lower urinary tract obstructions
have a mortality rate of up to 45%. We evaluated the clinical
usefulness of fetal urine analysis for the prediction of poor
postnatal renal function in two cases.
Methods: Patient 1: 26th week, diagnosis of left fetal abdominal
mass (suspected multicystic-dysplastic kidney). Patient 2: 14th
week, diagnosis of fetal megabladder. In both cases, 7
echoguided cystocentesis were performed. Urine fetal samples
were assayed for electrolytes, creatinine, albumin, osmolality,
β2-Microglobulin and CystatinC on Cobas311-Roche, BNII
nephelometer Siemens,Osmometer AI.
Results: In patient 1, the parameters of renal function were
elevated, supporting an impaired renal function (Na:130.1±3.1
mEq/L; K: 4.14±0.38 mEq/L; Cl:109.3±2.1 mEq/L; Osmolality:
258.1±7.4 mOsm/Kg; Creatinine: 8.8±1.4 mg/dl; β2-
Microglobulin: 0.47±0.11 mg/dL; CystatinC: 0.07±0.01 mg/dl).
At day 4 after birth, the child underwent left
nephroureterectomy, with a definitive diagnosis of segmental
form of renal dysplasia. The cystourethrography, performed at
3 months of age, showed a right healthy renal parenchyma,
with a normal renal function. In patient 2, the fetal urine
biochemical tests were normal (Na:61±16.6 mEq/L; K:2.57±0.5
mEq/L; Cl:50±18.4 mEq/L; Osmolality: 134.3±30.14 mOsm/Kg;
Creatinine: 13.14±4.4 mg/dL; β2 Microglobulin: 0.40±0.23
mg/dL; CystatinC: 0.03±0.02 mg/dL) suggesting a normal renal
function,even in the presence of megabladder, suggesting
Prune-Belly syndrome. At birth, general conditions were fair
with normal biochemical parameters and urinary tract
ultrasound. The statistical analysis of biochemical tests of the
two patients showed significant differences for Na, K, Cl,
Osmolality and CystatinC (P <0.05), but not for creatinine and
for β2-Microglobulin (Student’s test).
Discussion: The use of echo guided invasive techniques has
allowed to consider the fetus as a little patient and invasive
approaches can be made with a very low risk-benefit ratio.The
biochemical evaluations on fetal urines, have made possible
the monitoring of the disease,leading to pregnancies up to 37th
and 38th weeks,respectively, with appropriate approach and
without aggressive treatment. In conclusion, the biochemical
tests have been of great support to the formulation of the
diagnosis and to reduce the intra-bladder pressure.
AB - Background: Untreated fetal lower urinary tract obstructions
have a mortality rate of up to 45%. We evaluated the clinical
usefulness of fetal urine analysis for the prediction of poor
postnatal renal function in two cases.
Methods: Patient 1: 26th week, diagnosis of left fetal abdominal
mass (suspected multicystic-dysplastic kidney). Patient 2: 14th
week, diagnosis of fetal megabladder. In both cases, 7
echoguided cystocentesis were performed. Urine fetal samples
were assayed for electrolytes, creatinine, albumin, osmolality,
β2-Microglobulin and CystatinC on Cobas311-Roche, BNII
nephelometer Siemens,Osmometer AI.
Results: In patient 1, the parameters of renal function were
elevated, supporting an impaired renal function (Na:130.1±3.1
mEq/L; K: 4.14±0.38 mEq/L; Cl:109.3±2.1 mEq/L; Osmolality:
258.1±7.4 mOsm/Kg; Creatinine: 8.8±1.4 mg/dl; β2-
Microglobulin: 0.47±0.11 mg/dL; CystatinC: 0.07±0.01 mg/dl).
At day 4 after birth, the child underwent left
nephroureterectomy, with a definitive diagnosis of segmental
form of renal dysplasia. The cystourethrography, performed at
3 months of age, showed a right healthy renal parenchyma,
with a normal renal function. In patient 2, the fetal urine
biochemical tests were normal (Na:61±16.6 mEq/L; K:2.57±0.5
mEq/L; Cl:50±18.4 mEq/L; Osmolality: 134.3±30.14 mOsm/Kg;
Creatinine: 13.14±4.4 mg/dL; β2 Microglobulin: 0.40±0.23
mg/dL; CystatinC: 0.03±0.02 mg/dL) suggesting a normal renal
function,even in the presence of megabladder, suggesting
Prune-Belly syndrome. At birth, general conditions were fair
with normal biochemical parameters and urinary tract
ultrasound. The statistical analysis of biochemical tests of the
two patients showed significant differences for Na, K, Cl,
Osmolality and CystatinC (P <0.05), but not for creatinine and
for β2-Microglobulin (Student’s test).
Discussion: The use of echo guided invasive techniques has
allowed to consider the fetus as a little patient and invasive
approaches can be made with a very low risk-benefit ratio.The
biochemical evaluations on fetal urines, have made possible
the monitoring of the disease,leading to pregnancies up to 37th
and 38th weeks,respectively, with appropriate approach and
without aggressive treatment. In conclusion, the biochemical
tests have been of great support to the formulation of the
diagnosis and to reduce the intra-bladder pressure.
KW - Fetal urine
KW - cistocentesis
KW - Fetal urine
KW - cistocentesis
UR - http://hdl.handle.net/10807/62100
M3 - Conference article
SN - 0393-0564
SP - S408-S408
JO - Biochimica Clinica
JF - Biochimica Clinica
T2 - EuroMedLab 2013
Y2 - 19 May 2013 through 23 May 2013
ER -