A retrospective, observational multicentre trial on the nephrological outcome and associated congenital anomalies in children with Horseshoe Kidney.
Congenital abnormalities of the kidney and urinary tract (CAKUT) represent the main cause of CKD in children. Among them, the horseshoe kidney (HSK) represents one of the most frequent and is characterised by the presence of two distinct, functioning kidneys positioned on each side of the spine, fused together at one of the poles. The incidence of this condition is approximately 1 case every 400-600 new births with a prevalence in the male sex with a ratio of 2:1. Even though these children aregenerally asymptomatic and the diagnosis is often incidental , some may develop symptoms due to complications, such as infections, nephrolithiasis and urinary tract obstruction. More rarely risks of neoplastic degeneration and renal damage are described following trauma to the abdomen and lumbosacral spine. This condition is also associated in up to a third of cases with other abnormalities: the most frequent affect the urinary tract and genitals; however, abnormalities affecting other organs or systems as well as well-defined syndromic pictures. Due to its frequent asymptomatic nature, horseshoe kidney is historically considered a condition with a good prognosis and rarely as a risk factor capable of reducing survival or predisposing the kidney to long-term damage. The primary objective of the study is: To assess the 'nephrological outcome' understood as 'prevalence of patients who developed' and 'survival time free from": chronic renal failure, proteinuria, hypertension nephrolithiasis, UTI, renal neoplasms and renal trauma. The secondary objectives of the study are: 1. Prevalence of congenital and associated genito-urinary and systemic abnormalities; 2. Description of renal anatomical features; 3. Assessment of the usefulness of second level radiological investigations (VCUG, static renal scintigraphy, ddynamic renal scintigraphy).
Study Type
OBSERVATIONAL
Enrollment
500
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bologna, Italy
RECRUITINGChronic kidney disease
Defined as a reduction in eGFR \<90ml/min/1.73m2, calculated using the Schwartz formula(18) corrected for age: * δ= 0.45 for children \<1 yr * δ= 0.55 for children of both sexes from 2 to 12 yrs and for female children aged 13 to 18 yrs * δ= 0.70 for children aged 13 to 18 yrs The different stages of chronic kidney have been further defined according to eGFR: * Stage I: \>90ml/min/1.73m2 * Stage II: between 89 and 60ml/min/1.73m2 * Stage III: between 59 and 30ml/min/1.73m2 * Stage IV: between 30 and 15ml/min/1.73m2 * Stadio V: lower than15ml/min/1.73m2 or patient in dialysis
Time frame: at baseline
Proteinuria
Defined as the urinary protein:creatinine ratio (mg/mg) \>0.5 in chilrden up to 2 yrs of age and \>0.2 in chilrden older than 2 yrs
Time frame: at baseline
Hypertension
Arterial blood pressure ≥95th percentile for sex, age and height, on at least three different readings
Time frame: at baseline
Urinary tract infections
Confirmed by urine analysis and urine culture in a compatible clinical picture
Time frame: at baseline
Nephrolithiasis
Documented finding by imaging techniques (ultrasound and/or CT) of formations compatible with lithiasis formation
Time frame: at baseline
Renal neoplasms
Diagnosis confirmed by imaging and histology of the neoplasm of renal origin (especially Wilms' tumour)
Time frame: at baseline
Renal anatomical features
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Renal length measured as bipolar diameter with renal hypoplasia defined as the presence of kidneys with DBP \<5° centile reference for age and height
Time frame: at baseline
Renal anatomical features
Ultrasound description of abnormalities of the renal parenchyma with renal dysplasia defined by the presence of alterations such as: hyperechogenicity, reduced cortico-middular differentiation, reduced cortical thickness due to age, presence of multiple cystic formations
Time frame: at baseline
Renal trauma
Presence of instrumentally documented renal lesions (ultrasound and/or CT scan) following a traumatic episode
Time frame: at baseline