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Published on: October 12, 2017
CKD and bladder problems in children
1Vattikuti Urology Institute, Henry Ford Hospital, Detroit, MI, USA.
Insights
Approximately 35% of children with chronic kidney disease (CKD) needing renal replacement therapy have urological issues impacting kidney function. Coordinated pediatric urology and nephrology care, including regular evaluations, is crucial for managing these complex cases.
Area of Science:
- Pediatric Urology
- Pediatric Nephrology
- Renal Replacement Therapy
Background:
- Significant urological abnormalities are present in about 35% of children with chronic kidney disease (CKD) requiring renal replacement therapy.
- Abnormal bladder function in these children can severely damage renal function, particularly with bladder outlet obstruction leading to elevated intravesical pressure.
- Conditions like posterior urethral valves, neuropathic bladder, prune belly syndrome, and Hinman syndrome contribute to upper tract deterioration.
Purpose of the Study:
- To highlight the impact of urological abnormalities on renal function in children with CKD.
- To emphasize the need for coordinated care between pediatric urologists and nephrologists.
- To outline essential evaluations and management strategies for pediatric patients with CKD and urological issues.
Main Methods:
- Regular evaluation including renal sonography, urodynamics, urine culture, and serum chemistry.
- Behavioral modification and overnight continuous bladder drainage for valve bladder.
- Pharmacologic management and intermittent catheterization for neuropathic bladder.
- Thorough lower urinary tract evaluation, including voiding cystourethrogram and urodynamic studies, for renal transplant candidates.
Main Results:
- Overnight continuous bladder drainage can reduce hydronephrosis and stabilize or improve renal function in boys with posterior urethral valves.
- Neuropathic bladder management aims to prevent upper tract deterioration caused by detrusor-sphincter-dyssynergia, vesicoureteral reflux, and recurrent UTIs.
- Augmentation cystoplasty, while sometimes necessary, carries significant long-term risks.
Conclusions:
- Coordinated pediatric urological and nephrological care is essential for children with CKD and urological abnormalities.
- Early and regular evaluation of lower urinary tract function is critical for preserving renal health in affected children.
- Specific management strategies tailored to the underlying urological condition can significantly impact renal outcomes.
Abstract:
Approximately 35% of children with CKD who require renal replacement therapy have a significant urological abnormality, including posterior urethral valves, a neuropathic bladder, prune belly syndrome, Hinman syndrome, or severe vesicoureteral reflux. In such children, abnormal bladder function can have a significant deleterious effect on the renal function. In children with bladder outlet obstruction, bladder compliance and capacity often are abnormal, and a sustained intravesical pressure of >40 cm H(2)O impedes drainage from the upper urinary tract. Consequently, in these conditions, regular evaluation with renal sonography, urodynamics, urine culture, and serum chemistry needs to be performed. Pediatric urological care needs to be coordinated with pediatric nephrologists. Many boys with posterior urethral valves have severe polyuria, resulting in chronic bladder overdistension, which is termed as valve bladder. In addition to behavioral modification during the day, such patients may benefit from overnight continuous bladder drainage, which has been shown to reduce hydronephrosis and stabilize or improve renal function in most cases. In children with a neuropathic bladder, detrusor-sphincter-dyssynergia is the most likely cause for upper tract deterioration due to secondary vesicoureteral reflux, hydronephrosis, and recurrent urinary tract infection (UTI). Pharmacologic bladder management and frequent intermittent catheterization are necessary. In some cases, augmentation cystoplasty is recommended; however, this procedure has many long-term risks, including UTI, metabolic acidosis, bladder calculi, spontaneous perforation, and malignancy. Nearly half of children with prune belly syndrome require renal replacement therapy. Hinman syndrome is a rare condition with severe detrusor-sphincter discoordination that results in urinary incontinence, encopresis, poor bladder emptying, and UTI, often resulting in renal impairment. Children undergoing evaluation for renal transplantation need a thorough evaluation of the lower urinary tract, mostly including a voiding cystourethrogram and urodynamic studies.
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