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Published on: June 11, 2013
Imaging and surgical utilization for pediatric cystinuria patients: A single-institution cohort study
Briony K Varda1, Emilie K Johnson2, Kathryn L Johnson2
1Harvard Medical School, Brigham and Women's Hospital, Division of Urology, Boston, MA, USA.
Insights
Pediatric cystinuria patients face significant health issues, requiring frequent surgeries and extensive diagnostic imaging. Improved preventative therapies are crucial for managing this lifelong condition.
Area of Science:
- Pediatric Nephrology
- Urology
- Medical Genetics
Background:
- Cystinuria is a rare genetic disorder characterized by lifelong clinical manifestations.
- Healthcare utilization patterns in pediatric cystinuria patients are not well-understood.
Purpose of the Study:
- To investigate the healthcare utilization, including imaging and procedures, in pediatric patients with cystinuria.
- To highlight the clinical impact and management needs of this rare condition.
Main Methods:
- Retrospective review of billing records and patient charts for pediatric cystinuria cases.
- Analysis of demographics, comorbidities, presentation symptoms, stone characteristics, and subsequent imaging and surgical procedures.
- Calculation of median annual frequencies for procedures and imaging.
Main Results:
- Twenty-three pediatric patients with cystinuria were identified (1995-2011), with a median age of 12 years at presentation.
- High rates of surgical intervention (110 procedures in 15 patients) and diagnostic imaging (390 procedures) were observed.
- Radiation-associated imaging constituted half of all imaging tests, emphasizing potential exposure risks.
Conclusions:
- Pediatric cystinuria patients experience considerable disease morbidity, often necessitating multiple surgical procedures.
- Significant utilization of diagnostic imaging underscores the need for radiation exposure reduction strategies (e.g., ALARA principle).
- Development of improved preventive therapies and effective transitional care are essential for long-term management and reducing lifelong morbidity.
Objective:
Although cystinuria is rare, its clinical manifestations are life-long. Little is known about healthcare utilization in this population.
Study Design:
Through billing records and chart review, we identified pediatric patients with cystinuria treated at our institution. Variables included demographics, gender, race, comorbidities, location of presentation, presenting symptoms, initial laboratory data, and stone characteristics. Outcomes included the number and type of imaging tests and procedures performed. Descriptive statistics were performed. Median annual frequencies of procedures and imaging were calculated.
Results:
Twenty-three patients who presented between 1995 and 2011 were identified. The median age at presentation was 12 years, 48% of our patients were male, and 91% were Caucasian. Median follow-up was 4.6 years. Over half were diagnosed in clinic (13/23), while 30% (7/23) presented to the ED. Pain was the most common presenting symptom (13/23), followed by nausea/vomiting (6/23), gross hematuria (5/23), and fevers (5/23). Only one patient presented with acute renal failure. Five patients were discovered by sibling screening. The median number of stones at presentation was two and median size of the largest stone was 9 mm, with three staghorn calculi. During follow-up, a total of 110 stone procedures were performed in 15 patients. Five patients underwent 13 PCNLs, 11 patients underwent 44 ureteroscopy procedures, and nine underwent open or robotic surgery, including one nephrectomy. Among patients identified by sibling screening, most (4/5) were managed with medical therapy alone. A total of 390 imaging procedures were performed. Radiation-associated imaging comprised half of all imaging tests.
Discussion:
The high rates of imaging and surgical utilization among pediatric cystinuria patients reflect the morbidity of this condition and the need for preventative management. By practicing the ALARA principle during urologic procedures, urologists can reduce radiation exposure. Multiple procedures are often required to render patients stone-free. URS/LL and PCNL are likely to be more effective than ESWL. In complex cases, robotic-assist lithotomy provides the advantage of a minimally invasive approach. Both sibling screening and transitional care represent long-term strategies with the potential to reduce life-long morbidity. The limitations of this study include its small sample size, retrospective nature, and single-center experience.
Conclusions:
Our study demonstrates that the clinical impact of disease among pediatric patients presenting with cystinuria at our institution is considerable, with most requiring surgery. Our population also generates heavy utilization of diagnostic imaging. Given the lifelong nature of this disease, research on improved preventive therapies is urgently needed.
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