[Four years experience in the follow up of nursing children with urolithiasis]
Martha Medina-Escobedo1, Carolina Medina-Escobedo, Gloria Martín-Soberanis
11Hospital General "Agustín O'Horán," Servicios de Salud, Mérida, Yucatán, Mexico. marthamedinaescobedo@hotmail.com
Insights
Pediatric urolithiasis presents with urinary symptoms and can lead to renal failure. Hyperuricosuria was the most common metabolic alteration in this young cohort.
Area of Science:
- Pediatric Nephrology
- Urology
- Metabolic Disorders
Context:
- Urolithiasis in infants and young children is a growing concern.
- Understanding the clinical presentation and metabolic profile is crucial for early diagnosis and management.
- This study focuses on a cohort of very young children (≤36 months) with urolithiasis.
Purpose:
- To describe the clinical data, metabolic profile, treatment, and evolution of pediatric urolithiasis in children aged 36 months and younger.
- To identify common symptoms, calculus locations, complications, and metabolic alterations in this age group.
Summary:
- A prospective, longitudinal study followed 63 children (≤36 months) with urolithiasis.
- Common symptoms included crying upon urination and urinary retention. Kidney stones were most frequent.
- Complications included urinary tract infections and malnutrition. Hyperuricosuria was the predominant metabolic alteration.
Impact:
- Highlights the importance of suspecting urolithiasis in young children presenting with urinary symptoms.
- Emphasizes urolithiasis as a potential cause of renal failure in pediatrics.
- Identifies hyperuricosuria as a key metabolic finding requiring attention in pediatric stone disease.
Objective:
to describe clinical data, metabolic profile, treatment and evolution of a nursing children cohort with urolithiasis.
Methods:
using a descriptive, prospective and longitudinal design, were registered all patients with urolithiasis, of Pediatric Division at the Hospital General "Agustín O'Horán," in Yucatan, Mexico. We included all patients who were 36 months old and younger. We did not include children with malformations or associated disease which causes urolithiasis. Clinical and metabolic profiles, evaluation of the applied treatment as well as an evolution by four years period were done.
Results:
63 patients were recruited with ages ranging from 2 to 36 months; 39 (61.9 %) were male. The most common clinical signs were crying upon urination (49.2 %), urinary retention (31.7 %), hematuria (30.2 %), and pollakiuria (28.6 %). Calculus were most frequently located in the kidney (58.7 %). The most common complications were acute urinary tract infection (61.9 %), malnutrition (47.6 %) and acute renal failure (12.7 %). Documented metabolic alterations included hyperuricosuria (57.1 %), hypomagnesiuria (11.1 %) and hypercalciuria (9.5 %).
Conclusions:
urolithiasis should be suspected in children with crying upon urination and urinary symptoms; it should be considered among the different causes of renal failure; hyperuricosuria was the most frequent metabolic alteration.
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