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Etiology, urine metabolic risk factors, and urine oxalate patterns in patients with significant hyperoxaluria and recurrent nephrolithiasis.
Moore, Jonathan P; Mauler, David J; Narang, Gopal L; Stern, Karen L; Humphreys, Mitchell R; Keddis, Mira T.
Affiliation
  • Moore JP; Department of Urologic Surgery, UC Davis Medical Center, Sacramento, CA, USA.
  • Mauler DJ; Department of Urology, Mayo Clinic Arizona, Phoenix, AZ, USA.
  • Narang GL; Department of Urology, University of North Carolina, Chapel Hill, NC, USA.
  • Stern KL; Department of Urology, Mayo Clinic Arizona, Phoenix, AZ, USA. Stern.Karen@mayo.edu.
  • Humphreys MR; Department of Urology, Mayo Clinic Arizona, Phoenix, AZ, USA.
  • Keddis MT; Department of Nephrology, Mayo Clinic Arizona, Phoenix, AZ, USA.
Int Urol Nephrol ; 54(11): 2819-2825, 2022 Nov.
Article in En | MEDLINE | ID: mdl-35917078
PURPOSE: American Urology Association guidelines recommend genetic testing for patients with recurrent stones and urine oxalate > 75 mg/day. The goal of this study was to examine the treatment of patients in this category in a large multidisciplinary adult stone clinic. METHODS: Patients were evaluated from a single institution between 2006 and 2019. Those with at least one level of urinary oxalate excretion (uOx) above 75 mg/day were identified. A chart review identified enteric risk factors and genetic testing results. Patients without an identifiable enteric cause were considered idiopathic. RESULTS: A total of 4229 separate 24-h urine collections in 1302 patients were reviewed. At least one measurement of uOx above 75 mg/day was found in 103 (7.9%) patients. Enteric hyperoxaluria (EH) was seen in 28 (27%) and idiopathic hyperoxaluria (IH) in 76 (74%). 20 (71%) patients in the EH group had undergone gastric bypass. The median uOx was significantly higher level in the EH group (121.0 vs. 93.0 mg/day). For the entire cohort, there was a drop in uOx (- 33.8 mg/day) with medical and dietary therapy after a follow-up of 46.6 months. The final oxalate was higher in EH (88.9 vs. 60.1 mg/day). Only one patient had referral for genetic testing and was found to have primary hyperoxaluria type 2. CONCLUSIONS: The most common cause of significant hyperoxaluria in patients with recurrent nephrolithiasis remains idiopathic. Patients with IH have more significant improvement in uOx compared to EH; however, both groups had hyperoxaluria at last follow-up. Rate of genetic testing is low despite guideline recommendations.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperoxaluria / Kidney Calculi / Nephrolithiasis Type of study: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Humans Language: En Journal: Int Urol Nephrol Year: 2022 Document type: Article Affiliation country: United States Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hyperoxaluria / Kidney Calculi / Nephrolithiasis Type of study: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Humans Language: En Journal: Int Urol Nephrol Year: 2022 Document type: Article Affiliation country: United States Country of publication: Netherlands