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Outcomes and rates of dissolution therapy for uric acid stones

  • Technical Note
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Abstract

Introduction

To describe the outcomes and quantify the rate of uric acid stone medical dissolution therapy using automated, software-generated stone volume measurements.

Methods

A sample of patients treated with oral dissolution therapy was reviewed from a single institution between 2008 and 2019. Baseline patient demographics, metabolic urine testing and stone characteristics were collected. Computed tomography (CT) scan images were evaluated using the quantitative Stone Analysis Software (qSAS) to obtain total stone volume (TSV), maximum diameter (MD) and stone number. Rate of dissolution using total stone volume was calculated over the treatment period.

Results

Twenty-seven patients were started on oral dissolution therapy, corrected for renal function. After mean duration of 180 days (range 41–531), 16 patients failed treatment resulting in surgical therapy. Twenty stones in 11 patients showed complete or partial dissolution. Compared to those who failed treatment, patients with complete or partial dissolution had lower 24 h urinary uric acid and higher treatment urine pH. Thirteen (65%) stones showed complete dissolution after a mean 167.6 days. Rate of change for responders was 4.73 mm3 or 0.6% of total stone volume per day. Time to dissolution of one half of stone volume based on total stone volume was 86 days (12.30 weeks).

Discussion/conclusions

Software-calculated total stone volume may be an effective method of measuring uric acid stone response to oral alkalization therapy. Stone volume decreased by 50% after 12.3 weeks of treatment and could be an important benchmark for oral dissolution therapyoral dissolution therapy. Further studies with a larger sample and validation of the software are needed to confirm if this can be used to guide surveillance schedules for dissolution therapy.

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Fig. 1

Availability of data and material

Raw data are available upon request.

Code availability

qSAS software is available for investigational use at https://ctcicblog.mayo.edu/hubcap/qsas-stone-toolkit/.

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Acknowledgements

O’Brien Urology Research Center, funded by the National Institutes of Health (DK100277), and the CT Clinical Innovation Center at the Mayo Clinic.

Funding

No funding sources were used for the conduct of the study.

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Authors and Affiliations

Authors

Contributions

JM: study design, data collection, data analysis, manuscript preparation and review; AN study design, data collection, data analysis; SS data collection; MK manuscript preparation and review; KS manuscript preparation and review; MH study design, manuscript preparation and review.

Corresponding author

Correspondence to Mitchell Humphreys.

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Conflict of interest

Mitchell Humphreys disclosures unrelated to current research study with Boston Scientific (research support), Adva-Tech (research support), and J&J (consultant).

Ethical approval

Institutional Review Board approval was obtained for the conduct of this study.

Consent to participate

Individual consent from patients was not required due to the retrospective nature of study, as determined by the Institutional Review Board.

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Moore, J., Nevo, A., Salih, S. et al. Outcomes and rates of dissolution therapy for uric acid stones. J Nephrol 35, 665–669 (2022). https://doi.org/10.1007/s40620-021-01094-y

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  • DOI: https://doi.org/10.1007/s40620-021-01094-y

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