Preservation of urine specimens for metabolic evaluation of recurrent urinary stone formers

Author:

Šálek Tomáš12ORCID,Musil Pavel1,Vermeersch Pieter3ORCID,Marrington Rachel4,Dikmen Zeliha G.5,Poláchová Radka1,Kipman Ulrike6ORCID,Kouri Timo T.78ORCID,Cadamuro Janne9ORCID

Affiliation:

1. Department of Clinical Biochemistry and Pharmacology , 37742 Tomas Bata Hospital Zlín , Zlín , Czech Republic

2. Institute of Clinical Biochemistry and Diagnostics, Medical Faculty in Hradec Králové , Charles University , Prague , Czech Republic

3. Clinical Department of Laboratory Medicine , University Hospitals Leuven , Leuven , Belgium

4. Birmingham Quality (UK NEQAS) , University Hospitals NHS Foundation Trust , Birmingham , UK

5. Clinical Pathology Laboratory, Department of Medical Biochemistry and Hacettepe University Hospitals , Hacettepe University Faculty of Medicine , Ankara , Türkiye

6. College of Education , Salzburg , Austria

7. Department of Clinical Chemistry , University of Helsinki , Espoo , Finland

8. Hospital District of Helsinki and Uusimaa, HUS Diagnostic Center , HUSLAB , Helsinki , Finland

9. Department of Laboratory Medicine , Paracelsus Medical University , Salzburg , Austria

Abstract

Abstract Objectives Stability of concentrations of urinary stone-related metabolites was analyzed from samples of recurrent urinary stone formers to assess necessity and effectiveness of urine acidification during collection and storage. Methods First-morning urine was collected from 20 adult calcium-stone forming patients at Tomas Bata Hospital in the Czech Republic. Urine samples were analyzed for calcium, magnesium, inorganic phosphate, uric acid, sodium, potassium, chloride, citrate, oxalate, and urine particles. The single-voided specimens were collected without acidification, after which they were divided into three groups for storage: samples without acidification (“NON”), acidification before storage (“PRE”), or acidification after storage (“POST”). The analyses were conducted on the day of arrival (day 0, “baseline”), or after storage for 2 or 7 days at room temperature. The maximum permissible difference (MPD) was defined as ±20 % from the baseline. Results The urine concentrations of all stone-related metabolites remained within the 20 % MPD limits in NON and POST samples after 2 days, except for calcium in NON sample of one patient, and oxalate of three patients and citrate of one patient in POST samples. In PRE samples, stability failed in urine samples for oxalate of three patients, and for uric acid of four patients after 2 days. Failures in stability often correlated with high baseline concentrations of those metabolites in urine. Conclusions Detailed procedures are needed to collect urine specimens for analysis of urinary stone-related metabolites, considering both patient safety and stability of those metabolites. We recommend specific preservation steps.

Publisher

Walter de Gruyter GmbH

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