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The importance of sampling time in radionuclide measurement of glomerular filtration rate in adults using single blood sample

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F23%3A00084250" target="_blank" >RIV/00023001:_____/23:00084250 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00216208:11110/23:10466821 RIV/00064165:_____/23:10466821

  • Výsledek na webu

    <a href="https://link.springer.com/article/10.1007/s40336-023-00583-3" target="_blank" >https://link.springer.com/article/10.1007/s40336-023-00583-3</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s40336-023-00583-3" target="_blank" >10.1007/s40336-023-00583-3</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    The importance of sampling time in radionuclide measurement of glomerular filtration rate in adults using single blood sample

  • Popis výsledku v původním jazyce

    PurposeIn theory, radionuclide measurement of glomerular filtration rate (GFR) using bolus injection and a single blood sample results in GFR values close to the results of slope-intercept (SI) method using two or more blood samples, especially if the sample is collected at specific time. The aim of our study was to provide experimental validation of this assumption, to design the new single-sample methods potentially correcting for inadequate sampling time, and to validate them together with the method recommended by the British Nuclear Medicine Society (BNMS) guidelines.MethodsNew analytic and regression-based single-sample methods were developed using previously published concepts. In 373 patients, GFR measured by the new methods and by the method recommended by the BNMS guidelines was compared with the reference GFR measured by SI method using two blood samples. Prediction of the reference GFR was evaluated by cross-validation with all blood samples and with blood samples collected at time interval &amp; PLUSMN; 30 min around optimal sampling time.ResultsWith all 768 blood samples (regardless of sampling time), the method recommended by the BNMS guidelines performed significantly better than the new methods, predicting reference GFR with the mean absolute error (MAE) of 2.55 (versus 2.95-3.37) ml/min/1.73 m(2). In the subset of blood samples collected at time interval &amp; PLUSMN; 30 min around optimal sampling time derived from SI method (n = 247), performance of all methods was significantly improved. MAE was reduced to 1.18 (vs. 1.27-1.39) ml/min/1.73 m(2). Realistic estimate of optimal sampling time using creatinine prediction equation CKD-EPI (n = 235) resulted in MAE of 1.37 (vs. 1.53-1.76) ml/min/1.73 m(2).ConclusionThe study experimentally confirmed that collection of single blood sample near patient-specific optimal sampling time significantly improves accuracy of prediction of the reference SI GFR by all validated single-sample methods. The method recommended by the BNMS guidelines provided the best results with low prediction error that was further reduced by collecting blood sample at optimal sampling time. The new methods successfully corrected for small deviations from optimal sampling time.

  • Název v anglickém jazyce

    The importance of sampling time in radionuclide measurement of glomerular filtration rate in adults using single blood sample

  • Popis výsledku anglicky

    PurposeIn theory, radionuclide measurement of glomerular filtration rate (GFR) using bolus injection and a single blood sample results in GFR values close to the results of slope-intercept (SI) method using two or more blood samples, especially if the sample is collected at specific time. The aim of our study was to provide experimental validation of this assumption, to design the new single-sample methods potentially correcting for inadequate sampling time, and to validate them together with the method recommended by the British Nuclear Medicine Society (BNMS) guidelines.MethodsNew analytic and regression-based single-sample methods were developed using previously published concepts. In 373 patients, GFR measured by the new methods and by the method recommended by the BNMS guidelines was compared with the reference GFR measured by SI method using two blood samples. Prediction of the reference GFR was evaluated by cross-validation with all blood samples and with blood samples collected at time interval &amp; PLUSMN; 30 min around optimal sampling time.ResultsWith all 768 blood samples (regardless of sampling time), the method recommended by the BNMS guidelines performed significantly better than the new methods, predicting reference GFR with the mean absolute error (MAE) of 2.55 (versus 2.95-3.37) ml/min/1.73 m(2). In the subset of blood samples collected at time interval &amp; PLUSMN; 30 min around optimal sampling time derived from SI method (n = 247), performance of all methods was significantly improved. MAE was reduced to 1.18 (vs. 1.27-1.39) ml/min/1.73 m(2). Realistic estimate of optimal sampling time using creatinine prediction equation CKD-EPI (n = 235) resulted in MAE of 1.37 (vs. 1.53-1.76) ml/min/1.73 m(2).ConclusionThe study experimentally confirmed that collection of single blood sample near patient-specific optimal sampling time significantly improves accuracy of prediction of the reference SI GFR by all validated single-sample methods. The method recommended by the BNMS guidelines provided the best results with low prediction error that was further reduced by collecting blood sample at optimal sampling time. The new methods successfully corrected for small deviations from optimal sampling time.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30217 - Urology and nephrology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/GA303%2F07%2F0950" target="_blank" >GA303/07/0950: Kvantitativní hodnocení dynamické scintigrafie ledvin</a><br>

  • Návaznosti

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Ostatní

  • Rok uplatnění

    2023

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Clinical and Translational Imaging

  • ISSN

    2281-5872

  • e-ISSN

    2281-7565

  • Svazek periodika

    11

  • Číslo periodika v rámci svazku

    5

  • Stát vydavatele periodika

    IT - Italská republika

  • Počet stran výsledku

    12

  • Strana od-do

    493-504

  • Kód UT WoS článku

    001043657600002

  • EID výsledku v databázi Scopus

    2-s2.0-85166911253