An algorithm for individual dosage in cadmium–zinc–telluride spect-gated radionuclide angiography

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

An algorithm for individual dosage in cadmium–zinc–telluride spect-gated radionuclide angiography. / Hansen, Maria Normand; Haarmark, Christian; Kristensen, Bent; Zerahn, Bo.

In: Diagnostics, Vol. 11, No. 12, 2268, 2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hansen, MN, Haarmark, C, Kristensen, B & Zerahn, B 2021, 'An algorithm for individual dosage in cadmium–zinc–telluride spect-gated radionuclide angiography', Diagnostics, vol. 11, no. 12, 2268. https://doi.org/10.3390/diagnostics11122268

APA

Hansen, M. N., Haarmark, C., Kristensen, B., & Zerahn, B. (2021). An algorithm for individual dosage in cadmium–zinc–telluride spect-gated radionuclide angiography. Diagnostics, 11(12), [2268]. https://doi.org/10.3390/diagnostics11122268

Vancouver

Hansen MN, Haarmark C, Kristensen B, Zerahn B. An algorithm for individual dosage in cadmium–zinc–telluride spect-gated radionuclide angiography. Diagnostics. 2021;11(12). 2268. https://doi.org/10.3390/diagnostics11122268

Author

Hansen, Maria Normand ; Haarmark, Christian ; Kristensen, Bent ; Zerahn, Bo. / An algorithm for individual dosage in cadmium–zinc–telluride spect-gated radionuclide angiography. In: Diagnostics. 2021 ; Vol. 11, No. 12.

Bibtex

@article{1cd28c4f0db745f2a3c46398d26b81be,
title = "An algorithm for individual dosage in cadmium–zinc–telluride spect-gated radionuclide angiography",
abstract = "The aim of the present study was to test an individualised dose without compromising the ease of analysing data when performing equilibrium radionuclide angiography (ERNA) using cadmium–zinc–telluride (CZT) SPECT. From March 2018 to January 2019, 1650 patients referred for ERNA received either an individualised dose of99m Tc-labeled human serum albumin (HSA) according to their age, sex, height, and weight (n = 1567), or a standard dose of 550 MBq (n = 83). The target count rate (CRT ) was reduced every two months from 2.7 to 1.0 kcps. A final test with a CRT of 1.7 kcps was run for three months to test whether an agreement within 2% points for the determination of LVEF, on the basis of only two analyses, was obtainable in at least 95% of acquisitions. All the included ERNAs were performed on a dedicated cardiac CZT SPECT camera. When using the algorithm for an individualised dose, we found that agreement between the measured and predicted count rate was 80%. With a CRT of 1.7 kcps, the need for more than two analyses to obtain sufficient agreement for LVEF was 4.9%. Furthermore, this resulted in a mean dose reduction from 550 to 258 MBq. Patients{\textquoteright} weight, height, sex, and age can, therefore, be used for individualising a tracer dose while reducing the mean dose.",
keywords = "CZT SPECT, Gated SPECT, Personalised medicine, RNA",
author = "Hansen, {Maria Normand} and Christian Haarmark and Bent Kristensen and Bo Zerahn",
note = "Publisher Copyright: {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland.",
year = "2021",
doi = "10.3390/diagnostics11122268",
language = "English",
volume = "11",
journal = "Diagnostics",
issn = "2075-4418",
publisher = "MDPI AG",
number = "12",

}

RIS

TY - JOUR

T1 - An algorithm for individual dosage in cadmium–zinc–telluride spect-gated radionuclide angiography

AU - Hansen, Maria Normand

AU - Haarmark, Christian

AU - Kristensen, Bent

AU - Zerahn, Bo

N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

PY - 2021

Y1 - 2021

N2 - The aim of the present study was to test an individualised dose without compromising the ease of analysing data when performing equilibrium radionuclide angiography (ERNA) using cadmium–zinc–telluride (CZT) SPECT. From March 2018 to January 2019, 1650 patients referred for ERNA received either an individualised dose of99m Tc-labeled human serum albumin (HSA) according to their age, sex, height, and weight (n = 1567), or a standard dose of 550 MBq (n = 83). The target count rate (CRT ) was reduced every two months from 2.7 to 1.0 kcps. A final test with a CRT of 1.7 kcps was run for three months to test whether an agreement within 2% points for the determination of LVEF, on the basis of only two analyses, was obtainable in at least 95% of acquisitions. All the included ERNAs were performed on a dedicated cardiac CZT SPECT camera. When using the algorithm for an individualised dose, we found that agreement between the measured and predicted count rate was 80%. With a CRT of 1.7 kcps, the need for more than two analyses to obtain sufficient agreement for LVEF was 4.9%. Furthermore, this resulted in a mean dose reduction from 550 to 258 MBq. Patients’ weight, height, sex, and age can, therefore, be used for individualising a tracer dose while reducing the mean dose.

AB - The aim of the present study was to test an individualised dose without compromising the ease of analysing data when performing equilibrium radionuclide angiography (ERNA) using cadmium–zinc–telluride (CZT) SPECT. From March 2018 to January 2019, 1650 patients referred for ERNA received either an individualised dose of99m Tc-labeled human serum albumin (HSA) according to their age, sex, height, and weight (n = 1567), or a standard dose of 550 MBq (n = 83). The target count rate (CRT ) was reduced every two months from 2.7 to 1.0 kcps. A final test with a CRT of 1.7 kcps was run for three months to test whether an agreement within 2% points for the determination of LVEF, on the basis of only two analyses, was obtainable in at least 95% of acquisitions. All the included ERNAs were performed on a dedicated cardiac CZT SPECT camera. When using the algorithm for an individualised dose, we found that agreement between the measured and predicted count rate was 80%. With a CRT of 1.7 kcps, the need for more than two analyses to obtain sufficient agreement for LVEF was 4.9%. Furthermore, this resulted in a mean dose reduction from 550 to 258 MBq. Patients’ weight, height, sex, and age can, therefore, be used for individualising a tracer dose while reducing the mean dose.

KW - CZT SPECT

KW - Gated SPECT

KW - Personalised medicine

KW - RNA

U2 - 10.3390/diagnostics11122268

DO - 10.3390/diagnostics11122268

M3 - Journal article

C2 - 34943505

AN - SCOPUS:85121544775

VL - 11

JO - Diagnostics

JF - Diagnostics

SN - 2075-4418

IS - 12

M1 - 2268

ER -

ID: 290253293