2021
Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool
OPATŘIL, Lukáš; Roman PANOVSKÝ; Jan MÁCHAL; Tomas HOLECEK; Lucia MASÁROVÁ et al.Základní údaje
Originální název
Extracellular volume quantification using synthetic haematocrit assessed from native and post-contrast longitudinal relaxation T1 times of a blood pool
Autoři
OPATŘIL, Lukáš; Roman PANOVSKÝ; Jan MÁCHAL; Tomas HOLECEK; Lucia MASÁROVÁ; Vera FEITOVA; Vladimír KINCL; Marek HODĚJOVSKÝ a Lenka ŠPINAROVÁ
Vydání
BMC Cardiovascular Disorders, London, BMC, 2021, 1471-2261
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30201 Cardiac and Cardiovascular systems
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.174
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/21:00122063
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Extracellular volume; ECV; Synthetic haematocrit; Cardiovascular magnetic resonance; CMR
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 24. 8. 2021 13:38, Mgr. Tereza Miškechová
Anotace
V originále
Background In terms of cardiovascular magnetic resonance are haematocrit values required for calculation of extracellular volume fraction (ECV). Previously published studies have hypothesized that haematocrit could be calculated from T1 blood pool relaxation time, however only native T1 relaxation time values have been used and the resulting formulae had been both in reciprocal and linear proportion. The aim of the study was to generate a synthetic haematocrit formula from only native relaxation time values first, calculate whether linear or reciprocal model is more precise in haematocrit estimation and then determine whether adding post-contrast values further improve its precision. Methods One hundred thirty-nine subjects underwent CMR examination. Haematocrit was measured using standard laboratory methods. Afterwards T1 relaxation times before and after the application of a contrast agent were measured and a statistical relationship between these values was calculated. Results Different linear and reciprocal models were created to estimate the value of synthetic haematocrit and ECV. The highest coefficient of determination was observed in the combined reciprocal model “− 0.047 + (779/ blood native) − (11.36/ blood post-contrast)”. Conclusions This study provides more evidence that assessing synthetic haematocrit and synthetic ECV is feasible and statistically most accurate model to use is reciprocal. Adding post-contrast values to the calculation was proved to improve the precision of the formula statistically significantly.
Návaznosti
| MUNI/A/1685/2020, interní kód MU |
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