Cargando…

Pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume

BACKGROUND: Increased pulmonary blood volume (PBV) is a measure of congestion and is associated with an increased risk of cardiovascular events. PBV can be quantified using cardiovascular magnetic resonance (CMR) imaging as the product of cardiac output and pulmonary transit time (PTT), the latter m...

Descripción completa

Detalles Bibliográficos
Autores principales: Nelsson, Anders, Kanski, Mikael, Engblom, Henrik, Ugander, Martin, Carlsson, Marcus, Arheden, Håkan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554972/
https://www.ncbi.nlm.nih.gov/pubmed/34706735
http://dx.doi.org/10.1186/s12968-021-00809-1
_version_ 1784591888615997440
author Nelsson, Anders
Kanski, Mikael
Engblom, Henrik
Ugander, Martin
Carlsson, Marcus
Arheden, Håkan
author_facet Nelsson, Anders
Kanski, Mikael
Engblom, Henrik
Ugander, Martin
Carlsson, Marcus
Arheden, Håkan
author_sort Nelsson, Anders
collection PubMed
description BACKGROUND: Increased pulmonary blood volume (PBV) is a measure of congestion and is associated with an increased risk of cardiovascular events. PBV can be quantified using cardiovascular magnetic resonance (CMR) imaging as the product of cardiac output and pulmonary transit time (PTT), the latter measured from the contrast time-intensity curves in the right and left side of the heart from first-pass perfusion (FPP). Several methods of estimating PTT exist, including pulmonary transit beats (PTB), peak-to-peak, and center of gravity (CoG). The aim of this study was to determine the accuracy and precision for these methods of quantifying the PBV, taking the left atrium volume (LAV) into consideration. METHODS: Fifty-eight participants (64 ± 11 years, 24 women) underwent 1.5 T CMR. PTT was quantified from (1) a basal left ventricular short-axis image (FPP), and (2) the reference method with a separate contrast administration using an image intersecting the pulmonary artery (PA) and the LA (CoG(PA-LA)). RESULTS: Compared to the reference, PBV for (a) PTB(FPP) was 14 ± 17% larger, (b) peak-peak(FPP) was 17 ± 16% larger, and (c) CoG(FPP) was 18 ± 10% larger. Subtraction of the LAV (available for n = 50) decreased overall differences to − 1 ± 19%, 2 ± 18%, and 3 ± 12% for PTB(FPP), peak-peak(FPP), and CoG(FPP), respectively. Lowest interobserver variability was seen for CoG(FPP) (− 2 ± 7%). CONCLUSIONS: CoG(PA-LA) and FPP methods measured the same PBV only when adjusting for the LAV, since FPP inherently quantifies a volume consisting of PBV + LAV. CoG(FPP) had the best precision and lowest interobserver variability among the FPP methods of measuring PBV. GRAPHICAL ABSTRACT: [Image: see text]
format Online
Article
Text
id pubmed-8554972
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-85549722021-10-29 Pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume Nelsson, Anders Kanski, Mikael Engblom, Henrik Ugander, Martin Carlsson, Marcus Arheden, Håkan J Cardiovasc Magn Reson Research BACKGROUND: Increased pulmonary blood volume (PBV) is a measure of congestion and is associated with an increased risk of cardiovascular events. PBV can be quantified using cardiovascular magnetic resonance (CMR) imaging as the product of cardiac output and pulmonary transit time (PTT), the latter measured from the contrast time-intensity curves in the right and left side of the heart from first-pass perfusion (FPP). Several methods of estimating PTT exist, including pulmonary transit beats (PTB), peak-to-peak, and center of gravity (CoG). The aim of this study was to determine the accuracy and precision for these methods of quantifying the PBV, taking the left atrium volume (LAV) into consideration. METHODS: Fifty-eight participants (64 ± 11 years, 24 women) underwent 1.5 T CMR. PTT was quantified from (1) a basal left ventricular short-axis image (FPP), and (2) the reference method with a separate contrast administration using an image intersecting the pulmonary artery (PA) and the LA (CoG(PA-LA)). RESULTS: Compared to the reference, PBV for (a) PTB(FPP) was 14 ± 17% larger, (b) peak-peak(FPP) was 17 ± 16% larger, and (c) CoG(FPP) was 18 ± 10% larger. Subtraction of the LAV (available for n = 50) decreased overall differences to − 1 ± 19%, 2 ± 18%, and 3 ± 12% for PTB(FPP), peak-peak(FPP), and CoG(FPP), respectively. Lowest interobserver variability was seen for CoG(FPP) (− 2 ± 7%). CONCLUSIONS: CoG(PA-LA) and FPP methods measured the same PBV only when adjusting for the LAV, since FPP inherently quantifies a volume consisting of PBV + LAV. CoG(FPP) had the best precision and lowest interobserver variability among the FPP methods of measuring PBV. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2021-10-28 /pmc/articles/PMC8554972/ /pubmed/34706735 http://dx.doi.org/10.1186/s12968-021-00809-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Nelsson, Anders
Kanski, Mikael
Engblom, Henrik
Ugander, Martin
Carlsson, Marcus
Arheden, Håkan
Pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume
title Pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume
title_full Pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume
title_fullStr Pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume
title_full_unstemmed Pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume
title_short Pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume
title_sort pulmonary blood volume measured by cardiovascular magnetic resonance: influence of pulmonary transit time methods and left atrial volume
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554972/
https://www.ncbi.nlm.nih.gov/pubmed/34706735
http://dx.doi.org/10.1186/s12968-021-00809-1
work_keys_str_mv AT nelssonanders pulmonarybloodvolumemeasuredbycardiovascularmagneticresonanceinfluenceofpulmonarytransittimemethodsandleftatrialvolume
AT kanskimikael pulmonarybloodvolumemeasuredbycardiovascularmagneticresonanceinfluenceofpulmonarytransittimemethodsandleftatrialvolume
AT engblomhenrik pulmonarybloodvolumemeasuredbycardiovascularmagneticresonanceinfluenceofpulmonarytransittimemethodsandleftatrialvolume
AT ugandermartin pulmonarybloodvolumemeasuredbycardiovascularmagneticresonanceinfluenceofpulmonarytransittimemethodsandleftatrialvolume
AT carlssonmarcus pulmonarybloodvolumemeasuredbycardiovascularmagneticresonanceinfluenceofpulmonarytransittimemethodsandleftatrialvolume
AT arhedenhakan pulmonarybloodvolumemeasuredbycardiovascularmagneticresonanceinfluenceofpulmonarytransittimemethodsandleftatrialvolume