Non-invasive characterization of pleural and pericardial effusions using T1 mapping by magnetic resonance imaging
- 21 July 2021
- journal article
- research article
- Published by Oxford University Press (OUP) in European Heart Journal - Cardiovascular Imaging
- Vol. 23 (8) , 1117-1126
Abstract
Differentiating exudative from transudative effusions is clinically important and is currently performed via biochemical analysis of invasively obtained samples using Light’s criteria. Diagnostic performance is however limited. Biochemical composition can be measured with T1 mapping using cardiovascular magnetic resonance (CMR) and hence may offer diagnostic utility for assessment of effusions. A phantom consisting of serially diluted human albumin solutions (25–200 g/L) was constructed and scanned at 1.5 T to derive the relationship between fluid T1 values and fluid albumin concentration. Native T1 values of pleural and pericardial effusions from 86 patients undergoing clinical CMR studies retrospectively analysed at four tertiary centres. Effusions were classified using Light’s criteria where biochemical data was available (n = 55) or clinically in decompensated heart failure patients with presumed transudative effusions (n = 31). Fluid T1 and protein values were inversely correlated both in the phantom (r = −0.992) and clinical samples (r = −0.663, P < 0.0001). T1 values were lower in exudative compared to transudative pleural (3252 ± 207 ms vs. 3596 ± 213 ms, P < 0.0001) and pericardial (2749 ± 373 ms vs. 3337 ± 245 ms, P < 0.0001) effusions. The diagnostic accuracy of T1 mapping for detecting transudates was very good for pleural and excellent for pericardial effusions, respectively [area under the curve 0.88, (95% CI 0.764–0.996), P = 0.001, 79% sensitivity, 89% specificity, and 0.93, (95% CI 0.855–1.000), P < 0.0001, 95% sensitivity; 81% specificity]. Native T1 values of effusions measured using CMR correlate well with protein concentrations and may be helpful for discriminating between transudates and exudates. This may help focus the requirement for invasive diagnostic sampling, avoiding unnecessary intervention in patients with unequivocal transudative effusions.Keywords
Funding Information
- University College London Hospitals
- NIHR Biomedical Research Centre and Biomedical Research Unit
- British Heart Foundation (FS/18/83/34025)
- Barts Charity (MGU0422)
- University College London Hospitals NIHR Biomedical Research Centre and Biomedical Research Unit at Barts Hospital
- NIH
This publication has 34 references indexed in Scilit:
- Pearls and myths in pleural fluid analysisRespirology, 2010
- Imaging the pericardium: appearances on ECG-gated 64-detector row cardiac computed tomographyBritish Journal of Radiology, 2010
- Diagnostic Value of the Biochemical Composition of Pericardial Effusions in Patients Undergoing PericardiocentesisThe American Journal of Cardiology, 2007
- Accuracy of Computed Tomography Attenuation Values in the Characterization of Pleural FluidAcademic Radiology, 2005
- The composition of normal pericardial fluid and its implications for diagnosing pericardial effusionsThe American Journal of Medicine, 2005
- Is it Meaningful to use Biochemical Parameters to Discriminate Between Transudative and Exudative Pleural Effusions?Chest, 2002
- Consecutive 1127 Therapeutic Echocardiographically Guided Pericardiocenteses: Clinical Profile, Practice Patterns, and Outcomes Spanning 21 YearsMayo Clinic Proceedings, 2002
- Temperature- and pH-dependence of proton relaxation rates in rat liver tissueMagnetic Resonance Imaging, 1995
- Determinants of water proton T1 in blood serumMagnetic Resonance in Medicine, 1988
- Temperature dependence of proton relaxation times in vitroMagnetic Resonance Imaging, 1987