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Left ventricular end-diastolic and end-systolic volumes, reference values

Left ventricular end-diastolic and end-systolic volumes, reference values

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Radionuclide imaging of cardiac function represents a number of well-validated techniques for accurate determination of right (RV) and left ventricular (LV) ejection fraction (EF) and LV volumes. These first European guidelines give recommendations for how and when to use first-pass and equilibrium radionuclide ventriculography, gated myocardial pe...

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... ventricular end-diastolic volume QGS and 4D-MSPECT have been shown to underestimate LV EDV compared to the corresponding measurements from cMRI with 17 and 10ml, respectively [60]. Another comparison between the three software packages, 4D- MSPECT, ECT and QGS, have shown that 4D-MSPECT and ECT calculate LV EDV values that are 14-and 10-ml higher, respectively, than those calculated with QGS in patients with normal MPS [132] (Table 6). ...

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... Red blood cell (RBC) labeling is a commonly employed technique to assess red blood cell volume in the diagnostic evaluation of polycythemia, to measure the left ventricular ejection fraction [1,2], for gastrointestinal bleeding scintigraphy [3] and splenic function evaluation [4,5]. The accurate determination of RBC volume plays a crucial role in confirming the diagnosis of absolute polycythemia. ...
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... 47,48 In MUGA, cardiac volumes are derived from heart-centred images of the patient's own radiolabelled erythrocytes 49 and are therefore not influenced by geometric assumptions about the myocardial wall. 50 Three types of MUGA are distinguished: (i) first-pass MUGA, (ii) planar equilibrium radionuclide angiography (ERNA), and (iii) single-photon emission computed tomography (SPECT) ERNA. In practice, first-pass MUGA is limited to specific indications [right ventricular ejection fraction (RVEF) and shunt assessment 49,51 ], and only ERNA is used to assess CTRCD. ...
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... Currently, myocardial perfusion studies are acquired in a gated mode using an ECG trigger and separate computed tomography (CT) scans are performed for attenuation correction (available for SPECT/CT hybrid machines). This hybrid modality offers the evaluation of the ventricular volumes and function (including the regional contractility of the LV) with an improvement in the diagnostic accuracy of perfusion imaging [62]. ...
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... 74 years old man, with prostatic adenocarcinoma studied with equilibrium isotope ventriculoscintigraphy with [99mTc]NaTcO4labeled red blood cells (VEQ) 1 for evaluation of cardiac function, before starting treatment with cardiotoxic drugs (Figs. 1 and 2). In the parametric image of amplitude (white arrows) and phase (red arrows), an apical focus of a different color is visualized, suggesting delayed apical filling (B-C). ...
... Because of TTE's potential limitations in women, CMR is a useful alternative [127] to assess systolic and diastolic function and determine the type of HF. In chronic HF, ERNA is another option [132,136], although no longer mentioned in the latest European Society of Cardiology guidelines [114]. In case of HFrEF, the lower rate of ischemic origin in women stresses the importance of CMR with LGE to evaluate alternative etiologies, such as DCM, HCM, VHD [142], ARVC [144], myocarditis, sarcoidosis, and infiltrative diseases. ...
... In women with dyspnea and preserved systolic LVEF, an in-depth screen-ing for HFpEF must be considered, based on the four-step algorithm previously mentioned and established by the ESC [120,130]. Abbreviations: 18 [132]. However, scintigraphy tends to underestimate the value of LVEF compared to CMR in both sexes [133]. ...
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... An individual's EF measurement is not constant but varies, particularly as a function of the afterload and blood pressure (BP) (6)(7)(8). It is therefore generally recommended to record the bracial BP observed during individual EF measurements (9)(10)(11). ...
... Despite this limitation, EF remains extensively used to quantify LV systolic performance (1). The current recommendation therefore requires brachial BP to be reported for each EF measurement (9)(10)(11). The change in BP was a significant predictor of EF change but only for diastolic and mean BP levels. ...
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Introduction: This cardiovascular magnetic resonance (CMR) study aims to determine whether changes in systemic vascular resistance (SVR), obtained from CMR flow sequences, might explain the significant long-term changes in left ventricular (LV) ejection fraction (EF) observed in subjects with no cardiac disease history. Methods: Cohort subjects without any known cardiac disease but with high rates of hypertension and obesity, underwent CMR with phase-contrast sequences both at baseline and at a median follow-up of 5.2 years. Longitudinal changes in EF were analyzed for any concomitant changes in blood pressure and vascular function, notably the indexed SVR given by the formula: mean brachial blood pressure / cardiac output x body surface area. Results: A total of 118 subjects (53 ± 12 years, 52% women) were included, 26% had hypertension, and 52% were obese. Eighteen (15%) had significant EF variations between baseline and follow-up (7 increased EF and 11 decreased EF). Longitudinal changes in EF were inversely related to concomitant changes in mean and diastolic blood pressures ( p = 0.030 and p = 0.027, respectively) and much more significantly to SVR ( p < 0.001). On average, these SVR changes were −8.08 ± 9.21 and +8.14 ± 8.28 mmHg.min.m ² .L ⁻¹ , respectively, in subjects with significant increases and decreases in EF, and 3.32 ± 7.53 mmHg.min.m ² .L ⁻¹ in subjects with a stable EF (overall p < 0.001). Conclusions: Significant EF variations are not uncommon during the long-term CMR follow-up of populations with no evident health issues except for uncomplicated hypertension and obesity. However, most of these variations are linked to SVR changes and may therefore be unrelated to any intrinsic change in LV contractility. This underscores the benefits of specifically assessing LV afterload when EF is monitored in populations at risk of vascular dysfunction. Clinical Trial Registration: ClinicalTrials.gov , identifier: NCT01716819 and NCT02430805.
... Several techniques are currently available for this monitoring of LVEF [3,6]. Equilibrium radionuclide angiography (ERNA) is a well-validated non-invasive test [7], and in particular, cadmium-zinc-telluride single-photon emission tomography (CZT SPECT) radionuclide angiography ranks high, due to practicability, operator independency, and reproducibility [8][9][10]. ...
... This study successfully tested a combination of two equations for individualised dose planning in CZT ERNA, allowing for a reduction in the mean dose of at least 50% (to a mean effective dose of 1.6 mSv (range: 0.6 to 3.6 mSv)), without compromising the ability to produce reproducible analyses of LVEF. The average dose using a target count rate of 1.7 kcps is approximately half of the current recommendation for planar nuclear angiography [7,22], and as suggested possible by Duvall et al. [9]. Additionally, we found a level of the target count rate that minimises the need for a lower dose limit. ...
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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 of 99mTc-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.