Table 3.
Echocardiographic parameters characterizing patients with heart failure (HF) symptoms and normal or preserved left ventricular ejection fraction (LVEF) in left atrial (LA) phenotype
Echocardiographic parameter | Normal ranges—cut offs | Methodological aspects | Mandatory to determine (methods) | Why worth to do in routine |
---|---|---|---|---|
LA parameters and parameters of diastolic function | ||||
LAD—left atruial diameter (mm) |
♂ 31–39 Cut off < 39 ♀ 28–37 Cut off < 37 [85] |
“Old” parameter, which can only be used in normal LA geometry | No—only if LA dimensions are documented as normal | To document LA dimension—if LA geometry is normal |
LAD/BSA (mm/m2) |
♂ 13–23 Cut off < 23 ♀ 14–24 Cut off < 24 [85] |
“Old” parameter, which can only be used in normal LA geometry | No—only if LA dimensions are documented as normal | To document LA dimension—if LA geometry is normal |
LAVImax—maximum LA volume indexed to BSA (ml/m2) |
♂ 18–35 Cut off < 39 ♀ 18–36 Cut off < 38 (Cut off < 34) |
Avoid foreshortening, prefer triplane analysis or 3D volumetry. Increased LA volume predicts increased LV filling pressure | Yes | To document chronic diseases due to impaired LV filling |
LAVImin—minimum LA volume indexed to BSA (ml/m2) |
♂ 8–18 Cut off < 18 ♀ 18–18 Cut off < 18 [6] |
Avoid foreshortening, prefer triplane analysis or 3D volumetry. Increased LAVImin predicts impaired active LA contractility | Yes—under certain conditions | To document impact on active LA contraction on global LA function |
Total LA emptying fraction (LAEF) (%) |
51–61 Cut off > 38 [112] |
Avoid foreshortening, prefer triplane analysis or 3D volumetry. Reduced LA emptying fraction indicates LA dysfunction | Yes-—under certain conditions | To characterize LA function |
Average LA reservoir strain—reservoir LAS (%): LA reservoir function |
31–42 Cut off > 23 [89] |
LA strain analysis is only possible if image quality is adequate. 4ChV is usually used for LA strain analysis | Yes—especially in normal or LV phenotype—helpful to detect subclinical states of cardiac diseases | To characterize global LA function |
Passive LA conduit strain—passive LAS (%): LA conduit function |
15–23 Cut off > 11 [89] |
LA strain analysis is only possible if image quality is adequate. 4ChV is usually used for LA strain analysis | Yes—especially in normal or LV phenotype—helpful to detect subclinical states of cardiac diseases | To characterize passive LA filling properties |
Active LAS contraction strain—active LAS (%): LA contraction function |
14–21 Cut off > 8 [89] |
LA strain analysis is only possible if image quality is adequate. 4ChV is usually used for LA strain analysis | Yes—especially in normal or LV phenotype—helpful to detect subclinical states of cardiac diseases | To characterize active LA contractility |
LA stiffness—E/E´ devided by LAEF (%−1) |
0.13–0.17 Cut off < 0.27 [89] |
Standardize the Doppler assessment with respect to breathing to ensure comparability in follow-ups | No—especially in normal or LV phenotype—helpful in suspected infiltrative/storage diseases | To detect causes of LA stiffness by conventional parameters |
LA stiffness—E/E´ devided by LAS (%−1) |
0.18–0.29 Cut off < 0.55 [89] |
Standardize the Doppler assessment with respect to breathing to ensure comparability in follow-ups | No—especially in normal or LV phenotype—helpful in suspected infiltrative/storage diseases | To detect causes of LA stiffness using speckle tracking |
E-peak E-wave velocity (cm/sec) |
♂ 42–116 Cut off > 42 ♀ 43–115 Cut off > 43 [110] |
Acquire the pw Doppler spectra using Duplex mode to control correct positioning of the sample volume at the level of mitral valve (MV) coaptation | Yes—to differentiate between normal, abnormal relaxation, pseudo-normal, and restrictive | E reflects LA-LV gradient during early diastole |
Peak A-wave velocity (cm/sec) |
♂ 25–93 Cut off > 25 ♀ 29–93 Cut off > 29 [110] |
Acquire the pw Doppler spectra using Duplex mode to control correct positioning of the sample volume | Yes—to differentiate between normal, abnormal relaxation, pseudo-normal, and restrictive | A reflects LA-LV gradient during late diastole |
Transmitral A-duration (msec) |
100–176 Cut off > 100 |
Acquire an additional pw Doppler spectrum of blood LV inflow at the level of mitral anulus (MA). Time speed must be100mm/sec to ensure sufficient temporal resolution | Yes—especially in normal or LV phenotype | To be able to compare forward and retrograde LA blood flow during LA contraction |
Transmitral E/A ratio |
♂ 0.62–2.34 cut off > 0.62 ♀ 0.32–2.44 cut off > 0.32 [110] |
Acquire the pw Doppler spectrum with sharp contours (possibly highest Doppler frequencies) with a sample volume in the central blood stream of LV inflow | Yes—- to differentiate between normal, abnormal relaxation, pseudo-normal, and restrictive | To distinguish between impaired LV relaxation, pseudonormal conditions, and LV restriction |
Edt—E-wave deceleration time (msec) |
♂ 78–302 cut off > 78 ♀ 99–275 cut off > 99 [110] |
Acquire the pw Doppler spectrum with sharp contours (possibly highest Doppler frequencies) with a sample volume in the central blood stream of LV inflow | Yes- especially in normal or LV phenotype | To detect impaired LV relaxation and LV stiffness |
IVRT—isovolumetric relaxation time (msec) |
73–101 cut off ≤ 70 |
Acquire an additional pw Doppler spectrum with the sample volume positioned at the anterior mitral leaflet. IVRT estimates relaxation (τ) | Yes—especially in normal or LV phenotype | Prolonged in impaires relaxation; shortened if LAP increases |
L-wave (transmitral velocity spectrum and tissue doppler spectra) |
Qualitative sign of diastolic dysfunction |
The L-wave is documented in the transmitral pw Doppler spectrum and in the LV tissue Doppler spectra | Yes | If present, indicates increased LVEDP |
Peak E´-velocity basal septal (cm(sec) |
♂ 6–11 Cut off > 6 ♀ 5–10 Cut off > 5 [110] |
Acquire the pw tissue Doppler spectra using Duplex mode to control proper sample volume positioning of. Try to center the LV septum for optimal image quality | Yes | E´ includes LV relaxation, restoring forces and LV filling pressure |
Peak E´-velocity basal lateral [cm (sec)] |
♂ 5–16 Cut off > 5 ♀ 5–14 Cut off > 5 [110] |
Acquire the pw tissue Doppler spectra using Duplex mode to control proper sample volume positioning. Try to center the later LV segment for optimal image quality | Yes | E´ includes LV relaxation, restoring forces and LV filling pressure |
Average E/E´ratio |
< 8 normal 8–14 borderline > 14 pathological |
Check the respective positions of the sample volumes and standardize both documentation to comparable breathing periods | Yes | To estimate LVEDP. E/E’reflects normal or pathological relaxation |
TE´-E—time interval between E´- and E-onset (msec) |
0–8 Cut off > 8 [113] |
The estimation is within the limit of detection. Significant differences of time intervals in Doppler spectra can be detected by intervals > 20 ms | Optional—it can be used as a qualitative sign of diastolic dysfunction | TE´-E can distinguish between restriction (prolonged) and constriction (normal) |
IVRT/TE´-E ratio |
> 2 [113] |
The estimation should only be performed if TE´-E is > 20 | Optional—but helpful to detect increased LVEDP | If ratio is < 2, PCWP and LAP are increased |
ArD—retrograde pulmonary vein Ar-duration (msec) |
53–173 Cut off Ar < A |
Acquire pw Doppler spectrum using low pulse repetition frequency (LPRF). Prefer time speed of the spectrum at 100 mm/sec or more to ensure sufficient temporal resolution | Yes—especially in normal or LV phenotype | Prolonged ArD indicates diastolic dysfunction an increased VEDP |
Peak Ar velocity (cm/s) |
− 11to − 39 Cut off < 35 |
Acquire pw Doppler spectrum using LPRF. Try to increase contour sharpness by increasing Doppler frequencies in the range of LPRF | Yes—especially in normal or LV phenotype | Increased Ar velocity indicates increased VEDP |
Transmitral A duration–Ar duration |
0–20 cut Off < 30 |
For optimal documentation of sample volume position at the levels of MV coaptation and MA acquire both spectra using Duplex mode | Yes—especially in normal or LV phenotype |
Prolonged A—Ar indicates increased LVEDP |
Vp—left ventricular diastolic flow propagation (cm/sec) |
Cut off ≥ 50 |
Vp correlates with LV relaxation and the invasive parameter (τ. Adjust color Doppler setting and prefer time speed of the spectrum at 100 mm/sec or more | Yes—especially in normal or LV phenotype | Decreased Vp indicates LVEDP increase |
E/Vp ratio (sec) |
Cut off ≤ 2.5 |
Perform Measure E and Vp in transmitral pw spectra and mitral flow color M-modes at standardized comparable breathing intervals | Yes—especially in normal or LV phenotype | E/Vp correlates with LAP and PCWP. Decreased E/Vp indicates increases of LAP and PCWP |
For each echocardiographic parameter the normal ranges (and cut offs), methodological aspects, the importance of its determination, and the value to determine it in routine are listed. Mandatory parameters to be determined in clinical practice are labeled in bold print
LAD left atrial diameter, BSA body surface area, LAVImax maximum LA volume indexed to BSA, LA left atrial, LAVImin minimum LA volume indexed to BSA, LAEF total LA emptying fraction, LAS left atrial strain, E maximum early mitral flow velocity, E´ maximum early tissue Doppler lengthening velocity of the myocardium near to the mitral anulus, A maximum forward transmitral atrial flow velocity, Edt E-wave deceleration time, IVRT isovolumetric relaxation time, L flow velocity peak of transmitral flow during diastasis, TE´-E Time interval between E´ and E-onset, ArD retrograde pulmonary vein flow duration, Vp left ventricular diastolic flow propagation