Why the study?
Standard M-mode markers for left ventricular end-diastolic and end-systolic internal dimensions may not coincide with the true maximal or minimal chamber dimensions in dogs with myxomatous mitral valve disease, and the impact of alternative measurement methods on disease staging was unknown.
Do alternative M-mode echocardiographic timing methods (largest chamber diameter for LVIDd and minimum septal-to-free wall distance for LVIDs) alter left ventricular internal dimension measurements and disease staging compared to standard ACVIM-recommended methods in dogs with myxomatous mitral valve disease?
Observational (n=154)
Do alternative M-mode echocardiographic timing methods (largest chamber diameter for LVIDd and minimum septal-to-free wall distance for LVIDs) alter left ventricular internal dimension measurements and disease staging compared to standard ACVIM-recommended methods in dogs with myxomatous mitral valve disease?
Echocardiographic measurement timing significantly impacts LVIDd and LVIDs values in dogs with myxomatous mitral valve disease and could hypothetically alter ACVIM disease staging outcomes.
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M-mode LV measurements warrant caution in dogs with myxomatous mitral valve disease; leaves open validation of alternative echocardiographic standards.
INTRODUCTION/OBJECTIVES Echocardiographic assessment of myxomatous mitral valve disease (MMVD) includes measurement of the left ventricular internal dimension at the end-diastole (LVIDd) and at the end-systole (LVIDs), using established cardiac cycle markers. The LVIDd is measured at the QRS onset, which may not coincide with the maximal internal dimension. The LVIDs is obtained at maximum septal contraction, which in dogs with non-synchronous contraction (NSC) between the septal and free wall, may not correspond to the minimal internal dimension. This study investigates alternative measurement methods and their potential impact on MMVD staging. ANIMALS, MATERIALS AND METHODS A retrospective analysis of echocardiographic examinations from 154 dogs with MMVD was performed. Twenty-five dogs displayed NSC and were selected for LVIDs assessment. The LVIDd was measured at the onset of the QRS complex (method D1, recommended by the American College of Veterinary Internal Medicine [ACVIM]) and at the largest chamber diameter (method D2). In dogs with NSC, the LVIDs was measured using maximum septal contraction point (method S1) and minimum septal-to-free wall distance (method S2). RESULTS The LVIDd values were significantly lower with method D1 in 152 dogs (P<0.001). Using method D2, 12 dogs exceeded the the body-weight-normalized LVIDd threshold of 1.7. In NSC dogs, LVIDs values were significantly higher with method S1 (P<0.001). STUDY LIMITATIONS Limitations included operator subjectivity and observational NSC. CONCLUSIONS The measurement method influences LVIDd and LVIDs values. Although method D2 is not ACVIM- recommended, its application could hypothetically alter staging outcomes, highlighting the effect of measurement timing.
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Lobo et al. (2026) conducted an observational in Myxomatous mitral valve disease (MMVD) in dogs (n=154). Alternative M-mode measurement methods (largest chamber diameter [method D2] for LVIDd and minimum septal-to-free wall distance [method S2] for LVIDs) vs. Standard ACVIM-recommended M-mode measurement methods (QRS onset [method D1] for LVIDd and maximum septal contraction point [method S1] for LVIDs) was evaluated on Left ventricular internal dimension at end-diastole (LVIDd) and end-systole (LVIDs) (p=<0.001).
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