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Assessment of Right Ventricular Structure and Function in Mouse Model of Pulmonary Artery Constriction by Transthoracic Echocardiography
Published on: February 3, 2014
Defining minimal detectable difference in echocardiographic measures of right ventricular function in systemic
Monica Mukherjee1, Valentina Mercurio2, Aparna Balasubramanian2
1Divisions of Cardiology, Johns Hopkins University, 1830 E. Monument Street, Room 540, Baltimore, MD, 21205, USA.
Two-dimensional echocardiography (2DE) shows minimal measurement error in systemic sclerosis (SSc) patients with pulmonary arterial hypertension (PAH). This establishes reliable 2DE parameters for PAH screening and treatment monitoring in SSc.
Area of Science:
- Cardiology
- Rheumatology
- Medical Imaging
Background:
- Two-dimensional echocardiography (2DE) is crucial for screening and monitoring pulmonary arterial hypertension (PAH) in systemic sclerosis (SSc).
- Establishing the reliability and reproducibility of 2DE parameters is essential for accurate patient assessment.
Purpose of the Study:
- To determine the reliability, repeatability, and reproducibility of 2DE parameters in SSc patients with and without PAH.
- To define the minimal detectable difference (MDD) for these echocardiographic measures.
Main Methods:
- Systemic sclerosis patients with and without PAH underwent 2DE at two time points.
- Statistical analyses included ANOVA, coefficients of variation (CV), intraclass correlation, and Bland-Altman analysis.
- MDD was calculated using the standard error of measurement for each parameter.
Main Results:
- Most 2DE parameters demonstrated minimal differences between evaluations.
- Global right ventricular longitudinal systolic strain (GRVLSS) and fractional area change (FAC) showed the largest CVs.
- Excellent intra- and inter-observer agreement was observed, with defined MDD values for key parameters like TAPSE, FAC, and RVSP.
Conclusions:
- Clinically significant 2DE measures in SSc patients with/without PAH exhibit minimal measurement error.
- Defined MDD values are vital for accurate PAH screening, therapeutic response assessment, and clinical trial design in SSc.
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