What is the normal left ventricular (LV) longitudinal peak systolic strain average?

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Normal Left Ventricular Longitudinal Peak Systolic Strain Average

The normal left ventricular global longitudinal strain (GLS) average is between -18% and -22%, with a mean value of approximately -19.7% (more negative values indicate better function).

Understanding Left Ventricular Strain

Left ventricular (LV) longitudinal strain is a measure of myocardial deformation that assesses the function of longitudinal myocardial fibers, primarily located in the subendocardial layer. It is measured using speckle-tracking echocardiography (STE), which has become an important tool for evaluating subclinical cardiac dysfunction.

Normal Reference Values

According to comprehensive guidelines and meta-analyses:

  • The normal range for LV global longitudinal strain (GLS) is -15.9% to -22.1%, with a mean of -19.7% (95% CI, -20.4% to -18.9%) 1
  • Values better than (more negative than) -18% are generally considered normal 2
  • Values between -16% and -18% are considered borderline 2
  • Values worse than (less negative than) -16% are considered abnormal 2

The European Association of Cardiovascular Imaging (EACVI) guidelines indicate that LV GLS worse than -18% should be considered abnormal 3.

Factors Affecting Strain Measurements

Several factors can influence strain measurements:

  • Blood pressure: Meta-regression analysis has shown that systolic blood pressure is significantly associated with variations in normal GLS values 1
  • Heart rate: An inverse correlation exists between heart rate and GLS values (higher heart rates associated with lower absolute GLS values) 4
  • LV end-diastolic length: GLS is independently and inversely related to LV end-diastolic length 4
  • Age and gender: These have less consistent effects on strain measurements 1

Clinical Applications of Strain Measurement

Strain imaging provides valuable information in various clinical scenarios:

  • Subclinical LV dysfunction: Detecting early cardiac dysfunction in patients with preserved ejection fraction
  • Heart failure with preserved ejection fraction (HFpEF): GLS is often reduced despite normal LVEF 3
  • Cardiomyopathies: Distinguishing between physiological LVH in athletes from pathological LVH 3
  • Valvular heart disease: Monitoring LV function in conditions like aortic stenosis 5
  • Cardiotoxicity monitoring: Sequential follow-up during cardiotoxic treatments 2

Technical Considerations

When interpreting strain measurements, consider:

  • Vendor variability: Although reduced with modern software, some differences between vendors may exist
  • Image quality: High-quality images are essential for accurate strain measurements
  • Regional vs. global measurements: Global measurements are more reliable than regional strain values 2
  • Observer variability: Interobserver correlations for GLS (r = 0.71) are moderate compared to other measures of longitudinal function 4

Comparison with Other Measures of LV Function

  • GLS detects subtle changes in LV function before changes in ejection fraction become apparent
  • GLS correlates with other measures of longitudinal function such as mitral annular plane systolic excursion (MAPSE) and tissue Doppler-derived systolic velocity (s') 4, 5
  • In some clinical scenarios, MAPSE may provide similar diagnostic information to GLS and can be used when GLS is not available 5

Understanding normal strain values is essential for proper interpretation of cardiac function and early detection of subclinical myocardial dysfunction.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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