Point of Maximal Impulse at the 6th Intercostal Space
A point of maximal impulse (PMI) located at the 6th intercostal space at the mid-clavicular line indicates left ventricular enlargement and requires immediate echocardiographic evaluation to assess for dilated cardiomyopathy, left ventricular hypertrophy, or other structural cardiac pathology. 1
Clinical Significance
Lateral and inferior displacement of the apical impulse beyond the normal 5th intercostal space inside the mid-clavicular line strongly suggests left ventricular enlargement. 1 The American College of Cardiology states that lateral displacement of the apical impulse beyond the mid-clavicular line is a key physical finding for left ventricular enlargement. 1
Differential Diagnosis
The 6th intercostal space location indicates one of several pathological conditions:
Dilated cardiomyopathy is a primary consideration when the PMI is displaced laterally and inferiorly, as reported by the European Society of Cardiology. 1
Left ventricular hypertrophy from chronic pressure overload (hypertension, aortic stenosis) causes displacement of the apical impulse, according to the American Heart Association. 1
Chronic volume overload states including severe mitral regurgitation or aortic regurgitation can produce this finding. 1
In hypertrophic cardiomyopathy, a prominent point of maximal impulse is typically present, shifted laterally and either bifid or trifid, with the PMI often displaced. 2
Initial Investigations
Physical Examination Details
Beyond PMI location, assess these specific findings:
Measure the diameter of the apical impulse: A diameter ≥4.0 cm is 96% sensitive and 96% specific for left ventricular dilatation. 3
Assess the quality of the impulse: A sustained apical impulse indicates pressure overload (aortic stenosis, hypertension), while a hyperdynamic impulse suggests volume overload or high-output states. 1
Evaluate for parasternal heave/lift, which suggests right ventricular hypertrophy or enlargement. 1
Auscultate for a fourth heart sound (S4), which indicates a noncompliant left ventricle and is commonly present in hypertrophic cardiomyopathy. 2
Perform provocative maneuvers (Valsalva, standing from squatting) to assess for dynamic left ventricular outflow tract obstruction if hypertrophic cardiomyopathy is suspected. 2
Diagnostic Testing Algorithm
1. Transthoracic Echocardiography (First-Line, Mandatory)
Echocardiography is recommended as the initial evaluation in all patients with suspected cardiac enlargement based on PMI displacement. 2
Assess left ventricular dimensions, wall thickness, systolic function (ejection fraction), and diastolic function. 2
Evaluate for regional wall motion abnormalities suggesting prior myocardial infarction. 2
Measure left ventricular outflow tract gradient at rest and with provocative maneuvers if hypertrophic cardiomyopathy is suspected. 2
Assess mitral valve anatomy and function, particularly for mitral regurgitation. 2
2. 12-Lead Electrocardiogram
Obtain to assess for left ventricular hypertrophy voltage criteria, pathological Q waves, or conduction abnormalities. 2
Ensure proper lead placement: V4 should be at the 5th intercostal space in the midclavicular line, with V5 and V6 at the horizontal plane of V4. 2
Inferior placement of V5 and V6 in the 6th intercostal space or lower can alter amplitudes used in diagnosing ventricular hypertrophy and should be avoided. 2
3. Additional Testing Based on Echocardiographic Findings
Cardiac biomarkers (troponin, BNP/NT-proBNP) if acute decompensation or ischemia is suspected. 2
Cardiac MRI for tissue characterization if infiltrative disease (amyloidosis, sarcoidosis) or myocarditis is suspected based on echocardiographic findings. 2
Coronary angiography if ischemic cardiomyopathy is the suspected etiology. 2
Genetic testing if hypertrophic cardiomyopathy or familial dilated cardiomyopathy is diagnosed. 2
Common Pitfalls to Avoid
Do not dismiss PMI displacement as a normal variant: Research demonstrates that in the full left lateral position, the lateral margin of the apex beat in healthy adults is located in a 3-cm-wide area from the left anterior axillary line towards the mid-clavicular line, not beyond it. 3
Obesity, emphysema, or thick chest walls may obscure the apical impulse even when cardiac enlargement is present, so absence of a palpable PMI does not exclude cardiomegaly. 1
Avoid confusing ECG lead misplacement with actual cardiac pathology: Inferior placement of precordial leads can simulate or mask ventricular hypertrophy. 2
Management Priorities
The management strategy depends entirely on the underlying etiology identified by echocardiography, but initial steps include:
Assess volume status and optimize diuretic therapy if heart failure with volume overload is present. 2
Initiate guideline-directed medical therapy for heart failure with reduced ejection fraction if dilated cardiomyopathy is confirmed. 2
Control hypertension aggressively if left ventricular hypertrophy from pressure overload is identified. 2
Refer to cardiology for consideration of septal reduction therapy (surgical myectomy or alcohol septal ablation) if symptomatic hypertrophic cardiomyopathy with outflow tract obstruction is diagnosed. 2
Evaluate for implantable cardioverter-defibrillator if left ventricular systolic dysfunction is severe or if hypertrophic cardiomyopathy with high-risk features for sudden cardiac death is present. 2