Prognostic value of left-ventricular and peripheral vascular performance in patients with dilated cardiomyopathy

Tonino Bombardini1, Edoardo Nevola, Assuero Giorgetti

  • 1Consiglio Nazionale Ricerche (CNR), Institute of Clinical Physiology, Pisa, Italy.

Insights

In patients with idiopathic left-ventricular (LV) dysfunction, stress-induced increases in end-diastolic volume (EDV) and stroke volume indicate preserved pumping reserve. This finding offers powerful long-term death-risk stratification.

Area of Science:

  • Cardiology
  • Exercise Physiology
  • Heart Failure Research

Background:

  • The heart's primary role during exercise is to augment cardiac output to meet tissue metabolic demands.
  • Idiopathic left-ventricular (LV) dysfunction presents a challenge in maintaining adequate cardiac output.
  • Assessing the interplay of systolic and diastolic function is crucial for understanding cardiac output modulation in LV dysfunction.

Purpose of the Study:

  • To determine the relative contributions of systolic versus diastolic dysfunction in modulating cardiac output.
  • To investigate the mechanisms underlying cardiac output changes during exercise in patients with LV dysfunction.
  • To evaluate the prognostic significance of preserved LV functional reserve.

Main Methods:

  • 51 patients with idiopathic LV dysfunction (ejection fraction 36% ± 9%) and 24 controls were studied.
  • Exercise radionuclide angiography was used to assess LV functional reserve.
  • Patients were followed for a median of 129 months for clinical outcomes.

Main Results:

  • In controls, stroke volume increased via decreased end-systolic volume; in patients, it increased via end-diastolic volume (EDV) changes.
  • Patients with preserved stroke volume increase during stress (Group I) showed improved ventricular-arterial coupling and cardiac efficiency.
  • Group I had significantly better event-free survival (88%) compared to Group II (61%) (P = .03).

Conclusions:

  • Preserved LV pumping reserve in idiopathic LV dysfunction can be identified by stress-induced EDV and stroke volume variations.
  • These variations provide a powerful tool for long-term death-risk stratification in patients with LV dysfunction.
  • Understanding these mechanisms aids in managing heart failure and predicting patient outcomes.
Abstract

Related Concept Videos

Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
Imbalances in Cardiac Output01:26

Imbalances in Cardiac Output

The heart's primary function is to pump blood throughout the body, maintaining a balance between blood sent out (cardiac output) and blood returning (venous return). If this balance is disrupted, it can result in congestive heart failure (CHF), a severe condition where the heart becomes an inefficient pump, leading to inadequate blood circulation.
CHF can occur due to the failure of either side of the heart. Left-side failure leads to pulmonary congestion—the right side continues to send blood...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation01:21

Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation

Clinical manifestationsPeripheral Arterial Disease (PAD) manifests through a range of symptoms, from the characteristic intermittent claudication to atypical presentations and severe complications in advanced stages. Intermittent claudication, a hallmark symptom of PAD, presents as exercise-induced muscle pain that typically resolves within minutes of rest. This pain is reproducible and stems from inadequate blood flow, leading to the accumulation of lactic acid produced during anaerobic...
Aortic Regurgitation II: Clinical Features and Diagnostic Tests01:22

Aortic Regurgitation II: Clinical Features and Diagnostic Tests

Aortic valve regurgitation (AR) occurs when the aortic valve fails to close properly, allowing blood to flow backward from the aorta into the left ventricle. This backflow can result in two distinct clinical presentations: acute and chronic AR, each characterized by its own set of symptoms and physical findings.Acute Aortic RegurgitationAcute AR presents with a sudden onset of severe symptoms. Patients typically experience profound dyspnea (shortness of breath), chest pain, and signs of left...