The Psychometric Performance of the Kansas City Cardiomyopathy Questionnaire-12 in Symptomatic Obstructive

Andrew J Sauer1, Charles F Sherrod1, Kensey L Gosch1

  • 1University of Missouri Kansas City's Healthcare Institute for Innovations in Quality and Saint Luke's Mid America Heart Institute, Kansas City, Missouri, USA.

Journal of Cardiac Failure
|September 30, 2024
PubMed

Insights

The 12-item Kansas City Cardiomyopathy Questionnaire (KCCQ-12) shows strong psychometric performance in obstructive hypertrophic cardiomyopathy (oHCM) patients. This validated tool is comparable to the KCCQ-23, supporting its use in clinical practice.

Area of Science:

  • Cardiology
  • Patient-Reported Outcomes
  • Clinical Assessment

Background:

  • Improving symptoms, function, and quality of life is key in obstructive hypertrophic cardiomyopathy (oHCM) care.
  • The 23-item Kansas City Cardiomyopathy Questionnaire (KCCQ-23) has established psychometric properties in oHCM.
  • The shorter 12-item KCCQ-12 is increasingly used but requires psychometric validation in oHCM.

Purpose of the Study:

  • To evaluate the psychometric properties of the KCCQ-12 in patients with oHCM.
  • To determine if the KCCQ-12 is a reliable and valid measure for assessing oHCM patients.

Main Methods:

  • Analysis of data from the EXPLORER-HCM clinical trial.
  • Assessment of KCCQ-12 domain and summary scores against clinical and patient-reported measures.
  • Evaluation of internal consistency, test-retest reliability, and responsiveness to clinical change.

Main Results:

  • KCCQ-12 scores showed moderate correlations with key clinical (NYHA class, exercise duration, VO2 max) and patient-reported outcomes (EQ-5D-5L, WPAI, HCMSQ).
  • Strong internal consistency and test-retest reliability were observed for KCCQ-12 domain scores.
  • The KCCQ-12 demonstrated significant and proportional changes with clinical improvements and showed close equivalence to KCCQ-23 scores.

Conclusions:

  • The KCCQ-12 exhibits good psychometric performance in patients with oHCM.
  • Its performance is comparable to the KCCQ-23.
  • The KCCQ-12 is a suitable tool for use in clinical practice for managing oHCM patients.
Abstract

Related Concept Videos

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...
1
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...
2
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,...
1
Mitral Stenosis II: Clinical features and Diagnostic Tests01:23

Mitral Stenosis II: Clinical features and Diagnostic Tests

Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
6
Acute Coronary Syndrome III: Diagnostic studies01:30

Acute Coronary Syndrome III: Diagnostic studies

Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...
3
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
2