[Long-term outcome of patients with hypertrophic obstructive cardiomyopathy post percutaneous transluminal septal

S W Zheng1, H Y Shi1, J J Dai1

  • 1Department of Cardiology, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai 200030, China.

Insights

Percutaneous transluminal septal ablation (PTSMA) offers a safe and effective treatment for hypertrophic obstructive cardiomyopathy (HOCM), demonstrating long-term survival rates comparable to surgical myectomy. Age over 65 is identified as a risk factor for mortality post-PTSMA.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Cardiac Surgery

Background:

  • Hypertrophic obstructive cardiomyopathy (HOCM) is a significant cause of morbidity and mortality.
  • Percutaneous transluminal septal ablation (PTSMA) and surgical myectomy are primary treatment options for HOCM.
  • Long-term outcomes comparing PTSMA and surgical myectomy require further evaluation.

Purpose of the Study:

  • To evaluate the long-term outcomes of patients with HOCM treated with PTSMA.
  • To compare the efficacy and survival rates of PTSMA versus surgical myectomy in HOCM patients.
  • To identify risk factors associated with mortality after PTSMA in HOCM.

Main Methods:

  • Retrospective analysis of 104 HOCM patients undergoing PTSMA and 32 undergoing surgical myectomy.
  • Comparison of clinical data, procedural details, and complications between groups.
  • Multivariate Cox regression and Kaplan-Meier survival analysis were used to assess outcomes and risk factors.

Main Results:

  • PTSMA achieved an immediate success rate of 66%.
  • Long-term survival rates at 5, 10, and 15 years post-PTSMA were 90.1%, 78.3%, and 56.9% respectively.
  • Age ≥ 65 years was an independent risk factor for all-cause death (HR=2.697, P=0.020); no significant difference in survival rates was found between PTSMA and surgical myectomy groups (P > 0.05).

Conclusions:

  • PTSMA is a safe and effective treatment for HOCM.
  • Long-term survival following PTSMA is comparable to that of surgical myectomy.
  • Age is a critical factor influencing mortality risk in HOCM patients treated with PTSMA.

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...
278
Cardiomyopathy VII: Pre and Post Operative Nursing Management01:28

Cardiomyopathy VII: Pre and Post Operative Nursing Management

Patients with hypertrophic cardiomyopathy (HCM) and left ventricular outflow tract (LVOT) obstruction who remain symptomatic despite optimal medical therapy may undergo a septal myectomy (Morrow procedure). This procedure involves excising a portion of the hypertrophied septum below the aortic valve using a heart-lung machine to improve blood flow through the LVOT. Effective preoperative and postoperative nursing management ensures successful patient outcomes, minimizes complications, and...
199
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...
219
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,...
335