Objectives: The goals of this study were to assess late clinical outcome and left ventricular ejection fraction (LVEF) after transmyocardial revascularization with CO(2) laser (TMR).

Background: During the 1990s TMR emerged as a treatment option for patients with refractory angina not eligible for conventional revascularization. Few reports exist on clinical effects and LVEF >3 years after TMR.

Methods: One hundred patients with refractory angina not eligible for conventional revascularization were block-randomized 1:1 to receive continued medical treatment or medical treatment combined with TMR. The patients were evaluated at baseline and after 3, 12 and 43 (range: 32 to 60) months with end points to angina, hospitalizations due to acute myocardial infarctions or unstable angina, heart failure and LVEF. Mortality was registered and MOS 36 Short-Form Health Survey answered at baseline and after 3, 6 and 12 months.

Results: Forty-three months after TMR, angina symptoms were still significantly improved, and unstable angina hospitalizations reduced by 55% (p < 0.001). Heart failure treatment (p < 0.01) increased, whereas the number of acute myocardial infarctions, LVEF and mortality was not affected. Quality of life was improved 3, 6 and 12 months after TMR.

Conclusions: Forty-three months after TMR, angina symptoms and hospitalizations due to unstable angina were significantly reduced, heart failure treatment increased and LVEF and mortality were seemingly unaffected.

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0735-1097(02)01828-4DOI Listing

Publication Analysis

Top Keywords

transmyocardial revascularization
12
unstable angina
12
heart failure
12
lvef mortality
12
revascularization co2
8
co2 laser
8
late clinical
8
patients refractory
8
angina
8
refractory angina
8

Similar Publications

New Directions in Coronary Revascularization for Refractory Angina: Gene Therapy and the Lizard Heart.

Semin Thorac Cardiovasc Surg

December 2024

Department of Surgery, Division of Cardiac Surgery, The Ohio State University, Columbus, Ohio.. Electronic address:

Refractory angina is a debilitating disease with limited therapeutic options that is primarily caused by microvascular dysfunction and desertification. Toward addressing this unmet need, microvascular revascularization therapy has progressively evolved from the lizard heart-inspired transmyocardial revascularization to precisely inducing vascular endothelial growth factor with gene therapy. Gene therapy with adenoviral vehicles or naked modified ribonucleic acid is safe and shows early signs of clinical promise but has not yet been proven effective due to gaps in optimization.

View Article and Find Full Text PDF

Background Coronary artery disease (CAD) is a global health burden, contributing to mortality and morbidity. A proportion of patients with CAD suffer from diffuse CAD, where conventional revascularization techniques such as percutaneous coronary intervention and coronary artery bypass grafting (CABG) may be insufficient to adequately restore myocardial perfusion. Transmyocardial revascularization (TMR) uses a laser to create microscopic channels in the myocardium, inducing inflammation, angiogenesis, and neovascularization to improve perfusion to ischemic regions.

View Article and Find Full Text PDF
Article Synopsis
  • Coronary artery disease is common and severely impacts the quality of life, particularly through stable angina pectoris, which can be hard to manage despite treatment efforts.
  • Enhanced external counterpulsation and coronary sinus reduction are among the promising techniques developed to improve blood flow and alleviate chronic angina, though clinical trials are limited in size.
  • Other approaches, such as transmyocardial laser revascularization and spinal cord stimulation, have shown disappointing results and are not recommended, while angiogenic therapies show potential but require more substantial research for validation.
View Article and Find Full Text PDF

Objective: We tested the hypothesis that targeted TMLR combined with intramyocardial injection of autologous CD 133 progenitor cells is safe and feasible in patients with chronic ischemic cardiomyopathy (ICM) and no revascularization options.

Methods: Eight male patients (age 62 ± 2.4 years) with multivessel severe ischemic heart disease and no revascularization options were enrolled.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!