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1.
Clin Cardiol ; 27(5): 295-9, 2004 May.
Article in English | MEDLINE | ID: mdl-15188947

ABSTRACT

BACKGROUND: The number of patients awaiting heart transplantation is increasing in proportion to the waiting period for a donor. Studies have shown that coenzyme Q10 (CoQ10) has a beneficial effect on patients with heart failure. HYPOTHESIS: The purpose of the present double-blind, placebo-controlled, randomized study was to assess the effect of CoQ10 on patients with end-stage heart failure and to determine if CoQ10 can improve the pharmacological bridge to heart transplantation. METHODS: A prospective double-blind design was used. Thirty-two patients with end-stage heart failure awaiting heart transplantation were randomly allocated to receive either 60 mg U/day of Ultrasome--CoQ10 (special preparation to increase intestinal absorption) or placebo for 3 months. All patients continued their regular medication regimen. Assessments included anamnesis with an extended questionnaire based partially on the Minnesota Living with Heart Failure Questionnaire, 6-min walk test, blood tests for atrial natriuretic factor (ANF) and tumor necrosis factor (TNF), and echocardiography. RESULTS: Twenty-seven patients completed the study. The study group showed significant improvement in the 6-min walk test and a decrease in dyspnea, New York Heart Association (NYHA) classification, nocturia, and fatigue. No significant changes were noted after 3 months of treatment in echocardiography parameters (dimensions and contractility of cardiac chambers) or ANF and TNF blood levels. CONCLUSIONS: The administration of CoQ10 to heart transplant candidates led to a significant improvement in functional status, clinical symptoms, and quality of life. However, there were no objective changes in echo measurements or ANF and TNF blood levels. Coenzyme Q10 may serve as an optional addition to the pharmacologic armamentarium of patients with end-stage heart failure. The apparent discrepancy between significant clinical improvement and unchanged cardiac status requires further investigation.


Subject(s)
Cardiotonic Agents/therapeutic use , Heart Failure/drug therapy , Ubiquinone/analogs & derivatives , Ubiquinone/therapeutic use , Adult , Aged , Atrial Natriuretic Factor/blood , Coenzymes , Double-Blind Method , Exercise Tolerance , Female , Heart Failure/blood , Heart Failure/diagnostic imaging , Heart Transplantation , Humans , Male , Middle Aged , Prospective Studies , Quality of Life , Recovery of Function , Severity of Illness Index , Tumor Necrosis Factor-alpha/metabolism , Ultrasonography , Waiting Lists
2.
Ann Thorac Surg ; 76(5): 1523-7, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14602280

ABSTRACT

BACKGROUND: High-quality postoperative imaging of bypass conduits is essential when evaluating different types of conduits, anastomoses, and surgical techniques. We investigated the potential value of the newest generation of multidetector-row computer tomographic scanners in assessing bypass grafts. METHODS: From June to September 2002, 14 patients underwent scanning with a newly released 16-slice computed tomographic scanner (Mx8000 IDT; Philips Medical Systems) after coronary artery bypass grafting. Four patients had had minimally invasive direct coronary artery bypass grafting and 3, redo coronary artery revascularization. Contrast-enhanced computed tomographic angiography was performed using retrospective electrocardiographic gating. Scan length was 22 to 30 cm, and total scan time was 27 to 37 seconds. RESULTS: Of the 14 patients, 8 were scanned within 1 week after operation and 6, 1 month to 12 months postoperatively. Average heart rate during the scan was 82 beats per minute (range, 60 to 97 beats per minute), and all patients were able to hold their breath for the required time. Thirty conduits were studied: 26 arterial (18 in situ left and right internal mammary artery grafts, five free right internal mammary and radial artery grafts, and three in situ right gastroepiploic artery grafts) and four vein grafts. Excellent visualization of all 30 grafts was achieved. Thirty-four of the 35 distal anastomoses were patent; one vein graft was occluded. CONCLUSIONS: This new technology is a promising noninvasive measure to evaluate patency of bypass conduits, including the gastroepiploic artery where catheterization is usually difficult. The ability to display the vessel wall as well as its lumen might distinguish radial artery spasm from intimal hyperplasia. The superb resolution and increased scan length required to cover the entire internal mammary artery grafts-from origin to distal anastomoses-can be achieved easily in a single breath-holding owing to the increased number of slices per rotation and shortening of the gantry rotation time.


Subject(s)
Coronary Artery Bypass/methods , Coronary Disease/diagnostic imaging , Graft Occlusion, Vascular/diagnostic imaging , Magnetic Resonance Angiography/methods , Monitoring, Physiologic/methods , Aged , Cohort Studies , Coronary Disease/surgery , Female , Follow-Up Studies , Graft Rejection , Graft Survival , Humans , Male , Middle Aged , Postoperative Care/methods , Sensitivity and Specificity , Tomography, X-Ray Computed/methods , Vascular Patency/physiology
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