دورية أكاديمية

Final results of a phase IIa, randomised, open-label trial to evaluate the percutaneous intramyocardial transplantation of autologous skeletal myoblasts in congestive heart failure patients: the SEISMIC trial.

التفاصيل البيبلوغرافية
العنوان: Final results of a phase IIa, randomised, open-label trial to evaluate the percutaneous intramyocardial transplantation of autologous skeletal myoblasts in congestive heart failure patients: the SEISMIC trial.
المؤلفون: Duckers HJ; Thoraxcenter, Erasmus University Medical Center, Rotterdam, The Netherlands. h.duckers@erasmusmc.nl, Houtgraaf J, Hehrlein C, Schofer J, Waltenberger J, Gershlick A, Bartunek J, Nienaber C, Macaya C, Peters N, Smits P, Siminiak T, van Mieghem W, Legrand V, Serruys PW
المصدر: EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology [EuroIntervention] 2011 Feb; Vol. 6 (7), pp. 805-12.
نوع المنشور: Clinical Trial, Phase II; Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Société Europa édition Country of Publication: France NLM ID: 101251040 Publication Model: Print Cited Medium: Internet ISSN: 1969-6213 (Electronic) Linking ISSN: 1774024X NLM ISO Abbreviation: EuroIntervention Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Toulouse : Société Europa édition, c2005-
مواضيع طبية MeSH: Heart Failure/*therapy , Myoblasts, Skeletal/*transplantation, Adult ; Aged ; Amiodarone/therapeutic use ; Anti-Arrhythmia Agents/therapeutic use ; Arrhythmias, Cardiac/complications ; Arrhythmias, Cardiac/drug therapy ; Cells, Cultured ; Disease Progression ; Electrocardiography, Ambulatory ; Exercise Tolerance ; Female ; Heart Failure/physiopathology ; Humans ; Injections ; Male ; Middle Aged ; Myocardium ; Stroke Volume ; Transplantation, Autologous/adverse effects ; Transplantation, Autologous/methods ; Ventricular Function, Left
مستخلص: Aims: The SEISMIC study was an open-label, prospective, randomised study to assess the safety and feasibility of percutaneous myoblast implantation in heart failure patients with implanted cardioverter-defibrillators (ICD).
Methods and Results: Patients were randomised 2:1 to autologous skeletal myoblast therapy vs. optimal medical treatment. The primary safety end-point was defined as the incidence of procedural and device related serious adverse events, whereas the efficacy endpoints were defined as the change in global LVEF by MUGA scan, change in NYHA classification of heart failure and in the distance achieved during a six-minute walk test (6MW) at 6-month follow-up. Forty subjects were randomised to the treatment arm (n=26), or to the control arm (n=14). There were 12 sustained arrhythmic events and one death after episodes of ventricular tachycardia (VT) in the treatment group and 14 events in the control group (P=ns). At 6-month follow-up, 6MW distance improved by 60.3±54.1?meters in the treated group as compared to no improvement in the control group (0.4±185.7?meters; P=ns). In the control group, 28.6% experienced worsening of heart failure status (4/14), while 14.3% experienced an improvement in NYHA classification (2/14). In the myoblast-treatment arm, one patient experienced a deterioration in NYHA classification (8.0%), whereas five patients improved one or two classes (20.0%; P=0.06). However, therapy did not improve global LVEF measured by MUGA at 6-month follow-up.
Conclusions: These data indicate that implantation of myoblasts in patients with HF is feasible, appears to be safe and may provide symptomatic relief, though no significant effect was detected on global LVEF.
التعليقات: Comment in: EuroIntervention. 2011 Feb;6(7):789-93. (PMID: 21252009)
المشرفين على المادة: 0 (Anti-Arrhythmia Agents)
N3RQ532IUT (Amiodarone)
تواريخ الأحداث: Date Created: 20110122 Date Completed: 20110511 Latest Revision: 20131121
رمز التحديث: 20240628
DOI: 10.4244/EIJV6I7A139
PMID: 21252013
قاعدة البيانات: MEDLINE
الوصف
تدمد:1969-6213
DOI:10.4244/EIJV6I7A139