The aim of the present study is to investigate the effects of pentoxifylline on left ventricular
ejection fractions (EF) and volumes, New York Heart Association (NYHA) functional
class, left ventricular diastolic parameters and hospitalization for heart failure in patients
with ischemic or non-ischemic cardiomyopathy. A total of 60 patients were randomised
to either peroral 1200 mg/day pentoxifylline or control group. All patients were on optimal
heart failure therapy and their EF was <40% by transthoracic echocardiography. The
patients were followed up for 12 months. Twenty-one patients (70%) in pentoxifylline
group and 20 (66.7%) in control group completed the study. Baseline and 12 months’
end-diastolic volume, end-systolic volume, EF and NYHA class were as follows in pentoxifylline
group; 160.5±51.3 mL vs 156.6±43.1 mL, 109.1±40 mL vs 106.1±33.4 mL,
32.4±5.7% vs 33.2±5.2%, 2.4±0.5 vs 2.2±0.5, p=0.5411, 0.5257, 0.4099 and 0.1037; respectively.
There were also no difference in baseline and follow-up diastolic parameters.
Mean hospitalization numbers for heart failure were similar between groups (1.26±0.71
vs 1.60±1.04, p=0.1717). Contrary to previous reports, no beneficial effect of pentoxifylline
was observed on clinical or echocardiographic parameters.
Birincil Dil | İngilizce |
---|---|
Konular | Sağlık Kurumları Yönetimi |
Bölüm | Basic Medical Sciences |
Yazarlar | |
Yayımlanma Tarihi | 5 Haziran 2014 |
Gönderilme Tarihi | 27 Temmuz 2012 |
Yayımlandığı Sayı | Yıl 2014 Cilt: 31 Sayı: 1 |
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