Zick Suzanna M, Gillespie Brenda, Aaronson Keith D
Department of Family Medicine, University of Michigan, Ann Arbor, MI 48104, USA.
Eur J Heart Fail. 2008 Jun;10(6):587-93. doi: 10.1016/j.ejheart.2008.04.008. Epub 2008 May 19.
To examine whether hawthorn (Crataegus Special Extract WS 1442 {CSE}) inhibits progression in heart failure (HF) patients.
We performed a retrospective analysis of data from the HERB CHF study in which patients with mild to moderate HF were randomised to either CSE 900 mg or placebo for 6 months. The primary outcome was time to progression of HF (HF death, hospitalisation, or sustained increase in diuretics) as assessed by log-rank tests and by Cox modelling.
Progression of HF occurred in 46.6% of the CSE and 43.3% of the placebo groups (OR 1.14, 95% CI=0.56, 2.35: p=0.86). Patients receiving CSE were 3.9 times (95% CI=1.1-13.7: p=0.035) more likely to experience HF progression at baseline. In adjusted analysis, the risk of having early HF progression in the CSE group increased to 6.4 (95% CI=1.5, 26.5: p=0.011). In patients with LVEF< or =35%, those taking CSE were at significantly greater risk (3.2, 95% CI=1.3, 8.3: p=0.02) than the placebo group.
CSE does not reduce heart failure progression in patients who have HF. CSE appears to increase the early risk of HF progression.
研究山楂(山楂特殊提取物WS 1442 {CSE})是否能抑制心力衰竭(HF)患者病情进展。
我们对HERB CHF研究的数据进行了回顾性分析,该研究将轻至中度HF患者随机分为CSE 900毫克组或安慰剂组,为期6个月。主要结局是通过对数秩检验和Cox模型评估的HF进展时间(HF死亡、住院或利尿剂持续增加)。
CSE组中46.6%的患者出现HF进展,安慰剂组为43.3%(比值比1.14,95%置信区间=0.56,2.35:p = 0.86)。接受CSE治疗的患者在基线时发生HF进展的可能性高3.9倍(95%置信区间=1.1 - 13.7:p = 0.035)。在调整分析中,CSE组早期发生HF进展的风险增加至6.4(95%置信区间=1.5,26.5:p = 0.011)。在左心室射血分数(LVEF)≤35%的患者中,服用CSE的患者比安慰剂组的风险显著更高(3.2,95%置信区间=1.3,8.3:p = 0.02)。
CSE不能降低HF患者的心力衰竭进展。CSE似乎会增加HF进展的早期风险。