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Tolerability and effectiveness of every-other-day atorvastatin compared to daily atorvastatin in patients with muscle symptoms: A randomized controlled clinical trial

机译:与肌肉症状患者的每日阿托伐他汀相比每隔一天的阿托伐他汀的耐受性和有效性:随机对照临床试验

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摘要

Despite limited evidence, non-daily dosing of statins is recommended for managing muscle symptoms associated with statin therapy. We assessed the tolerability and effectiveness of every-other-day atorvastatin compared to daily atorvastatin in patients having muscle symptoms associated with atorvastatin therapy. A parallel-group, outcome-assessment-blinded, randomized controlled clinical trial was conducted at Colombo South Teaching Hospital, Sri Lanka. Patients with muscle pain, tenderness or cramps alone or in combination for ≥2 weeks while on daily atorvastatin for ≥1 month, with no alternative cause, were recruited. Patient's regular atorvastatin dose was given every-other-day to those in intervention group (IG) and daily to those in control group (CG). Primary outcomes were assessed at 24 weeks and included composite of myalgia and myositis, LDL-cholesterol level and percentage reduction of LDL-cholesterol from baseline. Number recruited was 49 to IG (women:79.6%; mean-age:60.6 ± 8.7years) and 52 to CG (women:73.1%; mean-age:61.7 ± 9.8years). Mean atorvastatin dose per day was 8.6 mg (SD = 4 mg) and 17.6 mg (SD = 8.4 mg) in IG and CG, respectively. Composite of myalgia and myositis at 24 weeks was 79.6% in IG and 69.2% in CG (OR = 1.7, 95% CI 0.7–4.3; p = 0.234). IG failed to show noninferiority for mean LDL-cholesterol (difference:0.31 mmol/L; upper limit 97.5% CI:0.61 mmol/L; p for noninferiority = 0.989) and for mean percentage reduction of LDL-cholesterol from baseline (difference:3.13%; upper limit 97.5% CI:15.5%; p for noninferiority = 0.718). At 24 weeks, mean creatine kinase and discomfort due to muscle symptoms (assessed with Visual Analogue Scale) were not different between the two groups. Findings of this study do not favor every-other-day atorvastatin as an option for managing patients with muscle symptoms associated with atorvastatin therapy.
机译:尽管有限的证据,建议使用他汀类药物的非日常剂量用于管理与他汀类药物治疗相关的肌肉症状。我们评估了每隔一天阿托伐他汀的耐受性和有效性与与阿托伐他汀治疗相关的肌肉症状的患者的日常阿托伐他汀相比。在科伦坡南教学医院,斯里兰卡科伦坡南教学医院进行了平行组,结果评估盲目的随机对照临床试验。患有肌肉疼痛,柔软或痉挛的患者或组合≥2周,同时在日常阿托伐他汀≥1个月,没有替代原因,被招募。患者的常规阿托伐他汀剂量为干预组(Ig)中的每隔一天给予,每天给予对照组(CG)。在24周内评估了主要结果,包括肌痛和肌炎,LDL-胆固醇水平和从基线的LDL-胆固醇的百分比。招募的数量为49岁(妇女:79.6%;卑鄙的年龄:60.6±8.7岁)和52至Cg(妇女:73.1%;卑鄙的年龄:61.7±9.8岁)。 IG和CG的平均Atorvastatin剂量每天每天为8.6mg(Sd = 4mg)和17.6mg(Sd = 8.4mg)。肌痛和肌炎的综合在24周的24周内为Ig的79.6%,Cg的69.2%(或= 1.7,95%CI 0.7-4.3; P = 0.234)。 Ig未能显示出平均LDL-胆固醇的非闭合性(差异:0.31mmol / L;上限97.5%CI:0.61mmol / L; f for NonInferiority = 0.989),从基线的LDL-胆固醇的平均百分比减少(差异:3.13 %;上限97.5%CI:15.5%;对于非金属突变度= 0.718)。在24周,两组之间的平均肌肉激酶和由于肌肉症状(评估)之间的不适在两组之间没有差异。本研究的结果不利于每隔除法过量伐他汀作为管理与阿托伐他汀治疗相关的肌肉症状的患者的选择。

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