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Primary benign back pain: supplementation with Pycnogenol?.

机译:原发性良性背痛:补充碧萝芷?。

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Back pain (BP) is one of the most common problems seen by general practitioners. The aim of this pilot registry study was to evaluate the effects of Pycnogenol~(?)(French Maritime Pine Bark extract) on pain, mobility and muscle spasm in patients with recurring episodes of back pain without any other clinical condition. The registry follow-up lasted 3 weeks. Subjects used either SM (standard management), including mild exercise and 3 days of resting or immobilization - or SM+Pycnogenol~(?)200 mg/day (4 cps/day). Eighty-two subjects were included in the study, 23 took Pycnogenol~(?)and 59 were in the SM group. No safety problems or tolerability problems were observed with Pycnogenol~(?)or with the SM. The two groups, SM and SM+Pycnogenol~(?), were comparable at inclusion. A prevalent localization to the lower part of the back/spine was observed in all patients of both groups. The improvement in Karnofsky performance status Scale - expressing the global physical capacity of the individuals - during the 3 weeks of follow-up was significantly higher and faster in the Pycnogenol~(?)group (P<0.05) compared to SM. Patients were able to restart physical training in 3 weeks with Pycnogenol~(?)(in comparison with 4.5 weeks with SM only). The decrease in back pain score (VASL score) was faster and more pronounced with Pycnogenol~(?)(P<0.05) compared to SM. Oxidative stress was significantly reduced in subjects using Pycnogenol~(?)(P<0.05) while it remained elevated in the control group. The use of the rescue medication doses (ibuprofen) was significantly higher in the SM only (P<0.05) in comparison with SM+Pycnogenol~(?). Pycnogenol~(?)appears to be an effective and safe supplementary management in healthy subjects with idiopathic BP. Mobility, pain, general physical capacity and oxidative stress improved in only a week with further improvements up to 4 weeks in most patients; results appear to be better and faster with Pycnogenol~(?)supplementation than with SM alone.
机译:背痛 (BP) 是全科医生最常见的问题之一。这项试点登记研究的目的是评估碧萝芷~(?)(法国海洋松树皮提取物)对反复发作的背痛患者没有任何其他临床状况的疼痛、活动能力和肌肉痉挛的影响。登记处随访持续了 3 周。受试者使用 SM(标准管理),包括轻度运动和 3 天的休息或固定 - 或 SM+碧萝芷~(?)200 毫克/天(4 cps/天)。本研究共纳入82名受试者,其中23名服用碧萝芷~(?)SM组59例。碧萝芷未发现安全问题或耐受性问题~(?)或使用 SM。SM和SM+碧萝芷~(?)两组在纳入时具有可比性。在两组的所有患者中都观察到普遍的背部/脊柱下部定位。在3周的随访中,Karnofsky体能状态量表(表示个体的整体身体能力)的改善在碧萝芷中明显更高,更快~(?)组(P<0.05)与SM组相比,患者在3周内能够重新开始碧萝芷的体能训练~(?)(与仅 SM 的 4.5 周相比)。碧萝芷组背痛评分(VASL评分)下降更快、更明显~(?)(P<0.05)与SM相比,使用碧萝芷的受试者氧化应激显著降低~(?)(P<0.05),而对照组仍保持升高。与SM+碧萝芷~(?)相比,SM中仅使用急救药物剂量(布洛芬)显著高于(P<0.05)。碧萝芷~(?)对于患有特发性血压的健康受试者来说,似乎是一种有效且安全的补充管理。 活动能力、疼痛、一般体能和氧化应激在短短一周内得到改善,大多数患者的进一步改善长达 4 周;使用碧萝芷的结果似乎更好更快~(?)补充比单独使用SM更好。

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