Istomina E V, Shikhkerimov R K
State budgetary healthcare institution 'City polyclinic #166 of Moscow Healthcare Department', Moscow, Russia.
Zh Nevrol Psikhiatr Im S S Korsakova. 2019;119(3):12-15. doi: 10.17116/jnevro201911903112.
To study the efficacy and safety of chondroitin sulfate (mucosat) in the treatment of chronic lower back pain.
The medical documentation of 46 outpatients with chronic lumbosacral dorsalgia, who received 25 intramuscular injections of 2 ml mucosat, was studied. The assessment of patients' condition and efficacy and safety of the treatment was conducted based on the data of four visits (1-st, 10-th and 25-th day and 3 months after the end of treatment). Results of the clinical-neurological examination, pain intensity at rest and at movement according to the Visual Analogue Scale (VAS) and the severity of Lasegue and Wasserman signs and limitation of movements in the lumbar spine were taken into account.
The use of mucosat at a dose of 2 ml intramuscularly 1 time in 2 days led to a significant decrease in the severity of pain syndrome and increased mobility in the lumbar spine (before treatment, the level of pain at rest according to the VAS was 4.22±1.28 scores, on the 25-th day 2.13±0.24, 3 month after treatment 2.37±0.31; the level of pain at movement: 5.78±1.15; 4.56±0.47; 4.78±0.22, respectively (p<0.01). There were a reduction of the dose of previously used non-steroidal anti-inflammatory drugs in the end of treatment and maintenance of the results of therapy for 3 months after the end of treatment. Good tolerability of the drug and the absence of significant side-effects were shown as well.
This study showed the efficacy and safety of chondroitin sulfate (mucosat) in the treatment of outpatients with chronic lower back pain.
研究硫酸软骨素(mucosat)治疗慢性下腰痛的疗效和安全性。
对46例慢性腰骶部疼痛门诊患者的医疗记录进行研究,这些患者接受了25次2ml mucosat的肌肉注射。根据四次就诊(治疗第1天、第10天、第25天以及治疗结束后3个月)的数据对患者病情、治疗的疗效和安全性进行评估。考虑了临床神经学检查结果、根据视觉模拟量表(VAS)评估的静息和运动时的疼痛强度、拉塞格征和瓦瑟曼征的严重程度以及腰椎活动受限情况。
每两天肌肉注射2ml mucosat可使疼痛综合征的严重程度显著降低,并增加腰椎活动度(治疗前,根据VAS静息时疼痛水平为4.22±1.28分,第25天时为2.13±0.24分,治疗后3个月为2.37±0.31分;运动时疼痛水平分别为:5.78±1.15分;4.56±0.47分;4.78±0.22分(p<0.01)。治疗结束时,先前使用的非甾体抗炎药剂量减少,且治疗结束后3个月疗效得以维持。该药物耐受性良好,未出现明显副作用。
本研究表明硫酸软骨素(mucosat)治疗慢性下腰痛门诊患者具有疗效和安全性。