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经皮椎间孔镜手术后辅助补气活血汤治疗腰椎间盘突出症的临床效果

2019-04-21黄志和

中外医学研究 2019年29期
关键词:腰椎间盘突出症

黄志和

【摘要】 目的:分析经皮椎间孔镜手术后辅助补气活血汤在腰椎间盘突出症治疗中的应用。方法:选择笔者所在医院收治的109例腰椎间盘突出症患者为研究对象,分为常规组、联合组,均给予常规经皮椎间孔镜手术治疗,联合组术后辅助补气活血汤治疗。结果:联合组术后4周腰椎功能优于常规组(P<0.05)。联合组术后4周生活质量及自理能力均优于常规组(P<0.05)。结论:经皮椎间孔镜手术后辅助补气活血汤用于腰椎间盘突出症的治疗,可促进患者腰椎功能的恢复,为其生活质量及自理能力的改善提供支持。

【关键词】 经皮椎间孔镜手术 补气活血汤 腰椎间盘突出症

doi:10.14033/j.cnki.cfmr.2019.29.020 文献标识码 B 文章编号 1674-6805(2019)29-00-03

[Abstract] Objective: To analyze the application of Buqi Huoxue Decoction in the treatment of lumbar disc herniation after percutaneous transforaminal endoscopy. Method: A total of 109 patients with lumbar intervertebral disc herniation admitted to our hospital were divided into the routine group and the combined group. They were treated with routine percutaneous transforaminal endoscopy and the combined group was supplementary Buqi Huoxue Decoction after percutaneous transforaminal endoscopy. Result: The lumbar function of combined group was better than that of routine group 4 weeks after operation (P<0.05). The quality of life and self-care ability of the combined group were better than those of the conventional group 4 weeks after operation (P<0.05). Conclusion: Supplementary Buqi Huoxue Decoction after percutaneous transforaminal endoscopy for the treatment of lumbar disc herniation can promote the recovery of lumbar function and provide support for the improvement of quality of life and self-care ability.

[Key words] Percutaneous transforaminal endoscopic surgery Buqi Huoxue Decoction Lumbar disc herniation

First-authors address: Fuzhou Gulou Hospital, Fuzhou 350000, China

作为一类常见的骨科疾病,腰椎间盘突出症的典型特征为:影响患者的活动功能[1]。如这一疾病未得到及时干预,患者的生活质量及自理能力均可能受到影响。经皮椎间孔镜手术是临床治疗腰椎间盘突出症的主要方法,其可于椎间孔镜引导下,纠正椎间盘的异常解剖结构[2]。补气活血汤作为经典中医方剂,其具有良好的补气、活血化瘀功效[3]。为验证经皮椎间孔镜手术后辅助补气活血汤治疗的价值,本研究主要针对109例患者进行分析。

1 资料与方法

1.1 一般资料

选择笔者所在医院于2018年1月-2019年2月收治的109例腰椎间盘突出症患者为研究对象。纳入标准:符合腰椎间盘突出症诊断标准。排除标准:(1)入组前2周内接受过其他治疗;(2)依从性差;(3)不耐受手术。依据治疗方法的异同,分为常规组(52例)和联合组(57例)。常规组男30例,女22例;年龄40~59岁,平均(49.3±8.7)岁;病程2~5年,平均(3.6±0.8)年。联合组男32例,女25例;年龄41~59岁,平均(49.5±8.8)岁;病程3~5年,平均(3.7±0.7)年。两组性别、年龄、病程比较,差异无统计学意义(P>0.05)。患者对本研究知情同意,且签署知情同意书。

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