首页|加巴喷丁联合血液灌流治疗老年维持性血液透析合并中重度不宁腿综合征患者的疗效分析

加巴喷丁联合血液灌流治疗老年维持性血液透析合并中重度不宁腿综合征患者的疗效分析

扫码查看
目的 观察加巴喷丁联合血液灌流治疗老年维持性血液透析合并中重度不宁腿综合征(RLS)患者的疗效.方法 40 例老年维持性血液透析合并中重度RLS患者,随机分为观察组和对照组,各 20 例.两组患者每周均行 2 次常规血液透析,1 次血液透析联合血液灌流治疗.观察组每晚口服加巴喷丁.比较两组治疗前后国际不宁腿综合征评定量表(IRLS)评分、匹兹堡睡眠指数量表(PSQI)评分、简明健康状况调查量表(SF-36)评分及实验室检查指标[甲状旁腺激素(iPTH)、血β2 微球蛋白(β2-MG)]水平,观察不良反应发生情况.结果 对照组治疗 1 周后IRLS评分较本组治疗前无改善(P>0.05);对照组治疗 4、8 周后IRLS评分较本组治疗期前降低,差异有统计学意义(P<0.05).观察组治疗 1、4、8 周后IRLS评分均较本组治疗前降低,且观察组治疗 1、4、8 周后IRLS评分(13.40±3.17)、(6.40±2.46)、(4.60±0.84)分低于对照组的(20.10±5.55)、(16.60±5.02)、(12.20±4.76)分,差异有统计学意义(P<0.05).治疗后,两组PSQI评分均较本组治疗前下降,且观察组PSQI评分(5.20±1.75)分低于对照组的(7.00±1.15)分,差异有统计学意义(P<0.05).治疗前,两组生理机能(PF)、生理职能(RP)、情感职能(RE)、社会功能(SF)、躯体疼痛(BP)、精力(VT)、精神健康(MH)和一般健康状况(GH)、健康变化(HT)评分及总分比较,差异无统计学意义(P>0.05).治疗后,对照组RE、VT评分及总分高于本组治疗前,差异有统计学意义(P<0.05);观察组RP、RE、SF、VT、MH、GH、HT评分及总分高于本组治疗前,差异有统计学意义(P<0.05).治疗后,观察组RE、SF、VT、MH评分及总分分别为(80.00±17.21)、(50.00±10.21)、(37.50±9.20)、(80.80±7.25)、(528.90±33.01)分,高于对照组的(60.00±21.08)、(38.75±12.43)、(29.00±7.38)、(72.20±10.17)、(437.65±36.73)分,差异有统计学意义(P<0.05).治疗前后,两组iPTH及β2-MG水平组间及组内比较差异无统计学意义(P>0.05).治疗后对照组无不良反应.观察组口服加巴喷丁治疗 1 周时出现 2 例嗜睡,1 例头晕,症状轻微均可耐受;1 例出现嗜睡伴双下肢无力、共济失调,行脑CT检查排除脑血管病,加巴喷丁渐减量,患者症状缓解,继续治疗.治疗 4 周时观察组1 例患者加巴喷丁调整药量至 300 mg/次、q.d.后出现嗜睡、头晕、恶心,症状可耐受.结论 加巴喷丁联合血液灌流能够快速有效缓解老年维持性血液透析患者RLS症状,并改善患者睡眠和生活质量,且耐受性良好.
Efficacy of gabapentin combined with hemoperfusion in the treatment of moderate to severe restless legs syndrome in elderly patients undergoing maintenance hemodialysis
Objective To observe the efficacy of gabapentin combined with hemoperfusion in the treatment of moderate to severe restless legs syndrome(RLS)in elderly patients undergoing maintenance hemodialysis.Methods 40 elderly patients with maintenance hemodialysis complicated with moderate to severe RLS were randomly divided into an observation group and a control group,with 20 cases in each group.Both groups were treated with conventional hemodialysis twice a week,and hemodialysis combined with hemoperfusion once a week.The observation group took gabapentin orally every night.The scores of International Restless Leg Syndrome Rating Scale(IRLS),Pittsburgh Sleep Quality Index(PSQI),36-Item Short-Form Health Survey(SF-36)and laboratory examination indicators[intact parathyroidism hormone(iPTH)and β2-microglobulin(β2-MG)]before and after treatment.Results IRLS score of the control group was not improved after 1 week of treatment compared with that before treatment in this group(P>0.05).IRLS scores in the control group after 4 and 8 weeks of treatment were lower than those before treatment in this group,and the difference was statistically significant(P<0.05).After 1,4 and 8 weeks of treatment,IRLS scores in the observation group were lower than those before treatment in this group;IRLS scores in the observation group were(13.40±3.17),(6.40±2.46)and(4.60±0.84)points,which were lower than(20.10±5.55),(16.60±5.02)and(12.20±4.76)points in the control group;the difference was statistically significant(P<0.05).After treatment,PSQI scores in both groups decreased compared with those before treatment in this group,and the observation group had lower PSQI score of(5.20±1.75)points than(7.00±1.15)points in the control group.The difference was statistically significant(P<0.05).Before treatment,there was no significant difference between the two groups in the scores of physical functioning(PF),role-physical(RP),role-emotional(RE),social functioning(SF),bodily pain(BP),vitality(VT),mental health(MH),general health(GH)and health transition(HT)and total scores(P>0.05).After treatment,RE and VT scores and total scores in the control group were higher than those before treatment in this group,and the difference was statistically significant(P<0.05).RP,RE,SF,VT,MH,GH,HT scores and total scores in the observation group were higher than those before treatment in this group,and the difference was statistically significant(P<0.05).After treatment,the RE,SF,VT and MH scores and total scores in the observation group were(80.00±17.21),(50.00±10.21),(37.50±9.20),(80.80±7.25)and(528.90±33.01)points,which were higher than(60.00±21.08),(38.75±12.43),(29.00±7.38),(72.20±10.17)and(437.65±36.73)points in the control group.The difference was statistically significant(P<0.05).Before and after treatment,there was no significant difference in iPTH and β2-MG levels between and within the two groups(P>0.05).There were no adverse reactions in the control group after treatment.In the observation group,there were 2 cases of drowsiness and 1 case of dizziness occurred after 1 week of oral gabapentin treatment,and the symptoms were mild and tolerable.1 case showed drowsiness accompanied by weakness of both lower limbs and ataxia.Brain CT examination was performed to rule out cerebrovascular disease,gabapentine gradually decreased,and the patient's symptoms were relieved and treatment continued.After 4 weeks of treatment,1 patient in the observation group had drowsiness,dizziness and nausea after adjusting the dosage of gabapentin to 300 mg/time,q.d,and the symptoms were tolerable.Conclusion Gabapentin combined with hemoperfusion can quickly and effectively relieve the RLS symptoms in elderly patients undergoing maintenance hemodialysis,and improve their sleep and quality of life,and it is well tolerated.

Restless legs syndromeGabapentinHemoperfusionHemodialysisOld age

朱虹、徐明成、闻君君

展开 >

100044 北京市西城区展览路医院血液净化中心

不宁腿综合征 加巴喷丁 血液灌流 血液透析 老年

2024

中国实用医药
中国康复医学会

中国实用医药

影响因子:0.797
ISSN:1673-7555
年,卷(期):2024.19(9)
  • 33