中国肿瘤临床
中國腫瘤臨床
중국종류림상
CHINESE JOURNAL OF CLINICAL ONCOLOGY
2014年
20期
1307-1311
,共5页
丁远远%姚鹏%兰培丽%马佳明%王志彬%洪涛
丁遠遠%姚鵬%蘭培麗%馬佳明%王誌彬%洪濤
정원원%요붕%란배려%마가명%왕지빈%홍도
芬太尼贴%加巴喷丁%癌性神经病理性疼痛
芬太尼貼%加巴噴丁%癌性神經病理性疼痛
분태니첩%가파분정%암성신경병이성동통
transdermal fentanyl%gabapentin%malignant neuropathic pain
目的:探讨芬太尼贴联合加巴喷丁治疗癌性神经病理性疼痛的临床疗效。方法:选择确诊为癌性神经病理性疼痛患者60例,随机分为单纯芬太尼贴治疗组(对照组)与芬太尼贴联合加巴喷丁组(联合组)。对照组对以前用过强阿片类药物的患者根据用药情况进行剂量转换,逐渐增量,直至疼痛缓解VAS<3分或爆发痛<3次;联合组在使用芬太尼贴的基础上加用加巴喷丁,初始剂量为100 mg 3次/日,逐渐增加剂量,直至疼痛缓解,但总用量≤2400 mg/日。观察治疗前、治疗后1、2、3和4W的VAS评分、生活质量评分(QOL)、疼痛缓解程度、阿片类药物的使用量及不良反应。结果:治疗后对照组与联合组VAS评分均有下降(P<0.05),联合组更明显(P<0.05);QOL两组较治疗前均有改善(P<0.05),联合组改善显著(P<0.05);对照组总有效率为83.3%,联合组为96.7%;联合组阿片类药物使用量较对照组明显减少,药物的不良反应明显降低P<0.05)。结论:芬太尼贴联合加巴喷丁治疗癌性神经病理性疼痛疗效显著,安全性高,不良反应低,值得临床推广。
目的:探討芬太尼貼聯閤加巴噴丁治療癌性神經病理性疼痛的臨床療效。方法:選擇確診為癌性神經病理性疼痛患者60例,隨機分為單純芬太尼貼治療組(對照組)與芬太尼貼聯閤加巴噴丁組(聯閤組)。對照組對以前用過彊阿片類藥物的患者根據用藥情況進行劑量轉換,逐漸增量,直至疼痛緩解VAS<3分或爆髮痛<3次;聯閤組在使用芬太尼貼的基礎上加用加巴噴丁,初始劑量為100 mg 3次/日,逐漸增加劑量,直至疼痛緩解,但總用量≤2400 mg/日。觀察治療前、治療後1、2、3和4W的VAS評分、生活質量評分(QOL)、疼痛緩解程度、阿片類藥物的使用量及不良反應。結果:治療後對照組與聯閤組VAS評分均有下降(P<0.05),聯閤組更明顯(P<0.05);QOL兩組較治療前均有改善(P<0.05),聯閤組改善顯著(P<0.05);對照組總有效率為83.3%,聯閤組為96.7%;聯閤組阿片類藥物使用量較對照組明顯減少,藥物的不良反應明顯降低P<0.05)。結論:芬太尼貼聯閤加巴噴丁治療癌性神經病理性疼痛療效顯著,安全性高,不良反應低,值得臨床推廣。
목적:탐토분태니첩연합가파분정치료암성신경병이성동통적림상료효。방법:선택학진위암성신경병이성동통환자60례,수궤분위단순분태니첩치료조(대조조)여분태니첩연합가파분정조(연합조)。대조조대이전용과강아편류약물적환자근거용약정황진행제량전환,축점증량,직지동통완해VAS<3분혹폭발통<3차;연합조재사용분태니첩적기출상가용가파분정,초시제량위100 mg 3차/일,축점증가제량,직지동통완해,단총용량≤2400 mg/일。관찰치료전、치료후1、2、3화4W적VAS평분、생활질량평분(QOL)、동통완해정도、아편류약물적사용량급불량반응。결과:치료후대조조여연합조VAS평분균유하강(P<0.05),연합조경명현(P<0.05);QOL량조교치료전균유개선(P<0.05),연합조개선현저(P<0.05);대조조총유효솔위83.3%,연합조위96.7%;연합조아편류약물사용량교대조조명현감소,약물적불량반응명현강저P<0.05)。결론:분태니첩연합가파분정치료암성신경병이성동통료효현저,안전성고,불량반응저,치득림상추엄。
Objective:To observe the effect of transdermal fentanyl combined with gabapentin for the treatment of malignant neu-ropathic pain (MNP). Methods:A total of 60 patients with MNP were randomly divided into two groups. A total of 30 cases in the con-trol group received transdermal fentanyl according to the dosages of opioid medicine that patients used. Such dosages were gradually in-creased until the pain relief visual analogue scale (VAS) fell below 3 or until the times of breakthrough pain became less than 3. For the combined group, gabapentin was co-administered with transdermal fentanyl, similar to the control group. Initially, 100 mg of gabapen-tin was administered thrice a day. This dosage was gradually increased until pain relief. However, gabapentin dosages were kept below 2,400 mg a day. VAS, quality of life (QOL), degree of pain relief, dosages of fentanyl and morphine, and side effects were evaluated be-fore treatment and at one, two, three, and four weeks after the treatment. Results:Both groups exhibited lower VAS after treatment (P<0.05), but the difference was observed to be more significant in the combined group than that in the control group (P<0.05). Both groups exhibited improved QOL (P<0.05), which was observed to be more significant in the combined group than in the control group (P<0.05). The effective rate was 96.7%in the combined group and 83.3%in the control group. The dosage of opioid medicine and the side effects in the combined group were less than those in the control group. Conclusion:Transdermal fentanyl combined with gabapen-tin is effective for the treatment of malignant neuropathic pain.