Acupuncture treatment for post-thoracotomy pain syndrome
Acupuncture treatment for post-thoracotomy pain syndrome
批准号:
7282665
负责人:
BARRIE R. CASSILETH
金额:
$13.3万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-01 至 2009-08-31
关键词:
Acupuncture procedureAcuteAffectBrief Pain InventoryCancer PatientCancer SurvivorChronicClinicalEffectivenessEnd PointExcisionHospitalsInterventionIntervention StudiesMalignant neoplasm of lungMethodsModalityNeedlesOperative Surgical ProceduresOpioidOpioid AnalgesicsPainPatientsPilot ProjectsPlacebo ControlPlacebosPlantsPost TechnicPostoperative PainQuality of lifeRandomizedRandomized Controlled Clinical TrialsRandomized Controlled TrialsRateRefractoryResearchSafetyScoreSurgeonSurvivorsSymptomsSyndromeTechniquesTestingThoracotomyVertebral columnWeekclinically relevantdayimprovedpainful neuropathyprospective
中文摘要
描述(由申请人提供):背景:开胸术后疼痛综合征影响许多肺癌患者和幸存者。在一些患者中,尽管目前可用治疗,但症状持续时间长且难治性,对他们的生活质量产生重大影响。针灸可以是一种有效的补充方式在某些类型的疼痛管理。癌症患者的术后疼痛和神经性疼痛都被证明对针灸治疗有反应。我们已经进行了一项试点研究,测试在围手术期植入小皮内针灸针以减少开胸术后疼痛的可行性。我们发现,在目前的临床实践环境中,干预是可行的,并受到患者和外科医生的好评。
目的:我们建议进行一项随机对照研究,以进一步评估这种针刺技术对开胸术后疼痛综合征的有效性。具体目的是1)确定与安慰剂相比,使用皮内针灸针的针灸是否减少了开胸术后慢性疼痛; 2)确定与安慰剂相比,使用皮内针灸针的针灸是否减少了开胸术后急性疼痛。
方法:对140例开胸手术的癌症患者进行前瞻性、随机、安慰剂对照的针刺干预研究。小的皮内针灸针或安慰剂针在手术前将主要沿着脊柱放置。针在原位停留总共四周。将在基线和术后评价疼痛数字评定量表、简明疼痛量表(BPI)、阿片类和非阿片类镇痛药的使用。主要比较的是真针组和安慰剂组在第30天的BPI评分。
意义:开胸术后疼痛综合征是肺癌外科治疗的一种难治性后遗症。这项拟议中的研究将测试针灸的有效性,一种补充方式,在治疗这种症状。如果结果是有希望的,我们将提出一个大的,多机构的随机试验。这项研究有可能导致一种新的治疗选择,以改善癌症患者和癌症幸存者的生活质量。
英文摘要
DESCRIPTION (provided by applicant): Background: Post-thoracotomy pain syndrome affects many lung cancer patients and survivors. In some patients, the symptom is long-lasting and refractory despite currently available treatment, having a significant impact on their quality of life. Acupuncture can be an effective complementary modality in the management of certain types of pain. Both post-operative pain and neuropathic pain in cancer patients have been shown to respond to acupuncture treatment. We have conducted a pilot study testing the feasibility of planting small intradermal acupuncture needles perioperatively to reduce post-thoracotomy pain. We found the intervention feasible in the current clinical practice setting and well received by patients and surgeons.
Objectives: We propose to conduct a randomized controlled study to further evaluate the effectiveness of such acupuncture technique for post-thoracotomy pain syndrome. The specific aims are to 1) determine whether acupuncture using intradermal acupuncture needles reduces chronic post-thoracotomy pain compared to placebo; 2) determine whether acupuncture using intradermal acupuncture needles reduces acute post-thoracotomy pain compared to placebo.
Methods: A prospective, randomized placebo-controlled intervention study of acupuncture in 140 cancer patients undergoing thoracotomy. Small intradermal acupuncture needles or placebo needles will be placed mainly along the spine prior to surgery. The needles stay in place for a total of four weeks. Numerical rating scale of pain, Brief Pain Inventory (BPI), use of opioids and non-opioids analgesics will be evaluated at baseline and postoperatively. The primary comparison is BPI scores at Day 30 between the true acupuncture group and the placebo acupuncture group.
Significance: Post-thoracotomy pain syndrome is a difficult-to-treat sequela of surgical treatment of lung cancer. The proposed study will test the effectiveness of acupuncture, a complementary modality, in treating this symptom. If results are promising, we would propose a large, multi-institutional randomized trial. The research has the potential of leading to a new treatment option to improve the quality of life of cancer patients and cancer survivors.
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Acupuncture treatment for post-thoracotomy pain syndrome
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