NYU School of Medicine, Departments of Anesthesiology and Psychiatry, Norman Marcus Pain Institute, New York, New York 10016, USA.
Pain Med. 2010 Jan;11(1):25-34. doi: 10.1111/j.1526-4637.2009.00752.x. Epub 2009 Dec 9.
A comprehensive protocol is presented to identify muscular causes of regional pain syndromes utilizing an electrical stimulus in lieu of palpation, and combining elements of Prolotherapy with trigger point injections.
One hundred seventy-six consecutive patients were evaluated for the presence of muscle pain by utilizing an electrical stimulus produced by the Muscle Pain Detection Device. The diagnosis of "Muscle Pain Amenable to Injection" (MPAI), rather than trigger points, was made if pain was produced for the duration of the stimulation. If MPAI was found, muscle tendon injections (MTI) were offered to patients along with post-MTI physical therapy, providing neuromuscular electrical stimulation followed by a validated exercise program [1]. A control group, evaluated 1 month prior to their actual consultation/evaluation when muscle pain was identified but not yet treated, was used for comparison.
Forty-five patients who met criteria completed treatment. Patients' scores on the Brief Pain Inventory decreased an average of 62%; median 70% (P < 0.001) for pain severity and 68%; median 85% (P < 0.001) for pain interference one month following treatment. These changes were significantly greater (P < 0.001) than those observed in the untreated controls.
A protocol incorporating an easily reproducible electrical stimulus to diagnose a muscle causing pain in a region of the body followed by an injection technique that involves the entirety of the muscle, and post injection restoration of muscle function, can successfully eliminate or significantly reduce regional pain present for years.
提出一种综合方案,利用电刺激代替触诊,结合增生疗法和触发点注射的元素,来识别区域疼痛综合征的肌肉原因。
利用肌肉疼痛探测装置产生的电刺激,对 176 例连续患者进行肌肉疼痛评估。如果刺激持续期间产生疼痛,则做出“可注射肌肉疼痛”(MPAI)的诊断,而不是触发点。如果发现 MPAI,则向患者提供肌肉肌腱注射(MTI)以及 MTI 后的物理治疗,提供神经肌肉电刺激,然后是经过验证的锻炼计划[1]。评估时已经存在肌肉疼痛但尚未治疗的对照组在实际就诊/评估前 1 个月进行评估,用于比较。
符合标准的 45 名患者完成了治疗。患者的简明疼痛量表评分平均下降 62%;中位数 70%(P<0.001)疼痛严重程度和 68%;中位数 85%(P<0.001)疼痛干扰一个月后治疗。这些变化明显大于(P<0.001)未治疗对照组。
一种方案包括一种易于复制的电刺激来诊断身体某一区域引起疼痛的肌肉,然后是一种涉及整个肌肉的注射技术,以及注射后肌肉功能的恢复,可以成功消除或显著减轻多年存在的区域疼痛。