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Sonography-guided trigger point injections in abdominal myofascial pain syndrome

机译:腹部肌菌疼痛综合征的超声波造影触发点注射

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摘要

Even though chronic abdominal pain is 1 of the most common reasons for hospital visits, diagnostic testing is often time-consuming and treatment is inadequate. Abdominal myofascial pain syndrome (AMPS) is usually not included as a differential diagnosis, but it should be considered in cases of chronic abdominal pain. The purpose of this study was to investigate the clinical characteristics of AMPS and to assess the effect of sonography-guided trigger point injections (TPI). A total of 100 patients with AMPS from 2012 to 2018 were retrospectively evaluated for clinical characteristics and TPI effects. AMPS was diagnosed using Srinivasan and Greenbaum's criteria, and the TPIs were performed at intervals of 2 to 4 weeks. The Visual Analog Scale (VAS) ratio was calculated by subtracting the final VAS from the initial VAS score and dividing it by the initial VAS score after injections, and the patients were divided into 4 groups: non-responders, mild, moderate, and good responders. The median duration of pain was 12 months, and the median number of hospital visits before TPI was 2. Of the 100 patients, 66 (66%) were categorized as good responders, 11 (11%) as moderate responders, 7 (6.9%) as mild responders, and 16 (15.7%) as non-responders. When the initial and final VAS scores were compared, the sonography-guided injections were found to be effective in alleviating pain ( P .001). Moreover, patients who received the injections 2 or more times tended to have more significant pain reduction than those who received a single injection ( P .001). Patients with AMPS suffer from long-term pain and undergo many hospital visits and diagnostic tests. TPI with lidocaine can be an effective and safe treatment for patients with chronic AMPS.
机译:尽管慢性腹痛是医院访问的最常见原因,但诊断测试通常是耗时的,并且治疗不足。腹部肌筋膜疼痛综合征(AMPS)通常不包括鉴别诊断,但应在慢性腹痛的情况下考虑。本研究的目的是研究安培的临床特征,并评估超声波引导触发点注射(TPI)的效果。回顾性评估了2012年至2018年2012年至2018年的100名AMPS患者进行临床特征和TPI效应。使用Srinivasan和Greenbaum标准诊断为AMPS,TPI以2至4周的间隔进行。通过从初始VAS评分中减去最终VAS来计算视觉模拟量表(VAS)比率,并通过注射后的初始VAS分数将其分成4组:非响应者,轻度,中等和良好的患者响应者。疼痛的中位数是12个月,TPI前的医院访问量中位数为2。在100名患者中,66名(66%)分类为良好的响应者,11(11%)为中度响应者,7(6.9%) )作为轻度响应者,16(15.7%)作为非响应者。当比较初始和最终的VAS分数时,发现超声波引导的注射有效减轻疼痛(P <.001)。此外,接受注射的患者2或更多次倾向于比接受一次注射的人更显着疼痛减少(P <.001)。患有安培患者患有长期疼痛,经历许多医院访问和诊断测试。利多卡因的TPI可以对慢性安培患者进行有效和安全的治疗方法。

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