光生物调节调节神经性疼痛和改善疤痕组织。

Scars, burns & healing Pub Date : 2022-10-26 eCollection Date: 2022-01-01 DOI:10.1177/20595131221134052
Ronaldo Santiago, Shannon Gomes, Jak Ozsarfati, Michael Zitney
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引用次数: 4

摘要

背景:本病例报告探讨光生物调节疗法(PBMT)对瘢痕组织愈合的影响。患者是一名32岁的女性,胆囊切除术后两年,造成15厘米的线状疤痕,引起剧烈疼痛。方法:使用BIOFLEX®治疗设备开始治疗,该设备由LED阵列和特定波长、功率和频率的激光探头组成,直接应用于疤痕覆盖的皮肤上。治疗的频率和持续时间是在诊所每隔一天进行一次,持续六周,然后在家中每周进行三次,持续两个月。然后患者继续在需要的基础上使用BIOFLEX®治疗师家用设备。结果:该患者治疗的最终结果是瘢痕明显变平,红肿减少。她自我报告的疼痛程度降至6/10。在一年的随访中,患者报告说她停止服用阿片类药物、抗抑郁药和安眠药,疼痛减轻到4/10。最后一次复查时,她的疼痛评分为1/10;她重返工作岗位,偶尔服用泰诺(对乙酰氨基酚)来缓解突发性疼痛。结论:我们将患者疤痕外观和疼痛症状的改善归因于PBMT。由于疼痛通常与抑郁情绪和睡眠障碍有关,因此无法确定PBMT是该患者情绪改善的直接原因还是间接原因。在未来的研究中,我们建议使用接受假治疗的疤痕相似的对照受试者,与接受PBMT的受试者进行相同时间的观察,并比较总体结果。概要:皮肤病学应用,特别是伤口愈合;是公认的光生物调节治疗(PBMT)适应症。扩展到其他临床应用,特别是神经学应用显示出潜在的益处。我们报告了一例伴有严重神经性疼痛和并发抑郁的增生性疤痕患者,所有这些都直接或间接地通过PBMT得到改善。虽然最初的治疗重点是皮肤病学,但疼痛的改善和治疗(阿片类药物、抗抑郁药和苯二氮卓类药物)的停止被认为是由于PBMT。
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Photobiomodulation for modulation of neuropathic pain and improvement of scar tissue.

Background: This case-report explores the effects of photobiomodulation therapy (PBMT) on the healing of scar tissue. The patient was a 32-year old female two years post cholecystectomy resulting in a 15 cm linear scar that was causing severe pain.

Methods: Treatment was initiated using the BIOFLEX® therapist device which consists of LED arrays and laser probes of a specific wavelength, power and frequency applied directly on the skin overlying the scar. The frequency and duration of treatment was every other day for six weeks in a clinic setting, followed by three times a week for two months at home. Then the patient continued to use the BIOFLEX® therapist home device on an as-needed basis.

Findings: The final result of this patient's treatment was significant flattening and decreased redness of her scar. Her self-reported pain decreased to a 6/10. At the one year follow up, the patient reported that she stopped taking her opioids, antidepressant and sleeping pills and that her pain decreased to a 4/10. At the last review her pain score was 1/10; and she had returned to work and took Tylenol (acetaminophen) occasionally for breakthrough pain.

Conclusions: We attribute the patient's improvement in scar appearance and pain symptoms to PBMT. Since pain is often associated with depressed mood and sleep disturbances, it cannot be determined whether PBMT was the direct or indirect cause of this patient's improved mood. For future studies, we propose the use of control subjects with similar scars treated with sham treatment compared to those who will receive the PBMT and observed for the same duration of time and compare the overall results.

Lay summary: Dermatological applications, especially wound healing; are accepted indications for photobiomodulation therapy (PBMT). The expansion into other clinical applications, particularly neurological ones show potential benefit. We present a case of a patient with a hypertrophic scar associated with severe neuropathic pain and concurrent depression, all of which improved directly or indirectly with PBMT. Although the original focus of treatment was dermatological the improvement in pain plus the discontinuation of therapy (opioids, antidepressants and benzodiazepines) were considered to be due to the PBMT.

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