de Alencar F Santos Joelita, Nicolau Renata A, Sant'Anna Luciana B, Paterno Josne C, Cristovam Priscila C, Gomes Jose Álvaro P, Santos José Diego Marques, Lo Schiavo Arisawa Emilia A
Department of Nursing, Federal University of Piaui, Teresina, Piaui, Brazil.
Universidade do Vale do Paraíba (UNIVAP), São José dos Campos, São Paulo, Brazil.
Wound Manag Prev. 2021 Aug;67(8):16-23.
Low-level laser therapy (LLLT) and human amniotic membrane (HAM) application have been shown to be viable options for use in wound healing.
This study sought to compare LLLT and HAM to a control treatment (hydrogel, saline, and gauze) in persons with diabetes mellitus (DM) and foot ulcers.
Using a prospective pilot clinical study design, patients receiving care at a health center that specializes in the treatment of diabetic foot wounds between November 2016 and August 2017 were recruited. Eligible patients had to be 30 to 59 years of age; diagnosed with type 2 DM (postprandial capillary glucose levels between 140 and 350 mg/dL); and have uninfected, granulating stage 2 or 3 foot ulcers measuring less than 7 cm by 3 cm. Immunosuppressed and malnourished patients or those with neoplasms or in critical condition were not eligible to participate. Patients received the control treatment (2 mg hydrogel, saline, and gauze), HAM (patches of thawed HAM, applied with overlapping edges), or LLLT (phototherapy session, 2 mg hydrogel, saline, and gauze) for 28 days. Variables, wound area measurements, Pressure Ulcer Scale for Healing (PUSH) scores, and Visual Analog Scale (VAS) scores were used to assess wound improvement progress and pain on days 7, 14, 21, and 28. Descriptive statistics were used to analyze the participant anthropometric and clinical profiles. The Kolmogorov-Smirnov test was used to analyze the sample distribution. The Kruskal-Wallis test with Dunn's post-test was used to evaluate differences in PUSH and VAS scores and wound size for intergroup analysis, and the Mann-Whitney U test was used for the same outcomes in intragroup analysis. The level of significance was 5% (P < .05).
Twenty-seven (27) patients participated (mean age, 51.4 years; mean body mass index, 26.5 kg/m2), with 9 patients in each treatment group. No statistically significant differences were noted in clinical or anthropometric variables among the groups, but mean baseline wound areas were different (2.6 cm² for the control, 1.9 cm² for the LLLT, and 5.5 cm² for the HAM groups). Intragroup comparisons showed a significant reduction in PUSH score in the LLT group between days 0 and 21 (8.2 vs 4.9; P < .01) and days 21 to 28 (4.9 vs 3.2; P < .001). In all treatment groups the percent reduction was significantly different between days 7 and 28. No outcomes were significantly different between groups.
Diabetic foot ulcer wound area as well as PUSH and VAS scores showed more improvement for patients with DM receiving LLLT or HAM than for the control group, but the differences were not significant. Larger studies are needed to compare these treatment modalities.
低强度激光疗法(LLLT)和人羊膜(HAM)应用已被证明是伤口愈合的可行选择。
本研究旨在比较低强度激光疗法和人羊膜与对照治疗(水凝胶、生理盐水和纱布)对糖尿病(DM)患者足部溃疡的疗效。
采用前瞻性试点临床研究设计,招募2016年11月至2017年8月期间在一家专门治疗糖尿病足伤口的健康中心接受治疗的患者。符合条件的患者年龄必须在30至59岁之间;被诊断为2型糖尿病(餐后毛细血管血糖水平在140至350mg/dL之间);且患有未感染、处于肉芽形成阶段的2期或3期足部溃疡,溃疡面积小于7cm×3cm。免疫抑制和营养不良的患者或患有肿瘤或处于危急状态的患者无资格参与。患者接受对照治疗(2mg水凝胶、生理盐水和纱布)、人羊膜(解冻的人羊膜贴片,边缘重叠应用)或低强度激光疗法(光疗疗程、2mg水凝胶、生理盐水和纱布),为期28天。在第7、14、21和28天,使用变量、伤口面积测量、愈合压力性溃疡量表(PUSH)评分和视觉模拟量表(VAS)评分来评估伤口改善进展和疼痛情况。描述性统计用于分析参与者的人体测量和临床特征。Kolmogorov-Smirnov检验用于分析样本分布。采用Kruskal-Wallis检验及Dunn事后检验评估组间分析中PUSH和VAS评分以及伤口大小的差异,组内分析中采用Mann-Whitney U检验评估相同结果。显著性水平为5%(P<.05)。
27名患者参与研究(平均年龄51.4岁;平均体重指数26.5kg/m²),每个治疗组9名患者。各组间临床或人体测量变量无统计学显著差异,但平均基线伤口面积不同(对照组为2.6cm²,低强度激光疗法组为1.9cm²,人羊膜组为5.5cm²)。组内比较显示,低强度激光疗法组在第0天至21天(8.2对4.9;P<.01)和第21天至28天(4.9对3.2;P<.001)PUSH评分显著降低。在所有治疗组中,第7天至28天的降低百分比有显著差异。组间无显著差异。
糖尿病足溃疡患者接受低强度激光疗法或人羊膜治疗时,伤口面积以及PUSH和VAS评分的改善比对照组更多,但差异不显著。需要更大规模的研究来比较这些治疗方式。