Li N, Yang L, Cheng J, Han J T, Hu D H
Burn Center of PLA, Department of Burns and Cutaneous Surgery, Xijing Hospital, Air Force Medical University, Xi'an 710032, China.
Zhonghua Shao Shang Za Zhi. 2018 Sep 20;34(9):603-607. doi: 10.3760/cma.j.issn.1009-2587.2018.09.009.
To compare the efficacy and safety of pulsed dye laser (PDL) and ultra-pulsed fractional carbon dioxide laser (UFCL) in treating hypertrophic scars after burns. Two hundred and twenty one patients with hypertrophic scar after burns conforming to the study criteria were admitted to our unit from February 2015 to October 2017, and their data were retrospectively analyzed. Patients were divided into group PDL (=122) and group UFCL (=99) according to the treatment method. Patients in group PDL were treated with PDL once every 3-4 weeks. Patients in group UFCL were treated with UFCL once every 6-12 weeks. Patients in both groups were treated until 12 months after having scar. Scars were scored by Vancouver Scar Scale (VSS) before and after treatment. Patients' pain was evaluated by Visual Analogue Scale (VAS) method before and after treatment. Blood flow in scar was monitored and recorded before treatment and in treatment months 6 and 12. Satisfaction degree of patients was recorded 3-6 months after treatment, and the satisfaction rate was calculated. Adverse reactions including duration of erythema/purpura, VAS in treatment, and loss of working time were recorded. Data were processed with one-way analysis of variance, test, and Chi-square test. (1) VSS scores of patients in groups PDL and UFCL after treatment were significantly lower than those before treatment in the same group (=11.34, 12.77, <0.05). The decreasing VSS scores of patients after treatment in groups PDL and UFCL were (5.8±1.1) and (6.0±1.4) points, respectively, and there was no statistically significant difference between the two groups (=1.91, >0.05). (2) VAS of patients in groups PDL and UFCL after treatment were significantly lower than those before treatment in the same group (=7.12, 5.23, <0.05). The decreasing VAS of patients after treatment in groups PDL and UFCL were (4.0±0.6) and (3.2±1.3) points, respectively, and there was no statistically significant difference between the two groups (=1.93, >0.05). (3) Scar blood flow of patients in group PDL in treatment months 6 had no obvious change compared with that before treatment (=1.59, >0.05), while that in treatment months 12 significantly decreased compared with that before treatment and that in treatment months 6 (=3.17, 6.96, <0.05). Scar blood flow of patients in group UFCL in treatment months 6 significantly increased compared with that before treatment (=6.01, <0.05), while that in treatment months 12 significantly decreased compared with that in treatment months 6 (=4.52, <0.05), but had no obvious change compared with that before treatment (=0.92, >0.05). (4) The satisfaction degree of patients in group PDL was 80.3% (98/122), which in group UFCL was 76.8% (76/99), and there was no statistically significant difference between the two groups ((2)=0.97, >0.05). (5) The duration of erythema/purpura of patients in group PDL was (5.2±0.7) d, significantly shorter than (6.1±0.5) d in group UFCL (=2.49, <0.05). The VAS of patients in group PDL during treatment was (1.9±0.9) points, significantly lower than (4.7±0.4) points in group UFCL (=4.85, <0.05). Loss of working time of patients in group UFCL was (9.17±0.72) d, which was significantly longer than (3.96±0.23) d in group PDL (=3.17, <0.05). PDL and UFCL have definite effects on hypertrophic scar, while PDL with light pain, minor wound, and fast recovery time, is safe and effective for treatment of early hypertrophic scar and worthy of clinical promotion and application, especially for children and patients with poor pain tolerance.
比较脉冲染料激光(PDL)与超脉冲分数二氧化碳激光(UFCL)治疗烧伤后增生性瘢痕的疗效及安全性。2015年2月至2017年10月,我科收治符合研究标准的烧伤后增生性瘢痕患者221例,对其资料进行回顾性分析。根据治疗方法将患者分为PDL组(n = 122)和UFCL组(n = 99)。PDL组患者每3 - 4周接受1次PDL治疗。UFCL组患者每6 - 12周接受1次UFCL治疗。两组患者均治疗至瘢痕形成后12个月。治疗前后采用温哥华瘢痕量表(VSS)对瘢痕进行评分。治疗前后采用视觉模拟评分法(VAS)评估患者疼痛情况。治疗前及治疗6个月、12个月时监测并记录瘢痕血流量。治疗后3 - 6个月记录患者满意度,并计算满意率。记录包括红斑/紫癜持续时间、治疗时VAS及误工时间等不良反应。数据采用单因素方差分析、t检验及卡方检验进行处理。(1)PDL组和UFCL组患者治疗后的VSS评分均显著低于同组治疗前(F = 11.34,12.77,P < 0.05)。PDL组和UFCL组患者治疗后VSS评分下降值分别为(5.8 ± 1.1)分和(6.0 ± 1.4)分,两组间差异无统计学意义(t = 1.91,P > 0.05)。(2)PDL组和UFCL组患者治疗后的VAS评分均显著低于同组治疗前(F = 7.12,5.23,P < 0.05)。PDL组和UFCL组患者治疗后VAS评分下降值分别为(4.0 ± 0.6)分和(3.2 ± 1.3)分,两组间差异无统计学意义(t = 1.93,P > 0.05)。(3)PDL组患者治疗6个月时瘢痕血流量与治疗前相比无明显变化(t = 1.59,P > 0.05),而治疗12个月时与治疗前及治疗6个月时相比显著降低(F = 3.17,6.96,P < 0.05)。UFCL组患者治疗6个月时瘢痕血流量与治疗前相比显著增加(t = 6.01,P < 0.05),治疗12个月时与治疗6个月时相比显著降低(t = 4.52,P < 0.05),但与治疗前相比无明显变化(t = 0.92,P > 0.05)。(4)PDL组患者满意度为80.3%(98/122),UFCL组为76.8%(76/99),两组间差异无统计学意义(χ² = 0.97,P > 0.05)。(5)PDL组患者红斑/紫癜持续时间为(5.2 ± 0.7)d,显著短于UFCL组的(6.1 ± 0.5)d(t = 2.49,P < 0.05)。PDL组患者治疗时VAS评分为(1.9 ± 0.9)分,显著低于UFCL组的(4.7 ± 0.4)分(t = 4.85,P < 0.05)。UFCL组患者误工时间为(9.17 ± 0.72)d,显著长于PDL组的(3.96 ± 0.23)d(t = 3.17,P < 0.05)。PDL和UFCL对增生性瘢痕均有确切疗效,而PDL疼痛轻、创伤小、恢复快,治疗早期增生性瘢痕安全有效,值得临床推广应用,尤其适用于儿童及疼痛耐受性差的患者。