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首页> 外文期刊>The Lancet >Pulsed-dye laser treatment for inflammatory acne vulgaris: randomised controlled trial.
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Pulsed-dye laser treatment for inflammatory acne vulgaris: randomised controlled trial.

机译:脉冲染料激光治疗寻常型炎性痤疮:随机对照试验。

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BACKGROUND: Low-fluence (low irradiation energy density) pulsed-dye lasers (PDLs) have been used for atrophic acne scarring, and anecdotal experience suggests that long-term improvements in inflammatory acne can be seen after one PDL treatment. Our aim was to compare the efficacy and tolerability of such PDL treatment with sham treatment in patients with facial inflammatory acne in a double-blind, randomised controlled trial. METHODS: We recruited 41 adults with mild-to-moderate facial inflammatory acne. We randomly assigned patients to PDL (n=31) or sham treatment (n=10). Treatment was given at baseline and patients were seen after 2, 4, 8, and 12 weeks. Assessors and participants were unaware of treatment allocations. Primary outcome measures were acne severity after 12 weeks and adverse events at any time. Secondary measures were change in lesion counts after 12 weeks and change in acne severity with time. Analysis was by intention-to-treat. FINDINGS: After 12 weeks, acne severity (measured by Leedsrevised grading system) was reduced from 3.8 (SD 1.5) to 1.9 (1.5) in the PDL group and 3.6 (1.8) to 3.5 (1.9) in the sham group (p=0.007). Treatment was well tolerated. Total lesion counts fell by 53% (IQR 19 to 64) in PDL patients and 9% (-16 to 38) in controls (p=0.023), and inflammatory lesion counts reduced by 49% (30 to 75) in PDL patients and 10% (-8 to 49) in controls (p=0.024). The most rapid improvements were seen in the first 4 weeks after treatment. INTERPRETATION: PDL therapy improves inflammatory facial acne 12 weeks after one treatment with no serious adverse effects.
机译:背景:低通量(低辐射能量密度)脉冲染料激光(PDL)已用于萎缩性痤疮疤痕形成,传闻经验表明,一种PDL治疗后可看到炎症性痤疮的长期改善。我们的目的是在一项双盲,随机对照试验中比较这种PDL治疗与假治疗在面部炎性痤疮患者中的疗效和耐受性。方法:我们招募了41名患有轻度至中度面部炎性痤疮的成人。我们随机分配患者接受PDL(n = 31)或假治疗(n = 10)。在基线进行治疗,并在2、4、8和12周后看到患者。评估者和参与者不知道治疗分配。主要结局指标为12周后痤疮严重程度以及任何时候的不良事件。次要措施是12周后病变计数的变化以及痤疮严重程度随时间的变化。分析是按意向性进行的。结果:在12周后,PDL组的痤疮严重程度(由Leedsrevised评分系统测量)从3.8(SD 1.5)降低到1.9(1.5),假手术组从3.6(1.8)降低到3.5(1.9)(p = 0.007) )。治疗耐受性良好。 PDL患者的总病灶数下降了53%(IQR 19到64),而对照组(p = 0.023)则下降了9%(-16至38),PDL患者的炎症病灶数减少了49%(30至75)。对照(p = 0.024)中的10%(-8至49)。在治疗后的最初4周内观察到了最快的改善。解释:PDL疗法在一种治疗后12周可改善面部炎症性痤疮,且无严重不良反应。

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