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LC-OCT imaging and application to energy based device therapy LC-OCT成像及其在基于能量的设备治疗中的应用。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-11-08 DOI: 10.1002/lsm.23738
Thomas M. Beachkofsky MD, James M. Grichnik MD, PhD, Peter R. Shumaker MD
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引用次数: 0
Needle-free electronically-controlled jet injector treatment with bleomycin and lidocaine is effective and well-tolerated in patients with recalcitrant keloids 用博来霉素和利多卡因进行无针电控喷射注射治疗顽固性瘢痕疙瘩是有效的,耐受性良好。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-11-07 DOI: 10.1002/lsm.23737
Vazula Zulfra Bekkers MD, Fatima Khan BSc, Pim Aarts MD, Katarzyna Zdunczyk MSc, Errol Prospero Prens MD, PhD, Albert Wolkerstorfer MD, PhD, Robert Rissmann PhD, Martijn Bastiaan Adriaan van Doorn MD, PhD

Objectives

The treatment of recalcitrant keloids is challenging. Although intralesional bleomycin using conventional needle injectors (CNI) is effective, it has important drawbacks, such as the need for repetitive and painful injections. Therefore, we aimed to evaluate the effectiveness, tolerability and patient satisfaction of intralesional bleomycin with lidocaine administered with a needle-free electronically-controlled pneumatic jet-injector (EPI) in recalcitrant keloids.

Methods

This retrospective study included patients with recalcitrant keloids who had received three intralesional EPI-assisted treatments with bleomycin and lidocaine. Effectiveness was assessed using the Patient and Observer Scar Assessment Scale (POSAS) at baseline and four to six weeks after the third treatment. Additionally, treatment related pain scores numeric rating scale, adverse effects, patient satisfaction and Global Aesthetic Improvement Scale (GAIS) were assessed.

Results

Fifteen patients with a total of >148 recalcitrant keloids were included. The median total POSAS physician- and patient-scores were respectively 40 and 41 at baseline, and reduced with respectively 7 and 6-points at follow-up ( p < 0.001; p < 0.001). The median pain scores during EPI-assisted injections were significantly lower compared to CNI-assistant injections, (2.5 vs. 7.0, respectively ( p < 0.001)). Adverse effects were mild. Overall, patients were “satisfied” or “very satisfied” with the treatments (14/15, 93.3%). The GAIS was “very improved” in one patient, “improved” in nine patients and “unaltered” in four patients.

Conclusions

EPI-assisted treatment with bleomycin and lidocaine is an effective, well tolerated, patient-friendly alternative for CNI in patients with recalcitrant keloid scars. Randomized controlled trials are warranted to confirm our findings and improve the clinical management of recalcitrant keloids.

目的:顽固性瘢痕疙瘩的治疗具有挑战性。尽管使用传统针头注射器(CNI)的病灶内博来霉素是有效的,但它也有重要的缺点,例如需要重复和痛苦的注射。因此,我们旨在评估病变内博来霉素与利多卡因在无针电控气动喷射注射器(EPI)治疗顽固性瘢痕疙瘩中的有效性、耐受性和患者满意度。方法:本回顾性研究纳入了接受过博莱霉素和利多卡因三次病灶内EPI辅助治疗的顽固性瘢痕疙瘩患者。在基线和第三次治疗后4-6周,使用患者和观察者疤痕评估量表(POSAS)评估疗效。此外,还评估了与治疗相关的疼痛评分数字评定量表、不良反应、患者满意度和整体美学改善量表(GAIS)。结果:纳入了15名患者,总计>148个顽固性瘢痕疙瘩。POSAS医师和患者的中位总分在基线时分别为40分和41分,在随访时分别降低了7分和6分( p 结论:EPI辅助博来霉素和利多卡因治疗顽固性瘢痕疙瘩是一种有效、耐受性好、患者友好的CNI替代方案。随机对照试验有助于证实我们的发现,并改善顽固性瘢痕疙瘩的临床管理。
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引用次数: 0
Comments on “Melasma treatment with a 1064 nm, picosecond-domain laser with a fractionated multibeam lens array” 评“用1064治疗黄褐斑” nm,皮秒域激光器”。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-10-27 DOI: 10.1002/lsm.23735
Manoj Pawar MD, Assel Satvaldinova MD, Mehak Singh MD
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引用次数: 0
Cover Image: Volume 55 Issue 9 封面图片:第55卷第9期
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-10-23 DOI: 10.1002/lsm.23734
Eric F. Bernstein MD, MSE, Lisa D. Basilavecchio RN, Jenny Wang BS

Cover micrograph: The cover image is based on the Clinical Report Melasma treatment with a 1064 nm, picosecond-domain laser with a fractionated multibeam lens array by Eric F. Bernstein et al., https://doi.org/10.1002/lsm.23723. Image Credit: Dr. Eric F. Bernstein of Main Line Center for Laser Surgery in Ardmore, PA.

封面显微照片:封面图像基于Eric F.Bernstein等人用1064nm皮秒域激光和分级多光束透镜阵列治疗黄褐斑的临床报告。,https://doi.org/10.1002/lsm.23723.图片来源:宾夕法尼亚州阿德莫尔主线激光外科中心的Eric F.Bernstein博士。
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引用次数: 0
Multimodal feedback systems for smart laser osteotomy: Depth control and tissue differentiation 智能激光截骨的多模式反馈系统:深度控制和组织分化。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-10-23 DOI: 10.1002/lsm.23732
Arsham Hamidi PhD, Yakub A. Bayhaqi PhD, Sandra Drusová PhD, Alexander A. Navarini MD, PhD, Philippe C. Cattin PhD, Ferda Canbaz PhD, Azhar Zam PhD

Objectives

The study aimed to improve the safety and accuracy of laser osteotomy (bone surgery) by integrating optical feedback systems with an Er:YAG laser. Optical feedback consists of a real-time visual feedback system that monitors and controls the depth of laser-induced cuts and a tissue sensor differentiating tissue types based on their chemical composition. The developed multimodal feedback systems demonstrated the potential to enhance the safety and accuracy of laser surgery.

Materials and Methods

The proposed method utilizes a laser-induced breakdown spectroscopy (LIBS) system and long-range Bessel-like beam optical coherence tomography (OCT) for tissue-specific laser surgery. The LIBS system detects tissue types by analyzing the plasma generated on the tissue by a nanosecond Nd:YAG laser, while OCT provides real-time monitoring and control of the laser-induced cut depth. The OCT system operates at a wavelength of 1288 ± 30 nm and has an A-scan rate of 104.17 kHz, enabling accurate depth control. Optical shutters are used to facilitate the integration of these multimodal feedback systems.

Results

The proposed system was tested on five specimens of pig femur bone to evaluate its functionality. Tissue differentiation and visual depth feedback were used to achieve high precision both on the surface and in-depth. The results showed successful real-time tissue differentiation and visualization without any visible thermal damage or carbonization. The accuracy of the tissue differentiation was evaluated, with a mean absolute error of 330.4 μm and a standard deviation of ±248.9 μm, indicating that bone ablation was typically stopped before reaching the bone marrow. The depth control of the laser cut had a mean accuracy of 65.9 μm with a standard deviation of ±45 μm, demonstrating the system's ability to achieve the pre-planned cutting depth.

Conclusion

The integrated approach of combining an ablative laser, visual feedback (OCT), and tissue sensor (LIBS) has significant potential for enhancing minimally invasive surgery and warrants further investigation and development.

目的:本研究旨在通过将光学反馈系统与Er:YAG激光器集成,提高激光截骨(骨外科)的安全性和准确性。光学反馈由一个实时视觉反馈系统和一个组织传感器组成,该系统监测和控制激光诱导切割的深度,该传感器根据组织的化学成分区分组织类型。所开发的多模式反馈系统证明了提高激光手术安全性和准确性的潜力。材料和方法:所提出的方法利用激光诱导击穿光谱(LIBS)系统和长程贝塞尔光束光学相干断层扫描(OCT)进行组织特异性激光手术。LIBS系统通过分析纳秒Nd:YAG激光器在组织上产生的等离子体来检测组织类型,而OCT则提供对激光诱导切割深度的实时监测和控制。OCT系统的工作波长为1288 ± 30 nm,并且具有104.17的A扫描速率 kHz,实现精确的深度控制。光学快门用于促进这些多模式反馈系统的集成。结果:所提出的系统在五个猪股骨标本上进行了测试,以评估其功能。组织分化和视觉深度反馈用于实现表面和深度的高精度。结果显示,成功的实时组织分化和可视化,没有任何可见的热损伤或碳化。对组织分化的准确性进行了评估,平均绝对误差为330.4 μm,标准偏差为±248.9 μm,表明骨消融通常在到达骨髓之前停止。激光切割的深度控制的平均精度为65.9 μm,标准偏差为±45 μm,展示了该系统实现预先计划的切割深度的能力。结论:消融激光、视觉反馈(OCT)和组织传感器(LIBS)相结合的综合方法在增强微创手术方面具有巨大潜力,值得进一步研究和开发。
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引用次数: 0
Biological effect of laser-assisted scar healing (LASH) on standardized human three-dimensional wound healing skin models using fractional non-ablative 1540 nm Er:Glass or 1550 nm diode lasers 激光辅助瘢痕愈合(LASH)对标准化人体三维创伤愈合皮肤模型的生物学效应 nm Er:玻璃或1550 nm二极管激光器。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-10-19 DOI: 10.1002/lsm.23731
Helena I. Riedemann MD, Yvonne Marquardt, Manuela Jansen, Jens M. Baron MD, Sebastian Huth PhD

Purpose

In postoperative wound healing after surgical operations or ablative laser treatments, recent studies suggest the timely use of non-ablative fractional laser treatments with the aim to improve wound healing and prevent pathological scar formation. However, the underlying molecular mechanisms are poorly understood. The aim of this study was to investigate the effects of laser-assisted scar healing (LASH) at the molecular level and to combine it with already established wound healing-promoting local treatments.

Methods

We irradiated full-thickness 3D skin models with a fractional ablative Er:YAG laser to set standardized lesions to the epidermal and upper dermal layer. Subsequently, LASH was induced by irradiating the models with either a fractional non-ablative 1540 nm Er:Glass or 1550 nm diode laser. In addition, we tested the combination of non-ablative fractional laser treatment and topical aftercare with a dexpanthenol-containing ointment (DCO).

Results

Histological analysis revealed that models irradiated with the 1540 nm Er:Glass or 1550 nm diode laser exhibited accelerated but not complete wound closure after 16 h. In contrast, additional topical posttreatment with DCO resulted in complete wound closure. At gene expression level, both non-ablative laser systems showed similar effects on epidermal differentiation and mild anti-inflammatory properties. The additional posttreatment with DCO enhanced the wound-healing effects of LASH, especially the upregulation of epidermal differentiation markers and anti-inflammatory cytokines at the gene expression level.

Conclusion

This in vitro study deciphers the biological effects of LASH with a fractional non-ablative 1540 nm Er:Glass or a 1550 nm diode laser in 3D skin models. These data help to better understand the biological properties of the LASH technique and is important to optimize its application.

目的:在外科手术或消融激光治疗后的术后伤口愈合中,最近的研究建议及时使用非消融部分激光治疗,以改善伤口愈合并防止病理性瘢痕形成。然而,人们对其潜在的分子机制知之甚少。本研究的目的是在分子水平上研究激光辅助瘢痕愈合(LASH)的效果,并将其与已经建立的促进伤口愈合的局部治疗相结合。方法:我们用部分消融Er:YAG激光照射全厚度3D皮肤模型,在表皮和上真皮层设置标准化病变。随后,通过用部分非消融1540照射模型来诱导LASH nm Er:玻璃或1550 nm二极管激光器。此外,我们测试了非消融部分激光治疗和含右泛醇软膏(DCO)的局部善后处理的组合。结果:组织学分析显示,1540 nm Er:玻璃或1550 nm二极管激光器在16岁后表现出加速但未完全闭合伤口 h.相反,DCO的额外局部后处理导致伤口完全闭合。在基因表达水平上,两种非消融激光系统对表皮分化和轻度抗炎特性表现出相似的效果。DCO的额外后处理增强了LASH的伤口愈合效果,特别是在基因表达水平上调表皮分化标志物和抗炎细胞因子。结论:这项体外研究用部分非消融1540破解了LASH的生物学效应 nm Er:玻璃或1550 纳米二极管激光在3D皮肤模型中的应用。这些数据有助于更好地了解LASH技术的生物学特性,对优化其应用非常重要。
{"title":"Biological effect of laser-assisted scar healing (LASH) on standardized human three-dimensional wound healing skin models using fractional non-ablative 1540 nm Er:Glass or 1550 nm diode lasers","authors":"Helena I. Riedemann MD,&nbsp;Yvonne Marquardt,&nbsp;Manuela Jansen,&nbsp;Jens M. Baron MD,&nbsp;Sebastian Huth PhD","doi":"10.1002/lsm.23731","DOIUrl":"10.1002/lsm.23731","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>In postoperative wound healing after surgical operations or ablative laser treatments, recent studies suggest the timely use of non-ablative fractional laser treatments with the aim to improve wound healing and prevent pathological scar formation. However, the underlying molecular mechanisms are poorly understood. The aim of this study was to investigate the effects of laser-assisted scar healing (LASH) at the molecular level and to combine it with already established wound healing-promoting local treatments.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We irradiated full-thickness 3D skin models with a fractional ablative Er:YAG laser to set standardized lesions to the epidermal and upper dermal layer. Subsequently, LASH was induced by irradiating the models with either a fractional non-ablative 1540 nm Er:Glass or 1550 nm diode laser. In addition, we tested the combination of non-ablative fractional laser treatment and topical aftercare with a dexpanthenol-containing ointment (DCO).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Histological analysis revealed that models irradiated with the 1540 nm Er:Glass or 1550 nm diode laser exhibited accelerated but not complete wound closure after 16 h. In contrast, additional topical posttreatment with DCO resulted in complete wound closure. At gene expression level, both non-ablative laser systems showed similar effects on epidermal differentiation and mild anti-inflammatory properties. The additional posttreatment with DCO enhanced the wound-healing effects of LASH, especially the upregulation of epidermal differentiation markers and anti-inflammatory cytokines at the gene expression level.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>This in vitro study deciphers the biological effects of LASH with a fractional non-ablative 1540 nm Er:Glass or a 1550 nm diode laser in 3D skin models. These data help to better understand the biological properties of the LASH technique and is important to optimize its application.</p>\u0000 </section>\u0000 </div>","PeriodicalId":17961,"journal":{"name":"Lasers in Surgery and Medicine","volume":null,"pages":null},"PeriodicalIF":2.4,"publicationDate":"2023-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lsm.23731","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49679052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single treatment scar resurfacing with a novel ablative fractional 2910 nm erbium-doped fluoride glass fiber laser 一种新型消融性2910分型瘢痕表面置换术 nm掺铒氟化物玻璃纤维激光器。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-10-17 DOI: 10.1002/lsm.23729
Taryn N. Murray MD, Emily L. Guo MD, Heather Richmond MD, Paul M. Friedman MD

Scars are a common dermatologic complaint that can adversely affect an individual's quality of life. With diverse etiologies and types of scars, treatment is often challenging. Myriad treatment options exist ranging from topical medications to surgical revision, however, no scar treatment has been as revolutionary as lasers. Since its introduction, ablative laser resurfacing technology has continually evolved including the development of fractional devices, new wavelengths, and expanding indications. Fractional and conventional ablative lasers cause direct destruction and debulking of scar tissue via vaporization. This tissue vaporization activates heat shock proteins, stimulates antifibrotic factors, and induces dermal matrix remodeling resulting in the reduction of scar tissue and improvement in skin texture.1 While ablative fractional lasers (AFLs) offer less discomfort and reduced downtime compared to conventional ablative lasers, depending on the scar size and anatomic location, they often still require sedation, regional nerve blocks, or intralesional injections of anesthetic solution. Moreover, they have limited utility in skin of color due to the degree of thermal damage. Thus there remains a need for an AFL that is less painful, safe in skin of color, and effectively resurfaces skin without a prolonged recovery.

This novel 2910 nm erbium-doped fluoride glass fiber laser (2910 nm fiber laser) (UltraClear; Acclaro Medical) targets water at its peak absorption between 2900 and 3100 nm. This highly selective wavelength and the novel pulse delivery system creates ablative microscopic thermal treatment zones while minimizing patient discomfort, recovery time, and residual thermal damage to surrounding tissue.2 This case series investigates the novel 2910 nm fiber laser for scars of various etiologies in Fitzpatrick skin types I–IV.

A retrospective case series was conducted with patients who underwent treatment for scars with the 2910 nm fiber laser at a single center in Houston, Texas between the years 2022–2023. Patients presenting for keloids or who had a history of keloids were excluded. A compounded topical anesthetic cream (20% benzocaine, 6% lidocaine, 6% tetracaine) was applied to the affected area for 30 min. The affected area was cleansed with 70% isopropyl alcohol or chlorhexidine gluconate 4% solution before treatment. Patients received a single treatment. A single patient underwent laser-assisted drug delivery with topical application of triamcinolone acetonide 40 mg/mL and 5-fluorouracil at a ratio of 1:9 to the treated surface. Photographs were taken at baseline and 1–3 months following treatment. Two independent nontreating physicians evaluated the degree of improvement between pretreatment and posttreatment photographs using a 5-point Global Aesthetic Improvement Scale (GAIS) as follows: (0) no improvement, (1) minor improvement, (2) moderate improvement, (3) marked

疤痕是一种常见的皮肤病,会对患者的生活质量造成不良影响。疤痕的病因和类型多种多样,治疗起来往往具有挑战性。现有的治疗方法多种多样,从局部用药到手术修复,但没有一种疤痕治疗方法能像激光一样具有革命性意义。自问世以来,激光烧蚀换肤技术一直在不断发展,包括点阵设备、新波长和适应症的开发。点阵激光和传统烧蚀激光通过汽化作用直接破坏和清除疤痕组织。这种组织汽化可激活热休克蛋白,刺激抗纤维化因子,诱导真皮基质重塑,从而减少疤痕组织,改善皮肤质地。1 虽然与传统的烧蚀激光相比,点阵激光(AFL)可减少不适感,缩短停工期,但根据疤痕的大小和解剖位置,它们通常仍需要镇静剂、区域神经阻滞或麻醉溶液的区域内注射。此外,由于热损伤的程度不同,激光对有色皮肤的作用也有限。这种新型的 2910 nm 掺铒氟化玻璃光纤激光器(2910 nm 光纤激光器)(UltraClear;Acclaro Medical)的目标是 2900 和 3100 nm 之间吸收峰值的水。2 本病例系列研究了新型 2910 nm 光纤激光治疗 Fitzpatrick I-IV 型皮肤上各种病因引起的疤痕。排除了因瘢痕疙瘩就诊或有瘢痕疙瘩病史的患者。在患处涂抹复方局部麻醉膏(20%苯佐卡因、6%利多卡因、6%四卡因)30分钟。治疗前用 70% 异丙醇或 4% 葡萄糖酸氯己定溶液清洗患处。患者只接受一次治疗。一名患者接受了激光辅助给药治疗,并在治疗部位局部使用了40毫克/毫升的曲安奈德和5-氟尿嘧啶,两者的比例为1:9。在基线和治疗后 1-3 个月拍摄照片。两名独立的非治疗医生采用 5 分全球美学改善量表(GAIS)对治疗前和治疗后照片的改善程度进行评估,具体如下:(共纳入 15 名疤痕患者。共纳入 15 名疤痕患者,其中 8 名女性,7 名男性。共有 15 名疤痕患者,其中 8 名女性,7 名男性,年龄从 13 岁到 59 岁不等,平均年龄为 33 岁。菲茨帕特里克皮肤类型为 II-IV 型。疤痕类型包括萎缩性(7 例)和增生性(8 例)。病因包括痤疮疤痕(4 例)、手术疤痕(3 例)、烧伤疤痕(3 例)、外伤疤痕(3 例)和切割疤痕(2 例)。疤痕年龄从3个月到18岁不等。患者采用深部激光模式或浅部和深部激光模式相结合的方法进行治疗。深层模式的深度和覆盖范围分别为 300 至 750 微米,每次通过的深度和覆盖范围分别为 1.0% 至 2.5%。表层深度和覆盖范围分别为 10 至 50 微米和 25%-40%。凝固率为 9.6%-32.0%。进行了 1 至 3 次扫描。两位独立的非治疗医生对数字图像进行评估后发现,所有疤痕的平均 GAIS 得分为 1.7。萎缩性疤痕的改善程度略高于增生性疤痕,平均 GAIS 分值分别为 2.0 和 1.43。在考虑疤痕病因时,外伤性疤痕的改善幅度最大(3.16 分),其次是痤疮疤痕(1.85 分)、切割疤痕(1.75 分)和烧伤疤痕(1.33 分)(图 1-3)。手术疤痕的改善程度最小,平均 GAIS 为 0.33。副作用是一过性的,包括轻度至中度红斑和水肿,以及偶尔的针尖出血和结痂。有两例短暂的炎症后红斑。本系列病例研究了用于疤痕重塑的新型 2910 nm 光纤激光的临床效果。该光纤传输系统可高度定制,通过分段式微光束消融组织,消融深度从角质层浅层的 5 μm 到真皮层深达 1500 μm。
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引用次数: 0
Conventional drilling versus ultrasound and laser osteotomy in mandibular third molar surgery: A comparative study 下颌第三磨牙手术中常规钻孔与超声和激光截骨的比较研究。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-10-09 DOI: 10.1002/lsm.23730
Bistra Blagova DDS, DMD, Dimo Krastev MD, PhD, Lina Malinova MD, PhD

Background

There are few research works with in-depth studies and direct simultaneous comparisons of the effects on tissue reactions and patients' recovery following in vivo conventional drilling, ultrasound- and laser-assisted osteotomy in humans.

Objective

The current study aims to compare bone cutting duration, pain, swelling, and trismus in patients following surgical mandible third molar extraction by bone removal using three different osteotomes—a conventional rotary device, an ultrasonic unit, and an Er:YAG laser.

Methods

A prospective, randomized three-group comparative clinical trial was performed. As an experimental setting for the study, аn open mandible third molar surgery was chosen because osteotomy is included in its protocol. Patients were divided into three groups according to the used device for bone removal. Bone cutting time intraoperatively, facial swelling, trismus, and pain on the first, second, and third postoperative days were assessed. The statistical analyses were performed using the SPSS v. 17.0—Kolmogorov–Smirnov test, one-way ANOVA, Student's t-test, Mann–Whitney test, and χ2 test. Statistical results were considered significant at p < 0.05 (confidence interval of difference, 95% CI).

Results

Eighty patients (34 males and 46 females with an average age of 25.18 years) were included in the study. The average time for bone removal by the conventional low-speed device (4.95 min), by the ultrasonic unit (5.13 min), and by the Er:YAG laser (9.00 min) differed significantly (p = 0.001). The mean postoperative facial swelling showed a marked difference between the groups (p < 0.05), in favor of the laser and piezo groups. The osteotome proved to influence pain intensity not only immediately after surgery (p = 0.002), but also during the followed-up period (p = 0.001), again in favor of the two above-mentioned groups. No association was found between trismus and the osteotome used by the followed-up patients (p > 0.05).

Conclusion

Bone-cutting mechanism and the biological influence of the laser beam and ultrasound on living tissues proved to be favorable factors for patients' pain levels and tissue swelling postoperatively independent of the longer osteotomy duration compared to conventional drilling.

背景:很少有研究工作对人体常规钻孔、超声和激光辅助截骨对组织反应和患者恢复的影响进行深入研究和直接同时比较。目的:本研究旨在比较使用三种不同的接骨器(传统旋转装置、超声装置和Er:YAG激光)进行下颌骨第三磨牙拔除术后患者的切骨持续时间、疼痛、肿胀和牙痛。方法:采用前瞻性随机三组比较临床试验。作为研究的实验环境,选择了开放式下颌第三磨牙手术,因为其方案中包括截骨。根据所使用的骨切除装置,将患者分为三组。评估术中切骨时间、术后第一天、第二天和第三天的面部肿胀、牙痛和疼痛。统计分析采用SPSS v.17.0-Kolmogorov-Smirnov检验、单因素方差分析、Student t检验、Mann-Whitney检验和χ2检验。统计结果在p时被认为是显著的 结果:80名患者(34名男性和46名女性,平均年龄25.18岁)被纳入研究。传统低速装置的平均骨去除时间(4.95 min),通过超声波单元(5.13 min)和Er:YAG激光器(9.00 min)差异显著(p = 0.001)。两组术后平均面部肿胀有显著差异(p  结论:骨切割机制以及激光束和超声对活体组织的生物学影响被证明是影响患者术后疼痛程度和组织肿胀的有利因素,与传统钻孔相比,截骨时间更长无关。
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引用次数: 0
Modified painless photodynamic therapy for facial multiple actinic keratosis in China: A prospective split-face control study 改良无痛光动力疗法治疗中国面部多发性光化性角化病:一项前瞻性分面对照研究。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-10-09 DOI: 10.1002/lsm.23728
Jiandan Li MM, Yunfeng Zhang MD, Guolong Zhang MD, PhD, Linglin Zhang MD, Zhongxia Zhou, Peiru Wang MD, PhD, Xiuli Wang MD, PhD

Background

Aminolevulinic acid photodynamic therapy (ALA-PDT) is an effective treatment for multiple actinic keratosis (AK). However, PDT-induced pain often discontinues the therapy to reduce its efficacy, limiting its application. If modified painless PDT schedule with shorter photosensitizer dressing and higher dose illumination could achieve good efficacy in AK, it is still unknown.

Objectives

To explore the efficacy and pain tolerance of the modified painless PDT (M-PDT) in facial multiple AK.

Methods

A split-face controlled clinical study including 14 patients with facial multiple AK was conducted. The patients received conventional PDT (C-PDT) on the left and M-PDT in the contralateral area. The left area (C-PDT) was illuminated by a red light-emitting diode light (144 J/cm2) after applying the 10% ALA cream for 3 h; the other had illumination for a total light dose of 288 J/cm2 after applying the 10% ALA cream for 0.5 h. The primary endpoint was the lesion clearance rate at 1-month postthree sessions of PDT. Secondary endpoints included pain scores, the incidence of adverse events during treatment, and cosmetic outcomes.

Results

At 1 month following three treatments, the total lesion clearance rate was comparable between M-PDT and C-PDT (91.6% vs. 89.0%). While the lesion clearance rate of M-PDT was higher than that of C-PDT in the Grade III lesions (86.5% vs. 72.0%, respectively) (p < 0.05). M-PDT achieved a 100% lesion clearance rate for Grade I lesions earlier than C-PDT, with M-PDT treated twice and C-PDT treated thrice. Moreover, the pain score during illumination was significantly lower for M-PDT than for C-PDT (p < 0.01). Regarding photoaging, the Global Subjective Skin Aging Assessment score showed that the total and atrophy scores of C-PDT and M-PDT were significantly improved, and M-PDT also reduced discoloration. There was no significant difference in adverse reactions between C-PDT and M-PDT.

Conclusions

M-PDT is comparable to C-PDT's efficacy for treating facial multiple AK, resulting in much lower pain scores.

背景:氨基乙酰丙酸光动力疗法(ALA-PDT)是治疗多发性光化性角化病(AK)的有效方法。然而,PDT引起的疼痛通常会中断治疗以降低其疗效,从而限制其应用。改良的无痛PDT方案,更短的光敏剂敷料和更高剂量的光照,是否能在AK中获得良好的疗效,目前尚不清楚。目的:探讨改良无痛PDT(M-PDT)治疗面部多发性AK的疗效和疼痛耐受性。患者在左侧接受常规PDT(C-PDT),在对侧接受M-PDT。左侧区域(C-PDT)由红色发光二极管照明(144 J/cm2) h;另一个的照明总剂量为288 在施用10%ALA乳膏0.5天后J/cm2 h.主要终点是PDT三个疗程后1个月的病变清除率。次要终点包括疼痛评分、治疗期间不良事件的发生率和美容效果。结果:在三种治疗后1个月,M-PDT和C-PDT的总病灶清除率相当(91.6%对89.0%),而M-PDT在III级病灶中的病灶清除率高于C-PDT(86.5%对72.0%)(p 结论:M-PDT治疗面部多发性AK的疗效与C-PDT相当,导致疼痛评分低得多。
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引用次数: 0
Rational of topical photodynamic therapy (PDT) with 5-aminolevulinic acid (5-ALA) for treatment of endocervical canal low-grade squamous intraepithelial lesion with high-risk human papillomavirus infection 5-氨基乙酰丙酸(5-ALA)局部光动力疗法(PDT)治疗宫颈管低级别鳞状上皮内病变伴高危人乳头瘤病毒感染的合理性。
IF 2.4 3区 医学 Q1 Medicine Pub Date : 2023-09-26 DOI: 10.1002/lsm.23727
Lin-Jing Yuan MD, Ke He MD, Cai-Xia Zhu MD, Tie-Feng Cao MD, Mian He MD

Background

The detection and continuous monitoring of low-grade squamous intraepithelial lesions (LSIL) within the endocervical canal pose considerable challenges, and the effectiveness of ablation treatment is also constrained. In this context, the potential efficacy of 5-aminolevulinic acid photodynamic therapy (5-ALA PDT) in targeting these concealed lesions merits exploration. The present study undertakes a comprehensive analysis of the clinical effectiveness and safety aspects associated with the utilization of 5-ALA PDT.

Methods

A retrospective analysis was conducted on a cohort of 13 patients who were diagnosed with LSIL within the endocervical canal, concomitant with high-risk human papillomavirus (hrHPV) infection. These patients were subjected to treatment with 5-ALA PDT and subsequently monitored over a period of 3−6 months following the intervention.

Results

The study cohort comprised 13 patients, among whom 4 presented with isolated lesions within the endocervical canal, 5 exhibited LSIL involving both the endocervical canal and the cervix vaginal portion, 3 displayed LSIL within the endocervical canal in conjunction with vaginal involvement, and 1 patient demonstrated lesions across all three of these anatomical sites. All identified lesions underwent therapeutic intervention via 5-ALA PDT. Before treatment initiation, 9 patients returned positive results in the liquid-based cytologic test (LBC), 4 displayed concurrent multiple hrHPV infections, and 5 manifested infections specifically with HPV 16/18. Subsequent to the application of 5-ALA PDT, regression was observed in the LBC results of all patients, with only 3 individuals retaining a singular type of hrHPV infection. Adverse reactions following treatment encompassed mild aberrant vaginal secretions and mild to moderately pronounced distending abdominal discomfort, all of which were remitted within a span of 7 days.

Conclusions

Within the context of LSIL within the endocervical canal in association with hrHPV infection, the findings affirm the efficacy and safety of 5-ALA PDT as a viable therapeutic modality.

背景:宫颈管内低度鳞状上皮内病变(LSIL)的检测和持续监测带来了相当大的挑战,消融治疗的有效性也受到限制。在这种情况下,5-氨基乙酰丙酸光动力疗法(5-ALA PDT)针对这些隐蔽性病变的潜在疗效值得探索。本研究对5-ALA PDT的临床有效性和安全性进行了全面分析。方法:对13名被诊断为宫颈管内LSIL并伴有高危型人乳头瘤病毒(hrHPV)感染的患者进行回顾性分析。这些患者接受5-ALA PDT治疗,随后在干预后3-6个月内进行监测。结果:研究队列包括13名患者,其中4名患者出现宫颈管内孤立性病变,5名患者同时出现宫颈管和宫颈阴道部分的LSIL,3名患者在宫颈管内出现LSIL并伴有阴道受累,1名患者在所有三个解剖部位都出现病变。所有确定的病变均通过5-ALA PDT进行治疗干预。在开始治疗之前,9名患者的液体细胞学检查(LBC)结果呈阳性,4名患者同时表现为多发性hrHPV感染,5名患者表现为HPV 16/18特异性感染。应用5-ALA PDT后,在所有患者的LBC结果中观察到回归,只有3人保留了单一类型的hrHPV感染。治疗后的不良反应包括轻度异常阴道分泌物和轻度至中度明显的腹胀不适,所有这些都在7天内缓解。结论:在宫颈管内LSIL与hrHPV感染相关的背景下,研究结果证实了5-ALA PDT作为一种可行的治疗方式的有效性和安全性。
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引用次数: 0
期刊
Lasers in Surgery and Medicine
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