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An Assessment and Comparison of Adverse Effect Rates in Differing Absorbable Thread Lift Suture Materials. 评估和比较不同可吸收线提升缝合材料的不良反应率。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-23 DOI: 10.1097/DSS.0000000000004466
Avaneesh Sean Ojha, Navid Farahbakhsh, Sami K Saikaly

Background: Thread lifting, a minimally invasive alternative to facial rhytidectomy, has shifted from using nonabsorbable to absorbable sutures. Although many thread lift options exist, the impact of these different properties on complication rates remains unclear.

Objective: To systematically compare thread lift complication rates across different suture materials, textures, fixation methods, and lift locations.

Materials/methods: A systematic review was conducted through February 2024, following PRISMA guidelines, using multiple databases. The study focused on absorbable sutures, excluding nonabsorbable materials. Statistical analysis used Chi-Square tests with Bonferroni correction.

Results: Nineteen studies, encompassing 1,406 patients, met inclusion criteria. A total of 876 complications were reported. Ecchymosis (19.49%), swelling (16.79%), and tenderness (9.96%) were the most frequent complications, while hematoma (0.64%), paresthesia (1.14%), and infection (2.49%) were least frequent. Complications varied significantly among the studied factors. Swelling and ecchymosis were more associated with polycaprolactone sutures, barbed threads, and midface lifts. Barbed threads were associated with more complications than smooth or coned threads, as were floating threads compared with fixed threads.

Conclusion: Variations in thread lift suture materials and fixation technique were associated with different complication rates. Thread lifts using absorbable sutures exhibited complication rates under 5%, suggesting a generally favorable safety profile.

背景:作为面部除皱术的微创替代方法,线提升术已从使用不可吸收缝合线转向可吸收缝合线。虽然有很多线提法可供选择,但这些不同特性对并发症发生率的影响仍不清楚:系统比较不同缝合材料、质地、固定方法和提升位置的线拉皮并发症发生率:根据 PRISMA 指南,使用多个数据库对截至 2024 年 2 月的研究进行了系统性回顾。研究重点是可吸收缝合线,不包括不可吸收材料。统计分析采用 Chi-Square 检验和 Bonferroni 校正:19项研究符合纳入标准,共涉及1406名患者。共报告了 876 例并发症。瘀斑(19.49%)、肿胀(16.79%)和压痛(9.96%)是最常见的并发症,而血肿(0.64%)、麻痹(1.14%)和感染(2.49%)是最少见的并发症。并发症在所研究的因素中差异很大。肿胀和瘀斑与聚己内酯缝合线、带刺线和中面部提升术的关系更大。与光滑线或锥形线相比,倒刺线的并发症更多,与固定线相比,浮动线的并发症也更多:结论:线拉提术缝合材料和固定技术的变化与不同的并发症发生率有关。使用可吸收缝线的线拉提术的并发症发生率低于 5%,表明其安全性总体良好。
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引用次数: 0
Comparing Google Trends Public Interest in Microcurrent Therapy Devices With Scientific Evidence for Microcurrents for Antiaging. 比较谷歌趋势中公众对微电流治疗设备的兴趣与微电流抗衰老的科学证据。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-23 DOI: 10.1097/DSS.0000000000004479
Aileen Park, Leo Wan, Peter Lio
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引用次数: 0
Microneedling With Topical Insulin Versus Microneedling With Placebo in the Treatment of Postacne Atrophic Scars: A Randomized Control Trial. 治疗痤疮后萎缩性疤痕的局部胰岛素微针疗法与安慰剂微针疗法:随机对照试验。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-23 DOI: 10.1097/DSS.0000000000004462
Rania Mounir Abdelhay, Manar Saeed Ali, Leila Zeiad Gad, Nahla Maher Mahran

Background: Among the treatment modalities for post-acne scars, microneedling is considered a safe and effective method.

Objective: To compare the efficacy and safety of combined microneedling with topical insulin versus microneedling with placebo (topical saline) in treating atrophic acne scars.

Methods and materials: Twenty-one patients with atrophic post-acne scars were randomized and treated in a split face manner with 4 sessions at 3-week intervals of microneedling using dermapen, followed by application of insulin on one side of the face and saline (placebo) on the other side. Evaluation of response was done before the sessions and after 1 month of the last session using the Global Scarring Grading System of Goodman & Baron and Lipper & Perez scores, Patient reported acne scar improvement using a 4-point scale, patient satisfaction, and the facial acne scar quality of life tools.

Results: Both therapeutic modalities yielded a statistically significant improvement of atrophic acne scars. By comparing both modalities, there was no statistical significance regarding clinical improvement and side effects.

Conclusion: Using topical insulin combined with microneedling may have a value in improving atrophic acne scars, suggesting further evaluation using different delivery systems, insulin formulations, and assessment modalities.

背景:在治疗痤疮后疤痕的方法中,微针疗法被认为是一种安全有效的方法:比较微针联合外用胰岛素与微针联合安慰剂(外用生理盐水)治疗萎缩性痤疮疤痕的有效性和安全性:21名萎缩性痤疮后疤痕患者被随机分为两组,每组4次,每次间隔3周,使用皮肤针进行微针治疗,然后一侧面部涂抹胰岛素,另一侧面部涂抹生理盐水(安慰剂)。在疗程前和最后一次疗程结束 1 个月后,使用 Goodman & Baron 的全球瘢痕分级系统和 Lipper & Perez 的评分标准对疗效进行评估,并使用 4 点量表对患者报告的痤疮疤痕改善情况、患者满意度和面部痤疮疤痕生活质量工具进行评估:结果:两种治疗方法都能显著改善萎缩性痤疮疤痕。结果:两种治疗方法对萎缩性痤疮疤痕的改善均有统计学意义,但两种治疗方法在临床改善和副作用方面的比较无统计学意义:结论:外用胰岛素结合微针疗法可能对改善萎缩性痤疮疤痕有一定价值,建议使用不同的给药系统、胰岛素配方和评估方式进行进一步评估。
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引用次数: 0
Reconstruction of a Wide Mental Defect. 大面积心理缺陷的重建。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-23 DOI: 10.1097/DSS.0000000000004460
Marcus G Tan, Stanislav N Tolkachjov
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引用次数: 0
Subcutaneous Leiomyosarcoma Presenting as Tophaceous Gout on the Left Knee. 表现为左膝痛风顶的皮下线粒体肉瘤
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-23 DOI: 10.1097/DSS.0000000000004465
Christine P Lin, Danny Linggonegoro, Hubert Lau, Kristin Nord
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引用次数: 0
Comparison of Patient Reported Sensory Hypersensitivity in Mohs and Interventional Pain Patients. 莫氏疗法和介入疗法疼痛患者感官过敏性报告的比较。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-23 DOI: 10.1097/DSS.0000000000004464
Caroline M Wilkowski, Elizabeth M Rao, Alexander K Maytin, Maira Bhatty, Roberta L Klatzky, Salim Hayek, Melinda Lawrence, Jeffrey Janata, Bryan T Carroll
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引用次数: 0
Point-of-Care Ultrasound's Implications for Dermatology: A Focus on POCUS. 护理点超声对皮肤病学的影响:聚焦 POCUS。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-23 DOI: 10.1097/DSS.0000000000004469
Baraa A Hijaz, Grant J Riew, Catherine Pisano, Emily S Ruiz, Vinod E Nambudiri
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引用次数: 0
Midface Projection Using Biostimulatory Poly-l-Lactic Acid Injectable Implant: A Subgroup Analysis of the Cheek Wrinkle Trial. 使用生物刺激性聚乳酸注射植入物进行面中部投影:面颊皱纹试验的分组分析。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-17 DOI: 10.1097/DSS.0000000000004434
Sabrina G Fabi, Jennifer Htd Le, Inna Prygova, Daniel Bråsäter

Background: Correction of cheek wrinkles using poly-l-lactic acid (PLLA-SCA) was demonstrated in a 12-month study.

Objective: This analysis assessed change from baseline in lifting effect of PLLA-SCA using a 3D camera to provide additional quantified data.

Methods: Subjects received PLLA-SCA (reconstituted in 8 mL of sterile water + 1 mL of 2% lidocaine) in both cheeks or no treatment (control). Assessments included the Galderma Cheek Wrinkle Scale (GCWS), aesthetic improvement, and 3D photography. In subjects with severe GCWS at baseline, Canfield software analyzed 3D images for change from baseline in midface volume projection and volume change of both cheeks at Month 9.

Results: The primary study showed a statistically significant higher at-rest GCWS responder rate at Month 12 for PLLA-SCA, 71.6%, versus control, 26.1% (p < .0001). In this Month 9 analysis, mean midface volume projection demonstrated a positive volume shift for PLLA-SCA (left: 0.45 mm; right: 0.34 mm; n = 46) versus control (left: 0.25 mm; right: -0.01 mm; n = 21). Midface volume and max projection changes for PLLA-SCA were +4.88 mL/+1.62 mm (left), +2.84 mL/+1.12 mm (right) versus +0.26 mL/+0.34 mm (left), +0.68 mL/+0.37 mm (right) for control.

Conclusion: Poly-l-lactic acid-treatment of subjects with severe GCWS had a clinically meaningful lifting effect in both cheeks (positive volume shift, positive volume change, and max projection) in the midface.

Clinical trial registry number: NCT04124692.

背景:一项为期 12 个月的研究显示,使用聚乳酸(PLLA-SCA)可矫正脸颊皱纹:一项为期12个月的研究显示,使用聚乳酸(PLLA-SCA)可矫正面颊皱纹:本分析使用三维照相机评估PLLA-SCA的提升效果与基线相比的变化,以提供更多量化数据:受试者双颊接受 PLLA-SCA(用 8 mL 无菌水+1 mL 2% 利多卡因重组)或不接受治疗(对照组)。评估包括Galderma面颊皱纹量表(GCWS)、美学改善和3D摄影。对于基线值为严重 GCWS 的受试者,Canfield 软件会分析三维图像,以确定与基线值相比,受试者在第 9 个月时的中面部容积投影和双颊容积变化:主要研究结果显示,在第 12 个月时,PLLA-SCA 的静息 GCWS 回复率为 71.6%,而对照组为 26.1%,差异有统计学意义(P < .0001)。在第 9 个月的分析中,PLLA-SCA(左:0.45 毫米;右:0.34 毫米;n = 46)与对照组(左:0.25 毫米;右:-0.01 毫米;n = 21)相比,平均中面部体积投影显示出正的体积移动。PLLA-SCA的中面体积和最大投影变化分别为+4.88 mL/+1.62 mm(左)、+2.84 mL/+1.12 mm(右),而对照组为+0.26 mL/+0.34 mm(左)、+0.68 mL/+0.37 mm(右):临床试验登记号:NCT04124692:临床试验登记号:NCT04124692。
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引用次数: 0
Squamous Cell Carcinoma Emerging From a Decades-Old Condyloma Acuminatum: A Rare Malignant Transformation of Low-Risk HPV. 从几十年前的尖锐湿疣演变而来的鳞状细胞癌:一种罕见的低风险 HPV 恶性转化。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-16 DOI: 10.1097/DSS.0000000000004459
Joseph Gofman, Colin Burnette, Daniel L Fischer, Sourab Choudhury
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引用次数: 0
Topical Therapies for Periorbital Dyschromia: A 30-Year Review of the Literature. 眶周畸形的局部疗法:30年文献回顾。
IF 2.5 3区 医学 Q2 DERMATOLOGY Pub Date : 2024-10-16 DOI: 10.1097/DSS.0000000000004429
Emily Woolhiser, Michelle Sobotka, Colin Burnette, Lauren Gawey, Cory A Dunnick

Background: Periorbital dyschromia (POD) is a prevalent dermatologic problem with multifactorial etiology, making treatment outcomes inconsistent and unclear.

Objective: To evaluate and compose a comprehensive review of topical ingredients proven to be effective in the treatment of POD.

Materials and methods: Scopus, PubMed, and OVID databases were searched in a span of 30 years through December 31, 2023, to identify articles with original findings of topical therapies for the treatment of POD. Findings of interest were objectively and subjectively measured regarding pigmentation, skin texture, aesthetic improvement, elasticity, hydration, and eye-bag volume.

Results: The database searches yielded 339 unique studies. After screening and review, 22 studies were included totaling 13 nonrandomized control trials, 7 randomized clinical trials, 1 retrospective case series, and 1 prospective single-arm study. Studies included all reported statistically significant results with topical therapies inclusive of acids, bark extract, bicyclic monoterpene diols, caffeine, combo ingredient serums, ethyl ximenynate, gentiopicroside, glycosaminoglycans, growth factors, topical PRP, and vitamins.

Conclusion: The findings of this review suggest that topical therapies can be effective in the treatment of POD. Future trials should focus on delineating specific etiology of POD and evaluation of therapies specific to their cause.

背景:眶周色素沉着症(POD)是一种普遍存在的皮肤病,其病因是多因素的,因此治疗效果不一致且不明确:材料与方法:对 Scopus、PubMed 和 OVID 数据库进行了检索,检索时间跨度为 30 年,截止日期为 2023 年 12 月 31 日,以确定治疗 POD 的外用疗法的原始研究结果的文章。感兴趣的研究结果是对色素沉着、皮肤质地、美学改善、弹性、水合作用和眼袋体积进行客观和主观测量的结果:结果:在数据库中搜索到 339 项独特的研究。经过筛选和审查,共纳入 22 项研究,包括 13 项非随机对照试验、7 项随机临床试验、1 项回顾性病例系列研究和 1 项前瞻性单臂研究。所有纳入的研究都报告了局部疗法(包括酸类、树皮提取物、双环单萜二醇、咖啡因、复合成分血清、西门酸乙酯、龙胆甙、糖胺聚糖、生长因子、局部 PRP 和维生素)在统计学上的显著效果:本综述的研究结果表明,局部疗法可以有效治疗 POD。未来的试验应侧重于明确 POD 的具体病因,并评估针对其病因的疗法。
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Dermatologic Surgery
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