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Extended Butterfly Graft for Functional and Cosmetic Correction of Saddle Nose Deformity. 扩展蝴蝶移植在鞍鼻畸形的功能和美容矫正中的应用。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.0815
Xavier Vega-Córdova, M. Brenner, Harrison C Putman
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引用次数: 2
Postoperative Antibiotic Use Among Patients Undergoing Functional Facial Plastic and Reconstructive Surgery. 功能性面部整形和重建手术患者术后抗生素的使用。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.1027
C. Olds, Emily A. Spataro, Kevin Li, Cherian K. Kandathil, Sam P. Most
ImportanceBest practices for antibiotic use after facial plastic and reconstructive procedures have been the subject of much debate, and there is a need for large-scale data to guide further development of evidence-based guidelines for antibiotic use in this setting.ObjectiveTo assess patterns of postoperative antibiotic prescriptions and infection rates after nasal and oculoplastic procedures.Design, Setting, and ParticipantsA retrospective population-based cohort study was conducted using IBM MarketScan Commercial and Medicare Supplemental research databases of 294 039 patients who underwent facial plastic surgery procedures between January 1, 2007, and December 31, 2015. Patients were excluded if they were younger than 18 years, lacked continuous insurance coverage for 1 year before and after the procedure, or underwent additional procedures on the surgery date of interest. Statistical analysis was performed from January 1, 2007, to December 31, 2016.Main Outcomes and MeasuresPrimary outcomes were antibiotic prescription patterns in the immediate postoperative period and rates of postoperative infectious complications. Explanatory variables included patient demographics, procedure type, and relevant comorbidities, which were used in multivariable logistic regression analysis.ResultsOf the 294 039 patients who met inclusion criteria (55.9% women and 44.1% men; mean [SD] age, 54.0 [18.6 years]), 45.2% filled prescriptions for postoperative antibiotics, including 55.3% of patients undergoing nasal procedures and 14.7% of patients undergoing oculoplastic procedures. Superficial surgical site infections occurred in 1.6% of patients, while deep surgical site infections occurred in 0.3% of patients. On multivariable logistic regression, patients receiving postoperative antibiotics were at significantly decreased risk of postoperative infections (nasal procedures: adjusted odds ratio [aOR], 0.144 [95% CI, 0.102-0.203]; oculoplastic procedures: aOR, 0.254 [95% CI, 0.104-0.622]) compared with those who did not receive postoperative antibiotics. Increased duration of postoperative antibiotics was not associated with reduced rates of infectious complications (nasal procedures: aOR, 1.000 [95% CI, 0.978-1.022]; oculoplastic procedures: aOR, 1.024 [95% CI, 0.959-01.092]). Despite being more likely to experience postoperative infections, patients with a history of tobacco use (aOR, 0.806 [95% CI, 0.747-0.870]), immunodeficiency (aOR, 0.774 [95% CI, 0.737-0.813]), or type 1 or 2 diabetes (aOR, 0.810 [95% CI, 0.772-0.850]) were less likely to be prescribed antibiotics than those without these conditions.Conclusions and RelevancePostoperative antibiotic prescriptions were associated with reduced rates of infections after facial plastic surgery. This study highlights the role of population-level data in the development of best practices for postoperative antibiotic use and identifies the need for additional examination of antibiotic use patt
重要性面部整形和重建手术后使用抗生素的最佳实践一直是争论的主题,需要大量数据来指导在这种情况下使用抗生素的循证指南的进一步发展。目的评估鼻、眼整形术后抗生素处方模式及感染率。设计、设置和参与者使用IBM MarketScan商业和医疗保险补充研究数据库进行了一项基于人群的回顾性队列研究,共294人 在2007年1月1日至2015年12月31日期间接受面部整形手术的039名患者。如果患者年龄小于18岁,在手术前后1年内没有持续保险,或者在感兴趣的手术日期接受了额外的手术,则将其排除在外。从2007年1月1日至2016年12月31日进行统计分析。主要结果和测量主要结果是术后即刻的抗生素处方模式和术后感染并发症的发生率。解释变量包括患者人口统计学、手术类型和相关合并症,这些变量用于多变量逻辑回归分析。294的结果 039名符合纳入标准的患者(55.9%的女性和44.1%的男性;平均[SD]年龄为54.0[18.6]),45.2%的患者开具了术后抗生素处方,其中55.3%的患者接受了鼻腔手术,14.7%的患者接受眼整形手术。1.6%的患者发生浅表手术部位感染,0.3%的患者发生深部手术部位感染。在多变量逻辑回归中,与未接受术后抗生素治疗的患者相比,接受术后抗菌药物治疗的患者术后感染风险显著降低(鼻腔手术:调整比值比[aOR],0.144[95%CI,0.102-0.203];眼整形手术:aOR,0.254[95%CI,0.104-0.622])。术后抗生素使用时间的延长与感染并发症发生率的降低无关(鼻腔手术:aOR,1.000[95%CI,0.978-1.022];眼整形手术:aOR1.024[95%CI:0.959-01.092])。尽管有吸烟史的患者更有可能经历术后感染(aOR,0.806[95%CI;0.747-0.870]),免疫缺陷(aOR,0.774[95%CI,0.737-0.813]。结论和相关性面部整形术后抗生素处方与降低感染率有关。这项研究强调了人群水平的数据在制定术后抗生素使用最佳实践中的作用,并确定了对抗生素使用模式进行额外检查的必要性,并为术后伤口感染风险增加的人群提出了建议。
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引用次数: 17
Alopecia Following Deoxycholic Acid Treatment for Submental Adiposity. 脱氧胆酸治疗颏下脂肪沉积后的脱发。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.0640
D. Sebaratnam, X. L. Wong, L. Kim, K. Cheung
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引用次数: 16
A Practical Precaution Relevant to Facial Injections-Reply. 与面部注射相关的实用预防措施回复。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.1082
V. Venning, K. Cheung, D. Sebaratnam
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引用次数: 0
Molecular Characterization of Lipoaspirates Used in Regenerative Head and Neck Surgery. 用于再生头颈部手术的吸脂剂的分子特性。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.0851
K. Sharaf, A. Kleinsasser, S. Schwenk-Zieger, O. Gires, H. Schinke, V. Kohlbauer, M. Jakob, M. Canis, F. Haubner
ImportanceAdipose-derived mesenchymal stem cells (ASCs) have been used commonly in regenerative medicine and increasingly for head and neck surgical procedures. Lipoaspiration with centrifugation is purported to be a mild method for the extraction of ASCs used for autologous transplants to restore tissue defects or induce wound healing. The content of ASCs, their paracrine potential, and cellular potential in wound healing have not been explored for this method to our knowledge.ObjectiveTo evaluate the characteristics of lipoaspirates used in reconstructive head and neck surgical procedures with respect to wound healing.Design, Setting, and ParticipantsThis case series study included 15 patients who received autologous fat injections in the head and neck during surgical procedures at a tertiary referral center. The study was performed from October 2017 to November 2018, and data were analyzed from October 2017 to February 2019.Main Outcomes and MeasuresExcessive material of lipoaspirates from subcutaneous abdominal fatty tissue was examined. Cellular composition was analyzed using immunohistochemistry (IHC) and flow cytometry, and functionality was assessed through adipose, osteous, and chondral differentiation in vitro. Supernatants were tested for paracrine ASC functions in fibroblast wound-healing assays. Enzyme-linked immunosorbent assay measurement of tumor necrosis factor (TNF), vascular endothelial growth factor (VEGF), stromal-derived factor 1α (SDF-1α), and transforming growth factor β3 (TGF-β3) was performed.ResultsAmong the 15 study patients (8 [53.3%] male; mean [SD] age at the time of surgery, 63.0 [2.8] years), the stromal vascular fraction (mean [SE], 53.3% [4.2%]) represented the largest fraction within the native lipoaspirates. The cultivated cells were positive for CD73 (mean [SE], 99.90% [0.07%]), CD90 (99.40% [0.32%]), and CD105 (88.54% [2.74%]); negative for CD34 (2.70% [0.45%]) and CD45 (1.74% [0.28%]) in flow cytometry; and negative for CD14 (10.56 [2.81] per 300 IHC score) and HLA-DR (6.89 [2.97] per 300 IHC score) in IHC staining; they differentiated into osteoblasts, adipocytes, and chondrocytes. The cultivated cells showed high expression of CD44 (mean [SE], 99.78% [0.08%]) and CD273 (82.56% [5.83%]). The supernatants were negative for TNF (not detectable) and SDF-1α (not detectable) and were positive for VEGF (mean [SE], 526.74 [149.84] pg/mL for explant supernatants; 528.26 [131.79] pg/106 per day for cell culture supernatants) and TGF-β3 (mean [SE], 22.79 [3.49] pg/mL for explant supernatants; 7.97 [3.15] pg/106 per day for cell culture supernatants). Compared with control (25% or 50% mesenchymal stem cell medium), fibroblasts treated with ASC supernatant healed the scratch-induced wound faster (mean [SE]: control, 1.000 [0.160]; explant supernatant, 1.369 [0.070]; and passage 6 supernatant, 1.492 [0.094]).Conclusions and RelevanceThe cells fulfilled the international accepted criteria for mesenc
重要性脂肪来源的间充质干细胞(ASCs)已广泛用于再生医学,并越来越多地用于头颈外科手术。离心抽脂被认为是一种温和的提取ASCs的方法,用于自体移植以修复组织缺陷或诱导伤口愈合。据我们所知,这种方法尚未探索ASCs的含量、其旁分泌潜力和伤口愈合中的细胞潜力。目的评价吸脂器在头颈部重建手术中的伤口愈合特点。设计、设置和参与者这项病例系列研究包括15名在三级转诊中心接受手术过程中头部和颈部自体脂肪注射的患者。该研究于2017年10月至2018年11月进行,数据分析于2017年11月至2019年2月。主要结果和测量方法检查了腹部皮下脂肪组织中脂肪抽吸物的过量物质。使用免疫组织化学(IHC)和流式细胞术分析细胞组成,并通过体外脂肪、骨和软骨分化评估功能。在成纤维细胞伤口愈合测定中测试上清液的旁分泌ASC功能。采用酶联免疫吸附法测定肿瘤坏死因子(TNF)、血管内皮生长因子(VEGF)、基质衍生因子1α(SDF-1α)和转化生长因子β3(TGF-β3)。结果在15名研究患者中(8名[55.3%]男性;手术时的平均[SD]年龄为63.0[2.8]岁),基质血管分数(平均[SE],53.3%[4.2%])是天然脂肪抽吸物中最大的分数。培养的细胞对CD73(平均[SE],99.90%[0.07%])、CD90(99.40%[0.32%])和CD105(88.54%[2.74%])呈阳性;流式细胞术中CD34(2.70%[0.45%])和CD45(1.74%[0.28%])呈阴性;在IHC染色中CD14(10.56[2.81]每300 IHC评分)和HLA-DR(6.89[2.97]每300 IHC评分)呈阴性;它们分化为成骨细胞、脂肪细胞和软骨细胞。培养的细胞显示出CD44(平均[SE],99.78%[0.08%])和CD273(82.56%[5.83%])的高表达。上清液对TNF(不可检测)和SDF-1α呈阴性,对VEGF呈阳性(外植体上清液的平均[SE]526.74[149.84]pg/mL;细胞培养上清液的平均每天528.26[131.79]pg/106)和TGF-β3(平均[SE],22.79[3.49]外植体上清液为pg/mL;细胞培养上清液每天7.97[3.15]pg/106)。与对照组(25%或50%间充质干细胞培养基)相比,ASC上清液处理的成纤维细胞愈合划痕诱导的伤口更快(平均[SE]:对照组,1.000[0.160];外植体上清液,1.369[0.070];传代6上清液,1.492[0.094])。脂肪抽吸物含有具有增殖和免疫调节特性的多分化潜能的ASCs。分离的ASCs的细胞因子谱具有促进伤口愈合的特征。吸脂器可能具有再生潜力,并在头颈部手术中应用。证据等级NA。
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引用次数: 7
Masseteric-to-Facial Nerve Transfer and Selective Neurectomy for Rehabilitation of the Synkinetic Smile. 面神经块转移和选择性神经切除治疗合动力微笑的康复。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.0689
A. Vincent, Scott E. Bevans, J. Robitschek, G. Wind, M. Hohman
ImportanceSynkinesis is the involuntary movement of 1 area of the face accompanying volitional movement of another; it is commonly encountered in patients affected by facial palsy. Current treatments for synkinesis include biofeedback for muscular retraining and chemodenervation via the injection of botulinum toxin. Chemodenervation is effective in reducing unwanted muscle movement, but it requires a commitment to long-term maintenance injections and may lose effectiveness over time. A permanent solution for synkinesis remains elusive.ObjectiveTo evaluate masseteric-to-facial nerve transfer with selective neurectomy in rehabilitation of the synkinetic smile.Design, Setting, and ParticipantsIn this case series, 7 patients at a tertiary care teaching hospital underwent masseteric-to-facial nerve transfer with selective neurectomy for synkinesis between September 14, 2015, and April 19, 2018. The medical records of these patients were retrospectively reviewed and demographic characteristics, facial palsy causes, other interventions used, and changes in eFACE scores were identified.InterventionMasseteric-to-facial nerve transfer.Main Outcomes and MeasuresChanges in eFACE scores (calculated via numeric scoring of many sections of the face, including flaccidity, normal tone, and hypertonicity; higher scores indicate better function and lower scores indicate poorer function) and House-Brackmann Facial Nerve Grading System scores (range, 1-6; a score of 1 indicates normal facial function on the affected side, and a score of 6 indicates absence of any facial function [complete flaccid palsy] on the affected side).ResultsAmong the 7 patients in the study (6 women and 1 man; median age, 49 years [range, 41-63 years]), there were no postoperative complications; patients were followed up for a mean of 12.8 months after surgery (range, 11.0-24.5 months). Patients experienced a significant improvement in mean (SD) eFACE scores in multiple domains, including smile (preoperative, 65.00 [8.64]; postoperative, 76.43 [7.79]; P = .01), dynamic function (preoperative, 62.57 [15.37]; and postoperative, 75.71 [8.48]; P = .03), synkinesis (preoperative, 52.70 [4.96]; and postoperative, 82.00 [6.93]; P < .001), midface and smile function (preoperative, 60.71 [13.52]; and postoperative, 78.86 [14.70]; P = .02), and lower face and neck function (preoperative, 51.14 [16.39]; and postoperative, 66.43 [20.82]; P = .046). Preoperative House-Brackmann Facial Nerve Grading System scores ranged from 3 to 4, and postoperative scores ranged from 2 to 3; this change was not significant.Conclusion and RelevanceThis study describes the application of masseteric-to-facial nerve transfer with selective neurectomy for smile rehabilitation in patients with synkinesis, with statistically significant improvement in smile symmetry and lower facial synkinesis as measured with the eFACE tool. This technique may allow for long-term improvement of synkinesis and smile. Th
同步运动是面部一个区域的不自主运动伴随另一个区域的意志运动;常见于面瘫患者。目前的治疗方法包括肌肉再训练的生物反馈和通过注射肉毒杆菌毒素的化学神经支配。化学神经支配在减少不必要的肌肉运动方面是有效的,但它需要长期维持注射,并且可能随着时间的推移而失去效果。永久解决联胞作用的方法仍然难以捉摸。目的探讨选择性按摩面神经移植联合神经切除术对联合运动微笑的康复作用。设计、环境和参与者:在该病例系列中,2015年9月14日至2018年4月19日期间,一家三级护理教学医院的7名患者接受了按摩至面神经移植和选择性神经切除术以治疗联动性。对这些患者的医疗记录进行回顾性分析,确定了人口统计学特征、面瘫原因、使用的其他干预措施以及eFACE评分的变化。介入:按摩-面神经转移。eFACE评分的变化(通过面部许多部分的数字评分计算,包括松弛、正常音调和高张力;分数越高,功能越好,分数越低,功能越差)和House-Brackmann面神经评分系统评分(范围:1-6;1分表示患侧面部功能正常,6分表示患侧没有任何面部功能(完全弛缓性麻痹)。结果本组7例患者(女6例,男1例;中位年龄49岁[范围41 ~ 63岁]),无术后并发症;术后平均随访12.8个月(11.0 ~ 24.5个月)。患者在多个领域的平均(SD) eFACE评分显著改善,包括微笑(术前,65.00 [8.64];术后76.43 [7.79];P = 0.01),动态函数(术前,62.57 [15.37];术后,75.71 [8.48];P = 0.03),综合运动(术前,52.70 [4.96];术后82.00 [6.93];P < 0.001),中脸和微笑功能(术前,60.71 [13.52];术后78.86 [14.70];P = .02),下面部和颈部功能(术前,51.14 [16.39];术后66.43 [20.82];p = .046)。术前House-Brackmann面神经评分系统评分为3 ~ 4分,术后评分为2 ~ 3分;这种变化并不显著。结论与相关性本研究描述了选择性神经切除术中咬面神经移植对伴联动患者微笑康复的应用,用eFACE工具测量的微笑对称性和下面部联动的改善具有统计学意义。这项技术可以长期改善肢体协调和微笑。这项研究只是初步的,更大的队列将允许对这种治疗方式进行更准确的评估。证据水平
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引用次数: 19
Clarification of a Suspension Technique for Unstable Nasal Bones. 不稳定鼻骨悬浮液技术的澄清。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.1110
Michele Ori, G. Ricci, L. D'Ascanio
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引用次数: 2
The Tripod Concept of the Upper Nasal Third. 上鼻三音的三脚架概念。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.0884
Laura E. T. Hetzler, Victoria B Givens, J. Sykes
ImportanceThe tripod theory of the upper nasal third parallels the concept of the well-known nasal tip tripod. We are evaluating the idea that one can simply alter the upper nasal angles reliably without the complex physics associated with the nasal tip to achieve a pleasing cosmetic result.ObjectiveTo describe a concept related to the well-known tripod theory with extrapolation to the upper nasal third as it pertains to cosmetic rhinoplasty.Design, Setting, and ParticipantsThis is a prospective study in which lateral photographs of 3 women who had not undergone surgery (age range, 20-50 years) were selected for digital manipulation of the nasal radix with subsequent alteration of the nasofrontal and nasofacial angles via imaging software. The altered images were analyzed by 20 blinded individuals between July 2009 and June 2017 to assess how changes in the height of the nasal dorsum and radix alone affect nasal appearance and the perception of ideal nasal angles. The study took place at a tertiary center, and the patients chosen for evaluation had nasal architecture that only required subtle changes rather than structure that demonstrated glaringly obvious overprojection or underprojection and rotation or a large dorsal bony hump. Analysis began June 2018.Main Outcomes and MeasuresOverall trend in recognition of objective and subjective alterations in projection and rotation for the rhinoplasty- and non-rhinoplasty-trained evaluators.ResultsTen medically trained and 10 lay individuals (13 women [65%]; mean [SD] age, 38 [8.6] years) analyzed digitally manipulated photographs of 3 women (age range, 20-50 years) who had not undergone surgery. Lay individuals were more likely to choose an ideal nasal profile based on surrounding facial architecture (28 of 30 [93%]), while individuals with rhinoplasty training tended to separate the ideal nose from the surrounding face (18 of 30 [60%]) (P < .001). Projection was consistently and accurately recognized as being altered by both rhinoplasty-trained and lay individuals (95% CI, -0.18 to 0.38; P = .60 and 95% CI, -0.26 to 0.33; P > .99 for most and least projected), whereas subjective changes in rotation were significantly more elusive to the lay individual (95% CI, -0.04 to 0.52; P = .12 and 95% CI, 0.11 to 0.65; P = .01 for most and least rotated).Conclusions and RelevancePredictable and consistent aesthetic results are the primary aim in rhinoplasty. Alterations in the upper nasal tripod are more reliable with extrapolated healing than with the tripod of the nasal tip. Ultimately, simple alteration of the upper nasal third can result in an improved nasal profile without specific alteration of tip architecture.Level of EvidenceNA.
重要性上鼻三分之一的三脚架理论与著名的鼻尖三脚架的概念相似。我们正在评估这样一种想法,即人们可以简单可靠地改变上鼻角度,而不需要与鼻尖相关的复杂物理,从而获得令人满意的美容效果。目的描述一个与著名的三脚架理论相关的概念,并将其外推到上鼻三分之一,因为它与美容鼻成形术有关。设计、设置和参与者这是一项前瞻性研究,选择了3名未接受手术的女性(年龄范围为20-50岁)的侧位照片,通过成像软件对鼻根进行数字操作,随后改变鼻额角和鼻面角。在2009年7月至2017年6月期间,20名盲人对改变后的图像进行了分析,以评估鼻背和鼻根高度的变化如何单独影响鼻腔外观和理想鼻角的感知。这项研究在一家三级中心进行,被选为评估对象的患者的鼻腔结构只需要细微的变化,而不是表现出明显的过度注射或注射不足和旋转或大的背侧骨隆起的结构。分析始于2018年6月。主要结果和衡量标准接受过隆鼻术和非隆鼻术培训的评估人员对投影和旋转的客观和主观变化的总体认识趋势。结果10名受过医学训练的非专业人员(13名女性[65%];平均[SD]年龄,38[8.6]岁)分析了3名未接受手术的女性(年龄范围,20-50岁)的数字处理照片。躺在床上的人更有可能根据周围的面部结构选择理想的鼻子轮廓(30人中有28人[93%]),而接受过隆鼻术训练的人倾向于将理想的鼻子与周围的面部分开(30人的18人[60%])(P  .99表示投影最多和投影最少),而旋转的主观变化对外行来说明显更难以捉摸(95%CI,-0.04至0.52;P=.12和95%CI,0.11至0.65;P=.01表示旋转最多和最少)。结论和相关性可预测和一致的美学结果是鼻整形术的主要目的。与鼻尖三脚架相比,上鼻三脚架的改变更可靠。最终,上鼻三分之一的简单改变可以在不改变尖端结构的情况下改善鼻腔轮廓。证据等级NA。
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引用次数: 4
Effect of a Vibratory Anesthetic Device on Pain Anticipation and Subsequent Pain Perception Among Patients Undergoing Cutaneous Cancer Removal Surgery: A Randomized Clinical Trial. 振动麻醉装置对接受皮肤癌切除手术患者疼痛预期和随后疼痛感知的影响:一项随机临床试验。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.0733
P. Govas, R. Kazi, Rachel M Slaugenhaupt, B. Carroll
ImportanceVibration has been shown to decrease injection site pain in patients; however, to date, this effect has not been assessed for patients who catastrophize pain (ie, patients who anticipate a higher pain level). The anticipation of a pain score greater than 4 on the 11-point Numeric Rating Scale (NRS) has been associated with an increase in a patient's perception of procedural pain.ObjectiveTo assess the efficacy of vibration during cutaneous anesthetic injection for dermatologic surgery for patients who catastrophize pain (NRS score >4) and patients who do not (NRS score ≤4).Design, Setting, and ParticipantsRandomized, parallel-group clinical trial from June 19 to September 4, 2018, at a tertiary dermatologic surgery clinic among 87 adults undergoing cutaneous cancer removal surgery. Patients completed a preprocedural questionnaire detailing their baseline pain, anticipated pain, and drug use. Analysis was performed on an intent-to-treat basis.InterventionsUse of a vibratory anesthetic device (VAD) on the treatment site prior to anesthetic injection in the on (VAD ON) or off (VAD OFF) mode.Main Outcomes and MeasuresPain was reported using the 11-point NRS (where 0 indicates no pain and 11 indicates the worst pain imaginable). A minimum clinically important difference of 22% or more and a substantial clinically important difference of 57% or more were used to assess the efficacy of vibration in patient-reported NRS score during anesthetic injection (iNRS score).ResultsA total of 87 patients were included, with 101 unique events reported (among the unique events, 37 were reported in women and 64 were reported in men; mean [SD] age, 66.0 [11.3] years). The mean (confidence level [CL]) iNRS score for patients who catastrophized pain was 2.27 (0.66) compared with 1.44 (0.39) for patients who did not (P = .03). A 38.9% decrease in mean (CL) iNRS score was reported with VAD ON compared with VAD OFF in all participants (1.24 [0.38] vs 2.04 [0.54]). Patients who catastrophized pain reported a 25.5% decrease in mean (CL) iNRS score with VAD ON vs VAD OFF (1.91 [0.99] vs 2.57 [0.98]), and patients who did not reported a 79.4% decrease (1.02 [0.40] vs 1.84 [0.66]). VAD ON was the only statistically significant variable to affect iNRS score (F statistic, 2.741; P = .03).Conclusions and RelevanceThis trial demonstrates that those who catastrophize pain prior to a procedure report a higher perceived level of pain. The application of vibration during local anesthetic injection resulted in a minimum clinically important difference in pain level for patients who catastrophize pain and a substantial clinically important difference in pain level for patients who do not.Level of Evidence2.Trial RegistrationClinicalTrials.gov identifier: NCT03467685.
重要的是,振动已被证明可以减少患者注射部位的疼痛;然而,到目前为止,这种影响还没有被评估的患者灾难的疼痛(即患者预期更高的疼痛水平)。在11分的数字评定量表(NRS)中,对疼痛评分大于4分的预期与患者对程序性疼痛的感知增加有关。目的评价震动对皮肤外科手术中出现巨痛(NRS评分≤4分)和无巨痛(NRS评分≤4分)患者注射皮麻的效果。设计、环境和参与者:2018年6月19日至9月4日,在一家三级皮肤外科诊所进行随机、平行组临床试验,共87名接受皮肤癌切除手术的成年人。患者完成了手术前问卷调查,详细说明了他们的基线疼痛、预期疼痛和药物使用情况。在意向治疗基础上进行分析。干预在麻醉注射前在治疗部位使用振动麻醉装置(VAD),打开(VAD on)或关闭(VAD off)模式。主要结果和测量方法使用11分NRS(0表示无疼痛,11表示可想象的最严重疼痛)报告疼痛。最小临床重要差异为22%或以上,显著临床重要差异为57%或以上,用于评估振动对麻醉注射期间患者报告的NRS评分(iNRS评分)的疗效。结果共纳入87例患者,报告独特事件101例(其中女性37例,男性64例;平均[SD]年龄,66.0[11.3]岁)。疼痛灾难化患者的平均iNRS评分(置信水平[CL])为2.27(0.66),而疼痛灾难化患者的平均iNRS评分为1.44 (0.39)(P = 0.03)。与VAD关闭组相比,VAD开启组的平均(CL) iNRS评分降低了38.9% (1.24 [0.38]vs 2.04[0.54])。严重疼痛的患者报告VAD ON与VAD OFF的平均(CL) iNRS评分下降25.5% (1.91 [0.99]vs 2.57[0.98]),未报告的患者报告下降79.4% (1.02 [0.40]vs 1.84[0.66])。VAD ON是影响iNRS评分的唯一有统计学意义的变量(F统计量,2.741;p = .03)。结论和相关性本试验表明,那些在手术前灾难化疼痛的人报告了更高的疼痛感知水平。在局部麻醉注射过程中,振动的应用对巨灾性疼痛患者的疼痛水平产生了最小的临床重要差异,而对非巨灾性疼痛患者的疼痛水平产生了重大的临床重要差异。2.证据水平临床试验注册号:NCT03467685。
{"title":"Effect of a Vibratory Anesthetic Device on Pain Anticipation and Subsequent Pain Perception Among Patients Undergoing Cutaneous Cancer Removal Surgery: A Randomized Clinical Trial.","authors":"P. Govas, R. Kazi, Rachel M Slaugenhaupt, B. Carroll","doi":"10.1001/jamafacial.2019.0733","DOIUrl":"https://doi.org/10.1001/jamafacial.2019.0733","url":null,"abstract":"Importance\u0000Vibration has been shown to decrease injection site pain in patients; however, to date, this effect has not been assessed for patients who catastrophize pain (ie, patients who anticipate a higher pain level). The anticipation of a pain score greater than 4 on the 11-point Numeric Rating Scale (NRS) has been associated with an increase in a patient's perception of procedural pain.\u0000\u0000\u0000Objective\u0000To assess the efficacy of vibration during cutaneous anesthetic injection for dermatologic surgery for patients who catastrophize pain (NRS score >4) and patients who do not (NRS score ≤4).\u0000\u0000\u0000Design, Setting, and Participants\u0000Randomized, parallel-group clinical trial from June 19 to September 4, 2018, at a tertiary dermatologic surgery clinic among 87 adults undergoing cutaneous cancer removal surgery. Patients completed a preprocedural questionnaire detailing their baseline pain, anticipated pain, and drug use. Analysis was performed on an intent-to-treat basis.\u0000\u0000\u0000Interventions\u0000Use of a vibratory anesthetic device (VAD) on the treatment site prior to anesthetic injection in the on (VAD ON) or off (VAD OFF) mode.\u0000\u0000\u0000Main Outcomes and Measures\u0000Pain was reported using the 11-point NRS (where 0 indicates no pain and 11 indicates the worst pain imaginable). A minimum clinically important difference of 22% or more and a substantial clinically important difference of 57% or more were used to assess the efficacy of vibration in patient-reported NRS score during anesthetic injection (iNRS score).\u0000\u0000\u0000Results\u0000A total of 87 patients were included, with 101 unique events reported (among the unique events, 37 were reported in women and 64 were reported in men; mean [SD] age, 66.0 [11.3] years). The mean (confidence level [CL]) iNRS score for patients who catastrophized pain was 2.27 (0.66) compared with 1.44 (0.39) for patients who did not (P = .03). A 38.9% decrease in mean (CL) iNRS score was reported with VAD ON compared with VAD OFF in all participants (1.24 [0.38] vs 2.04 [0.54]). Patients who catastrophized pain reported a 25.5% decrease in mean (CL) iNRS score with VAD ON vs VAD OFF (1.91 [0.99] vs 2.57 [0.98]), and patients who did not reported a 79.4% decrease (1.02 [0.40] vs 1.84 [0.66]). VAD ON was the only statistically significant variable to affect iNRS score (F statistic, 2.741; P = .03).\u0000\u0000\u0000Conclusions and Relevance\u0000This trial demonstrates that those who catastrophize pain prior to a procedure report a higher perceived level of pain. The application of vibration during local anesthetic injection resulted in a minimum clinically important difference in pain level for patients who catastrophize pain and a substantial clinically important difference in pain level for patients who do not.\u0000\u0000\u0000Level of Evidence\u00002.\u0000\u0000\u0000Trial Registration\u0000ClinicalTrials.gov identifier: NCT03467685.","PeriodicalId":14538,"journal":{"name":"JAMA facial plastic surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1001/jamafacial.2019.0733","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42519524","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Outcomes of Extracorporeal Septoplasty and Its Modifications in Treatment of Severe L-Strut Septal Deviation: A Systematic Review and Meta-analysis. 体外中隔成形术及其改良术治疗严重L型间隔偏移的疗效:系统评价和荟萃分析。
Q1 Medicine Pub Date : 2019-11-21 DOI: 10.1001/jamafacial.2019.1020
Emily A. Spataro, M. Saltychev, Cherian K. Kandathil, Sam P. Most
ImportanceWhile extracorporeal septoplasty (ECS) and its modifications have been previously studied, to our knowledge, no systematic review of surgical outcomes and complications of this technique has been performed.ObjectiveTo evaluate the evidence of surgical outcomes and complications of ECS (including modified techniques) to treat severe L-strut septal deviation defined as deviation within 1.0 cm of the caudal or dorsal septum.Data SourcesMEDLINE, Embase, CINAHL, CENTRAL, Scopus, and Web of Science databases and reference lists were searched from inception to April 2018 for clinical and observational studies. Search terms included extracorporeal, septoplasty, and septum.Study SelectionSelection criteria were defined according to the population, intervention, comparison, and outcome framework. Relevant studies were selected by 2 independent reviewers based on abstracts and full texts.Data Extraction and SynthesisData were extracted using standardized lists chosen by the authors according to Cochrane Collaboration guidelines. Data were collected and synthesized with ranges reported, as well as assessment of bias and heterogeneity when applicable. Analysis started in February 2019.Main Outcomes and MeasuresOutcomes assessed included functional nasal airway improvement by objective measurements and subjective measurements (Nasal Obstruction Symptom Evaluation [NOSE] and visual analog scale scores); complications including bleeding, infection, dorsal irregularities, and other functional or cosmetic deficits; and as revision surgery rates.ResultsOf 291 records initially obtained, 31 were considered relevant after review according to PRISMA guidelines. All studies except 1 randomized clinical trial (3.2%) were observational in nature, with 21 retrospective studies (67.7%) and 9 prospective studies (29.0%). Conventional ECS was performed in 16 studies (51.6%), and modified ECS was performed in 15 studies (48.4%). The sample size varied from 10 to 567, and the mean age varied from 22.5 to 46 years. Of 31 studies, 14 (45%) were of good methodology. Meta-analysis was performed on 5 studies reporting change in NOSE scores, with pooled effect of -60.0 (95% CI, -67.8 to -52.2) points, but heterogeneity was high, with I2 = 96%. When comparing complications between modified and conventional ECS, the relative risk for infections was 0.95 (95% CI, 0.34-2.7); for bleeding, 0; for nasal dorsal irregularities, 0.29 (95% CI, 0.16-0.53); for other cosmetic complications, 4.3 (95% CI, 0.87-21.1); for other functional complications, 0.47 (95% CI, 0.20-1.1); and for revision operations, 1.4 (95% CI, 0.83-2.3).Conclusions and RelevanceOf the 31 studies included in this systematic review, less than half were of good methodology, and a significant level of heterogeneity was found regarding type of outcome measure used and reporting of complications. To improve the level of evidence, better study methodology, standardization of surgical outcom
重要性虽然体外隔膜成形术(ECS)及其改良术之前已经进行了研究,但据我们所知,尚未对该技术的手术结果和并发症进行系统审查。目的评估ECS(包括改良技术)治疗严重L型鼻中隔偏曲(定义为尾中隔或背中隔1.0 cm以内的偏曲)的手术结果和并发症的证据。数据来源MEDLINE、Embase、CINAHL、CENTRAL、Scopus和Web of Science数据库和参考文献列表从开始到2018年4月进行了临床和观察性研究搜索。搜索词包括体外,隔膜成形术和隔膜。研究选择根据人群、干预、比较和结果框架确定选择标准。相关研究由2名独立评审员根据摘要和全文进行选择。数据提取和合成使用作者根据Cochrane协作指南选择的标准化列表提取数据。收集数据并将其与报告的范围进行综合,并在适用时评估偏差和异质性。分析始于2019年2月。主要结果和测量结果评估结果包括通过客观测量和主观测量(鼻阻塞症状评估[NOSE]和视觉模拟量表评分)改善鼻气道功能;并发症,包括出血、感染、背部不规则和其他功能或美容缺陷;以及作为翻修手术率。结果根据PRISMA指南,在最初获得的291份记录中,31份在审查后被认为是相关的。除1项随机临床试验(3.2%)外,所有研究均为观察性研究,其中21项为回顾性研究(67.7%),9项为前瞻性研究(29.0%)。16项研究(51.6%)采用常规ECS,15项研究(48.4%)采用改良ECS。样本量从10到567不等,平均年龄从22.5到46岁不等。在31项研究中,有14项(45%)采用了良好的方法。对5项报告NOSE评分变化的研究进行了荟萃分析,综合效应为-60.0(95%CI,-67.8至-52.2)分,但异质性很高,I2 = 96%。当比较改良ECS和传统ECS的并发症时,感染的相对风险为0.95(95%CI,0.34-2.7);出血,0;对于鼻背不规则性,0.29(95%CI,0.16-0.53);对于其他美容并发症,4.3(95%CI,0.87-21.1);对于其他功能性并发症,0.47(95%CI,0.20-1.1);对于翻修手术,为1.4(95%CI,0.83-2.3)。结论和相关性在本系统综述中纳入的31项研究中,只有不到一半的研究具有良好的方法学,并且在使用的结果测量类型和并发症报告方面发现了显著的异质性。为了提高证据水平,需要更好的研究方法、手术结果测量的标准化和并发症的报告。
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引用次数: 10
期刊
JAMA facial plastic surgery
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