Refractive surgery

屈光手术
  • 文章类型: Journal Article
    目的:使用WaveLightAllegrettoEX500准分子激光系统比较机械PRK(mPRK)和跨上皮PRK(tPRK)的屈光结果(Alcon实验室,沃思堡,TX,美国)。
    方法:圣保罗联邦大学眼科,巴西。
    方法:前瞻性随机研究。
    方法:对73例散光和近视患者151只眼,手术前双眼屈光相似,一只眼接受mPRK和对侧眼接受tPRK的消融差异最大为15μm。本研究患者的平均年龄为31.45±6.97岁(范围,22至54岁)。
    结果:对两组之间的所有变量进行比较,我们发现,6个月时,tPRK组的UDVA和SE比mPRK组要差.在mPRK组中,+/-0.50范围内的频率较高,+/-1.50范围内的频率较低.在tPRK组中,然而,+/-0.50范围内的频率较低,+/-1.50范围内的频率较高。关于视线的得失,两组之间没有关联(卡方检验,p=0.887)。
    结论:mPRK和tPRK似乎具有相似的安全性。然而,mPRK与术后6个月明显更好的UDVA和SE相关。
    OBJECTIVE: Compare refractive results between mechanical PRK (mPRK) and transepithelial PRK (tPRK) with WaveLight Allegretto EX500 excimer laser system (Alcon Laboratories, Fort Worth, TX, USA).
    METHODS: Department of Ophthalmology of the Federal University of Sao Paulo, Brazil.
    METHODS: Prospective and randomized study.
    METHODS: In 151 eyes of 73 patients with astigmatism and myopia, both eyes had similar refraction before surgery, with a maximum of 15-µm difference in ablation who underwent mPRK in one eye and tPRK in the contralateral eye. The mean age of the patients in this study was 31.45 ± 6.97 years (range, 22 to 54 years).
    RESULTS: A comparison was made with all variables between the two groups, and we found that UDVA and SE were worse in the tPRK group at six months than in the mPRK group. In the mPRK group, there was a higher frequency in the +/- 0.50 range and a lower frequency in the +/- 1.50 range. In the tPRK group, however, there was a lower frequency in the +/- 0.50 range and a higher frequency in the +/- 1.50 range. Concerning gain or loss of lines of sight, there was no association between the two groups (chi-square test, p = 0.887).
    CONCLUSIONS: Both mPRK and tPRK appear to have similar safety. However, mPRK was associated with significantly better UDVA and SE six months post-operatively.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    评估Zhang和Zheng的InnovEyes(ZZInnovEyes)策略与标准自动化策略相比优化光线追踪引导激光原位角膜磨镶术(LASIK)结果的有效性。
    在杭州MSK眼科医院接受治疗性屈光手术的38例患者(71只眼)被随机分配到ZZInnovEyes和使用双掩蔽随机化的自动组。这项研究评估了视力,屈光结果,术前和手术后1天的高阶像差,2周,1个月,和3个月的随访。用MicrosoftExcel和SPSS19.0进行统计学分析。
    暴露组和对照组包括36只和35只眼睛,分别。与自动方法组相比,ZZInnovEyes组在明显折射球面等效(MRSE)校正方面表现出显著优势(0.13±0.30Dvs0.62±0.40D,p<0.001),在3个月的随访中,实现97.22%的非矫正视力(UDVA)为20/16或更好,而自动化组为85.71%(p=0.08),在3个月的随访中,自动化组的UDVA为20/12.5或更好的50.00%,高于28.57%(p=0.06)。ZZInnovEyes组(0.00%)的术前矫正远距视力到术后UDVA的缺失线低于自动化组(8.57%;p=0.07)。两组均表现出相似的散光矫正和高阶像差。
    ZZInnovEyes战略,它结合了光线追踪引导的LASIK的明显和波前折射,与标准自动化策略相比,显示出较好的MRSE校正和在视力结果方面的潜在优势。这项研究强调了屈光手术中持续优化和研究的必要性。
    ChiCTR2300078709。
    UNASSIGNED: To evaluate the effectiveness of Zhang and Zheng\'s InnovEyes (ZZ InnovEyes) strategy for optimizing outcomes of ray-tracing-guided laser in situ keratomileusis (LASIK) compared to the standard automated strategy.
    UNASSIGNED: A total of 38 patients (71 eyes) undergoing therapeutic refractive surgery at Hangzhou MSK Eye Hospital were randomly assigned to the ZZ InnovEyes and automated groups using double-masked randomization. The study assessed visual acuity, refractive outcomes, and higher-order aberrations preoperatively and at 1-day, 2-week, 1-month, and 3-month follow-ups. Statistical analysis was done with Microsoft Excel and SPSS 19.0.
    UNASSIGNED: The exposure and control groups comprised 36 and 35 eyes, respectively. The ZZ InnovEyes group demonstrated significant advantages in manifest refraction spherical equivalent (MRSE) correction compared to the automated approach group (0.13 ± 0.30 D vs 0.62 ± 0.40 D, p < 0.001), achieving 97.22% uncorrected distance visual acuity (UDVA) of 20/16 or better compared to 85.71% in the automated group at the 3-month follow-up (p = 0.08), and achieving 50.00% UDVA of 20/12.5 or better compared to 28.57% in the automated group at the 3-month follow-up (p = 0.06). Loss lines from preoperative corrected distance visual acuity to postoperative UDVA were lower in the ZZ InnovEyes group (0.00%) than the automated group (8.57%; p = 0.07). Both groups exhibited similar astigmatism corrections and higher-order aberrations.
    UNASSIGNED: The ZZ InnovEyes strategy, which incorporates manifest and wavefront refraction for ray-tracing-guided LASIK, demonstrated superior MRSE correction and potential advantages in visual acuity outcomes compared to the standard automated strategy. This study highlights the need for ongoing optimization and research in refractive surgery.
    UNASSIGNED: ChiCTR2300078709.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    背景:在1年的随访中评估稳定性圆锥角膜(Stable-KCS)的角膜生物力学,并将其与亚临床圆锥角膜(SKC)的角膜生物力学进行比较。
    方法:这项前瞻性病例对照研究包括144例患者的眼睛。记录生物力学和层析成像参数(CorvisST和Pentacam)。稳定KCS组(n=72)包括双眼无圆锥角膜临床征象但有可疑断层扫描结果的患者。纵向随访用于评估Stable-KCS变化。SKC组包括单侧圆锥角膜对侧眼,可疑断层扫描(n=72)。使用T检验和非参数检验进行比较。使用多变量一般线性模型来调整混杂因素以进行进一步分析。使用受试者工作特征(ROC)曲线来分析可分辨性。
    结果:Stable-KCS的生物力学和层析成像参数在随访时间(13.19±2.41个月,p>0.05)。两组之间有15个生物力学参数和应力应变指数(SSI)差异(p<0.016)。Sable-KCS和SKC之间的A1dArc长度显示出最强的区分能力(ROC下的面积=0.888)。在-0.0175的截止值处具有90.28%的灵敏度和77.78%的特异性。
    结论:A1dArc长度可以区分Stable-KCS和SKC,表明在随访期间,有必要关注圆锥角膜嫌疑人的A1dArc长度的变化。虽然两者在断层成像上都有异常,Stable-KCS的角膜生物力学和SSI强于SKC,这可以解释稳定KCS缺乏进展。
    BACKGROUND: To evaluate the corneal biomechanics of stable keratoconus suspects (Stable-KCS) at 1-year follow-up and compare them with those of subclinical keratoconus (SKC).
    METHODS: This prospective case-control study included the eyes of 144 patients. Biomechanical and tomographic parameters were recorded (Corvis ST and Pentacam). Patients without clinical signs of keratoconus in both eyes but suspicious tomography findings were included in the Stable-KCS group (n = 72). Longitudinal follow-up was used to evaluate Stable-KCS changes. Unilateral keratoconus contralateral eyes with suspicious tomography were included in the SKC group (n = 72). T-tests and non-parametric tests were used for comparison. Multivariate general linear models were used to adjust for confounding factors for further analysis. Receiver operating characteristic (ROC) curves were used to analyze the distinguishability.
    RESULTS: The biomechanical and tomographic parameters of Stable-KCS showed no progression during the follow-up time (13.19 ± 2.41 months, p > 0.05). Fifteen biomechanical parameters and the Stress-Strain Index (SSI) differed between the two groups (p < 0.016). The A1 dArc length showed the strongest distinguishing ability (area under the ROC = 0.888) between Stable-KCS and SKC, with 90.28% sensitivity and 77.78% specificity at the cut-off value of -0.0175.
    CONCLUSIONS: The A1 dArc length could distinguish between Stable-KCS and SKC, indicating the need to focus on changes in the A1 dArc length for keratoconus suspects during the follow-up period. Although both have abnormalities on tomography, the corneal biomechanics and SSI of Stable-KCS were stronger than those of SKC, which may explain the lack of progression of Stable-KCS.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    白内障是晶状体中的混浊区域。白内障是导致失明的主要原因,也是世界范围内严重视力障碍的第二大原因。白内障手术期间,取出浑浊的晶状体并用人工人工晶状体代替,恢复光功率。使用现有的模制和车削技术制造人工晶状体是复杂且耗时的过程,其限制了新材料和设计的开发。为了克服这些限制,我们开发了一种基于立体光刻的工艺,用于生产没有折射功能的清晰透镜设计模型,作为概念的证明。这个过程有可能有助于新的镜片开发,允许无限的设计迭代和扩大的材料范围供科学家探索。
    通过使用立体光刻制造没有折射功能的透镜状3D物体。一种含有丙烯酸2-苯氧基乙酯的可光聚合树脂,聚(乙二醇)二甲基丙烯酸酯,并开发了合适的光引发剂用于生产透镜状3D物体原型。通过扫描电子显微镜表征印刷器件的形态。使用分光光度法和差示扫描量热法分析了透明度和热性能,分别。在培养的人晶状体细胞系(FHL-124)中研究了设备的生物相容性,使用标准的乳酸脱氢酶检测,将晶状体折叠并植入人体囊袋模型中。
    使用立体光刻(SLA)技术成功制造了没有折射功能且具有环形触觉设计的单片类透镜3D物体。生成的3D对象是透明的,通过紫外光谱测定。乳酸脱氢酶测试表明晶状体细胞对原型材料的耐受性,在直接注射到体外人囊袋模型中的过程中观察到明显的可折叠性和形状恢复。
    这项原理验证研究证明了快速成型过程对于研究和开发类似透镜的3D物体原型的潜力和意义,如人工晶状体。
    UNASSIGNED: A cataract is a cloudy area in the crystalline lens. Cataracts are the leading cause of blindness and the second cause of severe vision impairment worldwide. During cataract surgery, the clouded lens is extracted and replaced with an artificial intraocular lens, which restores the optical power. The fabrication of intraocular lenses using existing molding and lathing techniques is a complex and time-consuming process that limits the development of novel materials and designs. To overcome these limitations, we have developed a stereolithography-based process for producing models of clear lens designs without refractive function, serving as a proof of concept. This process has the potential to contribute toward new lens development, allowing for unlimited design iterations and an expanded range of materials for scientists to explore.
    UNASSIGNED: Lens-like 3D objects without refractive function were fabricated by using stereolithography. A photopolymerizable resin containing 2-phenoxyethyl acrylate, poly (ethylene glycol) dimethacrylate, and a suitable photoinitiator was developed for the production of lens-like 3D object prototypes. The morphology of the printed devices was characterized by scanning electron microscopy. The transparency and thermal properties were analyzed using spectrophotometry and differential scanning calorimetry, respectively. The biocompatibility of the devices was investigated in a cultured human lens cell line (FHL-124), using a standard lactate dehydrogenase assay, and the lenses were folded and implanted in the human capsular bag model.
    UNASSIGNED: One-piece lens-like 3D objects without refractive function and with loop-haptic design were successfully fabricated using Stereolithography (SLA) technique. The resulting 3D objects were transparent, as determined by UV spectroscopy. The lactate dehydrogenase test demonstrated the tolerance of lens cells to the prototyping material, and apparent foldability and shape recovery was observed during direct injection into a human capsular bag model in vitro.
    UNASSIGNED: This proof-of-principle study demonstrated the potential and significance of the rapid prototyping process for research and development of lens-like 3D object prototypes, such as intraocular lenses.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    目的:本文旨在描述在陆军训练医院进行的专家咨询中发现的军事服务中眼科不合格的原因。
    方法:这种观察,横截面,多中心回顾性研究包括在2020年1月至2021年12月期间在3个ATH进行的专家咨询中发现的因眼部疾病而被认为“不适合服兵役”的个人。收集的数据包括年龄,病史和手术史,眼科不合格的原因,未矫正的远距视力,最佳矫正视力和睫状肌麻痹屈光。
    结果:在此期间,包括133名受试者(98名男性和35名女性)。38名候选人(28.6%)因屈光不正超过要求的限制而被宣布不适合,包括30名超过-10屈光度(D)的近视受试者和8名超过8D的远视受试者。由于在所需年龄之前进行了角膜屈光手术,25名候选人(18.8%)不适合21岁以下。由于有晶状体眼内晶状体,四名受试者(3.0%)不适合。23名受试者(17.3%)观察到退化状况,包括21例严重圆锥角膜患者。丧失工作能力的其他原因与11名受试者(8.3%)的眼眶创伤有关,中度或重度弱视7例(5.3%),7名受试者的先天性原因(5.3%),7名候选人(5.3%)的炎症或传染病,6名受试者(4.5%)的遗传原因和4名受试者(3.0%)的未确定的视觉功能障碍。
    结论:眼科不合格的三个主要原因是高度屈光不正,在所需的年龄和圆锥角膜之前进行屈光手术。
    OBJECTIVE: This article aims to describe the causes of ophthalmological disqualification from the military services detected during specialist consultations conducted at Army Training Hospitals.
    METHODS: This observational, cross-sectional, multicenter study retrospectively included individuals deemed as \"unfit for military service\" due to eye diseases identified during the specialist consultation conducted at 3 ATHs between January 2020 and December 2021. The data collected included age, medical and surgical history, reasons for ophthalmological disqualification, uncorrected distance visual acuity, best corrected distance visual acuity and cycloplegic refraction.
    RESULTS: Over this period, 133 subjects (98 men and 35 women) were included. Thirty-eight candidates (28.6%) were declared unfit due to a refractive error beyond the required limits, including 30 myopic subjects in excess of -10 diopters (D) and 8 hypermetropic subjects over +8 D. Twenty-five candidates (18.8%) were unfit under the age of 21 years due to corneal refractive surgery performed before the required age. Four subjects (3.0%) were unfit due to phakic intraocular lenses. Degenerative conditions were observed in 23 subjects (17.3%), including 21 patients with severe keratoconus. Other causes of incapacity were linked to oculo-orbital trauma in 11 subjects (8.3%), moderate or severe amblyopia in 7 patients (5.3%), congenital causes in 7 subjects (5.3%), inflammatory or infectious diseases in 7 candidates (5.3%), hereditary causes in 6 subjects (4.5%) and undetermined visual dysfunctions in 4 subjects (3.0%).
    CONCLUSIONS: The three main causes of ophthalmological disqualification were high ametropia, refractive surgery performed before the required age and keratoconus.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    近几十年来,植入式Collamer晶状体(ICL)手术越来越多地用于近视矫正。这项研究,采用体内共聚焦显微镜(IVCM),目的评估ICL手术中角膜切口对角膜基底下神经丛(SNP)和邻近免疫树状细胞(DC)的影响。在这项纵向研究中,我们对53例接受ICL手术患者的眼睛进行了为期12个月的术前和术后评估.使用ACCMetricsV.2软件进行七个SNP参数的定量。最终,最终分析仅限于37例完成至少3个月术后随访的患者中的每只眼.术前调查显示DC密度与患者年龄呈正相关,与角膜神经纤维密度(CNFD)呈负相关。此外,DC和CNFD均与球面等效折射(SER)呈正相关,与轴向长度(AL)呈负相关。有趣的是,术前DC密度与基线和术后CNFD变化均有间接关系.手术后,观察到DC密度的初始浪涌,随后正常化。同时,CNFD等参数,角膜神经纤维长度(CNFL),角膜神经分形维数(CNFrD)最初显示手术后下降。然而,在一年的随访中,CNFL和CNFrD显示显著恢复,而CNFD没有恢复到基线水平。因此,这项研究描绘了SNP的再生模式和ICL手术后DC密度的改变,强调中央角膜的CNFD在一年内没有完全恢复到术前水平。鉴于这些发现,建议医生对老年患者谨慎行事,那些高度近视的人,或术前DC升高,可能经历SNP再生延迟。
    Implantable Collamer Lens (ICL) surgery has increasingly been adopted for myopia correction in recent decades. This study, employing in vivo confocal microscopy (IVCM), aimed to assess the impact of corneal incision during ICL surgery on the corneal sub-basal nerve plexus (SNP) and adjacent immune dendritiform cells (DCs). In this longitudinal study, eyes from 53 patients undergoing ICL surgery were assessed preoperatively and postoperatively over a twelve-month period. Quantification of seven SNP parameters was performed using ACCMetrics V.2 software. Ultimately, the final analysis was restricted to one eye from each of the 37 patients who completed a minimum of three months\' postoperative follow-up. Preoperative investigations revealed a positive correlation of DC density with patient age and a negative association with corneal nerve fiber density (CNFD). Additionally, both DCs and CNFD were positively linked to spherical equivalent refraction (SER) and inversely related to axial length (AL). Intriguingly, preoperative DC density demonstrated an indirect relationship with both baseline and postoperative CNFD changes. Post-surgery, an initial surge in DC density was observed, which normalized subsequently. Meanwhile, parameters like CNFD, corneal nerve fiber length (CNFL), and corneal nerve fractal dimension (CNFrD) initially showed a decline following surgery. However, at one-year follow-up, CNFL and CNFrD displayed significant recovery, while CNFD did not return to its baseline level. This study thus delineates the regeneration pattern of SNP and alterations in DC density post-ICL surgery, highlighting that CNFD in the central cornea does not completely revert to preoperative levels within a year. Given these findings, practitioners are advised to exercise caution in older patients, those with high myopia, or elevated preoperative DCs who may undergo delayed SNP regeneration.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    观察双侧飞秒激光辅助透明晶状体摘除联合三焦点人工晶状体(IOL)植入术矫正老花眼的效果,并评估其在早期老花眼成人中的可行性。
    经过飞秒激光辅助晶状体摘除和三焦点IOL的透明晶状体眼的前瞻性病例系列(AcrysofIQPanOptix,手术后随访2021年至2023年之间的模型TFNT00,Alcon)植入至少3个月。结果测量包括近处单眼未矫正视力(UNVA,40厘米),中间(UIVA,60厘米),和距离(UDVA,5m),单眼明显折射,矫正视力(CDVA),散焦曲线评估,近处和远处的眼镜独立性。
    共纳入30例连续患者的60只眼,他们的平均年龄为50.4±6.5岁。手术后,平均UNVA(LogMAR)从0.28±0.16增加到0.08±0.07,UIVA从0.25±0.12增加到0.09±0.06,UDVA从0.27±0.21增加到0.01±0.08。UNVA的增强,UIVA和UDVA均有统计学意义(P<0.05)。验光结果显示,术后平均球眼当量(SE)为-0.21±0.24D,术后平均CDVA(LogMAR)为-0.00±0.06。术前近距离和远距离视力的独立性分别为46.7%(14/30)和56.7%(17/30),分别,并且在手术后3个月都增加到100%。
    在这项研究中观察到满意的视觉结果和安全的外科手术,这表明双侧飞秒激光辅助下透明晶状体摘除并植入PanOptixIOL可能是中国工作年龄患者老花眼矫正的可行方法。
    UNASSIGNED: To observe the outcome of bilateral femtosecond laser-assisted clear lens extraction with trifocal intraocular lens (IOL) implantation for presbyopia correction and evaluate its feasibility in early presbyopic adults.
    UNASSIGNED: Prospective case series of eyes with clear crystalline lenses that underwent femtosecond laser-assisted lens extraction and trifocal IOL (Acrysof IQ PanOptix, Model TFNT00, Alcon) implantation between 2021 and 2023 were followed up for at least 3 months after surgery. Outcome measures included monocular uncorrected visual acuity at near (UNVA, 40 cm), intermediate (UIVA, 60 cm), and distance (UDVA, 5 m), monocular manifest refraction, corrected distance visual acuity (CDVA), defocus curve assessment, and spectacle independence at both near and distance.
    UNASSIGNED: A total of 60 eyes from 30 consecutive patients were included, and their mean age was 50.4±6.5 years. After surgery, the mean UNVA (LogMAR) increased from 0.28±0.16 to 0.08±0.07, UIVA increased from 0.25±0.12 to 0.09±0.06, and UDVA increased from 0.27±0.21 to 0.01±0.08. The enhancements of UNVA, UIVA and UDVA were all significant (P < 0.05). The optometric results showed that the mean postoperative spherical equivalent (SE) was -0.21±0.24 D, and the mean postoperative CDVA (LogMAR) was -0.00±0.06. The preoperative spectacle independences at near and distance were 46.7% (14/30) and 56.7% (17/30), respectively, and both increased to 100% at 3 months after surgery.
    UNASSIGNED: Satisfactory visual outcomes and safe surgical procedures were observed in this study, which demonstrate that bilateral femtosecond laser-assisted clear lens extraction with PanOptix IOL implantation could be a feasible approach for presbyopia correction in working-age Chinese patients.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    我们评估了在美国(US)批准的年龄和屈光范围内使用EVO/EVO+™(具有中央端口的后房型人工晶状体)的患者的视觉结果。
    这项单中心回顾性研究评估了一个月,2022年4月至10月,符合纳入标准并接受EVO/EVO+植入的225只眼的单中心术后数据.数据包括镜头尺寸(mm),透镜能力(球面和柱面屈光度的屈光度),术前最佳矫正视力,术前明显折射的等效球形,术后未矫正视力,术后屈光,眼内压(mmHg),和不良事件。
    从2022年4月至10月,共有225只眼睛接受了EVO/EVO植入式Collamer晶状体(ICL)植入,其中51.5%接受了复曲面晶状体。最常见的ICL尺寸为12.6mm(56.4%),其次是13.2mm(27.5%),12.1mm(15.1%),和13.7毫米(0.9%)。术前BCVA为20/20或更高的患者(149眼),95.2%的患者术后UCVA达到20/20或更好,术后1个月,99.3%的UCVA达到20/25或更好。约75%的眼睛在±0.50D的球形等效目标内,94%在±1.00D内。在116眼中植入了ToricICL(51.8%)。其中,在21只眼睛(18.1%)中观察到预期的残余圆柱体>1屈光度,导致3次旋转,三个外植体,和三个激光视力矫正(LVC)增强。术后调整率(包括旋转,交易所,和LVC增强)最小(4.8%)。主要不良事件发生率为0%。
    我们的研究,美国最大的EVO/EVO+ICL植入单中心分析,表现出强烈的早期结果和罕见的不良事件,支持ICL的安全性和有效性。高可预测性和良好的视觉效果,包括20/20或更高,突出了这项技术的可靠性。尽管研究有局限性,我们的发现强调了这项技术的有效性。未来的研究应该完善患者标准,并评估这一不断变化的景观中的长期结果。
    UNASSIGNED: We evaluate visual outcomes in patients with EVO/EVO+™ (posterior chamber phakic intraocular lens with a central port) within approved United States (US) age and refractive range indications.
    UNASSIGNED: This single-center retrospective study evaluated one-month, single-center postoperative data for 225 eyes meeting inclusion criteria and undergoing EVO/EVO+ implantation from April to October 2022. Data included lens size (mm), lens power (diopters of spherical and cylindrical power), preoperative best corrected visual acuity, preoperative spherical equivalent from manifest refraction, achieved postoperative uncorrected visual acuity, postoperative refraction, intraocular pressure (mmHg), and adverse events.
    UNASSIGNED: A total of 225 eyes underwent EVO/EVO+ Implantable Collamer Lens (ICL) implantation from April to October 2022, with 51.5% receiving toric lenses. The most common ICL size was 12.6mm (56.4%), followed by 13.2mm (27.5%), 12.1mm (15.1%), and 13.7mm (0.9%). Among patients with preoperative BCVA of 20/20 or better (149 eyes), 95.2% achieved postoperative UCVA of 20/20 or better, and 99.3% achieved UCVA of 20/25 or better at postoperative month one. About 75% of eyes were within a spherical equivalent target of ±0.50 D and 94% within ±1.00 D. Toric ICLs were implanted in 116 eyes (51.8%). Of these, anticipated residual cylinder >1 diopter was seen in 21 eyes (18.1%) resulting in three rotations, three explants, and three laser vision correction (LVC) enhancements. The postoperative adjustment rate (including rotations, exchanges, and LVC enhancement) was minimal (4.8%). Incidence of major adverse events was 0%.
    UNASSIGNED: Our study, the largest US single-center analysis of EVO/EVO+ ICL implantation, demonstrates strong early results and infrequent adverse events, supporting ICL safety and effectiveness. High predictability and favorable visual outcomes, including 20/20 or better, highlight the reliability of this technology. Despite study limitations, our findings underscore this technology\'s effectiveness. Future research should refine patient criteria and assess long-term outcomes in this evolving landscape.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    背景:屈光手术研究旨在根据患者对各种类型手术的适用性对患者进行最佳预分类。最近的进步导致了人工智能驱动的算法的发展,包括机器学习方法,评估风险并增强工作流程。像ChatGPT-4(OpenAILP)这样的大型语言模型(LLM)已经成为潜在的通用人工智能工具,可以跨各个学科提供帮助。可能包括屈光手术决策。然而,他们根据真实世界参数对屈光手术患者进行预分类的实际能力仍未得到探索.
    目的:这项探索性研究旨在验证ChatGPT-4根据常用临床参数对屈光手术患者进行预分类的能力。目的是评估ChatGPT-4在对批次输入进行分类时的性能是否与屈光外科医生的性能相当。比较了一组简单的二进制类别(是否适合激光屈光手术的患者)以及一组更详细的类别。
    方法:对来自屈光诊所的100名连续患者的数据进行匿名化和分析。参数包括年龄,性别,明显的折射,视敏度,以及Scheimpflug成像的各种角膜测量和指数。本研究使用科恩κ系数将ChatGPT-4的表现与临床医生的分类进行了比较,卡方检验,一个混淆矩阵,准确度,精度,召回,F1分数,曲线下的接收机工作特征面积。
    结果:在ChatGPT-4和临床医生的分类之间发现了具有统计学意义的非巧合,其中6个类别的Cohenκ系数为0.399(95%CI0.256-0.537),二元分类为0.610(95%CI0.372-0.792)。该模型显示了时间不稳定性和响应变异性,however.对6个类别的卡方检验表明2个评分者分布之间存在关联(χ²5=94.7,P<.001)。这里,准确率为0.68,准确率为0.75,召回率为0.68,F1评分为0.70.对于两个类别,准确率为0.88,精确度为0.88,召回率为0.88,F1评分为0.88,曲线下面积为0.79.
    结论:这项研究表明,ChatGPT-4在屈光手术中具有作为分类前工具的潜力,与临床医生分类显示出有希望的一致性。然而,其主要局限性包括,其中,只依赖一个人类评估者,小样本量,ChatGPT(OpenAILP)输出在迭代之间的不稳定性和可变性以及底层模型的不透明度。结果鼓励进一步探索ChatGPT-4等LLM在医疗保健中的应用,特别是在需要了解大量临床数据的决策过程中。未来的研究应该集中在定义模型的准确性与提示和插图标准化,检测混杂因素,并与其他版本的ChatGPT-4和其他LLM进行比较,为更大规模的验证和现实世界的实现铺平道路。
    BACKGROUND: Refractive surgery research aims to optimally precategorize patients by their suitability for various types of surgery. Recent advances have led to the development of artificial intelligence-powered algorithms, including machine learning approaches, to assess risks and enhance workflow. Large language models (LLMs) like ChatGPT-4 (OpenAI LP) have emerged as potential general artificial intelligence tools that can assist across various disciplines, possibly including refractive surgery decision-making. However, their actual capabilities in precategorizing refractive surgery patients based on real-world parameters remain unexplored.
    OBJECTIVE: This exploratory study aimed to validate ChatGPT-4\'s capabilities in precategorizing refractive surgery patients based on commonly used clinical parameters. The goal was to assess whether ChatGPT-4\'s performance when categorizing batch inputs is comparable to those made by a refractive surgeon. A simple binary set of categories (patient suitable for laser refractive surgery or not) as well as a more detailed set were compared.
    METHODS: Data from 100 consecutive patients from a refractive clinic were anonymized and analyzed. Parameters included age, sex, manifest refraction, visual acuity, and various corneal measurements and indices from Scheimpflug imaging. This study compared ChatGPT-4\'s performance with a clinician\'s categorizations using Cohen κ coefficient, a chi-square test, a confusion matrix, accuracy, precision, recall, F1-score, and receiver operating characteristic area under the curve.
    RESULTS: A statistically significant noncoincidental accordance was found between ChatGPT-4 and the clinician\'s categorizations with a Cohen κ coefficient of 0.399 for 6 categories (95% CI 0.256-0.537) and 0.610 for binary categorization (95% CI 0.372-0.792). The model showed temporal instability and response variability, however. The chi-square test on 6 categories indicated an association between the 2 raters\' distributions (χ²5=94.7, P<.001). Here, the accuracy was 0.68, precision 0.75, recall 0.68, and F1-score 0.70. For 2 categories, the accuracy was 0.88, precision 0.88, recall 0.88, F1-score 0.88, and area under the curve 0.79.
    CONCLUSIONS: This study revealed that ChatGPT-4 exhibits potential as a precategorization tool in refractive surgery, showing promising agreement with clinician categorizations. However, its main limitations include, among others, dependency on solely one human rater, small sample size, the instability and variability of ChatGPT\'s (OpenAI LP) output between iterations and nontransparency of the underlying models. The results encourage further exploration into the application of LLMs like ChatGPT-4 in health care, particularly in decision-making processes that require understanding vast clinical data. Future research should focus on defining the model\'s accuracy with prompt and vignette standardization, detecting confounding factors, and comparing to other versions of ChatGPT-4 and other LLMs to pave the way for larger-scale validation and real-world implementation.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    背景:老花眼矫正人工晶状体(PCIOL)植入是希望独立眼镜的白内障手术患者的一种流行治疗选择。这项研究旨在通过分析患者社交媒体帖子来了解患者对PCIOL的看法和结果。
    方法:这是一项非干预性回顾性研究,使用预定义的搜索字符串来识别公开可用的社交媒体数据,讨论患者对七个PCIOL的看法和结果(三个三焦,一个具有连续视觉范围的多焦点,和三个扩展的焦深[EDOF]PCIOL)。从Reddit搜索相关帖子,YouTube,和Facebook和病人论坛病人。info,Medicine.net,Optiker-Forum,和Medizin论坛从2020年9月到2022年10月以四种语言(英语,德语,法语,和西班牙语)。
    结果:共包括2237个帖子,全部用英语,68%的帖子被确定在患者身上。info.患者讨论最多的主题是视力质量(占总职位的69%),PCIOL植入后的患者体验(30%),PCIOL植入前患者的感知(26%),视力障碍(24%)。讨论最多的PCIOL是Vivity®(占总员额的58%),PanOptix®(38%),Synergy®(26%),和Symfony®(13%)。患者对PCIOL的感知最常受到医疗保健专业人员的影响,在线阅读,和在线视频(31%,18%,15%的帖子,分别)。共有215个帖子(占总数的10%)讨论了PCIOL手术后的眼镜使用:用于EDOF和三焦/多焦PCIOL,讨论眼镜使用的帖子中有37%和56%表示不戴眼镜,分别。共有537个帖子讨论了视觉障碍:光环/环(66%)和星爆(36%)是所有镜片类型中讨论最多的视觉障碍。PCIOL植入后不戴眼镜似乎是患者满意度的关键驱动因素。
    结论:社交媒体提供了丰富的患者感知信息来源,经验,和PCIOL的总体满意度,可用于补充和指导收集通过对照试验产生的进一步证据。
    老花眼是作为自然衰老过程的一部分的近视力逐渐丧失,这通常在40岁左右变得很明显。老花眼会降低一个人的自尊心,生活质量,工作效率,和社会互动。老花眼可以使用多种治疗方法进行矫正,包括手术。使用老花眼矫正人工晶状体(PCIOL)的白内障手术需要用合成晶状体替换患者的自然晶状体以改善视力。社交媒体收听正在成为一种了解疾病及其治疗如何直接影响患者的流行方法。患者在社交媒体上表达的想法和意见被认为反映了患者自发的观点,并且可能比传统研究更接近地反映患者在现实世界中的声音。在这项研究中,我们检查了老花眼患者的社交媒体帖子,以了解他们对PCIOL的看法和经验.患者讨论的主要主题是思想,问题,以及在进行PCIOL手术之前的担忧,PCIOL手术后的患者体验。患者描述,如果他们的独立视力得到改善,PCIOL手术后会很高兴,包括他们使用电子设备的能力。如果手术后仍然需要戴眼镜或视力障碍,患者的满意度会降低,特别是如果它影响日常活动,如夜间驾驶。社交媒体平台是关于患者对PCIOL的感知和体验的丰富信息来源;这些信息可用于补充和指导通过对照试验产生的进一步证据的收集。
    BACKGROUND: Presbyopia-correcting intraocular lens (PCIOL) implantation is a popular treatment option for cataract surgery patients who desire spectacle independence. This study aimed to understand patient perception and outcomes with PCIOLs by analyzing patient social media posts.
    METHODS: This was a non-interventional retrospective study that used predefined search strings to identify publicly available social media data discussing patient perceptions and outcomes with seven PCIOLs (three trifocal, one multifocal with continuous range of vision, and three extended depth-of-focus [EDOF] PCIOLs). Relevant posts were searched from Reddit, YouTube, and Facebook and patient forums Patient.info, Medicine.net, Optiker-Forum, and Medizin Forum from September 2020 to October 2022 in four languages (English, German, French, and Spanish).
    RESULTS: A total of 2237 posts were included, all in English, with 68% of posts identified on Patient.info. The themes most discussed by patients were quality of vision (69% of total posts), patient experience after PCIOL implantation (30%), patient perception before PCIOL implantation (26%), and visual disturbances (24%). Most discussed PCIOLs were Vivity® (58% of total posts), PanOptix® (38%), Synergy® (26%), and Symfony® (13%). Patient perception of PCIOLs was most frequently influenced by healthcare professionals, online reading, and online videos (31%, 18%, and 15% of posts, respectively). A total of 215 posts (10% of total) discussed glasses use after PCIOL surgery: for EDOF and trifocal/multifocal PCIOLs, 37% and 56% of posts discussing glasses use stated being glasses free, respectively. A total of 537 posts discussed visual disturbances: halos/rings (66%) and starbursts (36%) were the most discussed visual disturbances for all lens types. Being glasses free after PCIOL implantation appeared to be a key driver of patient satisfaction.
    CONCLUSIONS: Social media provides a rich source of information on patient perception, experience, and overall satisfaction of PCIOLs that can be used to complement and guide the collection of further evidence generated through controlled trials.
    Presbyopia is the gradual loss of near vision as part of the natural aging process, which typically becomes evident around 40 years of age. Presbyopia can lower a person’s self-esteem, quality of life, work productivity, and social interactions. Presbyopia can be corrected using a variety of treatments, including surgery. Cataract surgery with a presbyopia-correcting intraocular lens (PCIOL) entails replacing a patient’s natural lens with a synthetic lens to improve vision. Social media listening is becoming a popular method to understand how diseases and their treatments affect patients firsthand. The thoughts and opinions expressed by patients on social media are believed to reflect spontaneous patient perspectives and can potentially reflect the patient voice in the real-world setting closer than traditional research. In this study, we examined social media posts from patients with presbyopia to understand their perceptions and experiences with PCIOLs. The main topics discussed by patients were thoughts, questions, and concerns before pursuing PCIOL surgery, and patient experiences after PCIOL surgery. Patients described being happy after PCIOL surgery if their unaided vision improved, including their ability to use electronic devices. Patients were less satisfied if they still needed to wear glasses after surgery or if they experienced disturbances in their vision, particularly if it affected daily activities such as nighttime driving. Social media platforms are a rich source of information on patient perception and experience of PCIOLs; this information can be used to complement and guide the collection of further evidence generated through controlled trials.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

公众号