Henderson Bonnie An, Aramberri Jaime, Vann Robin, Abulafia Adi, Ainslie-Garcia Margaret, Berdahl John, Ferko Nicole, Gundersen Kjell Gunnar, Goto So, Gupta Preeya, Multack Samuel, Persaud Elizabeth, Raoof Duna, Savini Giacomo, Shammas H John, Wang Li, Wang Wendy Zhi
Department of Ophthalmology, Tufts University School of Medicine, Boston, MA, USA.
Ophthalmology Clinic Miranza Begitek, San Sebastian, Spain.
Clin Ophthalmol. 2023 Jul 24;17:2109-2124. doi: 10.2147/OPTH.S412847. eCollection 2023.
To obtain consensus on the key areas of burden associated with existing devices and to understand the requirements for a comprehensive next-generation diagnostic device to be able to solve current challenges and provide more accurate prediction of intraocular lens (IOL) power and presbyopia correction IOL success.
Thirteen expert refractive cataract surgeons including three steering committee (SC) members constituted the voting panel. Three rounds of voting included a Round 1 structured electronic questionnaire, Round 2 virtual face-to-face meeting, and Round 3 electronic questionnaire to obtain consensus on topics related to current limitations and future solutions for preoperative cataract-refractive diagnostic devices.
Forty statements reached consensus including current limitations (n = 17) and potential solutions (n = 23) associated with preoperative diagnostic devices. Consistent with existing evidence, the panel reported unmet needs in measurement accuracy and validation, IOL power prediction, workflow, training, and surgical planning. A device that facilitates more accurate corneal measurement, effective IOL power prediction formulas for atypical eyes, simplified staff training, and improved decision-making process for surgeons regarding IOL selection is expected to help alleviate current burdens.
Using a modified Delphi process, consensus was achieved on key unmet needs of existing preoperative diagnostic devices and requirements for a comprehensive next-generation device to provide better objective and subjective outcomes for surgeons, technicians, and patients.
就现有设备相关的关键负担领域达成共识,并了解综合下一代诊断设备的要求,以便能够解决当前的挑战,并更准确地预测人工晶状体(IOL)的屈光度和老花眼矫正IOL的成功率。
13名专家屈光性白内障外科医生,包括3名指导委员会(SC)成员,组成了投票小组。三轮投票包括第一轮结构化电子问卷、第二轮虚拟面对面会议和第三轮电子问卷,以就与术前白内障屈光诊断设备的当前局限性和未来解决方案相关的主题达成共识。
40项陈述达成了共识,包括与术前诊断设备相关的当前局限性(n = 17)和潜在解决方案(n = 23)。与现有证据一致,该小组报告了在测量准确性和验证、IOL屈光度预测、工作流程、培训和手术规划方面未满足的需求。一种有助于更准确地测量角膜、为非典型眼睛提供有效的IOL屈光度预测公式、简化工作人员培训并改善外科医生在IOL选择方面的决策过程的设备,有望帮助减轻当前的负担。
通过改进的德尔菲法,就现有术前诊断设备的关键未满足需求以及综合下一代设备的要求达成了共识,以为外科医生、技术人员和患者提供更好的客观和主观结果。