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An epidemiologic investigation of unexpected refractive errors following cataract surgery (see comments)

机译:白内障手术后意外屈光不正的流行病学调查(查看评论)

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摘要

OBJECTIVE: To determine the extent and magnitude of unexpected refractive errors following cataract surgery with intraocular lens (IOL) implantation and to determine what characteristics were associated with the errors. DESIGN: In this nonconcurrent prospective study, preoperative, intraoperative and postoperative information was collected from the charts of the 523 consecutive patients who underwent cataract extraction and polymethylmethacrylate IOL implantation performed by one of nine participating surgeons between Jan. 1 and Apr. 30, 1995, or the same dates in 1996. SETTING: University-affiliated eye care centre in Vancouver. OUTCOME MEASURE: Postoperative excess correction, calculated for each patient by subtracting the actual postoperative spherical equivalent from the expected spherical equivalent. Eyes with an excess correction of more than 1.00 dioptre were considered "overcorrected." RESULTS: Univariate analysis showed that the formula used to calculate the lens power, axial length, year of surgery, A-constant/surgeon factor used and lens manufacturer were associated with overcorrection. In a logistic regression model, lens manufacturer was the only variable independently associated with overcorrection. CONCLUSIONS: Routine reporting and follow-up is necessary to identify this kind of "outbreak" and the associated factors. The current guidelines of the Health Protection Branch, Health Canada, for evaluation of IOLs that have changed manufacturers are not adequate to identify the kind of error that we detected.
机译:目的:确定白内障人工晶状体(IOL)植入术后意外屈光不正的程度和大小,并确定与该误差相关的特征。设计:在这项非并行的前瞻性研究中,从1995年1月1日至4月30日由9位参与手术的外科医师之一进行的523例接受白内障摘除和聚甲基丙烯酸甲酯人工晶状体植入的连续患者的图表中收集了术前,术中和术后信息,或与1996年相同的日期。地点:温哥华的大学附属眼保健中心。观察指标:术后过量矫正,是通过从预期球面等效值中减去实际术后球面等效值而得出的,用于每个患者。过度矫正超过1.00屈光度的眼睛被视为“矫正过度”。结果:单因素分析表明,用于计算镜片度数,轴长,手术年限,所用的A常数/外科医生因素以及镜片制造商的公式与过度矫正相关。在逻辑回归模型中,镜片制造商是唯一与过度矫正相关的变量。结论:常规报告和随访对于确定这种“暴发”和相关因素是必要的。加拿大卫生部卫生保护处的现行准则,用于评估制造商已变更的IOL,不足以识别我们检测到的错误类型。

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