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Rotation of a toric intraocular lens with and without capsular tension ring: data from a multicenter non-inferiority randomized clinical trial (RCT)

机译:具有和无囊张力环的背心眼透镜的旋转:来自多中心非劣级性随机临床试验(RCT)的数据

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Evaluation of clinical outcome in cohorts with versus without simultaneous implantation of a capsular tension ring (CTR) and a toric lens (Tecnis Toric). Main parameter was rotation referring - in contrast to misalignment - to the IOL axis change from immediately after implantation to the final postoperative position. Lens position was measured at baseline with the patient still in recumbent position, postoperative rotation was calculated by software. Postoperative evaluation included measurement three months after surgery or prior to an indicated revision surgery. Explorative re-evaluation of the underlying RCT's intent-to-treat population was performed for the entire sample and stratified for cohorts by 95% confidence intervals for binary endpoints' incidences (primary endpoint: absolute postoperative rotation ≤5 degrees; secondary endpoints: absolute deviation between achieved cylinder and target cylinder ≤0.5 dpt, postoperative corrected distance visual acuity (CDVA)?≥?0.8). Data exploration was based on medians and quartiles. Outpatient study sites. Re-evaluation based on data from a multicenter non-inferiority randomized clinical trial (RCT). Sub cohorts (without CTR 89, with CTR 90 patients) did not present clinically relevant differences in preoperative characteristics: revision surgery was performed in 7 cases (3 without and 4 with CTR). Primary endpoint incidences for the total sample, without and with CTR were 90%/89%/90%; cylinder endpoint incidences were 46%/45%/46% and CDVA endpoint incidences 90%/92%/88%. Median absolute rotations were 1.74°/1.79°/1.72°, median absolute cylinder deviations 0.55/0.52/0.55 dpt and median visual acuity 1.0/1.0/1.0. No clinically relevant differences between CTR subgroups were found; a satisfying three months rotational stability was achieved. The trial was registered retrospectively in the trial registry DRKS, trial registration number DRKS00015316 , date of registration 27. August 2018.
机译:与同时植入胶囊张力环(CTR)和复曲面(TECNIS TORIC)的同时植入群体的临床结果评价。主要参数旋转引用 - 与未对准相比 - 对IOL轴从植入到最终术后位置后立即改变。在基线下测量镜头位置,患者仍处于旋转位置,通过软件计算术后旋转。术后评估包括手术后三个月或在指出的修订手术前测量。对潜在的RCT意图对治疗群体的探索性重新评估是对整个样本进行的,并为二元终点发病率的95%置信区间分层(主要终点:绝对术后旋转≤5度;辅助端点:绝对偏差在达到的圆筒和目标气缸之间≤0.5dpt,术后矫正距离视力(CDVA)?≥?0.8)。数据探索基于中位数和四分位数。门诊学习网站。基于来自多中心非劣级性随机临床试验(RCT)的数据重新评估。子群(没有CTR 89,随着CTR 90患者)在术前特征的临床上没有呈现临床相关差异:修正手术在7例中进行(3患者,4例没有4例CTR)。总样品的主要终点发病率,无需和CTR的发病率为90%/ 89%/ 90%;气缸终点发病率为46%/ 45%/ 46%,CDVA终点发病率为90%/ 92%/ 88%。中位绝对旋转为1.74°/ 1.79°/ 1.72°,中位绝对缸偏差0.55 / 0.52 / 0.55 DPT和中位视力1.0 / 1.0 / 1.0。没有发现CTR子组之间的临床相关差异;满足三个月的旋转稳定性。审判在试验登记处注册,试验登记渣,审判登记号码DRKS00015316,注册日期27。2018年8月。

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