From the Department of Ophthalmology, VIROS Vienna Institute for Research in Ocular Surgery, A Karl Landsteiner Institute, Hanusch Hospital, Vienna, Austria (Hienert, Amir-Asgari, Hirnschall, Findl); Carl Zeiss Meditec AG, Oberkochen, Germany (Matz).
J Cataract Refract Surg. 2022 Jun 1;48(6):663-666. doi: 10.1097/j.jcrs.0000000000000812.
To evaluate intraoperative aphakic eye axial length (AL) measurements using swept-source optical coherence tomography (SS-OCT).
Hanusch Hospital, Vienna, Austria.
Prospective single-center study.
Patients scheduled for cataract surgery were measured using SS-OCT (IOLMaster 700, Carl Zeiss Meditec AG) to assess the AL. Intraoperatively (intra-OP), SS-OCT measurements were performed with a prototype device (IOLMaster 700 connected to an OPMI Lumera 700 microscope, CZM) at the beginning of cataract surgery furthermore of the aphakic eye and 2 months after surgery.
106 patients were included. Of the 59 eyes of 59 patients, the phakic median AL preoperatively and intra-OP was 23.61 mm ± 0.96 (standard deviation [SD]) and 23.51 mm ± 0.96 (SD), respectively. The absolute median difference was 0.028 ± 0.02 (SD) (P = .049). Median phakic AL intra-OP vs 2 months postoperatively (post-OP) was 23.51 mm ± 0.97 (SD) vs 23.49 mm ± 0.95 (SD). The absolute median difference was 0.049 ± 0.04 (SD) (P = .000). Median AL intra-OP aphakic vs 2 months post-OP pseudophakic was 23.42 mm ± 0.97 (SD) vs 23.42 mm ± 0.97 (SD), respectively. Absolute median difference was 0.038 ± 0.04 (SD) (P = .379).
Intra-OP, SS-OCT technology of the phakic and aphakic eye shows excellent comparability to preoperative and postoperative measurements. This technique allows AL measurements with high precision in cases in which preoperative biometric measurements are not possible.
评估应用扫频源光学相干断层扫描(SS-OCT)进行术中无晶状体眼眼轴(AL)测量的效果。
奥地利维也纳 Hanusch 医院。
前瞻性单中心研究。
对计划行白内障手术的患者使用 SS-OCT(IOLMaster 700,卡尔蔡司 Meditec AG)进行 AL 评估。术中(IOP 内),在白内障手术开始时以及术后 2 个月,使用原型设备(连接至 OPMI Lumera 700 显微镜的 IOLMaster 700,CZM)对无晶状体眼进行 SS-OCT 测量。
共纳入 106 例患者。在 59 例患者的 59 只眼中,术前和 IOP 内的有晶状体眼中位 AL 分别为 23.61mm±0.96(标准差[SD])和 23.51mm±0.96(SD)。绝对中位差值为 0.028±0.02(SD)(P=0.049)。IOP 内与术后 2 个月(PO )的有晶状体眼中位 AL 分别为 23.51mm±0.97(SD)和 23.49mm±0.95(SD)。绝对中位差值为 0.049±0.04(SD)(P=0.000)。IOP 内无晶状体眼与术后 2 个月的人工晶状体眼中位 AL 分别为 23.42mm±0.97(SD)和 23.42mm±0.97(SD)。绝对中位差值为 0.038±0.04(SD)(P=0.379)。
IOP 内的 SS-OCT 技术在测量有晶状体眼和无晶状体眼时具有极好的可比性,与术前和术后测量结果相当。该技术可在无法进行术前生物测量的情况下,实现 AL 的高精度测量。