首页> 外文期刊>Canadian journal of ophthalmology >Repeated triamcinolone acetonide injection in the treatment of upper-lid retraction in patients with thyroid-associated ophthalmopathy
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Repeated triamcinolone acetonide injection in the treatment of upper-lid retraction in patients with thyroid-associated ophthalmopathy

机译:反复曲安奈德注射液治疗甲状腺相关性眼病患者上睑回缩

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Objective: To evaluate the efficacy and safety of repeated subconjunctival injections of triamcinolone in the treatment of upper-lid retraction with thyroid-associated ophthalmopathy. Design: Interventional controlled retrospective clinical study. Participants: We studied 23 eyes in 15 patients as the nontreatment control group and 35 eyes in 21 patients as the treatment group. Methods: In the treatment group, triamcinolone acetonide was subconjunctivally injected into each lid as 4 doses of 20 mg at 1-month intervals. After the treatment, the eyes were divided into 2 groups, response and nonresponse, based on the improvement in margin reflex distance. The eyes of the nontreatment group received no medicine. The eyes were examined regularly. Results: The rate of spontaneous improvement in the nontreatment group was 17.4%. The mean rate of effectiveness was 68.6%. The improvement of upper-lid retraction was 2.31 mm (0 to 7mm). The margin reflex distance was significantly smaller at 1 month after the initiation of treatment. Mean lid retraction time before treatment was 4.58 months in the response group versus 9.91 months in the nonresponse group. In the eyes presenting upper-lid retraction up to 6 months before treatment was initiated, the response rate was 83.3%. The response rate was only 36.4% when lid retraction developed more than 6 months before the procedure. The muscle thickness of the levator/superior rectus complex was significantly reduced after treatment in the response group (5.13 ± 0.85 mm at last follow-up vs. 5.69 ± 0.93 mm at baseline). Conclusions: Repeated subconjunctival injection of triamcinolone is an effective and safe treatment for upper-lid retraction due to thyroid-associated ophthalmopathy.
机译:目的:评价结膜下多次注射曲安奈德治疗甲状腺相关性眼病上睑回缩的疗效和安全性。设计:干预性对照回顾性临床研究。参与者:我们研究了15例患者的23眼作为非治疗对照组,研究了21例患者的35眼作为治疗组。方法:在治疗组中,以每1个月间隔4次20 mg的剂量将结膜曲康奈德皮下注射至每个眼睑。治疗后,根据边缘反射距离的改善,将眼睛分为响应和不响应两类。未治疗组的眼睛未接受药物治疗。定期检查眼睛。结果:未治疗组的自发改善率为17.4%。平均有效率为68.6%。上睑缩回的改善为2.31毫米(0至7毫米)。开始治疗后1个月的边缘反射距离明显变小。应答组治疗前的平均眼睑收缩时间为4.58个月,而无应答组为9.91个月。在开始治疗前6个月出现上睑回缩的眼睛,缓解率为83.3%。在手术前6个月以上进行眼睑回缩时,有效率仅为36.4%。响应组治疗后,提肌/上直肌复合体的肌肉厚度显着降低(最后一次随访为5.13±0.85 mm,而基线为5.69±0.93 mm)。结论:反复结膜下注射曲安奈德是一种安全有效的治疗甲状腺相关性眼病的上睑回缩的方法。

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