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Intravitreal bevacizumab during pregnancy.

机译:妊娠期间玻璃体内贝伐单抗。

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PURPOSE: To report the clinical course of four women treated with intravitreal bevacizumab during pregnancy. METHODS: Observational case series. RESULTS: Four pregnant women were treated with intravitreal bevacizumab for choroidal neovascularization (CNV) because of presumed ocular histoplasmosis syndrome punctate inner choroidopathy, or sarcoid uveitis. Patients received a mean of 2.6 +/- 2.3 injections (range, 1-6 injections) while pregnant. One patient was treated with five additional injections while breastfeeding. The mean follow-up duration after the most recent injection was 14 +/- 2.9 months (range, 11-18 months). Snellen visual acuity improved in all 4 patients with a mean of 5.75 +/- 2.2 lines (range, 3-8 lines). At the most recent follow-up, all patients had involuted CNV that did not require additional treatment. All patients had an uneventful prenatal course and delivered healthy full-term infants. All children have remained healthy, exhibiting normal development and growth during infancy. CONCLUSION: Offering pregnant patients intravitreal bevacizumab therapy during pregnancy for off-label ocular indications can result in significant visual improvement. No adverse events related to treatment occurred in any patient included in this study. Additional studies with more patients and longer follow-up duration are required to identify any risks associated with treatment.
机译:目的:报告四名妇女在妊娠期间接受玻璃体内贝伐单抗治疗的临床过程。方法:观察病例系列。结果:四名孕妇因玻璃体腔内贝氏体病综合征点状内脉络膜病变或结节性葡萄膜炎而接受玻璃体内贝伐单抗治疗脉络膜新生血管(CNV)。孕妇在怀孕期间平均接受2.6 +/- 2.3次注射(范围为1-6次注射)。一名患者在母乳喂养期间接受了五次额外的注射治疗。最近一次注射后的平均随访时间为14 +/- 2.9个月(范围11-18个月)。所有4例患者的Snellen视力均得到改善,平均为5.75 +/- 2.2线(范围3-8线)。在最近的随访中,所有患者均已感染CNV,不需要进一步治疗。所有患者的产前过程均顺利,并已分娩出健康的足月婴儿。所有儿童都保持健康,在婴儿期表现出正常的发育和成长。结论:在怀孕期间为妊娠患者提供玻璃体腔注射贝伐单抗治疗,以适应症外眼部适应症,可显着改善视力。在这项研究中,任何患者均未发生与治疗相关的不良事件。需要进行更多的研究,以更多的患者和更长的随访时间来确定与治疗相关的任何风险。

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