Evidence-based guidelines for drug dosing in intravitreal injections in silicone oil-filled eyes: Pharmacokinetics, safety, and optimal dosage

IF 5.1 2区 医学 Q1 OPHTHALMOLOGY Survey of ophthalmology Pub Date : 2024-09-27 DOI:10.1016/j.survophthal.2024.09.006
Lorenzo Ferro Desideri MD , Peng Yong Sim MD , Enrico Bernardi MD , Karin Paschon MD , Janice Roth MD , Adrian T. Fung MD , Xia Ni Wu MD , Hung-Da Chou MD , Robert Henderson MD , Edmund Tsui MD , Maria Berrocal MD , Jay Chhablani MD , Charles C. Wykoff MD, PhD , Chui Ming Gemmy Cheung MD , Giuseppe Querques MD, PhD , Gustavo Barreto Melo MD, PhD , Yousif Subhi MD, PhD , Anat Loewenstein MD , Jens Folke Kiilgaard MD, PhD , Martin Zinkernagel MD, PhD , Rodrigo Anguita MD
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Abstract

We evaluate the pharmacokinetics, safety, and optimal dosages of intravitreal agents in silicone oil (SO)-filled eyes, addressing challenges in administering such therapies. We assessed the pharmacological properties and safety profiles of intravitreal drugs in SO-filled eyes, deriving conclusions and guidance from available literature and expert consensus. Preclinical data suggest comparable half-lives of anti-vascular endothelial growth factoragents in SO-filled eyes, but clinical evidence is mainly from case reports and small series. Available research prioritizes standard dosages, particularly for bevacizumab (1.25 mg), supported by stronger evidence than aflibercept (2 mg) or ranibizumab (0.5 mg). Intravitreal steroids, especially dexamethasone at 0.7 mg, show efficacy and safety, while evidence for fluocinolone acetonide at 0.19 mg is limited. Intravitreal methotrexate has been reported at the dosage of 250–400 μg, with keratitis as the primary expected side effect. Case reports indicate tolerability of standard dosages of antivirals (foscarnet 1.2–2.4 mg/0.1 mL, ganciclovir 4 mg/0.1 mL) and the antibiotic combination piperacillin/tazobactam (250 μg/0.1 mL).
We offer guidance based on current, but limited, literature. Standard dosage of intravitreal agents should be carefully considered, along with close monitoring for potential side effects, which should be discussed with patients.
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基于证据的硅油填充眼玻璃体内注射药物剂量指南:药代动力学、安全性和最佳剂量。
我们评估了硅油(SO)填充眼内玻璃体内药物的药代动力学、安全性和最佳剂量,以应对此类疗法的挑战。我们评估了硅油填充眼内玻璃体内药物的药理特性和安全性,并根据现有文献和专家共识得出结论和指导意见。临床前数据表明,抗血管内皮生长因子药物在SO填充眼内的半衰期相当,但临床证据主要来自病例报告和小型系列研究。现有研究优先考虑标准剂量,尤其是贝伐珠单抗(1.25 毫克),其证据比阿弗利贝赛普(2 毫克)或雷尼珠单抗(0.5 毫克)更充分。玻璃体内类固醇,尤其是 0.7 毫克的地塞米松,显示出有效性和安全性,而 0.19 毫克的氟西酮缩丙酮的证据有限。有报告称,250-400 微克剂量的玻璃体内甲氨蝶呤的主要预期副作用是角膜炎。病例报告显示,标准剂量的抗病毒药物(福斯卡尼 1.2-2.4 毫克/0.1 毫升、更昔洛韦 4 毫克/0.1 毫升)和抗生素复方哌拉西林/他唑巴坦(250 微克/0.1 毫升)均可耐受。总之,我们将根据目前有限的文献资料提供指导。应仔细考虑玻璃体内药物的标准剂量,同时密切监测潜在的副作用,并与患者进行讨论。
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来源期刊
Survey of ophthalmology
Survey of ophthalmology 医学-眼科学
CiteScore
10.30
自引率
2.00%
发文量
138
审稿时长
14.8 weeks
期刊介绍: Survey of Ophthalmology is a clinically oriented review journal designed to keep ophthalmologists up to date. Comprehensive major review articles, written by experts and stringently refereed, integrate the literature on subjects selected for their clinical importance. Survey also includes feature articles, section reviews, book reviews, and abstracts.
期刊最新文献
Correspondence regarding the article: A major review of punctal stenosis: Updated anatomy, epidemiology, etiology, and clinical presentation. Clinical features, diagnosis, management, and prognosis of circumscribed choroidal hemangioma. An update on ocular effects of antidiabetic medications. Anatomical and functional changes after internal limiting membrane peeling. A comprehensive review of structure-function correlations in age-related macular degeneration: Contributions of microperimetry.
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