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
{"title":"Evidence-based guidelines for drug dosing in intravitreal injections in silicone oil-filled eyes: Pharmacokinetics, safety, and optimal dosage","authors":"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","doi":"10.1016/j.survophthal.2024.09.006","DOIUrl":null,"url":null,"abstract":"<div><div>We evaluate the pharmacokinetics, safety, and optimal dosages of intravitreal agents in silicone oil (SO)-filled eyes, addressing challenges in administering such therapies. <strong>We</strong> 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).</div><div>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.</div></div>","PeriodicalId":22102,"journal":{"name":"Survey of ophthalmology","volume":"70 1","pages":"Pages 96-105"},"PeriodicalIF":5.1000,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Survey of ophthalmology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S003962572400119X","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0
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.
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.