TY - JOUR
T1 - Evidence-based guidelines for drug dosing in intravitreal injections in silicone oil-filled eyes
T2 - Pharmacokinetics, safety, and optimal dosage
AU - Ferro Desideri, Lorenzo
AU - Sim, Peng Yong
AU - Bernardi, Enrico
AU - Paschon, Karin
AU - Roth, Janice
AU - Fung, Adrian T.
AU - Wu, Xia Ni
AU - Chou, Hung Da
AU - Henderson, Robert
AU - Tsui, Edmund
AU - Berrocal, Maria
AU - Chhablani, Jay
AU - Wykoff, Charles C.
AU - Cheung, Chui Ming Gemmy
AU - Querques, Giuseppe
AU - Melo, Gustavo Barreto
AU - Subhi, Yousif
AU - Loewenstein, Anat
AU - Kiilgaard, Jens Folke
AU - Zinkernagel, Martin
AU - Anguita, Rodrigo
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2025/1/1
Y1 - 2025/1/1
N2 - 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.
AB - 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.
KW - Anti-VEGF
KW - Antibiotics
KW - Antivirals, retinal detachment
KW - Intraocular steroids
KW - Intravitreal drugs
KW - Intravitreal injections
KW - Methotrexate
KW - Optimal dosage
KW - Silicone oil
UR - http://www.scopus.com/inward/record.url?scp=85205461183&partnerID=8YFLogxK
U2 - 10.1016/j.survophthal.2024.09.006
DO - 10.1016/j.survophthal.2024.09.006
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C2 - 39343316
AN - SCOPUS:85205461183
SN - 0039-6257
VL - 70
SP - 96
EP - 105
JO - Survey of Ophthalmology
JF - Survey of Ophthalmology
IS - 1
ER -