Table 9.
Clinical guidelines for anti-VEGF use across different systems
| System | Guidelines |
|---|---|
| Renal | Exercise caution in patients with significantly compromised renal function (eGFR < 30 mL/min/1.73m2) |
| Close monitoring is advised to detect potential renal impact | |
| Cardiovascular (CVS) | Prior stroke or MI within 6–12 months is a stronger predictor of cardiovascular risk than prolonged q4 injections |
| Long-term frequent injections (> 10 years) may contribute to gradual cardiac dysfunction | |
| — | |
| Central nervous system (CNS) | Most of the literature does not report significant long-term systemic side effects or neurological impairment associated with anti-VEGF use |
| Caution is advised when administering anti-VEGFs to patients with a recent history of stroke, as repeated injections may elevate stroke risk | |
| Pregnancy | Anti-VEGFs should be used only when the potential benefit to the woman justifies the potential fetal risks |
| A routine urinary pregnancy test can be considered before treatment in women of childbearing age | |
| Ranibizumab appears safer than other anti-VEGFs in pregnancy | |
| Avoid intravitreal anti-VEGF treatment during the first trimester, particularly in high-risk cases | |
| Breastfeeding | Ranibizumab appears to be a safer option than aflibercept for breastfeeding women |
| A 3-day “pump and dump” strategy is recommended after intravitreal injections | |
| Retinopathy of prematurity (ROP) | Anti-VEGF therapy can be considered for vision-threatening ROP cases after carefully weighing risks and benefits |
VEGF vascular endothelial growth factor, eGFR estimated glomerular filtration rate, MI myocardial infarction