Corticosteroid — Periocular or Intravitreal Injection
Pregnancy: Avoid — corticosteroids affect fetal development
Triamcinolone Acetonide (Intravitreal / Periocular)
Brand names: Kenalog, Triesence (preservative-free — intravitreal)
Adult dose
Dose: Intravitreal: 4 mg in 0.1 mL; Periocular (posterior sub-Tenon): 40 mg in 1 mL
Route: Intravitreal injection or posterior sub-Tenon injection
Frequency: Single injection; repeat at 3–4 months as required
Max: 4 mg per intravitreal injection; 40 mg per periocular injection
Use preservative-free preparation (Triesence) for intravitreal injection — Kenalog contains benzyl alcohol which is toxic to retinal cells. Sub-Tenon injection is preferred in phakic patients to reduce cataract risk. Duration: 3–4 months (shorter than Ozurdex).
Paediatric dose
Route:
Specialist paediatric ophthalmology guidance required — used in paediatric uveitis and cystoid macular oedema
Dose adjustments
Renal
No systemic adjustment — intravitreal/periocular use
Hepatic
No adjustment
Clinical pearls
- CRITICAL formulation difference: Kenalog (triamcinolone for intramuscular/intra-articular use) contains benzyl alcohol preservative — benzyl alcohol is directly retinotoxic; NEVER inject Kenalog intravitreally; ONLY use Triesence (preservative-free ophthalmic formulation) for intravitreal injection
- Pseudoendophthalmitis: triamcinolone crystals in vitreous can appear as white vitreous opacification mimicking endophthalmitis — distinguishing features: no anterior chamber cells/flare, no pain, no hypopyon, no systemic inflammation; resolves spontaneously
- IOP elevation: mandatory IOP check at week 8; topical IOP-lowering drugs started if IOP >25 mmHg; surgical IOP-lowering may be required in steroid responders (genetic predisposition to trabecular meshwork steroid response)
- Sub-Tenon vs intravitreal: posterior sub-Tenon injection provides periocular drug delivery without entering the eye — avoids endophthalmitis risk and cataract risk; IOP elevation still occurs; used for non-infectious posterior uveitis and CME
- Superseded in many indications: intravitreal triamcinolone has largely been replaced by Ozurdex (biodegradable implant) for sustained release with better safety profile and NICE approval
Contraindications
- Active ocular or periocular infection
- Glaucoma with poor IOP control
- Benzyl alcohol preparation (Kenalog) for INTRAVITREAL use — CRITICAL: use only preservative-free Triesence for intravitreal injection
- Phakic patient (cataract risk — relative; consider Ozurdex instead)
Side effects
- IOP elevation — common (30–50%); monitor at 8 weeks
- Cataract formation in phakic eyes
- Steroid-induced glaucoma — irreversible optic nerve damage if untreated
- Endophthalmitis (injection risk)
- Pseudoendophthalmitis (sterile): triamcinolone crystals in vitreous — white floaters mimicking endophthalmitis; differentiate by absence of hypopyon and absence of pain/inflammation signs
Interactions
- No clinically significant systemic drug interactions
Monitoring
- IOP at week 8 and monthly
- Lens status (cataract)
- OCT — retinal thickness
- Visual acuity
- Signs of endophthalmitis post-injection
Reference: BNFc; BNF 90; NICE TA229; RCOphth Uveitis Guidelines; SPC Triesence; SPC Kenalog. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Calculators
Pathways
- Acute Red Eye / Vision Loss Screen · RCOphth 2020; NICE CKS
- Idiopathic Intracranial Hypertension · ABN; consensus 2018
- Acute Red Eye Assessment · RCOphth / AAO
- Acute Angle Closure Glaucoma · RCOphth / EGS Guidelines
- Retinal Detachment · RCOphth Guidelines / EURETINA
- Diabetic Retinopathy — Screening and Management · NICE NG28 2016 / NHS DES Programme