Proper Usage and Dosage of Kenalog (Triamcinolone)
Kenalog (triamcinolone acetonide) is indicated for specific conditions with different dosages based on administration route, with intralesional injection using 2.5-10 mg/mL concentration for inflammatory skin conditions and 40 mg/mL for intramuscular administration for systemic effects. 1, 2
Intralesional Administration for Dermatologic Conditions
Dosing for Acne
- Concentration: 10 mg/mL (may be diluted to 5 or 3.3 mg/mL with sterile normal saline) 1
- Volume: 0.05 mL per lesion is most commonly used 3
- Technique: Inject into the center of the lesion 3
- Indication: Inflammatory nodulocystic acne (for occasional stubborn cystic lesions, not for multiple lesions) 1
- Response time: Flattens most acne nodules within 48-72 hours 1
Dosing for Other Dermatologic Conditions
- Acne keloidalis: Triamcinolone acetonide 10 mg/mL for inflammatory follicular lesions 1
- Hypertrophic scars/keloids: Triamcinolone acetonide 40 mg/mL 1
- Alopecia areata: Triamcinolone acetonide 5-10 mg/mL 1
- Psoriasis/Lichen planus affecting nails: Triamcinolone acetonide 5-10 mg/mL 1
- Gout (intra-articular): Triamcinolone acetonide 10 mg per affected joint 1
Intramuscular Administration
Dosing for Systemic Effects
- Concentration: Available as Kenalog-40 (40 mg/mL) and Kenalog-80 (80 mg/mL) 2
- Severe asthma: 360 mg as a single intramuscular injection (high-dose protocol for elderly patients with steroid-dependent asthma) 4, 5
- Atopic dermatitis (when necessary): 0.5-1.0 mg/kg 1
Contraindications
- Should not be injected at sites of active infections (impetigo, herpes) 1
- Previous hypersensitivity to triamcinolone 1
- Large injections should be avoided in patients with:
- Active tuberculosis or systemic fungal infection
- Extensive plaque psoriasis, pustular psoriasis, or erythrodermic psoriasis
- Active peptic ulcer disease
- Uncontrolled diabetes, heart failure, or severe hypertension
- Severe depression or psychosis 1
Adverse Effects
Local Effects (Intralesional)
- Skin atrophy, pigmentary changes, telangiectasias, hypertrichosis 1, 3
- Impaired wound healing 1
- Contact allergic dermatitis (from benzyl alcohol preservative) 1
- Sterile abscess, steroid acne 1
Systemic Effects
- Hypothalamic-pituitary-adrenal axis suppression with repeated injections 1
- Anaphylaxis, angioedema, urticaria (rare) 1
- Postinjection flares mimicking septic arthritis (rare but severe) 6
- Weight gain, menstrual disturbances, increased blood pressure, edema 5
Important Considerations
- Duration of effect: Triamcinolone acetonide has a uniquely long duration of action compared to other corticosteroids 7
- Atrophy risk: While observed skin atrophy rates are extremely low with proper technique, when it occurs, it can last over six months 3
- Patient counseling: 50.5% of dermatologists counsel patients about potential hypopigmentation and atrophy before every injection 3
- Systemic absorption: Even with local injections, some systemic absorption occurs, which may affect conditions like diabetes 1
- Rebound effects: Systemic steroids may cause rebound flares upon discontinuation, especially in atopic dermatitis 1
Monitoring
- For patients receiving repeated or high-dose injections, monitor for signs of systemic absorption
- For intralesional injections, follow up to assess response and potential adverse effects
- For children receiving long-term systemic steroids, monitor growth velocity 1
Remember that while triamcinolone is effective for many conditions, it should be used judiciously due to its potential for significant adverse effects, especially with repeated use.