Drug Guide
Hydrocortisone Butyrate
Classification
Therapeutic: Anti-inflammatory, corticosteroid
Pharmacological: Topical glucocorticoid
FDA Approved Indications
- Inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses
Mechanism of Action
Hydrocortisone Butyrate exerts anti-inflammatory, antipruritic, and vasoconstrictive effects by inducing synthesis of proteins that stabilize cell membranes, reduce inflammation, and suppress immune responses.
Dosage and Administration
Adult: Apply a thin film to affected area 2-4 times daily as directed by a physician.
Pediatric: Use with caution; consult specific pediatric guidelines and monitor for potential systemic absorption.
Geriatric: Use renal and hepatic functions to guide dosage; monitor for systemic effects.
Renal Impairment: No specific adjustment necessary, but caution advised.
Hepatic Impairment: No specific adjustment necessary; monitor for systemic effects.
Pharmacokinetics
Absorption: Minimal when used topically on intact skin; increased if applied to broken skin.
Distribution: Primarily localized; systemic absorption is low.
Metabolism: Metabolized in the liver.
Excretion: Excreted mainly in urine as metabolites.
Half Life: Approximately 1.5-2 hours once absorbed systemically.
Contraindications
- Hypersensitivity to hydrocortisone butyrate or any component of the formulation.
- Fungal or viral skin infections.
- Vaccine sites where immunization is active.
Precautions
- Use with caution in compromised skin, skin infections, or in children due to potential for systemic absorption. Avoid long-term or extensive use; monitor for signs of adrenal suppression. Use during pregnancy only if clearly needed; safety data are limited.
Adverse Reactions - Common
- Burning, itching, or dryness at application site (Common)
- Skin atrophy, striae (Less common)
Adverse Reactions - Serious
- Hypothalamic-pituitary-adrenal (HPA) axis suppression (Rare)
- Secondary infections (Rare)
- Contact dermatitis or allergic reactions (Rare)
Drug-Drug Interactions
- Potent topical or systemic corticosteroids
- Immunosuppressants
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess skin condition before and during therapy. Monitor for signs of irritation, skin atrophy, or systemic absorption.
Diagnoses:
- Risk for skin atrophy
- Impaired skin integrity
Implementation: Apply thin layer over affected area, avoiding surrounding healthy skin, eyes, and mucous membranes. Do not occlude unless directed.
Evaluation: Monitor skin improvement, adverse effects, and signs of systemic corticosteroid effects.
Patient/Family Teaching
- Use as prescribed, avoid covering with occlusive dressings.
- Do not use on large areas, broken skin, or for prolonged periods without medical advice.
- Report signs of skin thinning, growth disturbances in children, or systemic symptoms.
Special Considerations
Black Box Warnings:
- Long-term use of topical corticosteroids can cause hypothalamic-pituitary-adrenal (HPA) axis suppression.
- Extended or excessive use may lead to skin atrophy and secondary infections.
- Children are especially susceptible to systemic effects.
Genetic Factors: Patients with defective skin barriers or impaired healing may have altered absorption.
Lab Test Interference: May alter results of skin tests or immune function tests.
Overdose Management
Signs/Symptoms: Signs of systemic corticosteroid overdose include adrenal suppression, Cushingoid features, growth retardation in children.
Treatment: Discontinue use, provide supportive care, and monitor adrenal function. In severe cases, corticosteroid replacement therapy may be necessary.
Storage and Handling
Storage: Store at room temperature, 20-25°C (68-77°F). Keep container closed when not in use.
Stability: Stable for the shelf life indicated by the manufacturer.