Drug Guide

Generic Name

Hydrocortisone Butyrate

Brand Names Locoid, Locoid Lipocream

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/A

Drug-Herb Interactions

N/A

Nursing 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.

This guide is for educational purposes only and is not intended for clinical use.