endocrine:drugs:fluticasone
Differences
This shows you the differences between two versions of the page.
| Both sides previous revisionPrevious revisionNext revision | Previous revision | ||
| endocrine:drugs:fluticasone [2026/02/12 19:40] – andrew2393cns | endocrine:drugs:fluticasone [2026/02/12 20:04] (current) – created andrew2393cns | ||
|---|---|---|---|
| Line 1: | Line 1: | ||
| - | ====== | + | ====== |
| - | + | ||
| - | Corticosteroids are synthetic analogs of adrenal cortex hormones used for potent anti-inflammatory and immunosuppressive effects. | + | |
| - | + | ||
| - | They mimic: | + | |
| - | * Cortisol (glucocorticoid activity) | + | |
| - | * Aldosterone (mineralocorticoid activity — varies by agent) | + | |
| - | + | ||
| - | This page focuses on pharmacology. | + | |
| - | For disease-specific management, see linked clinical pages below. | + | |
| - | + | ||
| - | ---- | + | |
| ===== Classification ===== | ===== Classification ===== | ||
| + | * High-potency inhaled/ | ||
| - | ==== Systemic Glucocorticoids ==== | + | Parent class: |
| - | * [[endocrine:drugs: | + | * [[endocrine: |
| - | * [[endocrine: | + | |
| - | * [[endocrine: | + | |
| - | * [[endocrine: | + | |
| - | * [[endocrine: | + | |
| - | + | ||
| - | ==== Inhaled / Intranasal ==== | + | |
| - | * [[endocrine: | + | |
| - | * [[endocrine: | + | |
| - | * [[endocrine: | + | |
| - | * [[endocrine: | + | |
| - | + | ||
| - | ==== Topical ==== | + | |
| - | * Multiple potency classes (dermatologic use) | + | |
| ---- | ---- | ||
| - | ===== Mechanism of Action ===== | + | ===== Clinical |
| - | + | ||
| - | Corticosteroids act via intracellular glucocorticoid receptors. | + | |
| - | + | ||
| - | Stepwise: | + | |
| - | + | ||
| - | 1) Drug diffuses across cell membrane | + | |
| - | 2) Binds cytoplasmic glucocorticoid receptor | + | |
| - | 3) Complex translocates to nucleus | + | |
| - | 4) Alters gene transcription | + | |
| - | + | ||
| - | Primary effects: | + | |
| - | + | ||
| - | * ↓ IL-1, IL-2, IL-4, IL-5, IL-6, TNF-α | + | |
| - | * ↓ Eosinophil survival | + | |
| - | * ↓ T-cell activation | + | |
| - | * ↓ Mast cell mediator release | + | |
| - | * ↓ Phospholipase A2 → ↓ prostaglandins & leukotrienes | + | |
| - | + | ||
| - | Result: | + | |
| - | Broad suppression of inflammatory pathways. | + | |
| - | + | ||
| - | Onset: | + | |
| - | * Hours to days (genomic effect) | + | |
| - | + | ||
| - | ---- | + | |
| - | + | ||
| - | ===== Glucocorticoid vs Mineralocorticoid Activity ===== | + | |
| - | + | ||
| - | ^ Drug ^ Glucocorticoid Potency ^ Mineralocorticoid Activity ^ | + | |
| - | | Hydrocortisone | Low | Moderate | | + | |
| - | | Prednisone | Moderate | Low | | + | |
| - | | Methylprednisolone | Moderate | Minimal | | + | |
| - | | Dexamethasone | High | None | | + | |
| - | + | ||
| - | Clinical | + | |
| - | + | ||
| - | * Mineralocorticoid activity → fluid retention, edema, hypertension | + | |
| - | * Dexamethasone preferred when fluid retention undesirable | + | |
| - | + | ||
| - | ---- | + | |
| - | + | ||
| - | ===== Pharmacologic Roles Across Systems | + | |
| - | + | ||
| - | Corticosteroids are used in many disease states: | + | |
| + | * [[respiratory: | ||
| * [[allergy: | * [[allergy: | ||
| - | * [[respiratory: | ||
| - | * [[dermatology: | ||
| - | * [[rheumatology: | ||
| - | * [[gastroenterology: | ||
| - | * [[allergy: | ||
| - | * Transplant rejection prevention | ||
| - | |||
| - | This reflects their broad anti-inflammatory and immunosuppressive activity. | ||
| - | |||
| - | ---- | ||
| - | |||
| - | ===== Adverse Effects ===== | ||
| - | |||
| - | Short-term: | ||
| - | * Hyperglycemia | ||
| - | * Mood changes | ||
| - | * Fluid retention | ||
| - | * Insomnia | ||
| - | * Increased appetite | ||
| - | |||
| - | Long-term: | ||
| - | * Adrenal suppression | ||
| - | * Osteoporosis | ||
| - | * Cushingoid features | ||
| - | * Muscle wasting | ||
| - | * Increased infection risk | ||
| - | * Peptic ulcer disease | ||
| - | * Skin thinning | ||
| - | |||
| - | Mechanism: | ||
| - | Systemic metabolic and immune suppression. | ||
| - | |||
| - | ---- | ||
| - | |||
| - | ===== HPA Axis Suppression ===== | ||
| - | |||
| - | Chronic systemic corticosteroid use suppresses endogenous cortisol production. | ||
| - | |||
| - | Abrupt discontinuation may cause: | ||
| - | |||
| - | * Adrenal insufficiency | ||
| - | * Hypotension | ||
| - | * Fatigue | ||
| - | * Adrenal crisis (severe cases) | ||
| - | |||
| - | Taper required when: | ||
| - | * Therapy > 2–3 weeks | ||
| - | * Moderate to high doses | ||
| - | * Cushingoid features present | ||
| ---- | ---- | ||
| Line 133: | Line 18: | ||
| ===== Clinical Pearls ===== | ===== Clinical Pearls ===== | ||
| - | * Intranasal corticosteroids are first-line for nasal congestion in allergic rhinitis. | + | * Minimal systemic absorption when inhaled. |
| - | * Inhaled corticosteroids are foundational in asthma management. | + | * First-line for allergic |
| - | * Steroids suppress late-phase allergic | + | |
| - | * Epinephrine, | + | |
| - | * Always consider HPA suppression in prolonged systemic therapy. | + | |
| - | + | ||
| - | ---- | + | |
| - | + | ||
| - | ===== Related Pages ===== | + | |
| - | + | ||
| - | * [[allergy: | + | |
| - | * [[allergy: | + | |
| - | * [[autonomics: | + | |
endocrine/drugs/fluticasone.1770925229.txt.gz · Last modified: by andrew2393cns
