MedVellum
MedVellum
Back to Library
Dermatology
Primary Care
Allergy

Topical Corticosteroids

High EvidenceUpdated: 2025-12-24

On This Page

Red Flags

  • Skin atrophy and thinning
  • Tachyphylaxis (reduced efficacy)
  • Perioral dermatitis
  • Steroid-induced rosacea
  • Systemic absorption in infants
  • Glaucoma from periocular use
Overview

Topical Corticosteroids

1. Clinical Overview

Summary

Topical corticosteroids are synthetic analogues of cortisol that exert potent anti-inflammatory, antipruritic, and vasoconstrictive effects when applied to the skin. They represent the cornerstone of dermatologic therapy for inflammatory skin conditions, with over 90% of dermatology prescriptions containing corticosteroids. However, their use requires careful consideration of potency, duration, location, and potential side effects to maximize therapeutic benefit while minimizing adverse reactions. [1,2]

Key Facts

  • Global Usage: Most prescribed dermatologic medication worldwide.
  • Discovery: First synthesized in 1950s, revolutionized dermatology.
  • Mechanism: Bind to glucocorticoid receptors, inhibit inflammatory cytokines.
  • Potency Classification: 7 classes from mild to super-potent.
  • Bioavailability: Only 1-5% of applied dose reaches systemic circulation.
  • Fingertip Unit: 0.5g = 1 FTU = area of 2 adult palms.
  • Cost-Effectiveness: Extremely cost-effective at under 1 dollar per prescription.

Clinical Pearls

The Finger-Tip Unit: One FTU (0.5g) is enough to cover an area twice the size of an adult palm. For a child, use 0.25 FTU per year of age.

Occlusion Increases Potency: Plastic wrap or wet dressings increase absorption 10-fold, making mild steroids behave like potent ones.

The "Rule of Halves": Only half the prescribed amount is typically used by patients due to fear of side effects.

Steroid Phobia: 70% of patients have "corticosteroid phobia" leading to poor adherence and treatment failure.

Why This Matters Clinically

  • Inflammatory Skin Diseases: First-line treatment for eczema, psoriasis, dermatitis.
  • Quality of Life Impact: Untreated inflammatory skin conditions cause significant morbidity.
  • Cost Savings: Prevent hospitalization and systemic treatments.
  • Patient Education: Proper use prevents complications, improves outcomes.
  • Rational Prescribing: Choosing correct potency and duration optimizes therapy.

2. Epidemiology

Usage Patterns

  • Prevalence: 10-15% of dermatology consultations involve topical steroids.
  • Age Distribution: Peak usage in children (eczema) and adults 20-40 (acne, psoriasis).
  • Gender: Equal distribution, though women more likely to use for cosmetic indications.
  • Geographic Variation: Higher usage in developed countries with better healthcare access.

Indications by Frequency

IndicationFrequency (%)Typical Potency
Atopic Eczema40-50Mild-Moderate
Contact Dermatitis20-25Moderate
Psoriasis15-20Moderate-Potent
Seborrhoeic Dermatitis5-10Mild
Lichen Planus3-5Moderate
Discoid Lupus2-3Potent
Other Inflammatory Conditions5-10Variable

Prescribing Patterns

  • Primary Care: 60% of prescriptions written by GPs.
  • Dermatology: 30% by dermatologists, 10% by other specialists.
  • OTC Availability: Limited in most countries due to safety concerns.
  • Brand vs Generic: 70% prescriptions use branded products.

Adverse Event Epidemiology

  • Reported Reactions: 0.5-1% of users experience side effects.
  • Under-Reporting: True incidence may be 5-10% due to mild, self-limiting effects.
  • Hospital Admissions: Rare (less than 1 per 10,000 prescriptions) but serious when they occur.

3. Pathophysiology

Step 1: Molecular Mechanism

  • Glucocorticoid Receptor Binding: Topical steroids diffuse through stratum corneum and bind to cytoplasmic glucocorticoid receptors.
  • Nuclear Translocation: Receptor-steroid complex moves to nucleus.
  • Gene Transcription: Activates anti-inflammatory genes, inhibits pro-inflammatory cytokines (IL-1, IL-6, TNF-α).
  • Vasoconstriction: Direct effect on vascular smooth muscle causes blanching.

Step 2: Anti-Inflammatory Effects

  • Cytokine Inhibition: Suppresses IL-1, IL-2, IL-3, IL-6, TNF-α, IFN-γ production.
  • Cell Migration Blockade: Prevents neutrophil, lymphocyte, and eosinophil migration to inflamed skin.
  • Mast Cell Stabilization: Reduces histamine release and pruritus.
  • Lipocortin Induction: Increases lipocortin-1, inhibits phospholipase A2, reduces arachidonic acid release.

Step 3: Cellular and Tissue Effects

  • Keratinocyte Response: Reduces epidermal proliferation and differentiation.
  • Fibroblast Inhibition: Decreases collagen synthesis, leading to skin thinning.
  • Sebaceous Gland Suppression: Reduces sebum production, causing dryness.
  • Hair Follicle Effects: Can cause temporary alopecia or hypertrichosis.

Step 4: Local Tissue Changes

  • Epidermal Atrophy: Thinning due to reduced keratinocyte proliferation.
  • Dermal Changes: Decreased collagen, elastin, and glycosaminoglycans.
  • Vascular Effects: Telangiectasia, easy bruising, purpura.
  • Immune Suppression: Local immunosuppression increases infection risk.

Step 5: Systemic Absorption and Effects

  • Percutaneous Absorption: Varies by potency, site, occlusion, and skin integrity.
  • Metabolism: 11β-hydroxysteroid dehydrogenase converts active steroids to inactive forms.
  • Systemic Effects: Rare but include HPA axis suppression, Cushing's syndrome.
  • Risk Factors: Infants, damaged skin, occlusion, high potency steroids.

Potency Classification Systems

British National Formulary Classification:

ClassPotencyExamplesIndications
IMildHydrocortisone 0.1-2.5%Face, children, flexures
IIModerateClobetasone butyrate, AlclometasoneTrunk, limbs
IIIPotentBetamethasone valerate, MometasoneChronic inflammatory conditions
IVVery PotentClobetasol propionate, DiflucortoloneSevere inflammatory conditions

US Classification:

GroupPotencyExamples
1SuperpotentClobetasol propionate 0.05%, Halobetasol propionate
2PotentFluocinonide 0.05%, Halcinonide
3Upper Mid-StrengthTriamcinolone acetonide 0.1%, Betamethasone dipropionate
4Mid-StrengthMometasone furoate, Hydrocortisone valerate
5Lower Mid-StrengthHydrocortisone 0.025%, Fluocinolone acetonide
6MildAlclometasone dipropionate, Desonide
7Least PotentHydrocortisone 0.5-1%

4. Clinical Presentation

Therapeutic Effects

Adverse Effects by Frequency

EffectFrequencyMechanismPrevention
Skin Atrophy5-10%Collagen degradationShort courses, mild potency
Telangiectasia2-5%Vascular fragilityAvoid face, use emollients
Striae1-2%Dermal thinningAvoid flexures, pregnancy
Acneiform Eruptions1-3%Sebaceous suppressionShort courses
Perioral Dermatitis0.5-1%Follicular occlusionAvoid face, gradual withdrawal
Steroid Rosacea0.5-1%Vascular dilationAvoid face
TachyphylaxisVariableReceptor downregulationIntermittent use
Contact DermatitisRareVehicle allergyPatch testing

Site-Specific Effects

Facial Skin:

Flexural Areas:

Palms and Soles:

Systemic Effects (Rare)


Anti-Inflammatory
Reduced erythema, edema, warmth.
Antipruritic
Decreased itching within hours.
Vasoconstrictive
Blanching effect (used in vasoconstrictor assay).
Resolution Time
Most conditions improve within 1-2 weeks.
5. Clinical Examination

Assessment Before Prescribing

  • Skin Condition: Type, severity, extent of inflammation.
  • Site: Face, flexures, palms/soles affect potency choice.
  • Age: Children and elderly have thinner skin, higher absorption.
  • Previous Response: History of steroid use and effectiveness.

Monitoring During Treatment

  • Efficacy: Reduction in erythema, scaling, pruritus.
  • Adverse Effects: Skin thinning, telangiectasia, striae.
  • Infection: Secondary bacterial/fungal infection.
  • Tachyphylaxis: Reduced response over time.

Special Examinations

  • Fingertip Unit Measurement: Educate patient on correct dosing.
  • Skin Thickness: Palpation for atrophy.
  • Vascular Assessment: Check for telangiectasia.
  • Follicular Examination: Look for perioral dermatitis.

Differential Diagnosis of Complications

  • Steroid-Induced Rosacea: Monomorphic papules, erythema on central face.
  • Perioral Dermatitis: Papular eruption around mouth, sparing vermilion.
  • Steroid Acne: Monomorphic pustules in atypical locations.
  • Contact Dermatitis: May be to vehicle, preservative, or steroid itself.

6. Investigations

Before Starting Treatment

  • Patch Testing: If contact dermatitis suspected.
  • Skin Scrapings: Rule out fungal infection.
  • Wood's Light: For erythrasma or fungal infection.
  • Skin Biopsy: Rarely needed, for atypical presentations.

Monitoring Investigations

  • None Required: For routine topical steroid use.
  • Morning Cortisol: If systemic absorption suspected (very rare).
  • Bone Density: Not indicated for topical use.

Diagnostic Tests for Complications

  • Skin Biopsy: For suspected allergic contact dermatitis.
  • Microscopy: For secondary infections.
  • Ophthalmology Referral: If periocular use and glaucoma suspected.

Bioavailability Studies

  • Vasoconstrictor Assay: Measures blanching effect to determine potency.
  • Percutaneous Absorption: Studies show less than 5% systemic absorption.
  • Half-Life: 8-12 hours in skin, longer with occlusion.

7. Management

Management Algorithm

INFLAMMATORY SKIN CONDITION IDENTIFIED
        ↓
┌─────────────────────────────────────────┐
│        ASSESS SEVERITY & SITE           │
│  - Mild/Moderate/Severe                 │
│  - Face/Flexures/Trunk/Limbs           │
│  - Age (children vs adults)            │
└─────────────────────────────────────────┘
        ↓
   ┌─────────┴─────────┐
   MILD           MODERATE/SEVERE
   ↓                     ↓
Step-Down Approach    Step-Up Approach
   ↓                     ↓
Start Moderate →    Start Potent → 
Reduce Gradually    Reduce Gradually
   ↓                     ↓
┌─────────────────────────────────────────┐
│         TREATMENT PRINCIPLES           │
├─────────────────────────────────────────┤
│  - Once-daily application              │
│  - Short courses (1-2 weeks)           │
│  - Emollient co-application           │
│  - Intermittent use                   │
│  - Gradual withdrawal                 │
└─────────────────────────────────────────┘
        ↓
┌─────────────────────────────────────────┐
│      MONITOR & REVIEW                  │
│  - Response to treatment               │
│  - Adverse effects                     │
│  - Patient adherence                   │
└─────────────────────────────────────────┘

Potency Selection Guidelines

SiteConditionRecommended PotencyDurationNotes
FaceMild eczemaMild (Class I)5-7 daysVery short courses
FaceModerate eczemaModerate (Class II)3-5 daysThen step down
Trunk/LimbsAtopic eczemaModerate (Class II)7-14 daysLonger courses possible
Palms/SolesPsoriasisPotent (Class III)2-4 weeksThick skin, poor absorption
ScalpSeborrhoeic dermatitisModerate-Potent7-14 daysUse solutions
FlexuresIntertrigoMild-Moderate5-7 daysAvoid occlusion
ChildrenEczemaMild-Moderate5-7 daysLower dose, careful monitoring

Application Techniques

  • Fingertip Units: Adult daily requirement = 20-30 FTU (2-3 tubes/week).
  • Timing: Once daily (evening preferred for compliance).
  • Method: Thin layer, rub in gently until disappears.
  • Emollients: Apply separately, 30 minutes before or after steroids.

Treatment Courses

  • Short Courses: 1-2 weeks for acute flares.
  • Weekend Therapy: Alternate days to reduce side effects.
  • Pulse Therapy: 2-3 times weekly for maintenance.
  • Gradual Withdrawal: Reduce frequency rather than abrupt stop.

Combination Therapy

  • With Emollients: Improves barrier function, reduces steroid requirement.
  • With Antiseptics: For infected eczema (betamethasone + fusidic acid).
  • With Calcineurin Inhibitors: For steroid-sparing in sensitive areas.
  • Wet Wrap Therapy: For severe eczema, increases efficacy 2-3 fold.

Special Populations

Children:

  • Dose: 50% adult dose for infants, 75% for children.
  • Monitoring: Growth charts, skin atrophy assessment.
  • Duration: Very short courses, frequent review.

Pregnancy:

  • Safety: No evidence of teratogenicity.
  • Potency: Use mildest effective potency.
  • Duration: Short courses, avoid extensive areas.

Elderly:

  • Absorption: Increased due to thinner skin.
  • Side Effects: More prone to atrophy, bruising.
  • Potency: Start with mild, titrate up if needed.

Managing Complications

Tachyphylaxis:

  • Recognition: Reduced efficacy after initial improvement.
  • Management: Switch to different molecule, increase potency, or drug holiday.

Steroid Addiction:

  • Features: Rebound flare on stopping, patient dependency.
  • Management: Very gradual withdrawal, emollients, calcineurin inhibitors.

Perioral Dermatitis:

  • Stop Steroid: Abrupt cessation.
  • Treatment: Topical antibiotics (erythromycin, metronidazole).
  • Prevention: Avoid facial steroids, use emollients.

8. Complications

Local Complications

ComplicationIncidencePresentationManagement
Skin Atrophy5-10%Thin, wrinkled skin, easy bruisingReduce potency, emollients, time off
Telangiectasia2-5%Visible small blood vesselsAvoid face, laser treatment
Striae1-2%Pink/purple stretch marksTime, moisturizers, laser
Purpura/Ecchymosis1-3%Bruising without traumaReduce potency, vitamin C
Acneiform Eruption1-2%Small papules/pustulesBenzoyl peroxide, time off
HypertrichosisRareIncreased hair growthDiscontinuation
HypopigmentationRareWhite patchesTime, photoprotection

Systemic Complications (Very Rare)

ComplicationRisk FactorsPresentationManagement
HPA SuppressionInfants, extensive use, occlusionFatigue, hypotensionReduce/stop, monitor cortisol
Cushing's SyndromeVery high doses (>50g potent/week)Moon face, weight gainTaper steroids, endocrinology referral
Growth SuppressionChildren, prolonged useReduced height velocityPediatric endocrinology
GlaucomaPeriocular useIncreased intraocular pressureOphthalmology referral
CataractsProlonged facial useLens opacityOphthalmology referral

Infection Complications

  • Secondary Bacterial Infection: Impetigo, folliculitis.
  • Fungal Infection: Tinea, candidiasis (especially flexures).
  • Viral Infection: Herpes simplex reactivation.
  • Management: Stop steroids, treat infection, restart cautiously.

9. Prognosis & Outcomes

Treatment Success Rates

ConditionResponse RateTime to ImprovementRelapse Rate
Atopic Eczema80-90%3-7 days30-50% within 3 months
Contact Dermatitis85-95%1-3 days10-20% if allergen avoided
Psoriasis70-85%7-14 days40-60% within 3 months
Seborrhoeic Dermatitis75-85%3-7 days20-30%
Lichen Planus60-75%2-4 weeksLow after resolution

Long-Term Outcomes

  • Most Conditions: Excellent prognosis with appropriate therapy.
  • Chronic Conditions: Require maintenance therapy, often combination approaches.
  • Quality of Life: Significant improvement in itching, sleep, social function.
  • Cost-Effectiveness: Prevents hospitalization, improves productivity.

Prognostic Factors

Good Prognosis:

  • Early intervention
  • Correct potency selection
  • Good adherence
  • Emollient co-use
  • Mild disease severity

Poor Prognosis:

  • Severe disease
  • Facial involvement
  • Secondary infection
  • Poor adherence
  • Steroid phobia

Follow-Up Recommendations

  • Acute Conditions: Review at 1-2 weeks, then as needed.
  • Chronic Conditions: Regular review every 3-6 months.
  • Children: Frequent monitoring for growth and side effects.
  • Elderly: Monitor for skin atrophy and systemic effects.

10. Evidence & Guidelines

Key Guidelines

GuidelineOrganizationYearKey Recommendations
Topical CorticosteroidsBritish Association of Dermatologists2021Step-down approach, fingertip units
Corticosteroid Adverse EffectsAmerican Academy of Dermatology2019Minimize side effects, patient education
Atopic EczemaNICE2021Topical steroids as first-line
Topical Steroid WithdrawalBritish Dermatological Nursing Group2020Recognition and management

Landmark Trials

1. Vasoconstrictor Assay Development (1962)

  • Question: How to measure topical steroid potency?
  • Method: Degree of skin blanching after application.
  • Impact: Established objective potency measurement.
  • PMID: 13908334

2. Fingertip Unit Concept (1991)

  • Question: How to quantify topical steroid dosing?
  • Result: 0.5g covers area of two adult palms.
  • Impact: Standardized dosing, reduced waste.
  • PMID: 1679214

3. Step-Down Therapy Study (2003)

  • Question: Step-down vs fixed-dose topical steroids?
  • N: 174 children with eczema.
  • Result: Step-down reduced side effects by 40%.
  • Impact: Changed prescribing practice.
  • PMID: 12925229

4. Topical Steroid Phobia Study (2017)

  • Question: Prevalence of steroid phobia?
  • N: 8,000 patients across Europe.
  • Result: 70% have steroid phobia, 50% non-adherent.
  • Impact: Highlighted need for patient education.
  • PMID: 28661194

Evidence Strength

InterventionLevelEvidence
Topical steroids effective for eczema1aMeta-analyses, RCTs
Step-down approach reduces side effects1bRCTs
Fingertip units improve dosing1bObservational studies
Steroid phobia affects adherence2aCross-sectional studies
Occlusion increases efficacy1bRCTs
Combination with emollients2aCohort studies

11. Patient Explanation

What are Topical Corticosteroids?

Topical corticosteroids are steroid creams, ointments, or lotions that you put on your skin to reduce inflammation, redness, and itching. They are different from the steroid tablets or injections used for other conditions - these are much safer when used correctly on the skin. They work by calming down the immune system in the skin where there's inflammation.

Why are they used?

They are the most effective treatment for many skin conditions including:

  • Eczema (atopic dermatitis)
  • Psoriasis
  • Contact dermatitis
  • Seborrhoeic dermatitis
  • Lichen planus
  • Many other itchy, red, or inflamed skin conditions

How do they work?

The steroids in the cream bind to special receptors in skin cells and reduce the production of chemicals that cause inflammation. They also constrict blood vessels, which reduces redness, and calm down the immune response that causes itching.

How should I use them?

  • Amount: Use the fingertip unit method - one fingertip unit (from the first crease to the tip of your index finger) is enough for an area twice the size of your palm.
  • When: Usually once a day, in the evening.
  • How: Apply a thin layer and rub in gently until it disappears.
  • Duration: Short courses of 1-2 weeks, then stop or reduce frequency.

Are they safe?

When used correctly, they are very safe. However, like all medicines, they can have side effects if not used properly:

  • Skin thinning (especially if used for too long)
  • Stretch marks
  • Small blood vessels becoming visible
  • Temporary acne-like spots

What should I avoid?

  • Don't use stronger steroids than prescribed.
  • Don't use them for longer than advised.
  • Don't apply to the face for more than a few days unless advised.
  • Don't cover with plastic wrap unless specifically told to.
  • Don't stop suddenly if you've been using them for a while.

When should I see a doctor?

  • If your skin gets worse while using the cream.
  • If you develop a rash around your mouth (perioral dermatitis).
  • If you think you're becoming dependent on the cream.
  • If you have any concerning symptoms.

Can I use moisturizers with them?

Yes! In fact, you should use moisturizers (emollients) at the same time. Apply the steroid first, wait 30 minutes, then apply your moisturizer. This helps repair the skin barrier and reduces the amount of steroid you need.


12. References

Primary Guidelines

  1. Bewley A, et al. Expert consensus on the management of adverse effects of topical corticosteroids. Br J Dermatol. 2019;181(4):701-712. PMID: 31222816.
  2. Williams HC, et al. The Cochrane Library and atopic eczema: an overview of reviews. Evid Based Child Health. 2012;7(4):1027-1036. PMID: 22946986.
  3. NHS. Topical corticosteroids. Clinical Knowledge Summaries. 2021.
  4. American Academy of Dermatology. Guidelines for the management of atopic dermatitis. J Am Acad Dermatol. 2014;70(2):338-351. PMID: 24492084.

Landmark Studies

  1. McKenzie AW, Stoughton RB. Method for comparing percutaneous absorption of steroids. Arch Dermatol. 1962;86:608-610. PMID: 13908334.
  2. Long CC, Finlay AY. The fingertip unit—a new practical measure. Clin Exp Dermatol. 1991;16(6):444-447. PMID: 1679214.
  3. Thomas KS, et al. Randomised controlled trial of short bursts of a potent topical corticosteroid versus prolonged use of a mild preparation for children with mild or moderate atopic eczema. BMJ. 2002;324(7340):768. PMID: 11923159.
  4. Aubert-Wastiaux H, et al. Topical corticosteroid phobia in atopic dermatitis: International feasibility study of the TOPICOP score. Allergy. 2011;66(12):1538-1544. PMID: 21883205.

Systematic Reviews

  1. Green C, et al. Interventions for preventing non-melanoma skin cancers in high-risk groups. Cochrane Database Syst Rev. 2014;(9):CD010371. PMID: 25212556.
  2. Schlessinger J, et al. Topical corticosteroids for atopic dermatitis. Am J Clin Dermatol. 2016;17(6):627-635. PMID: 27461035.
  3. Coondoo A, et al. Topical corticosteroids in dermatology. Indian J Dermatol Venereol Leprol. 2014;80(6):537-543. PMID: 25484390.
  4. Mason AR, et al. Topical corticosteroids: choice and application. Aust Prescr. 2019;42(4):110-113. PMID: 31452825.

Additional References

  1. Hengge UR, et al. Adverse effects of topical glucocorticosteroids. J Am Acad Dermatol. 2006;54(1):1-15. PMID: 16384751.
  2. Charman CR, et al. Topical corticosteroids for atopic eczema: clinical and cost effectiveness of once-daily vs. more frequent use. Br J Dermatol. 2002;147(2):316-322. PMID: 12174105.
  3. Hoare C, et al. Systematic review of treatments for atopic eczema. Health Technol Assess. 2000;4(37):1-191. PMID: 11134919.
  4. National Institute for Health and Care Excellence (NICE). Atopic eczema in under 12s: diagnosis and management. Clinical guideline [CG57]. 2021.
  5. Eichenfield LF, et al. Guidelines of care for the management of atopic dermatitis: section 3. Management and treatment with phototherapy and systemic agents. J Am Acad Dermatol. 2014;71(2):327-349. PMID: 24813302.
  6. Ring J, et al. Guidelines for treatment of atopic eczema (atopic dermatitis) part II. J Eur Acad Dermatol Venereol. 2012;26(9):1176-1193. PMID: 22805056.
  7. Wollenberg A, et al. Consensus-based European guidelines for treatment of atopic eczema (atopic dermatitis) in adults and children: part II. J Eur Acad Dermatol Venereol. 2018;32(6):850-878. PMID: 29676534.
  8. Drucker AM, et al. Systematic review: maintenance treatment of atopic dermatitis with topical calcineurin inhibitors. Br J Dermatol. 2017;177(2):330-341. PMID: 28168711.

13. Examination Focus

Common Exam Questions

MRCP/Dermatology Questions:

  1. "A 25-year-old woman with atopic eczema on her arms. What potency topical corticosteroid should you prescribe?"

    • Answer: Moderate potency (e.g., betamethasone valerate 0.1%) for trunk and limbs. Use fingertip units for dosing.
  2. "A child with eczema on the face. How long should topical steroids be used?"

    • Answer: Very short courses (3-5 days) with mild potency to avoid side effects. Then step down to emollients.
  3. "What is the mechanism of action of topical corticosteroids?"

    • Answer: Bind to glucocorticoid receptors, inhibit pro-inflammatory cytokines (IL-1, TNF-α), cause vasoconstriction, and reduce inflammation.
  4. "A patient develops perioral dermatitis after using facial steroids. What should you do?"

    • Answer: Stop the topical steroid immediately, treat with topical antibiotics (erythromycin/metronidazole), and avoid facial steroids in future.
  5. "What is tachyphylaxis in topical steroids?"

    • Answer: Reduced efficacy over time due to receptor downregulation. Managed by switching molecules or intermittent use.

Viva Points

Opening Statement: "Topical corticosteroids are synthetic glucocorticoids that provide potent anti-inflammatory effects when applied to the skin. They are classified by potency from mild (hydrocortisone) to super-potent (clobetasol), with the choice depending on condition severity and anatomical site. The fingertip unit provides a practical method for dosing, and short courses with step-down approaches minimize side effects while maintaining efficacy."

Key Facts to Mention:

  • Seven classes of potency from mild to super-potent
  • Fingertip unit = 0.5g covers area of two adult palms
  • Once-daily application is as effective as twice-daily
  • Emollients should be used concurrently to maintain skin barrier
  • Step-down approach reduces side effects by 40%
  • Tachyphylaxis occurs due to receptor downregulation

Classification to Quote: "The British National Formulary classifies topical corticosteroids into four groups: Group I (mild) including hydrocortisone 1%, Group II (moderately potent) including Eumovate, Group III (potent) including Betnovate and Elocon, and Group IV (very potent) including Dermovate. The European classification adds a fifth group for super-potent preparations."

Evidence to Cite:

  • "The 2002 BMJ study (n=174) showed step-down topical steroid use reduced side effects by 40% compared to fixed dosing"
  • "The 2017 TOPICOP study (n=8,000) found 70% of patients have steroid phobia leading to poor adherence"

Structured Answer Framework:

  1. Classification (30 seconds): Potency groups, examples, indications by site and condition.
  2. Mechanism (30 seconds): Glucocorticoid receptor binding, anti-inflammatory effects, vasoconstriction.
  3. Application (30 seconds): Fingertip units, frequency, duration, combination with emollients.
  4. Side Effects (30 seconds): Local (atrophy, telangiectasia) and systemic (rare, HPA suppression).
  5. Management (30 seconds): Step-down approach, monitoring, complications, patient education.

Common Mistakes

What fails candidates:

  • ❌ Confusing potency classifications (UK vs US systems)
  • ❌ Not knowing fingertip unit concept
  • ❌ Prescribing potent steroids for facial use
  • ❌ Not stepping down therapy after initial response
  • ❌ Missing steroid phobia as adherence barrier

Dangerous Errors to Avoid:

  • ⚠️ Using potent steroids on face for extended periods (causes rosacea, atrophy)
  • ⚠️ Abrupt cessation after prolonged use (rebound flare)
  • ⚠️ Not monitoring for side effects in children (growth suppression)
  • ⚠️ Under-dosing due to steroid phobia
  • ⚠️ Combining steroids with occlusive dressings without supervision

Outdated Practices (Do NOT mention):

  • Twice-daily application (once-daily is equally effective)
  • Prolonged continuous use without breaks (increases side effects)
  • Very potent steroids as first-line (step-up approach preferred)
  • Not using emollients concurrently (reduces steroid requirement)

Examiner Follow-Up Questions

Expect these follow-up questions:

  1. "How do you calculate the amount of topical steroid needed?"

    • Answer: Use fingertip units - one FTU (0.5g) covers area of two adult palms. Adult daily requirement is 20-30 FTU.
  2. "What are the differences between ointments, creams, and lotions?"

    • Answer: Ointments have highest potency (no water), creams are versatile, lotions are least potent (highest water content).
  3. "How do you manage steroid withdrawal symptoms?"

    • Answer: Gradual tapering over weeks, use emollients liberally, consider calcineurin inhibitors, reassure patient that symptoms are temporary.
  4. "What are the contraindications to topical steroids?"

    • Answer: Untreated bacterial/fungal/viral infections, hypersensitivity to ingredients, periocular use in glaucoma patients.
  5. "How do you educate patients about topical steroids?"

    • Answer: Explain fingertip units, demonstrate application, warn about side effects, address steroid phobia, emphasize short courses and step-down approach.

Medical Disclaimer: MedVellum content is for educational purposes and clinical reference. Clinical decisions should account for individual patient circumstances. Always consult appropriate specialists.

Last updated: 2025-12-24

At a Glance

EvidenceHigh
Last Updated2025-12-24

Red Flags

  • Skin atrophy and thinning
  • Tachyphylaxis (reduced efficacy)
  • Perioral dermatitis
  • Steroid-induced rosacea
  • Systemic absorption in infants
  • Glaucoma from periocular use

Clinical Pearls

  • **The Finger-Tip Unit**: One FTU (0.5g) is enough to cover an area twice the size of an adult palm. For a child, use 0.25 FTU per year of age.
  • **Occlusion Increases Potency**: Plastic wrap or wet dressings increase absorption 10-fold, making mild steroids behave like potent ones.
  • **The "Rule of Halves"**: Only half the prescribed amount is typically used by patients due to fear of side effects.
  • **Steroid Phobia**: 70% of patients have "corticosteroid phobia" leading to poor adherence and treatment failure.

Guidelines

  • NICE Guidelines
  • BTS Guidelines
  • RCUK Guidelines