ATOPIC DERMATITIS MANAGEMENT | |||||
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Therapy | Strength | Dosage form | Dosing/frequency | Recommendations | |
NONPHARMACOLOGIC | |||||
Topical moisturizers | Emollients (glycol and glyceryl stearate, soy sterols) | — | crm, oint, gel, lotion, oil | Liberal and frequent reapplication. Apply soon after bathing to improve skin hydration. | • Mild AD: main primary treatment. • Moderate to severe AD: incorporated into regimen. |
Occlusives (petrolatum, dimethicone, mineral oil) | |||||
Humectants (glycerol, lactic acid, urea) | |||||
Prescription emollient devices | Palmitoylethanolamide-, glycyrrhetinic acid-, or other hydrolipid-containing preparations | — | crm | 2–3 times daily. | • Adjunct to treatment and maintenance. • More costly than topical moisturizers but not superior. |
Bathing | Water | — | — | Once daily for 5–10mins (warm water). Apply moisturizer immediately after bathing. Severely inflamed skin: up to 20mins; apply topical anti-inflammatory therapies (TCS) immediately after without towel drying. | • Use of nonsoap-based surfactants and synthetic detergents (syndets) are often recommended. • Limit use of neutral-to-low pH, hypoallergenic, and fragrance-free nonsoap cleansers. • Limited data on the addition of oils, emollients, and other related additives to bath water, and the use of acidic spring water (balneo-therapy) and water-softening devices; not recommended. |
Wet-wrap therapy | Topical agent covered by wetted first layer (tubular bandage, gauze, cotton suit) and dry second layer | — | — | Up to 24hrs at a time for up to 2wks. | • For significant flares and/or recalcitrant disease. • Use with or without TCS for moderate to severe AD (caution with medium to higher potency TCS).1 |
Phototherapy | UVB | Narrowband (309–312nm) | — | Administer to affected areas 2–5 times weekly | • Last-line therapy for non-immunocompromised patients with topical treatment failure. |
PHARMACOLOGIC2 | |||||
Topical Corticosteroids3 | |||||
Very high potency | augmented betamethasone dipropionate (oint) | 0.05% | crm, oint, lotion, foam, soln, gel | Treatment: apply twice daily until lesions improve, for up to 2–4wks at a time; for high potency TCS, may apply once daily. Use 0.5g for an area of 2 adult palms. Maintenance: apply 1–2 times weekly for frequent, repeated flares at same site. | • First-line pharmacologic therapy for mild to moderate AD if uncontrolled by moisturizers or irritant avoidance. • Use concomitantly with moisturizers. • Use least potent TCS that is effective. • Lower potency TCS should be used on the face and skin folds and medium to high potency TCS on the body. • Monitor cutaneous side-effects during long-term, potent steroid use. Routine monitoring of systemic effects is not recommended. |
clobetasol propionate | 0.05% | ||||
diflorasone diacetate (oint) | 0.05% | ||||
halobetasol propionate | 0.05% | ||||
High potency | amcinonide | 0.1% | |||
augmented betamethasone dipropionate (crm) | 0.05% | betamethasone dipropionate | 0.05% | ||
desoximetasone | 0.25% | ||||
desoximetasone (gel) | 0.05% | ||||
diflorasone diacetate (crm) | 0.05% | ||||
fluocinonide | 0.05% | ||||
halcinonide | 0.1% | ||||
mometasone furoate (oint) | 0.1% | ||||
triamcinolone acetonide | 0.5% | ||||
Medium potency | betamethasone valerate | 0.1% | |||
clocortolone pivalate | 0.1% | ||||
desoximetasone (crm) | 0.05% | ||||
fluocinolone acetonide | 0.025% | ||||
flurandrenolide | 0.05% | ||||
fluticasone propionate | 0.05%, 0.005% | ||||
mometasone furoate (crm) | 0.1% | ||||
triamcinolone acetonide | 0.1% | ||||
Lower-medium potency | hydrocortisone butyrate | 0.1% | |||
hydrocortisone probutate | 0.1% | ||||
hydrocortisone valerate | 0.2% | ||||
prednicarbate | 0.1% | ||||
Low potency | alclometasone dipropionate | 0.05% | |||
desonide | 0.05% | ||||
fluocinolone acetonide | 0.01% | ||||
Lowest potency | hydrocortisone acetate | 0.5–1% | |||
hydrocortisone base | 0.25–1% | ||||
Phosphodiesterase 4 (PDE4) Inhibitor | |||||
crisaborole | Eucrisa | 2% | oint | Mild to moderate: ≥3mos: apply a thin layer to affected areas twice daily; may consider reducing to once daily after clinical effect is achieved. | • First-line treatment |
Topical Calcineurin Inhibitors | |||||
tacrolimus | Protopic | 0.03%, 0.1% | oint | Moderate to severe: ≥2yrs4: apply a thin layer to affected areas twice daily. 2–15yrs: use 0.03% strength. ≥16yrs: use 0.03% or 0.1% strength. May use 2–3 times weekly as maintenance therapy to prevent recurrent flares. | • Second-line therapy for short-term and non-continuous chronic treatment of AD in non-immunocompromised patients with inadequate response to topical prescription therapies or when they are not advisable. • Preferred for sensitive areas (eg, face, skin folds). • Not recommended during active infections of lesions. • May be combined with TCS sequentially or concomitantly. • Long term safety has not been established due to association with skin malignancies and lymphoma; avoid continuous long-term use in any age group. |
pimecrolimus | Elidel | 1% | crm | Mild to moderate: ≥2yrs4: apply a thin layer to affected areas twice daily. May use 2–3 times weekly as maintenance therapy to prevent recurrent flares. | |
Interleukin-4 Receptor Alpha Antagonist | |||||
dupilumab | Dupixent | 100mg/0.67mL, 200mg/1.14mL, 300mg/2mL | SC inj | Moderate to severe: 6mos–5yrs (5–<15kg): 200mg every 4wks; (15–<30kg): 300mg every 4wks. 6–17yrs (15–<30kg): initially 600mg (two 300mg inj at different sites) followed by 300mg every 4wks; (30–<60kg): initially 400mg (two 200mg inj at different sites) followed by 200mg every other week; (≥60kg): initially 600mg followed by 300mg every other week. ≥18yrs: initially 600mg followed by 300mg every other week. | • Reserved for patients with inadequate response to topical prescription therapies or when they are not advisable. • May use with or without TCS. • Topical calcineurin inhibitors may also be used, but should be reserved only for problem areas (eg, face, neck, intertriginous and genital areas). |
tralokinumab-ldrm | Adbry | 150mg/mL | SC inj | Moderate to severe: ≥18yrs: initially 600mg (four 150mg inj), followed by 300mg (two 150mg inj) every other week. After 16wks, may consider 300mg every 4wks for patients weighing <100kg who achieve clear or almost clear skin. | |
Janus Kinase Inhibitor5 | |||||
abrocitinib | Cibinqo | 50mg, 100mg, 200mg | tabs | Moderate to severe: ≥12yrs:100mg once daily; may increase to max 200mg once daily if inadequate response after 12wks. | • Reserved for refractory patients with inadequate response to other systemic therapies, including biologics, or when they are not advisable. • May use with or without TCS. • Not recommended for use with biologics, other JAK inhibitors, or potent immunosuppressants (eg, azathioprine, cyclosporine). |
ruxolitinib | Opzelura | 1.5% | crm | Mild to moderate: ≥12yrs: apply a thin layer to the affected areas (up to 20% BSA) twice daily; max 60g per week or 100g per 2wks. Reevaluate if no improvement within 8wks. | • For short-term and non-continuous chronic treatment of AD in non-immunocompromised patients with inadequate response to topical prescription therapies or when they are not advisable. • Not recommended during active infections, and for use with biologics, other JAK inhibitors, or potent immunosuppressants (eg, azathioprine, cyclosporine). |
upadacitinib | Rinvoq | 15mg, 30mg, 45mg | ext-rel tabs | Moderate to severe: ≥12yrs (≥40kg): initially 15mg once daily; if inadequate response, consider increasing to 30mg once daily. Elderly (≥65yrs), severe renal impairment (CrCl <30mL/min), or concomitant strong CYP3A4 inhibitors: 15mg once daily. | • Reserved for refractory patients with inadequate response to other systemic therapies, including biologics, or when they are not advisable. • Not recommended for use with biologics, other JAK inhibitors, or potent immunosuppressants (eg, azathioprine, cyclosporine). |
NOTES | |||||
Key: AD = atopic dermatitis; BSA = body surface area; crm = cream; JAK = Janus kinase; MACE = major adverse cardiovascular events; oint = ointment; soln = solution; UVB = ultraviolet B; TCS = topical corticosteroid
1 Increased absorption of mid- to higher-potency TCS applied under the wraps may cause hypothalamic-pituitary-adrenal axis suppression. 2 Systemic immunosuppressants (eg, methotrexate, mycophenylate mofetil, azathioprine) have been recommended for severe AD in patients with topical treatment failure. 3 See Topical Steroid Potencies chart for more drug information. 4 For children aged <2yrs with mild to severe disease, off-label use of tacrolimus 0.03% or pimecrolimus 1% can be recommended. 5 Increased risk of serious infections, all-cause mortality, malignancies, MACE, and thrombosis in patients treated with JAK inhibitors for inflammatory conditions.
Not an inclusive list of medications and/or official indications. Please see drug monograph at www.eMPR.com and/or contact company for full drug labeling. |
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REFERENCES | |||||
Eichenfield LF, Tom WL, Berger TG, et al. Guidelines of care for the management of atopic dermatitis. American Academy of Dermatology, Inc. Published: May 07, 2014. http://dx.doi.org/10.1016/j.jaad.2014.03.023
Fleming P, Yang YB, Lynde C, O’Neill B, Lee KO. Diagnosis and management of atopic dermatitis for primary care providers. J Am Board Fam Med. 2020; 33 (4); 626-635.
(Rev. 6/2023) |
Atopic Dermatitis Management