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Atopic Dermatitis Treatment

Atopic dermatitis, often called eczema, is a chronic inflammatory skin condition marked by dry, itchy skin, redness, scaling, and sometimes thickened patches from repeated scratching. It is strongly associated with a weakened skin barrier and immune overactivity, which can allow moisture loss and make skin more reactive to irritants, allergens, and microbes. Because atopic dermatitis ranges from mild, intermittent flares to severe, widespread disease, treatment is typically stepwise and combines daily barrier support with targeted anti-inflammatory therapy. At Peak Skin Center, board-certified dermatologist Dr. Thomas Knackstedt builds treatment plans around severity, body location, infection risk, and long-term maintenance needs.

Topical therapy is the foundation for most atopic dermatitis, especially when disease is mild-to-moderate or localized. Peak Skin Center commonly emphasizes barrier repair while using prescription topicals to calm inflammation and reduce itch.

Moisturizers and barrier repair therapy

Moisturizers help by strengthening the skin barrier, reducing water loss, and decreasing exposure to triggers that drive itch and inflammation. Symptom comfort often improves within several days, with more durable improvements in dryness and flare frequency over 2–4 weeks of consistent use. Side effects are uncommon but can include stinging on very inflamed skin or contact sensitivity to fragrance or preservatives in certain products.

Topical corticosteroids

Topical steroids reduce eczema inflammation by suppressing immune signaling in the skin, which decreases redness, swelling, and itch during flares. Many individuals notice itch reduction within 2–7 days, with visible clearing over 1–3 weeks depending on potency and location. Common side effects include temporary burning or irritation; with prolonged or repeated use, thinning of the skin, stretch marks, and easy bruising can occur, especially on the face and skin folds.

Topical calcineurin inhibitors (tacrolimus, pimecrolimus)

Calcineurin inhibitors reduce T-cell–driven inflammation without the skin-thinning risks associated with long-term steroid use, which makes them useful for sensitive areas such as the face, eyelids, neck, groin, and skin folds. Improvement is often seen within 1–3 weeks, with itch relief sometimes occurring earlier. Common side effects include temporary burning or stinging during the first several days of application.

Crisaborole (topical PDE-4 inhibitor)

Crisaborole decreases inflammatory signaling by inhibiting phosphodiesterase-4 (PDE-4), helping reduce redness and itch in mild-to-moderate atopic dermatitis. Benefits often emerge over 1–2 weeks, with continued improvement over 4–6 weeks. The most common side effect is application-site burning or stinging, particularly when used on actively inflamed skin.

Roflumilast cream (topical PDE-4 inhibitor)

Roflumilast cream is a steroid-free topical that also inhibits PDE-4, which can lower cytokine signaling involved in eczema inflammation and itch. It is FDA-approved for mild-to-moderate atopic dermatitis (formulation-dependent), and may be considered when a non-steroidal option is preferred for maintenance or sensitive sites. Improvement is often noticed within the first 1–2 weeks, with broader reduction in redness and roughness over 4–8 weeks. Common side effects can include application-site discomfort (burning or stinging), and some people report headache or upper respiratory symptoms.

Topical JAK inhibitor (ruxolitinib cream)

Ruxolitinib cream reduces inflammation by blocking Janus kinase (JAK) pathways that transmit itch- and inflammation-related cytokine signals. Itch reduction can occur within days in some cases, with clearer skin developing over 2–8 weeks. Common side effects include application-site reactions and acne-like bumps; because it is an immunomodulating medication, selection, duration, and follow-up are individualized.

Wet wrap therapy during flares

Wet wraps help rehydrate skin and improve barrier function while enhancing penetration of topical anti-inflammatory medications, which can reduce itch quickly during more intense flares. Benefits can appear within 2–3 days, and wraps are typically used for several days to about a week. Side effects may include irritation or folliculitis if used too long or too often; wraps combined with steroids require clinical guidance to avoid excessive absorption.

Systemic therapy may be appropriate when atopic dermatitis is widespread, recurrent, or not adequately controlled with optimized topical care. Dr. Thomas Knackstedt and the team at Peak Skin Center consider medical history, infection risk, and monitoring needs when selecting systemic options.

Short courses of oral corticosteroids (selected situations)

Oral steroids rapidly suppress inflammation and can reduce severe flares within 24–72 hours. Rebound worsening can occur after stopping, so these are typically reserved for short, specific situations rather than long-term control. Common side effects include insomnia, mood changes, increased appetite, blood pressure or blood sugar elevation, and fluid retention.

Traditional immunosuppressants (cyclosporine, methotrexate, azathioprine, mycophenolate)

These medications reduce immune overactivity that drives chronic eczema inflammation. Cyclosporine often works within 1–2 weeks, while methotrexate and similar agents may take 4–12 weeks for fuller effect. Side effects vary by medication but may include nausea, fatigue, lab abnormalities, kidney or blood pressure effects (cyclosporine), and increased infection risk, which is why routine monitoring is standard.

Oral JAK inhibitors (upadacitinib, abrocitinib)

Oral JAK inhibitors reduce itch and inflammation by blocking cytokine signaling involved in atopic dermatitis. Itch improvement may occur within days to 2 weeks, with skin improvement continuing over 4–16 weeks. Common side effects include acne, headache, nausea, and increased risk of infections; laboratory monitoring may be recommended based on the specific medication and patient factors.

Biologics target specific immune pathways associated with atopic dermatitis and are commonly used for moderate-to-severe disease or persistent symptoms despite strong topical regimens. Peak Skin Center provides screening and ongoing follow-up to support safe, sustained control.

Dupilumab

Dupilumab blocks IL-4 and IL-13 signaling, key drivers of type-2 inflammation in atopic dermatitis. Itch often improves within 2–4 weeks, with progressive clearing over 8–16 weeks. Common side effects include injection-site reactions and eye symptoms such as conjunctivitis or eyelid inflammation, as well as oral herpes in some individuals.

Nemolizumab

Nemolizumab is an interleukin-31 receptor alpha antagonist approved for adults and adolescents aged 12 years and older with moderate-to-severe atopic dermatitis in combination with topical corticosteroids and/or topical calcineurin inhibitors when topical prescription therapy alone is not enough. Because IL-31 is closely linked to itch signaling, nemolizumab is thought to help by directly reducing pruritus pathways while also improving downstream inflammation; clinical analyses report itch and sleep improvements as early as Day 2 in some patients. Skin and symptom improvement typically continues over the first 8–16 weeks. Common side effects reported in trials include headache, joint pain, hives, and muscle aches, along with injection-site reactions and an overall increased susceptibility to infections typical of immune-targeting therapy.

Long-term eczema control often requires both flare treatment and prevention, including consistent moisturization, trigger reduction, and appropriately selected prescription therapy. Peak Skin Center provides individualized atopic dermatitis treatment plans for patients in Cary, Apex, Holly Springs and Fuquay-Varina. We integrate topical, oral, and biologic options, with board-certified dermatologist Dr. Thomas Knackstedt and the clinical team guiding medication selection, monitoring, and maintenance strategies as symptoms change over time.

At a Glance

Dr. Thomas Knackstedt

  • Double board certified in dermatology and Mohs Surgery
  • Over ten years of experience providing evidence-based care
  • Nationally renowned physician leader with numerous publications, lectures, and academic affiliations
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