|Year : 2019 | Volume
| Issue : 3 | Page : 166-181
|Guidelines on management of atopic dermatitis in India: An evidence-based review and an expert consensus
Murlidhar Rajagopalan1, Abhishek De2, Kiran Godse3, DS Krupa Shankar4, Vijay Zawar5, Nidhi Sharma6, Samipa Mukherjee7, Aarti Sarda8, Sandipan Dhar9
1 Department of Dermatology, Apollo Hospital, Chennai, Tamil Nadu, India
2 Department of Dermatology, Calcutta National Medical College, Kolkata, West Bengal, India
3 Department of Dermatology, D Y Patil Hospital, Navi Mumbai, Maharashtra, India
4 Department of Dermatology, Mallige Hospital, Bengaluru, Karnataka, India
5 Department of Dermatology, Skin Diseases Center, Nashik, Maharashtra, India
6 Department of Dermatology, The Medicity, Medanta Hospital, Gurugram, Haryana, India
7 Department of Dermatology, Cloud Nine Hospitals, Bengaluru, Karnataka, India
8 Department of Dermatology, Wizderm Specialty Skin and Hair Clinic, Kolkata, West Bengal, India
9 Department of Dermatology, Institute of Child Health, Kolkata, West Bengal, India
|Date of Web Publication||20-May-2019|
Dr. Abhishek De
Flat Number 3 A, Arcadia 1, Dream Park, Sonarpur Station Road Kolkata - 700 103, West Bengal
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Atopic dermatitis (AD) is a common and chronic, pruritic inflammatory skin condition that affects all age groups. There was a dearth of consensus document on AD for Indian practitioners. This article aims to provide an evidence-based consensus statement for the management of AD with a special reference to the Indian context. This guideline includes updated definition, etiological factors, classification, and management of atopic dermatitis. Methodology: The preparation of guidelines was done in multiple phases. Indian Dermatology Expert Board Members (DEBM), recommended by the Skin Allergy Society of India, prepared 26 evidence-based recommendations for AD. An extensive literature search was done in MEDLINE, Google scholar, Cochrane, and other resources. Articles published in the past 10 years were reviewed and recommendations were graded based on the quality of evidence as per GRADE. After forming the initial structure, DEBM met in Mumbai and gave their decisions on an agree and disagree scale with an Indian perspective. Finally, their suggestions were compiled for preparing the article. After DEBM finalized the draft, a treatment algorithm was formulated for the management of AD. Results: DEBM suggested a working definition for AD. The panel agreed that moisturizers should be used as mainstay of therapy and should be continued in all lines of therapy and in maintenance phase. Topical corticosteroids and topical calcineurin inhibitors should be considered as the first line of treatment. Among systemic therapies, cyclosporin should be considered first line, followed by azathioprine, methotrexate, and mycophenolate mofetil. Phototherapy can be an effecive alternative. Empirical food restriction was recommended against. Conclusion: These guidelines should form a reference for the management of patients with AD in an evidence-based manner.
Keywords: Atopic dermatitis, consensus, expert opinion, guidelines
|How to cite this article:|
Rajagopalan M, De A, Godse K, Krupa Shankar D S, Zawar V, Sharma N, Mukherjee S, Sarda A, Dhar S. Guidelines on management of atopic dermatitis in India: An evidence-based review and an expert consensus. Indian J Dermatol 2019;64:166-81
|How to cite this URL:|
Rajagopalan M, De A, Godse K, Krupa Shankar D S, Zawar V, Sharma N, Mukherjee S, Sarda A, Dhar S. Guidelines on management of atopic dermatitis in India: An evidence-based review and an expert consensus. Indian J Dermatol [serial online] 2019 [cited 2019 Aug 25];64:166-81. Available from: http://www.e-ijd.org/text.asp?2019/64/3/166/258637
| Introduction|| |
Indian Dermatology Expert Board Members (DEBM), who formulated the guidelines, agreed to use the term “atopic dermatitis” (AD), which can be used as a synonym for “atopic eczema” or “endogenous eczema.”
Why does India need a guiding tool for AD?
Globally, there are many guidelines established for AD. All guidelines have their own region-specific recommendations based on the ethnic, socioeconomic, resource-based, and demographic characteristics of AD. However, in India there is a paucity of published data about the natural history, etiopathogenesis, epidemiology, clinical patterns, and management of AD. There is yet no guideline on AD from India, published in any indexed journal. This article was developed by the Skin Allergy Research Society of India for an updated evidence-based consensus statement for the management of AD, with a special reference to the Indian context.
Scope of guidelines
This guideline addresses the management of pediatric and adult AD of all severities. Other forms of dermatitis, such as irritant dermatitis and allergic contact dermatitis, are outside of the purview of this document. The recommendations were prepared to cover an appraisal of all the relevant available literature until May 2018. This guideline is intended for specialists in dermatology, pediatric and adolescent medicine, general medicine, and all groups of physicians whose work includes the treatment of AD in India.
The preparation of guidelines was projected in multiple phases. An Indian DEBM, recommended by the Skin Allergy Society of India, prepared 26 evidence-based recommendations for AD. An extensive literature search was done in MEDLINE, Google Scholar, Cochrane, and other resources. Articles published in the past 10 years were reviewed and recommendations were graded based on the quality of evidence as per GRADE [Table 1]. After forming the initial discussion proforma, DEBM met in Mumbai. Their discussions were based on literature from clinical research articles and also from their experience and acumen. The members gave their independent views on the preselected recommendations in agree and disagree scale with an Indian perspective [Table 2]. Finally, their suggestions were complied for preparing the article. After DEBM finalized the draft, a treatment algorithm was formulated for the management of AD.
| Atopic Dermatitis: General Aspects|| |
AD, also known as atopic eczema, is a chronic, inflammatory, relapsing skin disorder with usually an early age of onset in infancy and early childhood. It follows a relapsing course with repeated exacerbation and remission, which is characterized by dermatitis with itch, and is often associated with elevated serum immunoglobulin (IgE) levels. Natural history of AD often involves typical progression including food allergy, allergic rhinitis (hay fever), and asthma. This sequence of events is referred to as the “atopic march.” It is accompanied in a majority of patients with a personal or family history of “atopic diathesis.”
The cumulative incidence of AD varies between 11% and 21% depending on age and region. In a clinicoepidemiological study in a north Indian pediatric population, the mean age at onset and mean duration of the disease were 4.2 and 3.3 months, respectively, in the “infantile AD” group, and in the “childhood AD” group, the corresponding figures were 4.1 and 1.9 years, respectively. Patients from urban areas significantly outnumbered those from rural background. Another hospital-based north Indian study documented that AD was the most common dermatosis in children registered to a pediatric dermatology clinic with a prevalence of 29.9% of the total patients. The male-to-female ratio was 2.25:1, with a mean onset of 4.5 months. The infants had more of facial involvement and acute eczema, whereas children had nonspecific distribution and chronic eczema, with overall mild to moderate AD being more prevalent. Winter exacerbation was noted in a majority of the population (62%). A lower prevalence 0.42% in the eastern part of the country was reported among dermatology outpatient department attendees.
Etiology and pathogenesis
The causes of AD are varied. Both a genetic predisposition and numerous trigger factors play an important role in the first manifestation and in exacerbations of the disease. Major candidate genes reported to date include CTLA4, interleukin (IL)-18, TLR9, CD14, CARD4, PHF11, TLR2, SCCE, MCC, IL-4R, GM-CSF, TIM1, CARD15, GSTT1, SPINK5, eotaxin, TGFb1, IL-13, RANTES, IL-4, and Fc 3RIb.
In the acute stage, the dominant mechanisms of AD are governed by Th2 cell–related cytokines, such as, IL-4 and IL-13, and chemokines, such as, TARC (thymus and activation-regulated chemokine) and eotaxin. Later, Th1 cells producing interferon (IFN)-γ and IL-12 perform a dominant role in the chronic stage. Langerhans cells and mast cells are also involved in the disease pathogenesis as they express a high-affinity IgE receptor (FcεRI) that causes antigen-presenting cells and mast cells to release histamine, cytokines, and so on. IL-4 and IL-13 stimulate fibroblasts to produce periostin, causing keratinocytes to produce thymic stromal lymphopoietin, which in turn induces TARC/CCL17 production by dendritic cells. In an eczematous lesion of AD, antimicrobial peptides (defensins, cathelicidins, etc.) are inhibited from being expressed by keratinocytes.
Expression of ceramide and filagrin decreases in skin with AD and is considered as a primary cause of barrier dysfunction. It is also considered as a secondary phenomenon associated with inflammation and as a cause of AD.
Environmental factors responsible for exacerbation of AD vary and include climatic changes, sweating, physical irritation (including scratching), microbes/fungi, contact allergens, stress, and foods.
Atopic dermatitis and vaccinations
It is recommended that children, adolescents, and adults with AD are vaccinated regularly according to the standard national vaccine program recommendation. In an acute exacerbation, postponement of the vaccination until the skin condition has stabilized is recommended.
AD dermatitis has a variable course, and informing patients/parents of the chronic and/or recurrent course is recommended. Spontaneous cure or remission is possible at any time, but about 30% of the children who suffer from the disease may have episodes in adulthood.
Infections can be frequent complications of AD and include secondary infections with bacteria, virus, and fungi. AD can rarely be complicated with eye diseases (glaucoma, keratoconus, retinal detachment, blindness), alopecia areata, and growth delay. AD can be associated with concomitant ichthyosis vulgaris.
| Diagnosis|| |
The diagnosis of AD is made clinically and is based on historical features, morphology and distribution of skin lesions, and associated clinical signs. Formal sets of criteria have been developed by various groups to aid in classification.
Diagnostics criteria for atopic dermatitis
Diagnostic criteria proposed by Hanifin and Rajka
One of the earliest and most recognized sets of diagnostic criteria is the 1980 Hanifin and Rajka criteria, which requires 3 of the 4 major criteria and 3 of the 23 minor criteria to be met.
Diagnostic criteria proposed by the United Kingdom Working Party
These consist of one mandatory and five major criteria, it is easy to use and do not require any laboratory testing. The original UK criteria cannot be applied to very young children, but revisions to include infants have since been proposed [Table 2] and [Table 3]. The Hanifin and Rajka diagnostic criteria were used in 44% of the trials and the UK diagnostic criteria in 12%.
|Table 3: Diagnostic criteria proposed by the United Kingdom Working Party|
Click here to view
Diagnostic criteria proposed by American Academy of Dermatology
A 2003 consensus conference spearheaded by the American Academy of Dermatology suggested revised Hanifin and Rajka criteria that are more streamlined and additionally applicable to the full range of ages affected [Table 3] and [Table 4].
|Table 4: Diagnostic criteria proposed by the American Academy of Dermatology|
Click here to view
Disease severity scales for atopic dermatitis
For the measurement of disease severity, more than 28 different scales were identified, with none of them being the gold standard. The most commonly used severity criteria for AD are the SCORAD index, the Eczema Area and Severity Index (EASI), Patient Oriented Eczema Measure, and the Six Area, Six Sign Atopic Dermatitis severity score.
SCORAD is an international severity criterion that has been most popularly adopted in the English written literature at present. SCORAD incorporates both objective physician estimates of extent and severity and subjective patient assessment of itch and sleep loss.
EASI uses only objective physician estimates of disease extent and severity.
Laboratory investigations for diagnosis
The diagnosis of AD remains clinical, because there is currently no reliable biomarker available to confirm the diagnosis.
Serum total IgE level
A high serum total IgE level is observed in approximately 80% of patients with AD, but is not present in about 20% of the affected individuals. AD was classified into “extrinsic” and “intrinsic” groups based on the presence or absence of IgE elevation; however, this delineation remains controversial. In many, elevation of IgE may be a secondary phenomenon, developed due to epicutaneous sensitization because of impaired skin barrier.
Allergen-specific IgE levels
Although patients with AD are known to produce IgE antibodies in response to various allergens such as mites, foods, and pets, these elevations are also nonspecific, because they are found in about 55% of the general population.
Increases in tissue mast cells and peripheral eosinophil counts
They have inconsistent association with disease severity.
Various studies have shown that serum levels of CD30, macrophage-derived chemoattractant, IL-12, IL-16, IL-18, and IL-31, and TARC may correlate with disease severity scores, but to date none has shown reliable sensitivity or specificity for AD to support general clinical use for diagnosis or monitoring.
Recommendation for the use of laboratory investigations for diagnosis and assessment of disease severity
There are no specific biomarkers available for AD that can be recommended for diagnosis and/or assessment of disease severity. Monitoring of IgE levels is not recommended. Routine allergy testing is not recommended as the results show many false positives and less reproducibility. Even with the Phadiatop or the enzyme-linked immunospot (ELISpot) assays, a negative value has a better predictive value rather than a positive value.
A skin biopsy taken from a site with acute atopic eczema is characterised by spongiosis, perivascular infiltrates primarily of lymphocytes, and parakeratosis. Chronic eczema is dominated by hyperkeratosis and acanthosis, but sparse lymphocytic infiltrates. Routine skin biopsy is NOT recommended.
Atopic patch tests
Skin tests with protein allergens (known as atopy patch test) are not recommended in routine diagnostics.
| Controlling Factors Responsible for Exacerbation of AD|| |
There are conflicting evidences available for associations of specific food with AD. Werfel et al. concluded a prevalence of food allergy from eight studies proven by double-blind placebo-controlled food challenge studies to be 33%–63%. The common food allergens identified for triggering AD are milk and milk products, peanuts, eggs, soy, wheat, seafood, and shellfish. The DEBM recommended against dietary exclusion for management of AD in patients not having confirmed food allergy (milk or egg). To diagnose a food allergy, clinical symptoms or signs after suspected food allergen intake or exposure must be reproducible, as broad-panel allergy testing unrelated to a clinical history of a reaction to certain foods should be avoided.
Coarse and irritating fabrics causing skin irritation are preferably avoided. Occlusive clothing that can induce heat sensation is not appropriate. Some studies suggest silver-coated textiles can significantly reduce the numbers of Staphylococcus aureus and improve the symptoms of AD. Another fabric, derma silk, is also suggested due to its sericin-free composition and nonirritating with antibacterial properties. However, keeping in mind the Indian context, the members suggested use of nonirritant cotton cloths.
Sweating is an important exacerbating factor for AD, hence washing away sweat by bathing and showering will lead to the improvement of symptoms. Avoiding occupational or recreational exposure to high temperature and humidity can help in controlling exacerbation.
Allergens such as mites, house dust, pollens, and organic solvents such as formaldehyde and toluene can become problematic. Being sensitized to mites in infancy is reportedly a marker for the development of asthma. Periocular pathological changes are often observed during airborne pollen seasons.
Occupational dermatology aspects
It is recommended to investigate potential occupational trigger factors of AD in working patients. It is also recommended to reduce potential occupational trigger factors of AD and/or implement skin preventive measures. If hand eczema has already occurred in adolescence in the context of AD, adoption of wet occupations is not recommended.
A randomized comparative study revealed that consumption of an elimination diet free of highly sensitized food antigens such as egg and cow milk by pregnant or lactating mothers has NO protective effect on newborns from developing sensitization to food allergens or AD. A meta-analysis provided evidence in support of a moderate role of probiotics in the prevention of AD and IgE-associated AD in infants. The favorable effect was similar regardless of the time of probiotic use (pregnancy or early life) or the subject(s) receiving probiotics (mother, child, or both).
| General Care|| |
Bathing and showering are important not only for washing away the components of perspiration but also for washing away allergens, such as, dust and pollens, and microbes on the skin surface. Bathing also allows removal of dirt and debris from the skin and thereby reduces the chance of infection. Swimming should be avoided in acute flares as the amount of free residual chlorine may impact the skin barrier and contribute to AD exacerbation.
The skin must be cleansed thoroughly, but gently and carefully to get rid of crusts and bacterial contaminants in case of bacterial superinfection. Strong scrubbing or rubbing immediately after bath should be avoided. Skin should be dried using soft towels.
Avoidance of perfumes, personal hygiene and cosmetic products
Fragrances, formaldehyde, lanolin, nickel, neomycin, preservatives, such as, parabens, and rubber chemicals are the common contact allergens which should be avoided in products manufactured for use by patients with AD.
Education (patients and parents)
Patient and parent education is effective in the management of AD and should aim to provide information about the clinical characteristics of AD (etiology, clinical manifestations, and disease course in common person language), aggravating and relieving factors, self-management and improving coping skills.
Psychological factors and psychosomatic interventions
Patients with AD often complain aggravation due to stress. Minimizing stress may be helpful in controlling the disease. Psychotherapeutic approaches and behavior therapy can be considered to manage individual emotional factors that trigger AD, such as, vicious itch-scratch cycles, comorbidity with anxiety and depression, and low quality of life (QOL).
Stepladder treatment in atopic dermatitis
Depending on the severity of the AD, topical treatment methods and/or systemic treatments are recommended. It is recommended to implement stepladder treatment appropriate to the clinical severity. Once remission is achieved, it is advisable to shift to proactive maintenance therapy to reduce the number of subsequent flare ups.
Their usefulness is controversial and debated. Published data from randomized controlled trials (RCTs) are available for both sedating and nonsedating antihistamines; the results of these trials generally suggest a limited role for antihistamines in the treatment of AD. Panel members suggested that a subset of patients with AD with allergic rhinitis and bronchial asthma benefit maximum from antihistamines. Sedating antihistamines (cetirizine) may be used short-term, under supervision where itch of eczema causes sleep disturbance especially in children under age of 2 years. Cetirizine also shows steroid-sparing effect. Addressing itch in young atopics is of primary importance. The nocturnal itch that accompanies AD leads to a fall in QOL indices. The active scratching can further disturb the skin barrier function. This will worsen the atopic state. Hydroxyzine and cetirizine will have an ameliorative effect by producing the required sedation and pruritus relief.
Use of systemic and topical antibiotic therapy
In the pathogenesis of AD, there is a significant role of microbial pathogens such as staphylococcus, streptococcus, herpes simplex, molluscum contagiosum, human papillomavirus, and Malassezia furfur infection. There is a lack of quality trials to support the use of antimicrobial and antiseptic preparations to treat AD and there were no reports available on the benefit of topical antibiotics/antiseptics, antibacterial soaps, or antibacterial bath additives in clinically uninfected AD. The DEBM recommends against the indiscriminate use of topical or oral antibiotics and also against the use of combinations of creams of steroids and antibiotics. Secondary infection should be suspected in patients with moderate-to-severe eczema who have weeping dermatitis, folliculitis and overt clinical signs of infection, or who are not responding to first-line topical therapy. Topical antibiotic therapy may be appropriate for localized areas of infection. Systemic antibiotics should be used according to clinical condition.
Wet wrap therapy
Wet wrap therapy (WWT) can be helpful to quickly reduce AD severity, and it is often useful for acute flares and/or recalcitrant disease. A recent RCT demonstrated that a 4-week proactive schedule of WWT with diluted topical corticosteroids (TCSs) was superior to WWT with moisturizer in children with severe AD. The first step of WWT is to apply topical agents to the lesion. Next, the skin is covered with a wet inner layer of tubular bandage followed by a dry outer layer. Gauze or a cotton suit can be used as an alternative. The WWT can be maintained from several hours to a day at a time.
The panel members suggested that its use might not be feasible in every region of India due to varied climatic conditions. However, wherever suitable, it can be used in severe or resistant patients older than 6 months of age, but if used with TCSs it may be associated with the risk of systemic absorption.
| First Line of Therapy|| |
Patients with AD suffer from dry skin and defective skin barrier function. Regular use of moisturizer constitutes the core of the management of AD. A moisturizer repairs the skin barrier, maintains skin integrity and appearance, reduces transepidermal water loss, and restores the lipid barrier's ability to attract, hold, and redistribute water [Table 5]. Data from RCTs show that moisturizers have a long- and short-term steroid-sparing effect in mild to moderate AD and in preventing AD flares.
Although no clinical trials have studied the proper amount or frequency of moisturizer use in patients with AD, moisturizer should be used at least twice daily and more frequently during acute flare-ups. Adult patients with AD should use approximately more than 250 g of moisturizer per week. It is recommended to use moisturizer within 3 min after taking a bath while the skin is still moist.
DEBM advised that moisturizers should be used in continuation, even when the AD is clear. It should be part of all treatment phases; mild, moderate, and severe.
Prescription emollient devices (PEDs) are a newer class of topical agents designed to target specific defects in skin barrier function observed in AD. There is limited evidence to suggest that PEDs lessen symptoms and signs of AD, including xerosis and inflammation. The results of few head to head trials of PED versus over-the-counter base moisturizers have shown no statistically significant differences. DEBM discussed the role of PEDs, which are expensive in comparison to moisturizers but can be helpful in selected scenario.
Moisturizers contain ingredients with anti-inflammatory properties that may reduce or substitute the use of TCS, thus minimizing their side effects. An RCT between aloe vera in olive oil cream versus 0.1% betamethasone cream in the treatment of chronic skin lesions following sulfur mustard exposure showed that aloe vera in olive oil cream was at least as effective as betamethasone 0.1% after 6 weeks of applications.
In acute inflammatory models, virgin coconut oil showed moderate anti-inflammatory effects on ethyl phenylpropiolate–induced ear edema in rats. The main nonglyceride constituents of shea butter have been reported to be triterpene alcohols. With regard to the emollient effect, in vivo and in vitro studies have shown that the biological activities of triterpene acetate and cinnamate esters include antiinflammatory and anti-tumor properties.
Thus, the most constructive way to spare steroids and avoid steroid-related side effects is through consequent baseline emollient skin care combined with early anti-inflammatory intervention to stabilize the disease and prevent treatment-intensive flares.
Topical corticosteroids (TCSs) are important anti-inflammatory drugs for managing AD, especially during acute stage. TCSs are first-line treatment for patients with AD who have failed good skin care, including moisturizer use.
Efficacy: RCTs have demonstrated safety and continued efficacy of repeated courses of low- to mid-potency TCS on active AD skin until clearance for up to 5 years in children and up to 1 year in adults.
Long-term proactive TCS: The proactive approach of applying low–mid potency TCS twice weekly for the prevention of flares in stabilized AD has been shown to be effective in both adults and children. Proactive treatment (along with reactive) was found to be superior to reactive only management in a year-long RCT in pediatric patients.
Classification: As per British National Formulary Classification, TCSs are classified as very potent, potent, moderate, and mild [Table 6]. A variety of factors should be considered when choosing a particular TCS for the treatment of AD, including patient age, areas of the body to which the medication will be applied, and other patient factors such as degree of xerosis, patient preference, and cost of medication.
Long-term TCS adverse effects: When used cautiously, long-term use of low to mid potency TCS is reasonably safe. However, the long term use of TCS, especially if high potency, may cause local side effects, such as, striae rubrae, skin atrophy, telangiectasia, skin burning, erythema and acneiform eruptions. In rare cases, systemic effects may occur including hypothalamic–pituitary–adrenal axis suppression, more frequently in children due to the high ratio of total body surface area to body mass, which is about 2.5 to 3 times higher than for adults. The use of twice-weekly proactive treatment has not been shown to cause skin atrophy.
Dosage: No universal standard exists for quantity of application, although suggested methods include use of the adult fingertip unit (the amount from the distal interphalangeal joint to the fingertip, or approximately 0.5 g, being applied over an area equal to two adult palms), following the rule of 9's that measures the percent of affected area and use of charts that propose amounts based on patient age and body site.
Frequency of application: Twice daily application of TCSs is generally recommended for the treatment of AD; however, evidence suggests that once-daily application of some TCSs may be sufficient. Proactive, intermittent use of TCSs as maintenance therapy (one to two times per week) on areas that commonly flare is recommended to help prevent relapses and is more effective than use of emollients alone.
Topical calcineurin inhibitors
Topical calcineurin inhibitors (TCIs) (pimecrolimus and tacrolimus) have been approved since 2002 for anti-inflammatory therapy in AD.
Efficacy: RCTs have demonstrated that TCIs are safe and effective when used twice daily for the intermittent treatment of AD flares in children and infants (3 months) for up to 5 years and in adults for up to 1 year. A meta-analysis of 25 RCTs found tacrolimus 0.1% to be as effective as the mid-potency TCS hydrocortisone butyrate 0.1%, whereas tacrolimus 0.03% is less effective than hydrocortisone butyrate 0.1% but more effective than the low-potency TCS hydrocortisone acetate 1%.
Strength: There are two available TCIs, tacrolimus ointment and pimecrolimus cream. Both agents have been shown to be more effective than vehicle in short-term (3–12 weeks) and long-term (up to 12 months) studies in adults and children with active disease.
The DEBM suggests that tacrolimus ointment 0.1% usage should not be restricted to above 12 years. It can safely be used for younger children.
Long-term proactive TCI: The proactive use of tacrolimus has been shown to be effective and safe for up to 1 year in both children and adults.
Long-term safety and adverse events of TCI: TCIs are very safe, the most common side effect being skin burning, which resolves in 80% of patients after 1 week. TCIs do not increase the risk of bacterial infections, but the risk of viral infections such as herpes simplex virus is slightly elevated. There was a boxed warning based on a theoretical risk of malignancy against TCI since 2006. However, there is no convincing evidence, either from controlled studies with follow-up of patients or from studies of patient databases that TCIs can induce malignant disease. The largest and longest trial looking at infants treated with pimecrolimus found no evidence of increased malignancy risk.
Although systemic corticosteroids (CSs) improve the clinical symptoms of AD, their administration should generally be avoided because of adverse effects and the rebound phenomenon. Their use should be limited to short courses as a transition to a more sustainable treatment. There are no long-term RCTs evaluating efficacy and safety of systemic corticosteroids in AD.
There are two RCTs which studied the efficacy of systemic CS in children. Both the trials were of low quality and none of them studied methylprednisolone, which is the most widely prescribed CS in clinical practice., The Practical Allergy (PRACTALL) Consensus Group guidelines published in 2006 suggested that patients with acute flares may benefit from a short course of systemic CSs, but their long-term use, especially in children, should be avoided. A slow taper is advisable to decrease the risk of rebound. There is no consensus on the duration of the taper, but it should overlap with a steroid-sparing agent. Special consideration should be made with pediatric patients because of concerns with delayed or reduced bone growth.
| Second Line of Therapy|| |
Cyclosporine (CsA) is an oral calcineurin inhibitor that suppresses the activation of the T-cell transcription factor, nuclear factor of activated T cells, inhibiting the transcription of a number of cytokines, including IL-2. It is approved for the treatment of adults with AD in European countries, Australia and Japan.
Efficacy: Studies in both adults and children have confirmed that cyclosporin is effective in the short-term management of severe AD, at doses of 3–5 mg/kg/day. RCT with 64 proven patients who received CsA had a decrease both in the surface area of involvement and in the degree of inflammation of the remaining dermatitis at the 6 week time mark. Based on seven long-term RCTs, CsA can be recommended as an effective second-line agent for AD for up to 1–2 years in both adults and children 2 years and older.
Dosage and scheduling
: CsA is applicable to patients 16 years of age or older with failure/resistance to first-line therapies. The drug should be administered twice a day at a daily dose of 3–5 mg/kg/day. CsA has been shown to be effective and relatively safe in four long-term RCTs in adults who received up to 1 year of continuous treatment. Low starting doses (3 mg/kg/day) and high starting doses (5 mg/kg/day) were found to be equally effective (EASI/body surface area improvement) after 2 weeks.
Adverse effects and monitoring:
Irreversible nephrotoxicity, infection, hypertension, electrolyte disturbances, dyslipidemia, tremor, hypertrichosis, headache, gingival hyperplasia, and nonmelanoma skin cancer are the major serious side effects of CsA. Two or more months with serum creatinine more than 30% above baseline may predict irreversible nephrotoxicity.
These adverse effects may occur regardless of daily dosage used, but high dose and low dose groups have only been compared and measured over short periods of time (up to 12 weeks).
CsA is an effective treatment for AD in the pediatric population, similar to adults. Both continuous long-term (up to 1 year) and intermittent short-term dosing schedules (3- to 6-month courses) are efficacious. CsA can be used in children older than 2 years of age. Long-term safety in children has not yet been established and caution should be exercised.
| Third Line of Therapy|| |
Morison et al. first attempted to treat refractory AD with oral psoralen and ultraviolet (UV) light, with success. Phototherapy can be used as monotherapy or in combination with emollients and topical steroids. Few clinical studies suggest that UV-B and UV-A1 are efficacious in the management of AD., The use of light therapy may decrease the need for topical steroid and topical immunomodulator use. The common adverse effects include actinic damage, local erythema and tenderness, pruritus, burning, and stinging. Rarer side efffects include nonmelanoma skin cancer, melanoma (mostly with PUVA), lentigines, photosensitive eruptions, folliculitis, photo-onycholysis, HSV reactivation, and facial hypertrichosis.,,
There is still no standard protocol for the optimal dose, duration, and frequency of narrowband (NB)-UVB treatment [Table 7]. The optimal treatment dose of UVA1 has not been determined yet. Considering the low accessibility of UVA1 devices compared with other modalities of phototherapy, NB-UVB offers the most efficacious and cost-effective evidence based treatment for patients with chronic AD.
Studies document the safe and effective use of both UVA and UVB phototherapy in children and adolescents. However, there is an increased risk of nonmelanoma skin cancer in children receiving PUVA treatment.
Off-label use of azathioprine (AZA) can be considered in adult patients unresponsive to, contraindicated to, or experiencing adverse effect with CsA. Double-blind placebo-controlled studies demonstrate that AZA improves both QOL and signs and symptoms of the disease when used in patients with AD as monotherapy.,
Measurement of the enzyme thiopurine methyltransferase (TPMT) is recommended before the initiation of treatment. A dose of 1–3 mg/kg/day is recommended depending on TPMT activity.
Nausea, vomiting and other gastrointestinal (GI) symptoms are common while on AZA. The other side effects include headache, hypersensitivity reactions, elevated liver enzymes and leukopenia. There is literature to support the use of AZA to treat AD in the pediatric population, but the dosage and optimal duration of therapy still needs to be defined.,
A long-term RCT investigating mycophenolic acid showed similar efficacy to CsA (3 mg/kg/day) in adults after the 10th week of therapy, but a delayed onset of action in the mycophenolic acid group. Insufficient data exist to make recommendations regarding the optimal mycophenolate mofetil (MMF) dosing or duration of therapy for patients with AD.
Dosing ranges from 0.5 to 3 g/day. MMF is generally well tolerated, with GI symptoms being the most commonly encountered. Hematologic (anemia, leukopenia, thrombocytopenia) and genitourinary (urgency, frequency, dysuria) symptoms were rarely reported.
The true efficacy of methotrexate (MTX) in the treatment of refractory AD is unknown, because of inadequate data. In an RCT comparing MTX (10–22 mg/week) with AZA (1.5–2.5 mg/kg/day) in adults with severe AD, both treatments were found to have similar effects on disease severity. Based on only two small long-term RCTs, MTX seems to be a well-tolerated and effective third-line option for the long-term treatment of moderate-to-severe AD in both children (above 8 years) and adults.
| Fourth Line of Therapy: Biologics and Emerging Therapies|| |
Crisaborole is a topical phosphodiesterase-4 inhibitor that reduces the production of proinflammatory cytokines. In two short-term (28 days), identically designed, multicenter, phase III studies in this patient population, topical therapy with crisaborole ointment 2% reduced disease severity and pruritus severity compared with vehicle, with the effect established early and sustained over the course of treatment.
Dupilumab is a fully human monoclonal antibody directed against the IL-4a receptor a-subunit, which blocks the signaling of both IL-4 and IL-13, the two key drivers of type 2 immune response. In 2017, dupilumab was approved by the US Food and Drug Administration (FDA) for treatment of moderate to severe AD in patients 18 years of age and older. A systematic review and meta-analysis of efficacy and safety of dupilumab treatment in moderate to severe AD provided evidence that dupilumab had an acceptable safety profile and resulted in clinically relevant improvements in signs and symptoms of AD.
Limited data exist to determine the efficacy of omalizumab in the treatment of AD. One double-blind, placebo-controlled study did not show clinical improvement in AD with its use despite reducing free serum IgE levels.In general, treatment of AD with omalizumab is not recommended.
On the basis of positive case reports, there is limited experience for the use of ustekinumab, rituximab, tocilizumab, and alefacept in AD. Current evidence does not allow use of these biologicals in AD, except for some exceptional situation.
Apremilast, an oral phosphodiesterase-4 inhibitor, was FDA-approved in September 2014 for the treatment of moderate-to-severe plaque psoriasis. However, its upstream anti-inflammatory effects, ease of use as an oral agent, and mild side effect profile make it an interesting treatment option for AD as well. Multiple open-labeled trials of apremilast in moderate-to-severe AD produce conflicting reports on efficacy, some showing fair and other showing limited efficacy.,
There are a few studies on IFN-γ that demonstrate its efficacy in the treatment of AD.
High-dose intravenous immunoglobulin
A review of literature showed improvement was observed in 61% of patients with AD treated with high-dose intravenous immunoglobulin (hdIvIg). Adults appeared less likely to respond (48%) than children (90%), and the duration of response was also more prolonged in children. Adjunctive therapy in adults was more effective than monotherapy (59% vs. 0%), whereas monotherapy was effective in 90% of children. HdIVIg may offer a safe potential therapeutic avenue for resistant cases of AD, particularly in children, but should be further assessed using double-blind placebo-controlled trials.
| Maintenance Therapy|| |
The proactive use of topical anti-inflammatory therapy to address subclinical inflammation is an effective, contemporary clinical strategy for the management of AD. Systematic review of RCTs reporting efficacy of TCSs and/or TCIs for flare prevention in AD reveals efficacy of proactive treatment with TCS and TCI to prevent AD flares. The trials, however, do not allow firm conclusions about long-term safety beyond 1 year. Indirect evidence from vehicle-controlled trials suggests that twice-weekly application of the potent TCS may be more efficacious to prevent AD flares than tacrolimus ointment.
| Adjunctive Treatment|| |
Alitretinoin, also known as 9-cis-retinoic acid, is a recently developed retinoid derivative. Alitretinoin is useful for the treatment of chronic hyperkeratotic atopic hand eczema.
Probiotics (Lactobacillus alone or Lactobacillus with Bifidobacterium) appeared to play a protective role in AD prevention upon administration in the pre- and postnatal periods. However, there is no evidence to support the benefit of probiotics in infants.
Essential fatty acids
Diet supplementation with evening primrose oil or an omega-3 fatty acid (docosahexaenoic acid) is safe and may be helpful in AD, but there are still insufficient RCT data assessing clinical efficacy for this method to be recommended.
RCTs have reported contradictory results for the therapeutic value of vitamin D supplementation in AD. One meta-analysis showed that serum vitamin D level was lower in the patients with AD, and vitamin D supplementation could be a new therapeutic option for AD. Vitamin D has a potentially significant role for improving the symptoms of AD. The results from this study suggest that vitamin D supplementation may help ameliorate the severity of AD and can be considered as a safe and tolerable therapy.
| Conclusion|| |
AD has a profound impact on the physical, mental, and social well-being of the patients and the parents. These guidelines suggest a treatment algorithm for patients with AD. However, to achieve high treatment efficacy, compliance, and patient satisfaction, treatment decisions should be made jointly by the treating physician and the patient or parents. It is of paramount importance to consider disease severity, socioeconomic factors, psychological status, and the patient's desire for treatment, before choosing an appropriate treatment for individual patient with AD.
The authors acknowledge Knowledge Isotopes Pvt. Ltd. (http://www.knowledgeisotopes.com) for the medical resources. Wockhardt Ltd., Mumbai, provided the scientific and financial support for the conduct of expert group meetings.
This guideline reflects the best available evidence at the time of preparation. Adherence to these guidelines may not ensure successful treatment in every situation. The treating physician must make the ultimate judgment regarding the choice of any specific therapy in the context of circumstances for individual case scenarios.
Financial support and sponsorship
Wockhardt Ltd., Mumbai, provided the scientific and financial support for the conduct of expert group meetings.
Conflicts of interest
There are no conflicts of interest.
| References|| |
Bieber T. Atopic dermatitis. Ann Dermatol 2010;22:125-37.
Werfel T, Heratizadeh A, Aberer W, Ahrens F, Augustin M, Biedermann T, et al
. S2k guideline on diagnosis and treatment of atopic dermatitis – Short version. Allergo J Int 2016;25:82-95.
Dhar S, Kanwar AJ. Epidemiology and clinical pattern of atopic dermatitis in a North Indian pediatric population. Pediatr Dermatol 1998;15:347-51.
Sarkar R, Kanwar AJ. Clinico-epidemiological profile and factors affecting severity of atopic dermatitis in north Indian children. Indian J Dermatol 2004;49:117-22. [Full text]
Dhar S, Mandal B, Ghosh A. Epidemiology and clinical pattern of atopic dermatitis in 100 children seen in a city hospital. Ind J Dermatol 2002;47:202-4.
Katayama I, Aihara M, Ohya Y, Saeki H, Shimojo N, Shoji S, et al.
Japanese guidelines fora topic dermatitis 2017. Allergol Int 2017;66:230-47.
Bieber T. Atopic dermatitis. N Engl J Med 2008;358:1483-94.
Grewe M, Bruijnzeel-Koomen CA, SchöpfE, Thepen T, Langeveld-Wildschut AG, Ruzicka T, et al.
A role for Th1 and Th2 cells in the immunopathogenesis of atopic dermatitis. Immunol Today 1998;19:359e61.
Ong PY, Ohtake T, Brandt C, Strickland I, Boguniewicz M, Ganz T, et al.
Endogenous antimicrobial peptides and skin infections in atopic dermatitis. N Engl J Med 2002;347:1151-60.
Rudzki E, Samochocki Z, Rebandel P, Saciuk E, Galecki W, Raczka A, et al.
Frequency and significance of the major and minor features of Hanifin and Rajka among patients with atopic dermatitis. Dermatology 1994;189:41-6.
Roguedas AM, Machet L, Fontes V, Lorette G. Atopic dermatitis: Which are the diagnostic criteria used in medical literature? [In French] Ann Dermatol Venereol 2004;131:161-4.
Eichenfield LF, Hanifin JM, Luger TA, Stevens SR, Pride HB. Consensus conference on pediatric atopic dermatitis. J Am Acad Dermatol 2003;49:1088-95.
Charman CR, Venn AJ, Williams H. Measuring atopic eczema severity visually: Which variables are most important to patients? Arch Dermatol 2005;141:1146-51.
Eichenfield LF, Tom WL, Chamlin SL, Feldman SR, Hanifin JM, Simpson EL, et al.
Guidelines of care for the management of atopic dermatitis: Section 1. Diagnosis and assessment of atopic dermatitis. J Am Acad Dermatol 2014;70:338-51.
Katta R, Schlichte M. Diet and dermatitis: Food triggers. J Clin Aesthet Dermatol 2014;7:30.
Gauger A, Mempel M, Schekatz A, Schäfer T, Ring J, Abeck D. Silver-coated textiles reduce Staphylococcus aureus
colonization in patients with atopic eczema. Dermatology 2003;207:15-21.
Fontanini C, Berti I, Monasta L, Longo G. DermaSilk in long-term control of infantile atopic dermatitis: A double blind randomized controlled trial. G Ital Dermatol Venereol 2013;148:293-7.
Sporik R, Holgate ST, Platts-Mills TA, Cogswell JJ. Exposure to house-dust mite allergen (Der p
I) and the development of asthma in childhood. A prospective study. N Engl J Med 1990;323:502e7.
Kramer MS, Kakuma R. Maternal dietary antigen avoidance during pregnancy or lactation, or both, for preventing or treating atopic disease in the child. Cochrane Database Syst Rev 2012;9:CD000133.
Pelucchi C, Chatenoud L, Turati F, Galeone C, Moja L, Bach JF, et al.
Probiotics supplementation during pregnancy or infancy for the prevention of atopic dermatitis: A meta-analysis. Epidemiology 2012;23:402-14.
Seki T, Morimatsu S, Nagahori H, Morohashi M. Free residual chlorine in bathing water reduces the water-holding capacity of the stratum corneum in atopic skin. J Dermatol 2003;30:196-202.
Ersser SJ, Cowdell F, Latter S, Gardiner E, Flohr C, Thompson AR, et al.
Psychological and educational interventions for atopic eczema in children. Cochrane Database Syst Rev 2014;1:CD004054.
Arndt J, Smith N, Tausk F. Stress and atopic dermatitis. Curr Allergy Asthma Rep 2008;8:312-7.
Darsow U, Wollenberg A, Simon D, Taïeb A, Werfel T, Oranje A, et al.
ETFAD/EADV eczema task force 2009 position paper on diagnosis and treatment of atopic dermatitis. J Eur Acad Dermatol Venereol 2010;24:317-28.
Munday J, Bloomfield R, Goldman M, Robey H, Kitowska G, Gwiezdziski Z, et al.
Chlorpheniramine is no more effective than placebo in relieving the symptoms of childhood atopic dermatitis with a nocturnal itching and scratching component. Dermatology 2002;205:40-5.
Bath-Hextall F, Birnie A, Ravenscroft J, Williams H. Interventions to reduce Staphylococcus aureus
in the management of atopic eczema: An updated Cochrane review. Br J Dermatol 2010;163:12-26.
Nicol NH, Boguniewicz M, Strand M, Klinnert MD. Wet wrap therapy in children with moderate to severe atopic dermatitis in a multidisciplinary treatment program. J Allergy Clin Immunol Pract 2014;2:400-6.
Nakamura M, Uemura K, Nemoto O, Miyachi Y. Evaluation of an optimal method for topical application of moisturizer. Skin Res 2006;5:311.
Grimalt R, Mengeaud V, Cambazard F; Study Investigators' Group. The steroid-sparing effect of an emollient therapy in infants with atopic dermatitis: A randomized controlled study. Dermatology 2007;214:61-7.
Hon KL, Ching GK, Leung TF, Choi CY, Lee KK, Ng PC. Estimating emollient usage in patients with eczema. Clin Exp Dermatol 2010;35:22-6.
Draelos ZD. An evaluation of prescription device moisturizers. J Cosmet Dermatol 2009;8:40-3.
Varothai S, Nitayavardhana S, Kulthanan K. Moisturizers for patients with atopic dermatitis. Asian Pac J Allergy Immunol 2013;31:91.
Panahi Y, Davoudi SM, Sahebkar A, Beiraghdar F, Dadjo Y, Feizi I, et al.
Efficacy of Aloe vera/olive oil cream versus betamethasone cream for chronic skin lesions following sulfur mustard exposure: A randomized double-blind clinical trial. Cutan Ocul Toxicol 2012;31:95-103.
Schempp CM, Hezel S, Simon JC. Topical treatment of atopic dermatitis with hypericum cream: Arandomized, placebo controlled, double blind half-side comparison study. Hautarz 2003;54:248-53.
Akihisa T, Kojima N, Kikuchi T, Yasukawa K, Tokuda H, T Masters E, et al.
Anti-inflammatory and chemopreventive effects of triterpene cinnamates and acetates from shea fat. J Oleo Sci 2010;59:273-80.
Luger TA, Lahfa M, Fölster-Holst R, Gulliver WP, Allen R, Molloy S, et al
. Long-term safety and tolerability of pimecrolimus cream 1% and topical corticosteroids in adults with moderate to severe atopic dermatitis. J Dermatolog Treat 2004;15:169-78.
Peserico A, Stadtler G, Sebastian M, Fernandez RS, Vick K, Bieber T. Reduction of relapses of atopic dermatitis with methylprednisolone aceponate cream twice weekly in addition to maintenance treatment with emollient: A multicentre, randomized, double-blind, controlled study. Br J Dermatol 2008;158:801-7.
Fukuie T, Hirakawa S, Narita M, Nomura I, Matsumoto K, Tokura Y, et al.
Potential preventive effects of proactive therapy on sensitization in moderate to severe childhood atopic dermatitis: A randomized, investigator-blinded, controlled study. J Dermatol 2016;43:1283-92.
British National Formulary (BNF) 69. 69th
edition. London: British Medical Association and Royal Pharmaceutical Society of Great Britain, March 2015. 2015.
Hong E, Smith S, Fischer G. Evaluation of the atrophogenic potential of topical corticosteroids in pediatric dermatology patients. Pediatr Dermatol 2011;28:393-6.
Sigurgeirsson B, Boznanski A, Todd G, Vertruyen A, Schuttelaar ML, Zhu X, et al.
Safety and efficacy of pimecrolimus in atopic dermatitis: A 5-year randomized trial. Pediatrics 2015;135:597-606.
Ashcroft DM, Dimmock P, Garside R, Stein K, Williams HC. Efficacy and tolerability of topical pimecrolimus and tacrolimus in the treatment of atopic dermatitis: Meta-analysis of randomized controlled trials. BMJ 2005;330:516.
Ring J, Alomar A, Bieber T, Deleuran M, Fink-Wagner A, Gelmetti C, et al.
Guidelines for treatment of atopic eczema (atopic dermatitis) Part II. J Eur Acad Dermatol Venereol 2012;26:1176-93.
Siegfried EC, Jaworski JC, Kaiser JD, Hebert AA. Systematic review of published trials: Long-term safety of topical corticosteroids and topical calcineurin inhibitors in pediatric patients with atopic dermatitis. BMC Pediatr 2016;16:75.
Heddle R, Soothill J, Bulpitt C, Atherton D. Combined oral and nasal beclomethasone diproprionate in children with atopic eczema: A randomised controlled trial. Br Med J (Clin Res Ed) 1984;289:651-4.
La Rosa M, Musarra I, Ranno C, Maiello N, Negri L, del Giudice MM Jr, et al.
A randomized, double-blind, placebo-controlled, crossover trial of systemic flunisolide in the treatment of children with severe atopic dermatitis. Curr Ther Res 1995;56:720-6.
Akdis CA, Akdis M, Bieber T, Bindslev-Jensen C, Boguniewicz M, Eigenmann P, et al.
Diagnosis and treatment of atopic dermatitis in children and adults: European Academy of Allergology and Clinical Immunology/American Academy of Allergy, Asthma and Immunology/PRACTALL Consensus Report. Allergy 2006;61:969-87.
Prezzano JC, Beck LA. Long-term treatment of atopic dermatitis. Dermatol Clin 2017;35:335-49.
Zonneveld IM, De R, Beljaars RC, Van Der HJ, Wuite J, Zeegelaar J, et al.
The long-term safety and efficacy of cyclosporin in severe refractory atopic dermatitis: A comparison of two dosage regimens. Br J Dermatol 1996;48 (135 Suppl):15-20.
Zachariae H, Kragballe K, Hansen HE, Marcussen N, Olsen S. Renal biopsy findings in long-term cyclosporin treatment of psoriasis. Br J Dermatol 1997;136:531-5.
Harper JI, Ahmed I, Barclay G, Lacour M, Hoeger P, Cork MJ, et al.
Cyclosporin for severe childhood atopic dermatitis: short course versus continuous therapy. Br J Dermatol 2000;142:52-8.
Morison WL, Parrish J, Fitzpatrick TB. Oral psoralen photochemotherapy of atopic eczema. Br J Dermatol 1978;98:25-30.
Bulur I, Erdogan HK, Aksu AE, Karapınar T, Saracoglu ZN. The efficacy and safety of phototherapy in geriatric patients: A retrospective study. An Bras Dermatol 2018;93:33-8.
Meduri NB, Vandergriff T, Rasmusssen H, Jacobe H. Phototherapy in the management of atopic dermatitis: A systematic review. Photodermatol Photoimmunol Photomed 2007;23:106-12.
Clayton TH, Clark SM, Turner D, Goulden V. The treatment of severe atopic dermatitis in childhood with narrowband ultraviolet B phototherapy. Clin Exp Dermatol 2007;32:28-33.
Menter A, Korman NJ, Elmets CA, Feldman SR, Gelfand JM, Gordon KB, et al.
Guidelines of care for the management of psoriasis and psoriatic arthritis, section 5: Guidelines of care for the treatment of psoriasis with phototherapy and photochemotherapy. J Am Acad Dermatol 2010;62:114-35.
Meggitt SJ, Gray JC, Reynolds NJ. Azathioprine dosed by thiopurine methyltransferase activity for moderate-to-severe atopic eczema: A double-blind, randomized controlled trial. Lancet 2006;367:839-46.
Berth-Jones J, Takwale A, Tan E, Barclay G, Agarwal S, Ahmed I, et al.
Azathioprine in severe adult atopic dermatitis: A double-blind, placebo-controlled, crossover trial. Br J Dermatol 2002;147:324-30.
Murphy LA, Atherton D. A retrospective evaluation of azathioprine in severe childhood atopic eczema, using thiopurine methyltransferase levels to exclude patients at high risk of myelosuppression. Br J Dermatol 2002;147:308-15.
Caufiel BAWL. Oral azathioprine for recalcitrant pediatric atopic dermatitis: Clinical response and thiopurine monitoring. Am Acad Dermatol 2013;68:29-35.
Haeck IM, Knol MJ, Ten Berge O, van Velsen SG, de Bruin-Weller MS, Bruijnzeel-Koomen CA. Enteric coated mycophenolate sodium versus cyclosporin A as long-term treatment in adult patients with severe atopic dermatitis: A randomized controlled trial. J Am Acad Dermatol 2011;64:1074-84.
Schram ME, Roekevisch E, Leeflang MM, Bos JD, Schmitt J, Spuls PI. A randomized trial of methotrexate versus azathioprine for severe atopic eczema. J Allergy Clin Immunol 2011;128:353-9.
Paller AS, Tom WL, Lebwohl MG, Blumenthal RL, Boguniewicz M, Call RS, et al.
Efficacy and safety of crisaborole ointment, a novel, nonsteroidal phosphodiesterase 4 (PDE4) inhibitor for the topical treatment of atopic dermatitis (AD) in children and adults. J Am Acad Dermatol 2016;75:494-503.e4.
Lake E. Game Changer: Dupilumab therapy provides clinically meaningful improvement in patient-reported outcomes (PROs): A phase IIb, randomized, placebo-controlled, clinical trial in adult patients with moderate to severe atopic dermatitis (AD). J Am Acad Dermatol 2018 Oct 30. pii: S0190-9622(18) 32822-6.
Wang FP, Tang XJ, Wei CQ, Xu LR, Mao H, Luo FM. Dupilumab treatment in moderate-to-severeatopic dermatitis: A systematic review and meta-analysis. J Dermatol Sci 2018;90:190-8.
Heil PM, Maurer D, Klein B, Hultsch T, Stingl G. Omalizumab therapy in atopic dermatitis: Depletion of IgE does not improve the clinical course – A randomized, placebo-controlled and double blind pilot study. J Dtsch Dermatol Ges 2010;8:990-8.
Samrao A, Berry TM, Goreshi R, Simpson EL.A pilot study of an oral phosphodiesterase inhibitor (apremilast) for atopic dermatitis in adults. Arch Dermatol 2012;148:890-7.
Volf EM, Au SC, Dumont N, Scheinman P, Gottlieb AB. A phase 2, open-label, investigator-initiated study to evaluate the safety and efficacy of apremilast in subjects with recalcitrant allergic contact or atopic dermatitis. J Drugs Dermatol 2012;11:341-6.
JollesS. A review of high-dose intravenous immunoglobulin treatment for atopic dermatitis. Clin Exp Dermatol 2002;27:3-7.
Panduru M, Panduru NM, Sălăvăstru CM, Tiplica GS. Probiotics and primary prevention of atopic dermatitis: A meta-analysis of randomized controlled studies. J Eur Acad Dermatol Venereol 2015;29:232-42.
Bath-Hextall FJ, Jenkinson C, Humphreys R, Williams HC. Dietary supplements for established atopic eczema. Cochrane Database Syst Rev 2012;2:CD005205.
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6], [Table 7]