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<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Asia Pac Allergy</journal-id>
<journal-id journal-id-type="publisher-id">APA</journal-id>
<journal-title-group>
<journal-title>Asia Pacific Allergy</journal-title>
</journal-title-group>
<issn pub-type="ppub">2233-8276</issn>
<issn pub-type="epub">2233-8268</issn>
<publisher>
<publisher-name>Asia Pacific Association of Allergy, Asthma and Clinical Immunology</publisher-name>
</publisher>
</journal-meta>

<article-meta>
<article-id pub-id-type="doi">10.5415/apallergy.2016.6.2.120</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Educational &#x0026; Teaching Material</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>A review on the role of moisturizers for atopic dermatitis</article-title>
</title-group>

<contrib-group>

<contrib contrib-type="author" corresp="yes">
<name>
<surname>Giam</surname>
<given-names>Yoke Chin</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Hebert</surname>
<given-names>Adelaide Ann</given-names>
</name>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Dizon</surname>
<given-names>Maria Victoria</given-names>
</name>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Van Bever</surname>
<given-names>Hugo</given-names>
</name>
<xref ref-type="aff" rid="A4">4</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Tiongco-Recto</surname>
<given-names>Marysia</given-names>
</name>
<xref ref-type="aff" rid="A5">5</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Kim</surname>
<given-names>Kyu-Han</given-names>
</name>
<xref ref-type="aff" rid="A6">6</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Soebono</surname>
<given-names>Hardyanto</given-names>
</name>
<xref ref-type="aff" rid="A7">7</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Munasir</surname>
<given-names>Zakiudin</given-names>
</name>
<xref ref-type="aff" rid="A8">8</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Diana</surname>
<given-names>Inne Arline</given-names>
</name>
<xref ref-type="aff" rid="A9">9</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Luk</surname>
<given-names>David Chi Kang</given-names>
</name>
<xref ref-type="aff" rid="A10">10</xref>
</contrib>

</contrib-group>

<aff id="A1"><label>1</label>National Skin Centre, Singapore 308205, Singapore.</aff>
<aff id="A2"><label>2</label>Departments of Dermatology and Pediatrics, University of Texas-Houston Medical School, Houston, TX 77030, USA.</aff>
<aff id="A3"><label>3</label>Department of Dermatology, College of Medicine and Surgery, University of Santo Tomas, Manila, the Philippines.</aff>
<aff id="A4"><label>4</label>Division of Paediatric Allergy, Immunology and Rheumatology, Khoo Teck Puat-National University Children's Medical Institute, Singapore 119228, Singapore.</aff>
<aff id="A5"><label>5</label>Section of Allergy and Immunology, Department of Pediatrics, University of the Philippines, Manila, the Philippines.</aff>
<aff id="A6"><label>6</label>Department of Dermatology, Seoul National University Hospital, Seoul 03080, Korea.</aff>
<aff id="A7"><label>7</label>Department of Dermatology Faculty of Medicine, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.</aff>
<aff id="A8"><label>8</label>Department of Allergy and Immunology, Department of Child Health, Medical Faculty, University of Indonesia, Jakarta, Indonesia.</aff>
<aff id="A9"><label>9</label>Faculty of Medicine, Padjadjaran University/Division of Paediatric Dermatology, Hospital Dr. Hasan Sadikin, Bandung, Indonesia.</aff>
<aff id="A10"><label>10</label>Department of Pediatrics and Adolescent Medicine, United Christian Hospital, Kwun Tong, Hong Kong.</aff>

<author-notes>
<corresp>
Correspondence: Yoke Chin Giam. National Skin Centre, 1 Mandalay Road, Singapore 308205, Singapore. Tel: +65-62534455, Fax: +65-62534455, <email>ycgiam@nsc.com.sg</email>
</corresp>
</author-notes>

<pub-date pub-type="ppub">
<month>04</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>28</day>
<month>04</month>
<year>2016</year>
</pub-date>
<volume>6</volume>
<issue>2</issue>
<fpage>120</fpage>
<lpage>128</lpage>

<history>
<date date-type="received">
<day>07</day>
<month>02</month>
<year>2016</year>
</date>
<date date-type="accepted">
<day>21</day>
<month>04</month>
<year>2016</year>
</date>
</history>

<permissions>
<copyright-statement>Copyright &#x00A9; 2016. Asia Pacific Association of Allergy, Asthma and Clinical Immunology.</copyright-statement>
<copyright-year>2016</copyright-year>
<license license-type="open-access" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/">
<license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/">http://creativecommons.org/licenses/by-nc/4.0/</ext-link>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>

<abstract>
<p>Effective management of atopic dermatitis (AD) involves the treatment of a defective skin barrier. Patients with AD are therefore advised to use moisturizers regularly. To date, there are few comparative studies involving moisturizers in patients with AD, and no classification system exists to objectively determine which types of moisturizers are best suited to specific AD phenotypes. With this in mind, a group of experts from allergy and immunology, adult and pediatric dermatology, and pediatrics centers within Southeast Asia met to review current data and practice, and to develop recommendations regarding the use of moisturizers in patients with AD within the Asia-Pacific region. Chronicity and severity of AD, along with patient age, treatment compliance, and economic background should all be taken into account when selecting an appropriate moisturizer for AD patients. Other considerations include adjuvant properties of the product, cosmetic acceptability, and availability over the counter. Well-defined clinical phenotypes of AD could optimally benefit from specific moisturizers. It is hoped that future studies may identify such differences by means of filaggrin mutation subtypes, confocal microscopic evaluation, pH, transepidermal water loss or presence of allergy specific IgE. Recommendations to improve the regular use of moisturizers among AD patients include measures that focus on treatment compliance, patient and caregiver education, appropriate treatment goals, avoidance of sensitizing agents, and collaboration with other relevant specialists.</p>
</abstract>

<kwd-group>
<kwd>Dermatitis, atopic</kwd>
<kwd>Compliance</kwd>
<kwd>Asia Pacific</kwd>
<kwd>Moisturizer</kwd>
<kwd>Classification</kwd>
</kwd-group>

</article-meta>
</front>

<body>

<sec sec-type="intro">
<title>INTRODUCTION</title>
  <p>Atopic dermatitis (AD) is a chronic pruritic inflammatory disorder characterized as a defect in the skin barrier [<xref ref-type="bibr" rid="B1">1</xref><xref ref-type="bibr" rid="B2">2</xref>]. This alteration in the barrier leads to increased penetration by environmental allergens and infective organisms that cause persistent inflammation in the skin. Although the barrier defect has been considered in the past as an epiphenomenon, it is now believed to play a major role in the pathophysiology of this disease [<xref ref-type="bibr" rid="B1">1</xref><xref ref-type="bibr" rid="B2">2</xref>].</p>
  <p>Since AD is chronic and relapsing, the most important treatment strategy involves treating and preventing flares, and repairing the skin barrier in the long term through adequate patient education and cooperation with the caregivers. Among the available treatment modalities, moisturizers are the basic requirement for optimal treatment of AD regardless of the severity [<xref ref-type="bibr" rid="B3">3</xref>]. These moisturizers hydrate the skin and repair skin barrier function [<xref ref-type="bibr" rid="B4">4</xref>]. Current AD management guidelines recommend moisturizer use as a key and basic step in the treatment of AD alongside avoidance of triggers and control of symptoms and inflammation [<xref ref-type="bibr" rid="B5">5</xref><xref ref-type="bibr" rid="B6">6</xref><xref ref-type="bibr" rid="B7">7</xref><xref ref-type="bibr" rid="B8">8</xref><xref ref-type="bibr" rid="B9">9</xref><xref ref-type="bibr" rid="B10">10</xref>].</p>
  <p>Treatment choice of moisturizers for AD patients is largely influenced by personal preference, with few well-designed comparative studies investigating the effects of moisturizers in these patients [<xref ref-type="bibr" rid="B11">11</xref>]. Moreover, there is currently no clinical classification system to objectively determine which types of moisturizers are most appropriate for specific AD phenotypes. In light of these issues and the wide variation observed in treatment of AD across the Asia-Pacific region, a panel of ten experts from allergy and immunology, adult and pediatric dermatology, and pediatrics from around the Asia-Pacific region convened for a one-day meeting in June 2014 to discuss the importance of the appropriate use of moisturizers in the treatment of AD. This review highlights the topics covered in these discussions, as well as presenting recommendations reached by the panel.</p>
</sec>

<sec>
<title>THE ROLE OF MOISTURIZERS IN AD</title>
  <p>A basic principle of treatment of AD is optimal skin care that adequately addresses the skin barrier defect. This skin barrier dysfunction manifests as an increase in transepidermal water loss (TEWL) and increased penetration of allergens and infectious agents, leading to inflammation and intense pruritus [<xref ref-type="bibr" rid="B3">3</xref>]. Contributing to this abnormality is a disturbed epidermal terminal differentiation leading to filaggrin deficiency and reduced natural skin lipids (<xref ref-type="fig" rid="F1">Fig. 1</xref>) [<xref ref-type="bibr" rid="B2">2</xref>].</p>
  <p>Moisturizers restore the ability of the intercellular lipid bilayers to absorb, retain and redistribute water [<xref ref-type="bibr" rid="B12">12</xref><xref ref-type="bibr" rid="B13">13</xref>]. These agents may penetrate and contribute to the reorganization of the structure of the skin layers [<xref ref-type="bibr" rid="B14">14</xref>]. Moisturizers increase the hydration of the skin as measured by subjective and objective parameters [<xref ref-type="bibr" rid="B15">15</xref><xref ref-type="bibr" rid="B16">16</xref><xref ref-type="bibr" rid="B17">17</xref>].</p>
  <p>Overall, the choice of moisturizers in practice has been dependent on the properties that physicians and their patients find most beneficial based on subjective considerations and outcomes [<xref ref-type="bibr" rid="B9">9</xref><xref ref-type="bibr" rid="B13">13</xref>]. Cosmetic acceptability of the moisturizer also has to be taken into consideration if compliance and outcomes are to be improved [<xref ref-type="bibr" rid="B3">3</xref><xref ref-type="bibr" rid="B16">16</xref>]. Other factors, like the availability of products over the counter and convenient packaging to carry around in adequate quantities have also been reported to be important [<xref ref-type="bibr" rid="B12">12</xref>].</p>
</sec>

<sec>
<title>CLASSIFICATION OF MOISTURIZERS</title>
  <p>Moisturizers can be divided into various groups (<xref ref-type="table" rid="T1">Table 1</xref>) [<xref ref-type="bibr" rid="B18">18</xref><xref ref-type="bibr" rid="B19">19</xref><xref ref-type="bibr" rid="B20">20</xref><xref ref-type="bibr" rid="B21">21</xref>]. The terms moisturizers and emollients may be used alternately; however, in this review, emollients are considered to be those moisturizers made up of lipids and their compounds. These products are formulated in a variety of delivery systems including gels, oils, creams, ointments, or lotions, and have different compositions and properties to enhance efficacy [<xref ref-type="bibr" rid="B20">20</xref><xref ref-type="bibr" rid="B21">21</xref>].</p>
</sec>

<sec>
<title>MOISTURIZERS AND ANTI-INFLAMMATORY MEDICATIONS</title>
  <p>There are multiple anti-inflammatory medication options available for treating AD. Corticosteroids which are considered appropriate for most patients [<xref ref-type="bibr" rid="B18">18</xref><xref ref-type="bibr" rid="B19">19</xref>]. Calcineurin inhibitors may provide alternative anti-inflammatory activity without the adverse effects associated with corticosteroids [<xref ref-type="bibr" rid="B21">21</xref><xref ref-type="bibr" rid="B22">22</xref><xref ref-type="bibr" rid="B23">23</xref>]. Recently, some of the newer anti-inflammatory agents have been added into the moisturizer formulations in order to alleviate mild-to-moderate AD [<xref ref-type="bibr" rid="B21">21</xref>]. These anti-inflammatory agents include glycyrrhetinic acid, palmitoylethanolamine, telmesteine, <italic>Vitis vinifera</italic>, ceramide-dominant barrier repair lipids and filaggrin breakdown products (e.g., ceramide precursor/pseudoceramide, 5-sphingosine-derived sphingolipid, niacinamide, vitamin B3, pyrrolidone carboxylic acid, and arginine) [<xref ref-type="bibr" rid="B24">24</xref>]. These active agents are combined with emollients or humectants, which may provide additional barrier repair and control of xerosis [<xref ref-type="bibr" rid="B24">24</xref><xref ref-type="bibr" rid="B25">25</xref><xref ref-type="bibr" rid="B26">26</xref>].</p>
  <p>Several such nonsteroidal, noncalcineurin inhibitor options are now available [<xref ref-type="bibr" rid="B22">22</xref>], of which MAS063DP was the first to be approved by the U.S. Food and Drug Administration for the relief of symptoms of AD and allergic contact dermatitis [<xref ref-type="bibr" rid="B27">27</xref><xref ref-type="bibr" rid="B28">28</xref>]. MAS063DP is a nonsteroidal barrier repair cream that contains glycyrrhetinic acid, <italic>Vitis vinifera</italic> extract and telmesteine in combination with shea butter (emollient) and hyaluronic acid (humectant). Randomized, vehicle-controlled studies have demonstrated that MAS063DP is an effective monotherapy for mild-to-moderate AD in pediatric and adult patients [<xref ref-type="bibr" rid="B26">26</xref><xref ref-type="bibr" rid="B29">29</xref>].</p>
</sec>

<sec>
<title>PATIENT PHENOTYPE AND MOISTURIZERS</title>
  <p>The severity of chronic diseases, especially AD, has an impact on the quality of life (QoL) of both the patient and the family [<xref ref-type="bibr" rid="B30">30</xref>]. In patients with AD, reduced QoL is commonly due to the scratching and sleep problems which are associated with a greater severity of the disease [<xref ref-type="bibr" rid="B30">30</xref>]. Certain priority patient groups with similar disease morphologies have been considered to benefit from specific moisturizer types [<xref ref-type="bibr" rid="B12">12</xref>]. However, a clinical classification system to objectively determine which types of moisturizers are best suited for these AD phenotypes has yet to be developed.</p>
  <p>There are several genes which contribute to skin types and mechanisms of repair implying the presence of distinct AD phenotypes; however, there is insufficient knowledge of the substrate that is necessary (i.e., moisturizer ingredients) to address the specific epidermal defect [<xref ref-type="bibr" rid="B31">31</xref>]. The choice of moisturizers has, therefore, been determined in clinical practice by individual preference, safety, efficacy and the absence of fragrances, additives or other sensitizing agents [<xref ref-type="bibr" rid="B18">18</xref>].</p>
  <p>A panel of clinical experts from the United Kingdom has developed recommendations to address the need for guidance regarding moisturizer choice for specific types of dry skin in patients with AD [<xref ref-type="bibr" rid="B12">12</xref>]. For mild-to-moderate cases of AD, occlusive emollient creams were recommended depending on the thickness of barrier, variable lipid content, severity of condition and body site. For more severe AD, occlusive emollient ointment was recommended, but the panel acknowledged that this may have limited acceptability. For very severe AD, occlusive ointment with no water content can be considered. Where simple emollients are ineffective or greasier products are unacceptable, humectant containing emollients may be applied. Lastly, for pruritus, emollients containing an antipruritic agent were recommended [<xref ref-type="bibr" rid="B12">12</xref>]. However, the panel acknowledged that there may be difficulty in the differentiation of skin types when using this approach (e.g., "dry" versus "very dry" skin).</p>
</sec>

<sec>
<title>THE ASIA-PACIFIC PERSPECTIVE</title>
  <p>AD is a relatively common disorder among patients in the Asia-Pacific region. In a 2-year survey in Singapore in 1989, dermatitis ranked top among the most common skin disorders amongst Chinese, Malay, and Indian patients [<xref ref-type="bibr" rid="B32">32</xref>]. More recently, data from an international cross-sectional survey of school children reported that the 12-month prevalence of AD in children aged 13&#x2013;14 years ranged from 0.9% in China to 9% in Malaysia and Singapore [<xref ref-type="bibr" rid="B33">33</xref>]. The prevalence of AD in Asia-Pacific countries appears to be increasing, a fact that has been attributed to environmental and socioeconomic factors [<xref ref-type="bibr" rid="B33">33</xref>]. The incidence and severity of AD among Asian patients may also be affected by environmental, cultural and dietary factors specific to the region [<xref ref-type="bibr" rid="B11">11</xref>]. Furthermore, evidence exists that a broader range of filaggrin gene mutations may be present in Asian populations [<xref ref-type="bibr" rid="B34">34</xref><xref ref-type="bibr" rid="B35">35</xref>]. Across the Asia-Pacific region, there are marked variations in skin types, as well as large differences in socioeconomic conditions. In this region of the world, the management of AD is likely to be influenced by differences in health-care systems and access to medical care, as well as cultural diversity and variable climate. Regional survey data indicate that there is substantial variation across Asia regarding treatment practices in AD [<xref ref-type="bibr" rid="B10">10</xref><xref ref-type="bibr" rid="B36">36</xref>].</p>
  <p>Recently published consensus guidelines have focused specifically on AD in the Asia-Pacific region [<xref ref-type="bibr" rid="B10">10</xref>]. These guidelines recommend the regular use of moisturizer as maintenance therapy and as an adjunct to other existing therapies such as topical steroids [<xref ref-type="bibr" rid="B10">10</xref>]. These region-specific guidelines also noted that moisturizer use should depend not only on skin type and degree of dryness, but also the humidity of the climate.</p>
</sec>

<sec>
<title>OBSTACLES TO AD TREATMENT</title>
  <p>Unsatisfactory treatment in AD has been attributed to misunderstanding of the disease, lack of information, inadequate self-management and nonadherence [<xref ref-type="bibr" rid="B37">37</xref>]. Various obstacles to patient adherence to treatment of patients with AD have been identified [<xref ref-type="bibr" rid="B38">38</xref><xref ref-type="bibr" rid="B39">39</xref><xref ref-type="bibr" rid="B40">40</xref><xref ref-type="bibr" rid="B41">41</xref>], and include the poor communication skills of the health-care providers; an inability to create a trusting patient-doctor relationship; a lack of adequate time to allow for patient education during the clinical visit; and the lack of effective mutual communication between patient and doctor. The lack of effective communication can lead to a failure to elicit the patient's point of view of the disease, as well as address the patient's concerns. A lack of discussion regarding the impact of the disease on the patient's QoL may be perceived by the patient as a lack of empathy on the part of the doctor. Other obstacles include the noninvolvement of the patient in the treatment plan and the failure of the clinician to recognize the patient's level of education/comprehension. The later may thereby affect self-care, as information may not have been delivered in an age-appropriate, or culturally-sensitive manner.</p>
  <p>Therefore, it is to be hope that the lessons learnt from overcoming the obstacles to AD treatment in general can be more specifically applied to the use of moisturizers in particular. The development of a functional doctor-patient relationship will more fully enable guided decision-making and hence, adherence to treatment, specifically the use of moisturizers.</p>
</sec>

<sec>
<title>EDUCATIONAL PROGRAMS FOR PATIENTS WITH AD</title>
  <p>Educational programs are necessary to improve awareness in AD patients. They are effective tools for improving treatment compliance, commonly providing psychological support for patients and their caregivers [<xref ref-type="bibr" rid="B37">37</xref>].</p>
  <p>Essential topics for any educational program in patients with AD include the causes or triggers of AD (particularly skin barrier dysfunction); the clinical manifestations and features of AD; treatment options and skin care focused on active disease management and a long-term maintenance plan; and environmental management.</p>
  <p>Various comprehensive education programs are available, for example therapeutic patient education, that help patients with chronic diseases acquire or maintain the skills they need to improve their therapeutic adherence, general health and QoL [<xref ref-type="bibr" rid="B41">41</xref><xref ref-type="bibr" rid="B42">42</xref><xref ref-type="bibr" rid="B43">43</xref>].</p>
  <p>In trials, intervention groups were shown to have positive improvement in the patient's coping behavior, sleeplessness symptoms, anxiety about corticosteroid usage, and other psychological variables [<xref ref-type="bibr" rid="B44">44</xref><xref ref-type="bibr" rid="B45">45</xref><xref ref-type="bibr" rid="B46">46</xref>]. Hence, outcomes may be improved by providing educational initiatives on top of conventional treatments for AD.</p>
  <p>In addition, the involvement of a dermatology nurses in the care and education of patients has been shown to improve the care and control of symptoms [<xref ref-type="bibr" rid="B47">47</xref>].</p>
  <p>Although originally used for nonmedical purposes, identification of specific, measurable, attainable, relevant, and time-based (SMART) goals has been increasingly used in medical practice to provide a structured guide for patients to set treatment objectives for chronic conditions [<xref ref-type="bibr" rid="B48">48</xref><xref ref-type="bibr" rid="B49">49</xref>].</p>
  <p>The objectives may be written down in the patient's personal journal. An example of this plan as applied in AD is shown in <xref ref-type="table" rid="T2">Table 2</xref>.</p>
  <p>Patients need to be education regarding the avoidance of ingredients that have caused skin irritation such as that in cleansers and detergents, or even moisturizers [<xref ref-type="bibr" rid="B12">12</xref>]. It has been found that some substances may induce a state of immunologically mediated hypersensitivity following a variable period of patient contact [<xref ref-type="bibr" rid="B50">50</xref>]. Thus, patients should be made aware of these irritants (e.g., neomycin, lavender, sodium lauryl sulphate, cetyl alcohol, etc.) and of allergens (e.g., peanut oil, which is an emerging cause of food allergy in Asia, fragrances, parabens).</p>
</sec>

<sec>
<title>EXPERT PANEL DISCUSSION OF CURRENT CLINICAL PRACTICE</title>
  <p>In terms of clinical factors, the expert panel concluded that chronicity and severity of AD are primary considerations when selecting treatment for AD. The majority of the panel agreed that patient age, compliance, QoL and economic background are also crucial concerns. Adjuvant properties, cosmetic acceptability, cost, accessibility over the counter, and availability of cream or ointment formulations were considered important by most panel members when selecting a moisturizer product for their patients. Other considerations in the choice of moisturizers in practice included the patient's personal preference, which may be influenced by weather conditions, time of day and cost. Some panel members noted that they offer a selection of suitable moisturizer products and leave the final choice to individual patients. Panel members emphasized that there is a need for better scientific studies to provide an evidence base for the selection of moisturizers for individual AD patients.</p>
  <p>The panel acknowledged that there could be well-defined clinical phenotypes of AD that would optimally benefit from specific moisturizers. However, there are currently limited data on any categorization system based on objective measures, but there may be identifiable differences based on filaggrin mutation subtypes, confocal microscopic evaluation, pH, TEWL levels, presence of allergy specific IgE in oriental versus non-oriental skin. Lastly, moisturizers prescribed to these phenotypes should be useful for both lesional and/or nonlesional skin.</p>
</sec>

<sec>
<title>EXPERT PANEL RECOMMENDATIONS</title>
  <p>Although the significance of moisturizer use in AD treatment is widely acknowledged, there is much variability in terms of prescription practices and patient comprehension [<xref ref-type="bibr" rid="B41">41</xref>]. Therefore, the panel formed recommendations for the use of moisturizer patients with AD within the Asia-Pacific region (<xref ref-type="table" rid="T3">Table 3</xref>).</p>
<sec>
<title>A patient-centered approach</title>
  <p>The need for moisturizers should be stressed to the patient and/or the caregiver during the clinic visit using a patient-centered approach. Time should be taken during clinic visits to discuss the objective and benefits of therapy. Instructional leaflets may be provided, along with guidance regarding the period when the patient may possibly grow out of AD (i.e., the allergy march in pediatric patients). Specific environmental triggers should be evaluated and detected to prevent future flare-ups and unnecessary dietary modification. All creams should be introduced to the patient (such as in a booklet), along with an explanation of how, and how much, should be applied. A Fingertip Unit chart can be used as guide [<xref ref-type="bibr" rid="B42">42</xref>].</p>
  <p>The patient's personal preference should be considered as a means of improving their treatment compliance. Patients should be informed of the cost of creams and other treatments and less expensive creams should be selected, especially if cost is an issue. Patients should be encouraged to try a range of appropriate moisturizers. Given that heavy sedation should be avoided in school children, the appropriate use of moisturizers alone may be sufficient to treat symptoms.</p>
</sec>
<sec>
<title>A holistic approach to education</title>
  <p>As highlighted above, moisturizing use in AD therapy can be optimized by developing SMART goals, explaining the long-term treatment plan, by being empathetic and motivating, and by being receptive to all queries from the patient and the caregiver. In order to discuss whether these goals have been met or not, a follow-up appointment should be scheduled early on during the treatment schedule.</p>
</sec>
<sec>
<title>Additional professional help</title>
  <p>Treatment of AD should entail collaboration among specialists (e.g., dermatologists, pediatricians, immunologists, pulmonologists, ENT, ophthalmologists, allergists) to address all interrelated conditions of the patient (e.g., AD, asthma, allergic rhinitis, allergic conjunctivitis, food allergy). This ensures a holistic and thorough management of the patient's conditions.</p>
</sec>
</sec>

<sec sec-type="conclusions">
<title>CONCLUSIONS</title>
  <p>AD is a chronic and relapsing condition requiring continuous care of the skin barrier defect. Management of this condition relies on effective preventive and therapeutic approaches, which need to be communicated well to the patient and the caregiver. Moisturizers are central to prevention and optimal use of the appropriate product could lead to better outcomes.</p>
  <p>AD patients and their physicians in the Asia-Pacific region face particular challenges, and wide variation has been noted across Asia regarding treatment practices in AD. Together, this supports the need for advice regarding both the appropriate selection of moisturizers for AD patients and steps clinicians can take to improve the success of treatment.</p>
  <p>Expert opinion from a panel of specialists from the Asia-Pacific region confirms that treatment choices in AD are largely influenced by treatment accessibility, cost considerations and subjective personal preference. There is evidence to support the existence of specific clinical phenotypes in AD and further research is needed to develop objective measures by which to identify these phenotypes to aid clinicians in making rationale treatment choices.</p>
  <p>The expert panel proposed a number of recommendations that support treatment compliance, patient education and the use of well-defined treatment goals to optimize outcomes of moisturizer treatment for AD. Treatment should also be holistic and should take into consideration other existing conditions of the patient.</p>
</sec>

</body>

<back>

<ack>
<title>ACKNOWLEDGEMENTS</title>
  <p>The authors would like to thank A. Menarini Asia-Pacific for providing an educational grant in support of the Asia-Pacific Expert Forum on the Choice of Moisturizers for Atopic Dermatitis. Meeting and editorial support was provided by Dennis Malvin H. Malgapo, MD, DFM of MIMS Pte Ltd through this grant.</p>
</ack>

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<floats-group>

<fig position="float" id="F1">
<label>Fig. 1</label>
<caption>
  <title>Skin barrier dysfunction in patients with atopic dermatitis. TSLP, thymic stromal lymphopoietin; Th2, T helper 2 cells; PAR-2, proteaseactivated receptor 2. Reprinted from Kabashima K. J Dermatol Sci 2013;70:3-11, with permission from Elsevier [<xref ref-type="bibr" rid="B2">2</xref>].</title>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="apa-6-120-g001"></graphic>
</fig>

<table-wrap position="float" id="T1">
<label>Table 1</label>
<caption>
  <title>Classification of moisturizers [<xref ref-type="bibr" rid="B20">20</xref><xref ref-type="bibr" rid="B21">21</xref>]</title>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="apa-6-120-i001"></graphic>
<table-wrap-foot>
<fn>
  <p>SC, subcutaneous layer; NMF, natural moisturizing factor; TEWL, transepidermal water loss.</p>
</fn>
</table-wrap-foot>
</table-wrap>

<table-wrap position="float" id="T2">
<label>Table 2</label>
<caption>
  <title>Example of SMART treatment objectives for atopic dermatitis patients using moisturizers</title>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="apa-6-120-i002"></graphic>
<table-wrap-foot>
<fn>
  <p>SMART, specific, measurable, attainable, relevant, and time-based.</p>
</fn>
</table-wrap-foot>
</table-wrap>

<table-wrap position="float" id="T3">
<label>Table 3</label>
<caption>
  <title>Recommendations for moisturizer use in patients with AD</title>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="apa-6-120-i003"></graphic>
<table-wrap-foot>
<fn>
  <p>AD, atopic dermatitis.</p>
</fn>
</table-wrap-foot>
</table-wrap>

</floats-group>

</article>