| Term 
 | Definition 
 
        | a common medical term used to describe patients at risk of developing allergic rhinitis, asthma, and atopic dermatitis |  | 
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        | Term 
 
        | THE EXACT CONTRIBUTING CAUSE OF ATOPIC DERMATITIS (AD) IS UNKNOWN 
 A COMBINATION OF GENETIC, ENVIRONMENTAL, AND IMMUNOLOGIC MECHANISMS ARE THE MOST LIKELY PRIMARY CAUSES OF AD
 |  | Definition 
 
        | patients with one atopic condition are at a higher risk of developing another atopic disease 
 patients with one or both parents that have an atopic condition are also at higher risk of developing another atopic disease
 
 patients with AD often also have elevated levels and/or abnormalities in function of immune mediators such as IgE, eosinophils, macrophages, lymphocytes, mast cells, or Langerhans cells
 
 AD's underlying immune mediated mechanisms occurs by both IgE and T helper cells
 
 since different immune mediated mechanisms can contribute to this condition, a wide variety of clinical presentations and high variation in response to treatments is seen with patients having AD
 
 immunologic and/or allergen triggers that commonly cause AD exacerbations include the following:
 
 ALLEROALLERGENS - dust mites, cat cander, molds, ragweed pollen, grass
 
 FOOD ALLERGENS - egg, milk, peanuts, soy, wheat
 
 OTHER - stress, soaps/detergents, abrasive clothing, smoking, extreme temperatures, humidity
 
 children will often "outgrow" food allergens.  parents should be careful in examining food labels in determining if they contain these allergens and/or related allergens
 
 breast fed infants have been shown to beat lower overall risk of developing allergies/atopic disease.  for infants at high risk of developing AD (family history of one or more atopic conditions), parents should be counseled that exclusive breastfeeding during the first 3-6 months of life may decrease the risk of developing AD
 
 greater air pollution, urbanization, industrialization, and higher socioeconomic status have also been correlated to increased rates of AD
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        | Term 
 | Definition 
 
        | a hallmark complaint of patients with AD 
 xerosis occurs ON A LARGE AREA OF THE BODY AND IS PRESENT MOST OF THE YEAR
 
 dry skin is primarily due to keratinocytes within the epidermis are unable to hold in water
 
 this abnormal skin barrier allows irritants (i.e. chemicals, allergens) to more easily penetrate and cause pruritus and inflammation of the skin
 
 xerosis can become progressively worse with time, in particular if not cared for properly
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        | Term 
 
        | overall treatment strategies for AD include: |  | Definition 
 
        | identification and avoidance of triggers 
 adequate skin hydration and patency
 
 prompt treatment of acute exacerbations
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        | Term 
 | Definition 
 
        | non medication measures should be tailored toward specific triggers of patients 
 skin hydration with moisturizers is an essential component of the treatment plan for AD management
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        | Term 
 
        | moisturizers can be classified as: |  | Definition 
 
        | OCCLUSIVE - provide an oily layer to protect skin from water loss; best moisturizer for AD 
 HUMECTANTS - increase water holding capacity of skin; not useful for AD
 
 EMOLLIENTS - smooth out skin surface by filling spaces with oil droplets; least effective for AD
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        | Term 
 
        | general non-pharm therapies for AD |  | Definition 
 
        | identify and eliminate potential allergens 
 limit overall length of bathing and potentially frequency of bathing
 
 use lukewarm water in baths/showers
 
 avoid soaps or detergents with irritants (ex. dyes, fragrances)
 
 avoid washcloths or irritating scrubs
 
 air dry skin or gently pat dry
 
 apply emollient therapy immediately after bathing
 
 keep fingernails short and clean
 
 consider cotton gloves to prevent scratching at night
 
 use cotton sheets and pajamas
 
 avoid temperature extremes
 
 use a second rinse cycle for laundry
 
 keep humidity at or above 50% at home
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        | Term 
 
        | topical corticosteroids:  MOA |  | Definition 
 
        | vasoconstrictive and anti-inflammatory effects aids in symptomatic relief and healing of skin manifestations |  | 
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        | Term 
 
        | topical corticosteroids:  ADRs |  | Definition 
 
        | often dependent on potency or strength used, quantity applied, frequency of applications, length of therapy, and areas of application (in particular in children) 
 systemic ADRs such as hypothalamus pituitary axis (HPA) suppression and growth retardation rarely occur
 
 long term ADRs:
 skin atrophy
 straie
 hypo-pigmentation
 steroid induced acne
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        | Term 
 
        | topical corticosteroids:  place in therapy for AD management |  | Definition 
 
        | 1st line agents for acute AD flares and only to be used for short term management 
 use for no more than 3 weeks
 
 do not use on face, mucous membranes, eyelids, or skin folds
 
 reserve use for lichenified (thickened lesions) or refractory exacerbations
 
 mild to moderate potency agents can be used for chronic AD
 
 children should be treated with low potency agents
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        | Term 
 
        | topical immunomodulators (tacrolimus, pimecrolimus):  MOA |  | Definition 
 
        | inhibit calcineurin receptors by forming a complex with FKBP-12, calcium, clamodulin, and calcineurin 
 calcineurin receptors are involved in T cell activation
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        | Term 
 
        | topical immunomodulators (tacrolimus, pimecrolimus):  ADRs |  | Definition 
 
        | burning 
 itching
 
 BBW:  long term safety of topical calcineurin inhibitors has not been established and rare cases of malignancy (e.g. skin and lymphoma) have been reported in patients treated with topical calcineurin inhibitors.  due to these un-established risks with chronic use, these medications are often reserved as a second line therapy for persistent or refractory disease
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        | Term 
 
        | topical immunomodulators (tacrolimus, pimecrolimus):  place in therapy |  | Definition 
 
        | second line therapy for AD 
 may be used for acute exacerbations for long term management of AD
 
 reductions in disease severity and acute AD flares have been evaluated with chronic use of both medications
 
 indications for use:
 
 tacrolimus - 2 years of age and older, use for moderate to severe AD disease
 
 pimecrolimus - 2 years of age and older, used for moderate to severe AD disease
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        | Term 
 | Definition 
 
        | block effects of histamine by competing for histamine receptors (inhibit effects of H1 and/or H2 receptors) |  | 
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        | Term 
 
        | antihistamines:  place in therapy for AD management |  | Definition 
 
        | adjunctive therapy for pruritus symptoms 
 sedating antihistamines (non-selective antihistamines) may be most effective in treating night itching
 
 topical preparations have shown variable therapeutic effectiveness; not recommended for use
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        | Term 
 | Definition 
 
        | possess anti-inflammatory and anti-pruritic properties |  | 
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        | Term 
 | Definition 
 
        | folliculitis 
 photosensitivity
 
 strong odor and stains clothing
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        | Term 
 
        | coal tar:  place in therapy |  | Definition 
 
        | used as a second line therapy option for AD 
 often used in combination with steroids and/or UV light therapies
 
 avoid use on acute purulent lesions
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        | Term 
 
        | potency of betamethasone dipropionate |  | Definition 
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        | Term 
 
        | potency of clobetasol propionate |  | Definition 
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        | Term 
 
        | potency of desoximetasone |  | Definition 
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        | Term 
 
        | potency of triamcinolone acetonide |  | Definition 
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        | Term 
 
        | potency of mometasone furoate |  | Definition 
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        | Term 
 
        | potency of hydrocortisone |  | Definition 
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