Jennifer D. Kaiser’s scientific contributions

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Publications (1)


Fig. 1 Systematic search strategy for published long-term (≥12 weeks) TCI trials in pediatric patients (<12 years) with AD. a Exclusions were based on review of MeSH terms, abstract, or (when necessary) the article text. b Meta-analyses and reviews were excluded if no new (previously unpublished) data were presented 
Table 1 Summary statements from review articles that assess TCI lymphoma risk a Citation Evidence of lymphoma risk with TCIs? Lymphoma risk summary statement 
Fig. 2 Systematic search strategy for published long-term (≥12 weeks) TCS trials in pediatric patients (<12 years) with AD. a Exclusions were based on review of MeSH terms, abstract, or (when necessary) the article text. b Meta-analyses and reviews were excluded if no new (previously unpublished) data were presented 
Table 3 Study designs for long-term (≥12 weeks) pimecrolimus trials in pediatric patients (<12 years) with AD 
Total subjects included in summary of long-term (≥12 weeks) pediatric trials by therapeutic agent and study duration. a Lighter shading indicates the proportion of patients that received TCS treatment as an active comparator in studies of a TCI. b One of the trials was a 1-yr OL extension of a 1-yr DB study. N = Number of studies. n = Number of subjects in respective treatment group
Systematic review of published trials: Long-term safety of topical corticosteroids and topical calcineurin inhibitors in pediatric patients with atopic dermatitis
  • Literature Review
  • Full-text available

June 2016

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268 Reads

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191 Citations

BMC Pediatrics

Elaine C. Siegfried

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Jennifer C. Jaworski

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Jennifer D. Kaiser

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Background Many clinicians have concerns about the safety of atopic dermatitis (AD) treatments, particularly in children requiring long-term daily maintenance therapy. Topical corticosteroids (TCS) have been widely used for >5 decades. Long-term TCS monotherapy has been associated with adverse cutaneous effects including atrophy, rebound flares, and increased percutaneous absorption with potential for adverse systemic effects. Topical calcineurin inhibitors (TCIs), tacrolimus and pimecrolimus, available for 1–2 decades, are not associated with atrophy or increased percutaneous absorption after prolonged use and have much lower potential for systemic effects. However, since 2006 TCIs have carried a controversial Boxed Warning based on a theoretical risk of malignancy (eg, skin and lymphoma) that has limited TCI use for standard-of-care maintenance therapy. Methods A comparative systematic search of PubMed was done for long-term (≥12 week) clinical trials of TCS or TCI treatment in patients <12 years with AD. Citations were reviewed for inclusion based on MeSH terms, abstracts, and relevant article text. Studies were excluded if they did not encompass subjects <12 years, or were <12 weeks’ duration, retrospective, meta-analyses, or limited to anecdotal case reports. Results Of 27 trials meeting criteria, 21 included 5825 pediatric patients treated with TCIs, and 6 included 1999 patients treated with TCS. TCS studies were limited to low- to mid-potency products, and all but one study lacked a vehicle control. Eight TCI studies were vehicle-controlled, and safety data were well reported, with ≤5 % of patients reporting discontinuation due to adverse effects (DAEs). Cutaneous and systemic adverse events (AEs) were similar in TCI and vehicle groups, with no reports of lymphoma. Safety data in TCS trials were less well reported. DAE incidence was addressed in just 2 trials, and systemic and cutaneous AEs were mostly unreported. Conclusions Data supporting long-term use of TCIs are robust, documenting safety and efficacy, while data supporting long-term TCS use are limited to low- to mid-potency products. Our review identifies a lack of information on the safety of commonly prescribed, long-term monotherapy with mid- to high-potency TCS in pediatric AD, and supports standard-of-care maintenance therapy with TCIs and intermittent use of low- to mid-potency TCS for flares.

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Citations (1)


... However, disruption of the hypothalamic-pituitary-adrenal axis has been reported, especially with high potency agents [24,25]. This is especially important to consider in the pediatric population, whose higher surface area-to-body weight ratio results in greater systemic absorption of topical corticosteroids [26]. This, combined with slower rates of steroid metabolism in children, puts them at higher risk of systemic adverse effects, such as adrenal suppression and stunting of growth [27,28]. ...

Reference:

Local Corticosteroids for Alopecia Areata: A Narrative Review
Systematic review of published trials: Long-term safety of topical corticosteroids and topical calcineurin inhibitors in pediatric patients with atopic dermatitis

BMC Pediatrics