Evaluation of emergency department utilization for dermatologic conditions in the pediatric population within the United States from 2009-2015.

Abstract:

BACKGROUND:Dermatologic conditions comprise a significant number of emergency department visits in the pediatric population in the United States. Understanding key predictors of emergency department utilization for dermatologic conditions is important to reduce inappropriate use. METHODS:A total of 44 554 sampled patient emergency department visits, consisting of patients less than 18 years of age, were collected from the National Hospital Ambulatory Medical Care Survey between 2009 to 2015. ICD-9 codes were used to define dermatologic conditions versus non-dermatologic conditions with univariate and multivariate analyses used to identify factors significantly correlated with dermatologic emergency department utilization. RESULTS:A total of 13 681 691 pediatric dermatologic emergency department visits (weighted) were evaluated over the seven-year period, representing 6.4% of total pediatric emergency department visits. The most common dermatologic diagnosis was cellulitis (25.6% of visits). The majority of patients were five years old or younger (54.4%). Patients with primary dermatologic conditions were more likely to be triaged as non-urgent (16.7%) or semi-urgent (45.8%) than patients without dermatologic conditions. Only 2.1% of patients with dermatologic conditions required further observation or admission. On further regression modeling, age ≤ 5, semi-urgent or non-urgent acuity, Medicaid insurance, and residence in the Northeastern or Midwestern United States were significantly associated with presentation to the emergency department with a dermatologic condition when compared to non-dermatologic condition. CONCLUSIONS:Dermatologic conditions continue to comprise a significant number of ED visits in the pediatric population. Increased ED utilization by vulnerable pediatric populations highlights the need to better direct or provide access to outpatient dermatologic care.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Collier EK,Yang JJ,Sangar S,Chen ST,Huang JT,Bach DQ

doi

10.1111/pde.14476

subject

Has Abstract

pub_date

2020-12-18 00:00:00

eissn

0736-8046

issn

1525-1470

pub_type

杂志文章
  • Trichophyton rubrum tinea capitis in a young child.

    abstract::While the primary etiologic agent of tinea capitis in the United States has varied over the past century, the last several decades have been marked by a predominance of infection with Trichophyton tonsurans. Related anthropophilic organisms commonly isolated in other dermatophytoses are infrequently observed in tinea ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21114.x

    authors: Abdel-Rahman SM,Penny J,Alander SW

    更新日期:2004-01-01 00:00:00

  • Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin.

    abstract::We report a family affected to the fourth generation by uncombable hair syndrome. This syndrome is characterized by unruly, dry, blond hair with a tangled appearance. The family pedigree strongly supports the hypothesis of autosomal dominant inheritance; some members of the family had, apart from uncombable hair, mino...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00385.x

    authors: Boccaletti V,Zendri E,Giordano G,Gnetti L,De Panfilis G

    更新日期:2007-05-01 00:00:00

  • Childhood granulomatous periorificial dermatitis with a good response to oral metronidazole.

    abstract::Childhood granulomatous periorificial dermatitis (CGPD) is a condition included in the spectrum of rosacea and perioral dermatitis that affects prepubescent children. It is characterized by papular eruptions located around the mouth, nose, and eyes that histopathologically show a granulomatous pattern. We report a 9-y...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12110

    authors: Rodriguez-Caruncho C,Bielsa I,Fernandez-Figueras MT,Ferrándiz C

    更新日期:2013-09-01 00:00:00

  • Polycystic Ovary Syndrome: Special Diagnostic and Therapeutic Considerations for Children.

    abstract::Polycystic ovary syndrome (PCOS) is an endocrine syndrome with variable phenotypic expression and important systemic associations and sequelae, including obesity, insulin resistance, infertility, risk of endometrial cancer, and possible risk of cardiovascular events. PCOS is recognized as a condition influenced by gen...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12566

    authors: Kamangar F,Okhovat JP,Schmidt T,Beshay A,Pasch L,Cedars MI,Huddleston H,Shinkai K

    更新日期:2015-09-01 00:00:00

  • Neonatal skin care: Developments in care to maintain neonatal barrier function and prevention of diaper dermatitis.

    abstract:BACKGROUND:Understanding the importance of the barrier function of the skin of preterm and term neonates is crucial in effective neonatal skin and diaper care. This literature search aimed to review the development of different practices in neonatal care to maintain skin barrier function, in turn preventing diaper derm...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13714

    authors: Burdall O,Willgress L,Goad N

    更新日期:2019-01-01 00:00:00

  • Frequency and severity of diaper dermatitis with use of traditional Chinese cloth diapers: observations in 3- to 9-month-old children.

    abstract::Chinese cloth diapers differ from disposable diapers in several respects that are central to our understanding of the etiology of diaper dermatitis (DD), yet there are no published reports on the dermatological correlates of this manner of infant care, which is prevalent among the world's second-largest pediatric popu...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01494.x

    authors: Liu N,Wang X,Odio M

    更新日期:2011-07-01 00:00:00

  • Propranolol-resistant infantile hemangioma successfully treated with sirolimus.

    abstract::Infantile hemangiomas are the most common benign vascular tumors in childhood. Propranolol is the first-line treatment for infantile hemangiomas, but failures may occur. Sirolimus, an mTOR inhibitor, is a promising drug for the treatment of vascular malformations and vascular tumors. We present the case of a child wit...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.14163

    authors: Dávila-Osorio VL,Iznardo H,Roé E,Puig L,Baselga E

    更新日期:2020-07-01 00:00:00

  • Hypercalcemia due to subcutaneous fat necrosis in a newborn after total body cooling.

    abstract::Subcutaneous fat necrosis is an inflammatory disorder of adipose tissue. Although patients need long-term follow-up to prevent hypercalcemia, the prognosis is generally favorable. We herein present a case of a newborn who developed subcutaneous fat necrosis-related hypercalcemia after hypothermia treatment for hypoxic...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01716.x

    authors: Akcay A,Akar M,Oncel MY,Kızılelma A,Erdeve O,Oguz SS,Uras N,Dılmen U

    更新日期:2013-01-01 00:00:00

  • Vesicular erythema multiforme-like reaction to para-phenylenediamine in a henna tattoo.

    abstract::Allergic contact dermatitis reaction to topical "black henna" tattoo is usually described secondary to the organic dye para-phenylenediamine, a derivative of analine. Allergic contact dermatitis reactions to para-phenylenediamine are well recognized and most commonly involve an eczematous reaction that may become gene...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00634.x

    authors: Sidwell RU,Francis ND,Basarab T,Morar N

    更新日期:2008-03-01 00:00:00

  • Effectiveness of Intralesional Triamcinolone in the Treatment of Keloids in Children.

    abstract:BACKGROUND:The current treatment of keloids includes surgery, intralesional steroids, and radiotherapy, among others. Radiotherapy is not recommended in children due to its effects on growing tissues. Our aim was to study intralesional triamcinilone therapy of keloids in children and analyze the impact of body location...

    journal_title:Pediatric dermatology

    pub_type: 临床试验,杂志文章

    doi:10.1111/pde.12746

    authors: Acosta S,Ureta E,Yañez R,Oliva N,Searle S,Guerra C

    更新日期:2016-01-01 00:00:00

  • Aeromonas hydrophila folliculitis associated with an inflatable swimming pool: mimicking Pseudomonas aeruginosa infection.

    abstract::Aeromonas species are ubiquitous, facultative, anaerobic, gram-negative flagellated rods, mainly found in aquatic ecosystems worldwide. Skin and soft-tissue infections, including cellulitis and wound infections, are the second most frequent location of isolations of Aeromonas spp. in clinical samples, after the gastro...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00993.x

    authors: Julià Manresa M,Vicente Villa A,Gené Giralt A,González-Enseñat MA

    更新日期:2009-09-01 00:00:00

  • Multiple familial pilomatricomas: a cutaneous marker for Gardner syndrome?

    abstract::A 40-year-old man and his 6-year-old only son had numerous, firm papulonodular lesions on their faces. Their medical histories were unremarkable and no family consanguinity was recorded. Surgical excision of several lesions was performed on each patient. All the lesions were solid tumors with the characteristic histop...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1995.tb00195.x

    authors: Pujol RM,Casanova JM,Egido R,Pujol J,de Moragas JM

    更新日期:1995-12-01 00:00:00

  • Crisaborole Topical Ointment, 2% in Patients Ages 2 to 17 Years with Atopic Dermatitis: A Phase 1b, Open-Label, Maximal-Use Systemic Exposure Study.

    abstract:BACKGROUND:Phosphodiesterase-4 (PDE4) is a promising target in atopic dermatitis (AD) treatment. The pharmacokinetics (PK), safety, and efficacy of crisaborole topical ointment, 2% (formerly AN2728) (Anacor Pharmaceuticals, Palo Alto, CA), a boron-based benzoxaborole PDE4 inhibitor, were evaluated in children with mild...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,多中心研究

    doi:10.1111/pde.12872

    authors: Zane LT,Kircik L,Call R,Tschen E,Draelos ZD,Chanda S,Van Syoc M,Hebert AA

    更新日期:2016-07-01 00:00:00

  • Bullous Impetigo Rapid Diagnostic and Therapeutic Quiz: A Model for Assessing Basic Dermatology Knowledge of Primary Care Providers.

    abstract:BACKGROUND/OBJECTIVES:Bullous impetigo (BI) is a common dermatologic condition, particularly in children, yet confusion regarding its diagnosis and treatment persists. This study measured pediatricians' ability to diagnose and appropriately treat BI and explored factors that might influence pediatricians' accuracy in m...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12974

    authors: Simkin DJ,Grossberg AL,Cohen BA

    更新日期:2016-11-01 00:00:00

  • Ear lobe bilateral necrosis by levamisole-induced occlusive vasculitis in a pediatric patient.

    abstract::We describe a bullous-hemorrhagic reaction of the ear lobes in a child with nephrosis after levamisole intake. This drug is used in children as an alternative treatment of corticosteroid-responsive nephrotic syndrome. Histologic evaluation of a lesion revealed necrotizing vasculitis involving mainly the large vessels ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1997.tb00695.x

    authors: Menni S,Pistritto G,Gianotti R,Ghio L,Edefonti A

    更新日期:1997-11-01 00:00:00

  • Erythema nodosum in association with celiac disease.

    abstract::We present a 16-year-old girl with a 4-year history of chronic persistent erythema nodosum. Recurrently low serum iron values suggested the possibility of a malabsorption syndrome. The presence of antitransglutaminase and antiendomysium antibodies and the jejunal biopsy specimen findings showed an underlying celiac di...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.0736-8046.2004.21307.x

    authors: Bartyik K,Várkonyi A,Kirschner A,Endreffy E,Túri S,Karg E

    更新日期:2004-05-01 00:00:00

  • Van der Woude syndrome. A case report.

    abstract::We describe several members of a family with Van der Woude syndrome, a genetic and congenital malformation syndrome with autosomal dominant inheritance and 70% to 80% penetrance with variable expressivity. It is characterized by clinical signs localized to the face, such as bilateral or unilateral pits on conical elev...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.1998.1998015459.x

    authors: Vignale R,Araujo J,Pascal G,Reissenweber N,Abulafia J,Quadrelli R,Vaglio A,Larrandaburo M,Reyno S

    更新日期:1998-11-01 00:00:00

  • PLACK syndrome resulting from a novel homozygous variant in CAST.

    abstract::PLACK syndrome (OMIM 616295) is a form of generalized peeling skin syndrome (GPSS; OMIM 270300). It is an autosomal recessive genodermatosis caused by pathogenic mutations in CAST, which encodes calpastatin, an endogenous specific inhibitor of calpain, a calcium-dependent cysteine protease. We present a 5-year-old gir...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.14383

    authors: Boggs JME,Irvine AD

    更新日期:2020-10-03 00:00:00

  • Fixed drug eruption in the genital area in 15 boys.

    abstract::Fixed drug eruption (FDE) is manifested as localized, circumscribed, round or oval plaques that characteristically recur in the same site with each use of the offending drug. The drugs most commonly implicated are phenolphthalein, barbiturates, antibiotics, salicylates, contraceptives, and anticonvulsants. FDE can app...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2002.00078.x

    authors: Nussinovitch M,Prais D,Ben-Amitai D,Amir J,Volovitz B

    更新日期:2002-05-01 00:00:00

  • Xp microdeletion syndrome characterized by pathognomonic linear skin defects on the head and neck.

    abstract::We describe a new case of a rare syndrome characterized by ocular abnormalities and pathognomonic linear skin defects. This syndrome is the result of an unbalanced translocation resulting in a deletion of the distal end of the short arm of the X chromosome. We report the thirteenth case and review the clinical and cyt...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1997.tb00422.x

    authors: Paulger BR,Kraus EW,Pulitzer DR,Moore CM

    更新日期:1997-01-01 00:00:00

  • Childhood lichen planus: a report of fifty cases.

    abstract::Lichen planus is an uncommonly encountered dermatosis in children. In the present study of 50 children the limbs were the most common site of involvement (70.0%). A majority of the children (60.0%) presented with the classic form of the disease. Hypertrophic lesions were present in 26.0% of children while linear lesio...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1046/j.1525-1470.1999.00074.x

    authors: Sharma R,Maheshwari V

    更新日期:1999-09-01 00:00:00

  • Urticating Hashimoto-Pritzker Langerhans cell histiocytosis.

    abstract::Red-brown papules developing during the neonatal period may present a diagnostic dilemma. The Darier sign has been a reliable feature in the diagnosis of mastocytosis. However, the cutaneous infiltrate of Hashimoto-Pritzker Langerhans cell histiocytosis (LCH) may contain a large number of mast cells, leading to confus...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2001.018001041.x

    authors: Butler DF,Ranatunge BD,Rapini RP

    更新日期:2001-01-01 00:00:00

  • Infantile Bullous Pemphigoid Treated Using Intravenous Immunoglobulin: Case Report and Review of the Literature.

    abstract::We report a 5-month-old girl diagnosed with bullous pemphigoid who initially did not respond to systemic corticosteroids and dapsone but rapidly improved after the addition of intravenous immunoglobulin (IVIG) infusions. A literature search revealed anecdotal cases of infantile bullous pemphigoid treated with IVIG, al...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12635

    authors: Tekin B,Yücelten AD

    更新日期:2015-09-01 00:00:00

  • Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement.

    abstract:BACKGROUND:Spiny hyperkeratosis refers to a rare clinical phenotype characterized by nonfollicular keratotic projections and sometimes associated with other acquired and inherited conditions. We describe a case of congenital patterned spiny hyperkeratosis. METHODS:To identify the cause of this disorder, we used a comb...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.12848

    authors: Eskin-Schwartz M,Metzger Y,Peled A,Weissglas-Volkov D,Malchin N,Gat A,Vodo D,Mevorah B,Shomron N,Sprecher E,Sarig O

    更新日期:2016-05-01 00:00:00

  • Vogt-Koyanagi-Harada syndrome in a 6-year-old Hispanic boy.

    abstract::A 6-year-old Hispanic boy presented to the ophthalmology department with complaints of pain, photophobia, and blurry vision of both eyes. He was found to have bilateral granulomatous panuveitis, cataracts, and high intraocular pressures. He later developed multiple asymptomatic, ovoid, hypopigmented patches over the m...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.2011.01571.x

    authors: Hernandez C,LePoole C,Tessler HH

    更新日期:2012-03-01 00:00:00

  • Childhood discoid lupus in identical twins.

    abstract::We report the exceptional case of 11-year-old identical male twins who both developed discoid lupus erythematosus lesions. Although systemic lupus erythematosus has often been reported in identical twins, discoid lupus erythematosus has only occasionally been described, with only one other case in twin children, as fa...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00794.x

    authors: Del Boz J,Martín T,Samaniego E,Vera A,Sanz A,Crespo V

    更新日期:2008-11-01 00:00:00

  • Neonatal linear immunoglobulin a bullous dermatosis: a rare presentation.

    abstract::Linear immunoglobulin A bullous dermatosis (LABD) is an autoimmune blistering disease that most commonly presents in preschool-aged children. There have been few neonatal reports, all of which had life-threatening aerodigestive complications requiring mechanical intervention and systemic therapy. We present a case of ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01507.x

    authors: Julapalli MR,Brandon KL,Rosales CM,Grover RK,Plunkett RW,Metry DW

    更新日期:2012-09-01 00:00:00

  • Successful Use of Cyclosporin A for Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Three Children.

    abstract:BACKGROUND/OBJECTIVES:Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are medical emergencies. Mainstays of treatment include removal of the offending agent, supportive care, and wound care. The use of immunosuppressive agents such as corticosteroids and intravenous immunoglobulin (IVIg) is controve...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13236

    authors: St John J,Ratushny V,Liu KJ,Bach DQ,Badri O,Gracey LE,Ho AW,Raff AB,Sugai DY,Schalock P,Kroshinsky D

    更新日期:2017-09-01 00:00:00

  • A practical review of dermoscopy for pediatric dermatology part II: Vascular tumors, infections, and inflammatory dermatoses.

    abstract::In addition to the evaluation of melanocytic growths (Part I), dermoscopy is helpful in the identification and management of vascular tumors, skin infections, and inflammatory conditions. In this practical review, we present the classic dermoscopic findings of the following: vascular tumors, infectious conditions (mol...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.14284

    authors: Natsis NE,Gordon SC,Kaushik A,Seiverling EV

    更新日期:2020-09-01 00:00:00

  • Ulerythema ophryogenes in Cornelia de Lange syndrome.

    abstract::A 17-year-old woman with Cornelia de Lange syndrome had asymptomatic skin lesions since the age of 4 years. These were multiple, follicular, horny papules, present on both cheeks, and surrounded by erythematous skin. Similar lesions were present on the external aspect of the arms, but amidst skin of normal coloration....

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2002.00003.x

    authors: Flórez A,Fernández-Redondo V,Toribio J

    更新日期:2002-01-01 00:00:00