![]() | Elaine C SiegfriedShow email addressDepartments of Pediatrics and Dermatology, Saint Louis University School of Medicine, St. Louis, Missouri, USA | Division of Dermatology, Department of Pediatrics, Cardinal ... |
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Elaine C Siegfried:Expert Impact
Concepts for whichElaine C Siegfriedhas direct influence:Atopic dermatitis,Pediatric patients,Eczema herpeticum,Pyoderma gangrenosum,Molluscum contagiosum,Systemic agents,Anatomical regions,Severe atopic dermatitis.
Elaine C Siegfried:KOL impact
Concepts related to the work of other authors for whichfor which Elaine C Siegfried has influence:Atopic dermatitis,Infantile hemangiomas,Acne vulgaris,Netherton syndrome,Oral propranolol,Pediatric psoriasis,Alopecia areata.
KOL Resume for Elaine C Siegfried
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2022 | Departments of Pediatrics and Dermatology, Saint Louis University School of Medicine, St. Louis, Missouri, USA |
2021 | Cardinal Glennon Children’s Hospital, St. Louis, Missouri, USA Department of Pediatrics and Dermatology, St Louis University, St Louis, Missouri |
2020 | Saint Louis University, Saint Louis, Missouri. Department of Pediatrics, St Louis University School of Medicine, St Louis, Missouri |
2019 | Saint Louis University, Saint Louis, Missouri |
2018 | Saint Louis University and Cardinal Glennon Children’s Hospital, St. Louis, MO, USA Cardinal Glennon Children's Hospital, St. Louis, MO |
2017 | Department of Dermatology, Saint Louis University School of Medicine, Saint Louis, Missouri Cardinal Glennon Children's Medical Center St. Louis MO USA |
2016 | Department of Pediatrics and Dermatology, Saint Louis University, Cardinal Glennon Children's Hospital, St Louis, Missouri Saint Louis University, Cardinal Glennon Children’s Hospital, 1465 South Grand Avenue, St Louis, MO 63104 USA |
2015 | Saint Louis University School of Medicine St. Louis Missouri |
2014 | Saint Louis University Cardinal Glennon Children's Hospital Department of Pediatrics St. Louis Missouri |
2013 | Department of Pediatrics, Saint Louis University School of Medicine, Cardinal Glennon Children's Medical Center, St Louis, Missouri Division of Dermatology, Cardinal Glennon Children's Medical Center and Saint Louis University School of Medicine, St. Louis, MO |
2012 | Departments of Dermatology and Pediatrics, St Louis University School of Medicine, St Louis, Missouri (Dr Siegfried). Dr Glenn was a medical student at the St Louis University School of Medicine and is now with the Department of Pediatrics at Children's Hospital and Research Center Oakland, Oakland, California. |
2011 | Department of Pediatrics and Dermatology, Saint Louis University School of Medicine, Saint Louis, Missouri |
2010 | Saint Louis, Missouri e‐mail: |
2009 | Saint Louis University, Department of Pediatrics and Dermatology, St. Louis, Missouri |
2008 | Professor of Pediatrics and Medicine (Dermatology), University of California, San Diego School of Medicine Cardinal Glennon Children's Hospital and Saint Louis University, St. Louis (E.C.S.) Chief, Division of Pediatric and Adolescent Dermatology, Rady Children's Hospital, San Diego, San Diego, California, USA Central Dermatology, St. Louis, Missouri |
2007 | Department of Dermatology, St Louis University School of Medicine, St Louis |
2006 | St Louis University School of Medicine and Kids Dermatology, St Louis, MO 63141, USA. Department of Dermatology, and Kids Dermatology, |
2005 | Professor of Pediatrics and Obstetrics and Gynecology, University of Pennsylvania School of Medicine, The Children's Hospital of Philadelphia, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania Kids Dermatology, 621 S. New Ballas Road, St. Louis, MO 63141, USA. Head, Division of Neonatology, University of Washington, Children's Hospital and Regional Medical Center, Seattle, Washington |
2004 | Department of Dermatology, St Louis University School of Medicine, St Louis, Missouri, USA |
2003 | From the Department of Dermatology, University of Cincinnati, Cincinnati, Ohio; the Department of Dermatology, Duke University, Durham, North Carolina; the Department of Dermatology, University of Missouri, and the Department of Pediatrics and Dermatology, St Louis University, St Louis, Missouri; and the Departments of Pathology and Dermatology, University of California, San Francisco, San Francisco, California, USA |
2002 | Department of Dermatology, Saint Louis University School of Medicine, St. Louis, Missouri |
2001 | Department of Pediatrics, Saint Louis University School of Medicine, St Louis, Missouri, U.S.A. |
2000 | Departments of *Dermatology and Pediatrics, Saint Louis University Medical Center, Saint Louis, Missouri, USA |
1999 | From the Departments of Dermatology,a Pediatrics,b and Internal Medicine,c Saint Louis University Health Sciences Center.*Ms Rogers is a medical student at Saint Louis University School of Medicine. **Dr Gibney was a resident in the Department of Dermatology at Saint Louis University Hospital during the study period and is currently in private practice in Quincy, Mass Department of Dermatology, St. Louis University Health Sciences Center, St. Louis, Missouri Dermatology, Pediatrics, and |
1998 | Department of Dermatology and Pediatrics, Saint Louis University Health Sciences Center, Missouri, USA. Pediatrics, St Louis University Health Sciences Center, St Louis, Missouri. |
1997 | Departments of Pediatrics and Dermatology Saint Louis University Health Sciences Center St. Louis, Missouri, USA |
1996 | Department of Internal Medicine/ Dermatology Division, St. Louis University Medical Center, St. Louis, Missouri, USA, US |
1995 | the Dermatology Associates of Cincinnati, Cincinnati, Ohio, USA St. Louis University Health Sciences Center, Division of Dermatology, St. Louis, Missouri |
Concept | World rank |
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skinrelated problem | #1 |
investigational nitric oxide | #1 |
newborn skin development | #1 |
confirmed eczema herpeticum | #1 |
tci data | #1 |
advance scheduling policy | #1 |
uncontrolled success rates | #1 |
label brimonidine | #1 |
18 nonattendance rate | #1 |
nonattendance rates | #1 |
average 6week time | #1 |
principles infant skin | #1 |
4 privately | #1 |
skinthis elaine siegfried | #1 |
37 nonattendance rate | #1 |
field pediatric dermatology | #1 |
binding cassette abca12 | #1 |
larger study efficacy | #1 |
longstanding shortage providers | #1 |
eczema anecdotal reports | #1 |
treated sb206 | #1 |
moderatesevere pediatric patients | #1 |
cutaneous congenital | #1 |
3 scheduling policies | #1 |
condyloma children | #1 |
skin evolving landscape | #1 |
insurance payment denial | #1 |
intramural pds | #1 |
material previous edition | #1 |
age systemic corticosteroids | #1 |
stem cellbased mutations | #1 |
publication brimonidine tartrate | #1 |
herpeticum response | #1 |
02timolol | #1 |
systemic therapy moderatesevere | #1 |
episode discontinuation | #1 |
defectsthis chapter material | #1 |
tci tcs | #1 |
flares administration | #1 |
brimonidine 02timolol | #1 |
pds period | #1 |
podophyllotoxin recurrence | #1 |
dupilumab pediatric patients | #1 |
02timolol 05 | #1 |
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Prominent publications by Elaine C Siegfried
Efficacy and Safety of Dupilumab in Adolescents With Uncontrolled Moderate to Severe Atopic Dermatitis
[ PUBLICATION ]
Importance: Adolescents with atopic dermatitis (AD) have high disease burden negatively affecting quality of life, with limited treatment options. The efficacy and safety of dupilumab, a monoclonal antibody, approved for treatment in adolescent patients with inadequately controlled AD, remain unknown in this patient population.
Objective: To assess the efficacy and safety of dupilumab monotherapy in adolescents with moderate to severe inadequately controlled AD.
Design, Setting, and ...
Known for Dupilumab Adolescents | 2 Weeks | Efficacy Safety | Severe Atopic | Quality Life |
BACKGROUND: Children with severe atopic dermatitis (AD) have limited treatment options.
OBJECTIVE: We report the efficacy and safety of dupilumab + topical corticosteroids (TCS) in children aged 6-11 years with severe AD inadequately controlled with topical therapies.
METHODS: In this double-blind, 16-week, phase 3 trial (NCT03345914), 367 patients were randomized 1:1:1 to 300 mg dupilumab every 4 weeks (300 mg q4w), a weight-based regimen of dupilumab every 2 weeks (100 mg q2w, baseline ...
Known for Severe Atopic Dermatitis | Dupilumab Tcs | Efficacy Safety | Topical Corticosteroids | 11 Years |
BACKGROUND: Etanercept, a soluble tumor necrosis factor receptor, has been shown to lessen disease severity in adult patients with psoriasis. We assessed the efficacy and safety of etanercept in children and adolescents with moderate-to-severe plaque psoriasis.
METHODS: In this 48-week study, 211 patients with psoriasis (4 to 17 years of age) were initially randomly assigned to a double-blind trial of 12 once-weekly subcutaneous injections of placebo or 0.8 mg of etanercept per kilogram ...
Known for Plaque Psoriasis | Etanercept Treatment | Placebo Pasi | Children Adolescents | 24 Weeks |
BackgroundAtopic dermatitis is a chronic inflammatory condition with substantial burden and limited treatment options for adolescents with moderate-to-severe disease. Significantly more patients treated with dupilumab vs. placebo achieved Investigator’s Global Assessment 0/1 at week 16.ObjectiveThe objective of this study was to assess the impact of dupilumab treatment vs. placebo on the achievement of clinically meaningful improvements in atopic dermatitis signs, symptoms and quality of ...
Known for Atopic Dermatitis | Quality Life | Dupilumab Placebo | Signs Symptoms | Clinically Meaningful |
The Comèl-Netherton syndrome is an autosomal recessive multisystemic disorder characterized by localized or generalized congenital ichthyosis, hair shaft abnormalities, immune deficiency, and markedly elevated IgE levels. Life-threatening complications during infancy include temperature and electrolyte imbalance, recurrent infections, and failure to thrive. To study the clinical presentations of the Comèl-Netherton syndrome and its molecular cause, we ascertained 19 unrelated families of ...
Known for Mutation Detection | Comèlnetherton Syndrome | Ichthyosiform Erythroderma | Preschool Codon | Prenatal Diagnosis |
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 ...
Known for Pediatric Patients | Topical Calcineurin Inhibitors | Atopic Dermatitis | Term Safety | Tcs Tci |
BACKGROUND: There is disparity in access to outpatient care for Medicaid beneficiaries. This inequity disproportionately impacts children. Access for children with skin disease may be especially limited.
OBJECTIVE: We sought to compare access to dermatologists for new pediatric patients insured by Medicaid versus a private plan.
METHODS: We surveyed 13 metropolitan markets by conducting secret-shopper scripted telephone calls to dermatology providers listed by Medicaid health plans. ...
Known for Private Insurance | Access Dermatologists | Health Medicaid | Insured Children | Paired Calls |
Importance: Molluscum contagiosum (MC) is a common viral skin infection that primarily affects children. Cantharidin, a topical vesicant, has a long history of use for MC in compounded formulations, but the safety and efficacy of doses, regimens, and application methods have not been demonstrated in large-scale trials.
Objective: To determine the safety and efficacy of VP-102, a drug-device combination containing cantharidin, 0.7% (w/v), compared with vehicle in individuals with ...
Known for Vp102 Vehicle | Complete Clearance | Molluscum Contagiosum | Cantharidin 07 | Device Combination |
Efficacy and Safety of Abrocitinib in Combination With Topical Therapy in Adolescents With Moderate-to-Severe Atopic Dermatitis
[ PUBLICATION ]
Importance: Dupilumab subcutaneous injection is approved for treating moderate-to-severe atopic dermatitis (AD) in adolescents, but there has been too little research on an efficacious systemic oral treatment with a favorable benefit-risk profile for adolescents with moderate-to-severe AD.
Objective: To investigate the efficacy and safety of oral abrocitinib plus topical therapy in adolescents with moderate-to-severe AD.
Design, Setting, and Participants: The phase 3, randomized, ...
Known for Adolescents Moderatetosevere | Oral Abrocitinib | Atopic Dermatitis | Topical Therapy | Placebo 12 Weeks |
OBJECTIVE: To assess early intervention with pimecrolimus combined with corticosteroid (CS) for major flares in patients with severe atopic dermatitis (AD).
METHODS: In this 6-month, double-blind, multicenter, randomized, vehicle-controlled, parallel-group in 35 US centers, 275 children aged 3 months to 11 years with mild to severe AD applied the study medication twice daily at first signs/symptoms of AD. For major flares not controlled with study medication, a mid-potency CS cream ...
Known for Pimecrolimus Cream | Preschool Dermatitis | Study Medication | Outcome Measure | Calcineurin Inhibitors |
Conjunctivitis in Dupilumab Clinical Trials for Adolescents with Atopic Dermatitis or Asthma
[ PUBLICATION ]
BackgroundConjunctivitis is a known comorbidity of atopic dermatitis. Dupilumab clinical trials for moderate-to-severe atopic dermatitis in adults showed a higher conjunctivitis incidence for dupilumab-treated patients than placebo-treated patients, whereas trials for uncontrolled asthma reported lower rates for both dupilumab and placebo.ObjectiveThe objective of this study was to evaluate the incidence and severity of conjunctivitis in dupilumab clinical trials in adolescents with ...
Known for Atopic Dermatitis | Dupilumab Placebo | Adolescents Moderate | Humanized Asthma | Lower Rates |
Timolol Maleate 0.5% or 0.1% Gel‐Forming Solution for Infantile Hemangiomas: A Retrospective, Multicenter, Cohort Study
[ PUBLICATION ]
Therapeutic options for superficial infantile hemangiomas (IH) are limited. Recently, timolol maleate gel, a topical nonselective beta-blocker, has been reported as a potentially effective treatment for superficial IH. This study is an extension of a previously published pilot study designed to further investigate the efficacy and safety and to identify predictors of good response of topical 0.5% or 0.1% timolol maleate gel-forming solution. This was a retrospective cohort study ...
Known for Timolol Maleate | Infantile Hemangiomas | Patients Superficial | Forming Solution | Study Efficacy |
BACKGROUND: No systemic therapies are approved by the US Food and Drug Administration for the treatment of psoriasis in children and adolescents.
OBJECTIVE: We sought to evaluate the long-term safety and efficacy of etanercept in pediatric patients (aged 4-17 years) with moderate to severe plaque psoriasis.
METHODS: Patients who completed or received substantial treatment benefit in a 48-week, randomized, double-blind, placebo-controlled study (N = 211) evaluating the efficacy and safety ...
Known for Pediatric Patients | Plaque Psoriasis | Efficacy Etanercept | Topic Receptors | Systemic Therapies |
Pimecrolimus in atopic dermatitis: Consensus on safety and the need to allow use in infants
[ PUBLICATION ]
Atopic dermatitis (AD) is a distressing dermatological disease, which is highly prevalent during infancy, can persist into later life and requires long-term management with anti-inflammatory compounds. The introduction of the topical calcineurin inhibitors (TCIs), tacrolimus and pimecrolimus, more than 10 yr ago was a major breakthrough for the topical anti-inflammatory treatment of AD. Pimecrolimus 1% is approved for second-line use in children (≥2 yr old) and adults with ...
Known for Atopic Dermatitis | Boxed Warning | Topical Corticosteroids | Anti Inflammatory | Term Safety |
Importance: Use of systemic therapies for moderate to severe psoriasis in children is increasing, but comparative data on their use and toxicities are limited.
Objective: To assess patterns of use and relative risks of systemic agents for moderate to severe psoriasis in children.
Design, Setting, and Participants: A retrospective review was conducted at 20 centers in North America and Europe, and included all consecutive children with moderate to severe psoriasis who used systemic ...
Known for Pediatric Psoriasis | Systemic Agents | Methotrexate Week | Folic Acid | Necrosis Factor |