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Dive into the research topics where Sarah L. Chamlin is active.

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Featured researches published by Sarah L. Chamlin.


Pediatrics | 2006

Prospective study of infantile hemangiomas: Clinical characteristics predicting complications and treatment

Anita N. Haggstrom; Beth A. Drolet; Eulalia Baselga; Sarah L. Chamlin; Maria C. Garzon; Kimberly A. Horii; Anne W. Lucky; Anthony J. Mancini; Denise W. Metry; Brandon Newell; Amy J. Nopper; Ilona J. Frieden

OBJECTIVES. Infantile hemangiomas are the most common tumor of infancy. Risk factors for complications and need for treatment have not been studied previously in a large prospective study. This study aims to identify clinical characteristics associated with complications and the need for therapeutic intervention. PATIENTS AND METHODS. We conducted a prospective cohort study at 7 US pediatric dermatology clinics with a consecutive sample of 1058 children, aged ≤12 years, with infantile hemangiomas enrolled between September 2002 and October 2003. A standardized questionnaire was used to collect data on each patient and each hemangioma, including clinical characteristics, complications, and treatment. RESULTS. Twenty-four percent of patients experienced complications related to their hemangioma(s), and 38% of our patients received some form of treatment during the study period. Hemangiomas that had complications and required treatment were larger and more likely to be located on the face. Segmental hemangiomas were 11 times more likely to experience complications and 8 times more likely to receive treatment than localized hemangiomas, even when controlled for size. CONCLUSIONS. Large size, facial location, and/or segmental morphology are the most important predictors of poor short-term outcomes as measured by complication and treatment rates.


Pediatrics | 2008

Growth characteristics of infantile hemangiomas: implications for management.

Linda C. Chang; Anita N. Haggstrom; Beth A. Drolet; Eulalia Baselga; Sarah L. Chamlin; Maria C. Garzon; Kimberly A. Horii; Anne W. Lucky; Anthony J. Mancini; Denise W. Metry; Amy J. Nopper; Ilona J. Frieden

OBJECTIVES. Infantile hemangiomas often are inapparent at birth and have a period of rapid growth during early infancy followed by gradual involution. More precise information on growth could help predict short-term outcomes and make decisions about when referral or intervention, if needed, should be initiated. The objective of this study was to describe growth characteristics of infantile hemangioma and compare growth with infantile hemangioma referral patterns. METHODS. A prospective cohort study involving 7 tertiary care pediatric dermatology practices was conducted. Growth data were available for a subset of 526 infantile hemangiomas in 433 patients from a cohort study of 1096 children. Inclusion criteria were age younger than 18 months at time of enrollment and presence of at least 1 infantile hemangioma. Growth stage and rate were compared with clinical characteristics and timing of referrals. RESULTS. Eighty percent of hemangioma size was reached during the early proliferative stage at a mean age of 3 months. Differences in growth between hemangioma subtypes included that deep hemangiomas tend to grow later and longer than superficial hemangiomas and that segmental hemangiomas tended to exhibit more continued growth after 3 months of age. The mean age of first visit was 5 months. Factors that predicted need for follow-up included ongoing proliferation, larger size, deep component, and segmental and indeterminate morphologic subtypes. CONCLUSIONS. Most infantile hemangioma growth occurs before 5 months, yet 5 months was also the mean age at first visit to a specialist. Recognition of growth characteristics and factors that predict the need for follow-up could help aid in clinical decision-making. The first few weeks to months of life are a critical time in hemangioma growth. Infants with hemangiomas need close observation during this period, and those who need specialty care should be referred and seen as early as possible within this critical growth period.


Journal of The American Academy of Dermatology | 2014

Guidelines of care for the management of atopic dermatitis: section 2. Management and treatment of atopic dermatitis with topical therapies.

Lawrence F. Eichenfield; Wynnis L. Tom; Timothy G. Berger; Alfons Krol; Amy S. Paller; Kathryn Schwarzenberger; James N. Bergman; Sarah L. Chamlin; David E. Cohen; Kevin D. Cooper; Kelly M. Cordoro; Dawn Marie R. Davis; Steven R. Feldman; Jon M. Hanifin; David J. Margolis; Robert A. Silverman; Eric L. Simpson; Hywel C. Williams; Craig A. Elmets; Julie Block; Christopher G. Harrod; Wendy Smith Begolka; Robert Sidbury

Atopic dermatitis is a common and chronic, pruritic inflammatory skin condition that can affect all age groups. This evidence-based guideline addresses important clinical questions that arise in its management. In this second of 4 sections, treatment of atopic dermatitis with nonpharmacologic interventions and pharmacologic topical therapies are reviewed. Where possible, suggestions on dosing and monitoring are given based on available evidence.


Pediatrics | 2013

Initiation and Use of Propranolol for Infantile Hemangioma: Report of a Consensus Conference

Beth A. Drolet; Peter C. Frommelt; Sarah L. Chamlin; Anita N. Haggstrom; Nancy M. Bauman; Yvonne E. Chiu; Robert H. Chun; Maria C. Garzon; Kristen E. Holland; Leonardo Liberman; Susan MacLellan-Tobert; Anthony J. Mancini; Denise W. Metry; Katherine B. Puttgen; Marcia Seefeldt; Robert Sidbury; Kendra M. Ward; Francine Blei; Eulalia Baselga; Laura D. Cassidy; David H. Darrow; Shawna Joachim; Eun Kyung M Kwon; Kari Martin; Jonathan A. Perkins; Dawn H. Siegel; Robert J. Boucek; Ilona J. Frieden

Infantile hemangiomas (IHs) are common neoplasms composed of proliferating endothelial-like cells. Despite the relative frequency of IH and the potential severity of complications, there are currently no uniform guidelines for treatment. Although propranolol has rapidly been adopted, there is significant uncertainty and divergence of opinion regarding safety monitoring, dose escalation, and its use in PHACE syndrome (PHACE = posterior fossa, hemangioma, arterial lesions, cardiac abnormalities, eye abnormalities; a cutaneous neurovascular syndrome characterized by large, segmental hemangiomas of the head and neck along with congenital anomalies of the brain, heart, eyes and/or chest wall). A consensus conference was held on December 9, 2011. The multidisciplinary team reviewed existing data on the pharmacologic properties of propranolol and all published reports pertaining to the use of propranolol in pediatric patients. Workgroups were assigned specific topics to propose protocols on the following subjects: contraindications, special populations, pretreatment evaluation, dose escalation, and monitoring. Consensus protocols were recorded during the meeting and refined after the meeting. When appropriate, protocol clarifications and revision were made and agreed upon by the group via teleconference. Because of the absence of high-quality clinical research data, evidence-based recommendations are not possible at present. However, the team agreed on a number of recommendations that arose from a review of existing evidence, including when to treat complicated IH; contraindications and pretreatment evaluation protocols; propranolol use in PHACE syndrome; formulation, target dose, and frequency of propranolol; initiation of propranolol in infants; cardiovascular monitoring; ongoing monitoring; and prevention of hypoglycemia. Where there was considerable controversy, the more conservative approach was selected. We acknowledge that the recommendations are conservative in nature and anticipate that they will be revised as more data are made available.


Journal of The American Academy of Dermatology | 2014

Guidelines of care for the management of atopic dermatitis: Section 3. Management and treatment with phototherapy and systemic agents

Robert Sidbury; Dawn Marie R. Davis; David E. Cohen; Kelly M. Cordoro; Timothy G. Berger; James N. Bergman; Sarah L. Chamlin; Kevin D. Cooper; Steven R. Feldman; Jon M. Hanifin; Alfons Krol; David J. Margolis; Amy S. Paller; Kathryn Schwarzenberger; Robert A. Silverman; Eric L. Simpson; Wynnis L. Tom; Hywel C. Williams; Craig A. Elmets; Julie Block; Christopher G. Harrod; Wendy Smith Begolka; Lawrence F. Eichenfield

Atopic dermatitis is a chronic, pruritic inflammatory dermatosis that affects up to 25% of children and 2% to 3% of adults. This guideline addresses important clinical questions that arise in atopic dermatitis management and care, providing recommendations based on the available evidence. In this third of 4 sections, treatment of atopic dermatitis with phototherapy and systemic immunomodulators, antimicrobials, and antihistamines is reviewed, including indications for use and the risk-benefit profile of each treatment option.


American Journal of Medical Genetics Part A | 2006

A prospective study of PHACE syndrome in infantile hemangiomas: demographic features, clinical findings, and complications.

Denise W. Metry; Anita N. Haggstrom; Beth A. Drolet; Eulalia Baselga; Sarah L. Chamlin; Maria Garzon; Kimberly A. Horii; Anne W. Lucky; Anthony J. Mancini; Brandon Newell; Amy J. Nopper; G. Heyer; Ilona J. Frieden

PHACE (OMIM no. 606519) is a neurocutaneous syndrome that refers to the association of large, plaque‐like, “segmental” hemangiomas of the face, with one or more of the following anomalies: posterior fossa brain malformations, arterial cerebrovascular anomalies, cardiovascular anomalies, eye anomalies, and ventral developmental defects, specifically sternal defects and/or supraumbilical raphe. The etiology and pathogenesis of PHACE is unknown, and potential risk factors for the syndrome have not been systematically studied. The purpose of this study was thus to determine (1) the incidence of PHACE and associated anomalies among a large cohort of hemangioma patients, (2) whether certain demographic, prenatal or perinatal risk factors predispose infants to this syndrome, and (3) whether the cutaneous distribution of the hemangioma can be correlated to the types of anomalies present. We undertook a prospective, cohort study of 1,096 children with hemangiomas, 25 of whom met criteria for PHACE. These 25 patients represented 20% of infants with segmental facial hemangiomas. Compared to previous reports, our PHACE patients had a higher incidence of cerebrovascular and cardiovascular anomalies. Two developed acute arterial ischemic stroke during infancy, while two with cardiovascular anomalies showed documented evidence of normalization, suggesting that both progressive and regressive vascular phenomena may occur in this syndrome. Correlation to the anatomic location of the hemangioma appears to be helpful in determining which structural abnormalities might be present. A comparison of demographic and perinatal data between our PHACE cases and the hemangioma cohort overall showed no major differences, except a trend for PHACE infants to be of slighter higher gestational age and born to slightly older mothers. Eighty‐eight percent were female, a finding which has been noted in multiple other reports. Further research is needed to determine possible etiologies, optimal evaluation, and outcomes.


Pediatrics | 2004

Effects of atopic dermatitis on young American children and their families

Sarah L. Chamlin; Ilona J. Frieden; Mary L. Williams; Mary-Margaret Chren

Objective. The psychologic, physical, and social impact of atopic dermatitis is complex and varies among children of different ages, and the effects of atopic dermatitis on the quality of life of very young American children and their families are not well understood. This study was conducted to document these effects of atopic dermatitis on young children and their families. Methods. Directed focus sessions were performed with parents of 26 young children with atopic dermatitis and 6 expert clinicians. Specific mentions of the ways in which atopic dermatitis affected the children and parents were reviewed, rank ordered, and categorized according to similarity in content. The categories were examined to determine the domains represented, and the domains were used to compose a conceptual framework of all of the ways that atopic dermatitis affects children and their families. Results. Parents and experts mentioned a total of 181 specific quality-of-life effects. A conceptual framework, developed from the 181 effects, contains the domains of physical health, emotional health, physical functioning, and social functioning; each domain includes effects on both the child and the parents. Conclusions. Atopic dermatitis greatly affects the quality of life of afflicted children and their families. The comprehensive conceptual framework summarizes the ways in which atopic dermatitis affects the quality of life in young American children. This conceptual framework forms the basis from which quality-of-life instruments can be developed.


Pediatric Dermatology | 2008

The Socioeconomic Impact of Atopic Dermatitis in the United States: A Systematic Review

Anthony J. Mancini; Kellee Kaulback; Sarah L. Chamlin

Abstract:  The aim of this study was to review studies examining the direct and indirect costs of atopic dermatitis in the United States. A search was performed using OVID MEDLINE, MEDLINE In‐Process and Other Non‐Indexed Citations, EMBASE, the International Agency for Health Technology Assessment (INAHTA) database, and the Cochrane Library. All abstracts were reviewed for the following criteria: original cost data, studies performed in the United States, and English language. The search yielded 418 papers. Fifty‐nine papers were reviewed in detail, and four studies were found that met the inclusion criteria. These cost‐identification analyses estimated the cost of atopic dermatitis heterogeneously and could not be compared directly. National cost estimates ranged widely, from


British Journal of Dermatology | 2007

A systematic review of the safety of topical therapies for atopic dermatitis

Jeffrey P. Callen; Sarah L. Chamlin; Lawrence F. Eichenfield; Charles N. Ellis; M. Girardi; M. Goldfarb; Jon M. Hanifin; P. Lee; David J. Margolis; Amy S. Paller; D. Piacquadio; W. Peterson; K. Kaulback; M. Fennerty; Bruce U. Wintroub

364 million to


Journal of The American Academy of Dermatology | 2014

Guidelines of care for the management of atopic dermatitis: Section 4. Prevention of disease flares and use of adjunctive therapies and approaches

Robert Sidbury; Wynnis L. Tom; James N. Bergman; Kevin D. Cooper; Robert A. Silverman; Timothy G. Berger; Sarah L. Chamlin; David E. Cohen; Kelly M. Cordoro; Dawn Marie R. Davis; Steven R. Feldman; Jon M. Hanifin; Alfons Krol; David J. Margolis; Amy S. Paller; Kathryn Schwarzenberger; Eric L. Simpson; Hywel C. Williams; Craig A. Elmets; Julie Block; Christopher G. Harrod; Wendy Smith Begolka; Lawrence F. Eichenfield

3.8 billion US dollars per year. The cost of atopic dermatitis is significant and will likely increase in proportion to increasing disease prevalence. Measurement of the cost of atopic dermatitis in the United States has been limited to direct cost‐identification analyses, with few studies measuring the indirect cost of disease.

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Beth A. Drolet

Medical College of Wisconsin

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Denise W. Metry

Baylor College of Medicine

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Eulalia Baselga

Autonomous University of Barcelona

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Amy J. Nopper

Children's Mercy Hospital

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