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From the Medical Board of the National Psoriasis Foundation: Treatment targets for plaque psoriasis.
Armstrong, April W; Siegel, Michael P; Bagel, Jerry; Boh, Erin E; Buell, Megan; Cooper, Kevin D; Callis Duffin, Kristina; Eichenfield, Lawrence F; Garg, Amit; Gelfand, Joel M; Gottlieb, Alice B; Koo, John Y M; Korman, Neil J; Krueger, Gerald G; Lebwohl, Mark G; Leonardi, Craig L; Mandelin, Arthur M; Menter, M Alan; Merola, Joseph F; Pariser, David M; Prussick, Ronald B; Ryan, Caitriona; Shah, Kara N; Weinberg, Jeffrey M; Williams, MaryJane O U; Wu, Jashin J; Yamauchi, Paul S; Van Voorhees, Abby S.
Afiliação
  • Armstrong AW; Keck School of Medicine, University of Southern California, Los Angeles, California. Electronic address: aprilarmstrong@post.harvard.edu.
  • Siegel MP; National Psoriasis Foundation, Portland, Oregon.
  • Bagel J; Windsor Dermatology, East Windsor, New Jersey; University Medical Center of Princeton at Plainsboro, Plainsboro, New Jersey.
  • Boh EE; Tulane University School of Medicine, New Orleans, Louisiana.
  • Buell M; National Psoriasis Foundation, Portland, Oregon.
  • Cooper KD; University Hospitals Case Medical Center, Cleveland, Ohio.
  • Callis Duffin K; University of Utah School of Medicine, Salt Lake City, Utah.
  • Eichenfield LF; University of California, San Diego School of Medicine, La Jolla, California.
  • Garg A; Northwell Health and Hofstra North Shore University Hospital, Long Island Jewish Medical Center School of Medicine, Manhasset, New York.
  • Gelfand JM; University of Pennsylvania, Philadelphia, Pennsylvania.
  • Gottlieb AB; Tufts University School of Medicine, Boston, Massachusetts.
  • Koo JY; University of California San Francisco Medical Center, San Francisco, California.
  • Korman NJ; University Hospitals Case Medical Center, Cleveland, Ohio.
  • Krueger GG; University of Utah School of Medicine, Salt Lake City, Utah.
  • Lebwohl MG; Icahn School of Medicine at Mount Sinai, New York, New York.
  • Leonardi CL; St Louis University Medical School, St Louis, Missouri.
  • Mandelin AM; Northwestern University Feinberg School of Medicine, Chicago, Illinois.
  • Menter MA; Baylor University Medical Center and Texas A&M Health Science Center, Dallas, Texas.
  • Merola JF; Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Pariser DM; Eastern Virginia Medical School, Norfolk, Virginia; Virginia Clinical Research Inc, Norfolk, Virginia.
  • Prussick RB; George Washington University, Washington, District of Columbia.
  • Ryan C; Baylor University Medical Center and Texas A&M Health Science Center, Dallas, Texas.
  • Shah KN; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Weinberg JM; Icahn School of Medicine at Mount Sinai, New York, New York.
  • Williams MO; Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Wu JJ; Kaiser Permanente Los Angeles Medical Center, Los Angeles, California.
  • Yamauchi PS; Division of Dermatology, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, California.
  • Van Voorhees AS; Eastern Virginia Medical School, Norfolk, Virginia.
J Am Acad Dermatol ; 76(2): 290-298, 2017 Feb.
Article em En | MEDLINE | ID: mdl-27908543
ABSTRACT

BACKGROUND:

An urgent need exists in the United States to establish treatment goals in psoriasis.

OBJECTIVE:

We aim to establish defined treatment targets toward which clinicians and patients with psoriasis can strive to inform treatment decisions, reduce disease burden, and improve outcomes in practice.

METHODS:

The National Psoriasis Foundation conducted a consensus-building study among psoriasis experts using the Delphi method. The process consisted of (1) literature review, (2) pre-Delphi question selection and input from general dermatologists and patients, and (3) 4 Delphi rounds.

RESULTS:

A total of 25 psoriasis experts participated in the Delphi process. The most preferred instrument was body surface area (BSA). The most preferred time for evaluating patient response after starting new therapies was at 3 months. The acceptable response at 3 months postinitiation was either BSA 3% or less or BSA improvement 75% or more from baseline. The target response at 3 months postinitiation was BSA 1% or less. During the maintenance period, evaluation every 6 months was most preferred. The target response at every 6 months maintenance evaluation is BSA 1% or less.

LIMITATIONS:

Although BSA is feasible in practice, it does not encompass health-related quality of life, costs, and risks of side effects.

CONCLUSION:

With defined treatment targets, clinicians and patients can regularly evaluate treatment responses and perform benefit-risk assessments of therapeutic options individualized to the patient.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Psoríase Tipo de estudo: Guideline / Prognostic_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Psoríase Tipo de estudo: Guideline / Prognostic_studies Limite: Humans País/Região como assunto: America do norte Idioma: En Revista: J Am Acad Dermatol Ano de publicação: 2017 Tipo de documento: Article