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Pilot phase results of a prospective, randomized controlled trial of narrowband ultraviolet B phototherapy in hospitalized COVID-19 patients.
Lau, Frank H; Powell, Catherine E; Adonecchi, Giacomo; Danos, Denise M; DiNardo, Andrew R; Chugden, Robert J; Wolf, Peter; Castilla, Carmen F.
Afiliação
  • Lau FH; Department of Surgery, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, USA.
  • Powell CE; Department of Surgery, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, USA.
  • Adonecchi G; School of Medicine, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, USA.
  • Danos DM; School of Public Health, Louisiana State University Health Sciences Center New Orleans, New Orleans, Louisiana, USA.
  • DiNardo AR; Baylor College of Medicine, Global TB program and William T Shearer Center for Human Immunobiology, Houston, Texas, USA.
  • Chugden RJ; West Jefferson Medical Center, Marrero, Louisiana, USA.
  • Wolf P; Department of Dermatology, Medical University of Graz, Graz, Austria.
  • Castilla CF; New York Dermatology Group; Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Exp Dermatol ; 31(7): 1109-1115, 2022 07.
Article em En | MEDLINE | ID: mdl-35638295
COVID-19 morbidity and mortality are driven by poor immune regulation. Narrowband ultraviolet B (NB-UVB) phototherapy is standard of care in a number of immune-dysregulated diseases. To assess the efficacy of NB-UVB phototherapy for improving COVID-19 outcomes in high-risk, hospitalized, we developed the Adaptive Photo-Protection Trial. This is a multi-center, prospective, double-blinded, randomized, placebo-controlled trial. The pilot phase results are reported here. Consecutive patients admitted with a positive COVID-19 PCR were screened for eligibility. Enrolled subjects were computer randomized 1:1 to NB-UVB or placebo phototherapy. Subjects were treated daily with escalating doses on 27% of their body surface area for up to 8 consecutive days. Primary outcomes were safety and efficacy, defined as persistent or painful erythema and 28-day mortality. Comparisons were made via non-parametric exact tests. Patients in treatment (n = 15) and placebo (n = 15) arms had similar demographics. No adverse events occurred. Twenty eight-day mortality was 13.3% in treatment vs. 33.3% in placebo arms (p = 0.39). NB-UVB phototherapy in hospitalized COVID-19 patients was safe. Decreased mortality was observed in treated patients but this was statistically non-significant. Given its low-cost, scalability, and adjunctive nature, NB-UVB has the potential to improve COVID-19 outcomes. Continuation of this trial is warranted.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terapia Ultravioleta / COVID-19 Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terapia Ultravioleta / COVID-19 Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article