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Randomized controlled trial of urinE chemiStry guided aCute heArt faiLure treATmEnt (ESCALATE): Rationale and design.
Cox, Zachary L; Siddiqi, Hasan K; Stevenson, Lynne W; Bales, Brian; Han, Jin H; Hart, Kimberly; Imhoff, Brant; Ivey-Miranda, Juan B; Jenkins, Cathy A; Lindenfeld, JoAnn; Shotwell, Matthew S; Miller, Karen F; Ooi, Henry; Rao, Veena S; Schlendorf, Kelly; Self, Wesley H; Siew, Edward D; Storrow, Alan; Walsh, Ryan; Wrenn, Jesse O; Testani, Jeffrey M; Collins, Sean P.
Afiliação
  • Cox ZL; Department of Pharmacy, Lipscomb University College of Pharmacy, Nashville, TN; Department of Pharmacy, Vanderbilt University Medical Center, Nashville, TN. Electronic address: Zachary.l.cox@vumc.org.
  • Siddiqi HK; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Stevenson LW; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Bales B; Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Han JH; Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN; Geriatric Research, Education and Clinical Center, Tennessee Valley Healthcare System, TN.
  • Hart K; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN.
  • Imhoff B; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN.
  • Ivey-Miranda JB; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT; Hospital de Cardiologia, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
  • Jenkins CA; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN.
  • Lindenfeld J; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Shotwell MS; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN.
  • Miller KF; Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Ooi H; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN; Department of Medicine, Veterans Affairs Tennessee Valley Healthcare System, TN.
  • Rao VS; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT.
  • Schlendorf K; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Self WH; Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Siew ED; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Storrow A; Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Walsh R; Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Wrenn JO; Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Testani JM; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT.
  • Collins SP; Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, TN; Geriatric Research, Education and Clinical Center, Tennessee Valley Healthcare System, TN.
Am Heart J ; 265: 121-131, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37544492
Diuresis to achieve decongestion is a central aim of therapy in patients hospitalized for acute decompensated heart failure (ADHF). While multiple clinical trials have investigated initial diuretic strategies for a designated period of time, there is a paucity of evidence to guide diuretic titration strategies continued until decongestion is achieved. The use of urine chemistries (urine sodium and creatinine) in a natriuretic response prediction equation accurately estimates natriuresis in response to diuretic dosing, but a randomized clinical trial is needed to compare a urine chemistry-guided diuresis strategy with a strategy of usual care. The urinE chemiStry guided aCute heArt faiLure treATmEnt (ESCALATE) trial is designed to test the hypothesis that protocolized diuretic therapy guided by spot urine chemistry through completion of intravenous diuresis will be superior to usual care and improve outcomes over the 14 days following randomization. ESCALATE will randomize and obtain complete data on 450 patients with acute heart failure to a diuretic strategy guided by urine chemistry or a usual care strategy. Key inclusion criteria include an objective measure of hypervolemia with at least 10 pounds of estimated excess volume, and key exclusion criteria include significant valvular stenosis, hypotension, and a chronic need for dialysis. Our primary outcome is days of benefit over the 14 days after randomization. Days of benefit combines patient symptoms captured by global clinical status with clinical state quantifying the need for hospitalization and intravenous diuresis. CLINICAL TRIAL REGISTRATION: NCT04481919.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: Am Heart J Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: Am Heart J Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos