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Vasopressin antagonism for decompensated right-sided heart failure.
Vidic, Andrija; Shuster, Jerrica E; Goff, Zackary D; Godishala, Anuradha; Joseph, Susan M; Chibnall, John T; Hauptman, Paul J.
Afiliação
  • Vidic A; The Department of Medicine, Florida Hospital, Orlando, FL, United States of America.
  • Shuster JE; The Department of Pharmacy, Barnes Jewish Hospital, St. Louis, MO, United States of America.
  • Goff ZD; The Department of Medicine, Johns Hopkins University, Baltimore, MD, United States of America.
  • Godishala A; The Department of Medicine, Barnes Jewish Hospital, St. Louis, MO, United States of America.
  • Joseph SM; The Department of Medicine, Baylor University, Dallas, TX, United States America.
  • Chibnall JT; The Department of Medicine, Saint Louis University, St. Louis, MO, United States of America.
  • Hauptman PJ; The Department of Medicine, Saint Louis University, St. Louis, MO, United States of America. Electronic address: hauptmpj@slu.edu.
Int J Cardiol ; 274: 245-247, 2019 Jan 01.
Article em En | MEDLINE | ID: mdl-30193794
ABSTRACT

BACKGROUND:

Targeted treatment for decompensated right heart failure (RHF) with or without left heart failure is lacking. Vasopressin antagonists (vaptans) may offer an option by increasing urine output and fluid mobilization when used in acute decompensated RHF without impacting blood pressure or renal function, both common complications of loop diuretics. METHODS AND

RESULTS:

We searched electronic medical records from 2 institutions over 4 years for patients with RHF treated with vaptans. Urine output, creatinine, BUN and sodium, 1 day pre- versus 1 day post-vaptan initiation were compared. Baseline (admission) pre-vaptan values for patients with RHF who met inclusion criteria (n = 112) were RAP, median (interquartile range) = 19 (13-24) mmHg; cardiac index, mean ±â€¯standard deviation = 1.8 ±â€¯0.4 L/min/m2; BNP, 1078 (523-1690) pg/ml; creatinine clearance of 51 (39-69) ml/min, BUN, 37 (26-54) mg/dl, and serum [Na+] 132 (126-135) mEq/L. Most patients (n = 103/112) received intravenous inotrope (prior to vaptan, n = 91). Overall length of stay was 27 (16-43) days. Vaptan treatment (90% tolvaptan, 10% conivaptan) was associated with increased 24 h urine output, 1517 (906-2394) vs 2337 (1425-3744) mL, p = 0.005, and [Na+], 127 (124-130) vs 130 (126-135) mEq/L, p = 0.001, without significant change in Cr or BUN. Furosemide IV dose equivalent decreased or remained unchanged in 75% of patients at 24 h and 64% at 72 h compared to the 24 h prior to vaptan use.

CONCLUSION:

Vaptans were associated with a significant increase in urine output and serum sodium with an apparent reduction or stabilization of furosemide equivalent dosing in the early treatment period in patients with decompensated RHF. Vaptans may offer a management option for patients failing conventional diuretic-based treatment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Função Ventricular Direita / Antagonistas dos Receptores de Hormônios Antidiuréticos / Insuficiência Cardíaca Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Volume Sistólico / Função Ventricular Direita / Antagonistas dos Receptores de Hormônios Antidiuréticos / Insuficiência Cardíaca Idioma: En Ano de publicação: 2019 Tipo de documento: Article