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Assessing Guideline-Directed Medication Therapy for Heart Failure in End-Stage Renal Disease.
Cutshall, B Tate; Duhart, Benjamin T; Saikumar, Jagannath; Samarin, Michael; Hutchison, Lydia; Hudson, Joanna Q.
Afiliação
  • Cutshall BT; The University of Alabama at Birmingham Medical Center, Birmingham, AL.
  • Duhart BT; Department of Clinical Pharmacy and Translational Science, The University of Tennessee College of Pharmacy, Memphis, TN.
  • Saikumar J; Department of Medicine (Nephrology), The University of Tennessee, Memphis, TN.
  • Samarin M; Department of Pharmacy, Methodist University Hospital, Memphis, TN.
  • Hutchison L; Department of Pharmacy, Methodist University Hospital, Memphis, TN.
  • Hudson JQ; Department of Clinical Pharmacy and Translational Science, The University of Tennessee College of Pharmacy, Memphis, TN; Department of Medicine (Nephrology), The University of Tennessee, Memphis, TN. Electronic address: jhudson@uthsc.edu.
Am J Med Sci ; 355(3): 247-251, 2018 03.
Article em En | MEDLINE | ID: mdl-29549927
ABSTRACT

BACKGROUND:

Treatment of heart failure with reduced ejection fraction (HFrEF) requires guideline-directed medication therapy (GDMT) consisting of either an angiotensin-converting enzyme inhibitor or an angiotensin receptor blocker in combination with an indicated beta-blocker. There is concern that end-stage renal disease (ESRD) patients are not being prescribed GDMT. The study aim was to determine whether outcomes differ for patients with HFrEF and ESRD receiving GDMT compared to those not receiving GDMT. MATERIALS AND

METHODS:

Adult patients with ESRD and HFrEF admitted to a tertiary teaching hospital over a 2-year period were included. Patients were categorized into GDMT or non-GDMT groups based on their home medications. The length of stay (LOS), mortality, and 30-day hospital readmissions were compared between groups. The incidence of hyperkalemia, hypotension and bradycardia were also evaluated.

RESULTS:

A total of 109 patients were included 88% African-American, 61% males, median age 63 (28-93) years with 25 in the GDMT group and 84 in the non-GDMT group. The LOS did not differ between the GDMT (5 days; 3-14) compared to the non-GDMT group (7 days; 3-28), P = 0.14. Thirty-day hospital readmission and in-hospital mortality were also similar. Hypotension occurred less frequently in the GDMT group compared to the non-GDMT group, 4% versus 27% (P = 0.01).

CONCLUSIONS:

Although there were no differences in the primary outcomes, the shorter LOS in the GDMT group may be clinically significant. The fact that most patients with ESRD and HFrEF were not receiving GDMT is a finding that requires further evaluation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores da Enzima Conversora de Angiotensina / Antagonistas Adrenérgicos beta / Fidelidade a Diretrizes / Antagonistas de Receptores de Angiotensina / Insuficiência Cardíaca Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores da Enzima Conversora de Angiotensina / Antagonistas Adrenérgicos beta / Fidelidade a Diretrizes / Antagonistas de Receptores de Angiotensina / Insuficiência Cardíaca Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2018 Tipo de documento: Article