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1.
Cleve Clin J Med ; 86(9): 621-632, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31498768

ABSTRACT

Cardiovascular disease has been the leading cause of death in the United States since the early 20th century. With advances in prevention and treatment, cardiovascular mortality rates are on the decline. Nevertheless, disparities in care persist, with devastating impact in select populations in the United States. This paper reviews the impact of disparate care on risk-factor burden, coronary artery disease, heart failure, and cardiovascular research.


Subject(s)
Cardiovascular Diseases/mortality , Coronary Artery Disease/mortality , Healthcare Disparities/trends , Cardiovascular Diseases/etiology , Coronary Artery Disease/etiology , Cost of Illness , Humans , Risk Factors , United States/epidemiology
2.
JACC Heart Fail ; 6(1): 65-70, 2018 01.
Article in English | MEDLINE | ID: mdl-29226816

ABSTRACT

OBJECTIVES: This study sought to determine the efficacy and safety of a novel, pH-neutral formulation of furosemide administered subcutaneously (SC) for treatment of acute decompensated heart failure (HF). BACKGROUND: Congestion requiring intravenous (IV) administration of a diuretic agent is the main reason patients with HF present for acute medical care. METHODS: Outpatients presenting with decompensated HF were randomized to receive a single SC or IV dose of furosemide. Primary outcome was 6-h urine output, and secondary outcomes were weight change, natriuresis, and adverse events. RESULTS: Forty-one patients were randomized: 19 were treated with IV (mean dose: 123 ± 47 mg) and 21 with SC furosemide (fixed dose of 80 mg over 5 h). The 6-h urine output in the IV group was not significantly different from that in the SC furosemide group (median IV: 1,425 ml; interquartile range [IQR]: 1,075 to 1,950 ml; vs. median SC: 1,350 ml; IQR: 900 to 1,900 ml; p = 0.84). Additionally, mean weight loss was not significantly different (-1.5 ± 1.1 kg in the IV group vs. -1.5 ± 1.2 kg in the SC group; p = 0.95). Hourly urine output was significantly higher in the IV group at hour 2 (425 ml in the IV group vs. 250 ml in the SC group; p = 0.02) and higher in the SC group at hour 6 (125 ml, IV group vs. 325 ml, SC group; p = 0.005). Natriuresis was higher in the SC group (IV: 7.3 ± 35.3 mEq/l vs. SC: 32.8 ± 43.6 mEq/l; p = 0.05). There was no worsening renal function, ototoxicity, or skin irritation with either formulation. Thirty-day hospitalization rates were similar. CONCLUSIONS: In this phase II trial, we did not identify significant differences between urine output obtained with pH-neutral furosemide administered SC and that obtained by IV. This method of decongestion may allow treatment at home and reduced HF resources and warrants further investigation. (Sub-Q Versus IV Furosemide in Acute Heart Failure; NCT02579057).


Subject(s)
Furosemide/administration & dosage , Heart Failure/drug therapy , Outpatients , Acute Disease , Diuretics/administration & dosage , Dose-Response Relationship, Drug , Female , Follow-Up Studies , Heart Failure/metabolism , Heart Failure/physiopathology , Humans , Hydrogen-Ion Concentration , Injections, Intravenous , Injections, Subcutaneous , Male , Middle Aged , Natriuresis/drug effects , Pilot Projects , Stroke Volume/physiology , Treatment Outcome
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