2018
DOI: 10.1016/j.jchf.2017.10.001
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Efficacy of Intravenous Furosemide Versus a Novel, pH-Neutral Furosemide Formulation Administered Subcutaneously in Outpatients With Worsening Heart Failure

Abstract: 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).

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Cited by 58 publications
(36 citation statements)
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“…The TRANSFORM‐HF will assess the superiority of torsemide in comparison to furosemide in reducing all‐cause mortality. Furthermore, ongoing studies are testing the effect of subcutaneous furosemide in comparison to oral furosemide …”
Section: Gaps In Knowledge and Future Directionsmentioning
confidence: 99%
“…The TRANSFORM‐HF will assess the superiority of torsemide in comparison to furosemide in reducing all‐cause mortality. Furthermore, ongoing studies are testing the effect of subcutaneous furosemide in comparison to oral furosemide …”
Section: Gaps In Knowledge and Future Directionsmentioning
confidence: 99%
“…There are several trials ongoing, including ADVOR (testing acetazolamide – NCT03505788), TRANSFORM‐HF (testing torsemide vs. furosemide – NCT03296813), EMPA‐RESPONSE‐AHF (testing empagliflozin in acute HF – NCT03200860), and a trial of metolazone vs. chlorothiazide (NCT03574857). The development of user‐friendly systems to deliver subcutaneous furosemide will require evaluation in clinical trials …”
Section: Pharmacotherapymentioning
confidence: 99%
“…The development of user-friendly systems to deliver subcutaneous furosemide will require evaluation in clinical trials. 38,39…”
Section: Supporting Evidencementioning
confidence: 99%
“…Aiming to further reduce healthcare utilization and to improve quality of life, a novel, pH-neutral subcutaneous formulation of furosemide has recently been developed. In a small, phase II, proof of concept study, a total of 80 mg furosemide was injected under the skin over 5 hours using an automated infusion pump (35). Upon direct comparison to a dose adjusted, single traditional IV furosemide injection, the new formulation provided comparable urine output with a more sustained diuretic effect.…”
Section: Subcutaneous Furosemide Therapymentioning
confidence: 99%