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Published on: July 28, 2018
A pilot randomised controlled trial evaluating the pharmacodynamic effects of furosemide versus acetazolamide in
Alastair Jw Brown1, Salvatore L Cutuli2, Glenn M Eastwood2
1Department of Intensive Care, Austin Hospital, Melbourne, VIC, Australia. alastair.brown3@austin.org.au.
Objective:
To compare the physiological and biochemical effects of a single intravenous dose of furosemide or acetazolamide in critically ill patients.
Design:
Single centre, pilot randomised controlled trial.
Setting:
Large tertiary adult intensive care unit (ICU).
Participants:
Twenty-six adult ICU patients deemed to require diuretic therapy.
Intervention:
Single dose of intravenous 40 mg furosemide or 500 mg acetazolamide.
Main Outcome Measures:
Data were collected on urine output, cumulative fluid balance, and serum and urine biochemistry for 6 hours before and 6 hours after diuretic administration.
Results:
Study patients had a median age of 55 years (IQR, 50-66) and median APACHE III score of 44 (IQR, 37-52). Furosemide caused a much greater increase in-urine output and much greater median mass chloride excretion (121.7 mmol [IQR, 81.1-144.6] 23.3 mmol [IQR, 20.4-57.3]; < 0.01) than acetazolamide. Furosemide also resulted in a progressively more negative fluid balance while acetazolamide resulted in greater alkalinisation of the urine (change in median urinary pH, +2 [IQR, 1.75-2.12] 0 [IQR, 0-0.5]; P = 0.02). In keeping with this effect, furosemide alkalinised and acetazolamide acidified plasma (change in median serum pH, +0.03 [IQR, 0.01-0.04] -0.01 [IQR, -0.04 to 0]; = 0.01; change in median serum HCO3-, +1.5 mmol/L [IQR, 0.75-2] -2 mmol/L [IQR, -3 to 0]; < 0.01).
Conclusions:
Furosemide is a more potent diuretic and chloriuretic agent than acetazolamide in critically ill patients, and achieves a threefold greater negative fluid balance. Compared with acetazolamide, furosemide acidifies urine and alkalinises plasma. Our findings imply that combination therapy might be a more physiological approach to diuresis in critically ill patients.
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