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©The Author(s) 2024.
World J Clin Cases. Dec 26, 2024; 12(36): 6892-6904
Published online Dec 26, 2024. doi: 10.12998/wjcc.v12.i36.6892
Published online Dec 26, 2024. doi: 10.12998/wjcc.v12.i36.6892
Agent | Onset | Half-life | Metabolism | Special considerations |
Midodrine, desglymidodrine | 1 hour | 0.5 hour, 3-4 hours | Rapid deglycination to desglymidodrine | Avoid during bradycardia. Dose reductions necessary in renal dysfunction |
Droxidopa | 1 hour | 2-3 hours | Metabolized to norepinephrine via the catecholamine pathway | Recent data suggests that capsule may be opened and administered via feeding tube |
Pseudoephedrine | 0.5 hour | 3-16 hours1 | Not substantially metabolized | Dose reductions should be considered in renal dysfunction |
Atomoxetine | 1 hour | 5-24 hours2 | Hepatic, cytochrome P4502D6 (major) and cytochrome P450 family 2 subfamily C member 19 (minor) | Avoid during agitated delirium. Dose reductions necessary in hepatic dysfunction |
- Citation: Robinson JC, ElSaban M, Smischney NJ, Wieruszewski PM. Oral blood pressure augmenting agents for intravenous vasopressor weaning. World J Clin Cases 2024; 12(36): 6892-6904
- URL: https://www.wjgnet.com/2307-8960/full/v12/i36/6892.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v12.i36.6892