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Missed dose: difference between revisions

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Revision 3 — 10:13, 17 Oct 2024
Chromatokid (talk)
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Revision 4 — 13:36, 28 Oct 2024
PuffRemoverPax (talk)
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10For a weekly agent with a half-life of several days, the concentration at the end of a normal dosing interval has fallen to a substantial fraction of its peak, and a missed week extends that decline rather than producing a sudden loss of exposure. For a daily agent with a half-life of hours, a missed day is a larger proportional change but is corrected within a day or two of resuming.{{r|knudsen2019}}10For a weekly agent with a half-life of several days, the concentration at the end of a normal dosing interval has fallen to a substantial fraction of its peak, and a missed week extends that decline rather than producing a sudden loss of exposure. For a daily agent with a half-life of hours, a missed day is a larger proportional change but is corrected within a day or two of resuming.{{r|knudsen2019}}
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+12Prescribing information for individual products states how a missed dose is to be handled, and those statements differ between products; general treatment guidance does not attempt to supply a single rule.{{r|ada2024}} This article describes the pharmacokinetic reasoning; it is not medical advice, and it is not a substitute for the labelling of any particular product. See [[Prescribing information]].{{r|drucker2018}}
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12== The governing arithmetic ==14== The governing arithmetic ==
13After a dose, concentration falls by half each half-life. For a peptide with a half-life of seven days on a weekly schedule, trough concentration is about half the peak and steady-state accumulation is roughly two-fold. Omitting one dose allows a further halving before the next dose is taken.{{r|knudsen2019}}15After a dose, concentration falls by half each half-life. For a peptide with a half-life of seven days on a weekly schedule, trough concentration is about half the peak and steady-state accumulation is roughly two-fold. Omitting one dose allows a further halving before the next dose is taken.{{r|knudsen2019}}
20| ≈2.4 hours | Twice daily | Essentially complete |22| ≈2.4 hours | Twice daily | Essentially complete |
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+24The final row explains why short-acting agents lose effect promptly on omission and long-acting agents do not. It also explains why a resumed long-acting agent does not need re-titration after a short gap while a resumed short-acting one may.{{r|drucker2018,lau2015}}
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22== References ==26== References ==
23{{reflist}}27{{reflist}}
24<ref name="drucker2018">Drucker DJ. "Mechanisms of action and therapeutic application of glucagon-like peptide-1." ''Cell Metabolism'' 27(4):740–756 (2018). PMID 29617641.</ref>28<ref name="drucker2018">Drucker DJ. "Mechanisms of action and therapeutic application of glucagon-like peptide-1." ''Cell Metabolism'' 27(4):740–756 (2018). PMID 29617641.</ref>
25<ref name="knudsen2019">Knudsen LB, Lau J. "The discovery and development of liraglutide and semaglutide." ''Frontiers in Endocrinology'' 10:155 (2019). PMID 31031702.</ref>29<ref name="knudsen2019">Knudsen LB, Lau J. "The discovery and development of liraglutide and semaglutide." ''Frontiers in Endocrinology'' 10:155 (2019). PMID 31031702.</ref>
+30<ref name="ada2024">American Diabetes Association. "Pharmacologic approaches to glycemic treatment: Standards of Care in Diabetes." ''Diabetes Care'' 47(Suppl 1) (2024).</ref>
+31<ref name="lau2015">Lau J, Bloch P, Schäffer L, et al. "Discovery of the once-weekly glucagon-like peptide-1 analog semaglutide." ''Journal of Medicinal Chemistry'' 58(18):7370–7380 (2015). PMID 26308095.</ref>
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27{{DEFAULTSORT:Missed dose}}33{{DEFAULTSORT:Missed dose}}