A reference interval is not a target, and a result outside one is not a diagnosis
Two sources of noise sit under every number: how reproducible the assay is, and how much the analyte varies within the same person on the same day.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Laboratory panels before, during and after treatment, and which changes are findings rather than artefacts.
Two sources of noise sit under every number: how reproducible the assay is, and how much the analyte varies within the same person on the same day.
Timing is the whole of the post-cessation panel: draw it too early and it measures the treatment period.
The arithmetic of the reference change value, worked for the analytes that matter here.
A monitoring schedule requires evidence about incidence. For this population, that evidence does not exist.
What the renal and hepatic outcome programmes actually measured, and over what duration.
Reduced intake is a plausible mechanism for deficiency. Reduced absorption is not, and the two are conflated in most of the advice.
A substantial proportion of the abnormal results generated during rapid weight loss are consequences of the weight loss rather than findings about the person.
The argument for a baseline panel is that it makes every subsequent result interpretable. The argument against frequent monitoring is that noise accumulates faster than…
A substantial proportion of the abnormal results generated during rapid weight loss are consequences of the weight loss rather than findings about the person.
HbA1c integrates roughly three months of glycaemia with the most recent weeks weighted most heavily. Almost every misreading of it is a misreading of that weighting.
A twelve-analyte panel in a perfectly healthy person has roughly even odds of producing at least one flagged result.
The alternatives with shorter windows, what they measure, and why they are rarely ordered.
A flag is a probability statement about a population. It is not a statement about the person holding the printout.
Reduced intake is a plausible mechanism for deficiency. Reduced absorption is not, and the two are conflated in most of the advice.
The assay is not the problem. The interpretation of a lagging integral as a current measurement is the problem.
The argument for a baseline panel is that it makes every subsequent result interpretable. The argument against frequent monitoring is that noise accumulates faster than…
Two sources of noise sit under every number: how reproducible the assay is, and how much the analyte varies within the same person on the same day.
Estimated glomerular filtration rate is a calculation with muscle mass in the denominator of its assumptions. In this population that matters.
Micronutrient guidance for this drug class is borrowed almost entirely from post-bariatric surveillance, where the anatomy is different and the deficiency mechanisms are not…
Two sources of noise sit under every number: how reproducible the assay is, and how much the analyte varies within the same person on the same day.