An honest declaration on building a sensible monitoring schedule: I have a prior here and it is strong enough that you should weight what I say downward. Stating it rather than hiding it.
Building a sensible monitoring schedule with your prescriber posts 91–109
This is a continuation of a long topic, addressed by post number rather than by page. Start at post 1.
Time of day: some biomarkers vary across the day. Cortisol in the morning differs from cortisol in the evening. Comparing results from different times of day is comparing things that are not the same.
Stating my assumptions rather than smuggling them in.
Distinguishing three things in the building a sensible monitoring schedule discussion that keep getting used interchangeably: the observation, the proposed mechanism, and the recommendation that gets attached to both.
Understood. Thank you for being specific about the limits of it.
Everything in post #94 holds. The case it does not cover is the one I have.
What I would tell a new member reading about building a sensible monitoring schedule for the first time: the confident posts are not the reliable ones, and the reliable ones are longer.
Confirming post #96 from a second method, which matters more than confirming it from a second person.
Glycaemic markers integrate over different periods. A point glucose and a longer-term marker disagreeing is not a contradiction; it is two different questions.
Not a conclusion. A place to stand while looking for one.
A trend needs at least three points to be a trend. Two points are a line and a line through noise is still a line.
Worth saying I have only my own numbers here, and n is small.
I would keep building a sensible monitoring schedule and the decision it usually gets used for separate in this thread. They are related and they are not the same question, and merging them is why the last one went badly.
Post #100 describes the usual case. This is about the unusual one.
Repeat before acting is standard practice for an isolated abnormal result on most analytes, and it is standard for a reason.
I have written this out at length because the short version keeps being misread.
On building a sensible monitoring schedule the community has more anecdote than the confidence in this thread implies, and I include my own contribution in that.
The practical version of building a sensible monitoring schedule is three sentences long. The rigorous version is three pages and reaches the same conclusion with the conditions attached.
A trend needs at least three points to be a trend. Two points are a line and a line through noise is still a line.
I would treat that as a working assumption and revisit it.
Grateful for the specificity. Vague answers to this question are what sent me looking.
Post #105 is the version of this I will quote in future. One addition.
Careful with the language on building a sensible monitoring schedule. "Not detected" and "not present" are different findings and the first is a statement about the method.
Building a sensible monitoring schedule looks different depending on whether you are reading the primary literature or the summaries of it, and the difference is not in our favour.
Glycaemic markers integrate over different periods. A point glucose and a longer-term marker disagreeing is not a contradiction; it is two different questions.
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