Weight regain is not a failure of willpower and it is not a mystery
The variance around the mean regain trajectory is large and unexplained, exactly as it is for the weight loss.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 7 of 8 of this archive, newest first.
The variance around the mean regain trajectory is large and unexplained, exactly as it is for the weight loss.
The regain trajectories, arm by arm, with the estimands named.
A supply interruption is a discontinuation with no notice, no taper and no plan. That is a distinct clinical situation.
A supply interruption is a discontinuation with no notice, no taper and no plan. That is a distinct clinical situation.
Regain begins immediately, proceeds at a decelerating rate, and does not usually return to baseline within the observed follow-up. Each of those three clauses matters.
Every withdrawal trial compared full dose against nothing. The clinically interesting comparison — full dose against a reduced one — has not been randomised.
Almost every practical recommendation in circulation was established in a population that does not resemble the people now following it.
Cost is the modal reason for discontinuation in every dataset we have seen, and it is absent from the clinical literature.
These agents produce no dependence and no withdrawal syndrome. What a taper would be for is therefore a real question rather than an obvious one.
Three randomised withdrawal designs have tested what happens when treatment stops. Their results are consistent and they are consistently misreported.
The schedules in circulation, described accurately, with their evidentiary status attached.
The gap between a defensible recommendation and a confident one is where most of the harm in this subject lives.
A supply interruption is a discontinuation with no notice, no taper and no plan. That is a distinct clinical situation.
Why the reason for stopping changes what happens afterwards.
Every withdrawal trial compared full dose against nothing. The clinically interesting comparison — full dose against a reduced one — has not been randomised.
These agents produce no dependence and no withdrawal syndrome. What a taper would be for is therefore a real question rather than an obvious one.
The commonest real-world strategy in this drug class is the least studied one.
The evidence on stopping is better than the evidence on almost anything else in this field, because somebody deliberately randomised it.
Cost is the modal reason for discontinuation in every dataset we have seen, and it is absent from the clinical literature.
The gap between a defensible recommendation and a confident one is where most of the harm in this subject lives.