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Psyclops said:Please discuss cogwheeling. I've rarely seen such a weird thing.
Solideliquid said:Although I wonder how giving something like Levodopa will interfere with a neuroleptic and or it's efficacy.
Doc Samson said:Badly... hallucinations are a common side effect with sinemet... full blown psychosis in overdose.
Solideliquid said:Cogwheeling, or muscle regidity at rest is part of parkinsonism. Probably due to the neuroleptic D2 blockage resulting in to much acetylcholine.
You can give cogentin or another anti-cholinergic drug. Or even parkinsons drugs for it.
Although I wonder how giving something like Levodopa will interfere with a neuroleptic and or it's efficacy.
Solideliquid said:Can you explain the pathophys behind the others? (Akathesia, Dystonia, and TD)
Thanks Samson!
It's fairly common on inpatient units.Psyclops said:Please discuss cogwheeling. I've rarely seen such a weird thing.
Poety said:Is this on a test Solid?![]()
pathophys freak 😱 😀 😛
Psyclops said:Thanks everyone, but I knew what casued it generally, being EPS and all. And I knew it could be treated with cogentin or another anti-cholinergic. What I was hoping to get is why it occurs in the "click, click, click" way, I find that so creepy.
Don't you remember the interns? They're the ones with the "deer caught int he headlights" syndrome 
Anasazi23 said:Some neurology texts classify cogwheeling as a variation of tremor, with the manifestation visible upon testing - either by wrist rotating or flexion of the arm. Evidence for this comes from that fact that cogwheeling can be seen in tremors without muscle tone increase.
Essential tremor, for example, demonstrates this finding.
If you approach these symptoms (dystonia, cogwheeling) from a Parkinson's perspective, it becomes more evident that this is a phenomena associated with a drop in intracerebral dopamine (<50% of normal). Subsequent mismatch of dopamine/cholinergic activity then contributes to symptoms.
The pathophysiology (stretch receptors, golgi tendon organs, etc, flower spray, annulospiral end organs) of the various symptoms are difficult to ascertain due to the differences in anatomic distrubition and individual differences in postsynaptic receptors for dopamine (of which there are 4 types).
