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just curious
None. The total I've ever had is probably less than 10. This is me being an attending for about 5-6 years and having some very treatment resistance patients. My biggest obstacle with it was the bridge for weeks with no antidepressant on someone that was already doing very bad. I'd rather try Venlafaxine + Mirtazapine before trying an MAO-I.
None. The total I've ever had is probably less than 10. This is me being an attending for about 5-6 years and having some very treatment resistance patients. My biggest obstacle with it was the bridge for weeks with no antidepressant on someone that was already doing very bad. I'd rather try Venlafaxine + Mirtazapine before trying an MAO-I.
I agree - that's why I haven't really had qualms about doing it when needed - if the antidepressant isn't working, then I'm not too worried about stopping it for a few days.1. If someone were considered for an MAOI, I'd imagine most people would have considered them treatment resistant and non-responders. Would the lack of an antidepressant onboard, that has proven ineffective in the patient, really matter?
In the STARD study, there was an arm that found venlafaxine+mirtazapine to be superior to tranylcypromine, both at therapeutic doses. I always try that before going to a MAOI. I've started a MAOI twice now, and both of them were already on venlafaxine, so the bridge was shorter because venlafaxine is short-acting. One was also on bupropion, which is also short-acting. The other was also on buspirone, which is also short-acting. One had been on mirtazapine but d/c'd because she didn't like the appetite stimulation. The other didn't want mirtazapine because of the appetite stimulation risk.2. A big gap between SNRI + mirtazapine and MAOI. Do you not see this utilized that often?
In the STARD study, there was an arm that found venlafaxine+mirtazapine to be superior to tranylcypromine, both at therapeutic doses. I always try that before going to a MAOI. I've started a MAOI twice now, and both of them were already on venlafaxine, so the bridge was shorter because venlafaxine is short-acting. One was also on bupropion, which is also short-acting. The other was also on buspirone, which is also short-acting. One had been on mirtazapine but d/c'd because she didn't like the appetite stimulation. The other didn't want mirtazapine because of the appetite stimulation risk.
I believe the STAR-D trial was flawed. If memory serves me correctly, there was a 2 week washout period for the MAOI and then there was an up titration period. Both of these occurred during the 4 week trial period. Thus, subjects were not at the recommended dose of the MAOI for much longer than 1 week.
Ha... you don't have any patients on linezolid long-term as an antidepressant, do you?Including linezolid?
Ha... you don't have any patients on linezolid long-term as an antidepressant, do you?
MRSA pneumonia can be kind of a downer... but no, not long term as an antidepressant per se...
I did have an interesting consult recently regarding discontinuing a patient's home SSRI during a prolonged course of linezolid. Since they were in-house for the foreseeable future we recc-ed continuing the home med, but monitoring closely for signs of seritonergic excess.
Does it really have to be two weeks on an inpatient basis if the patient isn't on Prozac? You could monitor them for side effects more closely...None, but I work in inpatient, so taking patients off meds for two weeks isn't really an option.
Not much love for Emsam in this thread apparently. ...
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Quick question for the group:
We know that clozapine is a reasonable/best option for TR Schizophrenia after 2 full adequate trials of an AP. STARD gave us multiple combo/switch strategies with diminishing returns. Knowing that, it seems ECT should be a discussion long before we get to an MAOI, no?
parnate and nardil inhibit both MAO isoforms. At doses used in depression, selegiline inhibits both MAO-A and -B. If using oral selegiline dose for parkisons is 5mg bid, for depression it is 15-30mg bid. I have treated patients with 60mg selegiline daily. It has a more favorable side-effect profile than the older MAOIs. I haven't used EMSAM yet because it's been cheaper for my patients to take the oral version.Because selegiline perferentially inhibits MAO-B, while Parnate and Nardil inhibit MAO-A. MAO-A has combined serotonin/norepinephrine/dopamine activity, while MAO-B is mostly dopaminergic. That's why selegiline is better for Parkinson's and also why we are less likely to use it for depression.
Does it really have to be two weeks on an inpatient basis if the patient isn't on Prozac? You could monitor them for side effects more closely....
Does it really have to be two weeks on an inpatient basis if the patient isn't on Prozac? You could monitor them for side effects more closely...
Doxepin is a TCA...I've started MAOIs, most often selegiline and doxepin. I've used other MAOIs, but less frequently.
In my opinion, psychiatrists tend to have disproportionately high thresholds to start MAOIs and low thresholds to start antipsychotics.