Apostacious
Bluelighter
I know that benzodiazepine withdrawal is a tired old subject. I hope that there might be some that have gone through a couple treatments and to see what the long-term effects as well as short-term effects that two treatments for intense benzodiazepine withdrawal are.
The only true drug that can help alleviate benzodiazepine withdrawal in patients has been flumazenil. As some may know this is a benzodiazepine antagonist and has the ability to reset the whole spectrum of gaba receptors within the brain. My main concern with this is the alarming lack of research and use of this method on patients. I've never come across a negative result from flumazenil, but there are no long-term checkups with patients to see if withdrawal symptoms dissipated entirely. Perhaps this can mean a good thing since patients do have the means to spread anything negative of the flumazenil treatment through various venues.
Since the medical community worldwide is in the dark ages when it comes to gaba-ergic drug withdrawal (well, for the most part benzodiazepine withdrawal, since benzodiazepines are used to treat alcohol, ghb, gbl, barbiturate, etc withdrawal therefore patients are stuck with another gaba-ergic addiction that isn't lethal when continuously prescribed) then flumazenil treatments are much more rare and the studies are as well.
Another temporary treatment that is rarely used, but is successful at least in detaching the person from benzodiazepine withdrawal without administration of a substance that causes dependence is through the use of nmda antagonists. I assume the issuing of ketamine to a patient (instead of another gaba-ergic drug to induce anaesthesia which can create a kindling effect on withdrawals) is to temporarily constrict the release of glutamate levels in the brain through nmda receptors. Glutamate is the primary reason patients go into seizures during gaba-ergic withdrawals since sensitivities of glutamte are drastically increased during an abrupt cessation of a benzodiazepine. I've yet to see a study where an nmda antagonist is administrated more than once. I assume this is to avoid delirium to an extent. But more information would be nice since I can't find anything of note.
The only true drug that can help alleviate benzodiazepine withdrawal in patients has been flumazenil. As some may know this is a benzodiazepine antagonist and has the ability to reset the whole spectrum of gaba receptors within the brain. My main concern with this is the alarming lack of research and use of this method on patients. I've never come across a negative result from flumazenil, but there are no long-term checkups with patients to see if withdrawal symptoms dissipated entirely. Perhaps this can mean a good thing since patients do have the means to spread anything negative of the flumazenil treatment through various venues.
Since the medical community worldwide is in the dark ages when it comes to gaba-ergic drug withdrawal (well, for the most part benzodiazepine withdrawal, since benzodiazepines are used to treat alcohol, ghb, gbl, barbiturate, etc withdrawal therefore patients are stuck with another gaba-ergic addiction that isn't lethal when continuously prescribed) then flumazenil treatments are much more rare and the studies are as well.
Another temporary treatment that is rarely used, but is successful at least in detaching the person from benzodiazepine withdrawal without administration of a substance that causes dependence is through the use of nmda antagonists. I assume the issuing of ketamine to a patient (instead of another gaba-ergic drug to induce anaesthesia which can create a kindling effect on withdrawals) is to temporarily constrict the release of glutamate levels in the brain through nmda receptors. Glutamate is the primary reason patients go into seizures during gaba-ergic withdrawals since sensitivities of glutamte are drastically increased during an abrupt cessation of a benzodiazepine. I've yet to see a study where an nmda antagonist is administrated more than once. I assume this is to avoid delirium to an extent. But more information would be nice since I can't find anything of note.