Guest guest Posted May 7, 2008 Report Share Posted May 7, 2008 (I'm updating Geri Hall's post so that I can keep saving them in the links w/out having her expired contact info on the post) " I am not trying to be sanctimonious here but wanted to comment about some of the things said this week: 1. Medications. Everything we know about mood controlling medications is changing dramatically in the past few weeks. In the recent past we had four atypical antipsychotics that we could use because the were " relatively safe " from Parkinsonain side-effects and neurleptic malignant syndrome. In the last few months [disclaimer = original post from 2003] we know that they produce many of the same side-effects as the typical antipsychotics...although perhaps some not as frequently. Thus the recent claims by Janssen that Risperdal has never been shown to be safe or effective with psychosis in the aged (although those of us who have been using it forever HAVE found it to be relatively safe and effective). So, to date we now have Seroquel -- which has very mixed results with LBD -- and Zyprexa -- which tends to zombify and change blood sugar. We have Geodon but that may cause some cardiac side-effects. And we have Clonazepam which tends to increase the patient's white blood cell count and blood should be drawn every week (or at very minimum every two weeks) for six months. This leaves us with a problem. There really are no " safe " drugs. The person with LBD tends to be extra sensitive to any medications that can have central nervous system (brain) side-effects. This may be due to the " most vulnerable system theory " of aging, whereby whenever a person is ill their most vulnerable system (the brain in LBD) takes the biggest hit in terms of symptoms. Most of these drugs affect not only the limbic system (where memory, perception, etc is found), but also the pyramidal tract (which means the person develops an associated movement disorder). NONE of these medications has been designed for or tested in people with LBD (or even AD -- except Ripseral which is now identified as too dangerous to use). So what the professional does is work VERY closely with the family and psychiatrists to develop a regimen that is least restrictive in terms of somnolence/chemical restraint, but helps the patient to be comfortable, not frightened, and safe to be around. So, with DLB patients who are very psychotic we usually see odd regimens, including a cholinergic, an atypical antipsychotic, a short-acting benzodiazapine, and or an SSRI antidepressant. And even then the control is not too good. One of the biggest issues is that once we get a medication regimen that is sort of working (after a lot of fine tuning) the minute someone from a nursing home tries to decrease it, all bets are off. We rarely see the same regimen in the rechallenge because the patient's response to it changes. Second is the issue of how long it takes the medications to work. The antipsychotics are tricky in that what you see for the first one to two weeks are the side-effects. It can take three to six weeks before you see the true effects of the drug. So for the first 48 hours the patient may be sleepy...but the med was given because the patient was up for days agitated and is actually physically exhausted. So the side-effect of drowsiness hits hard. The patient seems zombified, but does wake up in a few days. Our problem is getting families through that period without stopping the medication. 2. Violence/aggression LBD compared to most other dementias has the unique quality of producing a patient who has a high vulnerability to violent/aggressive behavior. Over the years I have had one caregiver killed and many many wounded. It is not unusual to be called by a caregiver who has locked themself in a closet with the phone to keep from being killed. The aggression in LBD is VERY dangerous. It should always be considered a medical emergency. I make sure my caregivers wear lifeline panic buttons at all times (I had one caregiver bludgeoned almost to death as she lay sleeping in a separate room from her spouse. The weapon? An alarm clock. My caregiver who was killed was stabbed by his wife with a steak knife. Placement is no cure for aggression. Placement only transfers the danger to other people. The patient who is aggressive towards other people poses significant risks to other residents and visitors. The risk to the staff is huge, making nursing home employment one of the most dangerous jobs in America. Most aids take the job because they want to help people but end up being bitten, slapped, pinched, hair pulled, and beaten. This places the patient at very high risk for abuse from staff. Then once facilities have a problem, all too often they try to discharge the patient, thus transferring the problem to other facilities. Moreover, nurses and families tend to want to blame the aide saying things like " Well, the aides weren't trained properly! " or " If you just know how to approach her, this wouldn't happen. " My point here are as follows: 1. Violence in any setting is unacceptable. it is a medical emergency and needs to be treated as such. Untreated aggression/violence only escalates. (I've had a lot of caregivers and professionals tell me that they won't treat because they think it's gonna pass -- two weeks later they call with a dire situation) It needs to be treated by a geriatric psychiatrist (if you have one available). And it needs to be followed carefully and closely. 2. When an antipsychotic is prescribed, it has to be given a few weeks to work. While we often " fiddle " with the dose, we try not to stop things until we see the true effect. 3. We have no right to expect nursing home staff to be beaten, bitten, or otherwise injured as a routine part of their job 4. If is the family's responsibility to " team " with the professionals to manage the behavior. If you are admitting a LO with LBD to a care center, you need to show the staff how to approach him/her to minimize potential for violence. You need to tell the staff is violence is a problem so they can prepare to manage it. If they choose not to manage it, this is a good thing as the facility should know its limits. 5. Most people with LBD should be off anti-Parkinsonian medications because they tend to produce psychosis and should be on a cholinergic (and soon memantine) to facilitate perception. Please please understand that violence is one the worst problems encountered with LBD. That and the psychosis are what really separates the people with LBD from the other dementias. Each dementia has its own problems and most have some psychosis in the later stages, but it is not as florid as in LBD. Thus, if aggression begins to rear its ugly head, treat early and treat often. Respectfully, Geri " Quote Link to comment Share on other sites More sharing options...
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