Is the Nursing Home Over-Medicating Your Elderly Parent?

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In the days before nursing homes were under so much regulation, many homes used heavy medication to "manage" residents. Elders who slept most of the day, as well as all night, didn't require as much staff time. Therefore, many homes considered drugging people efficient and cost containing.

Anti-psychotics were frequently prescribed when people had dementia. For some, a light dose may have been just the right thing, but one medication doesn't suit all elder issues. Gradually, nursing homes came under more intense scrutiny about safety and most states put strict guidelines in place about hygiene, restraints and, of course, medications for the convenience of the staff.

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There are still many states where these rules aren't strong enough, or if they exist they are not well enforced. Talk to any group of people with loved ones in a nursing home and you are bound to find a few who feel that too much medication is given.

They may be right. However, my experience was the reverse. My loved ones – several of them over many years – lived their last years at a nursing home just two blocks from my home. Whenever there was a medication change, I was notified. The reason for the prescription was discussed. If there was an antibiotic prescribed, the need was explained. Rarely, over the course of the full 15 years that I had loved ones in the home, did I have a medication complaint.

When I did, it was because the prescribing doctor made it too hard for the nursing home staff to get their hands on an "as needed" prescription for my dad's panic attacks. The physician didn't let them keep enough on hand. Of course, Dad's worst episodes were on weekends – Murphy's Law in action. Also, of course, the doctor wasn't around on weekends.

Getting Dad his desperately needed dose of a drug used to treat anxiety was often a nightmare. Dad had dementia that kicked in after brain surgery. Frequently, he would have panic attacks so severe that if people induced them on purpose, they would have to be accused of torture. The medication worked well to relax him and get him through the attacks.

However, it only worked if the staff could have a supply on hand to give to him. Those weekends with Dad in hell and the staff and me railing against the system, as we tried to get him his prescribed medications, live on in my brain. This was definitely a case where this excellent facility should have had more say over the amount of the drug needed to be kept on hand.

The flip side of my story comes from a friend of mine whose dad was living in another nursing home in our town. This home also had a very good reputation, though I'd heard a few more grumbles from people about over-medicating. My friend felt his dad was being over-medicated with an antipsychotics, even though the father was in a special dementia wing where they should have been able to handle his symptoms. My friend may have been right. At any rate, he moved his dad to a nursing home in a nearby small town. The home was run by a reputable non-profit area chain, and the family was happier with the care.

To medicate or not to medicate? The old practice of over-medicating just to keep people "manageable" so that they didn't need so much staff attention is, in my opinion, dead wrong. Still, if someone is in psychological agony, and a medication can help them feel calmer or more at peace, I think it should be used. Antipsychotics have come under fire lately as not being effective for people with Alzheimer's disease, but as soon as one study comes out with that finding, another appears contradicting it. So, I suggest we just stick with our elder and see what works best for that particular person. We can let the researchers duke it out at their leisure.

To me, human interaction comes first. Hands-on care and an attempt to find out what is bothering the person should be rule number one at all times. But if the person clearly needs a medication to feel better, and that medication improves quality of life, why shouldn't they have it? With dementia, this is not always a clear line, so family members need to be alert. But people who know the elder well need to be alert in any case. Medications that work for awhile can suddenly cause side effects. That happened to my dad. One medication he was given for nerve pain put him in far worse agony than he'd have been without it. It took some digging, but we found the source of his pain and "cured" him by withdrawing the medication.

Dosages are tricky. Allergies occur. Medicating elders is no walk in the park. Yet, that shouldn't put us in a mode where they are left to suffer needlessly because we have a "no medication" rule.

My dad's panic attacks were something I would not wish on anyone. He needed the medication to help make his life bearable. His need for the drug was episodic. But one hour of such misery shouldn't have to be suffered when relief is one tablet away. Medicating elders in nursing homes, or in their own homes, is about common sense and knowing the elders well so we can watch for unique reactions. Then we can work with modern medicine to limit unnecessary drugs, maximize human contact, but give medication where it is the most humane solution.

Elder care author, columnist and speaker Carol Bradley Bursack is an AgingCare.com contributing editor and moderator of the AgingCare.com community forum. Read her full biography

 
 
 

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  •  Comments 1 to 10 of 26 
 
 

AmazingGrace

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Mar 17, 2010

My mother is not in a nursing home. She lives with me and my husband. She has Alzheimer's disease and she gets very combative and hard to deal with at times. If I didn't have the anti-psychotic drugs to help her, I couldn't keep her with me, so how could I expect a nursing home to deal with her without that help. Often when people put their folks in a home, they don't realize how difficult things can become, because they haven't had to deal with it one on one. Without the help of these drugs, everyone would be upset and out of sorts, including the patient. I would much rather have her a little sedated than so upset and agitated. Dealing with that situation is not good for anyone.

 
 

PDdaughter

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Mar 17, 2010

Speaking from personal experience about my mother, who has Parkinson's Disease and, a few months ago, required in-patient rehabilitation for three weeks at a nursing facility following unrelated surgery subsequent to a fall, even reputable nursing facilities drug patients to subdue them merely for the convenience of their own nursing staff. My mother was not an unruly patient; she merely insisted on being given her PD medications at the required times (as did we when we were there with her) and required assistance with going to the bathroom and with picking something up off the floor that she may have dropped when my father and I were no longer visiting her.

Although we stayed by my mother's side for 10+ hours per day during the first week, I had to return to my city and my father had to shorten his visiting hours so as to have time to prepare the house for my mother's return. Therefore, neither my father or I were at my mother's bedside in the evenings. However, when I called to say good night between 7:30 and 8:00 p.m. each night, my mother sounded utterly drugged; she was confused, incoherent, and totally groggy. The nurses assured us that this was common for patients new to a facility environment, etc., but I didn't believe it. My mother was unaware of being given any additional drugs but the ones she normally took for PD at 7:00 p.m. plus the pain pill, but it was just too odd that my mother would be such a different person shortly after 7:00 p.m. each night during those remaining two weeks during her hospital stay. Something that was a "red flag" for me was what my father told me about a conversation that my mother had had with one of the night nurses, namely, that during a conversation that my mother had with that nurse about her PD medications, the nurse disagreed with my mother, stating that she (the nurse) knew better than the doctor. Anyway, I was there for my mother's return home and, from that evening on, she never again exhibited such signs of having been drugged. That's when we knew that our suspicion had been accurate. To our frustration, there is little we could do since, as so often happens in nursing facility situations, we have no proof. The only thing that is doable is to not only not return there but also to spread the word among friends and acquaintances so that others know what we wish we had known in time.

I'll go one step further than Carol Bradley Bursack did when she said, "The old practice of over-medicating just to keep people 'manageable' so that they didn’t need so much staff attention is, in my opinion, dead wrong." and say that it is ILLEGAL to dispense unprescribed medication and ethically and morally wrong to dispense any medications to a conscious and alert patient without the patient's consent.

 
 

mhmarfil

Give a Hug

Mar 18, 2010

Yup I understand the choice between sedating elderly patients or not sedating them. As always, there's something that has to give... Now that it's very expensive to hire additional staff, I am sure, the only triage option is to sedate unruly demanding patients. It's the most civil and possible way to keep things manageable without causing anyone too much tension to build up and explode. I know well based on my experience after my mom was hospitalized. I cherished the days when it was all quiet and peaceful at home, I can do whatever I want, while she was in the hospital. My daughter & I liked the feeling that we don't have a cantankerous grouchy old person at home. We can watch whatever channel on TV we like, eat whenever we want and let the dirty dishes stay at the sink longer unwashed, etc. We know the staff at the hospital kept my mom sedated strongly so they can handle other patients.

 
 

Lrock

Give a Hug

Mar 20, 2010

One size doesn't fit all. I just found out that my Mom was on a psychotropic drug. I had wondered why her behavior was getting worse. Seems the home was giving her the drug as needed I found out. You would have thought they would know better since it was making her behavior WORSE. I was NOT notified of this, and I have her power of attorney. They are now weaning her away from this drug. If Mom needs something to calm her then we can discuss this after she is weaned from this horrible drug. BTW Mom has a very low tolerance for meds to begin with.I had told them many,many times Mom has mild/moderate dementia and other medical issues..still ..she was never ,ever a problem. Yes I totally,agree the elderly are at times over medicated and one size doesn't fit all.

 
 

Carebuzz

Give a Hug

Apr 1, 2010

Good article, thank you, Carol.

It reminds me of the time my Dad was in a nursing home.. with last stages of Alzheimer's - dreaded place to be. The family was leery of the drug issue.. it seems my Dad was more distant each day. We also leery of other "staff behaviors" so we all pitched in and visited Dad every day. My sisters did most of the work during the week and I helped out on weekends... we were there everyday for lunches and dinners and of course breakfast too when we could make it. I spent hours with Dad on weekends during the day to make sure he was cared for properly.

In my opinion, this is what it takes... lots of dedicated effort by family to ensure your loved ones are safe and well cared for when they are living in a nursing home.

Thank you,

Carol
Carebuzz

 
 

anonymous13319

Give a Hug

Apr 1, 2010

This is why I am doing everything humanly possible to keep my mother out of these places.
Even the most reputable care facilities will never treat your parents like "family" so, therefore, they do not view overmedication as a problem.
Can you imagine how horrible it would be to be stuck in a bed, drugged out of your mind, and you cannot even express it to anyone?
I think that this practice is all too common and nh staff has no right to be medicating w/o both doctor's orders and family notification.
I think we need to install "granny" cams in all patient's rooms.

 
 

LynnPO

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Apr 1, 2010

My mother was over medicated in an attempt to save money and it nearly cost her life. She has epilepsy and takes a very specific dose of dilantin every 8 hours. She had to go to a rehab center to recouperate from hip replacement. She was fine but in a few days was completely out of it. I asked to SEE - physically LOOK AT - the pills they were giving her and noticed that the dilantin tablet was wrong. Come to find out, that they got a "deal" on a bunch of dilantin and substituted it for her prescribed pill. Though the active ingredient was only slightly more than her normal pill, it was enough to put her over the edge. After some screaming and yelling on my part - they sent someone to the pharmacy to purchase the correct pills and did blood work immediately. Her dilantin level was double what it should be - any more and it would have killed her. It took a week of tweaking and regular blood tests to get her back to normal. I took emergency leave from my job and be there daily to ensure they towed the line. Needless to say, I wrote letters of complaint to the state dept of healthy, Better Business Bureau, the state attorney general, and the local district attorney. Several years later Mom moved into assisted living and the director remembered me - she was employed at the rehab center during this fiasco. She made sure that everyone had training in dealing with seizures & seizure meds and they had a policy that they used EXACTLY what the physician described - no generics or substitutions without doctors permission. At least Mom's close call had a positive outcome for some one.

 
 

MyMomToo

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Apr 2, 2010

Medicating with mind altering drugs can also happen in the home. My mother, who still lives alone in her home, was prescribed a medication for "depression" at the request of my brother. The Pharmacist called her doctor and was given a prescription without a doctors visit. Even though I don't live near her I call her every day to see how she is. She has mild dementia so is confused but for months she was telling me about people in her home who were stealing her things. I asked my brother if she was on any new medication and he said no that she was making up stories to get attention. I became even more concerned when she expressed feelings of being harmed. I found out that she had been on a medication for Alzheimer's for 6 months and what I thought was real were really hallucinations. She has been taken off this mind altering drug but it has been 2 weeks and the hallucinations persist. Mother experienced hallucinations when she was put on an anti-depressant years ago but they subsided after the drug was removed.

Physicians will not take the time to explain the side effect or adverse effects of these drugs. Caregivers need to be vigilant and informed so our elderly are not robbed of what little memory they have left and end up in Nursing Homes and on more drugs.

 
 

CAtoodie

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Apr 24, 2010

My mother came to visit us in CA 81 days in the last 15 months. Then mom had eye surgery and couldn't drive so my sister had to do more. She resented it and talked my brothers into putting mom into a home against her wishes. Mom wanted an attorney to protect her and I called one. Unfortunately she fell and went to the hospital. Her doctor put her on a morphine patch PLUS pills and she went off her rocker. My sister falsified a power of attorney when mom was still hospitalized and they put her in a home. The longer mom got off the meds the clearer thinking she got. She terminated the power of attorney and wanted me come live with us in CA. My hateful siblings lied and went to court when I was in CA and told the court I stole $200K, I falsified a POA, not giving mom her meds, and I brought her against her will to CA. They came and forced her to return against her will to Texas. Now we are in a court battle and the doctor is over sedating her. He states in his report she suffers from hallucinations, memory loss and instability walking YET these are all listed as side effects of the drugs. On behalf of my siblings he is advising mom not to attend court because it will upset her (when she sees me) and they don't want the truth to come out. My phone number was listed on mom's pharmacy and they called that the new prescription her doctor order is approved and ready. So what else are they drugging her with? I also learned that my sister is telling mom's friends they will never get to see mom again. They also, based on lies, got the judge to rule against me - can't believe a 77 yr old judge would issue a permanent restraining order on the youngest daughter of her 83 year old mom. It's been heartbreaking for us. My son will never get to see his grandma and his daughter, my mom's great-granddaughter will never get to see her either. There is light at the end of this tunnel - we filed an appeal because I was violated my due process to defend myself. We have 11 affidavits and 3 testimonies and a doctor's report that argues my sister becoming mom's Guardian. I pray it becomes obvious to the court. However, the time clock is ticking and my mother is locked away for no one to see.

 
 

ckester

Give a Hug

May 22, 2010

My mother is sedated by the nursing home and it breaks my heart. They just don't want to deal with her requests so they drug her. We have found that some days she is still almost comotose by noon due to being heavily sedated. I do not understand why our states allow for this to go on. My mother doesn't deserve this and it makes me angry and sad.

 
  •  Comments 1 to 10 of 26 

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