“Dealing with Drooling” (Neurology Now article)

There’s a good article in the latest issue of Neurology Now magazine on the treatment of drooling in neurological disorders. Dr. Robert Miller (a neurologist at Stanford and at the ALS center at CPMC San Francisco) is quoted in the article as saying: “We tend to think that since some of these [neurologic] conditions are incurable, they’re also untreatable. That’s a big mistake. We have many treatments—for the breathing issues, the nutritional issues, treatments that slow the progression of disease, and yes, treatments for drooling.”

The article mentions the medication glycopyrrolate (brand name=Robinul). Generally speaking, caution should be exercised when giving an anticholinergic medication such as Robinul to someone to dementia (as there may already be a lack of acetylcholine in the brain of someone with dementia).

Neurology Now is a magazine written for laypeople. Subscriptions to the bimonthly publication are available at no charge; see:
http://journals.lww.com/neurologynow/Pa … vices.aspx

Robin

http://journals.lww.com/neurologynow/Fu … id.15.aspx

EYE ON THERAPY
Dealing with Drooling
Getting rid of excess saliva goes high-tech.
by Amy Paturel, MS, MPH

Neurology Now
February/March 2011; Volume 7(1); Pp 38,40

When 61-year-old Deborah Clark first experienced trouble swallowing, she didn’t think much of it. But six months later, when she began having symptoms like slurred speech and difficulty projecting her voice, she visited a neurologist. Diagnosed with amyotrophic lateral sclerosis (ALS, also called Lou Gehrig’s disease) in February 2008, Clark quickly discovered how integral the muscles in her mouth were to her quality of life. Not only did she have difficulty speaking, but she also experienced excess saliva pooling in her mouth. At its worst, Clark found herself changing clothes up to four times a day because she had drooled down the front of her shirt.

“I was reluctant to be in public or around strangers—especially when a meal was involved,” says Clark. “People were always offering me tissues to control the drooling. It was embarrassing.”

Drooling, or sialorrhea, can be a major problem for people with neurologic conditions ranging from Parkinson’s disease and cerebral palsy to certain types of stroke and ALS. People with these conditions may not have the brain control to coordinate muscle movements in the face and mouth.

“Any condition that affects the muscles and nerves of the bulbar area (the swallowing mechanism) could cause increased drooling,” says Steven Bachrach, M.D., co-director of the Cerebral Palsy Program for Alfred I. duPont Hospital for Children in Wilmington, DE. And if you’re not swallowing your saliva, it tends to pool and accumulate in the mouth, and then it starts overflowing.

Beyond the obvious social implications of incessant drooling, the overflow of saliva in the mouth can irritate tissues around the lips and even cause aspiration pneumonia, a serious condition where people breathe fluid (or other foreign materials) from the mouth into the lungs. But with recent advances in everything from oral medication to botulinum toxin injections, people have more options than ever to control sialorrhea.

SWALLOWING THERAPY
Speech and swallowing therapy is a great option for people who are mildly impaired and highly motivated to control their drooling. Most neurologists will advise patients to investigate this approach before considering invasive procedures. Through a series of sessions, therapists teach patients a variety of techniques to improve the safety of swallowing and minimize the risks of aspiration.

“There’s a lot that a swallowing therapist can do in this area,” says Robert Miller, M.D., professor of neurology at Stanford University and director of the Forbes Norris ALS Research Center at the California Pacific Medical Center in San Francisco. “If you tuck in your chin when you’re swallowing, for example, you’ll open up the airway, making it easier for fluid and food to go down.”

Even just becoming more aware of when and how you swallow can be effective. With regular training, people can learn to swallow more efficiently and get rid of excess saliva. Unfortunately, none of these techniques actually dries up the spit. If that’s your goal, medications or surgery are your best bets.

MEDICATION
When less invasive methods have failed, the next approach is medication, usually anti-cholinergic medications. This class of drugs is used for everything from seasickness to overactive bladder. But with dry mouth as one of the main side effects, anti-cholinergics have become a useful tool to control drooling. In fact, studies investigating glycopyrrolate (the most commonly prescribed medication for drooling) consistently find the drug reduces drooling for up to 95 percent of patients who try it.

“One of the biggest challenges was that glycopyrrolate was only available in tablet form, so it was hard to adjust the dose to very small amounts,” says Dr. Bachrach. But in January 2011, the Food and Drug Administration approved a liquid form of the drug, which will make it easier to take and easier to dose.

When Clark started taking glycopyrrolate, her drooling improved within a matter of days. Initially she took one tablet three times a day, but eventually she needed four tablets daily to experience the same effects. Over time, even four tablets didn’t reduce her drooling to an acceptable level.

“Even if the drugs do work initially, receptors on the cells and within the salivary glands change, so patients may end up requiring higher and higher doses to get the same result—and then they get side effects,” says Scott Brietzke, M.D., M.P.H., director of pediatric otolaryngology at the Walter Reed Army Medical Center in Washington D.C. While dry mouth is the most common side effect, some people also experience constipation, urinary retention, and cognitive side effects such as confusion and memory impairment.

If the anti-cholinergics stop working—or the side effects are intolerable—some physicians prescribe amitriptyline, an anti-depressant that dries up saliva. A bonus: amitriptyline improves sleep, which is often disrupted in patients with ALS, multiple sclerosis, and other neurologic disorders.

INJECTIONS
If meds can’t control drooling, botulinum toxin is another option. Using an ultrasound-guided approach, the physician injects the drug into the major salivary glands to paralyze the muscles that normally squeeze out saliva. In one study of 131 patients, published in the medical journal Archives of Otolaryngology Head and Neck Surgery in 2010, botulinum toxin injections in the submandibular glands (the two glands located in the lower jaw that produce most of the saliva) reduced drooling and improved quality of life among patients who received injections. Two months after the injections, nearly 50 percent of patients experienced significant improvement, with effects beginning to taper off at the eight-month mark.

Clark started with just two shots into the salivary glands on either side of her face. Within a week, her drooling had dissipated more than it had with glycopyrrolate alone, and the effects lasted for three months. On the heels of this success, Clark’s physician gradually increased her dose to a total of six shots (three on each side).

“With six shots, the results were much more dramatic,” says Clark. “I have very little drooling and the only side effect is dry mouth, which is easier to deal with than drooling.” After the last round of botulinum toxin, Clark discontinued the glycopyrrolate without any noticeable difference.

Studies suggest that combined injections in both the parotid glands (which are located in the cheeks) and submandibular glands are slightly more effective than injections into the submandibular glands alone. And after repeated injections, there have been some reports that the salivary glands actually stop working, resulting in a permanent reduction in drooling. “You can’t count on that,” says Dr. Bachrach, “but it does happen in some patients.”

For other people, though, botulinum toxin is just a trial procedure to determine whether surgery will be effective. “Botulinum toxin deactivates those major glands, so we can see if that helps the patient with either the social problem or aspiration,” says Dr. Brietzke. “If there’s significant improvement, then we can consider a potentially irreversible procedure, such as tying off the ducts or removing the glands.”

SURGERY
Surgical treatment for drooling may be even more effective than injections, without subjecting people to recurrent treatments. Studies show that people who have surgery are generally happy with the results. Unfortunately, there are a variety of approaches and little consensus about which ones work best. The most straightforward procedure involves the submandibular glands: Rerouting the ducts from these glands to the back of the mouth makes it easier to swallow saliva. Alternatively, surgeons can reroute the ducts from the parotid glands or remove the submandibular glands altogether.

“The evidence we have suggests that intra-oral procedures (like tying off the four ducts in the mouth) may not be as successful,” says Dr. Brietzke. According to a study he co-authored in Archives of Otolaryngology Head and Neck Surgery in 2009, removal of the submandibular glands and parotid duct rerouting appear to have the highest success rates at 87.8 percent while the success rates for tying off the four ducts varied wildly from 31 to 100 percent.

“The biggest downside is that surgery is not reversible,” says Dr. Bachrach. “Once you’ve tied off the ducts, or removed the glands altogether, you can’t undo that.” So while you can go from drooling to dry, you can’t go back. And dry mouth has its own set of complications.

Even so, treating symptoms like drooling still gets short shrift from some health care providers.

“We tend to think that since some of these [neurologic] conditions are incurable, they’re also untreatable,” says Dr. Miller. “That’s a big mistake. We have many treatments—for the breathing issues, the nutritional issues, treatments that slow the progression of disease, and yes, treatments for drooling.”

For Clark, that treatment has been invaluable. Today, she no longer carries a napkin with her at all times, she doesn’t shy away from social events, even with strangers, and her shirt stays dry throughout the day. “I’m very happy with the results,” she says.

“8 Life Issues You’re Bound to Face When Caring…”

This article on “8 Life Issues You’re Bound to Face When Caring for an Aging Parent” is written by Caring.com and published in “Parade” magazine.  The eight issues are:

1. Understanding your parents’ life stage
2. Talking about tough issues — from assisted living to adult diapers
3. Family disagreements
4. Having the “car talk”
5. Sex, drugs, and alcohol
6. Work-life balance
7. Death and dying
8. After the funeral

Here’s a link to the full article:

http://www.parade.com/health/caregiving/8-life-issues-youre-bound-to-face-when-caring-for-an-aging-parent.html

8 Life Issues You’re Bound to Face When Caring for an Aging Parent
by Connie Matthiessen, Caring.com Senior Editor
Parade Magazine

The article includes these Caring.com webpages that are related to some of the eight issues:

Demystifying Your Aging Parents’ New Stage of Life
http://www.caring.com/articles/elderly-communication

How to Talk to the Elderly
http://www.caring.com/articles/talking-to-elderly-parents

Caring for Elderly Relatives: How to Handle Family Conflicts
http://www.caring.com/articles/family-conflict

Difficult Conversations: How to Approach Older Adults With Concerns About Their Driving
http://www.caring.com/articles/when-should-seniors-stop-driving

Talking to a Loved One About Death
http://www.caring.com/articles/talking-to-a-dying-parent

How to Avoid Strained Sibling Relationships
http://www.caring.com/articles/sibling-relationships-strained

How to Help an Older Adult Create a Lasting Legacy.
http://www.caring.com/articles/creating-a-lasting-legacy

Lots to read!

“The Role of Caregivers in Parkinson’s” – lecture notes

Though this lecture focuses on the role of caregivers in Parkinson’s Disease, the content applies to all caregivers, regardless of disorder.

The 30-minute lecture by Elaine Lanier, RN, of UCSF’s Parkinson’s Center, presents an caregiver job description, lists the stresses of caregiving, and outlines practical ways to manage that stress. Here’s a link to the lecture, given at the UCSF Parkinson’s Conference in November 2010:

pdcenter.neurology.ucsf.edu/videos/role-caregivers-parkinsons-disease

Brain Support Network volunteer Denise Dagan listened to the lecture.  Denise’s takeaways from Ms. Lanier’s talk included:

  1. Assess your situation periodically.  Something that has worked for you might just not, anymore.  Employ the 3 R’s:

– Reassess!

– Recognize when you need to adjust to new circumstances.

– Request assistance from friends, family or services.  It’s the best way to care for both yourself and your loved one.

  1. Take get-aways and mini-breaks.

– Get-aways are scheduled times for your hobbies, church, personal grooming, friends, exercise, etc. (with or without your caree).

– Mini-breaks are anything to get your mind off the responsibilities of caregiving for 20 minutes, or so.  Some suggestions are, take a walk outside and a deep breath, grab some chocolate, or read.  De-stress, and then go back to it.

  1. Letting someone else help increases your creativity and skill set.  When you see how someone else is doing a task, you may wonder why you didn’t think to do it that way.
  1. Make a list of things to do and another list of people who can help.  Match the tasks with the most appropriate person to do it (by proximity, skill set, transportation, etc.) and ask the person to do that specific task.  Start with small things and ask them to do more if it goes well.  Some examples are:

– The neighbor kid who just got his driver’s license would probably love to pick up your prescription or some groceries.

– People who are far away can do your taxes, make your travel arrangements, buy Xmas gifts and ship them in your name, etc.

Think outside the box a bit for your own best health.

Denise’s extensive notes are copied below.

Robin


 

Denise’s Notes from

 

“The Role of Caregivers in Parkinson’s Disease”
Presented at the UCSF Conference on Parkinson’s Disease, November 13, 2010
Speaker, Elaine Lanier, RN, MS

Caregiver Job Description: A challenging “…job that takes place in an unstructured environment without coworkers…, no formal job description or training, and supervision by a boss that is by definition… ‘out sick.’”  (Fay Mikiska, the Caregiving Tool)

The Value of Family Caregivers

* Economic value of services family caregivers provide for “free” is approx. $375 billion per year.  This is almost double what is spent on home care and nursing home services combined (National Alliance for Caregiving and Evercare, 2009)

* Help to MD, nurse, clinicians is significant

* Service to loved one is beyond measure in terms of love, depth of care, and concern

* Your care is the person with Parkinson’s most valuable asset

What Do PD Caregivers Do?

* Help with Activities of Daily Living (ADLs), medication management & Administration, household chores, financial management, transportation, emotional support, medical plan management

* Cope with all PD symptoms – both motor (stiffness, tremor, rigidity, freezing, etc.) and non-motor (depression, anxiety, sleep disturbance, behavior and thinking changes, etc.)

* Role is a demanding,  24-hour job 7 days per week & duties increase with advancement of disease

Stresses of PD Caregiving

* Caregivers are often ill prepared to manage the emotional & physical demands of caregiving

* Face increasing demands due to PD progression

* Have their own aging processes and physical decline

* Caregiving can place constraints on social & family life, employment and finances

Story about the speaker having to give up visiting with her mother in the nursing home during meals because visiting at that time was just too stressful for both of them.  There are similar adjustments you will have to make as a Parkinson’s caregiver by being aware of circumstances as they change and being flexible.  Parkinson’s affects the entire family.  If you are still working as a PD caregiver, you’re juggling a lot – maybe too much.  Reducing your hours or quitting will affect your finances, but our work often contributes to our self esteem.  You have stress just in deciding whether to give that up, too.

Help for the PD Caregiver

* Be/get prepared

* Take care of yourself

* Get help – don’t try to do it all yourself, its too much.

* Keep good relationship/communication with the person who has Parkinson’s.  Its important for both of you.

Be/Get Prepared

* Education: internet, PD organizations, libraries, ask questions of doctors and nurses

* Evaluate present situation:  Whether you’re new to caregiving or not, assess your situation.

– Loved one’s needs.

– Home environment  Rearranging furniture to prevent falls, are there stairs in your home that will eventually be problematic?

– Your health, emotional state, commitments  (job, kids, parents, etc.)

– What you can and can’t do yourself  (Learn how to say, “No,” so you don’t take on too much.)

– What outside support needed

 

– Finance issues: health insurance (is PD covered, Is there a high deductible? Can you keep your coverage?), employment, paying bills, power of attorney (Don’t wait until there are cognitive issues before doing the paperwork for this.  Pick someone whom the person with PD trusts)

Have a Family Meeting

* Reasons/Benefits

– Parkinson’s affects the whole family

– Opens communication lines

– Helps everyone understand present & future situation

– Have early in decease, but never too late

– Include the person with PD whenever possible

Take Care of Yourself

* “Your own good health is the best present you can give your loved one” (Suzanne Mintz, caregiver of MS, president, Co-founder of the National Family Caregiver Alliance)  Call NFCA to find resources to help you.  Resources at the end of this talk.

* Maintain mental and physical health.  Make and keep medical and dental appointments.

* Keep your job whenever possible

* Join a support group for caregivers

* Get your sleep (even if PD person can’t)  Move to your own room/space if your sleep partner is keeping you awake.

* Take breaks – get-a-ways and mini-breaks. Walk outside and take a deep breath, grab some chocolate, or anything to get your mind off the responsibilities of caregiving for 20 minutes to de-stress, and then go back to it.

* Make and keep your social activities (even if the person with PD can no longer join you) and spiritual activities (church, yoga, or whatever)

* Keep (or develop) sense of humor.  It’s hard to have a sense of humor when you’re watching someone you love struggle and decline, but try.  Ms. Lanier shared a story about writing things her mom with Alzheimer’s said.  Sometimes there are funny things.  Recognize them.

Get Help – Don’t do it alone

* Benefits

– Lessens feelings of isolation and feeling like you’re the only one shouldering this responsibility.  You don’t have to be!

– Encourages independence of the person with PD.  If you’re not there to do everything, sometimes they might do it without you.  It may not be the way you want it done (messy, take longer, etc.) but its done!

– Gives you more confidence in your ability to caregive.

– Increases your creativity  (when you see how someone else is doing something, you wonder why you didn’t think to do it that way)

– Helps you be more peaceful & effective

How to Define and Get Help

* Asking for help is a sign of strength, not weakness

* Caregiving is a Job with individual tasks

* Make a list of caregiver tasks in a typical week

* Organize that list into categories

– Caregiving needs and how people can help

– Decide what to let go and what to keep

* Start with something small and specific like,pick up medicine at drug store, buy loaf of bread.  Match up what needs doing with who may be able to help and ask them to do something specific:

Make a list of tasks: pick up groceries, medication, mow the lawn, calling Kaiser about insurance issues, etc.

Make a list of the people who could help: grandson who just got his driver’s license; sister who lives at the other end of the state, has Kaiser, and great communication skills

Where to get help: Resources

* Local & Community

– Free to low cost: neighbors, friends, churches, synagogues, senior centers, adult day health, Meals on Wheels, door-to-door vans

– Fee based: In-home care (help with cooking, bathing, dressing, meal prep, etc.)

– Social Worker from health plan or hospital can connect you to these services

* Resources, State & National

– Family Caregiver Alliance, San Francisco  www.caregiver.org, 415-434-3388

– National Family Caregivers Association  www.nfcacares.org/index.cfm

– National Parkinson’s Foundation  www.parkinson.org/caregivers.aspx

– Michael J. Fox Foundation  www.michaeljfox.org  (Look under “Living with Parkinson’s,” guide for the caregiver)

* Each website gives information and other websites for resources

Relationship/Communication with Person with Parkinson’s

* Can be most difficult and rewarding part of caregiving

* Roles change  (e.g. adult children who must take an authoritative role with their parent)

* Research shows that despite high levels of strain, caregivers with good quality relationships have reduced depression & better physics health.

How PD Person Can Help Caregiver

* Appreciate caregiver and tell them – thank you’s go a long way

* Be an honest communicator

– Don’t minimize the situation

– Don’t avoid communication to “spare” the caregiver.  Caregivers/family want to know

Ms. Lanier shared a story about a support group.  The issue came up that a person with PD worries that if they ask for help now, it won’t be there later, when I really need it.  Caregivers all says they want to know what’s going on.

* Be Cooperative, be a team player

– Work with, not against caregiver

– Don’t expect things to be done exactly your way.  Ms. Lanier shared a story about asking her husband to go to the grocery store.  He didn’t come home with the sizes and/or brands she would have bought.  He saved her at least an hour, so it was good enough.

 

Summary

* Caregivers

– Get prepared with education, assess your situation as you go along, have regular family meetings

– Take care of yourself (take mini breaks, keep your medical appointments, reduce your stress)

– Get help (use the resources listed)

* Person’s with Parkinson’s

– Appreciate your caregiver(s)

– Be open and honest

– Be cooperative, you’re a team!

* To Both of You

– Work on having a positive relationship/communication with each other – for the health benefits.

“Bathroom Safety for Older People”

This post will be of interest to those looking to make a bathroom safer.

I ran across a webpage — with great figures — that addresses safety associated with the bath tub, showers, and toilets.

Three short personal notes about safety equipment in or modifications to a bathroom….

When we were remodeling our house ten years ago, we had my husband’s elderly aunt in mind when we installed grab bars in the shower.  We bought the grab bars and the contractor installed them in places he thought they should go.  We were disheartened to learn from the aunt that they were installed in the wrong places to be useful!  It’s important to consult with an occupational therapist or a contractor who specializes in aging-in-place about this sort of equipment!

Second was how we handled toilet safety for my father.  My father was tall and weighed 220 pounds so we needed a grab bar that went into the floor.  We liked the sturdiness of the L-bar (or P-bar) shown in Figure 14 for my father.  We bought a stainless steel grab bar from Adaptive Access (adaptiveaccess.com), and then found a welder to cut the stainless steel bar to the height and length we wanted.  We ended up running two identical bars, parallel to each other, on either side of the toilet.  This really helped my father to sit down on the toilet and stand up from the toilet.

Third is about a portable bidet.  This type of equipment is mentioned below.  We’ve had several local support group members use portable bidets for cleaning their family members’ back sides, and they all recommend the bidet.

So here’s what the experts say:

extension.missouri.edu/publications/DisplayPub.aspx?P=GH7060

Bathroom Safety for Older People
by Anna Cathryn Yost, Department of Consumer and Family Economics, and James Martinr, Physical Therapy Education
Published by the University of Missouri Extension
Reviewed April 1998

Robin

“When Sleep Apnea Masquerades as Dementia”

This short article is about the fact often sleep apnea goes undiagnosed in the elderly. In particular, the article reports on a case of a woman who had undiagnosed obstructive sleep apnea that was mimicking dementia symptoms. The impression I got from the article is that this is unusual; typically sleep apnea exacerbates dementia symptoms. Here’s the full article and a link to it.

http://newoldage.blogs.nytimes.com/2010 … -dementia/

The New Old Age
Caring and Coping

October 6, 2010, 3:44 PM
When Sleep Apnea Masquerades as Dementia
By Paula Span
The New York Times

The woman who came to see Dr. Ronald Petersen, an Alzheimer’s specialist at the Mayo Clinic, was only in her 60s but complained that she was having trouble concentrating. “Her attention was waning,” Dr. Petersen recalled. “She couldn’t follow a television program or stay focused during a conversation.”

She was probably developing dementia, Dr. Petersen thought as he took her history. But along the way he asked, as he usually does, how she was sleeping. The woman, who lived alone, hadn’t noticed any problems.

Her son, however, had stayed with her the previous night to drive her to the appointment. “She was snoring like a freight train,” he reported.

Aha. Overnight sleep testing determined that the woman had obstructive sleep apnea — nightlong interruptions in breathing that reduce oxygen flow to the brain and prevent deep sleep. The interruptions can happen 10 or more times an hour and are quite common in older adults, exacerbating — or sometimes mimicking — dementia symptoms.

Treated with a C.P.A.P. machine — the acronym stands for continuous positive airway pressure, a therapy that involves wearing a mask over the nose and/or mouth during sleep — the woman rapidly improved. Her scores on neuropsychological tests eventually climbed back into the normal range. A year later, Dr. Petersen said, “I can’t find any abnormalities.”

Most of the time, cognitive problems won’t evaporate when seniors are treated for sleep apnea. But researchers find that with C.P.A.P., many older patients see marked improvement. “They’re not dozing off during the day, they’re not dragging,” said Dr. Bradley Boeve, a neurologist at the Mayo Clinic. “Quality of life improves.”

Life gets easier for their caregivers, too, a key concern in trying to keep people out of nursing homes.

But apnea frequently goes undetected, especially in the elderly, although they are more likely to have it. Estimates of the percentage of older adults with sleep apnea are all over the map, in part because of varying definitions of the condition — but they’re always startlingly high. Sonia Ancoli-Israel, professor of psychiatry at the University of California, San Diego, has studied the disorder for 30 years and reports that almost half of older adults experience apnea to some degree, with even higher rates among those with dementia.

“It’s under-recognized in all age groups,” she told me in an interview. “But in older people, physicians are even less likely to recognize it.”

Why? Apnea in younger people frequently coincides with obesity; in elderly patients, that’s less often true. Loud snoring, often a tip-off, may go unnoticed when seniors live alone. And, as Dr. Ancoli-Israel pointed out, “there’s a belief that old people are supposed to be sleepy during the day.”

They’re not, and one reason she wants them and their caregivers to recognize the problem is the now-established connection between apnea and cognitive decline. “If you’re waking up hundreds of times a night and you’re not getting enough oxygen to the brain, of course you’ll see the effect,” Dr. Ancoli-Israel said.

She and her team, in a study published in 2008 in The Journal of the American Geriatrics Society, randomly assigned patients with Alzheimer’s disease to use real C.P.A.P. machines or fake ones for several weeks. The treatment produced “modest but statistically significant improvements,” particularly in vigilance (the ability to pay attention) and executive function (judgment and decision-making).

“We didn’t cure the dementia,” Dr. Ancoli-Israel cautioned. “But it wasn’t as severe as before.” As the researchers followed up months later, they also found that while all the patients continued to decline cognitively, in those using C.P.A.P. the decline was more gradual.

For years, physicians doubted that dementia patients could or would use these machines. Even younger people with apnea frequently find the C.P.A.P. mask uncomfortable, pulling it off during sleep or just not bothering to use it. But in recent studies, seniors diagnosed with Alzheimer’s disease did use the devices — not for as many hours each night as their doctors might wish, but long enough.

Now Dr. Ancoli-Israel is investigating whether C.P.A.P. therapy might help reduce the cognitive damage from Parkinson’s disease. “This isn’t just Alzheimer’s,” she said. “Any time there are symptoms of dementia, you should think about sleep apnea and discuss it with your doctor.”

Be forewarned: diagnosing sleep apnea can be complicated, requiring an overnight stay in a sleep center. If apnea proves to be the problem, technicians have to calibrate each C.P.A.P. machine’s settings and individually fit the mask. All those processes become harder with someone who’s cognitively impaired. (To find treatment centers, consult the American Academy of Sleep Medicine or the National Sleep Foundation.)

But when someone with apnea does stick with the treatment, “you’ll see the effects within a month or so,” Dr. Boeve said. “Sometimes even within a week.”

Paula Span is the author of “When the Time Comes: Families With Aging Parents Share Their Struggles and Solutions.”