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A Caregiver’s Guide to Inhalers

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A Caregiver’s Guide to Inhalers

Author: Mark Parkinson BsPharm:  President  AFC-CE

Credit Hours 4 - Approximate time required: 240 min.

 

Educational Goal

Enable caregiver to properly facilitate inhaler device therapy.

Educational Objectives

  • Present the basic anatomy and physiology of the respiratory tract.
  • Discuss the two main types of lung pathology
  • Prove through statics that the pathology is not well controlled despite readily available therapy.
  • List the reasons for inhaler therapy failure
  • Provide an understanding of inhaler types
  • Give information that will enable caregivers to facilitate proper inhaler device use.

Procedure:

Read the course materials.  2. Click on exam portal [Take Exam].  3. If you have not done so yet fill in Register form (username must be the name you want on your CE certificate).  4. Log in  5. Take exam.  6. Click on [Show Results] when done and follow the instructions that appear.  7. A score of 70% or better is considered passing and a Certificate of Completion will be generated for your records.

Disclaimer

   The information presented in this activity is not meant to serve as a guideline for patient management. All procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this article should not be used by care providers without evaluation of their patients’ Doctor. Some conditions and possible contraindications may be of concern. All applicable manufacturers’ product information should be reviewed before use. The author and publisher of this continuing education program have made all reasonable efforts to ensure that all information contained herein is accurate in accordance with the latest available scientific knowledge at the time of acceptance for publication. Nutritional products discussed are not intended for the diagnosis, treatment, cure, or prevention of any disease.

 

 

A Caregiver’s Guide to Inhalers

 

Quickly, take a breath. Taking a deep, cleansing breath always feels so good. Can you imagine trying to take a deep breath and that big inrush of air doesn’t happen? Instead, only a small wheezing trickle of air comes into your lungs. How terrible would that be if it happened over and over again? This is the health concern that is faced by many of your residents. Foster care providers are in a good position to help—but only if they understand how to help. Let us get started with a brief discussion about the respiratory system, its disorders, and how they are treated.

 

The Respiratory Tract

The respiratory system consists of the organs and structures used to exchange the gases we utilize to live and function. It is divided into two parts. The upper respiratory tract is the mouth, nose, sinuses, and throat. The lower respiratory tract is the throat below the vocal cords, lungs, and diaphragm. The lungs are subdivided into the trachea, bronchi, bronchioles, and alveola.  

Lining the respiratory system are several concentric layers of specialized tissue. Throughout the layers, you will find, to varying degrees, cartilage, muscle, nerves, blood vessels, mucosal cells, epithelium cells, and immunity cells, all of which have their part to play in taking in the oxygen we need to function. Once in the lungs, the oxygen can diffuse into the bloodstream and be transported around the body. In a reverse process, the carbon dioxide waste gas we produce diffuses out of the bloodstream and into the lungs, where it is exhaled. If all the parts work properly, respiration occurs. If something goes wrong, the whole body suffers.

 

Diseases and Disorders 

 

I’m not going to have a long, drawn-out discussion about everything that can go wrong in the lungs. For brevity, I am going to lump them into two broad categories and name them “asthma type” and “COPD type.” I know that I am taking quite a large medical literary liberty by doing so. Please don’t sweat the details, and instead, look at the broader picture I’m painting.

 

Asthma Type

Asthma is an inflammatory condition in the lungs. The layers lining the lungs become inflamed and swollen to the point that the airway paths are severely reduced. Along with the inflammation, extra mucus is produced. Together, these conditions block the capacity to breathe normally. Asthma symptoms can be triggered by environmental factors like allergies or pollutants, or they can be triggered by internal events like a sudden increase in exercise or strong emotions. The likelihood of an asthmatic condition manifesting itself can be increased by disease or genetic factors. The signs and symptoms of asthma are difficulty breathing, chest pain, cough, and wheezing. The symptoms can be seen as part of a chronic condition or a sudden flare-up called an asthma attack.

 

COPD Type

COPD, or chronic obstructive pulmonary disease, refers to a group of diseases that cause airflow blockage and a reduced capacity to exchange gases normally in the alveola. Exposure to toxins (like those in tobacco) and disease progression cause permanent damage to the lung tissues. The loss of lung tissue reduces the ability to breathe properly. Emphysema and chronic bronchitis are the two most common conditions that contribute to COPD. In emphysema, the alveoli have been damaged or destroyed. In bronchitis, the lining of the bronchial tubes is inflamed, and becomes mucus-filled. The signs and symptoms of COPD are shortness of breath, wheezing, chronic cough, and extra mucus production.

Asthma and COPD are both common respiratory disorders. Asthma can be seen in all ages, including the very young. COPD is usually seen in adults, with its prevalence increasing with age. Worldwide, approximately 300 million have asthma, and 10 percent of the adult population over the age of 40 years may have COPD. These conditions are common enough that, sooner or later, every foster caregiver will have to care for a resident with breathing difficulties.

 

 

Caregiving and Breathing Problems

 

Asthma and COPD are incurable diseases. The breathing problems—or the potential for breathing problems—will plague the resident for the rest of their life. Both conditions can be managed with the help of the right equipment, medication, and an understanding of how to use them. Medical oxygen can compensate for the reduced airflow, and medications can open airways by controlling the inflammation and reducing mucous production. Properly applied, these treatments can enable your resident to have a fairly normal life.

The majority of medications used for your residents with breathing problems are delivered via inhaler devices. They are the gold standard in respiratory care. Doctors prefer inhalers because they have several advantages over other treatment options.

  • They enable the medication to be delivered directly where it is needed immediately.
  • Doses of medication are small so that side effects can be reduced.
  • The inhalers are portable and convenient, and they require little if no preparation to dispense the drugs.

But (and this is a Big But) the patient has to be taught how to use them. Inhalers requires practice to properly deliver the medication where it is supposed to go. If inhalers are used incorrectly, the outcome is less than desirable.

 

 

The Problem

 

Even though effective inhaler-based treatment options are readily available, asthma and COPD patients continue to suffer from their diseases. Far too many deaths from these controllable conditions are still being reported. It is a tragedy that so much suffering still occurs from these largely preventable adverse conditions.

 

The Stats 

In medical studies, it has been shown that if patients use their inhalers correctly just 80 percent of the time, respiratory disorders can be controlled. But during recent research, it was observed that adherence to inhaler therapy rates are much lower, ranging from 73 percent to as low as 8 percent. It was also observed that when patients do use their inhalers, the majority of patients made errors in inhaler use. Non-adherence to therapy and improper inhaler use has resulted in a major health problem in the United States.

The impact of COPD:

  • Over 16 million doctor’s visits a year are related to COPD
  • It is the fourth-leading cause of death in the United States.
  • Direct costs for COPD are estimated to be over $18 billion annually.

 

The impact of asthma:

  • Asthma accounts for 9.8 million doctor’s office visits, 188,968 discharges from hospital inpatient care, and 1.8 million emergency department visits each year.

 

  • Asthma is the third-ranking cause of hospitalization among children younger than 16

 

  • Each day, ten Americans die from asthma, and in 2017, 3,564 people died from asthma. Many of these deaths are avoidable with proper treatment and care.

 

  • Adults are four times more likely to die from asthma than children.

 

  • Women are more likely to die from asthma than men and boys are more likely than girls.

 

  • From 2008–2013, the annual economic cost of asthma was more than $81.9 billion—including medical costs and loss of work and school days.

Source: https://www.aafa.org/asthma-facts

 

The Solution

 

How could this all have happened, and can it be prevented? That is where you, the in-home care provider, can step in and have a huge impact on those in your care. You can do what foster caregivers do better than anyone else, including family, doctors, nurses, therapists, and pharmacists. You are THE 24-7 therapy facilitator specialist. You can ensure that therapy is followed and done correctly. But you can’t facilitate anything until after you have the knowledge and skills required. So, let’s get to it and start learning what you need to know.

 

The Causes of Non-Compliance

The reasons for non-compliance in respiratory therapy are as complex and varied as humans are themselves. It can be a bit intimidating to caregivers to try to tackle such a huge subject. That is, until you simplify things by placing all various reasons for non-compliance into two categories: intentional non-compliance and unintentional non-compliance.

 

Intentional Non-Compliance

Intentional non-compliance is all the reasons a patient gives for not wanting to cooperate. Those who have been in the caregiving profession long enough will recognize the following list.

  • The belief that a particular medication is unnecessary
  • Concerns about side effects
  • Medication costs
  • Social stigmas
  • Unrealistic expectations of treatment
  • Dissatisfaction with health-care providers
  • General poor health that leads to grouchiness or just plain, old-fashioned grouchiness
  • Apathy (just doesn’t care or has a lifetime of poor health habits)

 

Intentional non-compliance is the easier category to understand and to manage … at least for foster care providers. Just perform your daily routine of good care practices, and eventually, even the grouchiest, most non-compliant resident will come around. New habits will be established, and greater understanding and acceptance will occur, but only if you maintain your good practices and persevere in your efforts. By the way, only foster care providers can apply this kind of behavior-altering pressure on the patient. Every other medical professional sees the client too infrequently to have as much of an impact on patient compliance as your caregiving efforts do.

 

Here are a few ideas for your caregiver’s mental toolbox.

  • Consistency is key. Stick to a regime—repeated actions lead to habits.

 

  • Appeal to an authority who is not there to argue with. Say that the doctor, nurse, family member, etc. said to do it. You’re just following orders. They can’t argue with you because you’re not the one giving the orders.
  • Give treats as a reward for compliance, thus reinforcing good behaviors.

 

  • If they complain of the taste, promise to wash it down with juice or a snack.

 

  • Point out the benefits. “Don’t you want to breathe better?”

 

  • Point out the consequences. “Do you really want to have difficulty breathing?”

 

  • Emphasize outcomes. “I’m glad to see you’re breathing so much better. That medicine sure is effective.”

 

  • Sincerely compliment efforts. “Now you’re getting the hang of it. Soon you’ll be teaching me how to use the inhaler.”

 

  • Empathy is rewarded with compliance, if done appropriately. Say things like, “I would think that using the inhaler all the time is a nuisance, but on the other hand, I would think that not breathing is worse.”

 

  • Educate the resident. Question them on what they think the inhaler is for, what side effects they think they have, and what benefits they think they are getting from the medication. Then correct any misconnections or fill in any missing information.

 

Unintentional Non-Compliance

Unintentional non-compliance is where the resident wants to cooperate but still falls short in their therapy. This type of non-compliance falls into three categories: forgetfulness, misunderstanding of the instructions, or poor inhaler technique.

In my opinion, this is where most of the problems with non-compliance occur. That may surprise you, considering these are the patients who want to cooperate. They think they are using the medication the way it was prescribed but, for one reason or another, they are falling short of full adherence to therapy. This leads to sub-optimal outcomes and the patient still suffers. Often, the patient gets frustrated with their therapy, wondering why it’s not working for them. If the frustration continues, they lose confidence in the treatment or the prescriber and become less willing to comply with instructions.

In one study of inner-city children with asthma, 87 percent showed they had poorly controlled symptoms. It is small wonder that the same study showed that only 1 percent of the children’s caregivers were able to demonstrate proper inhaler technique.

Stating again what is now more obvious, this is where foster care providers can have the greatest impact. You are in the unique position of being with the patient the most. You can remember for the client when to use the inhaler. You can objectively evaluate inhaler technique and catch errors in inhaler use. You can identify and report any handicaps and barriers that prevent optimal drug therapy. You can follow up with concerns, help overcome handicaps, and continually ensure that therapy is followed. With a little effort on your part, things will only get better for your residents. Let’s go over a few caregiving suggestions I have for you.  

 

Ways to Manage Forgetfulness

 

 Life events and activities of daily living tend to compete for the attention of every person, including residents and their caregivers. It’s only human to forget even the most important of action items. Here are a few ways to help you and your resident remember their inhaler medication in a foster care setting. These are by no means the only methods of remembering dosage times. The following ideas are meant to augment what you are currently doing.

 

The Caregiver

A caregiver tool to help you remember medication administration times is good recordkeeping techniques. That’s right, the MARS. You know, that annoying chore that every caregiver wants to avoid and is tempted to put off until the very last day before inspection. But you got it all wrong. The MARS is not a chore; rather, it is the most powerful memory tool you’ve got. If utilized properly, it’s the ultimate “to-do” list for medication administration.

I suggest making filling out the MARS a part of the drug-dispensing routine. Fill it out as you’re giving out the meds. Don’t hide away the MARS in a closet; pull it out and bring it with you when you grab the meds. Heck, use it as a tray to carry the meds. Put it right down in the middle of things where it can’t be overlooked. Tie a pen on a string and attach it to the MARS where it will be handy. As you dispense the drug, fill out the MARS, just like crossing off an item on a to-do list. Then, move on to the next medication to dispense. If you regularly use the MARS several times a day, you will never forget to dispense the resident’s medication. I promise you, if you avoid filling out the MARS in robot mode and use it instead as a to-do list, the resident will always be compliant with medication times. (And you will never again worry about being dinged during an inspection.)

Another powerful memory tool is timer alarms. You can buy medication delivery devices with sound reminders, but why spend the money? Just set up your smartphone with timer alerts apps. It’s not that much effort to download free versions to your cell phone.

 

The Resident

First things first: Get permission from the doctor to self-administer all inhaler medications. This is one of those details that can come back to bite you come inspection and relicense time. You will find it easier to obtain the necessary documentation if you do all the work for the doctor. Write out your own order and have a place for the doctor to sign.

It doesn’t have to be fancy, and you can certainly copy other self-admin orders you have seen. In fact, you can copy the format below:

 

__________________________________________________________________________________

Consent to Self-Administer Medication

 

_________________________

Resident’s name

 

_________________________________           __________

Medication                                                                               Dosage

           _________________________________

           Time of administration      

 

I have prescribed the specified medication to the patient listed above and authorize the patient to self-administer it as I have instructed.

 

________________________________

Signature of the prescriber

 

__________________________________________________________________________________

 

Please return to: Business name, address, email, fax, or include in patient’s return file.

A final note on self-admin forms: As a matter of courtesy and to avoid future problems, make a copy of yours and send it along with the resident if they participate in any event, work, or program where you are not present. That thought brings us to the next item.

 

There will always be times when you are not around to remind the resident to use their inhalers, such as recreational or work programs and family outings. During such events, your resident will experience extra distractions that will make them forget their medication. You will have to set things up so it is easy for the resident to remember their dose. Here are a few ideas that might help.  

  • Reminder notes are good, but timer alarms are better. Buy a cheap timer from Walmart and set it for them for when the inhaler dose is due. Slip it into their pocket before each trip and collect it when they get back. That way, you have control and can make time adjustments when needed. It will also give you an opportunity to visit with the resident about their inhaler use.

 

  • Educate the resident on what the medication does for them and when it is to be taken. Let them ask questions. If you don’t have the answers, ask the pharmacist or prescriber. The idea is to give them enough information so that they will buy into the need for taking the medication and alleviate any lingering fears.

 

  • Educate the person in charge of the outing. Make sure they have enough info to gain their cooperation. Supply them with a copy of the self-admin order from the doctor. If the outing is a repeated event, provide a mini MARS that requires filling out when doses are given. The responsible person will not really be responsible for filling it out, but it will be a motivational tool and give you information that you can follow up on.

  • Keep the inhaler noticeable. If the resident is responsible enough, slip the inhaler into their pocket, where it can be felt. If they will have trouble with that, give it to a responsible person for safekeeping. Another idea is to drill a hole in the plastic case of the inhaler and put a string through it, so it can be worn as a necklace. Have the resident place the inhaler necklace under their clothes for privacy reasons. When you are sending an inhaler with the person, it would be wise to get the prescriber to write the prescription for additional inhalers in case one gets lost.

 

  • Have them return and report. Tell them that you are required to keep track of when the inhaler gets used and are relying on them to help fulfill your responsibility. Have the MARS handy and fill it out as they report. It will give them a sense of importance and a feeling of control that will inspire further cooperation. You see, the MARS is a tool, not a burden.

 

Misunderstanding of the Instructions

 

As far as medications go, inhaler use is quite involved. It is a lot more complicated than just popping a pill every day and you’re done. In order to get the full benefit out of the medication, the patient has to know when to take it, how to use the device, and why they are taking it in the first place. The data in studies show that misunderstandings are occurring in far too many cases. Why is that? The doctor and/or the pharmacist are supposed to educate the patient in all these details to ensure the medication’s proper use. “Yeah, right. Like that happens 100 percent of the time.” At the very least, they are supposed to send home literature explaining everything. “Well, you know how often the patient reads those wonderful literary masterpieces.” 

Now consider understanding inhaler medication from the perspective of your resident’s point of view. How much medical training have they had? Add to that the mental acuity of your typical foster care resident. They are handicapped by their age (too old or too young) or impaired by their condition (developmentally disabled or mental-health challenged). In addition to those factors, think about how often they have seen their prescriber or pharmacist. “Once a year if you’re lucky.” Finally, think how long ago they received their initial instructions on inhaler use. “Months or even years, maybe.” Given these facts, it is small wonder that so many patients misunderstand their inhaler instructions.

You would be totally justified in thinking that none of your residents totally understand their inhaler medication instructions. In my expert opinion, you should assume that the resident doesn’t understand their inhaler medication. Start from scratch on every single inhaler prescription that comes into your home, no matter how long the resident has been on it. Even if I am proven wrong and they do understand the instructions, it is always wise to have a review of the details every so often.

If you are starting to get apprehensive about helping the residents with their inhalers, don’t be. It may appear that inhaler use is very difficult and impossible to get right. Quite the opposite is true. Inhalers are designed to be simply understood and used by almost anyone. You just need to be instructed on some of the basics and you will be good to go. As you read the following details about inhalers, remember, you’re not the prescriber, you’re the facilitator of therapy. You don’t have to understand the ins and outs of a drug. You just have to know enough to see that it’s used correctly.

  

The Prescription

As you know, the prescription contains the prescriber’s instructions on how the patient is to use the medication. When you first receive the medication from the pharmacy, read the instructions to see if you understand it. If you don’t fully understand it, ask the pharmacist questions until you do. Don’t worry about bothering the pharmacist. Remember, it’s your license on the line if you don’t ensure the doctor’s orders are followed as he or she intended.

 

Look for the hidden details that are not spelled out. For example:

  • Inhale by mouth 1 to 2 puffs as needed. Ask the pharmacist – How much time between puffs? As needed for what? How do you know when the second puff is needed? How long would you have to wait before giving the drug again? If the drug doesn’t seem to be working, then what do you do?

 

  • Take once daily. Ask the pharmacist – What time of day is the best time to take the medication? Why is that time the “best” time? What circumstances would justify a change in that time? How many days is the prescription supposed to last? When should I call in for refills?

 

  • Use as directed. Just hand the bag back to the pharmacist and say, “Call the doctor for better instructions.” Teach the pharmacist about what is required by foster care providers. If they are not cooperative, tell them you will have to go over their heads and call the doctor for a better written prescription.

 

  • If there are multiple inhalers prescribed, ask in which order they are to be used and how much time should be allowed between doses. (You might have to call the doctor for the answer to these questions.)

 

  • Rarely will the prescription label be placed on the inhaler itself. That means, when the inhaler is used away from your home, the instructions for use will be missing. If the patient is going to be taking the device outside your home on a regular basis, it would be wise to ask for a second label. From the second label, cut out the essential instructions and stick them directly on the device.

 

Patient Drug Information Insert

Every medication that comes from a pharmacy has to have an information sheet. Have you taken the time to read those papers from the perspective of a caregiver? It has listed almost everything you need to know to manage the resident’s medication use. It’s all spelled out in black and white in everyday language. How easy is that?

I went down to my local grocery store pharmacy and picked up an information sheet on an albuterol inhaler. Listen to how it is organized.

  • What is this drug used for?
  • How is this drug best taken?
  • What are some other side effects of this drug?
  • What are some things I need to know or do while I take this drug?
  • If overdose is suspected:
  • How should I store and/or throw out this drug?

It’s practically a caregiver’s training guide on albuterol. The only thing that is missing is how to fill out the MARS.

 

The Patient

Once the details are clear to you, set some time aside to counsel with the resident. Normally, caregivers don’t have to have a discussion with their residents about their drugs. But since inhaler devices are essentially self-administered, they require a degree of understanding and cooperation that must be verified by the caregiver. When you counsel with the resident, remember to be non-judgmental and use plenty of caring empathy in your discussion.

I suggest you start out by asking the following questions.

  • What do you think this inhaler is used for?
  • When do you usually take it?
  • How do you think the medication helps you?
  • How can you tell if the medication is working?
  • Could you show me how you use it?
  • Do you have any concerns about the drug?
  • Do you have any difficulties when using the inhaler device or devices?

As they answer your questions, you may start to notice misconceptions and misunderstandings the patient has collected over the course of their therapy. How you correct those misunderstandings will take some skill. I suggest that you do not try to make any corrections after each response. Wait until all the questions are done. If corrections need to be made, do not make the resident feel like they were wrong. You will get more cooperation if you do not make them feel bad about what they have done in the past. Tell them that there is a better way, better understanding, or better techniques that will help them get better outcomes from their therapy. 

Another counseling technique is not addressing the error in understanding at all. Make the correction appear to be something brand new. Say something like, “Well, it looks like there was a change somewhere along the way because I was told the doctor wants you to take the medication like this (add the correct detail). The doctor must have thought that you would feel better if you did it this way.”

Empathy can also be used to gain cooperation when changes are needed. Say something like, “I totally understand why you think (or feel) that way. Given your circumstance, I think I would have thought (felt) that way too. But there is a better way (better understanding) that will help you even more.”

There are circumstances when the mental abilities of the resident are so low that any discussion would just confuse the resident. In these cases, it is better to present the correct information as an authority figure. Confidence in your demeanor will be key for better outcomes.

Be careful not to blame any misconceptions on the doctor or pharmacist or you will undermine the resident’s confidence in them. That will only lead to problems down the road.

 

The Family or Other Responsible Person

Finally, do not forget to counsel with family members or other responsible persons who have influence on the resident in any significant way. If you do not include them in the conversation, they may undermine all your efforts to change the situation.

 

Poor Inhaler Technique

 

The vast majority of patients make at least one error in inhaler technique. Your residents either picked up some bad habits along the way, forgot their initial instructions, or were never shown the proper technique in the first place. If it wasn’t for the fact that inhalers are designed to be easily used, I don’t think that anyone would be close in getting it right.

The reality is that most health-care professionals are not very good at teaching their patients proper inhaler technique. In one study of pulmonologists (they are supposed to be the inhaler therapy specialists), it was discovered that only 43 percent were knowledgeable in teaching patients how to use inhalers. The problem is lack of available training. I remember as a practicing pharmacist I was never given any instructions on how to educate a patient when a new inhaler hit the market. I was supposed to just know what to say. I assume the same happens with doctors and nurses. Even if the resident was shown the proper technique, one education session is rarely enough to ensure proper inhaler use over the course of the therapy.

Knowing these facts should give you, the caregiver, the proper perspective when you start working with your residents. You are in a great position to teach what has not been taught and help remember what has been forgotten. After all, you have more time with and better access to the patient than any other health professional. Why shouldn’t foster caregivers be the ones to support proper inhaler technique? “But where is my training?” I hear you say. This CE is the start. I will show you how to access more training as we continue. All you will need is a computer, your good communication methods, and your keen observational skills. You will be able to help your resident have better inhaler technique.

 

Let us start with the basics. There are three varieties of inhalers: metered-dose inhalers (MDIs), dry powder inhalers (DPIs), and slow mist inhalers (SMIs). Each type relies on a different mechanism to deliver the medication into the lungs. I will give a general description of each category, but don’t get too caught up in the narrative. Each brand of inhaler will have its own set of specific instructions. I will cover how to get those instructions later.

 

MDIs

Metered-dose inhalers deliver the medication via a propellant from a pressurized canister. It works in the same way as an aerosol can of hairspray. By depressing the canister into the plastic mouthpiece, a measured dose of the drug is pushed into the lungs. This is the type of inhaler that most people are familiar with and, unfortunately, it is the most difficult type to get right.

Patient Instructions

  1. Remove the cap from the MDI and shake well.
  2. Breathe out all the way.
  3. Sit up or stand with your back straight.
  4. Place the mouthpiece of the inhaler between your teeth and seal your lips tightly around it.
  5. As you start to breathe in slowly, press down on the canister one time.
  6. Keep breathing in slowly and as deeply as you can. (It should take about 3–5 seconds for you to completely breathe in.)
  7. Hold your breath for 10 seconds (count to 10 slowly) to allow the medication to reach the airways of the lungs.
  8. Repeat the above steps for each puff ordered by your doctor. Wait about 1 minute between puffs.
  9. Replace the cap on the MDI when finished.
  10. If the inhaler is a corticosteroid MDI, rinse out the mouth after each use.

Caregiver Instructions

  • Make sure there is medication in the canister. The most accurate way is by keeping track of how many times it is used. Each box has listed how many total doses there are, and you just count it down each time it is used. The MARS will come in real handy for this. Remember to record when a new inhaler is used in the MARS. Once the number of doses is used up, don’t count on the inhaler working for symptom relief, even if the inhaler continues to spray.

 

  • New inhalers will have to be primed by shaking the inhaler and spraying it into the air one to two times. If the inhaler sits for over two weeks, prime it again. Don’t count the primer sprays in the dose countdown.

 

  • The plastic mouthpiece should be rinsed with warm water once a week and left to air-dry. Remove the canister before cleaning. If the canister can’t be removed, wipe its opening with a soft rag or cotton swab.

 

  • The timing and speed of breath intake is very important. If the resident inhales too late or too soon, the medication is sprayed on the back of the mouth or tongue. The medication is then swallowed into the stomach, where it doesn’t do much good. If the intake is too fast and strong, most of the medication ends up too deep in the lungs. The drug has to be deposited all along the airway to have full effect. Some residents are so used to tasting the medication as a result of bad technique that they think that they didn’t get the dose if they don’t taste it. You will have to educate them the opposite is true.

 

  • Make sure the resident is breathing through the mouth and not their nose. Make sure the tongue is placed under the mouthpiece and out of the way.

 

  • During times of stress, the resident will have difficulty with the timing and thinking clearly. Keep watch during these times and coach them along.

 

  • If the resident just can’t get the timing or breathing right, ask the doctor for a “spacer” prescription. It is a special hollow tube designed to hold the spray in the air of the tube. This makes it easier to breathe in the medication correctly. Pediatric versions can come with a mask for even easier use. Spacers also need to be periodically cleaned as per manufacturer instructions.

Spacer Instructions

  • Remove the cap from the MDI and chamber. Shake well.
  • Insert the MDI into the open end of the chamber (opposite the mouthpiece).
  • Place the mouthpiece of the chamber between your teeth and seal your lips tightly around it.
  • Breathe out completely.
  • Press the canister once.
  • Breathe in slowly and completely through your mouth. If you hear a horn-like or whistle sound, you are breathing too quickly and need to slow down.
  • Hold your breath for 10 seconds (count to 10 slowly) to allow the medication to reach all the airways of the lung.
  • If the resident is still having issues even with the spacer, ask the doctor for another type of inhaler or maybe even a nebulizer.
  • Monitor for effectiveness and side effects.

 

 

 

DPI

Dry powder inhalers deliver the medication as a fine powder mixed into the air of the inhaled breath. They come in either a multidose inhaler or as individual capsules that are placed into the devices with each use. In either case, the drug-containing capsule needs to be punctured by the device before a breath is inhaled. Most often, it makes a clicking sound. The medication is released only when the user takes a deep, fast breath in through the inhaler.

 

Patient Instructions

  1. Remove the cap.
  2. For single-use devices, load a capsule into the device as directed.
  3. Sit up or stand with your back straight.
  4. Breathe out slowly and completely (not into the mouthpiece).
  5. Place the mouthpiece between the front teeth and seal the lips around it. Hold it like a sandwich.
  6. Breathe in through the mouth quickly and deeply over two to three seconds. Suck like drinking through a straw.
  7. Remove the inhaler from the mouth. Hold your breath for as long as possible (10 seconds).
  8. Breathe out slowly.
  9. Rinse the mouth after use.

Caregiver Instructions

  • Do not shake the device or let the resident shake the device before use.
  • As you set up the device, listen for the telltale click that lets you know the drug-containing capsule has been broken. Then hand the DPI to your resident.
  • Do not let the resident blow into the device.
  • Never use a spacer with a DPI.
  • If the medication is a corticosteroid, make sure they rinse their mouth after use and spit out the water.
  • Clean the mouthpiece with a clean cloth but do not get the device wet.
  • Each multidose device comes with a counter so you know when to reorder the prescription.
  • The resident will most likely not taste or feel the medication. Assure them that they are getting the drug delivered to the proper area of the lungs.
  • The technology relies on a deep, strong breath. If the resident has trouble with that, consult with the doctor.
  • Monitor for effectiveness and side effects.

 

 

 

SMI

Soft mist inhalers deliver the medication via a sprayed mist. It does not have a propellant but has a spray of fine vapor, which is breathed into the lung. They are also known as Respimat inhalers and are the newest device type on the market.

 

 

Patient Instructions

  1. Hold the inhaler upright with one hand, with the cap closed. Use your other hand to turn the clear base to the right until it clicks.
  2. Open the cap.
  3. Sit upright or stand with your back straight.
  4. Breathe out slowly and completely.
  5. Put the mouthpiece in your mouth, holding the inhaler horizontally (pointing toward the back of your throat).
  6. Close your lips around the mouthpiece, making sure not to cover the air vents on the sides.
  7. Take a slow, deep breath in. As you start to inhale, press the button on the side of the inhaler.
  8. When your lungs are full, hold your breath for 10 seconds to keep the medicine in your lungs.
  9. Take the inhaler out of your mouth and breathe out slowly.
  10. Put the cap back on the mouthpiece.

Caregiver Instructions

  • Before you can start using the SMI, insert the medication cartridge. Press the safety catch on the side of the inhaler and remove the plastic base. Push the cartridge into the inhaler until it clicks. (To make sure it is inserted completely, push the cartridge against a firm surface, like a tabletop.) Once the cartridge is in, put the clear plastic base back on and press until you hear a click.
  • Brand-new devices need to be primed three times, as follows:
    • Hold the inhaler upright with the cap closed and twist the clear base clockwise (to the right) until it clicks.
    • Open the cap and point the inhaler at the floor, away from your face.
    • Press the button on the side until you see a mist come out.
  • Prime the device once if it has not been used in more than three days. If more than three weeks, prime it three times.
  • The medication does not need to be shaken, but it does not hurt anything if it is. Spacers are not required.
  • You may have to help the resident with step one.
  • Clean the mouthpiece with a damp cloth.
  • Monitor for effectiveness and side effects.

 

Foster Caregiver Considerations

 

You now have a basic understanding of the fundamental principles of inhaler therapy. You are by no means an expert, but you don’t have to be. You have enough info to get started. You certainly have more understanding than the resident has, and that is the whole point of foster care—taking better care of those who can’t take care of themselves. You may not be the authority on therapy and medication (that’s why you keep a doctor and pharmacist around) but you are the authority on “get ‘er done,”

Here are a few more ideas on “get ‘er done” and inhaler therapy.

 

Rescue vs. Regular

We have talked a lot about inhaler devices and technique. Now, let’s talk about the medication itself. I’ll spare you a long, drawn-out (and boring) discussion of the different classes of drugs and what they do. If you have a burning desire for that knowledge, ask the pharmacist for the package insert on the medication. What you do need to understand is rescue versus maintenance therapy.

Maintenance therapies are the drugs that prevent respiratory symptoms from occurring. Rescue medications are drugs that relieve breathing problems after they happen. Most likely that would be albuterol, but there are others. When you first receive the inhalers, ask which ones are the rescue inhalers. You can also tell which ones they are by the instructions on the prescription. They’re the ones that will be PRN (or as-needed).

There are two reasons why you ask about the rescue inhaler up front. First, you have to know what to reach for in breathing emergencies. Second, how often the PRN meds are being used is a great indicator of how the therapy is going. If the resident is having to be constantly “rescued,” you have to start thinking, “Why?” What is causing all the problems? Here are a few possibilities.

  • Poor technique is preventing the maintenance medication from getting to where it belongs. Solution: Observe inhaler use and educate the resident when needed.

 

  • Handicaps are interfering with therapy, especially in regard to how strong the breath needs to be for each type of inhaler. Solution: Make notes of your observations and consult with the doctor on what to do.

 

  • The resident may be using the rescue medication as a crutch. This one is tricky. Define as needed. Along with the medical need, there may also be emotional need, or a need to feel secure. It is clear that there will always be an emotional element in respiratory therapy. It is very hard not to be afraid when you can’t breathe. If this is a concern, the fear may lessen over time as you provide a caring, safe environment in your home. Of course, you can always discuss the matter with the doctor.

 

  • The resident may have developed a bad habit of relying on the rescue inhaler because they can feel it working, while the maintenance med can’t be immediately felt. Solution: Ensure proper use of the maintenance med, which will in turn reduce the need to be rescued. The problem will gradually take care of itself. If it doesn’t, concentrate on patient education.

 

  • Before they moved into your home, the patient may have skipped the maintenance med when they felt good. Of course, that is not going to happen after they move in, because you’ll see to it that the med is taken as prescribed. If they balk, explain how constant use of the maintenance medication is the reason they felt good in the first place.

 

 

 

Evaluating Inhaler Technique

Pay close attention to how the resident uses their inhalers when they first move into your home. Keep observing inhaler technique from then on. You should know that their technique will suffer during respiratory distress. School them with empathy and caring, or you might add to their anxiety. They may not be able to hold their breath for the full count. To ensure proper breath-hold times, have them concentrate on counting to 10 with their fingers.

 

 

These are common errors made by the patient to watch for.

  • Inhaler not shaken before use or shaken when it should not be.
  • Incorrect body positioning. If they’re hunched over, they cannot take a full breath in.
  • Failure to exhale fully prior to dosing.
  • Poor coordination of depressing the MDI and inhalation.
  • Breathing in too hard or too soft for the device they use.
  • Breath-hold is not long enough after dosing.
  • Failure to remember to rinse out the mouth.

Spacer Use and Care

Spacers are made of plastic, and plastic can build up an electrical static charge. The charge will make the medication stick to its side. Before using a spacer for the first time, you should wash the spacer with warm dilute soapy water. The device should be air-dried. Some brands are manufactured electrostatic-free, and no preparation is needed. Read the package instructions. When in doubt, wash them out. Cleaning the spacer with just warm water will cause the electrostatic charge to develop, reducing the effectiveness of the spacer. If you are using the pediatric version that comes with a mask, the same cleaning techniques apply. Also, when you use a mask, make sure there is a good seal around the entire mask. If you are careless, extra air will leak in and the entire dose of the med will not be inhaled.

 

When the Resident First Moves into Your Home

Inspect the inhalers and spacers. Determine which are the maintenance inhalers and which ones are the rescue inhalers. Do the inhalers need to be cleaned? Which ones are empty or close to being empty, expired, or broken and need to be replaced? When in doubt, replace them.

 

Determining How Full the Canister Is

Using the MARS to keep track of how many doses are left is the best way to determine when prescriptions should be renewed. But that’s not the only way. It is also not as useful when you cannot account for every dose used, for example, when they first move in or when the inhaler is used outside of the home. Two methods of estimating what remains in the MDI inhaler are:

  1. Remove the canister and drop it into a bowl of water. See how it floats. Straight up and down means the canister is full. Floating horizontally means empty. If you are forced to use this method, dry the canister completely before use and remember to prime the device.
  2. Read the package or call the pharmacist to find out how many doses there are in the inhaler. Then estimate how many puffs are used in a day. Find out how many days since the prescription was filled and do the math. Spraying the inhaler to see if something comes out will not work because even a medication-empty inhaler will continue to spray the propellant.

 

Rescue Inhaler Prescription Refill

For rescue inhalers, I recommend that you try to keep spares around just in case of emergencies. You can get around insurance refill issues by calling the pharmacy and finding out how many days’ supply they assigned the prescription. Most insurances will allow you to fill the prescription when 80 percent of the days assigned to the prescription fill have transpired. Keep ordering the rescue med early even if you don’t need it until you have a full extra prescription in reserve. Another method is to have the prescriber order two inhalers for a same-day’s supply. The insurance may not cooperate with that, though.

 

 

A Demonstration Is Worth a Thousand Words

 

Every brand of inhaler will come with its own specific set of instructions. You will find them tucked inside of the box that the inhaler comes in, written on a small paper insert. Take it out and become familiar with the device’s requirements. In my opinion, though, that is not good enough. The patient needs a demonstration. That is where you and your computer come into play.

 

There are thousands of demonstration videos on inhalers published by the drug manufacturers and knowledgeable health-care providers. The ways to find the good ones are:

 

  • Type in a browser search field (for example, Google) the phrase “(brand name) demonstration video”.

 

  • There will be a list of video websites that come up. Skip the “ad” ones unless it is the manufacturer’s website. Choose a likely candidate. Almost always, the video will be published on YouTube.

 

  • Select the video and review who presented the video. Choose only reputable sources, for example, medical or professional organization websites.

 

  • See how many views the video has. The larger the number, the more likely it will be a quality video.

 

  • View several videos and choose the best ones to show your resident.

 

After watching the video, have the resident use their inhaler. This show-and-tell session will be critical for you in evaluating their understanding of the instructions. Work with the resident until they get it right. It may take several sessions. Some habits are just hard to break.

Remember to be humble and helpful. After all, you are no therapy expert. You are just someone who is supporting the resident’s efforts to get it right. If there are difficulties, first evaluate your own understanding and communication techniques. Are you getting it right? If there are still difficulties that are too hard to overcome, report them to the doctor. When you talk to the doctor, be specific in reporting your observations.

I recommend that you repeat the video or demonstrate sessions periodically. Once or twice is never enough to ensure continued proper inhaler technique.

 

Conclusion

 

Asthma and COPD are significant health concerns in many residents of foster care homes. Inhaled medications are the gold standard for treating these conditions, but these devices require a greater effort from the patient to comply with therapy requirements. Studies have shown that the majority of patients are not compliant with their therapy, thus leading to increased mortality and morbidity issues.

The reasons for non-compliance are complex and are either intentional or unintentional. There is a great need to assist the patient in becoming compliant with therapy that is just not being met. Foster care providers are uniquely situated to effectively take care of this need. They can observe and evaluate the resident’s understanding and compliance with therapy. Facilitate the resident’s effort to become compliant and report back to the prescriber any significant difficulties the resident is having.

Caregivers are also best suited to ensure continued compliance over the course of the therapy. I hope that this CE has helped the caregiver along with internet resources to become THE expert on “getting it done.”

As always, good luck in your caregiving efforts.

Mark Parkinson, BS Pharm.

 

References:

Stephanie Watson. Inhalers for COPD. Healthline, Aug 14, 2018. https://www.healthline.com/health/copd/inhaler-nebulizer

Laura Koppen PharmD, BCPS. Advances in Inhaler Technology: Helping Patients Increase Adherence. Power-Pak CE. UAN: 0430-0000-19-138-H01-P. Dec 20, 2019 https://www.powerpak.com/course/preamble/119037

Aimee Simone. Many Caregivers Unable to Demonstrate Proper Use of Kids' Asthma Inhalers. Pharmacy Times. 2013-11-11 03:06:17.

https://www.pharmacytimes.com/news/Many-Caregivers-Unable-to-Demonstrate-Proper-Use-of-Kids-Asthma-Inhalers

How to Use a Metered Dose Inhaler. Family Doctor.org. American Academy of Family Physicians. 2020. https://familydoctor.org/how-to-use-a-metered-dose-inhaler/

Jane Scullion. The Nurse Practitioners’ Perspective on Inhaler Education in Asthma and Chronic Obstructive Pulmonary Disease. Hindawi. Canadian Respiratory Journal. Volume 2018 |Article ID 2525319. https://www.hindawi.com/journals/crj/2018/2525319/

Toby GD Capstick & Ian J Clifton. Inhaler technique and training in people with chronic obstructive pulmonary disease and asthma. Expert Review of Respiratory. Medicine, 6:1, 91-103, DOI: 10.1586/ers.11.89. https://www.tandfonline.com/doi/pdf/10.1586/ers.11.89

Lynn B Gerald, PhD, MSPHRajiv Dhand, MD. Patient education: Inhaler techniques in adults (Beyond the Basics). Up To Date, Sep 29, 2020.https://www.uptodate.com/contents/inhaler-techniques-in-adults-beyond-the-basics

 

 

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Medication Overload

Author: Mark Parkinson BsPharm:  President  AFC-CE

Credit Hours 2- Approximate time required: 120 min.

 

Educational Goal

Explain what Medication Overload is and ways that caregivers and reduce it’s negative effects on the residents.

Educational Objectives

  • Define Polypharmacy, Medication Overload and the Pill Burden
  • List contributing factors that cause medication overload
  • Tell what is being done by medical profession to reduce medication overload
  • Present idea about how caregivers can help manage the problem.

Procedure:

Read the course materials.  2. Click on exam portal [Take Exam].  3. If you have not done so yet fill in Register form (username must be the name you want on your CE certificate).  4. Log in  5. Take exam.  6. Click on [Show Results] when done and follow the instructions that appear.  7. A score of 70% or better is considered passing and a Certificate of Completion will be generated for your records.

Disclaimer

   The information presented in this activity is not meant to serve as a guideline for patient management. All procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this article should not be used by care providers without evaluation of their patients’ Doctor. Some conditions and possible contraindications may be of concern. All applicable manufacturers’ product information should be reviewed before use. The author and publisher of this continuing education program have made all reasonable efforts to ensure that all information contained herein is accurate in accordance with the latest available scientific knowledge at the time of acceptance for publication. Nutritional products discussed are not intended for the diagnosis, treatment, cure, or prevention of any disease.

 

Medication Overload

Three times in one year, a normally clear-thinking elderly woman was found wandering the neighborhood with her dog, unable to find her way back home. Upon review of her medication use, it was discovered that she had three different PRN (or, as-needed) medications for pain and anxiety. When all three were taken together, her ability to think clearly was so impaired that she would attempt to get into other people’s homes, thinking they were her own.

The adverse effects that arise from polypharmacy has been described as “America’s other drug problem.” Polypharmacy is loosely defined as the taking of at least five different medications together. As more and more drugs are prescribed to manage medical complaints, the chances of unforeseen side effects increase.

Iatrogenesis, or doctor-caused harm, is a perplexing problem that has always been associated with the prescribing of multiple medications together. Doctors find it hard to predict what side effects will arise when normally beneficial medications are taken together. Ironically, many doctors will prescribe even more medications to manage this “drug-caused” problem. What has been described as the “drug cascade” is an old problem of polypharmacy that is receiving new efforts to manage.

Not all polypharmacy is bad. There are certain disease states, like diabetes and mental health issues, where a multi-drug regime is required to manage the medical condition. To differentiate from those situations, a new term has been developed: medication overload. Medication overload is defined as the use of multiple medications for which the harm to the patient outweighs the benefit.

Harm to the patient can be more than just a biological side effect. Taking multiple medications can create a significant financial, emotional, and time burden for the patient to manage. Taken together, all these problems are known, in many medical publications, as the pill burden. A significant pill burden can greatly reduce the overall quality of life for a patient. As a practicing pharmacist, I witnessed firsthand the pill burden that many of my customers faced. It was heartbreaking to watch them struggle to decide whether to buy food or fill their prescriptions.

 

Major health institutions and medical associations are starting to recognize the problems of medication overload. They are beginning to take steps to try to understand the causes of iatrogenesis and reduce the pill burden their patients are experiencing. As with any scientific endeavor, the first step these organizations are taking is the gathering of data.

The Lown Institute of Canada reports that “Every day, 750 older people living in the United States (age 65 and older) are hospitalized due to serious side effects from one or more medications. Over the last decade, older people sought medical treatment more than 35 million times for adverse drug events, and there were more than 2 million hospital admissions.” Source: Medication Overload and Older Americans,” Lown Institute.

 In the same article, it was also reported that polypharmacy “has reached epidemic proportions. More than four in ten older adults take five or more prescription medications a day, tripling over the past two decades. Nearly 20 percent take ten drugs or more.” Similar data has also been reported in mental health and developmentally disabled patients who have multiple heath problems.

 

Why has this occurred?

 

No one in the medical field wants to cause the patient harm. Yet, for multiple reasons, harm is being experienced. To better manage the problem, a greater understanding of the causes must be considered. The many contributing factors can be more fully comprehended by placing them in three broad categories.

The Culture of Prescribing

The “a pill for every ill” culture of our modern society has it roots in several factors:

  • Pharmaceutical companies seeking profits. In order to stay in business, drug companies must sell products. They rely on salesmen that try to influence prescribers, and they advertise with slick commercials to try to influence consumers.

 

  • Overworked medical professionals. To treat all their patients in a profitable way, prescribers must be very efficient with how much time is spent with each patient. It is by far easier and quicker to write a prescription than manage a disease. “Take two pills and call me in the morning” is an easily recognized phrase.

 

  • The add-on therapy. Many treatment regimes call for adding drugs to therapy until the symptom is controlled. This leads to multiple drugs, all treating the same symptom. Doctors are trained to add a drug instead of replacing a drug.

 

  • Demanding patients. Patients, their families, and their caregivers often demand that the doctor “do something.” The perception of treatment is often linked to taking a drug.

 

  • Consumer culture. Consumers are used to buying their way out of problems. Have long grass, buy a lawnmower. Need food cooked quickly, buy a microwave. Have constipation, buy a laxative pill. The consumer finds it easier buy a drug to manage a medical problem than make changes to their lifestyle.

 

  • The vast majority of health-care costs are paid for by insurance companies. Health care is expensive. Insurance companies must impose limits on what they pay for or they will go out of business. They will try to save money by paying for older, cheaper medications that have more side effects and are more complicated to use than newer, expensive ones.

 

 

Information & Knowledge Gaps

The more medications that are consumed, the more information and knowledge is required by the prescriber and the patient. Yet when harm is caused, it is a clear indication that information was lacking.

  • Drug Companies: Pharmaceutical manufacturers cannot study the effect of combining their drug with every other drug or combination of drugs. It is an unknown and unknowable hazard factor in prescribing medication. Doctors are forced into prescribing blind to the consequences of combining medication.

 

  • Prescribers: Doctors are often unaware of the full list of the drugs the patient is taking. Doctors also lack reliable information on non-drug therapies. Therapy outcomes research is expensive and drug companies are often the only ones willing to pay for the research. Doctors are more willing to go with a proven drug therapy than experiment with an unproven non-drug therapy. Critical feedback from the patient about drug therapy outcomes is also dangerously lacking. If the patient does not call the doctor, the prescriber assumes that everything is okay.

 

  • Patients: The person receiving the drug is given instructions and written material about how to manage its use. But how often is that material read, and the instructions understood? The more pills that are taken, the greater amount of material there is to read. The little old lady who takes 1o different pills will not be able to appropriately manage all of them, especially when there are several medications that cause a drugged haze to her thinking. To complicate drug management even further, she may also use several health supplements and over-the-counter (OTC) medications that do not come with any medication literature to help her understand her medications.

 

Fragmentation of Care

The more advanced our medical knowledge becomes, the more specialized its practitioners become. You have cancer specialists, gerontologists, urologists, nurse practitioners, physician assistants, psychiatrists, and all the other “–ists” who have the ability to write prescriptions. Each has the same pressure to “do something.” Yet who is being held responsible to coordinate all these efforts? The primary care doctor (if there is one), the patient (who has no medical background), or the caregiver (who has no authority)? The coordination of American-style medicine and communication between its practitioners is lacking in many ways. Often, a “prescription cascade” occurs when one doctor will prescribe a medication that causes a side effect. Another doctor will prescribe an additional drug to manage the side effect, and around and around it goes until there is a significant medication overload.

Case in point, as reported by the Lown Institute:

“Killed by a Prescription Cascade

How did Joe Esposito go from a man in remarkable health, effortlessly running half marathons in his 50s, to being debilitated and incapacitated, struggling at death’s door, in just a few years? When Joe sought treatment for his mild to moderate Crohn’s disease, his list of medications cascaded from one to six to twenty, as each new medication brought on a new side effect. The steroids he was prescribed to treat Crohn’s led to bone loss and anal fistulas. He was given antibiotics for the fistulas, which caused peripheral neuropathy in his feet. He couldn’t sleep from the pain so he was prescribed benzodiazepines and Ambien for sleep, Lyrica for the nerve damage, and Tramadol for the pain. Several of the drugs gave him severe diarrhea. To treat his diarrhea, he was given opium drops, and other medications. Additional drugs weakened his kidneys, which in turn raised his blood pressure, so he was put on four blood pressure medications. And an experimental anti-inflammatory drug led to Joe contracting pericardial tuberculosis, which almost killed him.

At the end of his life, Joe was taking over 20 medications and 31 pills a day, but not one physician saw this as a problem worth addressing or even considered that his symptoms were caused by the drugs and not the Crohn’s disease.”

 

What can be done?

 

No one doctor can solve this problem. The training and tools are lacking. Medical societies and organizations are trying to step up to the plate and help manage medication overload. They are promoting new medical paradigms to counter the “pill for every ill” culture we live in.

 

 

Integrated Medical Records

In the past, prescribers kept their own records that other prescribers did not have easy access to. Larger health systems like Kaiser Permanente and the University of Utah now have medical record systems that are available via a shared computer system to everyone who has a need to know. Any prescriber, nurse, therapist, or pharmacist can see what the other clinicians are doing. In addition, since patient histories and lab values are readily available to other medical personnel, some of the more mundane doctor tasks are being done by other staff. This frees up prescribers to have more time with their patients.

 

Medication Management Services

Medical specialists are providing services that assist the doctor and patient in managing their medications. For example, diabetic educators and pharmacists actively work with patients to review all their medications, monitor outcomes, and report to the doctor any significant events and recommendations.

MTM – Medication Therapy Management is a program of several services provided to assist the doctor and patient and help them get the most out of drug therapy. Those services include:

  • A review of all medications prescribed by all prescribers providing care to the patient, and any over-the-counter and herbal products the patient may be taking to identify and address medication problems. Problems may include medications not being used correctly, duplication of medications, unnecessary medications, and the need for medication(s) for an untreated or inappropriately managed condition.

 

  • In-depth, medication-related education, consultation, and advice provided to patients, family, and/or caregivers to help assure proper use of medications.

 

  • Collaboration with the patient, physician, and other health-care providers to develop and achieve optimal goals of medication therapy.
  •  

 

Deprescribing

Deprescribing is the planned and supervised process of dose reduction or stoppage of medication that might be causing harm or is no longer of benefit. To encourage prescribers to incorporate deprescribing in their practice:

 

  • Deprescribing principles are being included in doctor education and continuing education courses

 

  • Research is being done to provide evidence-based protocols

 

  • Computer tools and practice protocols that assist in deprescribing are being made available to prescribers.

 

What can in-home caregivers do?

 

In-home caregivers are in a unique position. They are both part of the professional health-care team and can act as an advocate of the patient. This makes caregivers particularly suited to deal with medication overload problems. They can ensure drug therapy is followed and push for changing the therapy when it needs to be changed. Even if the patient is already part of an MTM program, there are still many things a caregiver can do to reduce the ill effects of medication overload.

 

Monitor and Report

  • Foster caregivers can ensure there is always a complete and up-to-date list of all the medications and supplements available for all medication prescribers to see. This simple action alone results in huge benefits. Prescribers will finally have a sure knowledge of what medications the patient is actually taking. It will also help prevent the fragmentation of medical care.

 

  • Caregivers can observe and report how the patient is reacting to therapy in a timely fashion.  

 

    • Side effects can be reported as they occur, not months down the road at the next scheduled doctor’s appointment. This will make it easier to determine that new symptoms are actually drug side effects and not a worsening of the disease state.  

 

    • PRN logs can be supplied to the doctor telling him or her exactly how much of drug is being taken and when. It will allow the doctor to see patterns of drug use that will help determine when therapies need to be changed.

Advocate and Action

Caregivers can act as the representative of the doctor and the resident, and can work to support the interests of both.

 

Caregivers representing the doctor:

  • You can support lifestyle changes so that the doctor does not have to rely on drugs for needed therapeutic effects.
  • You can guarantee the patient is not overtaking their medications.
  • You can control unauthorized over-the-counter medications and supplements.
  • You can stop the use of alcohol, tobacco, and other substances that can interfere with therapy.
  • You can control the overuse of PRN medications, ensuring they are used only when needed, not just when they are wanted.
  • You can help the patient understand their therapies better.
  • You will enforce doctor’s orders and ensure therapies are remembered and followed.

 

Ensuring the resident understands and remembers their medication instructions is a very important part of drug therapy. The lack of understanding and the failure to remember are major causes of medication overload. A study done in Italy in 2014 demonstrated how big this problem is. It looked at 100 patients (65 years of age or older) discharged from an internal medicine ward throughout 2012. The patients were followed for three months after discharge. The study found:

  • Non-adherence was reported to be 55.1% at first follow-up and 69.6% at three months.
  • Only 28.1% at first follow-up and 25.3% at second understood the reason for their medication.

When therapy is not followed, symptoms will continue. This leads to patients complaining to the doctor, demanding they “do something.” This leads to more medications being added, and the drug list grows and grows.

 

Caregivers representing the resident: 

  • You can request actions that need to be taken.
  • You can challenge questionable medical decisions.
  • You can ask the questions that will make the clinician rethink his or her interpretation of why symptoms are occurring and thus reduce over-prescribing to control new symptoms.
  • You can prevent family and friends from interfering with therapy.

Consider the following case.

Mrs. A was a 71-year-old widow with congestive cardiac failure and osteoarthritis. She was put on digoxin to help her heart function normally. Later, furosemide (a water pill) was added to reduce the amount of fluid that was building up. The daughter noticed over a two- to three-month period that her mother was becoming confused, easily fatigued, and very irritable. She also noticed that her mother had become compulsive about washing her curtains. Mrs. A said they always looked yellow-green and possibly moldy. The daughter, not knowing what was going on, assumed her mother was getting dementia and contemplated putting her in a nursing home. Fortunately, someone started asking what effect adding the furosemide had on Mrs. A’s symptoms. It turned out furosemide can cause digoxin poisoning, The poisoning caused confusion, irregular pulse, nausea, and a fast heartbeat. Mrs. A felt miserable and became irritable more often. Tellingly, digoxin poisoning can create vision changes. Mrs. A always saw her curtains as yellow and green, no matter how often she cleaned them.

Too bad there wasn’t a foster caregiver there to start asking the right questions earlier.

 

Medication Overload Action Steps for Caregivers

Caregivers have been working to prevent medication overload for decades. We just didn’t know what our efforts were called. All of us have, to one extent or another, been trying to control medications, promote healthy lifestyles, and fight with doctors over what is best for our residents.

To help make your efforts more effective, I recommend the following action steps. I do not intend this to be a step-by-step system that has to be followed in order to be effective. Rather, I present these action steps as suggestions to augment what you are currently doing.

 

New resident’s drug and supplement evaluation

When a new resident moves into your home, gather all their drugs (prescription and OTC) and supplements. Compile a list for the primary care physician to review. Look for the following information and make notes on the drug list you’re going to give to the doctor. The information will be very important, and it may be the first time that the doctor has seen it.

  • Write down the medication name, strength, instructions, and who prescribed it.

 

  • Note the expiration date of the drug. If it is expired, set it aside and don’t dispense it. Write on your list that the drug is expired, and ask the doctor if he wants to continue the drug.

 

  • Ask the resident why they think they are taking the drug.

 

  • Find out how often and when the resident last took each PRN drug.

 

  • Do all of the above for each OTC drug and supplement. Do not dispense these until the doctor gives you permission through a prescription.

 

  • After you compile your list, get it to the doctor. Follow up with the doctor until YOU are satisfied with the outcome. Don’t be afraid to act as the resident’s advocate. Politely push the doctor along and keep asking questions until you get results. If a doctor discontinues a drug or supplement, place a note about the order in the resident’s file. Pass the word on to the family so they will not try to give the discontinued drug to the resident.

 

Med list in resident’s file

After you get an “approved” drug list from the doctor, add the list to the resident’s file and make sure it goes with the resident to every medically related trip the resident takes. That includes therapy visits.

 

New order evaluation

Do not just accept a new prescription or therapy order. Find out the why’s and the what’s.

  • Why is the drug or therapy being prescribed?
  • What is the goal(s) of the therapy?
  • What are the key indicators to monitor for?
  • How often does the doctor want a report on outcomes?

Report to the doctor what you have observed.

  • Read the drug literature. Note the side effects and monitor closely for at least a month. You will be the first to notice any adverse reactions. You need to report them in a timely fashion. Reporting side effects can happen only if you’re looking for them.
  • Timely reporting will greatly help the doctor determine if a new or worsening symptom is drug-related or disease-related.
  • Don’t be afraid to challenge the need for a new prescription—especially if side effects start to occur or therapeutic goals are not being achieved.

 

Old order evaluation

Do not be afraid to ask questions about any drug or therapy order. Doctors have had plenty of training on how to prescribe a drug but little to no training on how to deprescribe a drug. I find the prevailing course of action in medical practice is to add a drug and just leave it there until it is forced off the list by an adverse event. Often, I find that the only person willing to ask the challenging questions surrounding the need for a drug is the caregiver.

 

Keep an eye on these drugs

Pay close attention to the following drugs:

Drug/Drug Class

Reason to pay attention

Digoxin

Digoxin poisoning can be caused by other drugs.

Blood thinners –

Warfarin, Heparin

Interaction with drugs, supplements, and even food can cause excessive bleeding and bruising.

Antidepressants –

Fluoxetine, Amitriptyline, Doxepin, Trazodone, Citalopram, Sertraline

Serotonin Syndrome: slurred speech, confusion, falls. Changes in behavior. Just not needed in the stable, supportive environment of a care home.

Antianxiety/Sedatives –

Lorazepam, Ativan, Diazepam, Zolpidem, Diphenhydramine, Haloperidol

 

Slurred speech, dizziness, falls, confusion. Changes in behavior. Just not needed in the stable supportive, environment of a care home.

Painkillers –

NSAIDS, Aspirin, Opioids, Narcotics

Can cause drowsiness, confusion, falls, constipation, nausea. Can interfere with other meds.

Protein-Pump Inhibitors (PPIs) –

Omeprazole, Lansoprazole, Pantoprazole

 

Just not needed for long-term therapy.

Nerve Pain/Antiseizure –

Gabapentin, Lamotrigine Phenytoin, Carbamazepine, Phenobarbital

Slurred speech, dizziness, falls, confusion, changes in behavior.

 

Manage the drugs

Foster care providers are not idle followers of other medical professionals’ orders. They are active participants in drug therapy management. The doctors may be the generals who give the orders, but you are the soldiers who actually turn those orders into actions. When those orders don’t fit neatly into the reality of the situation, you can push for a modification of those orders.

  • Change to a PRN. Drugs don’t always have to be given around-the-clock in order to achieve a therapeutic goal. There are those drugs that could be changed to PRNs as long as you are educated on what circumstances they need to be dispensed under.

 

  • Monitor the patient. Keep track of your resident’s condition. If therapy goals are not being achieved, ask why the drug is still being prescribed. Before reporting a new symptom, first look at the side-effect profile of the resident’s meds for possible causes. Point out these “possibilities” to the doctor and let him figure out what is actually going on.

 

  • Multiple meds of the same drug class. If you see two antidepressants, two diabetic drugs, two statins, or multiples of any drug class, I would consider that justification to ask why. Are both really needed? Does the marginal benefit outweigh the possible side effects?

 

  • Discontinue a drug no longer needed.
    • If the drug was needed to prevent a condition that you now manage with lifestyle changes, is the drug still needed? Examples: Are stool softeners still needed if you are controlling constipation through proper diet? Are antianxiety meds needed around-the-clock if you are keeping the resident calm through good caregiving?

 

    • If conditions have changed, is the drug need still there? Examples: Does an 85-year-old woman still need to take estrogen? Does a 90-year-old man still need to take anti-cholesterol statin drugs?

 

    • Make sure there is a need before a PRN pill is dispensed. I know it can be tricky to tell the difference between a perceived need and an actual need. Paying attention to how a resident reacts after taking the med will give important clues. For example, haloperidol (Haldol) taken for anxiety takes up to four hours to take effect. If the resident calms down after a few minutes, the calming effect did not come from the drug.

 

  • PRN logs as red flags. Medical concerns can be seen first in an increased use of PRN meds. Report sudden increases in PRN use to the doctor and ask the doctor if it is a sign of therapy failure or medication overload.

 

  • Take advantage of the pharmacists and visiting nurses. Sometimes changes can be made faster and more easily if the request comes from a pharmacist or nurse. Also, pharmacists are easily accessible drug encyclopedias. If you have questions or concerns over anything drug-related, run them by the pharmacist first—especially if a pharmacist is doing an MTM review in your home.

 

  • Use the terminology to make the point. I found that, as a caregiver, nothing gets a doctor’s attention faster than using proper medical terminology. Try it next time you communicate with the doctor and take note of their reactions.

 

Here are two more case studies that illustrate the need for active medication management by the caregiver.

CASE 1

A 39-year-old white woman with depression and panic attacks was being treated with fluoxetine, trazodone, clonazepam, and cimetidine. After fluoxetine and clonazepam were abruptly discontinued, venlafaxine and lorazepam were started. Within 24 hours, she developed diaphoresis, tremors, slurred speech, myoclonus, restlessness, impaired thinking, and diarrhea. These are all symptoms of drug-caused serotonin syndrome.

Case 2

An 83-year-old woman was taking 17 different medications. She started to show new signs of tremors, slurred speech, ataxia, and depression. Her symptoms started to manifest themselves after a recent stay in the hospital and the addition of several new medications.

 

Conclusion

 

When the pill burden and the side effects of medications outweigh their benefits, a medication overload condition exists. Foster caregivers are in a powerful position to start to manage and reduce this harmful effect of polypharmacy. For the good of the resident, caregivers need to actively monitor the drug effects, manage the drugs, and push for changes when needed.

As always, good luck in your caregiving.

Mark Parkinson, BS Pharm

 

References:

Medication overload and older Americans. Lown Institute, 2020

https://lowninstitute.org/projects/medication-overload-how-the-drive-to-prescribe-is-harming-older-americans/#:~:text=Scope%20of%20Medication%20Overload&text=The%20prescribing%20of%20multiple%20medications,over%20the%20past%20two%20decades.

Angie Eaton, PharmD, Polypharmacy in the Elderly. https://media.bcm.edu/documents/2015/c9/igcesession021815.pdf

Alice Bonner. How to Address the Harm of Medication Overload. Institute for Health Care Improvement. Feb 20, 2020.

http://www.ihi.org/communities/blogs/how-to-address-the-harm-of-medication-overload

Maria G. Tanzi. Eliminating medication overload. Pharmacy Today, Volume 26, Issue 4, P20-21, Apr 01, 2020

https://www.pharmacytoday.org/article/S1042-0991(20)30297-8/fulltext

Tackling Medication Overload. Aging 2.0. Sep 24, 2019 https://www.aging2.com/events/details/aging-20-baltimore-presents-tackling-medication-overload/

What is Deprescribing?. Deprescribing.org. 2020 https://deprescribing.org/what-is-deprescribing/

Wade Thompson, HBSc, Barbara Farrell, BScPhm, PharmD, FCSHP, Deprescribing: What Is It and What Does the Evidence Tell Us?. Can J Hosp Pharm. 2013 May-Jun; 66(3): 201–202., doi: 10.4212/cjhp.v66i3.126. PMCID: PMC3694945. PMID: 23814291 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694945/

Michael Steinman, MDEmily Reeve, BPharm(Hons) PhD. Deprescribing. Up To Date, Jan 21, 2020. https://www.uptodate.com/contents/deprescribing

 

 

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Vitamin E – An Advanced CE

Author: Mark Parkinson BsPharm:  President  AFC-CE

Credit Hours 3- Approximate time required: 180 min.

Educational Goal

To provide an advanced discussion on Vitamin E

Educational Objective

  • Provide a description of the chemical shape of the vitamin E molecule preferred by the body.
  • Explain Vitamin E’s roll as an antioxidant.
  • Supply the Recommended Daily Allowance and pertaining information
  • List and explain Caregiver concerns
  • Quote evidence based research

Procedure:

Read the course materials.  2. Click on exam portal [Take Exam].  3. If you have not done so yet fill in Register form (username must be the name you want on your CE certificate).  4. Log in  5. Take exam.  6. Click on [Show Results] when done and follow the instructions that appear.  7. A score of 70% or better is considered passing and a Certificate of Completion will be generated for your records.

Disclaimer

   The information presented in this activity is not meant to serve as a guideline for patient management. All procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this article should not be used by care providers without evaluation of their patients’ Doctor. Some conditions and possible contraindications may be of concern. All applicable manufacturers’ product information should be reviewed before use. The author and publisher of this continuing education program have made all reasonable efforts to ensure that all information contained herein is accurate in accordance with the latest available scientific knowledge at the time of acceptance for publication. Nutritional products discussed are not intended for the diagnosis, treatment, cure, or prevention of any disease.

 

 

Vitamin E – An Advanced CE

 

An advanced CE about vitamin E has been requested by a subscriber, and as you all know, I take requests. The requestor has a nursing degree and wanted to have a course with a little more meat on the bone to chew on. So as fair warning to all my other subscribers, this article will be a little more challenging. Struggle is good, though; it will make you stronger. As always, I will endeavor to make this pertinent to foster caregiving, with knowledge you can use in your homes. I also would like to think that this will not be beyond the understanding of the average caregiver. I do recommend that those without medical degrees take the CE The Vitality of Vitamins before tackling this one. If this is not your flavor of ice cream, then please enjoy my other CEs. So let’s get to it.

 

Vitamin E

There is a lot of useless chatter or downright inaccuracies surrounding vitamins, none more so than vitamin E. Don’t believe everything you hear—especially from those who want you to send them money for their miracle cure. It’s true that vitamin E is an essential vitamin, but it is not the cure-all that everyone says it is. What is needed is a conversation that is backed up by good, solid evidence so that caregivers can use the information in their practice without concerns for its validity.    

 

More Than One Vitamin E

Vitamin E is a chemical needed for good health that is not produced by the human body. It can be found naturally in foods, as a food additive, and as a dietary supplement. The fat-soluble organic compound known as vitamin E, chemically named tocopherol, comes in eight different isoforms. Isoforms are differentiated by slightly different shapes of the same organic compound. The version preferred by our bodies is alpha-tocopherol. When we consume vitamin E, it is absorbed through the wall of the small intestine and transported to the liver. In the liver, α-tocopherol is preferentially transported to the rest of the body via a special protein called the hepatic alpha-tocopherol transfer protein. All other versions are metabolized and removed by the liver. Natural, plant-produced, α-tocopherol comes as an RRR-shaped organic molecule. Synthetically produced vitamin E usually results in a combination of different racemic versions that may not be as bio-availably active as the naturally produced molecule.

To understand the impact different shapes of the same molecule have on your body, consider your hands. They are identical, but they come in a right- and a left-hand version. If you are right-handed and all you have available is a left-handed glove, it’s kind of hard to catch a baseball. The caregiver takeaway is that the natural version produced by plants is chemically better suited to be utilized by the body. Therefore, dietary intake of vitamin E in the foods we eat is medically preferred.

 

Antioxidation and Vitamin E

 

α-Tocopherol is used by the body primarily as a fat-soluble antioxidant. To understand the significance of this chemical property, let us consider the fat molecule. Fat molecules are utilized throughout the body. They are an integral part of all cell membranes. They are transported through the bloodstream as part of a larger molecule known as a lipoprotein. Unfortunately, fat molecules are highly susceptible to damage by other molecules called free radicals.

 

Free Radicals and Oxidation

Free radicals are molecules that have lost at least one of their electrons. When free radicals come in contact with other molecules, they steal an electron away. When a molecule loses an electron, the reaction is called oxidation. With a missing electron, the affected molecule is not able to function as well. In addition, it becomes a free radical itself and tries to steal an electron from its neighbors. Thus, the damage is passed to other molecules. When the damaged molecules are part of a cell wall or part of the nucleus, the entire cell can become damaged. In addition to cellular damage, oxidized fat molecules are also known contributing factors of many disease states.

Free-radical molecules are all around us and in us. They are a natural byproduct of the chemical process of turning our food into energy. Our immune system produces free radicals as a weapon, to damage or kill bacteria and viruses. Free radicals are also found in our environment. They come from sources such as smoking, ultraviolet radiation, sunlight radiation, power lines, and air pollution. Fortunately, we have a protection against free radicals: antioxidants.

 

Antioxidants

Antioxidants are molecules that can give an electron away without becoming a free radical themselves. They stop the oxidation chain reaction that can cause so much cellular damage. Vitamin E is one of our most potent antioxidant protections. As a fat-soluble molecule, vitamin E can freely mix with the rest of the body’s fat molecules. Being thus positioned, it is available to stop oxidation when it starts to occur. Other antioxidants like vitamin C cannot mix with fats and thus are not as readily available to protect our fat molecules. In addition, vitamin A, another fat-soluble vitamin, is easily destroyed by oxidation. The antioxidant effect of vitamin E enables vitamin A to survive longer, thus potentiating its essential effect in the body.

 

The caregiver takeaway is that free radicals are bad and antioxidants are good.

Other Known Functions

Vitamin E is also involved in other bodily functions, such as our immune system, regulation of gene expression, and the chemical pathways of cell signaling.

A few examples are:

  • It slows down the activity of protein kinase C, an enzyme involved in cell proliferation and differentiation in smooth muscle cells, platelets, and monocytes. In other words, it helps turn off those functions

 

  • When vitamin E combines with endothelial cells lining the inside surface of blood vessels, they are better able to resist blood-cell components adhering to their surface, making it harder for plaque to build up. Plaque leads to hardened and clogged arteries.

 

  • Vitamin E also increases the expression of two enzymes that suppress arachidonic acid metabolism. This reaction leads to an increase in the release of prostacyclin from the lining of blood vessel walls. Prostacyclin tends to dilate blood vessels and inhibit platelet aggregation.

 

Having Enough Vitamin E

 

Once the α-tocopherol molecule gives up its electron, it ceases to function as an antioxidant and must be replaced by the body. Also, the body’s regular metabolism will deplete its vitamin E stores. We find ourselves in a constant need to intake more vitamin E. But how much do we need?  

 

Recommended Daily Allowance (RDA)

The Food and Nutrition Board of the U.S. Institute of Medicine publishes guidelines that tell us a recommended daily allowance (RDA) of the essential vitamins and minerals we need to maintain good health. In 2000, it revised its recommendation for the daily allowance of vitamin E as follows.

 

Recommended Daily Allowance 

Age

mg/day

IU/day*

0–6 months

4

6

7–12 months

5

7.5

1–3 years

6

9

4–8 years

7

10.5

9–13 years

11

16.5

14 years and older

15

22.5

Nursing females

19

28.5

* IU – International Unit, as seen on the labels of some manufacturer’s bottles.

The RDA is based primarily on the concentration of α-tocopherol that protects red blood cells (erythrocytes) when exposed to hydrogen peroxide, a potent free radical source.

There are limitations to the usefulness of the RDA when it’s calculated using this method. It fails to measure the other needs of the body for vitamin E. There is also uncertainty caused by variability in what types of tocopherol are supplied to the body (remember the right- and left-hand molecule example above). In addition, the RDA amount will be inadequate when the need for vitamin E increases. For example, tobacco smoke puts extra free radicals into our bodies. Another example is that fat malabsorption conditions prevent normal absorption of vitamin E into the bloodstream. This is an important point that caregivers need to understand in greater depth.

 

Absorption into the Bloodstream

The full explanation of how vitamin E gets into the bloodstream from the food we eat remains unclear. We do know that bile acids and pancreatic enzymes are required for vitamin E to get from our gut into our bloodstream. We also know that when we consume a tocopherol molecule, it is combined with our dietary fat. The combination results in a chylomicron molecule that is transported through the intestinal wall. It has also been discovered that vitamin E absorption increases with the amount of fat ingested in our foods. The chylomicron then travels to the liver, where it is processed further. It is then sent into the bloodstream. Once in the bloodstream, the molecule can combine with circulating lipoproteins and be transported throughout the body.

 

Interference

There are numerous factors that can affect the absorption and transport of the vitamin E we consume. These factors are usually related to either genetic defects, or problems with the absorption or metabolism of dietary fats. For example, after the gall bladder is removed, the lack of bile acids will cause issues with fat- and fat-soluble vitamin metabolism. Symptoms of serious deficiencies are usually neurological problems, as seen in impaired balance and coordination, neuropathy, or muscle weakness. Retinopathy may also occur.

 

The caregiver takeaways are that the RDA intake of vitamin E is just the starting point—more may be needed. The caregiver should be ready to have a discussion with the resident’s doctor if deficiency symptoms start to appear.

 

Problems with Getting Enough Vitamin E

While serious deficiencies of vitamin E are rare, marginal deficiencies are quite common. The National Health and Nutrition Examination Surveys (NHANES) conducted by the National Center for Health Statistics demonstrated that vitamin E intake from the American diet is too low. In a series of studies conducted between 1980–1990 and 2003–2006, it was shown that more than 93 percent of American adults were below the RDA requirement. It can be concluded that a change in the average diet is needed. The question that remains is what specific changes are needed to consistently ensure that the RDA is achieved.

 

Vitamin E Food Sources

 

There are many foods that are rich in vitamin E that can be easily added to a normal diet. They include nuts, seeds, vegetable oils, green leafy vegetables, and vitamin-fortified cereals. Knowing how much of each item to add to the diet can be problematic. The FDA does not require food labels to list vitamin E content unless vitamin E has been added to the food. To determine how much of each food item to add to the diet, reference materials like the one listed below must be consulted.  

 

Vitamin E Quantities in Food

Food

Milligrams (mg)
per serving

Percent DV*

Wheat germ oil, 1 tablespoon

20.3

135

Sunflower seeds, dry roasted, 1 ounce

7.4

49

Almonds, dry roasted, 1 ounce

6.8

45

Sunflower oil, 1 tablespoon

5.6

37

Safflower oil, 1 tablespoon

4.6

31

Hazelnuts, dry roasted, 1 ounce

4.3

29

Peanut butter, 2 tablespoons

2.9

19

Peanuts, dry roasted, 1 ounce

2.2

15

Corn oil, 1 tablespoon

1.9

13

Spinach, boiled, ½ cup

1.9

13

Broccoli, chopped, boiled, ½ cup

1.2

8

Soybean oil, 1 tablespoon

1.1

7

Kiwifruit, 1 medium

1.1

7

Mango, sliced, ½ cup

0.7

5

Tomato, raw, 1 medium

0.7

5

Spinach, raw, 1 cup

0.6

4

Source: https://ods.od.nih.gov/factsheets/VitaminE-HealthProfessional/

 

About the DV

DV stands for daily value and is based on 15 mg per day from all food sources. It is a convenient way to compare which foods are good sources of vitamin E. Foods that contain 20 percent or more of the DV are considered to be rich sources.

 

Menu Planning

When considering vitamin E requirements, knowing which food and how much to add to the diet is the easy part. Trying to plan out a menu with a specific nutritional goal in mind is much more difficult. There are numerous factors that can interfere with achieving a nutritional goal, such as:

 

  • Food preferences and food allergies of the residents

 

  • Cooking skill of the chef

 

  • Cooking methods that affect how much vitamin E is consumed

 

  • Other dietary needs that affect vitamin E quantities (e.g., low-fat diets would reduce the amount of fat-dependent vitamin E absorption in the intestine)

 

  • Health conditions that affect digestion and fat absorption.

 

The caregiver takeaway is unless you’re a registered dietitian, achieving the RDA with just menu planning will be challenging. Taking a vitamin supplement may be required.

 

Supplements

 

The average American diet supplies about 7.2 mg of vitamin E per day for adults. This level is well below the 15 mg per day RDA. In addition, the typical foster care resident is far from average. Your residents have extra needs and special circumstances that warrant taking vitamin supplements. If one of your residents is not taking vitamin supplements, it might be time to have a conversation with the doctor about that. But first, let me share with you a few details about vitamin E and supplements in general so that you can have an informed conversation with the doctor.

 

Variety of Vitamins

There is an overwhelming number of choices in purchasing vitamin supplements. There are liquid vitamins, naturally sourced vitamins, synthetic vitamins, and chewable and gummy varieties. I even remember seeing a chewing gum vitamin for children. Here are a few considerations that will help make sense of it all.

  • Naturally sourced vitamins may be more potent. For example, vitamin E from plant sources will provide one form of α-tocopherol, while synthetic sources contain a variety of isoforms. The result is 100 IU of natural vitamin E provides 67 mg of RRR-α-tocopherol, the form preferred by the body, while 100 IU of a synthetic vitamin E provides only 45 mg of RRR-α-tocopherol.

 

  • Vitamin supplements are just that—supplemental to what you take in from your diet. Don’t get caught up in the details of a particular brand or trying get the exact amount to satisfy the RDA. The effort is just not necessary. For example, vitamin E supplements typically far exceed the RDA. I randomly looked at two common multivitamin brands. One had 167 percent and the other had 150 percent of the RDA. That’s more than enough, even if they are synthetic sources.

 

  • Vitamin supplements come in different forms that the caregiver can take advantage of, such as liquid and chewable varieties for those who have troubles swallowing, gummy varieties for those who hate pills, etc. Have the doctor write the prescription for that specific variety.

 

  • As a supplement, vitamins are not regulated by the FDA. That means the government regulates the quantities but not the quality of the supplement.

 

 

A Word About Topical Vitamin E

Vitamin E is added to many skin products. Its fat solubility and antioxidant properties make it a desirable ingredient in products that claim antiaging and healing abilities. There are some medical studies that back up some of these claims. The therapeutic effects of these products are mostly topical, though. Almost none of the vitamin E is absorbed into the bloodstream. The skin has both fat-soluble and water-soluble qualities. Being only fat-soluble, vitamin E cannot make it past the skin barrier. Since the effects are mostly cosmetic, I will not be covering any further details except for two items:

  1. There are those who like to pop the gel versions and spread the oil over the skin. Caregivers beware, that crosses over into the therapy zone and you have to get the doctor’s permission.
  2. There are some studies that show a therapeutic benefit of vitamin E for eczema and psoriasis sufferers. In these cases, it might be worth it to have the conversation with the doctor. See the following articles if you want more details.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976416/

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755091/

 

Other Caregiver Considerations

 

Can you take too much vitamin E? The answer is yes. Normally, in a foster care setting, it’s very hard to do, so it’s not really a caregiver concern. But there are some circumstances that need careful caregiver considerations. Most of the time, there will not be any significant health issues, though it is an easy thing for the doctor to have overlooked tocopherol’s side effects. If there are any concerns, have a talk with the doctor.

 

Blood Clotting

Vitamin E may inhibit vitamin K-dependent carboxylase activity and interfere with the coagulation cascade. This will lead to impaired blood clotting. Normally at doses less than 1,000 mg a day, the effect will be negligible. It might even be helpful in preventing strokes cause by blood clots (ischemic strokes). But there are circumstances when things aren’t normal.

 

  • Surgery – If the resident is scheduled for any type of procedure that may cause significant bleeding (including dental procedures), it may be wise to ask the doctor if they wish to discontinue the vitamin E supplement a few weeks before surgery.

 

  • Blood thinners – The doctor should be consulted about vitamin E supplements if the resident is on any of the following drugs: Heparin, warfarin (Coumadin), clopidogrel (Plavix), ticlopidine (Ticlid), tirofiban (Aggrastat), and dipyridamole (Aggrenox).

 

  • Painkillers – Non-steroidal anti-inflammatories (NSAIDS) and aspirin can also thin the blood. In my opinion, though, unless the resident is on a continual dose, it is not worth bringing the issue up with the doctor.

 

Retinitis Pigmentosa

Residents with retinitis pigmentosa should avoid higher doses of vitamin E. In a study of 601 patients with common forms of retinitis pigmentosa (RP) supplementation with 400 IU/day of synthetic vitamin E (equivalent to 180 mg/day of RRR-α-tocopherol) modestly but significantly accelerated the loss of retinal function compared to placebo. Any dose above the RDA of α-tocopherol would warrant a discussion with the doctor. 

 

Other Health Concerns

Caregivers should talk with the doctor about vitamin E supplements if the resident has any of the following conditions:

  • Liver failure
  • Bleeding peptic ulcer
  • Hemophilia
  • History of hemorrhagic stroke (stroke caused by bleeding in the brain area)

 

Drug Interactions

Vitamin E, in all its isomeric forms, is a chemical that can interact with and change the effect of other chemicals in the body. There are many drugs that interact with vitamin E. In my opinion, the following are the ones that can have a significant interaction:

  • Mephyton
  • Phenobarbital
  • Phenytoin (Dilantin)
  • Carbamazepine (Tegretol)
  • Cyclosporine (Neoral, Sandimmune)
  • Ketoconazole (Nizoral)
  • Itraconazole (Sporanox)
  • Cancer drugs (vitamin E might lessen their effects)

If you see any of these medications on the resident’s MARS, increase your side-effect monitoring until you’re satisfied that no issues are occurring. You can also bring up any drug concerns with your pharmacist.

 

Herbs

Just to be complete, there are herbs that can potentiate the blood-thinning side effect of vitamin E. These would be fish oil, garlic, or Ginkgo biloba supplements. In my opinion, they are not a big deal unless there are other serious underlying health concerns like the ones mentioned above.  

 

The caregiver takeaway is that vitamin E supplements can have significant interactions with health problems and other drugs and herbs. The larger the dose of vitamin E or the more serious the resident’s condition, the greater the need for close patient monitoring.

 

 

The Role of Vitamin E and Diseases

 

Many health claims have been attributed to the taking of vitamin E supplements. The reason for these assertions needs to be examined first to help determine which to pay attention to and which to ignore.

As an antioxidant, and as a chemical component of cellular mechanisms, vitamin E has the potential of affecting every cell in our body. Whether it actually affects a cell is hard to determine. In order to determine an actual event, you have to be able to measure an effected biomarker. A biomarker is a measurable substance in an organism whose presence is indicative of a biological occurrence. Currently, it is very hard to find biomarkers relating to vitamin E metabolism. Without vitamin E biomarkers, there are many who make claims that are based on the potential effect of vitamin E without the actual evidence that proves it. When such claims come under the scrutiny of outcomes research, some of these claims are questionable at best.  

 

Next Generation Researchers Initiative | grants.nih.govResearch Evidence

 

I am just an old country pharmacist who has spent a lot of time in care homes. I am in no way any kind of research specialist. I am uncomfortable writing in my own words about research studies I know little about. So, I am just going to quote verbatim from some trusted sources that I have found.

 

 

Vitamin E Fact Sheet for Health Professionals, National Institutes of Health (NIH)

Source:  https://ods.od.nih.gov/factsheets/VitaminE-HealthProfessional/

 

Coronary heart disease

Evidence that vitamin E could help prevent or delay coronary heart disease (CHD) comes from several sources. In vitro studies have found that the nutrient inhibits oxidation of low-density lipoprotein (LDL) cholesterol, thought to be a crucial initiating step for atherosclerosis. Vitamin E might also help prevent the formation of blood clots that could lead to a heart attack or venous thromboembolism.

Several observational studies have associated lower rates of heart disease with higher vitamin E intakes. One study of approximately 90,000 nurses found that the incidence of heart disease was 30 to 40 percent lower in those with the highest intakes of vitamin E, primarily from supplements. Among a group of 5,133 Finnish men and women followed for a mean of 14 years, higher vitamin E intakes from food were associated with decreased mortality from CHD.

However, randomized clinical trials cast doubt on the efficacy of vitamin E supplements to prevent CHD. For example, the Heart Outcomes Prevention Evaluation (HOPE) study, which followed almost 10,000 patients at high risk of heart attack or stroke for 4.5 years, found that participants taking 400 IU/day of natural vitamin E (268 mg) experienced no fewer cardiovascular events or hospitalizations for heart failure or chest pain than participants taking a placebo. In the HOPE-TOO follow-up study, almost 4,000 of the original participants continued to take vitamin E or placebo for an additional 2.5 years. HOPE-TOO found that vitamin E provided no significant protection against heart attacks, strokes, unstable angina, or deaths from cardiovascular disease or other causes after 7 years of treatment. Participants taking vitamin E, however, were 13 percent more likely to experience, and 21 percent more likely to be hospitalized for, heart failure, a statistically significant but unexpected finding not reported in other large studies.

The HOPE and HOPE-TOO trials provide compelling evidence that moderately high doses of vitamin E supplements do not reduce the risk of serious cardiovascular events among men and women >50 years of age with established heart disease or diabetes. These findings are supported by evidence from the Women’s Angiographic Vitamin and Estrogen study, in which 423 postmenopausal women with some degree of coronary stenosis took supplements with 400 IU vitamin E (form not specified) and 500 mg vitamin C twice a day or placebo for >4 years. Not only did the supplements provide no cardiovascular benefits, but all-cause mortality was significantly higher in the women taking the supplements.

The latest published clinical trial of vitamin E’s effects on the heart and blood vessels of women included almost 40,000 healthy women ≥45 years of age who were randomly assigned to receive either 600 IU of natural vitamin E (402 mg) on alternate days or placebo and who were followed for an average of 10 years. The investigators found no significant differences in rates of overall cardiovascular events (combined nonfatal heart attacks, strokes, and cardiovascular deaths) or all-cause mortality between the groups. However, the study did find two positive and significant results for women taking vitamin E: they had a 24 percent reduction in cardiovascular death rates, and those ≥65 years of age had a 26 percent decrease in nonfatal heart attack and a 49 percent decrease in cardiovascular death rates.

The most recent published clinical trial of vitamin E and men’s cardiovascular health included almost 15,000 healthy physicians ≥50 years of age who were randomly assigned to receive 400 IU synthetic alpha-tocopherol (180 mg) every other day, 500 mg vitamin C daily, both vitamins, or placebo. During a mean follow-up period of 8 years, intake of vitamin E (and/or vitamin C) had no effect on the incidence of major cardiovascular events, myocardial infarction, stroke, or cardiovascular morality. Furthermore, use of vitamin E was associated with a significantly increased risk of hemorrhagic stroke.

In general, clinical trials have not provided evidence that routine use of vitamin E supplements prevents cardiovascular disease or reduces its morbidity and mortality. However, participants in these studies have been largely middle-aged or elderly individuals with demonstrated heart disease or risk factors for heart disease. Some researchers have suggested that understanding the potential utility of vitamin E in preventing CHD might require longer studies in younger participants taking higher doses of the supplement. Further research is needed to determine whether supplemental vitamin E has any protective value for younger, healthier people at no obvious risk of CHD.

 

Cancer

Antioxidant nutrients like vitamin E protect cell constituents from the damaging effects of free radicals that, if unchecked, might contribute to cancer development. Vitamin E might also block the formation of carcinogenic nitrosamines formed in the stomach from nitrites in foods and protect against cancer by enhancing immune function. Unfortunately, human trials and surveys that have attempted to associate vitamin E intake with cancer incidence have found that vitamin E is not beneficial in most cases.

Both the HOPE-TOO Trial and Women’s Health Study evaluated whether vitamin E supplements might protect people from cancer. HOPE-TOO, which followed men and women ≥55 years of age with heart disease or diabetes for 7 years, found no significant differences in the number of new cancers or cancer deaths between individuals randomly assigned to take 400 IU/day of natural vitamin E (268 mg) or a placebo. In the Women’s Health Study, in which healthy women ≥45 years of age received either 600 IU of natural vitamin E (402 mg) every other day or a placebo for 10 years, the supplement did not reduce the risk of developing any form of cancer.

Several studies have examined whether vitamin E intake and/or supplemental vitamin E affects the risk of developing prostate cancer. A prospective cohort study of >29,000 men found no association between dietary or supplemental vitamin E intake and prostate cancer risk. However, among current smokers and men who had quit, vitamin E intakes of more than 400 IU/day (form not specified) were associated with a statistically significant 71 percent reduction in the risk of advanced prostate cancer. In a clinical trial involving 29,133 male smokers, men randomly assigned to take daily supplements of 111 IU of synthetic vitamin E (50 mg, as dl-alpha-tocopheryl acetate) for 5–8 years had 32 percent fewer prostate cancers compared to subjects who did not take the supplements. Based in part on the promising results of this study, a large randomized clinical trial, called the SELECT trial, began in 2001 to determine whether 7–12 years of daily supplementation with 400 IU of synthetic vitamin E (180 mg, as dl-alpha-tocopheryl acetate), with or without selenium (200 mcg, as L-selenomethionine), reduced the number of new prostate cancers in 35,533 healthy men age 50 and older. The trial was discontinued in October 2008 when an analysis found that the supplements, taken alone or together for about 5.5 years, did not prevent prostate cancer. Results from an additional 1.5 years of follow-up from this trial (during which the subjects no longer received vitamin E or selenium), showed that the men who had taken the vitamin E had a 17 percent increased risk of prostate cancer compared to men only taking placebos, a statistically significant difference. The risk of developing prostate cancer was also slightly increased in subjects taking vitamin E plus selenium or selenium alone, but the differences were not statistically significant. No differences were found among groups in the incidence of lung or colorectal cancers or all cancers combined. Study staff members will continue to monitor participants’ health for up to 5 more years. The National Cancer Institute website provides additional information on the SELECT trial.

One study of women in Iowa provides evidence that higher intakes of vitamin E from foods and supplements could decrease the risk of colon cancer, especially in women <65 years of age [34]. The overall relative risk for the highest quintile of intake (>35.7 IU/day, form not specified) compared to the lowest quintile (<5.7 IU/day, form not specified) was 0.32. However, prospective cohort studies of 87,998 women in the Nurses’ Health Study and 47,344 men in the Health Professionals Follow-up Study failed to replicate these results. Although some research links higher intakes of vitamin E with decreased incidence of breast cancer, an examination of the impact of dietary factors, including vitamin E, on the incidence of postmenopausal breast cancer in >18,000 women found no benefit from the vitamin.

The American Cancer Society conducted an epidemiologic study examining the association between use of vitamin C and vitamin E supplements and bladder cancer mortality. Of the almost one million adults followed between 1982 and 1998, adults who took supplemental vitamin E for 10 years or longer had a reduced risk of death from bladder cancer; vitamin C supplementation provided no protection.

Evidence to date is insufficient to support taking vitamin E to prevent cancer. In fact, daily use of large-dose vitamin E supplements (400 IU of synthetic vitamin E [180 mg]) may increase the risk of prostate cancer.

 

Eye Disorders

Age-related macular degeneration (AMD) and cataracts are among the most common causes of significant vision loss in older people. Their etiologies are usually unknown, but the cumulative effects of oxidative stress have been postulated to play a role. If so, nutrients with antioxidant functions, such as vitamin E, could be used to prevent or treat these conditions.

Prospective cohort studies have found that people with relatively high dietary intakes of vitamin E (e.g., 20 mg/day [30 IU]) have an approximately 20 percent lower risk of developing AMD than people with low intakes (e.g., <10 mg/day [<15 IU]). However, two randomized controlled trials in which participants took supplements of vitamin E (500 IU/day [335 mg] d-alpha-tocopherol in one study and 111 IU/day (50 mg) dl-alpha-tocopheryl acetate combined with 20 mg/day beta-carotene in the other or a placebo failed to show a protective effect for vitamin E on AMD. The Age-Related Eye Disease Study (AREDS), a large randomized clinical trial, found that participants at high risk of developing advanced AMD (i.e., those with intermediate AMD or those with advanced AMD in one eye) reduced their risk of developing advanced AMD by 25 percent by taking a daily supplement containing vitamin E (400 IU [180 mg] dl-alpha-tocopheryl acetate), beta-carotene (15 mg), vitamin C (500 mg), zinc (80 mg), and copper (2 mg) compared to participants taking a placebo over 5 years. A follow-up AREDS2 study confirmed the value of this and similar supplement formulations in reducing the progression of AMD over a median follow-up period of 5 years.

Several observational studies have revealed a potential relationship between vitamin E supplements and the risk of cataract formation. One prospective cohort study found that lens clarity was superior in participants who took vitamin E supplements and those with higher blood levels of the vitamin. In another study, long-term use of vitamin E supplements was associated with slower progression of age-related lens opacification. However, in the AREDS trial, the use of a vitamin E-containing (as dl-alpha-tocopheryl acetate) formulation had no apparent effect on the development or progression of cataracts over an average of 6.3 years. The AREDS2 study, which also tested formulations containing 400 IU (180 mg) vitamin E, confirmed these findings.

Overall, the available evidence is inconsistent with respect to whether vitamin E supplements, taken alone or in combination with other antioxidants, can reduce the risk of developing AMD or cataracts. However, the formulations of vitamin E, other antioxidants, zinc, and copper used in AREDS hold promise for slowing the progression of AMD in people at high risk of developing advanced AMD.

 

Cognitive Decline

The brain has a high oxygen consumption rate and abundant polyunsaturated fatty acids in the neuronal cell membranes. Researchers hypothesize that if cumulative free-radical damage to neurons over time contributes to cognitive decline and neurodegenerative diseases, such as Alzheimer’s disease, then ingestion of sufficient or supplemental antioxidants (such as vitamin E) might provide some protection. This hypothesis was supported by the results of a clinical trial in 341 patients with Alzheimer’s disease of moderate severity who were randomly assigned to receive a placebo, vitamin E (2,000 IU/day dl-alpha-tocopherol), a monoamine oxidase inhibitor (selegiline), or vitamin E and selegiline. Over 2 years, treatment with vitamin E and selegiline, separately or together, significantly delayed functional deterioration and the need for institutionalization compared to placebo. However, participants taking vitamin E experienced significantly more falls.

Vitamin E consumption from foods or supplements was associated with less cognitive decline over 3 years in a prospective cohort study of elderly, free-living individuals aged 65–102 years [49]. However, a clinical trial in primarily healthy older women who were randomly assigned to receive 600 IU (402 mg) d-alpha-tocopherol every other day or a placebo for ≤4 years found that the supplements provided no apparent cognitive benefits. Another trial in which 769 men and women with mild cognitive impairment were randomly assigned to receive 2,000 IU/day vitamin E (form not specified), a cholinesterase inhibitor (donepezil), or placebo found no significant differences in the progression rate of Alzheimer’s disease between the vitamin E and placebo groups.

In summary, most research results do not support the use of vitamin E supplements by healthy or mildly impaired individuals to maintain cognitive performance or slow its decline with normal aging. More research is needed to identify the role of vitamin E, if any, in the management of cognitive impairment.

 

 

 

 

 

 

Vitamin E, Oregon State University, Linus Pauling Institute

Source: https://lpi.oregonstate.edu/mic/vitamins/vitamin-E

 

Age-Related Deterioration of Immune Function

A randomized, placebo-controlled trial in 617 nursing home residents (≥65 years of age) reported that daily supplementation with 200 IU of synthetic α-tocopherol (90 mg of RRR-α-tocopherol) for one year significantly lowered the risk of contracting upper respiratory tract infections, especially the common cold, but had no effect on lower respiratory tract (lung) infections. More research is needed to examine whether supplemental vitamin E might enhance immune function and reduce risk of infection in older adults.

 

Type 2 Diabetes Mellitus

Oxidative stress contributes to the progression of type 2 diabetes mellitus and causes damage to many organs and tissues, including the pancreas, brain, eyes, peripheral nerves, and kidneys. Evidence from animal studies suggests that vitamin E supplementation could mitigate the role of oxidative damage in the occurrence of diabetes complications. In the Alpha-Tocopherol Beta-Carotene cancer prevention (ATBC) trial in male smokers, supplementation with 50 mg/day of synthetic α-tocopherol (25 mg/day of RRR-α-tocopherol) had no effect on the risk of incident type 2 diabetes mellitus during the 19-year post-intervention follow-up. Likewise, supplemental vitamin E intake during the trial made no difference on the incidence of macrovascular complications or mortality in participants with established type 2 diabetes. In addition, a meta-analysis of 14 heterogeneous randomized controlled trials, including 714 type 2 diabetic individuals, found that supplementation with vitamin E (200-1,800 IU/day for 6-27 weeks) had no effect on markers of glycemic control, including glycated hemoglobin A1c (HbA1c) level and measures of fasting glucose and fasting insulin concentrations. Further subgroup analyses indicated that higher doses of vitamin E (>400 IU/day) supplemented for longer periods (>12 weeks) significantly reduced HbA1c level and fasting insulin concentration, suggesting that vitamin E could possibly enhance insulin action and glucose disposal in type 2 diabetic individuals. Another recent meta-analysis of randomized controlled trials found that endothelial function in normal-weight and overweight—but not obese—patients with type 2 diabetes was significantly improved by supplementation with vitamin E and/or vitamin C. Although there is reason to suspect that vitamin E supplementation may have utility in the management of type 2 diabetes, evidence for benefit from large, well-controlled clinical trials is still lacking.

 

The caregiver takeaway is that many health claims of vitamin E products are in actuality just unproven theories of potential benefits. Only those claims based on actual clinical outcome studies are worth your attention.

 

Conclusion

 

How’s that for a CE with some meat on the bone? I hope that satisfied the appetites of my more advanced subscribers without losing the interest of everyone else. To recap, the topics I have covered are as follows:

  1. Vitamin E is an important component in maintaining the good health of your residents. The antioxidant properties and other chemical interactions are just too important to take for granted.
  2. As caregivers who control the menu, you are in a good position to plan diets that are rich in naturally occurring alpha-tocopherol. Even with good menu planning, supplementation may be required.
  3. Taking a vitamin E supplement is not the end to caregiver concerns. Monitoring the resident may be required if there are underlying conditions that warrant closer observations.
  4. With so many vitamin E products making medical claims, caregivers should concern themselves only with those whose claims are backed up by hard clinical evidence.

As always, good luck with your caregiving.

Mark Parkinson, BS Pharm.

 

References

Jane Higdon, Ph.D. Victoria J. Drake, Ph.D. Vitamin E. Oregon State University,  Linus Pauling Institute. Micronutrient Information Center. Nov 2008

https://lpi.oregonstate.edu/mic/vitamins/vitamin-E

Vitamin E, Fact Sheet for Health Professionals. National Institute of Health, Office of Dietary Supplements. 2020 https://ods.od.nih.gov/factsheets/VitaminE-HealthProfessional/

Vitamin E. MayoClinic.org. 2020 https://www.mayoclinic.org/drugs-supplements-vitamin-e/art-20364144

Zawn Villines. Ten benefits of vitamin E oil. MedicalNewsToday.com. Jan 29, 2020 https://www.medicalnewstoday.com/articles/318168#Risks-and-considerations

 

 

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