November 5, 2010

Emergency Hospitalization for People with Diabetes

Another hospitalization situation that can cause problems for people with diabetes is going into the hospital alone in an emergency situation and no medical alert identification. A case in an emergency room about 65 miles from here this summer really emphasized what can go wrong. These are the type of instances that get my feelings in an uproar when they should not have happened.

The person had collapsed and passed out from heat exhaustion (I'm guessing heat stroke). He was transported to the hospital with an IV in place per orders of the emergency room doctor. When they arrived at the hospital no alert identification was found so the IV was continued and a second one added and and then his billfold was opened. An emergency telephone number was found and called.

The person arrived at the hospital and went to the room where he had been admitted. This person was not aware he had diabetes so could give no insight into treatment or who the doctor was. So the IV's continued. The fellow did not come out of the heat exhaustion, so no changes were made. They did stop the IV's after the fifth one. On the second day the fellow still had not come around, but the emergency person had contacted an older brother, who arrived. Even he did not know about the diabetes, but knew of the doctor his brother was seeing.

Contact was made with the doctor then and it was discovered that he had diabetes Type 1. At that point they did a blood glucose test and if I understood correctly it was “HI”, so they had to do a test from a blood draw. This showed over 900 and I was not given a more accurate figure. Of course they administered insulin. Then they started testing every hour and administering more insulin every five hours. They also continued to test him regularly.

They continued monitoring him and on the fourth day he came to. When the nurse told me about the following, I nearly fell off the chair. The patient said nothing about having diabetes and asked for a Pepsi to drink. When he was told no, he got abusive, and asked for food. When he was told after his insulin, he went ballistic and refused to be treated. The fifth day he checked himself out against doctors wishes.

I don't understand totally what happened as I was not able to get more information. I do not understand why this person did not want to have diabetes identified and when it was, why he reacted this way. I know from the diabetes forums that some people will come out on them, but will not say anything to people near to them or wear a medical alert of any kind.

I can understand privacy, but not the extreme desire for it. He should be thankful that an older brother did know the doctor and that the doctor gave out the information. There are lots of unanswered questions about this, but the nurse would not identify anyone and only gave me a little that she could.

I think she was wanting me to see how important it was to have proper medical alert information on me. When I showed her mine, she asked to see it and thanked me for wearing it. I wear mine on a necklace and need to have it updated for sleep apnea which is not on it presently.

This is why I feel so strongly about educating close friends and family so that they can advocate for you and prevent these types of instances from occurring. And in this case, the person on the emergency notice did not have information. This is not what should have happened.

November 2, 2010

Enjoy Your Holiday Food!

It is interesting how families celebrate holidays. The question is how do you celebrate the holidays? Do you go overboard with the meal and deserts? For people with Type 2 diabetes holidays can be one of dread and fear of the diabetes police.

First, relax! This is not a rant about the holidays. Hopefully you have a few holidays under your belt and have found yourself able to cope or are looking for ways to do better. If you are new to diabetes, the holidays can be real problems. Hopefully this will provide some help and guidance.

For the parties and friends social gathering, read this for some tips. I would only emphasize that moderation is the key to these events. Do not overdo and select the serving size that is small enough to not raise you blood glucose into the stratosphere.

The next article is definitely for families and is one of the better articles for people with diabetes. I appreciate the statement by Marlene Schwartz, PhD, deputy director of the Rudd Center for Food Policy & Obesity at Yale University when she says “don't tell family members that they're eating more healthfully”. She calls it "stealth health".

This is sound and sage advice. If the food is just served without comment, everyone should be content. They also advise you to involve immediate family members in planning of the menu, especially if they are picky eaters and the younger generations.
There are many good tips and from experience I know that they will work for most families.

The third article is another take on planning for the holidays. It does suggest making a game plan to avoid problems and if you make it work, you can still enjoy the holidays. The best plan is sticking to the plan. Realize that this is the holidays and one day (at a time) is the best method for not being overwhelmed. If you happen to overindulge do not berate yourself. Just be careful the next few following days, and take care of yourself.

From Thanksgiving to at least New Year's Day is often very tempting for people with Type 2 diabetes. Be assured that you will find yourself being tempted, but by careful planning and conservative food selection you should survive. So relax and happy holidays!!!

October 28, 2010

Goals for the New Type 2 Organization

I am a bit disappointed in the response to the first blog on Type 2 diabetes needing their own organization, but just in the comments. The emails were only from one person and not very friendly.

Outside of the need to have an organization for those of us with Type 2 diabetes, I had hoped to get some more objectives and goals that would give us more ideas. So with that in mind, I will attempt to list a few of them and hope that we can draw some responses.

Besides raising funds for research, finding the proper research venues will be a big priority. There seems to be some areas that are coming to light now that may need more exploration that may lead to keys for managing diabetes. Being more accurate in the diagnosis of diabetes should not be overlooked as the ADA has opted to support the A1c test only.

Something will need to be done for educating the medical profession in being more aggressive in diagnosis, early treatment, and follow up. See this for some hope. Patient education also needs to be strongly promoted. I am not sure how this would be best accomplished, but one suggestion would be on line resources. This could be accomplished by having pamphlets or booklets that every doctor or endocrinologist can hand out when diagnosed.

Sadly in need of education are the insurance companies in preventative medicine and early work for patient education, patient followup, and working with other doctors for overall health. This may include, heart disease prevention, sleep apnea, kidney health, neuropathy, eye health, and many other related areas.

Research will need to be done to find out what other people with diabetes want for support, what education they want and need, and what services would better serve them. I suspect some work will be needed with government agencies, medical groups, and diabetes manufacturers of all types.

Because of the problems specific to women and to men, there should be special education and on line help for each. Education will need to be considered for the younger people now being diagnosed with Type 2 diabetes.

Education programs will need to be developed for hospitals and elder-care facilities. This will develop new standards for how patients with diabetes should be treated, allowed to be self-medicated while in these facilities, and procedures for reducing errors in IV solutions and medications. The attitudes of hospitals does need to be adjusted in many situations.

There has to be more objectives and goals. Help!

Which sweeteners are you consuming?

When I started this, I had no idea what I was getting into. The way the sweeteners are looked at and discussed varies more than a person might think. Much depends on site objectives and manufacturer influence. Sugar and sweeteners are generally viewed as a poison by some groups, and should not even be looked at for people with diabetes irregardless of type. So those articles have been ignored as I wanted something that made some sense and might be of interest.

While the glycemic index values may vary from what I have located, generally they are within a few points in the sources checked. A few values could not be found and I used (??) to indicate that. The value can also change when processed differently as in pasteurized and raw honey. The GI values listed are therefore only guides and can vary depending on method of processing.

Various sweeteners   Glycemic Index Value

Sugar                               GI  80

Other calorie containing sweeteners:
all have approximately 15 grams of carbohydrates per teaspoon
   Honey, pasteurized        GI  75
   Raw Honey                   GI  30
   Maple syrup                  GI  54
   Pancake syrup               GI (??)
   Malt syrup                     GI  42
   Karo syrup                    GI (??)
   Corn sweeteners            GI  62
   Molasses                       GI  58
   Jellies                           GI (??)
   Jams                             GI  46
   Marmalades                   GI  55
   Agave syrup, nectar       GI  15
   Brown Rice syrup          GI  25

Brown sugar                     GI  64
Fructose                           GI  22
Lactose                            GI  46
Glucose                           GI  96
Blackstrap Molasses          GI  55
Stevia – FOS Blend           GI  <1

Artificial sweeteners          GI <1
Name                          Brands
Aspartame              NutraSweet, Equal
                        People who have a condition called phenylketonuria should avoid
                        this sweetener.
Acesulfame K         Sunett, Sweet One, Swiss Sweet
Sucralose               Splenda
Saccharin               Sweet'nLow, Sugartwin
                        Avoid this sweetener if you are pregnant or breastfeeding

Sugar alcohols - These are neither sugars or alcohols, but pure carbohydrates. Examples of common sugar alcohols are maltitol, sorbitol, isomalt, and xylitol and are called “polyols”. There are other manufactured sugar alcohols, but these occur naturally in plants. This article explains more on sugar alcohols.

The key to non-artificial sweeteners is to use in moderation. Overuse of any sweetener is not good for maintaining tight management of diabetes and for many people will cause weight gain.

The above information is knowledge you should make use of when reading labels. While the GI values will not be listed, these are listed here to hopefully give you ideas when you are looking at labels. This article in WebMD may answer some more questions.

October 25, 2010

Hospital Awareness for People with Diabetes

Since the this post, more information keeps coming to light that people with diabetes need to be aware of when entering the hospital. There are some nasty situations that can arise even when the hospital is aware that you have diabetes. The nasty problems are life threatening if the hospital is unaware that you have diabetes.

If you are having an IV(intravenous therapy), please make yourself aware of what will be in the IV. You will want to be sure that dextrose or other sugars are not part of the IV. The IV should be saline, but many are five percent dextrose. For people without diabetes no harm will be done. For people with diabetes, this will play havoc with blood glucose levels (BG) management. Depending on how many you will be given, it could raise your BG to levels higher than manageable immediately, even with insulin, and will require close management for at least 24 hours or more.

So it does not matter whether you are Type 1 or Type 2, be careful of what you are given in your IV's. To assist in maintaining your independence and preventing the inadvertent problems, you should ask your doctor and the hospital administration for release forms to allow you to medicate yourself and to maintain control of your diabetes management. Drives hospitals crazy, but protects them as well as you.

Another area of concern, if you are having any surgeries, will be the medications you will be given (if any), and how they will react with BG levels. There are many medications that can raise BG and you should talk to the surgeons or physicians about your concerns and what medications you may be given.

If enough preparation time, have you doctor find out and discuss the medications you will be given. Be prepared to adjust your insulin needs or oral medications while in the hospital and your doctor can be of great assistance in making adjustments easier to handle. David Mendosa presented the list from Diabetes in Control dot com. This is a very good list to be aware of and use.

If you have surgeries that will involve body part replacements, steroids will probably be involved and this should be known. Steroids will elevate BG levels and for those on insulin, careful watch needs to be done and sometimes extra testing of BG is needed to adjust insulin. Those on oral medications should actually consider using insulin to manage BG levels while on steroids. If staying on oral medications, consult your doctor for dosage and possible addition of other oral medications.

Never be afraid to ask questions and ask for the advice from your doctor or endocrinologist as this assistance may keep you from making some serious mistakes. You may need to schedule another appointment to get this all in, but it will be worth the time and peace of mind for you. If you need to stand your ground, be ready to – it is your health.

This is worth repeating from the previous blog – try to get your medications approved and be prepared to sign any waivers necessary to have them with you. You will still need to guard them carefully. A local legal case brought this home for me. Patient had his medications approved and special warnings put on his chart and records that the medications were to be left with the patient as they were not available in the hospital and patient was allergic to certain comparable medications.

Evening shift nurse thought she knew everything and confiscated his medications and disposed of them in the medical waste. When this was discovered, the patient was suffering from an allergy attack from a substituted medication. When the doctor discovered this and the fact that his medications were gone, at least he had an internal investigation started. Outcome was patient recovered and needed three extra days in hospital at no cost, nurse lost her job, and hospital was out some money in the legal case plus had to replace the destroyed medications.

It is sad that only the bad get the publicity and those that do their jobs do not get the recognition they should. The attitude of the evening shift nurse does happen to be prevalent in more cases than we would like to acknowledge. I am not into speculating what the reasoning for this is; however, hospitals are beginning to slowly realize that with patients who are advocates for themselves, they must listen and facilitate, plus have the nursing staff in full cooperation mode.

The above is all written with the fact that you have knowledge of what is to happen and when. Remember that if you enter the hospital under emergency conditions, then hopefully your spouse, good friend, or other family member can act for you and determine that the above in handled for you. I will mention the limited medical power of attorney again to make sure that those you trust are able to act for you. They must be prepared to act for you and see to your health until you are able to assume that role.

October 22, 2010

Diabetic Wound Care of Feet

If this was not so serious, maybe we could all laugh about it, but taking care of foot injuries is very important if you have diabetes and no laughing matter.

Day 1 – stub your toes on the bed as you are hurrying to the bathroom. Nothing shows when you inspect while in lighted bathroom.

Day 2 – large red area on the two toes you banged the prior evening. They are tender, but you put your socks and shoes on and go to work. In the evening, you notice a spot of blood on the sock, so you wash the feet and go to bed.

Day 3 – toes are tender and inflamed, but you go to work anyhow. In the evening, more blood on the sock, again you wash your feet and spray a little antibiotic on the area.

Day 4 – toes are inflamed and very sore, painful when touched and a crust has formed over the bleeding area. You decide to tough it out as tomorrow is Saturday. Evening finds sock soaked in blood and another stain. Wash despite the pain and apply antibiotic and cover. Sleep is difficult as foot is sore now.

Day 5 – wife wants the lawn mowed, so you start, but cannot get far. The pain is too much and when you remove your shoe, the sock is a mixture of blood and more stain. Wife see this and decides to clean the area, apply antibiotic, and cover it. Now she tells you to get the yard mowed as her sister is having a surprise birthday party for her husband at 4 o'clock, and she does not want to be late. You do as told and are able to stay off you feet the rest of the day, but at home, tired and very sore you just fall into bed.

Day 6 – Wife wakes you for church, but you cannot stand on the foot. It is swollen and inflamed. You decide to go to the emergency room. There they clean and disinfect the wound, give you an antibiotic shot and a prescription for more antibiotics, tell you to stay off your feet for a few days. They tell you to see your regular doctor, and tell you not to work for a few days. You forget to tell them you have diabetes, don't see your doctor, and don't fill the prescription.

Day 12 – you wake in the hospital and realize that you are missing your foot. The doctor is telling you that they have saved your life and that the foot and part of the leg was a small sacrifice to be able to save your life.

The above is not a true story, but it could be. If you have diabetes, any small bruise, minor cut or scratch could end up putting you in the above story.

The importance of wound care cannot be emphasized enough, especially the lower part of the legs and feet. Even if your diabetes management is excellent, accidents do happen. For understanding the stages of wounds, burns, and the healing and treatments, see this article by diagnose-me dot com.

Then there are those that think nutrition is the end-all for people with diabetes and go to extremes to promote it as the only way of managing diabetes and try to scare those who don't manage diabetes with nutrition as poor candidates for wounds and other problems as they don't practice good glycemic control. Yes, nutrition is important, but exercise is also important and taking your medications if you cannot control diabetes with exercise and nutrition.

Then when we get past those that only have one line of thinking, we can get down to those that care and offer sound advice and directions for taking care of ourselves. Even if I often do not like WebMD, they have done an excellent job of outlining the problems and treatment of wounds for people with diabetes.

The article has a ten point checklist that make a lot of sense.

Check you feet daily.
Pay attention to your skin.
Moisturize your feet.
Wear proper footwear
Inspect your shoes every day
Chose the right socks
Wash your feet daily
Smooth away calluses
Keep toenails clipped and even
Manage your diabetes

They put a lot under manage your diabetes – monitoring blood glucose levels, blood pressure, and cholesterol levels. At least they went on to say a person with diabetes should eat healthy, exercise regularly, taking medications the doctor prescribed, not smoking, and having regular medical checkups. Too many writers stop at just manage your diabetes.

I also like that WebMD also covers burns as part of taking care of yourself. There are many parts to wound care and burns can certainly happen. Please read this carefully even if it is not all about your feet.

Two other sites worth reading are: Site 1 and Site 2.

Please take the extra time to inspect your feet and legs daily and treat every minor injury immediately. This could save a toe, a foot, and even your leg by taking care of minor bruise, cut, or ingrown toenail early. If the healing does not start promptly, get to the doctor for quick medical care. This should be done for good care and proper antibiotics or other treatments.
 
You should have regular appointments with a podiatrist to check your feet to prevent problems from starting.  Even for regular food care this should be done.  For injuries see your regular doctor promptly.

October 19, 2010

Sleep apnea and hospitalization Part 2

This part provides some issues you need to be aware of for treatment of sleep apnea in a hospital or out-patient setting whether for a surgical or other treatment. This is information I wished I have made myself aware of for past procedures. I will be ready for any future procedures.

Oral appliance users will need to consult with their prescriber for procedures to follow, but much of the following may apply. Just substitute oral appliance when CPAP is discussed.

When using the term CPAP it will be in the generic sense meaning all types of Positive Airway Pressure devices for the treatment of sleep apnea, including CPAP, bi-level PAP, variable PAP, and auto-titrating PAP devices. When reading about obstructive sleep apnea (OSA) please use the terms mild or moderate sleep apnea if applicable.

For all sleep apnea patients, knowledge is important to get proper care and treatment in the hospital or out-patient area. If at all possible - DO NOT LEAVE YOUR EQUIPMENT AT HOME. This is important in so many ways as sleep apnea therapy is as important in the hospital as it is at home.

If you do not inform your physicians or surgeon of your need for sleep apnea therapy
during and after medical procedures, this can create problems in healing and delay recovery time leading to longer hospital stays. Do not assume that the physicians and nurses will know how to manage your OSA. If they are not aware, they will not be prepared to care for OSA.

Please ask if you may use your own CPAP equipment. This will be when you will find out what the hospital policy says and you should talk to your doctor as well as your surgeon and the anesthesiologist if you are having surgery to confirm the hospital's policy. If they say no, then ask if they have a form called “Permission and Release for use of Outside Medical Equipment/Appliance for Patient Treatment” so that you may use your own equipment. At this time also ask if they will need a letter from your doctor or a consultation with your sleep doctor.

The only way you should accept the hospital's equipment is if clear that it has the same or better benefits as you equipment. If they cannot meet these requirements, you should be able to use your own equipment for your own well being and comfort. Always make every attempt to use your own mask to control leaks and for comfort.

If they allow your equipment, ask if they need to inspect the equipment to see that it is functioning correctly and does not pose any hazards. Ask when they want to inspect the equipment as you do not want to do this too far in advance.

Important - Label your equipment, CPAP carrying case, mask, and CPAP machine. When you are admitted, labels identifying you, and for your chart are printed. Be sure to ask for enough extras to label your equipment.

Again important, if supplemental oxygen is required, your mask may have ports for attaching an oxygen line. If your mask does not have oxygen ports, contact you equipment provider or the manufacturer to find out if an oxygen port adapter is available for your mask. Most of the time the hospital may have an adapter that will work with your mask.

If you are having surgery and will have a breathing tube inserted into your windpipe, your CPAP will not be required. After the tube is removed, you should be put on the CPAP machine. If you are not intubated, then remind the hospital staff that the CPAP need to be used.

Show your family and/or friends who will be visiting as well as the doctor and shift nurses how to use your equipment. Let them know and reinforce with them that if you are sedated or sleeping, your CPAP needs to be operating.

Normally while you are in what is termed pre-operation stage and being prepared by the nurse, your surgeon and anesthesiologist will stop by to discuss concerns and surgical plans. Do not forget to remind them that your CPAP needs to be in use at all times (if not intubated), and that they need to check your oxygen saturation and to monitor your heart rate.

Be ready if there are exceptions to any of the above when applied to your upper airway surgical procedures and if this should be cleared with the treating physicians and discussed with your sleep physician.

Good luck.

October 16, 2010

Sleep Apnea and Hospitalization Part 1

If you have sleep apnea and use a positive airway pressure machine, are you aware of what to do when if you are admitted to a hospital, or if you have an outpatient surgical procedure where you will be put under? I admit I was not! So it was with great interest that I read the article here from the American Sleep Apnea Association (ASAA).

Not included as part of the above link are the procedures for those who use oral appliances. This is the reason for making sure the dentist that prescribed your oral appliance is included in the following discussion.

When using the term CPAP it will be in the generic sense meaning all types of Positive Airway Pressure devices for the treatment of sleep apnea, including CPAP, bi-level PAP, variable PAP, and auto-titrating PAP devices.

The ASAA makes several recommendations for us as patients to accomplish prior to being admitted and what to do once we are admitted. I am concerned that this is aimed only a those of us with obstructive sleep apnea (OSA). So I will mention that this might will be considered by those with mild to moderate sleep apnea. It would be wise to consult with your doctor or dentist in charge of your sleep apnea to have their input in resolving any sleep apnea issues while undergoing medical procedures.

Know you patient rights to be properly treated for OSA and mild to moderate sleep apnea during all surgical procedures whether in a hospital setting or in an outpatient surgical center. This includes any same-day procedure that requires sedation or anesthesia, including but not limited to a colonoscopy or an angiogram.

You will need to determine whether you will be able to use your own CPAP equipment that is set to your prescribed pressure or whether the hospital or facility will supply an identical mask and/or identical or better equipment. You will also need to know whether you will be allowed to have humidification if you use this and whether there are any contraindications for its use. You will need to consult with your oral appliance prescriber for how to handle oral appliances.

To supplement the above, you, as the patient are required to notify your physicians and other caregivers that you have sleep apnea and what pressure the equipment must be set at. You will need to describe the therapy required and provide the contact information for your doctor or dentist so that they can provide the diagnosis information and prescribed pressure or equipment use.

Be prepared to provide your own clean mask and, if needed, your own CPAP machine. Be ready to label your equipment with your name and required identifying information. If possible meet with the surgeon and anesthesiologist to inform them that you have sleep apnea and require therapy.

Important! Make sure that your family, and if necessary friends, know that you are a sleep apnea patient and that they know you require the equipment. They should also know the parts of the equipment and how it is used for your sleep apnea treatment. Lastly, you should make sure that you have the information as part of your medical alert jewelry and on your wallet emergency information card so that medical emergency personnel will be able to take proper action for you.

Watch for Part 2