Challenge Diabetes
Thoughts about current approaches to managing diabetes

Diabetes Intervention Technology™
Challenge Diabetes » Blog Archive » Day 10 - Twelfth Camp Blog Entry

Day 10 - Twelfth Camp Blog Entry

July 27th, 2009 by Steve

Today’s Diabetes Challenge question of the day is for all parents of children or teens with type 1 diabetes. The role of being a parent of a child with diabetes may range between one of constant supervision to a state of complete detachment. Most parents simply feel they’re only fulfilling the role of parent as best as they know how. However, many teens with diabetes feel that their parents behave like the “Diabetes Police”. So the question today is: Rate yourself on a scale of 1 to 10, with 1 being like a diabetes “mall cop” to 10 like being the Diabetes “KGB”. Explain why your level of involvement in your child’s diabetes care is just right, not enough or perhaps excessive. Give examples.

Reflections on the first day of camp.

The second session of Diabetes Camp is underway. I’ve reviewed the state of the more than 200 campers under our care this week. As with the previous session, I saw lots of pumps and multi-dose insulin schedules. Both are what are referred to as “basal-bolus” insulin schedules. The “basal” is the long-acting insulin (Levemir or Lantus) and the “bolus” is the rapid-acting insulin (e.g., Humalog, Novolog, Apidra) taken before meals, large snacks and for correcting high BG levels.

The other approach, “split-mixed insulin therapy”, is rapidly becoming a relic of the past. Classic split-mixed regimens involved taking “intermediate-acting” insulin (NPH or the now defunct Lente) in the morning and evening, plus mixing in fast-acting insulin at the same times (2 shots a day). The total dose was “split” and “mixed”. Newer versions of split-mixed include NPH at bedtime instead of supper, with the rapid insulin still given before the evening meal. I have used a variant of this schedule quite effectively by substituting Lantus or Levemir for the bedtime dose of NPH. It has the advantage of causing much less middle of the night low blood sugar while avoiding the need for an injection at lunchtime.

Less than 10% of campers use an insulin regimen with NPH insulin at our camps. Analog insulin has trumped the old NPH insulin (which had been around since the 1940’s). And that was not an accident. Not only are most long acting analog insulin preparations much more predictable in their action compared to NPH, but they have had the marketing power of major pharmaceutical companies knocking doctor’s doors down to encourage them to prescribe their new and improved insulin analogs. NPH is also less expensive than insulins like Lantus, Levemir, Novolog and Humalog. That’s good for us, but bad for the insulin companies. In the end, NPH’s fate never had much of a chance.

But has there been a rush to judgment? Are the stories of NPH’s demise overstated? Much of the world still uses NPH insulin and classic split-mixed insulin schedules. If for no other reason than cost. NPH insulin costs a fraction of what a bottle of Lantus or Levemir costs. Here at camp last week, we had children using NPH regimens that had A1c values better than many of the campers on more sophisticated basal-bolus schedules or even pumps. The reason for the success of these simpler insulin schemes is consistency. If a diabetic can maintain a regular activity schedule and carbohydrate intake, then these regimens can be quite effective. Compared to the proven potential for better control with a basal-bolus regimen, we seem to be falling well short of realizing A1c values in the sub 7% range in most kids with type 1 diabetes on basal-bolus.

This fact begs a huge question: have we reached a point of diminishing returns as far as our ability to deliver a high quality injected insulin regimen (i.e., basal-bolus)?

Even a pump infuses insulin in a largely non-physiologic way. Insulin injected under the skin must first pass a gauntlet of tissues intent on destroying its action, starting with the skin and ending with the liver. This is why the amount of insulin injected under the skin is usually 10 times the amount of insulin that would be produced inside the body to produce a similar level of glucose control.

As I examined camper insulin regimens on Sunday, I found example after example of poorly applied basic diabetes insulin management principles. Some basal-bolus schedules were essentially fixed dose regimens with seemingly arbitrary rules for dosing extra insulin. Some had no correction factor or insulin to carbohydrate ratio included and dosing was based solely on glucose level and not carbs to be eaten. These factors are integral to any kind of quality basal-bolus or insulin pump regimen.

The frequency of blood sugar monitoring also fails in many cases to be frequent enough to allow for proper self-dosing calculations. Worse, campers in many cases didn’t know how to apply the proper decision making skills that are so essential for basal-bolus to work as expected. This is where parents must step in during childhood for sure, but also well into adolescence (through age 16 at least).

Don’t get me wrong: basal-bolus schedules are based on solid principles. But in many cases they are applied by people lacking the necessary training, skills, experience and motivation to make them work. As a result, A1c values still remain entrenched in the high 8 and mid-9% range for people on these regimens. Is this the kind of return on investment you want for your child or teen? Would you argue that the alternative is worse?

I think that as we look down the road for the next great hope for diabetes, we often lose sight of the tools we already have now and how well they can still work for us. New is not necessarily best or even better than what we have now. Plus, as I’ve said over and over, diabetes care is a series of informed choices, created by ongoing diabetes education and polished by personal experience.

So think twice about whether or not to be the first on your block to get on the bandwagon for the next great thing in diabetes care (whatever it may be). Beware of snake oil diabetes miracle therapies. They’re everywhere.

Stay in virtual touch with diabetes camp

I am posting daily blogs here about important diabetes issues that directly relate to the camp and posing controversial questions to you as above. I’m also tweeting very frequently from camp. Check out my twitter site: http://twitter.com/Dr_Steve_Ponder . My tweets are real time observations from camp (plus twitpics) as they happen, sent immediately from my mobile phone. I’m discussing how things are going and any special problems or situations that all parents of children with diabetes would benefit from. I’ll also answer questions posted to this blog site as quickly as I can. You can also check out the camp’s website at http://www.lionscamp.com where you can check out daily photographs from the day before. As always, we will be preparing a complementary DVD photo album for all campers to be provided at check out on Friday evening.

Parent’s Webinar on Wednesday Evening

A Parents Day Webinar will be held at 8-9PM CST on Wednesday July 29th 2009. Go to the TLC webinar site now for the details on how to participate. It’s totally free and can be accessed from the comfort of your home PC, laptop or just call in using your telephone. Even if you don’t have a webcam, you can dial in to the conference bridge. I’ll be discussing camper progress at camp to date, key observations about how campers are stacking up compared to each other, and address some major hot button issues in type 1 diabetes care of children in 2009. There are several hot topics I’ll be addressing. Join in and listen, or submit questions on line in the Q&A section of the Live Meeting toolbar during the webinar. See you in cyberspace! Also feel free to suggest topics via comments to the blog posts below. (New comments are approved so if this is your first time it may take an hour or two before you see your comment online).

Last 5 posts by Steve

4 Responses to “Day 10 - Twelfth Camp Blog Entry”

  1. Sandra Hall Says:

    Do you feel the OmniPod may be one of the “snake oil diabetes miracle therapies” discussed above? We are considering the OmniPod for our child and would appreciate hearing your thoughts on the product. Thank you.

  2. Melodi Henry Says:

    I would rate my involvement as a parent in my daughter’s care as an 8. I would have been rated a 10, probably, before we found a local endocrinologist and had my daughter’s pump training at their office. The nurse who completed our training and started her on the pump kept repeating to my daughter and to the rest of us there with her, “This is HER diabetes. She has to know how to do all of this. She has to remember to check blood sugars, learn how to count her own carbs, etc.” She didn’t intend for us to step out of the picture, but I do believe I was coddling her somewhat and needed to encourage her to take ownership in her care. Recently, she has gotten “lazy” about checking her blood sugar, skipping the before meal checks, so I’ve gotten back to asking her each time to give me the number after she checks. Her A1c was 6.8% at her checkup last week, which pleased her doctor. He said the current recommendation is not to have a child’s A1c below about 6.5%, but that he wouldn’t mind seeing her as low as 6.3% as long as she wasn’t have too many severe lows.

    This is her first time at diabetes camp, and I can say that as a parent, I am extremely grateful for the daily photos online! I had a very hard time leaving her - which actually surprised me - and just seeing her smiling face online has made it so much easier today. It is not the first time I’ve been away from her since her diagnosis, but something about walking away from her cabin on Sunday was very emotional for me. I’ve just heard so many wonderful things about this camp from other kids and parents that I knew it was a very good thing for her (and apparentely for my husband and I).

    One final comment: when she was initially diagnosed, our daughter was put on NPH and Novolog and gained 12 pounds right away. When that regimen was changed to Lantus and Novolog, the extra weight came off right away.

    Thank you for all that you’re doing to help our children and us!

  3. Steve Says:

    To answer Sandra’s question, I think that pumps all pretty much do the same things. Since very few people use pumps to their full capabilities, our current array of pumps meets the need. Omnipod has a unique attribute of being “tubeless”. This clearly appeals to people. It also self-inserts, which is another advantage. I have patients on all pump brands. I don’t restrict to one or the other. It’s a choice, after all. My number 1 rule of pumping is that an insulin pump is no better or worse than the human being operating it. Thanks for the comment.

  4. Cathy Salinas Says:

    I would rate myself a six. My husband and I had to learn to back off a bit after we attended the family camp held in Kerrville in April 2008. After listening to Dr. Anderson’s talk about diabetes and family dynamics, we discussed the way we monitored our daughter’s BG with her. Teenagers are easily annoyed by parents anyway, but she voiced how our constant inquiring about her BG made her feel like her diabetes was more important than she was. I try to pick up her meter and check her readings at the end of the day rather than asking her constantly throughout the day. I ask about her day before I ask about her BG readings for the day, and my husband runs the pump reports on the computer every two weeks so we can monitor her BG that way. As she enters high school, ironically, my husband and I are discussing giving her a little more freedom than we did our three older kids. Our reasoning is that we need to have her try out new situations independently while we are still around to provide a safety net.

Leave a Reply