Children and A1c targets

Two articles have appeared less than 2 years about children and A1c targets. The first appeared in January, 2013. It warns parents and medical staff that “only approximately one-third of participants (in a study of over 60,000) met the age specific ADA and ISPAD targets for HbA1c. Although the majority of participants did meet BP, lipid, and BMI targets” (Wood et al., 2013, p. 3). Now as a reminder these targets at the time of publication of this article were as follows:

“8.5% for those younger than 6 years,
8.0% for those 6 to younger than 13 years old, and
7.5% for those 13 to younger than 20 years old” (Wood et al., 2013, p. 1)

Obviously this represents a clinical problem. Since not meeting targets presents at least the possibility of a greater risk for complications.

Flash forward to 2014 and there was a new paper published at the June ADA Scientific conference. The new paper sets out the ADA’s position with regard to glycemic control mostly in children (Chiang, Kirkman, Laffel, & Peters, 2014). The new guideline is as follows:

“The ADA will harmonize its glycemic goals with those of ISPAD (as well as the Pediatric Endocrine Society and the International Diabetes Federation) by using a single A1C goal of <7.5% across all pediatric age-groups” (Chiang et al., 2014, p. 2044).

First a note here, the ADA was not in sync with the International Society for Pediatric and Adolescent Diabetes (ISPAD) as well as the other two organizations mentioned specifically in the statement which had already adopted the less than <7.5% standard (Chiang et al., 2014).

Second each pediatric target except for those 13 - 20 was higher than the new pediatric target adopted in July.

Their rationale for setting the lower target really comes down to one thing in my opinion. With the advent of CGM monitoring it has been generally felt that tighter control can be achieved without the significant fear of low blood sugar which prompted the establishment of the prior guidelines (Chiang et al., 2014).

I happen to know one the authors of the new ADA position paper and I know her to be a fine physician and a caring person. But in order to be taken seriously I believe the ADA paper should have addressed the broader issue present in January 2013, which is that around 2/3rds of pediatric type 1’s were not meeting the higher previous targets (Wood et al., 2013).

The new ADA positon is not unreasonable when viewed from a high altitude. It is easy to tell parents and schools that clinicians want tighter control. It is entirely different to be a parent who wakes up every night to check their child’s blood sugar. I know we have many parents who are fundamentally stressed about blood sugar lows. Imagine a child of less than 3 having a low without a parent to intercede. It is unimaginable to me. And yet promoting tighter controls moves a child closer to that threshold in a body that is growing, changing and developing daily. I just do not know if I could even have a blood sugar target for my child if they were under 3 and yet here is a tighter target? If I were a parent of a type 1 child my goal would be to make it too tomorrow.

Then the new guiltiness go on to say the following:

“CGM is a useful tool to reduce A1C levels in adults without increasing hypoglycemia and can reduce glycemic excursions in children. Glycemic improvements are correlated with frequency of CGM use across all ages.

Children should have additional blood glucose checks if the parent/
caregiver is concerned that the child’s behavior may be due to low/high
blood glucose levels.

School employees and caregivers should be knowledgeable about
SMBG and equipped with all necessary supplies.” (Chiang et al., 2014).

I had to chuckle about these items. Yeah you know I agree with these conclusions. School personnel need to be more familiar with Self Monitoring of Blood Glucose and CGM’s ought to have widespread use. I think we all need to work toward that end.

Of course there is the cost issue, something these authors did not consider when drafting this paper and yes school personnel should be better informed about SMBG practices.

You know I am not against saying this or that is the best practice. I am against telling parents and others they are failing and oh by the way guess what we are making it more difficult for you to hit targets. Come on ADA consider the whole child consequences before putting more stress on families to comply. Also if you want full adoption of CGM’s, maybe it is best to pursue federal legislation, and instead of starting with kids, why not start with Seniors who are denied CGM because of Medicare?

References



Chiang, J. L., Kirkman, M. S., Laffel, L. M. B., & Peters, A. L. (2014). Type 1 Diabetes Through the Life Span: A Position Statement of the American Diabetes Association. Diabetes Care, 37(7), 2034-2054. doi: 10.2337/dc14-1140


Wood, J. R., Miller, K. M., Maahs, D. M., Beck, R. W., DiMeglio, L. A., Libman, I. M., . . . Network, f. t. T. D. E. C. (2013). Most Youth With Type 1 Diabetes in the T1D Exchange Clinic Registry Do Not Meet American Diabetes Association or International Society for Pediatric and Adolescent Diabetes Clinical Guidelines. Diabetes Care. doi: 10.2337/dc12-1959

-30-




rick

Views: 84

Tags: a1c, blog, children, phillips, target

Comment by curlysarah on July 17, 2014 at 7:46am

AMEN!!!!!

Comment by Terrie on July 17, 2014 at 1:11pm

We didn't have A1c's when I was young or blood tests done. We lived in the rural area and our FD didn't request any tests from the hospital. I'd love to know what my A1c was back then.

I know that I'd rather be a PWD than a Parent of a Diabetic Child. What endless worry and work. I give them so much credit. God love the Parents(and the Kids). :)

Comment by shoshana27 on July 17, 2014 at 2:14pm

AMEN TO THAT
IMAGINE WHAT MY MOTHER WENT THROUGH WITH ME
T1 SINCE BEFORE I WAS 3 YEARS OLD

Comment

You need to be a member of Diabetes community by Diabetes Hands Foundation: TuDiabetes to add comments!

Join Diabetes community by Diabetes Hands Foundation: TuDiabetes

Advertisement



REsources

From the Diabetes Hands Foundation blog...

Meet The 2014 Big Blue Test Grant Recipients

  This year Diabetes Hands Foundation has pledged US$35,000 in Big Blue Test grants, continuing its support for programs aimed at providing lifesaving supplies, medical tests, treatment, and patient education to people living in need who have or at risk Read on! →

Kim Vlasnik: The Patient Voice

  Kim Vlasnik, you NAILED it! In this video, Kim Vlasnik takes our breath away as she describes what its like to be a person with diabetes. Fortunately, Stanford’s Medicine-X Conference gives ePatients, like Kim, a chance to speak since we carry the Read on! →

Diabetes Hands Foundation Team

DHF TEAM

Manny Hernandez
(Co-Founder, Editor, has LADA)

Emily Coles
(Head of Communities, has type 1)

Mila Ferrer
(EsTuDiabetes Community Manager, mother of a child with type 1)

Mike Lawson
(Head of Experience, has type 1)

Corinna Cornejo
(Development Manager, has type 2)

Desiree Johnson  (Administrative and Programs Assistant, has type 1)

DHF VOLUNTEERS


Lead Administrator

Brian (bsc) (has type 1)


Administrators

Lorraine (mother of type 1)
Marie B (has type 1)

DanP (has Type 1)

Gary (has type 2)

David (has type 2)

 

LIKE us on Facebook

Spread the word

Loading…

This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information: verify here.

© 2014   A community of people touched by diabetes, run by the Diabetes Hands Foundation.

Badges  |  Contact Us  |  Terms of Service