Diabetes mellitus type 2 Glycemic control: Difference between revisions

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Glycemic control is an important measure in [[diabetes]] [[treatment]]. There are general rules for glycemic control but they should be individualized for every patients based on provider decision and patient condition. [[HbA1c]] is one of the diagnostic tools with a strong predictive value for [[diabetes]] and also a laboratory method with 3 months average glycemic control. There are several guidelines defined glycemic goals. To name one, [[American Diabetes Association|ADA]] has suggested certain range of [[HbA1C]] for diabetic patients in order to have less [[complication(medicine)|complications]] and better [[prognose]].   
Glycemic control is an important measure in [[diabetes]] [[treatment]]. There are general rules for glycemic control but they should be individualized for every patients based on provider decision and patient condition. [[HbA1c]] is one of the diagnostic tools with a strong predictive value for [[diabetes]] and also a laboratory method with 3 months average glycemic control. There are several guidelines defined glycemic goals. To name one, [[American Diabetes Association|ADA]] has suggested certain range of [[HbA1C]] for diabetic patients in order to have less [[complication(medicine)|complications]] and better [[prognose]].   
==Measuring glycemic control==
==Measuring glycemic control==
*[[A1C|Hb A1C]] reflects average glycemia over approximately 3 months and has strong predictive value for [[diabetes]] [[complication(medicine)|complications]].<ref name="pmid20150297">{{cite journal |vauthors=Albers JW, Herman WH, Pop-Busui R, Feldman EL, Martin CL, Cleary PA, Waberski BH, Lachin JM |title=Effect of prior intensive insulin treatment during the Diabetes Control and Complications Trial (DCCT) on peripheral neuropathy in type 1 diabetes during the Epidemiology of Diabetes Interventions and Complications (EDIC) Study |journal=Diabetes Care |volume=33 |issue=5 |pages=1090–6 |year=2010 |pmid=20150297 |pmc=2858182 |doi=10.2337/dc09-1941 |url=}}</ref><ref name="pmid10938048">{{cite journal |vauthors=Stratton IM, Adler AI, Neil HA, Matthews DR, Manley SE, Cull CA, Hadden D, Turner RC, Holman RR |title=Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study |journal=BMJ |volume=321 |issue=7258 |pages=405–12 |year=2000 |pmid=10938048 |pmc=27454 |doi= |url=}}</ref> Therefore, [[HbA1C]] should be measured as baseline control and every 3 months to see whether the treatment goals have been achieved and maintained.
{{main|Blood glucose monitoring}}
(see also section on Continuous Blood Glucose Monitoring below)
 
[[A1C|Hb A1C]] reflects average glycemia over approximately 3 months and has strong predictive value for [[diabetes]] [[complication(medicine)|complications]].<ref name="pmid20150297">{{cite journal |vauthors=Albers JW, Herman WH, Pop-Busui R, Feldman EL, Martin CL, Cleary PA, Waberski BH, Lachin JM |title=Effect of prior intensive insulin treatment during the Diabetes Control and Complications Trial (DCCT) on peripheral neuropathy in type 1 diabetes during the Epidemiology of Diabetes Interventions and Complications (EDIC) Study |journal=Diabetes Care |volume=33 |issue=5 |pages=1090–6 |year=2010 |pmid=20150297 |pmc=2858182 |doi=10.2337/dc09-1941 |url=}}</ref><ref name="pmid10938048">{{cite journal |vauthors=Stratton IM, Adler AI, Neil HA, Matthews DR, Manley SE, Cull CA, Hadden D, Turner RC, Holman RR |title=Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study |journal=BMJ |volume=321 |issue=7258 |pages=405–12 |year=2000 |pmid=10938048 |pmc=27454 |doi= |url=}}</ref> Therefore, [[HbA1C]] should be measured as baseline control and every 3 months to see whether the treatment goals have been achieved and maintained.
 
ALternative measurements include:
*[[Fructosamine]] and glycated [[albumin]] can show mean [[blood sugar|blood glucose]] level over three weeks.  
*[[Fructosamine]] and glycated [[albumin]] can show mean [[blood sugar|blood glucose]] level over three weeks.  
*1,5-Anhydroglucitol can reflect [[Hyperglycemia|hyperglycemic]] changes in days to weeks.
*1,5-Anhydroglucitol can reflect [[Hyperglycemia|hyperglycemic]] changes in days to weeks.
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===Continuous glucose monitoring===
===Continuous glucose monitoring===
{{main|Blood glucose monitoring}} (see section on Continuous Blood Glucose Monitoring)
 
*The Miao Miao is a smartreader add on for the d-Nav that sends reading to a smartphone.
*The Miao Miao is a smartreader add on for the d-Nav that sends reading to a smartphone.
* Libre only tells you what your [[blood sugar]] was in the past.* The d-Nav Insulin Guidance System (Hygieia, Livonia, MI, USA) has shown benefit in a [[randomized controlled trial]]<ref name="pmid30808512">{{cite journal| author=Bergenstal RM, Johnson M, Passi R, Bhargava A, Young N, Kruger DF | display-authors=etal| title=Automated insulin dosing guidance to optimise insulin management in patients with type 2 diabetes: a multicentre, randomised controlled trial. | journal=Lancet | year= 2019 | volume= 393 | issue= 10176 | pages= 1138-1148 | pmid=30808512 | doi=10.1016/S0140-6736(19)30368-X | pmc=6715130 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30808512  }} </ref>.
* Libre only tells you what your [[blood sugar]] was in the past.* The d-Nav Insulin Guidance System (Hygieia, Livonia, MI, USA) has shown benefit in a [[randomized controlled trial]]<ref name="pmid30808512">{{cite journal| author=Bergenstal RM, Johnson M, Passi R, Bhargava A, Young N, Kruger DF | display-authors=etal| title=Automated insulin dosing guidance to optimise insulin management in patients with type 2 diabetes: a multicentre, randomised controlled trial. | journal=Lancet | year= 2019 | volume= 393 | issue= 10176 | pages= 1138-1148 | pmid=30808512 | doi=10.1016/S0140-6736(19)30368-X | pmc=6715130 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30808512  }} </ref>.

Revision as of 19:35, 9 September 2020

Diabetes mellitus main page

Diabetes mellitus type 2 Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Seyedmahdi Pahlavani, M.D. [2]

See also Glycemic Targets in Diabetes


Overview

Glycemic control is an important measure in diabetes treatment. There are general rules for glycemic control but they should be individualized for every patients based on provider decision and patient condition. HbA1c is one of the diagnostic tools with a strong predictive value for diabetes and also a laboratory method with 3 months average glycemic control. There are several guidelines defined glycemic goals. To name one, ADA has suggested certain range of HbA1C for diabetic patients in order to have less complications and better prognose.

Measuring glycemic control

(see also section on Continuous Blood Glucose Monitoring below)

Hb A1C reflects average glycemia over approximately 3 months and has strong predictive value for diabetes complications.[1][2] Therefore, HbA1C should be measured as baseline control and every 3 months to see whether the treatment goals have been achieved and maintained.

ALternative measurements include:

Self-monitoring blood glucose (SMBG)

Blood glucose, via self-monitoring of blood glucose (SMBG) is accurate and easy to use by patients. It allows patients to evaluate their individual response to therapy and assess whether glycemic targets are being achieved. SMBG is mostly used for patients with type 1 diabetes mellitus but some patients with type 2 diabetes who require basal insulin will benefit from this method of monitoring.

It is not clear that home monitoring is helpful in non-insulin treated diabetes mellitus type 2.

  • One randomized controlled trial found that self-monitoring of blood glucose did not improve the Hba1c among "reasonably well controlled non-insulin treated patients with type 2 diabetes".[3][4]
  • A more recent meta-analysis did not find benefit[5].


The following video shows how to apply glucometer devices for SMBG: {{#ev:youtube|rMMpeLLgdgY}}

Continuous glucose monitoring

  • The Miao Miao is a smartreader add on for the d-Nav that sends reading to a smartphone.
  • Libre only tells you what your blood sugar was in the past.* The d-Nav Insulin Guidance System (Hygieia, Livonia, MI, USA) has shown benefit in a randomized controlled trial[6].

smartphone.

Goals

Evidence from trials

Forest Plot showing meta-analysis of randomized controlled trials of differing target glucose control and mortality for diabetes mellitus type 2. Note the heterogeneity due to increased death when the glycosylated hemoglobin A (Hb A1c) target was 6.0% in the ACCORD trial

Clinical Practice Guidelines

  • There are opposing guidelines between the American College of Physicians (ACP) and the American Diabetes Association (ADA) on the goal for the HbA1c. Taking these guidelines into consideration, what is both an evidence-based and clinically practical HbA1c goal?​
  • The American College of Physicians published clinical practice guidelines in 2018 that states[22]:
    • "clinicians should aim to achieve an HbA1c level between 7% and 8% in most patients with type 2 diabetes and should consider de-intensifying pharmacologic therapy in patients with type 2 diabetes who achieve HbA1c levels less than 6.5%."
  • The American Diabetes Association (ADA) published clinical practice guidelines in 2020[23] that updated guidelines from 2019[24] and released a response statement in opposition to the ACP's guidelines:
    • “An HbA1C goal for many nonpregnant adults of <7% is appropriate”
    • On the basis of provider judgement and patient preference, achievement of lower HbA1C levels (such as <6.5%) may be acceptable if this can be achieved safely without significant hypoglycemia or other adverse effects of treatment
    • “Less stringent HbA1C goals may be appropriate for patients with a history of severe hypoglycemia, limited life expectancy, advanced microvascular or macrovascular complications, extensive comorbid conditions, or long-standing diabetes in whom the goal is difficult to achieve despite diabetes self-management education, appropriate glucose monitoring, and effective doses of multiple glucose-lowering agents including insulin
    • Regarding assessment of the trustworthiness of the methods[25] of the guideline[26], the ADA did not list author names, provide a statement of conflicts of interest nor describe methods or breadth of peer review.
  • Kaiser Permanente states[27]:
    • A1C goal of 7.0–8.0%
    • "Use clinical judgment to determine if a target lower than 7.0% is appropriate for an individual patient. It can be challenging to push a patient’s HbA1c levels from just above 7.0% to below 7.0%. There are potential benefits (decreased nonfatal myocardial infarction) and potential harms (hypoglycemia, weight gain, and possible increase in all-cause and cardiovascular-cause mortality) of intensive glucose therapy, especially in patients with known cardiovascular disease."
    • "For frail elderly patients, a target HbA1c of 7.0–9.0% is reasonable"

Frequency goals are achieved

Typical practice:

  • 35% of patients have an HbA1c of less than 7 per HEDIS measures[28]:
  • 59% according to NHANES (self-reported by patients[29])[30]

Best practice

  • 71% in the Veterans Affairs VISN16[31].
  • 69% according to Kaiser in Colorado[32] However, this is the proportion of patients "ever achieving" goal and not clear is this is equivalent to a cross-section of patients at goal.

References

  1. Albers JW, Herman WH, Pop-Busui R, Feldman EL, Martin CL, Cleary PA, Waberski BH, Lachin JM (2010). "Effect of prior intensive insulin treatment during the Diabetes Control and Complications Trial (DCCT) on peripheral neuropathy in type 1 diabetes during the Epidemiology of Diabetes Interventions and Complications (EDIC) Study". Diabetes Care. 33 (5): 1090–6. doi:10.2337/dc09-1941. PMC 2858182. PMID 20150297.
  2. Stratton IM, Adler AI, Neil HA, Matthews DR, Manley SE, Cull CA, Hadden D, Turner RC, Holman RR (2000). "Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study". BMJ. 321 (7258): 405–12. PMC 27454. PMID 10938048.
  3. Farmer A, Wade A, Goyder E; et al. (2007). "Impact of self monitoring of blood glucose in the management of patients with non-insulin treated diabetes: open parallel group randomised trial". doi:10.1136/bmj.39247.447431.BE. PMID 17591623.
  4. Farmer AJ, Perera R, Ward A, Heneghan C, Oke J, Barnett AH; et al. (2012). "Meta-analysis of individual patient data in randomised trials of self monitoring of blood glucose in people with non-insulin treated type 2 diabetes". BMJ. 344: e486. doi:10.1136/bmj.e486. PMID 22371867. Review in: Ann Intern Med. 2012 Jun 19;156(12):JC6-12
  5. Willett LR (2012). "ACP Journal Club. Meta-analysis: self-monitoring in non-insulin-treated type 2 diabetes improved HbA1c by 0.25%". Ann Intern Med. 156 (12): JC6–12. doi:10.7326/0003-4819-156-12-201206190-02012. PMID 22711113.
  6. Bergenstal RM, Johnson M, Passi R, Bhargava A, Young N, Kruger DF; et al. (2019). "Automated insulin dosing guidance to optimise insulin management in patients with type 2 diabetes: a multicentre, randomised controlled trial". Lancet. 393 (10176): 1138–1148. doi:10.1016/S0140-6736(19)30368-X. PMC 6715130 Check |pmc= value (help). PMID 30808512.
  7. "Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group". Lancet. 352 (9131): 837–53. 1998. doi:10.1016/S0140-6736(98)07019-6. PMID 9742976. Review by ACP Journal Club
  8. "Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). UK Prospective Diabetes Study (UKPDS) Group". Lancet. 352 (9131): 854–65. 1998. PMID 9742977.
  9. Duckworth W, Abraira C, Moritz T; et al. (2009). "Glucose control and vascular complications in veterans with type 2 diabetes". N. Engl. J. Med. 360 (2): 129–39. doi:10.1056/NEJMoa0808431. PMID 19092145. Unknown parameter |month= ignored (help)
  10. Abraira C, Duckworth W, McCarren M; et al. (2003). "Design of the cooperative study on glycemic control and complications in diabetes mellitus type 2: Veterans Affairs Diabetes Trial". Journal of diabetes and its complications. 17 (6): 314–22. PMID 14583175.
  11. "Intensive Blood Glucose Control and Vascular Outcomes in Patients with Type 2 Diabetes". N. Engl. J. Med. 358 (24): 2560–2572. 2008. doi:10.1056/NEJMoa0802987. PMID 18539916. Unknown parameter |month= ignored (help)
  12. Anonymous (February 6, 2008). "For Safety, NHLBI Changes Intensive [[Blood Sugar]] [[Treatment]] Strategy in Clinical Trial of [[Diabetes]] and [[Cardiovascular Disease]] -". National Institutes of Health (NIH). Retrieved 2008-02-07. URL–wikilink conflict (help)
  13. Gerstein HC, Miller ME, Byington RP; et al. (2008). "Effects of intensive glucose lowering in type 2 diabetes". N. Engl. J. Med. 358 (24): 2545–59. doi:10.1056/NEJMoa0802743. PMID 18539917. Unknown parameter |month= ignored (help)
  14. The ORIGIN Trial Investigators (2012). "Basal Insulin and Cardiovascular and Other Outcomes in Dysglycemia". N Engl J Med. doi:10.1056/NEJMoa1203858. PMID 22686416.
  15. Dormandy JA, Charbonnel B, Eckland DJ, Erdmann E, Massi-Benedetti M, Moules IK; et al. (2005). "Secondary prevention of macrovascular events in patients with type 2 diabetes in the PROactive Study (PROspective pioglitAzone Clinical Trial In macroVascular Events): a randomised controlled trial". Lancet. 366 (9493): 1279–89. doi:10.1016/S0140-6736(05)67528-9. PMID 16214598. Review in: ACP J Club. 2006 Mar-Apr;144(2):34 Review in: Evid Based Med. 2006 Apr;11(2):47
  16. Meinert CL, Knatterud GL, Prout TE, Klimt CR (1970). "A study of the effects of hypoglycemic agents on vascular complications in patients with adult-onset diabetes. II. Mortality results". Diabetes. 19: Suppl:789–830. PMID 4926376.
  17. "Effects of hypoglycemic agents on vascular complications in patients with adult-onset diabetes. VIII. Evaluation of insulin therapy: final report". Diabetes. 31 Suppl 5: 1–81. 1982. PMID 6757026.
  18. 18.0 18.1 Kilo C, Miller JP, Williamson JR (1980). "The Achilles heel of the University Group Diabetes Program". JAMA. 243 (5): 450–7. doi:10.1001/jama.1980.03300310038020. PMID 6985989.
  19. 19.0 19.1 19.2 Genuth S (1996). "Exogenous insulin administration and cardiovascular risk in non-insulin-dependent and insulin-dependent diabetes mellitus". Ann Intern Med. 124 (1 Pt 2): 104–9. PMID 8554200.
  20. Feinglos MN, Bethel MA (1999). "Therapy of type 2 diabetes, cardiovascular death, and the UGDP". Am Heart J. 138 (5 Pt 1): S346–52. doi:10.1016/S0002-8703(99)70034-7. PMID 10539796.
  21. Gaster B, Hirsch IB (1998). "[[complication(medicine)|complications]]". Arch Intern Med. 158 (2): 134–40. PMID 9448551. URL–wikilink conflict (help)
  22. Qaseem A, Wilt TJ, Kansagara D, Horwitch C, Barry MJ, Forciea MA; et al. (2018). "Hemoglobin A1c Targets for Glycemic Control With Pharmacologic Therapy for Nonpregnant Adults With Type 2 Diabetes Mellitus: A Guidance Statement Update From the American College of Physicians". Ann Intern Med. doi:10.7326/M17-0939. PMID 29507945.
  23. American Diabetes Association (2020). "6. Glycemic Targets: Standards of Medical Care in Diabetes-2020". Diabetes Care. 43 (Suppl 1): S66–S76. doi:10.2337/dc20-S006. PMID 31862749.
  24. American Diabetes Association (2019). "6. Glycemic Targets: Standards of Medical Care in Diabetes-2019". Diabetes Care. 42 (Suppl 1): S61–S70. doi:10.2337/dc19-S006. PMID 30559232.
  25. "Introduction: Standards of Medical Care in Diabetes-2020". Diabetes Care. 43 (Suppl 1): S1–S2. 2020. doi:10.2337/dc20-Sint. PMID 31862741.
  26. Institute of Medicine (US) Committee on Standards for Developing Trustworthy Clinical Practice Guidelines (2011). "Clinical Practice Guidelines We Can Trust". PMID 24983061.
  27. Kaiser Permanente Care Management Institute. Guidelines. Available at http://kpcmi.org/how-we-work/guidelines/
  28. Anonymous (2017). Comprehensive Diabetes Care
  29. Anonymous (2016). NHANES Participant Homepage. CDC/National Center for Health Statistics
  30. Selvin E, Parrinello CM, Sacks DB, Coresh J (2014). "Trends in prevalence and control of diabetes in the United States, 1988-1994 and 1999-2010". Ann Intern Med. 160 (8): 517–25. doi:10.7326/M13-2411. PMC 4442608. PMID 24733192.
  31. Shi L, Ye X, Lu M, Wu EQ, Sharma H, Thomason D; et al. (2015). "Glycemic and Cholesterol Control Versus Single-Goal Control in US Veterans with Newly Diagnosed Type 2 Diabetes: A Retrospective Observational Study". Diabetes Ther. 6 (3): 339–55. doi:10.1007/s13300-015-0122-2. PMC 4575310. PMID 26202185.
  32. Schroeder EB, Hanratty R, Beaty BL, Bayliss EA, Havranek EP, Steiner JF (2012). "Simultaneous control of diabetes mellitus, hypertension, and hyperlipidemia in 2 health systems". Circ Cardiovasc Qual Outcomes. 5 (5): 645–53. doi:10.1161/CIRCOUTCOMES.111.963553. PMC 3590111. PMID 22851534.