Type 2 diabetes mellitus: Difference between revisions

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== Management ==
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== Background ==
   
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=== Classification ===
* See also [[Diabetes mellitus#Management|Diabetes mellitus]]
 
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{| class="wikitable"
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!Test
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!Result
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!Category
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|-
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| rowspan="2" |fasting plasma glucose
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|6.1 to 6.9 mmol/L
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|impaired fasting glucose
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|-
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|≥7 mmol/L
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|diabetes
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|-
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| rowspan="2" |[[Hemoglobin A1c]]
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|6 to 6.4%
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|prediabetes
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|-
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|≥6.5%
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|diabetes
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|}
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==Management==
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*See also [[Diabetes mellitus#Management|Diabetes mellitus]]
   
=== Medical Management ===
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===Medical Management===
   
* At diagnosis: lifestyle changes, with nutritional therapy, weight management, and physical activity, and consider adding [[metformin]]
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*At diagnosis: lifestyle changes, with nutritional therapy, weight management, and physical activity, and consider adding [[metformin]]
* Determine A1c target (≤7% for most people)
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*Determine A1c target (≤7% for most people)
** A1c <1.5% above target
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**A1c <1.5% above target
*** Reassess after 3 months of lifestyle changes
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***Reassess after 3 months of lifestyle changes
*** If not at target, add [[metformin]]
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***If not at target, add [[metformin]]
** A1c ≥1.5% above target: start [[metformin]] immediately, and consider concurrent second agent
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**A1c ≥1.5% above target: start [[metformin]] immediately, and consider concurrent second agent
** Symptomatic hyperglycemia or metabolic decompensation: start [[metformin]] and [[insulin]]
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**Symptomatic hyperglycemia or metabolic decompensation: start [[metformin]] and [[insulin]]
* If not at target and has clinical CVD: add [[empagliflozin]], [[liraglutide]], or [[canagliflozin]]
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*If not at target and has clinical CVD: add [[empagliflozin]], [[liraglutide]], or [[canagliflozin]]
* If still not at target, add additional agents based on individualized considerations
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*If still not at target, add additional agents based on individualized considerations
** Avoidance of hypoglycemia and/or weight gain with adequate glycemic efficacy: [[DPP-4 inhibitors]], [[GLP-1 receptor agonists]], or [[SGLT2 inhibitors]]
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**Avoidance of hypoglycemia and/or weight gain with adequate glycemic efficacy: [[DPP-4 inhibitors]], [[GLP-1 receptor agonists]], or [[SGLT2 inhibitors]]
** Reduced eGFR or albuminuria
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**Reduced eGFR or albuminuria
** Clinical CVD or CV risk factors
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**Clinical CVD or CV risk factors
** Degree of hyperglycemia
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**Degree of hyperglycemia
** Other comorbidities, such as heart failure, cardiovascular disease, kidney disease, or liver disease
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**Other comorbidities, such as heart failure, cardiovascular disease, kidney disease, or liver disease
** Planning pregnancy
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**Planning pregnancy
** Cost to patient
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**Cost to patient
** Patient preference
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**Patient preference
   
 
{| class="wikitable"
 
{| class="wikitable"
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|$$$
 
|$$$
 
|}
 
|}
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===Target A1c===
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*≤6.5% for adults with T2DM to reduce with risk of CKD and retinopathy, if at low risk of hypoglycemia
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*≤7% for most adults with T1DM and T2DM
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*7.1-8% for functionally dependent elderly
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*7.1-8.5% for those with recurrent severe hypoglycemia or hypoglycemia unawareness
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*7.1-8.5% for those with a limited life expectancy (stop measuring, and target euglycemia for symptom control)
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*7.1-8.5% for those the frail elderly or those with dementia
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== Further Reading ==
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* [https://guidelines.diabetes.ca/docs/CPG-quick-reference-guide-web-EN.pdf Diabetes Canada 2018 Clinical Practice Guidelines Quick Reference]
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[[Category:Endocrinology]]
 
[[Category:Endocrinology]]

Latest revision as of 07:30, 25 February 2021

Background

Classification

Test Result Category
fasting plasma glucose 6.1 to 6.9 mmol/L impaired fasting glucose
≥7 mmol/L diabetes
Hemoglobin A1c 6 to 6.4% prediabetes
≥6.5% diabetes

Management

Medical Management

  • At diagnosis: lifestyle changes, with nutritional therapy, weight management, and physical activity, and consider adding metformin
  • Determine A1c target (≤7% for most people)
    • A1c <1.5% above target
      • Reassess after 3 months of lifestyle changes
      • If not at target, add metformin
    • A1c ≥1.5% above target: start metformin immediately, and consider concurrent second agent
    • Symptomatic hyperglycemia or metabolic decompensation: start metformin and insulin
  • If not at target and has clinical CVD: add empagliflozin, liraglutide, or canagliflozin
  • If still not at target, add additional agents based on individualized considerations
    • Avoidance of hypoglycemia and/or weight gain with adequate glycemic efficacy: DPP-4 inhibitors, GLP-1 receptor agonists, or SGLT2 inhibitors
    • Reduced eGFR or albuminuria
    • Clinical CVD or CV risk factors
    • Degree of hyperglycemia
    • Other comorbidities, such as heart failure, cardiovascular disease, kidney disease, or liver disease
    • Planning pregnancy
    • Cost to patient
    • Patient preference
Class CVD Outcomes Hypoglycemia Weight A1c Lowering Other Considerations Cost
GLP-1 receptor agonists liraglutide is superior in T2DM, LAR and lixiglutide are neutral rare ↓↓ ↓↓ to ↓↓↓ GI side effects, gallstones; contraindicated in personal/family history of medullary thyroid cancer or MEN-2; given by subcutaneous injection $$$$
SGLT2 inhibitors canagliflozin and empagliflozin are superior in T2DM rare ↓↓ ↓↓ to ↓↓↓ urogenital infections, hypotension, dose-related changes in LDL; caution with renal dysfunction, loop diuretics, and the elderly; dapagliflozin contrindicated in bladder caner; rarely caused euglycemic diabetic ketoacidosis; increased risk of fractures or amputations with canagliflozin; reduced progression of nephropathy and heart failure exacerbations with canaglizflozin and empagliflozin $$$
DPP-4 inhibitors rare ↓↓ avoid saxagliptin in heart failure; rare joint pain $$$
insulin yes ↑↑ ↓↓ to ↓↓↓↓ no dose ceiling; requires subcutaneous injection $ to $$$$
thiazolidinones rare ↑↑ ↓↓ CHF, edema, fractures, rare bladder cancer with pioglitazone, cardiovascular controversy with rosiglitazone, 6-12 weeks for maximum effect $$
alpha-glucosidase inhibitors rare GI side effects common; TID dosing $$
meglitinide yes ↓↓ lower glucose rapidly; reduced postprandial glycemia; TID to QID dosing $$
sulfonylureas yes ↓↓ gliclazide and glimepiride have less hypoglycemia than glyburide; poor durability $
orlistat none GI side effects; TID dosing $$$

Target A1c

  • ≤6.5% for adults with T2DM to reduce with risk of CKD and retinopathy, if at low risk of hypoglycemia
  • ≤7% for most adults with T1DM and T2DM
  • 7.1-8% for functionally dependent elderly
  • 7.1-8.5% for those with recurrent severe hypoglycemia or hypoglycemia unawareness
  • 7.1-8.5% for those with a limited life expectancy (stop measuring, and target euglycemia for symptom control)
  • 7.1-8.5% for those the frail elderly or those with dementia

Further Reading