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CLASSIFICATION
 Diabetes can be classified into the following general categories:
 Type 1 diabetes (due to autoimmune beta cell destruction, usually
leading to absolute insulin deficiency)
 Type 2 diabetes (due to a progressive loss of b-cell insulin secretion
frequently on the background of insulin resistance)
 Gestational diabetes mellitus (diabetes diagnosed in the second or
third trimester of pregnancy that was not clearly overt diabetes prior to
gestation)
 Specific types of diabetes due to other causes, e.g.,
 monogenic diabetes syndromes (such as neonatal diabetes and
maturity-onset diabetes of the young [MODY]),
 diseases of the exocrine pancreas (such as cystic fibrosis and
pancreatitis),
 and drug- or chemical-induced diabetes (such as with glucocorticoid
use, in the treatment of HIV/AIDS, or after organ transplantation)
CRITERIA FOR DIAGNOSIS

FPG > 126 mg/dL Fasting is defined as no caloric intake for
at least 8 h.* OR
 2-h PG >200 mg/dL during OGTT. The test should be
performed as described by the WHO, using a glucose load
containing the equivalent of 75-g anhydrous glucose
dissolved in water.* OR
 A1C >6.5% . The test should be performed in a laboratory
using a method that is NGSP certified and standardized to
the DCCT assay.* OR
 In a patient with classic symptoms of hyperglycemia or
hyperglycemic crisis, a random plasma glucose >200
mg/dL .
 *In the absence of unequivocal hyperglycemia, results
should be confirmed by repeat testing.
Marked discordance between measured A1C and plasma
glucose levels should raise the possibility of A1C assay
interference due to hemoglobin variants (i.e., hemoglo-
binopathies) and consideration of using an assay without
interference or plasma blood glucose criteria to diagnose
diabetes.
In conditions associated with increased red blood cell
turnover, such as sickle cell disease, pregnancy (second and
third trimesters), hemodialysis, recent blood loss or
transfusion, or erythropoietin therapy, only plasma blood
glucose criteria should be used to diagnose diabetes.
 A reasonable A1C goal for many nonpregnant adults is
<7%.
 Providers might reasonably suggest more stringent A1C
goals (such as <6.5% ) for selected individual patients if
this can be achieved without significant hypoglycemia or
other adverse effects of treatment (i.e., polypharmacy).
Appropriate patients might include those with short
duration of diabetes, type 2 diabetes treated with lifestyle
or metformin only, long life expectancy, or no significant
cardiovascular disease.
 Less stringent A1C goals (such as <8%) 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 maximal therapy.
CRITERIA IN
ASYMPTOMATIC ADULTS
 Testing should be considered in overweight or obese (BMI >25 kg/m2 or >23 kg/m2 in
Asian Americans) adults who have one or more of the following risk factors:
First-degree relative with diabetes
High-risk race/ethnicity (e.g., African American, Latino, Native American, Asian
American, Pacific Islander)
History of CVD
Hypertension (>140/90 mmHg or on therapy for hypertension)
HDL cholesterol level <35 mg/dL and/or a triglyceride level >250 mg/dL
Women with polycystic ovary syndrome
Physical inactivity
Other clinical conditions associated with insulin resistance (e.g., severe obesity,
acanthosis nigricans)
 Patients with prediabetes (A1C >5.7% ) should be
tested yearly.
 Women who were diagnosed with GDM should have
lifelong testing at least every 3 years.
 For all other patients, testing should begin at age 45
years.
 If results are normal, testing should be repeated at a
minimum of 3-year intervals, with consideration of
more frequent testing depending on initial results
and risk status.
ANTIDIABETIC DRUGS
TZDs
SGLT 2 INHIBITORS
 Metformin, if not contraindicated and if tolerated, is the preferred initial
pharmacologic agent for the treatment of type 2 diabetes.
 Long-term use of metformin may be associated with biochemical vitamin B12
deficiency, and periodic measurement of vitamin B12 levels should be
considered in metformin-treated patients, especially in those with anemia or
peripheral neuropathy.
 Consider initiating insulin therapy (with or without additional agents) in
patients with newly diagnosed type 2 diabetes who are symptomatic and/or
have A1C >10% and/or blood glucose levels >300 mg/dL.
 Consider initiating dual therapy in patients with newly diagnosed type 2
diabetes who have A1C > 9%.
 A patient-centered approach should be used to guide the choice of
pharmacologic agents. Considerations include efficacy, hypoglycemia risk,
history of atherosclerotic cardiovascular disease, impact on weight, potential
side effects, renal effects, delivery method (oral versus subcutaneous), cost,
and patient preferences
 In patients without atherosclerotic cardiovascular
disease, if mono- therapy or dual therapy does not
achieve or maintain the A1C goal over 3 months, add an
additional antihyperglycemic agent based on drug-
specific and patient factors.
 In patients with type 2 diabetes and established
atherosclerotic cardiovascular disease, antihyperglycemic
therapy should begin with lifestyle management and
metformin and subsequently incorporate an agent proven
to reduce major adverse cardiovascular events and
cardiovascular mortality (currently empagliflozin and
liraglutide).
 For patients with type 2 diabetes who are not achieving
glycemic goals, drug intensification, including consid-
eration of insulin therapy, should not be delayed.
 Metformin should be continued when used in combination
with other agents, including insulin, if not contra- indicated
and if tolerated.
BLOOD PRESSURE GOALS
 Most patients with diabetes and hypertension
should be treated to a systolic blood pressure goal
of <140 mmHg and a diastolic blood pressure goal of
<90 mmHg.
 Lower systolic and diastolic blood pressure targets,
such as 130/80 mmHg, may be appropriate for
individuals at high risk of cardiovascular disease, if
they can be achieved without undue treatment
burden.
 In pregnant patients with diabetes and preexisting
hypertension who are treated with antihypertensive
therapy, blood pressure targets of 120–160/80–105
mmHg are suggested in the interest of optimizing
long-term maternal health and minimizing impaired
fetal growth
 Patients with confirmed office based blood pressure
>140/90 mmHg should, in addition to lifestyle therapy, have
prompt initiation and timely titration of pharmacologic
therapy to achieve blood pressure goals.
 Patients with confirmed office-based blood pressure
>160/100 mmHg should, in addition to lifestyle therapy,
have prompt initiation and timely titration of two drugs or
a single pill combination of drugs demonstrated to reduce
cardiovascular events in patients with diabetes.
 Treatment for hypertension should include drug classes
demonstrated to reduce cardiovascular events in patients
with diabetes (ACE inhibitors, angiotensin receptor
blockers, thiazide- like diuretics, or dihydropyridine calcium
channel blockers).
 An ACE inhibitor or angiotensin receptor blocker, at the
maximumly tolerated dose indicated for blood pressure
treatment, is the recom- mended first-line treatment for hy-
pertension in patients with diabetes and urinary albumin-
to-creatinine ratio >300 mg/g creatinine or 30–299 mg/g
creatinine .
 For patients treated with an ACE inhibitor, angiotensin
receptor blocker, or diuretic, serum creatinine /estimated
glomerular filtration rate and serum potassium levels
should be monitored at least annually.
ROLE OF STATINS
 In adults not taking statins or other lipid-lowering
therapy, it is reasonable to obtain a lipid profile at
the time of diabetes diagnosis, at an initial medical
evaluation, and every 5 years thereafter if under the
age of 40 years, or more frequently if indicated.
 Obtain a lipid profile at initiation of statins or other
lipid-lowering therapy, 4–12 weeks after initiation or
a change in dose, and annually thereafter as it may
help to monitor the response to therapy and inform
adherence
 For patients of all ages with diabetes and atherosclerotic
cardiovascular disease, high-intensity statin therapy should
be added to lifestyle therapy.
 For patients with diabetes aged <40 years with additional
athero- sclerotic cardiovascular disease risk factors, the
patient and provider should consider using moderate-
intensity statin in addition to lifestyle therapy.
 For patients with diabetes aged 40– 75 years and >75 years
without atherosclerotic cardiovascular disease, use
moderate-intensity statin in addition to lifestyle therapy.
 For patients with diabetes and atherosclerotic
cardiovascular disease, if LDL cholesterol is >70 mg/dL on
maximally tolerated statin dose, consider adding additional
LDL- lowering therapy (such as ezetimibe or PCSK9
inhibitor) after evaluating the potential for further athero-
sclerotic cardiovascular disease risk reduction, drug-specific
adverse effects, and patient preferences. Ezetimibe may be
preferred due to lower cost.
 Statin therapy is contraindicated in pregnancy.
ROLE OF ANTIPLATELETS
 Use aspirin therapy (75–162 mg/day) as a secondary prevention
strategy in those with diabetes and a history of atherosclerotic
cardiovascular disease.
 For patients with atherosclerotic cardiovascular disease and
documented aspirin allergy, clopidogrel (75 mg/day) should be
used.
 Aspirin therapy (75–162 mg/day) may be considered as a
primary prevention strategy in those with type 1 or type 2
diabetes who are at increased cardiovascular risk. This includes
most men and women with diabetes aged >50 years who have
at least one additional major risk factor (family history of
premature atherosclerotic cardiovascular disease,
hypertension, dyslipidemia, smoking, or albuminuria) and are
not at increased risk of bleeding
SCREENING FOR CAD
 In asymptomatic patients, routine screening for
coronary artery disease is not recommended as it does
not improve outcomes as long as atherosclerotic
cardiovascular disease risk factors are treated.
 Consider investigations for coronary artery disease in
the presence of any of the following: atypical cardiac
symptoms ; signs or symptoms of associated vascular
disease including carotid bruits, transient ischemic
attack, stroke, claudication, or peripheral arterial
disease; or electrocardiogram abnormalities.
 In patients with type 2 diabetes with stable congestive
heart failure, metformin may be used if estimated
glomerular filtration rate remains >30 mL/min but
should be avoided in unstable or hospitalized patients
with congestive heart failure.
OLDER ADULTS GOALS
 Older adults who are otherwise healthy with few
coexisting chronic illnesses and intact cognitive
function and functional status should have lower
glycemic goals (A1C <7.5%), while those with multiple
coexisting chronic ill-nesses, cognitive impairment,
or functional dependence should have less stringent
glycemic goals (A1C ,8.0–8.5% )
 Treatment of hypertension to individualized target
levels is indicated in most older adults.
 Treatment of other cardiovascular risk factors should
be individualized in older adults considering the time
frame of benefit.
INDOOR PATIENTS
 Insulin therapy should be initiated for treatment of persistent
hyperglycemia starting at a threshold >180 mg/dL. Once insulin
therapy is started, a target glucose range of 140–180 mg/dL is
recommended for the majority of critically ill patients and
noncritically ill patients.
 More stringent goals, such as 110– 140 mg/dL, may be
appropriate for selected patients, if this can be achieved with-
out significant hypoglycemia.
 A basal plus bolus correction insulin regimen, with the addition
of nutritional insulin in patients who have good nutritional
intake, is the preferred treatment for noncritically ill patients.
 Sole use of sliding scale insulin in the inpatient hospital setting
is strongly discouraged
TAKE HOME MESSAGE
 Early diagnosis in asymptomatic adults.
 Intensive treatment(never delay insulin therapy if
indicated)
 Patient based treatment preferences
 Target risk factors like blood pressure goals , lipid
lowering and cardiovascular risk factors alongwith
hyperglycemia.

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Diagnosis and treatment of diabetes

  • 1.
  • 2. CLASSIFICATION  Diabetes can be classified into the following general categories:  Type 1 diabetes (due to autoimmune beta cell destruction, usually leading to absolute insulin deficiency)  Type 2 diabetes (due to a progressive loss of b-cell insulin secretion frequently on the background of insulin resistance)  Gestational diabetes mellitus (diabetes diagnosed in the second or third trimester of pregnancy that was not clearly overt diabetes prior to gestation)  Specific types of diabetes due to other causes, e.g.,  monogenic diabetes syndromes (such as neonatal diabetes and maturity-onset diabetes of the young [MODY]),  diseases of the exocrine pancreas (such as cystic fibrosis and pancreatitis),  and drug- or chemical-induced diabetes (such as with glucocorticoid use, in the treatment of HIV/AIDS, or after organ transplantation)
  • 3. CRITERIA FOR DIAGNOSIS  FPG > 126 mg/dL Fasting is defined as no caloric intake for at least 8 h.* OR  2-h PG >200 mg/dL during OGTT. The test should be performed as described by the WHO, using a glucose load containing the equivalent of 75-g anhydrous glucose dissolved in water.* OR  A1C >6.5% . The test should be performed in a laboratory using a method that is NGSP certified and standardized to the DCCT assay.* OR  In a patient with classic symptoms of hyperglycemia or hyperglycemic crisis, a random plasma glucose >200 mg/dL .  *In the absence of unequivocal hyperglycemia, results should be confirmed by repeat testing.
  • 4. Marked discordance between measured A1C and plasma glucose levels should raise the possibility of A1C assay interference due to hemoglobin variants (i.e., hemoglo- binopathies) and consideration of using an assay without interference or plasma blood glucose criteria to diagnose diabetes. In conditions associated with increased red blood cell turnover, such as sickle cell disease, pregnancy (second and third trimesters), hemodialysis, recent blood loss or transfusion, or erythropoietin therapy, only plasma blood glucose criteria should be used to diagnose diabetes.
  • 5.  A reasonable A1C goal for many nonpregnant adults is <7%.  Providers might reasonably suggest more stringent A1C goals (such as <6.5% ) for selected individual patients if this can be achieved without significant hypoglycemia or other adverse effects of treatment (i.e., polypharmacy). Appropriate patients might include those with short duration of diabetes, type 2 diabetes treated with lifestyle or metformin only, long life expectancy, or no significant cardiovascular disease.  Less stringent A1C goals (such as <8%) 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 maximal therapy.
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  • 9. CRITERIA IN ASYMPTOMATIC ADULTS  Testing should be considered in overweight or obese (BMI >25 kg/m2 or >23 kg/m2 in Asian Americans) adults who have one or more of the following risk factors: First-degree relative with diabetes High-risk race/ethnicity (e.g., African American, Latino, Native American, Asian American, Pacific Islander) History of CVD Hypertension (>140/90 mmHg or on therapy for hypertension) HDL cholesterol level <35 mg/dL and/or a triglyceride level >250 mg/dL Women with polycystic ovary syndrome Physical inactivity Other clinical conditions associated with insulin resistance (e.g., severe obesity, acanthosis nigricans)
  • 10.  Patients with prediabetes (A1C >5.7% ) should be tested yearly.  Women who were diagnosed with GDM should have lifelong testing at least every 3 years.  For all other patients, testing should begin at age 45 years.  If results are normal, testing should be repeated at a minimum of 3-year intervals, with consideration of more frequent testing depending on initial results and risk status.
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  • 20.  Metformin, if not contraindicated and if tolerated, is the preferred initial pharmacologic agent for the treatment of type 2 diabetes.  Long-term use of metformin may be associated with biochemical vitamin B12 deficiency, and periodic measurement of vitamin B12 levels should be considered in metformin-treated patients, especially in those with anemia or peripheral neuropathy.  Consider initiating insulin therapy (with or without additional agents) in patients with newly diagnosed type 2 diabetes who are symptomatic and/or have A1C >10% and/or blood glucose levels >300 mg/dL.  Consider initiating dual therapy in patients with newly diagnosed type 2 diabetes who have A1C > 9%.  A patient-centered approach should be used to guide the choice of pharmacologic agents. Considerations include efficacy, hypoglycemia risk, history of atherosclerotic cardiovascular disease, impact on weight, potential side effects, renal effects, delivery method (oral versus subcutaneous), cost, and patient preferences
  • 21.  In patients without atherosclerotic cardiovascular disease, if mono- therapy or dual therapy does not achieve or maintain the A1C goal over 3 months, add an additional antihyperglycemic agent based on drug- specific and patient factors.  In patients with type 2 diabetes and established atherosclerotic cardiovascular disease, antihyperglycemic therapy should begin with lifestyle management and metformin and subsequently incorporate an agent proven to reduce major adverse cardiovascular events and cardiovascular mortality (currently empagliflozin and liraglutide).  For patients with type 2 diabetes who are not achieving glycemic goals, drug intensification, including consid- eration of insulin therapy, should not be delayed.  Metformin should be continued when used in combination with other agents, including insulin, if not contra- indicated and if tolerated.
  • 22. BLOOD PRESSURE GOALS  Most patients with diabetes and hypertension should be treated to a systolic blood pressure goal of <140 mmHg and a diastolic blood pressure goal of <90 mmHg.  Lower systolic and diastolic blood pressure targets, such as 130/80 mmHg, may be appropriate for individuals at high risk of cardiovascular disease, if they can be achieved without undue treatment burden.  In pregnant patients with diabetes and preexisting hypertension who are treated with antihypertensive therapy, blood pressure targets of 120–160/80–105 mmHg are suggested in the interest of optimizing long-term maternal health and minimizing impaired fetal growth
  • 23.  Patients with confirmed office based blood pressure >140/90 mmHg should, in addition to lifestyle therapy, have prompt initiation and timely titration of pharmacologic therapy to achieve blood pressure goals.  Patients with confirmed office-based blood pressure >160/100 mmHg should, in addition to lifestyle therapy, have prompt initiation and timely titration of two drugs or a single pill combination of drugs demonstrated to reduce cardiovascular events in patients with diabetes.  Treatment for hypertension should include drug classes demonstrated to reduce cardiovascular events in patients with diabetes (ACE inhibitors, angiotensin receptor blockers, thiazide- like diuretics, or dihydropyridine calcium channel blockers).
  • 24.  An ACE inhibitor or angiotensin receptor blocker, at the maximumly tolerated dose indicated for blood pressure treatment, is the recom- mended first-line treatment for hy- pertension in patients with diabetes and urinary albumin- to-creatinine ratio >300 mg/g creatinine or 30–299 mg/g creatinine .  For patients treated with an ACE inhibitor, angiotensin receptor blocker, or diuretic, serum creatinine /estimated glomerular filtration rate and serum potassium levels should be monitored at least annually.
  • 25. ROLE OF STATINS  In adults not taking statins or other lipid-lowering therapy, it is reasonable to obtain a lipid profile at the time of diabetes diagnosis, at an initial medical evaluation, and every 5 years thereafter if under the age of 40 years, or more frequently if indicated.  Obtain a lipid profile at initiation of statins or other lipid-lowering therapy, 4–12 weeks after initiation or a change in dose, and annually thereafter as it may help to monitor the response to therapy and inform adherence
  • 26.  For patients of all ages with diabetes and atherosclerotic cardiovascular disease, high-intensity statin therapy should be added to lifestyle therapy.  For patients with diabetes aged <40 years with additional athero- sclerotic cardiovascular disease risk factors, the patient and provider should consider using moderate- intensity statin in addition to lifestyle therapy.  For patients with diabetes aged 40– 75 years and >75 years without atherosclerotic cardiovascular disease, use moderate-intensity statin in addition to lifestyle therapy.  For patients with diabetes and atherosclerotic cardiovascular disease, if LDL cholesterol is >70 mg/dL on maximally tolerated statin dose, consider adding additional LDL- lowering therapy (such as ezetimibe or PCSK9 inhibitor) after evaluating the potential for further athero- sclerotic cardiovascular disease risk reduction, drug-specific adverse effects, and patient preferences. Ezetimibe may be preferred due to lower cost.  Statin therapy is contraindicated in pregnancy.
  • 27. ROLE OF ANTIPLATELETS  Use aspirin therapy (75–162 mg/day) as a secondary prevention strategy in those with diabetes and a history of atherosclerotic cardiovascular disease.  For patients with atherosclerotic cardiovascular disease and documented aspirin allergy, clopidogrel (75 mg/day) should be used.  Aspirin therapy (75–162 mg/day) may be considered as a primary prevention strategy in those with type 1 or type 2 diabetes who are at increased cardiovascular risk. This includes most men and women with diabetes aged >50 years who have at least one additional major risk factor (family history of premature atherosclerotic cardiovascular disease, hypertension, dyslipidemia, smoking, or albuminuria) and are not at increased risk of bleeding
  • 28. SCREENING FOR CAD  In asymptomatic patients, routine screening for coronary artery disease is not recommended as it does not improve outcomes as long as atherosclerotic cardiovascular disease risk factors are treated.  Consider investigations for coronary artery disease in the presence of any of the following: atypical cardiac symptoms ; signs or symptoms of associated vascular disease including carotid bruits, transient ischemic attack, stroke, claudication, or peripheral arterial disease; or electrocardiogram abnormalities.  In patients with type 2 diabetes with stable congestive heart failure, metformin may be used if estimated glomerular filtration rate remains >30 mL/min but should be avoided in unstable or hospitalized patients with congestive heart failure.
  • 29. OLDER ADULTS GOALS  Older adults who are otherwise healthy with few coexisting chronic illnesses and intact cognitive function and functional status should have lower glycemic goals (A1C <7.5%), while those with multiple coexisting chronic ill-nesses, cognitive impairment, or functional dependence should have less stringent glycemic goals (A1C ,8.0–8.5% )  Treatment of hypertension to individualized target levels is indicated in most older adults.  Treatment of other cardiovascular risk factors should be individualized in older adults considering the time frame of benefit.
  • 30. INDOOR PATIENTS  Insulin therapy should be initiated for treatment of persistent hyperglycemia starting at a threshold >180 mg/dL. Once insulin therapy is started, a target glucose range of 140–180 mg/dL is recommended for the majority of critically ill patients and noncritically ill patients.  More stringent goals, such as 110– 140 mg/dL, may be appropriate for selected patients, if this can be achieved with- out significant hypoglycemia.  A basal plus bolus correction insulin regimen, with the addition of nutritional insulin in patients who have good nutritional intake, is the preferred treatment for noncritically ill patients.  Sole use of sliding scale insulin in the inpatient hospital setting is strongly discouraged
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  • 40. TAKE HOME MESSAGE  Early diagnosis in asymptomatic adults.  Intensive treatment(never delay insulin therapy if indicated)  Patient based treatment preferences  Target risk factors like blood pressure goals , lipid lowering and cardiovascular risk factors alongwith hyperglycemia.