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Pratap sagar Tiwari, MD, Internal Medcine,
Lecturer, NMCTH
UNDERSTANDING DIABETES..PART 3
CASE SUMMARY
• A 30 yrs old M was brought in ERD in the state of unconsciousness.
(Note: Coma is a symptom, not a diagnosis.)
Pic taken from http://censorbugbear-reports.blogspot.com/2010/03/shocking-neglect-of-comatose-patient-at.html
RECAP OF PREVIOUS PARTS
• Causes of patient in state of coma
• Definition of terms related to consciousness
• Causes of Coma in a Diabetic Patient
• Insulin Synthesis/ Secretion
• Regulation of Glucose hemostasis
• Response of hypoglycemia in normal & DM
• Hypoglycemia & symptoms
• DKA /HHS
• Abnormal respiration patterns
DIABETES MELLITUS
• Diabetes mellitus is a clinical syndrome characterised by
hyperglycaemia caused by absolute or relative deficiency of
insulin.
DIAGNOSTIC CRITERIA
• A1C ≥6.5%
• OR
• Fasting plasma glucose (FPG) ≥126 mg/dL (7.0 mmol/L)
OR
• 2-hour plasma glucose ≥200 mg/dL (11.1 mmol/L) during an OGTT
OR
• A random plasma glucose ≥200 mg/dL (11.1 mmol/L), in patients with
classic symptoms of hyperglycemia or hyperglycemic crisis
PRE DIABETES
1. IFG: fasting plasma glucose (FPG) levels of 100–
125 mg/dL (5.6–6.9 mmol/L)*
2. IGT: 2-hour plasma glucose (2-h PG) in the 75-g oral
glucose tolerance test (OGTT) of 140–199 mg/dL
(7.8–11.0 mmol/L)
3. A1c: 5.7-6.4%
Note: In 1997 and 2003, the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus recognized a
group of individuals whose glucose levels did not meet the criteria for DM, but were too high to be considered N.
These persons were defined as having IFG or IGT.
PREDIABETES
• Individuals with IFG and/or IGT have been referred to as
having pre-diabetes, indicating a relatively high risk for
future development of diabetes
• IFG and IGT are associated with obesity (especially
abdominal or visceral obesity), dyslipidemia with high
triglycerides and/or low HDL cholesterol, and
hypertension
• Note: WHO and a number of other diabetes organizations
define the cutoff for IFG at 110 mg/dL (6.1 mmol/L)
SCREENING FOR AND DIAGNOSIS OF GDM
• Perform a 75-g OGTT, with plasma glucose measurement fasting and at 1
and 2 h, at 24–28 weeks of gestation in women not previously diagnosed
with overt diabetes.
• The OGTT should be performed in the morning after an overnight fast of at
least 8 h.
• The diagnosis of GDM is made when any of the following plasma glucose
values are exceeded:
1. Fasting: ≥92 mg/dL (5.1 mmol/L)
2. 1 h: ≥ 180 mg/dL (10.0 mmol/L)
3. 2 h: ≥ 153 mg/dL (8.5 mmol/L)
CLASSIFICATION OF DIABETES
1. Type 1 diabetes (due to β-cell destruction, usually leading to absolute
insulin deficiency)
2. Type 2 diabetes (due to a progressive insulin secretory defect on the
background of insulin resistance)
3. Other specific types of diabetes due to other causes; e.g., genetic defects in
β-cell function, genetic defects in insulin action, diseases of the exocrine
pancreas (such as cystic fibrosis), and drug- or chemical-induced diabetes
(such as in the treatment of HIV/AIDS or after organ transplantation)
4. Gestational diabetes mellitus (GDM)(diabetes diagnosed during
pregnancy that is not clearly overt diabetes)
MANAGEMENT
• Dietary and lifestyle modification including exercise and
weight reduction if obese
• Manage hyperglycemia : OHA / Insulin therapy
• Management of complications of diabetes, including
treatment of HTN(<140/80) and dyslipidaemia.
• Patient Education / Vaccination (influenza,
pneumococcal , hepatitis b)
GOAL
• Attain individualized glycemic, blood pressure, and lipid goals.
General recommended goals from the ADA for these markers are
as follows:
• A1C < 7%.
• Blood pressure < 140/80 mmHg.
• LDL cholesterol < 100 mg/dL; triglycerides < 150 mg/dL;
• HDL cholesterol < 40 mg/dL for men; HDL cholesterol < 50
mg/dL for women.
• Achieve and maintain body weight goals.
ASPIRIN
• Consider aspirin therapy (75–162 mg/ day) as a primary
prevention strategy in those with type 1 or type 2 diabetes at
increased cardiovascular risk .
• This includes most men aged >50 years or women aged >60
years who have at least one additional major risk factor (family
history of CVD, hypertension, smoking, dyslipidemia, or
albuminuria).
STATIN
• Statin therapy should be added to lifestyle therapy,
regardless of baseline lipid levels, for diabetic patients:
1. with overt CVD
2. without CVD who are over the age of 40 years and
have one or more other CVD risk factors (family history
of CVD,hypertension, smoking, dyslipidemia,or
albuminuria).
ACE INHIBITOR
• An ACE inhibitor or ARB for the primary prevention of diabetic
kidney disease is not recommended in diabetic patients with
normal blood pressure and albumin excretion <30 mg/24 h. B
• Either ACE inhibitors or ARBs (but not both in combination) are
recommended for the treatment of the nonpregnant patient with
modestly elevated (30–299 mg/24 h) C or higher levels (.300
mg/24 h) of urinary albumin excretion. A
OHA
• Biguanides eg Metformin
• Thiazolidinediones eg Pioglitazone
• Sulfonylureas eg Glimepiride
• Meglitinide eg Mitiglinide, Repaglinide, Nateglinide
• Glucosidase inhibitors eg Acarbose, voglibose, miglitol
• Dipeptidyl peptidase IV inhibitors eg Sitagliptin
• SGLT2 inhibitor: eg Dapagliflogin, canagliflozin
DIPEPTIDYL PEPTIDASE IV INHIBITORS
PARENTERAL
• Insulin
• GLP-1 receptor agonists eg Exenatide, Liraglutide
• Amylin agonists eg pramlintide
END OF SLIDES
References:
1. Harrison's Principles of Internal Medicine, 18th Edition
2. Davidson Practice of Medicine
3. Uptodate 20.3
4. Standards of Medical Care in Diabetesd 2014. American Diabetes Association. Diabetes
Care Volume 37, Supplement 1, January 2014
5. Medscape.com
6. Mercksmanual

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Diabetes Mellitus..part 3

  • 1. Pratap sagar Tiwari, MD, Internal Medcine, Lecturer, NMCTH UNDERSTANDING DIABETES..PART 3
  • 2. CASE SUMMARY • A 30 yrs old M was brought in ERD in the state of unconsciousness. (Note: Coma is a symptom, not a diagnosis.) Pic taken from http://censorbugbear-reports.blogspot.com/2010/03/shocking-neglect-of-comatose-patient-at.html
  • 3. RECAP OF PREVIOUS PARTS • Causes of patient in state of coma • Definition of terms related to consciousness • Causes of Coma in a Diabetic Patient • Insulin Synthesis/ Secretion • Regulation of Glucose hemostasis • Response of hypoglycemia in normal & DM • Hypoglycemia & symptoms • DKA /HHS • Abnormal respiration patterns
  • 4. DIABETES MELLITUS • Diabetes mellitus is a clinical syndrome characterised by hyperglycaemia caused by absolute or relative deficiency of insulin.
  • 5. DIAGNOSTIC CRITERIA • A1C ≥6.5% • OR • Fasting plasma glucose (FPG) ≥126 mg/dL (7.0 mmol/L) OR • 2-hour plasma glucose ≥200 mg/dL (11.1 mmol/L) during an OGTT OR • A random plasma glucose ≥200 mg/dL (11.1 mmol/L), in patients with classic symptoms of hyperglycemia or hyperglycemic crisis
  • 6. PRE DIABETES 1. IFG: fasting plasma glucose (FPG) levels of 100– 125 mg/dL (5.6–6.9 mmol/L)* 2. IGT: 2-hour plasma glucose (2-h PG) in the 75-g oral glucose tolerance test (OGTT) of 140–199 mg/dL (7.8–11.0 mmol/L) 3. A1c: 5.7-6.4% Note: In 1997 and 2003, the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus recognized a group of individuals whose glucose levels did not meet the criteria for DM, but were too high to be considered N. These persons were defined as having IFG or IGT.
  • 7. PREDIABETES • Individuals with IFG and/or IGT have been referred to as having pre-diabetes, indicating a relatively high risk for future development of diabetes • IFG and IGT are associated with obesity (especially abdominal or visceral obesity), dyslipidemia with high triglycerides and/or low HDL cholesterol, and hypertension • Note: WHO and a number of other diabetes organizations define the cutoff for IFG at 110 mg/dL (6.1 mmol/L)
  • 8.
  • 9. SCREENING FOR AND DIAGNOSIS OF GDM • Perform a 75-g OGTT, with plasma glucose measurement fasting and at 1 and 2 h, at 24–28 weeks of gestation in women not previously diagnosed with overt diabetes. • The OGTT should be performed in the morning after an overnight fast of at least 8 h. • The diagnosis of GDM is made when any of the following plasma glucose values are exceeded: 1. Fasting: ≥92 mg/dL (5.1 mmol/L) 2. 1 h: ≥ 180 mg/dL (10.0 mmol/L) 3. 2 h: ≥ 153 mg/dL (8.5 mmol/L)
  • 10. CLASSIFICATION OF DIABETES 1. Type 1 diabetes (due to β-cell destruction, usually leading to absolute insulin deficiency) 2. Type 2 diabetes (due to a progressive insulin secretory defect on the background of insulin resistance) 3. Other specific types of diabetes due to other causes; e.g., genetic defects in β-cell function, genetic defects in insulin action, diseases of the exocrine pancreas (such as cystic fibrosis), and drug- or chemical-induced diabetes (such as in the treatment of HIV/AIDS or after organ transplantation) 4. Gestational diabetes mellitus (GDM)(diabetes diagnosed during pregnancy that is not clearly overt diabetes)
  • 11. MANAGEMENT • Dietary and lifestyle modification including exercise and weight reduction if obese • Manage hyperglycemia : OHA / Insulin therapy • Management of complications of diabetes, including treatment of HTN(<140/80) and dyslipidaemia. • Patient Education / Vaccination (influenza, pneumococcal , hepatitis b)
  • 12. GOAL • Attain individualized glycemic, blood pressure, and lipid goals. General recommended goals from the ADA for these markers are as follows: • A1C < 7%. • Blood pressure < 140/80 mmHg. • LDL cholesterol < 100 mg/dL; triglycerides < 150 mg/dL; • HDL cholesterol < 40 mg/dL for men; HDL cholesterol < 50 mg/dL for women. • Achieve and maintain body weight goals.
  • 13. ASPIRIN • Consider aspirin therapy (75–162 mg/ day) as a primary prevention strategy in those with type 1 or type 2 diabetes at increased cardiovascular risk . • This includes most men aged >50 years or women aged >60 years who have at least one additional major risk factor (family history of CVD, hypertension, smoking, dyslipidemia, or albuminuria).
  • 14. STATIN • Statin therapy should be added to lifestyle therapy, regardless of baseline lipid levels, for diabetic patients: 1. with overt CVD 2. without CVD who are over the age of 40 years and have one or more other CVD risk factors (family history of CVD,hypertension, smoking, dyslipidemia,or albuminuria).
  • 15. ACE INHIBITOR • An ACE inhibitor or ARB for the primary prevention of diabetic kidney disease is not recommended in diabetic patients with normal blood pressure and albumin excretion <30 mg/24 h. B • Either ACE inhibitors or ARBs (but not both in combination) are recommended for the treatment of the nonpregnant patient with modestly elevated (30–299 mg/24 h) C or higher levels (.300 mg/24 h) of urinary albumin excretion. A
  • 16. OHA • Biguanides eg Metformin • Thiazolidinediones eg Pioglitazone • Sulfonylureas eg Glimepiride • Meglitinide eg Mitiglinide, Repaglinide, Nateglinide • Glucosidase inhibitors eg Acarbose, voglibose, miglitol • Dipeptidyl peptidase IV inhibitors eg Sitagliptin • SGLT2 inhibitor: eg Dapagliflogin, canagliflozin
  • 18. PARENTERAL • Insulin • GLP-1 receptor agonists eg Exenatide, Liraglutide • Amylin agonists eg pramlintide
  • 19. END OF SLIDES References: 1. Harrison's Principles of Internal Medicine, 18th Edition 2. Davidson Practice of Medicine 3. Uptodate 20.3 4. Standards of Medical Care in Diabetesd 2014. American Diabetes Association. Diabetes Care Volume 37, Supplement 1, January 2014 5. Medscape.com 6. Mercksmanual

Notes de l'éditeur

  1. Extra notes: The precise mechanisms underlying gestational diabetes remain unknown. The hallmark of GDM is increased insulin resistance. Pregnancy hormones and other factors are thought to interfere with the action of insulin as it binds to the insulin receptor. Since insulin promotes the entry of glucose into most cells, insulin resistance prevents glucose from entering the cells properly. As a result, glucose remains in the bloodstream, where glucose levels rise . Because glucose travels across the placenta (through diffusion facilitated by GLUT1 carrier), If the untreated gestational diabetes fetus is exposed to consistently higher glucose levels, this leads to an increased fetal levels of insulin (insulin itself cannot cross the placenta). The growth-stimulating effects of insulin can lead to excessive growth and a large body (macrosomia). After birth, the high glucose environment disappears, leaving these newborns with ongoing high insulin production and susceptibility to low blood glucose levels (hypoglycemia). Women who have had gestational diabetes in a previous pregnancy should be offered early self-monitoring of blood glucose or an OGTT at 16–18 weeks, and a further OGTT at 28 weeks if the results are normal.