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hemorrhagic diathesis &
hematological
melignancy
 Diabetes mellitus (DM) is a group of diseases characterized
by high levels of blood glucose resulting from defects in
insulin production, insulin action, or both.
 The term diabetes mellitus describes a metabolic disorder
of multiple aetiology characterized by chronic
hyperglycaemia with disturbances of carbohydrate, fat and
protein metabolism resulting from defects in insulin
secretion, insulin action, or both.
 The effects of diabetes mellitus include long–term damage,
dysfunction and failure of various organs.
Diabetes mellitus
 Diabetes mellitus may present with characteristic
symptoms such as thirst, polyuria, blurring of vision,
and weight loss.
 In its most severe forms, ketoacidosis or a non–
ketotic hyperosmolar state may develop and lead to
stupor, coma and, in absence of effective treatment,
death.
 Often symptoms are not severe, or may be absent,
and consequently hyperglycaemia sufficient to cause
pathological and functional changes may be present
for a long time before the diagnosis is made.
 Type 1 Diabetes Mellitus
 Type 2 Diabetes Mellitus
 Gestational Diabetes
 Other types:
LADA
MODY (maturity-onset diabetes of youth)
Secondary Diabetes Mellitus
 Type 1 diabetes develops when the body’s
immune system destroys pancreatic beta cells, the
only cells in the body that make the hormone
insulin that regulates blood glucose.
 This form of diabetes usually strikes children and
young adults, although disease onset can occur at
any age.
 Type 1 diabetes may account for 5% to 10% of all
diagnosed cases of diabetes.
 Risk factors for type 1 diabetes may include
autoimmune, genetic, and environmental factors.
 Type 2 diabetes may account for about 90% to 95% of all
diagnosed cases of diabetes.
 It usually begins as insulin resistance, a disorder in which
the cells do not use insulin properly. As the need for insulin
rises, the pancreas gradually loses its ability to produce
insulin.
 Type 2 diabetes is associated with older age, obesity, family
history of diabetes, history of gestational diabetes, impaired
glucose metabolism, physical inactivity, and race/ethnicity.
 African Americans, Hispanic/Latino Americans, American
Indians, and some Asian Americans and Native Hawaiians
or Other Pacific Islanders are at particularly high risk for
type 2 diabetes.
 Type 2 diabetes is increasingly being diagnosed in children
and adolescents.
 A form of glucose intolerance that is diagnosed in some
women during pregnancy.
 Gestational diabetes occurs more frequently among African
Americans, Hispanic/Latino Americans, and American
Indians. It is also more common among obese women and
women with a family history of diabetes.
 During pregnancy, gestational diabetes requires treatment
to normalize maternal blood glucose levels to avoid
complications in the infant.
 After pregnancy, 5% to 10% of women with gestational
diabetes are found to have type 2 diabetes.
 Women who have had gestational diabetes have a 20% to
50% chance of developing diabetes in the next 5-10 years.
 TYPE 1:- viral infections
immunogenetic predisposition
autoimmune disorders
Type 2:-overeating
excessive carbohydrates
obesity
 Thirst,dry mouth
 Increased appetite
 Dry skin,itching of the skin
 Redness or rubeosis both cheeks
 Weight loss
 Redusing the level of insulin
 In laterstages:-
muscle weakness,pain in the
limbs,muscle in atropy,
 HBA1C content to 10% or more on the total
hemoglobin.
 Reducing the insulin c-peptide(diabates
mellitus type 1)
 The regime of physical activity
 Diet therapy
 Replacement therapy with insulin
 Oral hypoglycemic agents
 Treatment of complications
Short-term use:
 Acute illness, surgery, stress and emergencies
 Pregnancy
 Breast-feeding
 Insulin may be used as initial therapy in type 2 diabetes
 in marked hyperglycaemia
 Severe metabolic decompensation (diabetic ketoacidosis,
hyperosmolar nonketotic coma, lactic acidosis, severe
hypertriglyceridaemia)
Long-term use:
 If targets have not been reached after optimal dose of combination
therapy or BIDS, consider change to multi-dose insulin therapy.
When initiating this,insulin secretagogues should be stopped and
insulin sensitisers e.g. Metformin or TZDs, can be continued.

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diabetis mellitus

  • 2.  Diabetes mellitus (DM) is a group of diseases characterized by high levels of blood glucose resulting from defects in insulin production, insulin action, or both.  The term diabetes mellitus describes a metabolic disorder of multiple aetiology characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both.  The effects of diabetes mellitus include long–term damage, dysfunction and failure of various organs. Diabetes mellitus
  • 3.  Diabetes mellitus may present with characteristic symptoms such as thirst, polyuria, blurring of vision, and weight loss.  In its most severe forms, ketoacidosis or a non– ketotic hyperosmolar state may develop and lead to stupor, coma and, in absence of effective treatment, death.  Often symptoms are not severe, or may be absent, and consequently hyperglycaemia sufficient to cause pathological and functional changes may be present for a long time before the diagnosis is made.
  • 4.  Type 1 Diabetes Mellitus  Type 2 Diabetes Mellitus  Gestational Diabetes  Other types: LADA MODY (maturity-onset diabetes of youth) Secondary Diabetes Mellitus
  • 5.  Type 1 diabetes develops when the body’s immune system destroys pancreatic beta cells, the only cells in the body that make the hormone insulin that regulates blood glucose.  This form of diabetes usually strikes children and young adults, although disease onset can occur at any age.  Type 1 diabetes may account for 5% to 10% of all diagnosed cases of diabetes.  Risk factors for type 1 diabetes may include autoimmune, genetic, and environmental factors.
  • 6.  Type 2 diabetes may account for about 90% to 95% of all diagnosed cases of diabetes.  It usually begins as insulin resistance, a disorder in which the cells do not use insulin properly. As the need for insulin rises, the pancreas gradually loses its ability to produce insulin.  Type 2 diabetes is associated with older age, obesity, family history of diabetes, history of gestational diabetes, impaired glucose metabolism, physical inactivity, and race/ethnicity.  African Americans, Hispanic/Latino Americans, American Indians, and some Asian Americans and Native Hawaiians or Other Pacific Islanders are at particularly high risk for type 2 diabetes.  Type 2 diabetes is increasingly being diagnosed in children and adolescents.
  • 7.
  • 8.  A form of glucose intolerance that is diagnosed in some women during pregnancy.  Gestational diabetes occurs more frequently among African Americans, Hispanic/Latino Americans, and American Indians. It is also more common among obese women and women with a family history of diabetes.  During pregnancy, gestational diabetes requires treatment to normalize maternal blood glucose levels to avoid complications in the infant.  After pregnancy, 5% to 10% of women with gestational diabetes are found to have type 2 diabetes.  Women who have had gestational diabetes have a 20% to 50% chance of developing diabetes in the next 5-10 years.
  • 9.  TYPE 1:- viral infections immunogenetic predisposition autoimmune disorders Type 2:-overeating excessive carbohydrates obesity
  • 10.  Thirst,dry mouth  Increased appetite  Dry skin,itching of the skin  Redness or rubeosis both cheeks  Weight loss  Redusing the level of insulin  In laterstages:- muscle weakness,pain in the limbs,muscle in atropy,
  • 11.
  • 12.  HBA1C content to 10% or more on the total hemoglobin.  Reducing the insulin c-peptide(diabates mellitus type 1)
  • 13.
  • 14.
  • 15.  The regime of physical activity  Diet therapy  Replacement therapy with insulin  Oral hypoglycemic agents  Treatment of complications
  • 16. Short-term use:  Acute illness, surgery, stress and emergencies  Pregnancy  Breast-feeding  Insulin may be used as initial therapy in type 2 diabetes  in marked hyperglycaemia  Severe metabolic decompensation (diabetic ketoacidosis, hyperosmolar nonketotic coma, lactic acidosis, severe hypertriglyceridaemia) Long-term use:  If targets have not been reached after optimal dose of combination therapy or BIDS, consider change to multi-dose insulin therapy. When initiating this,insulin secretagogues should be stopped and insulin sensitisers e.g. Metformin or TZDs, can be continued.