Diabetes 1 Flashcards
(35 cards)
Diabetes Incidence (6)
- Affects approximately 193,000 youth <20 years
- 2.2/1,000 American youth
- Incidence of type 1 and type 2 diabetes in youth increasing in US and world
- Highest prevalence of DM is among older children
- T1DM remains a disease of white children for the most part
- T2DM doesn’t affect many young children; usually occurs around the time of puberty and adolesence
SEARCH Findings: DM in Youths (4)
- Majority of all new DM cases <10yrs had type 1 DM regardless of race/ethnicity
- Youth ≥10 yrs –> Type 1 most common form of DM for non-Hispanic white and Hispanic youth
- Type 2 DM –> More common after age of 10 years
* Higher rates among US minority populations - Implications for youth entering adulthood with disease duration, increased risk for complications, diabetes during reproductive years
T1DM onset age, race, islet autoimmunity, insulin secretion, insulin sensitivity, DKA at onset, obesity, and % of diabetes
Onset Age: throughout childhood
Race: All (lowest in NA)
Onset: Acute/severe
Islet Autoimmunity: present
Insulin Secretion: very low
Insulin Sensitivity: Normal (with BG control)
DKA at Onset: 20-40%
Obesity: as in population
% of diabetes: 87%
T2DM onset age, race, islet autoimmunity, insulin secretion, insulin sensitivity, DKA at onset, obesity, and % of diabetes
Onset Age: Pubertal/teen
Race: Highest in NA and Black
Onset: subtle to severe
Islet Autoimmunity: unusual
Insulin Secretion: variable
Insulin Sensitivity: decreased
DKA at Onset: more unusual
Obesity: >90%
% of diabetes: 10.5%
T1DM mode of inheritance, gender and biochemistry at dx
Mode of Inheritance: generally sporadic
Gender: male = female
Biochemistry at dx: hyperglycemia, ketosis common, acidosis common
T1DM Markers (4)
- Elevated HbA1c
- Low Insulin
- Low C peptide
- Antibodies common (anti-ICA, anti-GAD)
T2DM mode of inheritance, gender and biochemistry at dx
Mode of Inheritance: strongly familial
Gender: females > male
Biochemistry at dx: hyperglycemia, ketosis common, acidosis uncommon
T2DM Markers (4)
- Elevated HbA1c
- Normal Insulin
- High C-peptide
- Antibodies are uncommon
Genetic Syndromes associated with Type 1 Diabetes (10)
- Down syndrome
- Klinefelter syndrome*
- Turner syndrome
- Wolfram syndrome
- Friedreich’s ataxia
- Huntington’s chorea
- Lawrence-Moon Beidel syndrome
- Myotonic dystrophy
- Porphyria
- Prader-Willi syndrome
Type 1 Diabetes: Pathophysiology (6)
- Idiopathic; may have no family history
- Immune-mediated; Progressive autoimmune destruction of the β cells of the pancreas
* 75% of individuals with type 1 diabetes will test positive for the presence of autoantibodies at the time of diagnosis - Permanent loss of the body’s ability to produce insulin
- Insidious process of unknown duration
- Abrupt clinical onset and generally occurs over a two to three week period
* May begin to present with increased urination, thirst, etc, and then start to have the other manifestations - 20 to 40% of new cases of type 1 diabetes present in diabetic ketoacidosis
T1DM Inheritance Susceptibility (5)
- Most (85%) cases occur sporadically
- Increased risk if family member has type 1 diabetes
- Mother 10 fold risk
- Father 35 fold risk
- Siblings - 40 fold risk
Diabetes: Classic Symptoms (7)
- Polyuria; Getting rid of glucose in urine
- Nocturia; Parents may not understand why child is wetting the bed
- Polydipsia
- Polyphagia
- Blurred vision
- Weight loss or failure to gain weight
- Fatigue/Lethargy
Signs and symptoms As ketoacids accumulate…(6)
breaking down proteins that the body needs b/c can’t metabolize carbohydrates → ketones accumulate → following manifestations occurs:
- Abdominal pain
- Nausea/vomit
- Fruity smelling breath
- Weakness (caused by dehydration)
- Mental confusion
- Diabetic ketoacidosis
DKA: General (4)
- Type 1 Diabetes onset
- 20-40% hospital admissions
- More common in
a. Children <4 yrs of age
b. No family history of T1DM
c. Families of lower socioeconomic status (SES) or poorer access to care - More unusual in type 2 diabetes, but not impossible
DKA In Children with Known Diabetes (6)
- More common in children with poor metabolic control or previous episodes of DKA
- Adolescent girls
* Not taking insulin → won’t gain weight - Psychiatric comorbidity (including eating disorders)
- Lower SES, lack of or interrupted health insurance
- Inappropriate interruption of insulin pump therapy
* Occlusion alarms aren’t sensitive; can have poor infusion leading to DKA
* Need to change site - 75% episodes associated with insulin omission or treatment error; remainder inadequate insulin therapy during intercurrent illness
Diagnostic Studies at Diagnosis (4)
- Urine for glucose and ketones
- Metabolic screen for acid-base status to exclude DKA
- HemoglobinA1c
- Screen for presence of pancreatic auto-antibodies
a. Confirm diagnosis of type 1 diabetes in cases where there may be uncertainty regarding type of diabetes
Diabetes Diagnostic Criteria (4)
A1C >/= 6.5%
OR
FPG >/= 126 mg/dl (no caloric intake for at least 8 hours)
OR
2-h plasma glucose >/= 200 mg/dl during an OGTT (using 75g anhydrous glucose dissolved in water)
OR
In a patient with classic symptoms of hyperglycemia or hyperglycemic crisis, a random plasma glucose of >/= 200mg/dl
Diabetes Differential Dx (4)
Distinguish from
1. Stress-induced hyperglycemia **Can occur in as many as 4% of normal children during serious illness
- Maturity-onset diabetes of the young (MODY)
Identify co-occurrence of
- Thyroiditis
- Celiac disease
* Many centers will now screen for these two with diabetes because of the increased co-occurrence
Type 1 Diabetes: Long term Goals of Therapy (5)
- Normal growth, weight gain, sexual maturation
- Optimize glycemic control
- Maintain uniform glycemic level of HbA1c <7.5% for all youth
- Positive psychosocial adjustment to diabetes
- Minimize acute or chronic complications
A1 Goals for <6 years old, 6-12 years old and 13-19 years old
SHOULD BE <7.5% IN ALL AGES
Management of New Onset Type 1 Diabetes (5)
- Determining insulin regimen and dose
- Target range for blood glucose levels
- Managing child’s diet
- Education regarding insulin injection, blood glucose monitoring, carbohydrate counting, hypoglycemia prevention, managing diabetes during illness, adjusting insulin or carbohydrate intake for exercise
- Diabetes education tailored based on
a. Child’s age, family management priorities, health literacy
b. Child included in education – age 6 years
Management of New Onset Type 1 Diabetes: With ketoacidosis (4)
Hospitalized
i. IV insulin treatment
ii. Fluid replacement
iii. Monitoring to prevent cerebral edema
iv. Want to counteract acidosis prior to worrying about bringing down the blood glucose levels
Management of New Onset Type 1 Diabetes: With no ketoacidosis (2)
i. Insulin initiated
ii. Diabetes education initiated
Screening with New Onset T1DM (2)
- Hypothyroidism – 25% of youth with T1DM have + thyroid autoantibodies at time of diagnosis but may have normal thyroid function
- Celiac disease – tissue transglutaminase or anti-endomysial antibodies – occurs more frequently in children with diabetes (1%-16%) compared to those without diabetes (0.3% - 1%)
* Screen if suspicious → not growing well, belly pain, etc.