Module 7 Caring for Children with Alterations in Metabolism - Endocrine Chapter 29
Diabetes Mellitus Definition: metabolic disorder characterized by hyperglycemia because of lack of insulin or a resistance to insulin Classifications Type 1 Diabetes destruction on pancreatic beta cells Type 2 Diabetes insulin resistance
Impact of Diabetes leading cause of renal failure major cause of blindness most frequent cause of non-trauma amputations affects 17 million increasing prevalence of type 2 in children and adults >1/3 of all newly diagnosed diabetes in children
Historical Facts Diabetes is from the Greek word “to siphon” Mellitus is from Latin word “sweet” Usually died within 2-3 years from starvation Insulin discovery increased life span experiencing long term effects of diabetes self glucometers
Diabetes Type 1 Beta cells no longer produce insulin hyperglycemia fats and protein are broken down development of ketosis accounts for 10-15% of all cases occurs in childhood or adolescence
Diagnostic Tests 1. Symptoms of diabetes and random b.s. >200mg/dL 2. fasting glucose >126mg/dL 3. Oral glucose tolerance test - OGTT after 2 hrs glucose is >200mg/dL 4. Glycosylated hemoglobin - Hemoglobin A1C average glucose over 2-3 months Routine accu checks for management Type 1 3x/day
Hyperglycemia Hyperglycemia leads to polyuria glycosuria polydipsia polyphagia weight loss malaise and fatigue blurred vision
Diabetic Ketoacidosis DKA Results from a breakdown of fat occurs when undiagnosed or known diabetic has an increased energy need blood sugar >250mg/dL pH < 7.3 ketones and glucose in the blood and urine
DKA - Treatment Regular insulin - sub q or IV Restore fluid balance -.9NS IV Correct electrolyte imbalances - K+
Hypoglycemia verses Hyperglycemia
Long Term Complications of Diabetes Coronary Artery Disease Hypertension Stroke Peripheral Vascular Disease Diabetic Retinopathy retinal ischemia leading cause of blindness ages 25-74
Complications of Diabetes Diabetic nephropathy glomerular changes in kidneys leading to impaired renal function microalbuminuria most common cause ESRD in America
Therapeutic Management Monitoring keeping blood glucose levels close to normal Insulin Dietary management Exercise Future pancreatic transplant, beta cell transplant
Medications Insulin all type 1 Terms describing insulin onset, peak, duration Types rapid acting, short acting, intermediate, long and combinations
Injection sites
Nutrition Need consistent meal times Goals near-normal glucose levels optimal lipid levels adequate calories to maintain growth Meal planning eat less fat and saturated fat sugars and sweets in moderation
Diet Management Type 1 correlate eating with insulin onset Carb counting is main diet plan for children with diabetes “Illness Management Plan” change in insulin dosage attention to fluid balance
The Nursing Process Working together child/family individualized plan follow-up support community support
Growth Hormone Deficiency Decreased activity of pituitary gland Diagnosed in males earlier than females Short stature is noticed more often in males Causes of deficiency Infarct of pituitary gland (sickle cell) Central nervous system infection Tumors Brain trauma Chemotherapy Emotional deprevation
Signs and Symptoms Below the 3 rd percentile on growth chart in height by 1 year of age Overweight Higher pitched voices Delayed dentition Decreased muscle mass Delayed sexual maturation hypoglycemia
Treatment Treat underlying cause Growth hormone replacement Daily injections of hormone Possible delay of puberty to allow more time for growth hormone therapy to work
Precocious Puberty Appearance of any secondary sexual characteristics before 8 years of age in females and 9 years of age in males Hypothalamus is activated to secrete gonadtropin-releasing hormone In males is usually result of intracranial tumor Females is usually idiopathic
Children will have advanced bone age Stop growing prematurely Hormones stimulate early closure of epiphyseal plates Mood swings Emotional labilty
Treatment