Endocrine Disorders in the Pediatric Client Susan Beggs, MSN, CPN Susan Beggs, MSN, CPN
Understanding the endocrine system in children Puberty brings many changes ↑GH released ↑ production of LH and FSH in girls Development of sexual characteristics Feedback mechanism in place
Collecting data during an endocrine assessment Percentiles on weight and height Distinguishing facial features, abd. fat Onset of puberty Routine NB screening Blood glucose levels Detection of chromosomal disorders
Pancreatic dysfunctions Etiology Preclinical stage Manifestations Diagnosis
Therapy for diabetes in children Diagnosis: Under 18? Type I diabetes Clinical therapy combines: insulin nutrition exercise regimen psychosocial support
Insulin therapy
Insulin review Rapid (Lispro/Humalog) Short acting (regular) Intermediate acting (NPH, Lente) Long acting (Lantus/Ultralente)
Basal-bolus therapy ADA recommendations for children Basal insulin administered 1-2x day; bolus of rapid acting with each meal and snack Method of this therapy: Lower glucose levels Stabilize glucose levels Eliminate ketones Insulin dose adjusted to BS readings 4x day
Basal bolus, cont. BS monitored 4-8x day; 1x a week at midnight and 3AM Therapy can be achieved with 3+ insulin injections a day or by pump There must be consistent carb counts Routine exercise
Factors which may affect insulin dosage in children Stress Infection Illness Growth spurts (such as puberty) Meal coverage for finicky toddlers Adolescents concerned about weight gain not wanting to eat AM snack
External insulin infusion pump in children Advantages Delivers continuous infusion Maintain better control # of injection sites hypo/hyper episodes More flexible lifestyle Eat with more flexibility Improves growth in child Disadvantages Requires motivation Requires willingness to be connected to device Change sites every 2-4 days More time/energy to monitor BS Syringe, cath changes every 2-3 days Infection may occur at site Wt gain common when BS is controlled
Insulin therapy, cont. Monitored every 3 months by hemoglobin A1c Represents amt of glucose attached to hemoglb over period of time Roughly 120 days Good predictor of levels over 6-8 wks
Nursing Management at the time of diagnosis Child is admitted to hospital Nsg assessments directed toward: Hydration LOC Hourly monitoring of BS Dietary and caloric intake Ability of family to manage
“Sick Day guidelines” Days that child is ill Attention to glycemic control BS levels more often than routine DO NOT SKIP INSULIN! Factors key to preventing DKA
Home Teaching Incorporate into the family lifestyle “Honeymoon phase” Community resources Recognizing the cognitive levels at time of teaching levels at time of teaching
Diabetic Ketoacidosis Review of patho Causes Criteria for diagnosis of DKA BS levels> 300 Serum ketones ↓ bicarbonates Acidosis (pH <7.3)
Treatment for DKA Fluids (boluses) Wean off IV insulin when clinical stable Oral feedings introduced when alert Prevention of future episodes
Type II diabetes in children There is insulin resistance Fatty tissue produces hormone Hormone desensitized to insulin Can result in hyperinsulinism Signs and symptoms
Acanthosis nigricans
Inborn errors of metabolism Phenylketonuria Galactosemia Defects in Fatty Acid Oxidation Maple syrup urine disease
Phenylketonuria (PKU) Autosomal recessive Liver deficiency Treatment/education Counseling for future pregnancies
Galactosemia Carbohydrate metabolic dysfuntion Autosomal recessive Liver enzyme deficiency Implications/symptoms Treatment/management
Defects in fatty acid oxidation Defects result in fatty acid oxidation Most common of inborn errors Most common presentation Diagnosis/treatment
Maple syrup urine disease (MSUD) Disorder of amino acid metabolism Diagnosis made by UA Treatment/management
Nursing measures for metabolic disorders Genetic counseling Dietary teaching.compliance Mixing special preparations Mainly supportive