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A hereditary endocrine disorder characterized by inadequate or lack of insulin production that results in impaired glucose absorption & metabolism resulting in hyperglycemia.
Can either be Type 1 or type 2.
diabetes mellitus
Three cardinal symptoms of diabetes
polyuria
polydipsia
hyperglycemia
This forms the endocrine portion of the pancreas
islets of Langerhans
These cells secrete glucagon
alpha islet cells
These cells secrete insulin
beta islet cells
Involves an absolute or relative deficiency of insulin.
Formerly referred to as juvenile diabetes or insulin-dependent diabetes, occurs almost exclusively in childhood.
Must take insulin to replace what their pancreas cannot produce
Results from immunologic damage to insulin-producing cells in susceptible individuals
type 1 diabetes
S/S of type 1 diabetes
Hyperglycemia - due to glucose inability to enter body cells because of a lack of insulin, causing glucose build up in the bloodstream
Glycosuria - due to kidneys attempt to lower hyperglycemia by excreting excess glucose into the urine
Polyuria - 1st symptom in children together w/ polydipsia; also due to glycosuria
Polydipsia (thirst response) - results to dehydration & constipation
Weight loss, leading to short stature & underweight - body begins to break down protein and fat since glucose can’t be taken up by the body cells. if large amounts of fat are metabolized, weight loss occurs
Ketoacidosis, which results to acidic blood pH - due to ketone bodies, acid end product of fat breakdown, accumulating in the blood stream
Long-term effects DM: Vascular narrowing that leads to kidney, heart, and retinal dysfunction
Laboratory studies of type 1 diabetes
Random plasma glucose level greater than 200 mg/dL (normal range, 70 to 110 mg/dL fasting; 90 to 180 mg/dL not fasting) & significant glycosuria.
A diagnosis of diabetes is confirmed based on finding one of the following three criteria on two separate occasions:
symptoms of diabetes with a random blood glucose level greater 200 mg/dL
fasting blood glucose level greater than 126 mg/dL
two-hour plasma glucose level greater than 200 mg/dL during an oral glucose tolerance test
2 diagnostic tests to confirm diabetes
fasting blood glucose test
random blood glucose test
Diagnostics for type 1 diabetes
blood analysis for
pH
partial Pressure of carbon Dioxide (PCO2)
sodium & potassium levels
WBC count
Glycosylated Hemoglobin (HbA Evaluation)
electrocardiogram - if potassium is low
nose and throat cultures
Management of type 1 diabetes
Insulin administration
Regulation of nutrition and exercise
Stress management
Blood glucose monitoring
Urine ketone monitoring
more specific:
Nutrition - 55% carbohydrate, 15% protein, and 30% fat
Exercise - uses carbohydrates & helps reduce hyperglycemia
Stress Management - increase insulin if w/ stress
Blood Glucose Monitoring - SBGM can be done by early school age children
Urine Ketone Monitoring - done if glucose level is above 200mg/dL
Pancreas Transplantation - for severe cases or retinopathy
Nursing considerations when administering insulin
Regular/short acting should be drawn 1st (mixed).
Given SC; half of dose be given IV in emergencies.
Given @ rm temp; can be given 90degree angle if needle is less than 0.4in; admin site should be rotated.
Can also be given thru insulin pump & inhalation.
Administration site of insulin in children
subcutaneously on:
upper outer arms
outer aspects of the thighs
Types of human insulin
lispro (humalog)
aspart
regular (Humulin-r)
Lantus
Humulin-N
Humulin-L
Humulin-U
Onset, peak effect, and duration of effect of lispro
onset: immediate
peak effect: 30 mins-1 hour
duration of effect: 3-4 hours
Onset, peak effect, and duration of effect of aspart
onset: 15 mins
peak effect: 30-40 mins
duration of effect: 3-5 hours
Onset, peak effect, and duration of effect of regular Humulin-R
onset: 0.5-1.0
peak effect: 2-4 hours
duration of effect: 5-7 hours
Onset, peak effect, and duration of effect of Lantus
onset: 1 hour
peak effect: 5 hours
duration of effect: 24 hours
Onset, peak effect, and duration of effect of Humulin-N, L, U
humulin-N
onset: 1-2 hours
peak effect: 4-12 hours
duration of effect: 24+ hours
humulin-L
onset: 1-3 hours
peak effect: 6-14 hours
duration of effect: 24+ hours
humulin-U
onset: 6 hours
peak effect: 16-18 hours
duration of effect: 36+ hours
This is when only a minimal amount of insulin, or none at all, is needed for glucose regulation after blood glucose has been initially regulated by insulin.
“honeymoon” period
This is a sign fat tissue is being used for energy or that the child is becoming acidotic
acetone revealed by a test strip
Formerly known as non–insulin dependent diabetes.
Characterized by diminished insulin secretion & not caused by autoimmune factors.
Usually daily insulin not needed, because it can be managed with diet alone or with diet and an oral hypoglycemic agent.
Once thought to occur only in older adults, but is now seen in over- weight adolescents, termed maturity-onset diabetes of youth.
Development of PCOS is strongly associated with this disorder
type 2 diabetes
S/S of type 2 diabetes
symptoms often become apparent for the first time at puberty because increasing sex hormones increasing insulin resistance, creating a need for more insulin production
Sugar in urine but few ketones - due to hyperglycemia and kidneys can no longer reabsorb glucose, spiling or excreting in the urine
Lessened amounts of thirst & increased urination - fluid follows glucose in the urine through osmosis, leading to polyuria. in some people with long-term type 2 diabetes, the thirst mechanism may be reduced, causing less thirst despite increased urination.
Dark shiny patches on the skin (acanthosis nigricans) - high levels in the bloodstream can stimulate the growth of skin cells and melanocytes
most often found between the fingers and between the toes, on the back of the neck (“dirty neck”), and in axillary ceases
PCOS - insulin can stimulate the ovaries to produce more androgens, disrupt the normal development of follicles in the ovaries, and decrease the production of SHBG by the liver that binds to testosterone
Management of type 2 diabetes
nutrition and exercise
oral anti-glycemic agent: biguanide (metformin) - decreases the amount of glucose produced by the liver and increases insulin sensitivity in both the liver and muscle cells
sulfonylurea (glyburide) - if metformin is not effective
A lowered blood calcium level
May be caused by changes in either calcium or phosphorus metabolism
Occurs because phosphorus and calcium levels are always inverse proportion in the bloodstream
hypocalcemia
When does hypocalcemia usually happen?
occur in infants who experienced birth anoxia as phosphorus is released with anoxia
immature infants - parathyroid glands are immature
infants of people with diabetes - it tends to accompany the hypoglycemia that occurs in these infants shortly after birth
S/S of hypocalcemia
chief sign: latent tetany or neuromuscular irritability - occurs if blood calcium level falls below 7/5 mg per dL
jitteriness when handled or if the infant has been crying for an extended period
if blood calcium levels falls well below 7 mg per dL:
manifest tetany - muscular twitching
carpopedal spasm - abduction of the hand and flexion of the wrist with the thumb positioned across the palm
pedal spasm (foot spasm) - foot is extended, toes flex, sole of the foot cups
without therapy:
generalized seizures or spasm of the larynx, with the infant emitting a high-pitched, crowing sound on inspiration
These are 3 tests for detecting of hypocalcemia
Chvostek
trousseau
peroneal
This sign of hypocalcemia is when the skin anterior to external ear (just over sixth cranial nerve) is tapped, facial muscles surrounding the eye, nose, and mouth contract unilaterally
chvostek
This sign of hypocalcemia is when upper arm is constricted by tourniquet for 2-3 minutes and area becomes blanched, carpal spasm is elicited (hand abducts, wrist flexes, thumb is positioned across cupped palms)
trousseau
This sign of hypocalcemia is when fibular side of leg over peroneal nerve is tapped, foot abducts and dorsiflexes.
peroneal
Management of hypocalcemia
aimed at increasing the calcium level in the blood above the point of latent tetany
10% calcium chloride PO - if infant can suck
10% solution calcium gluconate IV - if the tetany has so progressed that the child does not have enough muscular coordination to take oral fluid safely
Anticonvulsant therapy - for generalized seizures
Emergency equipment for intubation - relieve laryngospasm
Oral calcium therapy - after immediate therapy to increase low blood calcium levels; until their calcium level stabilizes at greater than 7.5 mg per dL
Vit D (calcitriol) - vitamin D is necessary for the absorption of calcium from the GI tract