Flashcards in Chapter 17 - Endocrine / Hematologic Emergencies Deck (18):
Frequent and plentiful urination.
Frequent drinking of liquid to satisfy continuous thirst.
Excessive eating as a result of cellular "hunger."
Formed when fat is used as an immediate energy source.
ketones and fatty acids
diabetic ketoacidosis (DKA)
Body needs increased fluids and carbohydrate energy to avoid ketoacidosis leading to unconsciousness, hyperglycemic crisis and eventually, death.
Recognize DKA by sweet smell of breath.
Deep, rapid breathing.
In Type 2 diabetes, absence of insulin results in:
hyperosmolar hyperglycemic nonketotic coma (HHNC)
Typically slower onset that DKA with no sweet smell on breath.
A state of unconsciousness resulting from ketoacidosis, hyperglycemia and dehydration.
Hyperglycemic crisis (blood glucose > 800 mg/dL
dehydration (dry, warm, "tenting" skin and sunken eyes
sweet (acetone) odor on breath
rapid, weak (thready) pulse
normal to slightly low blood pressure
varying degrees of unresponsiveness
weakness, nausea, vomiting
polyuria, polydipsia, polyphagia
Result of insulin increase in absence of glucose.
hypoglycemic crisis (blood glucose <40 mg/dL)
declining mental status; aggressive or unusual behavior
unconsciousness and brain damage may follow
Children at high risk due to high activity and lack of attention to diet.
Signs of hypoglycemia
pale, moist (clammy) skin
altered mental status
seizure, fainting, coma
normal to shallow, or rapid respirations
Care of hyper/hypoglycemic patient.
Survey scene re: sharps
Clear airway, consider airway adjuvant if not conscious
High flow oxygen (15 L/min) via non-rebreathing mask
Check glucose level
Position patient on side if having seizures
Consider rapid transport if altered mental state and impaired ability to swallow
Blood is made up of two main components.
plasma is straw colored fluid
erythrocytes (red blood cells) 47% (male) and 42% female by voume
also contains leukocytes (WBC) and platelets
An inherited blood disorder affecting red blood cells.
Sickle cell disease
predominant in african americans
cells contain hemoglobin S (not normal Hb A)
cells are oblong or sickle shaped
cells lodge in smaller blood vessels or in spleen
Pain, ischemia and organ damage caused by restricted blood flow.
lasts 5 - 7 days
Worsening of a patients baseline anemia.
Aplastic crisis (reduced level of RBCs)
tachycardia, pallor and fatigue
parvovirus B19 can stop production of new cells for 2 - 3 days
Acute drop in patients hemoglobin levels.
caused by RBCs breaking down at a fast rate
common in patients with glucose-6-phosphate dehydrogenase deficiency (common in sickle cell disease)
Painful, acute enlargement of the spleen.
Splenic sequestration crisis
causes the abdomen to become very hard and bloated
Tendency to develop blood clots.
blood clots = thrombosis
affects 5% to 7% of Caucasians of European descent in US
Deep vein thromboses a leading cause of death in hospital
aspirin, heparin, coumadin decrease threat of thrombosis