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Acute respiratory failure
Condition that happens suddenly in which the exchange of O2 and/or CO2 between the alveoli and the pulmonary capillaries is inadequate.
Chronic obstructive pulmonary disease (COPD)
a group of lung diseases in which the bronchial airflow is chronically or recurrently obstructed, making it hard to breathe - dyspnea - as its major symptom
Forced Expiratory Volume (FEV)
used to measure and classify copd into
gold 1,,2,3,4
Emphysema
A serious disease that destroys lung tissue and causes breathing difficulties, characterized by abrnomal enlargement of air spaces
Bronchitis
Inflammation of the bronchi
Asthma
A condition in which a person's airways become inflamed, narrow and swell, and produce extra mucus, which makes it difficult to breathe; an immunological response to an allergen
Hypercapnea
High amounts of CO2 in the blood
Hypoxemia
Low levels of O2 in the blood
Cyanosis
a bluish discoloration of the skin resulting from poor circulation or inadequate oxygenation of the blood.
20-25 kcal/kg/day
Calorie recommendation for patients with COPD
SFF(air swallowing)
Frequency of feeding for patients with COPD
45-50% High fat(low RQ=0.7)
30-35% low carb(high RQ=1)
15% protein(RQ=0.8)
sodium restricted diet
avoid gas forming foods
avoid choking hazard foods(stringy/tough/crunchy)
Diet order for patients with COPD
Diabetes Mellitus
A group of metabolic disorders characterized by hyperglycemia resulting from defects in insulin secretion, insulin action, or both
Insulin
Hormone that lowers blood sugar levels
Beta cells
Cells in the Islets of Langerhans that secrete insulin
Hyperglycemia
Excess of sugar in the blood
type 1 diabetes mellitus
Diabetes caused by a total lack of insulin production; usually develops in childhood, and patients require insulin replacement therapy to control the disorder
- autoimmune
type 2 diabetes mellitus
Diabetes in which the body produces insulin, but not enough, or there is insulin resistance. The patient usually is not dependent on insulin for survival. Largely the result of sedentary lifestyle and excess body weight
Gestational diabetes
a form of diabetes mellitus that occurs during some pregnancies
impaired glucose tolerance (IGT)
A disorder in which blood glucose levels become elevated, and is the intermediate between normoglycemia and diabetes
180 mg/dL
Renal threshold for glucose
Somogyi phenomenon
A rebound phenomenon that occurs in clients with type 1 diabetes mellitus. Normal or elevated blood glucose levels are present at bedtime; hypoglycemia occurs at about 2 to 3 am. Counterregulatory hormones, produced to prevent further hypoglycemia, result in hyperglycemia (evident in the prebreakfast blood glucose level).
Polydipsia
excessive thirst
Polyuria
excessive urination
Polyphagia
excessive hunger
Ketosis
an abnormal accumulation of ketone bodies that is frequently associated with acidosis
Glycosuria
Excretion of sugar in urine
Ketonuria
Excretion of ketone bodies in the urine
>=200 mg/dL
RBS(random blood sugar) result indicative of DM
>126 mg/dL
FBS result indicative of DM
140-199 mg/dL
2hr OGTT/RBS result indicative of IGT
2hr OGTT/RBS result indicative of normal
>=200 mg/dL
2hr OGTT result indicative of
Oral Glucose Tolerance Test (OGTT)
Timed glucose challenge to examine efficiency of the body in metabolism of glucose
fasting blood sugar (FBS)
measurement of blood sugar level after fasting (not eating) for 12 hours
HbA1c
test to assess how well blood sugars have been controlled over the past 90-120 days.
HbA1c result for non-diabetics
5.7-6.4%
HbA1c result forpre-diabetics
>=6.5%
HbA1c for diabetes
Macroangiopathies
Damage to large blood vessels
Microangiopathies
Damage to the small blood vessels
Diabetic nephropathy
Damage to glomerular capillaries due to high blood sugar of diabetes mellitus
Diabetic retinopathy
Damage to the retina as a complication of uncontrolled diabetes
Diabetic Neuropathies
Cell damage from increased glucose levels leads to nerve degeneration & delayed conduction
Sensory deficits & symptoms (more than mator involvement)
Diabetic ketoacidosis
Acidity of the blood caused by the presence of ketone bodies produced when the body is unable to burn sugar; thus, it must burn fat for energy
- pH
Non-ketotic hyperosmolar coma
A syndrome of marked diabetic stupor, hyperglycemia, and hyperosmolarity in the absence due to dehydration of the brain cells caused by hyperosmolarity of blood due to excess sugar.
Gangrene
Death of tissue caused by loss of blood supply followed by bacterial invasion
Insulin shock
The result of too much insulin which causes a dangerous drop in blood glucose.
Sulphonylurea drugs
DM drugs contraindicated to pregenant DM patients due to risk of neonatal hypoglycemia and congenital anomalies
sulfonylureas
- ends in amide
diab drug
- stimulate insulin secretion
biguanides
- metformin
diab drug
- reduce glucose prod
- lessen insulin resistance
Short acting insulin
insulin that
starts 1hr or less
peaks 2-3hr
duration 3-6 hr
Intermediate acting insulin
insulin that
starts 2-4hr
peaks 4-12hr
duration 12-18 hr
long acting insulin
insulin that
starts 2hr
peaks no peak
duration 24 hr
1/3, 1/3, 1/3 or
2/5, 1/5, 2/5
CHO distribution for short-acting insulin
1/7, 2/7, 1/7, 2/7, 1/7
CHO distribution for intermediate-acting insulin
1/5, 2/5, 2/5;
1/3, 1/3, 1/3 both with 20-40 g h.s.
CHO distribution for long-acting insulin
20-30 g
Fiber recommendations for DM patients
Highly individualized diet
Diet prescribed to DM patients
Consistent carbohydrate diet
Diet which intends to keep intake of carbs at a constant level to avoid rapid increases or decreases in blood sugar levels.
- total carbs per day matter more
Make-up diet
Diet made from fruit/fruit juices foe insulin-requiring diabetics designed to make-up for missed meals to allay hypoglycemia
Limit to 30 g
Carbohydrate limit (g) during breakfast for GDM patients due to insulin resistance from hormonal action
1. Carb(normal=50-70%)
2. Protein(normal to high or 0.8kg if with dkd)
3. fat(25-30%)
4. Heart healthy
5. 20-30g fiber
6. soidum(
MNT for Diabetes
Metabolic Syndrome (Syndrome X)
Insulin Resistance Syndrome; A collection of risk factors that increase an individual's chance of developing cardiovascular disease and diabetes mellitus
Alternative sweeteners
Substances that are added to sweeten foods while providing few or no kilocalories and do not cause caries
low GI
56-69
medium GI
>=70
high GI
45-75 g
CHO allocation for meals for CC diet
15-30 g
CHO allocation for snacks for CC diet
reactive hypoglycemia
Decrease in blood sugar due to hypersecretion/dosing of insulin
Polyphagia, polyuria, polydipsia
3 P's of diabetes
Fasting hypoglycemia
Decrease in blood sugar due to insulin overdose, alcohol, tumor, heparic disease, or chronic renal insufficiency
Hyperthyroidism/Grave's disease
Abnormally high secretion of thyroid hormones
- weight loss
- high bmr(+50%)
- big thyroid and eyes
1. High kcal diet
2. vit and min supp
3. low iodine
Diet order for patients with hyperthyroidism
Hypothyroidism
condition of hyposecretion of the thyroid gland causing low thyroid levels in the blood that result in sluggishness, slow pulse, and often obesity
- due to lack of iodine
- decreased BMR(30-40%)
- weight gain
- puffy face and hands
Low calorie diet
Iodine(to meet deficiency)
MNT for hypothyroidism
Hyperparathyroidism
Hypersecretion of parathyroid hormone; may result in hypercalcemia and Recklinghausen(cell growth neural tissues) disease
- osteoporosis
- kidney stones
Acid ash diet
Diet which acidifies urine, and prevents Ca-stone formation -- presribed to patients with hyperparathyroidism
1. high fluid
2. Acid Ash diet
3. Na IV
4. phosphate(to prevent calcium release to blood)
MNT for hyperparathyroidism
parathormone (PTH)
Hormone secreted by the parathyroid glands; increases blood calcium
Phosphate binders
drugs that bind with phosphorus in food so the phosphorus is not absorbed in the intestines
Hypoparathyroidism
hyposecretion of parathyroid hormone; may result in hypocalcemia and tetany
-chvostek's - face spasm
-trousseau's - hand spasm
- cramps
-spasms
High calcium, high vitamin D
Dietary managment of hypoparathyroidism to normalize calcium levels
Addison's disease
A condition that occurs when the adrenal glands do not produce enough cortisol or aldosterone -
weight loss,
hyponatremia,
hyperkalemia,
hypoglycemia, and
hypotension occur
Aldosterone
A mineralcortocoid produced by the adrenal cortex that promotes sodium and water reabsorption by the kidneys and potassium excretion in urine.
1. high na
2. low potassium
3. high kcal if underweight
4. adequate fluids
MNT for addison's disease
High sodium, low potassium
Mineral recommendations for patients with Addison's disease
High kcal
Calorie recommendation for underweight patients with Addison's disease
Cushing's disease
Hypersecretion of the adrenal cortex causing
weight gain,
hypernatremia,
hypokalemia,
hyperglycemia,
hypertension
1. low na
2. high k
3. low kcal if obese
4. fluid restriction
MNT for cushings
Low Na, High K
Mineral recommendations foe patients with Cushing's disease
Low kcal
Calorie recommendation doe obese patients with Cushing's disease
Wilson's disease
Inherited disorder characterized by defective metabolism and excretion of Copper, caused by mutation of gene for coper transporting adenosine triphosphatase
- jaundice
- kayser fleischer rings(dark ring around iris)
Copper-restricted diet
(oysters, shellfish, organ meats, whole grains, nuts, legumes, potatoes, mushrooms)
Diet order for patient's with Wilson's disease
Hemochromatosis
Hereditary disorder with an excessive buildup of iron deposits as hemosiderin in the body
Iron-restricted diet
(meat, organs, eggs, legumes, green leafies)
Diet order for patients with hemochromatosis
Inborn Errors of Metabolism (IEM)
A group of congenital conditions that cause either accumulation of toxins or disorders of energy metabolism in the neonate due to defective enzymes. These conditions are characterized by an infant's failure to thrive and by vague signs such as poor feeding.
1. restrict substrate
2. supply amount of product or cofactor
3. combination of all these
General goals of MNT for IEM
Newborn screening
Tests used to screen newborn infants for a range of genetic and non-genetic disorders
- 24 hrs from birth