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Explain the reason for the laboratory tests listed below. Describe how these lab tests will assist
with a nutritional assessment. Identify which lab tests are affected by a change in hydration
status.
Lab Test and Values:
1. Albumin (normal adult level: 3.5-5 g/dL or 35-50 g/L) blood, urine
Albumin is a laboratory test to determine a measure of hepatic function. Albumin is synthesized in the
liver by hepatocytes; when the liver is compromised by disease, hepatocytes cannot properly produce
albumin thus a patients serum albumin level will be decreased. Because albumin composes
approximately 60% of total protein, it is also a measure of nutritional status. Burn patients,
malnourished patients, and patients with protein malabsorption issues will show low serum albumin
levels. An albumin blood or urine test assists with a nutritional assessment by identifying protein
status. May be elevated or reduced in response to dehydration. 21 day half-life
2. Transferrin (normal adult male level: 215-365 mg/dL or 2.15-3.65 g/L; normal adult female
level: 250-380 mg/dL or 2.50-3.80 g/L) blood
Transferrin is used as a lab test to measure iron. Iron is bound to transferrin and so when iron stores
are low, transferrin levels increase and vice versa. Other proteins are also available to bind mobile
iron however, transferrin represents the most available iron-binding protein. Transferrin, which is
produced by the liver, is a negative acute-phase reactant protein- during acute inflammatory reactions,
transferrin will lower. Transferrin is also low when a patient has a chronic illness such as liver
disease. Hypoproteinemia also may also reduce transferrin levels. Increased transferrin lab findings
may be due to oral contraceptives, iron deficiency anemia, or polycythemia vera. Will be elevated or
reduced in response to dehydration.
3. Pre-Albumin (normal adult level: 15-36 mg/dL or 150-360 mg/L) blood, CSF, 24 hr urine
Pre-albumin is used as a marker of nutritional status since this major plasma protein has a short halflife of 1.9 days. With the short half-life, prealbumin levels can show changes affecting protein
synthesis and catabolism. Thus, it is useful when monitoring patients on TPN. It is also used to
indicate protein-wasting diseases of intestines or kidneys, malnutrition, and inflammation
4. Serum Creatinine (normal adult female level: 0.5-1.1 mg/dL or 44-97 umol/L; normal adult
male level: 0.6-1.2 mg/dL or 53-106 umol/L) blood
Serum creatinine is a marker of renal function. Creatinine is excreted by the kidneys and is produced
in levels dependent upon muscle mass. Serum creatinine level should remain constant and normal in
patients with healthy renal excretory function. Dehydration and renal disorders such as
glomerulonephritis, pyelonephritis, acute tubular necrosis, and urinary obstruction will result in an
increased serum creatinine level. A creatinine test is used as an approximation of glomerular filtration
rate. Generally, double the amount of normal creatinine indicates a 50% reduction in GFR. If serum
creatinine is low, it may help nutritional assessment by reflecting decreased muscle mass. Will be
elevated in response to dehydration.
5. Blood Urea Nitrogen (normal adult level: 10-20 mg/dL or 3.6-7.1 mmol/L) blood
BUN is a measure of metabolic function of the liver and excretory function of the kidney. Together
with serum creatinine, BUN make up the renal function studies. BUN/creatinine ratio 6-25 for healthy
adults; the optimal adult value is 15.5. Specifically, BUN measures the amount of urea nitrogen in the
blood made from ammonia deposited by the liver. Patients with elevated levels of BUN have
azotemia. Generally all renal diseases cause blood concentration of urea to rise above normal. Other
conditions cause elevated BUN as well such as GI bleeding or excessive consumption of protein.
Hydration status affects BUN levels. BUN is elevated in dehydration and reduced in overhydration.
Patients with severe liver disease also decreases BUN status. Patients with both renal and liver
disease may falsely show a normal BUN because poor hepatic functioning has resulted in decreased
formation of urea. Other examples causing reduced BUN may be due to negative nitrogen balance,
pregnancy, and nephrotic syndrome. Examples causing elevated BUN may be due to CHF, GI
bleeding, starvation, and sepsis. Will be elevated in response to dehydration.
6. Serum Uric Acid (normal adult male level: 4.0-8.5 mg/dL or 0.24-0.51 mmol/L; normal adult
female level: 2.7-7.3 mg/dL or 0.16-0.43 mmol/L) blood urine
The product of purine catabolism, uric acid is excreted mostly by the kidney and to some extent by
the intestinal tract. Often when a patient has hyeruricemia, the patient has gout with a serum urate
measurement > 6.8mg/dL (exceeding the physical saturation threshold). With gout, monosodium
urate crystals may form and be deposited in joints and soft tissues. The overproduction or decreased
excretion of uric acid which causes hyperuricemia may be due to kidney failure, alcoholism,
leukemia, metastatic cancer, hyperlipoporoteinemia, DM, stress, lead poisoning, and dehydration.
Elevated uric acid in the urine, uricosuria, depends on uric acid levels in the blood, GFR, and tubular
secretion of uric acid into the urine. As the urine pH rises, more uric acid can exist without
crystallization and stone formation.
% in mm3
55-70
Lymphocyte (NG)
20-40
1000-4000
Monocytes (NG)
2-8
100-750
Eosinophils
1-4
Basophils
0.5-1
50-500
25-100
Function
Produced in 7-14 days, in circulation for 6 hours;
phagocytosis of bacterial microorganisms
T cells: cellular-type immune reactions; B-cells:
humoral immunity (antibody production); fight
chronic bacterial and acute viral infections
Fight bacteria in way similar to that of neutrophils;
produced rapidly, spend longer time in circulation
Involved in allergic reaction; phagocytosis of
antigen-antibody complexes; do not respond to
bacterial or viral infections
malnutrition and severe liver diseases. This is because the liver is required to make cholesterol so low
levels indicate a problem. Furthermore, diet is the main source of cholesterol so malnourished
patients will show low levels.
9. Triglycerides (normal adult male level: 40-160 mg/dL or 0.45-1.81 mmol/L; normal adult
female level 35-135 mg/dL or 0.40-1.52 mmol/L) blood
TGs is a form of fat transported in the bloodstream by VLDL or LDL. It is part of the lipid profile
that elevates cholesterol. TGs are produced in the liver. The level of TGs is increased after ingestion
of fatty meals and alcohol, pregnancy, glycogen storage disease, hyperlipidemia, hypothyroidism,
high CHO diet, poorly controlled DM, risk of arteriosclerosis, HTN, MI, and nephrotic syndrome.
The level of TGs is decreased during malnutrition, malabsorption syndrome, and hyperthyroidism.
10. Glucose (normal adult level: 74-106 mg/dL or 4.1-5.9 mmol/L) blood
Levels of glucose in the blood are controlled by hormones insulin and glucagon. In the fasting state,
glucose levels are low so glucagon is excreted to raise glucose. In the fed state, glucose levels are
high so insulin is secreted to drive glucose into cells to be metabolized to glycogen, aa, and FA.
Serum glucose levels fluctuate by the time of day they are taken; for example, levels will be high if
taken right after a meal. True glucose elevations indicate DM but hyperglycemia is also caused by
acute stress response, cushing syndrome, chronic renal failure, acute pancreatitis, and diuretic
therapy. Hypoglycemia, on the other hand, may be caused by insulinoma, hypothyroidism, extensive
liver disease, and starvation.
11. Hemoglobin (normal adult male level: 14-18 g/dL or 8.7-11.2 mmol/L; normal adult female
level: 12-16 g/dL or 7.4-9.9 mmol/L) blood
Hgb in peripheral blood reflects the number of RBCs in blood. Hgb test is part of a complete blood
count. Hgb also serves as a vehicle for oxygen and carbon dioxide transport. Reduced levels of Hgb
indicate anemia, hemorrhage, hemolysis, nutritional deficiency, lymphoma, systemic lupus
erythematosus, kidney disease, splenomegaly, and neoplasia. Elevated levels of Hgb indicate
congenital heart disease, chronic obstructive pulmonary disease, CHF, high altitudes, severe burns,
and dehydration. Will be elevated in response to dehydration.
12. Hematocrit (normal adult male level: 42-52% or 0.42-0.52 volume fraction; normal adult
female level: 37-47% or 0.37-0.47 volume fraction) blood
Hct is the measure of the percentage of total blood volume that is made up by RBCs. The ratio of the
height of the RBC column compared with the original total blood column after centrifugation is
multiplied by 100%-- this is Hct. Hct in percentage points usually is about three times the Hgb
concentration in g/dL when RBCs are of normal size and contain normal amounts of Hgb. Decreased
HCT indicates anemia, cirrhosis, hemorrhage, dietary deficiency, bone marrow failure, pregnancy,
leukemia, renal disease, lymphoma, and Hodgkin disease. Increased HCT indicates congenital heart
disease, polycythemia vera, erythrocytosis, eclampsia, burns, severe dehydration, and COPD.
Hemodilution and dehydration may affect Hct levels. Will be elevated in response to dehydration.
of the problem; the patient is given pancreatic enzymes for three days and then a radioactive
dose of vitamin B12. Considerations: patients cannot eat 8 hours before the test. Urinating 840% of radioactive B12 within 24 hr is normal result
14. Urinary Ketones (normal: negative) urine
Normally no ketones are in the urine. Kteones are the end product of fatty acid catabolism. Ketones
will spill over into the urine if blood levels of ketones in a patient with DM are elevated (as with
glucose). The excess production of ketones in urine is usually associated with poorly controlled DM.
This part of a urinalysis is important to evaluate ketoacidosis associated with alcoholism, fasting,
starvation, high PRO diets, and isopropanol ingestion. Ketonuria may also occur with acute febrile
illnesses, esp. in infants and children, dehydration, anorexia nervosa, prolonged vomiting, and
excessive aspirin ingestion.
15. Urinary Glucose (normal: negative in fresh specimen, 50-300 mg/d or 0.3-1.7 mmol/d in 24
hr specimen) urine
Glucose in the urine tests for DM or other causes of glucose intolerance. Usually glucose is filtered
from the blood by the glomeruli of the kidney and then all of it is resorbed in the proximal renal
tubules. However, when blood glucose exceeds the capability of the renal threshold to resorb glucose
(>180 mg/dL), glycosuria occurs. Glucosuria can be seen in patients with DM, pregnancy, renal
glycosuria, and hereditary defects in metabolism of reducing substances such as galactose, fructose,
and pentose.
16. Urinary Proteins (normal: 0-8 mg/dL, 50-80 mg/24 hr at rest, <250 mg/24 hr exercise) Urine
Part of a urinalysis. Abnormalities detected by urinalysis may reflect either UTI (ex. Infection, loss of
concentrating capacity) or extrarenal disease processes (glucosuria in DM< proteinuria in monoclonal
gammopathies, bilirubinuria in liver disease). Protein is a sensitive indicator of glomerular and
tubular renal function. Normally, <30 mg of PRO/d is in urine. In glomerulonephritis where
glomerular filtration membrane is injured, larger particles can go through so protein seeps out into
filtrate and then into urine. Proteinuria is the major indicator of renal disease. Urinary protein also
tests for complications of DM, glomerulonephritis, amyloidosis, preeclampsia, CHF, malignant HTN,
SLE, bladder tumor, and multiple myeloma.
17. Total Iron Binding Capacity (normal: 250-460 mcg/dL or 45-82 umol/L) blood
TIBC is a measurement of all proteins available for binding mobile iron. Transferrin makes up most
of TIBC. Ferritin is not included in TIBC because it only binds stored iron. TIBC varies minimally
according to iron intake and is more of a reflection of liver function and nutrition than of iron
metabolism. TIBC is increased in 70% of pt with iron deficiency. Chronic illness is characterized by
decreased TIBC as well as hemolytic anemia, pernicious anemia, and sickle cell anemia. It is not
uncommon to find high TIBC in late pregnancy
19. C-reactive Protein (normal findings: <1.0 mg/dL or < 10.0mg/L) blood
CRP is protein produced by the liver during an acute inflammatory process and other diseases. It is
used to diagnose bacterial infectious disease and inflammatory disorders as a nonspecific, acute-phase
reactant. The synthesis of CRP is initiated by antigen-immune complexes, bacteria, fungi, and trauma.
Failure of CRP to normalize is associated with heart tissue damage. Increased levels of CRP also
indicate arthritis, acute rheumatic fever, Crohn disease, SLE, MI, UTI, TB, and bacterial meningitis.
List the nutritional interactions of the following medications and their indications for use.
Medications:
1. Prednisone/Solumedrol: corticosteroid taken by mouth
Indication for use: anti-inflammatory, immunosuppressant; treats severe allergies, adrenal problems,
endocrine problems, bone marrow problems, lupus, skin conditions, kidney problems, arthritis,
asthma, stomach or bowel problems, ulcerative colitis, and flare-ups of MS.
Nutritional interactions: lower sodium, increase Ca, increase vit D, increase protein. May need
increased potassium, increased vitamin A, C. Caution with grapefruit, limit caffeine. . Interferes with
DM medicine, diuretics, NSAIDs, blood thinners. May increase appetite.
(used
in
combination
or
alone):
Indication for use: treats edema or HTN. Do not use with AC inhibitor or other BP medicine, blood
thinners, DM medicine, laxatives, NSAIDs, or steroids.
Nutritional interactions: may cause kidney problems, high or low levels of Ca, Mg, K, or NA, and
gout. May also cause dizziness, allergic reaction, dry mouth, N/V, fever, sore throat, stomach pain,
fever, and/or problems urinating.
Nutritional interactions: careful with salt substitutes that contain potassium. Do not use if pt has
Addison disease. May cause weakness, drowsiness, dry mouth, increased thirst, N/V, tingling in
hands, lips, blood in stools, allergic reaction.
Type
Class
Intraven
ous
Name
Brand
Maker
Onset
Peak
Duration
Comments
Uman
regular (U100)
Humulin R
Lilly
Immediate
Novolog
<10
min
Aspart
Apidra
NovoNordis
k
Immedia
te
30-90
min
< 5 hr
< 5 hr
At mealtime; pump
indication/CSII; control
glycemia following
meal/food intake
Sanofi
Glulisine
Bolus
(subcuta
neous)
Rapid
acting
Lispro
Humalog
Lilly
5-15 min
Aspart
Novolog
novoNordisk
5-15 min
Glulisine
Apidra
Sanofi
5-15 min
30-90
min
< 5 hr
30-90
min
Basal
(subcuta
neous)
Short
acting
Human
regular (U100)
Humulin R
Lilly
30-60 min
2-4 hr
5-8 hr
Novolin R
NovoNordis
k
30-60 min
2-4 hr
5-8 hr
Interme
diate
Human NPH
Humulin N
Lilly
2-4 hr
4-10 hr
Human
regular (U500)
Novolin N
NovoNordis
k
2-4 hr
4-10 hr
10-18
hr
Humulin R
(U-500)
2-4 hr
4-10 hr
Lilly
10-18
hr
10-16
hr
Mixed
(subcuta
neous)
Long
acting
Glargine
Lantus
Sanofi
2-4 hr
None
24 hr
Detemir
Levemir
novoNordisk
3-6 hr
None
18-24
hr
Premixed
Human
NPH/regular
Humulin
70/30
Lilly
30-60 min
Dual
NovoNordis
k
30-60 min
Dual
10-18
hr
Lilly
5-15 min
Dual
Lilly
5-15 min
Dual
NovoNordisk
5-15 min
Dual
Novolin
70/30
Lispro
protamine/Li
spro
Lispro
protamine/
Lispro
Aspart
protamine/
Aspart
Humalog
Mix 75/25
Humalog
mix 50/50
Novolog mix
70/30
10-18
hr
10-18
hr
10-18
hr
10-18
hr
Indications for use: improper functioning of pancreas, body does not produce enough insulin
as it should
Nutritional interactions: risk of hypoglycemia; caution should be used when consuming
alcohol; general weight gain may occur
13. Heparin: anticoagulant
Indications for use: prevents and treats blood clots. Caution with other blood thinners, aspirin,
nicotine, and some allergy meds and certain antibiotics.
Nutritional interactions: may cause N/V, abdominal pain, GI bleeding, constipation, black tarry
stools. Caution with DM, ESRD, hyperkalemia, and decrease hepatic or renal function. May also
cause bleeding, dizziness, headache, fever, osteoporosis, decrease platelets, increased AST and ALT,
increase potassium, decreased TG, and increased FFA.
14. Digoxin: cardiotonic, antiarrhythmic, CHF treatment, inotropic agent (oral or parentral)
Indications for use: congestive heart failure, heart rhythm problems; often used in combination with
diuretic and ACE inhibitor.
Nutritional interactions: maintain diet with increase potassium, decreased sodium, and adequate Mg
and Ca. Take at least 2 hours before antacids or Mg supplement, otherwise may have decreased
absorption of drug. Caution with Ca or Vit D supplement, some herbal products such as aloe. Avoid
St. Johns Wort and natural licorice. May cause decreased appetite, stomach pain, weight loss, Ca and
Vit D induced hypercalcemia, N/V, diarrhea. May also cause weakness, headache, depression,
drowsiness, and apathy. Monitor electrolytes.
15. Kayexalate/ sodium polystyrene sulfonate: antihyperkalemia, cation exchange resin (oral or
rectal)
Indications for use: Treats hyperkalemia. Caution in pt with high BP, CHF, heart rhythm problems,
severe swelling, kidney disease, low Ca, low Mg, or stomach or bowel problems.
Nutritional interactions: Diets should be low in potassium and pt should avoid potassium
supplementations. Patients should be wary of sodium intake and should adhere to a low sodium diet.
IF patient is taking a calcium or magnesium supplement or antacids, these should be taken several
hours before or after taking kayexalate. Kayexalate should not be taken with salt substitutes or
sorbitol. May cause hypokalemia, N/V, SOB, chest pain, constipation, loss of appetite, stomach pain,
dry mouth, and increased thirst. This drug will lower potassium, Mg, and Ca in the blood while
raising serum sodium concentration. Electrolytes should be monitored.
Nutritional interactions: If pt is allergic to eggs, egg products, soybeans, or soy products, this
anesthetic should not be used. May cause fever, pain or fullness in upper stomach, weakness,
seizures, SOB, irregular heartbeat, swelling in extremities, decreased urination, lightheadedness, and
N/V.
Indication for use: increases calcium, if needed. Also helps to prevent osteoporosis. Caution if pt has
kidney disease or kidney stones, or hypercalcemia.
Nutritional interactions: Supplement should be taken with food. Take other medications 2 hours
before or after supplement. Do not take supplement with high-fiber meals or caffeine. Avoid large
amounts of alcohol. May cause stomach or digestion problems, diarrhea, malabsorption of nutrients,
headache,dry mouth, loss of appetite, constipation, or flatulence.
constipation drowsiness, low sodium levels, and dyspnea. Cholesterol and TG will increase in blood
while WBC and platelets will decrease, possibly causing anemia. Urination will increase in
frequency. Avoid alcohol.
32. Ace Inhibitors: angiotensin converting enzyme inhibitors lower blood pressure and
decrease blood volume; perindopril, captopril, lisinopril
Indication for use: HTN, CKD, CHF, HF, stroke, DM
Nutritional interactions: possible hypotension, reduction in GFR, hyperkalemia, loss of appetite, upset
stomach, diarrhea
rapid weight loss post bariatric surgery (inadequate PRO, Fe, zinc, biotin), thyroid
disease, and polycystic ovary syndrome; telogen effluvium- hair loss in handfuls
o Alopecia areata: autoimmune disorder- immune system attacks hair follicles;
starts as patchy hair loss and can lead to total baldness
o Medications may increase hair loss- warfarin, gemfibrozil, antidepressants, betablockers, NSAIDs, drugs for gout, arthritis, birth control, and high BP
o Telogen effluvium: hair follicles in resting phase and fall out too early; pt shed
100-150 hairs/d
o Anagen effluvium: hair falls out during active phase of growth; matrix cells which
produce new hairs cannot divide normally (common side effect of chemo)
Tenting of skin: elevated skin common in pt with dehydration; pink skin to check for
turgor/elasticity, if skin remains tented for more than 3 seconds then turgor is decreased
o Turgor is naturally slower in older adults and is not a reliable indicator of
dehydration
o Preferred sites to check for tenting: sternum and inner aspect of thigh, also top of
hand
o Sign of severe dehydration
Xerosis: dry skin; deficiency of essential fatty acid
Diabetic Ulcer: foot ulcers; due to arterial insufficiency or neuropathy leading cause of
hospitalization and amputation in pt with DM
Venous Ulcer: most common type of chronic wounds treated; may be caused by valve
incompetence in perforating veins or when history of deep vein thrombophlebitis and/or
thrombosis; associated with edema; found on lower leg or ankle
Arterial Ulcer/ ischemic ulcer: caused by poor perfusion to lower extremities; overlying
skin and tissues deprived of oxygen, killing tissues and causing area to form open wound
Surgical Wound: cut made into skin during operation wound infection
Necrosis:
o may benefit wound by providing stable barrier to infection
o necrotic tissues on heels of feet considered stable eschar and shouldnt be
removed
o as tissue becomes necrotic, turns from light yellow and nonadherent to loosely
adherent yellow slough to finally black eschar
Debridement
o Enzymatic, surgical, mechanical, autolytic
o Remove nonliving necrotic or black eschar tissue to allow living tissue to heal
o Afterwards, wound usually becomes larger
Unstageable Wound
o Wound base covered by slough or necrotic tissue
o Depth and stage difficult to determine until base of wound exposed
o Full thickness tissue loss, base of ulcer covered by slough
Deep Tissue Injury
o Purple/maroon localized area of discolor intact skin or blood-filled blister d/t
damage of underlying soft tissue from pressure and/or shear
o Area may be painful, firm, muhys, warmer or cooler than surrounding tissue
Ecchymosis: discoloration of skin resulting from bleeding underneath usually caused by
bruising
Abrasion: superficial damage to skin no deeper than epidermis
Wound dehiscence
o Increased with infection; infection impairs collagen formation thus delaying
healing process
MRSA: methicillin-resistant Staphylococcus aureus; causes staph infection
Dx: inadequate oral intake, fluid intake, protein intake, vitamin intake (such as vit C),
mineral intake (such as zinc); increased nutrient needs; malnutrition
Sources: Nutrition, Physical Assessment, and Wound Healing. Megan Tempest, Erika
Siesennop, Kristin Howard, Hatherine Hartoin. Support Line. June 2010 22-29
Diabetes (Lakeside)
1. List risk factors for type 2 diabetes.
Age, obesity (fat accumulation. Larger adipocytes dont respond to insulin),
family history, genetic predisposition, history of GDM, impaired glucose
metabolism, physical inactivity, dyslipidemia
2. Describe lab values involved with the diagnosis of type 2 diabetes.
Glycated hbg level of 6.5% or more
Fasting plasma glucose level of 126 mg/dL or more (7.0 mmol/L)
2 hr plasma glucose level of 200 mg/dL or more during OGTT (11.1 mmol/L)
administering 75 g glucose
Classic symptoms of hyperglycemia or hyperglycemic crisis: random plasma
glucose value of greater than 200 mg/dL
Symptoms: polyuria, polydipsia, unexplained weight loss
Category
FPG test
HbA1c
2 Hr Plasma
Glucose test
Normal
<5.7%
Impaired fasting
glucose and
impaired glucose
tolerance
100-125 mg/dL
(5.6-6.9 mmol/L)
140-199 mg/dL
(7.8-11.0 mmol/L)
Pre-DM 5.7-6.4%
DM
> 6.5%
3. List symptoms of hypo- (plasma glucose lower than 70 mg/dL or 4.0 mmol/L) and
hyperglycemia (first elevated postprandial glucose conc. Caused by insulin resistance at
cellular level then elevated fasting glucose conc.).
Hyper: glucotoxicity of inulin sensitivity and insulin secretion; caused by
impaired beta cell insulin secretion d/t functional defect in glucose secretion;
moderate decrease in beta cell mass; rates of hepatic glucose production elevated
d/t increased gluconeogenesis; skeletal muscle becomes insulin resistant; any
blood glucose level in excess of 110 mg/dL
o Frequent urination, increased thirst
o High levels of sugar in urine and high blood glucose
Hypo: sweating, trembling, difficulty concentrating, light-headedness, lack of
coordination alleviated by eating CHO foods; severe hypoinability to selftreat because of mental confusion, lethargy, unconsciousness
o Eat or drink 15-20 g glucose to raise glucose levels to 45-50 mg/dL
response to treatment apparent in 10-20 minutes
4. List complications associated with prolonged poor glycemic control.
Microvascular: Retinopathy, cataract, glaucoma blindness
Class
Intraven
ous
Name
Brand
Maker
Onset
Peak
Duration
Comments
Uman
regular (U100)
Humulin R
Lilly
Immediate
Novolog
<10
min
Aspart
Apidra
NovoNordis
k
Immedia
te
30-90
min
< 5 hr
< 5 hr
At mealtime; pump
indication/CSII; control
glycemia following
meal/food intake
Sanofi
Glulisine
Bolus
(subcuta
neous)
Rapid
acting
Lispro
Humalog
Lilly
5-15 min
Aspart
Novolog
novoNordisk
5-15 min
Glulisine
Apidra
Sanofi
5-15 min
30-90
min
< 5 hr
30-90
min
Basal
(subcuta
neous)
Short
acting
Human
regular (U100)
Humulin R
Lilly
30-60 min
2-4 hr
5-8 hr
Novolin R
NovoNordis
k
30-60 min
2-4 hr
5-8 hr
Interme
diate
Human NPH
Humulin N
Lilly
2-4 hr
4-10 hr
Human
regular (U500)
Novolin N
NovoNordis
k
2-4 hr
4-10 hr
10-18
hr
Humulin R
(U-500)
2-4 hr
4-10 hr
Lilly
10-18
hr
10-16
hr
Mixed
(subcuta
neous)
Long
acting
Glargine
Lantus
Sanofi
2-4 hr
None
24 hr
Detemir
Levemir
novoNordisk
3-6 hr
None
18-24
hr
Premixed
Human
NPH/regular
Humulin
70/30
Lilly
30-60 min
Dual
NovoNordis
k
30-60 min
Dual
10-18
hr
Novolin
70/30
10-18
hr
Lispro
protamine/Li
spro
Lispro
protamine/
Lispro
Humalog
Mix 75/25
Humalog
mix 50/50
Novolog mix
70/30
Lilly
5-15 min
Dual
Lilly
5-15 min
Dual
NovoNordisk
5-15 min
Dual
10-18
hr
10-18
hr
independent manipulation of
insulin components; usually
bid
10-18
hr
Aspart
protamine/
Aspart
Renal (Lakeside)
1. Briefly define Hemodialysis and Peritoneal Dialysis
a. HD: removes excess toxic by-products of metabolism from blood through
selective membrane with use of artificial kidney dialyzer made out of hollow fiber
or parallel-plate dialyzers; ultrafiltration and diffusion; access site is either
arteriovenous fistula (AVF), arteriovenous graft (AVG), or catheter; treatments
usually 3x/wk for avg. 4 hr/treatment
b. PD: selective membrane is pts peritoneal wall (**be sure pt has adequate protein
due to albumin and aa losses here); dialysate introduced into peritoneum through
peritoneal catheter; three typescontinuous ambulatory peritoneal dialysis
(CAPD- dwell time of 4 to 6 hr followed by draining and replacement with fresh
solutionchange 4x/d), continuous cyclic peritoneal dialysis (CCPD- cycler fills
and empties abdomen 3-5x/night, once exchange during day with daylong dwell
time), and intermittent peritoneal dialysis; range of dextrose concentrations that
alter osmolality and assist in fluid removal (glucose absorption needs to be
considered when calculating energy)
2. Review the Renal Diet Patient Education Materials on Share Drive
a. Diet and Kidney Disease
i. PRO: HBV such as eggs, meat, fish, milk, poultry in proper amounts,
check urea
ii. Kcal: focus on CHO and fats (candies, oils, butters)
iii. Potassium: cant be too high; found in dried fruits, citrus fruits, bananas,
tomatoes, dried beans, green leafy vegetables, potatoes, nuts, milk,
chocolate, salt substitutes
iv. Sodium: low sodium, probably less than 1500 mg/d
v. Ca and Phos: phos binder to lower serum concentration as to not take
calcium from bones; take phos binder with food
vi. Fluid: measured amount in ccs; includes water, milk, cream, juices, pop,
alcohol, koolaid, gelatin, ice cream, soups, ice cubes, popsicle
b. Eating Right for Kidney Health: Tips for People with CKD
i. Grill, broil, bake, roast, stir-fry instead of frying for heart health
c. High Magnesium Diet
i. Important for proper nerve, muscle, heart, bone function
ii. Nuts, beans, unrefined grains, green vegetables, molasses, avocado
d. Kidney Test Results
i. GFR: kidneys filtering blood
ii. Urine albumin-to-creatinine ratio (UACR): checks for kidney damage
(want low number)
iii. Blood pressure: checks possible damage to heart
iv. Serum albumin: checks malnourishment
v. Bicarbonate: acid in blood
vi. BUN: urea in blood
vii. K: checks nerve and muscle function
viii. Ca: checks bone health
ix. Phos: checks bone and heart health
x. PTH: checks control of Ca and Phos in blood
Creatinine criteria
Urine output criteria
>0.3 mg/dl or increase to 150-200% from
<0.5 ml/kg/hr for > 6 hr
baseline
2
Increase to > 200-300% from baseline
<0.5 ml/kg/hr for > 12 hr
3
Increase to > 300% from baseline or 4.0
<0.3 ml/kg/hr x 24 hrs or
mg/dl with acute rise of at least 0.5 mg/dl
anuria x 12 hr
ESRD (end stage renal disease): kidneys can no longer support bodys needs, after last
stage of CKD; treatment involves dialysis or transplant; collective signs and symptoms
called uremia
o Anorexia, N/V, pericarditis, central nervous system abnormalities, peripheral
neuropathy
o GFR < 15
Glomerulonephritis: inflammation of glomeruli that damage function to filter waste and
fluids from blood
o Blood and PRO lost in urine
o Leading cause of nephrotic syndrome in adults
PCKD (polycystic kidney disease): cyst in kidney, strong positive family history, cyst
enlarges kidneys, reducing function and leading to kidney failure
o Cyst damages surrounding tissue, other cysts may form in liver
Nephrotic syndrome: urinary losses of albumin and other plasma proteins (> 3 g/d)
o Hyperlipidemia: increased synthesis of lipids
o Edema
o Causes: DM, lupus, infections, medications, PEC, neoplasms
o Want to avoid proteinuria so lower protein diet recommended
HIV associated nephropathy: failure of kidney cells due to HIV infection
o Usually begins with proteinuria and quickly progresses to kidney failure
o Especially prominent in black pt with HIV
PRO: 1.0-1.5 g/kg/d, likely to have PEM (this is usually well tolerated, protein
restriction not needed)
Leucine, valine, isoleucine: one study found that high dose of oral BCAA (12 g/d)
given to pt with cirrhosis without history of hepatocellular carcinoma lower
incidence of HCC after 6 months of therapy
Another study: improve quality of life, increased event-free, improved serum
albumin concentrations
Improve intractable encephalopathy
11. Describe how TPN can lead to liver dysfunction.
Infection, metabolic complications
Young pt on TPN especially at risk for liver dysfunction
Theories: nutrients delivered to body first and not intestines/liver; loss of
hormones given to liver after passage through GI tract; increase in bacteria that
reach liver; altered blood flow to liver
o
o
o
2.
3.
4.
5.
Fluids: 35 mL/kg/d
Complications: heart arrhythmia, acute heart failure, cardiogenic shock, mitral
regurgitation, Dresslers syndrome (fever, pleuritic, pericarditis, caused by
autoimmune rxn to damage), chronic heart failure
Meds: opiate analgegics, anti-platelets, anti-coagulants, beta-blockers (reduce HR,
BP), nitrates (vasodilators, pain relief), statins, ACE inhibitors, coronary angiography
stroke and heart failure; may be caused by high blood pressure, CHD,
rheumatic heart disease, inflammation, overactive thyroid, heavy alcohol
use; risk increases with age
ii. Atrial flutter: electrical signals spread through atria in fast and regular
rhythm; similar complications and symptoms as AF but less common
iii. PSVT: very fast heart rate with sudden onset and end; caused by issues
with electrical connection between atria and ventricles; can happen during
intense physical activity
iv. WPW: electrical signals travel along extra pathway from atria to
ventriclesdisrupts timing, causes ventricles to beat very fast (life
threatening)
d. 3. Ventricular arrhythmias: start in lower chambers, very dangerous, require
immediate medical attention
i. Ventricular tachycardia: fast, regular beating of ventricles that lasts for
only a few seconds or for much longer (only a few seconds dont lead to
other problems but if they last long, can turn into more serious
arrhythmias)
ii. Ventricular fibrillation (v-fib): abnormal electrical signals make ventricles
quiver rather than pump (adequate blood flow not supplied to body); can
lead to SCA and death within few minute; condition must be treated
immediately with heart defibrillator; may occur during or after heart attack
or in those with weak hearts
e. 4. Bradyarrhythmias: heart rate slower than normal, may not allow blood to reach
brain if beat is too slow (<60 BPM); may be caused by heart attacks, underactive
thyroid gland, aging, chemical/electrolyte imbalance, medications (beta blockers,
calcium channel blockers, anti-arrhythmics, digoxin)
i. Bradycardias, sinus bradycardia
f. Atrioventricular block
g. Non-sustained ventricular tachycardia
6. What is cardiopulmonary arrest? See above for cardiac arrest
7. Define cardiopulmonary resuscitation (CPR)
a. Chest compressions, cleared airway, rescue breathing
b. Needed seconds after cardiac arrest to prevent brain damage or death
c. Pt who received bystander CPR had better survival than pt who had delayed CPR
from EMS
8. What is angina pectoris? (CP)
a. Chest pain, usually occurs with activities or stress due to impaired blood flow
through blood vessels in heart
b. Associated with myocardial ischemia
i. Oxygen demand exceeds supply
c. Causes: coronary arteries blocked by atherosclerosis or blood clot; most common
causeCAD
d. Risk factors: DM, HTN, high LDL low HDL, smoking, arrhythmias, anemia,
coronary artery spasms, heart failure, heart valve disease, hyperthyroidism, pt
with heart diseasecold weather, exercise, emotional stress, large meals
Stage
A
B
C
D
o Heart cant pump enough blood to meet bodys needs, can affect one
side of heart or both result from cardiac dysfunction
o Blood flow to kidneys diminished problematic hormonal response
vasoconstriction fatigue, edema, SOB, CP
o Causes: CAD, HTN, DM, MI, in elderly: elevated natriuretic peptides
Classification Description
High risk
Pt doesnt have structural heart disease or symptoms. Pt has HTN,
atherosclerosis, DM, obesity, MS
Asymptomatic Pt doesnt experience symptoms although structural damage to
heart such as enlarged left ventricle (LV hypertrophy or previous
MI)
Symptomatic Pt has structural changes in heart, experiences symptoms such as
SOB, fatigue, reduced tolerance to activity
Advanced
Structural changes, experiencing symptoms at rest despite
disease
medications and treatment
Descriptor
Asymptomatic, pt not SOB or fatigued during activity
Pt SOB/ fatigued after moderate activity (climbing two flights
of stairs, carrying load of laundry)
Pt SOB/fatigued after mild exertion (walking around house or
up half flight of stairs)
Pt exhausted, SOB, fatigued at rest
active for at least 30 min day most days of week; reduce alcohol consumption (2
drinks/d for men and 1 drink/d for women)
Intervention for pt with disorders of lipid metabolism: saturated and trans fat less
than 7% total energy intake (no trans fat) focus on whole grains and
unsaturated fat; total fat limited to 25-35% of total kcal intake; cholesterol <200
mg/d; plant sterols/stanols 2-3xd for total of 2-3g/d; antioxidant rich foods;
omega-3 fatty acids (two or more servings of 4oz fish per week); total fiber intake
21-25 g/d females and 25-38 g/d men with emphasis on soluble fiber (7-13 g/d)
such as whole grains
Intervention for pt with metabolic syndrome: kcal controlled diet, energy
reduction for 7-10% weight reduction from baseline, limited added sugar and fat;
physical activity most days of week for 30 minutes
Intervention for pt with elevated TG: kcal controlled diet, energy reduction,
limited added sugar and fat; use of omega-3 fatty acids
Intervention for pt with HTN: DASH diet1600 to 2300 mg Na/d
Warfarin and vitamin K: need consistency; RDA is 65-80 mcg/d (1 cup of green
leafy vegetables will exceed this); high doses of Vit E contraindicated in pt taking
warfarin
o With ischemic stroke, prothrombin time may need to be increased
o With hemorrhagic stroke, PT may need to be decreased
3. What is dysphagia and explain the pathophysiology of dysphagia following stroke.
Dysphagia: difficulty swallowing caused by issue in swallowing mechanism
Phase one of swallowing: oralbolus propelled into pharynx where swallow
triggered
o voluntary
Phase two of swallowing: pharyngealswallow triggered and bolus moves
through pharynx to cricopharyngeal sphincter (upper esophageal sphincter) which
opens to allow food to enter esophagus
o Voluntaryaffected during stroke
Phase three of swallowing: esophagealbolus propelled from upper esophageal
sphincter to LES by peristalsis
4. Please describe the national dysphagia guidelines incorporating the different diet levels.
Grade of dysphagia:
o 1: middle but can eat regular diet
o 2: pureed, soft, or liquid diet
o 3: need for feeding tube, IV hydration
Liquid consistencies
o Thin: regular liquids, no adjustment needed (ex. Tomato juice, water)
o Nectar: falls slowly from spoon and can be sipped through straw or from
cup
o Honey: drops from spoon but too thick to drink through straw (ex. Tomato
sauce)
o Spoon: maintains shape, needs to be eaten with spoon, too thick to drink
(ex. Pudding)
Food consistencies
o Dysphagia level 1: pureed pudding-like texture; add gravies, sauces,
vegetable broth, milk, cream to puree
Pulmonary (MICU)
Define and answer the following:
1. Pneumonia: infection in one or both of lungs
a. Are there different types of pneumonia? If so, what are they?
Aspiration pneumonia: food/liquid/salvia gets into lungs
Hospital acquired pneumonia/health-care acquired pneumonia (HCAP):
occurs 48 hours or more after admission to hospital that wasnt present at
time of admission
o In pt with IV therapy or chemotherapy or wound care within
previous 30 days
o At risk: residents of nursing homes or LTC, pts in acute care
hospitals for two or more days within previous 90 days or in
hemodialysis clinic within last 30 days
Community-acquired pneumonia (CAP): most common, infectious from
streptococcus pneumoniae, viruses, haemophilus influenzae
b. What is the appropriate medical abbreviation for pneumonia? PNA
c. Nutrition recommendations:
pt are in hypermetabolic/catabolic state
1.0-1.5 g pro/kg
o PNA complicated by sepsis: 1.6-2.0 g pro/kg; watch for urine urea
nitrogen
Small frequent snacks may be better tolerated d/t SOB
Goals are to prevent anorexia, SOB, N/V
2. Pneumonitis: inflammation of alveoli in lungs
a. May be caused by airborne irritants, medications, or cancer treatment
b. Symptoms: difficulty breathing and dry cough
3. Pneumothorax: collapsed lungair gets into space between lungs and chest wall; may be
caused by chest injury
a. What is the appropriate medical abbreviation for pneumothorax? PTX
4. Hemopneumothorax: air and blood in chest cavity
5. Chest tube: hollow, flexible tube in chest that acts as drain for blood, fluid or air from
around lungs to allow full expansion
a. Tube placed between ribs and into space between pleural space
6. Asthma: walls of airways sore, swollen, sensitive react strongly to allergies and
irritants; airways contract under irritation making it more difficult to take in air
7. COPDumbrella term for chronic bronchitis, emphysema, and other lung disorders;
lungs elastic recoil reduced and airway resistance increased
a. What does it stand for? Chronic obstructive pulmonary disease
b. How is it staged? Global Initiative for Chronic Obstructive Lung Disease (GOLD)
use forced expiratory volume in one second but FEV only captures one
component of COPD; symptom severity assessed using mMRC or CAT (number
of exacerbations in previous year used to predict future risk)
Group A: low risk, less symptoms, GOLD 1 or GOLD 2 (mild or
moderate airflow limitation) and/or 0-1 exacerbation per year
Group B: low risk, more symptoms, GOLD 1 or 2 and/or 0-1 exacerbation
per year
Group C: high risk, less symptoms, GOLD 3 or 4 (severe or very severe
airflow limitation), and/or 2 exacerbations per year
Venturimask: mask mixes oxygen with room air to create high-flow enriched oxygen; used
when CO2 retention is a concernprovides accurate and constant inspiratory oxygen fraction
12. Hypercapnia or hypercarbia: abnormally high carbon dioxide levels in blood
13. Identify the following abbreviations:
a. SOB: shortness of breath
b. WOB: work of breathing
c. DOE: dyspnea on exertion
References: NCM, Up-to-date, MedlinePlus NLM
Medical GI
(LT 9, SICU)
ii. Intermediate dumping: 20-30 min after eating gas, ab pain, cramping,
diarrhea
iii. Late dumping: 1-3 hours after eating, common when consuming simple
CHO insulin release but no substrate for insulin to act on
hypoglycemia shakiness, sweating, confusion, weakness
iv. Meds to treat: acarbose, octreotide, etc.
v. How to avoid: no simple sugars; no clear liquids beside broth for first
meal; no sucrose, fructose, sugar alcohols; chew thoroughly; meals should
contain protein, fat, complex CHO but only 1-2 food items at time; 5-6
small meals per day; liquids 30-60 min after solids; lie down after eating;
functional fibers to delay gastric emptying and assist with diarrhea; may
need liquid MVM
c. What is gastroparesis? Delayed gastric emptying from stomach into small
intestine
i. Caused by issue relating to vagus nerve which controls involuntary
movement of food through digestion track
ii. DM most common cause (diabetic gastropathy)
iii. Symptoms: N/V of undigested food, early satiety, bloating, ab pain,
fluctuations in blood glucose levels, hyperglycemia, electrolyte
imbalances
iv. Treatment: manage glucose; small frequent meals; low-fat and low-fiber
options, soft foods, liquid meals; Reglan; jejeunostomy EN; exercise;
chew foods well; may need supplements for Mg, Fe, B12, D
4. Explain how absorption of medium chain triglycerides is different than long-chain
triglycerides.
a. Easily to absorb than long-chain: passively diffuse from GI tract and do not need
bile salts for digestions (no energy needed for absorption, use, or storage)
b. Used often for pt with malnutrition, malabsorption, or fatty-acid metabolism
disorders
c. Examples: coconut oil, palm oil, dairy fat
5. What is diverticulitis and diverticulosis?
a. Diverticulosis: presence of sac-like pouches or herniations in mucosal layer of
colon (esp. descending)
i. Advanced age or Meckels diverticulum (usually present at birth)
ii. Usually asymptomatic
iii. May be developed through history of constipation, high red meat intake,
obesity, decreased physical activity, low fiber intake
iv. Signs and symptoms: fever, ab pain in left lower quadrant, GI bleeding,
elevated white blood cell count
v. Complications: bleeding abscess, obstruction, fistula, perforation
vi. Treatment: fiber intake and pro/prebiotics
vii. Nutrition therapy: 6-10 g beyond 25-35 g fiber per day; probiotic foods
such as yogurt, miso, kefir; proper fluid intake
b. Diverticulitis: inflammation of diverticulum
i. Treatment: NPO until bleeding and diarrhea absolve clear liquid diet
ii. Nutrition therapy: possible need for folic acid, B12, Fe; flow-fiber diet;
high probiotic foods
6. Define Crohns disease and Ulcerative colitis: environmental trigger causes abnormal
inflammatory autoimmune response within GI tract
a. Crohns disease: can affect any portion of GI tract but most commonly affects
ileum and colon
i. Development of fistulas which results in fibrotic tissue strictures and
bowel obstructions
ii. Symptoms: ab pain, fever, diarrhea, oral aphthous ulcerations, pyroderma
gangrenosa
iii. Complications: abscesses, anal fissures, bowel obstruction, bowel
perforation, bowel resection, colon cancer, fistulas, hyperoxaluria,
malnutrition, steatorrhea, strictures, ulcers
b. UC: usually affects lower bowel (colon and rectum), no areas of normal mucosa
i. Symptoms: pain, cramping, bloody diarrhea, N/V, fever
c. Treatments: aminosalicylates, immunomodulators, antibiotics, biological
modifiers, corticosteroids, surgical intervention
d. Comparative standards: 25-35 kcal/kg, 1.0-1.5 g pro/kg/d; may need
supplementation of B12, folate, thiamin, riboflavin, niacin, vit C, vit E, vit D, vit
K, Fe, zinc, Mg, Se, K; omega-3 fatty acids, glutamine, prebiotics, probiotics
(fructooligosaccharides)
e. Nutrition prescription for exacerbation: EN, TPN if needed; low-fat, low-fiber
(during acute exacerbations), high kcal; small frequent meals; supplementation of
Vit D, Zn, Ca, Mg, folate, B12, Fe if needed
f. Nutrition for remission: avoid foods high in oxalate (beer, beans, beets, berries,
chocolate, coffee, cranberries, nuts, dark green veggies, oranges, dark pop, soy,
wheat bran); increase antioxidant intake; supplementation with omega-3s and
glutamine; pre/probiotics
g. Common problems: anorexia, malnutrition, increased protein needs, ab pain,
diarrhea, catabolism, short bowel syndrome, blood loss, long-term steroid use,
surgical resections of stomach
7. Define IBS. What is the FODMAP diet?
a. IBS: irritable bowel syndrome IBS-C, IBS-D, IBS-M (mixed), IBS-U
(unspecified)
b. Rome III criteria: recurrent ab pain/discomfort 3 days per month in last 3 months
and two or more change in frequency/onset/form of stool
c. ACG: ab pain or discomfort that occurs in association with altered bowel habits
over period of at least 3 months
d. Symptoms: lower ab pain, constipation, diarrhea, bloating, mucus in stools,
incomplete evacuation, chest discomfort, excessive gas, fatigue, headache, urinary
incontinence
e. Medications: antidiarrheal agents, antispasmodics, clonidine, tricyclic
antidepressants
f. FODMAPs: fermentable oligosaccharides, disaccharides, monosaccharides,
polyols such as fruits, dried fruits, fruit juice, fructose as sweetener, HFCS,
honey, coconuts, onion, leek , asparagus, artichokes, cabbage, brussel sprouts,
beans, legumes, sorbitol, mannitol, isomalt, xylitol
i. These foods enter distal small bowel and colon where they ferment
increased intestinal permeability and possibly inflammation
g. Treatment: probiotics; reduce lactose; may need MVM; avoid foods that increase
gas
8. Celiac disease: autoimmune disordersensitivity to aa in prolamin of wheat, barley, rye
(gliadin, hordein, secalin, respectively)
a. Diagnostic tests: serologic tests such as IgA, biopsy of small intestine (look for
increased density of intraepithelial lymphocytes, partial/total villous atrophy,
crypt hyperplasia); genetic markers such as DQ2, DQ8
b. Treatment: lifelong adherence to gluten-free diet; may need supplementation of
Ca, Vit D, Fe, folate if deficient
c. Symptoms: gas, constipation, bloating, indigestion, steatorrhea, ab pain, anemia,
bone disease, dental enamel defects, joint pain, anxiety, depression, infertility,
miscarriage, delayed puberty, short stature
d. May have secondary form of lactose intolerance
e. Grains and plant foods to include in diet: rice, corn, amaranth, quinoa, teff, millet,
soy, arrowroot, buckwheat, flax, sago, potato, wild rice, tapioca, mesquite,
legumes, cassava, yucca, nuts, seeds, potential oats
f. To avoid when shopping: flour, white flour, plain flour, bromated flour, enriched
flour, phosphate flour, self-rising flour, durum flour, farina, semolina, graham
flour, beer, malt
g. Careful of bouillon cubes, brown rice syrup, candy, cold cuts/processed meat,
communion wafers, French fries, gravy, imitation fish, licorice, matzo, rice mixes,
sauces, seasoned snack foods, soups, soy sauce, vegetables in sauce
9. Discuss the following and how they affect stool output:
a. Psyllium: bulk-forming laxative to treat constipation
i. Absorbs liquid in intestines to form bulky stool easy to pass
b. Docusate: stool softener to treat constipation
i. Absorbs liquid in intestines to form bulky stool easy to pass
c. Miralax: stool softener/ osmotic laxative to treat constipation
i. Absorbs liquid in intestines to form bulky stool easy to pass
d. Senna: stimulant laxative to empty bowels and treat constipation
i. Increases activity of intestines to cause bowel movement
e. Bisacodyl: stimulant laxative to empty bowels and treat constipation
i. Increases activity of intestines to cause bowel movement
ii. Normally causes BM within 6-12 hours
f. Lactulose (synthetic sugar): stool softener to treat constipation
i. Breaks down in colon then pulls water from body into colon
g. Magnesium citrate: osmotic laxatives
i. often used to empty colon before colonoscopy
ii. soften stools
10. Discuss the 4 general types of diarrhea
a. Osmotic: poorly absorbed, osmotically active solutes in gut lumen, disrupting
osmotic forces, substrates drawn across intestinal epithelium; stools large and
water and resolve with elimination of osmotically active agent; may be caused by
sorbitol, Mg-based antacids, lactulose, hyperosmolar EN feedings
b. Malabsorption: alteration in luminal/mucosal integrity of gut (ex. Enzyme
deficiency); may be seen with lactose intolerance, pancreatic insufficiency, blind
loop syndrome after bowel resection or short-bowel syndrome
c. Resulting from defective ion absorption: small intestine and colon brush border
membranes have gradients for ion absorption need more than two ion brush
border
exchangers,
otherwise
congenital
diarrhea
(http://www.ncbi.nlm.nih.gov/pmc/articles/PMC152597/)
d. Secretory: large volume of stool output >1000 mL/d despite little food intake
intestinal oversecretion of fluid and electrolytes exceeding absorptive capacity of