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BCP
a group of select tests that can screen for certain conditions - patterns of abnormal values provide data for arriving at a diagnosis - CMP is like the same thing
glucose
primary energy source - blood glucose levels are held within a fairly constant range by regulatory hormones and metabolic activity - disorders of glucose metabolism result in hypoglycemia and hyperglycemia - insulin decreases blood glucose concentrations - levels controlled by feedback mechanism
what things increase blood glucose levels
glucagon (secreted in the fasting state), epinephrine, growth hormone, ACTH, and cortisol
insulin
secreted to drive glucose into the cells to be metabolized to glycogen. amino acids, and fatty acids = reduces glucose
reasons for hyperglycemia
diabetes mellitus, acute stress response, cushing’s syndrome, pheochromocytoma, renal failure, acromegaly, pancreatitis
reasons for hypoglycemia
insulin overdose, pancreatic islet cell tumor, starvation, liver disease, addison’s disease, hypothyroidism
diabetes symptoms
polydipsia (thirsty), polyuria, polyphagia, fatigue, weight loss, blurred vision, slow healing, dizziness, nausea
ranges for fasting blood glucose
normal is under 100 mg/dl (really between 70-99), pre-diabetes is ≥100 mg/dl to <126 mg/dl, diabetes is ≥126 mg/dl
symptoms of hypoglycemia
sweating, hunger, trembling, anxiety, confusion, blurred vision
glucose tolerance test (OGTT)
used if diabetes is suspected - usually a 2hr OGTT (most commonly used) - patient fasts, then a FBS is taken and then is given an oral glucose load (75 g of glucose in 300 ml water) - tested 30 min, 1hr, 2hr, 3hr, and sometimes 4hr - normally there is a rapid insulin increase in response to the glucose load and peaks within the first hour and returns to normal in about 3 hours - 2hr mark should be less than 140
results of OGTT
patient with an appropriate insulin response are able to tolerate the glucose load and glucose does not spill into the urine - patient’s with diabetes will not tolerate the load and serum levels will be greatly elevated from 1 to 5 hours and glucose spills out in the urine
ranges for OGTT
normal is under 140 mg/dl, pre-diabetes is ≥140 mg/dl and <200 mg/dl, diabetes is ≥200 mg/dl
hemoglobin A1c test (HbA1c)
blood test used to determine how well a patient’s diabetes/blood sugar levels are being controlled - provides an average of your blood sugar control over a 6-12 seek period - normal range is 4-6% for those without diabetes - goal for patients with diabetes should be less than 7% (low A1c level means a significantly lower likelihood of experiencing complications from diabetes
what test is being recommended to becoming the new gold standard for diagnosing diabetes?
A1c assay
A1c ranges
normal is <5.6%, pre-diabetes is ≥5.7% to <6.5%, diabetes is ≥6.5%
diabetes mellitus diagnosis
diagnosis is <200 mg/dl or a FBS >126 or a ≥200 mg/dl on OGTT or ≥6.5 A1c - glycosuria is present when glucose levels exceed the renal threshold values (RTV may rise in some diabetics)
diabetes
patients often present with musculoskeletal and neurological complaints - only half of patients are aware of their disorder - the leading cause of kidney failure, lower-limb amputations, and adult-onset blindness
type 1 diabetes mellitus
insulin dependent - polyuria, polydipsia, hyperglycemia - most commonly seen in juveniles, circulating insulin is absent and plasma glucagon is elevated - autoimmune destruction of pancreatic islet beta cells, although the etiology is unknown - dependent on exogenous insulin to sustain life
type 2 diabetes mellitus
most common type, most patients are over 40 and obese with a family history - polyuria, polydipsia, hyperglycemia = circulating insulin is present but inadequate in times of increased need - insulin resistance or decreased amounts - may be controlled by diet, lifestyle, exercise, maybe oral hypoglycemic agents
gestational diabetes mellitus
occurs during pregnancy and disappears after delivery - tested between 24th-28th week - imbalance occurs between the mother’s ability to secrete insulin ad the diabetogenic hormones of pregnancy (estrogen and progesterone) which results in insulin resistance and glucose levels ride (hyperglycemia) - extra blood glucose goes through the placenta, giving the baby high blood glucose levels, which causes baby’s pancreas to make extra insulin to get rid of the blood glucose - since baby is getting more energy than it needs to grow and develop, the extra energy is stored as fat
what percent chance do people who had gestational diabetes have of developing diabetes in the next 10-20 years?
35-60%
diabetes mellitus complications
diabetic catarcts, diabetic retinopathy, glaucoma, diabetic nephropathy, diabetic neuropathy, vascular disease, skin lesions, foot gangrene, diabetic coma
diabetic coma/DKA - diabetic ketoacidosis
from a shortage of insulin - glycosuria, ketonuria, hyperglycemia, polyuria, polydipsia, fatigue, vomiting, mental stupor and can progress to coma, rapid breathing, fruity breath odor
hypoglycemia
blood glucose levels below 70 mg/dl - more common in a diabetic patient - anxiety, sweating, palpitations, tremor, hunger - if it persists, CNS glucose deprivation occurs and they may exhibit lethargy, headaches, confusion, visual disturbances convulsions, and coma - symptoms of reactive and fasting hypoglycemia are similar to diabetes-related hypoglycemia
reactive hypoglycemia
occurs within 4 hours after meals - under 70 mg/dl - also called postprandial hypoglycemia - relief of symptoms when glucose returns to normal (eat small meals and snacks about every 3 hours) - high blood sugar can result in excessive insulin secretion and results in lowered glucose levels - exercise regularly
fasting hypoglycemia
often related to underlying disease, various medications, excess insulin or carbohydrate deprivation, tumors like insulinoma, insulin overdose in diabetic, hormonal deficiencies, hepatic or renal disease - under 50 mg/dl - also called postabsorptive hypoglycemia - may need a 5 or 6 hour glucose tolerance test with measurements hourly
whipple’s triad
symptoms known or likely to be caused by hypoglycemia - a low plasma glucose measured at the time of symptoms - relief of symptoms when the glucose is raised
blood urea nitrogen BUN
measures the amount of urea nitrogen in the blood - urea is formed in the liver as an end product of protein metabolism and transported to the kidneys for excretion - this test is related to the metabolic function of the liver and excretory function of the kidneys - nearly all renal disease will elevate this - high protein diet may also elevate and severe liver disease and overhydration will decrease levels
azotemia
elevated blood levels of BUN
what 2 tests are the renal function tests
BUN and creatinine
creatinine
measures the amount of creatinine in the blood - catabolic product of creatine phosphate which is used in muscle contraction - only renal disorders can elevate this (so better indicator of renal disease than BUN) - levels tend to rise later and indicate chronicity
uric acid
nitrogenous compound that is a product of purine catabolism excreted by the kidney and a little by the intestinal tract - hyperuricemia (elevated levels) is associated with gout - may also be elevated in renal disease, metastasis, multiple myeloma, alcoholism, leukemias
radiographic findings of gout
soft tissue swelling, decreased joint space, nonmarginal erosions (overhang sign)
gout of the big toe is called what?
podagra
proteins
constituents of muscle, enzymes, hormones, hemoglobin, etc. - most significant factor for osmotic pressure, keeping fluids within the vascular space - increased in multiple myeloma, dehydration, chronic infections, and malignancies - decreased in liver disease, kidney disease, and malabsorption diseases
what 2 proteins constitute most of the protein in the body and are measured as the total protein?
albumin and globulin
albumin
formed in the liver and makes up 60% of the total protein and helps regulate colloidal osmotic pressure and transports important blood constituents - measure of liver function - levels are decreased in liver disease, malnutrition, overhydration, inflammatory diseases - increased levels with dehydration
globulins
the key building block of antibodies and some are used in transport of various proteins
example patients who would have decreased levels of total proteins
malnourished, burn, and protein losing uropathy patients
albumin/globulin ratio
if albumin is low and globulins are high, then the total proteins may be normal - normally the ratio exceeds 1.0 - diseases that reduce albumin reduce the ratio - diseases that increase total proteins particularly the globulins (MM, malignancy, inflammatory diseases) can reverse the ratio
what are some symptoms of hypercalcemia?
nausea, confusion, constipation, polyuria, and fatigue
biomarkers for multiple myeloma
hypercalcemia, hypercelciuria, elevated ESR, elevated protein in blood and urine, M spike on PEP, rouleaux formation, normocytic normochromic anemia, reversed A/G ratio, phosphorus is normal, alkaline phosphatase usually is normal or low, increased BUN and creatinine (kidney dysfunction), uric acid may be increased
biomarker stats for lytic metastasis
urine calcium often increased, serum calcium and phosphate usually normal or increased, serum ALP normal or increased, normocytic normochromic anemia
biomarkers for blastic metastasis
serum calcium usually normal, urine calcium is low, ALP is increased, acid phosphatase increased (prostate - PSA), serum phosphorus variable, normocytic normochromic anemia
bilirubin
measures excretory function of the liver - metabolism for this begins with the breakdown of RBC in the RES, hemoglobin released from RBCs is broken down into heme and iron, heme is transformed into bilirubin (unconjugated) in the liver it is converted to conjugated bilirubin - increased levels may be due to unconjugated or conjugated bilirubin - total serum bilirubin is the sum of both types
elevated bilirubin
causes jaundice and need to determine if conjugated or not - hepatocellular dysfunction results in elevated unconjugated bilirubin as does increased RBC hemolysis - liver disease and extrahepatic obstruction such as gallstones, tumor blocking bile ducts, results in elevated conjugated bilirubin
urobilinogen parameters
increased in liver/biliary disease, absent with biliary obstruction, increased in hemolytic anemia - these findings are from the urine
bilirubin parameters
positive with liver/biliary disease, positive with biliary obstruction, negative/absent in hemolytic anemia
primarily unconjugated hyperbilirubinemia
increased production (from hemolysis, intravascular or extravascular, ineffective erythropoiesis, hematoma, or pulmonary embolus), decreased hepatic uptake, decreased glucuronidation
primarily conjugated hyperbilirubinemia
decreased liver excretion (intrahepatic), extrahepatic biliary obstruction, external compression - increased in conjugated bilirubin are highly specific for disease of the liver or bile ducts
alkaline phosphatase ALP
found in many tissues, the highest concentrations are found in the liver, bone, biliary tract epithelium, placenta, and intestinal mucosa - detection of this enzyme is important in detecting liver and bone disorders (particularly blastic problems)
when is ALP elevated?
in intrahepatic and extrahepatic obstructions, biliary disease, and cirrhosis, tumors, hepatitis, liver metastasis
what is the most important site for extrahepatic ALP?
bone - new bone growth is associated with elevated ALP (osteoblastic activity) - high in adolescents, pathological new bone growth like blastic mets, Paget’s, bone disease, healing fractures, and hyperparathyroidism - decreased in hypothyroidism and pernicious anemia
what should you do if there is elevated ALP?
a liver function test (GGTP) - is normal LFT, then non-liver problem - if abnormal LFT, then liver/biliary tract problem
osteopoikilosis
multiple bone islands
chondrocalcinosis etiologies
cartilage degeneration = DJD
crystal deposition = primary is CPPD, then gout
cation disease = hemochromatosis Fe++, hyperparathyroidism HPT Ca++, wilson’s disease Cu++
acid phosphates - prostatic acid phosphatase PAP
this is found in many tissues but highest levels are found in the prostate gland - levels primarily used to diagnose, stage, and monitor treatment of metastatic cancer of the prostate
when are PAP levels elevated
with prostatic cancer that has metastasized beyond the prostate capsule to other parts of the body, especially to bone - may also be seen in MM and benign prostatic hypertrophy or a recent prostate exam - PAP is normal in a confined tumor with enlargement
prostate specific antigen
glycoprotein found in the cytoplasm of prostate epithelial cells - can be detected in all males - elevated levels are seen with prostate cancer, the higher the levels, the greater the tumor burden - a sensitive test to monitor treatment, more sensitive and specific than other tumor markers like PAP - may be elevated in benign prostatic hypertrophy and prostatitis
PSA level parameters
between 4-10 ng/mL is considered suspicious - levels >10 ng/mL has high probability of being cancer
PSA velocity
change in PSA level over time - a sharp rise raises the suspicion of cancer
signs indicating prostate cancer metastasis to bone
markedly elevated PAP and PSA with elevated ALP
age dependent ranges
slide 189 - ask if he’ll provide normal ranges
lactate dehydrogenase
catalyzes lactate to pyruvate - is found in many tissues - total LDH is not a specific indicator of any one disease - disease affects cells that contain LDH, the cell lyses and releases LDH
gamma-glutamyl transpeptidase GGTP
an enzyme that participates in transfer of amino acids and peptides across cell membranes - highest concentrations are found in the liver and biliary tract - lesser concentrations are found in the kidneys, spleen, and heart - test is used to detect liver cell dysfunction (sensitive to liver disease) - sensitive to chronic alcohol ingestion and is the most sensitive test for alcohol induced liver disease
when is GGTP not elevated?
on bone disease - if ALP is elevated with GGTP, it would imply skeletal disease
elevated GGTP and ALP implies what?
hepatobiliary disease
aspartate aminotransferase AST
enzyme which removes the amino group from aspartate - when diseased cells lyse, they release AST - AST/SGOT is one of the cardiac enzymes - widely used for suspected coronary occlusive heart disease or suspected hepatocellular disease - found in heart, liver, and skeletal muscles - rises uickly and returns to normal in 3-4 days
is AST/SGOT or ALT/SGPT more sensitive for the liver?
ALT/SGPT
is AST/SGOT or ALT/SGPT more sensitive for the heart?
AST/SGOT
alanine aminotransferase ALT
found predominantly in the liver and in lesser quantities the heart, kidneys, and skeletal muscles - injury or disease of the liver will release this enzyme - generally elevated with liver disease
components of liver panel
AST (heart), ALT (liver), ALP, LDH, GGTP, protein (especially albumin), bilirubin - a UA would also be helpful
electrolytes
substances whose molecules dissociate into ions when in solution - total cations equal total anions to maintain electroneutrality - major functions are to maintain osmotic pressure, water distribution, proper pH, regulation of proper heart and muscle function - profile includes sodium, potassium, chloride, and bicarbonate
sodium
major extracellular cation and is important for water distribution and osmotic pressure in plasma
potassium
major intracellular cation and is important to cellular metabolism and normal neuromuscular function, particularly of the heart
chloride
major extracellular anion and is important in maintaining cellular integrity through water balance and osmotic pressure
bicarbonate
major component of carbon dioxide in plasma, helps regulate acid-base balance
minerals
calcium: 99% in bone and involved with neurotransmission and muscular contraction
phosphorus: 80-85% in bone
magnesium: 50-60% in bone, cofactor for enzymes, activator for some enzymes, neurotransmission and muscular contraction
calcium
can evaluate parathyroid function - hypercalcemia typically associated with muscle weakness and disorientation seen with skeletal metastasis, HPT, MM, hyperthyroidism, renal transplant - hypocalcemia typically associated with tetany and seen with hypoalbuminemia (alcoholics), renal failure, vitmain D deficiecny, hypoparathyroidism
2 most common causes of hypercalcemia
primary hyperparathyroidism, then malignancy - make up >90% of cases
hyperparathyroidism
overactivity of the parathyroid gland - PTH is a strong osteoclastic hormone - primary cause is adenoma - secondary is chronic renal disease (hemodialysis - renal osteodystrophy (secondary and tertiary HPT))
primary HPT
most common type and cause of hypercalcemia in ambulatory patients - parathyroid adenoma in 90% of cases - elevated PTH, hypercalcemia, hypophosphatemia
sestamibi parathyroid scan
procedure of nuclear medicine performed to identify hyperparathyroidism
secondary HPT
complication of chronic renal disease - persistent loss of calcium and phosphorus - stimulates PTH release (high PTH and low to normal calcium) - hyperphosphatemia (kidney’s can’t excrete it as well)
tertiary HPT
seen in dialysis patients, parathyroid gland acts independent of serum calcium levels (high PTH and calcium)
demographics for HPT
30-40 women more than men - bone pain, fractures, weakness, lethargy, polydipsia, polyuria, may have renal stones, pancreatitis, elevated ALP and PTH - hypercalcemia in primary, normal to low in secondary, elevated in tertiary
parathormone physiology
maintains the circulating level of calcium ion - stimulates osteoclasts to resorb bone and release calcium and phosphorus ion into the blood stream = increased calcium absorption through small intestine —> renal tubular phosphate excretion and calcium absorption which upsets homeostasis - in secondary HPT, calcium loss and abnormal vit D formation leads to hypocalcemia and release of PTH
HPT radiography
osteopenia, subperiosteal resorption, distal tuft resorption (acro-osteolysis), accentuated trabeculation, brown tumors (cystic accumulations of fibrous tissue), loss of cortical definition, soft tissue calcification (metastatic calcification - vascular calcification), salt and pepper skull
subperiosteal resorption
most definitive radiographic sign of HPT (pathognomonic) - seen especially at the radial margins of middle and proximal phalanges of the 2nd and 3rd digits - outer cortical erosion may appear frayed or lace life - widened joint spaces and osteolysis especially of AC and SI joints
what kind of relationship do phosphorus and calcium have?
inverse one
hyperphosphatemia
seen with renal failure, hypoparathyroidism, excess vit D, bone metastasis, myeloma, and cell destruction
hypophosphatemia
seen with decreased intestinal absorption, increased renal excretion, HPT
hypermagnesemia
seen with dehydration, renal insufficiency, uncontrolled diabetes
hypomagnesemia
seen with malabsorption, malnutrition, alcoholism, cirrhosis typically accompanied by tetany, muscle weakness, and cardiac arrhythmias
a decrease in magnesium results in what?
calcium being released from bone and increased deposition in aorta and kidney
chamberlain’s line
odontoid can go no further than 3mm above this line
mcgregor’s line
odontoid can go no further than 4.5mm above this line
what does a bone panel consist of?
calcium, phosphorus, alkaline phosphatase, acid phosphatase (male), PSA (male), uric acid, total proteins, A/G ratio, serology, CBC/ESR/CRP
amylase
most specific for pancreatitis (upper quadrant, epigastric severe pain, mid back pain) - normally secreted by pancreas and aids in catabolism of carbohydrates - damage to pancreatic cells (pancreatitis and tumor) cause outpouring of this enzyme - rises quickly and returns to normal rapidly unless it’s a persistent condition
lipase
most common cause of elevated levels if acute pancreatitis - secreted by pancreas into duodenum to break down triglycerides into fatty acids - increased levels are released with damage to pancreatic cells - elevates a littler later and lasts a little longer than amylase