medsurg exam 1

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174 Terms

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1/3 americans
living w chronic stress
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Hans selye
stress theorist; began early research on stress in 1940 at McGill; studied stressors to animals -- formulated stress as a response which turned into GAS theory
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GAS theory (general adaptation syndrome)
describes the process your body goes through when you are exposed to any kind of stress, positive or negative
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stress definition
a response of the body to any demand made on it
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stressors
anything that induces stress - physical or emotional, pleasant, or unpleasant
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examples of stressors (physiologic)
skin burn, chronic pain, hypothermia, infectious disease, excessive noise, starvation
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examples of stressors (emotional/psychologic)
dx of cancer, marital probs, failing an exam, grief, winning lottery
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3 stages of gas theory
alarm, resistance, exhaustion
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alarm phase
in response to

activation of ___ “fight or flight”
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stage of resistance determined by
physical state of person, number of stressors they have, coping abilities; goal is adaptation
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stage of exhaustion
all energy for ____ is exhausted; may seen return of alarm phase, can be fatal
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holmes, rahe, and masuda
stress as a stimulus
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richard lazarus
stress as a transaction
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mediators of stress
hardiness, sense of coherence, resilience, hassles vs uplifts (attitude/optimism)
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hardiness
pt has clear sense of personal goals and values; has strong tendency toward interaction with an env; sense of meaningfulness is important; internal rather than external locus of ctrl
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sense of coherence
seen as more powerful than hardiness - refers to how person sees the world and their place in it
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SOC terms
comprehensibility, manageability, meaningfulness
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comprehensibility
the sense that internal and external stimuli are ordered and make sense
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manageability
that there are resources available as needed
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meaningfulness
sense that demands that one faces are worthy of taking on
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resilience
ones is resourceful, flexible, and a good problem-solver
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hassles vs uplifts (attitude)
balance of the two within one’s life and how the stressors are viewed
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attitude
positive = can mean quicker recovery

pessimism can = poorer health
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link bt stress and illness
positive relationship bt stress and infection

latent viruses

aids

breast cancer incidence and recurrence

heart disease

accidents and suicide
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immune system
acute and chronic stress can cause immunosuppression
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immunosuppression from stress bc
decreasing # and function of natural killer cells

decreasing lymphocyte proliferation

altering production of cytokines

decreasing phagocytosis
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theories?
not as important as how you will recognize stress in your pt at the bedside and how you’ll manage that stress
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assist pt to handle stress by
relaxation, imagery, medication, therapeutic touch, 4x4 breathing techniques, prayer + spiritual encouragement
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relaxation
opposite of fight or flight
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imagery
seeing the fight (ex: cancer patients)
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therapeutic touch
systematic manipulation of soft tissue to reduce tension
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hematology
study of blood and blood forming tissues, including the blood cells, bone marrow, spleen, and lymph system
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bone marrow
soft center of bones, home of stem cells; located in sternum, ribs, scapulae, clavicle, pelvis, flat cranial bones end of long bones
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yellow matter
sponge that helps protect bone
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red marrow
stem cells stimulate from; gives us white & red cells & platelets
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3 types of blood cells
erythrocytes (RBCs), leukocytes (WBCs), thrombocytes (platelets)
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complete blood count (CBC)
erythrocytes; males: 4.3-5.7 million/ul; females: 3.8-5.1
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hemolysis
destruction of damaged/abnormal RBCs
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2 reasons for decreased RBCS
age or immunocompromised
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hemoglobin
combo of heme (iron) and globin (protein); binds with oxygen and carbon dioxide and represents oxygen carrying capacity of RBCs; low in anemia and hemodilution
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HGB levels women
11\.7-16 g/dL
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HGB levels men
13\.2-17.3 g/dL
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hematocrit
measured as %; percentage of RBCs in relationship to total blood volume; best representative of blood volume loss
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HCT levels women
35-47%
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HCT levels men
39-50%
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when HCT goes down (in hydrated pts)
RBCs go down
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in dehydrated pts HCT
elevates with normal RBCs
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mean corpuscular volume (MCV)
measure of average volume or size of single RBC and is used in classifying anemias; NORMAL: 80-100 fL
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mean corpuscular hemoglobin (MCH)
measure of average amount (weight) of hemoglobin within an RBC; NORM: 27-34 pg
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mean corpuscular hemoglobin concentration (MCHC)
measure of average concentration or percentage of hemoglobin within a single RBC; NORM: 32-36%
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WBC levels
5,000-10,000 ul
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neutropenia (or leukopenia)
WBC
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platelets levels
normal: 150,000-400,000

critical values:
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platelets clotting
activated by interstitial collagen, aggregate and form a plug, vascular response + plug + clotting factors = fibrin clot
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spleen
filters out old RBCs and takes hemoglobin and hemolysis and catabolizes the iron; contains lots of lymphocytes and monocytes; sequesters 30% of platelets
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effects of aging
stem cells drop after age 30 & again after 65; hemoglobin drops after middle age; WBC increase less w infection
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assess
hx, meds, surgeries, family hx, nutrional hx, signs of bleeding, exercise level, reproductive pattern, lab values
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erythrocytes sedimentation rate (ESR)
rate at which RBCs setting in saline over specified perioid (1hr); nonspecific measure of inflammatory conditions
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ESR normal range
less than 30 mm/hr - usually women higher than men
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serum iron lab test
iron + proteins; 50-175 mcg/dl
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TIBC
proteins available to bind to iron; 250-425 mcg/dl
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Ferritin
major iron storage protein; 10-250 mcg/dl
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transferrin
largest protein that binds w iron (190-380 mcg/dl)
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serum iron goes up
TIBC down
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Serum iron up
ferritin up (& vice versa)
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prothrombin time (PT)
assessment of clotting times for factors I, II, V, VII, X
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normal PT
11-16 seconds; above normal associated w vit. K deficiency or therapeutic coumadin dose
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activated partial thromboplastin time (PTT)
assessment of clotting times for factors I, II, V, VIII, IX, X, XI, and XII
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normal PTT
25-35 sec; therapeutic 60-70 sec
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international normalized ratio
standard method of reporting PT; normal: 0.5
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hemophilia
men get; hereditary bleeding disorder due to deficient clotting factors; A type - classic, factor VIII (80%), B type - christmas disease, factor IX
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von willebrand disease
involves congenitally acquired deficiency of coagulation protein
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medical mgmt of hemophilia
primary means of tx: replace clotting factor;

given during crisis and before procedures; assess for blood born infections, thrombosis; minor bleeds, tx for 72 hr, surgeries for 10-14 days; DDAVP may be used for mild type A and some von willeb. subtypes
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hemophilia joint bleed mgmt
rest joint, pack in ice, analgesics without aspirin, mobilize as soon as bleeding under ctrl without weight bearing (ROM)
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hemophilia nurs mgmt
genetic counsel referral, only female carriers, stop acute bleeds, assess for intracranial bleeds & airway obstruction from hemorrhage into neck and pharynx
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anemia
deficiency of # of erythrocytes, the quantity of HGB, and/or volume of packed RBCs (HCT)
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anemia compensation
shift oxygen from tissues to blood; shunt blood from tissues that dont need as much; increase cardiac output, HR, and stroke volume; increase # of RBCs produced
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iron deficiency
most common type; caused by inadequate diet, poor absorption, GI bleed, menstruation
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iron deficiency s/s
pallor, glossitis, burning of tongue, chelitis, headache, paresthesia
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tx for iron deficiency
treat underlying cause and iron replacement; may be given PO (give in acidic env like orange juice), IM (using Z-track method), or IV
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thalassemia etiology
genetics, mediterranean and equatorial regions of asian, middle easter, and african cultures
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thalassemia
inadequate production of HGB
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s/s of thalassemia
pale, thickening of cranium & maxillary cavity, hyperplasia of bone marrow, growth retardation and ultimately death
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tx for thalassemia
palliative transfusions and IV desferal/ferriprox; goal to keep Hgb bt 9-10 & prevent buildup of iron
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cobalamin deficiency (pernicious anemia)
insufficient amt of intrinsic factor; can be d/t gi surgery, crohns, chronic alcoholism
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s/s pernicious anemia
paraesthesia, ataxia, weakness, confusion or dementia
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normal b12 levels
190-950 pg/mL
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folic acid deficiency causes
Poor diets

Malabsorption disorders

Oral contraception

Patients on anti-seizure drugs

__Alcohol__ abuse / anorexia

Hemodialysis patients
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anemia of chronic disease causes
inflammatory, autoimmune, infectious, and malignant disease; treat underlying disease
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aplastic anemia
life threatening stem cell disorder resulting in pancytopenia
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aplastic anemia etiology
Congenital or Acquired (through Cancer treatment, infections tx, pregnancy, idiopathic)
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aplastic anemia sequelae
risk for infection, fatigue and dyspnea, cardiovas and cerebral vascular response, thrombocytopenia
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sickle cell anemia
family of __genetic__ disorders caused by the abnormal properties conveyed to RBC by mutated sickle cell hemoglobin; affects african americas, mediterranean, caribbean, s and central america, arabian or east indian
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incidence of sickle cell
1 in 375 births; incurable and often fatal by middle age;

´If both parents have the trait, ___25__% chance that each pregnancy will result in a child with sickle cell

´If only one parent has the trait, then __50%__ of children will have one trait
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prsentation of sickle cell
much like chronic anemia until crisis (v__ascular occlusion__ leading to pain and tissue death.  Lasts days to weeks.  Often without known cause, may result in shock)
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mgmt of sickle cell
\-Teamwork is essential

\-Lifestyle: avoid high altitudes, __hydrate__ well, treat infections promptly, Pneumovax and H flu __vaccines__

\-Treat the areas of tissue necrosis – ex. Chronic leg ulcers

\-Large doses of continuous narcotics to control pain during crisis

\-\`Stem Cell Transplant
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stems cells form new cells
when cells are damaged/die; when body needs mroe (like WBCs)
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all tissue
has stem cells
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initiation phase
inherited mutation; when host exposed to carcinogen, may be environmental, physical, or biological; sets cellular change into motion
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promotion phase
presence of agent creates correct env for dev; reversible