Exam 2 Flashcards

(158 cards)

1
Q

Malignant

A

capable of metastasis

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2
Q

tumor

A

a non-specific term meaning lump or swelling

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3
Q

metastasis

A

discontinuous spread of malignant neoplasm

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4
Q

neoplasm

A

uncontrolled growth of cells

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5
Q

cancer

A

any malignant tumor/neoplasm

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6
Q

carcinoma in situ (CIS)

A
  • cancer in place
  • has not through basement membrane yet
  • if caught in this stage it can be cut out to cure it
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7
Q

TNM system

A
  • describes staging
  • T: describes tumor (0-3)
  • N: lymph nodes (0-2)
  • M: metastasis (0-2)
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8
Q

staging

A

describes extent of spreed

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9
Q

Dysplasia

A
  • premalignant state
  • if it stays there it will become cancer
  • doesn’t necessarily progress to malignancy
  • usually occurs in the epithelium
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10
Q

carcinogenesis

A

the creation of cancer

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11
Q

cachexia

A

generalized wasting that occurs in terminal cancer

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12
Q

grading of tumor

A
  • shows how differentiated or undifferentiated cells are

- degree of differentiation roughly estimates tumors malignant potential

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13
Q

CAUTION

A
  • Changes in bowel/bladder habits or functions
  • A sore that doesn’t heal
  • Unusual bleeding or discharge
  • Thickening or lump in breast or elsewhere
  • Indigestion or difficulty swallowing
  • Obvious changes in a wart or mole
  • Nagging cough or horseness
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14
Q

lifestyle choices that reduce risk of cancer

A
  • don’t use tobacco
  • sun safely
  • diet (processed foods are carcinogens)
  • drink alcohol moderately
  • exercise regularly
  • vaccinations (HPV)
  • safe sex practices
  • maintain a healthy weight
  • self-examinations
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15
Q

what is the most deadly cancer in adults?

A

lung cancer

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16
Q

which cancer is the most common in women?

A

breast cancer

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17
Q

which cancer is the most common in men?

A

prostate cancer

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18
Q

proto-oncogene

A

a normal gene

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19
Q

oncogene

A
  • mutated proto-oncogene

- “green light”

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20
Q

KRAS oncogene

A
  • mutation of the RAS proto-oncogene
  • mutated RAS leads to activation of protein which stimulates transcription
  • mutation in RAS causes it to always be “on” making cells grow really fast
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21
Q

tumor suppressor genes

A
  • they detect and repair DNA damage before they can go through mitosis
  • “red light”
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22
Q

mutation of Tumor Suppressor p53

A
  • mutation causes the levels of p53 to increase in a cell
  • results in:
    1. ) recruit in DNA repair
    2. ) senescence
    3. ) death by apoptosis
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23
Q

what is the most mutated tumor suppressor gene?

A

p53

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24
Q

what is the function of tumor suppressor gene p53

A

stops the cell cycle and usually found in low amount in cells

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25
senescence
the cell is still alive but it will never divide again
26
how is cancer a multi-hit development?
in order for cancer to acquire a malignant phenotype it needs to have multiple mutations (hits) to genome
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etiology of cancer
-cancer occurs due to mutations in DNA
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what cells does cancer occur in
somatic or germ cells
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why is cancer hard to treat?
each cancer is genetically unique, not everyone's is the same
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manifestations of cancer
1. ) mass 2. ) hormone production 3. ) systemic manifestation 4. ) cachexia
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paraneoplastic syndrome
manifestation of aberrant and uncontrolled hormone production by a malignant neoplasm EX: lung cancer produces unregulated cortisol, so it can be misdiagnosed as Cushings syndrome
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Surgery for treating cancer
- prevent cancer - cure depending on localization - biopsy for diagnosis - debulking surgery - palliative surgery: surgery to manage symptoms
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hormone therapy for cancer treatment
- activation or blockage of a receptor | - interferes with cellular growth and signaling
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ionizing radiation for cancer treatment
-targets cells in S phase so mutated DNA can't divide goals: -eradicate cancer without excessive toxicity -avoid damage to normal structure
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chemotherapy for cancer treatment
- given via IV - chemicals target ALL rapidly dividing cells (can't target only cancer dividing cells) - puts a base analogue in DNA that won't work
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symptoms of chemotherapy
- hair loss - low white blood cell count, can get sick more often - low red blood cell count, anemia - loss of appetite
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immunotherapy
- immune system sees mutant cell as foreign - it then stimulates own immune system to better recognize cancer cells - tumor antibodies
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targeted therapy
- "precession medicine": acts on specific molecular targets | - EX: HER2
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mammography
screening for breast cancer recommenced at age 40
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pap smear
screening for cervical cancer
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colonoscopcy/fecal occulta test
screening for colon cancer recommened at age 50
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what cancers are the most deadly?
cancers that don't have screening tests
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congenital disease
a disease that you are born with
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allele
variation form of a gene (EX: eye color)
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Non-disjuction
DNA doesnt pull apart correctly in meiosis
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Genetic disease
disease caused by abnormal DNA
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Karyotype
illustration of chromosomes that is used to visualize them and look for abnormailites and alterations
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Aneuploidy
when there is one or more extra or missing chromosomes which results in abnormal number
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what are the main causes of developmental diseases?
1.) birth defects/congenital anomalies
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how does a genetic disease develop?
- inherited by parents | - can occur in gamete development
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fetal alcohol syndrome causes and effects
- Cause: when mom consumes alcohol during pregnancy | - effects: fetal growth restriction, CNS abnormalities, and distinctive facial features
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what is Amniocentesis
- a sample of amniotic fluid is taken via needle to check for disease - has risk for miscarriage
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what is chorionic villi testing
- sample of projections (chorionic villi) of placenta are taken to test for disease - greater risk for pregnancy loss
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is Amniocentesis or CVT more accurate and why?
amniocentesis is more accurate because in CVT it takes samples of the placenta not direct samples of fetus
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who is recommended to have amniocentesis or CVT done?
- mother 35 or older - parents who have a child with genetic disease - family history
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Trisomy 21
- Down syndrome - 3 21 chromosomes (extra) - cause due to non-disjunction in mieosis 1
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what are manifestations of down syndrome
- intellectual impairment that varie - round face and slanted eyes - small stature - congenital heart defects - intestinal defects - increased risk for alzheimers
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Turners syndrome
- sex chromosome abnormalities - females only has 1 x (x)chromosome instead of 1 - causes: non disjunction - features: short in stature, webbing at neck, secondary sex organ don't develop, infertile/don't through puberty
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Kleinfelter syndrome
- sex chromosome abnormalitie - male has extra x chromosome (xxy) - causes: non disjunction features: tall, long limbs, breast development, secondary sex organs don't develop, infertile
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Autosomal dominant inheritance
- disease is expressed if only one copy is present | - affected person has 50% of passing disease to off spring
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Martan syndrome
- autosomal dominant disease - effects: tall w long limbs and fingers/toes, heart valves don't close correctly, eyes can detach from retinas, blood vessels more likely yo stretch, increase in cardiac death
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autosomal recessive inheritance
- need two copies of genes | - both parents must be carriers
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cystic fibrosis
- autosomal recessive disease - most common ARD affecting white mothers - causes mutation in chloride channels which regulates chloride and sodium movement - effects: thick, sticky mucus that doesn't move
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Sickle cell disease
- mutation in hemoglobin that alters RBC' shape - leads to microinfarct due to ischemia - RBC's will be removed by body but can result in anemia
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Sex-linked inheritance
- mutation on the X or Y chromosome | - more likely to occur on the X chromosome because it is bigger
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Duchenne Muscular Dystrophy
- mutation on X chromosome causing neuromuscular disease - diagnosis: around 2-3 years - wheelchair bound at 12 years
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teratogen
- harmful drug/chemical that affects the development of a fetus - EX: cigarettes, alcohol, radiation, and infections
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when is the embryonic period
first 8 weeks after fertilization
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when is the fetal period
9-38th weeks of pregnancy
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when is the perinatal period
- "around birth" | - 2 weeks before birth to 1 month after birth
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when is infancy
after birth to one year
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when is childhood
- after infancy to before adolescene | - 1 to puberty
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when does adolescence begin
once child hits puberty
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what is the most common embryonic and fetal disease?
congenital heart defects
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Sudden Infant Death Syndrome (SIDS)
- unexpected, sudden death of child under age of 1 - risk factors: co-sleeping, sleeping on stomach, premature birth, cigarettes, sibling who had SIDS, teen mom, no prenatal care, live in poverty
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what is the most common cause of death in children?
drowning
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what is a common disease pf a premature baby?
cerebral palsy
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edema
increase in fluid for the interstitial space
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effusion
accumulation of fluid in a body cavity
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Thrombus
an abnormal intravascular clot which can occur in any vessel within the heart (stationary)
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embolus
"traveling blood clot" | -detaches from thrombus and is carried into the pulmonary or systemic circulation
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Arterioscelorsis
hardening of the arteries
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Atherosclerosis
- type of arterioscelrosis | - inflammation/degenerative disease
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Ascites
fluid in abdonmial cavity (effusion)
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Aneurysm
ballooning/weakening of an artery
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Common causes of edema
1. ) increase in hydrostatic pressure 2. ) decrease in osmotic pressure due to loss of albumin 3. ) kidney/liver disease 4. ) lack of protein in diet
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hydrostatic pressure
blood pressure pushes fluid out of vessels
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osmotic pressure
- water move into vessels due to concentration gradient | - determined by amount of albumin in blood
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lymph
fluid that comes out of blood composed of water, proteins, and white blood cells, that the lymphatic system will return back to blood
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hemangioma
capillaries that divide locally and form a red spot on the skin (painless, benign, won't grow
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lymphangioma
dilated pass of lymphatics (lump on skin, not red)
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how does atherosclerosis develop?
injury to endothelial cells in arteries which eventually lead to endothelial cell dysfunction
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what occurs in atherosclerosis?
1. increase in permeability causing accumulation of macrophages and smooth cells 2. ) lipid accumulation (fatty streaks) and possibly plaque
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how does atheroscelorsis harm?
1. ) narrows lumen causing ischemia 2. ) weakens vessels wall causing aneuryam 3. ) rupturing plaque causing exposure to collagen forming a thrombus
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what are the complications of atherscelrosis
1. ) coronary arteries can narrow and cause heart attack 2. )abdominal aorta can develop aneurysm 3. )arteris of lower limbs can cause decreased blood flow leadng to intermittent claudication
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what is hypertension
high blood pressure above 140/90
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primary hypertension
- hypertension that is the main problem - majority of cases - idiopathic
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secondary hypertension
- hypertension that is due to another disease | - EX: tumor on adrenal causes extra cortisol which increase blood pressure
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what organ systems are effected by hypertension?
1. ) CNS: more likely to have stroke 2. ) cardiovascular system 3. ) kidneys: main cause of dialysis
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aortic dissection
- tunica media of the aorta splits into two - fatal - feels like ripping sensation in chest anf dizziness
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medication for hypertension
1. ) diuretics | 2. ) ACE inhibitors
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diuretics
increase urination which decreases cardiac output by lowering mean arterial pressure
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ACE inhibitors
- cause lower levels of angiotensin 2 - increases TPR - lowers cardiac output by causing less sodium and water retention
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treatments of hypertension that is not medication
1. ) physical activity 2. ) diet: reduce sodium, increase fruits and veggies (magnesium and potassium) - parts of DASH diet
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risk factors of atherscelrosis
1. ) major: - elevated blood lipids - hypertension - cigarette smoking - diabetes - obesity 2. ) Minor: - age - gender - stress - family history
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venous thrombus
- thrombophlebits - clot forming in deep leg veins bc blood os stationary - caused by prolonged bed rest, cramped position for long time, genetic factors
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what is the risk for a venous thrombus?
deep vein thrombus: peice of clot comes off and can get into heart causing pulmonary embolsim
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varicose veins
- dialted, cury veins - due to incompetent valve - causes: genetics, standing - complication: pain and visibility - treatment is surgery
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what is shock
failure to maintain adequate blood pressure
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how is shock manifested?
- decreased blood flow - increased heart rate - decreased urine output - altered state of conscicousness
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cardiogenic shock
pump fails due to heart attach
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hemorrhagic shock
loss of blood volume, usually due to truama
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anaphylactic shock
- systemic allergic reaction causing WBC's to release vasodilators everywhere - blood pressure drops quickly
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septic (sepsis) shock
-blood infections leading to massive vasodilation
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treatment of shock
- remove stressor - fluids (saline) - vasoconstriction agents - antibiotics - surgically repair beelding arteries
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where is the mitral valve located?
between the left atrium and ventricle
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where is the tricuspid valve located?
between the right atrium and ventricle
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where is the pulmonary valve located
between the right ventricle and pulmonary artery
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where is the aortic valve located
between the left ventricle and aorta
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angina
chest pain
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cardiomyopathy
disorder involving the chambers of the heart
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valvular stenosis
valves doesn't open all of the way
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valvular regurgitation
valve doesn't close all the way
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echcardiography
uses ultrasound to see the heart and look for valve and chamber abnormalities
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angiogram
a catheter is placed up the femoral artery and into the heart to view it
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fibrillation
"quivering" of the chambers instead of contractions
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what are the most common cardiac disorders?
1. ) athersclerosis 2. ) hypertension heart disease 3. ) aortic stenosis 4. ) Afib 5. ) heart failure
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signs and symptoms of heart faillure
- fluid build up in lungs and other tissues - shortness of breath due to pulmonary edema - edema in extremities
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Chest X-ray
can view if there is any fluid in lungs
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serum enzyme level
when cells die via infarct they release enzymes
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electrocardiogram (ECG/EKG)
- looks at the electrical activity of the heart - track rhythm and look arrythmia - detect heart attack
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what is the P wave
atrial depolarization
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what is the QRS complex
ventricular depolarization
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what is the T wave
ventricular repolarization
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atrial and ventricular septal defects
- defect in the septum between the atria and ventricle | - mixes CO2 and O2 blood
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manifestations of atrial and ventricle septal defects
- murmur - easily fatigues - heart failure: due to hypertrophy of ventricles
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defects of Tetralogy of Fallot
1. ) ventricular septum defect 2. ) pulmonary stenosis: pulmonary valve can't open all the way 3. ) hypertrophy of right ventricle 4. ) overriding aorta: aorta is located above both ventricle
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manifestations of tetralogy fallot
1. ) cyanosis (blue) 2. ) slow growth 3. ) heart failure 4. )reduced like expectancy
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pulmonary circuit
on the right side of heart | -receives and pumps CO2 blood from body to lungs
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systemic circuit
on left side of heart | -recieves O2 blood from the lungs and pumps it to the body
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Aortic regurgitation
- most common vavlular disorder - leaflets of aortic valve undergo changes that restrict mobility - causes left ventricle to work harder resulting in hypertrophy - can lead to heart failure
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Rheumatic Fever (scarlet fever)
- streptococcal bacteria - WBC's invade the - valves look like the bacteria so WBC's attach to valve and cause damage - disease does not cause the damage the immune system does
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what is the most common cause coronary heart disease?
arrhythmia's
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hypertensive heart disease
- hypertension causes an increase in work load on the heart | - in order for heart to drive blood flow it must overcome the systolic pressure
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manifestations of hypertension heart disease
- enlarged heart - heart failure - ischemia
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Myocardial infarct
- death of cells due to ischemia | - "heart attack"
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symptoms of Myocardial infarct
- angina - sympathetic NS response: increased HR, anxiety, vomiting - Hypotension and shock: weakness in arms/legs
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symptoms of MI in men and women
men are more likely to have the symptoms than women
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diagnosis of MI
1. ) EKG: look to see if in between the S and T wave is abnormal 2. ) enzyme serum test (creatine kinase, lactase dehydrogenase, and troponin) 3. ) coronary angiogram
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treatment of MI
- stent: holds wall of coronary artery open - angiopasy: destroys clot - cardiac bypass - lifestyle changes
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what is the goal of treatment in MI
restore blood flow immediately
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Bradycardia
slow resting heart rate
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tachycardia
increased resting heart rate
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Atrial Fibrillation
- atria "quivers" instead of contracting - blood will stay in the atria - increased risk for thrombus - caused by a disorganized electrical impulse
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ventricular fibrillation
- more serious - there is no coordination in the electrical impulses at all - no blood flow to body - need to use paddles to shock and reset the heart
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dilated cardiomyopathy
- dilation of the chamber - causes problem when contracting (systole) - muscles too far apart
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hypertonic cardiomyopathy
- chamber wall thickens - chambers can't hold as much blood - can lead to sudden cardiac arrest - leading cause of death in young athletes
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restrictive cardiomyopathy
- chambers are rigid which restricts stretching | - chambers can't relax and fill with blood (diastolic)