Exam 1 (3/1) Flashcards

1
Q

components of a cardiac assessment

A

gather health history:
Chest pain/discomfort
Pain/discomfort in other areas of the upper body
SOB/dyspnea
Peripheral edema, weight gain, abdominal distention
Palpitations
Unusual fatigue, dizziness, syncope, change in LOC

gather past health, family and social history:
Medications
Nutrition
Elimination
Activity, exercise
Sleep, rest
Self-perception/self-concept
Roles and relationships
Coping and stress
Physical assessment: 
General appearance
Skin and extremities
Pulse pressure
Blood pressure; orthostatic changes
Arterial pulses
Jugular venous pulsations
Heart inspection, palpation, auscultation
Assessment of other systems
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2
Q

Lab tests for the heart

A

Biomarkers—cardiac enzymes (CK, CK-MB, trop)- from myocardial cells r/t prolonged ischemia or trauma.

BUN—Blood urea nitrogen (and creatine)– kidneys

Lipids monitored in the development of CAD

Brain (B-type) natriuretic peptide- a neurohormone that helps regulate BP and fluid volume.

C-reactive protein- Liver Inflammation noted with atherosclerosis.

Homocysteine— atherosclerosis

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3
Q

age related changes in the cardiac system

A

Loss of function of the cells leading to slower heart rate
Size of heart increases due to hypertrophy
Reduced volume of blood
Reduced strength of contraction
Valves stiffen
Backflow of blood creates heart murmurs

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4
Q

cardiac tests

A

-Exercise stress test:
Pt walks on treadmill with intensity progressing according to protocols
ECG, V/S, symptoms monitored
Terminated when target HR is achieved

  • Echocardiogram:
    Noninvasive ultrasound test that is used to:
    Measure the ejection fraction
    Examine the size, shape, and motion of cardiac structures
  • Transthoracic endocardiogram
  • Transesophageal endocardiogram
  • Chest X-Ray (CXR)
  • Fluoroscopy: moving images on xray
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5
Q

What is an (ECG)?

A

12 lead ECG:
graphic representation of the electrical currents of the heart
diagnose dysrhythmias, conduction abnormalities, and chamber enlargement, as well as myocardial ischemia, injury, or infarction

All ECG’s:
Monitor more than one ECG lead simultaneously
Monitor ST segments (ST-segment depression is a marker of myocardial ischemia; ST-segment elevation provides evidence of an evolving MI)
Provide graded visual and audible alarms (based on priority, asystole merits the highest grade of alarm)
Interpret and store alarms
Trend data over time
Print a copy of rhythms from one or more specific ECG leads over a set time (called a rhythm strip)

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6
Q

What are cardiac enzymes? What are the expectations and concerns related to these?

A

Myocardial cells that become necrotic from prolonged ischemia or trauma release specific enzymes
These substances leak into the interstitial spaces of the myocardium and are carried by the lymphatic system into general circulation. As a result, abnormally high levels of these substances can be detected in serum blood samples

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7
Q

Heart catheterization

A

Invasive procedure used to diagnose structural and functional diseases of the heart and great vessels
Right Heart Cath: Pulmonary artery pressure and oxygen saturations may be obtained; biopsy of myocardial tissue may be obtained
Left Heart Cath: Involves use of contrast age

Post procedure care:
Observe cath site for bleeding, hematoma
Peripheral Neurovascular assessment
Evaluate temp, color, and cap refill of affected extremity
Screen for dysrhythmias
Maintain bed rest 2 to 6 hours
Instruct patient to report chest pain, bleeding
Monitor for contrast-induced nephropathy
Ensure patient safety
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8
Q

age-related changes in cardiac system

A

Loss of function of the cells leading to slower heart rate
Size of heart increases due to hypertrophy
Reduced volume of blood
Reduced strength of contraction
Valves stiffen
Backflow of blood creates heart murmurs

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9
Q

Causes of Heart failure

A

causes: coronary artery disease, hypertension, cardiomyopathy, valvular disorders, renal dysfunction, diabetes, atherosclerosis
patho: body activates compensatory hormines, structure of heart changes leading to low CO

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10
Q

Manifestions of Heart Failure

A
RIGHT SIDED:
viscera & peripheral conjestion
JVD
dependent edema
hepatomegaly
ascites (accumulation of fluid in abdomen)
weight gain
LEFT SIDED: 
pulmonary congestion "crackles"
S3 or "ventricular gallops"
dyspnea on exertion
low O2 sat
dry nonproductive cough
oliguria (small amount of urine only)
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11
Q

Management of Heart Failure

A

Angiotensin-converting enzyme (ACE) inhibitors: vasodilation; diuresis; decreases afterload; monitor for hypotension, hyperkalemia, and altered renal function; cough

Angiotensin II receptor blockers: prescribed as an alternative to ACE inhibitors; work similarly

Hydralazine and isosorbide dinitrate: alternative to ACE inhibitors

Beta-blockers: prescribed in addition to ACE inhibitors; may be several weeks before effects seen; use with caution in patients with asthma

Diuretics: decreases fluid volume, monitor serum electrolytes

Digitalis: improves contractility, monitor for digitalis toxicity especially if patient is hypokalemic

IV medications: indicated for hospitalized patients admitted for acute decompensated HF

Milrinone: decreases preload and afterload; causes hypotension and increased risk of dysrhythmias

Dobutamine: used for patients with left ventricular dysfunction; increases cardiac contractility and renal perfusion

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12
Q

Nursing Process with HF

A
Assessment: 
Focus on:
-Effectiveness of therapy
-Patient’s self-management 
-S&S of increased HF
-Emotional or psychosocial response
Health history
Physical Exam
Mental status
 lung sounds: crackles and wheezes
heart sounds: S3; fluid status or signs of fluid overload
daily weight and I&O
assess responses to medications

Diagnosis:
Activity intolerance related to decreased CO
Excess fluid volume related to the HF syndrome
Anxiety-related symptoms related to complexity of the therapeutic regimen
Powerlessness related to chronic illness and hospitalizations
Ineffective family therapeutic regimen management

Planning:
-Goals-
-Promote activity and reduce fatigue
-Relieving fluid overload symptoms
-Decrease anxiety or increase the patient’s ability to manage anxiety
-Encourage the patient to verbalize his or her ability to make decisions and influence outcomes
-Educate the patient and family about management of the therapeutic regimen
-interventions-
activity intolerance:
Bed rest for acute exacerbations
Encourage regular physical activity; 30 to 45 minutes daily
Exercise training
Pacing of activities
Wait 2 hours after eating for physical activity
Avoid activities in extreme hot, cold, or humid weather
Modify activities to conserve energy
Positioning; elevation of the head of bed to facilitate breathing and rest, support of arms
Fluid volume excess:
Assessment for symptoms of fluid overload
Daily weight
I&O
Diuretic therapy; timing of meds
Fluid intake; fluid restriction
Maintenance of sodium restriction

Potential complications:
Hypotension
poor perfusion
cardiogenic shock 
Dysrhythmias 
Thromboembolism 
Pericardial effusion
cardiac tamponade
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13
Q

Heart failure pt education & end of life considerations

A

-education-
Medications
Diet: low-sodium diet and fluid restriction
Monitoring for signs of excess fluid, hypotension, and symptoms of disease exacerbation, including daily weight
Exercise and activity program
Stress management
Prevention of infection
Know how and when to contact health care provider
Include family in education

-end of life-
HF is a chronic and often progressive condition:
Need to consider issues related to the end of life
When palliative or hospice care should be considered

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14
Q

Pulmonary edema Patho

A

Acute event results in LV failure
As LV begins to fail, blood backs up into the pulmonary circulation, causing pulmonary interstitial edema
Results in hypoxemia, often severe

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15
Q

manifestations of Pulmonary edema

A

restlessness, anxiety, dyspnea, cool and clammy skin, cyanosis, weak and rapid pulse, cough, lung congestion (moist, noisy respirations), increased sputum production (sputum may be frothy and blood tinged), decreased level of consciousness

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16
Q

Management of pulmonary edema (fluid in the lungs)

A

Easier to prevent than to treat
Early recognition: monitor lung sounds and for signs of decreased activity tolerance and increased fluid retention
Minimize exertion and stress
Oxygen; nonrebreather
Medications: Diuretics (furosemide), vasodilators (nitroglycerin)

Nursing Management:
Positioning the patient to promote circulation- Positioned upright with legs dangling
Providing psychological support- Reassure patient and provide anticipatory care
Monitoring medications- I&O

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17
Q

Risk factors of Peripheral Areterial Occlusive Disease (PAD)

A
Modifiable:
Nicotine, diet
Hypertension
Diabetes
Obesity 
Stress
Sedentary lifestyle
C-reactive protein
Hyperhomocysteinemia

Non-modifiable
Age
Gender
Familial predisposition and genetics

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18
Q

Manifestations of PAD

A

Intermittent claudication (aching, cramping, fatigue/weakness)
Occurs with activity, relieved with rest
Pain is due to critical ischemia
Persistent, aching, boring (rest pain)
Usually worse at night

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19
Q

Nursing Prosess for PAD

A

Assessment:
Health history
- Intermittent claudication
- Location of the pain (persistent in forefoot)
Physical assessment
- Skin (blue color (rubor) and cool/pale)
- Pulses (you cant feel it so use a doppler)

Diagnosis:
Ineffective Tissue Perfusion

Diagnostic evaluation:
Doppler Ultrasound
Magnetic Resonance Angiography
Angiography-
- confirms location of an obstruction or aneurysm
-Allergy to contrast:
- normal-sensation of warmth, local irritation at injection site
- Allergy reaction may be immediate or delayed—Dyspnea, nausea and vomiting, sweating, tachycardia, and numbness of the extremities
any reactions should be reported to the interventionalist immediately
Treatment generally includes epinephrine, antihistamines, and/or corticosteroids

Planning:
Medical Management
-Low-fat diet
-Controlled exercise
-Medication
-Antilipemics
-Anti-hypertensives
Surgical/Radiologic Interventions
-Angioplasty
-Atherectomy
-Stent grafts
Implementation:
Lower extremities below the level of the heart
Promote vasodilation
Application of warmth
Smoking cessation
Stress reduction
Encourage walking
Relieve pain (analgesics)
Maintain tissue integrity
Evaluation:
Extremities warm to touch & improved color
Walks further & with less pain
Reports less pain
Absence of injury or ulceration

Educate: lower the extremity below the heart, encourage moderate exercise, don’t be on extremity for too long

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20
Q

Venous Insufficiency

A
Chronic venous stasis:
Edema
Altered pigmentation
Pain
Stasis dermatitis
Prevention:
Application of graduated compression stockings
	Pneumatic compression devices
	Early ambulation
	Subcutaneous heparin or LMWH
	Lifestyle changes
		Weight loss
		Smoking cessation
		Regular exercise
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21
Q

Varicose veins

A
Dilated, tortuous veins:
Dull aches
Muscle cramps
Muscle fatigue lower legs
Nocturnal cramps

Prevention:
Avoid activities that cause venous stasis (wearing socks that are too tight at the top or that leave marks on the skin, crossing the legs at the thighs, and sitting or standing for long periods)
Elevate the legs 3 to 6 inches higher than heart level
Encourage to walk 30 minutes each day if there are no contraindications
Wear graduated compression stockings
Overweight patients should be encouraged to begin weight reduction plans

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22
Q

Leg Ulcers

A

Venous insufficiency can result from obstructed venous valves
Edema, altered pigmentation, pain, stasis dermatitis
Assessment: H & P
Diagnosis: Impaired skin integrity

Plan: Restoration of skin integrity

Interventions     
Medication - antiseptic agents, oral antibiotics, topical agents
GCS, elastic wraps, Unna boots
Debridement
Dressings
Hyperbaric oxygen
Negative pressure wound therapy
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23
Q

Lymphangitis

A

inflammation or infection of the lymphatic channels
Hemolytic streptococcus
Red streaks
Treat with antibiotics

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24
Q

Lymphadenitis

A

tissue swelling related to obstruction of lymphatic flow
Hemolytic streptococcus
Red streaks
Treat with antibiotics

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25
Q

Cellulitis

A

S&S: localized swelling or redness, fever, chills, sweating
Treat with oral or IV antibiotics based on severity
Nursing interventions:
Elevate affected area
Warm, moist packs to site every 2 to 4 hours
Educate regarding prevention of recurrence
Reinforce education about skin and foot care
look for points of entry

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26
Q

Lymphedema and elephantiasis

A

Tissue swelling due to increase lymph that results from obstruction of lymphatic vessels

  • Exercise
  • GCS
  • Manual lymphatic drainage
  • Diuretics
  • Surgery
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27
Q

Venous Thromboemolism (VTE) preventiosn risk factors

A
Endothelial damage (trauma, surgery, central venous or dialysis catheters, pacing wires, local vein damage, repetitive motion injury)
Venous stasis (bed rest/immobilization, obesity, spinal cord injury, age >65)
Altered coagulation (cancer, pregnancy, oral contraceptives, sepsis, polycythemia, protein C or S deficiency, factor V leiden defect)
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28
Q

Manifestation VTE

A
Swelling 
Throbbing pain 
Warm skin
Red or darkened skin 
Swollen veins that are hard/sore when touched
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29
Q

Nursing Process for VTE

A
Planning: 
Decrease Venous Congestion
Medical/Nursing Management:
Anti-gravity activities
Graduated compression stockings
Encourage walking
Maintain tissue integrity

Diasgnosis:
Ineffective Tissue Perfusion
Duplex Ultrasonography
Contrast Phlebography (Venography)

Implementation
Elevate extremities above the level of the heart
Discourage standing or sitting for prolong periods
Discourage constrictive clothing
Avoid crossing legs

evaluation: decreased edema

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30
Q

Management of VTE

A

Elevate extremity, GCS, SCDs
Warm, moist packs
Anticoagulants:
Monitor lab values
Monitor for bleeding
Know how to reverse anticoagulation effects
Encourage walking AFTER anticoagulation therapy has been started
Prophylactic medication- heparin, enoxaparin

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31
Q

DVT

A
Prevention:
Identify high-risk patients—Endothelial damage (trauma, surgery, central venous or dialysis catheters, pacing wires, local vein damage, repetitive motion injury), venous stasis (bed rest/immobilization, obesity, spinal cord injury, age >65), altered coagulation (cancer, pregnancy, oral contraceptives, sepsis, polycythemia, protein C or S deficiency, factor V leiden defect. 
GCS
Early ambulation
Leg exercises
Prophylactic medication
Heparin, Enoxaparin
Management:
Elevate extremity, GCS, SCDs
Warm, moist packs
Anticoagulants
Monitor lab values
Monitor for bleeding
Know how to reverse anticoagulation effects
Encourage walking AFTER anticoagulation therapy has been started
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32
Q

Hypertension categories

A

Primary or essential (95%)
secondary (5%)
gestational

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33
Q

Manifestations of hypertension & complications

A
vague symptoms
headaches
shortness of breath
nosebleeds
flushing
dizziness
chest pain
visual changes
blood in the urine
complications: 
Left ventricular hypertrophy
Myocardial infarction
Heart failure
Transient ischemic attack (TIA)
Cerebrovascular disease (CVA, stroke, or brain attack)
Renal insufficiency and chronic kidney disease
Retinal hemorrhage
34
Q

how to treat HTN

A
  1. try to change lifestyle, 2. if that does not work then add medication 3. if that doesnt work add or change med 4. add more meds

older adults start taking meds if SBP 150mm HG or > or if DBP 90 mmHg or >

interventions: Emphasize control, not cure.
Emphasize medication compliance, for rest of life- Discuss consequences of noncompliance.
Diet changes: Reduce salt & fat. Increase fruits & vegetables.
Regular physical activity.
Meds: Teach to identify, report, & minimize SE/AE:
- Orthostasis, sexual dysfunction, dry mouth, frequent urination
-Inform about rebound hypertension: Need adequate supply of meds available, esp. when traveling.
Support groups: AHA, National Heart, Lung & Blood Institute
Inform about need for regular follow-ups.

35
Q

Hypertensive Crisis

A
Symptoms:
Neuro: ha, confusion, change in LOC
blurred vision
CV: tachycardia
Resp: tachypnea & dyspnea

Assess:
BP every 5-30 min.
Hemodynamic monitoring
I & O

Have emergency equipment available.

Slowly reduce BP:
20%-25% in first hr
Over next 6 hr, reduce to goal 160/100 mm Hg
Then further reduction

Pharmacologic therapy:
vasodilators (sodium nitroprusside, nicardipine, enalapril, NTG)
HTN urgency: oral agents

Position: bed rest, HOB 45 degrees

Assess for hypotension r/t vasodilators
Fluid replacement, if needed

36
Q

Symptoms of Hypoxia (do not have enough oxygen in their system)

A

Early
R- restlessness
A- anxiety
T- tachycardia /tachypnea

is late to
B- bradycardia
E- extreme restlessness
D- dyspnea

(in prediatrics) 
F- feeding difficulty
I- inspiratory stridor
N- nares flare
E- expiratory grunting
S- sternal retractions
37
Q

3 P’s of dyspnea

A

Pulmonary bronchial constriction
possible foreign body
pulmonary emboulus
pump failure
Pneumothorax: Do not have enough room for the lungs to expand.
Pneumonia: Do not have enough capacity for air to get into lungs.

38
Q

Physical assessment of Respiratpry system

A

Normal breath sounds (vesicular, bronchovesicular, bronchial)

Abnormal breath sounds:
Crackles:
Short, discrete, crackling or bubbling sounds
Noted in pneumonia, bronchitis, CHF
Wheezes:
Continuous, musical sounds
Heard in bronchitis, emphysema, asthma
Rhonchi:
Deep, low-pitched rumbling sounds heard primarily during expiration.
Caused by air moving through narrowed tracheobronchial passages

39
Q

Diagnostic tests for the respiratory system

A
Pulmonary Function Tests
Cultures- throat, nasal, nasopharyngeal
Sputum Studies
Endoscopic Procedures
Bronchoscopy: For invasive procedures we need consent, nothing by mouth, pre and post procedure considerations. 
Thoracoscopy
Thoracentesis
Imaging studies:
Chest X-Ray
Computed tomography (CT)
Magnetic resonance imaging (MRI)
VQ Scan
Preparation, consent, NPO, Pre & Post-procedure considerations
Pulmonary angiography- To diagnose a PE
40
Q

Laryngectomy Nursing Process

A

Assessment:
H&P

Nursing Diagnoses:
Ineffective airway clearance
Impaired verbal communication
Imbalanced nutrition
Risk for aspiration

Plan:
Airway
Alternative means of communication
Nutrition and hydration

Interventions:
Monitor respiratory status
Position in semi-fowler or Fowler’s 
Perform laryngectomy/tracheostomy tube care 
Provide humidification
Utilize writing, hand gestures
Administer IV fluids, enteral (NG or GT), and/or parenteral  nutrition
Obtain swallow study before PO
41
Q

Atelectasis

A
I = incentive spirometry
C = cough and deep breathing
O = oral care
U = understanding
G = getting out of bed
H = head of bed elevated
42
Q

Aspiration

A

Inhalation of foreign material into the lungs
Risk Factors- seizure activity, brain injury, decreased LOC, flat body positioning, enteral tube feedings, swallowing disorders (dysphagia)

prevention:
HOB 30-45 degrees
Use sedatives sparingly
Enteral tubes - confirm tip location, check for residuals, avoid bolus feedings
Swallow evaluation before initiating PO feedings in patients intubated >2 days
Maintain endotracheal cuff pressure and suction before deflating

Tests: Bedside Swallow Screen

43
Q

Pneumonia classifications

A

inflammation of lung parenchyma from bacteria, fungi and viruses:

Community acquired (vaccine only good for this)
Health care associated
Hospital acquired (resistant to some antibiotics)
Ventilator associated

44
Q

Pneumonia risk factors

A
PREVENTION IS KEY 
Elderly, 
Chronic health or coexisting condition 
Not vaccinated, Immunocompromised, 
Immobility, CVA, decreased LOC
Tobacco, alcohol use, 
Upper airway infections
NPO status,
placement of NG/OG, endotracheal, or tracheostomy tube, 
Mechanical ventilation 
CAUSED A LOT BY ASPIRATION
45
Q

Nursing interventions for pneumonia

A

antibiotics (bacterial pneumonia)
supportive (viral pneumonia): rest, hydration, antipyretics, antitussive, antihistamines, decongestants
Airway – oxygen, chest physiotherapy, TCDB (turn, cough, deep breath)
Fluid – at least 2L/day
Nutrition – small, frequent meals

46
Q

Physical exam for pneumonia

A

Flushed cheeks, anxiety
Myalgia, headache, chills
Pleuritic pain
Accessory muscle use- Chest muscle weakness (from coughing)
Cough, sputum (purulent, blood-tinged or rust-colored)

47
Q

Diagnosic tests of pneumonia

A

CXR: Most common dx test
(may not show changes until 2 or more days after sx are present)
Sputum: gram stain & culture: obtain sputum culture prior to antibiotic therapy
Blood culture: bacteremia occurs frequently
CBC: WBC > 11,000 w/bacterial
Oximetry; ABGs
Fiberoptic bronchoscopy: Obtain sputum specimen or remove secretions, use this when pneumonia is bad

48
Q

Pneumonia symtpoms

A
cough
fever
chills 
tachycardia
tachypnea
dyspnea
pleural pain 
malaise
respiratory distress
decresed blood sounds
49
Q

complications of pneumonia

A

obstruction of broncioles
decreased gas exchange
increased exudate

50
Q

Tuberculosis risk factors

A

Constant frequent contact with people
Congregate settings (ex. Jails, shelters)
Medically underserved
Poor nutrition
Immune dysfunction or sick with other diseases
HIV+
Immigrants
Age: Babies or children under 15 or elderly
People living in or traveling to Mexico, Philippines, Latin American, Cuba, or Southeast Asia, plus more
Being infected with TB bacteria within the last 2 years
Illegal drug use

51
Q

TB manifestations

A
Low-grade fever (late-afternoon)
Cough: nonproductive to sputum filled
Night sweats 
Fatigue 
Weight loss 
Pleuritic chest pain
Hemoptysis (advanced state)- coughing up blood
52
Q

TB diagnostic tests

A

TB Skin Test (Mantoux test): Intradermal Prified protein Derivative (PPD)
only shows if person was ever exposed, not that they are necessarily infected. If skin test is + then one must get a chest xray.
measures delayed cell-mediated (Type IV) hypersensitivity reaction (develops within 3-10 weeks after infection)
Once a person becomes positive, they usually remain so for life.
If pt received the BCG vaccine, TB skin test is not contraindicated, but may need further evaluation (CXR) to diagnose TB
POSITIVE SKIN TEST RESULT:
Measure diameter of the induration (not erythema- bump/hard center).
>10 mm induration
> 5 mm if high-risk (HIV)
Exposed but not infected
Infected but no active disease
Active TB disease
NEGATIVE SKIN TEST RESULT
0-10 mm induration
“Never exposed”

Calcified Lesions on CXR: Chest X-ray to look for any lesions on the lungs (usually in upper lobes)

QuantiFERON- TB Gold:
Whole-blood test
If TB +: Enzyme-linked immunosorbent assay (ELISA) detects release of interferon-gamma by WBCs
Results available in 24 hours
Results not affected by prior BCG vaccination
THIS IS EXPENSIVE, USE ONLY IS REALLY NEEDED

Sputum Studies
•Sputum smear- Acid-fast Bacilli (AFB)
•Sputum culture- TB

Biopsy

findings: lesions on upper lobes

53
Q

TB nursing process

A

assessment:
complete history: Past and present medical history is assessed as well as both of the parents’ histories.
physical examination: A TB patient loses weight dramatically and may show the loss in physical appearance.
tuberculin skin test
chest x-ray
Drug susceptibility testing
If symptoms are present then further assessment will be done on respiratory function: breathing sounds, fremitus (vibrations), and egophony (increased resonance to voice sounds when auscultating)

Interventions:
Promote airway clearance: postural drainage: sit up right and increase fluid intake
Promote adherence to treatment regimen: must stick to exact regimen in order to be most effective and prevent transmission
Promoting activity and adequate nutrition
Prevent transmission of TB infection: instruct the patient about important hygiene measures, including mouth care, covering the mouth and nose when coughing and sneezing, proper disposal of tissues, and hand hygiene. Also educate that it can spread to nonpulmonary sites on the infected as well as be transmitted to others.

Diagnosis:
Risk for infection related to inadequate primary defenses and lowered resistance.
Ineffective airway clearance related to thick, viscous, or bloody secretions.
Risk for impaired gas exchange related to decrease in effective lung surface.
Activity intolerance related to imbalance between oxygen supply and demand.
Imbalanced nutrition: less than body requirements related to inability to ingest adequate nutrients.

54
Q

TB medical management

A

People with disease: treated with 4 medications for 2 months and then 2 medications for 4-7 months
Other people exposed or recent positive skin test: use a med just a few months
Treated with Anti-TB agent for 6-12 months (total time)

  • Isoniazid (INH) - dose, SE (peripheral neuritis, hepatic enzyme elevation, hepatitis), interactions (pg. 603), teaching, use for 6-9 months unless for prevention Effects Liver
  • Rifampin- SE (hepatitis, orange-red coloration of body secretions) Effects Liver
  • Rifabutin
  • Rifapentine
  • Pyrazinamide (PZA)- hyperuricemia (monitor uric acid) Effects Liver
  • Ethambutol
  • Combination drugs
55
Q

clinical manifestations of Pulmonary Embolism

A
Dyspnea 
Chest pain
Tachycardia
Hemoptysis
Tachypnea
hypoxia
56
Q

Nursing process with pulmonary embolism

A

assessment:
Death commonly comes 1 hr after symptoms start so early detection is key
clinical assessment: focus on the clinical probability of risk, clinical history, symptoms, signs, and testing
Health history:
Family history:
Medication record:
Physical exam: Extremities are evaluated for warmth, redness, and inflammation.

Diagnostic Findings: can show abnormal lung function
CXR:
ECG:
ABG:
V/Q scan: most important, evaluates the different regions of the lung and allows comparisons of the percentage of ventilation and perfusion in each area.

Diagnosis:
Ineffective peripheral tissue perfusion related to obstructed pulmonary artery.
Risk for shock related to increased workload of the right ventricle.
Acute pain related to pleuritic origin.

Goals:
Increase perfusion
Verbalize understanding of condition, therapy regimen, and medication side effects.
Display hemodynamic stability.
Report pain is relieved or controlled.
Follow prescribed pharmacologic regimen.

Interventions:
Prevent venous stasis: Encourage ambulation and active and passive leg exercises to prevent venous stasis.
Monitor thrombolytic therapy:Monitoring thrombolytic and anticoagulant therapy through INR or PTT.
Manage pain: Turn patient frequently and reposition to improve ventilation-perfusion ratio.
Manage oxygen therapy: Assess for signs of hypoxemia and monitor the pulse oximetry values.
Relieve anxiety: Encourage the patient to talk about any fears or concerns related to this frightening episode.

evaluate:
Increased perfusion.
Verbalized understanding of condition, therapy regimen, and medication side effects.
Displayed hemodynamic stability.
Reported pain is relieved or controlled.
Followed prescribed pharmacologic regimen.

57
Q

Management of Pulmonsry embolism

A

Anticoagulation therapy: Heparin, and warfarin sodium has been traditionally been the primary method for managing acute DVT and PE.

Thrombolytic therapy: Urokinase, streptokinase, alteplase are used in treating PE, particularly in patients who are severely compromised.

Surgical embolectomy: the removal of the actual clot and must be performed by a cardiovascular surgical team with the patient on cardiopulmonary bypass.

Transvenous catheter embolectomy: a technique in which a vacuum-cupped catheter is introduced transvenously into the affected pulmonary artery.

Interrupting the vena cava: prevents dislodged thrombi from being swept into the lungs while allowing adequate blood flow.

58
Q

risk factors of COPD

A
Smoking
Environmental exposure: aire pollution, second hand smoke, chemicals, allergens
Recurrent URI
Age
Genetic predisposition
Air-way hyper-responsiveness
No gender predisposition
59
Q

Manifestations of COPD

A
Dyspnea, persistent and progressive
Chronic cough
Sputum productions
Increase A to P diameter (AKA:Barrel Chest)
Intercostal retractions
Wheezing, rhonchi
Body position; tripod
Weight loss
Fatigue
Use of accessory muscles to breath
Clubbing
Pursed-lip breathing
60
Q

Nursing process for COPD

A

Assessment:
Health history: obtain a thorough health history from patients with known or potential COPD.
Assess patient’s exposure to risk factors.
Assess the patient’s past and present medical history.
Assess the signs and symptoms of COPD and their severity.
Assess the patient’s knowledge of the disease.
Assess the patient’s vital signs.
Assess breath sounds and pattern.

Diagnosis:
Blood Tests
-ABG
-CBC- will affect how it correlates with PaO2
Sputum studies
Chest x-ray (CXR)
Pulse Oximetry- fingers, toes, ear lobe, or forehead
Pulmonary function test/Spirometry
Bronchoscopy

Planning/goals
Improvement in gas exchange.
Achievement of airway clearance.
Improvement in breathing pattern.
Independence in self-care activities.
Improvement in activity intolerance.
Ventilation/oxygenation adequate to meet self-care needs.
Nutritional intake meeting caloric needs.
Infection treated/prevented.
Disease process/prognosis and therapeutic regimen understood.
Plan in place to meet needs after discharge.

Interventions:
High Fowler’s position and Tripod position
Monitor vital signs, pulse ox, and sputum
Encourage diaphragmatic & pursed lip breathing
Encourage “Huff” coughing
Respiratory treatments
Bronchodilators
LOW concentration of O2 (1-2 L/min) as ordered
Chest physiotherapy
Suction if necessary
Monitor weight
Promote nutrition
Small, frequent meals (High cal., high protein)
Activity as tolerated
Medications as prescribed
Prevent infection: flu & pneumonia vaccines
Smoking cessation
Self-care strategies

Evaluation
Identifies the hazards of cigarette smoking
Identifies resources for smoking cessation
Enrolls in smoking cessation program
Minimizes or eliminates exposures
Verbalizes the need for fluids
Is free of infection
Practices breathing techniques
Performs activities with less shortness of breath

61
Q

Managing COPD

A

Smoking cessation
Education/Self-Management
Pharmacologic Therapy: alpha1-antitrypsin augmentation therapy, antibiotic agents, mucolytic agents, antitussive agents, vasodilators, and narcotics
Bronchodilators: relieve bronchospasm by altering the smooth muscle tone and reduce airway obstruction by allowing increased oxygen distribution throughout the lungs and improving alveolar ventilation
Corticosteroids: A short trial course of oral corticosteroids may be prescribed for patients to determine whether pulmonary function improves and symptoms decrease
Pulmonary rehab
Oxygen
surgery

62
Q

clinical manifestations of asthma

A
Cough 
Wheezing (initially on expiration, severe=inspiration too
Dyspnea
Chest tightness
Tachypnea
Tachycardia
Use of accessory muscles 
Restlessness
Decreased O2 sat
Cyanosis
Hyperresonance
Diaphoresis (if severe)
Widened pulse pressure (if severe)
63
Q

Nursing Process for asthma

A
Assessment: 
fam history
hisotry
Assess respiratory status: Assess the patient’s respiratory status by monitoring the severity of symptoms, breath sounds, peak flow, pulse oximetry, and vital signs.
assess medications
Diagnostic Tests:
Spirometry:
Forced vital capacity (FVC)
Forced expiratory volume in 1 second (FEV 1)
FEV1/FVC ratio (FEV1/FVC): % <70% 
Blood tests:
IgE immunoglobulin: because asthma is an allergic reaction 
Arterial Blood Gas (ABG)
Chest x-ray (CXR)
Pulse oximetry:
Peak Flow: measure the highest airflow during a forced expiration,  helps measure asthma severity and, when added to symptom monitoring, indicates the current degree of asthma control
Measure same time everyday 
Repeat 3 times
Record highest reading
Zones for assessment 

Diagnosis:
Nursing Diagnoses:
Ineffective airway clearance related to increased production of mucus and bronchospasm.
Impaired gas exchange related to altered delivery of inspired O2.
Anxiety related to perceived threat of death.

Interventions:
Pharmacologic therapy: Administer medications as prescribed and monitor patient’s responses to medications.
Fluid therapy: Administer fluids if the patient is dehydrated.

Planning/Goals:
Maintenance of airway patency.
Expectoration of secretions.
Demonstration of absence/reduction of congestion with breath sounds clear, respirations noiseless, improved oxygen exchange.
Verbalization of understanding of causes and therapeutic management regimen.
Demonstration of behaviors to improve or maintain clear airway.
Identification of potential complications and how to initiate appropriate preventive or corrective actions.

Evaluation:
Maintenance of airway patency.
Expectoration or clearance of secretions.
Absence /reduction of congestion with breath sound clear, noiseless respirations, and improved oxygen exchange.
Verbalized understanding of causes and therapeutic management regimen.
Demonstrated behaviors to improve or maintain clear airway.
Identified potential complications and how to initiate appropriate preventive or corrective actions.

64
Q

Managing Asthma

A
High Fowler’s position
Vital signs & Pulse ox
Peak flow
O2 as ordered
Patient education: 
ID triggers and measures to prevent exposure
Lifelong management
Medication administration
Use of peak flow meter
Asthma Action Plan: Help pt to develop their asthma action plan so they can prevent attacks and have a better quality of life
A- adrenergics
S- steroids
T- theophylline
H- Hydration (IV)
M- mask O2
A- anticholingergics
65
Q

Triggers for asthma

A
hypersensitivty
URI
exercise
air pollutants
GERD
66
Q

GI Assessment

A

-Pain: duration, pattern, frequency, location, referred
-Previous GI disorders, abdominal surgeries
-GI symptoms:
Change in appetite, weight (gain or loss)
-Medications
-Social history
-Travel history
-Nutritional history
Special diet needs
Food alleergies, intolerances
Change in eating habits
socioeconomic status
Culture/ethnicity

67
Q

GI Physical Examination

A

-Inspection: Mouth, tongue, buccal mucosa, teeth and gums, abdominal skin
-Auscultation: Always precedes percussion and palpation
-Percussion: Percussion of entire abdomen
-Palpation:
Assess area of tenderness last.
Murphy’s sign and rebound tenderness
-Rectal examination
Last part, most uncomfortable

68
Q

Diagnostic Evaluation of GI System

A
-Serum labs:
CBC and metabolic profile 
Liver enzymes (AST & ALT) and cholesterol and triglycerides, PT/PTT
Bilirubin; amylase and lipase
Ammonia
-Stool tests: FOBT, steatorrhea, ova parasites, C. Diff
-Abdominal ultrasonography
-Imaging Studies:
Upper and lower GI tract studies
CT, MRI, PET, motility studies
69
Q

Barium Enema

A

Purpose:

  • Identify structural abnormalities of rectum, colon
  • Barium enema enhances radiographic visualization

Before Test:

  • Clear liquid diet 24 hours
  • NPO 8 hours
  • Bowel cleansing with laxatives, enemas, suppositories evening before

After the test:

  • Increase fluids to wash out enema.
  • Stool may be chalky white for 24 to 72 hours when it comes out.
70
Q

Small Bowel Series

A
Before test:
-Low-residual diet for 48 hrs. 
-No food for 8 hrs. No fluids for 4 hrs.
-Withhold analgesics & anticholinergics for 24 hr.
-Patient drinks 16 oz. of barium
During:
-Films taken every 20min. until medium reaches terminal ileum
-Rotate examination table
After test:
-Increase fluids
-Mild laxative or stool softener
-Stools may be chalky white for 24 to 72 hr.
71
Q

Esophagogastroduodenoscopy

A

Purpose: visualize esophagus, stomach, & duodenum
Before test:
-Avoid anticoagulants, ASA, NSAIDs for several days
-NPO 8 hr. Position left lateral.
-Conscious sedation: spray anesthetic, midazolam IV, atropine, glucagon
After test:
-Assess VS, O2 sat, LOC, & pain every 30 min.
-NPO until gag reflex returns.
-Throat discomfort possible for several days.
-Must be transported home by another person.
Complications: perforation (pain, bleeding), dysphagia, rapidly elevated temperature

72
Q

Colonoscopy

A

Purpose: Visualize entire colon to ileocecal valve. Identify tumors, polyps, inflammatory bowel disease
-Before test:
Bowel prep varies by physician/clinic
Liquid diet for 12-24 hr before; NPO for 6 to 8 hr
-During test: Same as for EGD
-After test: Same as for EGD
If polypectomy or tissue biopsy, visible blood in stool is possible
Teach: flatus
Complications: perforation
Report: abd. pain, chills, fever, rectal bleeding, mucopurulent discharge

73
Q

Hiatal Hernia

A

Patho: upper stomach and gastroesophageal junction pushes through diaphragm and moves into thorax.
Causes: Increased abdominal cavity pressure (coughing, straining, lifting, pregnancy, obesity)
Manifestations:
-50% asymptomatic
-Heartburn, pyrosis, regurgitation, dysphagia
Complications:
-hemorrhage, obstruction, strangulation

Assessment:
-Differentiate chest pain (angina) from CP caused by reflux
-Auscultate lungs (asthma)
Diagnosis:
-Barium swallow with fluaroscopy
-EGD
-Esophageal manometry
-pH test
-Gastric emptying study

Management:
-Frequent, small meals
Avoid eating late in evening
-Avoid acidic and fatty foods. Avoid caffeine, alcohol, ketchup and mustard, vinegar
-Elevate head after eating. Do not recline for at least 1 hr pc
-Elevate HOB
-Lose weight
-Quit smoking
-Avoid wearing a tight belt, clothing. Avoid straining
-Take meds that reduce acid in stomach

74
Q

Gastroesophageal Reflux Disease (GERD)

A

Contents flow back into esophagus

Causes:

  • Incompetent Les or relaxation of LES
  • Increased gastric volume (after meals)
  • Positioning (bending over, lying down)
  • Increased gastric pressure (pregnancy, obesity)
  • Hiatal hernia

Risk Factor: Obesity

Medications: 
-PPI (omeprazole) most effective!
take 30 minutes before eating
twice daily dosing
-gaviscon (antacid)
-carafate
-H2 receptor antagonists (cimetidine)
-baclofen

endoluminal therapies
-Transoral incisionless fundoplication (TIF)

Surgery: fundoplication

Manifestations:
-Dyspepsia: “heartburn” (usually after meals, when bending over or reclining)
Regurgitation of sour substance into mouth
-Hypersalivation (water brash)
-Eructation (belching)
-Flatulence (gas)
-Bloating
-Odynophagia (painful swallowing)
-Pain after eating
-Dysphagia
-N & V

other manifestations:

  • Chest pain
  • Wheezing
  • Coughing
  • Dyspnea
75
Q

GERD Teaching

A
  • Lose weight
  • Diet: small, more frequent. Avoid carbonated drinks, alcohol, caffiene, tobacco, high-fiber and low fat diet recommended.
  • After you eat don’t lay down
  • Avoid tight clothing
  • Regular sleeping patterns, don’t stay up late
  • Avoid eating right before bed
76
Q

Fundoplication

A

Fundus is wrapped around distal esophagus: Nissen fundoplication for GERD or hiatal hernia repair.

Post-op management:

  • Respiratory care
  • NG managment
  • Nutrional care

Post-op Teaching:
-Activity restrictions: no driving for 1 week, do not drive if taking opioids, walk every day, no heavy lifting.

  • Complications:
  • Temp greater than 101. 100 for elderly
  • N/V, uncontrollable bloating, pain
  • Temporary dysphagia
  • gas bloat syndrome
  • atelectasis, pneumonia
  • Obstructed NG tube
77
Q

GERD: Complications

A
  • Acidic stomach contents damage esophagus
  • Leads to Esophagitis and ulcers develop. Healing occurs, but may substitute Barrett’s epithelium for normal squamous cell epithelium
  • Barrett’s esophagus (Premalignant)-> esophageal scarring and strictures -> esophageal cancer -> hemorrhage, aspiration penumonia, asthma laryngitis, dental decay, cardiac disease
  • Asthma
78
Q

Barrett’s esophagus

A

Lining of the esophageal mucosa is altered

  • Manifestations and Assessment:
  • Complains of s/s of GERD
  • Frequent heartburn

Management

  • EGD performed
  • Monitoring
79
Q

Gastritis

A
  • Inflammation of gastric mucosa
  • Impaired mucosal barrier allows HCl to come into contact with gastric mucosa
  • Epigastric pain, anorexia, hiccups, n/v
80
Q

Peptic Ulcer Disease (PUD)

A

Risk Factors:

  • 40-60 years old
  • H. pylori infection
  • familial tendancy (type O blood)
  • chronic use of NSAIDs, alcohol, smoking

Manifestations:

  • May be asymptomatic
  • dull, gnawing pain, burning in midepigastrium or back
  • Pain often relieved by eating
  • heartburn, V/C/D, bleeding

Treatment:

  • combination of antibiotics to eradicate H. pylori
  • H2 receptor antagonists
  • PPIs
  • Surgery
Assessment:
-Pain
-72 hour diet recall
-VS
-Meds? NSAIDS?
Gi: melena, occult?
Lifestyle? Habits?

Nursing Dx:
-Acute pain
-Anxiety
Imbalance Nutrition

Interventions:

  • Relieve pain
  • Lifestyle management: reduce anxiety, adeq. rest, smoking cessation
  • Maintain optimal nutrition
  • Manage complications
  • Home Care

Evaluation

81
Q

Complications of PUD:

A

Hemorrhage

Perforation