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pulmonary system functions 3
1. Ventilation of the alveoli w/ air
2. Diffusion of gases into and out of the blood (co2 and o2)
3. Perfusion of the lungs to allow organs and tissues of the
body receive blood that is rich in oxygen and low in carbon
dioxide
pleura 2
visceral » surrounds lungs (INNER)
parietal » lines chest cavity
SPACE INBETWEEN IS PLEURAL SPACE - has some fluid so lungs can comfortably expand
signs of increased work of breathing
nasal flairing
indrawing - intercostal and clavicular muscles go INWARDS
both common in peds
abdo muscle use
pursed lip breathing - will actually reduce workload
VQ mismatch
V = VENTILATION - Air into lungs
Q = PERF - blood flow to alveolar CAP
Vent to lungs/ min over perf to lungs /min
Rule 1 » Perfusion is Gravity Dependent - IF BLOCKED VENTILATE THE SIDE OF THE GOOD LUNG
Rule 2» Match Good Ventilation to Good Perfusion
IF HIGH OR LOW ALWAYS LOOK AT V
LOW VQ
low vent, normal perf » blockage of air coming into lungs, cap perf is normal
Pneumonia, asthma, bronch COPD, etc
SHUNT » perforation of alveoli with 0 ventilation
High VQ
normal vent, low perf
air flowing into alveoli, but capillarys arent able to recieve o2 - BLOCKAGE OF BLOOD IN PULMONARY ARTERIES
PE, Pulmonar HTN, emphasemic COPD -
Dead space » vent of alveoli with 0 PERF
hypoxemia vs hypoxia
hypoxemia » low o2 TO BLOOD
hypoxia » low o2 to PERIPH tissues + organs (ex. o2 sat to finger)
ABG calculation steps
PH
ROME - resp = opposite, metabolic = same (PH → CO2 vs PH → hco3)
compensation (body will comp with opposite system
- fully comp » PH normal but CO₂ and HCO₃ abnormal.
- partial comp » pH abnormal AND both CO₂ and HCO₃ abnormal.
- uncomp »PH abnormal and only one of CO₂ or HCO₃ abnormal
Ph range
7.35-7.45
too low = ACIDIC
too high = ALKALOTIC
pco2
35-45
IF YOU KNOW PH YOU CAN KNOW co2
low = ALKALOTIC
high = ACIDOTIC
po2 range
70-100
<70 = hypoxemia
ACCEPTABLE PERCENTAGE GRADE RANGE
bicarb range
22-26 - ACTS AS BUFFER
low = ACIDOTIC
high = ALKALOTIC
atelectasis overview
aspiration overview
foreign material - typically food enters lungs
airway obstruction inflammation injury or infection
commonly due to dsyphagia » elderly pop, peds, post op and neurological issues GERD
can follow infectios process - fever, chills WBC SOB
hearing crackles wheezez rhonchi or diminished breath sounds
prevent with swallowing assessments, upright positioning during meals, proper oral hygiene &
feeding techniques, elevated HOB
atelectasis overview
collapse of alveoli
common in recent surge, bed rest obesity, immobility airway obstruction, hypoventillation
SOB, chest tightness, tachypnea, tachy decreased o2 sat
diminished or absent breath sounds,
prevent with incentive spiro, deep breathing and coughing, early ambulation and adequate pain management
pneumothorax general
AIR in pleural space resulting in collapsed lung (partial or complete
can be open closed or tension
- closed » no external wound
- open » air enters through chest wall opening
- tension » SERIOUS, open pneumo with RAPID air accumulation ↑↑ pressure
pneumothorax HTT
Inspection» Unequal chest expansion, tachypnea, cyanosis, apprehension,
Palpation: Subcutaneous emphysema, crepitus, chest expansion decreased on affected side,
tachycardia, and decreased blood pressure.
Percussion: Hyper-resonant DUE TO AIR
Auscultation: Breath sounds decreased or absent, voice sounds decreased or absent.
tension pneumo SS
SIGNS WILL BE SAME AS REST OF ASSESSMENT IN ADDITION TO NIGHT SWEATS
Tracheal shift to opposite side (unaffected side), severe respiratory distress, tachycardia and hypotension
hemothorax vs chylothorax
hemothorax » BLOOD in pleural space » PE, trauma, cancer
chylothorax» LYMPHATIC fluid in pleural space, white or light pink - trauma, surge, cancer
pleural effusions - general 3
FLUID BUILDUP IN PLEURAL SPACE (like pericarditis of lungs)
exudative » FLUID AND CELLS FROM INFECTION - pulmonary cancer, infection PE
transudative » PRESSURE CHANGE FROM BLOODSTREAM - common in CHF or cirrhosis
empyema » PUS - creamy green or yellow, common with TB pneumonia or abcess
pleural effusion HTT
Inspection: Unequal chest expansion, tachypnea, increased WOB, accessory muscle use.
Palpation: chest expansion decreased on affected side
Auscultation: Breath sounds decreased or absent over fluid, pleural rub
Percussion: Dullness over fluid.
diagnostics (effusion and chest wall disorders)
xray » air or fluid confirmation, chest tube placement
CT» better imaging
thoracentesis » colour characterstics and PH of fluid, allows for Culture and sensistivity
labs
CBC
CRP/ESR
ABG
BNP and LFT
planning + interventions
lung assessment and expansion
o2 as prescribed
monitor o2 rest status lung sounds
high fowlers + encourage resp
monitor for complications
Chest tube care
Patient assessment » RR, depth, effort Breath sounds, symmetry and expansion
Dressing – dry, drainage, secured (3 SIDES NOT 4 IN EMERGENCY), anchor intact, no redness or emphysema
drainage//system » no leaks or tubing issues, colour consistency and amount of drainage, suction and emergency equip present
Patient teaching » Ambulation, DB&C exercises, splinting Chest tube safety Symptoms to report immediately?
- tracheal shift, SOB low sats, increase work of breathing
pneumonia - general
infection of LOWER resp tract caused by bacteria viral fungal protozoa parasitic
enter via inhalation aspiration or blood
immune response initiated leading to damaged mucous membranes and alveoli-capillary membranes
FLUID AND GUNK BUILDUP - leads to VQ mismatch hypoxemia and dyspnea
community, hospital or aspiration aquired
can be lobar or broncho (patchy all over)
pneumonia SS// HTT
fever chills fatigue - INFECTION
productive PURULENT cough
tachypnea SOB chest pain
changes in perf and o2
dullness in areas with gunk buildup
decreased breath sounds, bronchial sounfds or crackles
pneumonia risk factors
aging » lowered immune sys, weaker muscles, asperation risk
prolonged immobility » up risk for atelectasis
decreased immune sys//transplant rejection drugs
environmental » chemical exposure, vaping, smoking, pollution
TB - genreal
infection by mycobacterium tuberculosis, an acid-fast bacillus
HIGHLY CONTAGIOUS - airborne precautions
Will become latent - PEOPLE WITH HEALTHY IMMUNE SYS are able to live with TB without passing it on - asymp
if activated or reduced immunity TB will reactivate
TB SS
symptoms are similar to that of pneumonia
Productive cough with purulent sputum, fever, night sweats, general anxiety, dyspnea, chest pain, hemoptysis, decreased O2 sats, hypoxemia
TB HTT
Inspection: Cough initially nonproductive, later
productive of purulent, yellow-green sputum, may be blood-tinged. Dyspnea, orthopnea, fatigue, weakness.
Palpation: Skin moist at night from night sweats.
Auscultation: Normal or decreased breath
sounds.
Percussion: Resonant initially. Dull over any effusion.
Adventitious sounds: Crackles over upper lobes common, persist after full expiration and cough
pneumonia and TB diagnostivs
xray » identifies infiltraites monitors improvement//complications
CT » more detailed image
TB vs pneumonia labs
TB » CBC, ABG, ACID FAST BACILLI SPUTUM
pneumonia » CBC, viral + sputum+ blood cultures, ABG
testing for infection and VQ mismatch
guides treatement esp pneumonia if viral bacterial etc
resp tract infections treatment
med regime
prevent spread
PFT & chest xrays
isolation - esp TB
prevent and manage complications
ARDS - general
acute lung inflammation and extensive alveolar cap injury
MOST COMMON CAUSE IS SEPSIS
- trauma burns aspiration, surge, gas inhalation, fat emboli overuse of supp o2 DIC (clotting across body)
ARDS patho
MASSIVE inflammation causing severe pulmonary edema due to damage to alveolar cap membrane
SHUNTING - low VQ (low to no vent, normal perf) & hypoxemia
Lungs become less compliant increasing thework of breathing, ventilation of alveoli decrease and hypercapnia develops leading to acute respiratory failure
ARDS SS// assessment
dyspnea
inspiratory crackles
resp alk - will turn into resp acid due to co2 buildup (unable to clear)
hypoxemia unresponsive to O2
alveolar infiltrates WOUT Cardiac disease
productive cough with thin frothy sputum
indrawing of chest
tachycardia and hypotn
ARDS labs and diagnostics
diagnostics» ground glass or whiteout on XRay
labs » CBC, blood cultures, ABG, CRP + ESR, plts (if intubating
ARDS nursing management
lung ventilation - postioning (prone)
monitor ABG and o2 sats
patent airway- vent and intubation'
nutrition and fluid balance » IV TPN esp if intubated'
CO and tissue perf maintenance
vent care
resp assessment » ET tube secure, RR depth and effort, breath sounds and expansion equal
o2 sats and ABG
Ventialtor and suction settings
pain» distress and sedation management
prevent complications » semi fowlers, oral hygiene, suction, reposistioning
CF general
Autosomal recessive disorder (1/4 chance if both parents are carriers)
Mutation of CFTR gene - protien that regualtes NA and CL movement in and out of cells
less water due to cl + sodium not going out = sticky secretions
affects lungs pancreas billiary and reproductive tract - mucus, sweat saliva tears and diegestive enzymes are affected
mucous secretions block bronchioles - cillia impaired + unable to clear ↑ risk for lung infections
chronic infection and inflammation leads to airway destruction over time
CF resp SS
recurrent wheezing, pneumonia np cough
cough will eventually have purulent grey sputum due to ↑ WBC and debris
↑ obstruction and mucus accumulation
bronchiectasis (widening and scarring of bronchioles), dyspnea, hemoptysis. chest pain recurrent sinusitis and infection, nasal polyps
Barrel shaped chest, cyanosis, clubbing of fingers and toes DUE TO CHRONIC HYPOXEMIA
CF GI SS
thickened secretions block ducts - pancreatitis, billiary issues, gallstones, etc
meconium illeus in babies » bowel perf with first BM
Large, bulky, loose, frothy, foul smelling stool (steatorrhea)
Rectal prolapse & incontinence - excessive coughing
Small bowel obstruction
Pancreatic insufficiency
Biliary cirrhosis with portal hypertension » blockage in bile trunk can lead to
Voracious appetite (early); loss of appetite (late)
FTT: Lack of weight gain, skeletal muscle wasting and weakness, failure to grow, distended abdomen
Nutritional deficiencies, vitamin deficiencies, anemia
CF PANCREAS
Chronic cough and wheezing
Failure to thrive
Pancreatic insufficiency
Alkalosis and hypotonic dehydration » alkalosis as comp (can also trap CO2), dehydration due to NACL loss
Neonatal intestinal obstruction (meconium ileus)// Nasal polyps
Clubbing of fingers//chest radiograph with characteristics changes
Rectal prolapse
Electrolyte elevation in sweat, salty skin
Absence or congenital atresia of vas deferens OR increased viscocity of cervical secretions (secretions thickened and blocked)
Sputum with Staph or Pseudomonas
CF HTT
NEURO: Concerns with self image, confidence, depression, anxiety
CV: edema, risk for cor Pulmonale, PAH
RESP: breathing quality, increased work of breathing, crackles, wheezes, productive sputum –greyish , ↓ oxygen saturation, nasal polyps, high risk for infections, pneumothorax
GI: GERD, pancreatic insufficiency-diabetes, pain, bloating, anorexia, wt loss, rectal prolapse, small bowel obstruction, meconium ileus in newborns, require high protein/high calorie diet
GU: stress incontinence
CF Diagnostics
NEWBORN SCREENINGS
genetic testing for CTFR gene mutation
SWEAT CL test » must be 2 weeks + for suffecient sweat
PFT
if older » family history, pmhx of pancreatitis, chronic infections FTT, infertility
CF labs 6
CBC » infection, anemia, inflamm
lytes » nutrition and hydration
BG//A1C » gluc or panc insuff
LFT » liver and panc insufficiences
lipase » elevated in pancreatitis- spill over into blood stream + unable to digest fat soluble vits
sputum cultures » pathogen testing
CF complications
cysts caused by mucus pooling and trapping can rupture - CAUSE CLOSED PNEUMOTHORAX
blockage in billiary tract - gall stones
absorption issues in bones - OP
intussception » telescoping of intestine - more common in peds - gut secretions are also affected turning stool hard intestines struggle to push allong and slide inwards
volvulus » bowel twisting
CF pharm
CFTR Modulators » Improve CFTR protein function Improves lung function and nutritional status Reduces exacerbations
Vitamin supplements » A,D,E,K
Pancreatic enzymes » Aid in digestion allowing for proper absorption
Mucolytics » Thin secretions
Bronchodilators
Antibiotics - can also be prophylactic
Diabetes management
CF nursing management 5
Promote clearance of secretions
Manage and minimize lung infections
Provide adequate nutrition
Minimize complications
Promote coping independence
CF interventions 7
Chest physiotherapy
Feeding & Chest tube care
Airway clearance support
Proper hydration and nutrition
Medication administration
Infection prevention
Support groups
Pulmonary fibrosis general
Chronic, progressive, fibrosing disorder of the lower respiratory tract (limited to lungs).
High incidence in occupations with environmental exposures.
Usually onset 50 to 70 years of age; more frequent in males
Median survival is only 2-4 years after diagnosis
Characterized by irreversible scarring of the lung parenchyma
Leads to decreased lung compliance and impaired gas exchange
PF risk factors
Cigarette smoking
Viral infection
Environmental pollutants
Chronic aspiration
GERD: acid reflux/heartburn
Genetic predisposition
More common in men than women - traditional trade exposure
PF patho
exposure to triggering agent - damages lung epithelium
fibro and myofibroblasts activated to heal the damage but are left ON - excessive scar tissue production leading to tissue stiffness, decreased O2 diffusion, hypoxemia, increased WOB, low TC and hypervent with hypercapnia
PF SS
history of environmental exposure
BILATERAL VELCRO CRACKLES, clubbing hypoxemia, cyanosis?
exertional dsyspnea, tachypnea, dry persistent cough
bilateral honeycomb//netting on CXR
diagnostics PF
PFT » testing tidal volume and o2 absorption
CXR » netting or honeycomb pattern, monitors progression
CT » better image - scarring of lungs
bronchoscopy » tube via mouth nose to lungs - ROOT OF INFECTION NOT DIAGNOSIS
lung biopsy
PF labs 5
WBC » infection and inflamm
lytes » monitor nutrtion and hydration
CRP » inflammation monitoring - ↑ in progression
LFT » toxic effects from medications
ABG » monitor O2 needs hypercapnia and progression
PF HTT
NEURO: anxiety, fatigue
CV: cor pulmonale, dysrrhythmias (afib or tachy)
RESP: dyspnea, cough, respiratory failure
GI: loss of appetite, anorexia
PF treatment
o2 » o2 89-92 BUT ALSO DEPENDS ON PT BASELINE
corticosteroids (lowers inflamm)
antifibrotics » manages exacerbation and NEW scarring
cytotoxic meds » can be secondary to cancer
PF nursing management 6
Improve oxygenation
Reduce dyspnea and fatigue
Promote activity tolerance
Prevent respiratory infections
Support medication adherence
Optimize quality of life
PF interventions 7
Monitor respiratory status
Adequate oxygenation
Manage dyspnea
Promote airway clearance
Medication administration
Infection prevention
Support group
COPD general
chronic obstructive airway diseases - includes emphysema and chronic bronchitis
AIR TRAPPING - prolonged exhalation period leading to VQ mismatch (LOW)
causes » smoking, irritant exposure, infection, aging or genetics
COPD brochitis
Hypersecretion of mucous glands
narrowed airways
Obstructed airflow
AIR TRAPPING IN ALVEOLI - cant go in and out
BUILD UP OF CO2 CAN LEAD TO PULMONARY CONSTRICTION
COPD emphysema
DESTRUCTION OF ALVEOLI WALLS
LOSS OF RECOIL
alvioli collapse duing exhalation
air trapping in alveoli
COPD HTT
NEURO: Fatigue, anxiety
CV: cor pulmonale, dysrhythmias
RESP: dyspnea, chronic cough, wheezing, barrel-shaped chest, cyanosis, respiratory failure
GI: loss of appetite, anorexia
GU: stress incontinence
COPD treatment
Oxygen therapy
Bronchodilators
Anticholinergics » DRY SECRETIONS
Corticosteroids
Antibiotics
COPD interventions
Assess respiratory status
Position High Fowler's » NEVER TRENDELENBURG FOR ANYONE WITH RESP
Administer prescribed oxygen
Encourage pursed-lip breathing
Administer bronchodilators –rescue inhalers vs maintenance
Promote airway clearance
Monitor ABGs and SpO₂ » 88-92
Teach smoking cessation and exacerbation prevention
pulmonary artery HTN general
Mean elevated pulmonary artery pressures (PAP) > 25 mmHg at rest or > 30 mmHg with exercise
caused by abnormalities in pulmonary arterioles - - increased pulmonary vascular resistance or increased pulmonary venous pressure
Leads to right ventricular (RV) dilation and remodeling-- then RV failure and death [when RV compensation cannot sustain normal cardiac function]
common causes
ideopathic
LV disease failure
Chronic lung disease - COPD
hypoxia
![<ul><li><p>Mean elevated pulmonary artery pressures (PAP) > 25 mmHg at rest or > 30 mmHg with exercise</p></li><li><p>caused by abnormalities in pulmonary arterioles - - increased pulmonary vascular resistance or increased pulmonary venous pressure</p></li><li><p> Leads to right ventricular (RV) dilation and remodeling-- then RV failure and death [when RV compensation cannot sustain normal cardiac function]</p></li></ul><p></p><p>common causes</p><ul><li><p>ideopathic</p></li><li><p>LV disease failure</p></li><li><p>Chronic lung disease - COPD</p></li><li><p>hypoxia</p></li></ul><p></p>](https://assets.knowt.com/user-attachments/3a92a4b1-7825-44bc-ad38-e57c02fab49a.png)
pulmonary artery HTN SS early vs late
Early Symptoms may include: » Progressive exertional dyspnea, Fatigue, Chest discomfort, Tachypnea
Later Symptoms [signs of Right heart failure]
cyanosis
Exertional presyncope
Peripheral edema
RV heave // S3
Jugular vein distention
Tricuspid regurgitation murmur » hear blood flow back into RA
pulmonary artery HTN HTT
NEURO: fatigue, anxiety
CV: chest discomfort, syncope, JVD, murmurs, dysrhythmias, cor pulmonale
RESP: dyspnea, tachypnea, hypoxemia, respiratory failure
pulmonary HTN labs/diagnosticcs
CBC » anemia and plt (venous stasis)
serum antibodies » autoimmune ruleout
ecg » R axis deviation (widening) peaked P waves
CXR
PFT
R heart catheterization » to diagnose, but also treatment to relieve pressure and widen artery
cor pumonale
Right ventricle enlargement (hypertrophy, dilation or both)
Secondary to a lung disorder that causes pulmonary artery hypertension increasing pressure on RV and leading to RV failure
ENLARGEMENT AND FAILURE OF RV DUE TO ↑ BP IN PULMONARY ARTERIES
Injury or predefining factors cause vasoconstriction, pulmonary HTN, RV hypertrophy
Symptoms of dyspnea or exertional fatigue due to underlying lung disorder
Symptoms occur with exercise when cardiac output falls
Cor pulmonale SS // diagnostics
As pressure increases so do signs of RHF
Edema
s3 & s4
Tricuspid regurgitation murmur/pulmonic valve murmur
Chest pain
JVD
Hepatosplenomegaly
diagnostics = CXR ECG
cor pulmonale treatment
O2 therapy, diuretics, anticoag BB
BB treatment dependant on HR and pt baseline
cor pulmonale interventions
Assess oxygenation and respiratory status
Administer supplemental oxygen
Monitor for right-sided heart failure
Assess edema, JVD, and daily weight
Administer pulmonary vasodilators and diuretics Monitor BNP, renal function, and electrolytes Encourage energy conservation
Teach medication adherence and symptom monitoring
post op care for R heart cath
Assess airway, breathing, and circulation (ABCs) Monitor insertion site for bleeding
Monitor for dysrhythmias
Assess for pneumothorax (if jugular/subclavian access)
Maintain ordered bedrest and positioning
Perform ongoing neurovascular assessments (CSM)
upper resp tract diseases
disease above thoracic inlet » 1st rib
Characterized by inspiratory stridor, hoarseness, and suprasternal retractions - indrawing
Croup - general
group of acute infections processes
1-7 yo peak occurance in fall and winter
Bacterial, Viral(Influenza A and B, RSV), Allergic component
Clinical manifestations: Bark-like cough, brassy cough, Hoarseness, inspiratory stridor, varying degrees of respiratory distress due to larynx swelling
Diagnostics: CXR, nasopharyngeal swab for viral respiratory panel, C&S swab for bacterial respiratory, sputum sample, CBC
NOT TREATED WITH ANTIBIOTICS
foreign body aspiration
most common in ages 1-3 - kids stick stuff in mouths
Culprits of Foreign body aspiration: Beads, paper clips, food, marbles, magnets, batteries, hot dogs//meat, peanuts heard candy
initial signs include choking gaggin wheeze or cough
diagnosed via CXR direct laryngoscopy or bronchoscopy
types of obstructions and signs 3
Laryngotracheal obstruction: dyspnea, cough, stridor, and hoarseness, with worsening of obstruction- cyanosis
Bronchial obstruction: cough, wheezing, asymmetrical breath sounds, decreased air entry, dyspnea.
Complete obstruction of larynx: Face becomes livid, child may fall unconscious, cardiac arrest
epiglottitis
inflammation of epiglottis - seals off resp tract when swallowing
cant swallow - will cause drooling
‘thumb’ on xray due to swellinng
typically go to bed asymp with flu symptoms - progresses quickly
AVOID TOUNGE DEPRESSOR AND THROAT EXAM - INCREASE IN PRESSURE AND WORSENING SYMPTOMS
General upper resp treatment 6
corticosteroids - dexamethasone
epinephrine as nebulizer - VASODIALATES
antibiotics
humidified o2
calm environment
family education
lower resp tract infections general
Obstruction of airways below thoracic inlet, produces more expiratory sounds.
Classic symptom: wheezing
Common differential diagnosis of wheezing:-Bronchiolitis: first episode of wheezing.
-Pneumonia: fever, cough, fatigue
.-Asthma: recurrent wheezing episodes, identifiable triggers
RSV general
symptoms and lower respiratory infection of the bronchioles due to inflammation
Epidemiology: <3 yrs, Indigenous children have high rates of RSV hospitalization
Etiology: most cases are RSV, adenoviruses and parainfluenza viruses; associated cases of Human metapneumovirus
Diagnostics: CXR, nasopharyngeal swab for viral respiratory panel, CBC
RSV inital vs progression vs severe
Initial: Rhinorrhea, pharyngitis, coughing, sneezing, chest wheezing, ear and/or eye drainage, intermittent fever
With Progression: Increased coughing and wheezing, tachypnea, retractions, cyanosis
Severe Illness: Tachypnea >70 breaths/min, listlessness, apneic spells, poor air exchange, decreased breath sounds
RSV management
Oxygen therapy to maintain adequate oxygen saturation
Nasal suctioning to clear secretions
Hydration (oral or IV fluids)
Humidified oxygen Antipyretics
pedatric pneumonia
inflammation of the pulmonary parenchyma.
Epidemiology: occurs more frequently in infancy and early childhood.
Etiology: Virus, or Bacterial pathogen
Diagnostics: CXR, Nasopharyngeal swab for respiratory panel, CBC, C&S sputum
peds pneumonia ss
cough Tachypnea, Breath sounds-crackles, decreased air entry, dullness with percussion,
chest pain,
pallor to cyanosis,
indrawing and nasal flaring
behaviour: irritable, restless, lethargic,
GI: anorexia, vomiting , diarrhea, abdominal pain
pneumonia management
Monitor resp rate, breath sounds, O2 sats, ABGs Antibiotics
asthma
Asthma is a chronic inflammatory disorder of the airways characterized by recurring symptoms, airway obstruction, bronchial hyperresponsiveness, and an underlying inflammation process
MUCOUS PRODUCTION - like COPD
influenced by allergies
recurrent episodes of wheezing, breathlessness, chest tightness, and cough;
symptoms occurring most frequently at night or in the early morning + with exercise
asthma assessment
Inspection: increased respiratory rate, shortness of breath with audible wheeze, use of accessory neck muscles, cyanosis, indrawing Expiration laboured, prolonged. barrel chest may develop.
Palpation: Tactile fremitus decreased (CANT FEEL CHEST WALL MOVE WITH VOICE tachycardia.
Percussion:Resonant. May be hyperresonant if asthma is chronic.
Auscultation:Diminished air movement. Breath sounds decreased, with prolonged expiration. Voice sounds decreased
. Adventitious sounds:Bilateral wheezing on expiration; sometimes inspiratory and expiratory
asthma management
Monitor resp rate, breath sounds, accessory muscle use, O2 sats, ABGs
Bronchodilators, corticosteroids
Order of brain meninges and spacing - out to in
skull
epidural space
dura
subdural space
arachnoid
subarachnoid space - contains CSF
pia
brain
levels of LOC 7
alert » a&o x4
confusion» shorten attention span, difficuty following commands
disorientation » no longer a&ox4, lost track of person place time
lethargy » drowsy and sluggish, CAN BE ROUSED
obtundation». difficult to rouse, needs constant stimulation
stupor» semiconciousness, respond to strong noxious or painful stimuli
coma » no response to internal or external stimuli or needs
occulocephalic - dolls eye
DO NOT USE IF SUSPECTED OR KNOWN SPINAL AS IT TESTS BRAINSTEM FUNCTION
hold head with two hands and turn
eyes go to opp side of head = NORMAL
occulovestibular test - caloric ice water
TYPICALLY USED IN BRAIN DEATH DETERMINATION
OR IF SUS SPINAL WHEN DOLLS EYE CANT BE DONE
eyes move to opposite side where water was injected = normal
breathing patterns 5
cheyne-stokes » crescendo decrescendo (hypervent to apnea)
cluster » clusters of disorganized breathing, irregular pauses
apneustic » brief inspiratory expiratory pause
agonal » dying gasp-like breathing
ataxic » completly irregular pattern, some shallow, some deep slow rate
damage to lower brainstem
vomiting WITHOUT nausea, yawning uncontrollably
can happen with compression, diseases or damage
ACUTE NEURO HTT GENERAL
NEURO: LOC and monitoring for deterioration pupillary changes unilaterally and bilaterally PERRLA , vision changes, heachache, hyperthermia seizures.
CV: bradycardia hypertensive, widening pulse
pressure (sign of Cushing’s triad) changes to perf, cap refill, pulses
RESP: monitor for changes in respirations: bradypnea, tachypnea,
irregular, Cheyne’s stoke present or absent,
RENAL: urine output
GI » projectile vomit w/out nausea