CSE Flashcards
(96 cards)
Emphysema
irreversible destruction of the alveolar walls causing enlargement of the distal air spaces, collapse of the small airways, air trapping, and hyperinflation
Chronic bronchitis
productive cough for at least 3 months per year for at least 2 years
COPD patient assesment
- barrel chest
- increased AP diameter
- clubbing
- cyanosis
- pursed lip breathing
- tympanic or hyperresonant
- productive cough
COPD diagnostic testing
- CXR –> hyperluceny, hyperinflation, flat diaphragms
- ABG –> compensated respiratory acidosis with hypoxemia
- PFT –> decreased flows
COPD stage 1 care: mild
FEV1/FVC <70%
FEV1 >80% predicted
- SABA or inhaled anticholinergic (tiotropium PRN)
COPD stage 2 care: moderate
FEV1/FVC <70%
FEV1= 50-79% predicted
SOB on exertion
- regular use of LABA
- combined LABA and long acting anticholinergic
COPD stage 3 care: severe
FEV1/FVC <70%
FEV1=30-49%
SOB on exertion
Frequent exacerbations
- inhaled steriod for exacerbation
- steriod + LABA (fluticasone+salmeterol)
COPD stage 4 care: very severe
FEV1?FVC <70%
FEV1 <30%
FEV1 <50% predicted + chronic respiratory failure
- long term O2
- lung volume reduction surgery (EMPHYSEMA ONLY)
COPD emergency
- dyspnea at rest
- cyanosis
- RR > 25
- heart rate > 110
- use of accessory muscle
COPD emergency treatments
- Provide supplemental O2 to maintain PaO2 of 60–65 torr/SpO2 of 88–92%.
- Recommend increasing the beta-agonist dose.
- Recommend adding inhaled anticholinergic (if not already prescribed).
- Recommend systemic steroids (in addition to inhaled steroids).
- Recommend antibiotic therapy if secretions copious and purulent
COPD BIPAP
- IF patient is getting worse
- IPAP= 10 cm H2O, EPAP = 5 cm H2O
- Backup rate = 10/min
- Sufficient expiratory time to allow complete exhalation
- FIO2 to assure SpO2 ≥ 90%
COPD ventilator
- Worsening of ABGs in first 1 to 2 hrs
- Lack of improvement in ABGs after 4 hrs
- Severe acidosis (pH < 7.25) and hypercapnia (PaCO2 > 60 torr)
- Severe hypoxemia (P/F ratio < 200)
- Severe tachypnea (> 35 breaths/min)
- Other complications (e.g., metabolic abnormalities, sepsis, pneumonia, pulmonary embolism, barotrauma, or massive pleural effusion)
Asthma patient assessment
- SOB, pursed lip breathing, chest tightness
- increased AP diameter
- retractions (seen in children)
- hyperresonant, tympanic
- dimished breath sounds
- diaphoresis
- pulus paradoxus
Asthma diagnostic testing
- CXR –> translucent lung fields, depressed or flat diaphragms
- ABG –> acute alveolar hyperventilation with hypoxemia then hypercarbia
- PFT –> reduced flow rates
Asthma green zone: level 1 treatment
Peak flow= 80-100%
- no symptoms
- able to perform activites
- no coughing, wheezing, chest tightness
- continue medication plan
- use preventative (anti-inflammatory steriod)
Asthma yellow zone: level 2 care
Peak flow= 50-80%
- increased need for inhaled quixk relief
- increased asthma symptoms at night
- awakening at night with symptoms
- preventative (anti inflammatory) inhaler
- quick relief
- oral steriod
- return to level 1 when improved
Asthma red zone: level 3 care
Peak flow <50%
- no improvement after increasing level 2 (yellow) treatment
- quick relief
- oral steriod
Bronchiectasis patient assessment
- history of pulmonary infections or cystic fibrosis
- cyanosis
- barrel chest
- clubbing
- wheezing, diminished breath sounds
- hyperresonat/tympanic
- purluent, foul smelling secretions, hemoptysis
Bronchiectasis diagnostic tests
*best confirmed via high-resolution CT scan)
1. CXR –> hyperlucent lung fields, depressed or flat diaphragms, enlarged heart
- ABG –> mild to moderate= acute alveolar hyperventilation with hypoxemia
severe= chronic ventilatory faliure with hypoxemia - CT scan –> dilated bronchi, increased bronchial wall
Bronchiectasis treatment
- O2 therapy
- bronchial hygiene
- lung expansion therapy
- antibiotics
- expertorants
- SABA and anticholinergic
- surgical resection if necessary
Cystic Fibrosis patient assessment
- Chronic cough with sputum production
- History of sinusitis
- History of bowel obstruction or steatorrhea (fatty stool)
- Wheezes, crackles, rhonchi
- Body mass index (BMI) < 19
- Presence of nasal polyps
- Digital clubbing
- Signs of pancreatic
- Abdominal distension and flatulence
- fatigue
Cystic Fibrosis diagnostic testing
- Recommend a sweat chloride test (positive for CF if > 60 mmol/L)
- Recommend sputum Gram stain as well as culture and sensitivity –> The presence of P. aeruginosa supports a diagnosis of CF
- CXR –> translucent, right ventricular enlargment, atelectasis, fibrosis
- ABG –> acute alveolar hyperventilation then chronic ventilatory faliure
- PFT –> decreased flow rates
- CBC –> increased HCT and HB
Cystic Fibrosis acute respiratory distress
Recent history:
- Development of fever
- Increase in productive cough with purulent sputum
- Increased fatigue, weakness, or poor appetite or weight loss
- New-onset or increased hemoptysis
Physical assessment:
- Labored breathing with intercostal retractions and use of accessory muscles
- Severe wheezing, rhonchi, or rhonchial fremitus
Diagnostic tests:
- New infiltrate on chest x-ray
- Labs: leukocytosis; low Na+, Cl–, and K+; hypochloremic metabolic acidosis
- ABG/pulse oximetry: moderate hypoxemia, SpO2 < 90% on room air
Cystic Fibrosis treatment
- Provide supplemental O2 to maintain a SpO2 above 90%
- An aerosolized bronchodilator (e.g., albuterol) –> aerosolized dornase alfa (Pulmozyme) or hypertonic saline –> airway clearance therapy (PEP)
1. bronchodilator
2. mucolytic
3. corticosteriod
4. antibiotic
5. digestive enzymes
*If P. aeruginosa confirmed –> Tobramycin (TOBI) via breath-enhanced nebulizer, Polymyxin E (Colistin), or Aztreonam (Cayston) via mesh nebulizer (e.g., Altera)