Chapter 27 - Chronic Respiratory Problems
Chapter 27 - Chronic Respiratory Problems
1. Emphysema:
CHRONIC RESPIRATORY - Defined by permanent enlargement
PROBLEMS of air spaces and wall destruction
without fibrosis
Types
Pulmonary Diseases Overview:
1. Centriacinar emphysema: Destruction
• Chronic pulmonary diseases have risen
confined to respiratory bronchioles and
dramatically, expected to increase as the
central acinus
older adult population grows
2. Panacinar emphysema: Whole acinus
• Many respiratory diseases, like asthma
affected; often in AAT-deficient
and COPD, are not reportable, making
individuals
full prevalence estimates challenging
• Chronic pulmonary diseases are a major
Pathogenesis
health issue, contributing to productivity
➢ Protease-antiprotease imbalance
losses and disability payments—
leads to connective tissue destruction in
second only to heart disease
the lung
• COPD is the fourth leading cause of ➢ Cigarette smoke inhibits AAT,
death in the U.S. after heart disease, attracting neutrophils which release
cancer, and stroke elastase, damaging lung elastin
• Symptoms such as cough, breathing
difficulty, sputum production, Clinical Signs
shortness of breath, and irritation in • Increased lung compliance: Loss of
the nose and throat should not be elastic recoil from elastin destruction,
ignored if they persist over two weeks leading to overdistended lungs
• Increased airway resistance: Small
Chronic Obstructive Pulmonary airways collapse during expiration,
Disease (COPD) trapping air and requiring accessory
muscle use
➢ COPD includes chronic bronchitis and
emphysema, leading to airflow
Altered oxygen-CO2 exchange:
limitation
➢ Decreased surface area from alveolar
➢ COPD progresses slowly with stable
destruction impairs gas diffusion
phases and acute exacerbations of
symptoms
Early compensation with increased
➢ Asthma differs due to its unique
respiratory rate; later, respiratory acidosis
inflammation and reversibility
and hypoxemia develop
characteristics
Symptoms include:
Etiology and Epidemiology:
• Insidious onset of dyspnea (initially on
➢ Cigarette smoking is the primary
exertion)
cause, with 90% of COPD patients
• Minimal cough and sputum production.
affected
• Appearance of barrel chest, thin body
➢ Protease-antiprotease imbalances
habitus, pursed-lip breathing, and use
contribute, with alpha-1 antitrypsin
of accessory muscles
(AAT) deficiency leading to
emphysema
Pulmonary function studies
➢ Secondhand smoke, air pollution,
occupational toxins, and infections are • Increased residual volume (RV),
additional risk factors • Functional residual capacity (FRC)
• Total lung capacity (TLC)
Pathophysiology of COPD:
Hallmarks include lung parenchyma Decreased FEV1 and FEV1/VC ratio
destruction (emphysema) and central ✓ Arterial blood gases (ABGs) often near
airway inflammation (chronic bronchitis) normal early; respiratory alkalosis from
hyperventilation
Chronic Bronchitis Diagnostic and Collaborative Care
Definition: Chronic bronchitis is defined by a Management
chronic productive cough lasting for 3 Underdiagnosis is common (up to 50%
months in each of 2 successive years undiagnosed)
after other causes of chronic cough have
been excluded Pulmonary Function and Spirometry
Tests: Diagnose and monitor progression
Pathologic Changes
➢ Hypertrophy and hyperplasia of 1. Chest X-Ray: Shows flat diaphragm,
mucus-secreting glands increased AP diameter, and
➢ Chronic inflammatory changes in small overdistention of lungs
airways. 2. Arterial Blood Gas (ABG): Early COPD
➢ Excessive mucus production and shows hypoxemia without hypercapnia
impaired ciliary movement increase 3. Sputum Studies: Identify pathogens (S.
susceptibility to infection pneumoniae, H. influenzae).
➢ Bacteria (e.g., Streptococcus 4. Complete Blood Count (CBC): May
pneumoniae, Haemophilus influenzae) show erythrocytosis due to hypoxia
proliferate, causing neutrophilic
chemotaxis and mucopurulent Medications and Treatment
exudate in bronchi. ✓ Bronchoactive Medications: Improve
➢ Granulation tissue and peribronchial airflow and symptoms
fibrosis result in airway obstruction ✓ Anticholinergic Agents: First-line
therapy for bronchodilation (e.g.,
Clinical Manifestations Ipratropium)
➢ Increased airway resistance due to ✓ Beta-Agonists: Second-line therapy
bronchial wall changes, mucosal edema, (e.g., albuterol for short-acting,
and excess mucus salmeterol for long-acting)
➢ Altered oxygen-carbon dioxide exchange ✓ Methylxanthines (e.g., theophylline):
causing V/Q mismatch Enhance respiratory muscle strength but
➢ Obstructed airways may lead to require monitoring
atelectasis (lung collapse) ✓ Combination Therapy: Anticholinergics
➢ Hypercapnia, hypoxemia, and respiratory and beta-agonists
acidosis occur due to altered gas ✓ Corticosteroids: Reduce exacerbations
exchange in moderate-to-severe cases
➢ Cor pulmonale (right ventricular ✓ Mucolytics: Limited evidence for
failure) may develop due to pulmonary effectiveness
hypertension ✓ Antibiotics: For acute exacerbations
with purulent sputum
Early symptom: Productive cough, often ✓ Alpha1-Antitrypsin (AAT)
ignored by smokers as "cigarette cough" Replacement: For patients with AAT
Late-stage symptoms: Constant dyspnea, deficiency
use of accessory muscles, cyanosis due to ✓ Antidepressants and Anxiolytics:
chronic hypoxemia, right-sided heart Treat depression and anxiety in COPD
failure (cor pulmonale), and dusky skin
Smoking Cessation
Disease Progression and Complications • The only intervention proven to slow
✓ Typically progresses over 30 years due lung function decline in COPD
to tobacco smoke exposure • Older adults may respond well to regular,
✓ Major complications: Infection and brief counseling and encouragement
respiratory failure • Nicotine replacement should be carefully
✓ Common in the fifth decade with monitored for overdose signs in older
productive cough or acute chest illness patients
✓ Dyspnea on exertion typically begins in
the sixth or seventh decade
Oxygen Therapy Transtracheal oxygen (TTO) reduces dead
✓ Supplemental oxygen is the only space and oxygen use but requires specific
therapy proven to improve outcomes patient criteria
in advanced COPD
✓ Indications: Patients unable to Aerosol Therapy
maintain PaO₂ > 55 mm Hg or O₂ Delivers bronchoactive medications
saturation > 85% at rest, or unable to effectively with minimal side effects
complete ADLs without shortness of
breath Vaccination
✓ Dosage: Usually 1-2 L/min via nasal Pneumococcal and influenza vaccines
prongs to relieve hypoxemia, reduce are recommended for COPD patients and
pulmonary hypertension, and decrease their close contacts
the right heart load
✓ Goal: Maintain O₂ saturation > 90% Additional Therapy and Rehabilitation
ideally 24 hours per day Encourage mobility: Patients should stay
✓ Activity-related hypoxemia may require active with portable oxygen when needed.
supplemental O₂ during activity or sleep Pulmonary rehabilitation: Enhances
✓ Continuous oxygen therapy is quality of life, reduces hospital stays, and
recommended for patients with cor improves exercise capacity
pulmonale or arrhythmias Sleep and rest: Assess for sleep disorders,
✓ Portable oxygen systems preferred for common in COPD
mobility to improve exercise and cardiac Hospice/Palliative Care: Important as
output. COPD is progressive and ultimately fatal;
focus on comfort and symptom management
Patient Education
Misunderstanding: Patients may think Surgical Management
oxygen should be used only when Lung Transplantation: Considered for
symptomatic to avoid "habituation," which is patients with severe COPD; highest survival
incorrect rate with bilateral transplantation
Lung Volume Reduction Surgery (LVRS):
High-flow oxygen (≥6 L/min or >40% ➢ For patients with severe emphysema
concentration) may risk respiratory failure to ease breathing and improve lung
by reducing the stimulus to breathe in function
patients with chronic CO₂ retention ➢ Criteria: Severe limitation in
pulmonary function, impaired
Oxygen Therapy Assessment & ADLs, non-responsive to medical
Discharge management, and 6-12 weeks of
Before discharge: Check ABG and O₂ rehab completed
saturation at rest, during activity, and sleep
to determine need for home oxygen Health Promotion and Prevention
✓ Education on smoking cessation and
CMS Reimbursement Criteria: respiratory irritants
1. PaO₂ ≤ 55 mm Hg or O₂ saturation ≤ 88% ✓ Screening for AAT deficiency in patients
at rest on room air with family history of emphysema.
2. PaO₂ ≤ 55 mm Hg or O₂ saturation ≤ 88% ✓ Regular influenza and pneumococcal
during exercise vaccines for high-risk individuals.
3. PaO₂ 56-59 mm Hg with heart failure,
pulmonary hypertension, cor
pulmonale, or hematocrit > 56%
Complications
Status asthmaticus: Uncontrolled severe
attack leading to respiratory failure
Symptoms: Severe distress, cyanosis,
inability to speak.
Requires immediate medical intervention.
Nursing Management of the Patient with Respiratory Failure
Cystic Fibrosis Respiratory failure is the impairment of
the lung's ability to maintain adequate
Nursing Diagnosis: Risk for Infection oxygen and carbon dioxide homeostasis
✓ Maintain environment as pathogen-
free as possible ✓ Diagnosis requires ABGs and pulse
✓ Encourage frequent handwashing for oximetry analysis
the patient, especially after coughing
✓ Provide frequent mouth care, Classified into:
especially after postural drainage. 1. Acute Respiratory Failure (ARF):
✓ Instruct visitors to wash hands before Rapid onset of hypoxemia, hypercarbia,
touching the patient or both, occurring over hours to days
✓ Minimize exposure to people with upper 2. Chronic Respiratory Failure (CRF):
respiratory infections Develops over months to years, with
✓ Monitor temperature regularly, along compensatory mechanisms improving
with sputum color, volume, and oxygen transport and buffering
consistency respiratory acidemia
✓ Collect sputum specimens accurately 3. Acute-on-Chronic Respiratory Failure
for culture and sensitivity (AOCF): ARF superimposed on CRF,
✓ Administer antibiotics on time to maintain e.g., in patients with COPD experiencing
adequate blood levels acute exacerbation
3. Intubation
• Required if NIV is not effective or
patient is not a candidate for NIV
• Intubation is necessary for
mechanical ventilation
4. Ventilator Modes 3. PSV weaning: Gradually reduce
• Common modes include: the preset positive pressure to
1. Assist/Control (A/C): Full ventilatory ease breathing
support, ventilator delivers breath if
patient cannot trigger it 10. Noninvasive Ventilation During
2. Synchronized Intermittent Mandatory Weaning:
Ventilation (SIMV): Patient can take • Use in patients who can breathe
additional breaths over the set rate comfortably post-weaning and
3. CPAP: Set airway pressure throughout have satisfactory ABGs
the respiratory cycle, with the patient
controlling the breaths Failure to Wean
Possible due to:
5. Ventilator Types: ➢ Obstructive lung disease,
➢ Pressure-cycled ventilators: neuromuscular diseases, severe
Deliver positive pressure to reach chest wall deformities
preset pressure, volume varies ➢ Factors like malnutrition,
➢ Volume-cycled ventilators: Deliver electrolyte abnormalities, and
constant volume of air, with recurrent aspiration
pressure adjusted as needed
Nursing diagnoses: Dysfunctional
6. Suctioning the Patient Ventilatory Weaning Response and Impaired
• Use a closed system for suctioning Spontaneous Ventilation
to maintain oxygen supply, stability
of PEEP, and reduce risk of Care for Patients Who Cannot Be Weaned:
ventilator-associated pneumonia ✓ Managed in specialized respiratory units
or long-term care facilities
7. General Care of the Patient on a ✓ Planning for home ventilation requires
Ventilator careful preparation for the equipment and
• Regular assessment of the patient's a responsible caregiver
respiratory status and ventilator
settings Diet
• Alarm troubleshooting: Start with ➢ Diet as tolerated, may be NPO
the patient, then move to the depending on the severity of respiratory
ventilator failure
• Manual ventilation with an Ambu ➢ Proper nutritional support is critical for
bag if needed weaning