Module 9 Respiratory Flashcards
Name the structures of the upper respiratory tract
•Nose
•Mouth
•Pharynx
•Larynx
•Trachea
Name the structures of the lower respiratory tract
•Bronchi
•Bronchioles
•Alveolar ducts
•Alveoli
Lungs :
Left = 2 lobes
Right = 3 lobes
Explain Gas exchange in the lungs
•Alveoli – primary site of gas exchange (over 300 million in the body)
•Gases exchange across the alveolar-capillary membrane
•Surfactant – reduces the amount of pressure needed to inflate alveoli. (Surfactant makes alveoli less likely to collapse. Every few breathes we take a larger one and this ‘sigh’ increases surfactant secretion/stretches the alveoli)
What is Atelectasis?
•Collapsed, airless alveoli
Interventions: cough/deep breath, IS, ambulation
•Causes: reduction of surfactant or obstruction of airways with secretions
•At risk: Post-op or bedridden patients
What are the structures of the chest wall?
•Thoracic Cage 24 ribs total, 12 each side, sternum in the middle. Protects heart & lungs
•Mediastinum
•Parietal Pleura
•Visceral Pleura
•Diaphragm
What are pleurae? (Important to know to several disease processes/test!)
•2 Parietal Pleura – lines the chest cavity
•Visceral pleura – lines the lungs
•Intrapleural space – space between the layers
•Provides lubrication (allows movement & expansion w/o friction of organs)
•Increases unity between the layers
•Fluid drains from the pleural space via the lymphatic circulation.
Physiology of respiration
•Oxygenation – process of obtaining air from the atmosphere and making it available to the organs and tissues of the body
•Ventilation =
-Inspiration (inhale!)
-Expiration (exhale!)
•Compliance (measure of how easy it is for lung expansion)
•Resistance (how much the lung needs to overcome to expand)
Explain central/peripheral chemoreceptors in the control of Respiration
•Chemoreceptors = central (medulla) peripheral (carotid/aortic arch).
-Central Receptors respond to change in hydrogen ion concentration and either increase or decrease RR based upon PH levels (acidosis or alkalosis)
-peripheral receptors respond to a decrease in blood oxygen levels (pao2) or an increase in CO2 (paco2) and PH levels.
Explain mechanical receptors and where they’re found.
•Mechanical receptors =
Irritant, stretch, & juxtacapillary receptors
-located in structures of the lungs & respond to physiologic factors
-irritant = conducting airways (sensitive to inhaled particles)
-stretch = smooth muscle (activate respiratory center to inhibit over-expansion of the lungs)
-Juxta = capillaries of the alveoli. Stimulated with increased pulmonary capillary pressure.
Respiratory Defense Mechanisms
“Keep us from getting sick/keeps things out of our lungs”
•Filtration of air (nose hairs filter dust particles)
•Mucociliary Clearance System (moves mucus. Goblet cells secrete mucus that assist in the clearance of debris. Cilia help)
•Cough Reflex (is a back up to the clearance system to expel mucus and debris)
•Reflex Bronchoconstriction (close in response to irritating substances)
•Alveolar Macrophages (primary defense below level of the bronchioles. They phagocytize inhaled particles like bacteria to fight infection)
Gero considerations - respiratory
•Changes in :
-Structures (chest wall stiffening, decrease elastic recoil and compliance decreasing vital capacity. Decreased Breath sounds or barrel chest)
-Defense Mechanisms (overall decrease. Force of cough, ciliary function, macrophage ability, cough effectiveness, secretion clearance)
-Respiratory Control (decrease in response to hypoxemia /increased CO2
•TABLE 25.2 Pg. 460* important!
Subjective/physical assessment of respiratory
Subjective:
•Shortness of breath
•Pain with breathing
•Cough/Sputum production (color, quality)
•Physical Assessment:
•Inspection*
•Palpation
•Percussion
•Auscultation*
Diagnostic studies - respiratory
•Sputum Studies (common: culture & sensitivity to help diagnose bacterial infection and choose antibiotic)
•Chest X-Ray (screening/ evaluation)
•CT Scan (evaluate PE)
•Bronchoscopy (Dr)
•Thoracentesis (Dr)
•Pulmonary Function Tests
•ABGs (tells acid base levels & blood co2 /o2)
•Lung Biopsy (surgical)
Signs of respiratory distress
•Central Nervous System (symptoms are a progression. Early
Onset = restlessness/irritability—> confused & lethargic
•Respiratory ( onset: tachypnea & dyspnea on exertion—-> dyspnea at rest/using accessory muscles)
•Cardiovascular (onset: tachycardia/HTN—> hypotension)
•TABLE 25.1 Manifestations of Inadequate O2* important*
Ventilation interventions
•Oxygenation Administration
-Nasal Cannula
-Simple Mask
-Non-rebreather
-High-Flow Nasal Cannula
-Incentive spirometry
•Chest physiotherapy (done by RT: postural drainage, percussion, vibration for Pt’s w/excessive secretions
•Closed chest drainage (thoracentesis, chest tube)
•Intubation (emergency airway)
TB overview
•Organism: Mycobacterium Tuberculosis (Gram + Bacillus)
•Aerobic organism (oxygen loving)
•Airborne droplets viable from minutes to hours
•Spread by breathing, talking, sneezing or coughing
•Usually requires close contact
•Only infects humans
•Lungs are prime site but can infect any organ (brain, kidneys, bone)
•Can be carried by lymphatic system
MDR-TB
•Multi-drug resistant TB (BAD!)
•Does not respond to first-line treatment**
•Cases of MDR-TB increasing annually
•Treatment 9-20 months with second-line drugs (expensive, chemo-based drugs)
•if 2nd line doesn’t work, there’s no other options
TB Risk Factors
•Poor, homeless, medically underserved
•Foreign-born individuals
•People living or working in institutions or in overcrowded living conditions*
•Those with less-than-optimal sanitation
•Immunosuppression (HIV, cancer, corticosteroid use)
•IV drug use, smoking(impacts lungs), alcohol use disorder
•Malnutrition
TB- Factors Affecting Transmission
•Number of organisms expelled into the air
•Concentration of organisms (higher risk)- Small spaces with limited ventilation
•Length of time of exposure
•Immune system of the person exposed
TB- Progression
•Once inhaled, bacteria lodges into bronchioles & alveoli
•Local inflammatory reaction
•Ghon lesion or ’focus’ – calcified TB granuloma*
•Body’s defense to wall off infection & stop the spread
•Most immune systems can completely kill the bacillus
•Dormancy
•5-10 % develop active TB (bc of calcified ganuloma)
•Can occur months to years later
•Can spread to other organs