Escolar Documentos
Profissional Documentos
Cultura Documentos
College of Nursing
MENTORING ACTIVITY: SY 2014-2015
Mentee: Patricia Joy Guinto, Batch 2016
Mentor: Leslie Masaya, Batch 2015
MED-SURG: RESPIRATORY SYSTEM
2.
3.
1.
2.
3.
4.
5.
6.
7.
II.
4.
Bronchi
Subsegmental Bronchi
Bronchioles
Terminal Bronchioles
Respiratory Bronchioles, considered
to be the transitional passageways
between the
conducting airways and the gas exchange
Alveoli
functional cellular units or gas-exchange
units of the
lungs.
O2 and CO2 exchange takes place
Made up of about 300 million
TYPE 1 - provide structure to the alveoli
collapse
TYPE 3 alveolar cell macrophages, destroys
foreign material, such as bacteria
Nasopharynx
Oropharynx
Laryngopharynx
Lecithin
Sphingomyelin
increases
alveoli stability & prevents their
L/S ratio indicates lung maturity
2:1 normal
1:2 immature lungs
PULMONARY CIRCULATION
Cricoid cartilage
Arythenoid cartilage
Vocal cords
Trachea - consists of cartilaginous
rings
Passageway of air
th th
Right 3 lobes, 10
segments
Pleural cavity
Parietal
Visceral
RESPIRATORY MUSCLES
PRIMARY: diaphragm and external intercostal muscles
ACCESORY:
sternocleidomastoid
(elevated
sternum), the scalene muscles (anterior, middle
and posterior scalene) and the nasal alae
PHYSIOLOGY OF RESPIRATORY SYSTEM
airways.
NEUROCHEMICAL CONTROL
MEDULLA OBLONGATA respiratory center
initiates each breath by sending messages to
primary respiratory muscles over the phrenic nerve
has inspiration and expiration centers
PONS has 2 respiration centers that work
with the inspiration center to produce normal rate
of breathing
1. PNEUMOTAXIC CENTER
affects the
inspiratory effort by limiting the volume of air
inspired
2. APNEUSTIC CENTER
prolongs
inhalation
NOTE: Chemoreceptors responds to changes in ph,
increased
PaCO2 = increase
RR
Background
information
A. Abnormal patterns of
breathing
1. Sleep Apnea
cessation of airflow for more than 10 seconds
more than 10 times a night during sleep
causes: obstructive (e.g. obesity with upper
narrowing, enlarged tonsils, pharyngeal soft
tissue changes in
acromegaly or hypothyroidism)
2. Cheyne-Stokes
periods of apnoea alternating with
periods of hyperpnoae
pathophysiology: delay in medullary
chemoreceptor response to blood gas changes
AIRWAY RESISTANCE
Resistance is determined chiefly by the radius size
of the airway.
Causes of Increased Airway
1.
2.
3.
4.
Resistance
Contraction of bronchial mucosa
Thickening of bronchial mucosa
Obstruction of the airway
Loss of lung elasticity
RESPIRATION
The
process
of
gas
exchange
between
atmospheric air and the blood at the alveoli, and
between the blood cells and the cells of the body.
3.
4.
5.
6.
causes
left ventricular failure
brain damage (e.g. trauma,
cerebral, haemorrhage)
high altitude
Kussmaul's (air hunger)
deep rapid respiration due to stimulation of
respiratory centre
causes: metabolic acidosis (e.g. diabetes
mellitus, chronic renal failure)
Hyperventilation
complications: alkalosis and tetany
causes: anxiety
Ataxic (Biot)
irregular in timing and deep
causes: brainstem damage
Apneustic
post-inspiratory pause in breathing
7.
Paradoxical
the abdomen sucks with respiration
(normally, it pouches uotward due to
diaphragmatic descent)
causes: diaphragmatic paralysis
B. Cyanosis
1.
Refers to blue discoloration of skin and
mucous membranes , is due to presence of
deoxygenated haemoglobin in superficial
blood vessels
2. Central cyanosis = abnromal amout of
deoxygenated
haemoglobin in arteries and that blue
discoloration is present in parts of body with
good circulation such as tongue
3. Peripheral cyanosis = occurs when blood supply
to a
certain part of body is reduced, and the tissue
extracts more oxygen from normal from the
circulating blood, e.g. lips in cold weather are often
blue, but lips are spared
4. Causes of cyanosis
Central cyanosis
decreased arterial saturation
decreased concentration of inspired
oxygen:
high
altitude
lung disease: COPD with cor
pulmoale, massive pulmonary
embolism
right to left cardiac shunt (cyanotic
congenital
heart
disease)
polycythaemia
haemoglobin abnromalities (rare):
methaemoglobinaemia,
sulphaemoglobinaemia
Peripheral cyanosis
all causes of central cyanosis cause
peripheral
cyanosis
exposure to cold
reduced cardiac output: left ventricular
failure or shock
arterial or venous obstruction
Position: patient sitting over edge of bed
General appearance
look for the following
Dyspnea
normal respiratory rate < 14 each
minute tachypnoea = rapid
respiratory rate
are accessory muscles being used
(sternomastoids, platysma, strap muscles of
neck) - characteristically, the accessory
muscles cause elevation of shoulders with
inspiration and aid respiration by increasing
chest expansion
Cyanosis
Character of cough
ask patient to cough several times
with:
chest infection
- asthma
- carcinoma of bronchus
- left ventricular failure
- interstitial lung disease
- ACE inhibitors
Sputum
volume
type (purulent, mucoid, mucopurulent)
presence or absence of blood?
Stridor
croaking noise loudest on
inspiration is a sign that requires
urgent attention
causes: (obstruction of larynx, trachea or
large broncus)
- acute onset (minutes)
inhaled foreign body
acute epiglottitis
anaphylaxis
toxic gas inhalation
- gradual onset (days, weeks)
laryngeal and pharyngeal tumours
crico-arytenoid rheumatoid arthritis
bilateral vocal cord palsy
tracheal carcinoma
paratracheal compression by lymph
nodes
post-tracheostomy or
intubation granulomata
Hoarseness
causes
include:
- laryngitis
- laryngeal nerve palsy associated
with carcinoma of lung
laryngeal carcinoma
The Hands
Clubbing
commonly cause by respiratory disease (but
NOT
emphysema or chronic
bronchitis)
occasionally, clubbing is associated with
hypertrophic pulmonary osteoarthropathy (HPO)
characterised by periosteal inflammation at distal
ends
of long bones, wrists, ankles,
metacarpals and metatarsals
sweelling and tenderness over wrists and
other involved areas
Staining
staining of fingers - sign of cigarette smoking
(caused by tar, not nicotine)
Wasting and weakness
Pulse rate
Flapping tremor (asterixis) - unreliable sign
ask patient to dorsiflex wrists and spread out
fingers, with arms outstretched
flapping tremor may occur with severe carbon
dioxide retention (severe chronic airflow
limitation)
The Face
Eyes
Horner's syndrome? (constricted pupil, partial
ptosis and loss of sweating which can be due to
apical lung tumour
compressing sympathetic nerves in neck)
Nose
polpys? (associated with asthma)
engorged turbinates? (various allergic conditions)
deviated septum? (nasal obstruction)
Mouth and tongue
look for central cyanosis
evidence of upper respiratory tract infection (a
reddened pharynx and tonsillar enlargement with
or without a coating of pus)
broken tooth - may predispose to lung
abscess or pneumonia
sinusitis is indicated by tenderness over the
sinuses on palpation
some patients with obstructive sleep apnoea will be
obese
with a receding chin, a small pharynx and a short
thick neck
The Trachea
causes of tracheal displacement:
toward the side of the lung lesion
upper lobe collapse
upper lobe fibrosis
pneumonectomy
upper mediastinal masses, such as retrosternal
goitre
tracheal tug (finger resting on trachea feels it move
inferiorly with each inspiration) is a sign of gross
overexpansion of the
chest because of airflow obstruction
The Chest: inspection
Shape and symmetry of chest
Barrel shaped
anteroposterior (AP) diameter is increased
compared
with lateral
diameter
causes: hyperinflation due to asthma,
emphysema
Harrison's sulcus
innar depression of lower ribs just above costal
margins
at site of attachment of diaphragm
causes:
severe asthma in
childhood rickets
Kyphosis , exaggerated forward curvature of spine
Scoliosis , lateral bowing
Kyphoscoliosis: causes:
idiopathic (80%)
secondary to poliomyelitis (inflammation
involving grey matter of cord)
(note: severe thoracic kyphoscoliosis may reduce
lung
capacity and increase work of breathing)
Lesions of chest wall
scars - previous thoracic operations or chest drains
for a
previous pneumothorax or pleural efusion
thoracoplasty (was once performed to remove
TB, but no longer is because of efective
antituberculosis chemotherapy) invovled
removal of large number of
ribs on one side to achieve permanent
collapse of afected lung
erythema and thickening of skin may occur
in radiotherapy; there is a sharp demarcation
between
abnormal and normal skin
Difuse swelling of chest wall and neck
diffuse pulmonary
The Abdomen
pulmonary
thromboembolism marked
obesity
sleep apnoea
severe kyphoscoliosis
Permberton's sign
ask patient to lift arms over head
look for development of facial plethora,
inspiratory stridor, non-pulsatile elevation of
jugular venous pressure
occurs in vena caval obstruction
Feet
DIAGNOSTIC EVALUATION
2. Pulse Oximeter
Non-invasive method of continuously
monitoring he oxygen saturation of
hemoglobin
A probe or sensor is attached to the fingertip,
forehead, earlobe or bridge of the nose
Sensor detects changes in O2 sat levels by
monitoring light signals generated by the
oximeter and reflected by the blood pulsing
through the tissue at the probe
Cardiac arrest
Shock
Use of dyes or
vasoconstricto
rs
Severe anemia
High carbon
monoxide
Level
3. Chest X-ray
Nursing
8. Bronchoscopy
This is the direct inspection and observation of the
Therapeutic uses
9. Lung Scan
the
tracheobronchial tree
To Excise lesions
To remove tenacious secretions obstructing
abnormalities
tracheobronchial
To drain abscess tree
To treat post-operative atelectasis
Laboratory test
Nursing interventions:
Early morning sputum specimen
is to be collected (suctioning or
expectoration)
Scalene or cervicomediastinal
Non-invasive test
Measurement of lung volume, ventilation, and
difusing capacity
Nursing interventions:
Document bronchodilators or narcotics
used before testing
LUNG CAPACITIES:
Functional Residual Capacity (ERV 1100 mL + RV 1200
mL =
2300 mL )
The volume of air that remains in the lungs after
normal, quiet exhalation
Inspiratory Capacity (TV 500 mL + IRV 3000 mL = 3500
mL )
The amount of air that a person can inspire
maximally after a normal expiration
Vital capacity (IRV 3000 mL + TV 500 mL + ERV 1100 mL =
4600 mL )
The maximum volume of air that can be exhaled
after a maximum inhalation
Reduced in COPD
Total Lung Capacity (IRV 3000 mL + TV 500 mL + ERV
1100 mL + RV 1200 mL = 5800 mL )
Laboratory test
Nursing interventions:
Utilize a 10-ml. Pre-heparinized
syringe to prevent clotting of
specimen
17. Thoracentesis
Secure consent
site
1. Oxygen Therapy
Indication: Hypoxemia
Signs of Hypoxemia
o Increased pulse rate
o Rapid, shallow respiration and dyspnea
o Increased restlessness or lightheadedness
o Flaring of nares
o Substernal or intercostals retractions
o Cyanosis
Low fow oxygen provides partial oxygenation with
patient breathing a combination of supplemental
oxygen and room air. Low-flow administration devices:
o Nasal Cannula 24-45% 2-6 LPM
o Simple Face Mask 0-60%
5-8 LPM
o Partial Rebreathing Mask 60-90%
6-10 LPM
o Non-rebreathing Mask
95-100% 6-15 LPM
o Croupette
o Oxygen Tent
High fow oxygen provides all necessary
oxygenation, with patients breathing only oxygen
supplied from the mask and exhaling through a oneway vent.
High flow administration devices
o Venturi Mask
24-40% 4-10 LPM
2. Tracheobronchial suctioning
Postural drainage
a. Steam inhalation
b. Aerosol inhalation
Percussion
Produces energy wave that is transmitted through the
chest wall to the bronchi.
The chest is struck rhythmically with cupped hands over
the areas were secretions are located.
Avoid percussion over the spine, kidneys, breast or
incision and broken ribs. Areas should be percussed for
1-2 minutes
Vibration
Works similarly to percussion, where hands are placed on
clients chest and gently but firmly rapidly vibrate hands
against thoracic wall especially during clients exhalation.
This may help dislodge secretions and stimulate cough.
This should be done at least 5-7 times during patient
exhalation.
Suctioning
Nursing Interventions in CPT
Nursing care
Positioning
of
patient,
teach
and
encourage use, set realistic goals for the
patient, and record the results.
Three-bottle system
If there is NO
mean
TWO things
Ambulate
I.
PNEUMONIA
inflammation
of
the
lung
parenchyma leading to pulmonary consolidation
because alveoli is filled with exudates
A.
ETIOLOGIC AGENTS
1.
Streptococcus
pneumoniae
(pneumococcal
pneumonia
)
2.
Hemophilus influenzae (bronchopneumonia)
3.
Klebsiella pneumoniae
4.
Diplococcus pneumoniae
5.
Escherichia coli
6.
Pseudomonas aeruginosa
B.
C.
PREDISPOSING FACTORS
1.
Smoking
2.
Air pollution
3.
Immunocompromised
(+) AIDS
Kaposis Sarcoma
Bronchogenic Ca
4. Prolonged immobility (hypostatic pneumonia)
5. Aspiration of food (aspiration pneumonia)
6. Over fatigue
D.
E.
DIAGNOSTICS
1.
Sputum GS/CS confirmatory; type and
sensitivity;
2.
3.
4.
F.
Elevated
ABG PO2 decreased (hypoxemia)
NURSING MANAGEMENT
1.
Enforce CBR (consistent to all respi disorders)
2.
Strict respiratory isolation
3.
Administer medications as ordered
Broad spectrum
antibiotics
Tetracycline
Macrolides
Azithromycin (OD x
3/days)
1.
Too costly
2. Only se: ototoxicity
transient hearing loss
4.
5.
6.
7.
8.
9.
Anti-pyretics
Mucolytics/expectorants
Administer O2 inhalation as ordered
Force fluids to liquefy secretions
Institute pulmonary toilet measures to
promote expectoration of secretions
DBE,
Coughing
exercises,
CPT
(clapping/vibration), Turning and
repositioning
Nebulize and suction PRN
Place client of semi-fowlers to high fowlers
Provide a comfortable and humid environment
Monitor VS and BS
Encourage DBE
Unstable VS
Hemoptysis
Increased
ICP
Avoidance of precipitating
factors
Prevention of complications
Atelectasis
Meningitis
Internal
External
RETROLENTAL
FIBROPLASIA
II.
A.
PRECIPITATING FACTORS
1.
Malnutrition
2.
Overcrowding
3. Alcoholism: Depletes VIT B1 (thiamin) alcoholic
beriberi malnutrition
4.
Physical and emotional stress
5.
6.
B.
C.
D.
E.
Mantoux test
PPD
8-10 mm (DOH)
10-14 mm (WHO)
5 mm in AIDS patients is +
indicates
previous
exposure
tubercle bacilli
2.
Sputum AFB (+) tubercle bacilli
3.
CXR (+) pulmo infiltrated due to caseous
necrosis
4.
CBC elevated WBC
9.
to
NURSING MANAGEMENT
1.
Enforce CBR
2.
Institute strict respiratory isolation
3.
Administer O2 inhalation
4.
Forced fluids
5.
Encourage DBE and coughing
NO CLAPPING in chronic PTB
d/t hemoptysis may lead to
hemorrhage
6.
Nebulize and suction PRN
7.
Provide comfortable and humid environment
8.
Institute short course chemotherapy
Intensive
phase
INH
Rifampicin
SE:
red
orange
color
of
bodily secretions
PZA
May
be
replaced
with
Ethambutol (SE: optic neuritis) if
(+) hypersensitivity to drug
SE:
allergic
reactions;
hepatotoxicity and nephrotoxicity
1.
Monitor liver enzymes
2.
Monitor BUN and CREA
INH given for 4 months, PZA
and Rifampicin is given for 2 months,
A.C. to facilitate absorption
These
3
drugs
are
given
simultaneously
to
prevent
development of resistance
Standard
Regimen
Streptomycin injection
(aminoglycosides)
Neomycin, Amikacin,
Gentamycin
th
1. common
SE:
8
CN
damage
tinnitus
b.
CREA (N = 8-10)
Health teaching and d/c planning
Atelectasis
Military
TB
(extrapulmonary
TB:
meningeal, Potts, adrenal glands,
skin,
cornea
)
Strict compliance to medications
Never double the dose! Continue
taking the meds if missed a day)
Diet modifications: increased CHON,
CHO, Calories, Vit C
Importance of ffup care
3.
4.
SIGNS AND
SYMPTOMS
PTB like symptoms
Productive cough
Fever, chills, anorexia,
body malaise
Cyanosis
Chest and joint pains
Dyspnea
NURSING MANAGEMENT
Enforce CBG
Antifungal agents
Amphotericin B (Fungizone)
SE:
nephrotoxicity and hypokalemia
PREDISPOSING FACTORS
DIAGNOSTICS
Hemoptysis
Bronchiectasis, atelectasis
Prevention of spread
generalized
1.
2.
3.
4.
Chronic Bronchitis
Bronchial Asthma
Bronchiectasis
Pulmonary Emphysema
I.
CHRONIC
BRONCHITIS
(Blue
Bloaters)
II.
A.
PREDISPOSING FACTORS
A.
PREDISPOSING FACTORS
1.
Smoking
2.
Air pollution
B.
Peripheral edema
Cor pulmonale
C.
NURSING MANAGEMENT
1.
Enforce CBR
2.
Administer medications as ordered
Bronchodilators
Antimicrobials
Corticosteroids
Mucolytics/expectorants
3. Low inflow O2 admin; high inflow will
cause respiratory arrest
4.
Force fluids
5.
Nebulize and suction client as needed
6.
Provide comfortable and humid environment
7.
Health teaching and d/c planning
avoidance of smoking
prevent complications
Drugs
(aspirin, penicillin, B-blockers)
Genetics
DIAGNOSTICS
1. ABG analysis: decreased PO2, increased
PCO2, respiratory acidosis; hypoxemia
cyanosis
D.
1.
SIGNS AND
SYMPTOMS
Cough that is productive
Dyspnea
Wheezing on expiration
Tachycardia, palpitations and diaphoresis
Mild apprehension, restlessness
Cyanosis
C.
DIAGNOSTICS
1.
PFT decreased vital lung capacity
2.
ABG analysis PO2 decreased
D.
NURSING MANAGEMENT
1.
Enforce CBR
2.
Administer medications as ordered
Bronchodilators administer first to
facilitate absorption of corticosteroids
Inhalation
MDI
Corticosteroids
Mucolytics/expectorants
Mucomyst
Antihistamine
3.
4.
5.
6.
7.
8.
Prevention of complications
III.
Status asthmaticus
DOC:
Epinephrine
Aminophylline
drip
Emphysema
Regular adherence to medications
Importance of ffup care
D.
E.
A.
PREDISPOSING FACTORS
1.
Recurrent lower respiratory tract infection
Histoplasmosis
2.
Congenital disease
3.
Presence of tumor
4.
Chest trauma
B.
1.
2.
3.
4.
5.
6.
C.
SIGNS AND
SYMPTOMS
Consistent productive cough
Dyspnea
Presence of cyanosis
Rales and crackles
Hemoptysis
Anorexia and generalized body malaise
DIAGNOSTICS
1.
ABG analysis reveals low PO2
2. Bronchoscopy direct visualization of
bronchi lining using a fibroscope
Pre-op
Secure consent
Explain procedure
Post-operative
Atelectasis
Cardiac tamponade: muffled heart
sounds, pulsus paradoxus, HPN
NURSING MANAGEMENT
1.
Enforce CBR
2. Low inflow O2 admin; high inflow will
cause respiratory arrest
3.
Administer medications as ordered
Bronchodilators
Antimicrobials
Corticosteroids
(5-10
minutes
after bronchodilators)
Mucolytics/expectorants
4.
Force fluids
5.
Nebulize and suction client as needed
6.
Provide comfortable and humid environment
7.
Health teaching and d/c planning
Avoidance of
smoking
Prevent
complications
Atelectasis
Cor
pulmonale
Pleural
efusion
Pneumothorax
Importance of ffup
care
Inelasticity of alveoli
Air trapping
A.
PREDISPOSING FACTORS
1.
Smoking
2.
Air pollution
3. Hereditary: involves alpha-1 antitrypsin
for elastase production for recoil of the
alveoli
4.
Allergy
5. High risk group elderly degenerative
decreased
vital
lung
capacity
and
thinning of alveolar lobes
SIGNS AND
SYMPTOMS
1.
Productive cough
2.
Dyspnea at rest
3.
Prolonged expiratory grunt
4.
Resonance to hyperresonance
5.
Decreased tactile fremitus
6.
Decreased breath sounds ( if (-) BS lung
collapse)
7.
Barrel chest
8.
Anorexia and generalized body malaise
9.
Rales or crackles
10. Alar flaring
11. Pursed-lip breathing (to eliminate excess CO2)
TYPES
1. Spontaneous air enters pleural space
without an obvious cause
B.
PREDISPOSING FACTORS
1.
Chest trauma
2.
Inflammatory lung condition
3.
tumors
SIGNS AND SYMPTOMS
1.
Sudden sharp chest pain, dyspnea, cyanosis
2.
Diminished breath sounds
3.
Cool, moist skin
4.
Mild restlessness and apprehension
5.
Resonance to hyperresonance
B.
C.
D.
DIAGNOSTICS
1.
ABG analysis reveal
Panlobular, centrilobular PO2 elevation
and PCO2 depression respiratory
acidosis (blue bloaters)
Panacinar/centriacinar PCO2
depression and
PO2 elevation (pink pufers hyperaxemia)
2.
Pulmo function test decreased vital lung
capacity
NURSING MANAGEMENT
1.
Enforce CBR
2.
Administer medications as ordered
Bronchodilators
Antimicrobials
Corticosteroids
Mucolytics/expectorants
3. Low inflow O2
admin; high inflow will
cause respiratory arrest and oxygen toxicity
4.
Force fluids
5.
Pulmonary toilet
6.
Nebulize and suction client as needed
7.
Institute PEEP in mechanical ventilation
Avoidance of smoking
Prevent complications
Atelectasis
Cor
pulmonale
Pleural
efusion
Pneumothorax
C.
D.
DIAGNOSTICS
1.
ABG analysis: PO2 decreased
2.
CXR confirms collapse of lungs
E.
NURSING MANAGEMENT
1.
Assist in endotracheal intubation
2.
Assist in thoracentesis
3.
Administer meds as ordered
Antibiotics
4.
Assist in CTT to H20 sealed drainage