Pedia 3.1 Pediatric Pulmo
Pedia 3.1 Pediatric Pulmo
Pedia 3.1 Pediatric Pulmo
Weight loss
Contact with tuberculosis
Chronic ear or nose symptoms (is there a problem with the cilia
function?)
Relieving factors, such as bronchodilators or antibiotics
Exposure to cigarette smoke
Possible allergies and triggers
Family history of atopy (is this ashma?) Or chronic respiratory
disorders
Relation to feeding and swallowing (is there a problem with
aspiration?)
Foreign body aspiration
SPECIFIC COUGH
DIAGNOSIS
clinical, X-ray of the neck subglottic narrowing “Steeple sign”
YES Reversible airway
ASTHMA obstruction? TREATMENT
airway management, tx of hypoxia
NO cold steam- no evidence supporting use of cold mist
Assess risk factors for: nebulized racemic epinephrine-fluid resorption and dec laryngeal mucosal
edema
Bronchiectasis recurrent pneumonia
Aspiration steroids- oral dexamethasone 0.6 mk single dose -dec edema in the
Chronic or less common infections laryngeal mucosa
Protracted bacterial bronchitis o IM dexamethasone and inhaled budesonide same effect
Airway abnormality antibiotics, sedatives, expectorants and antihistamine – not indicated
Other less common pulmonary conditions
Cardiac disease RADIOGRAPH
DIAGNOSIS
Polysomnography
o gold standard
o assess gas exchange impairment CO2 and O2 saturation,
thoracoabdominal movement, resp pattern
lateral neck-evaluates size of adenoids
TREATMENT
adenotonsillectomy (T and A)
continous or bilevel positive airway pressure
(nasal CPAP or BiPAP)
TREATMENT
COMPLICATIONS
• Airway management- endo or naso tracheal intubation for 2-3 days
pulmonary hypertension, right sided hearth failure and cor pulmonale
• Ceftriaxone, cefotaxime,or meropenem for 10 days
Failure to diagnose and treat: serious but generally reversible
• Racemic epinephrine and steroids- ineffective
consequences
• Chemoprophylaxis when exposed child develops febrile illness
Attentional capacity, memory, and cognitive function, and increased
• Rifampicin 20mg/kg OD for 4 days: max dose 600mg
behavior problems
o all household members
o child <4 y.o incomplete immunized
DISEASES OF THE LOWER RESPIRATORY TRACT o younger than 12 mos not completed primary vaccine series
CROUP: LARYNGOTRACHEOBRONCHITIS (LTB) o immunocompromised
most common, caused by parainfluenza viruses in 75%
affects children 3 mos to 5 yrs peak at 2yr
mild URTI, low grade fever for 1-3 days
barking cough hoarseness with inspiratory stridor
other family members have mild respiratory illness with laryngitis
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PEDIATRICS II: PEDIATRIC PULMONOLOGY
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PEDIATRICS II: PEDIATRIC PULMONOLOGY
Defined by the history of respiratory symptoms i.e. wheeze, shortness Initial Assessment of Acute Asthma Exacerbation in ≤ 5 years
of breath, chest tightness and cough that vary over time and in
intensity SYMPTOMS MILD SEVERE
With widespread, variable and reversible expiratory airflow limitation Altered consciousness No Agitated confused or
drowsy
Variations are often triggered by factors: exercise, allergen or irritant
exposure, change in weather or viral respiratory infections Oximetry on >95% <92%
presentation **
Speech + Sentences Words
Pulse rate <100 beats / minute >200 bpm (0-3 years
old) >180bpm (4-5 yo)
Central cyanosis Absent Likely to be present
Wheeze intesity Variable Chest may be quiet
*Any of theses indicates a severe exacerbation.
** Oximetry pre )2 or BD + normal development abnormality must be
considered
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PEDIATRICS II: PEDIATRIC PULMONOLOGY
BRONCHIECTASIS
Irreversible abnormal dilatation of the bronchial tree.
Pathogenesis – three basic mechanism
1. Obstruction – because of foreign body, impacted mucuos poor
mucocillary clearance, external compression.
2. Infection – measles, TB, pertussis induce chronic inflammation,
bronchial wall damage and dilatation.
3. Chronic inflammation similar to obstruction leads to
bronchiectasis
Most Common Cause:
o Difficulty clearing secretions and recurrent infections
TYPES
Cylindrical
o Diffuse dilatation of bronchial unit affect muscles and
connected tissue
Saccular
o Affects the cartilage of the airway causing ballooning of
bronchi
o Most severe form of bronchiectasis
SYMPTOMS AND PHYSICAL FINDINGS
Cough and copious purulent sputum production-most common
complaint.
Hemptysis
Crackles, wheezing, digital clubbing
DIAGNOSIS
CXR – non specific, cystic spaces with air fluid level
HRCT – gold standard, provides disease location mediastinal lesion
and extent of involvement
TREATMENT
COUGH VARIANT ASTHMA Medical – dec airway obstruction and control infection chest
physiotherapy, bronchodilators
Frequently under diagnosed if no Hx of recurrent wheezing. antibiotics two -4 weeks parenteral
Cough may be the main symptom. Surgical – localized lesion more severe resistant to med treatment.
Dyspnea usually absent or minimal DISEASE OF THE PLEURA
PE: mostly normal Inflammatory process of the pleura
Chest xray : normal o Dry or plastic
o Serofibrinous pleurisy
PFTs may be diagnostic proof with increased in FEV1 after SABA of
o Empyema
>20%. Dry or Plastic Pleurisy
Trial on ICS on LTRA w/ salbutamol. Most commonly associated with infection of the lung
Small amount of yellow serous fluid and adhesion
ATELECTASIS Pain exaggerated by deep breathing coughing and straining.
Rough friction rub, dullness and suppressed breath sounds.
Incomplete expansion or complete collapse of the air-breathing Serofibrinous Pleurisy
tissue. Associated with acute bacterial pulmonary infection
Results from obstruction of air intake into the alveolar sac Pleuritic pain is absent as fluid accumulates
Associated with the absorption of air contained in the alveoli, which Cough, dyspnea, retractions during large fluid collections.
are no longer ventilated. Chest x-ray shows homogenous density
CLINICAL SYMPTOMS AND FINDINGS Purulent Pleurisy (Empyema)
Small area – asymptomatic Pus in the pleural space
Associated with pneumococci and H. Influenzae or staph aureus.
Large area – dyspnea, rapid shallow breathing, cough and often
Most patients are febrile
cyanosis. Older children have greater respiratory difficulty
Chest appears flat on affected side.
Limitation of chest excursion decreased breath sound and coarse
crackles dullness to percussion.
DIAGNOSIS
Chest Xray- Opacity, wedge-shaped density.
TREATMENT:
Antibiotics
Bronchodilator / corticosteroid – in asthma
Bronchoscopy
Postural drainage
RIGHT MIDDLE LOBE SYNDROME
Absent or aeration and bronchial obstruction
Associated with PTB and Asthma
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PEDIATRICS II: PEDIATRIC PULMONOLOGY
PLEURAL EFFUSION
Types
Antibiotics
• empirical treatment
GASTROESOPHAGEAL REFLUX
• S. pneumoniae – most common
• Increased incidence of CPE from 1996 –1999 then declined with use
reduced lower esophageal sphincter tone
of pneumococcal vaccine
Closed thoracostomy drainage indications cough occurs when there’s an acid reflux in the distal esophagus
- gross pus stimulate the vagus nerve
- + organism on gram stain Symptoms: cough occurs while awake and upright
- pH < 7.0 - regurgitation of food , dysphagia.
- glucose < 40mg/dl Pathophysiology
- LDH > 1000 IU Microaspiration and vagal reflexes elicited in the esophagus may
- volume ? result in respiratory symptoms like cough and wheezes
- respiratory distress? PE: failure to thrive, wheezing
Dx:
Barium esophagogram,
24 hr pH-gold standard
Treatment: Supportive
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PEDIATRICS II: PEDIATRIC PULMONOLOGY
Medical- Domperidone,PPI
Surgery - Fundoplication
Physical examination
o Dark discolouration of
the periorbital skin
(allergic shiners).
o Horizontal wrinkle near
the tip of the nose
(allergic crease).
o Pale and swollen inferior
turbinates with clear
nasal discharge.
o Total serum Ig E 300 (<
100 kiu/ml), with
eosinophilia on nasal
smear.
o Positive skin prick test
for dog, cat dander,
House dust mites mix,
feather mix.
Clinical diagnosis
o “PND, nasal discharge, throat-clearing” caused by rhinosinusitis
o Historical reports of post nasal or pharyngeal syndromes –unreliable
CHRONIC SINUSITIS
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PEDIATRICS II: PEDIATRIC PULMONOLOGY
APPENDIX
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