DISORDERS OF THE RESPIRATORY SYSTEM PART 2.2 (based on T) Flashcards

1
Q

What are the two layers of the pleura?

A

Parietal pleura (lines the chest wall) and visceral pleura (lines the lung)

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2
Q

What is the function of pleural fluid?

A

Allows smooth movement of the lungs during normal ventilation

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3
Q

How is pleural fluid produced?

A

By filtration from systemic capillaries within the parietal interstitium, with production greatest at the lung apex

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4
Q

What maintains pleural fluid balance?

A

Pulmonary capillary hydrostatic and oncotic pressure, lymphatic drainage, and integrity of pleural and capillary membranes

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5
Q

What can cause excess pleural fluid formation?

A

Disturbance in hydrostatic/oncotic pressures, lymphatic drainage, or membrane integrity

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6
Q

What is pleural effusion?

A

Accumulation of fluid between the parietal and visceral pleura

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7
Q

What are the clinical manifestations of a small pleural effusion?

A

Usually asymptomatic

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8
Q

What are the clinical manifestations of a large pleural effusion?

A

Respiratory distress, dyspnea, dry cough, chest/shoulder pain worsened by inspiration

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9
Q

What are general causes of pleural effusion due to increased pleural fluid formation?

A

LV failure, pneumonia, pulmonary embolus, increased capillary permeability, lung atelectasis, ascites, peritoneal dialysis

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10
Q

What can cause decreased pleural fluid absorption?

A

Lymphatic obstruction, right ventricular failure, superior vena cava syndrome, aquaporin system disruption

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11
Q

What are the diagnostic tests for pleural effusion?

A

Pleural fluid analysis (protein, LDH, bacterial culture, gram stain, glucose, pH, WBC/RBC counts, amylase, cytology) and serum tests (CBC, LDH, total protein, glucose)

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12
Q

What are Light’s criteria for exudative pleural effusion?

A

Pleural fluid/serum LDH >0.6, Pleural fluid/serum protein >0.5, Pleural fluid LDH >2/3 upper limit of normal serum LDH, Pleural fluid cholesterol >55 mg/dL

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13
Q

What is the key difference between exudative and transudative pleural effusion?

A

Exudative effusions fulfill at least one Light’s criteria, while transudative effusions do not

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14
Q

What procedure is used to obtain pleural fluid for analysis?

A

Thoracentesis

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15
Q

What is the first-line management of pleural effusion?

A

Thoracentesis if the cause is unresolved

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16
Q

What is the preferred method for draining pleural effusion in chest trauma?

A

Tube thoracostomy

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17
Q

What are some pleural fluid appearances and their causes?

A

Grossly purulent: Empyema;
Thick tan brown: Staphylococcus aureus;
Putrid: Anaerobes;
Bloody: Hemothorax, Malignancy;
Milky: Chylothorax;
Yellow-green: Rheumatoid arthritis;
Black: Aspergillus nigricans

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18
Q

What is the key feature of transudative pleural effusion?

A

Results from imbalance of hydrostatic or oncotic pressures,
contains little protein and few cells (<500 cells/mm³), and
has serum-like glucose and hydrogen ion concentrations

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19
Q

What are common causes of transudative pleural effusion in children?

A

Atelectasis, LV failure, nephrotic syndrome, free peritoneal fluid, hypothyroidism

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20
Q

What distinguishes exudative pleural effusions from transudative?

A

Exudative effusions result from inflammation or lymphatic obstruction, causing fluid leakage with higher protein and cellular content

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21
Q

What are parapneumonic effusions?

A

Pleural effusions as a complication of bacterial pneumonia, especially in children under 2 years old

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22
Q

What are clinical signs of parapneumonic effusion?

A

Initially low WBC count, later high WBC count, elevated LDH, low glucose and pH, progressive fibrin deposition

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23
Q

What is the management of parapneumonic effusion?

A

IV antibiotics for infection, thoracotomy if massive effusion

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24
Q

What is pneumothorax?

A

Abnormal presence of air in the pleural space

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25
Q

What are causes of pneumothorax?

A

Traumatic, iatrogenic, spontaneous, post-infectious, inhalation toxins, congenital

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26
Q

What are clinical manifestations of pneumothorax?

A

Sudden chest pain, tachypnea, dyspnea, cyanosis, ipsilateral shoulder pain, hyperresonance on percussion

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27
Q

What is the diagnostic test for pneumothorax?

A

Chest radiograph (CXR), CT scan for bullae and blebs

28
Q

What is the treatment for pneumothorax?

A

Evacuating air from the pleural space and sealing the leakage”

29
Q

What causes disorders of ventilation in short limb dwarfism?

A

Reduced thoracic cage size, lateral narrowing, and sometimes shortening of the thoracic spine.

30
Q

Do most patients with short limb dwarfism survive?

A

Most patients do not survive, but some with asphyxiating thoracic dystrophy improve their ventilation as they grow up.

31
Q

What is Werdnig-Hoffman disease caused by?

A

A decrease in motor neurons, chromatolysis, proliferation of astrocytes and microglia, and diminution of spinal cord ventral roots due to the loss of myelinated fibers.

32
Q

What is a common symptom of Werdnig-Hoffman disease?

A

Severe skeletal muscle weakness with or without diaphragm involvement.

33
Q

What does childhood interstitial lung disease (ILD) cause?

A

Rare respiratory disorders that are mostly chronic and associated with high morbidity and mortality.

34
Q

What is the typical presentation of childhood ILD?

A

Insidious onset with symptoms like cough, dyspnea, exercise limitation, respiratory crackles, and wheezing.

35
Q

What can be seen in the advanced stage of childhood ILD?

A

Finger clubbing and cyanosis during exercise or rest.

36
Q

What diagnostic test is used for childhood ILD?

A

High-resolution CT, pulmonary function tests, bronchoalveolar lavage, and lung biopsy (gold standard).

37
Q

What is the first-line management for childhood ILD?

A

Oxygen, nutrition, immunization, and avoidance of air pollution.

38
Q

What are superior mediastinal tumors commonly associated with?

A

Thymus masses and cystic hygromas.

39
Q

Where are cystic hygromas typically located?

A

In the superior and anterior mediastinum.

40
Q

Which tumors are most commonly found in the middle mediastinum in children?

A

Lymphatic tumors, which are most common childhood malignancies.

41
Q

What is the management for posterior mediastinum neurogenic tumors?

A

Surgery and radiation therapy, as they are often radiosensitive.

42
Q

What are common primary benign pulmonary tumors?

A

Hamartomas, plasma cell granulomas, bronchial adenomas, papillomas, and hemangiomas.

43
Q

What are the symptoms of obstructive sleep apnea (OSA)?

A

Loud snoring, difficulty breathing during sleep, and sleep-related breathing pauses.

44
Q

How is obstructive sleep apnea (OSA) diagnosed?

A

Lateral neck radiograph and sleep study.

45
Q

What is the treatment for obstructive sleep apnea (OSA)?

A

Tonsilloadenoidectomy, nasal continuous positive airway pressure (NCPAP), nasopharyngeal intubation, and craniofacial operations.

46
Q

What are the symptoms of alveolar hypoventilation?

A

Sleep-related cyanosis, hypoventilation without snoring, and unexplained cor pulmonale.

47
Q

How is congenital central hypoventilation syndrome treated?

A

With ventilatory support and, in some cases, diaphragmatic pacing.

48
Q

What is a common complication of pneumonia in children?

A

Lung abscess, often involving mixed flora of aerobes and anaerobes.

49
Q

What are the physical exam findings in lung abscess?

A

Decreased breath sounds (effusion and empyema), increased breath sounds (consolidation), scattered crackles, rhonchi, and finger clubbing in ⅓ of cases.

50
Q

What is the treatment for a lung abscess?

A

Broad-spectrum antibiotics for 4-6 weeks, chest physiotherapy, postural drainage, and surgical drainage if no response to antibiotics.

51
Q

What is pneumothorax?

A

Presence of gas in the pleural cavity.

52
Q

Which type of pneumothorax occurs without underlying lung disease?

A

Primary spontaneous pneumothorax, commonly observed in tall males and smokers.

53
Q

What is the treatment for pneumothorax?

A

Supplemental oxygen and chest tube thoracostomy (CTT) if the area is large.

54
Q

What is atelectasis?

A

Partial or total collapse of a previously expanded alveolus or lung segment.

55
Q

Which diagnostic sign is seen in atelectasis?

A

Ipsilateral mediastinal shift on chest x-ray (CXR).

56
Q

What is bronchiectasis caused by?

A

Abnormal dilation, distortion, and destruction of the bronchial tree due to chronic infections or inflammation.

57
Q

Which organisms are involved in bronchiectasis?

A

Necrotizing bacterial infections.

58
Q

What are common symptoms of bronchiectasis?

A

Chronic cough, increased sputum production, progressive shortness of breath, easy fatigability, hypoxia, and hemoptysis.

59
Q

What is the treatment for bronchiectasis?

A

Beta-2 agonists (salbutamol), broad-spectrum antibiotics, 2D echo, and annual vaccinations for influenza and pneumococcus.

60
Q

What defines respiratory failure in children?

A

Inability to deliver oxygen and remove carbon dioxide from the pulmonary capillary bed, often indicated by PaCO2 >50 mmHg or PaO2 <60 mmHg on room air.

61
Q

What are the types of respiratory failure?

A

Type I (Non-ventilatory): PaO2 is low; Type II (Ventilatory): PaCO2 is elevated.

62
Q

What is the management for acute respiratory failure in children?

A

Oxygen, intubation, mechanical ventilation, and treatment of the underlying cause.

63
Q

What is ARDS?

A

Acute non-cardiogenic pulmonary edema with bilateral infiltrates on CXR and a PaO2 to FiO2 ratio of <200.

64
Q

How is ARDS in children different from adults?

A

Pediatric ARDS has a different pathophysiology and response to treatment.

65
Q

What are the signs of respiratory failure?

A

Tachypnea, bradypnea, apnea, nasal flaring, chest retraction, head bobbing, and cyanosis.

66
Q

What is the treatment for chronic respiratory failure in children?

A

Continuous oxygen supplementation at home or tracheostomy.

67
Q

What is BiPAP used for in children?

A

Ventilatory support during sleep, especially for those with sleep apnea or intrinsic lung disease.