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Pleural Effusion, Pediatric


Basics


Description


Accumulation of fluid in the pleural cavity ‚  

Pathophysiology


  • Normally 1 " “15 mL of fluid in the pleural space
  • Alterations in the flow and/or absorption of this fluid lead to its accumulation.
  • Mechanisms that influence this flow of fluid:
    • Increased capillary hydrostatic pressure (i.e., congestive heart failure [CHF], overhydration)
    • Decreased pleural space hydrostatic pressure (i.e., after thoracentesis, atelectasis)
    • Decreased plasma oncotic pressure (i.e., hypoalbuminemia, nephrosis)
    • Increased capillary permeability (i.e., infection, toxins, connective tissue diseases, malignancy)
    • Impaired lymphatic drainage from the pleural space (i.e., disruption of the thoracic duct)
    • Passage of fluid from the peritoneal cavity through the diaphragm to the pleural space (i.e., hepatic cirrhosis with ascites)
  • 2 types of pleural effusion:
    • Transudate: Mechanical forces of hydrostatic and oncotic pressures are altered, favoring liquid filtration.
    • Exudate: Damage to the pleural surface occurs that alters its ability to filter pleural fluid; lymphatic drainage is diminished.
  • Stages associated with parapneumonic effusions (infectious exudates):
    • See Appendix, Table 3.
    • Exudative stage
      • Free-flowing fluid
      • Pleural fluid glucose, protein, lactate dehydrogenase (LDH) level, and pH are normal.
    • Fibrinolytic stage
      • Loculations are forming.
      • Increase in fibrin, polymorphonuclear leukocytes, and bacterial invasion of pleural cavity are occurring.
      • Pleural fluid glucose and pH falls while protein and LDH levels increase.
    • Organizing stage (empyema)
      • Fibroblasts grow.
      • Pleural peal forms.
      • Pleural fluid parameters worsen.

Diagnosis


History


  • Underlying disease determines most systemic symptoms.
  • Patient may be asymptomatic until the amount of fluid is large enough to cause cardiorespiratory compromise/distress.
  • Dyspnea and cough are associated with large effusions.
  • Fever (if infectious etiology)
  • Pleuritic pain (pneumonia may cause irritation of the parietal pleura, causing pleural pain; as the effusion increases and separates the pleural membrane, the pain may disappear)

Physical Exam


  • Decreased thoracic wall excursion on the ipsilateral side
  • Fullness of intercostal spaces on the ipsilateral side
  • Trachea and cardiac apex displaced toward the contralateral side (may produce a mediastinal shift that can reduce venous return and compromise the cardiac output)
  • Dull or flat percussion on the ipsilateral side (suggesting the presence of consolidation of pleural effusion)
  • Decreased tactile and vocal fremitus
  • Decreased whispering pectoriloquy
  • Pleural rub during early phase (may resolve as fluid accumulates in the pleural space)
  • Decreased breath sounds

Diagnostic Tests & Interpretation


  • Cytologic exam of pleural fluid
    • Fresh and heparinized specimen should be refrigerated at 4 ‚ °C (39.2 ‚ °F) until it can be processed.
    • Fixatives should not be added.
  • Pleural fluid parameters to be routinely measured include the following (Appendix, Table 4):
    • pH
    • LDH
    • Protein
    • Glucose
      • Note: Glucose of <40 mg/dL suggests a para-pneumonic, tuberculosis, malignant, or rheumatic etiology to the effusion.

Lab
Initial lab tests
Serology values to follow the degree of inflammation and the response to therapy: ‚  
  • Erythrocyte sedimentation rate (ESR)
  • C-reactive protein (CRP)

Imaging
  • Chest radiograph
    • Anteroposterior projection can show >400 mL of pleural fluid.
    • Lateral projection can show <200 mL of pleural fluid.
    • Lateral decubitus film to evaluate for free-flowing pleural fluid can show as little as 50 mL of pleural fluid.
  • Ultrasound
    • Reveals small (3 " “5 mL) loculated collections of pleural fluid
    • Useful as a guide for thoracentesis
    • Aids in distinguishing between pleural thickening and pleural effusion
  • CT scan
    • Clearly reveals effusions/empyemas, abscess, or pulmonary consolidations
    • Useful for defining the extent of loculated effusions

Diagnostic Procedures/Other
  • Thoracentesis
    • Indicated whenever etiology is unclear or if the effusion causes symptoms (e.g., prolonged fever or respiratory distress)
  • Pleural biopsy
    • If thoracentesis is nondiagnostic
    • Most useful for diseases that cause extensive involvement of the pleura (i.e., tuberculosis, malignancies)
    • Confirms neoplastic involvement in 40 " “70% of cases

Differential Diagnosis


  • Transudate
    • Cardiovascular
      • CHF
      • Constrictive pericarditis
    • Nephrotic syndrome with hypoalbuminemia
    • Cirrhosis
    • Atelectasis
  • Exudate
    • Infection
      • Staphylococcus aureus (increasing incidence of methicillin-resistant species)
      • Streptococcus pneumoniae (increasing incidence of penicillin-resistant species)
      • Haemophilus influenzae (decreasing incidence since introduction of H. influenzae type b [Hib] vaccine)
      • Group A Streptococcus
      • Anaerobes
      • Gram-negative enterics
      • No identified organisms (all cultures sterile)
      • Tuberculous effusion
      • Viral effusions (adenovirus, influenza)
      • Fungal effusions: most not associated with effusions; Nocardia and Actinomyces are most commonly seen.
      • Parasitic effusions
    • Neoplasm: seen mostly in leukemia and lymphoma; uncommon in children
    • Connective tissue disease
      • Rheumatoid arthritis
      • Systemic lupus erythematosus
      • Wegener granulomatosis
    • Pulmonary embolus
    • Intra-abdominal disease
      • Subdiaphragmatic abscess
      • Pancreatitis
    • Sarcoidosis
    • Esophageal rupture
    • Hemothorax
    • Chylothorax
    • Drugs
    • Chemical injury
    • Postirradiation effusion

Treatment


Medication


  • Antibiotics
    • Used when effusion is caused by a bacterial infection
    • Specific antibiotics dictated by organism identified
    • If effusion is sterile, broad-spectrum antibiotics are indicated to cover for the usually seen organisms.
    • Clinical improvement usually begins within 48 " “72 hours of therapy.
    • Continue IV antibiotics until afebrile.
    • Complete remainder of therapy on oral antibiotics.
  • Duration of antibiotic therapy depends on the infectious organism and the degree of illness:
    • Total duration is controversial.
    • Usually, at least 2 " “4 weeks of total IV and PO

Additional Treatment


General Measures
  • Supportive measures:
    • Maintain adequate
      • Oxygenation
      • Fluid status
      • Nutritional balance
    • Antipyretic agents when febrile
    • Pain control
  • Treat the underlying disease:
    • Antibiotics for infections
    • Cardiac medications for CHF
    • Chemotherapeutic agents for malignancies
    • Anti-inflammatory agents (i.e., steroids) for connective tissue diseases
    • Medium-chain triglycerides and low-fat diet for chylothorax
  • Effective drainage of pleural fluid
    • Thoracentesis
    • Chest tube drainage
    • Surgical drainage
  • Duration of chest tube drainage
    • Discontinue when patient is asymptomatic (afebrile, no distress) and drainage <50 mL/h
    • Thick, loculated empyema requires prolonged drainage (and possibly a video-assisted thoracic surgery [VATS] procedure if effusion not improving).

Complementary & Alternative Therapies


  • Thoracentesis
    • For diagnosis purposes
      • To distinguish between a transudate and an exudate
      • For culture material (if infection is suspected)
      • For cytology (if malignancy is suspected)
    • For relief of dyspnea or cardiorespiratory distress
  • Chest tube thoracostomy
    • Reduce reaccumulation of fluid.
    • Drain parapneumonic effusion (before loculations develop which will prevent fluid drainage).
  • Intrapleural fibrinolytics
    • Adjunct to aid in drainage of complicated (i.e., multiloculated empyema) pleural effusions
    • Streptokinase, urokinase, and tPA are the agents of choice.

Surgery/Other Procedures


  • VATS
    • Alternative to more invasive procedures (e.g., open thoracotomy/decortication)
    • Debridement through pleural visualization and lysis of adhesions/loculations
    • Useful when
      • Initial drainage is delayed
      • Loculations prevent adequate drainage by chest tube alone
      • Patient is failing more conservative therapy
  • Pleurectomy
    • Chylothorax
    • Malignant effusions
  • Pleurodesis
    • For recurrent effusions
    • Chemical agents frequently used include talc, tetracycline, doxycycline, and quinacrine.
    • Surgical methods include the following:
      • Mechanical abrasion
      • Pleurectomy via VATS
      • Open thoracotomy route
    • In cases of malignant effusion:
      • Sclerosing procedures are usually ineffective.
      • Chest tube drainage can create a pneumothorax because the lung is incarcerated by the tumor.

Ongoing Care


Follow-up Recommendations


  • Clinical improvement usually within 1 " “2 weeks
  • With empyemas, the patient may have fever spikes for up to 2 " “3 weeks after improvement is noted.

Diet


When the effusion is a chylothorax: ‚  
  • Medium-chain triglycerides
  • Nutritional replacement
  • At least 4 " “5 weeks on this regimen

Prognosis


Depends on underlying disease process: ‚  
  • Properly treated infectious cause: excellent prognosis
  • Malignancy: poor prognosis

Complications


  • Hypoxia
  • Respiratory distress
  • Persistent fevers
  • Decreased cardiac function
  • Malnutrition (seen in chylothorax)
  • Shock (secondary to blood loss in cases of hemothorax)
  • Trapped lung

Additional Reading


  • Beers ‚  SL, Abramo ‚  TJ. Pleural effusions. Pediatr Emerg Care.  2007;23(5):330 " “334. ‚  [View Abstract]
  • Buckingham ‚  SC, King ‚  MD, Miller ‚  ML. Incidence and etiologies of complicated parapneumonic effusions in children. Pediatr Infect Dis.  2003;22(6):499 " “504. ‚  [View Abstract]
  • Calder ‚  A, Owens ‚  CM. Imaging of parapneumonic pleural effusions and empyema in children. Pediatr Radiol.  2009;39(6):527 " “537. ‚  [View Abstract]
  • Doski ‚  JJ, Lou ‚  D, Hicks ‚  BA, et al. Management of parapneumonic collections in infants and children. J Pediatr Surg.  2000;35(2):265 " “268; discussion 269 " “270. ‚  [View Abstract]
  • Heffner ‚  JE. Discriminating between transudates and exudates. Clin Chest Med.  2006;27(2):241 " “252. ‚  [View Abstract]
  • Krenke ‚  K, Peradzynska ‚  J, Lange ‚  J. Local treatment of empyema in children: a systematic review of randomized controlled trials. Acta Paediatr.  2010;99(10):1449 " “1453. ‚  [View Abstract]
  • Merino ‚  JM, CarpinteroI ‚  I, Alvarez ‚  T, et al. Tuberculous pleural effusion in children. Chest.  1999;115(1):26 " “30. ‚  [View Abstract]
  • Proesmans ‚  M, De Boeck ‚  K. Clinical Practice: Treatment of childhood empyema. Eur J Pediatr.  2009;168(6):639 " “645. ‚  [View Abstract]
  • Rocha ‚  G. Pleural effusions in the neonate. Curr Opin Pulm Med.  2007;13(4):305 " “311. ‚  [View Abstract]

Codes


ICD09


  • 511.9 Unspecified pleural effusion
  • 510.9 Empyema without mention of fistula
  • 511.81 Malignant pleural effusion
  • 012.00 Tuberculous pleurisy, unspecified
  • 511.89 Other specified forms of effusion, except tuberculous

ICD10


  • J90 Pleural effusion, not elsewhere classified
  • J86.9 Pyothorax without fistula
  • J91.0 Malignant pleural effusion
  • A15.6 Tuberculous pleurisy
  • J91.8 Pleural effusion in other conditions classified elsewhere

SNOMED


  • 60046008 Pleural effusion (disorder)
  • 58554001 Empyema of pleura
  • 83270006 Neoplastic pleural effusion (disorder)
  • 446986002 Tuberculous pleural effusion (disorder)

FAQ


  • Q: When will the chest radiograph findings become normal?
  • A: They may take up to 6 months (or longer) to return to normal appearance.
  • Q: When will the pulmonary function tests normalize?
  • A: Depending on extent of effusion, they may take up to 6 " “12 months.
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