Acute chest syndrome: Difference between revisions

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==See Also==
==See Also==
*[[Sickle Cell Crisis]]
*[[Sickle Cell Crisis]]
==References==


==Video==
==Video==
{{#widget:YouTube|id=pKxAsqj4GOE}}
{{#widget:YouTube|id=pKxAsqj4GOE}}
==References==


[[Category:Heme/Onc]]
[[Category:Heme/Onc]]

Revision as of 21:59, 2 November 2015

Background

  • A leading cause of hospitalization and death in adults with sickle cell disease
  • Occurs most commonly in the 2-4yr old age group and then declines with age
  • Due to pulmonary ischemia and infarction; complication of PNA

Causes

Clinical Features

Differential Diagnosis

Sickle cell crisis

Diagnosis

Work-Up

  • CBC
  • Retic count
  • VBG / ABG
  • Bcx /sputum cx
  • CXR

Evaluation

  • New infiltrate on CXR with at least one of the following:
    • Fever >38.5
    • Cough
    • Wheezing
    • Tachypnea
    • Chest pain
  • Note: CXR findings may lag behind the clinical features

Treatment

  1. O2
    • Titrate to pulse oximetry
  2. Incentive Spirometer
  3. Hydration
    • Oral hydration preferred
    • IV hydration with hypotonic fluid if pt unable to tolerate PO
  4. Analgesia
    • Pulmonary toilet is important but avoid excessive sedation
  5. Bronchodilators
  6. Antibiotics
  7. Transfusion (leukocycte depleted)
    • Consider transfusion to goal of Hb 11 / Hct 30 for:
      • O2 Sat <92% on room air
      • Hct 10-20% below pt's usual Hct or dropping Hct
  8. Exchange transfusion
    • Consider for:
      • Progression of acute chest syndrome despite simple transfusion
      • Severe hypoxemia
      • Multi-lobar disease
      • Previous history of severe acute chest syndrome or cardiopulmonary disease

Complications

See Also

Video

{{#widget:YouTube|id=pKxAsqj4GOE}}

References