Systemic corticosteroids in acute chest syndrome: friend or foe?

Folasade Ogunlesi1, Matthew M Heeney2, Anastassios C Koumbourlis1

  • 1Division of Pulmonary & Sleep Medicine, Children's National Medical Center/George Washington University, Washington DC.

Insights

Corticosteroids may benefit acute chest syndrome (ACS) in sickle cell disease (SCD) patients by reducing inflammation. However, their use is debated due to serious adverse effects like pain crises and stroke.

Area of Science:

  • Hematology
  • Pulmonology
  • Pharmacology

Background:

  • Acute chest syndrome (ACS) is a severe pulmonary complication in sickle cell disease (SCD).
  • ACS is a leading cause of hospitalization and mortality in SCD patients, particularly in children.
  • Potential triggers for ACS include infections, fat embolism, asthma, and ischemic reperfusion injury, all linked to inflammation.

Purpose of the Study:

  • To review the evidence supporting and opposing the use of corticosteroids in managing ACS.
  • To analyze the risk-benefit profile of different corticosteroids, dosing strategies, and the impact of comorbidities.

Main Methods:

  • Literature review of studies investigating corticosteroid use in ACS.
  • Analysis of reported benefits, adverse effects, and influencing factors.

Main Results:

  • Corticosteroids demonstrate anti-inflammatory properties that can benefit ACS.
  • Significant adverse effects, including rebound pain, stroke, and renal complications, lead to reluctance in their use.
  • The choice of corticosteroid, dosage, and patient comorbidities influence the risk-benefit balance.

Conclusions:

  • The use of corticosteroids in ACS requires careful consideration of potential benefits against serious risks.
  • Further research is needed to optimize corticosteroid therapy for ACS in SCD patients.

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