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Acute Chest Syndrome
- ACS is the leading cause of morbidity and mortality in children and adults with Sickle Cell Disease.
- Definition: ==> A new infiltrate on CXR (excluding atelectasis) PLUS one or more of the following:
- Tachpnea
- Fever (>101 degrees F)
- Chest Pain
- Cough
- Wheezing
- Hypoxemia
- Treatment
- Bronchodilators
- Trial of beta-agonists for clinical response is advocated even in those without wheezing.
- Antibiotics
- Broad Spectrum: Ceftriaxone PLUS Azithromycin
- Evidence demonstrates a significant amount of these patients have atypical bacterial infections
- Vanco is warranted for severe disease unresponsive to therapy
- Steroids
- Use for patients with Reactive Airway Disease or severe distress
- They may cause a rebound of Vaso-occlusive Crisis and need to be tapered.
- Prednisone 2mg/kg/Day x 5 then taper
- Pain Control
- Need to optimize pulmonary toilet by providing adequate pain management, but avoid over-sedation leading to hypoventilation.
- NSAIDs have proven to be useful in conjunction opiods.
- Transfusion of PRBCs
- Simple
- For pts who have a >10-20% drop from their baseline Hgb
- For pts who are symptomatic, but not in impending respiratory failure
- Try not to EXCEED Hgb of 10g/dL post transfusion
- Exchange
- For pts with impending respiratory failure
- For pts with Hgb > 10g/dL and significant symptoms (to avoid hyperviscosity)
- The decision to transfuse these patients needs to be made in conjunction with the consulting Hematologist.
- Simple
- Bronchodilators
References
NHLBI. Acute chest syndrome and other pulmonary complications. Management of Sickle Cell Disease. June 2003; 25 – 29. http://www.nhlbi.nih.gov/health/prof/blood/sickle/index.htm.
Kathleen Ryan, RN, MPH, Anju Chawla, MD and Matthew Heeney, MD. Management of Acute Chest Syndrome in Sickle Cell Disease. New England Pediatric Sickle Cell Consortium. 2005.