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Clinical presentation of acute chest syndrome in sickle cell disease

C Taylor, F Carter, J Poulose, S Rolle, S Babu, S Crichlow

Derriford Hospital, Plymouth, Devon, UK

Correspondence to:
Correspondence to:
Dr C Taylor
Derriford Hospital, Plymouth, Devon PL6 8DH, UK; charlesy7{at}hotmail.com

In this study the records of 45 patients with sickle cell disease involved in 63 presentations of acute chest syndrome at the Princess Margaret Hospital in Nassau, the Bahamas, between 1997 and 2001 were examined. Patients were divided into three groups on the basis of age (<13 years, 13–18 years, 19 years) with a view to assessing clinical presentation. The incidence of symptoms, physical signs, and laboratory findings were enumerated and significant differences between age groups determined. The data were analysed using analysis of variance, t test, and ² test and compared with existing knowledge on the subject.

 This study proposed to evaluate the clinical presentation of acute chest syndrome with emphasis on historical and physical findings, and to encourage the physician to maintain a high index of suspicion for the condition in susceptible patients. It was found that presentation varied significantly with age groups, children presenting most classically with fever and cough and adults, with chest pain. The 13–18 age group emerged as the group which presented most frequently with the typical symptoms of chest infection, thus potentially making diagnosis easier. Of note, the most frequent finding was a normal examination, while the second commonest physical finding was crepitations on auscultation of the chest.

Abbreviations: ACS, acute chest syndrome; LOS, length of stay

Keywords: acute chest syndrome; sickle cell disease

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