Background This study was designed to determine the incidenceof thoracic bone infarction in patients with sickle cell diseaseswho were hospitalized with acute chest or back pain above thediaphragm and to test the hypothesis that incentive spirometrycan decrease the incidence of atelectasis and pulmonary infiltrates.
Methods We conducted a prospective, randomized trial in 29 patientsbetween 8 and 21 years of age with sickle cell diseases whohad 38 episodes of acute chest or back pain above the diaphragmand were hospitalized. Each episode of pain was considered tobe an independent event. At each hospitalization, patients withnormal or unchanged chest radiographs on admission were randomlyassigned to treatment with spirometry or to a control nonspirometrygroup. Each patient in the spirometry group took 10 maximalinspirations using an incentive spirometer every two hours between8 a.m. and 10 p.m. and while awake during the night until thechest pain subsided. A second radiograph was obtained threeor more days after admission, or sooner if clinically necessary,to determine the incidence of pulmonary complications. Bonescanning was performed no sooner than two days after hospitaladmission to determine the incidence of thoracic bone infarction.
Results The incidence of thoracic bone infarction was 39.5 percent(15 of 38 hospitalizations). Pulmonary complications (atelectasisor infiltrates) developed during only 1 of 19 hospitalizationsof patients assigned to the spirometry group, as compared with8 of 19 hospitalizations of patients in the nonspirometry group(P = 0.019). Among patients with thoracic bone infarction, nopulmonary complications developed in those assigned to the spirometrygroup during a total of seven hospitalizations, whereas theydeveloped during five of eight hospitalizations in the nonspirometrygroup (P = 0.025).
Conclusions Thoracic bone infarction is common in patients withsickle cell diseases who are hospitalized with acute chest pain.Incentive spirometry can prevent the pulmonary complications(atelectasis and infiltrates) associated with the acute chestsyndrome in patients with sickle cell diseases who are hospitalizedwith chest or back pain above the diaphragm.
Source Information
From the Division of General Pediatrics (P.S.B.), the Division of HematologyOncology and the Cincinnati Comprehensive Sickle Cell Center (K.A.K., D.L.R.), and the Department of Radiology (M.J.G.), Children's Hospital Medical Center; and the Department of Environmental Health, Division of Biostatistics and Epidemiology, University of Cincinnati College of Medicine (R.S.) all in Cincinnati.
Address reprint requests to Dr. Bellet at the Department of Pediatrics, Children's Hospital Medical Center, 3333 Burnet Ave., Cincinnati, OH 45229-3039.
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