Wheezing and asthma are independent risk factors for increased sickle cell disease morbidity
Wheezing and asthma are independent risk factors for increased sickle cell disease morbidity
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DOI:
10.1111/bjh.12049
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发表时间:
2012-11-01
影响因子:
6.5
通讯作者:
Richardson, Lynne D.
中科院分区:
文献类型:
--
作者:
Glassberg, Jeffrey A.;Chow, Annie;Richardson, Lynne D.
To assess the associations between a doctor diagnosis of asthma and wheezing (independent of a diagnosis of asthma) with sickle cell disease (SCD) morbidity, we conducted a retrospective review of Emergency Department (ED) visits to the Mount Sinai Medical Center for SCD between 1 January 2007 and 1 January 2011. Outcomes were ED visits for pain and acute chest syndrome. The cohort included 262 individuals, median age 23.8 years, (range: 6 months to 67.5 years). At least one episode of wheezing recorded on a physical examination was present in 18.7% (49 of 262). Asthma and wheezing did not overlap completely, 53.1% of patients with wheezing did not carry a diagnosis of asthma. Wheezing was associated with a 118% increase in ED visits for pain (95% confidence interval [CI]: 56-205%) and a 158% increase in ED visits for acute chest syndrome (95% CI: 11-498%). A diagnosis of asthma was associated with a 44% increase in ED utilization for pain (95% CI: 2-104%) and no increase in ED utilization for acute chest syndrome (rate ratio 1.00, 95%CI 0.41-2.47). In conclusion, asthma and wheezing are independent risk factors for increased painful episodes in individuals with SCD. Only wheezing was associated with more acute chest syndrome.