N-acetylcysteine reduces the risk of re-hospitalisation among patients with chronic obstructive pulmonary disease

被引:60
作者
Gerrits, CMJM
Herings, RMC
Leufkens, HGM
Lammers, JWJ
机构
[1] Utrecht Inst Pharmaceut Sci, Dept Pharmacoepidemiol & Pharmacotherapy, NL-3508 TB Utrecht, Netherlands
[2] Heart Lung Ctr Utrecht, PHARMO Inst, Utrecht, Netherlands
[3] Heart Lung Ctr Utrecht, Dept Pulm Dis, Utrecht, Netherlands
关键词
chronic obstructive pulmonary disease; exacerbation; hospitalisation; mucolytics N-acetylcysteine pharmacoepidemiology;
D O I
10.1183/09031936.03.00063402
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The aim of this study was to evaluate the effect of oral N-acetylcysteine in the prevention of re-hospitalisation for chronic obstructive pulmonary disease (COPD) exacerbations. Using the PHARmacoMOrbidity linkage (PHARMO) system the authors included all patients aged greater than or equal to55 yrs who had been dispensed medication, labelled for respiratory indications (anatomical therapeutic chemical (ATC) classification system: R03), between 1986-1998 and who had also been hospitalised for COPD (international Classification of Diseases (ICD)-9: 491, 492, 496) in this time frame. These subjects were subsequently divided into two groups, those who had received N-acetyleysteine following discharge from their first admission between 1986-1998 and those who had not. All the patients were studied starting from their initial discharge, until their first readmission, death or end of data collection period. The maximum follow-up period was 1 yr. A total of 1,219 patients, who were hospitalised for COPD between 1986-1998, were included in this study. After adjustment for disease severity, it was observed that the use of N-acetylcysteine was significantly associated with a reduced risk of readmission. The readmission risk was significantly lower in patients with high average daily doses of N-acetyicysteine. In conclusion it was observed that N-acetylcysteine reduces the risk of rehospitalisation for chronic obstructive pulmonary disease by similar to30% and that this risk reduction is dose-dependent.
引用
收藏
页码:795 / 798
页数:4
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