Rogues A M, Dumartin C, Lashéras A, Venier A G, Fourrier A, Parneix P, Gachie J P
Unité INSERM 657, Pharmacoépidémiologie et évaluation de l'impact des produits de santé sur les populations, IFR Santé Publique Université Victor Ségalen Bordeaux 2, France.
Microb Drug Resist. 2007 Fall;13(3):199-203. doi: 10.1089/mdr.2007.754.
The aim of this study was to describe consumption of glycopeptides and to study factors associated with their use in 47 French hospitals. Consumption of glycopeptides for systemic use (defined daily doses per 1,000 patient-days: DDD/1,000 PD and per 100 admissions), number of methicillin-resistant Staphylococcus aureus (MRSA) (percentage and incidence per 1,000 patient-days), and number of venous central lines and hospital characteristics (size, length of stay, number of beds: total and for each hospital inpatient areas and antibiotic policies) were recorded from January, 2002, through December, 2002. Multiple linear regression was performed to check for hospital characteristics. The median rate of total consumption of glycopeptides was 4.11(range 0.21-27.22) DDD per 1,000 PD with higher consumption in large public hospitals and in intensive care areas (median 46.51; range 7.19-134) than in surgery areas (median 4.5; range 0.17-24.76). The consumption of glycopeptides correlated with MRSA incidence, but not with the proportion of MRSA. In the multivariate analysis, the incidence of MRSA and the number of beds in surgery areas were independent predictors of total glycopeptides use in the hospital, expressed in DDD per 1,000 PD (R2 adjusted, 0.39). The incidence of MRSA, the number of venous central lines, and the number of beds in the medicine areas were significant determinants associated with higher consumption of glycopeptides expressed in DDD per 100 admissions (R2 adjusted, 0.73). To reduce glycopeptides use in hospitals, the first effort required is that hospitals focus increased attention on the prevention of cross transmission for MRSA between patients but also on the use of the venous central line. Furthermore, hospitals have to compare their data with others to identify overuse of glycopeptides and to plan control interventions.
本研究旨在描述糖肽类药物的使用情况,并研究法国47家医院中与糖肽类药物使用相关的因素。记录了2002年1月至2002年12月期间全身用糖肽类药物的使用情况(每1000患者日限定日剂量数:DDD/1000 PD以及每100例住院患者的DDD数)、耐甲氧西林金黄色葡萄球菌(MRSA)的数量(每1000患者日的百分比和发病率)、静脉中心导管的数量以及医院特征(规模、住院时间、床位数:总数以及各医院住院区域的床位数和抗生素政策)。进行多元线性回归以检验医院特征。糖肽类药物总使用量的中位数为每1000 PD 4.11(范围0.21 - 27.22)DDD,大型公立医院和重症监护区域的使用量(中位数46.51;范围7.19 - 134)高于手术区域(中位数4.5;范围0.17 - 24.76)。糖肽类药物的使用与MRSA发病率相关,但与MRSA的比例无关。在多变量分析中,MRSA的发病率和手术区域的床位数是医院中糖肽类药物总使用量(以每1000 PD的DDD数表示)的独立预测因素(调整后的R2为0.39)。MRSA的发病率、静脉中心导管的数量以及内科区域的床位数是与每100例住院患者中以DDD数表示的糖肽类药物较高使用量相关的显著决定因素(调整后的R2为0.73)。为减少医院中糖肽类药物的使用,首先需要医院更加关注预防患者之间MRSA的交叉传播,同时也要关注静脉中心导管的使用。此外,医院必须将自己的数据与其他医院的数据进行比较,以识别糖肽类药物的过度使用情况并规划控制干预措施。