Conly John M, Stiver H Grant, Weiss Karl A, Becker Debbie L, Rosner Andrew J, Miller Elizabeth
Division of Infectious Diseases, Department of Medicine, Toronto General Hospital, University Health Network, University of Toronto, Toronto, Ontario.
Can J Infect Dis. 2003 Nov;14(6):315-21. doi: 10.1155/2003/103682.
Methicillin-resistant Staphylococcus aureus (MRSA) infections are increasingly being encountered and pose an increasing burden to the health care system in Canada.
To elucidate and characterize the factors influencing the current MRSA treatment patterns in patients with skin and soft tissue infections (SSTIs) before linezolid became available on the Canadian market.
A retrospective study collected demographic, treatment and resource use data on patients hospitalized at one of three geographically distinct tertiary care facilities, where MRSA SSTI treatment was initiated with intravenous (IV) vancomycin. Analysis of opportunities for IV-to-oral switch therapy was based on eligibility criteria.
Of 89 patients identified over a 43-month period, the mean (+/-SD) durations of anti-infective treatment and hospitalization were 22.4+/-21 days and 28.9+/-20.8 days, respectively. An infected surgical wound was most common, representing 62.9% of infections. The mean duration of vancomycin treatment was 19.5 days and the mean number of 1 g doses received was 29.0+/-32.9. The majority of patients (55.1%) initiated vancomycin therapy a mean of 5.4+/-8.9 days after confirmation of MRSA. Of the 70% of patients meeting criteria for IV-to-oral switch therapy, only 10% received oral treatment. The most common reason cited for not switching was lack of an effective oral alternative. Analysis of switch therapy criteria found that IV treatment continued for a mean of 13 days despite the appropriateness of the oral route.
Considerable variation exists in treatment patterns for MRSA infections. Improvements in the initiation of therapy and the use of IV-to-oral switch therapy may improve care and reduce the duration of hospitalization for MRSA SSTIs.
耐甲氧西林金黄色葡萄球菌(MRSA)感染日益常见,给加拿大医疗保健系统带来越来越大的负担。
在利奈唑胺于加拿大市场上市之前,阐明并描述影响皮肤和软组织感染(SSTI)患者当前MRSA治疗模式的因素。
一项回顾性研究收集了在三个地理位置不同的三级医疗设施之一住院患者的人口统计学、治疗和资源使用数据,这些患者的MRSA SSTI治疗均从静脉注射(IV)万古霉素开始。基于入选标准分析静脉转口服转换治疗的机会。
在43个月期间确定的89例患者中,抗感染治疗和住院的平均(±标准差)持续时间分别为22.4±21天和28.9±20.8天。感染的手术伤口最为常见,占感染病例的62.9%。万古霉素治疗的平均持续时间为19.5天,接受的1g剂量的平均数量为29.0±32.9。大多数患者(55.1%)在确认MRSA后平均5.4±8.9天开始使用万古霉素治疗。在符合静脉转口服转换治疗标准的患者中,只有10%接受了口服治疗。未进行转换的最常见原因是缺乏有效的口服替代药物。对转换治疗标准的分析发现,尽管口服途径合适,但静脉治疗平均持续了