Schuetz Philipp, Christ-Crain Mirjam, Wolbers Marcel, Schild Ursula, Thomann Robert, Falconnier Claudine, Widmer Isabelle, Neidert Stefanie, Blum Claudine A, Schönenberger Ronald, Henzen Christoph, Bregenzer Thomas, Hoess Claus, Krause Martin, Bucher Heiner C, Zimmerli Werner, Müller Beat
Department of Internal Medicine, Diabetes and Clinical Nutrition, University Hospital Basel, Petersgraben 4, Basel, Switzerland.
BMC Health Serv Res. 2007 Jul 5;7:102. doi: 10.1186/1472-6963-7-102.
Lower respiratory tract infections like acute bronchitis, exacerbated chronic obstructive pulmonary disease and community-acquired pneumonia are often unnecessarily treated with antibiotics, mainly because of physicians' difficulties to distinguish viral from bacterial cause and to estimate disease-severity. The goal of this trial is to compare medical outcomes, use of antibiotics and hospital resources in a strategy based on enforced evidence-based guidelines versus procalcitonin guided antibiotic therapy in patients with lower respiratory tract infections.
We describe a prospective randomized controlled non-inferiority trial with an open intervention. We aim to randomize over a fixed recruitment period of 18 months a minimal number of 1002 patients from 6 hospitals in Switzerland. Patients must be >18 years of age with a lower respiratory tract infections <28 days of duration. Patients with no informed consent, not fluent in German, a previous hospital stay within 14 days, severe immunosuppression or chronic infection, intravenous drug use or a terminal condition are excluded. Randomization to either guidelines-enforced management or procalcitonin-guided antibiotic therapy is stratified by centre and type of lower respiratory tract infections. During hospitalization, all patients are reassessed at days 3, 5, 7 and at the day of discharge. After 30 and 180 days, structured phone interviews by blinded medical students are conducted. Depending on the randomization allocation, initiation and discontinuation of antibiotics is encouraged or discouraged based on evidence-based guidelines or procalcitonin cut off ranges, respectively. The primary endpoint is the risk of combined disease-specific failure after 30 days. Secondary outcomes are antibiotic exposure, side effects from antibiotics, rate and duration of hospitalization, time to clinical stability, disease activity scores and cost effectiveness. The study hypothesis is that procalcitonin-guidance is non-inferior (i.e., at worst a 7.5% higher combined failure rate) to the management with enforced guidelines, but is associated with a reduced total antibiotic use and length of hospital stay.
Use of and prolonged exposure to antibiotics in lower respiratory tract infections is high. The proposed trial investigates whether procalcitonin-guidance may safely reduce antibiotic consumption along with reductions in hospitalization costs and antibiotic resistance. It will additionally generate insights for improved prognostic assessment of patients with lower respiratory tract infections.
ISRCTN95122877.
像急性支气管炎、慢性阻塞性肺疾病急性加重以及社区获得性肺炎等下呼吸道感染,常常不必要地使用抗生素进行治疗,主要原因是医生难以区分病毒感染与细菌感染病因,以及难以评估疾病严重程度。本试验的目的是比较在基于强化循证指南的策略与降钙素原指导下的抗生素治疗策略中,下呼吸道感染患者的医疗结局、抗生素使用情况及医院资源利用情况。
我们描述了一项采用开放干预的前瞻性随机对照非劣效性试验。我们的目标是在18个月的固定招募期内,从瑞士6家医院随机选取至少1002例患者。患者必须年满18岁,患有病程小于28天的下呼吸道感染。排除无知情同意书、德语不流利、在过去14天内曾住院、严重免疫抑制或慢性感染、静脉吸毒或处于终末期疾病的患者。根据中心和下呼吸道感染类型,将患者随机分为强化指南管理组或降钙素原指导下的抗生素治疗组。住院期间,在第3、5、7天及出院当天对所有患者进行重新评估。在30天和180天后,由盲法医学生进行结构化电话访谈。根据随机分组情况,分别依据循证指南或降钙素原临界值范围,鼓励或不鼓励开始及停用抗生素。主要终点是30天后合并疾病特异性失败的风险。次要结局包括抗生素暴露情况、抗生素副作用、住院率和住院时长、临床稳定时间、疾病活动评分及成本效益。研究假设是降钙素原指导治疗不劣于强化指南管理(即最差情况下合并失败率高7.5%),但抗生素总使用量和住院时长会减少。
下呼吸道感染中抗生素的使用及长期暴露情况很高。拟进行的试验调查降钙素原指导治疗是否能安全地减少抗生素消耗,同时降低住院成本和抗生素耐药性。它还将为改善下呼吸道感染患者的预后评估提供见解。
ISRCTN95122877。