Pinzone Marilia Rita, Cacopardo Bruno, Abbo Lilian, Nunnari Giuseppe
Division of Infectious Diseases, Department of Clinical and Molecular Biomedicine, University of Catania, Via Palermo 636, ARNAS Garibaldi Nesima, 95125 Catania, Italy.
Division of Infectious Diseases, Department of Medicine, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.
ScientificWorldJournal. 2014 Jan 21;2014:759138. doi: 10.1155/2014/759138. eCollection 2014.
Community acquired pneumonia (CAP) represents the most common cause of infection-related morbidity and mortality worldwide. Appropriate treatment of CAP is challenging and sometimes limited by the availability to obtain rapid and timely identification of the etiologic agent in order to initiate or deescalate the correct antimicrobial therapy. As a consequence, prescribers frequently select empiric antimicrobial therapy using clinical judgment, local patterns of antimicrobial resistance, and, sometimes, individual patient expectations. These issues may contribute to prolonged courses of inappropriate therapy. In this review, we discuss the evidence and recommendations from international guidelines for the management of CAP and the clinical trials that specifically addressed duration of antimicrobial therapy for CAP in adults. In randomized controlled trials comparing the clinical efficacy of a short-course antimicrobial regimen versus an extended-course regimen, no differences in terms of clinical success, bacterial eradication, adverse events, and mortality were observed. The use of biomarkers, such as procalcitonin, to guide the initiation and duration of antimicrobial therapy may reduce total antibiotic exposure and treatment duration, healthcare costs, and the risk of developing antimicrobial resistance. In clinical practice, antimicrobial stewardship interventions may improve the management of CAP and may help in reducing treatment duration. Sometimes "less is more" in CAP.
社区获得性肺炎(CAP)是全球感染相关发病和死亡的最常见原因。CAP的恰当治疗具有挑战性,有时会因难以快速及时鉴定病原体以启动或调整正确的抗菌治疗而受到限制。因此,开处方者常常根据临床判断、当地的抗菌药物耐药模式,有时还会考虑患者个人期望来选择经验性抗菌治疗。这些问题可能导致不恰当治疗疗程延长。在本综述中,我们讨论了国际CAP管理指南的证据和建议,以及专门针对成人CAP抗菌治疗疗程的临床试验。在比较短疗程抗菌方案与长疗程方案临床疗效的随机对照试验中,未观察到临床成功率、细菌清除率、不良事件和死亡率方面的差异。使用生物标志物(如降钙素原)来指导抗菌治疗的启动和疗程,可能会减少抗生素总暴露量和治疗疗程、医疗费用以及产生抗菌药物耐药性的风险。在临床实践中,抗菌药物管理干预措施可能会改善CAP的管理,并有助于缩短治疗疗程。在CAP治疗中,有时“少即是多”。