School of Pharmacy and Health Professions, Creighton University, Omaha, NE, USA.
Memorial Hermann-Texas Medical Center, Houston, TX, USA.
Int J Antimicrob Agents. 2019 May;53(5):644-649. doi: 10.1016/j.ijantimicag.2019.01.014. Epub 2019 Jan 31.
The clinical experience of ceftaroline fosamil (CPT-F) therapy for Gram-positive infective endocarditis is reported from CAPTURE, a retrospective study conducted in the USA.
Data, including patient demographics, medical history, risk factors, microbiological aetiology and clinical outcomes, were collected by review of patient charts between September 2013 and February 2015.
Patients (n=55) with Gram-positive endocarditis were treated with CPT-F. The most common risk factors were intravascular devices (43.6%), diabetes mellitus (40.0%) and injection drug use (38.2%). The most commonly isolated pathogens were meticillin-resistant Staphylococcus aureus (MRSA; 80%), meticillin-susceptible S. aureus (MSSA; 7.3%) and coagulase-negative staphylococci (7.3%). CPT-F was given as first-line therapy in 7.3% of patients and as second-line or later therapy in 92.7% of patients, and as monotherapy in 41.8% of patients and as concurrent therapy in 58.2% of patients. Clinical success was observed in 82.6% (19/23) of patients treated with CPT-F as monotherapy. In patients treated with CPT-F as first-line therapy or second-line or later therapy, 75.0% (3/4) and 70.6% (36/51) achieved success, respectively. Clinical success was observed in 77.3% (34/44) of patients with MRSA and 25% (1/4) of patients with MSSA. Two patients discontinued treatment with CPT-F due to an adverse event.
CPT-F treatment was associated with a high rate of clinical success in patients with Gram-positive infective endocarditis, including those with risk factors and infections caused by MRSA. A high rate of clinical success was observed in patients treated with CPT-F used as first- line therapy or second-line or later therapy, or as monotherapy or in combination with other antibiotics.
从美国进行的回顾性研究 CAPTURE 中报告了头孢洛林酯(CPT-F)治疗革兰氏阳性感染性心内膜炎的临床经验。
通过回顾 2013 年 9 月至 2015 年 2 月之间的患者病历,收集了包括患者人口统计学、病史、危险因素、微生物病因和临床结果在内的数据。
55 例革兰氏阳性心内膜炎患者接受了 CPT-F 治疗。最常见的危险因素是血管内装置(43.6%)、糖尿病(40.0%)和注射吸毒(38.2%)。最常分离出的病原体是耐甲氧西林金黄色葡萄球菌(MRSA;80%)、甲氧西林敏感金黄色葡萄球菌(MSSA;7.3%)和凝固酶阴性葡萄球菌(7.3%)。CPT-F 作为一线治疗药物应用于 7.3%的患者,作为二线或更后的治疗药物应用于 92.7%的患者,作为单一治疗药物应用于 41.8%的患者,作为联合治疗药物应用于 58.2%的患者。在接受 CPT-F 单一治疗的 19/23 例患者中观察到临床治疗成功。在接受 CPT-F 一线或二线或更后治疗的 3/4 例患者和 36/51 例患者中,分别有 75.0%和 70.6%获得成功。在 MRSA 感染的 44 例患者中有 77.3%观察到临床治疗成功,而在 MSSA 感染的 1 例患者中仅观察到 25%的临床治疗成功。有 2 例患者因不良事件停止了 CPT-F 治疗。
CPT-F 治疗与革兰氏阳性感染性心内膜炎患者的高临床成功率相关,包括具有危险因素和由 MRSA 引起的感染患者。在接受 CPT-F 一线或二线或更后治疗、单一治疗或联合其他抗生素治疗的患者中,观察到高的临床成功率。