Heizmann W R, Löschmann P-A, Eckmann C, von Eiff C, Bodmann K-F, Petrik C
Orgamed Laborsysteme GmbH, Maria-Schmid-Str. 14b, 94086, Bad Griesbach, Germany,
Infection. 2015 Feb;43(1):37-43. doi: 10.1007/s15010-014-0691-4. Epub 2014 Nov 4.
Tigecycline is an established treatment option for infections with multiresistant bacteria (MRB). It retains activity against many strains with limited susceptibility to other antibiotics. Efficacy and safety of tigecycline as monotherapy or in combination regimens were investigated in a prospective noninterventional study involving 1,025 severely ill patients in clinical routine at 137 German hospitals.
Data on the full population have been published; our present analysis focuses on infections caused by MRB. The study population included patients with complicated infections, high disease severity (APACHE II > 15: 65 %) and high MRB prevalence. Most patients had comorbidities, including cardiovascular disease, renal insufficiency, and/or diabetes mellitus. Treatment success was defined as cure/improvement without requirement of further antibiotic therapy.
Pathogens isolated from 215 evaluable patients with documented MRB infections included 132 methicillin-resistant Staphylococcus aureus (MRSA), 42 vancomycin-resistant Enterococci (VRE) and 67 Gram-negative extended beta-lactamase (ESBL) producers. Of the MRB subpopulation, 140 patients received tigecycline monotherapy, 75 were treated with combination regimens. High overall clinical success rates were recorded for MRB infections treated with tigecycline alone (94 %) or in combinations (88 %); in detail intraabdominal infections (monotherapy: 90 %; combinations: 93 %), skin/soft tissue infections (93; 100 %), community-acquired pneumonia (100; 100 %), hospital-acquired pneumonia (94,7; 72,7 %), diabetic foot infections (89; 33 %), blood stream infections (100; 100 %) and multiple-site infections (92; 71 %).
Tigecycline achieved high clinical success rates in patients with documented infections involving MRB strains despite high disease severity. These results add to the evidence indicating that tigecycline is a valuable therapeutic option for complicated infections in severely ill patients with a high likelihood of multidrug-resistant pathogen involvement.
替加环素是治疗多重耐药菌(MRB)感染的既定治疗选择。它对许多对其他抗生素敏感性有限的菌株仍具有活性。在一项前瞻性非干预性研究中,对德国137家医院临床常规治疗的1025例重症患者,研究了替加环素单药治疗或联合治疗方案的疗效和安全性。
关于全部人群的数据已发表;我们目前的分析重点是由MRB引起的感染。研究人群包括患有复杂感染、疾病严重程度高(急性生理与慢性健康状况评分系统II>15:65%)和MRB患病率高的患者。大多数患者有合并症,包括心血管疾病、肾功能不全和/或糖尿病。治疗成功定义为治愈/改善且无需进一步抗生素治疗。
从215例有记录的MRB感染的可评估患者中分离出的病原体包括132株耐甲氧西林金黄色葡萄球菌(MRSA)、42株耐万古霉素肠球菌(VRE)和67株产超广谱β-内酰胺酶(ESBL)的革兰阴性菌。在MRB亚组中,140例患者接受替加环素单药治疗,75例接受联合治疗方案。单用替加环素(94%)或联合治疗(88%)的MRB感染总体临床成功率较高;具体而言,腹腔内感染(单药治疗:90%;联合治疗:93%)、皮肤/软组织感染(93%;100%)、社区获得性肺炎(100%;100%)、医院获得性肺炎(94.7%;72.7%)、糖尿病足感染(89%;33%)、血流感染(100%;100%)和多部位感染(92%;71%)。
尽管疾病严重程度高,但替加环素在有记录的涉及MRB菌株感染的患者中取得了较高的临床成功率。这些结果进一步证明,替加环素是重症患者复杂感染的一种有价值的治疗选择,这些患者很可能感染多重耐药病原体。