Todi Subhash, Sathe Prachee, V Ramasubramanian, Swaminathan Subramanian, Talwar Deepak, Prayag Parikshit, Rao Polati Vishnu, Sabnis Kirti, Kamat Shweta, Mane Akshata, Thanusubramanian Harish
Department of Critical Care Medicine, Advanced Medical Research Institute (AMRI) Hospital Dhakuria, Kolkata, IND.
Department of Critical Care Medicine, Ruby Hall Clinic, Pune, IND.
Cureus. 2024 Sep 26;16(9):e70234. doi: 10.7759/cureus.70234. eCollection 2024 Sep.
There is limited real-world data from India examining the treatment characteristics, safety, and efficacy of ceftazidime-avibactam against Gram-negative organisms especially multidrug-resistant pathogens including carbapenem-resistant and carbapenem-resistant . In this retrospective study, the real-world treatment patterns, effectiveness, and safety of ceftazidime-avibactam in treating Gram-negative infections were assessed. Data was extracted from electronic health records of adult patients admitted to the hospital with documented Gram-negative infection who had received treatment for at least 48 hours with ceftazidime-avibactam as a part of routine clinical management. Among the 189 patients, on Day 3, clinical symptom improvement was recorded in 79.6% of patients who received ceftazidime-avibactam within 72 hours of hospital admission. Clinical success was achieved in 79.5% and 76.3% of assessed patients on Day 7 and Day 14/end-of-treatment (EOT), respectively. Microbiological success was reported in 76% of patients on Day 7 and in 60.3% of patients on Day 14 or EOT. The mean treatment duration of ceftazidime-avibactam therapy was 6.92 (± 4.1) days. No new safety concerns were identified. In conclusion, this study provides real-world evidence on treatment patterns and clinical outcomes associated with ceftazidime-avibactam in India, complementing the previously reported literature. The results suggest ceftazidime-avibactam is an effective and tolerable option for the management of multidrug-resistant (MDR) Gram-negative infections in critically ill patients.
在印度,关于头孢他啶-阿维巴坦针对革兰氏阴性菌尤其是多重耐药病原体(包括碳青霉烯耐药菌和耐碳青霉烯类肠杆菌科细菌)的治疗特性、安全性和有效性的真实世界数据有限。在这项回顾性研究中,评估了头孢他啶-阿维巴坦治疗革兰氏阴性菌感染的真实世界治疗模式、有效性和安全性。数据从因记录在案的革兰氏阴性菌感染而入院的成年患者的电子健康记录中提取,这些患者作为常规临床管理的一部分接受了至少48小时的头孢他啶-阿维巴坦治疗。在189名患者中,在入院72小时内接受头孢他啶-阿维巴坦治疗的患者中,第3天有79.6%的患者临床症状得到改善。在评估的患者中,第7天和第14天/治疗结束(EOT)时的临床成功率分别为79.5%和76.3%。第7天76%的患者和第14天或EOT时60.3%的患者报告微生物学成功。头孢他啶-阿维巴坦治疗的平均持续时间为6.92(±4.1)天。未发现新的安全问题。总之,本研究提供了印度与头孢他啶-阿维巴坦相关的治疗模式和临床结果的真实世界证据,补充了先前报道的文献。结果表明,头孢他啶-阿维巴坦是治疗重症患者多重耐药(MDR)革兰氏阴性菌感染的有效且可耐受的选择。