Arjun Rajalakshmi, Gopalakrishnan Ram, Nambi P Senthur, Kumar D Suresh, Madhumitha R, Ramasubramanian V
Department of Infectious Diseases, Apollo Hospitals, Chennai, Tamil Nadu, India.
Indian J Crit Care Med. 2017 May;21(5):317-321. doi: 10.4103/ijccm.IJCCM_454_16.
As the use of colistin to treat carbapenem-resistant Gram-negative infections increases, colistin resistance is being increasingly reported in Indian hospitals.
Retrospective chart review of clinical data from patients with colistin-resistant isolates (minimum inhibitory concentration >2 mcg/ml). Clinical profile, outcome, and antibiotics that were used for treatment were analyzed.
Twenty-four colistin-resistant isolates were reported over 18 months (January 2014-June 2015). A history of previous hospitalization within 3 months was present in all the patients. An invasive device was used in 22 (91.67%) patients. Urine was the most common source of the isolate, followed by blood and respiratory samples. constituted 87.5% of all isolates. Sixteen (66.6%) were considered to have true infection, whereas eight (33.3%) were considered to represent colonization. Susceptibility of these isolates to other drugs tested was tigecycline in 75%, chloramphenicol 62.5%, amikacin 29.17%, co-trimoxazole 12.5%, and fosfomycin (sensitive in all 4 isolates tested). Antibiotics that were used for treatment were combinations among the following antimicrobials-tigecycline, chloramphenicol, fosfomycin, amikacin, ciprofloxacin, co-trimoxazole, and sulbactam. Among eight patients who were considered to have colonization, there were no deaths. Bacteremic patients had a significantly higher risk of death compared to all nonbacteremic patients ( = 0.014).
Colistin resistance among Gram-negative bacteria, especially , is emerging in Indian hospitals. At least one-third of isolates represented colonization only rather than true infection and did not require treatment. Among patients with true infection, only 25% had a satisfactory outcome and survived to discharge. Fosfomycin, tigecycline, and chloramphenicol may be options for combination therapy.
随着黏菌素用于治疗耐碳青霉烯革兰阴性菌感染的情况增多,印度医院中黏菌素耐药的报道也日益增加。
对分离出黏菌素耐药菌株(最低抑菌浓度>2 mcg/ml)的患者临床资料进行回顾性图表审查。分析临床特征、转归以及用于治疗的抗生素。
在18个月(2014年1月至2015年6月)期间共报告了24株黏菌素耐药菌株。所有患者均有在3个月内曾住院的病史。22例(91.67%)患者使用了侵入性装置。尿液是分离菌株最常见的来源,其次是血液和呼吸道样本。 占所有分离菌株的87.5%。16株(66.6%)被认为存在真正感染,而8株(33.3%)被认为仅代表定植。这些分离菌株对其他测试药物的敏感性为替加环素75%、氯霉素62.5%、阿米卡星29.17%、复方新诺明12.5%,磷霉素(在所有4株测试菌株中均敏感)。用于治疗的抗生素是以下抗菌药物的联合使用——替加环素、氯霉素、磷霉素、阿米卡星、环丙沙星、复方新诺明和舒巴坦。在8例被认为是定植的患者中,无死亡病例。与所有非菌血症患者相比,菌血症患者的死亡风险显著更高( = 0.014)。
革兰阴性菌尤其是 中的黏菌素耐药性在印度医院中正在出现。至少三分之一的分离菌株仅代表定植而非真正感染,不需要治疗。在真正感染的患者中,只有25%的患者有满意的转归并存活至出院。磷霉素、替加环素和氯霉素可能是联合治疗的选择。