Umair Muhammad, Walsh Timothy R, Mohsin Mashkoor
Institute of Microbiology, University of Agriculture, Faisalabad, 38000, Pakistan.
INEOS Oxford Institute for Antimicrobial Research, Department of Biology, University of Oxford, Oxford, OX1 3SZ, UK.
Heliyon. 2024 Mar 17;10(7):e28052. doi: 10.1016/j.heliyon.2024.e28052. eCollection 2024 Apr 15.
Carbapenem resistance is epidemic worldwide, these last resort antimicrobials are listed in the WHO 'watch group' with higher resistance potential. During the years 2017-18 Pakistan Antimicrobial Resistance Surveillance System reported an increase in carbapenem resistance. However, a comprehensive information on prevalence and molecular epidemiology of carbapenem resistance in Pakistan is not available. This systematic review and meta-analysis is aimed to report the current carbapenem resistance situation in Pakistan and its treatment options.
In this systematic review and meta-analysis, we investigated the pooled prevalence (PPr) of carbapenem resistance in and non- by organizing available data, from Web of Science and PubMed by April 2, 2020, in various groups and subgroups including species, years, provinces, extended spectrum β-lactamase production, clinical presentation, carbapenemase and metallo-β-lactamase production, and New Delhi metallo-β-lactamase (NDM) prevalence. Literature review was updated for the studies publisehd by December 07, 2023. Moreover, we descriptively reviewed the molecular epidemiology of carbapenem resistance in and non- in Pakistan. Lastly, we statistically explored different treatment options available for carbapenem resistant infections. We used R package 'metafor' for performing meta-analysis and influence diagnostics and determining treatment options.
From two academic databases Web of Science and PubMed we identified 343 studies. Eighty-eight studies were selected for the systematic review and meta-analysis. Seventy-four studies were selected for phenotypic analysis, 36 for genotypic analysis, and 31 for available treatment options. PPr-ID of 12% [0.12 (0.07, 0.16)] was observed for phenotypic carbapenem resistance in with more prevalence recorded in 24% [0.24 (0.05, 0.44)] followed by 9% [0.09 (-0.03, 0.20)] in . During the last two decades we observed a striking increase in carbapenem resistance PPr i.e., from 0% [0.00 (-0.02, 0.03)] to 36% [0.36 (0.17, 0.56)]. with PPr 15% [0.15 (0.06, 0.23)] in naive isolates was found to be the fundamental genetic determinant for carbapenem resistance in in Pakistan. Polymyxin B, colistin, tigecycline, and fosfomycin were identified as the suggested treatment options available for multidrug resistant infections not responding to carbapenems. Various studies reported carbapenem resistance from human, animal, and environment sources.
In conclusion, we found that NDM-1 producing carbapenem resistant are increasing in Pakistan. Meta-analysis showed that metallo-β-lactamases producing ST405 and sequence type11 are the major resistant clones. Number of reported studies in various subgroups and inconsistency in following CLSI guidelines are the potential limitations of this meta-analysis. A National antimicrobial resistance (AMR) surveillance strategy based on One Health is urgently needed to check any future AMR crisis in Pakistan.
碳青霉烯类耐药在全球范围内流行,这些作为最后手段的抗菌药物被列入世界卫生组织的“监测组”,具有较高的耐药潜力。2017 - 18年期间,巴基斯坦抗菌药物耐药监测系统报告碳青霉烯类耐药有所增加。然而,关于巴基斯坦碳青霉烯类耐药的流行情况和分子流行病学的全面信息尚不可得。本系统评价和荟萃分析旨在报告巴基斯坦目前的碳青霉烯类耐药情况及其治疗选择。
在本系统评价和荟萃分析中,我们通过整理截至2020年4月2日从科学网和PubMed获取的可用数据,调查了不同组和亚组(包括菌种、年份、省份、超广谱β - 内酰胺酶产生情况、临床表现、碳青霉烯酶和金属β - 内酰胺酶产生情况以及新德里金属β - 内酰胺酶(NDM)流行情况)中碳青霉烯类耐药的合并患病率(PPr)。对截至2023年12月7日发表的研究进行了文献综述更新。此外,我们对巴基斯坦碳青霉烯类耐药在肺炎克雷伯菌和非肺炎克雷伯菌中的分子流行病学进行了描述性综述。最后,我们对碳青霉烯类耐药感染可用的不同治疗选择进行了统计学探索。我们使用R包“metafor”进行荟萃分析、影响诊断和确定治疗选择。
从科学网和PubMed这两个学术数据库中,我们识别出343项研究。88项研究被选入系统评价和荟萃分析。74项研究被选用于表型分析,36项用于基因型分析,31项用于可用治疗选择分析。观察到肺炎克雷伯菌中碳青霉烯类耐药的表型PPr为12% [0.12(0.07,0.16)],其中更多耐药情况记录在大肠埃希菌中为24% [0.24(0.05,0.44)],其次在肺炎克雷伯菌中为9% [0.09( - 0.03,0.20)]。在过去二十年中,我们观察到碳青霉烯类耐药PPr显著增加,即从0% [0.00( - 0.02,0.03)]增至36% [0.36(0.17,0.56)]。在巴基斯坦,未接触过抗菌药物的分离株中PPr为15% [0.15(0.06,0.23)]的肺炎克雷伯菌被发现是碳青霉烯类耐药的主要遗传决定因素。多粘菌素B、黏菌素、替加环素和磷霉素被确定为对碳青霉烯类无反应的多重耐药感染的建议治疗选择。各项研究报告了来自人类、动物和环境来源的碳青霉烯类耐药情况。
总之,我们发现巴基斯坦产NDM - 1的碳青霉烯类耐药肺炎克雷伯菌正在增加。荟萃分析表明,产生金属β - 内酰胺酶的肺炎克雷伯菌ST405和大肠埃希菌序列类型11是主要的耐药克隆。本荟萃分析的潜在局限性在于各亚组报告的研究数量以及遵循CLSI指南方面的不一致性。迫切需要基于“同一健康”理念的国家抗菌药物耐药(AMR)监测策略,以应对巴基斯坦未来可能出现的AMR危机。