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ICU病人耐碳青霉烯类肺炎克雷伯菌血流感染的危险因素与预后分析(附81例报告)

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  • 上海交通大学医学院附属瑞金医院 a.重症医学科,b. 老年医学科,c.微生物科,d.急诊科,上海 200025

收稿日期: 2023-08-16

  网络出版日期: 2024-01-04

Risk factors and prognosis of carbapenem-resistant Klebsiella pneumoniae bloodstream infection in ICU patients: a report of 81 cases

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  • Department of Critical Care Medicine, b. Department of Geriatry, c. Department of Clinical Microbiology, d. Department of Emergency, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China

Received date: 2023-08-16

  Online published: 2024-01-04

摘要

目的:分析真实世界中重症病人耐碳青霉烯类肺炎克雷伯菌血流感染(carbapenem-resistant Klebsiella pneumonia bloodstream infection, CRKP-BSI)的死亡危险因素以及治疗效果,为病人个体化治疗提供参考。方法:回顾性分析2016年7月至2020年6月我院重症监护病房内81例CRKP-BSI病人的临床特征,评估死亡危险因素及不同抗菌药物方案的治疗效果。结果:CRKP-BSI以腹腔来源和呼吸道来源的占比较多,分别为56.79%(46例)、22.22%(18例)。CRKP-BSI病人28 d死亡率及住院死亡率分别为54.32%(44例)、65.43%(53例)。多因素回归分析结果提示入院前患胆道疾病(P=0.026)、病人BSI发生时SOFA评分升高(P=0.006)为28 d死亡率独立危险因素。接受以替加环素为基础(44例)或以多黏菌素B(26例)为基础的抗生素治疗,两组28 d死亡率差异无统计学意义[56.82%(25/44)比57.69%(15/26), P=0.943]。根据病人的年龄(≤65岁比>65岁)、性别、体质量指数(≤25 kg/m2比 >25 kg/m2)、APACHE Ⅱ评分(≤20分比>20分)、肾脏替代治疗及机械通气的使用分为不同亚组,各亚组间死亡率差异无统计学意义。结论:SOFA评分及入院前胆道疾病病史是CRKP-BSI 28 d死亡率的危险因素。以替加环素为基础与以多黏菌素B为基础的抗菌药物治疗效果无差异。

本文引用格式

刘萌, 徐文, 戴赟麒, 谭若铭, 刘嘉琳, 顾飞飞, 陈尔真, 王晓丽, 瞿洪平, 邱毓祯 . ICU病人耐碳青霉烯类肺炎克雷伯菌血流感染的危险因素与预后分析(附81例报告)[J]. 外科理论与实践, 2023 , 28(05) : 454 -462 . DOI: 10.16139/j.1007-9610.2023.05.11

Abstract

Objective Comprehensive mortality risk analyses and therapeutic assessment in real-world practice are beneficial to guide individual treatment in patients with Carbapenem-resistant Klebsiella pneumoniae bloodstream infections (CRKP-BSI). Methods Retrospective analysis of the clinical characteristics of 81 CRKP-BSI patients in our intensive care unit from July 2016 to June 2020, to indentify the risk factors of death and treatment effects of different antibiotic regimens. Results In 81 CRKP-BSI cases, the majority source were from abdominal and respiratory, accounting for 56.79% (46 cases) and 22.22% (18 cases), respectively. The 28-day mortality and hospitalization mortality of CRKP-BSI were 54.32% (44 cases) and 65.43% (53 cases). Multivariate regression analysis suggested that biliary tract disease before admission (P=0.026) and increased SOFA score at the onset of BSI (P=0.006) were independent risk factors for 28-day mortality. There was no statistically significant difference in 28-day mortality between the groups of antibiotic treatment based on tigecycline (44 cases) and polymyxin B (26 cases) [56.82% (25/44) vs. 57.69% (15/26), P=0.943]. Patients were evaluated based on their age (≤ 65 years vs. >65 years), gender, body mass index (≤25 kg/m2 vs. >25 kg/m2), and APACHE Ⅱ score (≤20 vs. >20), the use of renal replacement therapy and mechanical ventilation, there was no difference in the mortality among each subgroup. Conclusions Biliary tract disease before admission and SOFA score were independent risk factors for 28-day mortality. There was no significant difference outcomes between tigecycline- and polymyxin B-based therapy.

参考文献

[1] BRINK A J. Epidemiology of carbapenem-resistant Gram-negative infections globally[J]. Curr Opin Infect Dis, 2019, 32(6):609-616.
[2] HU F, YUAN L, YANG Y, et al. A multicenter investigation of 2,773 cases of bloodstream infections based on China antimicrobial surveillance network (CHINET)[J]. Front Cell Infect Microbiol, 2022, 12:1075185.
[3] TIAN L, TAN R, CHEN Y, et al. Epidemiology of Klebsiella pneumoniae bloodstream infections in a teaching hospital: factors related to the carbapenem resistance and patient mortality[J]. Antimicrob Resist Infect Control, 2016, 5:48.
[4] ZHEN X, LUNDBORG C S, SUN X, et al. Economic burden of antibiotic resistance in ESKAPE organisms: a systematic review[J]. Antimicrob Resist Infect Control, 2019, 8:137.
[5] XIAO T, ZHU Y, ZHANG S, et al. A retrospective analysis of risk factors and outcomes of carbapenem-resistant Klebsiella pneumoniae bacteremia in nontransplant patients[J]. J Infect Dis, 2020, 221(Suppl 2):S174-S183.
[6] LI Y, LI J, HU T, et al. Five-year change of prevalence and risk factors for infection and mortality of carbapenem-resistant Klebsiella pneumoniae bloodstream infection in a tertiary hospital in North China[J]. Antimicrob Resist Infect Control, 2020, 9(1):79.
[7] KARAKONSTANTIS S, KRITSOTAKIS E I, GIKAS A. Treatment options for K. pneumoniae, P. aeruginosa and A. baumannii co-resistant to carbapenems, aminoglycosides, polymyxins and tigecycline: an approach based on the mechanisms of resistance to carbapenems[J]. Infection, 2020, 48(6):835-851.
[8] TRECARICHI E M, TUMBARELLO M. Therapeutic options for carbapenem-resistant Enterobacteriaceae infections[J]. Virulence, 2017, 8(4):470-484.
[9] GUAN X, HE L, HU B, et al. Laboratory diagnosis,clinical management and infection control of the infections caused by extensively drug-resistant Gram-negative bacilli: a Chinese consensus statement[J]. Clin Microbiol Infect, 2016, 22(Suppl 1):S15-S25.
[10] GU F, HE W, XIAO S, et al. Antimicrobial resistance and molecular epidemiology of staphylococcus aureus causing bloodstream infections at Ruijin Hospital in Shanghai from 2013 to 2018[J]. Sci Rep, 2020, 10(1):6019.
[11] Clinical and Laboratory Standards Institute (CLSI). Performance standards for antimicrobial susceptibility testing: twenty-four informational supplement[S]. CLSI document,2014,M100-S24.
[12] TIMSIT J F, RUPPé E, BARBIER F, et al. Bloodstream infections in critically ill patients: an expert statement[J]. Intensive Care Med, 2020, 46(2):266-284.
[13] KELLUM J A, LAMEIRE N, KDIGO AKI Guideline Work Group. Diagnosis,evaluation,and management of acute kidney injury: a KDIGO summary (Part 1)[J]. Crit Care, 2013, 17(1):204.
[14] SHEN L, LIAN C, ZHU B, et al. Bloodstream infections due to carbapenem-resistant Klebsiella pneumoniae: a single-center retrospective study on risk factors and therapy option[J]. Microb Drug Resist, 2021, 27(2):227-233.
[15] NIU T, LUO Q, LI Y, et al. Comparison of tigecycline or cefoperazone/sulbactam therapy for bloodstream infection due to carbapenem-resistant Acinetobacter baumannii[J]. Antimicrob Resist Infect Control, 2019, 8:52.
[16] WANG X, WANG Q, CAO B, et al. Retrospective observational study from a chinese network of the impact of combination therapy versus monotherapy on mortality from carbapenem-resistant Enterobacteriaceae bacteremia[J]. Antimicrob Agents Chemother, 2018,21, 63(1):e01511-e015118.
[17] GUTIéRREZ-GUTIéRREZ B, SALAMANCA E, DE CUETO M, et al. Effect of appropriate combination therapy on mortality of patients with bloodstream infections due to carbapenemase-producing Enterobacteriaceae (INCREMENT): a retrospective cohort study[J]. Lancet Infect Dis, 2017, 17(7):726-734.
[18] SEO H, LEE S C, CHUNG H, et al. Clinical and microbiological analysis of risk factors for mortality in patients with carbapenem-resistant Enterobacteriaceae bacteremia[J]. Int J Antimicrob Agents, 2020, 56(4):106126.
[19] STEWARDSON A J, MARIMUTHU K, SENGUPTA S, et al. Effect of carbapenem resistance on outcomes of bloodstream infection caused by Enterobacteriaceae in low-income and middle-income countries (PANORAMA): a multinational prospective cohort study[J]. Lancet Infect Dis, 2019, 19(6):601-610.
[20] TABAH A, KOULENTI D, LAUPLAND K, et al. Characteristics and determinants of outcome of hospital-acquired bloodstream infections in intensive care units: the EUROBACT international cohort study[J]. Intensive Care Med, 2012, 38(12):1930-1945.
[21] SOLOMKIN J S, RISTAGNO R L, DAS A F, et al. Source control review in clinical trials of anti-infective agents in complicated intra-abdominal infections[J]. Clin Infect Dis, 2013, 56(12):1765-1773.
[22] LIANG C A, LIN Y C, LU P L, et al. Antibiotic strategies and clinical outcomes in critically ill patients with pneumonia caused by carbapenem-resistant Acinetobacter baumannii[J]. Clin Microbiol Infect, 2018, 24(8):908.e1-908.e7.
[23] GUTIéRREZ-GUTIéRREZ B, SALAMANCA E, DE CUETO M, et al. A predictive model of mortality in patients with bloodstream infections due to carbapenemase-producing Enterobacteriaceae[J]. Mayo Clin Proc, 2016, 91(10):1362-1371.
[24] FALCONE M, BASSETTI M, TISEO G, et al. Time to appropriate antibiotic therapy is a predictor of outcome in patients with bloodstream infection caused by KPC-producing Klebsiella pneumoniae[J]. Crit Care, 2020, 24(1):29.
[25] MARTíNEZ M L, FERRER R, TORRENTS E, et al. Impact of source control in patients with severe sepsis and septic shock[J]. Crit Care Med, 2017, 45(1):11-19.
[26] CHANG D, SHARMA L, DELA CRUZ C S, et al. Clinical epidemiology, risk factors, and control strategies of Klebsiella pneumoniae infection[J]. Front Microbiol, 12:750662.
[27] TSUJI B T, POGUE J M, ZAVASCKI A P, et al. International consensus guidelines for the optimal use of the polymyxins: endorsed by the American College of Clinical Pharmacy (ACCP), European Society of Clinical Microbiology and Infectious Diseases (ESCMID), Infectious Diseases Society of America (IDSA), International Society for Anti-infective Pharmacology (ISAP), Society of Critical Care Medicine (SCCM), and Society of Infectious Diseases Pharmacists (SIDP)[J]. Pharmacotherapy, 2019, 39(1):10-39.
[28] MEDEIROS G S, RIGATTO M H, FALCI D R, et al. Combination therapy with polymyxin B for carbapenemase-producing Klebsiella pneumoniae bloodstream infection[J]. Int J Antimicrob Agents, 2019, 53(2):152-157.
[29] DICKSTEIN Y, LELLOUCHE J, SCHWARTZ D, et al. Colistin resistance development following colistin-meropenem combination therapy versus colistin monotherapy in patients with infections caused by carbapenem-resistant organisms[J]. Clin Infect Dis, 2020, 71(10):2599-2607.
[30] GIAMARELLOU H, POULAKOU G. Pharmacokinetic and pharmacodynamic evaluation of tigecycline[J]. Expert Opin Drug Metab Toxicol, 2011, 7(11):1459-1470.
[31] WANG J, PAN Y, SHEN J, et al. The efficacy and safety of tigecycline for the treatment of bloodstream infections: a systematic review and meta-analysis[J]. Ann Clin Microbiol Antimicrob, 2017, 16(1):24.
[32] NI W, HAN Y, LIU J, et al. Tigecycline treatment for carbapenem-resistant Enterobacteriaceae infections: a systematic review and meta-analysis[J]. Medicine (Baltimore), 2016, 95(11):e3126.
[33] TUMBARELLO M, VIALE P, VISCOLI C, et al. Predictors of mortality in bloodstream infections caused by Klebsiella pneumoniae carbapenemase-producing K. pneumoniae: importance of combination therapy[J]. Clin Infect Dis, 2012, 55(7):943-950.
[34] LIN Y T, SU C F, CHUANG C, et al. Appropriate treatment for bloodstream infections due to carbapenem-resistant Klebsiella pneumoniae and Escherichia coli: a nationwide multicenter study in Taiwan[J]. Open Forum Infect Dis, 2019, 6(2):ofy336.
[35] ALRADDADI B M, SAEEDI M, QUTUB M, et al. Efficacy of ceftazidime-avibactam in the treatment of infections due to carbapenem-resistant Enterobacteriaceae[J]. BMC Infect Dis, 2019, 19(1):772.
[36] TAMMA P D, AITKEN S L, BONOMO R A, et al. Infectious Diseases Society of America guidance on the treatment of extended-spectrum β-lactamase producing Enterobacterales (ESBL-E), carbapenem-resistant Enterobacterales (CRE), and Pseudomonas aeruginosa with difficult-to-treat resistance (DTR-P. aeruginosa)[J]. Clin Infect Dis, 2021, 72(7):1109-1116.
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