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分子分型在医院感染控制中的作用 ( the Role of Molecular Typing in Nosocomial Infection Control )

分子分型在医院感染控制中的作用 ( the Role of Molecular Typing in Nosocomial Infection Control ). 瑞金医院临床微生物科 瑞金医院医院感染办公室 杨 莉. 分子分型(分子流行病学研究). 从核酸分子水平上分析医院感染的发生、发展规律及机理,更加准确有效地进行医院感染管理控制,已成为当前国际医院感染管理研究中的重要方向。. 从患者分离株到病区周围环境株的比较分析; 从外源性感染到内源性感染 从某一医院的医院感染暴发到大范围甚至世界范围的感染菌株流行变迁;.

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分子分型在医院感染控制中的作用 ( the Role of Molecular Typing in Nosocomial Infection Control )

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  1. 分子分型在医院感染控制中的作用(the Role of Molecular Typing inNosocomial Infection Control) 瑞金医院临床微生物科 瑞金医院医院感染办公室 杨 莉

  2. 分子分型(分子流行病学研究) • 从核酸分子水平上分析医院感染的发生、发展规律及机理,更加准确有效地进行医院感染管理控制,已成为当前国际医院感染管理研究中的重要方向。 • 从患者分离株到病区周围环境株的比较分析; • 从外源性感染到内源性感染 • 从某一医院的医院感染暴发到大范围甚至世界范围的感染菌株流行变迁; • 基因多态性分析技术已成为医院感染监测控制的高水平研究领域。

  3. 微生物室在医院感染中的作用 • accurately identifying nosocomial pathogens • detecting unexpected antimicrobial-drug resistance • epidemiologic typing • 鉴定 • 特殊耐药菌的检出 • 流行病学分型 Pfaller MA et al. The clinical microbiology laboratory and infection control: emerging pathogens, antimicrobial resistance, and new technology. Clin Infect Dis 1997;25:858-70.

  4. PFGE(脉冲场凝胶电泳) • RAPD(随机扩增DNA多态性) • REA(限制性酶切) • ribotyping (核糖体分型) • 分子分型 • 基因分型 • 分子流行病学研究

  5. 1、脉冲场凝胶电泳(PFGE) 制备琼脂糖栓块 消 化 酶 切 脉冲电泳 结果解释

  6. 消化、释放出DNA PFGE原理

  7. PFGE原理 酶切 Enzyme • 约5~20个、长度10~800kb的大片段DNA

  8. Tenover FC.et al.J Clin Microbiol,1995;33(9):2233~2239

  9. PFGE原理 脉冲电泳

  10. 原理: 常规凝胶电泳 DNA 脉冲场凝胶电泳

  11. PFGE原理 染色、拍照 时间消耗 • 从分离菌株到出结果平均 2.5 天 • 标本准备、细胞裂解--第一天 • 酶切--第二天 • 染色、拍照--第三天

  12. PFGE结果判读 • 目测法: • 按美国疾病控制和预防中心(CDC)Tenover等人推荐的方法判读。 • 图谱完全相同的定为一个型,彼此之间相差一个带的定为同一型的不同亚型,相差2-3个带的认为亲缘关系密切,相差4-6个带的认为可能相关,条带相差7个以上的认为无亲缘关系。并随机地选择不同的字母如A、B、C、D等的字母顺序分型。 • 聚类分析 • 计算机输入SPSS,做树状图

  13. PFGE同源性分析

  14. PFGE特点: • DNA原位提取法,减少了断裂 • 利用细菌全基因组信息 • 细菌分型金标准

  15. 2、RAPD(随机扩增DNA多态性) • 1990年 • Williams:RAPD • Welsh:AP-PCR • 本质上相同 • 引物: • “短” 、“单一” 和“非特异性”,一般9~10bp • 扩增条件:“非严格性” • 退火温度一般较低,25~35℃

  16. ESHWAR MAHENTHIRALINGAM.et al.J Clin Microbiol,1996;34(5):1129~1135

  17. ESHWAR MAHENTHIRALINGAM.et al.J Clin Microbiol,1996;34(5):1129~1135

  18. ESHWAR MAHENTHIRALINGAM.et al.J Clin Microbiol,1996;34(5):1129~1135

  19. 分子分型在医院感染控制中的作用

  20. Special Issue New Technology for Detecting Multidrug-Resistant Pathogens in the Clinical Microbiology Laboratory Lance R. Peterson*† and Gary A. Noskin*†*Northwestern Memorial Hospital and †Northwestern University Medical School, Chicago, Illinois, USA EID, 2001, 7: 306

  21. Northwestern Memorial Hospital, Chicago • 700-bed, university-affiliated medical center • 出院:>39,000/年 • 急诊:56,000例/年 • 门诊量:260,000/年

  22. 分型确认后及干预效果 5.79 P=0.002 LR Peterson et al, EID, 2001, 7: 306

  23. 指标 • the total number of nosocomial infections per 1,000 patient days每千住院日医院感染数 • the number of patients with nosocomial infections per 100 patient discharges 每100出院病人医院感染病人数 (percentage of patients with nosocomial infection) (医院感染病人百分比)

  24. 感染控制工作小组成员: • We formed a permanent, integrated infection control and prevention program that fully incorporates • 感染控制 • 感染性疾病 • 药学 • 临床微生物 • infection control personnel, • infectious disease personnel, • pharmacy personnel, • clinical microbiology personnel • into a single working group to minimize hospital infections. Hacek DM et al. Am J Clin Pathol 1999;111:647-54.

  25. 资料收集方法(Methods for data collection): • review of microbiology reports • review of patients' medical records, • direct observation of medical and nursing practice, • active surveillance of rectal cultures of patients in nursing units for high-risk patients, • evaluation of suspected nosocomial infections reported by health-care providers. • 查阅微生物报告 • 查阅病史记录 • 对医护人员操作的直接观察 • 高危病人直肠培养的动态连续观察 • 对上报的可疑医院感染的评估鉴定 由三位专职感染控制人员对资料进行汇总分析,并制定出相应控制措施,并在医院感染控制和预防部门主管的指导下实施。

  26. Two interventions: • a molecular typing laboratory • a weekly planning meeting • infection control • diagnostic medical microbiology (molecular epidemiology) • Pharmacy • and infectious diseases • 两个主要的干预措施: • 分子分型 • 周会 • 包括以下方面的代表: • 感染控制 • 微生物诊断(分子流行病学) • 药学 • 感染性疾病

  27. weekly meetings: • the ongoing short- and long-term trends in nosocomial infections within the center • activities of the infection control professionals and microbiology laboratory personnel; • any needed changes were determined. • The organizational structure for selecting microbes for typing was shared by the medical directors of infection control and clinical microbiology 周会内容: • 医院感染动向(短期、长期) • 感染控制专职人员和微生物实验室的工作 • 决定需要做的调整 • 需分型的病原体与主管讨论决定

  28. 需基因分型的微生物: • 常规基因分型:VRE • 周期性分型: • 氟喹诺酮耐药的铜绿 • MRSA • 阴沟肠杆菌 • 难辨梭菌 • 其他:根据微生物报告并在周会上讨论后决定需基因分型的病原体 • routinely genomically typed:VRE • Periodic routine typing: • fluoroquinolone-resistant P. aeruginosa, • methicillin-resistant Staphylococcus aureus (MRSA), • Enterobacter cloacae, • Clostridium difficile • Additional organisms for typing:selected through surveillance of microbiology culture reports discussed at the weekly meeting. 任何时候工作小组要求进行基因分型,临床微生物实验室即将菌株提供给分子分型部门并执行

  29. 实验方法 REA analysis restriction of genomic DNA with conventional electrophoresis DNA限制性酶切

  30. 基因分型相关费用 成本-效益分析(Analysis of Cost Data) • the cost of equipment, remodeling, • reagent and other supplies, • salaries and benefits for three technologists, • plus all the institutional assessments (e.g., full-cost basis) required to operate a hospital laboratory. • 仪器配制及维修、实验室改造等; • 试剂及其他消耗品 • 三位实验员的薪水 • 所有的评估分析(如full-cost basis )需要动用全院系统 分析方法:t检验

  31. 结果: • 1、VRE • 最初调查:VRE医院感染严重 • 分型结果提示: • 多型别、小规模(mini)病人间流行 • 而不是一个型别的流行 • 1、VRE • initial impetus: serious nosocomial problem---VRE's emergence • molecular typing results: • a pattern of numerous “mini” patient-to-patient outbreaks of distinct clones • rather than the spread of a single persisting strain

  32. 结果: • 基因分型:可将可能的医院感染分组: • 病人之间交叉感染(high conality, >90%) • 感染爆发(moderate clonality, 35%-75%) • 无水平传播(<20% clonality). • 在此基础上,决定采取哪种控制措施 • genomic typing: • patient-to-patient transmission; • nosocomial outbreak; • little evidence of horizontal spread • Using this information, we determined what intervention was likely to control an apparent outbreak (20).

  33. similarity

  34. 通过基因分型,共鉴别25起微生物感染爆发 • VRE • 氟喹诺酮耐药的铜绿 • MRSA • 阴沟 • 难辩梭菌 • During the last 2 years of this study, • 25 possible microbial outbreaks were investigated by the typing laboratory • VRE, • fluoroquinolone-resistant P. aeruginosa, • MRSA, • E. cloacae, • C. difficile.

  35. 典型的医院感染传播 • VRE: 19株, 来自16个病人,2个月时间内; • 其中十四株:为两个型别中的一个型别 (88%) • 高度提示感染传播 • 检查分析: • 微生物实验室: 培养过程无密切联系 • 患者:14人中有11人有直接联系 • 感染控制:中止暴发 • Classic Spread of Nosocomial Infection • VRE: 19 strains, from 16 patients, in a 2-month period; • 14 strains: from one of two clones (88%) • Indicating: a high probability of nosocomial spread • Review: • microbiology laboratory: culture requisitions---no close contact. • Patients: existing direct connection between 11/14 patients (14). • infection control practices: aborted the outbreak

  36. Moderate Likelihood of Spread of Nosocomial Infections • 较有可能为NI传播 • 1个月时间内,特殊病房 • 侵入性操作感染: • 肺炎克雷伯菌 • 表皮葡萄球菌 • 溶血葡萄球菌 • 40%-60% clonality • 分析:分离出相同型别菌株的患者病床临近 • 措施: • 病房设立屏障 • 医护人员教育 • 结果:感染中止 • During a 1-month period, in a special-care unit • invasive infections, caused by five isolates • Klebsiella pneumoniae, • S. epidermidis, and • S. hemolyticus • DNA typing indicated 40% to 60% for each of the bacterial species. • patients with genetically identical organisms occupied adjacent beds. • Erecting a barrier on the unit, along with educating medical staff, halted the spread of these infections (15).

  37. Outbreaks not Caused by Patient-to-Patient Spread • 2个医院的ICU病房 • 4株肺克,64株粘质沙雷菌 • 21% clonality • 提示:非病人之间传播indicating unlikely patient-to-patient spread. • 调查分析:机械通气相关操作不规范 • 措施:规范操作 • 结果:感染中止 • Suspected outbreaks consisting of four isolates of K. pneumonia and 64 strains of Serratia marcescens were investigated in the ICUs of two hospitals. Both investigations showed 21% clonality, indicating unlikely patient-to-patient spread. • Investigation suggested suboptimal handling of ventilator equipment, and both outbreaks were stopped by retraining of personnel using this equipment

  38. 2个医院,特殊护理病房,每个医院都有自己的分子分型部门2个医院,特殊护理病房,每个医院都有自己的分子分型部门 • 7株金葡 • 迅速分子分型rapid typing • no (20%) clonality • 没有采取措施 • 节省: • 医护人员携菌情况调查(培养) • 关闭病房30天,消毒、清洁 • Pseudooutbreaks • Possible outbreaks occurred in the special-care nursery units of two hospitals, each of which had its own molecular typing section. • seven S. aureus strains, and the other of four isolates of gram-negative bacilli. • immediately typed and no (20%) clonality existed. • No interventions were instituted, and the apparent outbreaks were determined to be normal variation in infections (15,21). • avoided culture-based surveillance investigation of staff by the state department of health, and the other avoided closing the unit for a 30-day full disinfection and cleaning (done in previous suspected outbreaks). • 4株G-菌

  39. 分型确认后及干预效果 P=0.000006 LR Peterson et al, EID, 2001, 7: 306

  40. 分型确认后及干预效果 5.79 P=0.002 LR Peterson et al, EID, 2001, 7: 306

  41. nosocomial infection: 3.3%-2.6% (national rate: 4.4%-5%) • >1,400 fewer patients acquired infections during this time, • averting more than 50 expected deaths • Even with endemic VRE, most of our outbreaks involve three or fewer patients (19). • 医院感染:3.3%下降至2.6%(全国医院感染率:4.4%-5%) • 减少>1,400的病人感染 • 死亡:减少了>50 • VRE:涉及的病人也比其他医院少

  42. 成本 • The mean number of patients with nosocomial infections decreased by 283 per year, a reduction of more than 1,100 inpatient days. • The costs avoided by using this calculation averaged more than $2,150,000/year, based on 1999 dollars. • 医院感染患者数量平均每年下降 283,住院天数下降超过1100天 • 因此节省的费用平均每年超过$2,150,000(与1999年相比)

  43. 小组聚会逐渐转为每周开会,45min,讨论 • 微生物室成立分子分型实验室(设备及人员)的费用为$180,050. • 每年分子分型相关支出为$400,000 • 医院承担 • Representatives now meet together for 45 minutes each week • For Microbiology, opening the typing laboratory totaled $180,050. By the fifth year, costs in the laboratory section were stable. • The cost for the laboratory, includng three medical technologists, is $400,000 yearly. • Virtually all these costs are borne by the hospital.

  44. While such a grant program would cost up to $2 billion each year if all U.S. hospitals participated, • the projected reduction in cost of treating nosocomial infections could reach over five times that amount. • a savings of $5.00 for each dollar spent. • 假设:美国所有医院 • 进行基因分型相关费用达到20亿美元 • 节省下来的治疗医院感染的费用将超过5倍(100亿)! • 每使用1美元节省5美元

  45. 时间:1周,48h • 如没有流行相关线索,可能是其他原因: • 抗生素压力, • 护理操作不当(非感染相关), • 仅仅是感染数量的随机变化 • 早发现、及早确定调查范围、采取合适的干预措施 • Typing time: within 1 week 48 hours. • Lack of clonality: suggests other reasons for the apparent outbreak, • antimicrobial-agent use pressure, • failure of appropriate nursing-care practices, • or simply random variation in the number of infections. • Early knowledge of whether microbial clonality is present or absent focuses the scope of an investigation and facilitates appropriate intervention.

  46. cost of rapid detection using the polymerase chain reaction (PCR) • =one day of glove isolation • could be completed in a single 8-hour workday. • As gene chip technology moves into clinical use, detecting a large number of resistance determinants soon after a patient is admitted to the hospital should be possible. • PCR分型 • 费用=一天的手套费用 • 8小时的工作时间内可完成 • 基因芯片: • 大规模 • 耐药监测 • 病人入院后即实施

  47. 分子分型在医院感染中的应用: • technically possible • medically useful • economically justified

  48. 医院感染的分子流行病学研究方法 • 分子流行病学方法在医院感染中的应用 • 医院感染控制的人员安排 • 成本-效益研究 • 临床医院感染控制 • 科研

  49. 实验研究: • 瑞金医院 04年~05年 • 全耐药鲍曼不动杆菌(PRAB) 各个科室的突然增多 • 经脉冲场凝胶电泳(PFGE)证实 • 烧伤科为单独一个型别PRAB科室内流行 • 除烧伤科以外的其他科室为科室间同一型别PRAB流行。 • 由此可见,分子流行病学方法: • 为医院感染控制提供准确的实验数据 • 有效判断感染来源和流行趋势 • 为更好的做好医院感染控制工作打下了基础。

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