Hotchkiss John R, Strike David G, Simonson Dana A, Broccard Alain F, Crooke Philip S
CRISMA Laboratory, Department of Critical Care, University of Pittsburgh, USA.
Crit Care Med. 2005 Jan;33(1):168-76; discussion 253-4. doi: 10.1097/01.ccm.0000150658.05831.d2.
To develop and disseminate a spatially explicit model of contact transmission of pathogens in the intensive care unit.
A model simulating the spread of a pathogen transmitted by direct contact (such as methicillin-resistant Staphylococcus aureus or vancomycin-resistant Enterococcus) was constructed. The modulation of pathogen dissemination attending changes in clinically relevant pathogen- and institution-specific factors was then systematically examined.
The model was configured as a hypothetical 24-bed intensive care unit. The model can be parameterized with different pathogen transmissibilities, durations of caregiver and/or patient contamination, and caregiver allocation and flow patterns.
Pathogen- and institution-specific factors examined included pathogen transmissibility, duration of caregiver contamination, regional cohorting of contaminated or infected patients, delayed detection and isolation of newly contaminated patients, reduction of the number of caregiver visits, and alteration of caregiver allocation among patients.
The model predicts the probability that a given fraction of the population will become contaminated or infected with the pathogen of interest under specified spatial, initial prevalence, and dynamic conditions. Per-encounter pathogen acquisition risk and the duration of caregiver pathogen carriage most strongly affect dissemination. Regional cohorting and rapid detection and isolation of contaminated patients each markedly diminish the likelihood of dissemination even absent other interventions. Strategies reducing "crossover" between caregiver domains diminish the likelihood of more widespread dissemination.
Spatially explicit discrete element models, such as the model presented, may prove useful for analyzing the transmission of pathogens within the intensive care unit.
开发并推广一种重症监护病房内病原体接触传播的空间明确模型。
构建了一个模拟通过直接接触传播的病原体(如耐甲氧西林金黄色葡萄球菌或耐万古霉素肠球菌)传播的模型。然后系统地研究了临床相关病原体和机构特定因素变化对病原体传播的调节作用。
该模型被配置为一个假设的拥有24张床位的重症监护病房。该模型可以根据不同的病原体传播性、护理人员和/或患者污染持续时间以及护理人员分配和流动模式进行参数化设置。
研究的病原体和机构特定因素包括病原体传播性、护理人员污染持续时间、受污染或感染患者的区域分组、新受污染患者的延迟检测和隔离、护理人员探视次数的减少以及护理人员在患者之间分配的改变。
该模型预测在特定的空间、初始患病率和动态条件下,给定比例的人群被感兴趣的病原体污染或感染的概率。每次接触时病原体获得风险和护理人员病原体携带持续时间对传播的影响最为强烈。即使没有其他干预措施,污染患者的区域分组以及快速检测和隔离也会显著降低传播的可能性。减少护理人员区域之间“交叉”的策略会降低更广泛传播的可能性。
如本文所呈现的空间明确离散元素模型,可能被证明对分析重症监护病房内病原体的传播有用。