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Article

Synergistic Effect of Combination Interventions for Methicillin-Resistant Staphylococcus aureus Transmission Control in Nursing Homes: A Computation Modelling Evaluation with Heterogeneous Contact Mixing

1
Department of Software, Sungkyunkwan University, Suwon 16419, Korea
2
JC School of Public Health and Primary Care, The Chinese University of Hong Kong, Hong Kong 999077, China
3
Stanley Ho Centre for Emerging Infectious Diseases, The Chinese University of Hong Kong, Hong Kong 999077, China
4
Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen 518057, China
5
Centre for Health Protection, Department of Health, Hong Kong 999077, China
6
Alice Lee Centre for Nursing Studies, National University of Singapore, Singapore 117597, Singapore
*
Author to whom correspondence should be addressed.
Antibiotics 2021, 10(3), 227; https://doi.org/10.3390/antibiotics10030227
Submission received: 25 January 2021 / Revised: 12 February 2021 / Accepted: 18 February 2021 / Published: 24 February 2021
(This article belongs to the Special Issue Antibiotic Resistance and Treatment of MRSA Infection)

Abstract

:
The endemic threat of methicillin-resistant Staphylococcus aureus (MRSA) in nursing homes poses a serious and escalating challenge to public health administration in infection control. Nursing homes are considered as major reservoirs for MRSA colonization, with considerable high levels of colonization prevalence. We employed a computation model to evaluate effects of three intervention scenarios on MRSA colonization prevalence rate in nursing homes. Simulations were conducted using a deterministic compartmental model featuring heterogeneous contact matrix between residents and health-care workers (HCWs). Contact parameters were derived from a nursing home survey. Three intervention scenarios were simulated: (1) hand-hygiene compliance by HCWs, (2) screening-and-isolation upon admission, and (3) implementing both interventions at the same time. For every 10% reduction in average contamination duration in HCWs, the estimated average reduction in prevalence rate was 1.29 percentage point compared with the prevalence rate before the intervention was implemented. Screening-and-isolation intervention resulted in an average reduction of 19.04 percentage point in prevalence rate (S.D. = 1.58; 95% CI = 18.90–19.18). In intervention scenario 3, synergistic effects were observed when implementing hand-hygiene compliance by HCWs and screening-and-isolation together. Our results provide evidence showing that implementing multiple interventions together has a synergistic effect on colonization prevalence reduction.

1. Introduction

Antimicrobial resistance (AMR) has become one of the major pressing public health threats and challenges globally. Antibiotics are widely used to combat life-threatening bacterial diseases. However, the imprudent use of antibiotics contributes to resistance among pathogenic microorganisms which in turn threatens the effective treatment of bacterial, parasitic, viral, and fungal infection. Methicillin-resistant Staphylococcus aureus (MRSA) is a multi-drug resistant strain of Staphylococcus aureus, and is regarded as one of the major AMR pathogens. Among the 18 drug-resistant threats identified by the United States Centers for Disease Control and Prevention, MRSA is regarded as a serious threat, where patients in healthcare settings frequently have severe or potentially life-threatening infections [1].
MRSA is commonly associated with the morbidity and mortality among elderly individuals. The overall incidence rates of MRSA infection among elderly individuals were consistently highest among other age groups globally [2,3,4]. Its strains were commonly identified in health care facilities, especially in nursing homes [5], which are considered as major reservoirs for MRSA [6]. MRSA was endemic at high levels in nursing homes [7,8]. Previous research works reported that MRSA colonization prevalence rate in nursing homes can be as high as 52% in the United States [9,10,11], significantly higher than that of 1.5% in the general population. Residents in nursing homes were shown to carry MRSA for a considerably long period of time: asymptomatic colonization could last for more than 3 years [12,13].
The endemic threat of MRSA in nursing homes along with the trend in global population aging pose a serious and escalating challenge to public health administration in infection control. Compared to acute care hospital settings, little was known about the epidemiology of MRSA in nursing homes. A primary effort in MRSA control of nursing homes is to drive down the endemic prevalence rate. Two key MRSA infection control measures for nursing-home are hand-hygiene by healthcare workers (HCWs) and screening followed by isolation for residents upon their admissions. One of the concerns for nursing homes’ administration is how to evaluate effectiveness among different interventions in reducing the colonization prevalence rate. As a natural experiment studying infectious diseases transmission is neither possible nor ethical, computational modelling becomes an essential tool to simulate how infectious diseases progress and to evaluate the impact of infection control policies with different intervention implementations.
The major transmission mode of MRSA infections is through direct contact with wounds, discharge, and soiled areas [14]. A recent systematic review on mathematical modelling of AMR summarizes computation models simulating MRSA transmission in nursing home settings [15]. Social contact in these models was mostly assumed to be homogeneous, except one modelling study in nursing home setting that explicitly represents the contact between residents and healthcare workers (HCWs) [6]. Our study further extended this computation model to evaluate the effect of two interventions to MRSA colonization prevalence: (1) hand-hygiene compliance by HCWs and (2) screening-and-isolation upon admission. Our study further evaluated a potential synergistic effect for implementing both of these two interventions together. We used the aggregate social contact information among residents and staff obtained in the previous contact survey [16] and demographics of nursing homes as parameters of our simulation model.

2. Results

The results of the simulations in intervention scenario 1, hand-hygiene compliance for HCWs, are summarized in Table 1 and illustrated in Figure 1. It is further estimated that for every 10% reduction in average contamination duration, there is an average reduction of 1.29 percentage point in prevalence rate compared with the prevalence rate before the intervention was implemented.
The results of the simulations in intervention scenario 2, screening-and-isolation upon admission, are illustrated in Figure 2. Our simulation results estimated that the screening-and-isolation intervention results in an average reduction of 19.04 percentage point in prevalence rate (S.D. = 1.58; 95% CI = 18.90–19.18) compared with the prevalence rate before the intervention was implemented.
The results of the simulations in intervention scenario 3, implementing both interventions at the same time, are illustrated in Figure 3 and summarized in Table 2. A synergistic effect is observed; the effect of scenario 3 is larger than the combined effect of scenario 1 and scenario 2.

3. Discussion

Close contact is the major transmission route of MRSA infections. The primary considerations in this study are how to represent the heterogeneity of contact mixing between residents and HCWs in the model, and the availability of social contact matrix data for parameters estimation. The modeling framework of this study employed explicit representation of the heterogeneous contact mixing between residents and HCWs. The contact parameters of this study were estimated based on the results of a nursing home survey conducted for residents and HCWs of 53 nursing homes. These approaches provide more legitimate simulation results of MRSA transmission in nursing homes. The model and methodology of this study also provide an instantaneous framework to evaluate hypothetical scenarios and to conduct “what-if” analyses. Nursing home administrators can employ the methodology of our study to make informed judgment and decision on infection control strategies accordingly.
Our simulation results suggest that the two simulated interventions, (1) hand-hygiene compliance for HCWs and (2) screening-and-isolation upon admission, are effective in driving down MRSA colonization prevalence. Quantitative data shows that every 10% reduction in average contamination duration for HCWs results in a reduction of 1.29 percentage points in prevalence on average. The screening-and-isolation upon admission intervention was also shown to be effective in driving prevalence down, with a 19.04 percentage point reduction on average. In intervention scenario 3, a synergistic effect is observed when implementing both interventions together. The magnitude of effect in prevalence reduction in scenario 3 is larger than the sum of the magnitude of effect in scenarios 1 and 2. The synergistic effects observed by implementing both interventions together in scenario 3 is quite encouraging. We are not aware of any evidence showing this kind of synergistic effect in prior literature. This result should be brought to broader attention as hand-hygiene based intervention is relatively convenient to be implemented and is shown to be effective in bringing down MRSA colonization prevalence. Our simulation results provide quantitative data for nursing home administrators in interventions planning, design, adjustment, and effect estimation and comparison.
To the best of our knowledge, the latest systematic review about MRSA transmission control in nursing homes was conducted in 2013 [17]. One clinical study [18] was included in this systematic review. We further identified two additional clinical studies about MRSA transmission control in nursing homes [19,20]. Currently, there is a lack of prior clinical studies evaluating effectiveness of different interventions on MRSA prevalence in nursing home. While there exists a sizable amount of clinical studies evaluating MRSA intervention effectiveness in hospital settings, MRSA epidemiology in hospitals is quite different from that in nursing homes. Infection control measures for MRSA used in hospital settings should be applied with caution to nursing home before being validated by clinical data.
The three prior clinical studies evaluating MRSA transmission control in nursing homes employed different intervention strategies, including hand-hygiene training program for HCWs, screening-and-isolation, and environmental cleaning. The study by Baldwin et al. [18] employed hand-hygiene training program for HCWs, screening-and-isolation, and environmental cleaning in their intervention program, and their interventions program has no significant effect on MRSA prevalence. The study by Hequet et al. [19] employed hand-hygiene and training program for HCWs in their intervention program, and their intervention program has no significant effect on MRSA prevalence. The study by Peterson et al. employed hand-hygiene training program for HCWs, screening-and-isolation, and environmental cleaning in their intervention program, and their intervention program has a significant reduction on MRSA prevalence with the interventions employed. Results in intervention effectiveness among these three clinical studies are inconclusive. Prior research in MRSA control in hospital settings suggests that hand hygiene compliance is crucial in reducing healthcare associated infections [21]. The results from our simulation also demonstrated that different level of hand hygiene compliance results in different levels of long term MRSA prevalence reduction. Intervention compliance could be the crucial factor in MRSA control, rather than the choice of intervention methods [22].
Hand-hygiene intervention in health-care settings is beyond merely providing hand-hygiene facilities and implementing policy for HCWs. A prior study [23] reported that a one-hour lecture plus 30-min hands-on session could effectively improve the hand-hygiene compliance from 9.3% to 30.4%. The World Health Organization (WHO) published guidelines in 2009 for implementing and evaluating hand hygiene programmes in healthcare settings [24]. The guidelines had identified five components to be implemented in healthcare-setting, including (1) using soap and water or alcohol-based hand rub at point of care or carried by the HCWs, (2) training and education, (3) observation and performance feedback, (4) reminders, and (5) administrative support/institutional safety climate. A recent systematic review reported that multimodal interventions that include some or all strategies recommended in the WHO guidelines might slightly improve hand hygiene compliance [25]. As to screening-and-isolation, although it was advocated by many researchers [26,27], studies in nursing homes were limited, but some studies reported the effectiveness of such measure in hospital settings [28,29].

4. Materials and Methods

4.1. The Computational Model

A two-level compartmental model with deterministic framework was employed. Nursing home residents are considered as hosts of MRSA, and HCWs are considered as transmission vectors. Residents are categorized into two mutually exclusive states: (a) uncolonized or (b) colonized; whereas HCWs are categorized into two mutually exclusive states: (c) contaminated or (d) uncontaminated. The model features the residents’ admission from community/hospital and discharge/death of the residents who are susceptible and colonized. Different routes of transmission were taken into account via the close contact among HCWs and residents: (i) HCWs-residents contacts, (ii) residents-residents contacts, and (iii) residents-HCWs contacts. Two types of transmission were defined in the model: Colonization and Contamination. MRSA can be transmitted to uncolonized residents by contact made with colonized residents or contaminated HCWs. Uncontaminated HCWs can be contaminated by contact made with colonized residents. Schematic of the transmission model is illustrated in Figure 4.
The model is described with the following set of nonlinear differential equations:
d U ( t ) d t =   β r r U ( t )   C ( t ) N r β h r U ( t ) H c ( t ) N h + ω C ( t ) + ( 1 λ ) Λ γ u U ( t )
d C ( t ) d t =   β r r U ( t )   C ( t ) N r + β h r U ( t )   H c ( t ) N h ω C ( t ) + λ Λ γ c C ( t )
d H ( t ) d t =   β r h H ( t )   C ( t ) N r β h h H ( t )   H c ( t ) N h + µ H c ( t )
d H c ( t ) d t = β r h H ( t )   C ( t ) N r µ H c ( t )
where U(t), C(t), H(t), and Hc(t) denote the population size of uncolonized-residents, colonized-residents, uncontaminated-HCWs, and contaminated-HCWs, respectively in a nursing home at time t; 1/μ denotes the mean duration of contamination, while 1/ω denotes the mean duration of colonization. Nr denotes the population of residents and Nh denotes the population of healthcare-workers, where Nr = U(t) + C(t) and Nh = H(t) + Hc(t).
The average length of stay of colonized residents and uncolonized residents are denoted by γu and γc, respectively. Residents are admitted at the rate of Λ, and the probability of admitted residents being colonized is λ. It is assumed that the number of residents and HCWs remain constant, and the occupancy rate is 100%. Therefore, residential admission rate equals to residents’ discharge rate; i.e., Λ = γuU + γcC.
Three transmission rates were defined in the model. βr-r and βh-r denoted the residents-to-residents transmission rate and HCWs-to-residents transmission rate respectively, whereas βr-h denoted the residents-to-HCWs transmission rate. The values of these three transmission rates were defined as the estimated number of contacts multiplied by the transmission probability via contact, as summarized in Table 3 and Table 4. Three types of contact and transmission probability were defined; ar-r, ar-h, and ah-r denote the average number of residents-to-residents contact, residents-to-HCWs contact, and HCWs-to-residents contact, respectively; pr-r, pr-h, and ph-r denote the transmission probability via residents-to-residents contact, residents-to-HCWs contact, and HCWs-to-residents contact, respectively.

4.2. Parameterization

4.2.1. Parameter Identification

Fourteen parameters were incorporated in the model. Values of 12 of the 14 parameters were identified in the parameterization process. Values of 2 parameters cannot be identified and were estimated. Table 5 summarizes the 14 parameters.

4.2.2. Parameter Estimation

No best estimates of two key parameters were identified from prior studies: (a) transmission probability via residents-to-residents contact and (b) transmission probability via HCWs-to-residents contact. We estimated these two parameters by fitting the mathematical transmission model to the prevalence data. Four MRSA point-prevalence rates and their 95% confidence interval (CI) of nursing homes in Hong Kong were identified from prior studies (Table 6) [30,34,35,36]. We denoted the date of these four point-prevalence rates as Day 1, Day 108, Day 1600, and Day 2239.
Simulations using the computational model described in the previous section were conducted by varying the two unknown transmission probabilities and the prevalence of Day 1. The combinations of the three variables used in the simulations are constructed based on 3-dimensional hypercube, varying the two transmission probabilities from 0% to 100% (with 0.1% increments) and the prevalence of Day 1 from 16.2% to 19.4% (with 0.1% increment); 33,066,033 simulations (1001 × 1001 × 33) were conducted. Each simulation was conducted to simulate prevalence for 2500 days where the prevalence rates reached equilibrium. Of the 33,066,033 simulation generated results, 487 fitted within the 95% confidence interval of the four point-prevalence rate on their respective day. These 487 sets of parameters were used to further conduct simulations of interventions. Figure 5 illustrates simulation results of these 487 simulations.

4.3. Simulations of Interventions

Three types of intervention scenarios were evaluated using the computational model: (1) hand-hygiene compliance by HCWs, (2) screening-and-isolation upon all admission, and (3) implementing both interventions at the same time. Assuming interventions implemented on Day 2501, we simulated the long term impact of different hypothetical intervention scenarios on MRSA transmission dynamics. The 487 sets of parameters that fitted within 95% CI of the four point-prevalence rates were used as the input parameters for the computational model. Effects of interventions were evaluated by comparing the point prevalence of Day 2500 and Day 7500 for each of the simulations.

4.3.1. Intervention Scenario 1: Hand-Hygiene Compliance by HCWs

Hand-hygiene compliance by HCWs was simulated by reducing the average contamination duration 1/μ. Five levels of hand-hygiene compliance by HCWs were evaluated by reducing the average contamination duration by 10%, 20%, 30%, 40%, or 50%. Computational model defined in the previous section was used to simulate effects of hand-hygiene by HCWs compliance to prevalence in our study; 2435 simulations (5 levels of compliance ×487 set of parameters) were conducted for this scenario.

4.3.2. Intervention Scenario 2: Screening-and-Isolation Upon Admission

The model was further extended in order to study effects of screening-and-isolation upon admission to prevalence rate. We assumed a 100% screening success rate, a 5-day isolation period, and a 100% decolonization rate after 5 days in isolation. An additional compartment was added in the model in order to represent the screening-and-isolation upon admission. All colonized admissions were put into an isolation compartment I, and they were forwarded to compartment U after 5 days. Schematic of the extended model is illustrated in Figure 6; 487 simulations were conducted for this scenario.

4.3.3. Intervention Scenario 3: Implementing Both Interventions at the Same Time

Simulation of intervention scenario 2 was run with five levels of hand-hygiene compliance by HCWs (reducing the average contamination duration by 10%, 20%, 30%, 40%, or 50%); 2435 simulations were conducted for this scenario.

5. Conclusions

We presented a computational model with heterogeneous social contact mixing to simulate the transmission of MRSA in nursing homes. This approach can be used to conduct scenario analyses for MRSA transmission in nursing homes, and can also be generalized to other settings including hospitals and households as well as multi-drug resistance organisms such as extended spectrum beta-lactamases and Carbapenem-resistant enterobacteriaceae. Several limitations of the study are noteworthy. First, the potential super-spreading events and transmissibility variation in individual or sub-groups were not considered in this model. Second, this study mainly employed the survey data of nursing homes in Hong Kong to parameterize the model. Region or country specific data including point prevalence, characteristics of nursing home, and social mixing matrix is needed to study the situations in different countries/regions. Finally, we are not aware of any prior study about the efficacy of MRSA screening and decolonization of nursing homes and 100% efficacy was assumed in this study. Further study is needed to parameterize these two factors accurately.

Supplementary Materials

The following are available online at https://www.mdpi.com/2079-6382/10/3/227/s1, Supplementary Material S1: Parameterization.

Author Contributions

Conceptualization, A.T., K.O.K.; methodology, A.T., K.O.K.; software, A.T., W.W.S.T.; validation, A.T., K.O.K., V.W.I.W., and W.W.S.T.; formal analysis, A.T., K.O.K.; investigation, A.T., K.O.K.; resources, A.T., K.O.K., V.W.I.W., H.C., S.Y.S.W., and W.W.S.T.; data curation, A.T., V.W.I.W.; writing—original draft preparation, A.T., K.O.K.; writing—review and editing, A.T., K.O.K., H.C., S.Y.S.W., and W.W.S.T.; visualization, A.T.; supervision, K.O.K., H.C., S.Y.S.W., and W.W.S.T.; project administration, A.T., K.O.K., V.W.I.W., and W.W.S.T.; funding acquisition, A.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research was solely funded by Sungkyun Research Fund, Sungkyunkwan University, 2018 (S-2018-2558-000-01).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data sharing not applicable. No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Acknowledgments

Arthur Tang acknowledges support by Sungkyun Research Fund, Sungkyunkwan University, 2019 (S-2018-2558-000-01). Kin On Kwok acknowledges Health and Medical Research Fund of the Health, Welfare and Food Bureau of the Hong Kong SAR Government (grant nos. CU-17-C18, CID-CUHK-A), Wellcome Trust (200861/Z/16/Z), and Li Ka Shing Institute of Health Sciences.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. US Centers for Disease Control and Prevention. Biggest Threats and Data—Antibiotic/Antimicrobial Resistance (AR/AMR). Available online: https://www.cdc.gov/drugresistance/biggest_threats.html (accessed on 3 August 2020).
  2. Bradley, S.F. Methicillin-resistant Staphylococcus aureus in nursing homes. Epidemiology, prevention and management. Drugs Aging 1997, 10, 185–198. [Google Scholar] [CrossRef]
  3. O’Sullivan, N.R.; Keane, C.T. The prevalence of methicillin-resistant staphylococcus aureus among the residents of six nursing homes for the elderly. J. Hosp. Infect. 2000, 45, 322–329. [Google Scholar] [CrossRef]
  4. Wong, J.W.; Ip, M.; Tang, A.; Wei, V.W.; Wong, S.Y.; Riley, S.; Read, J.M.; Kwok, K.O. Prevalence and risk factors of community-associated methicillin-resistant Staphylococcus aureus carriage in Asia-Pacific region from 2000 to 2016: A systematic review and meta-analysis. Clin. Epidemiol. 2018, 10, 1489–1501. [Google Scholar] [CrossRef] [Green Version]
  5. Boucher, H.W.; Corey, G.R. Epidemiology of methicillin-resistant Staphylococcus aureus. Clin. Infect. Dis. 2008, 46, S344–S349. [Google Scholar] [CrossRef] [Green Version]
  6. Chamchod, F.; Ruan, S. Modeling the spread of methicillin-resistant Staphylococcus aureus in nursing homes for elderly. PLoS ONE 2012, 7, e29757. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Datta, R.; Huang, S.S. Risk of infection and death due to methicillin-resistant Staphylococcus aureus in long-term carriers. Clin. Infect. Dis. 2008, 47, 176–181. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Hawkins, G.; Stewart, S.; Blatchford, O.; Reilly, J. Should healthcare workers be screened routinely for meticillin-resistant Staphylococcus aureus? A review of the evidence. J. Hosp. Infect. 2011, 77, 285–289. [Google Scholar] [CrossRef] [PubMed]
  9. Garazi, M.; Edwards, B.; Caccavale, D.; Auerbach, C.; Wolf-Klein, G. Nursing homes as reservoirs of MRSA: Myth or reality? J. Am. Med. Dir. Assoc. 2009, 10, 414–418. [Google Scholar] [CrossRef] [PubMed]
  10. Mody, L.; Kauffman, C.A.; Donabedian, S.; Zervos, M.; Bradley, S.F. Epidemiology of Staphylococcus aureus colonization in nursing home residents. Clin. Infect. Dis. 2008, 46, 1368–1373. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Reynolds, C.; Quan, V.; Kim, D.; Peterson, E.; Dunn, J.; Whealon, M.; Terpstra, L.; Meyers, H.; Cheung, M.; Lee, B.; et al. Methicillinresistant Staphylococcus aureus (MRSA) carriage in 10 nursing homes in Orange County, California. Infect. Control Hosp. Epidemiol. 2011, 32, 91–93. [Google Scholar] [CrossRef]
  12. Bradley, S.F.; Terpenning, M.S.; Ramsey, M.A.; Zarins, L.T.; Jorgensen, K.A.; Sottile, W.S.; Schaberg, D.R.; Kauffman, C.A. Methicillinresistant Staphylococcus aureus: Colonization and infection in a long-term care facility. Ann. Intern. Med. 1991, 115, 417–422. [Google Scholar] [CrossRef]
  13. Sanford, M.D.; Widmer, A.F.; Bale, M.J.; Jones, R.N.; Wenzel, R.P. Efficient detection and long-term persistence of the carriage of methicillin-resistant Staphylococcus aureus. Clin. Infect. Dis. 1994, 19, 1123–1128. [Google Scholar] [CrossRef]
  14. Hong Kong Centre for Health Protection. Methicillin-resistant Staphylococcus Aureus (MRSA) Infection. Available online: https://www.chp.gov.hk/en/healthtopics/content/24/10688.html (accessed on 3 August 2020).
  15. Kwok, K.O.; Read, J.M.; Tang, A.; Chen, H.; Riley, S.; Kam, K.M. A systematic review of transmission dynamic studies of methicillin-resistant Staphylococcus aureus in non-hospital residential facilities. BMC Infect. Dis. 2018, 18, 188. [Google Scholar] [CrossRef] [Green Version]
  16. Kwok, K.O.; Tang, A.; Chan, H.H.; Wong, S.Y.S.; Wei, W.I. A Longitudinal Contact Survey in Residential Care Homes for the Elderly in Hong Kong. Available online: https://www.cuhk.edu.hk/sphpc/kkokwok/manuscript_rche_contact.pdf (accessed on 23 February 2021).
  17. Hughes, C.; Tunney, M.; Bradley, M.C. Infection control strategies for preventing the transmission of methicillin-resistant Staphylococcus aureus (MRSA) in nursing homes for older people. Cochrane Database Syst. Rev. 2013, 11, CD006354. [Google Scholar]
  18. Baldwin, N.S.; Gilpin, D.F.; Tunney, M.M.; Kearney, M.P.; Crymble, L.; Cardwell, C.; Hughes, C.M. Cluster randomised controlled trial of an infection control education and training intervention programme focusing on meticillin-resistant Staphylococcus aureus in nursing homes for older people. J. Hosp. Infect. 2010, 76, 36–41. [Google Scholar] [CrossRef] [PubMed]
  19. Hequet, D.; Rousson, V.; Blanc, D.S.; Bula, C.; Qalla-Widmer, L.; Masserey, E.; Zanetti, G.; Petignat, C. Universal screening and decolonization for control of MRSA in nursing homes: Follow-up of a cluster randomized controlled trial. J. Hosp. Infect. 2017, 96, 69–71. [Google Scholar] [CrossRef]
  20. Peterson, L.R.; Boehm, S.; Beaumont, J.L.; Patel, P.A.; Schora, D.M.; Peterson, K.E.; Burdsall, D.; Hines, C.; Fausone, M.; Robicsek, A.; et al. Reduction of Methicillin-Resistant Staphylococcus aureus (MRSA) Infection in Long Term Care is Possible While Maintaining Patient Socialization: A Prospective Randomized Clinical Trial. Am. J. Infect. Control 2017, 44, 1622–1627. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Ojanperä, H.; Kanste, O.I.; Syrjala, H. Hand-hygiene compliance by hospital staff and incidence of health-care-associated infections, Finland. Bull. World Health Organ. 2020, 98, 475–483. [Google Scholar] [CrossRef] [PubMed]
  22. Wong, V.W.Y.; Huang, Y.; Wei, W.I.; Wong, S.Y.S.; Kwok, K.O. Approaches to Multidrug-Resistant Organism Prevention and Control in Long-Term Care Facilities for Older People: A Systematic Review and Meta-Analysis. Available online: https://www.researchsquare.com/article/rs-207428/v1 (accessed on 23 February 2021).
  23. Huang, T.T.; Wu, S.C. Evaluation of a training programme on knowledge and compliance of nurse assistants’ hand hygiene in nursing homes. J. Hosp. Infect. 2010, 68, 164–170. [Google Scholar] [CrossRef] [PubMed]
  24. World Health Organization. World Health Organization Guidelines on Hand Hygiene in Health Care. First Global Patient Safety Challenge Clean Care is Safer Care. 2009. Available online: https://www.who.int/gpsc/5may/tools/en/ (accessed on 31 July 2020).
  25. Gould, D.J.; Moralejo, D.; Drey, N.; Chudleigh, J.H.; Taljaard, M. Interventions to improve hand hygiene compliance in patient care. Cochrane Database Syst. Rev. 2017, 9, CD005186. [Google Scholar] [CrossRef]
  26. Boyce, J.M.; Havill, N.L.; Kohan, C.; Dumigan, D.G.; Ligi, C.E. Do infection control measures work for methicillin-resistant Staphylococcus aureus? Infect. Control Hosp. Epidemiol. 2004, 25, 395–401. [Google Scholar] [CrossRef]
  27. Verbrugh, H.A. Value of screening and isolation for control of methicillin-resistant Staphylococcus aureus. Clin. Infect. Dis. 2005, 41, 268–271. [Google Scholar] [CrossRef] [Green Version]
  28. Ahmed, M.O.; Elramalli, A.K.; Amri, S.G.; Abuzweda, A.R.; Abouzeed, Y.M. Isolation and screening of methicillin-resistant Staphylococcus aureus from health care workers in Libyan hospitals. East. Mediterr. Health J. 2012, 18, 37–42. [Google Scholar] [CrossRef]
  29. Popiel, K.Y.; Miller, M.A. Evaluation of vancomycin-resistant enterococci (VRE)-associated morbidity following relaxation of VRE screening and isolation precautions in a tertiary care hospital. Infect. Control Hosp. Epidemiol. 2014, 35, 818–825. [Google Scholar] [CrossRef] [PubMed]
  30. Cheng, V.C.; Tai, J.W.; Wong, Z.S.; Chen, J.H.; Pan, K.B.; Hai, Y.; Ng, W.-C.; Chow, D.M.K.; Yau, M.C.Y.; Chan, J.F.W.; et al. Transmission of methicillin-resistant Staphylococcus aureus in the long term care facilities in Hong Kong. BMC Infect. Dis. 2013, 13, 205. [Google Scholar] [CrossRef] [Green Version]
  31. Shenoy, E.S.; Paras, M.L.; Noubary, F.; Walensky, R.P.; Hooper, D.C. Natural history of colonization with methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE): A systematic review. BMC Infect. Dis. 2014, 14, 177. [Google Scholar] [CrossRef] [PubMed]
  32. Kwok, C.L.; Lee, C.K.M.; Lo, W.T.L.; Yip, P.S.F. The Contribution of Ageing to Hospitalisation Days in Hong Kong: A Decomposition Analysis. Int. J. Health Policy Manag. 2017, 6, 155–164. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Pineles, L.; Morgan, D.J.; Lydecker, A.; Johnson, J.K.; Sorkin, J.D.; Langenberg, P.; Blanco, N.; Lesse, A.; Sellick, J.; Gupta, K.; et al. Transmission of methicillin-resistant Staphylococcus aureus to health care worker gowns and gloves during care of residents in Veterans Affairs nursing homes. Am. J. Infect. Control 2017, 45, 947–953. [Google Scholar] [CrossRef]
  34. Kwok, K.O.; Wei, W.I.; Yu, C.H.; Hsu, E.K.; Wong, S.Y.S.; Lee, S.S.; Chen, H. Prevalence of Methicillin-Resistant Staphylococcus Aureus in Residential Care Homes for the Elderly in Hong Kong. Available online: https://www.cuhk.edu.hk/sphpc/kkokwok/manuscript_rche_mrsa_prevalence.pdf (accessed on 23 February 2021).
  35. Chen, H.; Au, K.M.; Hsu, K.E.; Lai, C.K.; Myint, J.; Mak, Y.F.; Lee, S.Y.; Wong, T.Y.; Tsang, N.C. Multidrug-resistant organism carriage among residents from residential care homes for the elderly in Hong Kong: A prevalence survey with stratified cluster sampling. Hong Kong Med. J. 2018, 24, 350–360. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Cheng, V.C.C.; Chen, H.; Wong, S.C.; Chen, J.H.K.; Ng, W.C.; So, S.Y.C.; Chan, T.-C.; Wong, S.C.Y.; Ho, P.-L.; Mody, L.; et al. Role of Hand Hygiene Ambassador and Implementation of Directly Observed Hand Hygiene Among Residents in Residential Care Homes for the Elderly in Hong Kong. Infect. Control Hosp. Epidemiol. 2018, 39, 571–577. [Google Scholar] [CrossRef]
Figure 1. Plots of effect of five levels of hand-hygiene compliance to MRSA colonization prevalence. Hand-hygiene compliance interventions were implemented on Day 2501.
Figure 1. Plots of effect of five levels of hand-hygiene compliance to MRSA colonization prevalence. Hand-hygiene compliance interventions were implemented on Day 2501.
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Figure 2. Plot of effect of screening-and-isolation upon admission to MRSA colonization prevalence.
Figure 2. Plot of effect of screening-and-isolation upon admission to MRSA colonization prevalence.
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Figure 3. Plots of combined effect of hand-hygiene compliance and screening-and-isolation upon admission to MRSA colonization prevalence. Interventions were implemented on Day 2500.
Figure 3. Plots of combined effect of hand-hygiene compliance and screening-and-isolation upon admission to MRSA colonization prevalence. Interventions were implemented on Day 2500.
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Figure 4. Schematic of the transmission model.
Figure 4. Schematic of the transmission model.
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Figure 5. Plot of 487 simulation results that fitted within 95% CI of the four point-prevalence rates on their respective day.
Figure 5. Plot of 487 simulation results that fitted within 95% CI of the four point-prevalence rates on their respective day.
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Figure 6. Schematic of the extended model for screening-and-isolation upon admission.
Figure 6. Schematic of the extended model for screening-and-isolation upon admission.
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Table 1. Effect of five levels of hand-hygiene compliance to Methicillin-Resistant Staphylococcus aureus (MRSA) colonization prevalence.
Table 1. Effect of five levels of hand-hygiene compliance to Methicillin-Resistant Staphylococcus aureus (MRSA) colonization prevalence.
Hand-Hygiene Compliance LevelAverage Reduction in Prevalence (In Percentage Point)Standard
Deviation
95% C.I.
10% reduction in average contamination duration for HCWs1.380.921.30–1.46
20% reduction in average contamination duration for HCWs2.841.912.67–3.01
30% reduction in average contamination duration for HCWs4.372.934.10–4.62
40% reduction in average contamination duration for HCWs5.913.965.56–6.26
50% reduction in average contamination duration for HCWs7.444.937.01–7.88
Table 2. Combined effect of hand-hygiene compliance and screening-and-isolation upon admission to MRSA colonization prevalence.
Table 2. Combined effect of hand-hygiene compliance and screening-and-isolation upon admission to MRSA colonization prevalence.
Hand-Hygiene Compliance LevelAverage Reduction in Prevalence (In Percentage Point)Standard
Deviation
95% C.I.
10% reduction in average contamination duration for HCWs21.990.6521.93–22.05
20% reduction in average contamination duration for HCWs25.342.6025.11–25.57
30% reduction in average contamination duration for HCWs28.314.1427.94–28.67
40% reduction in average contamination duration for HCWs30.004.4929.60–30.40
50% reduction in average contamination duration for HCWs30.944.4430.55–31.34
Table 3. The three transmission rates defined in the computational model.
Table 3. The three transmission rates defined in the computational model.
DescriptionSymbolValue
Residents-to-residents transmission rateβr-rar-rpr-r
HCWs-to-residents transmission rateβh-rah-rph-r
Residents-to-HCWs transmission rateβr-har-hpr-h
Table 4. The six parameters used in the three transmission rates.
Table 4. The six parameters used in the three transmission rates.
DescriptionSymbol
Average number of residents-to-residents contactar-r
Average number of HCWs-to-residents contactah-r
Average number of residents-to-HCWs contactar-h
Transmission probability via residents-to-residents contactpr-r
Transmission probability via HCWs-to-residents contactph-r
Transmission probability via residents-to-HCWs contactpr-h
Table 5. List of the 14 parameter values used in the computational model.
Table 5. List of the 14 parameter values used in the computational model.
DescriptionSymbolValueReference
Number of residentsNr75.10[16]
Number of HCWsNhcw8.61[16]
Probability of admission of colonized residentsΛ15.8%[30]
Average duration of colonization (days)1/ω268.8[31]
Average length of stay for uncolonized residents (days)1/γu233.89 *[30,32]
Average length of stay for colonized residents (days)1/γc233.89 *[30,32]
Average contamination duration (hours)1/μ4.1 *[16]
Average number of residents-to-residents contactar-r0.2[16]
Average number of HCWs-to-residents contactah-r1.2[16]
Average number of residents-to-HCWs contactar-h12.7[16]
Average number of HCWs-to-HCWs contactah-h0.6[16]
Transmission probability via residents-to-residents contactpr-rNot identified
Transmission probability via HCWs-to-residents contactph-rNot identified
Transmission probability via residents-to-HCWs contactpr-h20%[33]
* Average length of stay for uncolonized residents and average length of stay for colonized residents were calculated based on data presented in Kwok et al. [18]. Average contamination duration was calculated based on data presented in Kwok et al. [15]. Detail of calculations of these three parameters is included in Supplementary Material S1.
Table 6. Point-prevalence of MRSA in Hong Kong nursing homes.
Table 6. Point-prevalence of MRSA in Hong Kong nursing homes.
Study PeriodMid-Date of Study PeriodDay CountPrevalence95% C.I.Reference
3 March–26 September 201114 June 2011117.8%16.2–19.4%[34]
1 July–31 December 201130 September 201110821.6%19.8–23.4%[30]
1 September–31 December 201531 October 2015160030.1%25.1–35.6%[35]
1 July–31 August 201731 July 2015223937.9%33.7–42.1%[36]
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Tang, A.; Kwok, K.O.; Wei, V.W.I.; Chen, H.; Wong, S.Y.S.; Tam, W.W.S. Synergistic Effect of Combination Interventions for Methicillin-Resistant Staphylococcus aureus Transmission Control in Nursing Homes: A Computation Modelling Evaluation with Heterogeneous Contact Mixing. Antibiotics 2021, 10, 227. https://doi.org/10.3390/antibiotics10030227

AMA Style

Tang A, Kwok KO, Wei VWI, Chen H, Wong SYS, Tam WWS. Synergistic Effect of Combination Interventions for Methicillin-Resistant Staphylococcus aureus Transmission Control in Nursing Homes: A Computation Modelling Evaluation with Heterogeneous Contact Mixing. Antibiotics. 2021; 10(3):227. https://doi.org/10.3390/antibiotics10030227

Chicago/Turabian Style

Tang, Arthur, Kin On Kwok, Vivian Wan In Wei, Hong Chen, Samuel Yeung Shan Wong, and Wilson Wai Sun Tam. 2021. "Synergistic Effect of Combination Interventions for Methicillin-Resistant Staphylococcus aureus Transmission Control in Nursing Homes: A Computation Modelling Evaluation with Heterogeneous Contact Mixing" Antibiotics 10, no. 3: 227. https://doi.org/10.3390/antibiotics10030227

APA Style

Tang, A., Kwok, K. O., Wei, V. W. I., Chen, H., Wong, S. Y. S., & Tam, W. W. S. (2021). Synergistic Effect of Combination Interventions for Methicillin-Resistant Staphylococcus aureus Transmission Control in Nursing Homes: A Computation Modelling Evaluation with Heterogeneous Contact Mixing. Antibiotics, 10(3), 227. https://doi.org/10.3390/antibiotics10030227

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