key: cord-0331499-iuu8vmwy authors: Rios, Patricia; Radhakrishnan, Amruta; Thomas, Sonia M.; Darvesh, Nazia; Straus, Sharon E.; Tricco, Andrea C. title: Preventing respiratory illness in older adults aged 60 years and above living in long-term care: A rapid overview of reviews date: 2020-03-26 journal: nan DOI: 10.1101/2020.03.19.20039081 sha: 012daf6c5795683b3d82e9b58bf346daa6af4612 doc_id: 331499 cord_uid: iuu8vmwy Background: The overall objective of this rapid overview of reviews (overview hereafter) was to identify evidence from systematic reviews (SRs) for infection control and prevention practices for adults aged 60 years and older in long-term care settings. Methods: Comprehensive searches in MEDLINE, EMBASE, the Cochrane Library, biorxiv.org/medrxiv.org, clinicaltrials.gov and the Global Infectious Disease Epidemiology Network (GIDEON) were carried out in early March 2020. Title/abstract and full-text screening, data abstraction, and quality appraisal (AMSTAR 2) were carried out by single reviewers. Results: A total of 6 SRs published between 1999 and 2018 were identified and included in the overview. The SRs included between 1 and 37 primary studies representing between 140 to 908 patients. All of the primary studies included in the SRs were carried out in long-term care facilities (LTCF) and examined pharmacological, non-pharmacological, or combined interventions. One high quality SR found mixed results for the effectiveness of hand hygiene to prevent infection (2 studies statistically significant positive results, 1 study non-statistically significant results). One moderate quality SR with meta-analysis found a moderate non-statistically significant effect for personal protective equipment (PPE) in preventing infection and found no statistically significant results for the effectiveness of social isolation. One moderate quality SR reported statically significant evidence for the effectiveness of amantadine and amantadine + PPE to prevent infection with respiratory illness in LTCF. Conclusion: The current evidence suggests that with antiviral chemoprophylaxis with adamantine is effective in managing respiratory illness in residents of long-term care facilities. The rest of the strategies can be used in long-term care facilities, yet have limited evidence supporting their use from systematic reviews. The Infection Prevention & Control of the World Health Organization (WHO) Health Emergency Programme presented a query on preventing and managing COVID-19 in older adults aged 60 years and above living in long-term care facilities including privately paid for and publicly paid for settings with a 5-business day timeline. According to the WHO, "long-term care covers those activities undertaken by others to ensure that people with, or at risk of, a significant ongoing loss of intrinsic capacity can maintain a level of functional ability consistent with their basic rights, fundamental freedoms and human dignity" (https://www.who.int/ageing/long-term-care/WHO-LTC-series-subsaharan-africa.pdf?ua=1). Examples of long-term care include nursing homes, charitable homes, municipal homes, long-term care hospitals, long-term care facilities, skilled nursing facilities, convalescent homes, and assisted living facilities (https://www.canada.ca/en/health-canada/services/home-continuing-care/long-term-facilitiesbased-care.html). The overall objective of this rapid overview of reviews (overview hereafter) was to identify evidence on infection protection and control measures for adults aged 60 years and older in long-term care settings from systematic reviews. In order to focus the research question to increase feasibility, we proposed the following key research questions: 1. What are the infection prevention and control practices/measures for preventing or reducing respiratory viruses (including coronavirus and influenza) in older adults aged 60 years and above living in long-term care? 2. How do infection prevention and control practices differ for adults aged 60 years and above living in long-term care with respiratory illness and severe comorbidities or frailty differ than those without such severe comorbidities/frailty? 3. How do infection prevention and control practices differ for adults aged 60 years and above living in long-term care with respiratory illness from low-and middle-income economy countries (LMIC) differ than those living in high-income economy countries and do differences exist across different cultural contexts? The rapid overview was guided by the Cochrane Handbook for Systematic Reviews of Interventions 1 along with the Rapid Review Guide for Health Policy and Systems Research 2 . The team used an integrated knowledge translation approach, with consultation from the knowledge users from the WHO at the following stages: question development, interpretation of results, and draft report. We used the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Statement 3 to guide the reporting of our rapid overview results; a PRISMA extension for rapid reviews and a reporting guideline on overviews are currently under development. This rapid overview was completed in conjunction with a rapid review of clinical practice guidelines published in a separate report titled: Guidelines for preventing respiratory illness in older adults aged 60 years and above living in long-term care: A rapid review of clinical practice guidelines. . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. (which was not certified by peer review) The copyright holder for this preprint this version posted March 26, 2020 . . https://doi.org/10.1101 /2020 We prepared a brief protocol for this query that is available in Appendix 1. If publication in a peer-reviewed journal is planned in the future, we will register this rapid review with the Open Science Framework (https://osf.io/). Comprehensive literature searches addressing all research questions were developed by an experienced librarian for MEDLINE, EMBASE, the Cochrane Library, and biorxiv.org/medrxiv.org databases. Grey (i.e., difficult to locate or unpublished) literature was located using keyword searches of relevant terms (e.g. respiratory illness, MERS, coronavirus, SARS, long-term care facilities) in clinicaltrials.gov and GIDEON (Global Infectious Diseases and Epidemiology Network). The full MEDLINE search strategy can be found in Appendix 2. Due to the rapid timelines for this overview, a peer review of the literature search was not conducted. The Eligibility criteria followed the PICOST framework and consisted of: Population: Individuals aged 60 years and above residing in long-term care facilities. The age cut-off for an older adult might be 50 years and above in different LMIC and/or cultural settings. As such, we included these in level 1 screening of titles and abstracts and presented potentially relevant studies in an appendix. Intervention: Any form of infection control and prevention, such as hand hygiene, respiratory hygiene/etiquette, personal protective equipment (for patients and health care providers), triage (on arrival), source control, isolation, daily monitoring/surveillance for signs and symptoms of respiratory illness (e.g., in residence, environmental cleaning, cleaning of linen and medical equipment used by patients, restrictions on resident movement and transportation, restrictions on visitors, restrictions on travel for health care providers and other long-term care facility staff, waste management, dead body management. Only those measures used to prevent and control respiratory illnesses, including influenza and coronavirus (e.g., COVID-19, MERS, SARS) were included. Interventions focused on preventing bacterial respiratory outbreaks (e.g., strep, pneumonia, klebsiella) or aspiration pneumonia were excluded. Interventions specifically focused on vaccination were excluded, as a vaccine for the coronavirus currently does not exist. Comparator: One of the interventions listed above or no intervention Outcomes: Lab-confirmed respiratory illness due to the virus (e.g., SARS, MERS, COVID-19, influenza) [primary outcome], secondary bacterial infection, symptoms, secondary transmission (e.g., other patients, healthcare workers, visitors), goal concordant care, hospitalization, intensive-care unit (ICU) admission, and mortality. Study designs: We limited inclusion to systematic reviews using the Cochrane definition of a systematic review (https://www.cochrane.org/news/what-are-systematic-reviews). Time periods: All periods of time and duration of follow-up were eligible. . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020 . . https://doi.org/10.1101 /2020 Other: No other restrictions were imposed. For both level 1 (title/abstract) and level 2 (full-text) screening, a screening form was prepared based on the eligibility criteria and pilot-tested by the review team using 25 citations prior to level 1 screening and 5 full text articles prior to level 2 screening. Agreement between reviewers was sufficiently high (>75%) in both cases so no further pilot-testing was required. Full screening was completed by a single reviewer for both level 1 and level 2 using Synthesi.SR, the team's proprietary online software (https://breakthroughkt.ca/login.php). Items for data abstraction included characteristics (e.g., duration of follow-up, study design, country of conduct, multi-center vs. single site, long-term care setting characteristics, such as availability of medical support, characteristics of care staff, family/community engagement, accommodation characteristics, collective practices), patient characteristics (e.g., mean age, age range, co-morbidities), intervention details (e.g., type of intervention, duration and frequency of intervention, timing of intervention), comparator details (e.g., comparator intervention, duration and frequency of intervention, timing of intervention), and outcome results (e.g., lab-confirmed viral respiratory infection, symptoms, secondary transmission, hospitalization, ICU admission, mortality) at the longest duration of follow-up. A standardized data abstraction form was developed. Prior to data abstraction, a calibration exercise was completed to test the form amongst the entire review team using two randomly selected full-text systematic reviews. Following successful completion of the calibration exercise, included reviews were abstracted by single reviewers. Risk of bias appraisal was carried out by single reviewers using the AMSTAR-2 tool (https://amstar.ca/Amstar-2.php). The AMSTAR-2 tool includes 16 items, plus an overall risk of bias rating that ranges from low risk of bias to high risk of bias, with moderate risk of bias in between. The items focus on methods related to the research question, protocol, literature search, study selection, risk of bias appraisal, data abstraction, meta-analysis, and conflicts of interest. Included studies were synthesized descriptively including summary statistics and detailed tables of study characteristics and results. Tables of study results are organized according to study design and where available, information on relevant subgroups were highlighted. The database search returned a total of 3,309 citations, while the grey literature searches returned 42 citations for level 1 screening. A total of 3,225 citations were excluded after level 1 . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020. . https://doi.org/10. 1101 /2020 screening. Of the 126 articles screened at level 2, 6 systematic reviews were included ( Figure 1 ). The six systematic reviews were published between 1999 and 2018 (Appendix 3). The number of studies included in the systematic reviews ranged from 1 to 37 (not reported in one systematic review). Only two systematic reviews reported the number of included patients, which ranged from 140 to 908. The systematic reviews included studies that were conducted in long-term care facilities and the interventions were pharmacological (e.g., antiviral chemoprophylaxis), non-pharmacological (e.g., increasing hand hygiene, personal protective equipment, social distancing), and a combination of pharmacological and non-pharmacological. The six systematic reviews varied in their quality according to the AMSTAR-2 tool, with two being assessed as having a high risk of bias, one with a moderate risk of bias, and three with a low risk of bias ( Figure 2 , Appendix 4). Citations identified through database search (n = 3,309) Citations identified through other sources (n = 42) Full-text articles screened for eligibility (n=126) Systematic reviews included (n = 6) Full-text articles excluded (n = 120) Duplicates (n=3) Citations excluded (n = 3,225) . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020. Preventing respiratory illness in long-term care facilities: One high quality SR found mixed results for the effectiveness of hand hygiene to prevent infection with 2 studies reporting statistically significant positive results in favour of hand hygiene and 1 study reporting nonstatistically significant results. One moderate quality SR with meta-analysis found a moderate non-statistically significant effect in favour of personal protective equipment (PPE) in preventing infection. The same SR and meta-analysis also examined the effectiveness of social isolation to prevent infection and found no statistically significant results. One moderate quality SR reported statically significant evidence for the effectiveness of amantadine and amantadine + PPE to prevent the spread of viral respiratory infections in long-term care facilities. Managing respiratory illness in long-term care facilities: Statistically significant results were found from one moderate and one high quality systematic review for the use of amantadine as antiviral chemoprophylaxis for individuals diagnosed with lab-confirmed influenza (Table 1 ). In addition, statistically significant results were found from one high quality systematic review for the use of amantadine plus personal protective equipment to prevent spread of infection from individuals diagnosed with lab-confirmed influenza. Statistically significant results were not observed in one moderate and one high quality systematic review regarding rimantadine or neuraminidase inhibitors as antiviral chemoprophylaxis. However, statistically significant results were observed in one low quality systematic review for rimantadine as antiviral chemoprophylaxis. Mixed evidence was identified from two low quality systematic reviews for zanamivir as antiviral chemoprophylaxis that reported non-statistically significant reductions in viral respiratory infection rates. The full systematic review results are available in Appendix 5. . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020. . https://doi.org/10. 1101 /2020 The WHO commissioned a rapid overview to address the urgent question of the infection prevention and control practices/measures for respiratory viruses in long-term care facilities that could be applied to COVID-19. A comprehensive literature search of both electronic databases and grey literature sources resulted in six included systematic reviews, none of which specifically focused on issues related to residents with respiratory illness and severe comorbidities or frailty. Furthermore, none focused on issues in LMIC or different cultural contexts. Overall, the results of the included systematic reviews suggest that high quality evidence supports treating residents with antiviral chemoprophylaxis with adamantine, as well as adamantine in combination with personal protective equipment. For the rest of the strategies, there was either no evidence of effectiveness (e.g., social isolation) or mixed evidence of effectiveness (e.g., rimantadine, zanamivir, hand hygiene, personal protective equipment). The mixed evidence on hand hygiene and use of personal protective equipment does not imply these should not be used in outbreaks. There are several limitations to the overview methods employed here, single screening and abstraction for example, however they were selected to thoughtfully tailor our methods according to our knowledge user needs and the urgent nature of the request to provide timely results. . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020 . . https://doi.org/10.1101 /2020 The current evidence suggests that with antiviral chemoprophylaxis with adamantine is effective in managing respiratory illness in residents of long-term care facilities. The rest of the strategies can be used in long-term care facilities, yet have limited evidence supporting their use. . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020. The Infection Prevention & Control of the WHO WHE Programme has presented a query on the transmission of COVID-19 in older adults aged 60 years and above living in long-term care including privately paid for and publicly paid for settings with a 5business day timeline. According to the World Health Organization, "long-term care covers those activities undertaken by others to ensure that people with, or at risk of, a significant ongoing loss of intrinsic capacity can maintain a level of functional ability consistent with their basic rights, fundamental freedoms and human dignity" (https://www.who.int/ageing/long-term-care/WHO-LTC-series-subsaharanafrica.pdf?ua=1) Examples of long-term care will include nursing homes, charitable homes, municipal homes, long-term care hospitals, long-term care facilities, skilled nursing facilities, convalescent homes, and assisted living facilities (https://www.canada.ca/en/health-canada/services/home-continuing-care/long-termfacilities-based-care.html). The proposed research questions are: 1. What are the infection prevention and control practices/measures for preventing or reducing respiratory viruses (including coronavirus and influenza) in older adults aged 60 years and above living in long-term care? 2. How do infection prevention and control practices differ for adults aged 60 years and above living in long-term care with respiratory illness and severe comorbidities or frailty differ than those without such severe comorbidities/frailty? 3. How do infection prevention and control practices differ for adults aged 60 years and above living in long-term care with respiratory illness from low-and middle-income economy countries (LMIC) differ than those living in high-income economy countries and do differences exist across different cultural contexts? . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020. . https://doi.org/10. 1101 /2020 The research question will be addressed through a rapid review informed by the methods proposed by the WHO Guide to rapid reviews (https://www.who.int/alliancehpsr/resources/publications/rapid-review-guide/en/). Due to the urgent nature of the request and limited time frame to complete the work, this document will serve as the protocol for this query. If publication in a peer-reviewed journal is planned in the future, we will register this rapid review with the Open Science Framework (https://osf.io/). Comprehensive literature searches will be developed by an experienced librarian for MEDLINE, EMBASE, the Cochrane Library, biorxiv.org/medrxiv.org, and GIDEON (Global Infectious Diseases and Epidemiology Network). Grey (i.e., difficult to locate or unpublished) literature will be searched via clinicaltrials.gov. Due to the rapid timelines for this review a peer review of the literature search will not be conducted. The Eligibility criteria will follow the PICOST framework and will consist of: Population: Individuals aged 60 years and above residing in long-term care facilities. The age cut-off for an older adult might be 50 years and above in some LMIC and/or cultural settings. As such, we will include these in level 1 screening of titles and abstracts and include anything deemed relevant at level 2 screening of full-text articles in an appendix. Interventions: Any form of infection control and prevention, such as hand hygiene, respiratory hygiene/etiquette, personal protective equipment (for patients and health care providers), triage (on arrival), source control, isolation, daily monitoring/surveillance for signs and symptoms of respiratory illness (e.g., in residence, environmental cleaning, cleaning of linen and medical equipment used by patients, restrictions on resident movement and transportation, restrictions on visitors, restrictions on travel for health care providers and other long-term care facility staff, waste management, dead body management. Only those measures used to prevent and control respiratory illnesses, including influenza and coronavirus (e.g., COVID-19, MERS, SARS) will be included. Interventions focused on preventing bacterial respiratory outbreaks (e.g., strep, pneumonia, klebsiella) will be excluded. Comparator: One of the interventions listed above or no intervention . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020 . . https://doi.org/10.1101 /2020 Outcomes: Lab-confirmed respiratory illness due to the virus (e.g., SARS, MERS, COVID-19, influenza) [primary outcome], secondary bacterial infection, symptoms, secondary transmission (e.g., other patients, healthcare workers, visitors), goal concordant care, hospitalization, intensive-care unit (ICU) admission, mortality Study designs: Due to the rapid nature of this request, we will limit inclusion to clinical practice guidelines and systematic reviews, using the Cochrane definition of a systematic review. If there is scant evidence from these study designs, we will expand inclusion to include the following study designs: o Randomized controlled trials (RCTs) o NRCTs (e.g., such as quasi-RCTs, non-randomized trials, interrupted time series, controlled before after), o Observational studies (e.g., cohort, case control, cross-sectional) o Case studies, case reports, and case series, including outbreak reports Time periods: All periods of time and duration of follow-up will be included. Other limitations: No other limitations will be imposed. If possible, we will translate studies written in languages other than English (e.g., Mandarin, Cantonese) that are deemed relevant. In order to meet the requested timeline of 5 working days a streamlined approach to study selection will be employed. A screening form based on the eligibility criteria will be prepared and a brief calibration exercise will be conducted prior to citation and full-text screening. Screening will be completed by single reviewers using Synthesi.SR, the team's proprietary online software (https://breakthroughkt.ca/login.php). Items for data abstraction will include study characteristics (e.g., duration of follow-up, study design, country of conduct, multi-center vs. single site, long-term care setting characteristics, such as availability of medical support, characteristics of care staff, family/community engagement, accommodation characteristics, collective practices), patient characteristics (e.g., mean age, age range, co-morbidities), intervention details (e.g., type of intervention, duration and frequency of intervention, timing of intervention), comparator details (e.g., comparator intervention, duration and frequency of intervention, timing of intervention), and outcome results (e.g., lab-confirmed viral respiratory infection, symptoms, secondary transmission, hospitalization, ICU admission, mortality) at the longest duration of follow-up. For the clinical practice . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020 . . https://doi.org/10.1101 /2020 guidelines, we will abstract the recommendations and level of evidence for reach recommendation. Prior to data abstraction, we will complete a calibration exercise of the form amongst all reviewers using a random sample of 2 included articles. Following calibration, included studies will be abstracted by single reviewers. Risk of bias appraisal will be carried out by single reviewers using the AMSTAR-2 tool (https://amstar.ca/Amstar-2.php) for systematic reviews and the AGREE-2 tool (https://www.agreetrust.org/resource-centre/agree-reporting-checklist/) for clinical practice guidelines. The synthesis will involve providing a descriptive summary of included studies with summary tables and detailed tables of study results. Tables of study results will be organized according to interventions of interest and reported outcomes and where available, information on relevant subgroups will be presented separately. The summary of results will be sent to the WHO and other relevant policy-makers as a brief summary report (1-5 pages) and 1-page policy brief (see http://www.cihrirsc.gc.ca/e/documents/dsen-abstract-en.pdf for an example). We will work with the WHO team to consider submitting this paper to an open-access, peer-reviewed journal for publication (e.g. British Medical Journal). Five business days (March 16, 2020) Updates provided to the WHO: Daily emails will be sent to the WHO Funding will be obtained from the WHO and the Canadian Institutes of Health Research Strategy for Patient Oriented Research Evidence Alliance (https://sporevidencealliance.ca/). . CC-BY-NC-ND 4.0 International license It is made available under a is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. The copyright holder for this preprint this version posted March 26, 2020. . readiness, Each LTCF should designate a person whose responsibility it is to create, coordinate, and track staff training on emergency management, Ideally, LTCF should have the ability to be self-sustaining for at least 96 hours. To do this, the facility EOP must address resource assessment and management. PubMed was searched. Studies of any design reporting influenza outbreaks among elderly individuals in LTCFs were considered for inclusion. During full text review, articles were included if they contained the number of influenza cases occurring on a specific date or within a 3-day period, such as through an epidemic curve or a line list of symptom onset dates 37 studies N = NR Long term care facilitiesdefined as any residential environment that housed older adults or elderly individuals with the assistance of medical staff and included facilities referred to as 'assisted living' or 'nursing homes' but excluded community centers and daytime-only facilities serving older adults living in the outside community. Chemoprophylaxis was defined as offering antiviral drugs to asymptomatic individuals in the facility; Personal protective equipment (PPE) included glove and mask use, hand hygiene, and droplet precautions; Social distancing included patient isolation and restrictions on staff, visitors, admissions and ward transfers. Isolation was defined as restriction of movement within the facility by symptomatic individuals through the use of room, unit, or ward quarantine or cohorting. coronaviridae infections/ or coronavirus infections/ or SARS Virus/ 3 (coronavirus* or "corona virus*" or mers or "middle east respiratory syndrome*" or "Severe Acute Respiratory Syndrome*" or SARS or CoV or SARS-CoV or MERS-CoV or 2019-nCoV or COVID-19 or "2019 novel coronavirus disease" or "2019 ncov disease" or "2019 ncov infection" or "coronavirus disease 19" or "severe acute respiratory syndrome coronavirus 2" or "severe acute respiratory syndrome coronavirus 2" or "wuhan" or "sars cov 2").tw,kf. 4 (flu or influenza or "respiratory tract infection*" or "respiratory infection*" or bronchitis or "common cold" or laryngitis or pharyngitis or pneumonia or rhinitis or rhinoscleroma or sinusitis or supraglottitis or tracheitis or "whooping cough").tw,kf. prevent* or "respiratory hygiene" or "respiratory etiquette " or "cough etiquette" or "Hand Hygiene" or "hand wash*" or "handwash*" or "patient isolation" or "quarant*" or "infection control" or "blood safety" or steril* or disinfect* or "contract tracing" or "disease notification" or fumigat* or "personal protective equipment" or triage or "source control" or isolation or "daily monitoring" or surveillance or "waste management" or cadaver or body or corpse or "face mask*" or facemask* or Long-Term Care/ or exp Nursing Homes/ or Homes for the Aged/ or Assisted Living Facilities/ 21 ("long-term care" or "long term care" or "senior* home*" or "senior* residence*" or "nursing home*" or "old age home*" or Rimantadine did not show any prophylactic effect in the elderly. The quality of evidence was very low: 103 participants (RR 0.45; 95% CI 0.14 to 1.41). The assumed risk was 17 per 100. The corresponding risk in the rimantadine group was 7 per 100 (95% CI 2 to 23). There was no evidence of adverse effects caused by treatment with amantadine or rimantadine Dunn, 1999; AMSTAR Rating: Low, Condition: Influenza A/B During the 14-day prophylaxis period, there were 9 new cases of respiratory illness in volunteers in units affected by influenza A.None of these were confirmed as influenza in 65 volunteers receiving zanamivir, whereas there was 1 confirmed case among the 23 volunteers receiving rimantadine. Of the 35 volunteers randomised to zanamivir and the 17 randomised to supportive care on units affected by influenza B, there was 1 case of laboratoryconfirmed influenza in the supportive care group. Gould, 2017; AMSTAR Rating: High, Condition: Viral respiratory illness 1 RCT reported reduced respiratory outbreaks and MRSA infections requiring hospitalisation (IRR 0.12 to 0.61) favouring the intervention, while 1 ITS study reported no reduction in MRSA clinical isolates or infection. 1 RCT reported reductions of 0.27 to 0.77 cases per 1000 resident-days in serious infections, pneumonia and death in the intervention group compared to no change or an increase of 0.57 cases per 1000 resident-days in the control groupWith the identified variability in certainty of evidence, interventions, and methods, there remains an urgent need to undertake methodologically robust research to explore the effectiveness of multimodal versus simpler interventions to increase hand hygiene compliance, and to identify which components of multimodal interventions or combinations of strategies are most effective in a particular context Marshall, 2018; AMSTAR Rating: Low, Condition: Influenza The CDC, APIC and CMS recommend antiviral treatment for residents with confirmed or suspected influenza and antiviralThe LTC pharmacist can play a key role in influenza management by helping identify outbreaks, distributing Overall Conclusions chemoprophylaxis for non-ill residents exposed during outbreaks.Oseltamivir, zanamivir and peramivir were the antivirals recommended for the 2017-2018 season. Oseltamivir has been the prescribed antiviral in LTC despite mixed reports of effectiveness in residents. Treatment should begin within 48 hours of symptom onset or exposure. Oseltamivir dosage should be decreased for patients with creatinine clearance less than 60 mL/minute and it's not recommended for end stage renal disease patients not on dialysis. The most common oseltamivir prophylaxis/treatment ADRs reported were nausea, vomiting, headache and pain but neuropsychiatric ADRs of hallucinations, abnormal behavior, confused state, and delirium have occurred, resulting in discontinuation in some cases. Of 10,218 cumulative ADRs reported to the FDA, 2,412 were psychiatric and 2,019 were nervous system; 12% of the cumulative reports involved patients aged 65 and older medication in a timely manner, providing information regarding oseltamivir benefits/risks and dosages, identifying potential ADRs, and suggesting discontinuation when warranted Rainwater-Lovett, 2014; AMSTAR Rating: High, Condition: Influenza Individuals in facilities where chemoprophylaxis was used were significantly less likely to develop influenza A or B than those in facilities with no interventions [odds ratio (OR) 0.48, 95% CI: 0.28, 0.84]. Considered by drug class, amantadine significantly reduced infection risk (OR 0.22, 95% CI: 0.12, 0.42), while neuraminidase inhibitors did not show a significant effect. Although NPI showed no significant effect, the results suggest that personal protective equipment may produce modest protective effects. After adjusting for NPI, use of any antiviral drug halved attack rates among outbreaks consisting of influenza A cases [OR: 0 52 (95% CI: 0.29, 0 93)] and influenza A and B cases [OR: 0 48 (95% CI: 0 28, 0 84)] compared with outbreaks that did not implement influenza control measures. More specifically, the use of amantadine produced statistically significant protective effects among outbreaks with cases of influenza A [OR: 0 33 (95% CI: 0 17, 0 62)] and influenza This analysis provides further evidence that antiviral prophylaxis is one of the most effective ways to control influenza in populations at high risk of complications and where vaccine efficacy is reduced. While antiviral prophylaxis is highly effective, it may fail in the face of a novel, resistant strain. In such a scenario, NPI will be our only option for control and the importance of understanding which measures are most effective, and how effective they are, is paramount. Antiviral prophylaxis significantly reduced influenza attack rates, reducing the odds of developing influenza by 50% among LTCF residents. While our results were consistent with a protective effect of PPE, this effect was not statistically significant. We suspect the lack of statistically significant protective effects of PPE and social distancing was the result of broad definitions as NPI were rarely reported in detail Whereas there were multiple publications related to the difficulties and risk factors LTCFs face in disasters, there were no publications that specifically addressed infection prevention in disasters or planning specific to infection prevention concerns in disasters in long-term care. All health care settings need to have comprehensive emergency operations plans that address all hazards. LTCFs have unique challenges not experienced by other health care settings, and these issues need to be addressed as part of facility emergency management planning. Protocols need to be in place that will minimize infection transmission risk among patients, visitors, and staff during disasters. This article summarizes disaster planning considerations related to infection prevention for LTCFs, including having an infection prevention program, developing and assessing an emergency operations plan that is coordinated with regional and federal plans, creating and implementing an infection prevention education program related to disaster preparedness, and managing supplies. LTCFs should use this article to develop and assess their EOP and staff training as it relates to infection prevention procedures and protocols.