Reducing Morbidity and Mortality Rates from COVID-19, Influenza and Pneumococcal Illness in Nursing Homes and Long-Term Care Facilities by Vaccination and Comprehensive Infection Control Interventions
Abstract
:1. Introduction
Purposes
2. Materials and Methods
Literature Search
3. Results
3.1. Frail Health Status of Nursing Home and LTCF Residents
3.2. Infections and Respiratory Infections in Nursing Homes and LTCFs
Infections and Respiratory Infections in LTCFs and Nursing Homes | ||
---|---|---|
Author, Date | Setting | Disabilities and Mortality Rates |
Lee 2020 [15] | Systematic review of 37 studies of infections in LCTFs: Risk of bias assessed with Risk of Bias Assessment tool for Nonrandomized Study (RoBANS) [16]. Only 6 studies at low risk for all criteria, with problems with recall bias and self-reported measurement in 7 studies, problems with confounders in 4 studies and missing data in 5 studies. No meta-analysis performed. | 1332 infection outbreaks: most commonly reported pathogens influenza and Group A streptococcus. In 29 studies median attack rate 15.7% (8.3% for bacterial and 19.3% for viral outbreaks); 25 studies identified causes, half documented person-to-person transmission (involving poor hand hygiene and decontamination), only 9 promptly involved public health authorities, 5 studies reported creation of outbreak control teams; 60% of studies reported cases among staff, few studies implemented work restrictions. |
Childs 2019 [17] | Systematic review of 26 articles reporting respiratory infections in LCTFs: in unvaccinated residents ≥ 60 years in LCTFs 1964–2019 to assess burden of respiratory infections in unvaccinated residents; average ages 70.8 to 90.1 years. | Respiratory infection incidence and prevalence rates in LTCFs: varied widely and attributed partly to seasonality. Influenza incidence rates ranged from 5.9% to 85.2%, RSV incidence 1.1% to 13.5%, pneumonia incidence rates 4.8% to 41.2%. Policy recommendations need to be based on well-designed epidemiologic studies in large populations with assessments for seasonality and risk factors in specific homes and populations. |
Influenza Rates in the Community and in LCTFs | ||
Shen 2019 [18] | Retrospective cohort study of >26 million US Medicare fee-for-service patients ≥ 65: 2015–2017 | Influenza vaccination by age quintiles: 65–69 (44.2%), 70–74 (52.2%), 75–79 (56.3%), 80–84 (57.9%), 85–89 (57.9%), 90–94 (54.8%), 95–99 (49.9%), and 100+ (35.8%) [20]. For US nursing homes the Minimum Data Set of the US Centers for Medicare and Medicaid Services found influenza vaccination coverage increased from 71.4% in the 2005–2006 influenza season to 75.7% in the 2014–2015 season, but there were large variations by state in influenza vaccination coverage (50.0% to 89.7%) in the 2014–2015 influenza season. |
Public Health Agency of Canada 2021 [19] | National survey of influenza vaccination rates, Canada: 2019–2020 | Vaccination rate by age groups: for 18–64 34.1% (95% CI 31.8, 36.5); 18–64 with serious health conditions 43.6% (95% CI 39.0, 48.1); ≥65 70.3% (95% CI 66.7, 73.8). |
Ramos 2016 [20] | Retrospective study of 219 influenza patients: admitted to General University Hospital of Alicante, Spain, 1 January to 31 April 2015, diagnosed with influenza by molecular biology tests. | Risk factors for patients ≥ 80 compared to those < 65: had lower average glomerular filtration rates (49.7 mL/min vs. 62.2 mL/min; p = 0.006), higher rates of non-invasive mechanical ventilation (22% vs. 9.3%; p = 0.02), higher rates of cardiac insufficiency (40.5% vs. 16.4%; p < 0.001), chronic renal disease (32.9 vs. 20%; p = 0.03), and mortality (19% vs. 2.9%; p < 0.001; adjusted OR 9.2 (95% Confidence Interval [CI] 1.65 to 51.1)). |
Coronavirus in LCTFs | ||
Shi 2020 [21] | Retrospective COVID-19 cohort study in LCTF: March 2020 of patients in an academic long-term chronic care facility in Boston, USA. Patient data and clinical symptoms from electronic medical records and Minimum Data Set, COVID-19 status by PCR testing of nasopharyngeal swabs; staff residence from zip codes. | Higher mortality rates among the frail patients: Of 389 long-stay residents 146 (37.5%) tested positive for COVID-19 and of these 66 of the 146 (45.5%) were asymptomatic. Wide variation between nursing units in COVID-19 rates: Nursing units varied widely (0–90.5%) in percentage COVID-19 positive. Of the COVID-19 positive residents 44 (30.1%) died (22.2% of the moderately frail and 50.0% of the frail; p < 0.001). In LCTF units 6% (95% CI 1.04, 1.08) increase in positive COVID-19 tests for each 10% increase in percentage of staff living in communities with high COVID-19 prevalence. |
McMichael 2020 [22] | Progression of COVID-19 epidemic in LTCF: King County, Washington State, USA. Confirmed COVID-19 case identified 28 February 28 2020. | By 18 March 18 167 confirmed COVID-19 cases (101 residents, 50 HCWs, 16 visitors) epidemiologically linked to the facility. Hospitalisation rates for COVID-19 positive residents: 54.5%, visitors 50.0%, staff 6.0%; 34 deaths in the 101 residents and one in a visitor. |
Kennelly 2021 [23] | National point-prevalence COVID-19 testing programme in Ireland: residents and staff conducted 18 April to 5 May 2020 in all nursing homes and then if a new COVID-19 case was discovered every two weeks. For 45 nursing homes in Dublin and eastern Ireland complete surveys received from 28 homes (62.2%) for 2043 residents. | Progression of epidemic: First laboratory-confirmed community COVID-19 case in Ireland 29 February 2020. In the national survey the confirmed COVID-19 rate for residents 40.8% (25% asymptomatic); case fatality rate 25.8%; for staff confirmed rate 33.6% within the first 28 days of an outbreak and 28.9% subsequently (27.6% asymptomatic). |
Garibaldi 2021 [25] | Retrospective cohort study in 5 hospitals: 832 consecutive COVID-19 admissions 4 March to 24 April 2020, five hospitals Maryland and Washington, DC. | Progression to more severe COVID-19: 787 admitted with mild to moderate disease, 45 with severe disease (WHO scale) [23]. At discharge 523 (63%) had experienced mild to moderate disease, 171 (20%) severe disease and 131 (16%) died. Progression to severe disease or death rapid and occurred in 181 (60%) by day 2 and 238 (79%) by day 4. Progression to severe disease or death correlated with BMI, respiratory symptoms, respiratory rate, C-reactive protein (CRP) level, albumin level, and temperature > 38.0 °C and for those 60 to 74 years a detectable troponin level. Older age and nursing home residence were associated with high comorbidity levels and risk of death. |
Telle 2021 [26] | National study in Norway: all 8569 individuals who tested positive for SARS-CoV-2 by end of June 2020. | Outcomes for ≥90 year olds compared to <50 year olds: risks of hospitalisation (RR = 9.5; 7.1, 12.7) and death (RR = 607.9; 145.5, 2540.1) much higher and risk of death for nursing home residents was higher (RR = 4.2; 3.1, 5.7) |
Tarteret 2020 [27] | Comparison of 3 nursing homes in France: 2 hospital-dependent nursing homes in France with permanent physicians and connections with infection prevention and control departments and a nursing home without permanent physicians, infection control practitioner home or direct connection with a general hospital. | Mortality rates: During first 3 months of the COVID-19 outbreak 224/375 (59.7%) residents classified as COVID-19 and 57/375 (15.2%) died with rates of 6.6% in the hospital-dependent homes and 25.8% in the non-hospital-dependent home, OR = 0.20 (0.11, 0.38; p = 0.001). Risk factors for mortality: in COVID-19 patients during first 3 weeks of outbreak lower if received a daily clinical examination OR = 0.09 (0.03, 0.35; p = 0.01), three vital signs measured daily OR = 0.06 (0.01, 0.30; p = 0.001) and prophylactic anticoagulation OR = 0 (0.00, 0.24; p = 0.001). |
Gopal 2021 [28] | COVID-19 outbreak sizes in 713 LCTFs: California to 1 May 2020. | Outbreak sizes: 12.7 times larger in for-profit than non-profit LCTFs (p <.001). Higher ratings for approved Centers for Medicare and Medicaid services correlated with fewer infections in residents (p < 0.001) and staff (p < 0.05). |
Castriotta 2020 [29] | Community COVID-19 mortality rates in Italy: Friuli Venezia Giulia region, northern Italy. | COVID-19 mortality rates higher in older seniors: for those 70–79 SMR = 16.13 (95% CI 9.73, 26.74) and for those ≥80 SMR = 35.58 (95% CI 21.77, 58.15) compared to those <70 years. No significant differential mortality for seniors in nursing homes. Mortality variations between provinces: Standardised mortality rates as of 23 June 2020 varied from high of 2.92 (95% CI 2.88, 2.97) in Lombardia, and 1.95 (95% CI 1.64, 3.30) in Valle D’Aosta to a low of 0.71 (95% CI 0.68, 0.74) in Veneto, and in central Italy SMR = 0.13 (95% CI 0.11, 0.17) in Umbria and 0.26 (95% CI 0.24, 0.28) in Lazio, with unexplained local transmission patterns. |
3.3. Rates of Community Acquired Pneumococcal Pneumonia (CAP) and Invasive Pneumococcal Disease (IPD) in Seniors in the Community and in Nursing Homes and LCTFs
4. Results: Improving the Health Status and Outcomes of Patients in LTCFs
4.1. Interventions to Increase Vaccination Rates in Seniors and HCWs
Author, Date | Setting | Interventions | Outcomes or Observations |
---|---|---|---|
Thomas 2018 [39] | Systematic review of 61 RCTs to increase influenza vaccination rates in ≥60 years | (1) Increase demand from individuals, (2) increase vaccine access, (3) increase provision. 38% of RCTs assessed low risk of bias for randomisation, 11% allocation concealment, 44% blinding, 51% missing data, 0% selective reporting; overall evidence low quality. | Three types of interventions to increase influenza vaccination rates: (1) 41 RCTs (767,460 participants) increasing patient demand: invitations by clinic receptionists (OR 2.72; 1.55 to 4.76); nurses or pharmacists educated, and nurses vaccinated patients (OR 152.95; 9.39 to 2490.67); medical students counselled patients (OR 1.62; 1.11 to 2.35); multiple recall questionnaires (OR 1.13; 1.03 to 1.24). (2) 8 RCTs increasing vaccine access (9353 participants); invitations during home visits (OR 1.30; 1.05 to 1.61), free vaccine (OR 2.36; 1.98 to 2.82), invitations during consultations with patient groups. (3) 15 RCTs tested interventions with HCWs or medical systems; payments to physicians (OR 2.22; 1.77 to 2.77), reminding physicians to vaccinate all patients (OR 2.47; 1.53 to 3.99); clinic posters of vaccination rates and encouraging doctor competition (OR 2.03; 1.86 to 2.22); chart reviews benchmarking to rates of top 10% of physicians (OR 3.43; 2.37 to 4.97). |
Gravenstein 2017 [40] | 823 nursing homes in USA, Medicare-certified (92,269 residents; 75,917 ≥ 65 years) | 409 homes randomised to high-dose influenza vaccination, 414 homes to standard-dose vaccine | Respiratory-related hospital admissions rate: significantly lower (3.4% over 6 months) in homes whose residents received high-dose influenza vaccines vs. 3.9% in standard-dose influenza vaccines; adjusted (RR) = 0.873 (0.776 to 0.982; p = 0.023). |
Interventions to Increase Seniors’ Pneumococcal Vaccination Rates | |||
Naito 2020 [41] | Japan, national vaccination campaign, 2014 | Public subsidy for pneumococcal vaccination (PPV23) for ≥65 years | Vaccination rates: 0% in 2009, 10% in 2011, 40.6% after campaign in 2015, 74% 2018. Child vaccination programme included PCV7 then PCV13 resulting in increase in community prevalence of serotypes 8, 9N and 12F (which comprise 40% of serotypes causing Invasive Pneumococcal Disease (IPD) in elderly). However, these serotypes are included in PPV23 which thus provides protection to elderly. |
Murakami 2019 [42] | Japanese Health Ministry survey influenza vaccine coverage all municipalities (n = 1741); 1010 municipalities (58.0%) responded | Direct mail offer of subsidised PPV23 vaccination | Median PPV23 coverage for ≥65 years for responding municipalities 2016 41.8%. Differences in response rates: 18.7% higher in municipalities which sent direct mail notification to targeted adults. Rate decreased by 3.02% for every ¥1000 increase in out-of-pocket costs to individuals and coverage inversely related to municipality unemployment rates and average per capita income. |
Interventions to Increase Influenza Vaccination Rates of Health Care Workers in LCTFs | |||
Thomas 2013 [46], 2016 [47] | Systematic review of four c-RCTs and one cohort study (n = 12,742) of influenza vaccination for HCWs caring for individuals ≥ 60 years of age in LTCFs. Studies similar in study populations, interventions and outcome measures [48,49,50,51]. | Vaccination offered to residents and HCWs in intervention arms and usual care in control arms. Bias in studies due to attrition, lack of blinding, contamination in control groups and low rates of vaccination coverage in intervention arms. GRADE quality assessments downgraded for all outcomes due to serious risk of bias. | Laboratory-proven influenza: HCW influenza vaccination in LTCFs may have little or no effect on number of residents who develop compared with those living in care homes where no vaccination offered (RD 0 (95% CI −0.03 to 0.03)) (2 studies, 752 participants; low quality evidence); Lower respiratory tract infection: HCW vaccination probably leads to reduction in residents from 6% to 4% (RD −0.02 (95% CI −0.04 to 0.01)) (one study, n = 3400 people, moderate quality evidence); Number of residents admitted to hospital for respiratory illness: HCW vaccination programmes may have little or no effect on (RD 0 (95% CI −0.02 to 0.02)) (one study n = 1059; low quality evidence). Deaths from lower respiratory tract infection: Data not combined (two studies, n = 4459) or all cause deaths (four studies, n = 8468). Very low quality of evidence because direction and size of difference in risk varied between studies and uncertainty about the effect of vaccination on these outcomes. |
4.2. Implementation of Comprehensive Infection Control Policies for COVID-19 in Nursing Homes and LTCFs
Author, Date | Setting | Interventions | Outcomes or Observations |
---|---|---|---|
Goto 2021 [67] | US Veterans’ Affairs Midwest HealthCare Network | (1) Admit patients from hospitals or communities with no COVID-19 cases. (2) Quarantine admissions in single-patient rooms 14 days. (3) Daily screening for temperature, symptoms. (4) Only visitors critical to care-giving. (5) No temporary staff. (6) Hand and respiratory education. (7) Supervised by full-time infection on-site preventionists and infectious disease specialists. | Minimal COVID-19 infections: All residents from 6 March to 1 September 2020 reverse-transcriptase polymerase chain reaction (RT-PCR) for SARS-CoV-2 negative; 4 employees positive and asymptomatic and furloughed. |
Vijh 2021 [68] | 75 LTCFs in British Columbia | (1) Symptom assessment, testing all residents and staff; contact tracing; isolation of high risks. (2) Universal personal protective equipment (PPE) all staff; contact and droplet precautions all COVID-19 cases (confirmed, suspected or exposed) and residents with significant exposure. (3) COVID-19 mobile team provided assessment and education. (4) No admissions or community discharges. (5) Residents restricted to rooms; staff cohorted to wards; COVID-19 residents cohorted to rooms. (6) Enhanced cleaning rooms, common spaces, high-touch surfaces. (7) Check-in with staff provision additional staff/resources. Daily | Initial outbreak: 28 February to 30 May 2020, 18 (24%) LTCFs had at least 1 documented exposure from a COVID-19 case (total n = 165 staff and 110 residents). During the two weeks after outbreak significant increase in COVID-19 incidence RR = 1.07 (1.03 to 1.11; p < 0.001). Results 14 days and onwards after interventions were implemented: significant decrease in cases RR = 0.68 (0.62 to 0.75; p < 0.001) and 27% decrease in incidence rate every 2 days RR = 0.73 (0.67 to 0.80; p < 0.001). |
Telford 2020 [69] | 24 LTCFs, Fulton County, Georgia, which had 85% of COVID-19 positive residents of all LTCFs in the county | CDC COVID-19 tool indicators assessed prevalence [59,60]: 11 LTCFs with higher prevalence: (1310 residents, 817 cases) average infection rate 62% (range 46–74%), 196 hospitalisations, 124 deaths. 13 LCTFs with lower prevalence: (1270 residents, 187 cases) average infection rate 15% (range 1–33%), 51 hospitalisations, 38 deaths. | Prevention implementation in lower COVID-19 prevalence LTCFs compared to higher prevalence LTCFs: 69% implementation of hand hygiene indicators (55% in higher prevalence group), 77% disinfection indicators (36%), 74% social distancing indicators (54%), personal protective equipment indicators 72% (41%), 82% screening indicators (64%). |
Belmin 2020 [70] | 17 nursing homes in France compared to national survey of 9513 LTCFs (385,290 staff; 695,060 residents) | 17 nursing homes in which 794 staff members voluntarily confined themselves to the facility with their 1250 residents. | 17 nursing homes in which staff confined themselves with patients: 1/17 (5.8%) homes had 5 (0.4%) COVID-19 resident cases; 5 (0.4%) deaths; confirmed or possible COVID-19 in 12 (1.6%) staff members. National survey of nursing homes: 30,569 (4.4%) COVID-19 resident cases (p < 0.001); self-confinement of 31,799 (4.6%) residents; 12,516 (1.8%) resident deaths (OR = 0.22 (95% CI 0.09 to 0.53; p < 0.001); confirmed or possible COVID-19 in 29,463 staff members (7.6%) (p < 0.001). |
Brown 2021 [71] | 618 nursing homes Ontario, Canada (78,607 residents) = 99% of all 623 homes | Assessment of effect of crowding (crowding index assessed single-bedded to four-bedded rooms). | 29 March to 20 May 2020 5218 (6.6%) residents developed COVID-19 infection; 4496 (86%) of infections occurred in only 63 (10%) homes; 1452 (1.8%) residents died of COVID-19 infection to May 20 2020. Low crowding index homes: COVID-19 incidence 4.5%; mortality 1.3%. High crowding index homes: COVID-19 incidence 9.7% (p < 0.001), mortality 2.7%; (p < 0.001). |
Jones 2021 [73] | 623 LCTFs in Ontario, Canada | Policy to prevent staff working in multiple LTCFs | Before policy: 266 (42.7%) homes had staff working in at least 1 other home. After policy instituted: 79 (12.7%) homes had staff working in 1 other home (decrease 70.3% (p < 0.001)); average number of connections between homes declined 3.90 to 0.77 (decrease of 80.3%, p < 0.001) |
4.3. Increasing the Use of Medical or Surgical Masks and Hand Hygiene to Reduce the Transmission of Respiratory Viruses
Interventions to Decrease Respiratory Disease Transmission Using Masks, Hand Washing, and Isolation | |||
---|---|---|---|
Author, Date | Setting | Interventions | Outcomes or Observations |
Jefferson 2020 [75] | Hospital wards in high-income countries, suburban schools, and inner cities in low-income countries. | Comparison of medical or surgical masks to no masks: 8 c-RCTs, 1 RCT (2 trials with healthcare workers and 7 in the community). | Low certainty evidence mask wearing may make little or no difference in influenza-like illness (ILI): compared to not wearing masks RR = 0.99 (0.82, 1.18; 6 trials, 3507 participants). Moderate certainty evidence mask wearing probably makes little or no difference to laboratory-confirmed influenza: compared to not wearing masks RR = 0.91 (0.66, 1.26; 6 trials; 3005 participants). |
Jefferson 2020 [75] | Comparison of respirators and masks. | Comparison of N95/P2 respirators to medical/surgical masks. | Clinical respiratory illness: very low certainty evidence: RR = 0.70 (0.45, 1.10; 3 trials; 7779 participants); ILI: low-certainty evidence: due to imprecision and heterogeneity RR = 0.82 (0.66, 1.03; 5 trials; 8407 participants); Laboratory-confirmed influenza: little or no difference and moderate-certainty evidence: RR = 1.10 (0.90, 1.34; 5 trials; 8407 participants) with no differences for health care workers (HCWs). |
Jefferson 2020 [75] | Hand hygiene studies in schools, childcare centres, homes, and offices. | Hand hygiene interventions compared to no intervention. | Acute respiratory infections (ARIs): hand hygiene interventions compared to no intervention: 16% relative reduction in number of people with RR = 0.84 (0.82, 0.86; 7 trials; 44,129 participants; probable benefit with moderate-certainty evidence); ILI: RR = 0.98 (0.85, 1.13; 10 trials; 32,641 participants; little or no difference with low-certainty evidence); Laboratory-confirmed influenza: RR = 0.91 (0.63, 1.30; 8 trials; 8332 participants; little or no difference with low-certainty evidence). |
Cheng 2018 [79] | 10 residential care homes for the elderly, Hong Kong. | 5 homes randomised to directly observe hand hygiene (DOHH) of residents’ hands by hand hygiene ambassador nurses, and 5 homes randomised to usual care control group. Intervention: (515/774 residents participated) hand cleaning by hand hygiene ambassador nurse at two-hourly intervals and also before meals and medication rounds 9 am to 6 pm weekdays; during 8-week intervention samples collected twice weekly immediately before environmental cleaning from communal areas (blood pressure cuff, meal table-top, activity table-top, chair armrest, corridor hand rail, remote TV control), and in staff areas (station table top, computer keyboard and mouse, trolley-top and handle, telephone handle). | Baseline colonisation: 33% of 100 samples culture-positive for methicillin-resistant Staphylococcus aureus (MRSA); 26% of 100 specimens for carbapenem-resistant Acinetobacter species (CRA). Serial monitoring of colonisation during 2 month intervention: MRSA: present in 79/600 (13.2%) of samples in intervention homes and in 197/600 (32.8%; p < 0.001) in control homes, and CRA: present in 56/600 (9.3%) of samples in intervention homes and 94/600 (15.7%; p = 0.001) in control homes. Volume of Alcohol Based Hand Rub (ABHR): consumed/resident/week 3 times higher in intervention group (59.3 ± 12.9 mL) compared with baseline (19.7 ± 12.6 mL; p < 0.001) and significantly higher than in control group (23.3 ± 17.2 mL; p = 0.006). Hand hygiene compliance: improved from 27% to 60% during study period, but adherence to WHO Five Moments hand hygiene campaign not sustained, and bacterial contamination occurred with return from hospital care. |
Chu 2020 [80] | Systematic review of physical distancing, face masks and eye protection on spread of SARS-CoV-2. | Search of 21 WHO-specific and COVID-19 sources: 172 observational studies; 44 non-randomised studies selected for meta-analysis, no RCTs identified. | Virus transmission: Lower rates with physical distancing ≥ 1 metre: (n = 10,736, OR = 0.18 (0.09 to 0.38); risk difference (RD) −10.2% (−11.5 to −7.5; moderate certainty); Protection increased with distance RR = 2.02 per metre (p = 0.041); moderate certainty). Lower rates with face mask use: (n = 2647; OR = 0.15 (0.07 to 0.34, RD −14.3%, −15.9 to −10.7; low certainty)). Lower rates with N95 or similar respirators compared with disposable surgical or cotton masks: (p = 0·090); low certainty. Lower rates with eye protection: (n = 3713; OR = 0.22 (0.12 to 0.39, RD −10.6%, 95% CI −12.5 to −7.7; low certainty)). |
Interventions and Models of Interventions to Isolate Infected Patients | |||
Author, Date | Setting | Interventions | Outcomes or Observations |
Kim 2020 [81] | Emergency department, Chungbuk National University Hospital, Cheongju, South Korea. | 27 February to 31 March 2020, 2455 patients assessed for potential COVID-19 and if fever or respiratory symptoms they were screened in triage room, and if indicated COVID-19, test and chest X-ray obtained. Transported on isolation stretcher to CT unit. | Before isolation strategies implemented: emergency department shut down for 2 hours of cleaning 1.6 times/day; after isolation strategies 0.6 times/day. |
Cho 2019 [82] | Model of infection control room for airborne infectious. Manikin used to assess flow of potentially contaminated air from patient in bed directed to HCW providing care. | Fresh external air flowed over patient’s bed from ceiling vent and vented externally: venting either ceiling vent, single vent under bed, or two vents 1.2m above floor behind patient’s bed. Air flows visualised by fog generator from manikin’s mouth using SF6 (sodium hexafluoride). | For HCW 1.4m from patient concentration of SF6 with ceiling exhaust 33.1 to 72.7 ppm, with exhaust under bed 25.1 to 34.4 ppm, with dual exhausts in wall behind the bed 21.2 to 24.4 ppm and for two exhausts in the wall either side of bed with a Fan Filter Unit (FFU) with a 0.3-micron pore size HEPA filter (rated 99.997% efficient at retaining particles) concentration 1.4m and 0.9m above the floor was 2.0 to 8.9 ppm, 85.2% lower than without the FFU and for the whole room 79.6% lower than without the FFU. |
Kalliomäki 2016 [83] | Model of model isolation room. | Air flowed into the room and was exhausted by vents at the top of the room. Air flows were filmed and change in air flows visualised with smoke generator as door opened, manikin entered and doors closed. | During 24 second period as doors opened and manikin entered room the plume of smoke was dragged by the manikin into the room, the plume passed in front of manikin and mixed with the room air and doors closed. More air influx occurred with hinged doors than sliding doors. |
Shao 2020 [84] | Model clean room with air pressure 15 Pa > anteroom and anteroom 10 Pa > surrounding room. | Manikin walking speed 0 m/s, 0.5 m/s, 1.0 m/s (=fast walking; airflow rates in cleanroom 200 L/s, 400 L/s, 580 L/s; TSI Atomizer 9302 particle generator generated particles 0.5 to 3.0 μm with 25 psi pressure. | Particle concentration in clean room before door opening range 18,519 to 100,482 /m3 (meets ISO 14644 specification for classes 6 and 7). With door closed no particles entered cleanroom due to overpressure of 15 Pa; few particles entered with door opening and closing. When manikin entered walking at 0.5 m/s and airflow rate 210 L/s 840,994 particles/m3 entered cleanroom; at 400L/s 83,774 particles/m3 and at 580 L/s 42,407 particles/m3 (meets ISO 14644 Class 7 specification); Particle counts in cleanroom tripled with manikin entering at fast walking speed of 1 m/s: 1,745,142/m3 at 210 L/s; 247,580/m3 at 440 L/s and 120,417/m3 at 580 L/s. |
Mousavi 2020 [85] | Model conversion of patient room to an isolation room with a temporary anteroom and air purifier. | Two High Efficiency Particulate Air (HEPA) machines drew air from patient room at 1500 m3 h−1 to exterior yielding 20 air changes/hour and a negative pressure of 2.5 Pa. Particle concentration in patient room < 1000 for particle size 0.3 μm Nebuliser released aerosols at 105 particles/L from manikin’s head lying in bed (1000 above room concentration to simulate a SARS-CoV-2 virus count from a cough). | Marked increase in concentration within patient room with aerosol simulating coughing. Highest migration rate from patient room for particles < 3 μm compared to > 3 μm. Plastic barrier in anteroom without HEPA filters prevented spread of 80% of particles. HEPA filters markedly reduced particle counts in anteroom and hallway. |
Author, Date | Setting | Interventions | Outcomes or Observations |
---|---|---|---|
Anderson 2017 [98], 2018 [99] | C-RCT, 9 hospitals, SE USA, single rooms from which patients had been discharged who had had positive cultures of four target organisms in previous 12 months. | 21,395 patients randomised to 4 study arms: (1) quaternary ammonium disinfectant (QUAD) (except bleach for C. difficile); (2) UV and QUAD (or UV and bleach for C. difficile); (3) bleach; (4) bleach and UV. Randomisation by random-number generator, 99% power to detect 20% decrease in incidence rates, microbiological identification used standard protocols, environmental services personnel trained on use of disinfectants, cleaning protocols, UV lights; compliance with protocols, hand hygiene and cleaning similar across study groups, cleaning compliance 90%; QUAD applied using microfibre cloths (which remove more bacteria than cotton or synthetic fibres). | New patients admitted to rooms which had been occupied by patients who had had methicillin-resistant Staphylococcus aureus, vancomycin-resistant enterococcus, C. difficile, or multidrug-resistant Acinetobacter. Patients in the QUAD arm: had 51.3 cases of the targeted organisms/10,000 patient days. Patients in UV + QUAD arm: 33.9 cases/10,000 exposure days, RR = 0.70 (0.50–0.98; p = 0.036). Patients in bleach arm: 41.6 cases/10,000 exposure days, RR = 0.85 (0.69–1.04; p = 0.116). Patients in UV + bleach arm: 45·6 cases/10,000 exposure days, RR = 0.91 (0.76–1.09; p = 0.303). Incidence of C. difficile infections: among exposed patients unchanged for UV plus bleach compared to bleach with 30.4 cases vs. 31.6 cases/10,000 exposure days RR = 1.0 (0.57 to 1.75; p = 0·997). |
Ethington 2018 [97] | Before-after study of special care unit of a long-term acute care hospital. | Airborne bacterial colony forming units (CFU)/m3 of air were measured in 16 patient rooms, hallway and biohazard room. Ultra-violet germicidal irradiation equipment installed in these locations. | On resampling 81 days later 42% decline in number of airborne bacteria CFU/m3 (average 175 vs. 102 CFU/m3), rate of infections/month in the home declined from 20.3 to 8.6 (p = 0.001), annual number of Clostridium difficile cases declined from 8 to 1 (p = 0.01), annual number of cases of catheter-associated urinary infections declined from 20 to 9 (p = 0.012). No significant decreases in cases of methicillin-resistant Staphylococcus aureus (13 vs. 6) or central line-associated bloodstream infections (16 vs. 9). |
Buchan 2020 [101] | Model of 3 meter3 room with air entry top left, air exit top right standard ventilation compared to ultra-violet. | Far-UVC light from excimer lamps or light-emitting diodes is safe to use with humans because it generates narrow bandwidth short wavelength UVC (207–222 nm) which does not affect cornea. | Far-UVC: Disinfection rates increased by 50–85%. Far-UVC and high ventilation (8 air changes/hour): time to achieve 90% reduction in viral count = 6 minutes; 8 air changes/hour results in 99% reduction in 11.5 minutes. |
5. Discussion
6. Conclusions
6.1. Detection
6.2. Identification of Nursing Homes Most in Need of Help Implementing Comprehensive Infection Control Plans
6.3. Implementation of Comprehensive Infection Control Plans
6.4. Restructuring Nursing Homes to Reduce Crowding
6.5. Upgrading Ventilation Systems in Nursing Homes
6.6. Increasing Influenza, Pneumococcal and SARS-CoV-2 Vaccination Rates in Seniors
6.7. Identifying Interventions Programmed to Function Automatically
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Crowe, J.E., Jr. Common Viral Respiratory Infections. In Harrison’s Principles of Internal Medicine, 20th ed.; Jameson, J.L., Fauci, A.S., Kasper, D.L., Hauser, S.L., Longo, D.L., Loscalzo, J., Eds.; McGraw-Hill Education: New York, NY, USA, 2018. [Google Scholar]
- Centers for Disease Control and Prevention. Older Adults at Greater Risk of Requiring Hospitalization or Dying If Diagnosed with COVID-19. Available online: https://www.cdc.gov/coronavirus/2019-ncov/need-extra-precautions/older-adults.html (accessed on 12 February 2021).
- Yanez, N.D.; Weiss, N.S.; Romand, J.A.; Treggiari, M.M. COVID-19 mortality risk for older men and women. BMC Public Health 2020, 20, 1742. [Google Scholar] [CrossRef]
- Vossius, C.; Selbæk, G.; Benth, J. Šaltytė; Bergh, S. Mortality in nursing home residents: A longitudinal study over three years. PLoS ONE 2018, 13, e0203480. [Google Scholar] [CrossRef] [Green Version]
- McCann, M.; O’Reilly, D.; Cardwell, C. A Census-based longitudinal study of variations in survival amongst residents of nursing and residential homes in Northern Ireland. Age Ageing 2009, 38, 711–717. [Google Scholar] [CrossRef] [Green Version]
- Wieland, D.; Boland, R.; Baskins, J.; Kinosian, B. Five-Year Survival in a Program of All-Inclusive Care for Elderly Compared with Alternative Institutional and Home-and Community-Based Care. J. Gerontol. A Biol. Sci. Med. Sci. 2010, 65, 721–726. [Google Scholar] [CrossRef] [Green Version]
- Hjaltadottir, I.; Hallberg, I.R.; Ekwall, A.K.; Nyberg, P. Predicting mortality of residents at admission to nursing home: A longitudinal cohort study. BMC Health Serv. Res. 2011, 19, 1–86. [Google Scholar] [CrossRef] [Green Version]
- Li, S.; Middleton, A.; Ottenbacher, K.J.; Goodwin, J.S. Trajectories Over the First Year of Long-Term Care Nursing Home Residence. J. Am. Med Dir. Assoc. 2018, 19, 333–341. [Google Scholar] [CrossRef]
- Gambassi, G.; Landi, F.; Lapane, K.L.; Sgadari, A.; Mor, V.; Bernabei, R. Predictors of mortality in patients with Alzheimer’s disease living in nursing homes. J. Neurol. Neurosurg. Psychiatry 1999, 67, 59–65. [Google Scholar] [CrossRef] [Green Version]
- Vossius, C.; Nilsen, O.B.; Larsen, J.P. Parkinson’s disease and nursing home placement: The economic impact of the need for care. Eur. J. Neurol. 2009, 16, 194–200. [Google Scholar] [CrossRef] [PubMed]
- Tabue-Teguo, M.; Kelaiditi, E.; Demougeot, L.; Dartigues, J.F.; Vellas, B.; Cesari, M. Frailty Index and Mortality in Nursing Home Residents in France: Results from the INCUR Study. J. Am. Med Dir. Assoc. 2015, 16, 603–606. [Google Scholar] [CrossRef] [PubMed]
- Dwyer, R.; Gabbe, B.; Stoelwinder, J.U.; Lowthian, J. A systematic review of outcomes following emergency transfer to hospital for residents of aged care facilities. Age Ageing 2014, 43, 759–766. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Canadian Institute of Health Information. Profile of Residents in Residential and Hospital-Based Continuing Care, 2019–2020. 2020. Available online: ccrs-qick-stats-2019-2020-en-xlsx (accessed on 10 January 2021).
- Harris-Kojetin, L.; Sengupta, M.; Lendon, J.P.; Rome, V.; Valverde, R.; Caffrey, C. Long-Term Care Providers and Services Users in the United States, 2015–2016. Vital Health Stat. 2019, 38, 1–105. [Google Scholar]
- Lee, M.H.; Lee, G.A.; Lee, S.H.; Park, Y.H. A systematic review on the causes of the transmission and control measures of outbreaks in long-term care facilities: Back to basics of infection control. PLoS ONE 2020, 15, e0229911. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kim, S.Y.; Park, J.E.; Lee, Y.J.; Seo, H.J.; Sheen, S.S.; Hahn, S.; Jang, B.H.; Son, H.J. Testing a tool for assessing the risk of bias for nonrandomized studies showed moderate reliability and promising validity. J. Clin. Epidemiol. 2013, 66, 408–414. [Google Scholar] [CrossRef] [PubMed]
- Childs, A.; Zullo, A.R.; Joyce, N.R.; McConeghy, K.W.; van Aalst, R.; Moyo, P.; Bosco, E.; Mor, V.; Gravenstein, S. The burden of respiratory infections among older adults in long-term care: A systematic review. BMC Geriatr. 2019, 19, 210. [Google Scholar] [CrossRef] [Green Version]
- Shen, A.K.; Warnock, R.; Selna, W.; MaCurdy, T.E.; Chu, S.; Kelman, J.A. Vaccination among Medicare-fee-for service beneficiaries: Characteristics and predictors of vaccine receipt, 2014–2017. Vaccine 2019, 37, 1194–1201. [Google Scholar] [CrossRef]
- Public Health Agency of Canada. Seasonal Influenza Vaccination Coverage in Canada, 2019–2020. Available online: https://www.canada.ca/en/public-health/services/immunization-vaccines/vaccination-coverage/2019-2020-seasonal-influenza-flu-vaccine-coverage.html#vaccination_coverage (accessed on 24 January 2021).
- Ramos, J.M.; García-Navarro, M.M.; González de la Aleja, M.P.; Sánchez-Martínez, R.; Gimeno-Gascón, A.; Reus, S.; Merino, E.; Rodríguez-Díaz, J.C.; Portilla, J. Seasonal influenza in octogenarians and nonagenarians admitted to a general hospital: Epidemiology, clinical presentation and prognostic factors. Rev. Esp. Quimioter. 2016, 29, 296–301. [Google Scholar] [PubMed]
- Shi, S.M.; Bakaev, I.; Chen, H.; Travison, T.G.; Berry, S.D. Risk Factors, Presentation, and Course of Coronavirus Disease 2019 in a Large, Academic Long-Term Care Facility. J. Am. Med. Dir. Assoc. 2020, 21, 1378–1383.e1. [Google Scholar] [CrossRef]
- McMichael, T.M.; Currie, D.W.; Clark, S.; Pogosjans, S.; Kay, M.; Schwartz, N.G.; Lewis, J.; Baer, A.; Kawakami, V.; Lukoff, M.D.; et al. Epidemiology of Covid-19 in a Long-Term Care Facility in King County, Washington. N. Engl. J. Med. 2020, 382, 2005–2011. [Google Scholar] [CrossRef]
- Kennelly, S.P.; Dyer, A.H.; Noonan, C.; Martin, R.; Kennelly, S.M.; Martin, A.; O’Neill, D.; Fallon, A. Asymptomatic carriage rates and case fatality of SARS-CoV-2 infection in residents and staff in Irish nursing homes. Age Ageing 2021, 50, 49–54. [Google Scholar] [CrossRef]
- World Health Organization. WHO R&D Blueprint: Novel Coronavirus COVID-19 Therapeutic Trial Synopsis. 2020. Available online: https://apps.who.int/iris/bitstream/handle/10665/330694/WHO-HEO-RDBlueprintnCoV-2020.4-eng.pdf?sequence=1&isAllowed=y (accessed on 12 February 2021).
- Garibaldi, B.T.; Fiksel, J.; Muschelli, J.; Robinson, M.L.; Rouhizadeh, M.; Perin, J.; Schumock, G.; Nagy, P.; Gray, J.H.; Malapati, H.; et al. Patient Trajectories Among Persons Hospitalized for COVID-19: A Cohort Study. Ann. Intern. Med. 2021, 174, 33–41. [Google Scholar] [CrossRef]
- Telle, K.E.; Grøsland, M.; Helgeland, J.; Håberg, S.E. Factors associated with hospitalization, invasive mechanical ventilation treatment and death among all confirmed COVID-19 cases in Norway: Prospective cohort study. Scand. J. Public Health 2021, 49, 41–47. [Google Scholar] [CrossRef]
- Tarteret, P.; Strazzulla, A.; Rouyer, M.; Gore, C.; Bardin, G.; Noel, C.; Benguerdi, Z.E.; Berthaud, J.; Hommel, M.; Aufaure, S.; et al. Clinical features and medical care factors associated with mortality in French nursing homes during the COVID-19 outbreak. Int. J. Infect. Dis. 2021, 104, 125–131. [Google Scholar] [CrossRef] [PubMed]
- Gopal, R.; Han, X.; Yaraghi, N. Compress the curve: A cross-sectional study of variations in COVID-19 infections across California nursing homes. BMJ Open 2021, 11, e042804. [Google Scholar] [CrossRef]
- Castriotta, L.; Rosolen, V.; Barbiero, F.; Tomietto, M.; De Dottori, M.; Barbone, F.; Zamaro, G. Impact of the COVID-19 epidemic in Friuli Venezia Giulia Region (Northern Italy): Assessment of factors associated with the risk of death by competing risks analysis. Epidemiol. Prev. 2021, 44, 128–135. [Google Scholar]
- US Centers for Medicare and Medicaid Services. Quality ID #111: Pneumococcal Vaccination Status for Older Adults. Available online: https://qpp.cms.gov/docs/QPP_quality_measure_specifications/Claims-Registry-Measures/2020_Measure_111_MedicarePartBClaims.pdf (accessed on 27 December 2020).
- Chalmers, J.D.; Campling, J.; Dicker, A.; Woodhead, M.; Madhava, H. A systematic review of the burden of vaccine pre-ventable pneumococcal disease in UK adults. BMC Pulm. Med. 2016, 16, 1–11. [Google Scholar] [CrossRef] [Green Version]
- Van Hoek, A.J.; Andrews, N.; Waight, P.A.; George, R.; Miller, E. Effect of serotype on focus and mortality of invasive pneumococcal disease: Coverage of different vaccines and insight into non-vaccine serotypes. PLoS ONE 2012, 7, e39150. [Google Scholar] [CrossRef]
- Waight, P.A.; Andrews, N.J.; Ladhani, S.N.; Sheppard, C.L.; Slack, M.P.; Miller, E. Effect of the 13-valent pneumococcal conjugate vaccine on invasive pneumococcal disease in England and Wales 4 years after its introduction: An observational cohort study. Lancet Infect. Dis. 2015, 15, 535–543. [Google Scholar] [CrossRef] [Green Version]
- Norris, T.; Vahratian, A.; Cohen, R.A.; US Centers for Disease Control. Vaccination Coverage among Adults Aged 65 and Over: United States. 2015. Available online: www.cdc.gov/nchs/data/databriefs/db281.pdf (accessed on 27 December 2020).
- Black, C.L.; Williams, W.W.; Arbeloa, I.; Kordic, N.; Yang, L.; MaCurdy, T.; Worrall, C.; Kelman, J.A. Trends in Influenza and Pneumococcal Vaccination Among US Nursing Home Residents, 2006–2014. J. Am. Med. Dir. Assoc. 2017, 18, 735. [Google Scholar] [CrossRef]
- Vila-Córcoles, A.; Ochoa-Gondar, O.; De Diego, C.; Satué, E.; Vila-Rovira, A.; Aragón, M. Pneumococcal vaccination coverages by age, sex and specific underlying risk conditions among middle-aged and older adults in Catalonia, Spain, 2017. Eurosurveillance 2019, 24, 24. [Google Scholar] [CrossRef]
- Wang, Y.; Cheng, M.; Wang, S.; Wu, F.; Yan, Q.; Yang, Q.; Li, Y.; Guo, X.; Fu, C.; Shi, Y.; et al. Vaccination coverage with the pneumococcal and influenza vaccine among persons with chronic diseases in Shanghai, China, 2017. BMC Public Health 2020, 20, 1–9. [Google Scholar] [CrossRef]
- Djennad, A.; Ramsay, M.E.; Pebody, R.; Fry, N.K.; Sheppard, C.; Ladhani, S.N.; Andrews, N.J. Effectiveness of 23-Valent Polysaccharide Pneumococcal Vaccine and Changes in Invasive Pneumococcal Disease Incidence from 2000 to 2017 in Those Aged 65 and Over in England and Wales. E Clin. Med. 2018, 6, 42–50. [Google Scholar] [CrossRef] [Green Version]
- Thomas, R.E.; Lorenzetti, D.L. Interventions to increase influenza vaccination rates of those 60 years and older in the community. Cochrane Database Syst. Rev. 2018, 5, CD005188. [Google Scholar] [CrossRef] [PubMed]
- Gravenstein, S.; Davidson, H.E.; Taljaard, M.; Ogarek, J.; Gozalo, P.; Han, L.; Mor, V. Comparative effectiveness of high-dose versus standard-dose influenza vaccination on numbers of US nursing home residents admitted to hospital: A cluster-randomised trial. Lancet Respir. Med. 2017, 5, 738–746. [Google Scholar] [CrossRef]
- Naito, T.; Suzuki, M.; Fujibayashi, K.; Kanazawa, A.; Takahashi, H.; Yokokawa, H.; Watanabe, A. The estimated impact of the 5-year national vaccination program on the trend of 23-valent pneumococcal polysaccharide vaccine vaccination rates in the elderly in Japan, 2009–2018. J. Infect. Chemother. 2020, 26, 407–410. [Google Scholar] [CrossRef]
- Murakami, Y.; Kanazu, S.; Petigara, T.; Oba, M.S.; Nishiwaki, Y.; Watanabe, A. Factors associated with PPSV23 coverage among older adults in Japan: A nationwide community-based survey. BMJ Open 2019, 9, e030197. [Google Scholar] [CrossRef] [Green Version]
- Public Health England. Pneumococcal Polysaccharide Vaccine (ppv) Coverage Report, England, April 2017 to March 2018. Health Protection Report. Available online: https://www.gov.uk/government/publications/pneumococcalpolysaccharide-vaccineppv-vaccine-coverage-estimates (accessed on 20 December 2020).
- Dyda, A.; Karki, S.; Hayen, A.; MacIntyre, C.R.; Menzies, R.; Banks, E.; Kaldor, J.M.; Liu, B. Influenza and pneumococcal vaccination in Australian adults: A systematic review of coverage and factors associated with uptake. BMC Infect. Dis. 2016, 16, 1–15. [Google Scholar] [CrossRef]
- Yang, T.U.; Kim, E.; Park, Y.-J.; Kim, D.; Kwon, Y.H.; Shin, J.K.; Park, O. Successful introduction of an underutilized elderly pneumococcal vaccine in a national immunization program by integrating the pre-existing public health infrastructure. Vaccine 2016, 34, 1623–1629. [Google Scholar] [CrossRef]
- Thomas, R.E.; Jefferson, T.; Lasserson, T.J. Influenza vaccination for healthcare workers who care for people aged 60 or older living in long-term care institutions. Cochrane Database Syst. Rev. 2013, 7. [Google Scholar] [CrossRef] [Green Version]
- Thomas, R.E.; Jefferson, T.; Lasserson, T.J. Influenza vaccination for healthcare workers who care for people aged 60 or older living in long-term care institutions. Cochrane Database Syst. Rev. 2016, 6. [Google Scholar] [CrossRef] [PubMed]
- Potter, J.; Stott, D.J.; Roberts, M.A.; Elder, A.G.; O’Donnell, B.; Knight, P.V.; Carman, W.F. Influenza Vaccination of Health Care Workers in Long-Term-Care Hospitals Reduces the Mortality of Elderly Patients. J. Infect. Dis. 1997, 175, 1–6. [Google Scholar] [CrossRef] [PubMed]
- Carman, W.F.; Elder, A.G.; Wallace, L.A.; McAulay, K.; Walker, A.; Murray, G.D.; Stott, D.J. Effects of influenza vaccination of health-care workers on mortality of elderly people in long-term care: A randomized controlled trial. Lancet 2000, 355, 93–97. [Google Scholar] [CrossRef]
- Hayward, A.C.; Harling, R.; Wetten, S.; Johnson, A.M.; Munro, S.; Smedley, J.; Murad, S.; Watson, J.M. Effectiveness of an influenza vaccine programme for care home staff to prevent death, morbidity, and health service use among residents: Cluster randomised controlled trial. BMJ 2006, 333, 1241. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Lemaitre, M.; Meret, T.; Rothan-Tondeur, M.; Belmin, J.; Lejonc, J.L.; Luquel, L.; Piette, F.; Salom, M.; Verny, M.; Vetel, J.M.; et al. Effect of Influenza Vaccination of Nursing Home Staff on Mortality of Residents: A Cluster-Randomized Trial. J. Am. Geriatr. Soc. 2009, 57, 1580–1586. [Google Scholar] [CrossRef]
- Thomas, R.E. Is influenza-like illness a useful concept and an appropriate test of influenza vaccine effectiveness? Vaccine 2014, 32, 2143–2149. [Google Scholar] [CrossRef]
- Thomas, R.E. Do we have enough evidence how seasonal influenza is transmitted and can be prevented in hospitals to implement a comprehensive policy? Vaccine 2016, 34, 3014–3021. [Google Scholar] [CrossRef] [PubMed]
- Lytras, T.; Kopsachilis, F.; Mouratidou, E.; Papamichail, D.; Bonovas, S. Interventions to increase seasonal influenza vaccine coverage in healthcare workers: A systematic review and meta-regression analysis. Hum. Vaccin Immunother. 2016, 12, 671–681. [Google Scholar] [CrossRef] [Green Version]
- De Serres, G.; Skowronski, D.M.; Ward, B.J.; Gardam, M.; Lemieux, C.; Yassi, A.; Patrick, D.M.; Krajden, M.; Loeb, M.; Collignon, P.; et al. Influenza Vaccination of Healthcare Workers: Critical Analysis of the Evidence for Patient Benefit Underpinning Policies of Enforcement. PLoS ONE 2017, 12, e0163586. [Google Scholar] [CrossRef] [Green Version]
- World Health Organization Regional Office for Europe. Prevention and Control of Outbreaks of Seasonal Influenza in Long-term Care Facilities: A Review of the Evidence and Best Practice Guidance. 2017. Available online: http://www.euro.who.int/__data/assets/pdf_file/0015/330225/LTCF-best-practice-guidance.pdf?ua=1 (accessed on 24 January 2021).
- Lansbury, L.E.; Brown, C.S.; Nguyen-Van-Tam, J.S. Influenza in long-term care facilities. Influ. Other Respir. Viruses 2017, 11, 356–366. [Google Scholar] [CrossRef]
- Corace, K.M.; Srigley, J.A.; Hargadon, D.P.; Yu, D.; MacDonald, T.K.; Fabrigar, L.R.; Garber, G.E. Using behavior change frameworks to improve healthcare worker influenza vaccination rates: A systematic review. Vaccine 2016, 34, 3235–3242. [Google Scholar] [CrossRef] [Green Version]
- US Centers for Disease Control and Prevention. Testing and Management Considerations for Nursing Home Residents with Acute Respiratory Illness Symptoms When Sars-CoV-2 and Influenza Viruses Are Cocirculating. Available online: https://www.cdc.gov/coronavirus/2019-ncov/hcp/nursing-home-long-term-care.html (accessed on 9 March 2021).
- US Centers for Disease control and Prevention. Similarities and Differences between Flu and COVID-19. Available online: https://www.cdc.gov/flu/symptoms/flu-vs-covid19.htm (accessed on 9 March 2021).
- World Health Organisation. Considerations for Implementing and Adjusting Public Health and Social Measures in the Context of COVID-19. Interim Guidance. 2020. Available online: WHO-2019-nCov-Adjusting_PH_measures-2020.2-eng (accessed on 9 March 2021).
- Dugdale, C.M.; Rubins, D.M.; Lee, H.; McCluskey, S.M.; Ryan, E.T.; Kotton, C.N.; Hurtado, R.M.; Ciaranello, A.L.; Barshak, M.B.; McEvoy, D.S.; et al. Coronavirus Disease 2019 (COVID-19) Diagnostic Clinical Decision Support: A Pre-Post Implementation Study of CORAL (COvid Risk cALculator). Clin. Infect. Dis. 2021, ciab111. [Google Scholar] [CrossRef]
- Echeverria, P.; Mas Bergas, M.A.; Puig, J.; Isnard, M.; Massot, M.; Vedia, C.; Peiro, R.; Ordorica, Y.; Pablo, S.; Ulldemolins, M.; et al. COVIDApp as an Innovative Strategy for the Man-agement and Follow-Up of COVID-19 Cases in Long-Term Care Facilities in Catalonia: Implementation Study. JMIR Public Health Surveill. 2020, 6, e21163. [Google Scholar] [CrossRef]
- Bigelow, B.F.; Tang, O.; Barshick, B.; Peters, M.; Sisson, S.D.; Peairs, K.S.; Katz, M.J. Outcomes of Universal COVID-19 Testing Following Detection of Incident Cases in 11 Long-term Care Facilities. JAMA Intern. Med. 2021, 181, 127. [Google Scholar] [CrossRef] [PubMed]
- CDC. Interim Infection Prevention and Control. Recommendations for Healthcare Personnel during the Coronavirus Disease 2019 (COVID-19) Pandemic. 2020. Available online: https://www.cdc.gov/coronavirus/2019-ncov/hcp/infectioncontrol-recommendations.html (accessed on 30 January 2021).
- CDC. Preparing for COVID-19 in Nursing Homes. 2020. Available online: https://www.cdc.gov/coronavirus/2019-ncov/hcp/long-term-care.html (accessed on 30 January 2021).
- Michihiko Goto, M.; Ueckert, N.; Meiches, R.K.; Perencevich, E.I. Successful multimodal measures preventing coronavirus disease 2019 (COVID-19) outbreaks without universal frequent testing within long-term care units in the Midwestern Veterans’ Health Care Network. Inf. Control H. Epidemiol. 2021, 1–3. [Google Scholar] [CrossRef]
- Vijh, R.; Prairie, J.; Otterstatter, M.C.; Hu, Y.; Hayden, A.S.; Yau, B.; Daly, P.; Lysyshyn, M.; McKee, G.; Harding, J.; et al. Evaluation of a multisectoral intervention to mitigate the risk of severe acute respiratory coronavirus virus 2 (SARS-CoV-2) transmission in long-term care facilities. Infect. Control Hosp. Epidemiol. 2021, 1, 1–8. [Google Scholar] [CrossRef] [PubMed]
- Telford, C.T.; Onwubiko, U.; Holland, D.P.; Turner, K.; Prieto, J.; Smith, S.; Yoon, J.; Brown, W.; Chamberlain, A.; Gandhi, N.; et al. Preventing COVID-19 Outbreaks in Long-Term Care Facilities Through Preemptive Testing of Residents and Staff Members: Fulton County, Georgia, March–May 2020. MMWR. Morb. Mortal. Wkly. Rep. 2020, 69, 1296–1299. [Google Scholar] [CrossRef] [PubMed]
- Belmin, J.; Um-Din, N.; Donadio, C.; Magri, M.; Nghiem, Q.D.; Oquendo, B.; Pariel, S.; Lafuente-Lafuente, C. Coronavirus Disease 2019 Outcomes in French Nursing Homes That Implemented Staff Confinement with Residents. JAMA Netw. Open 2020, 3, e2017533. [Google Scholar] [CrossRef] [PubMed]
- Brown, K.A.; Jones, A.; Daneman, N.; Chan, A.K.; Schwartz, K.L.; Garber, G.E.; Costa, A.P.; Stall, N.M. Association Between Nursing Home Crowding and COVID-19 Infection and Mortality in Ontario, Canada. JAMA Intern. Med. 2021, 181, 229–236. [Google Scholar] [CrossRef] [PubMed]
- Federgruen, A.; Naha, S. Crowding Effects Dominate Demographic Attributes in COVID-19 Cases. Int. J. Infect. Dis. 2021, 102, 509–516. [Google Scholar] [CrossRef]
- Jones, A.; Watts, A.G.; Khan, S.U.; Forsyth, J.; Brown, K.A.; Costa, A.P.; Bogoch, I.I.; Stall, N.M. Impact of a Public Policy Restricting Staff Mobility Between Nursing Homes in Ontario, Canada During the COVID-19 Pandemic. J. Am. Med. Direct Assoc. 2021, 22, 494–497. [Google Scholar] [CrossRef]
- Panagiotou, O.A.; Kosar, C.M.; White, E.M.; Bantis, L.E.; Yang, X.; Santostefano, C.M.; Feifer, R.A.; Blackman, C.; Rudolph, J.L.; Gravenstein, S.; et al. Risk Factors Associated With All-Cause 30-Day Mortality in Nursing Home Residents With COVID-19. JAMA Intern. Med. 2021, 181, 439–448. [Google Scholar] [CrossRef] [PubMed]
- Jefferson, T.; Del Mar, C.B.; Dooley, L.; Ferroni, E.; Al-Ansary, L.A.; Bawazeer, G.A.; van Driel, M.L.; Jones, M.A.; Thorning, S.; Beller, E.M.; et al. Physical interventions to interrupt or reduce the spread of respiratory viruses. Cochrane Database Sys Rev. 2020, 11, CD006207. [Google Scholar]
- McConeghy, K.W.; Baier, R.; McGrath, K.P.; Baer, C.J.; Mor, V. Implementing a Pilot Trial of an Infection Control Program in Nursing Homes: Results of a Matched Cluster Randomized Trial. J. Am. Med. Dir. Assoc. 2017, 18, 707–712. [Google Scholar] [CrossRef]
- Temime, L.; Cohen, N.; Ait-Bouziad, K.; Denormandie, P.; Dab, W.; Hocine, M.N. Impact of a multicomponent hand hygiene–related intervention on the infectious risk in nursing homes: A cluster randomized trial. Am. J. Infect. Control 2018, 46, 173–179. [Google Scholar] [CrossRef]
- Yeung, W.K.; Tam, W.S.W.; Wong, T.W. Clustered Randomized Controlled Trial of a Hand Hygiene Intervention Involving Pocket-Sized Containers of Alcohol-Based Hand Rub for the Control of Infections in Long-Term Care Facilities. Infect. Control Hosp. Epidemiol. 2011, 32, 67–76. [Google Scholar] [CrossRef]
- 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] [PubMed]
- Chu, D.K.; Duda, S.; Solo, K.; Yacoub, S.; Schünemann, H.J. Physical distancing, face masks, and eye protection to prevent per-son-to-person transmission of SARS-CoV-2 and COVID-19: A systematic review and meta-analysis. Lancet 2020, 395, 1973–1987. [Google Scholar] [CrossRef]
- Kim, S.C.; Kong, S.Y.; Park, G.J.; Lee, J.H.; Lee, J.K.; Lee, M.S.; Han, H.S. Effectiveness of negative pressure isolation stretcher and rooms for SARS-CoV-2 nosocomial infection control and maintenance of South Korean emergency department capacity. Am. J. Emerg. Med. 2020. [Google Scholar] [CrossRef] [PubMed]
- Cho, J. Investigation on the contaminant distribution with improved ventilation system in hospital isolation rooms: Effect of supply and exhaust air diffuser configurations. Appl. Therm. Eng. 2019, 148, 208–218. [Google Scholar] [CrossRef] [PubMed]
- Kalliomäki, P.; Saarinen, P.; Tang, J.W.; Koskela, H. Airflow patterns through single hinged and sliding doors in hospital isolation rooms: Effect of ventilation, flow differential and passage. Build. Environ. 2016, 107, 154–168. [Google Scholar] [CrossRef]
- Shao, X.; Hashimoto, K.; Fang, L.; Melikov, A.K.; Naydenov, K.G.; Rasmuseen, C. Experimental study of airborne particle transmission through the doorway of a cleanroom due to the movement of a person. Build. Environ. 2020, 183, 107205. [Google Scholar] [CrossRef]
- Mousavi, E.S.; Pollitt, K.J.G.; Sherman, J.; Martinello, R.A. Performance analysis of portable HEPA filters and temporary plastic anterooms on the spread of surrogate coronavirus. Build. Environ. 2020, 183, 107186. [Google Scholar] [CrossRef]
- Zhou, Y.; Zhang, Z.; Wang, B.; Ren, G.; Qi, H.; Wang, X. Construction time, cost and testing data of a prefabricated isolation medical unit for COVID-19. Data Brief. 2020, 32, 106068. [Google Scholar] [CrossRef] [PubMed]
- Hao, L.; Wu, J.; Zhang, J.; Liu, Z.; Yi, Y.; Zhang, Z.; Zhang, E.; Qi, J. Development of a negative pressure hood for isolation and transportation of individual patient with respiratory infectious disease. Biosaf. Health 2019, 1, 144–149. [Google Scholar] [CrossRef] [PubMed]
- Knibbs, L.D.; Morawska, L.; Bell, S.C.; Grzybowski, P. Room ventilation and the risk of airborne infection transmission in 3 health care settings within a large teaching hospital. Am. J. Infect. Control 2011, 39, 866–872. [Google Scholar] [CrossRef] [Green Version]
- Rosenbaum, R.A.; Benyo, J.S.; O’Connor, R.E.; Passarello, B.A.; Williams, D.R.; Humphrey, B.D.; Ross, R.W.; Berry, J.M.; Krebs, J.G. Use of a portable forced air system to convert existing hospital space into a mass casualty isolation area. Ann. Emerg. Med. 2004, 44, 628–634. [Google Scholar] [CrossRef]
- Silich, B.A. Method to Reduce Aerosolized Contaminant Concentration Exposure to Healthcare Workers During the COVID-19 Pandemic when Temporary Isolation Systems Are Required. West. J. Emerg. Med. 2020, 21, 93–98. [Google Scholar] [CrossRef]
- Yen, M.Y.; Lin, Y.E.; Su, I.J.; Huang, F.Y.; Huang, F.Y.; Ho, M.S.; Chang, S.C.; Tan, K.H.; Chen, K.T.; Chang, H.; et al. Using an integrated infection control strategy during outbreak control to minimize nosocomial infection of severe acute respiratory syndrome among healthcare workers. J. Hosp. Infect. 2006, 62, 195–199. [Google Scholar] [CrossRef] [Green Version]
- Miller, S.L.; Mukherjee, D.; Wilson, J.; Clements, N.; Steiner, C. Implementing a negative pressure isolation space within a skilled nursing facility to control SARS-CoV-2 transmission. Am. J. Infect. Control 2020, 49, 438–446. [Google Scholar] [CrossRef]
- Mendes, A.; Papoila, A.L.; Carreiro-Martins, P.; Bonassi, S.; Caires, I.; Palmeiro, T.; Aguiar, L.; Pereira, C.; Neves, P.; Mendes, D.; et al. The impact of indoor air quality and contaminants on respiratory health of older people living in long-term care residences in Porto. Age Ageing 2016, 45, 136–142. [Google Scholar] [CrossRef] [Green Version]
- Aguiar, L.; Mendes, A.; Pereira, C.; Neves, P.; Mendes, D.; Teixeira, J.P. Biological air contamination in elderly care centers: Geria project. J. Toxicol. Environ. Health A 2014, 77, 944–958. [Google Scholar] [CrossRef] [PubMed]
- Rodriguez, M.; Valero, A.; Posada-Izquierdo, G.D.; Carrasco, E.; Zurera, G. Evaluation of food handler practices and microbio-logical status of ready-to-eat foods in long term care facilities in the Andalusia region of Spain. J. Food Protect. 2011, 74, 1504–1512. [Google Scholar] [CrossRef]
- Kampf, G.; Todt, D.; Pfaender, S.; Steinmann, E. Persistence of coronaviruses on inanimate surfaces and their inactivation with biocidal agents. J. Hosp. Infect. 2020, 4, 246–251. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kampf, G.; Jatzwauk, L. Ist die Desinfektion öffentlicher Flächen zur Prävention von SARS-CoV-2 - Infektionen sinnvoll? Gesundheitswesen 2021, 83, 180–185. [Google Scholar]
- Anderson, D.J.; Chen, L.F.; Weber, D.J.; Moehring, R.W.; Lewis, S.S.; Triplett, P.F.; Blocker, M.; Becherer, P.; Schwab, J.C.; Knelson, L.P.; et al. Enhanced terminal room disinfection and acquisition and infection caused by multidrug-resistant organisms and Clostridium difficile (the Benefits of Enhanced Terminal Room Disinfection study): A cluster-randomised, multicentre, crossover study. Lancet 2017, 389, 805–814. [Google Scholar] [CrossRef]
- Anderson, D.J.; Knelson, L.P.; Moehring, R.K.; Lewis, S.L.; Weber, D.K.; Chen, L.F.; Triplett, P.F.; Blocker, M.; Cooney, R.M.; Schwab, J.C.; et al. For the CDC Prevention Epicenters Program. Implementation Lessons Learned from the Benefits of Enhanced Terminal Room (BETR) Disinfection Study: Process and Perceptions of Enhanced Disinfection with Ultraviolet Disinfection Devices. Infect. Control Hosp. Epidemiol. 2018, 39, 157–163. [Google Scholar] [CrossRef]
- Ethington, T.; Newsome, S.; Waugh, J.; Lee, L.D. Cleaning the air with ultraviolet germicidal irradiation lessened contact infections in a long-term acute care hospital. Am. J. Infect. Control 2018, 46, 482–486. [Google Scholar] [CrossRef] [Green Version]
- Buchan, A.G.; Yang, L.; Atkinson, K.D. Predicting airborne coronavirus inactivation by far-UVC in populated rooms using a high-fidelity coupled radiation-CFD model. Sci. Rep. 2020, 10, 1–7. [Google Scholar] [CrossRef]
- Coutureau, C.; Pascard, M.; Kanagaratnam, L.; Jolly, D.; de Champs, C. Does Copper Prevent Nosocomial Transmission of COVID-19? J. Am. Med Dir. Assoc. 2021, 22, 219–220. [Google Scholar] [CrossRef]
- Mantlo, E.K.; Paessler, S.; Seregin, A.; Mitchell, A. Luminore CopperTouch™ surface coating effectively inactivates SARS-CoV-2, Ebola, and Marburg viruses in vitro. MedRxiv Prepr. Serv. Health Sci. 2020. [Google Scholar] [CrossRef]
- Salgado, C.D.; Sepkowitz, K.A.; John, J.F.; Cantey, J.R.; Attaway, H.H.; Freeman, K.D.; Sharpe, P.A.; Michels, H.T.; Schmidt, M.G. Copper surfaces reduce the rate of healthcare-acquired infections in the intensive care unit. Infect. Control Hosp. Epidemiol. 2013, 34, 479–486. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Noyce, J.O.; Michels, H.; Keevil, C.W. Inactivation of Influenza A Virus on Copper versus Stainless Steel Surfaces. Appl. Environ. Microbiol. 2007, 73, 2748–2750. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Warnes, S.L.; Keevil, C.W. Inactivation of Norovirus on Dry Copper Alloy Surfaces. PLoS ONE 2013, 8, e75017. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Warnes, S.L.; Summersgill, E.N.; Keevil, C.W. Inactivation of Murine Norovirus on a Range of Copper Alloy Surfaces Is Accompanied by Loss of Capsid Integrity. Appl. Environ. Microbiol. 2015, 81, 1085–1091. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sugg, M.M.; Spaulding, T.J.; Lane, S.J.; Runkle, J.D.; Harden, S.R.; Hege, A.; Iyer, L.S. Mapping community-level determinants of COVID-19 transmission in nursing homes: A multi-scale approach. Sci. Total Environ. 2021, 752, 141946. [Google Scholar] [CrossRef] [PubMed]
- Waternews Europe. Netherlands: Covid-19 Sewage Measurements Difficult to Interpret. Available online: https://www.waternewseurope.com/netherlands-covid-19-sewage-measurements-difficult-to-interpret/ (accessed on 12 February 2021).
Age Group | Hospitalisation Rate | Death Rate |
---|---|---|
18–29 years | Comparison Group | Comparison Group |
30–39 years | 2x higher | 4x higher |
40–49 years | 3x higher | 10x higher |
50–64 years | 4x higher | 30x higher |
65–74 years | 5x higher | 90x higher |
75–84 years | 8x higher | 220x higher |
85+ years | 13x higher | 630x higher |
Search Term | Medline | Embase | |
---|---|---|---|
1 | coronavirus.mp. | 81468 | 125824 |
2 | Sars-CoV-2.mp. or exp SARS-CoV-2/ | 68254 | 35064 |
3 | Covid-19.mp. | 107186 | 96515 |
4 | 1 or 2 or 3 | 125192 | 131716 |
5 | nursing home.mp. | 22862 | 63414 |
6 | homes for the aged.mp. | 14435 | 746 |
7 | long term care.mp. | 39334 | 142648 |
8 | long term care facilities.mp. | 4389 | 5579 |
9 | 5 or 6 or 7 or 8 | 67177 | 195407 |
10 | 4 and 9 | 722 | 1288 |
11 | mortality.mp. | 1206828 | 1564538 |
12 | 10 and 11 | 186 | 383 |
13 | Disease transmission | 40060 | 107336 |
14 | disease transmission, infectious.mp. | 10443 | 58 |
15 | respiratory tract infections.mp. | 47170 | 22062 |
16 | negative pressure isolation.mp. | 73 | 94 |
17 | systematic review.mp. | 206869 | 364785 |
18 | meta-analysis.mp. | 208052 | 312070 |
19 | 17 or 18 | 318737 | 513093 |
20 | 10 and 19 | 9 | 27 |
21 | 13 or 14 or 15 | 87017 | 129231 |
22 | 10 and 21 | 37 | 42 |
Numbers of Patients in LCTFs and Nursing Homes, Disabilities and Mortality Rates | ||
---|---|---|
Author, Date | Setting | Disabilities and Mortality Rates |
Vossius 2018 [4] | 47 small and large nursing homes in urban and rural areas in 4 Norwegian counties followed for 3 years. Average age 84.5 years, 83.9% dementia at baseline. Assessment: Trained healthcare workers (74% registered nurses, 2 days of training) collected data using structured interviews with patient and caregiver, supervised by 10 research nurses (5 days training). Dementia assessments by 2 psychiatrists (adjudicated by a 3rd), ICD-10, Clinical Dementia Rating Scale (CDR), neuropsychiatric symptoms by the Neuropsychiatric Inventory nursing home version (NPI-NH), self-care by the Physical Self-Maintenance Scale (PSMS), general health by General Medical Health Rating (GMHR), comorbidities by Charlson’s comorbidity index. | Survival: median Kaplan–Meier survival 2.2 years (95% CI 1.9 ± 2.4) with stable median yearly mortality 31.8%. Assessed mortality rate may be an underestimate. Hazard ratios for mortality: Charlson comorbidity index (HR 1.13; 1.06, 1.22; p <0.001), physical self-maintenance (PSMS scores) (HR 1.07; 1.03, 1.12; p = 0.001), age (HR 1.04; 1.01, 1.06; p = 0.002), residing on a nonspecialised ward (with more patients) (HR 1.03; 1.01, 1.05; p = 0.016). |
Dwyer 2014 [12] | Systematic review of 83 studies of emergency transfers to hospital of residents of LTCFs ≥ 65 years. | Triage assessment in emergency departments: 59% triaged urgent or emergent compared to 45% of all emergency department presentations. Reasons for admission: multiple illnesses: respiratory tract infections (12–37% of all presentations), other infections (6–24%), falls (12–23%), fractures and orthopedic injuries (7–24%), cardiovascular illness (11–28%), altered mental state (7–12%). Mortality: 1–5% died in the emergency department, 5–34% after admission to hospital and 12–29% within a month of discharge. |
Canadian Institute of Health Information 2020 [13] | Numbers of nursing home patients in Canada: 2019–2020 there were 189,662 residents in 1318 nursing homes; average age 83 years, 54% ≥ 85, 65% female. Risk factors: Cognitive Performance Scale (CPS) ≥4, Index of Social Engagement (ISE) ≤ 2, the Aggressive Behaviour Scale (ABS) ≥1, and the Pain Scale ≥ 2. | Morbidities: 61.6% dementia, 59% hypertension, 24.5% signs of depression, 24.8% diabetes, 9% cancer, 77% some urinary incontinence, 59% some bowel incontinence, 42.9% little or no social engagement, 12% total dependence for Activities of Daily Living (ADLs), 9% daily pain. |
Harris-Kojetin 2018 [14] | Numbers of nursing home patients: 1,347,600 residents in 15,600 nursing homes. Multiple types of long-term care: In US in 2016 there were 65,600 remunerated regulated long-term care services, providing care for >8.3 million people in five sectors: estimated 286,300 individuals in 4600 adult day services centers, 811,500 residents in residential care communities, 1,426,000 patients receiving services from 4300 hospices and residents in 28,900 assisted living residential care communities. In 2015, ~4,455,700 patients discharged annually from home health agencies. | Morbidities in nursing home patients: 72% hypertension, 48% dementia, 46% depression, 38% heart disease, 32% diabetes, 26% arthritis, and 12% osteoporosis. Hours of staff care time: If staff used every hour for patient care, in nursing homes daily per patient RNs could provide 0.54 hours of care, licensed practical or vocational nurses 0.85, aides 2.4, social workers 0.08; in residential care, 0.2, 0.17, 2.27 and 0.03 h, respectively. |
|
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2021 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Thomas, R.E. Reducing Morbidity and Mortality Rates from COVID-19, Influenza and Pneumococcal Illness in Nursing Homes and Long-Term Care Facilities by Vaccination and Comprehensive Infection Control Interventions. Geriatrics 2021, 6, 48. https://doi.org/10.3390/geriatrics6020048
Thomas RE. Reducing Morbidity and Mortality Rates from COVID-19, Influenza and Pneumococcal Illness in Nursing Homes and Long-Term Care Facilities by Vaccination and Comprehensive Infection Control Interventions. Geriatrics. 2021; 6(2):48. https://doi.org/10.3390/geriatrics6020048
Chicago/Turabian StyleThomas, Roger E. 2021. "Reducing Morbidity and Mortality Rates from COVID-19, Influenza and Pneumococcal Illness in Nursing Homes and Long-Term Care Facilities by Vaccination and Comprehensive Infection Control Interventions" Geriatrics 6, no. 2: 48. https://doi.org/10.3390/geriatrics6020048
APA StyleThomas, R. E. (2021). Reducing Morbidity and Mortality Rates from COVID-19, Influenza and Pneumococcal Illness in Nursing Homes and Long-Term Care Facilities by Vaccination and Comprehensive Infection Control Interventions. Geriatrics, 6(2), 48. https://doi.org/10.3390/geriatrics6020048