| Literature DB >> 34316581 |
C M Rooney1,2, J McIntyre3, L Ritchie3, M H Wilcox1,2.
Abstract
We review the evidence base for two newly introduced Infection prevention and control strategies within UK hospitals. The new standard infection control precaution of 2 metres physical distancing and the use of partition screens as a means of source control of infection for SARS-CoV-2. Following review of Ovid-MEDLINE and governmental SAGE outputs there is limited evidence to support the use of 2 metres physical distancing and partition screens within healthcare.Entities:
Keywords: Engineering controls; Partition screens; Physical distancing; SARS-CoV-2; Social distancing
Year: 2021 PMID: 34316581 PMCID: PMC8081747 DOI: 10.1016/j.infpip.2021.100144
Source DB: PubMed Journal: Infect Prev Pract ISSN: 2590-0889
Summary of droplet/airborne transmission with respect to physical distance.
| Author | Setting | Infectious agent | Sampling method | Distance (M) | Result | Limitations |
|---|---|---|---|---|---|---|
| Ai [ | Simulation room with thermal manikins | Tracer gas technique | N/A | 0.35, 1.0, 1.5 | Time average exposure mostly decreases with an increase in separation distance, this effect was more prominent in steady state rather than short term events. | Tracer gas. Still Manikins, limited measurements, risk calculation relying on stable dosing flow rate, short term events limited to building up from background concentration. |
| Bischoff [ | Human participants. Hospital ward and A&E | Influenza | Air sampling with rRT-PCR | 0.30, 0.914, 1.829 | Influenza virus was detected in 43% of known positive patient rooms. Exposure was mainly small particles. (diameter, <4.7 μm), with concentrations decreasing with increasing distance from the patient's head, -p value < 0.05, at 0.30 versus 1.8 metres. | All equipment removed from patients. Single time point. Assess exposure to virus rather than transmission. No asymptomatic individuals included. |
| Kunkel [ | Simulation room | Bacteriophage T4 | aerosol sampling, culture and qPCR | 0.5, 3, 5, 7 | Particle size distribution between 40-70um. 49% of T4 DNA was extracted from 0.5um sized particles at 0.5M and 90% from <1um. No substantial size distribution of mass demonstrated at different locations but there was a decrease in magnitude of aerosols with increasing distance. | Surrogate organisms used. Not healthcare environment. |
| Lindsley [ | Simulation air chamber | Influenza | Aerosol sampling, qPCR | 0.46, 1.83 | Increased distance from cough simulator to breathing simulator significantly reduced the amount of inhaled virus (P = 0.009). Analysis of longer exposure of 30mins duration, increased distance increased the overall particle inhalation | Two sizes of aerosol particles used. Uniform concentration of influenza within aerosols. |
| Liu [ | simulation with thermal manikins | Tracer gas technique | Aerosol sampling. Computational fluid dynamics | 0.5, 1.0, 1.5, 2.0, 3.0 | Substantial increase in droplet nuclei exposure when within 1–1.5M of infection source. | Exposure not transmission. The 1.5M threshold does not account for the cough scenario. |
| Savory [ | cough test chamber using human participants | None | Particle image velocimetry | 1.0 | Following a cough air motion of 0.5m/s is identified at 1m away | Small sample size (12), single distance measured. Healthy volunteers without respiratory infection were studied. Particle size not studied. |
| Tang [ | Human participants, simulated exposure manikins | Influenza | RT-PCR | 0.1, 0.5 | Failed to detect any influenza RNA landing on, or inhaled by, a life-like, human manikin target, after exposure to naturally influenza-infected volunteers. | Low PCR CT values in participants (visible droplets were present on the manikins after exposure). Experiment did not capture the entire exhaled breath/cough. Short exposure time and significant variability (10 seconds–15mins) |
| Xie [ | Mathematical modelling | None | N/A | 0.5, 1.0, 1.5, 2.0, 2.5 | Particles between 60 and 100um in size totally evaporate before falling 2M. Particles of the same size are carried more than 6 m away by exhaled air at a velocity of 50 m/s (sneezing), more than 2 m away at a velocity of 10 m/s (coughing) and less than 1 m away at a velocity of 1 m/s (breathing). | Mathematical modelling based on multiple theoretical assumptions. |
Summary of partition use in multi-bedded bay environments.
| Author | Setting | Partition | Infectious agent | Sampling method | Result |
|---|---|---|---|---|---|
| Noakes [ | Two bedded bay | Full length vertical partition extending to the foot of bed | Computational fluid dynamics | Physical barrier inserted between bed spaces could reduce the transmission of infection, but this was dependant on the location of outflow extractor | |
| King [ | Two bedded bay | Plastic sheet hung between the patients bed spaces; gaps of 20 cm were left above and below the sheet (partial partition) and 80 cm at the end of the sheet from the wall | Settle plates and computational fluid dynamics | Univariate linear regression model based on normalised deposition counts predicted a halving of pathogen deposition per surface (r= -0.32, p= 0.0254) for patient 2 (using a partial partition, when the source of infection is patient 1) | |
| Ching [ | Two and four bedded bay | fully extended, bed length (2.1 metre) and partial bed length (1.2 metre) curtains | Tracer gas | Computational fluid dynamics | In a two-bedded bay, without curtains, the concentration of bioaerosols on the adjacent bed was 11,503 cfu m3; this reduced to 9865 cfu m3 with partially extended curtains, and to 3782 cfu m3 with fully extended curtains. For the four-bedded bay configuration, the results showed a similar trend for both partial and full extended curtains |
| Gilkeson [ | Six bedded bay | Extended vertically from the floor to 2 feet below the ceiling and horizontally to beyond the foot of the bed | Tracer gas | Pulse injection technique | The cross ventilated partitioned ward led to a more heterogeneous tracer distribution compared with the open ward environment, but did demonstrate the ability of the partitions to effectively contain the source of infection |
| Nielsen [ | Two bedded bay | Partial vertical textile partition, 10 cm opening above the floor, and 40 cm below the ceiling | Tracer gas | Calibrated multi-gas monitor and multipoint sampler | In a multitude of ventilation layouts, the partition was shown not to decrease cross infection between patients, and may increase infection exposure to simulated healthcare workers. |