Introduction
The ability to measure airborne bacteria and viruses in real time could serve as a crucial tool in alerting individuals to potential airborne infection transmission, thereby prompting behavior modifications to mitigate risks. While biosensors have been proposed for this purpose [1], current models are not sufficiently compact, lightweight, or cost-effective. Hence, we developed a Pocket Carbon Dioxide (CO2) Logger, a portable recording device with a built-in CO2 sensor, and conducted a field experiment on city sensing by attaching it to participants in Tokyo, Japan. We aimed to visualize areas with poor ventilation and, therefore, a high risk of airborne transmission, by analyzing data on indoor CO2 concentrations using citizen sensing.
Exhaled human breath contains CO2 concentrations of approximately 30,000 ppm, which is two orders of magnitude higher than the atmospheric level of 400 ppm, thereby, making it a reliable tracer gas to indicate indoor ventilation capacity [2, 3]. Furthermore, the exhaled breath of infected individuals contains droplet nuclei containing viruses and high concentrations of CO2, both of which have spreading and translocation properties. Hence, CO2 concentrations can be regarded as a proxy indicator of aerosol risks [4]. Several developed countries recommend maintaining CO2 concentrations below 800 ppm as a special exception in pandemic situations [5] as CO2 concentrations are recognized as an indicator of indoor ventilation and airborne transmission.
In Japan, control of indoor CO2 concentrations has been proposed since 1902 in the Meiji period [6]. Today, Japan’s Building Standards Act (revised and enforced in 2003) requires the installation of 24-h ventilation systems in all living rooms to prevent sick house syndrome. Moreover, it requires a ventilation capacity of at least 0.5 times/h in the living rooms of residential buildings. A ventilation capacity of 0.5 times/h is, for example, the ventilation capacity that would result in a steady-state CO2 concentration of 800 ppm when two people are in a room, 1,000 ppm when three people are in a room, and approximately 1,200 ppm when four people with standard activity levels are present in a 70 m2 space, which is the minimum standard for infection control. Maintaining CO2 concentrations consistently below 1000 ppm proves challenging for an average household [7]. Conversely, the Act on Maintenance of Sanitation in Buildings (enforced in 1970), which specifies environmental sanitation requirements for buildings used and occupied by a large number of people, sets standards for the control of CO2 concentrations across various types of buildings including entertainment venues, department stores, offices, and schools, where the area of the portion used for these specified purposes is ≥ 3,000 m2 (≥8,000 m2 for schools) (defined as specified buildings), the CO2 concentration is regulated at ≤1,000 ppm and periodic inspections are conducted [8].
Du et al. reported that improving the ventilation system in a poorly ventilated university building, where a tuberculosis (TB) outbreak (27 patients with TB and 1,665 contacts) occurred, and reducing the maximum CO2 concentration from 3,204 ± 50 to 591–603 ppm would reduce the rate of secondary infection among new contacts to zero (average follow-up period: 5.9 years); moreover, controlling CO2 concentrations below 1,000 ppm would reduce the incidence of TB in contacts by 97% (95% confidence interval (CI):50–99.9%) [9]. Multiple studies have reported airborne transmission of coronavirus disease (COVID-19), particularly in poorly ventilated indoor spaces [10–15]; hence, the application of CO2 concentration as an indicator of risk for the airborne transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has also been proposed [16, 17].
The Wells–Riley Eq (1) is the classic model for quantitatively evaluating the risk of airborne infections [18, 19].(1)Where P is the probability that an infected person will be infected, I is the number of infected persons in a closed space, p is the volume of breath per person (㎥/h), q is the rate of infectious droplets (/h) (where the q in a person infected with SARS-CoV-2 will be ≥100 pieces/h [20]), t is the time stayed by the infected person (h), θ is the time spent by the infected person (h), V is the room volume (m3), and Q is the ventilation rate (m3/h). The Wells–Riley equation models the probability of exposure due to a person breathing in infectious droplets emitted by an infected person as a risk quantity. Eq (1) explains that increasing Q, i.e., improving ventilation, is effective in reducing airborne infection risk P.
Fieldwork using CO2 sensors as a countermeasure against airborne transmission has been conducted worldwide. Wiryasaputra et al. [21] conducted a systematic review of studies that monitored indoor environments, particularly CO2, to reduce the risk of COVID-19 infection. According to a systematic review of 19 articles in urban spaces, CO2 is the primary reference for the spread of novel coronaviruses in buildings [22]. Studies have been conducted to visualize areas at high risk of COVID-19 infection using the CO2 tracer gas method [23–27]. In South Africa, where TB is widely prevalent, CO2 sensors have been installed in public buildings, and the application of Eq (1) to estimate the risk of TB transmission has confirmed that the chances of transmission in schools is relatively large [28, 29]. Additionally, attempts have been made in South Africa to utilize portable CO2 sensors with a built-in global positioning system (GPS) [30] and combine them with a geographic information system to visualize the risk of TB transmission on a map [31]. However, to the best of our knowledge, no attempts have been made to employ citizens with mobile CO2 sensors to measure the adequacy of ventilation in developed countries or metropolitan areas during the COVID-19 pandemic.
Therefore, this study aimed to demonstrate the feasibility of visualizing the risk of airborne infection with mobile citizen sensing using a Pocket CO2 Logger to identify locations with poor ventilation in the Tokyo area, the largest megacity in the world.
Materials and methods
Pocket CO2 Logger
The Pocket CO2 Logger (Fig 1), which we developed originally, measures 76.5 mm wide, 30 mm height, and 43 mm in depth and weighs 40 g for easy portability. The device is equipped with a nondispersive infrared CO2 sensor module, SCD30 (Sensirion AG., Stäfa, Switzerland), a lithium polymer battery, a low-power microcontroller in deep-sleep mode (PIC24FJ128GB204, Microchip Technology, Arizona), a real-time clock (RX8900CE, Seiko Epson, Tokyo, Japan), and a 1 GB SD card.
[Figure omitted. See PDF.]
By default setting, intermittent operation every 10 min and a 10 s pre-measurement warm-up ensure continuous operation for at least one week, since the sensor consumes no power except while measuring. These variables for intermittent operation and warm-up time can be changed arbitrarily in the configuration file on the SD card. The built-in real-time clock has low power consumption and long-term operation by virtue of its deep-sleeping qualities outside the measurement time.
Yasuda et al. [30] have developed the Portable CO2 Measurement Device with a handle and powered by six AA cell batteries, although it is considered excessively large and not portable enough for participants to carry with them at all times. Wood et al. [31] developed a true portable CO2 logger that can be carried by participants for TB prevention in Cape Town, South Africa; however, the Pocket CO2 logger is 34% smaller in volume and has 3.5 times longer continuous operating time than Wood’s logger. Ishigaki and Kitamura et al. [25–27] deployed TR-76Ui sensors (T&D Corporation, Nagano, Japan) for mobile CO2 logging to estimate the risk of airborne transmission of COVID-19; however, the Pocket CO2 logger is 66% smaller in volume and 92% lighter in weight than TR-76Ui. The USB connector can be used for both charging and data transfer in accordance with the USB mass storage mode. The measured results were recorded on the SD card in a comma-separated value (CSV) format as log file(s), with one file generated per day with the name of that date. The log files could subsequently be transferred to a computer via USB connection.
Nondispersive infrared sensing is a method of estimating CO2 concentration by measuring the attenuation of the absorption wavelength (4.26 μm) of CO2 molecules using a photodiode. The internal sensor module (SCD30) also contained temperature and humidity sensors that were used to compensate for the CO2 concentration measurements. The CO2 measurement range of SCD30 is 400–10,000 ppm, with a measurement accuracy of ±30 ppm, typical relative humidity accuracy of 3% RH, and operating relative humidity range of 0–95% RH; hence, it is unlikely to be significantly inhibited in everyday temperature and humidity environments.
Participants
With the cooperation of a local restaurant in Tokyo, Japan, we have requested 11 customers to participate in the experiment. Those who consented were lent a Pocket CO2 Logger and asked to carry it with them at all times for the intended one-week experimental period, except when directly exposed to water, such as when taking a bath. The Pocket CO2 Logger can operate for more than a week without requiring a recharge and could be carried at all times.
The participants were instructed to carry the Pocket CO2 Logger in one of three possible ways: hang it around their neck with a strap, attach it to a carabiner, or tie it to a bag or pouch. During the experiment, the participants recorded in the logger the location and time of their stay. This allowed the continuous collection of data on the participant’s locations and CO2 concentrations. However, for privacy protection reasons, we did not collect any GPS or location information, nor record the names or contact information of the participants, except for sex and history of COVID-19 infection. Thus, the data of the measurement results were not linked to any specific individual.
This study was approved by the Ethics Committee of the University of Electro-Communications, Chofugaoka, Chofu, Tokyo, Japan (approval number: 21006 and 21006 [2]). The need for consent was waived by the ethics committee. Participants were provided with written information about the purpose of the experiment and contact information for questions. The participants did not include minors. The recruitment period for this study started June 2, 2021and ended March 31, 2022.
Data analysis
Based on the data of the participant’s identification (ID), CO2 concentration [ppm], and location listed in the ledger, we performed an analysis using JMP Pro 16.2.0 (SAS Institute, North Carolina) with a generalized linear mixed model (GLMM). The objective variable was set to the logarithm of CO2 concentration, participant ID was assigned as the random effect, and location was assigned as the fixed effect. Because the description of the location was expected to vary between participants, it was screened in advance and set as a factor after roughly classifying the genres as follows: cinema, gyms, halls, homes, hospitals, pubs, restaurants, universities, stores, transportation, workplaces, other indoors, and other outgoings.
The data may have contained participant-specific biases owing to the different carrying methods used by each participant. Therefore, as a preliminary analysis, we estimated the covariance parameter of the random effect of participant ID, checked the validity of conducting an analysis incorporating the random effect, determined whether individual differences were significant based on the Wald p-values (double-sided), and confirmed that significant individual differences were found.
In parallel with the above analysis, quantile plots and histograms were generated for the residuals and random effects of the estimated GLMM, respectively, to validate the use of the GLMM and the normality of the variable. A priori determination of the necessary sample size or post-hoc power analysis was not performed as this was a pilot study.
Results
An average of 8 days of data per participant was collected from the 11 participants (seven males and four females, none with a history of COVID-19 infection) from December 8, 2021 to January 14, 2022, resulting in a total of 12,253 records. The start date of the experiment varied between participants. As an example, Fig 2 plots the CO2 concentration for one participant (ID: C05), color-coded according to location. It shows the trend of CO2 concentration changing at different locations; at home, the CO2 concentration increased monotonically with time spent at home, whereas at a restaurant and store, the CO2 concentration was steady at a lower level than at home.
[Figure omitted. See PDF.]
Measurements are color-coded for each location and connected by a line graph.
The data collected from all participants were tabulated and the number of records per location in descending order was as follows: home, 8081 records (66.0%); workplace, 1963 records (16.0%); other outgoings, 866 records (7.1%); transportation, 368 records (3.0%); restaurant, 343 records (2.8%); hall, 191 records (1.6%); store, 186 records (1.5%); gym, 75 records (0.6%); pub, 69 records (0.6%); other indoors, 48 records (0.4%); hospital, 39 records (0.3%); cinema, 12 records (0.1%); and university, 12 records (0.1%).
A Wald p-value of 0.0342 for participant ID in the covariance parameter estimates of the variant effects showed significant individual differences, confirming the validity of setting participant ID as a random effect in the GLMM. S1 Fig in S1 File shows a box-and-whisker diagram of the variation in CO2 concentration for each participant over the study period.
The histogram and quantile plot of the estimated GLMM residuals are shown in S2 Fig in S1 File, and the histogram and quantile plot of random effects indicating individual differences are shown in S3 Fig in S1 File. In both cases, the distributions were considered approximately normal; therefore, the application of GLMMs was considered reasonable.
Table 1 summarizes the parameter estimators for the fixed effects. These estimators show the interaction of each factor, sorted in ascending order by the estimator. The factors indicating locations that significantly (p < 0.0001) contributed to CO2 concentrations were, in ascending order, workplaces, halls, homes, gyms, other indoors, pubs, other outgoings, stores, and universities. Conversely, the results for hospitals, transportation, restaurants, and cinemas were not significant.
[Figure omitted. See PDF.]
Fig 3 shows a box-and-whisker plot of the CO2 concentrations plotted by location. Factors that contributed significantly to the CO2 concentration obtained from the parameter estimates above are marked with an asterisk (*).
[Figure omitted. See PDF.]
The locations are sorted in descending order of average values. Asterisk (*) indicates that the factor contributed significantly (p < 0.05) to the CO2 concentration.
Discussion
Of the locations considered relatively poorly ventilated, with a median CO2 concentration exceeding 1,000 ppm in all measurements (Fig 3), those contributing significantly (p < 0.0001) (Table 1) were: homes (1,316 ppm), halls (1,173 ppm), gyms (1,005 ppm), and other outgoings (972 ppm). Conversely, the locations with relatively good ventilation, with a median value <1,000 ppm, and continued to significantly contribute to CO2 concentrations were: pubs (864 ppm), other indoors (835 ppm), workplaces (705 ppm), cinemas (663 ppm), universities (652 ppm), and stores (620 ppm).
Our study highlights homes as being poorly ventilated enclosed spaces, despite a previous study examining the risk of TB transmission in South Africa pointing to schools and public facilities [32]. Although Japan’s Building Standards Act requires 0.5 times/h ventilation to prevent sick house syndrome, this alone is not enough to maintain CO2 concentrations <1,000 ppm. A study conducted in China by the World Health Organization [33] indicated that 80% of COVID-19 outbreaks could be attributed to household infections. The actual risk of secondary infection at home is 12.1% in Japan (Okinawa), 4.6% in Taiwan, 10.5% in the USA, 11.8% in Korea, and 17.2% in China [33–38]. These findings of a relatively high risk of infection at home are consistent with the results of this study.
Outbreaks due to airborne transmission during choruses have been confirmed in the U.S. and Australia [13, 39]. Clusters also occurred during yoga sessions in poorly ventilated gyms in South Korea [40]. In developed countries, halls and gyms are often built in dense residential areas; hence, windows may not be opened to prevent sound pollution and promote privacy. Such urban-specific environments are thought to increase the CO2 concentrations in homes, halls, and gyms.
For other outgoings, a relatively large amount of data was collected– 866 records (7.1%)–but the classification was rather ambiguous and included incidences when participants walked outdoors or in other unclassified buildings. Future studies should analyze data in a more detail by specifically stating the type of building.
For pubs, the median CO2 concentration was <1,000 ppm, which was relatively low. The Tokyo Metropolitan Government issued multiple emergency declarations requiring pubs to reduce business hours or refrain from operating in cooperation with the police and fire department, with business owners who cooperated receiving financial subsidies [41]. To deter airborne transmission of infection, concurrent measures should be considered for high-risk locations such as homes, halls, and gyms. For example, the Kyoto Prefecture installed CO2 sensors free of charge in 2,836 restaurants in the prefecture, and based on the data on collected, made individual visits and provided guidance on specific measures to improve ventilation [42]. To deter infections in family members during home care, it may be effective to conduct surveillance based on CO2 concentrations at home.
In contrast, CO2 concentrations were relatively low in workplaces and stores. This could be attributed to the Act on Maintenance of Sanitation in Buildings (enforced in 1970), which mandates CO2 concentrations of 1,000 ppm or less in entertainment venues, large-scale stores, offices, and school, along with periodic inspections.
The data for "other indoors, cinemas, and universities" is not sufficient because only one participant visited these places. This may be because the activities of the participants were restricted because of the Japanese government’s request for a voluntary curfew.
Notably, certain hidden variables, including the number of people staying, metabolic rate, air area of the space where the participants stayed, and ventilation frequency, were not addressed in this study, indicating its weakness. The CO2 concentration fluctuates and stabilizes with these variables [43]. It would be possible to adopt the CO2 concentration as a reliable risk proxy by knowing what the steady-state CO2 concentration is in the space where the participant temporarily stays. For this purpose, installing fixed CO2 sensors and human detection cameras on the space side are necessary.
This study had several limitations. First, it did not capture the demographic characteristics of the participants (excluding sex and history of COVID-19); hence, we were unable to analyze characteristics according to age group or employment status. Second, since the location information was identified by self-report, it may contain errors or mistakes. Future research should link the indoor and outdoor location estimation functions of smartphones using GPS and Wi-Fi to automatically collect location information. If smartphones and sensors can automatically synchronize via Bluetooth and periodically collect data in the Cloud, the workload of the participants can be significantly reduced, resulting in large-scale, long-term monitoring with a larger number of individuals. This can contribute to field epidemiology and administrative decision-making.
In this study, the CO2 concentration was classified as high or low based on a cut-off of 1,000 ppm; however, for future social implementation, a method to adaptively calculate the excess CO2 threshold based on the number of occupants, community prevalence, and activity level should be adopted [44].
Conclusions
Using our newly developed, compact, and lightweight Pocket CO2 Logger, we found that homes, halls, and gyms, were relatively poorly ventilated and significantly (p < 0.0001) contributed to elevated CO2 concentrations, with average values >1,000 ppm. As several cases of outbreaks due to airborne transmission in these locations have been reported in previous studies, it can be inferred that they have a relatively high risk of transmission.
In contrast, workplaces and stores had significantly lower (p < 0.0001) CO2 concentrations. This may be due to the ventilation regulations under Japan’s Act on the Maintenance of Sanitation in Buildings.
Our results may be used to make policy recommendations for infection control, such as human flow restrictions and ventilation measures, in locations identified as relatively high-risk. In the future, we plan to conduct a large-scale survey and the sensor may be linked to a smartphone to automatically collect indoor and outdoor location information to reduce the workload on the participant.
Supporting information
S1 File.
https://doi.org/10.1371/journal.pone.0303790.s001
(DOCX)
Acknowledgments
We would like to thank Ms. Yasuyo Shikata and Editage [http://www.editage.com] for their writing support on the manuscript.
Citation: Ishigaki Y, Yokogawa S (2024) Monitoring the ventilation of living spaces to assess the risk of airborne transmission of infection using a novel Pocket CO2 Logger to track carbon dioxide concentrations in Tokyo. PLoS ONE 19(5): e0303790. https://doi.org/10.1371/journal.pone.0303790
About the Authors:
Yo Ishigaki
Roles: Conceptualization, Methodology, Project administration, Resources, Supervision, Writing – original draft
E-mail: [email protected]
Affiliation: Research Center for Realizing Sustainable Societies, The University of Electro-Communications, Chofu, Tokyo, Japan
ORICD: https://orcid.org/0000-0001-7284-0381
Shinji Yokogawa
Roles: Formal analysis, Investigation, Validation, Visualization, Writing – review & editing
Affiliation: Info-Powered Energy System Research Center (iPERC), The University of Electro-Communications, Chofu, Tokyo, Japan
ORICD: https://orcid.org/0000-0003-2956-3600
[/RAW_REF_TEXT]
[/RAW_REF_TEXT]
1. Puthussery JV, Ghumra DP, McBrearty KR, Doherty BM, Sumlin BJ, Sarabandi A, et al. Real-time environmental surveillance of SARS-CoV-2 aerosols. Nat Commun. 2023;14:3692. pmid:37429842
2. Batterman S. Review and extension of CO₂-based methods to determine ventilation rates with application to school classrooms. Int J Environ Res Public Health. 2017;14:145. https://doi.org/10.3390/ijerph14020145.
3. Rudnick SN, Milton DK. Risk of indoor airborne infection transmission estimated from carbon dioxide concentration. Indoor Air. 2003;13:237–245. pmid:12950586
4. Peng Z, Jimenez JL. Exhaled CO2 as a COVID-19 infection risk proxy for different indoor environments and activities. Environ Sci Technol Lett. 2021;8:392–397. https://doi.org/10.1021/acs.estlett.1c00183.
5. Eykelbosh A. Indoor CO2 sensors for COVID-19 risk mitigation: current guidance and limitations. Vancouver, BC: National Collaborating Centre for Environmental Health; 2021 [cited Jul 25 2021]. Available from: https://ncceh.ca/documents/field-inquiry/indoor-co2-sensors-COVID-19-risk-mitigation-current-guidance-and.
6. Okuda T, Murakami M, Naito W, Shinohara N, Fujii K. Interpretation of carbon dioxide concentration values for applying it as a management index of infection control. Jpn J Risk Anal. 2021;30:207–212. https://doi.org/10.11447/jjra.SRA-0364.
7. Tanabe S. Measuring methods and standardization for chemical emission. J Jpn Air Clean Assoc. 2008;46:38–44 ISSN: 0023-5032, https://www.jaca-1963.or.jp/English/tosyo(e)-ab46.htm.
8. Azuma K, Yanagi U, Kagi N, Kim H, Ogata M, Hayashi M. Environmental factors involved in SARS-CoV-2 transmission: effect and role of indoor environmental quality in the strategy for COVID-19 infection control. Environ Health Prev Med. 2020;25:66, https://link.springer.com/article/10.1186/s12199-020-00904-2. https://doi.org/10.1186/s12199-020-00904-2. pmid:33143660
9. Du CR, Wang SC, Yu MC, Chiu TF, Wang JY, Chuang PC, et al. Effect of ventilation improvement during a tuberculosis outbreak in underventilated university buildings. Indoor Air. 2020;30:422–432. pmid:31883403
10. Prather KA, Marr LC, Schooley RT, McDiarmid MA, Wilson ME, Milton DK. Airborne transmission of SARS-CoV-2. Science. 2020;370:303–304. pmid:33020250
11. Tang JW, Bahnfleth WP, Bluyssen PM, Buonanno G, Jimenez JL, Kurnitski J, et al. Dismantling myths on the airborne transmission of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). J Hosp Infect. 2021;110:89–96. pmid:33453351
12. Morawska L, Milton DK. It is time to address airborne transmission of coronavirus disease 2019 (COVID-19). Clin Infect Dis. 2020;71:2311–3. pmid:32628269
13. Miller SL, Nazaroff WW, Jimenez JL, Boerstra A, Buonanno G, Dancer SJ, et al. Transmission of SARS-CoV-2 by inhalation of respiratory aerosol in the Skagit Valley Chorale superspreading event. Indoor Air. 2021;31:314–323. pmid:32979298
14. Lu J, Gu J, Li K, Xu C, Su W, Lai Z, et al. COVID-19 outbreak associated with air conditioning in restaurant, Guangzhou, China, 2020. Emerg Infect Dis. 2020;26:1628–1631. pmid:32240078
15. Smith SH, Somsen GA, Van Rijn C, Kooij S, Van Der Hoek L, Bem RA, et al. Aerosol persistence in relation to possible transmission of SARS-CoV-2. Phys Fluids (1994). 2020;32:107108. pmid:33154612
16. Iwamura N, Tsutsumi K. SARS-CoV-2 airborne infection probability estimated by using indoor carbon dioxide. Environ Sci Pollut Res Int. 2023;30:79227–79240. pmid:37286835
17. Park S, Song D. CO2 concentration as an indicator of indoor ventilation performance to control airborne transmission of SARS-CoV-2. J Infect Public Health. 2023;16:1037–1044. pmid:37196366
18. Wells WF. Airborne contagion and air hygiene: an ecological study of droplet infections. Commonwealth Fund; 1955.
19. Riley EC, Murphy G, Riley RL. Airborne spread of measles in a suburban elementary school. Am J Epidemiol. 1978;107:421–432. pmid:665658
20. Buonanno G, Stabile L, Morawska L. Estimation of airborne viral emission: quanta emission rate of SARS-CoV-2 for infection risk assessment. Environ Int. 2020;141:105794. pmid:32416374
21. Wiryasaputra R, Huang CY, Kristiani E, Liu PY, Yeh TK, Yang CT. Review of an intelligent indoor environment monitoring and management system for COVID-19 risk mitigation. Front Public Health. 2022;10:1022055. pmid:36703846
22. Saeedi R, Ahmadi E, Hassanvand MS, Mohasel MA, Yousefzadeh S, Safari M. Implemented indoor airborne transmission mitigation strategies during COVID-19: a systematic review. J Environ Health Sci Eng. 2023;21:11–20. pmid:37152068
23. Tang H, Pan Z, Li C. Tempo-spatial infection risk assessment of airborne virus via CO2 concentration field monitoring in built environment. Build Environ. 2022;217:109067. https://doi.org/10.1016/j.buildenv.2022.109067.
24. Vanhaeverbeke J, Deprost E, Bonte P, Strobbe M, Nelis J, Volckaert B, et al. Real-time estimation and monitoring of COVID-19 aerosol transmission risk in office buildings. Sensors (Basel). 2023;23:2459. pmid:36904663
25. Ishigaki Y, Kawauchi Y, Yokogawa S, Saito A, Kitamura H, Moritake T. Ventilatory effects of excessive plastic sheeting on the formation of SARS-CoV-2 in a closed indoor environment. EOH-P. 2023;5. https://doi.org/10.1539/eohp.2022-0024-OA.
26. Ishigaki Y, Yokogawa S, Minamoto Y, Saito A, Kitamura H, Kawauchi Y. Pilot evaluation of possible airborne transmission in a geriatric care facility using carbon dioxide tracer gas: case study. JMIR Form Res. 2022;6:e37587. pmid:36583933
27. Kitamura H, Ishigaki Y, Ohashi H, Yokogawa S. Ventilation improvement and evaluation of its effectiveness in a Japanese manufacturing factory. Sci Rep. 2022;12:17642. pmid:36271253
28. Taylor JG, Yates TA, Mthethwa M, Tanser F, Abubakar I, Altamirano H. Measuring ventilation and modelling M. tuberculosis transmission in indoor congregate settings, rural KwaZulu-Natal. Int J Tuberc Lung Dis. 2016;20:1155–1161. pmid:27510239
29. Andrews JR, Morrow C, Walensky RP, Wood R. Integrating social contact and environmental data in evaluating tuberculosis transmission in a South African township. J Infect Dis. 2014;210:597–603. pmid:24610874
30. Yasuda T, Yonemura S, Tani A. Comparison of the Characteristics of Small Commercial NDIR CO2 Sensor Models and Development of a Portable CO2 Measurement Device. Sensors. 2012; 12(3):3641−3655. pmid:22737029
31. Wood R, Morrow C, Ginsberg S, Piccoli E, Kalil D, Sassi A, et al. Quantification of shared air: a social and environmental determinant of airborne disease transmission. PLOS ONE. 2014;9:e106622. pmid:25181526
32. Patterson B, Morrow CD, Kohls D, Deignan C, Ginsburg S, Wood R. Mapping sites of high TB transmission risk: integrating the shared air and social behaviour of TB cases and adolescents in a South African township. Sci Total Environ. 2017;583:97–103. pmid:28109661
33. WHO, Report of the WHO-China joint mission on coronavirus disease 2019 (COVID-19), https://www.who.int/publications/i/item/report-of-the-who-china-joint-mission-on-coronavirus-disease-2019-(covid-19), [accessed 17 July 2020]; 2020.
34. Kuba Y, Nihei M, Tetsuya K, Minori O, Maeshiro N, Kudeken T, et al. Household transmission of novel coronavirus infection (COVID-19) in Okinawa Prefecture [in Japanese]. IASR. Available from: https://www.niid.go.jp/niid/ja/2019-ncov/2502-idsc/iasr-in/9880-487d04.html. Vol. 41(9); 2020. p. 173−174.
35. Cheng HY, Jian SW, Liu DP, Ng TC, Huang WT, Lin HH, et al. Contact tracing assessment of COVID-19 transmission dynamics in Taiwan and risk at different exposure periods before and after symptom onset. JAMA Intern Med. 2020;180:1156–1163. pmid:32356867
36. Burke RM, Midgley CM, Dratch A, Fenstersheib M, Haupt T, Holshue M, et al. Active monitoring of persons exposed to patients with confirmed COVID-19—United States, January–February 2020. MMWR Morb Mortal Wkly Rep. 2020;69:245–246. pmid:32134909
37. Park YJ, Choe YJ, Park O, Park SY, Kim YM, Kim J, et al. Contact tracing during coronavirus disease outbreak, South Korea, 2020. Emerg Infect Dis. 2020;26:2465–2468. pmid:32673193
38. Jing QL, Liu MJ, Zhang ZB, Fang LQ, Yuan J, Zhang AR, et al. Household secondary attack rate of COVID-19 and associated determinants in Guangzhou, China: a retrospective cohort study. Lancet Infect Dis. 2020;20:1141–1150. pmid:32562601
39. Katelaris AL, Wells J, Clark P, Norton S, Rockett R, Arnott A, et al. Epidemiologic evidence for airborne transmission of SARS-CoV-2 during church singing, Australia, 2020. Emerg Infect Dis. 2021;27:1677–1680. pmid:33818372
40. Jang S, Han SH, Rhee JY. Cluster of coronavirus disease associated with fitness dance classes, South Korea. Emerg Infect Dis. 2020;26:1917–1920. pmid:32412896
41. Saikawa H. Tokyo police, officials visit eateries not complying with requests to cut hours amid virus, Mainichi Japan, https://mainichi.jp/english/articles/20210807/p2a/00m/0na/005000c [accessed 17 July 2023]; 2021.
42. Kyoto Prefecture website [cited Jul 17 2023]. Available from: https://www.pref.kyoto.jp/sanroso/news/co2monitoring-data.html
43. Endo S, Yokogawa S. Analysis of the trends between indoor carbon dioxide concentration and plug-level electricity usage through topological data analysis. IEEE Sens J. 2021;22(2):1424–1434. https://doi.org/10.1109/JSEN.2021.3130570.
44. Lyu X, Luo Z, Shao L, Awbi H, Lo Piano SL. Safe CO2 threshold limits for indoor long-range airborne transmission control of COVID-19. Build Environ. 2023;234:109967. https://doi.org/10.1016/j.buildenv.2022.109967.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2024 Ishigaki, Yokogawa. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
We employed carbon dioxide (CO2) concentration monitoring using mobile devices to identify location-specific risks for airborne infection transmission. We lent a newly developed, portable Pocket CO2 Logger to 10 participants, to be carried at all times, for an average of 8 days. The participants recorded their location at any given time as cinema, gym, hall, home, hospital, other indoors, other outgoings, pub, restaurant, university, store, transportation, or workplace. Generalized linear mixed model was used for statistical analysis, with the objective variable set to the logarithm of CO2 concentration. Analysis was performed by assigning participant identification as the random effect and location as the fixed effect. The data were collected per participant (seven males, four females), resulting in a total of 12,253 records. Statistical analysis identified three relatively poorly ventilated locations (median values > 1,000 ppm) that contributed significantly (p < 0.0001) to CO2 concentrations: homes (1,316 ppm), halls (1,173 ppm), and gyms (1005ppm). In contrast, two locations were identified to contribute significantly (p < 0.0001) to CO2 concentrations but had relatively low average values (<1,000 ppm): workplaces (705 ppm) and stores (620 ppm). The Pocket CO2 Logger can be used to visualize airborne infectious transmission risk by location to help guide recommendation regarding infectious disease policies, such as restrictions on human flow and ventilation measures and guidelines. In the future, large-scale surveys are expected to utilize the global positioning system, Wi-Fi, or Bluetooth of an individual’s smartphone to improve ease and accuracy.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer