Experimental
Experimental
Original Article
a r t i c l e i n f o a b s t r a c t
Article history: Background: Many health care workers around the world tackled with COVID-19, however sadly, the
Received 27 January 2021 infection of many medical care workers were reported. To reduce the risk of infection, we launched
Received in revised form 27 July 2021 selected team (Team COVID) of non-specialists and brought in active telemedicine method and computed
Accepted 15 August 2021
tomography (CT)-first protocol. We describe our actual practice and the health status of medical doctors
dealing with COVID-19 patients.
Keywords:
Methods: Between April 17, 2020 and May 24, 2020, 10 doctors worked with COVID-19 patients as part
COVID-19
of Team COVID. The Team COVID doctors used a CT-first triage protocol for outpatients and telemedicine
CT-first triage
Health of medical stuff
for inpatients and outpatients. We evaluated paired serum-specific antibodies for SARS-CoV-2 at the
Medical care team initial and end of the study duration and PCR results for SARS-CoV-2 at the end of the study duration.
Telemedicine Furthermore, 36-item short-form of the Medical Outcome Study Questionnaire (SF-36) at the beginning
and end of the study period were evaluated.
Results: Ten doctors worked as Team COVID: seven internal medicine doctors and three surgeons. During
the study period, Team COVID treated 165 individuals in the outpatient clinic and isolated hospital-
ized patients for 315 person-days. There were no positive results of serum-specific antibody testing and
PCR testing for SARS-CoV-2 in Team COVID doctors. Furthermore, the SF-36 showed no deterioration in
physical and mental QOL status. No in-hospital infection occurred during the study period.
Conclusions: The Team COVID fulfilled the treatment using the active telemedicine and CT-first triage
protocol without in hospital infection and excess stress. The combination strategy seems acceptable for
both the protection and stress relief among the medical staff.
© 2021 The Author(s). Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for
Health Sciences. This is an open access article under the CC BY-NC-ND license ([Link]
org/licenses/by-nc-nd/4.0/).
Abbreviations: CO-RADS, coronavirus disease 2019 reporting and data system; COVID-19, coronavirus disease 2019; CT, computed tomography; ELISA, enzyme linked
immunosorbent assay; MCS, Mental Component Summary; PCR, polymerase chain reaction; PCS, Physical Component Summary; PPE, personal protective equipment; QOL,
quality of life; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; SF-36, 36-item short form of the medical outcome study questionnaire.
∗ Corresponding author at: Department of Gastroenterology and Hepatology, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa, Yokohama
2360004, Japan.
E-mail address: takuma h@[Link] (T. Higurashi).
[Link]
1876-0341/© 2021 The Author(s). Published by Elsevier Ltd on behalf of King Saud Bin Abdulaziz University for Health Sciences. This is an open access article under the CC
BY-NC-ND license ([Link]
S. Miyake et al. Journal of Infection and Public Health 14 (2021) 1212–1217
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Table 1
Participants characteristics.
Team COVID
Number 10
Age 33.8 ± 6.5
Sex (male, female) 9, 1
Internal medicine 7
Specialty Surgery 3
Infection 0
History of overseas 0
Rich contact with COVID-19 0
extraction was used for the reaction of Real Time quantitative PCR
(RT-qPCR). The RT-qPCR Reaction Mix was prepared with TaqMan
Fast Virus 1-Step Master Mix (Thermo Fisher Scientific, City) and
Primer/Probe N2 (2019-nCoV) (TAKARA, City, japan) according to
the manufacture’s protocol. The sequences of the primers were
shown in the supplementary Table 1. Denature and anneal/extend
steps were repeated 45 cycles. Absolutely quantified artificial syn-
thetic template RNA was used as positive control, whereas the well
that contain no template RNA was used as negative control. Accord-
ing to the Manual [23], the assay was considered valid when the
assay meets the following criteria; the 50 copies/well of template
RNA was successfully detected before 40 cycles. (b) The nonspe-
cific amplification was not detected in the well with no template
RNA until 45 cycles. The sample that was detected the amplifica-
tion of COVID-19 genomic RNA before 40 cycles was determined as
positive for COVID-19 in this study.
We previously reported the methodology of serological testing
[24,25]. In brief, enzyme linked immunosorbent assay (ELISA) was
performed to detect and quantify anti–SARS-CoV-2 antibodies in
plasma. We used n coronavirus-N-terminally truncated nucleocap-
sid protein as the antigen. In serological test, cut-off of COVID-19
Fig. 1. Active telemedicine method for COVID-19 suspected patients. antibody positive was over 0.45.
The applications for the active telemedicine method were shown. (A) The temporary
tent for the feverish outpatients. (B) The intercom in the temporary tent. The inter-
com connected outpatient and medical staff without contact. (C) The room camera
Statistical analysis
of isolating inpatient. (D) The medical question through the nurse call phone. (E)
The isolating inpatient area.
The results are presented as means for the quantitative
data and as frequencies (percentage) for categorical data. The
Calculation Mann–Whitney U test was used for continuous data. A p value <0.05
was considered statistically significant. All statistical analyses were
Outcome performed using JMP® 15 (SAS Institute Inc., Cary, NC, USA).
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