COVID-19 Surveillance Program
Background:
COVID-19 workplace clusters, particularly in large industry factories, have been frequently reported over the last year, despite preventative measures and workplace guidelines being published1, 2. On-site employee screening using RT-PCR and RTK-Antigen testing have been adopted by organizations, but is not conducted on a repeated basis due to the costs involved from mass testing as well as resources required for coordination. Therefore, unless repeat tests and close monitoring take place, the risk of COVID-19 transmission and exposure among employees still remains. Lengthy quarantine periods and decontamination of premises reduces productivity levels which ultimately leads to financial losses suffered by an organization.
COVID-19 Surveillance Program
Our Pathology Partner, one of the first laboratories accredited by the Ministry of Health to conduct the ‘gold standard’ RT-PCR test for COVID-19, has taken the initiative to develop a COVID-19 Surveillance Program which is a cost-competitive and effective way to routinely screen employees to reduce the risk of economic downtime. Details are as follows:
- Minimum duration of 6 months.
- Employees are grouped (e.g. department / work shifts) and a test schedule is provided.
- Employees in each group are required to provide an initial blood sample to test for COVID-19 antibody levels. Baseline antibody levels provide visibility to which employees have been previously exposed to COVID-19 and would enable employee classification into higher and lower risk groups. Blood antibody levels are encouraged to be repeated midway and at the end of the surveillance program.
- Employees in each group are required to provide a small sample of saliva (2 mls) in a specimen container once a week throughout the entire duration of the program. These samples will be picked up by our courier services and transported to our laboratory for RT-PCR testing. Alternatively, arrangements can be made whereby employees can provide samples at the nearest Gribbles branch.
- A list of employee results will be electronically delivered to the Company after each weekly session within 24 hours upon sample arrival at the laboratory.
- Employees who are found to be positive from the saliva test will go through the standard process of notifying the relevant Health authorities.
Benefits to Company
- Ability to identify low / high risk groups which will help in work shift planning purposes
- Early detection of positive cases which will help facilitate rapid and effective quarantine measures for affected groups only, thereby minimizing economic downtime
- Testing is done in a reliable manner, as RT-PCR methodology is used3
- Minimum resources required for saliva testing (also less discomfort experienced)
- Significant cost-savings compared to traditional on-site screening (Appendix 1)
Internal Findings
- Our Pathology Partner had begun conducting the Surveillance Program beginning 18th January 2021 on a total of 799 employees across 43 sites nationwide.
- To date, a total of 9 asymptomatic employees were detected positive via the Surveillance Program.
- All 9 employees were also found to be positive in the confirmatory RT-PCR test which demonstrates 100% correlation between saliva and conventional method of RT-PCR testing.
References:
- https://www.malaymaicom/news/malaysia/2021/02/08/occupational-hazard-health-ministry-shows- 11-out-of-13-covid-19-clusters-ac/1948071
- ANNEX 25 : COVID-19 Management Guidelines For Workplace (Ministry of Health)
- ANNEX 4i : GuidelineOn The Use Of Deep Throat Saliva To Test For COVID-19 By RT-qPCR (Ministry of Health)
Appendix 1 – Pricing
|
Pax (Per Site) |
Saliva rt PCR / Pax (RM) |
Total Antibody / Pax (RM) |
|
< 100 |
100.00 |
50.00 |
|
100-199 |
90.00 |
45.00 |
|
200-499 |
80.00 |
40.00 |
|
>500 |
70.00 |
35.00 |
Note:
- Any positive result will incur additional surcharge of RM 100.00 per pax for retesting purposes (for PCR only)
- Results electronically delivered within 24 hours upon sample arrival at laboratory
- Additional 10% discount off invoice if Company agrees to commit to 12 months surveillance period