Literature DB >> 32299521

Environmental cleaning is effective for the eradication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus in contaminated hospital rooms: A patient from the Diamond Princess cruise ship.

Yosuke Hirotsu1, Makoto Maejima2, Masumi Nakajima3, Hitoshi Mochizuki1,4, Masao Omata4,5.   

Abstract

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Year:  2020        PMID: 32299521      PMCID: PMC7308617          DOI: 10.1017/ice.2020.144

Source DB:  PubMed          Journal:  Infect Control Hosp Epidemiol        ISSN: 0899-823X            Impact factor:   3.254


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To the Editor—Doctors, nurses, and other medical staff are greatly concerned about nosocomial outbreaks of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Environmental contamination is a possible source of nosocomial transmission.[1,2] However, how effective environmental cleaning is against SARS-CoV-2 remains unclear. A 75-year-old man infected with SARS-CoV-2 was diagnosed with COVID-19 during the quarantine period on the Diamond Princess cruise ship. He was transferred directly to our hospital on February 11, 2020. He resided in patient room A for 2 days then was moved to room B, where he stayed for 19 days. After cleaning the rooms thoroughly with disinfectant (Rely+On Virkon, LANXESS, or RUBYSTA in Japan), we tested 15 areas that were in close contact with the patient and medical staff. Swabs were used to transfer 5 environmental samples from room A and 10 samples from room B to universal transport media (Copan, Murrieta, CA). Cleaning was conducted immediately after the patient left the rooms. Environmental sampling was conducted within 5 days and 30 min after the patient left rooms A and B, respectively. Nucleic acids were extracted using MagMAX Viral/Pathogen Nucleic Acid Isolation Kit (ThermoFisher Scientific, Waltham, MA) and were tested using real-time reverse transcription polymerase chain reaction (RT-PCR) targeting the nucleocapsid (N) gene of SARS-CoV-2. Seven sets of primers and probes (CDC-N1, CDC-N2, CDC-N3, YCH-N1, YCH-N2, NIID-N1, and NIID-N2) were used to detect SARS-CoV-2 as previously described (Supplemental Table 1 online).[3] For the internal positive control, the human ribonuclease P 30 subunit (RPP30) gene was used. The patient’s records, timing of cleaning and sampling, and RT-PCR results were collated. On admission, the patient had fever (39°C) and a mild cough (Supplemental Table 2 online). The chest X-ray and computed tomography scan on day 1 showed signs of pneumonia in both lungs. He received lopinavir/ritonavir and antibacterial therapy on day 2, but showed respiratory failure. He received supplemental oxygen from day 4 to day 15. After careful clinical management, the patient’s overall status improved. RT-PCR showed that his sputum was positive for SARS-CoV-2 on day 11. Subsequently, nasopharyngeal swabs were negative on days 17, 22, and 29. The patient stayed in room A for 3 days, during which he had the SARS-CoV-2 infection. After cleaning room A, 5 environmental samples were examined by RT-PCR. All samples were negative for SARS-CoV-2 and were positive or negative for RPP30 (Table 1).
Table 1.

Real-Time RT-PCR Analysis of Environmental Samples

LocationRT-PCR (No. of Samples)
Patient room A SARS-CoV-2Human RPP30
 Light switchNegative (0/1)Negative (0/1)
 Nurse call attached to the bedNegative (0/1)Positive (1/1)
 Toilet door handleNegative (0/1)Negative (0/1)
 Bed guardNegative (0/1)Positive (1/1)
Anterior room A
 Dust boxNegative (0/1)Positive (1/1)
Patient room B
 Bed deskNegative (0/1)Negative (0/1)
 Bed guardNegative (0/1)Negative (0/1)
 Door handleNegative (0/1)Positive (1/1)
 Dust box, room sideNegative (0/1)Negative (0/1)
 Dust box, corridorNegative (0/1)Positive (1/1)
 Control panel on mechanical ventilationNegative (0/1)Positive (1/1)
 Light switchNegative (0/1)Negative (0/1)
 Nurse callNegative (0/1)Positive (1/1)
 Hand soap dispenserNegative (0/1)Negative (0/1)
Anterior room B
 Sink, external rim and internal bowlNegative (0/1)Positive (1/1)

Note. PCR, polymerase chain reaction; RPP30, ribonuclease P 30 subunit; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

Real-Time RT-PCR Analysis of Environmental Samples Note. PCR, polymerase chain reaction; RPP30, ribonuclease P 30 subunit; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2. After the patient left room A, he resided in room B for 20 days. Ten environmental samples were collected after cleaning. All 10 samples from room B were negative for SARS-CoV-2 and were positive or negative for RPP30 (Table 1). SARS-CoV-2 is detectable in several types of clinical samples including bronchial lavage fluid, nasopharyngeal swab, pharyngeal swab, sputum, saliva, and feces.[4,5] Transmission of SARS-CoV-2 via surfaces in hospitals is of great concern to medical staff and patients. Blocking the potential routes of transmission is essential for preventing the spread of SARS-CoV-2.[6] A recent study showed that environmental contamination can occur via contact with patients with SARS-CoV-2 and upper respiratory tract symptoms.[7] After cleaning, all areas were negative for SARS-CoV-2; therefore, thorough cleaning is sufficient for SARS-CoV-2 decontamination. This study had several limitations. First, RT-PCR was not performed before cleaning because of the risk of nosocomial transmission. Therefore, a comparison of the viral loads of high-touch areas before and after cleaning is required. Second, this study involved a single patient, and further studies are required to confirm these findings. In summary, our data indicate the effectiveness of environmental cleaning for SARS-CoV-2 decontamination. This information is useful for infection control strategies and may alleviate the concerns of medical staff.
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