key: cord-0829021-7iufbaxy authors: Kerimov, Dominik; Tamminen, Pekka; Viskari, Hanna; Lehtimäki, Lauri; Aittoniemi, Janne title: Sampling site for SARS-CoV-2 RT-PCR—An intrapatient four-site comparison from Tampere, Finland date: 2021-11-16 journal: PLoS One DOI: 10.1371/journal.pone.0260184 sha: 93fde21fc952ee33accdcd2b6e00a013a653ca24 doc_id: 829021 cord_uid: 7iufbaxy BACKGROUND: SARS-CoV-2 diagnosis relies on the performance of nasopharyngeal swabs. Alternative sample sites have been assessed but the heterogeneity of the studies have made comparing different sites difficult. OBJECTIVES: Our aim was to compare the performance of four different sampling sites for SARS-CoV-2 samples with nasopharynx being the benchmark. STUDY DESIGN: COVID-19 positive patients were recruited prospectively, and samples were collected and analysed for SARS-CoV-2 with RT-PCR from all four anatomical sites in 43 patients, who provided written informed consent. RESULTS: All anterior nasal and saliva samples were positive, while two oropharyngeal samples were negative. There was no significant difference in the cycle threshold values of nasopharyngeal and anterior nasal samples while saliva and oropharynx had higher cycle threshold values. CONCLUSIONS: Anterior nasal swab performs as good as nasopharynx swab with saliva also finding all the positives but with higher cycle threshold values. Thus, we can conclude that anterior nasal swabs can be used for SARS-CoV-2 detection instead of nasopharyngeal swabs if the situation would require so. Background After the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first identified in China in late 2019 [1] , the procedure for its reverse transcription polymerase chain reaction (RT-PCR) detection was quickly shared and a robust diagnostic methodology was established [2] . Initially, nasopharyngeal swab sample for RT-PCR was the recommended sample. Subsequently alternative sample types have been assessed and saliva and anterior nasal swab have been suggested comparable in performance to nasopharyngeal samples. [3] [4] [5] [6] [7] . However, comparing different sample sites across different studies is difficult owing to the heterogeneity of the studies [8] . Our aim was to ascertain if alternative sampling sites (oropharynx, anterior nasal or saliva) are viable for SARS-CoV-2 detection via RT-PCR in comparison to nasopharyngeal swab, and if self-collection of anterior nasal samples is feasible. The study population consisted of 43 outpatients with COVID-19 and upper respiratory symptoms including loss of smell [mean age 40 years (age range 20-70 years); 19 males], who took part in CANNAS-study from January 15th to March 25th, 2021 (R20090, NCT04728919). All patients were RT-PCR positive for SARS-CoV-2 from nasopharyngeal swab, and they had been recruited to the study during contact tracing phone call by the infectious diseases unit. The patients were from the Tampere University Hospital region, and they were recruited only if they could arrive to the study visit without exposing others. The exclusion criteria were the absence of upper respiratory symptoms, onset of symptoms over ten days ago, pregnancy or breastfeeding, and previous vaccination against COVID-19. The duration of symptoms until sample collection was on average 5.4 days (1.82 days SD). Four sampling sites per patient were selected for the study: nasopharynx, oropharynx, anterior nasal and spat saliva. Nasopharyngeal and oropharyngeal samples were collected by the same physician (D.K.) following established sample collecting guidelines. Nasopharyngeal swab samples were collected unilaterally with FLOQSwabs 503CS01 (Copan Italia SpA, Brescia, Italy) flocked swabs. Oropharyngeal samples were collected with FLOQSwabs 502CS01 (Copan Italia SpA, Brescia, Italy) or HydraFlock 25-3506-H (Puritan Medical Products Company LLC, Guilford, USA) flocked swabs. The anterior nasal samples were collected by the patients themselves with FLOQSwabs 502CS01 or HydraFlock 25-3506-H flocked swabs. The sampling site in this study refers to the area behind the nasal vestibulum, confined by medial and superior aspect of the inferior turbinate, the nasal septum, anterior aspect of the middle turbinate and the dorsum. The same swab was applied to both nares and the patient was instructed to rotate the swab at the site for 10 seconds. For saliva samples, patients were asked to clear their throat and then proceed to collect saliva in their mouths for ten seconds. Saliva was spat into a 50-millilitre conical-bottom polypropylene centrifuge tube. The collection was repeated three times or until the bottom cone of the tube was full (approximately four millilitres). When self-collecting samples (saliva and anterior nasal), patients followed written and illustrated instructions under physician supervision. The physician did not need to intervene in the sample self-collection process as no safety issues were encountered. The transport medium used for the swab samples was UTM Mini 3 ml 353C (Copan Italia SpA, Brescia, Italy). Swab sample transport medium was analysed undiluted whereas all saliva samples were diluted with phosphate buffered saline with a ratio of 1:1 regardless of the sample volume collected to reduce sample viscosity. The analysis of all the samples was performed at Fimlab Laboratories alongside regular COVID-19-samples with standard operating procedures and personnel with Allplex™ 2019-nCoV Assay (Seegene Inc, Seoul, South Korea) RT-PCR for SARS-CoV-2 with three target genes (N-, Rdrp-and E-genes). The cycle threshold (Ct) values of each target were given by the RT-PCR protocol. A sample site was defined positive if at least one target gene other than E had Ct value �40. All tests were done in accordance with the manufacturer's instructions. The study was approved by the Tampere University Hospital Ethical committee (R20090, registered at clinicaltrials.gov NCT04728919) and all the patients provided written informed consent. Out of the 43 patients with positive nasopharyngeal sample, all gave a positive anterior nasal and saliva samples while two oropharyngeal samples were negative ( exact test). There were no statistically significant differences between the median Ct values of self-collected anterior nasal cavity samples when compared to the nasopharynx. However, the median Ct values of oropharyngeal and saliva samples were higher in comparison to nasopharyngeal samples (Table 1 , Fig 1) . The two self-collected sample types, anterior nasal cavity and saliva showed no statistically significant difference in Ct values (p = 0.316). The Ct values of anterior nasal, oropharyngeal and saliva samples correlated significantly with those of the nasopharyngeal in the whole group level. Previous studies have identified saliva [9] and anterior nasal swabs [10] as viable alternatives to nasopharyngeal swab in SARS-CoV-2-diagnosis. The current results are in line with this. The Sampling site comparison for SARS-CoV-2 RT-PCR less invasive, self-collected anterior nasal swab was comparable to nasopharyngeal swab in symptomatic and relatively high viral load patients: all positive cases were found with no significant difference in median Ct values. Saliva samples also found all positives, but at higher Ct values. Anterior nasal samples had wider inter-quartile ranges in Ct values, which we assume to result from the self-collection of samples. Confounding factors were controlled by using the same type of swab device in certain anatomical site, same transport medium across all swab samples, having the same person collecting all the nasopharyngeal and oropharyngeal samples and using the same RT-PCR assay and laboratory. Pandemic has continued for over a year, refusal of testing seems to be emerging as a new challenge [11] . Providing a possibility of a less invasive sample collection method might be helpful in improving test compliance. Alternative testing sites may also be needed e.g. for people with coagulation disorders predisposed to bleeding or for children. Even though nasopharyngeal sampling is safe, serious complications can occur [12] and compared to the nasopharynx, anterior nasal cavity is easier to access if local treatment of sampling site trauma is needed. Also, self-collected samples open additional avenues to improving testing coverage and by implementing controlled self-testing, the need of protective equipment and medical staff is reduced, and patients might be more willing to get themselves tested if the sample was self-collected. The challenge, though, is maintaining high standards of testing so that results are still reliable. The study included 43 SARS-CoV-2 RT-PCR positive outpatients. Confounding factors were carefully controlled but due to the sample size we cannot rule out the possibility of minor differences. In addition, our study did not recruit any asymptomatic patients so the behaviour of their samples could differ from those of symptomatic patients. Writing -review & editing: Dominik Kerimov, Pekka Tamminen, Hanna Viskari, Lauri Lehtimäki, Janne Aittoniemi. A Novel Coronavirus from Patients with Pneumonia in China Detection of 2019 -nCoV by RT-PCR Saliva as a noninvasive specimen for detection of sars-cov-2 Saliva or Nasopharyngeal Swab Specimens for Detection of SARS-CoV-2 Comparing saliva and nasopharyngeal swab specimens in the detection of COVID-19: A systematic review and meta-analysis Diagnostic performance of different sampling approaches for SARS-CoV-2 RT-PCR testing: a systematic review and meta-analysis Performance of Saliva, Oropharyngeal Swabs, and Nasal Swabs for SARS-CoV-2 Molecular Detection: a Systematic Review and Meta-analysis Diagnosis of SARS-CoV-2 Infection Using Specimens Other than Naso-and Oropharyngeal Swabs: A Systematic Review and Meta-Analysis Comparison of Saliva and Nasopharyngeal Swab Nucleic Acid Amplification Testing for Detection of SARS-CoV-2: A Systematic Review and Meta-analysis Self-collected anterior nasal and saliva specimens versus health care worker-collected nasopharyngeal swabs for the molecular detection of SARS-CoV-2 First It Was Masks; Now Some Refuse Testing for SARS-CoV-2 Complications of COVID-19 Nasopharyngeal Swab Test The authors would like to thank study nurses Merja Rumpunen and Tiina Mäki as well as the contact tracing unit from Tampere University Hospital for patient management and guidance. The authors would also like to thank statistician Mika Helminen from Tampere University Hospital for his advice on statistical analysis.