Detection of Severe Acute Respiratory Syndrome Coronavirus 2 on Self-Collected Saliva or Anterior Nasal Specimens Compared With Healthcare Personnel–Collected Nasopharyngeal Specimens
BACKGROUNDNasopharyngeal specimens (NPS) are commonly used for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing but can be uncomfortable for patients. Self-collected saliva specimens (SS) or anterior nasal specimens (ANS) for SARS-CoV-2 detection are less invasive, but the sensit...
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creator | Marx, Grace E Biggerstaff, Brad J Nawrocki, Courtney C Totten, Sarah E Travanty, Emily A Burakoff, Alexis W Scott, Tracy De Hey, Jesse Chavez-Van Carlson, Jesse J Wendel, Karen A Harcourt, Jennifer L Tamin, Azaibi Thomas, Jennifer D Rowan, Sarah E Matzinger, Shannon R Hudziec, Meghan Hetherington-Rauth, Molly C Pysnack, Nicholas J Delmonico, Christopher Huynh-Templeman, Kimberly Stitzlein, Tara M Rossheim, Alexandria E B Folster, Jennifer Medrzycki, Magdalena Wong, Phili Jain, Shilpi Thornburg, Natalie |
description | BACKGROUNDNasopharyngeal specimens (NPS) are commonly used for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing but can be uncomfortable for patients. Self-collected saliva specimens (SS) or anterior nasal specimens (ANS) for SARS-CoV-2 detection are less invasive, but the sensitivity of these specimen types has not been thoroughly evaluated. METHODSDuring September-November 2020, 730 adults undergoing SARS-CoV-2 testing at community testing events and homeless shelters in Denver provided self-collected SS and ANS before NPS collection and answered a short survey about symptoms and specimen preference. Specimens were tested for SARS-CoV-2 by means of real-time reverse-transcription polymerase chain reaction (rRT-PCR); viral culture was performed on a subset of specimens positive by rRT-PCR. The sensitivity of SS and ANS for SARS-CoV-2 detection by rRT-PCR was measured against that of NPS. Subgroup analyses included test outcomes by symptom status and culture results. RESULTSSensitivity for SARS-CoV-2 detection by rRT-PCR appeared higher for SS than for ANS (85% vs 80%) and higher among symptomatic participants than among those without symptoms (94% vs 29% for SS; 87% vs 50% for ANS). Among participants with culture-positive SARS-CoV-2 by any specimen type, the sensitivities of SS and ANS by rRT-PCR were 94% and 100%, respectively. SS and ANS were equally preferred by participants; most would undergo NPS collection again despite this method's being the least preferred. CONCLUSIONSSS were slightly more sensitive than ANS for SARS-CoV-2 detection with rRT-PCR. With both SS and ANS, SARS-CoV-2 was reliably detected among participants with symptoms. Self-collected SS and ANS offer practical advantages, are preferred by patients, and might be most useful for testing people with coronavirus disease 2019 symptoms. |
doi_str_mv | 10.1093/cid/ciab330 |
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Self-collected saliva specimens (SS) or anterior nasal specimens (ANS) for SARS-CoV-2 detection are less invasive, but the sensitivity of these specimen types has not been thoroughly evaluated. METHODSDuring September-November 2020, 730 adults undergoing SARS-CoV-2 testing at community testing events and homeless shelters in Denver provided self-collected SS and ANS before NPS collection and answered a short survey about symptoms and specimen preference. Specimens were tested for SARS-CoV-2 by means of real-time reverse-transcription polymerase chain reaction (rRT-PCR); viral culture was performed on a subset of specimens positive by rRT-PCR. The sensitivity of SS and ANS for SARS-CoV-2 detection by rRT-PCR was measured against that of NPS. Subgroup analyses included test outcomes by symptom status and culture results. RESULTSSensitivity for SARS-CoV-2 detection by rRT-PCR appeared higher for SS than for ANS (85% vs 80%) and higher among symptomatic participants than among those without symptoms (94% vs 29% for SS; 87% vs 50% for ANS). Among participants with culture-positive SARS-CoV-2 by any specimen type, the sensitivities of SS and ANS by rRT-PCR were 94% and 100%, respectively. SS and ANS were equally preferred by participants; most would undergo NPS collection again despite this method's being the least preferred. CONCLUSIONSSS were slightly more sensitive than ANS for SARS-CoV-2 detection with rRT-PCR. With both SS and ANS, SARS-CoV-2 was reliably detected among participants with symptoms. Self-collected SS and ANS offer practical advantages, are preferred by patients, and might be most useful for testing people with coronavirus disease 2019 symptoms.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/ciab330</identifier><language>eng</language><ispartof>Clinical infectious diseases, 2021-07, Vol.73 (Supplement_1), p.S65-S73</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c331t-f3568a9ec4aa86a63071c6f6923140e07879c568da48c7d502e6bef254f22a6c3</citedby><cites>FETCH-LOGICAL-c331t-f3568a9ec4aa86a63071c6f6923140e07879c568da48c7d502e6bef254f22a6c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Marx, Grace E</creatorcontrib><creatorcontrib>Biggerstaff, Brad J</creatorcontrib><creatorcontrib>Nawrocki, Courtney C</creatorcontrib><creatorcontrib>Totten, Sarah E</creatorcontrib><creatorcontrib>Travanty, Emily A</creatorcontrib><creatorcontrib>Burakoff, Alexis W</creatorcontrib><creatorcontrib>Scott, Tracy</creatorcontrib><creatorcontrib>De Hey, Jesse Chavez-Van</creatorcontrib><creatorcontrib>Carlson, Jesse J</creatorcontrib><creatorcontrib>Wendel, Karen A</creatorcontrib><creatorcontrib>Harcourt, Jennifer L</creatorcontrib><creatorcontrib>Tamin, Azaibi</creatorcontrib><creatorcontrib>Thomas, Jennifer D</creatorcontrib><creatorcontrib>Rowan, Sarah E</creatorcontrib><creatorcontrib>Matzinger, Shannon R</creatorcontrib><creatorcontrib>Hudziec, Meghan</creatorcontrib><creatorcontrib>Hetherington-Rauth, Molly C</creatorcontrib><creatorcontrib>Pysnack, Nicholas J</creatorcontrib><creatorcontrib>Delmonico, Christopher</creatorcontrib><creatorcontrib>Huynh-Templeman, Kimberly</creatorcontrib><creatorcontrib>Stitzlein, Tara M</creatorcontrib><creatorcontrib>Rossheim, Alexandria E B</creatorcontrib><creatorcontrib>Folster, Jennifer</creatorcontrib><creatorcontrib>Medrzycki, Magdalena</creatorcontrib><creatorcontrib>Wong, Phili</creatorcontrib><creatorcontrib>Jain, Shilpi</creatorcontrib><creatorcontrib>Thornburg, Natalie</creatorcontrib><creatorcontrib>Centers for Disease Control and Prevention COVID-19 Laboratory Response Team</creatorcontrib><creatorcontrib>Colorado Department of Public Health and Environment COVID-19 Laboratory Response Team</creatorcontrib><title>Detection of Severe Acute Respiratory Syndrome Coronavirus 2 on Self-Collected Saliva or Anterior Nasal Specimens Compared With Healthcare Personnel–Collected Nasopharyngeal Specimens</title><title>Clinical infectious diseases</title><description>BACKGROUNDNasopharyngeal specimens (NPS) are commonly used for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing but can be uncomfortable for patients. Self-collected saliva specimens (SS) or anterior nasal specimens (ANS) for SARS-CoV-2 detection are less invasive, but the sensitivity of these specimen types has not been thoroughly evaluated. METHODSDuring September-November 2020, 730 adults undergoing SARS-CoV-2 testing at community testing events and homeless shelters in Denver provided self-collected SS and ANS before NPS collection and answered a short survey about symptoms and specimen preference. Specimens were tested for SARS-CoV-2 by means of real-time reverse-transcription polymerase chain reaction (rRT-PCR); viral culture was performed on a subset of specimens positive by rRT-PCR. The sensitivity of SS and ANS for SARS-CoV-2 detection by rRT-PCR was measured against that of NPS. Subgroup analyses included test outcomes by symptom status and culture results. RESULTSSensitivity for SARS-CoV-2 detection by rRT-PCR appeared higher for SS than for ANS (85% vs 80%) and higher among symptomatic participants than among those without symptoms (94% vs 29% for SS; 87% vs 50% for ANS). Among participants with culture-positive SARS-CoV-2 by any specimen type, the sensitivities of SS and ANS by rRT-PCR were 94% and 100%, respectively. SS and ANS were equally preferred by participants; most would undergo NPS collection again despite this method's being the least preferred. CONCLUSIONSSS were slightly more sensitive than ANS for SARS-CoV-2 detection with rRT-PCR. With both SS and ANS, SARS-CoV-2 was reliably detected among participants with symptoms. Self-collected SS and ANS offer practical advantages, are preferred by patients, and might be most useful for testing people with coronavirus disease 2019 symptoms.</description><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpNkdFK5DAUhous4KzulS-Qy4WlmjRN2l4Os6sjDCrWxctyTE93sqRJN8kMzJ3v4NP4Oj6JkRHWi8P5Ofz_x4E_y04ZPWO04edK92ngkXN6kM2Y4FUuRcO-JE1FnZc1r4-yryH8pZSxmopZ9vITI6qonSVuIC1u0SOZq01Ecodh0h6i8zvS7mzv3Yhk4byzsNV-E0hBUqpFM-QLZ0yiYE9aMHoLxHkytxG9TuIaAhjSTqj0iDYkxDiBT94HHddkiWDiWqUDuUUfnLVoXp-e_xNT3E1r8Dv7Bz9zTrLDAUzAbx_7OPt98et-scxXN5dXi_kqV5yzmA9cyBoaVCVALUFyWjElB9kUnJUUaVVXjUqWHspaVb2gBcpHHApRDkUBUvHj7PueO3n3b4MhdqMOCo0Bi24TukKwpmoaIWmy_thblXcheBy6yesxvd4x2r0X1KWCuo-C-BsziYnw</recordid><startdate>20210715</startdate><enddate>20210715</enddate><creator>Marx, Grace E</creator><creator>Biggerstaff, Brad J</creator><creator>Nawrocki, Courtney C</creator><creator>Totten, Sarah E</creator><creator>Travanty, Emily A</creator><creator>Burakoff, Alexis W</creator><creator>Scott, Tracy</creator><creator>De Hey, Jesse Chavez-Van</creator><creator>Carlson, Jesse J</creator><creator>Wendel, Karen A</creator><creator>Harcourt, Jennifer L</creator><creator>Tamin, Azaibi</creator><creator>Thomas, Jennifer D</creator><creator>Rowan, Sarah E</creator><creator>Matzinger, Shannon R</creator><creator>Hudziec, Meghan</creator><creator>Hetherington-Rauth, Molly C</creator><creator>Pysnack, Nicholas J</creator><creator>Delmonico, Christopher</creator><creator>Huynh-Templeman, Kimberly</creator><creator>Stitzlein, Tara M</creator><creator>Rossheim, Alexandria E B</creator><creator>Folster, Jennifer</creator><creator>Medrzycki, Magdalena</creator><creator>Wong, Phili</creator><creator>Jain, Shilpi</creator><creator>Thornburg, Natalie</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20210715</creationdate><title>Detection of Severe Acute Respiratory Syndrome Coronavirus 2 on Self-Collected Saliva or Anterior Nasal Specimens Compared With Healthcare Personnel–Collected Nasopharyngeal Specimens</title><author>Marx, Grace E ; Biggerstaff, Brad J ; Nawrocki, Courtney C ; Totten, Sarah E ; Travanty, Emily A ; Burakoff, Alexis W ; Scott, Tracy ; De Hey, Jesse Chavez-Van ; Carlson, Jesse J ; Wendel, Karen A ; Harcourt, Jennifer L ; Tamin, Azaibi ; Thomas, Jennifer D ; Rowan, Sarah E ; Matzinger, Shannon R ; Hudziec, Meghan ; Hetherington-Rauth, Molly C ; Pysnack, Nicholas J ; Delmonico, Christopher ; Huynh-Templeman, Kimberly ; Stitzlein, Tara M ; Rossheim, Alexandria E B ; Folster, Jennifer ; Medrzycki, Magdalena ; Wong, Phili ; Jain, Shilpi ; Thornburg, Natalie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c331t-f3568a9ec4aa86a63071c6f6923140e07879c568da48c7d502e6bef254f22a6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marx, Grace E</creatorcontrib><creatorcontrib>Biggerstaff, Brad J</creatorcontrib><creatorcontrib>Nawrocki, Courtney C</creatorcontrib><creatorcontrib>Totten, Sarah E</creatorcontrib><creatorcontrib>Travanty, Emily A</creatorcontrib><creatorcontrib>Burakoff, Alexis W</creatorcontrib><creatorcontrib>Scott, Tracy</creatorcontrib><creatorcontrib>De Hey, Jesse Chavez-Van</creatorcontrib><creatorcontrib>Carlson, Jesse J</creatorcontrib><creatorcontrib>Wendel, Karen A</creatorcontrib><creatorcontrib>Harcourt, Jennifer L</creatorcontrib><creatorcontrib>Tamin, Azaibi</creatorcontrib><creatorcontrib>Thomas, Jennifer D</creatorcontrib><creatorcontrib>Rowan, Sarah E</creatorcontrib><creatorcontrib>Matzinger, Shannon R</creatorcontrib><creatorcontrib>Hudziec, Meghan</creatorcontrib><creatorcontrib>Hetherington-Rauth, Molly C</creatorcontrib><creatorcontrib>Pysnack, Nicholas J</creatorcontrib><creatorcontrib>Delmonico, Christopher</creatorcontrib><creatorcontrib>Huynh-Templeman, Kimberly</creatorcontrib><creatorcontrib>Stitzlein, Tara M</creatorcontrib><creatorcontrib>Rossheim, Alexandria E B</creatorcontrib><creatorcontrib>Folster, Jennifer</creatorcontrib><creatorcontrib>Medrzycki, Magdalena</creatorcontrib><creatorcontrib>Wong, Phili</creatorcontrib><creatorcontrib>Jain, Shilpi</creatorcontrib><creatorcontrib>Thornburg, Natalie</creatorcontrib><creatorcontrib>Centers for Disease Control and Prevention COVID-19 Laboratory Response Team</creatorcontrib><creatorcontrib>Colorado Department of Public Health and Environment COVID-19 Laboratory Response Team</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marx, Grace E</au><au>Biggerstaff, Brad J</au><au>Nawrocki, Courtney C</au><au>Totten, Sarah E</au><au>Travanty, Emily A</au><au>Burakoff, Alexis W</au><au>Scott, Tracy</au><au>De Hey, Jesse Chavez-Van</au><au>Carlson, Jesse J</au><au>Wendel, Karen A</au><au>Harcourt, Jennifer L</au><au>Tamin, Azaibi</au><au>Thomas, Jennifer D</au><au>Rowan, Sarah E</au><au>Matzinger, Shannon R</au><au>Hudziec, Meghan</au><au>Hetherington-Rauth, Molly C</au><au>Pysnack, Nicholas J</au><au>Delmonico, Christopher</au><au>Huynh-Templeman, Kimberly</au><au>Stitzlein, Tara M</au><au>Rossheim, Alexandria E B</au><au>Folster, Jennifer</au><au>Medrzycki, Magdalena</au><au>Wong, Phili</au><au>Jain, Shilpi</au><au>Thornburg, Natalie</au><aucorp>Centers for Disease Control and Prevention COVID-19 Laboratory Response Team</aucorp><aucorp>Colorado Department of Public Health and Environment COVID-19 Laboratory Response Team</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Severe Acute Respiratory Syndrome Coronavirus 2 on Self-Collected Saliva or Anterior Nasal Specimens Compared With Healthcare Personnel–Collected Nasopharyngeal Specimens</atitle><jtitle>Clinical infectious diseases</jtitle><date>2021-07-15</date><risdate>2021</risdate><volume>73</volume><issue>Supplement_1</issue><spage>S65</spage><epage>S73</epage><pages>S65-S73</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>BACKGROUNDNasopharyngeal specimens (NPS) are commonly used for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing but can be uncomfortable for patients. Self-collected saliva specimens (SS) or anterior nasal specimens (ANS) for SARS-CoV-2 detection are less invasive, but the sensitivity of these specimen types has not been thoroughly evaluated. METHODSDuring September-November 2020, 730 adults undergoing SARS-CoV-2 testing at community testing events and homeless shelters in Denver provided self-collected SS and ANS before NPS collection and answered a short survey about symptoms and specimen preference. Specimens were tested for SARS-CoV-2 by means of real-time reverse-transcription polymerase chain reaction (rRT-PCR); viral culture was performed on a subset of specimens positive by rRT-PCR. The sensitivity of SS and ANS for SARS-CoV-2 detection by rRT-PCR was measured against that of NPS. Subgroup analyses included test outcomes by symptom status and culture results. RESULTSSensitivity for SARS-CoV-2 detection by rRT-PCR appeared higher for SS than for ANS (85% vs 80%) and higher among symptomatic participants than among those without symptoms (94% vs 29% for SS; 87% vs 50% for ANS). Among participants with culture-positive SARS-CoV-2 by any specimen type, the sensitivities of SS and ANS by rRT-PCR were 94% and 100%, respectively. SS and ANS were equally preferred by participants; most would undergo NPS collection again despite this method's being the least preferred. CONCLUSIONSSS were slightly more sensitive than ANS for SARS-CoV-2 detection with rRT-PCR. With both SS and ANS, SARS-CoV-2 was reliably detected among participants with symptoms. Self-collected SS and ANS offer practical advantages, are preferred by patients, and might be most useful for testing people with coronavirus disease 2019 symptoms.</abstract><doi>10.1093/cid/ciab330</doi><oa>free_for_read</oa></addata></record> |
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title | Detection of Severe Acute Respiratory Syndrome Coronavirus 2 on Self-Collected Saliva or Anterior Nasal Specimens Compared With Healthcare Personnel–Collected Nasopharyngeal Specimens |
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