Long‐term pulmonary sequelae in adolescents post‐SARS‐CoV‐2 infection

Rationale Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) causes long‐term pulmonary sequelae in adults, but little is known about pulmonary outcomes in pediatrics. Objective(s) The aim of this study was to describe long‐term subjective and objective pulmonary abnormalities after SARS‐C...

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Veröffentlicht in:Pediatric pulmonology 2022-10, Vol.57 (10), p.2455-2463
Hauptverfasser: Palacios, Sabrina, Krivchenia, Katelyn, Eisner, Mariah, Young, Bailey, Ramilo, Octavio, Mejias, Asuncion, Lee, Simon, Kopp, Benjamin T.
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container_end_page 2463
container_issue 10
container_start_page 2455
container_title Pediatric pulmonology
container_volume 57
creator Palacios, Sabrina
Krivchenia, Katelyn
Eisner, Mariah
Young, Bailey
Ramilo, Octavio
Mejias, Asuncion
Lee, Simon
Kopp, Benjamin T.
description Rationale Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) causes long‐term pulmonary sequelae in adults, but little is known about pulmonary outcomes in pediatrics. Objective(s) The aim of this study was to describe long‐term subjective and objective pulmonary abnormalities after SARS‐CoV‐2 infection in pediatric populations. Methods Single‐center, retrospective cohort of patients seen in post‐coronavirus disease 2019 (COVID‐19) pulmonary clinic in 2021. Subjects evaluated had persistent pulmonary symptoms 4 weeks or more after initial infection. Clinical testing included a 6‐min walk test (6MWT), chest X‐ray, pre‐ and postbronchodilator spirometry, plethysmography, and diffusion capacity. Patients were followed 2‐to‐3‐months after the initial visit with repeat testing. The primary outcome was the presence of abnormal pulmonary function testing. Secondary measures included variables associated with pulmonary outcomes. Results Eighty‐two adolescents were seen at a median of 3.5 months postinfection, with approximately 80% reporting two or more symptoms at clinic presentation (cough, chest pain, dyspnea at rest, and exertional dyspnea). At follow‐up (~6.5 months) exertional dyspnea persisted for most (67%). Spirometry was normal in 77% of patients, but 31% had a positive bronchodilator response. No abnormalities were noted on plethysmography or diffusion capacity. Clinical phenotypes identified included inhaled corticosteroid responsiveness, paradoxical vocal fold motion disorder, deconditioning, and dysautonomia. Multivariable modeling demonstrated that obesity, anxiety, and resting dyspnea were associated with reduced 6MWT, while female sex and resting dyspnea were associated with higher Borg Dyspnea and Fatigues scores. Conclusions This is the largest study to date of pediatric patients with long‐term pulmonary sequelae post‐COVID‐19. Identified clinical phenotypes and risk factors warrant further study and treatment.
doi_str_mv 10.1002/ppul.26059
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Objective(s) The aim of this study was to describe long‐term subjective and objective pulmonary abnormalities after SARS‐CoV‐2 infection in pediatric populations. Methods Single‐center, retrospective cohort of patients seen in post‐coronavirus disease 2019 (COVID‐19) pulmonary clinic in 2021. Subjects evaluated had persistent pulmonary symptoms 4 weeks or more after initial infection. Clinical testing included a 6‐min walk test (6MWT), chest X‐ray, pre‐ and postbronchodilator spirometry, plethysmography, and diffusion capacity. Patients were followed 2‐to‐3‐months after the initial visit with repeat testing. The primary outcome was the presence of abnormal pulmonary function testing. Secondary measures included variables associated with pulmonary outcomes. Results Eighty‐two adolescents were seen at a median of 3.5 months postinfection, with approximately 80% reporting two or more symptoms at clinic presentation (cough, chest pain, dyspnea at rest, and exertional dyspnea). At follow‐up (~6.5 months) exertional dyspnea persisted for most (67%). Spirometry was normal in 77% of patients, but 31% had a positive bronchodilator response. No abnormalities were noted on plethysmography or diffusion capacity. Clinical phenotypes identified included inhaled corticosteroid responsiveness, paradoxical vocal fold motion disorder, deconditioning, and dysautonomia. Multivariable modeling demonstrated that obesity, anxiety, and resting dyspnea were associated with reduced 6MWT, while female sex and resting dyspnea were associated with higher Borg Dyspnea and Fatigues scores. Conclusions This is the largest study to date of pediatric patients with long‐term pulmonary sequelae post‐COVID‐19. Identified clinical phenotypes and risk factors warrant further study and treatment.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/ppul.26059</identifier><identifier>PMID: 35775163</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc</publisher><subject>Bronchodilators ; Coronaviruses ; COVID-19 ; Dyspnea ; Infections ; Original ; PASC ; Pediatrics ; Severe acute respiratory syndrome coronavirus 2 ; Spirometry</subject><ispartof>Pediatric pulmonology, 2022-10, Vol.57 (10), p.2455-2463</ispartof><rights>2022 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4259-aa550b4deb962fb78b545afac55c15c9c80cc338c5effccbbfa3f21dd76a99fc3</citedby><cites>FETCH-LOGICAL-c4259-aa550b4deb962fb78b545afac55c15c9c80cc338c5effccbbfa3f21dd76a99fc3</cites><orcidid>0000-0002-5983-8006 ; 0000-0002-9817-2710 ; 0000-0002-2021-7990</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fppul.26059$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fppul.26059$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Palacios, Sabrina</creatorcontrib><creatorcontrib>Krivchenia, Katelyn</creatorcontrib><creatorcontrib>Eisner, Mariah</creatorcontrib><creatorcontrib>Young, Bailey</creatorcontrib><creatorcontrib>Ramilo, Octavio</creatorcontrib><creatorcontrib>Mejias, Asuncion</creatorcontrib><creatorcontrib>Lee, Simon</creatorcontrib><creatorcontrib>Kopp, Benjamin T.</creatorcontrib><title>Long‐term pulmonary sequelae in adolescents post‐SARS‐CoV‐2 infection</title><title>Pediatric pulmonology</title><description>Rationale Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) causes long‐term pulmonary sequelae in adults, but little is known about pulmonary outcomes in pediatrics. Objective(s) The aim of this study was to describe long‐term subjective and objective pulmonary abnormalities after SARS‐CoV‐2 infection in pediatric populations. Methods Single‐center, retrospective cohort of patients seen in post‐coronavirus disease 2019 (COVID‐19) pulmonary clinic in 2021. Subjects evaluated had persistent pulmonary symptoms 4 weeks or more after initial infection. Clinical testing included a 6‐min walk test (6MWT), chest X‐ray, pre‐ and postbronchodilator spirometry, plethysmography, and diffusion capacity. Patients were followed 2‐to‐3‐months after the initial visit with repeat testing. The primary outcome was the presence of abnormal pulmonary function testing. Secondary measures included variables associated with pulmonary outcomes. Results Eighty‐two adolescents were seen at a median of 3.5 months postinfection, with approximately 80% reporting two or more symptoms at clinic presentation (cough, chest pain, dyspnea at rest, and exertional dyspnea). At follow‐up (~6.5 months) exertional dyspnea persisted for most (67%). Spirometry was normal in 77% of patients, but 31% had a positive bronchodilator response. No abnormalities were noted on plethysmography or diffusion capacity. Clinical phenotypes identified included inhaled corticosteroid responsiveness, paradoxical vocal fold motion disorder, deconditioning, and dysautonomia. Multivariable modeling demonstrated that obesity, anxiety, and resting dyspnea were associated with reduced 6MWT, while female sex and resting dyspnea were associated with higher Borg Dyspnea and Fatigues scores. Conclusions This is the largest study to date of pediatric patients with long‐term pulmonary sequelae post‐COVID‐19. Identified clinical phenotypes and risk factors warrant further study and treatment.</description><subject>Bronchodilators</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Dyspnea</subject><subject>Infections</subject><subject>Original</subject><subject>PASC</subject><subject>Pediatrics</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Spirometry</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kd9KwzAYxYMobk5vfIKCNyJ0Jk2TNjfCGP6DisM5b0OaJrOjbWrTKrvzEXxGn8TUDUEvvMl38f1yOOc7ABwjOEYQBud13RXjgELCdsAQQcZ8GDK6C4ZxRIhPY4oH4MDaFYRux9A-GGASRQRRPAR3iamWn-8frWpKz-mUphLN2rPqpVOFUF5eeSIzhbJSVa31amNbR88nD3M3pubJvYGDtJJtbqpDsKdFYdXRdo7A4urycXrjJ_fXt9NJ4sswIMwXghCYhplKGQ10GsUpCYnQQhIiEZFMxlBKjGNJlNZSpqkWWAcoyyIqGNMSj8DFRrfu0lJlvbdGFLxu8tK550bk_Pemyp_50rxyhkMWxcwJnG4FGuOS2paXuYtYFKJSprM8oHGIIIJR7NCTP-jKdE3l4vEgQgTT_paOOttQsjHWNkr_mEGQ9y3xviX-3ZKD0QZ-ywu1_ofks9ki2fz5AgFSmY0</recordid><startdate>202210</startdate><enddate>202210</enddate><creator>Palacios, Sabrina</creator><creator>Krivchenia, Katelyn</creator><creator>Eisner, Mariah</creator><creator>Young, Bailey</creator><creator>Ramilo, Octavio</creator><creator>Mejias, Asuncion</creator><creator>Lee, Simon</creator><creator>Kopp, Benjamin T.</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5983-8006</orcidid><orcidid>https://orcid.org/0000-0002-9817-2710</orcidid><orcidid>https://orcid.org/0000-0002-2021-7990</orcidid></search><sort><creationdate>202210</creationdate><title>Long‐term pulmonary sequelae in adolescents post‐SARS‐CoV‐2 infection</title><author>Palacios, Sabrina ; Krivchenia, Katelyn ; Eisner, Mariah ; Young, Bailey ; Ramilo, Octavio ; Mejias, Asuncion ; Lee, Simon ; Kopp, Benjamin T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4259-aa550b4deb962fb78b545afac55c15c9c80cc338c5effccbbfa3f21dd76a99fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Bronchodilators</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Dyspnea</topic><topic>Infections</topic><topic>Original</topic><topic>PASC</topic><topic>Pediatrics</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Spirometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Palacios, Sabrina</creatorcontrib><creatorcontrib>Krivchenia, Katelyn</creatorcontrib><creatorcontrib>Eisner, Mariah</creatorcontrib><creatorcontrib>Young, Bailey</creatorcontrib><creatorcontrib>Ramilo, Octavio</creatorcontrib><creatorcontrib>Mejias, Asuncion</creatorcontrib><creatorcontrib>Lee, Simon</creatorcontrib><creatorcontrib>Kopp, Benjamin T.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Palacios, Sabrina</au><au>Krivchenia, Katelyn</au><au>Eisner, Mariah</au><au>Young, Bailey</au><au>Ramilo, Octavio</au><au>Mejias, Asuncion</au><au>Lee, Simon</au><au>Kopp, Benjamin T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long‐term pulmonary sequelae in adolescents post‐SARS‐CoV‐2 infection</atitle><jtitle>Pediatric pulmonology</jtitle><date>2022-10</date><risdate>2022</risdate><volume>57</volume><issue>10</issue><spage>2455</spage><epage>2463</epage><pages>2455-2463</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><abstract>Rationale Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) causes long‐term pulmonary sequelae in adults, but little is known about pulmonary outcomes in pediatrics. Objective(s) The aim of this study was to describe long‐term subjective and objective pulmonary abnormalities after SARS‐CoV‐2 infection in pediatric populations. Methods Single‐center, retrospective cohort of patients seen in post‐coronavirus disease 2019 (COVID‐19) pulmonary clinic in 2021. Subjects evaluated had persistent pulmonary symptoms 4 weeks or more after initial infection. Clinical testing included a 6‐min walk test (6MWT), chest X‐ray, pre‐ and postbronchodilator spirometry, plethysmography, and diffusion capacity. Patients were followed 2‐to‐3‐months after the initial visit with repeat testing. The primary outcome was the presence of abnormal pulmonary function testing. Secondary measures included variables associated with pulmonary outcomes. Results Eighty‐two adolescents were seen at a median of 3.5 months postinfection, with approximately 80% reporting two or more symptoms at clinic presentation (cough, chest pain, dyspnea at rest, and exertional dyspnea). At follow‐up (~6.5 months) exertional dyspnea persisted for most (67%). Spirometry was normal in 77% of patients, but 31% had a positive bronchodilator response. No abnormalities were noted on plethysmography or diffusion capacity. Clinical phenotypes identified included inhaled corticosteroid responsiveness, paradoxical vocal fold motion disorder, deconditioning, and dysautonomia. Multivariable modeling demonstrated that obesity, anxiety, and resting dyspnea were associated with reduced 6MWT, while female sex and resting dyspnea were associated with higher Borg Dyspnea and Fatigues scores. Conclusions This is the largest study to date of pediatric patients with long‐term pulmonary sequelae post‐COVID‐19. 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subjects Bronchodilators
Coronaviruses
COVID-19
Dyspnea
Infections
Original
PASC
Pediatrics
Severe acute respiratory syndrome coronavirus 2
Spirometry
title Long‐term pulmonary sequelae in adolescents post‐SARS‐CoV‐2 infection
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