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...
Gespeichert in:
Veröffentlicht in: | Pediatric pulmonology 2022-10, Vol.57 (10), p.2455-2463 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9349789</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2684101078</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4259-aa550b4deb962fb78b545afac55c15c9c80cc338c5effccbbfa3f21dd76a99fc3</originalsourceid><addsrcrecordid>eNp9kd9KwzAYxYMobk5vfIKCNyJ0Jk2TNjfCGP6DisM5b0OaJrOjbWrTKrvzEXxGn8TUDUEvvMl38f1yOOc7ABwjOEYQBud13RXjgELCdsAQQcZ8GDK6C4ZxRIhPY4oH4MDaFYRux9A-GGASRQRRPAR3iamWn-8frWpKz-mUphLN2rPqpVOFUF5eeSIzhbJSVa31amNbR88nD3M3pubJvYGDtJJtbqpDsKdFYdXRdo7A4urycXrjJ_fXt9NJ4sswIMwXghCYhplKGQ10GsUpCYnQQhIiEZFMxlBKjGNJlNZSpqkWWAcoyyIqGNMSj8DFRrfu0lJlvbdGFLxu8tK550bk_Pemyp_50rxyhkMWxcwJnG4FGuOS2paXuYtYFKJSprM8oHGIIIJR7NCTP-jKdE3l4vEgQgTT_paOOttQsjHWNkr_mEGQ9y3xviX-3ZKD0QZ-ywu1_ofks9ki2fz5AgFSmY0</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2715365775</pqid></control><display><type>article</type><title>Long‐term pulmonary sequelae in adolescents post‐SARS‐CoV‐2 infection</title><source>Wiley Journals</source><creator>Palacios, Sabrina ; Krivchenia, Katelyn ; Eisner, Mariah ; Young, Bailey ; Ramilo, Octavio ; Mejias, Asuncion ; Lee, Simon ; Kopp, Benjamin T.</creator><creatorcontrib>Palacios, Sabrina ; Krivchenia, Katelyn ; Eisner, Mariah ; Young, Bailey ; Ramilo, Octavio ; Mejias, Asuncion ; Lee, Simon ; Kopp, Benjamin T.</creatorcontrib><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><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 & 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. Identified clinical phenotypes and risk factors warrant further study and treatment.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35775163</pmid><doi>10.1002/ppul.26059</doi><tpages>9</tpages><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><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 8755-6863 |
ispartof | Pediatric pulmonology, 2022-10, Vol.57 (10), p.2455-2463 |
issn | 8755-6863 1099-0496 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9349789 |
source | Wiley Journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T04%3A37%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Long%E2%80%90term%20pulmonary%20sequelae%20in%20adolescents%20post%E2%80%90SARS%E2%80%90CoV%E2%80%902%20infection&rft.jtitle=Pediatric%20pulmonology&rft.au=Palacios,%20Sabrina&rft.date=2022-10&rft.volume=57&rft.issue=10&rft.spage=2455&rft.epage=2463&rft.pages=2455-2463&rft.issn=8755-6863&rft.eissn=1099-0496&rft_id=info:doi/10.1002/ppul.26059&rft_dat=%3Cproquest_pubme%3E2684101078%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2715365775&rft_id=info:pmid/35775163&rfr_iscdi=true |