Bronchiectasis in chronic pulmonary aspiration: Risk factors and clinical implications

Introduction Bronchiectasis is a well‐known sequela of chronic pulmonary aspiration (CPA) that can result in significant respiratory morbidity and death. However, its true prevalence is unknown because diagnosis requires high resolution computed tomography which is not routinely utilized in this pop...

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Veröffentlicht in:Pediatric pulmonology 2012-05, Vol.47 (5), p.447-452
Hauptverfasser: Piccione, Joseph C., McPhail, Gary L., Fenchel, Matthew C., Brody, Alan S., Boesch, Richard P.
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container_end_page 452
container_issue 5
container_start_page 447
container_title Pediatric pulmonology
container_volume 47
creator Piccione, Joseph C.
McPhail, Gary L.
Fenchel, Matthew C.
Brody, Alan S.
Boesch, Richard P.
description Introduction Bronchiectasis is a well‐known sequela of chronic pulmonary aspiration (CPA) that can result in significant respiratory morbidity and death. However, its true prevalence is unknown because diagnosis requires high resolution computed tomography which is not routinely utilized in this population. This study describes the prevalence, time course for development, and risk factors for bronchiectasis in children with CPA. Materials and Methods Using a cross‐sectional design, medical records were reviewed for all patients with swallow study or airway endoscopy‐confirmed aspiration in our airway center over a 21 month period. All patients underwent rigid and flexible bronchoscopy, and high resolution chest computed tomography. Prevalence, distribution, and risk factors for bronchiectasis were identified. Results One hundred subjects age 6 months to 19 years were identified. Overall, 66% had bronchiectasis, including 51% of those less than 2 years old. The youngest was 8 months old. Severe neurological impairment (OR 9.45, P 
doi_str_mv 10.1002/ppul.21587
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However, its true prevalence is unknown because diagnosis requires high resolution computed tomography which is not routinely utilized in this population. This study describes the prevalence, time course for development, and risk factors for bronchiectasis in children with CPA. Materials and Methods Using a cross‐sectional design, medical records were reviewed for all patients with swallow study or airway endoscopy‐confirmed aspiration in our airway center over a 21 month period. All patients underwent rigid and flexible bronchoscopy, and high resolution chest computed tomography. Prevalence, distribution, and risk factors for bronchiectasis were identified. Results One hundred subjects age 6 months to 19 years were identified. Overall, 66% had bronchiectasis, including 51% of those less than 2 years old. The youngest was 8 months old. Severe neurological impairment (OR 9.45, P &lt; 0.004) and history of gastroesophageal reflux (OR 3.36, P = 0.036) were identified as risk factors. Clinical history, exam, and other co‐morbidities did not predict bronchiectasis. Sixteen subjects with bronchiectasis had repeat chest computed tomography with 44% demonstrating improvement or resolution. Discussion Bronchiectasis is highly prevalent in children with CPA and its presence in young children demonstrates that it can develop rapidly. Early identification of bronchiectasis, along with interventions aimed at preventing further airway damage, may minimize morbidity and mortality in patients with CPA. Pediatr Pulmonol. 2012; 47:447–452. © 2011 Wiley Periodicals, Inc.</description><identifier>ISSN: 8755-6863</identifier><identifier>EISSN: 1099-0496</identifier><identifier>DOI: 10.1002/ppul.21587</identifier><identifier>PMID: 22028069</identifier><identifier>CODEN: PEPUES</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; aspiration pneumonia ; Biological and medical sciences ; Bronchiectasis - diagnosis ; Bronchiectasis - epidemiology ; Bronchoscopy - methods ; Child ; Child, Preschool ; children ; Chronic Disease ; Cross-Sectional Studies ; deglutition disorders ; Deglutition Disorders - diagnosis ; Deglutition Disorders - epidemiology ; Esophagus ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; General aspects ; Humans ; Infant ; Male ; Medical sciences ; Other diseases. 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Pulmonol</addtitle><description>Introduction Bronchiectasis is a well‐known sequela of chronic pulmonary aspiration (CPA) that can result in significant respiratory morbidity and death. However, its true prevalence is unknown because diagnosis requires high resolution computed tomography which is not routinely utilized in this population. This study describes the prevalence, time course for development, and risk factors for bronchiectasis in children with CPA. Materials and Methods Using a cross‐sectional design, medical records were reviewed for all patients with swallow study or airway endoscopy‐confirmed aspiration in our airway center over a 21 month period. All patients underwent rigid and flexible bronchoscopy, and high resolution chest computed tomography. Prevalence, distribution, and risk factors for bronchiectasis were identified. Results One hundred subjects age 6 months to 19 years were identified. Overall, 66% had bronchiectasis, including 51% of those less than 2 years old. The youngest was 8 months old. Severe neurological impairment (OR 9.45, P &lt; 0.004) and history of gastroesophageal reflux (OR 3.36, P = 0.036) were identified as risk factors. Clinical history, exam, and other co‐morbidities did not predict bronchiectasis. Sixteen subjects with bronchiectasis had repeat chest computed tomography with 44% demonstrating improvement or resolution. Discussion Bronchiectasis is highly prevalent in children with CPA and its presence in young children demonstrates that it can develop rapidly. Early identification of bronchiectasis, along with interventions aimed at preventing further airway damage, may minimize morbidity and mortality in patients with CPA. Pediatr Pulmonol. 2012; 47:447–452. © 2011 Wiley Periodicals, Inc.</description><subject>Adolescent</subject><subject>aspiration pneumonia</subject><subject>Biological and medical sciences</subject><subject>Bronchiectasis - diagnosis</subject><subject>Bronchiectasis - epidemiology</subject><subject>Bronchoscopy - methods</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>children</subject><subject>Chronic Disease</subject><subject>Cross-Sectional Studies</subject><subject>deglutition disorders</subject><subject>Deglutition Disorders - diagnosis</subject><subject>Deglutition Disorders - epidemiology</subject><subject>Esophagus</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>General aspects</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Pneumology</subject><subject>Prevalence</subject><subject>Respiratory Aspiration - diagnosis</subject><subject>Respiratory Aspiration - epidemiology</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><subject>Risk Factors</subject><subject>Tomography, X-Ray Computed</subject><subject>Young Adult</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90E1PVDEUBuDGaGRAN_4A042JIbnQ7966E6JAMsGJirhrzm17Q-V-2d6J8u_tMAPuWLVpn3NOzovQG0qOKCHseJrW3RGjstbP0IISYyoijHqOFrWWslK14ntoP-dfhJQ_Q1-iPcYIq4kyC_TjJI2Du4nBzZBjxnHA7qY8RYdL134cIN1hyFNMMMdx-IC_xnyLW3DzmDKGwWPXxaKhw7GfunLZsPwKvWihy-H17jxAV58_fT89r5Zfzi5OPy4rx43WFXiqOJO64SCDV0CFpB6a0CgVmKLBeFc3GoyWnGnfSkWFp0IQJikRjZf8AL3f9p3S-Hsd8mz7mF3oOhjCuM625EMEUYLUhR5uqUtjzim0dkqxL-sVtHHMbnK09zkW_HbXd930wT_Sh-AKeLcDkMvybYLBxfzfSW2k5Lw4unV_YhfunhhpV6ur5cPwalsT8xz-PtZAurVKcy3t9eWZPbn8Kb6dX6-s5P8AthqakQ</recordid><startdate>201205</startdate><enddate>201205</enddate><creator>Piccione, Joseph C.</creator><creator>McPhail, Gary L.</creator><creator>Fenchel, Matthew C.</creator><creator>Brody, Alan S.</creator><creator>Boesch, Richard P.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201205</creationdate><title>Bronchiectasis in chronic pulmonary aspiration: Risk factors and clinical implications</title><author>Piccione, Joseph C. ; McPhail, Gary L. ; Fenchel, Matthew C. ; Brody, Alan S. ; Boesch, Richard P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3977-ad163257b3a5ed6a1451dabeb66e261e9dc8b7a975327df5614d144025104bd53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>aspiration pneumonia</topic><topic>Biological and medical sciences</topic><topic>Bronchiectasis - diagnosis</topic><topic>Bronchiectasis - epidemiology</topic><topic>Bronchoscopy - methods</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>children</topic><topic>Chronic Disease</topic><topic>Cross-Sectional Studies</topic><topic>deglutition disorders</topic><topic>Deglutition Disorders - diagnosis</topic><topic>Deglutition Disorders - epidemiology</topic><topic>Esophagus</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>General aspects</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><topic>Pneumology</topic><topic>Prevalence</topic><topic>Respiratory Aspiration - diagnosis</topic><topic>Respiratory Aspiration - epidemiology</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><topic>Risk Factors</topic><topic>Tomography, X-Ray Computed</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Piccione, Joseph C.</creatorcontrib><creatorcontrib>McPhail, Gary L.</creatorcontrib><creatorcontrib>Fenchel, Matthew C.</creatorcontrib><creatorcontrib>Brody, Alan S.</creatorcontrib><creatorcontrib>Boesch, Richard P.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Piccione, Joseph C.</au><au>McPhail, Gary L.</au><au>Fenchel, Matthew C.</au><au>Brody, Alan S.</au><au>Boesch, Richard P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bronchiectasis in chronic pulmonary aspiration: Risk factors and clinical implications</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr. Pulmonol</addtitle><date>2012-05</date><risdate>2012</risdate><volume>47</volume><issue>5</issue><spage>447</spage><epage>452</epage><pages>447-452</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><coden>PEPUES</coden><abstract>Introduction Bronchiectasis is a well‐known sequela of chronic pulmonary aspiration (CPA) that can result in significant respiratory morbidity and death. However, its true prevalence is unknown because diagnosis requires high resolution computed tomography which is not routinely utilized in this population. This study describes the prevalence, time course for development, and risk factors for bronchiectasis in children with CPA. Materials and Methods Using a cross‐sectional design, medical records were reviewed for all patients with swallow study or airway endoscopy‐confirmed aspiration in our airway center over a 21 month period. All patients underwent rigid and flexible bronchoscopy, and high resolution chest computed tomography. Prevalence, distribution, and risk factors for bronchiectasis were identified. Results One hundred subjects age 6 months to 19 years were identified. Overall, 66% had bronchiectasis, including 51% of those less than 2 years old. The youngest was 8 months old. Severe neurological impairment (OR 9.45, P &lt; 0.004) and history of gastroesophageal reflux (OR 3.36, P = 0.036) were identified as risk factors. Clinical history, exam, and other co‐morbidities did not predict bronchiectasis. Sixteen subjects with bronchiectasis had repeat chest computed tomography with 44% demonstrating improvement or resolution. Discussion Bronchiectasis is highly prevalent in children with CPA and its presence in young children demonstrates that it can develop rapidly. Early identification of bronchiectasis, along with interventions aimed at preventing further airway damage, may minimize morbidity and mortality in patients with CPA. Pediatr Pulmonol. 2012; 47:447–452. © 2011 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22028069</pmid><doi>10.1002/ppul.21587</doi><tpages>6</tpages></addata></record>
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subjects Adolescent
aspiration pneumonia
Biological and medical sciences
Bronchiectasis - diagnosis
Bronchiectasis - epidemiology
Bronchoscopy - methods
Child
Child, Preschool
children
Chronic Disease
Cross-Sectional Studies
deglutition disorders
Deglutition Disorders - diagnosis
Deglutition Disorders - epidemiology
Esophagus
Female
Gastroenterology. Liver. Pancreas. Abdomen
General aspects
Humans
Infant
Male
Medical sciences
Other diseases. Semiology
Pneumology
Prevalence
Respiratory Aspiration - diagnosis
Respiratory Aspiration - epidemiology
Respiratory system : syndromes and miscellaneous diseases
Risk Factors
Tomography, X-Ray Computed
Young Adult
title Bronchiectasis in chronic pulmonary aspiration: Risk factors and clinical implications
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