In vivo real-time imaging of airway dynamics during bronchial challenge test
Background and Objective Asthmatic patients exhibit airway hyper‐responsiveness, which induces bronchoconstriction and results in a ventilation defect. The bronchial challenge test using methacholine is a useful way to measure airway hyper‐responsiveness with airway constriction. Anatomical optical...
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creator | Hwang, Sang Seok Chae, Yu-Gyeong Oak, Chulho Jung, Jaechul Lee, Hae-Young Kim, Sung Won Chun, Bong-Kwon Kim, Hee-Kyoo Jung, Mannhong Ahn, Yeh-Chan , Park |
description | Background and Objective
Asthmatic patients exhibit airway hyper‐responsiveness, which induces bronchoconstriction and results in a ventilation defect. The bronchial challenge test using methacholine is a useful way to measure airway hyper‐responsiveness with airway constriction. Anatomical optical coherence tomography has been used to image airway hyper‐responsiveness of medium sized bronchus with the aid of an endoscopic probe. Recently, a thoracic window was reported that allows direct visualization of terminal airway such as alveolus. A multi‐scale integrated airway dynamics was assessed in this study. We imaged in vivo changes in the right intermedius bronchus and alveolar structure during the bronchial challenge test using two optical coherence tomography systems and correlated the changes with airway resistance.
Materials and Methods
Rabbits intubated with a non‐cuffed endotracheal tube on a ventilator sequentially inhaled normal saline and methacholine (2 or 5 μg/ml). The airway resistance was measured by mechanical ventilation and airway structures were monitored by a commercial endoscopic optical coherence tomography system (1,310 nm) and a house‐made table‐top spectral‐domain optical coherence tomography system (850 nm).
Results
We demonstrated an early decrease in the size of the right intermedius bronchus and alveoli in accordance with increased airway resistance after methacholine inhalation. OCT image after inhalation of 2 μg/ml methacholine showed some segmental narrowing of the right intermedius bronchus and the image after inhalation of 5 μg/ml methacholine showed even greater segmental narrowing. The cross‐sectional areas were 7.2 ± 3.3 mm2 (normal saline), 3.7 ± 2.1 mm2 (2 μg/ml methacholine), and 2.4 ± 1.1 mm2 (5 μg/ml methacholine), respectively (P = 0.04). Most of the alveolar space was collapsed under elevated airway resistance with methacholine inhalation. The averaged areas per alveolus at the end of inspiration were 0.0244 ±0.0142 mm2 (normal saline), 0.0046 ±0.0026 mm2 (2 μg/ml methacholine), and 0.0048 ±0.0028 mm2 (5 μg/ml methacholine), respectively (P = 0.03). Methacholine induced a dose‐dependent increase in airway resistance (1.1 ± 0.3 cmH2O sec/ml for 2 μg/ml methacholine, 1.5 ± 0.5 cmH2O sec/ml for 5 μg/ml methacholine) (P = 0.03). These results were obtained from normal rabbits during the bronchial challenge test with a non‐cuffed endotracheal tube on a ventilator. With this setup increased airway resistance possibly res |
doi_str_mv | 10.1002/lsm.22345 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1673396400</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1673396400</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3625-b86ac9afb8fa841d0cd3db723705b1fce2bf73d701181e4ba6191b0b711284b53</originalsourceid><addsrcrecordid>eNqFUTtPwzAQthAISmHgDyCPLKF3dhInI6qgVASQKAg2y06cYnASiNtC_j0pBVamO-l73OMj5AjhFAHYyPnqlDEeRltkgJDGQYqA22QA2PcJpGyP7Hv_AgCcgdgleywSIhUiGZBsWtOVXTW0NcoFC1sZais1t_WcNiVVtv1QHS26WlU297RYtmtEt02dP1vlaP6snDP13NCF8YsDslMq583hTx2Sh4vz-_FlkN1OpuOzLMh5zKJAJ7HKU1XqpFRJiAXkBS-0YFxApLHMDdOl4IUAxARNqFWMKWrQApEloY74kJxsfN_a5n3ZD5aV9blxTtWmWXqJseA8jcP-3v-psUjjiMPa9fiHutSVKeRb23-i7eTvs3rCaEP4sM50fziCXKcg-xTkdwoym11_N70i2CisX5jPP4VqX2W_oojk481EZk-zO3Y_TuQV_wI47IgW</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1667965305</pqid></control><display><type>article</type><title>In vivo real-time imaging of airway dynamics during bronchial challenge test</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>Hwang, Sang Seok ; Chae, Yu-Gyeong ; Oak, Chulho ; Jung, Jaechul ; Lee, Hae-Young ; Kim, Sung Won ; Chun, Bong-Kwon ; Kim, Hee-Kyoo ; Jung, Mannhong ; Ahn, Yeh-Chan ; , Park</creator><creatorcontrib>Hwang, Sang Seok ; Chae, Yu-Gyeong ; Oak, Chulho ; Jung, Jaechul ; Lee, Hae-Young ; Kim, Sung Won ; Chun, Bong-Kwon ; Kim, Hee-Kyoo ; Jung, Mannhong ; Ahn, Yeh-Chan ; , Park</creatorcontrib><description>Background and Objective
Asthmatic patients exhibit airway hyper‐responsiveness, which induces bronchoconstriction and results in a ventilation defect. The bronchial challenge test using methacholine is a useful way to measure airway hyper‐responsiveness with airway constriction. Anatomical optical coherence tomography has been used to image airway hyper‐responsiveness of medium sized bronchus with the aid of an endoscopic probe. Recently, a thoracic window was reported that allows direct visualization of terminal airway such as alveolus. A multi‐scale integrated airway dynamics was assessed in this study. We imaged in vivo changes in the right intermedius bronchus and alveolar structure during the bronchial challenge test using two optical coherence tomography systems and correlated the changes with airway resistance.
Materials and Methods
Rabbits intubated with a non‐cuffed endotracheal tube on a ventilator sequentially inhaled normal saline and methacholine (2 or 5 μg/ml). The airway resistance was measured by mechanical ventilation and airway structures were monitored by a commercial endoscopic optical coherence tomography system (1,310 nm) and a house‐made table‐top spectral‐domain optical coherence tomography system (850 nm).
Results
We demonstrated an early decrease in the size of the right intermedius bronchus and alveoli in accordance with increased airway resistance after methacholine inhalation. OCT image after inhalation of 2 μg/ml methacholine showed some segmental narrowing of the right intermedius bronchus and the image after inhalation of 5 μg/ml methacholine showed even greater segmental narrowing. The cross‐sectional areas were 7.2 ± 3.3 mm2 (normal saline), 3.7 ± 2.1 mm2 (2 μg/ml methacholine), and 2.4 ± 1.1 mm2 (5 μg/ml methacholine), respectively (P = 0.04). Most of the alveolar space was collapsed under elevated airway resistance with methacholine inhalation. The averaged areas per alveolus at the end of inspiration were 0.0244 ±0.0142 mm2 (normal saline), 0.0046 ±0.0026 mm2 (2 μg/ml methacholine), and 0.0048 ±0.0028 mm2 (5 μg/ml methacholine), respectively (P = 0.03). Methacholine induced a dose‐dependent increase in airway resistance (1.1 ± 0.3 cmH2O sec/ml for 2 μg/ml methacholine, 1.5 ± 0.5 cmH2O sec/ml for 5 μg/ml methacholine) (P = 0.03). These results were obtained from normal rabbits during the bronchial challenge test with a non‐cuffed endotracheal tube on a ventilator. With this setup increased airway resistance possibly resulted in larger leakage around the endotracheal tube, decreased inhaled volumes, and, in turn, alveolar collapse.
Conclusion
We performed a feasibility study of in vivo visualization of real‐time airway dynamics. To our best knowledge, this is the first report of real‐time integrated airway dynamics including the right intermedius bronchus and alveoli during a bronchial challenge test. OCT showed bronchial constriction and alveolar collapse with a higher methacholine dose. OCT images correlated with the measured airway resistance. Therefore, OCT could be a potential diagnostic device for airway hyper‐responsiveness and airway remodeling. Lasers Surg. Med. 47:252–256, 2015. © 2015 Wiley Periodicals, Inc.</description><identifier>ISSN: 0196-8092</identifier><identifier>EISSN: 1096-9101</identifier><identifier>DOI: 10.1002/lsm.22345</identifier><identifier>PMID: 25779778</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; Bronchi - physiology ; bronchial challenge test ; Bronchial Provocation Tests ; Computer Systems ; in vivo airway dynamics ; Male ; optical coherence tomography ; Rabbits ; thoracic window ; Tomography, Optical Coherence</subject><ispartof>Lasers in surgery and medicine, 2015-03, Vol.47 (3), p.252-256</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3625-b86ac9afb8fa841d0cd3db723705b1fce2bf73d701181e4ba6191b0b711284b53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Flsm.22345$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Flsm.22345$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25779778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hwang, Sang Seok</creatorcontrib><creatorcontrib>Chae, Yu-Gyeong</creatorcontrib><creatorcontrib>Oak, Chulho</creatorcontrib><creatorcontrib>Jung, Jaechul</creatorcontrib><creatorcontrib>Lee, Hae-Young</creatorcontrib><creatorcontrib>Kim, Sung Won</creatorcontrib><creatorcontrib>Chun, Bong-Kwon</creatorcontrib><creatorcontrib>Kim, Hee-Kyoo</creatorcontrib><creatorcontrib>Jung, Mannhong</creatorcontrib><creatorcontrib>Ahn, Yeh-Chan</creatorcontrib><creatorcontrib> , Park</creatorcontrib><title>In vivo real-time imaging of airway dynamics during bronchial challenge test</title><title>Lasers in surgery and medicine</title><addtitle>Lasers Surg. Med</addtitle><description>Background and Objective
Asthmatic patients exhibit airway hyper‐responsiveness, which induces bronchoconstriction and results in a ventilation defect. The bronchial challenge test using methacholine is a useful way to measure airway hyper‐responsiveness with airway constriction. Anatomical optical coherence tomography has been used to image airway hyper‐responsiveness of medium sized bronchus with the aid of an endoscopic probe. Recently, a thoracic window was reported that allows direct visualization of terminal airway such as alveolus. A multi‐scale integrated airway dynamics was assessed in this study. We imaged in vivo changes in the right intermedius bronchus and alveolar structure during the bronchial challenge test using two optical coherence tomography systems and correlated the changes with airway resistance.
Materials and Methods
Rabbits intubated with a non‐cuffed endotracheal tube on a ventilator sequentially inhaled normal saline and methacholine (2 or 5 μg/ml). The airway resistance was measured by mechanical ventilation and airway structures were monitored by a commercial endoscopic optical coherence tomography system (1,310 nm) and a house‐made table‐top spectral‐domain optical coherence tomography system (850 nm).
Results
We demonstrated an early decrease in the size of the right intermedius bronchus and alveoli in accordance with increased airway resistance after methacholine inhalation. OCT image after inhalation of 2 μg/ml methacholine showed some segmental narrowing of the right intermedius bronchus and the image after inhalation of 5 μg/ml methacholine showed even greater segmental narrowing. The cross‐sectional areas were 7.2 ± 3.3 mm2 (normal saline), 3.7 ± 2.1 mm2 (2 μg/ml methacholine), and 2.4 ± 1.1 mm2 (5 μg/ml methacholine), respectively (P = 0.04). Most of the alveolar space was collapsed under elevated airway resistance with methacholine inhalation. The averaged areas per alveolus at the end of inspiration were 0.0244 ±0.0142 mm2 (normal saline), 0.0046 ±0.0026 mm2 (2 μg/ml methacholine), and 0.0048 ±0.0028 mm2 (5 μg/ml methacholine), respectively (P = 0.03). Methacholine induced a dose‐dependent increase in airway resistance (1.1 ± 0.3 cmH2O sec/ml for 2 μg/ml methacholine, 1.5 ± 0.5 cmH2O sec/ml for 5 μg/ml methacholine) (P = 0.03). These results were obtained from normal rabbits during the bronchial challenge test with a non‐cuffed endotracheal tube on a ventilator. With this setup increased airway resistance possibly resulted in larger leakage around the endotracheal tube, decreased inhaled volumes, and, in turn, alveolar collapse.
Conclusion
We performed a feasibility study of in vivo visualization of real‐time airway dynamics. To our best knowledge, this is the first report of real‐time integrated airway dynamics including the right intermedius bronchus and alveoli during a bronchial challenge test. OCT showed bronchial constriction and alveolar collapse with a higher methacholine dose. OCT images correlated with the measured airway resistance. Therefore, OCT could be a potential diagnostic device for airway hyper‐responsiveness and airway remodeling. Lasers Surg. Med. 47:252–256, 2015. © 2015 Wiley Periodicals, Inc.</description><subject>Animals</subject><subject>Bronchi - physiology</subject><subject>bronchial challenge test</subject><subject>Bronchial Provocation Tests</subject><subject>Computer Systems</subject><subject>in vivo airway dynamics</subject><subject>Male</subject><subject>optical coherence tomography</subject><subject>Rabbits</subject><subject>thoracic window</subject><subject>Tomography, Optical Coherence</subject><issn>0196-8092</issn><issn>1096-9101</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUTtPwzAQthAISmHgDyCPLKF3dhInI6qgVASQKAg2y06cYnASiNtC_j0pBVamO-l73OMj5AjhFAHYyPnqlDEeRltkgJDGQYqA22QA2PcJpGyP7Hv_AgCcgdgleywSIhUiGZBsWtOVXTW0NcoFC1sZais1t_WcNiVVtv1QHS26WlU297RYtmtEt02dP1vlaP6snDP13NCF8YsDslMq583hTx2Sh4vz-_FlkN1OpuOzLMh5zKJAJ7HKU1XqpFRJiAXkBS-0YFxApLHMDdOl4IUAxARNqFWMKWrQApEloY74kJxsfN_a5n3ZD5aV9blxTtWmWXqJseA8jcP-3v-psUjjiMPa9fiHutSVKeRb23-i7eTvs3rCaEP4sM50fziCXKcg-xTkdwoym11_N70i2CisX5jPP4VqX2W_oojk481EZk-zO3Y_TuQV_wI47IgW</recordid><startdate>201503</startdate><enddate>201503</enddate><creator>Hwang, Sang Seok</creator><creator>Chae, Yu-Gyeong</creator><creator>Oak, Chulho</creator><creator>Jung, Jaechul</creator><creator>Lee, Hae-Young</creator><creator>Kim, Sung Won</creator><creator>Chun, Bong-Kwon</creator><creator>Kim, Hee-Kyoo</creator><creator>Jung, Mannhong</creator><creator>Ahn, Yeh-Chan</creator><creator> , Park</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>201503</creationdate><title>In vivo real-time imaging of airway dynamics during bronchial challenge test</title><author>Hwang, Sang Seok ; Chae, Yu-Gyeong ; Oak, Chulho ; Jung, Jaechul ; Lee, Hae-Young ; Kim, Sung Won ; Chun, Bong-Kwon ; Kim, Hee-Kyoo ; Jung, Mannhong ; Ahn, Yeh-Chan ; , Park</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3625-b86ac9afb8fa841d0cd3db723705b1fce2bf73d701181e4ba6191b0b711284b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Bronchi - physiology</topic><topic>bronchial challenge test</topic><topic>Bronchial Provocation Tests</topic><topic>Computer Systems</topic><topic>in vivo airway dynamics</topic><topic>Male</topic><topic>optical coherence tomography</topic><topic>Rabbits</topic><topic>thoracic window</topic><topic>Tomography, Optical Coherence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hwang, Sang Seok</creatorcontrib><creatorcontrib>Chae, Yu-Gyeong</creatorcontrib><creatorcontrib>Oak, Chulho</creatorcontrib><creatorcontrib>Jung, Jaechul</creatorcontrib><creatorcontrib>Lee, Hae-Young</creatorcontrib><creatorcontrib>Kim, Sung Won</creatorcontrib><creatorcontrib>Chun, Bong-Kwon</creatorcontrib><creatorcontrib>Kim, Hee-Kyoo</creatorcontrib><creatorcontrib>Jung, Mannhong</creatorcontrib><creatorcontrib>Ahn, Yeh-Chan</creatorcontrib><creatorcontrib> , Park</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Lasers in surgery and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hwang, Sang Seok</au><au>Chae, Yu-Gyeong</au><au>Oak, Chulho</au><au>Jung, Jaechul</au><au>Lee, Hae-Young</au><au>Kim, Sung Won</au><au>Chun, Bong-Kwon</au><au>Kim, Hee-Kyoo</au><au>Jung, Mannhong</au><au>Ahn, Yeh-Chan</au><au> , Park</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo real-time imaging of airway dynamics during bronchial challenge test</atitle><jtitle>Lasers in surgery and medicine</jtitle><addtitle>Lasers Surg. Med</addtitle><date>2015-03</date><risdate>2015</risdate><volume>47</volume><issue>3</issue><spage>252</spage><epage>256</epage><pages>252-256</pages><issn>0196-8092</issn><eissn>1096-9101</eissn><abstract>Background and Objective
Asthmatic patients exhibit airway hyper‐responsiveness, which induces bronchoconstriction and results in a ventilation defect. The bronchial challenge test using methacholine is a useful way to measure airway hyper‐responsiveness with airway constriction. Anatomical optical coherence tomography has been used to image airway hyper‐responsiveness of medium sized bronchus with the aid of an endoscopic probe. Recently, a thoracic window was reported that allows direct visualization of terminal airway such as alveolus. A multi‐scale integrated airway dynamics was assessed in this study. We imaged in vivo changes in the right intermedius bronchus and alveolar structure during the bronchial challenge test using two optical coherence tomography systems and correlated the changes with airway resistance.
Materials and Methods
Rabbits intubated with a non‐cuffed endotracheal tube on a ventilator sequentially inhaled normal saline and methacholine (2 or 5 μg/ml). The airway resistance was measured by mechanical ventilation and airway structures were monitored by a commercial endoscopic optical coherence tomography system (1,310 nm) and a house‐made table‐top spectral‐domain optical coherence tomography system (850 nm).
Results
We demonstrated an early decrease in the size of the right intermedius bronchus and alveoli in accordance with increased airway resistance after methacholine inhalation. OCT image after inhalation of 2 μg/ml methacholine showed some segmental narrowing of the right intermedius bronchus and the image after inhalation of 5 μg/ml methacholine showed even greater segmental narrowing. The cross‐sectional areas were 7.2 ± 3.3 mm2 (normal saline), 3.7 ± 2.1 mm2 (2 μg/ml methacholine), and 2.4 ± 1.1 mm2 (5 μg/ml methacholine), respectively (P = 0.04). Most of the alveolar space was collapsed under elevated airway resistance with methacholine inhalation. The averaged areas per alveolus at the end of inspiration were 0.0244 ±0.0142 mm2 (normal saline), 0.0046 ±0.0026 mm2 (2 μg/ml methacholine), and 0.0048 ±0.0028 mm2 (5 μg/ml methacholine), respectively (P = 0.03). Methacholine induced a dose‐dependent increase in airway resistance (1.1 ± 0.3 cmH2O sec/ml for 2 μg/ml methacholine, 1.5 ± 0.5 cmH2O sec/ml for 5 μg/ml methacholine) (P = 0.03). These results were obtained from normal rabbits during the bronchial challenge test with a non‐cuffed endotracheal tube on a ventilator. With this setup increased airway resistance possibly resulted in larger leakage around the endotracheal tube, decreased inhaled volumes, and, in turn, alveolar collapse.
Conclusion
We performed a feasibility study of in vivo visualization of real‐time airway dynamics. To our best knowledge, this is the first report of real‐time integrated airway dynamics including the right intermedius bronchus and alveoli during a bronchial challenge test. OCT showed bronchial constriction and alveolar collapse with a higher methacholine dose. OCT images correlated with the measured airway resistance. Therefore, OCT could be a potential diagnostic device for airway hyper‐responsiveness and airway remodeling. Lasers Surg. Med. 47:252–256, 2015. © 2015 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25779778</pmid><doi>10.1002/lsm.22345</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Bronchi - physiology bronchial challenge test Bronchial Provocation Tests Computer Systems in vivo airway dynamics Male optical coherence tomography Rabbits thoracic window Tomography, Optical Coherence |
title | In vivo real-time imaging of airway dynamics during bronchial challenge test |
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