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Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy
Diffuse alveolar damage (DAD) is the pathological hallmark of acute respiratory distress syndrome (ARDS), however, the presence of DAD in the clinical criteria of ARDS patients by Berlin definition is little known. This study is designed to investigate the role of DAD in ARDS patients who underwent...
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Published in: | Critical care (London, England) England), 2015-05, Vol.19 (1), p.228-228, Article 228 |
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description | Diffuse alveolar damage (DAD) is the pathological hallmark of acute respiratory distress syndrome (ARDS), however, the presence of DAD in the clinical criteria of ARDS patients by Berlin definition is little known. This study is designed to investigate the role of DAD in ARDS patients who underwent open lung biopsy.
We retrospectively reviewed all ARDS patients who met the Berlin definition and underwent open lung biopsy from January 1999 to January 2014 in a referred medical center. DAD is characterized by hyaline membrane formation, lung edema, inflammation, hemorrhage and alveolar epithelial cell injury. Clinical data including baseline characteristics, severity of ARDS, clinical and pathological diagnoses, and survival outcomes were analyzed.
A total of 1838 patients with ARDS were identified and open lung biopsies were performed on 101 patients (5.5 %) during the study period. Of these 101 patients, the severity of ARDS on diagnosis was mild of 16.8 %, moderate of 56.5 % and severe of 26.7 %. The hospital mortality rate was not significant difference between the three groups (64.7 % vs 61.4 % vs 55.6 %, p = 0.81). Of the 101 clinical ARDS patients with open lung biopsies, 56.4 % (57/101) patients had DAD according to biopsy results. The proportion of DAD were 76.5 % (13/17) in mild, 56.1 % (32/57) in moderate and 44.4 % (12/27) in severe ARDS and there is no significant difference between the three groups (p = 0.113). Pathological findings of DAD patients had a higher hospital mortality rate than non-DAD patients (71.9 % vs 45.5 %, p = 0.007). Pathological findings of DAD (odds ratio: 3.554, 95 % CI, 1.385-9.12; p = 0.008) and Sequential Organ Failure Assessment score on the biopsy day (odds ratio: 1.424, 95 % CI, 1.187-1.707; p |
doi_str_mv | 10.1186/s13054-015-0949-y |
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fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4449559</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A541584749</galeid><sourcerecordid>A541584749</sourcerecordid><originalsourceid>FETCH-LOGICAL-c564t-45d6b9621af365e887a8c0a6b616ca23fd05b66f883c5f3bdbc063fcf2f301e03</originalsourceid><addsrcrecordid>eNptUk1rFTEUHUSxtfoD3EjAjZupycvHZDZCqfUDCm4U3IVM5uY1JZOMSaYy-Oeb4dVqRUK4uTfnnJsbTtO8JPiUECneZkIxZy0mvMU969v1UXNMmBCtwP33x_VMBWslp_yoeZbzNcakk4I-bY52vJek7uPm13tn7ZIBaX8D0euERj3pfc1zjsbpAiOaYirau7IiF1AGD2ararMUQAny7JIuMa1odLnUPKO8hjHFCdCsi4NQMvrpyhWKMwTkl7BHg4tzXp83T6z2GV7cxZPm24eLr-ef2ssvHz-fn122hgtWWsZHMfRiR7SlgoOUnZYGazEIIozeUTtiPghhpaSGWzqMg8GCWmN3lmICmJ407w668zJMMJr6oqS9mpObdFpV1E49vAnuSu3jjWKM9Zz3VeDNnUCKPxbIRU0uG_BeB4hLVkRI3jHWCVqhr_-BXsclhTqeIj0nAu9q-IPaaw_KBRtrX7OJqjPOCJesY1vb0_-g6hphciYGsK7WHxDIgWBSzDmBvZ-RYLU5Rh0co6pj1OYYtVbOq78_557x2yL0Finwv1s</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1951602195</pqid></control><display><type>article</type><title>Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central</source><creator>Kao, Kuo-Chin ; Hu, Han-Chung ; Chang, Chih-Hao ; Hung, Chen-Yiu ; Chiu, Li-Chung ; Li, Shih-Hong ; Lin, Shih-Wei ; Chuang, Li-Pang ; Wang, Chih-Wei ; Li, Li-Fu ; Chen, Ning-Hung ; Yang, Cheng-Ta ; Huang, Chung-Chi ; Tsai, Ying-Huang</creator><creatorcontrib>Kao, Kuo-Chin ; Hu, Han-Chung ; Chang, Chih-Hao ; Hung, Chen-Yiu ; Chiu, Li-Chung ; Li, Shih-Hong ; Lin, Shih-Wei ; Chuang, Li-Pang ; Wang, Chih-Wei ; Li, Li-Fu ; Chen, Ning-Hung ; Yang, Cheng-Ta ; Huang, Chung-Chi ; Tsai, Ying-Huang</creatorcontrib><description>Diffuse alveolar damage (DAD) is the pathological hallmark of acute respiratory distress syndrome (ARDS), however, the presence of DAD in the clinical criteria of ARDS patients by Berlin definition is little known. This study is designed to investigate the role of DAD in ARDS patients who underwent open lung biopsy.
We retrospectively reviewed all ARDS patients who met the Berlin definition and underwent open lung biopsy from January 1999 to January 2014 in a referred medical center. DAD is characterized by hyaline membrane formation, lung edema, inflammation, hemorrhage and alveolar epithelial cell injury. Clinical data including baseline characteristics, severity of ARDS, clinical and pathological diagnoses, and survival outcomes were analyzed.
A total of 1838 patients with ARDS were identified and open lung biopsies were performed on 101 patients (5.5 %) during the study period. Of these 101 patients, the severity of ARDS on diagnosis was mild of 16.8 %, moderate of 56.5 % and severe of 26.7 %. The hospital mortality rate was not significant difference between the three groups (64.7 % vs 61.4 % vs 55.6 %, p = 0.81). Of the 101 clinical ARDS patients with open lung biopsies, 56.4 % (57/101) patients had DAD according to biopsy results. The proportion of DAD were 76.5 % (13/17) in mild, 56.1 % (32/57) in moderate and 44.4 % (12/27) in severe ARDS and there is no significant difference between the three groups (p = 0.113). Pathological findings of DAD patients had a higher hospital mortality rate than non-DAD patients (71.9 % vs 45.5 %, p = 0.007). Pathological findings of DAD (odds ratio: 3.554, 95 % CI, 1.385-9.12; p = 0.008) and Sequential Organ Failure Assessment score on the biopsy day (odds ratio: 1.424, 95 % CI, 1.187-1.707; p<0.001) were significantly and independently associated with hospital mortality. The baseline demographics and clinical characteristics were not significantly different between DAD and non-DAD patients.
The correlation of pathological findings of DAD and ARDS diagnosed by Berlin definition is modest. A pathological finding of DAD in ARDS patients is associated with hospital mortality and there are no clinical characteristics that could identify DAD patients before open lung biopsy.</description><identifier>ISSN: 1364-8535</identifier><identifier>EISSN: 1466-609X</identifier><identifier>EISSN: 1364-8535</identifier><identifier>EISSN: 1366-609X</identifier><identifier>DOI: 10.1186/s13054-015-0949-y</identifier><identifier>PMID: 25981598</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acute respiratory distress syndrome ; Adult ; Aged ; Biopsy ; Care and treatment ; Comparative analysis ; Complications and side effects ; Critical care ; Data analysis ; Female ; Hospital Mortality - trends ; Hospitals ; Humans ; Intensive care ; Lung - pathology ; Lung - surgery ; Lungs ; Male ; Medical centers ; Medical prognosis ; Medical research ; Medicine, Experimental ; Middle Aged ; Mortality ; Mortality - trends ; Patient outcomes ; Patients ; Pulmonary Alveoli - pathology ; Respiratory distress syndrome ; Respiratory Distress Syndrome, Adult - diagnosis ; Respiratory Distress Syndrome, Adult - mortality ; Respiratory Distress Syndrome, Adult - surgery ; Respiratory therapy ; Retrospective Studies ; Risk factors ; Smoke inhalation ; United Kingdom ; Ventilators</subject><ispartof>Critical care (London, England), 2015-05, Vol.19 (1), p.228-228, Article 228</ispartof><rights>COPYRIGHT 2015 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2015</rights><rights>Kao et al.; licensee BioMed Central. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c564t-45d6b9621af365e887a8c0a6b616ca23fd05b66f883c5f3bdbc063fcf2f301e03</citedby><cites>FETCH-LOGICAL-c564t-45d6b9621af365e887a8c0a6b616ca23fd05b66f883c5f3bdbc063fcf2f301e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449559/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1951602195?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25981598$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kao, Kuo-Chin</creatorcontrib><creatorcontrib>Hu, Han-Chung</creatorcontrib><creatorcontrib>Chang, Chih-Hao</creatorcontrib><creatorcontrib>Hung, Chen-Yiu</creatorcontrib><creatorcontrib>Chiu, Li-Chung</creatorcontrib><creatorcontrib>Li, Shih-Hong</creatorcontrib><creatorcontrib>Lin, Shih-Wei</creatorcontrib><creatorcontrib>Chuang, Li-Pang</creatorcontrib><creatorcontrib>Wang, Chih-Wei</creatorcontrib><creatorcontrib>Li, Li-Fu</creatorcontrib><creatorcontrib>Chen, Ning-Hung</creatorcontrib><creatorcontrib>Yang, Cheng-Ta</creatorcontrib><creatorcontrib>Huang, Chung-Chi</creatorcontrib><creatorcontrib>Tsai, Ying-Huang</creatorcontrib><title>Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy</title><title>Critical care (London, England)</title><addtitle>Crit Care</addtitle><description>Diffuse alveolar damage (DAD) is the pathological hallmark of acute respiratory distress syndrome (ARDS), however, the presence of DAD in the clinical criteria of ARDS patients by Berlin definition is little known. This study is designed to investigate the role of DAD in ARDS patients who underwent open lung biopsy.
We retrospectively reviewed all ARDS patients who met the Berlin definition and underwent open lung biopsy from January 1999 to January 2014 in a referred medical center. DAD is characterized by hyaline membrane formation, lung edema, inflammation, hemorrhage and alveolar epithelial cell injury. Clinical data including baseline characteristics, severity of ARDS, clinical and pathological diagnoses, and survival outcomes were analyzed.
A total of 1838 patients with ARDS were identified and open lung biopsies were performed on 101 patients (5.5 %) during the study period. Of these 101 patients, the severity of ARDS on diagnosis was mild of 16.8 %, moderate of 56.5 % and severe of 26.7 %. The hospital mortality rate was not significant difference between the three groups (64.7 % vs 61.4 % vs 55.6 %, p = 0.81). Of the 101 clinical ARDS patients with open lung biopsies, 56.4 % (57/101) patients had DAD according to biopsy results. The proportion of DAD were 76.5 % (13/17) in mild, 56.1 % (32/57) in moderate and 44.4 % (12/27) in severe ARDS and there is no significant difference between the three groups (p = 0.113). Pathological findings of DAD patients had a higher hospital mortality rate than non-DAD patients (71.9 % vs 45.5 %, p = 0.007). Pathological findings of DAD (odds ratio: 3.554, 95 % CI, 1.385-9.12; p = 0.008) and Sequential Organ Failure Assessment score on the biopsy day (odds ratio: 1.424, 95 % CI, 1.187-1.707; p<0.001) were significantly and independently associated with hospital mortality. The baseline demographics and clinical characteristics were not significantly different between DAD and non-DAD patients.
The correlation of pathological findings of DAD and ARDS diagnosed by Berlin definition is modest. A pathological finding of DAD in ARDS patients is associated with hospital mortality and there are no clinical characteristics that could identify DAD patients before open lung biopsy.</description><subject>Acute respiratory distress syndrome</subject><subject>Adult</subject><subject>Aged</subject><subject>Biopsy</subject><subject>Care and treatment</subject><subject>Comparative analysis</subject><subject>Complications and side effects</subject><subject>Critical care</subject><subject>Data analysis</subject><subject>Female</subject><subject>Hospital Mortality - trends</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Intensive care</subject><subject>Lung - pathology</subject><subject>Lung - surgery</subject><subject>Lungs</subject><subject>Male</subject><subject>Medical centers</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Mortality - trends</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Pulmonary Alveoli - pathology</subject><subject>Respiratory distress syndrome</subject><subject>Respiratory Distress Syndrome, Adult - diagnosis</subject><subject>Respiratory Distress Syndrome, Adult - mortality</subject><subject>Respiratory Distress Syndrome, Adult - surgery</subject><subject>Respiratory therapy</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>Smoke inhalation</subject><subject>United Kingdom</subject><subject>Ventilators</subject><issn>1364-8535</issn><issn>1466-609X</issn><issn>1364-8535</issn><issn>1366-609X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptUk1rFTEUHUSxtfoD3EjAjZupycvHZDZCqfUDCm4U3IVM5uY1JZOMSaYy-Oeb4dVqRUK4uTfnnJsbTtO8JPiUECneZkIxZy0mvMU969v1UXNMmBCtwP33x_VMBWslp_yoeZbzNcakk4I-bY52vJek7uPm13tn7ZIBaX8D0euERj3pfc1zjsbpAiOaYirau7IiF1AGD2ararMUQAny7JIuMa1odLnUPKO8hjHFCdCsi4NQMvrpyhWKMwTkl7BHg4tzXp83T6z2GV7cxZPm24eLr-ef2ssvHz-fn122hgtWWsZHMfRiR7SlgoOUnZYGazEIIozeUTtiPghhpaSGWzqMg8GCWmN3lmICmJ407w668zJMMJr6oqS9mpObdFpV1E49vAnuSu3jjWKM9Zz3VeDNnUCKPxbIRU0uG_BeB4hLVkRI3jHWCVqhr_-BXsclhTqeIj0nAu9q-IPaaw_KBRtrX7OJqjPOCJesY1vb0_-g6hphciYGsK7WHxDIgWBSzDmBvZ-RYLU5Rh0co6pj1OYYtVbOq78_557x2yL0Finwv1s</recordid><startdate>20150515</startdate><enddate>20150515</enddate><creator>Kao, Kuo-Chin</creator><creator>Hu, Han-Chung</creator><creator>Chang, Chih-Hao</creator><creator>Hung, Chen-Yiu</creator><creator>Chiu, Li-Chung</creator><creator>Li, Shih-Hong</creator><creator>Lin, Shih-Wei</creator><creator>Chuang, Li-Pang</creator><creator>Wang, Chih-Wei</creator><creator>Li, Li-Fu</creator><creator>Chen, Ning-Hung</creator><creator>Yang, Cheng-Ta</creator><creator>Huang, Chung-Chi</creator><creator>Tsai, Ying-Huang</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150515</creationdate><title>Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy</title><author>Kao, Kuo-Chin ; Hu, Han-Chung ; Chang, Chih-Hao ; Hung, Chen-Yiu ; Chiu, Li-Chung ; Li, Shih-Hong ; Lin, Shih-Wei ; Chuang, Li-Pang ; Wang, Chih-Wei ; Li, Li-Fu ; Chen, Ning-Hung ; Yang, Cheng-Ta ; Huang, Chung-Chi ; Tsai, Ying-Huang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c564t-45d6b9621af365e887a8c0a6b616ca23fd05b66f883c5f3bdbc063fcf2f301e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acute respiratory distress syndrome</topic><topic>Adult</topic><topic>Aged</topic><topic>Biopsy</topic><topic>Care and treatment</topic><topic>Comparative analysis</topic><topic>Complications and side effects</topic><topic>Critical care</topic><topic>Data analysis</topic><topic>Female</topic><topic>Hospital Mortality - trends</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Intensive care</topic><topic>Lung - pathology</topic><topic>Lung - surgery</topic><topic>Lungs</topic><topic>Male</topic><topic>Medical centers</topic><topic>Medical prognosis</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Mortality - trends</topic><topic>Patient outcomes</topic><topic>Patients</topic><topic>Pulmonary Alveoli - pathology</topic><topic>Respiratory distress syndrome</topic><topic>Respiratory Distress Syndrome, Adult - diagnosis</topic><topic>Respiratory Distress Syndrome, Adult - mortality</topic><topic>Respiratory Distress Syndrome, Adult - surgery</topic><topic>Respiratory therapy</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Smoke inhalation</topic><topic>United Kingdom</topic><topic>Ventilators</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kao, Kuo-Chin</creatorcontrib><creatorcontrib>Hu, Han-Chung</creatorcontrib><creatorcontrib>Chang, Chih-Hao</creatorcontrib><creatorcontrib>Hung, Chen-Yiu</creatorcontrib><creatorcontrib>Chiu, Li-Chung</creatorcontrib><creatorcontrib>Li, Shih-Hong</creatorcontrib><creatorcontrib>Lin, Shih-Wei</creatorcontrib><creatorcontrib>Chuang, Li-Pang</creatorcontrib><creatorcontrib>Wang, Chih-Wei</creatorcontrib><creatorcontrib>Li, Li-Fu</creatorcontrib><creatorcontrib>Chen, Ning-Hung</creatorcontrib><creatorcontrib>Yang, Cheng-Ta</creatorcontrib><creatorcontrib>Huang, Chung-Chi</creatorcontrib><creatorcontrib>Tsai, Ying-Huang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Critical care (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kao, Kuo-Chin</au><au>Hu, Han-Chung</au><au>Chang, Chih-Hao</au><au>Hung, Chen-Yiu</au><au>Chiu, Li-Chung</au><au>Li, Shih-Hong</au><au>Lin, Shih-Wei</au><au>Chuang, Li-Pang</au><au>Wang, Chih-Wei</au><au>Li, Li-Fu</au><au>Chen, Ning-Hung</au><au>Yang, Cheng-Ta</au><au>Huang, Chung-Chi</au><au>Tsai, Ying-Huang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy</atitle><jtitle>Critical care (London, England)</jtitle><addtitle>Crit Care</addtitle><date>2015-05-15</date><risdate>2015</risdate><volume>19</volume><issue>1</issue><spage>228</spage><epage>228</epage><pages>228-228</pages><artnum>228</artnum><issn>1364-8535</issn><eissn>1466-609X</eissn><eissn>1364-8535</eissn><eissn>1366-609X</eissn><abstract>Diffuse alveolar damage (DAD) is the pathological hallmark of acute respiratory distress syndrome (ARDS), however, the presence of DAD in the clinical criteria of ARDS patients by Berlin definition is little known. This study is designed to investigate the role of DAD in ARDS patients who underwent open lung biopsy.
We retrospectively reviewed all ARDS patients who met the Berlin definition and underwent open lung biopsy from January 1999 to January 2014 in a referred medical center. DAD is characterized by hyaline membrane formation, lung edema, inflammation, hemorrhage and alveolar epithelial cell injury. Clinical data including baseline characteristics, severity of ARDS, clinical and pathological diagnoses, and survival outcomes were analyzed.
A total of 1838 patients with ARDS were identified and open lung biopsies were performed on 101 patients (5.5 %) during the study period. Of these 101 patients, the severity of ARDS on diagnosis was mild of 16.8 %, moderate of 56.5 % and severe of 26.7 %. The hospital mortality rate was not significant difference between the three groups (64.7 % vs 61.4 % vs 55.6 %, p = 0.81). Of the 101 clinical ARDS patients with open lung biopsies, 56.4 % (57/101) patients had DAD according to biopsy results. The proportion of DAD were 76.5 % (13/17) in mild, 56.1 % (32/57) in moderate and 44.4 % (12/27) in severe ARDS and there is no significant difference between the three groups (p = 0.113). Pathological findings of DAD patients had a higher hospital mortality rate than non-DAD patients (71.9 % vs 45.5 %, p = 0.007). Pathological findings of DAD (odds ratio: 3.554, 95 % CI, 1.385-9.12; p = 0.008) and Sequential Organ Failure Assessment score on the biopsy day (odds ratio: 1.424, 95 % CI, 1.187-1.707; p<0.001) were significantly and independently associated with hospital mortality. The baseline demographics and clinical characteristics were not significantly different between DAD and non-DAD patients.
The correlation of pathological findings of DAD and ARDS diagnosed by Berlin definition is modest. A pathological finding of DAD in ARDS patients is associated with hospital mortality and there are no clinical characteristics that could identify DAD patients before open lung biopsy.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>25981598</pmid><doi>10.1186/s13054-015-0949-y</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acute respiratory distress syndrome Adult Aged Biopsy Care and treatment Comparative analysis Complications and side effects Critical care Data analysis Female Hospital Mortality - trends Hospitals Humans Intensive care Lung - pathology Lung - surgery Lungs Male Medical centers Medical prognosis Medical research Medicine, Experimental Middle Aged Mortality Mortality - trends Patient outcomes Patients Pulmonary Alveoli - pathology Respiratory distress syndrome Respiratory Distress Syndrome, Adult - diagnosis Respiratory Distress Syndrome, Adult - mortality Respiratory Distress Syndrome, Adult - surgery Respiratory therapy Retrospective Studies Risk factors Smoke inhalation United Kingdom Ventilators |
title | Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy |
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