Pneumonia risk and use of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers
Recent studies have shown that use of angiotensin-converting enzyme (ACE) inhibitors may decrease pneumonia risk in various populations. We investigated the effect of ACE inhibitors and angiotensin II receptor blockers (ARBs) on pneumonia hospitalization in the general population of Taiwan. We condu...
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Veröffentlicht in: | Journal of epidemiology 2013, Vol.23 (5), p.344-350 |
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description | Recent studies have shown that use of angiotensin-converting enzyme (ACE) inhibitors may decrease pneumonia risk in various populations. We investigated the effect of ACE inhibitors and angiotensin II receptor blockers (ARBs) on pneumonia hospitalization in the general population of Taiwan.
We conducted a case-crossover study using the Taiwan Longitudinal Health Insurance Database for the year 2005. Data from patients hospitalized for the first time for pneumonia during 1997-2007 were analyzed. The case period was defined as the 30 days before admission; the periods 90 to 120 days and 180 to 210 days before admission were used as control periods. Prescribing status of ACE inhibitors and ARBs during the 3 periods was assessed for each patient. Conditional logistic regression was used to estimate the odds ratio (OR) for pneumonia associated with use of ACE inhibitors and ARBs.
We identified 10 990 cases of hospitalization for new pneumonia. After adjustment for time-variant confounding factors, pneumonia was not associated with use of ACEI or ARBS: the ORs were 0.99 (95% CI, 0.81-1.21) and 0.96 (0.72-1.28), respectively. No association was seen for cumulative defined daily doses (DDDs), as compared with nonusers, for 0 to 30, 31 to 60, or more than 60 DDDs. The results were found to be robust in sensitivity analysis.
Neither the use nor cumulative dose of ACE inhibitors or ARBs was associated with pneumonia among the Taiwanese general population. |
doi_str_mv | 10.2188/jea.JE20120112 |
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We conducted a case-crossover study using the Taiwan Longitudinal Health Insurance Database for the year 2005. Data from patients hospitalized for the first time for pneumonia during 1997-2007 were analyzed. The case period was defined as the 30 days before admission; the periods 90 to 120 days and 180 to 210 days before admission were used as control periods. Prescribing status of ACE inhibitors and ARBs during the 3 periods was assessed for each patient. Conditional logistic regression was used to estimate the odds ratio (OR) for pneumonia associated with use of ACE inhibitors and ARBs.
We identified 10 990 cases of hospitalization for new pneumonia. After adjustment for time-variant confounding factors, pneumonia was not associated with use of ACEI or ARBS: the ORs were 0.99 (95% CI, 0.81-1.21) and 0.96 (0.72-1.28), respectively. No association was seen for cumulative defined daily doses (DDDs), as compared with nonusers, for 0 to 30, 31 to 60, or more than 60 DDDs. The results were found to be robust in sensitivity analysis.
Neither the use nor cumulative dose of ACE inhibitors or ARBs was associated with pneumonia among the Taiwanese general population.</description><identifier>ISSN: 0917-5040</identifier><identifier>EISSN: 1349-9092</identifier><identifier>DOI: 10.2188/jea.JE20120112</identifier><identifier>PMID: 23912052</identifier><language>eng</language><publisher>Japan: Japan Epidemiological Association</publisher><subject>Adult ; Aged ; Angiotensin Receptor Antagonists - adverse effects ; Angiotensin Receptor Antagonists - therapeutic use ; Angiotensin-Converting Enzyme Inhibitors - adverse effects ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Antagonist drugs ; Case-Control Studies ; Clinical Epidemiology ; Cross-Over Studies ; Databases, Factual ; Drug use ; Female ; Hospitalization - statistics & numerical data ; Humans ; Inhibitor drugs ; Male ; Middle Aged ; Original ; Pharmacology ; Pneumonia ; Pneumonia - chemically induced ; Pneumonia - therapy ; Risk ; Risk assessment ; Taiwan ; Treatment Outcome</subject><ispartof>Journal of epidemiology, 2013, Vol.23 (5), p.344-350</ispartof><rights>Copyright Japan Epidemiological Association 2013</rights><rights>2013 Chia-Lin Liu et al. 2013 Chia-Lin Liu et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c576t-6f2fcde5278b6082a435bf18e7863cc6a48aecb64b447a66ca9f4bfe93397e253</citedby><cites>FETCH-LOGICAL-c576t-6f2fcde5278b6082a435bf18e7863cc6a48aecb64b447a66ca9f4bfe93397e253</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/PMC3775528/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775528/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,4010,27900,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23912052$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Chia-Lin</creatorcontrib><creatorcontrib>Shau, Wen-Yi</creatorcontrib><creatorcontrib>Chang, Chia-Hsuin</creatorcontrib><creatorcontrib>Wu, Chi-Shin</creatorcontrib><creatorcontrib>Lai, Mei-Shu</creatorcontrib><title>Pneumonia risk and use of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers</title><title>Journal of epidemiology</title><addtitle>J Epidemiol</addtitle><description>Recent studies have shown that use of angiotensin-converting enzyme (ACE) inhibitors may decrease pneumonia risk in various populations. We investigated the effect of ACE inhibitors and angiotensin II receptor blockers (ARBs) on pneumonia hospitalization in the general population of Taiwan.
We conducted a case-crossover study using the Taiwan Longitudinal Health Insurance Database for the year 2005. Data from patients hospitalized for the first time for pneumonia during 1997-2007 were analyzed. The case period was defined as the 30 days before admission; the periods 90 to 120 days and 180 to 210 days before admission were used as control periods. Prescribing status of ACE inhibitors and ARBs during the 3 periods was assessed for each patient. Conditional logistic regression was used to estimate the odds ratio (OR) for pneumonia associated with use of ACE inhibitors and ARBs.
We identified 10 990 cases of hospitalization for new pneumonia. After adjustment for time-variant confounding factors, pneumonia was not associated with use of ACEI or ARBS: the ORs were 0.99 (95% CI, 0.81-1.21) and 0.96 (0.72-1.28), respectively. No association was seen for cumulative defined daily doses (DDDs), as compared with nonusers, for 0 to 30, 31 to 60, or more than 60 DDDs. The results were found to be robust in sensitivity analysis.
Neither the use nor cumulative dose of ACE inhibitors or ARBs was associated with pneumonia among the Taiwanese general population.</description><subject>Adult</subject><subject>Aged</subject><subject>Angiotensin Receptor Antagonists - adverse effects</subject><subject>Angiotensin Receptor Antagonists - therapeutic use</subject><subject>Angiotensin-Converting Enzyme Inhibitors - adverse effects</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Antagonist drugs</subject><subject>Case-Control Studies</subject><subject>Clinical Epidemiology</subject><subject>Cross-Over Studies</subject><subject>Databases, Factual</subject><subject>Drug use</subject><subject>Female</subject><subject>Hospitalization - statistics & numerical data</subject><subject>Humans</subject><subject>Inhibitor drugs</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Pharmacology</subject><subject>Pneumonia</subject><subject>Pneumonia - chemically induced</subject><subject>Pneumonia - therapy</subject><subject>Risk</subject><subject>Risk assessment</subject><subject>Taiwan</subject><subject>Treatment Outcome</subject><issn>0917-5040</issn><issn>1349-9092</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpVUUlLAzEUDqJoXa4eJeB5arbJZC6CFJdKQQ96Dpn0TZvaJjWZEfTXG60rPHgPvuV98CF0TMmQUaXOFmCGt5eM0DyUbaEB5aIualKzbTQgNa2Kkgiyh_ZTWhDCpWJkF-0xXmdByQZodu-hXwXvDI4uPWHjp7hPgEObz5kLHfjkfGGDf4HYOT_D4N9eV4Cdn7vGdSGmT80fMh6PcQQL6wziZhnsE8R0iHZas0xw9LUP0OPV5cPoppjcXY9HF5PClpXsCtmy1k6hZJVqJFHMCF42LVVQKcmtlUYoA7aRohGiMlJaU7eiaaHmvK6AlfwAnW98132zgqkF30Wz1OvoVia-6mCc_o94N9ez8KJ5VZUlU9ng9MsghuceUqcXoY8-Z9ZUcCqYFERm1nDDsjGkFKH9-UCJ_ihG52L0bzFZcPI31w_9uwn-DtqujJo</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Liu, Chia-Lin</creator><creator>Shau, Wen-Yi</creator><creator>Chang, Chia-Hsuin</creator><creator>Wu, Chi-Shin</creator><creator>Lai, Mei-Shu</creator><general>Japan Epidemiological Association</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>7QL</scope><scope>7QP</scope><scope>7TS</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BVBZV</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope></search><sort><creationdate>2013</creationdate><title>Pneumonia risk and use of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers</title><author>Liu, Chia-Lin ; Shau, Wen-Yi ; Chang, Chia-Hsuin ; Wu, Chi-Shin ; Lai, Mei-Shu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c576t-6f2fcde5278b6082a435bf18e7863cc6a48aecb64b447a66ca9f4bfe93397e253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Angiotensin Receptor Antagonists - adverse effects</topic><topic>Angiotensin Receptor Antagonists - therapeutic use</topic><topic>Angiotensin-Converting Enzyme Inhibitors - adverse effects</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Antagonist drugs</topic><topic>Case-Control Studies</topic><topic>Clinical Epidemiology</topic><topic>Cross-Over Studies</topic><topic>Databases, Factual</topic><topic>Drug use</topic><topic>Female</topic><topic>Hospitalization - statistics & numerical data</topic><topic>Humans</topic><topic>Inhibitor drugs</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Pharmacology</topic><topic>Pneumonia</topic><topic>Pneumonia - chemically induced</topic><topic>Pneumonia - therapy</topic><topic>Risk</topic><topic>Risk assessment</topic><topic>Taiwan</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Chia-Lin</creatorcontrib><creatorcontrib>Shau, Wen-Yi</creatorcontrib><creatorcontrib>Chang, Chia-Hsuin</creatorcontrib><creatorcontrib>Wu, Chi-Shin</creatorcontrib><creatorcontrib>Lai, Mei-Shu</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>East & South Asia Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Chia-Lin</au><au>Shau, Wen-Yi</au><au>Chang, Chia-Hsuin</au><au>Wu, Chi-Shin</au><au>Lai, Mei-Shu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pneumonia risk and use of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers</atitle><jtitle>Journal of epidemiology</jtitle><addtitle>J Epidemiol</addtitle><date>2013</date><risdate>2013</risdate><volume>23</volume><issue>5</issue><spage>344</spage><epage>350</epage><pages>344-350</pages><issn>0917-5040</issn><eissn>1349-9092</eissn><abstract>Recent studies have shown that use of angiotensin-converting enzyme (ACE) inhibitors may decrease pneumonia risk in various populations. We investigated the effect of ACE inhibitors and angiotensin II receptor blockers (ARBs) on pneumonia hospitalization in the general population of Taiwan.
We conducted a case-crossover study using the Taiwan Longitudinal Health Insurance Database for the year 2005. Data from patients hospitalized for the first time for pneumonia during 1997-2007 were analyzed. The case period was defined as the 30 days before admission; the periods 90 to 120 days and 180 to 210 days before admission were used as control periods. Prescribing status of ACE inhibitors and ARBs during the 3 periods was assessed for each patient. Conditional logistic regression was used to estimate the odds ratio (OR) for pneumonia associated with use of ACE inhibitors and ARBs.
We identified 10 990 cases of hospitalization for new pneumonia. After adjustment for time-variant confounding factors, pneumonia was not associated with use of ACEI or ARBS: the ORs were 0.99 (95% CI, 0.81-1.21) and 0.96 (0.72-1.28), respectively. No association was seen for cumulative defined daily doses (DDDs), as compared with nonusers, for 0 to 30, 31 to 60, or more than 60 DDDs. The results were found to be robust in sensitivity analysis.
Neither the use nor cumulative dose of ACE inhibitors or ARBs was associated with pneumonia among the Taiwanese general population.</abstract><cop>Japan</cop><pub>Japan Epidemiological Association</pub><pmid>23912052</pmid><doi>10.2188/jea.JE20120112</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Angiotensin Receptor Antagonists - adverse effects Angiotensin Receptor Antagonists - therapeutic use Angiotensin-Converting Enzyme Inhibitors - adverse effects Angiotensin-Converting Enzyme Inhibitors - therapeutic use Antagonist drugs Case-Control Studies Clinical Epidemiology Cross-Over Studies Databases, Factual Drug use Female Hospitalization - statistics & numerical data Humans Inhibitor drugs Male Middle Aged Original Pharmacology Pneumonia Pneumonia - chemically induced Pneumonia - therapy Risk Risk assessment Taiwan Treatment Outcome |
title | Pneumonia risk and use of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers |
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