Statins and Mortality in COPD: A Methodological Review of Observational Studies
Randomized controlled trials and observational studies have reported conflicting results on the potential beneficial effects of statins on mortality in patients with chronic obstructive pulmonary disease (COPD). We performed a systematic search of the literature to review all observational studies r...
Saved in:
Published in | Chronic obstructive pulmonary disease Vol. 20; no. 1; pp. 284 - 291 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
Taylor & Francis Group
01.12.2023
|
Subjects | |
Online Access | Get full text |
ISSN | 1541-2555 1541-2563 1541-2563 |
DOI | 10.1080/15412555.2023.2242489 |
Cover
Abstract | Randomized controlled trials and observational studies have reported conflicting results on the potential beneficial effects of statins on mortality in patients with chronic obstructive pulmonary disease (COPD). We performed a systematic search of the literature to review all observational studies reporting relative risks of death with statin use in COPD, focusing on potential sources of bias. We identified 15 observational studies, out of 2835, of which 12 were affected by time-related and other biases and the remaining 3 by confounding bias. All 15 studies were also subject to confounding bias due to lack of adjustment for important COPD-related factors. The risk of death associated with statin use was reduced across all 15 studies (pooled relative risk (PRR) 0.66; 95% CI: 0.59-0.74). The reduction was observed in 7 studies with immortal time bias (PRR 0.62; 95%: 0.53-0.72), two with collider-stratification bias (PRR 0.60; 95% CI: 0.45-0.80), one with time-window bias (RR 0.61; 95% CI: 0.38-0.98), one with immeasurable time bias (RR 0.50; 95% CI: 0.40-0.62), and one with exposure misclassification (RR 0.86; 95% CI: 0.72-1.03). The three studies that avoided these biases were, however, affected by confounding bias resulting in a PRR of 0.77 (95% CI: 0.61-0.98). In conclusion, the observational studies investigating statin use and mortality in COPD are affected by major biases, many of which can result in spurious protective effects. Well-designed observational studies that carefully emulate randomized trials are needed to resolve this uncertainty regarding the potential beneficial benefits of statins on mortality in patients with COPD. |
---|---|
AbstractList | Randomized controlled trials and observational studies have reported conflicting results on the potential beneficial effects of statins on mortality in patients with chronic obstructive pulmonary disease (COPD). We performed a systematic search of the literature to review all observational studies reporting relative risks of death with statin use in COPD, focusing on potential sources of bias. We identified 15 observational studies, out of 2835, of which 12 were affected by time-related and other biases and the remaining 3 by confounding bias. All 15 studies were also subject to confounding bias due to lack of adjustment for important COPD-related factors. The risk of death associated with statin use was reduced across all 15 studies (pooled relative risk (PRR) 0.66; 95% CI: 0.59-0.74). The reduction was observed in 7 studies with immortal time bias (PRR 0.62; 95%: 0.53-0.72), two with collider-stratification bias (PRR 0.60; 95% CI: 0.45-0.80), one with time-window bias (RR 0.61; 95% CI: 0.38-0.98), one with immeasurable time bias (RR 0.50; 95% CI: 0.40-0.62), and one with exposure misclassification (RR 0.86; 95% CI: 0.72-1.03). The three studies that avoided these biases were, however, affected by confounding bias resulting in a PRR of 0.77 (95% CI: 0.61-0.98). In conclusion, the observational studies investigating statin use and mortality in COPD are affected by major biases, many of which can result in spurious protective effects. Well-designed observational studies that carefully emulate randomized trials are needed to resolve this uncertainty regarding the potential beneficial benefits of statins on mortality in patients with COPD.Randomized controlled trials and observational studies have reported conflicting results on the potential beneficial effects of statins on mortality in patients with chronic obstructive pulmonary disease (COPD). We performed a systematic search of the literature to review all observational studies reporting relative risks of death with statin use in COPD, focusing on potential sources of bias. We identified 15 observational studies, out of 2835, of which 12 were affected by time-related and other biases and the remaining 3 by confounding bias. All 15 studies were also subject to confounding bias due to lack of adjustment for important COPD-related factors. The risk of death associated with statin use was reduced across all 15 studies (pooled relative risk (PRR) 0.66; 95% CI: 0.59-0.74). The reduction was observed in 7 studies with immortal time bias (PRR 0.62; 95%: 0.53-0.72), two with collider-stratification bias (PRR 0.60; 95% CI: 0.45-0.80), one with time-window bias (RR 0.61; 95% CI: 0.38-0.98), one with immeasurable time bias (RR 0.50; 95% CI: 0.40-0.62), and one with exposure misclassification (RR 0.86; 95% CI: 0.72-1.03). The three studies that avoided these biases were, however, affected by confounding bias resulting in a PRR of 0.77 (95% CI: 0.61-0.98). In conclusion, the observational studies investigating statin use and mortality in COPD are affected by major biases, many of which can result in spurious protective effects. Well-designed observational studies that carefully emulate randomized trials are needed to resolve this uncertainty regarding the potential beneficial benefits of statins on mortality in patients with COPD. Randomized controlled trials and observational studies have reported conflicting results on the potential beneficial effects of statins on mortality in patients with chronic obstructive pulmonary disease (COPD). We performed a systematic search of the literature to review all observational studies reporting relative risks of death with statin use in COPD, focusing on potential sources of bias. We identified 15 observational studies, out of 2835, of which 12 were affected by time-related and other biases and the remaining 3 by confounding bias. All 15 studies were also subject to confounding bias due to lack of adjustment for important COPD-related factors. The risk of death associated with statin use was reduced across all 15 studies (pooled relative risk (PRR) 0.66; 95% CI: 0.59-0.74). The reduction was observed in 7 studies with immortal time bias (PRR 0.62; 95%: 0.53-0.72), two with collider-stratification bias (PRR 0.60; 95% CI: 0.45-0.80), one with time-window bias (RR 0.61; 95% CI: 0.38-0.98), one with immeasurable time bias (RR 0.50; 95% CI: 0.40-0.62), and one with exposure misclassification (RR 0.86; 95% CI: 0.72-1.03). The three studies that avoided these biases were, however, affected by confounding bias resulting in a PRR of 0.77 (95% CI: 0.61-0.98). In conclusion, the observational studies investigating statin use and mortality in COPD are affected by major biases, many of which can result in spurious protective effects. Well-designed observational studies that carefully emulate randomized trials are needed to resolve this uncertainty regarding the potential beneficial benefits of statins on mortality in patients with COPD. |
Author | Sule, Naheemot Olaoluwa Suissa, Samy |
Author_xml | – sequence: 1 givenname: Naheemot Olaoluwa surname: Sule fullname: Sule, Naheemot Olaoluwa organization: Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Québec, Canada – sequence: 2 givenname: Samy orcidid: 0000-0002-1281-5296 surname: Suissa fullname: Suissa, Samy organization: Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Québec, Canada, Centre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, Montreal, Québec, Canada |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37555454$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkUtvUzEQhS1U1Bf9CSAv2STYY_teG1ZVeFVqFUTbteVncXVzXWynqP-emybNgg2rGR1954w05wQdjHkMCL2lZE6JJB-o4BSEEHMgwOYAHLhUr9DxRp-B6NjBfhfiCJ3Uek8ICM7EITpi_SRywY_R8rqZlsaKzejxVS7NDKk94TTixfLH54_4HF-F9iv7POS75MyAf4bHFP7gHPHS1lAeJ3ceJ_26rX0K9Q16Hc1Qw9lunqLbr19uFt9nl8tvF4vzy5njUrZZ73mkKhLfAfOBCTAeYqe4s8wz45TkwqpOBGo76iKTlitLCI2RG0Z7Gdkputjm-mzu9UNJK1OedDZJPwu53GlTWnJD0AYc9JyA6aXigTJJQEHnO2t73kXLpqz326yHkn-vQ216laoLw2DGkNdVg-QSGOmZmtB3O3RtV8HvD788dALEFnAl11pC3COU6E1x-qU4vSlO74qbfJ_-8bnUnn_biknDf9x_AYjrmk4 |
CitedBy_id | crossref_primary_10_5551_jat_RV22021 crossref_primary_10_1093_ije_dyae176 crossref_primary_10_1080_15412555_2024_2317380 |
Cites_doi | 10.1002/pds.5083 10.1183/16000617.0057-2018 10.4104/pcrj.2011.00095 10.1136/bmj.j4587 10.1183/13993003.01798-2020 10.1161/01.cir.103.15.1933 10.1186/1465-9921-15-80 10.1016/j.jclinepi.2016.01.021 10.1016/j.jacc.2006.04.039 10.1183/09031936.00106406 10.1097/maj.0000000000000435 10.1016/j.arbr.2017.02.001 10.5812/ircmj.8267 10.1186/1471-2466-9-32 10.1186/1465-9921-10-45 10.1111/j.1742-1241.2008.01731.x 10.1378/chest.09-0194 10.2147/copd.s296472 10.1016/j.pupt.2011.06.003 10.1002/14651858.cd011959.pub2 10.1136/bmjopen-2015-007866 10.1002/pds.1357 10.1016/j.chest.2017.02.002 10.1159/000315387 10.1016/j.clinthera.2011.12.014 10.1164/rccm.200705-656oc 10.1097/01.ede.0000042804.12056.6c 10.1093/ije/dyp334 10.1136/thoraxjnl-2011-201518 10.1080/15412555.2021.1963696 10.1371/journal.pone.0114866 10.1016/j.clinthera.2011.08.010 10.1093/aje/kwm324 10.1164/rccm.201208-1565oc 10.1161/circulationaha.108.824151 10.1002/pds.4107 10.1111/j.1541-0420.2011.01619.x 10.1093/aje/kwj275 10.1136/bmj.d549 10.1016/j.pupt.2012.10.008 10.1007/s40801-016-0101-6 10.1056/nejmoa1403086 10.1136/bmjopen-2021-050757 10.1056/nejmsb1609216 10.1038/sj.ki.5002650 10.1371/journal.pone.0037483 10.1136/bmjresp-2016-000142 10.3390/jpm12020299 10.1183/13993003.02112-2018 |
ContentType | Journal Article |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 DOA |
DOI | 10.1080/15412555.2023.2242489 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1541-2563 |
EndPage | 291 |
ExternalDocumentID | oai_doaj_org_article_a2c27402a7894e13802926d6bb746fb3 37555454 10_1080_15412555_2023_2242489 |
Genre | Research Support, Non-U.S. Gov't Journal Article Review |
GroupedDBID | --- 00X 03L 0YH 29B 4.4 5GY AALUX AAYXX ABDBF ABEIZ ABLKL ABUPF ACGEJ ACGFS ACUHS ADCVX ADRBQ ADXPE AECIN AEOZL AGYJP AIJEM ALMA_UNASSIGNED_HOLDINGS ALQZU BABNJ BLEHA BOHLJ CCCUG CITATION CS3 DKSSO EBD EBS EMOBN ESX F5P GROUPED_DOAJ H13 HZ~ KRBQP KSSTO KWAYT KYCEM LJTGL M4Z O9- OK1 SV3 TDBHL TFDNU TFL TFW TUS V1S ~1N 53G 5VS AALIY ACKZS ADFZZ AFFVI AWYRJ CAG CGR COF CUY CVF CZDIS DRXRE DWTOO ECM EIF EJD M44 NPM S70 7X8 |
ID | FETCH-LOGICAL-c488t-7d4f19f0d623de352ad2f694cb3d3ac9845b965e1b61cf38b49b001ff4a3178f3 |
IEDL.DBID | DOA |
ISSN | 1541-2555 1541-2563 |
IngestDate | Wed Aug 27 01:22:54 EDT 2025 Wed Oct 01 17:16:04 EDT 2025 Thu Apr 03 07:01:21 EDT 2025 Tue Jul 01 01:04:15 EDT 2025 Thu Apr 24 22:58:09 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Keywords | selection bias Confounding immortal time bias database studies |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c488t-7d4f19f0d623de352ad2f694cb3d3ac9845b965e1b61cf38b49b001ff4a3178f3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
ORCID | 0000-0002-1281-5296 |
OpenAccessLink | https://doaj.org/article/a2c27402a7894e13802926d6bb746fb3 |
PMID | 37555454 |
PQID | 2848230739 |
PQPubID | 23479 |
PageCount | 8 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_a2c27402a7894e13802926d6bb746fb3 proquest_miscellaneous_2848230739 pubmed_primary_37555454 crossref_primary_10_1080_15412555_2023_2242489 crossref_citationtrail_10_1080_15412555_2023_2242489 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2023-12-00 |
PublicationDateYYYYMMDD | 2023-12-01 |
PublicationDate_xml | – month: 12 year: 2023 text: 2023-12-00 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | Chronic obstructive pulmonary disease |
PublicationTitleAlternate | COPD |
PublicationYear | 2023 |
Publisher | Taylor & Francis Group |
Publisher_xml | – name: Taylor & Francis Group |
References | e_1_3_2_28_1 e_1_3_2_49_1 e_1_3_2_20_1 e_1_3_2_41_1 e_1_3_2_22_1 e_1_3_2_43_1 e_1_3_2_24_1 e_1_3_2_45_1 e_1_3_2_26_1 e_1_3_2_47_1 e_1_3_2_16_1 e_1_3_2_39_1 e_1_3_2_9_1 e_1_3_2_18_1 e_1_3_2_7_1 e_1_3_2_31_1 e_1_3_2_10_1 e_1_3_2_33_1 e_1_3_2_12_1 e_1_3_2_35_1 e_1_3_2_5_1 e_1_3_2_14_1 e_1_3_2_37_1 e_1_3_2_3_1 e_1_3_2_50_1 e_1_3_2_27_1 e_1_3_2_29_1 e_1_3_2_42_1 e_1_3_2_21_1 e_1_3_2_44_1 e_1_3_2_23_1 e_1_3_2_46_1 e_1_3_2_25_1 e_1_3_2_48_1 e_1_3_2_40_1 e_1_3_2_17_1 e_1_3_2_38_1 e_1_3_2_8_1 e_1_3_2_19_1 e_1_3_2_2_1 e_1_3_2_30_1 e_1_3_2_11_1 e_1_3_2_32_1 e_1_3_2_6_1 e_1_3_2_13_1 e_1_3_2_34_1 e_1_3_2_4_1 e_1_3_2_15_1 e_1_3_2_36_1 |
References_xml | – ident: e_1_3_2_42_1 doi: 10.1002/pds.5083 – ident: e_1_3_2_4_1 doi: 10.1183/16000617.0057-2018 – ident: e_1_3_2_19_1 doi: 10.4104/pcrj.2011.00095 – ident: e_1_3_2_45_1 doi: 10.1136/bmj.j4587 – ident: e_1_3_2_10_1 doi: 10.1183/13993003.01798-2020 – ident: e_1_3_2_5_1 doi: 10.1161/01.cir.103.15.1933 – ident: e_1_3_2_8_1 doi: 10.1186/1465-9921-15-80 – ident: e_1_3_2_13_1 doi: 10.1016/j.jclinepi.2016.01.021 – ident: e_1_3_2_15_1 doi: 10.1016/j.jacc.2006.04.039 – ident: e_1_3_2_16_1 doi: 10.1183/09031936.00106406 – ident: e_1_3_2_24_1 doi: 10.1097/maj.0000000000000435 – ident: e_1_3_2_2_1 doi: 10.1016/j.arbr.2017.02.001 – ident: e_1_3_2_48_1 doi: 10.5812/ircmj.8267 – ident: e_1_3_2_7_1 doi: 10.1186/1471-2466-9-32 – ident: e_1_3_2_17_1 doi: 10.1186/1465-9921-10-45 – ident: e_1_3_2_38_1 doi: 10.1111/j.1742-1241.2008.01731.x – ident: e_1_3_2_12_1 doi: 10.1378/chest.09-0194 – ident: e_1_3_2_27_1 doi: 10.2147/copd.s296472 – ident: e_1_3_2_18_1 doi: 10.1016/j.pupt.2011.06.003 – ident: e_1_3_2_47_1 doi: 10.1002/14651858.cd011959.pub2 – ident: e_1_3_2_41_1 doi: 10.1136/bmjopen-2015-007866 – ident: e_1_3_2_31_1 doi: 10.1002/pds.1357 – ident: e_1_3_2_26_1 doi: 10.1016/j.chest.2017.02.002 – ident: e_1_3_2_11_1 doi: 10.1159/000315387 – ident: e_1_3_2_20_1 doi: 10.1016/j.clinthera.2011.12.014 – ident: e_1_3_2_6_1 doi: 10.1164/rccm.200705-656oc – ident: e_1_3_2_33_1 doi: 10.1097/01.ede.0000042804.12056.6c – ident: e_1_3_2_34_1 doi: 10.1093/ije/dyp334 – ident: e_1_3_2_37_1 doi: 10.1136/thoraxjnl-2011-201518 – ident: e_1_3_2_30_1 doi: 10.1080/15412555.2021.1963696 – ident: e_1_3_2_23_1 doi: 10.1371/journal.pone.0114866 – ident: e_1_3_2_40_1 doi: 10.1016/j.clinthera.2011.08.010 – ident: e_1_3_2_32_1 doi: 10.1093/aje/kwm324 – ident: e_1_3_2_21_1 doi: 10.1164/rccm.201208-1565oc – ident: e_1_3_2_50_1 doi: 10.1161/circulationaha.108.824151 – ident: e_1_3_2_49_1 doi: 10.1002/pds.4107 – ident: e_1_3_2_43_1 doi: 10.1111/j.1541-0420.2011.01619.x – ident: e_1_3_2_36_1 doi: 10.1093/aje/kwj275 – ident: e_1_3_2_14_1 doi: 10.1136/bmj.d549 – ident: e_1_3_2_22_1 doi: 10.1016/j.pupt.2012.10.008 – ident: e_1_3_2_39_1 doi: 10.1007/s40801-016-0101-6 – ident: e_1_3_2_9_1 doi: 10.1056/nejmoa1403086 – ident: e_1_3_2_28_1 doi: 10.1136/bmjopen-2021-050757 – ident: e_1_3_2_46_1 doi: 10.1056/nejmsb1609216 – ident: e_1_3_2_44_1 doi: 10.1038/sj.ki.5002650 – ident: e_1_3_2_3_1 doi: 10.1371/journal.pone.0037483 – ident: e_1_3_2_25_1 doi: 10.1136/bmjresp-2016-000142 – ident: e_1_3_2_29_1 doi: 10.3390/jpm12020299 – ident: e_1_3_2_35_1 doi: 10.1183/13993003.02112-2018 |
SSID | ssj0025435 |
Score | 2.3714619 |
SecondaryResourceType | review_article |
Snippet | Randomized controlled trials and observational studies have reported conflicting results on the potential beneficial effects of statins on mortality in... |
SourceID | doaj proquest pubmed crossref |
SourceType | Open Website Aggregation Database Index Database Enrichment Source |
StartPage | 284 |
SubjectTerms | confounding database studies Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use immortal time bias Observational Studies as Topic Pulmonary Disease, Chronic Obstructive - drug therapy selection bias |
Title | Statins and Mortality in COPD: A Methodological Review of Observational Studies |
URI | https://www.ncbi.nlm.nih.gov/pubmed/37555454 https://www.proquest.com/docview/2848230739 https://doaj.org/article/a2c27402a7894e13802926d6bb746fb3 |
Volume | 20 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
journalDatabaseRights | – providerCode: PRVAON databaseName: DOAJ Directory of Open Access Journals customDbUrl: eissn: 1541-2563 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025435 issn: 1541-2555 databaseCode: DOA dateStart: 20220101 isFulltext: true titleUrlDefault: https://www.doaj.org/ providerName: Directory of Open Access Journals – providerCode: PRVEBS databaseName: Academic Search Ultimate customDbUrl: https://search.ebscohost.com/login.aspx?authtype=ip,shib&custid=s3936755&profile=ehost&defaultdb=asn eissn: 1541-2563 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025435 issn: 1541-2555 databaseCode: ABDBF dateStart: 20040501 isFulltext: true titleUrlDefault: https://search.ebscohost.com/direct.asp?db=asn providerName: EBSCOhost – providerCode: PRVAWR databaseName: Taylor & Francis Open Access customDbUrl: eissn: 1541-2563 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0025435 issn: 1541-2555 databaseCode: 0YH dateStart: 20221201 isFulltext: true titleUrlDefault: https://www.tandfonline.com providerName: Taylor & Francis |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV07a8MwEBYlQ-lS-m76QoWuTqKHZatb-gih4KZDA9mMZEsQKE5pkv_fO1sOWUqWrodsyaeT7zud9B0hD4lgTDilIqc4BCjWJpEplIwsc9qy2PDY4T5k9q7GU_k2i2dbpb7wTFhDD9worm94AYHTgJsk1dIxkQ645qpU8FapvK15PsGNtcFUCLViWZfWBHzAIgDNcXt3Jx30UYaiHhYO73G8HoE13re8Uk3e_zfirD3P6IgcBshIh81Qj8meq07IfhaS4qdkgoBxXi2pqUqa1XAaoDWdV_R58vHySIc0q8tEt7852uQD6MLTid1syoI8nCk8I9PR6-fzOAp1EqIClt8qSkrpmfaDEqBM6QBRmZJ7pWVhRSlMoVMZW61ix6xihReplUiEyLyXBtBD6sU56VSLyl0S6nyqvGfKag2tGLNI4QUoptTcQR-sS2Srp7wIJOJYy-IrZ4FrtFVvjurNg3q7pLd57Lth0dj1wBNOwqYxkmDXAjCNPJhGvss0uuS-ncIcFg1mQkzlFutlDj4ZE4yJgI4umrnddCUSGIyM5dV_DOGaHOBnNedfbkhn9bN2t4BiVvauNthfSozk0Q |
linkProvider | Directory of Open Access Journals |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Statins+and+Mortality+in+COPD%3A+A+Methodological+Review+of+Observational+Studies&rft.jtitle=Chronic+obstructive+pulmonary+disease&rft.au=Sule%2C+Naheemot+Olaoluwa&rft.au=Suissa%2C+Samy&rft.date=2023-12-01&rft.issn=1541-2555&rft.eissn=1541-2563&rft.volume=20&rft.issue=1&rft.spage=284&rft.epage=291&rft_id=info:doi/10.1080%2F15412555.2023.2242489&rft.externalDBID=n%2Fa&rft.externalDocID=10_1080_15412555_2023_2242489 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1541-2555&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1541-2555&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1541-2555&client=summon |