Oral anticoagulation in patients with hypertrophic cardiomyopathy and non-valvular atrial fibrillation in Japan
There are limited data to support direct oral anticoagulant (DOAC) use in patients with hypertrophic cardiomyopathy (HCM) and non-valvular atrial fibrillation (NVAF). The current study investigated the safety and effectiveness of DOACs versus warfarin in patients in Japan. This retrospective observa...
Saved in:
Published in: | ESC Heart Failure |
---|---|
Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
19-09-2024
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | There are limited data to support direct oral anticoagulant (DOAC) use in patients with hypertrophic cardiomyopathy (HCM) and non-valvular atrial fibrillation (NVAF). The current study investigated the safety and effectiveness of DOACs versus warfarin in patients in Japan.
This retrospective observational study assessed a Japanese cohort of patients diagnosed with HCM and NVAF between July 2011 and June 2021 using a Japanese claims database. Propensity score (PS) matching (2:1 DOAC:warfarin) using the nearest-neighbour method was applied to balance demographic and clinical characteristics between treatment groups. The primary outcomes were the risk of major bleeding and any bleeding (major or minor). Secondary outcomes included describing baseline demographic and clinical characteristics and the risk of stroke/systemic embolism (SE).
After PS matching, 2955 DOAC- and 1603 warfarin-treated patients were assessed. The mean [standard deviation (SD)] age in the DOAC and warfarin groups was 74.8 (10.5) and 75.3 (10.2) years, respectively. The majority of patients were male (DOAC, 58.8%; warfarin, 59.6%), had comorbidities (DOAC, 97.5%; warfarin, 96.6%), and were treated with β-blockers (DOAC, 62.5%; warfarin, 62.3%). The risk of major and any bleeding was similar across cohorts [hazard ratio (HR), 0.80; 95% confidence interval (CI), 0.50-1.27; P = 0.336 and HR, 0.93; 95% CI, 0.78-1.11; P = 0.420] while the risk of stroke/SE was lower among patients treated with DOACs (HR, 0.67; 95% CI, 0.47-0.96; P = 0.027). Factors associated with an increased risk of major bleeding included prior bleeding (HR, 1.97; 95% CI, 1.22-3.17) and chronic kidney disease (HR, 1.87; 95% CI, 1.10-3.18). An increased risk of stroke/SE was associated with prior ischaemic stroke (HR, 2.97; 95% CI, 2.05-4.29), peripheral arterial disease (HR, 1.88; 95% CI, 1.22-2.88) and chronic kidney disease (HR, 1.87; 95% CI, 1.24-2.83).
DOAC-treated patients had a lower risk of stroke/SE and a comparable risk of bleeding compared with warfarin-treated patients. Prior stroke was shown to augment stroke risk by approximately three-fold. This large real-world study suggests that patients diagnosed with HCM and NVAF can be safely and effectively treated with DOACs in Japan. |
---|---|
AbstractList | There are limited data to support direct oral anticoagulant (DOAC) use in patients with hypertrophic cardiomyopathy (HCM) and non-valvular atrial fibrillation (NVAF). The current study investigated the safety and effectiveness of DOACs versus warfarin in patients in Japan.AIMSThere are limited data to support direct oral anticoagulant (DOAC) use in patients with hypertrophic cardiomyopathy (HCM) and non-valvular atrial fibrillation (NVAF). The current study investigated the safety and effectiveness of DOACs versus warfarin in patients in Japan.This retrospective observational study assessed a Japanese cohort of patients diagnosed with HCM and NVAF between July 2011 and June 2021 using a Japanese claims database. Propensity score (PS) matching (2:1 DOAC:warfarin) using the nearest-neighbour method was applied to balance demographic and clinical characteristics between treatment groups. The primary outcomes were the risk of major bleeding and any bleeding (major or minor). Secondary outcomes included describing baseline demographic and clinical characteristics and the risk of stroke/systemic embolism (SE).METHODSThis retrospective observational study assessed a Japanese cohort of patients diagnosed with HCM and NVAF between July 2011 and June 2021 using a Japanese claims database. Propensity score (PS) matching (2:1 DOAC:warfarin) using the nearest-neighbour method was applied to balance demographic and clinical characteristics between treatment groups. The primary outcomes were the risk of major bleeding and any bleeding (major or minor). Secondary outcomes included describing baseline demographic and clinical characteristics and the risk of stroke/systemic embolism (SE).After PS matching, 2955 DOAC- and 1603 warfarin-treated patients were assessed. The mean [standard deviation (SD)] age in the DOAC and warfarin groups was 74.8 (10.5) and 75.3 (10.2) years, respectively. The majority of patients were male (DOAC, 58.8%; warfarin, 59.6%), had comorbidities (DOAC, 97.5%; warfarin, 96.6%), and were treated with β-blockers (DOAC, 62.5%; warfarin, 62.3%). The risk of major and any bleeding was similar across cohorts [hazard ratio (HR), 0.80; 95% confidence interval (CI), 0.50-1.27; P = 0.336 and HR, 0.93; 95% CI, 0.78-1.11; P = 0.420] while the risk of stroke/SE was lower among patients treated with DOACs (HR, 0.67; 95% CI, 0.47-0.96; P = 0.027). Factors associated with an increased risk of major bleeding included prior bleeding (HR, 1.97; 95% CI, 1.22-3.17) and chronic kidney disease (HR, 1.87; 95% CI, 1.10-3.18). An increased risk of stroke/SE was associated with prior ischaemic stroke (HR, 2.97; 95% CI, 2.05-4.29), peripheral arterial disease (HR, 1.88; 95% CI, 1.22-2.88) and chronic kidney disease (HR, 1.87; 95% CI, 1.24-2.83).RESULTSAfter PS matching, 2955 DOAC- and 1603 warfarin-treated patients were assessed. The mean [standard deviation (SD)] age in the DOAC and warfarin groups was 74.8 (10.5) and 75.3 (10.2) years, respectively. The majority of patients were male (DOAC, 58.8%; warfarin, 59.6%), had comorbidities (DOAC, 97.5%; warfarin, 96.6%), and were treated with β-blockers (DOAC, 62.5%; warfarin, 62.3%). The risk of major and any bleeding was similar across cohorts [hazard ratio (HR), 0.80; 95% confidence interval (CI), 0.50-1.27; P = 0.336 and HR, 0.93; 95% CI, 0.78-1.11; P = 0.420] while the risk of stroke/SE was lower among patients treated with DOACs (HR, 0.67; 95% CI, 0.47-0.96; P = 0.027). Factors associated with an increased risk of major bleeding included prior bleeding (HR, 1.97; 95% CI, 1.22-3.17) and chronic kidney disease (HR, 1.87; 95% CI, 1.10-3.18). An increased risk of stroke/SE was associated with prior ischaemic stroke (HR, 2.97; 95% CI, 2.05-4.29), peripheral arterial disease (HR, 1.88; 95% CI, 1.22-2.88) and chronic kidney disease (HR, 1.87; 95% CI, 1.24-2.83).DOAC-treated patients had a lower risk of stroke/SE and a comparable risk of bleeding compared with warfarin-treated patients. Prior stroke was shown to augment stroke risk by approximately three-fold. This large real-world study suggests that patients diagnosed with HCM and NVAF can be safely and effectively treated with DOACs in Japan.CONCLUSIONSDOAC-treated patients had a lower risk of stroke/SE and a comparable risk of bleeding compared with warfarin-treated patients. Prior stroke was shown to augment stroke risk by approximately three-fold. This large real-world study suggests that patients diagnosed with HCM and NVAF can be safely and effectively treated with DOACs in Japan. There are limited data to support direct oral anticoagulant (DOAC) use in patients with hypertrophic cardiomyopathy (HCM) and non-valvular atrial fibrillation (NVAF). The current study investigated the safety and effectiveness of DOACs versus warfarin in patients in Japan. This retrospective observational study assessed a Japanese cohort of patients diagnosed with HCM and NVAF between July 2011 and June 2021 using a Japanese claims database. Propensity score (PS) matching (2:1 DOAC:warfarin) using the nearest-neighbour method was applied to balance demographic and clinical characteristics between treatment groups. The primary outcomes were the risk of major bleeding and any bleeding (major or minor). Secondary outcomes included describing baseline demographic and clinical characteristics and the risk of stroke/systemic embolism (SE). After PS matching, 2955 DOAC- and 1603 warfarin-treated patients were assessed. The mean [standard deviation (SD)] age in the DOAC and warfarin groups was 74.8 (10.5) and 75.3 (10.2) years, respectively. The majority of patients were male (DOAC, 58.8%; warfarin, 59.6%), had comorbidities (DOAC, 97.5%; warfarin, 96.6%), and were treated with β-blockers (DOAC, 62.5%; warfarin, 62.3%). The risk of major and any bleeding was similar across cohorts [hazard ratio (HR), 0.80; 95% confidence interval (CI), 0.50-1.27; P = 0.336 and HR, 0.93; 95% CI, 0.78-1.11; P = 0.420] while the risk of stroke/SE was lower among patients treated with DOACs (HR, 0.67; 95% CI, 0.47-0.96; P = 0.027). Factors associated with an increased risk of major bleeding included prior bleeding (HR, 1.97; 95% CI, 1.22-3.17) and chronic kidney disease (HR, 1.87; 95% CI, 1.10-3.18). An increased risk of stroke/SE was associated with prior ischaemic stroke (HR, 2.97; 95% CI, 2.05-4.29), peripheral arterial disease (HR, 1.88; 95% CI, 1.22-2.88) and chronic kidney disease (HR, 1.87; 95% CI, 1.24-2.83). DOAC-treated patients had a lower risk of stroke/SE and a comparable risk of bleeding compared with warfarin-treated patients. Prior stroke was shown to augment stroke risk by approximately three-fold. This large real-world study suggests that patients diagnosed with HCM and NVAF can be safely and effectively treated with DOACs in Japan. |
Author | Kubo, Toru Teixeira, Bruno Casaes Kitaoka, Hiroaki Eugene, Natalie Carroll, Robert Matsuo, Yukako |
Author_xml | – sequence: 1 givenname: Hiroaki surname: Kitaoka fullname: Kitaoka, Hiroaki organization: Department of Cardiology and Geriatrics, Kochi Medical School, Kochi University, Nankoku, Japan – sequence: 2 givenname: Robert surname: Carroll fullname: Carroll, Robert organization: Centre for Observational Research and Data Sciences, Bristol Myers Squibb, Uxbridge, UK – sequence: 3 givenname: Natalie surname: Eugene fullname: Eugene, Natalie organization: Centre for Observational Research and Data Sciences, Bristol Myers Squibb, Uxbridge, UK – sequence: 4 givenname: Bruno Casaes surname: Teixeira fullname: Teixeira, Bruno Casaes organization: Real-World-Data Analytics, Bristol Myers Squibb, London, UK – sequence: 5 givenname: Yukako surname: Matsuo fullname: Matsuo, Yukako organization: Medical Department, Bristol Myers Squibb K.K., Chiyoda, Japan – sequence: 6 givenname: Toru surname: Kubo fullname: Kubo, Toru organization: Department of Cardiology and Geriatrics, Kochi Medical School, Kochi University, Nankoku, Japan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39300752$$D View this record in MEDLINE/PubMed |
BookMark | eNpNkMtOwzAQRS1UREvphg9AXiKkwNhO6nSJKp6q1A2sI9exiVESB9spyt_j0vJYzV2cObq6p2jU2lYhdE7gmgDQG1Vpek0yYIsjNKGQZUmWUzr6l8do5v07AJBsTjKanqAxWzAAntEJsmsnaizaYKQVb30tgrEtNi3uYlJt8PjThApXQ6dccLarjMRSuNLYZrCRqYb4XOJYKtmKehsFDovgTJRqs3Gm_jM-i060Z-hYi9qr2eFO0ev93cvyMVmtH56Wt6tEUkJDQsu8JARkzjQRXDGQhOtSMxALmEtKFecMdAxaccqFlJEvU5KTRZ6qNOVsii733s7Zj175UDTGSxXrtMr2vmAEOMnyOaMRvdqj0lnvndJF50wj3FAQKHYbF7uNi--NI3xx8PabRpW_6M-i7AvmiXq5 |
Cites_doi | 10.1056/NEJMra1710575 10.1056/NEJMoa1009638 10.1056/NEJMoa1107039 10.1253/circj.CJ‐20‐1212 10.1253/circrep.CR‐21‐0001 10.1056/NEJMoa0905561 10.1016/j.jacc.2016.04.026 10.1161/CIR.0b013e318223e230 10.1161/01.cir.92.4.785 10.1016/j.jacc.2015.01.019 10.1016/j.amjcard.2017.01.005 10.1016/s0735‐1097(01)01727‐2 10.1111/j.1538‐7836.2005.01204.x 10.1136/heartjnl‐2013‐304276 10.1016/j.amjmed.2015.07.013 10.1002/joa3.12184 10.1016/j.jjcc.2018.09.003 10.1161/CIRCULATIONAHA.117.033200 10.14744/AnatolJCardiol.2016.6752 10.1016/j.chest.2018.11.009 10.1253/circj.CJ‐20‐0910 10.1093/ehjqcco/qcx032 10.1093/eurheartj/ehaa612 10.1016/j.ijcard.2017.08.010 10.1002/ehf2.13563 10.1161/JAHA.114.001002 10.1016/j.ijcard.2008.06.029 10.1253/circj.CJ‐21‐0682 10.1093/eurheartj/ehu284 10.1111/jth.13140 10.1016/j.jjcc.2022.09.015 10.1161/hc4601.097997 10.1714/4127.41209 10.1056/NEJMoa1310907 10.1001/jamanetworkopen.2020.2881 |
ContentType | Journal Article |
Copyright | 2024 The Author(s). ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. |
Copyright_xml | – notice: 2024 The Author(s). ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. |
DBID | NPM AAYXX CITATION 7X8 |
DOI | 10.1002/ehf2.15039 |
DatabaseName | PubMed CrossRef MEDLINE - Academic |
DatabaseTitle | PubMed CrossRef MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 2055-5822 |
ExternalDocumentID | 10_1002_ehf2_15039 39300752 |
Genre | Journal Article |
GrantInformation_xml | – fundername: Bristol Myers Squibb K.K. |
GroupedDBID | 0R~ 1OC 24P 53G 5VS 7X7 8FI 8FJ AAHHS ABUWG ACCFJ ACXQS ADBBV ADKYN ADZMN ADZOD AEEZP AEQDE AFKRA AIWBW AJBDE ALIPV ALMA_UNASSIGNED_HOLDINGS ALUQN AOIJS AVUZU BAWUL BCNDV BENPR BPHCQ BVXVI CCPQU DIK EBS EMOBN FYUFA GROUPED_DOAJ HMCUK HYE IAO IHR INH ITC KQ8 M~E NPM OK1 PIMPY PQQKQ RPM UKHRP WIN AAYXX CITATION 7X8 |
ID | FETCH-LOGICAL-c212t-2d8d110c83f1a7e30c17fdf30a906c22e7730fc22fe727accd8dd4181984e4473 |
ISSN | 2055-5822 |
IngestDate | Sat Oct 26 03:57:28 EDT 2024 Fri Nov 22 01:40:16 EST 2024 Sat Nov 02 12:19:20 EDT 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | atrial fibrillation ischaemic stroke hypertrophic cardiomyopathy direct oral anticoagulant |
Language | English |
License | 2024 The Author(s). ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c212t-2d8d110c83f1a7e30c17fdf30a906c22e7730fc22fe727accd8dd4181984e4473 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | https://doi.org/10.1002/ehf2.15039 |
PMID | 39300752 |
PQID | 3107158632 |
PQPubID | 23479 |
ParticipantIDs | proquest_miscellaneous_3107158632 crossref_primary_10_1002_ehf2_15039 pubmed_primary_39300752 |
PublicationCentury | 2000 |
PublicationDate | 2024-Sep-19 2024-09-19 20240919 |
PublicationDateYYYYMMDD | 2024-09-19 |
PublicationDate_xml | – month: 09 year: 2024 text: 2024-Sep-19 day: 19 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | ESC Heart Failure |
PublicationTitleAlternate | ESC Heart Fail |
PublicationYear | 2024 |
References | e_1_2_8_28_1 e_1_2_8_29_1 e_1_2_8_24_1 e_1_2_8_25_1 e_1_2_8_26_1 e_1_2_8_27_1 e_1_2_8_3_1 e_1_2_8_2_1 e_1_2_8_5_1 e_1_2_8_4_1 e_1_2_8_7_1 e_1_2_8_6_1 e_1_2_8_9_1 e_1_2_8_8_1 e_1_2_8_20_1 e_1_2_8_21_1 e_1_2_8_22_1 e_1_2_8_23_1 e_1_2_8_17_1 e_1_2_8_18_1 e_1_2_8_19_1 e_1_2_8_13_1 e_1_2_8_36_1 e_1_2_8_14_1 e_1_2_8_35_1 e_1_2_8_15_1 e_1_2_8_16_1 e_1_2_8_37_1 e_1_2_8_32_1 e_1_2_8_10_1 e_1_2_8_31_1 e_1_2_8_11_1 e_1_2_8_34_1 e_1_2_8_12_1 e_1_2_8_33_1 e_1_2_8_30_1 |
References_xml | – ident: e_1_2_8_7_1 doi: 10.1056/NEJMra1710575 – ident: e_1_2_8_30_1 doi: 10.1056/NEJMoa1009638 – ident: e_1_2_8_37_1 – ident: e_1_2_8_20_1 doi: 10.1056/NEJMoa1107039 – ident: e_1_2_8_15_1 doi: 10.1253/circj.CJ‐20‐1212 – ident: e_1_2_8_25_1 doi: 10.1253/circrep.CR‐21‐0001 – ident: e_1_2_8_31_1 doi: 10.1056/NEJMoa0905561 – ident: e_1_2_8_16_1 doi: 10.1016/j.jacc.2016.04.026 – ident: e_1_2_8_2_1 doi: 10.1161/CIR.0b013e318223e230 – ident: e_1_2_8_5_1 doi: 10.1161/01.cir.92.4.785 – ident: e_1_2_8_6_1 doi: 10.1016/j.jacc.2015.01.019 – ident: e_1_2_8_35_1 doi: 10.1016/j.amjcard.2017.01.005 – ident: e_1_2_8_9_1 doi: 10.1016/s0735‐1097(01)01727‐2 – ident: e_1_2_8_18_1 doi: 10.1111/j.1538‐7836.2005.01204.x – ident: e_1_2_8_34_1 doi: 10.1136/heartjnl‐2013‐304276 – ident: e_1_2_8_21_1 doi: 10.1016/j.amjmed.2015.07.013 – ident: e_1_2_8_32_1 doi: 10.1002/joa3.12184 – ident: e_1_2_8_23_1 doi: 10.1016/j.jjcc.2018.09.003 – ident: e_1_2_8_8_1 doi: 10.1161/CIRCULATIONAHA.117.033200 – ident: e_1_2_8_22_1 doi: 10.14744/AnatolJCardiol.2016.6752 – ident: e_1_2_8_17_1 doi: 10.1016/j.chest.2018.11.009 – ident: e_1_2_8_4_1 doi: 10.1253/circj.CJ‐20‐0910 – ident: e_1_2_8_36_1 doi: 10.1093/ehjqcco/qcx032 – ident: e_1_2_8_14_1 doi: 10.1093/eurheartj/ehaa612 – ident: e_1_2_8_26_1 doi: 10.1016/j.ijcard.2017.08.010 – ident: e_1_2_8_11_1 doi: 10.1002/ehf2.13563 – ident: e_1_2_8_10_1 doi: 10.1161/JAHA.114.001002 – ident: e_1_2_8_24_1 doi: 10.1016/j.ijcard.2008.06.029 – ident: e_1_2_8_28_1 doi: 10.1253/circj.CJ‐21‐0682 – ident: e_1_2_8_3_1 doi: 10.1093/eurheartj/ehu284 – ident: e_1_2_8_19_1 doi: 10.1111/jth.13140 – ident: e_1_2_8_12_1 doi: 10.1016/j.jjcc.2022.09.015 – ident: e_1_2_8_33_1 doi: 10.1161/hc4601.097997 – ident: e_1_2_8_13_1 doi: 10.1714/4127.41209 – ident: e_1_2_8_29_1 doi: 10.1056/NEJMoa1310907 – ident: e_1_2_8_27_1 doi: 10.1001/jamanetworkopen.2020.2881 |
SSID | ssj0001561524 |
Score | 2.3200617 |
Snippet | There are limited data to support direct oral anticoagulant (DOAC) use in patients with hypertrophic cardiomyopathy (HCM) and non-valvular atrial fibrillation... |
SourceID | proquest crossref pubmed |
SourceType | Aggregation Database Index Database |
Title | Oral anticoagulation in patients with hypertrophic cardiomyopathy and non-valvular atrial fibrillation in Japan |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39300752 https://www.proquest.com/docview/3107158632 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3dT9swELeASdNeEPvuYMjT9laFpbbTJI8TtKoGgweCxFvk-oNGgxilzbT99zvbadIMTWIPe4miU3N17369_GzfnRH6FHMIeikbB3psS3LSOA14yuGPx0Q4l3MmiTvOZ3YZn18nJxM26ZLYO9l_9TTIwNe2cvYfvN0qBQHcg8_hCl6H66P8flG56n-QG37TnM017BqoNtVsC5h-VqvK3C8KYbtTy8Lc_TL2eGLfj6k0ZQCj-uGSVLk_2kPb6oDbTuNXeM-WvZX9S_sagzENp7y4rbu02tNixc13R1NnRWWAtHZbH1Vl_M6Hz_FuGX4Nv1D5-G-bNLa6MlX8VEXFG2CWZnjMl1z1li8Is7kWTZB0UY6EURREiS9OPlIPZQ9ivO8ZqxaaHAGb9a2Q-o20zy_y6dXZWZ5NrrNt9IRADKIbCzlNATkwF5tz0H5Z27yWfO6U9-nKX-Ygjotke2i3mUTgL977z9GWKl-gp9-aNImXyFgQ4D9AgIsSr0GALQjwJghwHwTwsMSbIMAeBHgTBFajA8ErdDWdZMezoDlZIxBAVVYBkYkE3icSqkc8VjQUo1hLTUOehmNBiIoh8Gu40Qr4LRcCPi8ZkME0YYqxmL5GOzAG9RbhSAqSKBrxyJL_kZ5zIhWjcq6SCITpAH1cGzC_9w1Uct8qm-TWzLkz8wB9WNs2h_hmN614qUy9zGH6EY-iZEzJAL3xRm_10JRaykvePeLpffSsg98B2llVtXqPtpeyPnTrMIcOH78BapF9JQ |
link.rule.ids | 315,782,786,866,27933,27934 |
linkProvider | National Library of Medicine |
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=Oral+anticoagulation+in+patients+with+hypertrophic+cardiomyopathy+and+non-valvular+atrial+fibrillation+in+Japan&rft.jtitle=ESC+Heart+Failure&rft.au=Kitaoka%2C+Hiroaki&rft.au=Carroll%2C+Robert&rft.au=Eugene%2C+Natalie&rft.au=Teixeira%2C+Bruno+Casaes&rft.date=2024-09-19&rft.issn=2055-5822&rft.eissn=2055-5822&rft_id=info:doi/10.1002%2Fehf2.15039&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2055-5822&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2055-5822&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2055-5822&client=summon |