Impact of ACEI/ARB use on COVID-19 mortality in patients with ischaemic heart disease: insights from South Korean National health insurance service data

Background The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:BMC infectious diseases Ročník 25; číslo 1; s. 1529 - 12
Hlavní autoři: Kim, Shin-Woo, Goo, Taewan, Noh, Seunghwan, Lee, Seungyeoun, Oh, Bumjo, Park, Taesung
Médium: Journal Article
Jazyk:angličtina
Vydáno: London BioMed Central 10.11.2025
BioMed Central Ltd
BMC
Témata:
ISSN:1471-2334, 1471-2334
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Abstract Background The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the use of angiotensin receptor blockers (ARBs) and angiotensin-converting-enzyme inhibitors (ACEIs) by leveraging the South Korean National Health Insurance Service (NHIS) big data. Methods We conducted a retrospective cohort study of 30,056 patients with COVID-19 from the NHIS. The study population was stratified into four groups based on IHD status and the use of ACEI/ARBs. To assess their effects on mortality, we applied inverse probability of treatment weighting (IPTW) to balance baseline covariates, followed by a weighted logistic regression. The interaction between IHD and ACEI/ARB use was evaluated on both multiplicative (interaction term) and additive scales (Relative Excess Risk Due to Interaction, RERI), supplemented by an age-stratified analysis (≤ 70 vs. >70 years). Results Among 30,056 COVID-19 patients, we identified a significant interaction between IHD and ACEI/ARB use on mortality after adjusting for confounders. The main finding revealed that among patients with IHD, ACEI/ARB treatment was associated with 74% lower odds of mortality compared to non-treatment (Adjusted OR: 0.26, 95% CI: 0.08–0.92, p  = 0.037). This protective interaction was strongly age-dependent, remaining statistically significant only in patients older than 70 (Interaction OR: 0.53, 95% CI: 0.27–0.99; p  = 0.048). Furthermore, a significant antagonistic interaction on the additive scale (RERI: − 1.77, 95% CI − 3.04 to − 0.51; p  = 0.006) confirmed a combined protective effect greater than the sum of the individual effects. Conclusions This study leverages the NHIS big data to provide a comprehensive analysis of the complex interactions among IHD, ACEI/ARB use, demographic factors, and comorbidities in the context of COVID-19 mortality. Our findings suggest a 45% reduction in the odds of mortality for IHD patients taking ACEI/ARB, particularly those over 70 years, but randomised controlled trials are needed before clinical guideline changes. The findings highlight the protective effect of ACEI/ARB in patients with IHD and emphasize the importance of personalized treatment approaches considering patient characteristics, pre-existing conditions, and medication use.
AbstractList The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the use of angiotensin receptor blockers (ARBs) and angiotensin-converting-enzyme inhibitors (ACEIs) by leveraging the South Korean National Health Insurance Service (NHIS) big data. We conducted a retrospective cohort study of 30,056 patients with COVID-19 from the NHIS. The study population was stratified into four groups based on IHD status and the use of ACEI/ARBs. To assess their effects on mortality, we applied inverse probability of treatment weighting (IPTW) to balance baseline covariates, followed by a weighted logistic regression. The interaction between IHD and ACEI/ARB use was evaluated on both multiplicative (interaction term) and additive scales (Relative Excess Risk Due to Interaction, RERI), supplemented by an age-stratified analysis (≤ 70 vs. >70 years). Among 30,056 COVID-19 patients, we identified a significant interaction between IHD and ACEI/ARB use on mortality after adjusting for confounders. The main finding revealed that among patients with IHD, ACEI/ARB treatment was associated with 74% lower odds of mortality compared to non-treatment (Adjusted OR: 0.26, 95% CI: 0.08-0.92, p = 0.037). This protective interaction was strongly age-dependent, remaining statistically significant only in patients older than 70 (Interaction OR: 0.53, 95% CI: 0.27-0.99; p = 0.048). Furthermore, a significant antagonistic interaction on the additive scale (RERI: - 1.77, 95% CI - 3.04 to - 0.51; p = 0.006) confirmed a combined protective effect greater than the sum of the individual effects. This study leverages the NHIS big data to provide a comprehensive analysis of the complex interactions among IHD, ACEI/ARB use, demographic factors, and comorbidities in the context of COVID-19 mortality. Our findings suggest a 45% reduction in the odds of mortality for IHD patients taking ACEI/ARB, particularly those over 70 years, but randomised controlled trials are needed before clinical guideline changes. The findings highlight the protective effect of ACEI/ARB in patients with IHD and emphasize the importance of personalized treatment approaches considering patient characteristics, pre-existing conditions, and medication use.
Abstract Background The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the use of angiotensin receptor blockers (ARBs) and angiotensin-converting-enzyme inhibitors (ACEIs) by leveraging the South Korean National Health Insurance Service (NHIS) big data. Methods We conducted a retrospective cohort study of 30,056 patients with COVID-19 from the NHIS. The study population was stratified into four groups based on IHD status and the use of ACEI/ARBs. To assess their effects on mortality, we applied inverse probability of treatment weighting (IPTW) to balance baseline covariates, followed by a weighted logistic regression. The interaction between IHD and ACEI/ARB use was evaluated on both multiplicative (interaction term) and additive scales (Relative Excess Risk Due to Interaction, RERI), supplemented by an age-stratified analysis (≤ 70 vs. >70 years). Results Among 30,056 COVID-19 patients, we identified a significant interaction between IHD and ACEI/ARB use on mortality after adjusting for confounders. The main finding revealed that among patients with IHD, ACEI/ARB treatment was associated with 74% lower odds of mortality compared to non-treatment (Adjusted OR: 0.26, 95% CI: 0.08–0.92, p = 0.037). This protective interaction was strongly age-dependent, remaining statistically significant only in patients older than 70 (Interaction OR: 0.53, 95% CI: 0.27–0.99; p = 0.048). Furthermore, a significant antagonistic interaction on the additive scale (RERI: − 1.77, 95% CI − 3.04 to − 0.51; p = 0.006) confirmed a combined protective effect greater than the sum of the individual effects. Conclusions This study leverages the NHIS big data to provide a comprehensive analysis of the complex interactions among IHD, ACEI/ARB use, demographic factors, and comorbidities in the context of COVID-19 mortality. Our findings suggest a 45% reduction in the odds of mortality for IHD patients taking ACEI/ARB, particularly those over 70 years, but randomised controlled trials are needed before clinical guideline changes. The findings highlight the protective effect of ACEI/ARB in patients with IHD and emphasize the importance of personalized treatment approaches considering patient characteristics, pre-existing conditions, and medication use.
The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the use of angiotensin receptor blockers (ARBs) and angiotensin-converting-enzyme inhibitors (ACEIs) by leveraging the South Korean National Health Insurance Service (NHIS) big data. We conducted a retrospective cohort study of 30,056 patients with COVID-19 from the NHIS. The study population was stratified into four groups based on IHD status and the use of ACEI/ARBs. To assess their effects on mortality, we applied inverse probability of treatment weighting (IPTW) to balance baseline covariates, followed by a weighted logistic regression. The interaction between IHD and ACEI/ARB use was evaluated on both multiplicative (interaction term) and additive scales (Relative Excess Risk Due to Interaction, RERI), supplemented by an age-stratified analysis ([less than or equal to] 70 vs. >70 years). Among 30,056 COVID-19 patients, we identified a significant interaction between IHD and ACEI/ARB use on mortality after adjusting for confounders. The main finding revealed that among patients with IHD, ACEI/ARB treatment was associated with 74% lower odds of mortality compared to non-treatment (Adjusted OR: 0.26, 95% CI: 0.08-0.92, p = 0.037). This protective interaction was strongly age-dependent, remaining statistically significant only in patients older than 70 (Interaction OR: 0.53, 95% CI: 0.27-0.99; p = 0.048). Furthermore, a significant antagonistic interaction on the additive scale (RERI: - 1.77, 95% CI - 3.04 to - 0.51; p = 0.006) confirmed a combined protective effect greater than the sum of the individual effects. This study leverages the NHIS big data to provide a comprehensive analysis of the complex interactions among IHD, ACEI/ARB use, demographic factors, and comorbidities in the context of COVID-19 mortality. Our findings suggest a 45% reduction in the odds of mortality for IHD patients taking ACEI/ARB, particularly those over 70 years, but randomised controlled trials are needed before clinical guideline changes. The findings highlight the protective effect of ACEI/ARB in patients with IHD and emphasize the importance of personalized treatment approaches considering patient characteristics, pre-existing conditions, and medication use.
Background The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the use of angiotensin receptor blockers (ARBs) and angiotensin-converting-enzyme inhibitors (ACEIs) by leveraging the South Korean National Health Insurance Service (NHIS) big data. Methods We conducted a retrospective cohort study of 30,056 patients with COVID-19 from the NHIS. The study population was stratified into four groups based on IHD status and the use of ACEI/ARBs. To assess their effects on mortality, we applied inverse probability of treatment weighting (IPTW) to balance baseline covariates, followed by a weighted logistic regression. The interaction between IHD and ACEI/ARB use was evaluated on both multiplicative (interaction term) and additive scales (Relative Excess Risk Due to Interaction, RERI), supplemented by an age-stratified analysis ([less than or equal to] 70 vs. >70 years). Results Among 30,056 COVID-19 patients, we identified a significant interaction between IHD and ACEI/ARB use on mortality after adjusting for confounders. The main finding revealed that among patients with IHD, ACEI/ARB treatment was associated with 74% lower odds of mortality compared to non-treatment (Adjusted OR: 0.26, 95% CI: 0.08-0.92, p = 0.037). This protective interaction was strongly age-dependent, remaining statistically significant only in patients older than 70 (Interaction OR: 0.53, 95% CI: 0.27-0.99; p = 0.048). Furthermore, a significant antagonistic interaction on the additive scale (RERI: - 1.77, 95% CI - 3.04 to - 0.51; p = 0.006) confirmed a combined protective effect greater than the sum of the individual effects. Conclusions This study leverages the NHIS big data to provide a comprehensive analysis of the complex interactions among IHD, ACEI/ARB use, demographic factors, and comorbidities in the context of COVID-19 mortality. Our findings suggest a 45% reduction in the odds of mortality for IHD patients taking ACEI/ARB, particularly those over 70 years, but randomised controlled trials are needed before clinical guideline changes. The findings highlight the protective effect of ACEI/ARB in patients with IHD and emphasize the importance of personalized treatment approaches considering patient characteristics, pre-existing conditions, and medication use. Keywords: COVID-19 mortality, Ischaemic heart disease, Angiotensin receptor blockers, Angiotensin-Converting enzyme inhibitors, National health insurance data
The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the use of angiotensin receptor blockers (ARBs) and angiotensin-converting-enzyme inhibitors (ACEIs) by leveraging the South Korean National Health Insurance Service (NHIS) big data.BACKGROUNDThe COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the use of angiotensin receptor blockers (ARBs) and angiotensin-converting-enzyme inhibitors (ACEIs) by leveraging the South Korean National Health Insurance Service (NHIS) big data.We conducted a retrospective cohort study of 30,056 patients with COVID-19 from the NHIS. The study population was stratified into four groups based on IHD status and the use of ACEI/ARBs. To assess their effects on mortality, we applied inverse probability of treatment weighting (IPTW) to balance baseline covariates, followed by a weighted logistic regression. The interaction between IHD and ACEI/ARB use was evaluated on both multiplicative (interaction term) and additive scales (Relative Excess Risk Due to Interaction, RERI), supplemented by an age-stratified analysis (≤ 70 vs. >70 years).METHODSWe conducted a retrospective cohort study of 30,056 patients with COVID-19 from the NHIS. The study population was stratified into four groups based on IHD status and the use of ACEI/ARBs. To assess their effects on mortality, we applied inverse probability of treatment weighting (IPTW) to balance baseline covariates, followed by a weighted logistic regression. The interaction between IHD and ACEI/ARB use was evaluated on both multiplicative (interaction term) and additive scales (Relative Excess Risk Due to Interaction, RERI), supplemented by an age-stratified analysis (≤ 70 vs. >70 years).Among 30,056 COVID-19 patients, we identified a significant interaction between IHD and ACEI/ARB use on mortality after adjusting for confounders. The main finding revealed that among patients with IHD, ACEI/ARB treatment was associated with 74% lower odds of mortality compared to non-treatment (Adjusted OR: 0.26, 95% CI: 0.08-0.92, p = 0.037). This protective interaction was strongly age-dependent, remaining statistically significant only in patients older than 70 (Interaction OR: 0.53, 95% CI: 0.27-0.99; p = 0.048). Furthermore, a significant antagonistic interaction on the additive scale (RERI: - 1.77, 95% CI - 3.04 to - 0.51; p = 0.006) confirmed a combined protective effect greater than the sum of the individual effects.RESULTSAmong 30,056 COVID-19 patients, we identified a significant interaction between IHD and ACEI/ARB use on mortality after adjusting for confounders. The main finding revealed that among patients with IHD, ACEI/ARB treatment was associated with 74% lower odds of mortality compared to non-treatment (Adjusted OR: 0.26, 95% CI: 0.08-0.92, p = 0.037). This protective interaction was strongly age-dependent, remaining statistically significant only in patients older than 70 (Interaction OR: 0.53, 95% CI: 0.27-0.99; p = 0.048). Furthermore, a significant antagonistic interaction on the additive scale (RERI: - 1.77, 95% CI - 3.04 to - 0.51; p = 0.006) confirmed a combined protective effect greater than the sum of the individual effects.This study leverages the NHIS big data to provide a comprehensive analysis of the complex interactions among IHD, ACEI/ARB use, demographic factors, and comorbidities in the context of COVID-19 mortality. Our findings suggest a 45% reduction in the odds of mortality for IHD patients taking ACEI/ARB, particularly those over 70 years, but randomised controlled trials are needed before clinical guideline changes. The findings highlight the protective effect of ACEI/ARB in patients with IHD and emphasize the importance of personalized treatment approaches considering patient characteristics, pre-existing conditions, and medication use.CONCLUSIONSThis study leverages the NHIS big data to provide a comprehensive analysis of the complex interactions among IHD, ACEI/ARB use, demographic factors, and comorbidities in the context of COVID-19 mortality. Our findings suggest a 45% reduction in the odds of mortality for IHD patients taking ACEI/ARB, particularly those over 70 years, but randomised controlled trials are needed before clinical guideline changes. The findings highlight the protective effect of ACEI/ARB in patients with IHD and emphasize the importance of personalized treatment approaches considering patient characteristics, pre-existing conditions, and medication use.
Background The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease (IHD), and mortality risk. This study aims to investigate the associations among COVID-19 mortality, the presence of IHD, and the use of angiotensin receptor blockers (ARBs) and angiotensin-converting-enzyme inhibitors (ACEIs) by leveraging the South Korean National Health Insurance Service (NHIS) big data. Methods We conducted a retrospective cohort study of 30,056 patients with COVID-19 from the NHIS. The study population was stratified into four groups based on IHD status and the use of ACEI/ARBs. To assess their effects on mortality, we applied inverse probability of treatment weighting (IPTW) to balance baseline covariates, followed by a weighted logistic regression. The interaction between IHD and ACEI/ARB use was evaluated on both multiplicative (interaction term) and additive scales (Relative Excess Risk Due to Interaction, RERI), supplemented by an age-stratified analysis (≤ 70 vs. >70 years). Results Among 30,056 COVID-19 patients, we identified a significant interaction between IHD and ACEI/ARB use on mortality after adjusting for confounders. The main finding revealed that among patients with IHD, ACEI/ARB treatment was associated with 74% lower odds of mortality compared to non-treatment (Adjusted OR: 0.26, 95% CI: 0.08–0.92, p  = 0.037). This protective interaction was strongly age-dependent, remaining statistically significant only in patients older than 70 (Interaction OR: 0.53, 95% CI: 0.27–0.99; p  = 0.048). Furthermore, a significant antagonistic interaction on the additive scale (RERI: − 1.77, 95% CI − 3.04 to − 0.51; p  = 0.006) confirmed a combined protective effect greater than the sum of the individual effects. Conclusions This study leverages the NHIS big data to provide a comprehensive analysis of the complex interactions among IHD, ACEI/ARB use, demographic factors, and comorbidities in the context of COVID-19 mortality. Our findings suggest a 45% reduction in the odds of mortality for IHD patients taking ACEI/ARB, particularly those over 70 years, but randomised controlled trials are needed before clinical guideline changes. The findings highlight the protective effect of ACEI/ARB in patients with IHD and emphasize the importance of personalized treatment approaches considering patient characteristics, pre-existing conditions, and medication use.
ArticleNumber 1529
Audience Academic
Author Kim, Shin-Woo
Noh, Seunghwan
Oh, Bumjo
Goo, Taewan
Lee, Seungyeoun
Park, Taesung
Author_xml – sequence: 1
  givenname: Shin-Woo
  surname: Kim
  fullname: Kim, Shin-Woo
  organization: Department of Internal Medicine, School of Medicine, Kyungpook National University
– sequence: 2
  givenname: Taewan
  surname: Goo
  fullname: Goo, Taewan
  organization: Interdisciplinary Program in Bioinformatics, Seoul National University
– sequence: 3
  givenname: Seunghwan
  surname: Noh
  fullname: Noh, Seunghwan
  organization: Department of Economics, College of Social Sciences, Seoul National University
– sequence: 4
  givenname: Seungyeoun
  surname: Lee
  fullname: Lee, Seungyeoun
  organization: Department of Mathematics & Statistics, Sejong University
– sequence: 5
  givenname: Bumjo
  surname: Oh
  fullname: Oh, Bumjo
  organization: Department of Family Medicine, Seoul National University College of Medicine, Department of Family Medicine, SMG-SNU Boramae Medical Center
– sequence: 6
  givenname: Taesung
  surname: Park
  fullname: Park, Taesung
  email: tspark@stats.snu.ac.kr
  organization: Department of Statistics, Seoul National University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/41214606$$D View this record in MEDLINE/PubMed
BookMark eNqNks9u1DAQxiNURNuFF-CALHGBQ1o7tvOH27IUiKhYqYVeLa8z3nWV2FvbAfomPC5Ot1SshBCaw9ij3_dJM_qOswPrLGTZc4JPCKnL00CKumpyXPA8_Wues0fZEWEVyQtK2cEf78PsOIRrjElVF82T7JCRgrASl0fZz3bYShWR02i-OGtP5xdv0RgAOYsWy6v2XU4aNDgfZW_iLTIWbWU0YGNA303cIBPURsJgFNqA9BF1JoAM8CaRwaw3CdPeDejSjQn-5DxIiz4nB2dlP0n6ycOG0UurAAXw30zqnYzyafZYyz7As_s-y76-P_uy-JifLz-0i_l5rjjjMSe8oqWmkmJNdV1WXcUJpVVRAFNNQ3RTMVwTXKqmruUKV6VizYonAetq4IDpLGt3vp2T12LrzSD9rXDSiLuB82uRFjOqB6EbroGzsgKiWUHoitUaGkY6ULJpmEper3ZeW-9uRghRDOlA0PfSghuDoEWFK05Zqln2coeuZXI2VrvopZpwMa9LikuewESd_IVK1U03T2nQJs33BK_3BImJ8COu5RiCaC8v_p9dXu2zL-43G1cDdA93-h2kBBQ7QHkXggf9gBAsprSKXVpFSqu4S6uYjkB3opBguwYvrt3oUzTCv1S_AJ5b58o
Cites_doi 10.1016/j.ijcha.2020.100627
10.1007/s10654-020-00698-1
10.1002/cpt.1863
10.3346/jkms.2017.32.5.718
10.3389/fmed.2021.703661
10.1093/aje/kwq439
10.34133/2020/2402961
10.1038/s41569-020-0413-9
10.1001/jamanetworkopen.2021.3594
10.3390/life14050545
10.1161/HYPERTENSIONAHA.120.15572
10.1016/j.puhe.2020.05.006
10.1161/CIRCRESAHA.120.317134
10.1016/j.annepidem.2006.10.009
10.18632/aging.103000
10.1016/j.jinf.2020.04.021
10.4093/dmj.2022.0193
10.1371/journal.pone.0238215
10.1161/CIRCRESAHA.121.317997
10.1159/000512592
10.3390/jpm11020116
10.1038/s41467-020-19741-6
10.1093/ije/dyr218
10.1002/prp2.666
10.3390/bdcc5030030
10.1177/2047487320915663
10.1161/JAHA.121.023535
10.1001/jama.2020.25864
10.1214/aos/1176346391
10.1161/JAHA.122.025289
ContentType Journal Article
Copyright The Author(s) 2025
2025. The Author(s).
COPYRIGHT 2025 BioMed Central Ltd.
Copyright_xml – notice: The Author(s) 2025
– notice: 2025. The Author(s).
– notice: COPYRIGHT 2025 BioMed Central Ltd.
DBID C6C
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
IOV
ISR
7X8
DOA
DOI 10.1186/s12879-025-11885-4
DatabaseName Springer Nature OA Free Journals (WRLC)
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Gale In Context: Opposing Viewpoints
Gale In Context: Science
MEDLINE - Academic
DOAJ Directory of Open Access Journal Collection
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE



MEDLINE - Academic



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: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1471-2334
EndPage 12
ExternalDocumentID oai_doaj_org_article_f95fe5467e1f4213b48fe941deca994c
A863065753
41214606
10_1186_s12879_025_11885_4
Genre Journal Article
GeographicLocations Republic of Korea
South Korea
GeographicLocations_xml – name: Republic of Korea
– name: South Korea
GrantInformation_xml – fundername: National Research Foundation
  grantid: RS-2023 00227944
– fundername: Mid-Career Bridging Program through Seoul National University
– fundername: Ministry of Science and ICT, South Korea
  grantid: No. 2021M3E5E3081425
GroupedDBID ---
0R~
23N
2WC
53G
5VS
6J9
6PF
7X7
88E
8C1
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAWTL
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AEAQA
AENEX
AEUYN
AFFHD
AFKRA
AFPKN
AFRAH
AHBYD
AHMBA
AHYZX
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BCNDV
BENPR
BFQNJ
BMC
BPHCQ
BVXVI
C6C
CCPQU
CS3
DIK
DU5
E3Z
EAD
EAP
EAS
EBD
EBLON
EBS
EMB
EMK
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
IAO
IHR
INH
INR
IOV
ISR
ITC
KQ8
M1P
M~E
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PJZUB
PPXIY
PQQKQ
PROAC
PSQYO
RBZ
RNS
ROL
RPM
RSV
SMD
SOJ
SV3
TR2
TUS
UKHRP
W2D
WOQ
WOW
XSB
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
ID FETCH-LOGICAL-c545t-15736f3a30f3f867d75133722e4c991f97408106c988ab076c49b5f3a4d8e5e03
IEDL.DBID RSV
ISICitedReferencesCount 0
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=001613984700005&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1471-2334
IngestDate Mon Nov 17 19:35:29 EST 2025
Tue Nov 11 20:31:51 EST 2025
Thu Nov 20 00:40:39 EST 2025
Sat Nov 29 10:28:47 EST 2025
Thu Nov 13 04:41:01 EST 2025
Thu Nov 13 04:40:58 EST 2025
Fri Nov 14 01:40:53 EST 2025
Thu Nov 13 04:17:27 EST 2025
Tue Nov 11 01:10:28 EST 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords COVID-19 mortality
National health insurance data
Angiotensin-Converting enzyme inhibitors
Ischaemic heart disease
Angiotensin receptor blockers
Language English
License 2025. The Author(s).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c545t-15736f3a30f3f867d75133722e4c991f97408106c988ab076c49b5f3a4d8e5e03
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://link.springer.com/10.1186/s12879-025-11885-4
PMID 41214606
PQID 3270753434
PQPubID 23479
PageCount 12
ParticipantIDs doaj_primary_oai_doaj_org_article_f95fe5467e1f4213b48fe941deca994c
proquest_miscellaneous_3270753434
gale_infotracmisc_A863065753
gale_infotracacademiconefile_A863065753
gale_incontextgauss_ISR_A863065753
gale_incontextgauss_IOV_A863065753
pubmed_primary_41214606
crossref_primary_10_1186_s12879_025_11885_4
springer_journals_10_1186_s12879_025_11885_4
PublicationCentury 2000
PublicationDate 2025-11-10
PublicationDateYYYYMMDD 2025-11-10
PublicationDate_xml – month: 11
  year: 2025
  text: 2025-11-10
  day: 10
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
– name: England
PublicationTitle BMC infectious diseases
PublicationTitleAbbrev BMC Infect Dis
PublicationTitleAlternate BMC Infect Dis
PublicationYear 2025
Publisher BioMed Central
BioMed Central Ltd
BMC
Publisher_xml – name: BioMed Central
– name: BioMed Central Ltd
– name: BMC
References Jordan Loader (11885_CR10) 2022; 11
RD Lopes (11885_CR30) 2021; 325
Z Zheng (11885_CR22) 2020; 81
MJ Funk (11885_CR17) 2011; 173
MK Chung (11885_CR1) 2021; 128
AT Levin (11885_CR13) 2020; 35
J. N. K. Rao (11885_CR18) 1984; 12
11885_CR26
K Sriram (11885_CR3) 2020; 108
JA Patel (11885_CR25) 2020; 183
TK Oh (11885_CR14) 2021; 11
B Wang (11885_CR28) 2020; 12
Michael Pan (11885_CR4) 2021; 10
H Peckham (11885_CR24) 2020; 11
R Li (11885_CR20) 2007; 17
D Riswantini (11885_CR21) 2021; 5
Daniel Caldeira (11885_CR8) 2020; 31
JA Kim (11885_CR15) 2017; 32
M Gatti (11885_CR12) 2021; 28
P Karakasis (11885_CR27) 2024; 14
MJ Knol (11885_CR19) 2012; 41
R Baral (11885_CR23) 2021; 4
M Nishiga (11885_CR2) 2020; 17
MK Kim (11885_CR16) 2022; 46
P Zhang (11885_CR5) 2020; 126
11885_CR9
A Kurdi (11885_CR7) 2020; 8
X Guo (11885_CR6) 2020; 76
Mohitosh Biswas (11885_CR11) 2021; 64
P Ssentongo (11885_CR29) 2020; 15
References_xml – volume: 31
  start-page: 100627
  year: 2020
  ident: 11885_CR8
  publication-title: International Journal of Cardiology Heart & Vasculature
  doi: 10.1016/j.ijcha.2020.100627
– volume: 35
  start-page: 1123
  issue: 12
  year: 2020
  ident: 11885_CR13
  publication-title: Eur J Epidemiol
  doi: 10.1007/s10654-020-00698-1
– volume: 108
  start-page: 236
  issue: 2
  year: 2020
  ident: 11885_CR3
  publication-title: Clin Pharmacol Ther
  doi: 10.1002/cpt.1863
– volume: 32
  start-page: 718
  issue: 5
  year: 2017
  ident: 11885_CR15
  publication-title: J Korean Med Sci
  doi: 10.3346/jkms.2017.32.5.718
– ident: 11885_CR9
  doi: 10.3389/fmed.2021.703661
– volume: 173
  start-page: 761
  issue: 7
  year: 2011
  ident: 11885_CR17
  publication-title: Am J Epidemiol
  doi: 10.1093/aje/kwq439
– ident: 11885_CR26
  doi: 10.34133/2020/2402961
– volume: 17
  start-page: 543
  issue: 9
  year: 2020
  ident: 11885_CR2
  publication-title: Nat Rev Cardiol
  doi: 10.1038/s41569-020-0413-9
– volume: 4
  start-page: e213594
  issue: 3
  year: 2021
  ident: 11885_CR23
  publication-title: JAMA Netw Open
  doi: 10.1001/jamanetworkopen.2021.3594
– volume: 14
  start-page: 545
  issue: 5
  year: 2024
  ident: 11885_CR27
  publication-title: Life
  doi: 10.3390/life14050545
– volume: 76
  start-page: 13
  issue: 2
  year: 2020
  ident: 11885_CR6
  publication-title: Hypertension
  doi: 10.1161/HYPERTENSIONAHA.120.15572
– volume: 183
  start-page: 110
  year: 2020
  ident: 11885_CR25
  publication-title: Public Health
  doi: 10.1016/j.puhe.2020.05.006
– volume: 126
  start-page: 1671
  issue: 12
  year: 2020
  ident: 11885_CR5
  publication-title: Circ Res
  doi: 10.1161/CIRCRESAHA.120.317134
– volume: 17
  start-page: 227
  issue: 3
  year: 2007
  ident: 11885_CR20
  publication-title: Ann Epidemiol
  doi: 10.1016/j.annepidem.2006.10.009
– volume: 12
  start-page: 6049
  issue: 7
  year: 2020
  ident: 11885_CR28
  publication-title: Aging
  doi: 10.18632/aging.103000
– volume: 81
  start-page: 16
  issue: 2
  year: 2020
  ident: 11885_CR22
  publication-title: J Infect
  doi: 10.1016/j.jinf.2020.04.021
– volume: 46
  start-page: 552
  issue: 4
  year: 2022
  ident: 11885_CR16
  publication-title: Diabetes Metab J
  doi: 10.4093/dmj.2022.0193
– volume: 15
  start-page: e0238215
  issue: 8
  year: 2020
  ident: 11885_CR29
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0238215
– volume: 128
  start-page: 1214
  issue: 8
  year: 2021
  ident: 11885_CR1
  publication-title: Circ Res
  doi: 10.1161/CIRCRESAHA.121.317997
– volume: 64
  start-page: 36
  issue: 1
  year: 2021
  ident: 11885_CR11
  publication-title: Intervirology
  doi: 10.1159/000512592
– volume: 11
  start-page: 116
  issue: 2
  year: 2021
  ident: 11885_CR14
  publication-title: J Pers Med
  doi: 10.3390/jpm11020116
– volume: 11
  start-page: 6317
  issue: 1
  year: 2020
  ident: 11885_CR24
  publication-title: Nat Commun
  doi: 10.1038/s41467-020-19741-6
– volume: 41
  start-page: 514
  issue: 2
  year: 2012
  ident: 11885_CR19
  publication-title: Int J Epidemiol
  doi: 10.1093/ije/dyr218
– volume: 8
  start-page: e00666
  issue: 6
  year: 2020
  ident: 11885_CR7
  publication-title: Pharmacol Res Perspect
  doi: 10.1002/prp2.666
– volume: 5
  start-page: 30
  issue: 3
  year: 2021
  ident: 11885_CR21
  publication-title: Big Data Cogn Comput
  doi: 10.3390/bdcc5030030
– volume: 28
  start-page: 983
  issue: 9
  year: 2021
  ident: 11885_CR12
  publication-title: Eur J Prev Cardiol
  doi: 10.1177/2047487320915663
– volume: 10
  start-page: e023535
  issue: 24
  year: 2021
  ident: 11885_CR4
  publication-title: Journal of the American Heart Association
  doi: 10.1161/JAHA.121.023535
– volume: 325
  start-page: 254
  issue: 3
  year: 2021
  ident: 11885_CR30
  publication-title: JAMA
  doi: 10.1001/jama.2020.25864
– volume: 12
  start-page: 46
  issue: 1
  year: 1984
  ident: 11885_CR18
  publication-title: The Annals of Statistics
  doi: 10.1214/aos/1176346391
– volume: 11
  start-page: e025289
  issue: 11
  year: 2022
  ident: 11885_CR10
  publication-title: Journal of the American Heart Association
  doi: 10.1161/JAHA.122.025289
SSID ssj0017829
Score 2.438873
Snippet Background The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic...
The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic heart disease...
Background The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as ischaemic...
Abstract Background The COVID-19 pandemic has highlighted the importance of understanding the complex interactions between pre-existing conditions, such as...
SourceID doaj
proquest
gale
pubmed
crossref
springer
SourceType Open Website
Aggregation Database
Index Database
Publisher
StartPage 1529
SubjectTerms Adult
Aged
Aged, 80 and over
Angiotensin II receptor blockers
Angiotensin Receptor Antagonists - therapeutic use
Angiotensin receptor blockers
Angiotensin-Converting enzyme inhibitors
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Cardiac patients
Care and treatment
Comorbidity
COVID-19 - complications
COVID-19 - mortality
Diagnosis
Dosage and administration
Enzyme inhibitors
Female
Humans
Infectious Diseases
Internal Medicine
Ischaemic heart disease
Male
Medical Microbiology
Medicine
Medicine & Public Health
Middle Aged
Myocardial Ischemia - complications
Myocardial Ischemia - drug therapy
Myocardial Ischemia - epidemiology
Myocardial Ischemia - mortality
National health insurance data
National Health Programs
Parasitology
Republic of Korea - epidemiology
Retrospective Studies
SARS-CoV-2
Tropical Medicine
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journal Collection
  dbid: DOA
  link: http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3fb9MwELbQhBAviN8UBjoQEg8QNU6c2OatK5uogA0NmPZmOY49VWIJqlv-Fv5czo4zrSDghcc2V6n2ne--i---I-S5bmQlhTMZ19JhgkJtJnmcmlrQthJaCBdJXN_zw0Nxeio_Xhr1FWrCBnrgYeOmTlbOVnicLXWsoGXDhLOS0dYaLSUzwfvmXI7JVLo_wLgnxxYZUU89emEuszC6FT-LKmNbYSiy9f_uky8FpV9uSWPwObhJbiTUCLPh394iV2x3m1z7kO7F75Afi9jsCL2D2Xx_MZ0d78HGW-g7mB-dLN5kVMJ5BNoIumHZQaJT9RDew8LSh9r586WBMN96DenW5jVK-pC8ewhdKBDH7cG7HnFmB4lQ-ysMnZRBdBOGdFjwg_uBUHx6l3w52P88f5ulmQuZQSy1zmjFy9qVusxd6UTNWx4GwKDmLDMIJR2mHwgi8tpIIXST89ow2VT4A9YKW9m8vEd2ur6zDwjwOjcIIAyXVDNquNaFzNFiXFNT27T5hLwcVaC-DdQaKqYkolaDwhQqTEWFKTYhe0FLF5KBFjt-gcaikrGofxnLhDwLOlaB-KILlTVneuO9WhydqJmoMXtC8Fr-SejT8ZbQiyTk-vVKG526GXDpgVBrS3J3SxKPr9l6_HS0NxUehZq3zvYbr8qCI54rWYlrvz8Y4sXqGQ0D2fN6Ql6NlqmS8_F_2cSH_2MTH5HrxXCSMIbvkp31amMfk6vm-3rpV0_iOfwJ8iIyZg
  priority: 102
  providerName: Directory of Open Access Journals
Title Impact of ACEI/ARB use on COVID-19 mortality in patients with ischaemic heart disease: insights from South Korean National health insurance service data
URI https://link.springer.com/article/10.1186/s12879-025-11885-4
https://www.ncbi.nlm.nih.gov/pubmed/41214606
https://www.proquest.com/docview/3270753434
https://doaj.org/article/f95fe5467e1f4213b48fe941deca994c
Volume 25
WOSCitedRecordID wos001613984700005&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVADU
  databaseName: BioMedCentral
  customDbUrl:
  eissn: 1471-2334
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0017829
  issn: 1471-2334
  databaseCode: RBZ
  dateStart: 20010101
  isFulltext: true
  titleUrlDefault: https://www.biomedcentral.com/search/
  providerName: BioMedCentral
– providerCode: PRVAON
  databaseName: DOAJ Directory of Open Access Journals
  customDbUrl:
  eissn: 1471-2334
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0017829
  issn: 1471-2334
  databaseCode: DOA
  dateStart: 20010101
  isFulltext: true
  titleUrlDefault: https://www.doaj.org/
  providerName: Directory of Open Access Journals
– providerCode: PRVHPJ
  databaseName: ROAD: Directory of Open Access Scholarly Resources
  customDbUrl:
  eissn: 1471-2334
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0017829
  issn: 1471-2334
  databaseCode: M~E
  dateStart: 20010101
  isFulltext: true
  titleUrlDefault: https://road.issn.org
  providerName: ISSN International Centre
– providerCode: PRVPQU
  databaseName: Health & Medical Collection
  customDbUrl:
  eissn: 1471-2334
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0017829
  issn: 1471-2334
  databaseCode: 7X7
  dateStart: 20090101
  isFulltext: true
  titleUrlDefault: https://search.proquest.com/healthcomplete
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: ProQuest Central
  customDbUrl:
  eissn: 1471-2334
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0017829
  issn: 1471-2334
  databaseCode: BENPR
  dateStart: 20090101
  isFulltext: true
  titleUrlDefault: https://www.proquest.com/central
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: Public Health Database
  customDbUrl:
  eissn: 1471-2334
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0017829
  issn: 1471-2334
  databaseCode: 8C1
  dateStart: 20090101
  isFulltext: true
  titleUrlDefault: https://search.proquest.com/publichealth
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: Publicly Available Content Database
  customDbUrl:
  eissn: 1471-2334
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0017829
  issn: 1471-2334
  databaseCode: PIMPY
  dateStart: 20090101
  isFulltext: true
  titleUrlDefault: http://search.proquest.com/publiccontent
  providerName: ProQuest
– providerCode: PRVAVX
  databaseName: SpringerLink Journals
  customDbUrl:
  eissn: 1471-2334
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0017829
  issn: 1471-2334
  databaseCode: RSV
  dateStart: 20011201
  isFulltext: true
  titleUrlDefault: https://link.springer.com/search?facet-content-type=%22Journal%22
  providerName: Springer Nature
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lj9MwELbYXYS48H4UlsogJA4Qbdw4sc2tLV1RwXarLqzKyXJce1WJTVDd8lv4uYwdp6K8JLhESjKRYns8843nhdBzVYpccKsTpoQFA4WYRLDQNbVHFjlXnNtQxPU9m0z4fC6mMSnMtdHurUsySOqwrXlx5ECSMpH49qtwz_OE7qEDUHfcN2yYnZ1vfQeg80SbHvPb73ZUUKjU_6s8_kEh_eQhDYrn-Ob__fItdCMCTdxvOOM2umKqO-jaSXSl30XfxiE_EtcW94ej8VF_NsAbZ3Bd4eHp-fhNQgS-DNgccDpeVjhWYHXYH93ipfPh9pdLjX1L7DWOjp7XQOm8ve-wT1zBoUMfflcDNK1wrMH9GTfJl5504_t6GOwaiYV9vOo99PF49GH4NoltGhIN8GudkJxlhc1UltrM8oItmO8ZA4ttqAb0acFiAdyRFlpwrsqUFZqKMocP6IKb3KTZfbRf1ZV5iDArUg2YQzNBFCWaKdUTKTCZLQtiykXaQS_blZNfmmocMlgxvJDNZEuYbBkmW9IOGvjF3VL6StrhQb26kHFjSitya3JQF4ZY2iNZSbk1gpKF0UoIqjvomWcN6WtlVD4Y50JtnJPj03PZ5wUYXIB3sz8Rnc12iF5EIluvV0qrmAABQ_c1uHYoD3coYcfrnddPWzaV_pUPk6tMvXEy6zGAgBnNYOwPGv7djp4S38M9LTroVcusMsor95dJfPRv5I_R9V7D76DgD9H-erUxT9BV_XW9dKsu2mNzFq4crnxIuuhgMJpMZ91wFgJ30_HJ9FM3bOjv12E89Q
linkProvider Springer Nature
linkToHtml http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLZgIOCF-6UwwCAkHiBa0jixzVtXNq1a16Fuq_ZmOY49VWIJqhN-Cz-XY8epKDcJHtt8kWr7-Jzv9NwQeiMLnnFmVEQlN-CgJDri1E9NHSZlxiRjxjdxndLZjJ2f80-hKMz22e59SNJran-tWb5jQZNSHrnxq_CZZRG5iq4RsFiuY_78ZLGOHYDN4315zG_f2zBBvlP_r_r4B4P0U4TUG579O__3k--i24Fo4lEnGffQFV3dRzeOQij9Afo28fWRuDZ4NN6b7Izmu7i1GtcVHh8vJh-jhONLz82Bp-NlhUMHVovdX7d4aV26_eVSYTcSu8Eh0PMBkNb5-xa7whXsJ_ThwxqoaYVDD-7PuCu-dNDWzfXQ2HYaC7t81YfobH_vdHwQhTENkQL61URJRtPcpDKNTWpYTkvqZsbAYWuigH0a8FiAd8S54ozJIqa5IrzI4AVSMp3pOH2Etqq60k8QpnmsgHMoyhNJEkWlHPIYhMwUeaKLMh6gd_3JiS9dNw7hvRiWi26zBWy28JstyADtusNdI10nbf9FvboQ4WIKwzOjMzAXOjEgTWlBmNGcJKVWknOiBui1Ew3hemVULhnnQrbWisnxQoxYDg4X8N30T6CT-QbobQCZullJJUMBBCzd9eDaQG5vIOHGq43Hr3oxFe6RS5OrdN1akQ4pUMCUpLD2x538rldPEjfDPc4H6H0vrCLoK_uXTXz6b_CX6ObB6dFUTCezw2fo1rCTfTD222irWbX6ObquvjZLu3rhL-13dbs4_A
linkToPdf http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1bb9MwFLZgoIkX7pfCAIOQeICoSePENm9dt4pqo5s2qPZmOY49VWLJVKf8Fn4u5zhptXKTEI9Nvki1c3zOd3JuhLzRhcykcCbiWjpwUBIbSR6mpg6SMhNaCBeauB7y6VScncnjK1X8Idt9FZJsaxqwS1PV9C9L1x5xkfc9aFUuIxzFCr9FFrHr5AbDRHr0109n6zgC2D-5KpX57XMb5ih07f9VN18xTj9FS4MRGt_5_79_l9zuCCgdthJzj1yz1X2y_akLsT8g3yehbpLWjg5H-5P-8GSXLr2ldUVHR7PJXpRIehE4O_B3Oq9o15nVU_ykS-ce0_Av5obiqOyGdgGgD4D0-B3AUyxooWFyHz2ogbJWtOvN_ZW2RZkIXeK8D0t9q8ko5rE-JF_G-59HH6NufENkgJY1UZLxNHepTmOXOpHzkuMsGRACywywUgeeDPCRODdSCF3EPDdMFhk8wEphMxunj8hWVVf2CaE8jw1wEcNlolliuNYDGYPwuSJPbFHGPfJu9RbVZdulQwXvRuSq3WwFm63CZivWI7v4otdI7LAdLtSLc9UdWOVk5mwGZsQmjg2StGDCWcmS0hotJTM98hrFRGEPjQqTdM710ns1OZqpocjBEQMenP4JdHqyAXrbgVzdLLTRXWEELB17c20gdzaQoAnMxu1XK5FVeAvT5ypbL71KBxyoYcpSWPvjVpbXq2cJznaP8x55vxJc1ekx_5dNfPpv8Jdk-3hvrA4n04Nn5NagFX3gADtkq1ks7XNy03xr5n7xIpzfH0KGQeA
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=Impact+of+ACEI%2FARB+use+on+COVID-19+mortality+in+patients+with+ischaemic+heart+disease%3A+insights+from+South+Korean+National+health+insurance+service+data&rft.jtitle=BMC+infectious+diseases&rft.au=Kim%2C+Shin-Woo&rft.au=Goo%2C+Taewan&rft.au=Noh%2C+Seunghwan&rft.au=Lee%2C+Seungyeoun&rft.date=2025-11-10&rft.pub=BioMed+Central+Ltd&rft.issn=1471-2334&rft.eissn=1471-2334&rft.volume=25&rft.issue=1&rft_id=info:doi/10.1186%2Fs12879-025-11885-4&rft.externalDocID=A863065753
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-2334&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-2334&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-2334&client=summon