Evolutionary perspective of drug eluting stents: from thick polymer to polymer free approach

Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the...

Full description

Saved in:
Bibliographic Details
Published inJournal of cardiothoracic surgery Vol. 17; no. 1; pp. 65 - 20
Main Authors Hassan, Sadia, Ali, Murtaza Najabat, Ghafoor, Bakhtawar
Format Journal Article
LanguageEnglish
Published London BioMed Central 04.04.2022
BioMed Central Ltd
BMC
Subjects
Online AccessGet full text
ISSN1749-8090
1749-8090
DOI10.1186/s13019-022-01812-y

Cover

Loading…
Abstract Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the DES in the stent market is the degree of improvement with which it evolves. New and better stents come into the market every year, surpassing their predecessors by many folds. Literature review This review paper discusses the journey of DES with supporting clinical trials in detail. In the first generation, there were stainless-steel stents with thicker coatings. Although they had superior results compared to BMS, there was still room for improvement. Afterward came the second-generation stents, which had superior metal platforms with thinner struts and thin coatings. The drugs were also changed from Paclitaxel and Sirolimus to Zotrolimus and Everolimus. These stents performed best; however, there was an issue of permanent coating, which remained intact over the stent surface after complete drug elution and started to cause issues in longer-term studies. Hence, an improved version of DES was introduced to these permanent coatings called the third generation of drug eluting stents, which initially utilized biodegradable polymer and ultimately moved towards polymer free drug coatings. This generation has introduced a unique amalgam of technologies to achieve its polymer free coatings; however, researchers have numerous prospects of growth in this field. This review paper highlights the major coups of stent technology evolution from BMS to DES, from thick polymeric coatings to thin coatings and from durable polymers to polymer free DES. Conclusion In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology.
AbstractList Abstract Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the DES in the stent market is the degree of improvement with which it evolves. New and better stents come into the market every year, surpassing their predecessors by many folds. Literature review This review paper discusses the journey of DES with supporting clinical trials in detail. In the first generation, there were stainless-steel stents with thicker coatings. Although they had superior results compared to BMS, there was still room for improvement. Afterward came the second-generation stents, which had superior metal platforms with thinner struts and thin coatings. The drugs were also changed from Paclitaxel and Sirolimus to Zotrolimus and Everolimus. These stents performed best; however, there was an issue of permanent coating, which remained intact over the stent surface after complete drug elution and started to cause issues in longer-term studies. Hence, an improved version of DES was introduced to these permanent coatings called the third generation of drug eluting stents, which initially utilized biodegradable polymer and ultimately moved towards polymer free drug coatings. This generation has introduced a unique amalgam of technologies to achieve its polymer free coatings; however, researchers have numerous prospects of growth in this field. This review paper highlights the major coups of stent technology evolution from BMS to DES, from thick polymeric coatings to thin coatings and from durable polymers to polymer free DES. Conclusion In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology.
Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the DES in the stent market is the degree of improvement with which it evolves. New and better stents come into the market every year, surpassing their predecessors by many folds. Literature review This review paper discusses the journey of DES with supporting clinical trials in detail. In the first generation, there were stainless-steel stents with thicker coatings. Although they had superior results compared to BMS, there was still room for improvement. Afterward came the second-generation stents, which had superior metal platforms with thinner struts and thin coatings. The drugs were also changed from Paclitaxel and Sirolimus to Zotrolimus and Everolimus. These stents performed best; however, there was an issue of permanent coating, which remained intact over the stent surface after complete drug elution and started to cause issues in longer-term studies. Hence, an improved version of DES was introduced to these permanent coatings called the third generation of drug eluting stents, which initially utilized biodegradable polymer and ultimately moved towards polymer free drug coatings. This generation has introduced a unique amalgam of technologies to achieve its polymer free coatings; however, researchers have numerous prospects of growth in this field. This review paper highlights the major coups of stent technology evolution from BMS to DES, from thick polymeric coatings to thin coatings and from durable polymers to polymer free DES. Conclusion In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology.
Literature review In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology.
Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the DES in the stent market is the degree of improvement with which it evolves. New and better stents come into the market every year, surpassing their predecessors by many folds. This review paper discusses the journey of DES with supporting clinical trials in detail. In the first generation, there were stainless-steel stents with thicker coatings. Although they had superior results compared to BMS, there was still room for improvement. Afterward came the second-generation stents, which had superior metal platforms with thinner struts and thin coatings. The drugs were also changed from Paclitaxel and Sirolimus to Zotrolimus and Everolimus. These stents performed best; however, there was an issue of permanent coating, which remained intact over the stent surface after complete drug elution and started to cause issues in longer-term studies. Hence, an improved version of DES was introduced to these permanent coatings called the third generation of drug eluting stents, which initially utilized biodegradable polymer and ultimately moved towards polymer free drug coatings. This generation has introduced a unique amalgam of technologies to achieve its polymer free coatings; however, researchers have numerous prospects of growth in this field. This review paper highlights the major coups of stent technology evolution from BMS to DES, from thick polymeric coatings to thin coatings and from durable polymers to polymer free DES. In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology.
Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the DES in the stent market is the degree of improvement with which it evolves. New and better stents come into the market every year, surpassing their predecessors by many folds.BACKGROUNDIntroduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the DES in the stent market is the degree of improvement with which it evolves. New and better stents come into the market every year, surpassing their predecessors by many folds.This review paper discusses the journey of DES with supporting clinical trials in detail. In the first generation, there were stainless-steel stents with thicker coatings. Although they had superior results compared to BMS, there was still room for improvement. Afterward came the second-generation stents, which had superior metal platforms with thinner struts and thin coatings. The drugs were also changed from Paclitaxel and Sirolimus to Zotrolimus and Everolimus. These stents performed best; however, there was an issue of permanent coating, which remained intact over the stent surface after complete drug elution and started to cause issues in longer-term studies. Hence, an improved version of DES was introduced to these permanent coatings called the third generation of drug eluting stents, which initially utilized biodegradable polymer and ultimately moved towards polymer free drug coatings. This generation has introduced a unique amalgam of technologies to achieve its polymer free coatings; however, researchers have numerous prospects of growth in this field. This review paper highlights the major coups of stent technology evolution from BMS to DES, from thick polymeric coatings to thin coatings and from durable polymers to polymer free DES.LITERATURE REVIEWThis review paper discusses the journey of DES with supporting clinical trials in detail. In the first generation, there were stainless-steel stents with thicker coatings. Although they had superior results compared to BMS, there was still room for improvement. Afterward came the second-generation stents, which had superior metal platforms with thinner struts and thin coatings. The drugs were also changed from Paclitaxel and Sirolimus to Zotrolimus and Everolimus. These stents performed best; however, there was an issue of permanent coating, which remained intact over the stent surface after complete drug elution and started to cause issues in longer-term studies. Hence, an improved version of DES was introduced to these permanent coatings called the third generation of drug eluting stents, which initially utilized biodegradable polymer and ultimately moved towards polymer free drug coatings. This generation has introduced a unique amalgam of technologies to achieve its polymer free coatings; however, researchers have numerous prospects of growth in this field. This review paper highlights the major coups of stent technology evolution from BMS to DES, from thick polymeric coatings to thin coatings and from durable polymers to polymer free DES.In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology.CONCLUSIONIn conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology.
Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the DES in the stent market is the degree of improvement with which it evolves. New and better stents come into the market every year, surpassing their predecessors by many folds. Literature review This review paper discusses the journey of DES with supporting clinical trials in detail. In the first generation, there were stainless-steel stents with thicker coatings. Although they had superior results compared to BMS, there was still room for improvement. Afterward came the second-generation stents, which had superior metal platforms with thinner struts and thin coatings. The drugs were also changed from Paclitaxel and Sirolimus to Zotrolimus and Everolimus. These stents performed best; however, there was an issue of permanent coating, which remained intact over the stent surface after complete drug elution and started to cause issues in longer-term studies. Hence, an improved version of DES was introduced to these permanent coatings called the third generation of drug eluting stents, which initially utilized biodegradable polymer and ultimately moved towards polymer free drug coatings. This generation has introduced a unique amalgam of technologies to achieve its polymer free coatings; however, researchers have numerous prospects of growth in this field. This review paper highlights the major coups of stent technology evolution from BMS to DES, from thick polymeric coatings to thin coatings and from durable polymers to polymer free DES. Conclusion In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology.
Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained its superiority over BMS in every aspect from restenosis rate to late lumen loss. The reason behind the magnanimous position of the DES in the stent market is the degree of improvement with which it evolves. New and better stents come into the market every year, surpassing their predecessors by many folds. Literature review This review paper discusses the journey of DES with supporting clinical trials in detail. In the first generation, there were stainless-steel stents with thicker coatings. Although they had superior results compared to BMS, there was still room for improvement. Afterward came the second-generation stents, which had superior metal platforms with thinner struts and thin coatings. The drugs were also changed from Paclitaxel and Sirolimus to Zotrolimus and Everolimus. These stents performed best; however, there was an issue of permanent coating, which remained intact over the stent surface after complete drug elution and started to cause issues in longer-term studies. Hence, an improved version of DES was introduced to these permanent coatings called the third generation of drug eluting stents, which initially utilized biodegradable polymer and ultimately moved towards polymer free drug coatings. This generation has introduced a unique amalgam of technologies to achieve its polymer free coatings; however, researchers have numerous prospects of growth in this field. This review paper highlights the major coups of stent technology evolution from BMS to DES, from thick polymeric coatings to thin coatings and from durable polymers to polymer free DES. Conclusion In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has provided even better results than BMS. In DES, the first and second generation has ruled the technology for many years and are still on the shelves. Still, the issues aroused due to durable polymer shifted the attention towards biodegradable drug eluting stents, the third generation growing rapidly. But the scientific community has not restricted themselves and is investigating bioresorbable stents that completely eliminate the polymer intervention in drug eluting stent technology. Keywords: Bare metal stents, Angioplasty, Xience, Sirolimus, Stents, Cardiovascular disease
ArticleNumber 65
Audience Academic
Author Ali, Murtaza Najabat
Ghafoor, Bakhtawar
Hassan, Sadia
Author_xml – sequence: 1
  givenname: Sadia
  surname: Hassan
  fullname: Hassan, Sadia
  organization: Department of Biomedical Engineering and Sciences (BMES), School of Mechanical and Manufacturing Engineering (SMME), National University of Sciences and Technology (NUST)
– sequence: 2
  givenname: Murtaza Najabat
  orcidid: 0000-0002-3829-8215
  surname: Ali
  fullname: Ali, Murtaza Najabat
  email: murtaza.bme@hotmail.com
  organization: Department of Biomedical Engineering and Sciences (BMES), School of Mechanical and Manufacturing Engineering (SMME), National University of Sciences and Technology (NUST)
– sequence: 3
  givenname: Bakhtawar
  surname: Ghafoor
  fullname: Ghafoor, Bakhtawar
  organization: Department of Biomedical Engineering and Sciences (BMES), School of Mechanical and Manufacturing Engineering (SMME), National University of Sciences and Technology (NUST)
BackLink https://www.ncbi.nlm.nih.gov/pubmed/35379273$$D View this record in MEDLINE/PubMed
BookMark eNp9kktr3DAUhU1JaB7tH-iiGLrJxoletqUuCiGkbSDQTbsrCEmWPJralivZA_PveyfOa0IJXlhI53zWuT4n2cEQBptlHzA6x5hXFwlThEWBCCkQ5pgU2zfZMa6ZKDgS6ODZ-ig7SWmNECspKt9mR7SktSA1Pc5-X29CN08-DCpu89HGNFoz-Y3Ng8ubOLe53R0PbZ4mO0zpc-5i6PNp5c2ffAzdtrcxn8Lj0kVrczWOMSizepcdOtUl-_7-fZr9-nr98-p7cfvj283V5W1hKlRPBTMN001Z1tYwuDLhrHaVotSwEnPGmGo011oLajDWFCntGBe2wZjoiiik6Gl2s3CboNZyjL6HMDIoL-82QmylipM3nZWIoZLipuaEKKBo7pzhDWIKO62JKIH1ZWGNs-5tYyB0VN0edP9k8CvZho3kgsNPQAA4uwfE8He2aZK9T8Z2nRpsmJMkFasJJqziIP30QroOcxxgVKAqsahhGtWTqlUQwA8uwHfNDiovKyFgZITt7n3-HxU8je29geI4D_t7ho_Pgz4mfOgGCPgiMDGkFK2Txk9qVxUg-05iJHc1lEsNJdRQ3tVQbsFKXlgf6K-a6GJKIB5aG5-m8YrrHxgX74c
CitedBy_id crossref_primary_10_1002_ccd_30636
crossref_primary_10_3390_jcm12031238
crossref_primary_10_1080_17425247_2023_2190580
crossref_primary_10_1097_CRD_0000000000000705
crossref_primary_10_7759_cureus_35651
crossref_primary_10_3390_molecules29204927
crossref_primary_10_1016_j_cpcardiol_2024_102568
crossref_primary_10_1002_wnan_1941
crossref_primary_10_1016_j_amjcard_2024_01_019
crossref_primary_10_3390_jpm13050753
crossref_primary_10_1021_acsapm_4c03734
crossref_primary_10_1186_s43044_023_00408_8
crossref_primary_10_3389_fcvm_2024_1288659
crossref_primary_10_36660_abc_20230302
crossref_primary_10_1038_s41598_024_51192_7
crossref_primary_10_1016_j_mtbio_2024_101259
crossref_primary_10_1007_s13770_024_00646_0
crossref_primary_10_3390_biomedicines10082047
crossref_primary_10_1016_j_cclet_2024_110492
crossref_primary_10_1007_s42823_023_00496_1
crossref_primary_10_7759_cureus_52004
crossref_primary_10_3390_biomimetics8010072
crossref_primary_10_1080_14796678_2024_2370688
crossref_primary_10_3390_ijms252413345
crossref_primary_10_1016_j_ejmech_2024_117172
crossref_primary_10_1109_JIOT_2022_3215884
crossref_primary_10_3390_pharmaceutics16030432
crossref_primary_10_1126_sciadv_abq0997
crossref_primary_10_1016_j_ijpharm_2024_124572
crossref_primary_10_3390_jcm11175079
crossref_primary_10_3390_polym17030420
Cites_doi 10.1016/j.amjcard.2009.02.011
10.4049/jimmunol.177.10.6667
10.1161/CIRCULATIONAHA.118.038065
10.17925/HI.2019.13.2.17
10.1007/s10856-009-3705-5
10.1161/CIRCULATIONAHA.109.849877
10.1111/j.1540-8183.1994.tb00498.x
10.1016/j.ahj.2012.08.010
10.1001/jama.294.10.1215
10.1016/j.jcin.2015.12.076
10.1002/ccd.22509
10.1161/01.CIR.0000047700.58683.A1
10.1111/j.1540-8183.2009.00450.x
10.1161/CIRCINTERVENTIONS.110.946426
10.1007/s40204-018-0097-y
10.1016/S0952-7915(98)80172-6
10.1016/j.jacc.2012.09.004
10.1016/j.jcin.2017.06.070
10.1007/BF03091792
10.1007/s10439-015-1380-x
10.1016/S0140-6736(14)61038-2
10.5694/mja16.00444
10.1161/CIRCULATIONAHA.105.591206
10.1093/ehjci/jes025
10.2147/vhrm.2008.04.01.31
10.1016/j.carrev.2016.04.001
10.1161/CIRCINTERVENTIONS.119.008024
10.1016/S0142-9612(01)00297-6
10.1111/j.1540-8183.2006.00184.x
10.1056/NEJMoa012843
10.1016/S0002-9149(98)00004-6
10.4244/EIJY14M08_06
10.1056/NEJM199408253310801
10.4244/EIJ-D-17-00796
10.2147/vhrm.2007.3.2.191
10.1016/B978-0-323-47671-3.00006-5
10.1093/neuonc/nov152
10.1016/S0140-6736(16)32050-5
10.1016/j.jcin.2009.02.009
10.1161/CIRCINTERVENTIONS.119.008152
10.1016/S0041-1345(01)02369-7
10.1001/jamacardio.2018.3573
10.1161/CIRCINTERVENTIONS.113.000120
10.1016/j.actbio.2015.02.006
10.1016/j.jcin.2008.07.003
10.4244/EIJ-D-18-00336
10.1056/NEJMoa1607991
10.1016/j.amsu.2018.12.003
10.1016/j.jacc.2014.11.053
10.1016/j.jcin.2010.12.014
10.1161/01.CIR.103.23.2816
10.1002/ccd.25993
10.1016/S0735-1097(97)00511-1
10.1093/eurheartj/ehv511
10.2174/1389557514666140530093620
10.1161/CIRCULATIONAHA.110.003210
10.4244/EIJV9I6A116
10.1111/j.1755-5922.2010.00144.x
10.1016/j.amjcard.2016.06.061
10.1016/S0735-1097(03)00119-0
10.1517/17425247.4.3.287
10.1001/jama.295.8.895
10.1016/0735-1097(95)00473-4
10.1016/j.ihj.2013.08.031
10.1007/s12928-015-0366-9
10.1016/j.jacc.2011.12.016
10.3390/ijms17091490
10.1517/14656566.2014.948844
10.1093/eurheartj/ehp044
ContentType Journal Article
Copyright The Author(s) 2022
2022. The Author(s).
COPYRIGHT 2022 BioMed Central Ltd.
2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Copyright_xml – notice: The Author(s) 2022
– notice: 2022. The Author(s).
– notice: COPYRIGHT 2022 BioMed Central Ltd.
– notice: 2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
DBID C6C
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7X7
7XB
88E
8FD
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FR3
FYUFA
GHDGH
K9.
M0S
M1P
M7Z
P64
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.1186/s13019-022-01812-y
DatabaseName Springer Nature OA Free Journals
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Technology Research Database
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One Community College
ProQuest Central
Engineering Research Database
Health Research Premium Collection (UHCL Subscription)
Health Research Premium Collection (Alumni)
ProQuest Health & Medical Complete (Alumni)
ProQuest Health & Medical Collection
Medical Database
Biochemistry Abstracts 1
Biotechnology and BioEngineering Abstracts
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
Technology Research Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Central China
ProQuest Central
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Health & Medical Research Collection
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Biochemistry Abstracts 1
Engineering Research Database
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
Publicly Available Content Database

MEDLINE
MEDLINE - Academic


Database_xml – sequence: 1
  dbid: C6C
  name: Springer Nature OA Free Journals
  url: http://www.springeropen.com/
  sourceTypes: Publisher
– sequence: 2
  dbid: DOA
  name: DOAJ Open Access Full Text
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 3
  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: 4
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 5
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1749-8090
EndPage 20
ExternalDocumentID oai_doaj_org_article_040531d7822a489b8ffc8d04a1fbb295
PMC8981810
A699417245
35379273
10_1186_s13019_022_01812_y
Genre Journal Article
Review
GroupedDBID ---
0R~
29K
2WC
53G
5GY
5VS
7X7
88E
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAWTL
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACIWK
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AEAQA
AENEX
AFKRA
AFPKN
AFRAH
AHBYD
AHMBA
AHYZX
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BCNDV
BENPR
BFQNJ
BMC
BPHCQ
BVXVI
C6C
CCPQU
CS3
D-I
DIK
DU5
E3Z
EBD
EBLON
EBS
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
IAO
IHR
INH
INR
ITC
KQ8
M1P
M48
M~E
O5R
O5S
OK1
OVT
P2P
P6G
PGMZT
PHGZM
PHGZT
PIMPY
PJZUB
PPXIY
PQQKQ
PROAC
PSQYO
PUEGO
RBZ
RNS
ROL
RPM
RSV
SMD
SOJ
SV3
TR2
TUS
UKHRP
WOQ
WOW
~8M
AAYXX
ALIPV
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
PMFND
3V.
7XB
8FD
8FK
AZQEC
DWQXO
FR3
K9.
M7Z
P64
PKEHL
PQEST
PQUKI
PRINS
7X8
5PM
ID FETCH-LOGICAL-c607t-4cd4bd557ec41742847f6a33c4518444adb8bbb93c11b30abf489ed112b62a0a3
IEDL.DBID M48
ISSN 1749-8090
IngestDate Wed Aug 27 01:30:56 EDT 2025
Thu Aug 21 18:21:33 EDT 2025
Thu Sep 04 20:30:36 EDT 2025
Fri Jul 25 20:07:17 EDT 2025
Tue Jun 17 21:00:26 EDT 2025
Tue Jun 10 20:40:33 EDT 2025
Mon Jul 21 05:46:05 EDT 2025
Thu Apr 24 22:58:25 EDT 2025
Tue Jul 01 02:57:07 EDT 2025
Sat Sep 06 07:23:24 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Bare metal stents
Cardiovascular disease
Sirolimus
Angioplasty
Xience
Stents
Language English
License 2022. The Author(s).
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c607t-4cd4bd557ec41742847f6a33c4518444adb8bbb93c11b30abf489ed112b62a0a3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
ORCID 0000-0002-3829-8215
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.1186/s13019-022-01812-y
PMID 35379273
PQID 2651971746
PQPubID 55047
PageCount 20
ParticipantIDs doaj_primary_oai_doaj_org_article_040531d7822a489b8ffc8d04a1fbb295
pubmedcentral_primary_oai_pubmedcentral_nih_gov_8981810
proquest_miscellaneous_2647212468
proquest_journals_2651971746
gale_infotracmisc_A699417245
gale_infotracacademiconefile_A699417245
pubmed_primary_35379273
crossref_citationtrail_10_1186_s13019_022_01812_y
crossref_primary_10_1186_s13019_022_01812_y
springer_journals_10_1186_s13019_022_01812_y
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-04-04
PublicationDateYYYYMMDD 2022-04-04
PublicationDate_xml – month: 04
  year: 2022
  text: 2022-04-04
  day: 04
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
– name: England
PublicationTitle Journal of cardiothoracic surgery
PublicationTitleAbbrev J Cardiothorac Surg
PublicationTitleAlternate J Cardiothorac Surg
PublicationYear 2022
Publisher BioMed Central
BioMed Central Ltd
BMC
Publisher_xml – name: BioMed Central
– name: BioMed Central Ltd
– name: BMC
References RA Byrne (1812_CR7) 2015; 36
JJ Wu (1812_CR64) 2018; 38
B O’Brien (1812_CR69) 2016; 44
JR Costa (1812_CR77) 2009; 2
RA Schatz (1812_CR4) 1994; 7
A Villa (1812_CR11) 2009; 103
AB Mehta (1812_CR49) 2013; 65
PI Meredith Am (1812_CR59) 2012; 59
PW Serruys (1812_CR2) 1994; 331
CR Kelly (1812_CR47) 2017; 10
N Ding (1812_CR40) 2009; 22
VA Jiménez (1812_CR53) 2016; 17
GW Stone (1812_CR20) 2005; 294
HA Sharar (1812_CR39) 2016; 9
MWZ Basalus (1812_CR44) 2010; 18
CJ George (1812_CR5) 1998; 81
JA Ormiston (1812_CR70) 2010; 3
JJ Wu (1812_CR61) 2019; 13
J Pache (1812_CR25) 2003; 41
A Abizaid (1812_CR71) 2013; 9
IM Singh (1812_CR10) 2010; 76
B AL-Mangour (1812_CR26) 2013; 4
M-C Morice (1812_CR21) 2006; 295
JP MacKeigan (1812_CR30) 2015; 17
JA Rymer (1812_CR9) 2016; 118
C Macaya (1812_CR3) 1996; 27
JF Iglesias (1812_CR24) 2019; 12
A Akinapelli (1812_CR56) 2017; 13
1812_CR16
L Räber (1812_CR68) 2011; 29
MJ Eppihimer (1812_CR58) 2013; 6
A Abizaid (1812_CR15) 2007; 3
MM Kok (1812_CR62) 2018; 14
E Guerra (1812_CR28) 2014; 15
IBA Menown (1812_CR50) 2020; 26
A Chisari (1812_CR51) 2016; 17
PW Serruys (1812_CR45) 2016; 388
S McGinty (1812_CR67) 2015; 18
T Pilgrim (1812_CR63) 2014; 384
C Mcormick (1812_CR74) 2018
M-C Morice (1812_CR75) 2002; 346
M Boden (1812_CR17) 2009; 20
RA Byrne (1812_CR48) 2009; 30
I Neamtu (1812_CR34) 2014; 14
R Diletti (1812_CR41) 2012; 164
KH Bønaa (1812_CR12) 2016; 375
DJ Kereiakes (1812_CR8) 2018; 3
DJ Kereiakes (1812_CR60) 2019; 12
RT Abraham (1812_CR72) 1998; 10
JR Costa (1812_CR76) 2008; 1
I Sheiban (1812_CR38) 2008; 4
1812_CR27
DE Kandzari (1812_CR37) 2011; 4
K Kolandaivelu (1812_CR31) 2011; 123
M Klein (1812_CR73) 2006; 177
M Valgimigli (1812_CR33) 2015; 65
GD Baura (1812_CR14) 2013
M Natsuaki (1812_CR43) 2016; 31
E Grube (1812_CR18) 2003; 107
J Bennett (1812_CR46) 2013; 7
A Kastrati (1812_CR23) 2001; 103
DE Kandzari (1812_CR35) 2006; 19
GW Stone (1812_CR54) 2012; 60
1812_CR1
B Nashan (1812_CR29) 2001; 33
S Kufner (1812_CR55) 2019; 139
J Fajadet (1812_CR36) 2006; 114
MP Savage (1812_CR6) 1998; 31
B Xu (1812_CR42) 2018; 14
I Tsujino (1812_CR66) 2007; 4
S Borhani (1812_CR13) 2018; 7
E Barbato (1812_CR52) 2015; 11
J Gutiérrez-Chico (1812_CR22) 2012; 13
GJ Wilson (1812_CR57) 2015; 86
AL Lewis (1812_CR32) 2002; 23
S Silber (1812_CR19) 2009; 120
D Chen (1812_CR65) 2016; 205
References_xml – volume: 103
  start-page: 1651
  issue: 12
  year: 2009
  ident: 1812_CR11
  publication-title: Am J Cardiol
  doi: 10.1016/j.amjcard.2009.02.011
– volume: 177
  start-page: 6667
  issue: 10
  year: 2006
  ident: 1812_CR73
  publication-title: J Immunol
  doi: 10.4049/jimmunol.177.10.6667
– volume: 139
  start-page: 325
  issue: 3
  year: 2019
  ident: 1812_CR55
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.118.038065
– volume: 13
  start-page: 17
  issue: 2
  year: 2019
  ident: 1812_CR61
  publication-title: Heart Int
  doi: 10.17925/HI.2019.13.2.17
– volume: 20
  start-page: 1553
  issue: 7
  year: 2009
  ident: 1812_CR17
  publication-title: J Mater Sci Mater Med
  doi: 10.1007/s10856-009-3705-5
– volume: 120
  start-page: 1498
  issue: 15
  year: 2009
  ident: 1812_CR19
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.109.849877
– volume: 7
  start-page: 575
  issue: 6
  year: 1994
  ident: 1812_CR4
  publication-title: J Interv Cardiol
  doi: 10.1111/j.1540-8183.1994.tb00498.x
– volume: 164
  start-page: 654
  issue: 5
  year: 2012
  ident: 1812_CR41
  publication-title: Am Heart J
  doi: 10.1016/j.ahj.2012.08.010
– volume: 294
  start-page: 1215
  issue: 10
  year: 2005
  ident: 1812_CR20
  publication-title: JAMA
  doi: 10.1001/jama.294.10.1215
– volume: 9
  start-page: S16
  issue: 4
  year: 2016
  ident: 1812_CR39
  publication-title: JACC Cardiovasc Interv
  doi: 10.1016/j.jcin.2015.12.076
– volume: 76
  start-page: 257
  issue: 2
  year: 2010
  ident: 1812_CR10
  publication-title: Catheter Cardiovasc Interv
  doi: 10.1002/ccd.22509
– volume: 107
  start-page: 38
  issue: 1
  year: 2003
  ident: 1812_CR18
  publication-title: Circulation
  doi: 10.1161/01.CIR.0000047700.58683.A1
– volume: 22
  start-page: S18
  issue: 1
  year: 2009
  ident: 1812_CR40
  publication-title: J Interv Cardiol
  doi: 10.1111/j.1540-8183.2009.00450.x
– volume: 3
  start-page: 556
  issue: 6
  year: 2010
  ident: 1812_CR70
  publication-title: Circ Cardiovasc Interv
  doi: 10.1161/CIRCINTERVENTIONS.110.946426
– volume: 7
  start-page: 175
  issue: 3
  year: 2018
  ident: 1812_CR13
  publication-title: Prog Biomater
  doi: 10.1007/s40204-018-0097-y
– volume: 10
  start-page: 330
  issue: 3
  year: 1998
  ident: 1812_CR72
  publication-title: Curr Opin Immunol
  doi: 10.1016/S0952-7915(98)80172-6
– start-page: 1418
  volume-title: Corporate considerations on biomaterials and medical devices: case studies in regulation and reimbursement. Biomaterials science
  year: 2013
  ident: 1812_CR14
– volume: 60
  start-page: 1975
  issue: 19
  year: 2012
  ident: 1812_CR54
  publication-title: J Am Coll Cardiol
  doi: 10.1016/j.jacc.2012.09.004
– volume: 10
  start-page: 2392
  issue: 23
  year: 2017
  ident: 1812_CR47
  publication-title: JACC Cardiovasc Interv
  doi: 10.1016/j.jcin.2017.06.070
– volume: 18
  start-page: 360
  issue: 7–8
  year: 2010
  ident: 1812_CR44
  publication-title: Neth Heart J
  doi: 10.1007/BF03091792
– volume: 44
  start-page: 523
  issue: 2
  year: 2016
  ident: 1812_CR69
  publication-title: Ann Biomed Eng
  doi: 10.1007/s10439-015-1380-x
– volume: 384
  start-page: 2111
  issue: 9960
  year: 2014
  ident: 1812_CR63
  publication-title: Lancet
  doi: 10.1016/S0140-6736(14)61038-2
– volume: 205
  start-page: 277
  issue: 6
  year: 2016
  ident: 1812_CR65
  publication-title: Med J Aust
  doi: 10.5694/mja16.00444
– volume: 114
  start-page: 798
  issue: 8
  year: 2006
  ident: 1812_CR36
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.105.591206
– volume: 13
  start-page: 370
  year: 2012
  ident: 1812_CR22
  publication-title: Eur Heart J Cardiovasc Imaging
  doi: 10.1093/ehjci/jes025
– volume: 4
  start-page: 31
  issue: 1
  year: 2008
  ident: 1812_CR38
  publication-title: Vasc Health Risk Manag
  doi: 10.2147/vhrm.2008.04.01.31
– volume: 17
  start-page: 355
  issue: 6
  year: 2016
  ident: 1812_CR53
  publication-title: Cardiovasc Revasc Med
  doi: 10.1016/j.carrev.2016.04.001
– volume: 12
  start-page: e008024
  issue: 8
  year: 2019
  ident: 1812_CR24
  publication-title: Circ Cardiovasc Intervent
  doi: 10.1161/CIRCINTERVENTIONS.119.008024
– volume: 23
  start-page: 1697
  issue: 7
  year: 2002
  ident: 1812_CR32
  publication-title: Biomaterials
  doi: 10.1016/S0142-9612(01)00297-6
– volume: 19
  start-page: 405
  issue: 5
  year: 2006
  ident: 1812_CR35
  publication-title: J Interv Cardiol
  doi: 10.1111/j.1540-8183.2006.00184.x
– volume: 346
  start-page: 1773
  issue: 23
  year: 2002
  ident: 1812_CR75
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa012843
– volume: 81
  start-page: 860
  issue: 7
  year: 1998
  ident: 1812_CR5
  publication-title: Am J Cardiol
  doi: 10.1016/S0002-9149(98)00004-6
– volume: 11
  start-page: 541
  issue: 5
  year: 2015
  ident: 1812_CR52
  publication-title: EuroIntervention
  doi: 10.4244/EIJY14M08_06
– volume: 331
  start-page: 489
  issue: 8
  year: 1994
  ident: 1812_CR2
  publication-title: New Engl J Med
  doi: 10.1056/NEJM199408253310801
– volume: 14
  start-page: e554
  issue: 5
  year: 2018
  ident: 1812_CR42
  publication-title: EuroIntervention
  doi: 10.4244/EIJ-D-17-00796
– volume: 3
  start-page: 191
  issue: 2
  year: 2007
  ident: 1812_CR15
  publication-title: Vasc Health Risk Manag
  doi: 10.2147/vhrm.2007.3.2.191
– ident: 1812_CR27
  doi: 10.1016/B978-0-323-47671-3.00006-5
– volume: 17
  start-page: 1550
  issue: 12
  year: 2015
  ident: 1812_CR30
  publication-title: Neuro Oncol
  doi: 10.1093/neuonc/nov152
– volume: 388
  start-page: 2479
  issue: 10059
  year: 2016
  ident: 1812_CR45
  publication-title: Lancet
  doi: 10.1016/S0140-6736(16)32050-5
– volume: 2
  start-page: 422
  issue: 5
  year: 2009
  ident: 1812_CR77
  publication-title: JACC Cardiovasc Interv
  doi: 10.1016/j.jcin.2009.02.009
– volume: 12
  start-page: e008152
  issue: 9
  year: 2019
  ident: 1812_CR60
  publication-title: Circ Cardiovasc Interv
  doi: 10.1161/CIRCINTERVENTIONS.119.008152
– volume: 33
  start-page: 3215
  issue: 7–8
  year: 2001
  ident: 1812_CR29
  publication-title: Transplant Proc
  doi: 10.1016/S0041-1345(01)02369-7
– volume: 3
  start-page: 1039
  issue: 11
  year: 2018
  ident: 1812_CR8
  publication-title: JAMA Cardiol
  doi: 10.1001/jamacardio.2018.3573
– start-page: 343
  volume-title: Functionalised cardiovascular stents
  year: 2018
  ident: 1812_CR74
– volume: 6
  start-page: 370
  issue: 4
  year: 2013
  ident: 1812_CR58
  publication-title: Circ Cardiovasc Interv
  doi: 10.1161/CIRCINTERVENTIONS.113.000120
– volume: 18
  start-page: 213
  year: 2015
  ident: 1812_CR67
  publication-title: Acta Biomater
  doi: 10.1016/j.actbio.2015.02.006
– volume: 1
  start-page: 545
  issue: 5
  year: 2008
  ident: 1812_CR76
  publication-title: JACC Cardiovasc Interv
  doi: 10.1016/j.jcin.2008.07.003
– volume: 14
  start-page: 915
  issue: 8
  year: 2018
  ident: 1812_CR62
  publication-title: EuroIntervention
  doi: 10.4244/EIJ-D-18-00336
– volume: 375
  start-page: 1242
  issue: 13
  year: 2016
  ident: 1812_CR12
  publication-title: New Engl J Med
  doi: 10.1056/NEJMoa1607991
– volume: 26
  start-page: 100472
  year: 2020
  ident: 1812_CR50
  publication-title: Int J Cardiol Heart Vasc
– ident: 1812_CR16
– volume: 38
  start-page: 13
  year: 2018
  ident: 1812_CR64
  publication-title: Ann Med Surg (Lond)
  doi: 10.1016/j.amsu.2018.12.003
– volume: 65
  start-page: 805
  issue: 8
  year: 2015
  ident: 1812_CR33
  publication-title: J Am Coll Cardiol
  doi: 10.1016/j.jacc.2014.11.053
– volume: 4
  start-page: 543
  issue: 5
  year: 2011
  ident: 1812_CR37
  publication-title: JACC Cardiovasc Interv
  doi: 10.1016/j.jcin.2010.12.014
– volume: 103
  start-page: 2816
  issue: 23
  year: 2001
  ident: 1812_CR23
  publication-title: Circulation
  doi: 10.1161/01.CIR.103.23.2816
– volume: 86
  start-page: E247
  issue: 6
  year: 2015
  ident: 1812_CR57
  publication-title: Catheter Cardiovasc Interv
  doi: 10.1002/ccd.25993
– volume: 31
  start-page: 307
  issue: 2
  year: 1998
  ident: 1812_CR6
  publication-title: J Am Coll Cardiol
  doi: 10.1016/S0735-1097(97)00511-1
– volume: 36
  start-page: 3320
  issue: 47
  year: 2015
  ident: 1812_CR7
  publication-title: Eur Heart J
  doi: 10.1093/eurheartj/ehv511
– volume: 14
  start-page: 505
  year: 2014
  ident: 1812_CR34
  publication-title: Mini Rev Med Chem
  doi: 10.2174/1389557514666140530093620
– volume: 123
  start-page: 1400
  issue: 13
  year: 2011
  ident: 1812_CR31
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.110.003210
– volume: 9
  start-page: 721
  issue: 6
  year: 2013
  ident: 1812_CR71
  publication-title: EuroIntervention
  doi: 10.4244/EIJV9I6A116
– volume: 29
  start-page: 176
  issue: 3
  year: 2011
  ident: 1812_CR68
  publication-title: Cardiovasc Ther
  doi: 10.1111/j.1755-5922.2010.00144.x
– volume: 118
  start-page: 959
  issue: 7
  year: 2016
  ident: 1812_CR9
  publication-title: Am J Cardiol
  doi: 10.1016/j.amjcard.2016.06.061
– volume: 41
  start-page: 1283
  issue: 8
  year: 2003
  ident: 1812_CR25
  publication-title: J Am Coll Cardiol
  doi: 10.1016/S0735-1097(03)00119-0
– volume: 4
  start-page: 287
  issue: 3
  year: 2007
  ident: 1812_CR66
  publication-title: Expert Opin Drug Deliv
  doi: 10.1517/17425247.4.3.287
– volume: 295
  start-page: 895
  issue: 8
  year: 2006
  ident: 1812_CR21
  publication-title: JAMA
  doi: 10.1001/jama.295.8.895
– ident: 1812_CR1
– volume: 27
  start-page: 255
  issue: 2
  year: 1996
  ident: 1812_CR3
  publication-title: J Am Coll Cardiol
  doi: 10.1016/0735-1097(95)00473-4
– volume: 65
  start-page: 593
  issue: 5
  year: 2013
  ident: 1812_CR49
  publication-title: Indian Heart J
  doi: 10.1016/j.ihj.2013.08.031
– volume: 31
  start-page: 196
  issue: 3
  year: 2016
  ident: 1812_CR43
  publication-title: Cardiovasc Interv Ther
  doi: 10.1007/s12928-015-0366-9
– volume: 13
  start-page: 139
  issue: 2
  year: 2017
  ident: 1812_CR56
  publication-title: Curr Cardiol Rev
– volume: 59
  start-page: 1362
  year: 2012
  ident: 1812_CR59
  publication-title: J Am Coll Cardiol
  doi: 10.1016/j.jacc.2011.12.016
– volume: 7
  start-page: 149
  year: 2013
  ident: 1812_CR46
  publication-title: Biologics Targets Ther
– volume: 4
  start-page: 16
  issue: 10
  year: 2013
  ident: 1812_CR26
  publication-title: Mater Sci Appl
– volume: 17
  start-page: 1490
  issue: 9
  year: 2016
  ident: 1812_CR51
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms17091490
– volume: 15
  start-page: 2155
  year: 2014
  ident: 1812_CR28
  publication-title: Expert Opin Pharmacother
  doi: 10.1517/14656566.2014.948844
– volume: 30
  start-page: 923
  issue: 8
  year: 2009
  ident: 1812_CR48
  publication-title: Eur Heart J
  doi: 10.1093/eurheartj/ehp044
SSID ssj0045305
Score 2.4287705
SecondaryResourceType review_article
Snippet Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES)...
Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES) maintained...
Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting Stents (DES)...
Literature review In conclusion, though the medical industry promptly accepted BMS as the best treatment option for cardiovascular diseases; however, DES has...
Abstract Background Introduction of Bare Metal Stents (BMS) was itself a revolutionary step in the history of the medical industry; however, Drug Eluting...
SourceID doaj
pubmedcentral
proquest
gale
pubmed
crossref
springer
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 65
SubjectTerms Angioplasty
Bare metal stents
Biocompatibility
Biodegradability
Biomedical materials
Cardiac Surgery
Cardiovascular disease
Cardiovascular diseases
Catheters
Clinical outcomes
Clinical trials
Coatings
Diabetes
Drug delivery
Drug-Eluting Stents
Everolimus
Heart attacks
Humans
Hyperplasia
Implants
Inhibitor drugs
Literature reviews
Medical research
Medicine
Medicine & Public Health
Paclitaxel
Pharmaceutical industry
Pharmaceuticals
Polymer coatings
Polymer industry
Polymers
Rapamycin
Restenosis
Review
Sirolimus
Sirolimus - pharmacology
Stainless steels
Stent (Surgery)
Stents
Struts
Thoracic Surgery
Thrombosis
Veins & arteries
Xience
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NaxUxEA_SkxdR_FqtJYLgQZfu20yySW9VWoqgJws9CCHJJlWsu499-4T33zvJfrRbUS_e9m1mIfnlN5kZ3syEkFcVD7IqbZUrZE8OwE1umeS5MVJJBsGE1GLj4ydxdg4fLvjFjau-Yk7Y0B54AO4QSYY0qaMhMyCVlSE4WRdgVsHaUqXupWjzpmBqOIOBI42nEhkpDjd4UsdinTKmIaBJy3cLM5S69f9-Jt8wSrcTJm_9a5qM0el9cm_0IunxMPsH5I5vHpIvJz9HHpluR9fXVZS0DbTutpfUx-HmkuLONv3miMbaEhoT3r_TdXu1--E72rfzY-i8p1PP8Ufk_PTk8_uzfLw8IXeiqPocXA225rzyDjDqiFYoCMOYA45BHYCprbTWKuZWK8sKYwOi62t0v6woTWHYY7LXtI1_SqhytYFQGcvAgLBeopdmwBQ8AP7gNiOrCUvtxs7i8YKLK50iDCn0gL9G_HXCX-8y8mb-Zj301fir9Lu4RbNk7ImdXiBT9MgU_S-mZOR13GAdNRen58xYgICLjD2w9LFQCqEqASX3F5KocW45PFFEjxq_0aWIJcCItMjIy3k4fhmz2BrfbqMMYMBdgpAZeTIwal4S46xS6EtmpFpwbbHm5Ujz7WvqB45ahTAVGXk7sfJ6Wn_G9Nn_wPQ5uVsmrYrZTPtkr--2_gV6ab09SAr5C_MrOCM
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: ProQuest Central
  dbid: BENPR
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfR1di9QwMOjeiy-i-FU9JYLgg5brtpM09UXuZI9D8BDx4B6EkKTJnXi2a3dX2H_vTDfdtSfeW9uZQGcyX0lmJoy9KkVQZW7LtELpSQGESW2hRGqMqlQBwYS-xcanU3lyBh_PxXnccFvEtMrBJvaGum4d7ZEf5JJKLDF-lu_nv1K6NYpOV-MVGrfZHppgJSZs72h2-vnLYItBoDgPpTJKHizQYlPRTk7pCOja0vXIHfVd-_-1zX85p-uJk9dOT3undHyP3Y3RJD_cTP99dss3D9i32e8oT6Zb8_mumpK3gdfd6oJ7AjcXHGe4WS7ecaox4ZT4_oPP26v1T9_xZbt9DJ33fOg9_pCdHc--fjhJ4yUKqZNZuUzB1WBrIUrvALlH3ihIUxQOBC7uAExtlbW2Ktx0aovM2ACq8jWGYVbmJjPFIzZp2sY_YbxytYFQGluAAWm9wmjNgMlEAHwRNmHTgZfaxQ7jdNHFle5XGkrqDf818l_3_NfrhL3Zjplv-mvciH1EU7TFpN7Y_Ye2u9BR1TSaJTQsNYU-BmmxKgSn6gzMNFibVyJhr2mCNWkw_p4zsRABiaReWPpQVhWyKgfE3B9houa5MXgQER01f6F3cpqwl1swjaRstsa3K8IBXHjnIFXCHm8kaktSIYqywpgyYeVI1kY0jyHN98u-LzhqF7IpS9jbQSp3v_V_nj69mYpn7E7e6wvlK-2zybJb-ecYhy3ti6hsfwAmqTFg
  priority: 102
  providerName: ProQuest
– databaseName: Springer Nature OA Free Journals
  dbid: C6C
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3da9UwFA86QXwRv61OiSD4oMW2OUlT3-bYGMJ8crAHISRpMoezvfTeK9z_3nN6226dH-Bb25xAc75DzvmFsdeljLosXJlWqD0pgLSpE1qm1upKC4g29hAbx5_V0Ql8OpWnA0wO9cJcPb_PtXq_RB9LbTYFFRBgMEo3N9ktSThjdDCr9kevCxIVd2yK-eO8WeDp8fl_98JXwtD1Eslr56R9-Dm8x-4OeSPf2wr6PrsRmgfs9vFwMv6QfT34OSiR7TZ8cdlCydvI6259xgMNN2ccxdqslh84NZZwqnb_zhftxeZH6PiqnR5jFwIfAccfsZPDgy_7R-lwc0LqVVauUvA1uFrKMnjALQeFoKisEB4k7ugAbO20c64SPs-dyKyLoKtQY-7lVGEzKx6znaZtwlPGK19biKV1AiwoFzSmaBZsJiPgi3QJy0e2Gj_AitPtFhem315oZbaiMCgK04vCbBL2dpqz2IJq_JP6I0lroiRA7P4D6okZ7MugL0JvUlO-Y3EtTsfodZ2BzaNzRSUT9oZkbchs8fe8HboPcJEEgGX2VFUhqwpAyt0ZJZqbnw-P2mIGc1-aQlH_L3JaJezVNEwzqYStCe2aaAB32wUonbAnW-WaliSkKCtMJBNWztRutub5SHP-rQcDR5NCNmUJezcq6OVv_Z2nz_6P_Dm7U_SmREVLu2xn1a3DC0zGVu5lb4W_AJb1LHs
  priority: 102
  providerName: Springer Nature
Title Evolutionary perspective of drug eluting stents: from thick polymer to polymer free approach
URI https://link.springer.com/article/10.1186/s13019-022-01812-y
https://www.ncbi.nlm.nih.gov/pubmed/35379273
https://www.proquest.com/docview/2651971746
https://www.proquest.com/docview/2647212468
https://pubmed.ncbi.nlm.nih.gov/PMC8981810
https://doaj.org/article/040531d7822a489b8ffc8d04a1fbb295
Volume 17
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3di9NAEF_uA-ReRPErepYVBB80mmY_shFEeqXHUbhD1EIfhGU32a1iTWraivnvnd0mOXPe-dQ2Owu7M7_ZmWlmZhF6njArklgnYQroCSllKtREsFApkQpCrbK-xcb5BT-b0emczfdQe91Rw8D1taGdu09qVi1f__5ZvweFf-cVXvA3aziHXSlO7JIMwGCF9T46BMvEHcrPafdWgTIAd1s4c-28I3SLMJKkcUJ6dsq38__30P7Lal3NqLzyWtVbq9M76HbjZuLRDhd30Z4p7qEvk18N0FRV49VlmSUuLc6r7QIbN1wsMIi-2KzfYld8gl1G_He8Kpf1D1PhTdl9tZUxuG1Kfh_NTiefx2dhc7tCmPEo2YQ0y6nOGUtMRiEscWbKckVIRhlEfZSqXAutdUqy4VCTSGlLRWpy8M80j1WkyAN0UJSFeYRwmuWK2kRpQhXl2ghw4xRVEbMUfjAdoGHLS5k1rcfdDRhL6UMQweVOFBJEIb0oZB2gl92c1a7xxn-pT5yIOkrXNNs_KKuFbHRQwnkFJ07ufCIFe9HC2kzkEVVDq3WcsgC9cAKWDmywvEw1FQqwSdckS454mgKrYgqUxz1KUMmsP9xCRLaIljF3NcLAaR6gZ92wm-nS3ApTbh0NhYg8plwE6OEOUd2WWmAGKOlhrbfn_kjx7atvGA5qB2yKAvSqReXlsm7m6eMbl_AEHcVea1wO0zE62FRb8xR8s40eoP1kngzQ4Wg0_TSFz5PJxYeP8HTMxwP_f8fAq-QfShM5HA
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwELfG9gAvCMRXYICRQDxAtDSxHQcJoQ06dWyrENqkPSAZ27HLtJGUtAX1n-Jv5C5NWjLE3vbW1pcod_7dh5v7IOR5yr1MY5OGGaAnZIzr0CSSh1rLTCbMa1-32DgcisEx-3jCT9bI77YWBtMqW5tYG-q8tPgf-VYssMQS4mfxbvwjxKlR-Ha1HaGxgMW-m_-CI9vk7d4H2N8XcbzbP3o_CJupAqEVUToNmc2ZyTlPnWVwOzTPXugksYzDaYcxnRtpjMkS2-uZJNLGM5m5HOISI2Id6QTue41sQJiRgRZt7PSHnz63tp9xUJ-2NEeKrQl4CCwSijH9AVxpOO-4v3pKwL--4C9neDFR88Lb2toJ7t4iN5volW4v4HabrLniDvnS_9ngV1dzOl5Vb9LS07yajajD5WJEAVHFdPKGYk0LxUT7Mzouz-ffXUWn5fKjr5yjba_zu-T4SsR7j6wXZeEeEJrZXDOfapMwzYRxEqJDzXTEPYMv3ASk18pS2aajOQ7WOFf1yUYKtZC_AvmrWv5qHpBXy2vGi34el1Lv4BYtKbEXd_1DWY1Uo9oKzCAYshxDLQ28GOm9lXnEdM8bE2c8IC9xgxVaDHg8q5vCB2ASe2-pbZFlIKqYAeVmhxI03XaXW4ioxtJM1EovAvJsuYxXYvZc4coZ0jA46MdMyIDcXyBqyVLCkzSDGDYgaQdrHZ67K8Xpt7oPOWgziCkKyOsWlavH-r9MH17OxVNyfXB0eKAO9ob7j8iNuNYdzJXaJOvTauYeQww4NU8axaPk61Xr-h82FW4_
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Zb9QwELagSBUvFTeBAkZC4gGi5hg7Dm9l6aocrXigUh-QLDuxF0SbrLK7SPvvmcmxbcoh8bZZj6XM6Rl55gtjLzLhVZbYLMzRekIAYUKbKhEao3KVgje-hdg4OpaHJ_DhVJxemuJvu92HK8lupoFQmqrl3rz0nYsrubfAyEvDNwm1FeARFa6vsxtYqcSEnj-RkyEWg0BzHkZl_rhvdBy1qP2_x-ZLh9PVxskrt6ftoTS9xXb6bJLvd-q_za656g7bPurvy--yrwc_e9MyzZrPLwYree152axm3NFyNeML4n7xhtO4Cace-B98Xp-tz13Dl_Xmp2-c4wMM-T12Mj34MjkM--8phIWMsmUIRQm2FCJzBWAhQgeTlyZNCxBY5wGY0iprbZ4WcWzTyFgPKnclZmRWJiYy6X22VdWVe8h4XpQGfGZsCgakdQoTNwMmEh7wQdiAxYNYddGDjdM3L850W3QoqTtVaFSFblWh1wF7tdkz76A2_kn9lrS1oSSY7PaPupnp3us0RiiMMSVlQQZ5scr7QpURmNhbm-QiYC9J15qcGV-vMP1MAjJJsFh6X-Y5iioBpNwdUaITFuPlwVp0HwQWOpE0FYySlgF7vlmmndTYVrl6RTSANXgCUgXsQWdcG5ZSkWY5ppcBy0ZmN-J5vFJ9_9ZChKOjoZiigL0eDPTitf4u00f_R_6MbX9-N9Wf3h9_fMxuJq1XUVfTLttaNiv3BLO1pX3aOuQvwng3rw
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=Evolutionary+perspective+of+drug+eluting+stents%3A+from+thick+polymer+to+polymer+free+approach&rft.jtitle=Journal+of+cardiothoracic+surgery&rft.au=Hassan%2C+Sadia&rft.au=Ali%2C+Murtaza+Najabat&rft.au=Ghafoor%2C+Bakhtawar&rft.date=2022-04-04&rft.eissn=1749-8090&rft.volume=17&rft.issue=1&rft.spage=65&rft_id=info:doi/10.1186%2Fs13019-022-01812-y&rft_id=info%3Apmid%2F35379273&rft.externalDocID=35379273
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1749-8090&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1749-8090&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1749-8090&client=summon