Supplementary Appendix Supplement Table S1. Search Strategy on Medline, Embase and CENTRAL Supplement Table S2. Main Characteristics of Included Trials Supplement Table S3. Patient Characteristics of Included Trials Supplement Table S4. Sensitivity Analysis of Definite or Probable Stent Thrombosis Within 1 Year Supplement Figure S1. Risk of Bias Assessment Summary Supplement Figure S2. Ranks for Study Stents Regarding Definite or Probable Stent Thrombosis Supplement Figure S3. Definite or Probable Stent Thrombosis at the Longest Follow-Up Available Supplement Figure S4. Definite or Probable Stent Thrombosis, Early (≤30 days) Supplement Figure S5. Definite or Probable Stent Thrombosis, Late (31-365 days) Supplement Figure S6. Definite or Probable Stent Thrombosis, Very Late (>365 days) Supplement Figure S7. Definite or Probable Stent Thrombosis, Late and Very Late (>30 days) Supplement Figure S8. Definite Stent Thrombosis with Reference to Bare Metal Stent Supplement Figure S9. Inconsistency Plot for Triangular Loops Supplement Figure S10. Target Vessel Revascularization Within 1 Year Supplement Figure S11. All-Cause Death Within 1 Year Supplement Figure S12. Cardiac Death Within 1 Year Supplement Figure S13. Network Plot of Sensitivity Analysis for Trials with Low Risk of Bias Supplement Figure S14. Sensitivity Analysis for Trials with Low Risk of Bias Supplementary Table S1. Search Strategy on Medline, Embase and Central Medline #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17 #18 #19 (randomized controlled trial[Publication Type] OR (randomized[Title/Abstract] AND controlled[Title/Abstract] AND trial[Title/Abstract])) "stents"[MeSH Terms] OR "stents"[tiab] OR "stent"[tiab] (#1) AND (#2) "bare metal"[All Fields] "drug-eluting stents"[All Fields] OR "drug-eluting stent"[All Fields] OR "drug-coated stents"[All Fields] OR "drug-coated stent"[All Fields] OR "drug eluting"[All Fields] (("sirolimus-eluting" OR "rapamycin-eluting" OR "paclitaxel-eluting" OR "zotarolimus-eluting" OR "everolimus-eluting") AND ("stents" OR "stent")) OR ("cypher" OR "taxus" OR "endeavor" OR "resolute" OR "xience" OR "xience-V" OR "promus" OR "promus-element") (#5) OR (#6) ("bioabsorbable"[tiab] OR "biodegradable"[tiab]) AND ("polymers"[MeSH Terms] OR "polymers"[All Fields] OR "polymer"[All Fields]) "drug-eluting stent"[All Fields] OR "drug-eluting stent"[All Fields] OR "drug-coated stents"[All Fields] OR "drug-coated stent"[All Fields] OR "drug eluting"[All Fields] (#8) AND (#9) (("biolimus-eluting" OR "everolimus-eluting") AND ("stents" OR "stent")) OR ("biomatrix" OR "nobori" OR "synergy") (#10) OR (#11) ("Peripheral Arterial Disease"[Mesh] OR "Peripheral Vascular Diseases"[Mesh]) OR ("Peripheral Arterial Disease"[TIAB] OR "Peripheral Vascular Diseases"[TIAB]) registries[MeSH Terms] OR "registries"[All Fields] OR "registry"[All Fields] observational[All Fields] AND ("clinical trials as topic"[MeSH Terms] OR ("clinical"[All Fields] AND "trials"[All Fields] AND "topic"[All Fields]) OR "clinical trials as topic"[All Fields] OR "study"[All Fields] OR "biomedical research"[MeSH Terms] OR ("biomedical"[All Fields] AND "research"[All Fields]) OR "biomedical research"[All Fields]) ((#13) OR (#14)) OR (#15) ((#4) OR (#7)) OR #12 (#3) AND (#17) (18) NOT (#16) Embase #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 ‘randomized controlled trial’/exp AND [embase]/lim ‘stent’/exp AND [embase]/lim #1 AND #2 ‘bare metal stent’/exp AND [embase]/lim ‘drug eluting stent’/exp AND [embase]/lim bioabsorbable AND ‘polymer’/exp AND ‘drug’/exp AND eluting and ‘stent’/exp AND [embase]/lim biodegradable AND ‘polymer’/exp AND ‘drug’/exp AND eluting and ‘stent’/exp AND [embase]/lim #4 OR #5 OR #6 OR #7 ‘peripheral occlusive artery disease’/exp AND [embase]/lim ‘register’/exp AND [embase]/lim ‘observational study’/exp AND [embase]/lim #9 OR #10 OR #11 #3 AND #8 NOT #12 CENTRAL #1 MeSH descriptor: Stents] explode all trees #2 bare metal stent #3 #4 #5 drug-eluting stent sirolimus-eluting or rapamycin-eluting or paclitaxel-eluting or zotarolimus-eluting or everolimus-eluting or cypher or taxus or endeavor or resolute or xience or xience-V or promus or promus-element bioabsrobable or biodegradable or polymer #6 biolimus-eluting or everolimus-eluting or biomatrix or nobori or synergy #7 #2 or #3 or #4 or #5 or #6 #8 MeSH descriptor: [Peripheral Arterial Disease] explode all trees #9 MeSH descriptor: [Registries] explode all trees #10 MeSH descriptor: [Comparative Study] explode all trees #11 #8 or #9 or #10 #12 (#1 and #7) not #11 Supplementary Table S2. Main Characteristics of Included Trials Trials Stent Comparison (Patient Number) Primary Endpoint Design Major Inclusion Criteria Main Results Follow-Up SES vs. BMS (120:118) In-stent LL at 6 months Multicenter, superiority Stable or unstable angina SES superior to BMS 5 years PES vs. BMS (118:59) % stenosis at 4-6 months Three-center, superiority Stable or unstable angina PES superior to BMS 6 months E-SIRIUS SES vs. BMS (175:177) MLD at 8 months Multicenter, superiority Stable or unstable angina SES superior to BMS 9 months SIRIUS SES vs. BMS (533:525) TVF at 9 months Multicenter, superiority Stable or unstable angina SES superior to BMS 5 years TAXUS I PES vs. BMS (31:30) MACE (death Q-wave MI, TVR, ST) at 30 days Three-center, feasibility Stable or unstable angina Promising results of PES 2 years TAXUS II BMS vs. PES (270:266) %NIH by IVUS at 6 months Multicenter, superiority Stable or unstable angina PES superior to BMS 5 years SES vs. BMS (50:50) MLD at 8 months Multicenter, superiority Stable or unstable angina SES superior to BMS 9 months SES-SMART SES vs. BMS (129:128) In-segment binary restenosis at 8 months Multicenter, superiority Stable angina, ACS SES superior to BMS 2 years TAXUS IV BMS vs. PES (652:662) TVR at 9 months Multicenter, superiority Stable or unstable angina PES superior to BMS 5 years SES vs. PES (264:281) Cost-effectiveness after 6 months Single-center, superiority All-comer design DES (SES and PES) not superior to BMS 18 months Published in 2002 RAVEL Published in 2003 ASPECT Published in 2004 C-SIRIUS Published in 2005 BASKET DIABETES SES vs. BMS (80:80) in-segment LL at 9 months Multicenter, superiority Diabetes SES superior to BMS 5 years ISAR-DESIRE SES vs. PES (100:100) Binary restenosis at 6 months Multicenter, superiority ISR DES superior to balloon angioplasty; SES superior to PES 1 year ISAR-DIABETES PES vs. SES (125:125) In-segment LL at 9 months Multicenter, non-inferiority (PES over SES) Diabetes SES superior to PES 9 months Pache et al. SES vs. BMS (250:250) Binary restenosis at 6 months Multicenter, superiority Stable or unstable angina SES superior to BMS 1 year SIRTAX SES vs. PES (503:509) MACE (cardiac death, MI, TLR) at 9 months Multicenter, superiority Stable angina or ACS SES superior to PES 5 years CoCr-EES vs. BMS (28:32) in-stent LL at 6 months Multicenter, superiority Stable or unstable angina CoCr-EES superior to BMS 5 years BP-BES vs. BMS (80:40) In-stent LL at 6 months Multicenter, superiority Stable or unstable angina BP-BES superior to BMS 6 months STRATEGY BMS vs. SES (88:87) Composite of death, MI, stroke, binary restenosis at 8 months Single-center, superiority STEMI (SES + tirofiban) superior to (BMS + abciximab) 5 years TAXi PES vs. SES (100:102) MACE (Death, MI, TLR, ST) Singer-center, superiority All-comer design SES similar to PES 3 years TAXUS V PES vs. BMS (586:586) TVR at 9 months Multicenter, superiority Stable or unstable angina PES superior to BMS 9 months TAXUS VI PES vs. BMS (219:227) TVR at 9 months Multicenter, superiority Stable or unstable angina PES superior to BMS 5 years SES vs. PES (37:33) %NIH by 3D IVUS at 6 months Single-center, superiority Complex lesions or complex patients SES superior to PES 6 months ZES-E vs. BMS (598:599) TVF at 9 months Multicenter, superiority Stable or unstable angina ZES-E superior to BMS 5 years SPIRIT FIRST STEALTH Published in 2006 Cervinka et al. ENDEAVOR II ENDEAVOR III ZES-E vs. SES (323:113) In-segment LL at 8 months Multicenter, non-inferiority Stable or unstable angina ZES-E inferior to SES 5 years HAAMU-STENT (abstract only) BMS vs. PES (82:82) Not specified Single-center, superiority STEMI PES (angiographically) superior to BMS; (clinically) similar with BMS 1 year ISAR-SMART 3 PES vs. SES (180:180) In-stent LL between 6 and 8 months Two-center, non-inferiority Stable or unstable angina PES inferior to SES 1 year LONG-DES-II SES vs. PES (250:250) In-segment binary restenosis at 6 months Multicenter, superiority Long lesion (≥25 mm) SES superior to PES 9 months Pasceri et al. SES vs. BMS (32:33) ST at 6 months Single-center, superiority STEMI SES similar to BMS 6 months PASSION PES vs. BMS (310:309) MACE (cardiac death, MI, TLR) at 12 months Two-center, superiority STEMI PES not superior to BMS 5 years PRISON II BMS vs. SES (100:100) In-segment binary restenosis at 6 months Two-center, superiority Chronic total occlusion SES superior to BMS 5 years REALITY SES vs. PES (684:669) In-lesion binary restenosis at 8 months Multicenter, superiority Stable or unstable angina SES similar to PES 1 year RRISC BMS vs. SES (37:38) In-stent LL 6 months Single-center, superiority Saphenous vein grafts SES superior to BMS 3 years SCANDSTENT SES vs. BMS (163:159) MLD at 6 months Multicenter, superiority Stable or unstable angina, recent NSTEMI SES superior to BMS 3 years TYPHOON SES vs. BMS (355:357) TVF at 1 year Multicenter, superiority STEMI SES superior to BMS 4 years BMS vs. SES (60:60) Composite of death, MI, and recurrent ischemia at 1 year Single-center, superiority STEMI SES superior to BMS 1 year SES vs. BMS (54:29) In-stent LL at 6 months Multicenter, superiority Diabetes SES superior to BMS 1 year Published in 2007 de la Llera et al. DECODE Erglis et al BMS vs. PES (50:53) clinical, angiographic, and IVUS results at 6 months Single-center, superiority Unprotected LMCA PES superior to BMS 3 years BP-BES vs. PES (85:35) In-stent LL at 9 months Multicenter, non-inferiority Stable or unstable angina BP-BES non-inferior to PES 2 years Ortolani et al. BMS vs. SES (52:52) In-segment LL at 9-month Single-center, superiority Stable or unstable angina, NSTEMI, STEMI (> 48 hours) SES superior to BMS 1 year Pan et al (2007) SES vs. PES (103:102) Binary restenosis & TLR at 1 year single-center, superiority Bifurcation lesions SES superior to PES 1 year Petronio et al. SES vs. PES (51:50) NIHA% at 9 months Single-center, superiority Complex lesions SES superior to PES 9 months SCORPIUS SES vs. BMS (98:102) In-segment LL at 8 months Multicenter, superiority Diabetes SES superior to BMS 5 years SELECTION PES vs. BMS (40:40) %NIH by IVUS at 7 months Single-center, superiority STEMI SESAMI SES vs. BMS (160:160) Binary restenosis at 1 year Single-center, superiority STEMI SES superior to BMS 5 years Strozzi et al. SES vs. BMS (39:40) Angiographic restenosis at 6 months Single-center, superiority (stent graft vs. SES vs. BMS) ACS SES superior to BMS 6 months SES vs. PES (200:200) In-segment binary restenosis at 6 months Multicenter, superiority Diabetes SES superior to PES 4 years DESSERT BMS vs. SES (75:75) in-stent LL at 8 months Multi-center, superiority Diabetes SES superior to BMS 1 year Hong et al. SES vs. PES (85:84) In-segment LL at 6 months Multicenter, superiority Diabetes SES not superior to PES 3 years LEADERS BP-BES vs. SES (857:850) Composite of cardiac death, MI, TVR at 9 months Multicenter, non-inferiority Stable angina, ACS BP-BES noninfeior to SES 5 years NOBORI 1 - Phase 1 Published in 2008 DES-DIABETES PES superior to BMS 7 months Li et al. (2008) SES vs. BMS (24:24) Plasma CRP & IL-6 MISSION! SES vs. BMS (158:152) In-segment LL at 9 months MULTISTRATEGY BMS vs. SES (372:372) PROSIT SORT OUT II Single-vessel disease SES superior to BMS 8 months Single-center, superiority STEMI SES superior to BMS 5 years MACE (death, MI TVR) at 8 months Multicenter, superiority STEMI SES superior to BMS 3 years SES vs. PES (154:154) MACE (death, MI, ST, TLR) at 12 months Three-center, superiority STEMI Superiority no shown 3 years SES vs. PES (1065:1033) MACE (cardiac death, MI, TLR, TVR) at 5 years Multicenter, superiority All-comer design Superiority not proven 5 years CoCr-EES vs. PES (669:333) In-segment LL at 8 months Multicenter, non-inferiority Stable or unstable angina CoCr-EES superior to PES 3 years PES vs. BMS (2257:749) 1) TLR, 2) composite of death, MI, stroke, ST at 12 months Multicenter, superiority STEMI PES superior to BMS 3 years PES vs. SES (302:305) Composite of death, MI, TLR at 1 year Multicenter, non-inferiority Unprotected LMCA PES non-inferior to SES 2 years ISAR-TEST-2 SES vs. ZES-E (335:339) Binary restenosis at 6–8 months Two-center, superiority de novo stenosis Dual-DES & SES superior to ZES-E 2 years ISAR-TEST-4 CoCr-EES vs. SES (652:652) Composite of cardiac death, MI, TLR Multicenter, non-inferiority Stable angina, ACS BP-DES non-inferior to PPDES (SES, CoCr EES) 3 years Juwana et al. SES vs. PES (196:201) In-stent LL at 9 months Single-center, superiority STEMI SES superior to PES 1 year Li et al. (2009) SES vs. PES (16:16) Plasma CRP & IL-6 Single-center, superiority Stable angina with single-vessel disease SES superior to PES 8 months BP-BES vs. PES (153:90) In-stent LL at 9 months Multicenter, non-inferiority Stable or unstable angina BP-BES non-inferior to PES 9 months SPIRIT III Published in 2009 HORIZONS-AMI ISAR-LEFT-MAIN NOBORI 1 - Phase 2 Single-center, superiority PASEO BMS vs. PES vs. SES (90:90:90) TLR at 1 year Single-center, superiority STEMI SES and PES superior to BMS 5 years BMS vs. PES (39:41) In-segment binary restenosis at 12 months Multicenter, superiority Saphenous Vein Graft Lesions PES superior to BMS 5 years SPIRIT II CoCr-EES vs. PES (223:77) In-stent LL at 6 months Multi-center, non-inferiority Stable or unstable angina CoCr-EES non-inferior and superior to PES 4 years ZEST-AMI ZES-E vs. SES vs. PES (108:110:110) MACE (death, MI, TVR) at 12 months Multicenter, superiority (SES over ZES-E, PES over ZES-E) STEMI Superiority not shown 1 year Multicenter, superiority Large coronary artery (stents ≥3.0 mm) No difference among SES, CoCr-EES, BMS 2 years SOS Published in 2010 BASKET-PROVE COMPARE SES vs. CoCr-EES vs. BMS composite of cardiac death, MI at 2 (775:774:765) years CoCr-EES vs. PES (897:903) Composite of death, MI, TVR at 12 months Single-center, superiority All-comer design CoCr-EES superior to PES 2 years ENDEAVOR IV ZES-E vs. PES (773:775) TVF at 9 months Multicenter, non-inferiority Stable or unstable angina ZES-E non-inferior to PES 3 years GISSOC II-GISE BMS vs. SES (78:74) in-segment MLD at 8 months Multicenter, superiority Chronic total occlusion SES superior to BMS 2 years GRACIA-3 BMS vs. PES (216:217) Binary restenosis at 12 months Multicenter, superiority STEMI PES similar to BMS 1 year ISAR-DESIRE 2 SES vs. PES (225:225) In-stent LL at 6-8 months Multicenter, superiority (PES over SES) ISR of SES PES not superior to SES 1 year ZES-E vs. BMS (33:11) % of uncovered stent struts by OCT at 6 months Single-center, superiority STEMI ZES-E similar with BMS 1 year ZES-R vs. CoCr-EES (1140:1152) TLF at 12 months Multicenter, non-inferiority All-comer design ZES-R non-inferior to CoCrEES 2 years ZES-E vs. SES (1162:1170) MACE (cardiac death, MI, CDTVR) at 9 months Multicenter, superiority All-comer design SES superior to ZES-E 3 years OCTAMI RESOLUTE All Comers SORT OUT III SPIRIT IV CoCr-EES vs. PES (2458:1229) TLF at 1 year Multicenter, non-inferiority and superiority Stable or unstable angina CoCr-EES non-inferior & superior to PES 2 years ZES-E vs. SES vs. PES (883:878:884) MACE (death, MI, TVR) at 12 months Multicenter, non-inferiority (ZES-E vs. SES) and superiority (ZES-E vs. PES) Stable angina or ACS ZES-E non-inferior to SES; ZES-E superior to PES 2 years CoCr-EES vs. SES (149:151) In-segment LL at 8 months Multicenter, non-inferiority Diabetes CoCr-EES non-inferior to SES 1 year EXCELLENT CoCr-EES vs. SES (1079:364) In-segment LL at 9 months Multicenter, non-inferiority Stable or unstable angina, recent MI CoCr-EES were non-inferior to SES 1 year GARA-GARA SES vs. PES (400:400) MACE (cardiac death, MI, CABG or TLR) at 1 year Single-center, superiority All-comer design SES superior to PES 1 year ZES-E vs. SES vs. PES (205:204:202) MACE (cardiac death, MI, TLR) at 12 months Multicenter, superiority STEMI Superiority not shown 18 months CoCr-EES vs. SES (224:226) In-segment LL at 9 months Multicenter, non-inferiority Long lesion (≥ 25 mm) 1 year Naples-Diabetes SES vs. PES vs. ZES-E (76:75:75) MACE (death, MI, TVR) at 3 years Single-center, pilot study Diabetes CoCr-EES not non-inferior to SES (SES superior to CoCrEES) ZES-E inferior to SES, PES PLATINUM CoCr-EES vs. PtCr-EES (762:768) TLF at 12 months Multicenter, non-inferiority Stable or unstable angina PtCr-EES non-inferior to CoCrEES 3 years SES vs. PES (152:149) QCA and IVUS parameters Multicenter, superiority de novo lesion SES superior to PES 5 years Phase I: SES vs. ZES-E (51:46) Phase II: SES vs. ZES-R (103:104) In-segment LL at 8 months Multicenter, superiority Chronic total occlusion SES superior to ZES-E 1 year SES vs. BMS (30:30) MACE (death, MI, TVR) at 9 months Single-center, pilot trial Bifurcation (provisional stenting) SES similar to BMS 9 months ZEST Published in 2011 ESSENCE-DIABETES KOMER LONG-DES-III POET PRISON III (abstract only) PROSUMER 3 years SEA-SIDE SES vs. CoCr-EES (75:75) Procedural and angiographic results Single-center, superiority Bifurcated lesions CoCr-EES similar to SES 18 months ZES-E vs. SES (80:80) in-segment binary restenosis rate at 9-month Multicenter, non-inferiority Chronic total occlusion ZES-E is non-inferior to SES 1 year BP-BES vs. BMS (575:582) MACE (cardiac death, MI, TLR) at 1 year Multicenter, superiority AMI BP-BES superior to BMS 1 year ZES-R vs. CoCr-EES (22:22) % strut coverage (OCT) at 9 months Multicenter, superiority de novo lesions ZES-R similar to PtCr-EES 9 moths SES vs. PES (441:466) MACCE (death, MI, stroke, RR, bleeding) at 1 year Single-center, superiority STEMI SES superior to BMS 1 year CoCr-EES vs. BMS (751:747) POCE at 1-year Multicenter, superiority STEMI Superiority not shown 1 year ZES-R vs. CoCr-EES (324:326) MACE (death, MI , TLR) at 1 year Multicenter, non-inferiority unprotected LMCA ZES-R non-inferior to CoCrEES 1 year LONG-DES-IV ZES-R vs. SES (250:250) In-segment LL at 9 months Multicenter, non-inferiority Long lesion (≥ 25 mm) ZES-R non-inferior to SES 1 year NOBORI JAPAN BP-BES vs. SES (198:137) TVF at 9 months Multicenter, non-inferiority Stable or unstable angina BP-BES non-inferior to SES 9 months SES vs. CoCr-EES (145:148) MACE (cardiac death, MI, TLR) at 1 year Single-center, noninferiority Bifurcation lesions with provisional SB stenting SES similar with CoCr-EES 1 year ZES-E vs. SES (4357:4352) Definite or probable ST at 3 years Multicenter, superiority All-comer design ZES-E not superior to SES 3 years RESET CoCr-EES vs. SES (1597:1600) TLR at 1 year Multicenter, non-inferiority All-comer design CoCr-EES non-inferior to SES 1 year Sakakibara et al. SES vs. CoCr-EES (50:50) Angiographic binary restenosis at 8 months Single-center, superiority Stable angina on maintenance hemodialysis CoCr-EES superior to SES 1 year Published in 2012 CATOS COMFORTABLE AMI COVER OCT DEBATER EXAMINATION ISAR-LEFT MAIN 2 (abstract only) Pan et al PROTECT SEZE ZES-E vs. SES (60:61) In-stent LL at 9 month Multicenter, superiority STEMI ZES-E inferior to SES 1 year Song et al SES vs. CoCr-EES (32:34) In-segment LL at 9 months Multicenter, superiority ISR of DES with diffuse lesion (>10 mm) CoC-EES similar with SES 1 year SORT OUT IV CoCr-EES vs. SES (1390:1384) Composite of cardiac death, MI, definite ST, TVR at 18 months Multicenter, non-inferiority All-comer design CoCr-EES non-inferior to SES 2 years SPIRIT V Diabetic CoCr-EES vs. PES (218:106) in-stent LL at 9 months Multicenter, non-inferiority and superiority Diabetes CoCr-EES non-inferior & superior to PES 1 year ZES-R vs. CoCr-EES (697:694) TVF at 1 year Single-center, noninferiority Stable or unstable angina, NSTEMI ZES-R non-inferior to CoCrEES 2 years X-AMI CoCr-EES vs. SES (404:221) MACE (cardiac death, MI, TVR) at 12 months Multicenter, non-inferiority AMI CoCr-EES non-inferior & superior to SES 1 year XIMA (abstract only) BMS vs. CoCr-EES (401:399) Composite of death, MI, CVA, TVR, haemorrhage at 1 year Multicenter, superiority Octarians (age≥80) CoCr-EES not superior (similar) to BMS 1 year SES vs. CoCr-EES (101:106) In-stent LL at 9-month Multicenter, non-inferiority Chronic total occlusion CoCr-EES non-inferior to SES 1 year COMPARE II BP-BES vs. CoCr-EES (1795:912) Composite cardiac death, MI, TVR at 12 months Multicenter, non-inferiority All-comer design BES non-inferior to SES 1 year COVER OCT II ZES-R vs. CoCr-EES (20:20) % strut coverage (OCT) at 3 months Multicenter, superiority Stable or unstable angina ZES-R similar to CoCr-EES 3 months HOST-ASSURE (abstract only) PtCr-EES vs. ZES-R (2503:1252) TLF Multicenter, non-inferiority All-comer design PtCr-EES non-inferior to ZESR 1 year NEXT (abstract only) BP-BES vs. CoCr-EES (1617:1618) TLR at 1 year Multicenter, non-inferiority All-comer design BP-BES non-inferior to CoCrEES 1 year BP-BES vs. SES (1229:1239) composite of cardiac death, MI, definite ST, TVR at 9 months Multicenter, non-inferiority All-comer design BP-BES not non-inferior to SES 1 year TWENTE Published in 2013 CIBELES SORT OUT V BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimus-eluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents; MACE, major adverse cardiac events; TVF, target vessel failure; TLF, target lesions failure; MI, myocardial infarction; TVR, target vessel revacularization; TLR, target lesion revascularization; ST, stent thrombosis; MLD, minimum luminal diameter; LL, late loss; NIH, neointimal hyperplasia; IVUS, intravascular ultrasound; ACS, acute coronary syndrome; NSTEMI, non ST-segment elevation MI; STEMI, ST-segment elevation MI; LMCA, left main coronary artery; ISR, in-stent restenosis Supplementary Table S3. Patient Characteristics of Included Trials Trials Published in 2002 1. RAVEL1-3 Published in 2003 2. ASPECT4 3. E-SIRIUS5, 6 4. SIRIUS7-10 5. TAXUS I11-13 6. TAXUS II13-15 Published in 2004 7. C-SIRIUS16 8. SES-SMART17, 18 9. TAXUS IV13, 19, 20 Published in 2005 10. BASKET21-23 11 DIABETES24-28 12. ISAR-DESIRE29, 30 13. ISAR-DIABETES30, 31 14. Pache et al.32 15. SIRTAX33-35 16. SPIRIT FIRST36-39 17. STEALTH40 18. STRATEGY41-44 19. TAXi45, 46 20. TAXUS V13, 47 21. TAXUS VI48-52 Published in 2006 22. Cervinka et al.53 23. ENDEAVOR II54-58 Mean Male Diabetes Age (%) (%) Antiplatelet Regimen Mandatory Follow-Up Angiography 19 DAPT ≥8 weeks Yes 76 20 Yes 62 62 65 60 71 71 89 79 23 26 18 16 DAPT ≥1 month (2 centers) ≥6 months (1 center) DAPT ≥2 months DAPT ≥3 months DAPT ≥6 months DAPT ≥6 months 50:50 129:128 652:662 60 64 62 68 72 72 24 25 24 DAPT ≥2 months DAPT ≥2 months DAPT ≥6 months Yes Yes Yes SES vs. PES SES vs. BMS SES vs. PES PES vs. SES SES vs. BMS SES vs. PES 264:281 80:80 100:100 125:125 250:250 503:509 64 67 64 68 67 62 79 63 79 73 78 77 19 100 29 100 31 20 DAPT for 6 months DAPT ≥12 months DAPT ≥6 months DAPT ≥6 months DAPT ≥6 months DAPT ≥12 months CoCr-EES vs. BMS BP-BES vs. BMS BMS vs. SES PES vs. SES PES vs. BMS PES vs. BMS 28:32 80:40 88:87 100:102 586:586 219:227 63 62 62 64 63 63 73 71 67 81 70 76 11 25 15 34 31 22 DAPT ≥3 months DAPT ≥3 months DAPT ≥3 months DAPT for 2-12 months DAPT ≥6 months DAPT ≥6 months No Yes Yes Yes Yes Partially yes: angiographic substudy (1/2 of patients) Yes Yes Yes No Yes Yes SES vs. PES ZES-E vs. BMS 37:33 598:599 56 62 73 76 36 20 DAPT for 6 months DAPT ≥3 months Yes Partially yes: angiographic follow-up Stent Comparison Sample Size SES vs. BMS 120:118 61 76 PES vs. BMS 118:59 59 SES vs. BMS SES vs. BMS PES vs. BMS BMS vs. PES 175:177 533:525 31:30 270:266 SES vs. BMS SES vs. BMS BMS vs. PES Yes Yes Yes Yes 24. ENDEAVOR III59-61 25. HAAMU-STENT62 (from other work63) 26. ISAR-SMART 330, 64 27. LONG-DES-II65 subgroup (1/2 of patients) Yes Yes ZES-E vs. SES BMS vs. PES 323:113 82:82 61 63 69 72 29 15 DAPT ≥6 months DAPT for 12 months PES vs. SES SES vs. PES 180:180 250:250 67 61 72 64 0 33 Yes Yes 28. Pasceri et al.66 (from other works63, 67) 29. PASSION68-70 SES vs. BMS 32:33 62 74 23 DAPT ≥6 months DAPT ≥ 6 months; Cilostazol randomized (2-by-2 factorial design) Insufficient information PES vs. BMS 310:309 61 74 31 DAPT ≥6 months No 30. PRISON II71-74 BMS vs. SES 100:100 59 80 14 DAPT ≥6 months Yes 31. REALITY75, 76 SES vs. PES 684:669 62 73 28 Yes 32. RRISC77, 78 33. SCANDSTENT79 34. TYPHOON80, 81 BMS vs. SES SES vs. BMS SES vs. BMS 37:38 163:159 355:357 73 63 59 89 77 78 14 18 16 DAPT ≥6 months for PES ≥ 2 months for SES DAPT ≥2 months DAPT ≥12 months DAPT ≥6 months BMS vs. SES 60:60 48 79 28 SES vs. BMS 54:29 60 68 BMS vs. PES BP-BES vs. PES BMS vs. SES SES vs. PES SES vs. PES SES vs. BMS PES vs. BMS SES vs. BMS SES vs. BMS 50:53 85:35 52:52 103:102 51:50 98:102 40:40 160:160 39:40 62 64 66 62 63 66 61 63 58 SES vs. PES 200:200 61 Published in 2007 35. de la Llera et al.82 (from other works63, 67) 36. DECODE83 37. Erglis et al84, 85 38. NOBORI 1 - Phase 186, 87 39. Ortolani et al.88 40. Pan et al. (2007)89 41. Petronio et al.90 42. SCORPIUS91, 92 43. SELECTION93 44. SESAMI94-96 45. Strozzi et al.97 Published in 2008 46. DES-DIABETES98-100 No Yes Yes Partially yes: follow-up angiographic substudy (1/4 of patients) 100 DAPT ≥1 month for BMS ≥9 months for SES DAPT ≥3 months No Yes 83 68 76 82 35 64 80 80 79 12 20 16 37 25 100 13 20 32 DAPT ≥6 months DAPT ≥ 6 months DAPT ≥3 months DAPT ≥12 months DAPT ≥6 months DAPT ≥6 months DAPT ≥9 months DAPT ≥12 months DAPT ≥6 months Yes Yes Yes Yes Yes Yes Yes Yes Yes 58 100 DAT ≥6 month Yes DESSERT101 47. 48. Hong et al.102, 103 49. LEADERS104-109 50. Li et al. (2008)110 51. MISSION!111-113 52. MULTI-STRATEGY114-116 53. PROSIT117, 118 54. SORT OUT II119 55. SPIRIT III120-123 Published in 2009 56. HORIZONS-AMI124-126 57. ISAR-LEFT-MAIN127 58. ISAR-TEST-2128, 129 59. ISAR-TEST-4130, 131 60. Juwana et al.132 61. Li et al. (2009)133 62. NOBORI 1 - Phase 2134 63. PASEO135, 136 64. SOS137, 138 65. SPIRIT II120, 139-142 66. ZEST-AMI143 Published in 2010 67. BASKET-PROVE144, 145 68. COMPARE146, 147 69. ENDEAVOR IV148-150 70 GISSOC II-GISE151 71. GRACIA-3152 72. ISAR-DESIRE 2153 73. OCTAMI154 74. RESOULTE All Comers155, 156 BMS vs. SES SES vs. PES BP-BES vs. SES 75:75 85:84 857:850 70 62 64 56 74 75 100 100 24 randomly allocated to TAPT and DAPT DAPT ≥2 months for BMS, ≥6 months SES DAPT ≥6 months DAPT ≥12 months SES vs. BMS SES vs. BMS BMS vs. SES SES vs. PES SES vs. PES 24:24 158:152 372:372 154:154 1065:1033 47 59 64 60 64 73 78 76 76 75 13 10 14 25 15 DAPT ≥6 months DAPT ≥12 months DAPT ≥3 months DAPT ≥6 months DAPT ≥12 months CoCr-EES vs. PES 669:333 63 70 28 DAPT ≥6 months PES vs. BMS PES vs. SES SES vs. ZES-E CoCr-EES vs. SES SES vs. PES SES vs. PES BP-BES vs. PES BMS vs. PES vs. SES BMS vs. PES 2257:749 302:305 335:339 652:652 196:201 16:16 153:90 90:90:90 39:41 60 69 67 67 61 51 63 62 67 77 78 23 76 82 78 72 71 100 16 29 27 29 9 13 21 26 44 Yes Yes Yes Yes Yes Yes Yes No Yes CoCr-EES vs. PES ZES-E vs. SES vs. PES 223:77 108:110:110 62 60 73 83 23 26 DAPT ≥6 months DAPT indefinitely DAPT ≥6 months DAPT ≥6 month DAPT ≥6 months DAPT ≥9 months DAPT ≥6 months DAPT ≥6 months DAPT ≥6 months for PES ≥1 month for BMS DAPT ≥6 months DAPT ≥12 months. 775:774:765 897:903 773:775 66 63 64 76 69 68 16 17 31 DAPT ≥12 months DAPT ≥12 months DAPT ≥6 months 78:74 216:217 225:225 33:11 1140:1152 64 61 67 61 64 83 83 77 77 77 22 18 36 14 23 DAPT ≥6 months DAPT ≥12 months DAPT ≥6 months DAPT ≥6 months DAPT ≥6 months No No Partially yes: angiographic follow-up subgroup (1/5 of patients) Yes Yes Yes Yes Partially yes: angiographic follow-up SES vs. CoCr-EES vs. BMS CoCr-EES vs. PES ZES-E vs. PES BMS vs. SES BMS vs. PES SES vs. PES ZES-E vs. BMS ZES-R vs. CoCr-EES Yes Yes Partially yes: angiographic follow-up subgroup (1/4 of patients) Yes Yes No Yes Partially yes: angiographic follow-up subgroup (0.5% of patients) Partially yes: angiographic follow-up cohort (1/2 of patients) Yes Yes 75. SORT OUT III157, 158 76. SPIRIT IV122, 159, 160 77. ZEST161, 162 Published in 2011 78. ESSENCE-DIABETES163 79. EXCELLENT164, 165 80. GARA-GARA166 81. KOMER167 80. LONG-DES-III168 83. Naples-Diabetes169 84. PLATINUM170 85. POET171 86. PRISON III172, 173 87. PROSUMER174 88. SEA-SIDE175 Published in 2012 89. CATOS176 90. COMFORTABLE AMI177, 178 91. COVER OCT179 92. DEBATER180 subgroup (1/5 of patients) No No Yes ZES-E vs. SES CoCr-EES vs. PES ZES-E vs. SES vs. PES 1162:1170 2458:1229 883:878:884 64 63 62 73 68 66 13 32 29 DAPT ≥12 months DAPT ≥6 months DAPT ≥12 months CoCr-EES vs. SES CoCr-EES vs. SES SES vs. PES ZES-E vs. SES vs. PES CoCr-EES vs. SES SES vs. PES vs. ZES-E CoCr-EES vs. PtCr-EES SES vs. PES 149:151 1079:364 400:400 205:204:202 224:226 76:75:75 762:768 152:149 63 63 69 60 63 64 64 62 59 65 71 79 70 57 71 36 100 38 46 21 30 100 24 30 Yes Yes Yes Yes Yes No No Yes 51:46 30:30 75:75 62 62 65 84 23 80 28 DAPT ≥12 months Randomized to 6- vs. 12-months DAPT (1:1) DAPT ≥6 months DAPT ≥12 months DAPT ≥12 months DAPT ≥6 months DAPT ≥6 months DAPT ≥6 months for PES ≥3 months for SES DAPT ≥12 months Insufficient information DAPT ≥12 months 80:80 575:582 22:22 441:466 63 61 59 60 71 79 70 76 32 15 34 10 Yes No Yes No SES vs. ZES-E SES vs. BMS SES vs. CoCr-EES ZES-E vs. SES BP-BES vs. BMS ZES-R vs. CoCr-EES SES vs. PES 93. EXAMINATION181, 182 94. ISAR-LEFT MAIN 2183 95. LONG-DES-IV184 96. NOBORI JAPAN185 97. Pan et al. (2012) 186 98. PROTECT187, 188 99. RESET189 CoCr-EES vs. BMS ZES-R vs. CoCr-EES ZES-R vs. SES BP-BES vs. SES SES vs. CoCr-EES ZES-E vs. SES CoCr-EES vs. SES 751:747 324:326 250:250 198:137 145:148 4357:4352 1597:1600 61 70 63 67 63 62 69 84 75 73 72 80 76 77 18 29 29 39 32 28 45 DAPT ≥12 months DAPT ≥12 months DAPT ≥9 months DAPT ≥ 6-12 months for SES ≥ 1 month for BMS DAPT ≥12 months DAPT ≥12 months DAPT ≥12 months DAPT ≥3 months DAPT ≥12 months DAPT 3-12 months DAPT ≥ 3 months 100. Sakakibara et al.190 101. SEZE191 102. Song et al.192 103. SORT OUT IV193-195 SES vs. CoCr-EES ZES-E vs. SES SES vs. CoCr-EES CoCr-EES vs. SES 50:50 60:61 32:34 1390:1384 66 61 63 64 70 81 52 76 70 22 30 14 DAPT ≥12 months DAPT ≥12 months DAPT ≥6 months DAPT ≥12 months Yes Yes No No Yes Yes Yes No No Partially yes: angiographic substudy (1/6 of patients) Yes Yes Yes No 104. SPIRIT V Diabetic Study196 105. TWENTE197-199 106. X-AMI200 107. XIMA201 Published in 2013 108. CIBELLES202, 203 109. COMPARE II204 110. COVER OCT II205 111. HOST-ASSURE206, 207 112. NEXT208 113. SORT OUT V209 CoCr-EES vs. PES ZES-R vs. CoCr-EES CoCr-EES vs. SES BMS vs. CoCr-EES 218:106 697:694 404:221 401:399 65 64 61 83 70 72 74 60 100 22 10 25 DAPT ≥6 months DAPT ≥12 months DAPT ≥12 months DAPT ≥12 months for EES ≥1 month for BMS Yes No No No SES vs. CoCr-EES BP-BES vs. CoCr-EES ZES-R vs. CoCr-EES PtCr-EES vs. ZES-R 101:106 1795:912 20:20 2503:1252 64 63 64 63 84 74 68 68 36 22 38 32 Yes No Yes No BP-BES vs. CoCr-EES 1617:1618 69 77 46 DAPT ≥9 months DAPT ≥12 months DAPT ≥ 3 months DAPT ≥12 months randomized to DDAT vs. TAT (1:1) unclear BP-BES vs. SES 1229:1239 65 75 15 DAPT ≥12 months Partially yes: angiographic substudy (1/4 of patients) No BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimus-eluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents; DAPT, dual antiplatelet therapy; DDAT, douuble-dose dual antiplatelet therapy; TAT, triple antiplatelet therapy Supplement Table S4. Sensitivity Analysis of Definite or Probable Stent Thrombosis Within 1 Year Comparison BMS as reference BMS vs. BMS PES vs. BMS ZES-E vs. BMS BP-BES vs. BMS SES vs. BMS ZES-R vs. BMS CoCr-EES vs. BMS PtCr-EES vs. BMS PES as reference BMS vs. PES PES vs. PES ZES-E vs. PES BP-BES vs. PES SES vs. PES ZES-R vs. PES CoCr-EES vs. PES PtCr-EES vs. PES ZES-E as reference BMS vs. ZES-E PES vs. ZES-E ZES-E vs. ZES-E BP-BES vs. ZES-E SES vs. ZES-E ZES-R vs. ZES-E CoCr-EES vs. ZES-E PtCr-EES vs. ZES-E BP-BES as reference BMS vs. BP-BES PES vs. BP-BES ZES-E vs. BP-BES BP-BES vs. BP-BES SES vs. BP-BES ZES-R vs. BP-BES CoCr-EES vs. BP-BES PtCr-EES vs. BP-BES SES as reference BMS vs. SES PES vs. SES ZES-E vs. SES BP-BES vs. SES SES vs. SES ZES-R vs. SES CoCr-EES vs. SES PtCr-EES vs. SES ZES-R as reference BMS vs. ZES-R PES vs. ZES-R ZES-E vs. ZES-R All trials Low risk of bias Excluding studies with diabetes Excluding studies with STEMI 0.85 (0.60-1.19) 0.75 (0.45-1.19) 0.55 (0.32-0.89) 0.53 (0.39-0.73) 0.52 (0.24-1.18) 0.35 (0.23-0.52) 0.31 (0.10-0.89) 0.87 (0.59-1.32) 0.95 (0.54-1.74) 0.54 (0.30-0.91) 0.54 (0.36-0.80) 0.51 (0.21-1.22) 0.34 (0.21-0.53) 0.30 (0.09-0.95) 0.84 (0.60-1.20) 0.74 (0.44-1.18) 0.54 (0.31-0.88) 0.53 (0.38-0.74) 0.52 (0.24-1.14) 0.35 (0.22-0.52) 0.31 (0.10-0.91) 0.89 (0.48-1.65) 0.83 (0.41-1.68) 0.49 (0.24-0.92) 0.47 (0.28-0.78) 0.48 (0.17-1.21) 0.31 (0.17-0.57) 0.28 (0.07-1.03) 1.17 (0.84-1.67) 0.88 (0.54-1.42) 0.64 (0.37-1.08) 0.63 (0.46-0.87) 0.61 (0.29-1.34) 0.40 (0.27-0.60) 0.35 (0.12-1.07) 1.15 (0.76-1.71) 1.09 (0.62-1.98) 0.63 (0.33-1.08) 0.62 (0.41-0.91) 0.59 (0.25-1.38) 0.39 (0.25-0.59) 0.35 (0.10-1.10) 1.19 (0.83-1.68) 0.88 (0.54-1.39) 0.65 (0.37-1.08) 0.63 (0.45-0.88) 0.62 (0.29-1.33) 0.41 (0.27-0.61) 0.37 (0.12-1.09) 1.13 (0.60-2.07) 0.93 (0.48-1.82) 0.55 (0.25-1.07) 0.53 (0.32-0.86) 0.54 (0.20-1.28) 0.35 (0.20-0.58) 0.32 (0.08-1.09) 1.33 (0.84-2.21) 1.14 (0.70-1.84) 0.73 (0.40-1.33) 0.70 (0.48-1.10) 0.70 (0.30-1.66) 0.46 (0.27-0.78) 0.40 (0.13-1.28) 1.05 (0.57-1.86) 0.92 (0.51-1.61) 0.57 (0.26-1.11) 0.57 (0.33-0.94) 0.54 (0.19-1.44) 0.36 (0.18-0.66) 0.32 (0.08-1.08) 1.35 (0.85-2.26) 1.13 (0.72-1.86) 1.00 (1.00-1.00) 0.72 (0.48-1.11) 0.73 (0.39-1.34) 0.42 (0.13-1.30) 0.70 (0.31-1.67) 1.21 (0.59-2.43) 1.08 (0.55-2.10) 1.00 (1.00-1.00) 0.57 (0.31-1.01) 0.59 (0.25-1.24) 0.34 (0.08-1.26) 0.58 (0.20-1.54) 1.83 (1.12-3.08) 1.56 (0.93-2.69) 1.36 (0.75-2.53) 0.98 (0.60-1.59) 0.97 (0.40-2.23) 0.63 (0.37-1.07) 0.55 (0.18-1.76) 1.84 (1.10-3.37) 1.60 (0.93-3.01) 1.74 (0.90-3.80) 1.00 (0.61-1.71) 0.94 (0.38-2.48) 0.63 (0.36-1.13) 0.56 (0.16-1.89) 1.85 (1.14-3.22) 1.55 (0.93-2.73) 1.36 (0.75-2.59) 0.98 (0.63-1.62) 0.97 (0.41-2.27) 0.64 (0.38-1.10) 0.58 (0.18-1.78) 2.04 (1.09-4.23) 1.82 (0.94-3.95) 1.69 (0.81-4.07) 0.97 (0.56-1.85) 0.97 (0.36-2.65) 0.64 (0.34-1.27) 0.57 (0.16-2.21) 1.88 (1.37-2.58) 1.60 (1.14-2.18) 1.42 (0.91-2.08) 1.03 (0.63-1.67) 0.98 (0.46-2.20) 0.65 (0.45-0.93) 0.57 (0.19-1.66) 1.84 (1.25-2.77) 1.60 (1.09-2.41) 1.75 (1.06-3.07) 1.00 (0.59-1.64) 0.94 (0.41-2.21) 0.63 (0.42-0.94) 0.55 (0.17-1.75) 1.88 (1.36-2.64) 1.58 (1.13-2.21) 1.39 (0.90-2.10) 1.02 (0.62-1.60) 0.98 (0.46-2.09) 0.65 (0.45-0.93) 0.59 (0.18-1.67) 2.11 (1.28-3.55) 1.88 (1.16-3.15) 1.74 (0.99-3.21) 1.03 (0.54-1.79) 1.01 (0.41-2.36) 0.66 (0.42-1.03) 0.59 (0.17-2.01) 1.91 (0.85-4.13) 1.64 (0.75-3.48) 1.42 (0.60-3.31) 1.94 (0.82-4.74) 1.70 (0.73-4.08) 1.85 (0.70-5.29) 1.92 (0.88-4.22) 1.62 (0.75-3.48) 1.42 (0.60-3.28) 2.09 (0.83-5.81) 1.86 (0.78-4.92) 1.73 (0.65-5.11) BP-BES vs. ZES-R SES vs. ZES-R ZES-R vs. ZES-R CoCr-EES vs. ZES-R PtCr-EES vs. ZES-R CoCr-EES as reference BMS vs. CoCr-EES PES vs. CoCr-EES ZES-E vs. CoCr-EES BP-BES vs. CoCr-EES SES vs. CoCr-EES ZES-R vs. CoCr-EES CoCr-EES vs. CoCr-EES PtCr-EES vs. CoCr-EES PtCr-EES as reference BMS vs. PtCr-EES PES vs. PtCr-EES ZES-E vs. PtCr-EES BP-BES vs. PtCr-EES SES vs. PtCr-EES ZES-R vs. PtCr-EES CoCr-EES vs. PtCr-EES PtCr-EES vs. PtCr-EES 1.04 (0.45-2.48) 1.02 (0.45-2.15) 0.66 (0.35-1.25) 0.57 (0.23-1.47) 1.06 (0.40-2.62) 1.07 (0.45-2.45) 0.67 (0.31-1.38) 0.58 (0.22-1.59) 1.04 (0.44-2.45) 1.02 (0.48-2.19) 0.66 (0.34-1.26) 0.59 (0.23-1.48) 1.03 (0.38-2.75) 0.99 (0.42-2.47) 0.66 (0.31-1.43) 0.59 (0.20-1.76) 2.90 (1.91-4.38) 2.47 (1.68-3.66) 2.17 (1.28-3.69) 1.58 (0.93-2.69) 1.55 (1.07-2.22) 1.52 (0.80-2.88) 0.87 (0.31-2.43) 2.93 (1.89-4.74) 2.56 (1.69-4.03) 2.78 (1.53-5.45) 1.59 (0.89-2.76) 1.60 (1.06-2.39) 1.50 (0.72-3.22) 0.88 (0.29-2.62) 2.89 (1.93-4.46) 2.45 (1.65-3.68) 2.15 (1.26-3.61) 1.56 (0.91-2.64) 1.54 (1.08-2.23) 1.51 (0.80-2.96) 0.90 (0.31-2.51) 3.19 (1.75-6.04) 2.84 (1.72-4.95) 2.62 (1.36-5.49) 1.56 (0.79-2.93) 1.51 (0.97-2.39) 1.52 (0.70-3.18) 0.89 (0.27-2.88) 2.69 (0.97-6.93) 2.49 (0.87-6.46) 2.04 (0.74-5.19) 1.72 (0.60-4.66) 1.54 (0.65-3.63) 1.49 (0.50-3.94) 1.03 (0.39-2.52) - 3.31 (1.05-11.05) 2.90 (0.91-9.60) 3.16 (0.93-12.16) 1.80 (0.53-6.12) 1.80 (0.57-5.81) 1.71 (0.63-4.58) 1.14 (0.38-3.39) - 3.20 (1.10-9.99) 2.68 (0.92-8.23) 2.37 (0.77-7.88) 1.73 (0.56-5.65) 1.69 (0.60-5.47) 1.68 (0.67-4.38) 1.11 (0.40-3.24) - 3.56 (0.97-13.65) 3.17 (0.92-11.78) 2.94 (0.79-11.87) 1.75 (0.45-6.42) 1.68 (0.50-6.00) 1.70 (0.57-5.01) 1.12 (0.35-3.66) - BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents; STEMI, STsegment elevation myocardial infarction Supplement Figure S1. Risk of Bias Assessment Summary Risk of bias of each included trial was assessed with the Cochrane Collaboration’s tool. This ‘risk of bias summary’ figure presents all of the judgements in a cross-tabulation of study by entry. Green represents ‘Yes (low risk of bias)’; yellow, ‘Unclear’; red, ‘No (high risk of bias)’. Supplement Figure S2. Ranks for Study Stents Regarding Definite or Probable Stent Thrombosis (A) Rankograms for the study stents. On the horizontal axis are the 8 possible ranks and on the vertical axis the probability of a treatment to achieve each rank. (B) Barplots for the ranking probabilities of competing stents. On the horizontal axis is the possible rank of each treatment (from best to worse according to the outcome). The size of each bar corresponds to the probability of each treatment to be at a specific rank. % probability to rank at each place BMS PES SES ZES-E 2 3 CoCr-EES PtCr-EES ZES-R BP-BES 100% 80% 60% 40% 20% 0% 1 4 Ranks 5 6 7 8 Supplement Figure S3. Definite or Probable Stent Thrombosis at the Longest Follow-Up Available The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for definite or probable stent thrombosis at the longest follow-up available estimated with multiple-treatment meta-analysis. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S4. Definite or Probable Stent Thrombosis, Early (≤30 days) The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for early definite or probable stent thrombosis within 30 days estimated with multiple-treatment meta-analysis. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S5. Definite or Probable Stent Thrombosis, Late (31-365 days) The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for late definite or probable stent thrombosis (31-365 days) estimated with multiple-treatment meta-analysis. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S6. Definite or Probable Stent Thrombosis, Very Late (>365 days) The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for very late definite or probable stent thrombosis (>365 days) estimated with multiple-treatment meta-analysis. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S7. Definite or Probable Stent Thrombosis, Late and Very Late (>30 days) The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for late and very late definite or probable stent thrombosis (>30 days) estimated with multiple-treatment meta-analysis. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S8. Definite Stent Thrombosis (ST) with Reference to Bare Metal Stent The squares and horizontal lines indicate odds ratios and their 95% credible intervals for definite or probable stent thrombosis estimated with multiple-treatment meta-analysis. All comparisons are presented with reference to bare metal stent. ST denotes stent thrombosis; BMS, bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimus-eluting stents; CoCr-EES, Cobaltchromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S9. Inconsistency Plot for Triangular Loops BMS, bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimus-eluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S10. Target Vessel Revascularization Within 1 Year The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for target vessel revascularization within 1 year estimated with multiple-treatment meta-analysis. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S11. All-Cause Death Within 1 Year The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for all-cause death within 1 year estimated with multiple-treatment meta-analysis. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S12. Cardiac Death Within 1 Year The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for cardiac death within 1 year estimated with multiple-treatment meta-analysis. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S13. Network Plot of Sensitivity Analysis for Trials with Low Risk of Bias Each stent is represented by a node. The size of the node is proportional to the sample size randomized to each stent, while the thickness of the line connecting the nodes is to the total randomized sample size in each pairwise treatment comparison. A total of 48 trials including 60,911 patients were analyzed with exclusion of trials with any potential risk of bias (unclear or no) in the 6 domains assessed according the Cochrane Collaboration’s tool (random sequence generation, allocation concealment, blinding of clinical outcome assessment, incomplete outcome data addressed, free of selective reporting, free of other bias). BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents Supplement Figure S14. Sensitivity Analysis for Trials with Low Risk of Bias The squares and horizontal lines indicate pairwise odds ratios and their 95% credible intervals for definite or probable stent thrombosis within 1 year estimated with multiple-treatment meta-analysis. Gray squares and lines represent the analysis with all trials included, while red squares and lines do the sensitivity analysis including trials with low risk of bias. BMS denotes bare metal stents; PES, paclitaxel-eluting stents; SES, sirolimus-eluting stents; ZES-E, Endeavor zotarolimuseluting stents; CoCr-EES, Cobalt-chromium everolimus-eluting stents; PtCr-EES, Platinum-chromium everolimus-eluting stents; ZES-R: Resolute zotarolimus-eluting stents; BP-BES, biodegradable polymer biolimus-eluting stents References 1. Morice MC, Serruys PW, Sousa JE, Fajadet J, Ban Hayashi E, Perin M, Colombo A, Schuler G, Barragan P, Guagliumi G, Molnar F, Falotico R. A randomized comparison of a sirolimus-eluting stent with a standard stent for coronary revascularization. N Engl J Med 2002;346(23):1773-80. 2. Fajadet J, Morice MC, Bode C, Barragan P, Serruys PW, Wijns W, Constantini CR, Guermonprez JL, Eltchaninoff H, Blanchard D, Bartorelli A, Laarman GJ, Perin M, Sousa JE, Schuler G, Molnar F, Guagliumi G, Colombo A, Ban Hayashi E, Wulfert E. Maintenance of long-term clinical benefit with sirolimus-eluting coronary stents: three-year results of the RAVEL trial. Circulation 2005;111(8):1040-4. 3. Morice MC, Serruys PW, Barragan P, Bode C, Van Es GA, Stoll HP, Snead D, Mauri L, Cutlip DE, Sousa E. Long-term clinical outcomes with sirolimus-eluting coronary stents: five-year results of the RAVEL trial. J Am Coll Cardiol 2007;50(14):1299-304. 4. Park SJ, Shim WH, Ho DS, Raizner AE, Park SW, Hong MK, Lee CW, Choi D, Jang Y, Lam R, Weissman NJ, Mintz GS. A paclitaxel-eluting stent for the prevention of coronary restenosis. N Engl J Med 2003;348(16):1537-45. 5. Schofer J, Schluter M, Gershlick AH, Wijns W, Garcia E, Schampaert E, Breithardt G, Investigators ES. Sirolimus-eluting stents for treatment of patients with long atherosclerotic lesions in small coronary arteries: double-blind, randomised controlled trial (E-SIRIUS). Lancet 2003;362(9390):1093-9. 6. Schofer J, Breithardt G, Garcia E, Gershlick AH, Schlüter M, Wichter T, W. Wijns. The European multicenter, randomized, double-blind study of the Sirolimus-eluting stent in the treatment of patients with de novo coronary artery lesions (E-SIRIUS): 4-year clinical outcomes. http://www.crtonline.org/flash.aspx?PAGE_ID=3336. 7. Moses JW, Leon MB, Popma JJ, Fitzgerald PJ, Holmes DR, O'Shaughnessy C, Caputo RP, Kereiakes DJ, Williams DO, Teirstein PS, Jaeger JL, Kuntz RE, Investigators S. Sirolimus-eluting stents versus standard stents in patients with stenosis in a native coronary artery. N Engl J Med 2003;349(14):1315-23. 8. Holmes DR, Jr., Leon MB, Moses JW, Popma JJ, Cutlip D, Fitzgerald PJ, Brown C, Fischell T, Wong SC, Midei M, Snead D, Kuntz RE. Analysis of 1-year clinical outcomes in the SIRIUS trial: a randomized trial of a sirolimus-eluting stent versus a standard stent in patients at high risk for coronary restenosis. Circulation 2004;109(5):634-40. 9. Weisz G, Leon MB, Holmes DR, Jr., Kereiakes DJ, Clark MR, Cohen BM, Ellis SG, Coleman P, Hill C, Shi C, Cutlip DE, Kuntz RE, Moses JW. Two-year outcomes after sirolimus-eluting stent implantation: results from the Sirolimus-Eluting Stent in de Novo Native Coronary Lesions (SIRIUS) trial. J Am Coll Cardiol 2006;47(7):1350-5. 10. Weisz G, Leon MB, Holmes DR, Jr., Kereiakes DJ, Popma JJ, Teirstein PS, Cohen SA, Wang H, Cutlip DE, Moses JW. Five-year follow-up after sirolimus-eluting stent implantation results of the SIRIUS (Sirolimus-Eluting Stent in De-Novo Native Coronary Lesions) Trial. J Am Coll Cardiol 2009;53(17):1488-97. 11. Grube E, Silber S, Hauptmann KE, Mueller R, Buellesfeld L, Gerckens U, Russell ME. TAXUS I: sixand twelve-month results from a randomized, double-blind trial on a slow-release paclitaxel-eluting stent for de novo coronary lesions. Circulation 2003;107(1):38-42. 12. Grube E, Silber S, Hauptmann KE, Buellesfeld L, Mueller R, Lim V, Gerckens U, Russell ME. Twoyear-plus follow-up of a paclitaxel-eluting stent in de novo coronary narrowings (TAXUS I). Am J Cardiol 2005;96(1):79-82. 13. Stone GW, Ellis SG, Colombo A, Grube E, Popma JJ, Uchida T, Bleuit JS, Dawkins KD, Russell ME. Long-term safety and efficacy of paclitaxel-eluting stents final 5-year analysis from the TAXUS Clinical Trial Program. JACC Cardiovasc Interv 2011;4(5):530-42. 14. Colombo A, Drzewiecki J, Banning A, Grube E, Hauptmann K, Silber S, Dudek D, Fort S, Schiele F, Zmudka K, Guagliumi G, Russell ME, Group TIS. Randomized study to assess the effectiveness of slow- and moderate-release polymer-based paclitaxel-eluting stents for coronary artery lesions. Circulation 2003;108(7):788-94. 15. Silber S, Colombo A, Banning AP, Hauptmann K, Drzewiecki J, Grube E, Dudek D, Baim DS. Final 5-year results of the TAXUS II trial: a randomized study to assess the effectiveness of slow- and moderaterelease polymer-based paclitaxel-eluting stents for de novo coronary artery lesions. Circulation 2009;120(15):1498-504. 16. Schampaert E, Cohen EA, Schluter M, Reeves F, Traboulsi M, Title LM, Kuntz RE, Popma JJ, Investigators CS. The Canadian study of the sirolimus-eluting stent in the treatment of patients with long de novo lesions in small native coronary arteries (C-SIRIUS). J Am Coll Cardiol 2004;43(6):1110-5. 17. Ardissino D, Cavallini C, Bramucci E, Indolfi C, Marzocchi A, Manari A, Angeloni G, Carosio G, Bonizzoni E, Colusso S, Repetto M, Merlini PA, Investigators S-S. Sirolimus-eluting vs uncoated stents for prevention of restenosis in small coronary arteries: a randomized trial. JAMA 2004;292(22):2727-34. 18. Menozzi A, Solinas E, Ortolani P, Repetto A, Saia F, Piovaccari G, Manari A, Magagnini E, Vignali L, Bonizzoni E, Merlini PA, Cavallini C, Ardissino D, Investigators S-S. Twenty-four months clinical outcomes of sirolimus-eluting stents for the treatment of small coronary arteries: the long-term SES-SMART clinical study. Eur Heart J 2009;30(17):2095-101. 19. Stone GW, Ellis SG, Cox DA, Hermiller J, O'Shaughnessy C, Mann JT, Turco M, Caputo R, Bergin P, Greenberg J, Popma JJ, Russell ME, Investigators T-I. A polymer-based, paclitaxel-eluting stent in patients with coronary artery disease. N Engl J Med 2004;350(3):221-31. 20. Ellis SG, Stone GW, Cox DA, Hermiller J, O'Shaughnessy C, Mann T, Turco M, Caputo R, Bergin PJ, Bowman TS, Baim DS, Investigators TI. Long-term safety and efficacy with paclitaxel-eluting stents: 5-year final results of the TAXUS IV clinical trial (TAXUS IV-SR: Treatment of De Novo Coronary Disease Using a Single Paclitaxel-Eluting Stent). JACC Cardiovasc Interv 2009;2(12):1248-59. 21. Kaiser C, Brunner-La Rocca HP, Buser PT, Bonetti PO, Osswald S, Linka A, Bernheim A, Zutter A, Zellweger M, Grize L, Pfisterer ME. Incremental cost-effectiveness of drug-eluting stents compared with a third-generation bare-metal stent in a real-world setting: randomised Basel Stent Kosten Effektivitäts Trial (BASKET). The Lancet;366(9489):921-929. 22. Rocca HPB-L, Kaiser C, Bernheim A, Zellweger MJ, Jeger R, Buser PT, Osswald S, Pfisterer M. Cost-effectiveness of drug-eluting stents in patients at high or low risk of major cardiac events in the Basel Stent KostenEffektivitäts Trial (BASKET): an 18-month analysis. The Lancet;370(9598):1552-1559. 23. Schomig A, Dibra A, Windecker S, Mehilli J, Suarez de Lezo J, Kaiser C, Park SJ, Goy JJ, Lee JH, Di Lorenzo E, Wu J, Juni P, Pfisterer ME, Meier B, Kastrati A. A meta-analysis of 16 randomized trials of sirolimus-eluting stents versus paclitaxel-eluting stents in patients with coronary artery disease. J Am Coll Cardiol 2007;50(14):1373-80. 24. Sabaté M, Jiménez-Quevedo P, Angiolillo DJ, Gómez-Hospital JA, Alfonso F, Hernández-Antolín R, Goicolea J, Bañuelos C, Escaned J, Moreno R, Fernández C, Fernández-Avilés F, Macaya C, Investigators ftD. Randomized Comparison of Sirolimus-Eluting Stent Versus Standard Stent for Percutaneous Coronary Revascularization in Diabetic Patients: The Diabetes and Sirolimus-Eluting Stent (DIABETES) Trial. Circulation 2005;112(14):2175-2183. 25. Jiménez-Quevedo P, Sabaté M, Angiolillo DJ, Alfonso F, Hernández-Antolín R, SanMartín M, Gómez-Hospital JA, Bañuelos C, Escaned J, Moreno R, Fernández C, Fernández-Avilés F, Macaya C. Longterm clinical benefit of sirolimus-eluting stent implantation in diabetic patients with de novo coronary stenoses: long-term results of the DIABETES trial. European Heart Journal 2007;28(16):1946-1952. 26. de Waha A, Dibra A, Kufner S, Baumgart D, Sabate M, Maresta A, Schomig A, Kastrati A. Long-term outcome after sirolimus-eluting stents versus bare metal stents in patients with diabetes mellitus: a patient-level meta-analysis of randomized trials. Clin Res Cardiol 2011;100(7):561-70. 27. Jimenez-Quevedo P, Hernando L, Iniguez A, SanRoman A, Antolin RH, Alfonso F, Banuelos C, Escaned J, Macaya C, Sabate M. Four years follow-up of DIABETES trial. Journal of the American College of Cardiology 2009;53(10):A33. 28. Tuesday, 30 August 2011. European Heart Journal 2011;32(suppl 1):633-933. 29. Kastrati A, Mehilli J, von Beckerath N, Dibra A, Hausleiter J, Pache J, Schuhlen H, Schmitt C, Dirschinger J, Schomig A, Investigators I-DS. Sirolimus-eluting stent or paclitaxel-eluting stent vs balloon angioplasty for prevention of recurrences in patients with coronary in-stent restenosis: a randomized controlled trial. JAMA 2005;293(2):165-71. 30. Birkmeier KA, Kastrati A, Byrne RA, Holle H, Schulz S, Tiroch K, Kufner S, Massberg S, Laugwitz KL, Schomig A, Mehilli J. Five-year clinical outcomes of sirolimus-eluting versus paclitaxel-eluting stents in high-risk patients. Catheter Cardiovasc Interv 2011;77(4):494-501. 31. Dibra A, Kastrati A, Mehilli J, Pache J, Schuhlen H, von Beckerath N, Ulm K, Wessely R, Dirschinger J, Schomig A, Investigators I-DS. Paclitaxel-eluting or sirolimus-eluting stents to prevent restenosis in diabetic patients. N Engl J Med 2005;353(7):663-70. 32. Pache J, Dibra A, Mehilli J, Dirschinger J, Schomig A, Kastrati A. Drug-eluting stents compared with thin-strut bare stents for the reduction of restenosis: a prospective, randomized trial. Eur Heart J 2005;26(13):1262-8. 33. Windecker S, Remondino A, Eberli FR, Juni P, Raber L, Wenaweser P, Togni M, Billinger M, Tuller D, Seiler C, Roffi M, Corti R, Sutsch G, Maier W, Luscher T, Hess OM, Egger M, Meier B. Sirolimus-eluting and paclitaxel-eluting stents for coronary revascularization. N Engl J Med 2005;353(7):653-62. 34. Billinger M, Beutler J, Taghetchian KR, Remondino A, Wenaweser P, Cook S, Togni M, Seiler C, Stettler C, Eberli FR, Luscher TF, Wandel S, Juni P, Meier B, Windecker S. Two-year clinical outcome after implantation of sirolimus-eluting and paclitaxel-eluting stents in diabetic patients. Eur Heart J 2008;29(6):718- 25. 35. Raber L, Wohlwend L, Wigger M, Togni M, Wandel S, Wenaweser P, Cook S, Moschovitis A, Vogel R, Kalesan B, Seiler C, Eberli F, Luscher TF, Meier B, Juni P, Windecker S. Five-year clinical and angiographic outcomes of a randomized comparison of sirolimus-eluting and paclitaxel-eluting stents: results of the Sirolimus-Eluting Versus Paclitaxel-Eluting Stents for Coronary Revascularization LATE trial. Circulation 2011;123(24):2819-28, 6 p following 2828. 36. Serruys PW, Ong AT, Piek JJ, Neumann FJ, van der Giessen WJ, Wiemer M, Zeiher A, Grube E, Haase J, Thuesen L, Hamm C, Otto-Terlouw PC. A randomized comparison of a durable polymer Everolimuseluting stent with a bare metal coronary stent: The SPIRIT first trial. EuroIntervention 2005;1(1):58-65. 37. Tsuchida K, Piek JJ, Neumann FJ, van der Giessen WJ, Wiemer M, Zeiher AM, Grube E, Haase J, Thuesen L, Hamm CW, Veldhof S, Dorange C, Serruys PW. One-year results of a durable polymer everolimuseluting stent in de novo coronary narrowings (The SPIRIT FIRST Trial). EuroIntervention 2005;1(3):266-72. 38. Beijk MA, Neumann FJ, Wiemer M, Grube E, Haase J, Thuesen L, Hamm C, Veldhof S, Dorange C, Serruys PW, Piek JJ. Two-year results of a durable polymer everolimus-eluting stent in de novo coronary artery stenosis (The SPIRIT FIRST Trial). EuroIntervention 2007;3(2):206-12. 39. Wiemer M, Serruys PW, Miquel-Hebert K, Neumann FJ, Piek JJ, Grube E, Haase J, Thuesen L, Hamm C. Five-year long-term clinical follow-up of the XIENCE V everolimus eluting coronary stent system in the treatment of patients with de novo coronary artery lesions: the SPIRIT FIRST trial. Catheter Cardiovasc Interv 2010;75(7):997-1003. 40. Grube E, Hauptmann KE, Buellesfeld L, Lim V, Abizaid A. Six-month results of a randomized study to evaluate safety and efficacy of a Biolimus A9 eluting stent with a biodegradable polymer coating. EuroIntervention 2005;1(1):53-7. 41. Valgimigli M, Percoco G, Cicchitelli G, Ferrari F, Barbieri D, Ansani L, Guardigli G, Parrinello G, Malagutti P, Soukhomovskaia O, Bettini A, Campo G, Ferrari R. High-dose bolus tirofiban and sirolimus eluting stent versus abiciximab and bare metal stent in acute myocardial infarction (STRATEGY) study--protocol design and demography of the first 100 patients. Cardiovasc Drugs Ther 2004;18(3):225-30. 42. Valgimigli M, Percoco G, Malagutti P, Campo G, Ferrari F, Barbieri D, Cicchitelli G, McFadden EP, Merlini F, Ansani L, Guardigli G, Bettini A, Parrinello G, Boersma E, Ferrari R, Investigators S. Tirofiban and sirolimus-eluting stent vs abciximab and bare-metal stent for acute myocardial infarction: a randomized trial. JAMA 2005;293(17):2109-17. 43. Valgimigli M, Campo G, Arcozzi C, Malagutti P, Carletti R, Ferrari F, Barbieri D, Parrinello G, Percoco G, Ferrari R. Two-year clinical follow-up after sirolimus-eluting versus bare-metal stent implantation assisted by systematic glycoprotein IIb/IIIa Inhibitor Infusion in patients with myocardial infarction: results from the STRATEGY study. J Am Coll Cardiol 2007;50(2):138-45. 44. Tebaldi M, Arcozzi C, Campo G, Percoco G, Ferrari R, Valgimigli M, Investigators S. The 5-year clinical outcomes after a randomized comparison of sirolimus-eluting versus bare-metal stent implantation in patients with ST-segment elevation myocardial infarction. J Am Coll Cardiol 2009;54(20):1900-1. 45. Goy JJ, Stauffer JC, Siegenthaler M, Benoit A, Seydoux C. A prospective randomized comparison between paclitaxel and sirolimus stents in the real world of interventional cardiology: the TAXi trial. J Am Coll Cardiol 2005;45(2):308-11. 46. Berger A, Stauffer JC, Seydoux C, Siegenthaler M, Benoit A, Goy JJ. Three-year follow-up of the first prospective randomized comparison between paclitaxel and sirolimus stents: the TAXi-LATE trial. Catheter Cardiovasc Interv 2007;70(2):163-6. 47. Stone GW, Ellis SG, Cannon L, Mann JT, Greenberg JD, Spriggs D, O'Shaughnessy CD, DeMaio S, Hall P, Popma JJ, Koglin J, Russell ME, Investigators TV. Comparison of a polymer-based paclitaxel-eluting stent with a bare metal stent in patients with complex coronary artery disease: a randomized controlled trial. JAMA 2005;294(10):1215-23. 48. Dawkins KD, Grube E, Guagliumi G, Banning AP, Zmudka K, Colombo A, Thuesen L, Hauptman K, Marco J, Wijns W, Popma JJ, Koglin J, Russell ME, Investigators TV. Clinical efficacy of polymer-based paclitaxel-eluting stents in the treatment of complex, long coronary artery lesions from a multicenter, randomized trial: support for the use of drug-eluting stents in contemporary clinical practice. Circulation 2005;112(21):3306-13. 49. Grube E, Dawkins KD, Guagliumi G, Banning AP, Zmudka K, Colombo A, Thuesen L, Hauptman K, Marco J, Wijns W, Popma JJ, Buellesfeld L, Koglin J, Russell ME. TAXUS VI 2-year follow-up: randomized comparison of polymer-based paclitaxel-eluting with bare metal stents for treatment of long, complex lesions. Eur Heart J 2007;28(21):2578-82. 50. Dawkins KD. Long-Term Outcomes in Complex Patients Treated with the TAXUS Moderated Release Stent: TAXUS IV Three Year Clinical Results. 51. Grube E, Dawkins KD, Guagliumi G, Banning AP, Zmudka K, Thuesen L, Hauptmann KE, Marco J, Wijns W, Koglin J. Long-Term Outcomes in Complex Patients Treated with the TAXUS Moderated Release Stent: TAXUS IV 4-Year. http://www.crtonline.org/flash.aspx?PAGE_ID=4464. 52. Grube E, Dawkins KD, Guagliumi G, Banning A, Zmudka K, Colombo A, Thuesen L, Hauptman K, Marco J, Wijns W, Joshi A, Mascioli S. TAXUS VI final 5-year results: a multicentre, randomised trial comparing polymer-based moderate-release paclitaxel-eluting stent with a bare metal stent for treatment of long, complex coronary artery lesions. EuroIntervention 2009;4(5). 53. Červinka P, Costa MA, Angiolillo DJ, Špaček R, Bystroň M, Kvašňák M, Veselka J, Nanda H, Futamatsu H, Futamatsu K. “Head-to-head comparison between sirolimus-eluting and paclitaxel-eluting stents in patients with complex coronary artery disease: An intravascular ultrasound study”. Catheterization and Cardiovascular Interventions 2006;67(6):846-851. 54. Fajadet J, Wijns W, Laarman GJ, Kuck KH, Ormiston J, Munzel T, Popma JJ, Fitzgerald PJ, Bonan R, Kuntz RE, Investigators EI. Randomized, double-blind, multicenter study of the Endeavor zotarolimus-eluting phosphorylcholine-encapsulated stent for treatment of native coronary artery lesions: clinical and angiographic results of the ENDEAVOR II trial. Circulation 2006;114(8):798-806. 55. Meredith I. ENDEAVOR Clinical Program Update. http://www.crtonline.org/flash.aspx?PAGE_ID=1953. 56. Zeiher A. ENDEAVOR I & II Update. http://www.crtonline.org/flash.aspx?PAGE_ID=4454. 57. Fajadet J. ENDEAVOR Clinical Program Update. http://www.crtonline.org/flash.aspx?PAGE_ID=5360. 58. Fajadet J, Wijns W, Laarman G-J, Kuck K-H, Ormiston JA, Baldus S, Hauptmann K-E, Suttorp M, Drzewiecki J, Pieper M, Schultheiss H-P, Mauri L. Long-term follow-up of the randomised controlled trial to evaluate the safety and efficacy of the zotarolimus-eluting driver coronary stent in de novo native coronary artery lesions: five year outcomes in the ENDEAVOR II study. EuroIntervention 2010;6(5):562-567. 59. Kandzari DE, Leon MB, Popma JJ, Fitzgerald PJ, O'Shaughnessy C, Ball MW, Turco M, Applegate RJ, Gurbel PA, Midei MG, Badre SS, Mauri L, Thompson KP, LeNarz LA, Kuntz RE, Investigators EI. Comparison of zotarolimus-eluting and sirolimus-eluting stents in patients with native coronary artery disease: a randomized controlled trial. J Am Coll Cardiol 2006;48(12):2440-7. 60. Eisenstein EL, Leon MB, Kandzari DE, Mauri L, Edwards R, Kong DF, Cowper PA, Anstrom KJ, Investigators EI. Long-term clinical and economic analysis of the Endeavor zotarolimus-eluting stent versus the cypher sirolimus-eluting stent: 3-year results from the ENDEAVOR III trial (Randomized Controlled Trial of the Medtronic Endeavor Drug [ABT-578] Eluting Coronary Stent System Versus the Cypher Sirolimus-Eluting Coronary Stent System in De Novo Native Coronary Artery Lesions). JACC Cardiovasc Interv 2009;2(12):1199-207. 61. Kandzari DE, Mauri L, Popma JJ, Turco MA, Gurbel PA, Fitzgerald PJ, Leon MB. Late-term clinical outcomes with zotarolimus- and sirolimus-eluting stents. 5-year follow-up of the ENDEAVOR III (A Randomized Controlled Trial of the Medtronic Endeavor Drug [ABT-578] Eluting Coronary Stent System Versus the Cypher Sirolimus-Eluting Coronary Stent System in De Novo Native Coronary Artery Lesions). JACC Cardiovasc Interv 2011;4(5):543-50. 62. Tierala I, Syvänne M, Kupari M. Comparison of Paclitaxel-Eluting with Bare Metal Stents in Acute Myocardial Infarction: The HAAMU-STENT-study. http://www.tctmd.com/show.aspx?id=56036. 63. Kalesan B, Pilgrim T, Heinimann K, Raber L, Stefanini GG, Valgimigli M, da Costa BR, Mach F, Luscher TF, Meier B, Windecker S, Juni P. Comparison of drug-eluting stents with bare metal stents in patients with ST-segment elevation myocardial infarction. Eur Heart J 2012;33(8):977-87. 64. Mehilli J, Dibra A, Kastrati A, Pache J, Dirschinger J, Schomig A, Intracoronary Drug-Eluting Stenting to Abrogate Restenosis in Small Arteries Study I. Randomized trial of paclitaxel- and sirolimus-eluting stents in small coronary vessels. Eur Heart J 2006;27(3):260-6. 65. Kim YH, Park SW, Lee SW, Park DW, Yun SC, Lee CW, Hong MK, Kim HS, Ko JK, Park JH, Lee JH, Choi SW, Seong IW, Cho YH, Lee NH, Kim JH, Chun KJ, Park SJ, Long DESIISI. Sirolimus-eluting stent versus paclitaxel-eluting stent for patients with long coronary artery disease. Circulation 2006;114(20):2148-53. 66. Pasceri V, Granatelli A, Pristipino C, Pelliccia F, Speciale G, Pironi B, Roncell A, Richichi G. A Randomized Trial of a Rapamycin-Eluting Stent in Acute Myocardial Infarction: Preliminary Results. The American Journal of Cardiology 2003;92(6, Supplement 1):1-4. 67. Luca G, Valgimigli M, Spaulding C, Menichelli M, Rocca H-L, Hoeven B, Lorenzo E, Llera L-SD, Pasceri V, Pittl U, Percoco G, Violini R, Stone G. Short and long-term benefits of sirolimus-eluting stent in STsegment elevation myocardial infarction: a meta-analysis of randomized trials. Journal of Thrombosis and Thrombolysis 2009;28(2):200-210. 68. Laarman GJ, Suttorp MJ, Dirksen MT, van Heerebeek L, Kiemeneij F, Slagboom T, van der Wieken LR, Tijssen JG, Rensing BJ, Patterson M. Paclitaxel-eluting versus uncoated stents in primary percutaneous coronary intervention. N Engl J Med 2006;355(11):1105-13. 69. Dirksen MT, Vink MA, Suttorp MJ, Tijssen JG, Patterson MS, Slagboom T, Kiemeneij F, Laarman GJ, Paclitaxel-Eluting Stent versus Conventional S, in Myocardial Infarction with STSEi. Two year follow-up after primary PCI with a paclitaxel-eluting stent versus a bare-metal stent for acute ST-elevation myocardial infarction (the PASSION trial): a follow-up study. EuroIntervention 2008;4(1):64-70. 70. Vink MA, Dirksen MT, Suttorp MJ, Tijssen JG, van Etten J, Patterson MS, Slagboom T, Kiemeneij F, Laarman GJ. 5-year follow-up after primary percutaneous coronary intervention with a paclitaxel-eluting stent versus a bare-metal stent in acute ST-segment elevation myocardial infarction: a follow-up study of the PASSION (Paclitaxel-Eluting Versus Conventional Stent in Myocardial Infarction with ST-Segment Elevation) trial. JACC Cardiovasc Interv 2011;4(1):24-9. 71. Rahel BM, Laarman GJ, Suttorp MJ, investigators PIs. Primary stenting of occluded native coronary arteries II--rationale and design of the PRISON II study: a randomized comparison of bare metal stent implantation with sirolimus-eluting stent implantation for the treatment of chronic total coronary occlusions. Am Heart J 2005;149(3):e1-3. 72. Suttorp MJ, Laarman GJ, Rahel BM, Kelder JC, Bosschaert MA, Kiemeneij F, Ten Berg JM, Bal ET, Rensing BJ, Eefting FD, Mast EG. Primary Stenting of Totally Occluded Native Coronary Arteries II (PRISON II): a randomized comparison of bare metal stent implantation with sirolimus-eluting stent implantation for the treatment of total coronary occlusions. Circulation 2006;114(9):921-8. 73. Rahel BM, Laarman GJ, Kelder JC, Ten Berg JM, Suttorp MJ. Three-year clinical outcome after primary stenting of totally occluded native coronary arteries: a randomized comparison of bare-metal stent implantation with sirolimus-eluting stent implantation for the treatment of total coronary occlusions (Primary Stenting of Totally Occluded Native Coronary Arteries [PRISON] II study). Am Heart J 2009;157(1):149-55. 74. Van den Branden BJ, Rahel BM, Laarman GJ, Slagboom T, Kelder JC, Ten Berg JM, Suttorp MJ. Five-year clinical outcome after primary stenting of totally occluded native coronary arteries: a randomised comparison of bare metal stent implantation with sirolimus-eluting stent implantation for the treatment of total coronary occlusions (PRISON II study). EuroIntervention 2012;7(10):1189-96. 75. Morice MC, Colombo A, Meier B, Serruys P, Tamburino C, Guagliumi G, Sousa E, Stoll HP, Investigators RT. Sirolimus- vs paclitaxel-eluting stents in de novo coronary artery lesions: the REALITY trial: a randomized controlled trial. JAMA 2006;295(8):895-904. 76. Morice MC, Serruys PW, Colombo A, Meier B, Tamburino C, Guagliumi G, Sousa E, Mendiz O, Grube E. Prospective Randomized Multicenter Head-to-Head Comparison of the Sirolimus-Eluting Stent and the Paclitaxel-Eluting Stent: 2-Year Outcome of the REALITY Trial. http://www.crtonline.org/flash.aspx?PAGE_ID=3389. 77. Vermeersch P, Agostoni P, Verheye S, Van den Heuvel P, Convens C, Bruining N, Van den Branden F, Van Langenhove G. Randomized double-blind comparison of sirolimus-eluting stent versus bare-metal stent implantation in diseased saphenous vein grafts: six-month angiographic, intravascular ultrasound, and clinical follow-up of the RRISC Trial. J Am Coll Cardiol 2006;48(12):2423-31. 78. Vermeersch P, Agostoni P, Verheye S, Van den Heuvel P, Convens C, Van den Branden F, Van Langenhove G, Investigators DR. Increased late mortality after sirolimus-eluting stents versus bare-metal stents in diseased saphenous vein grafts: results from the randomized DELAYED RRISC Trial. J Am Coll Cardiol 2007;50(3):261-7. 79. Kelbaek H, Thuesen L, Helqvist S, Clemmensen P, Klovgaard L, Kaltoft A, Andersen B, Thuesen H, Engstrom T, Botker HE, Saunamaki K, Krusell LR, Jorgensen E, Hansen HH, Christiansen EH, Ravkilde J, Kober L, Kofoed KF, Terkelsen CJ, Lassen JF, Investigators D. Drug-eluting versus bare metal stents in patients with st-segment-elevation myocardial infarction: eight-month follow-up in the Drug Elution and Distal Protection in Acute Myocardial Infarction (DEDICATION) trial. Circulation 2008;118(11):1155-62. 80. Spaulding C, Henry P, Teiger E, Beatt K, Bramucci E, Carrie D, Slama MS, Merkely B, Erglis A, Margheri M, Varenne O, Cebrian A, Stoll HP, Snead DB, Bode C, Investigators T. Sirolimus-eluting versus uncoated stents in acute myocardial infarction. N Engl J Med 2006;355(11):1093-104. 81. Spaulding C, Teiger E, Commeau P, Varenne O, Bramucci E, Slama M, Beatt K, Tirouvanziam A, Polonski L, Stella PR, Clugston R, Fajadet J, de Boisgelin X, Bode C, Carrie D, Erglis A, Merkely B, Hosten S, Cebrian A, Wang P, Stoll HP, Henry P. Four-year follow-up of TYPHOON (trial to assess the use of the CYPHer sirolimus-eluting coronary stent in acute myocardial infarction treated with BallOON angioplasty). JACC Cardiovasc Interv 2011;4(1):14-23. 82. Diaz de la Llera LS, Ballesteros S, Nevado J, Fernandez M, Villa M, Sanchez A, Retegui G, Garcia D, Martinez A. Sirolimus-eluting stents compared with standard stents in the treatment of patients with primary angioplasty. Am Heart J 2007;154(1):164 e1-6. 83. Chan C, Zambahari R, Kaul U, Lau CP, Whitworth H, Cohen S, Buchbinder M, Investigators D. A randomized comparison of sirolimus-eluting versus bare metal stents in the treatment of diabetic patients with native coronary artery lesions: the DECODE study. Catheter Cardiovasc Interv 2008;72(5):591-600. 84. Erglis A, Narbute I, Kumsars I, Jegere S, Mintale I, Zakke I, Strazdins U, Saltups A. A randomized comparison of paclitaxel-eluting stents versus bare-metal stents for treatment of unprotected left main coronary artery stenosis. J Am Coll Cardiol 2007;50(6):491-7. 85. Narbute I, Jegere S, Kumsars I, Mintale I, Zakke I, Bumeistere K, Sondore D, Grave A, Erglis A. Are paclitaxel-eluting stents better in unprotected left main coronary artery disease? Three-year clinical and intravascular imaging results from a randomized study. Medicina (Kaunas) 2011;47(10):536-43. 86. Chevalier B, Serruys PW, Silber S, Garcia E, Suryapranata H, Hauptmann K, Wijns W, Schuler G, Fath-Ordoubadi F, Worthley S, Thuesen L, Meredith I, Bressers M, Nagai H, Paunovic D. Randomised comparison of Nobori, biolimus A9-eluting coronary stent with a Taxus(R), paclitaxel-eluting coronary stent in patients with stenosis in native coronary arteries: the Nobori 1 trial. EuroIntervention 2007;2(4):426-34. 87. Silber S. No Late and no Very Late Stent Thrombosis with a Drug-Eluting Stent of the Second Generation: 2 Years Results from the Randomized NOBORI-I trial. http://www.crtonline.org/flash.aspx?PAGE_ID=5903. 88. Ortolani P, Marzocchi A, Marrozzini C, Palmerini T, Saia F, Taglieri N, Aquilina M, Baldazzi F, Silenzi S, Cooke RM, Reggiani ML, Branzi A. Randomized comparative trial of a thin-strut bare metal cobaltchromium stent versus a sirolimus-eluting stent for coronary revascularization. Catheter Cardiovasc Interv 2007;69(6):790-8. 89. Pan M, Suarez de Lezo J, Medina A, Romero M, Delgado A, Segura J, Ojeda S, Mazuelos F, Hernandez E, Melian F, Pavlovic D, Esteban F, Herrador J. Drug-eluting stents for the treatment of bifurcation lesions: A randomized comparison between paclitaxel and sirolimus stents. American Heart Journal 2007;153(1):15.e1-15.e7. 90. Petronio AS, De Carlo M, Branchitta G, Papini B, Ciabatti N, Gistri R, Cortese B, Gherarducci G, Barsotti A. Randomized comparison of sirolimus and paclitaxel drug-eluting stents for long lesions in the left anterior descending artery: an intravascular ultrasound study. J Am Coll Cardiol 2007;49(5):539-46. 91. Baumgart D, Klauss V, Baer F, Hartmann F, Drexler H, Motz W, Klues H, Hofmann S, Volker W, Pfannebecker T, Stoll HP, Nickenig G, Investigators SS. One-year results of the SCORPIUS study: a German multicenter investigation on the effectiveness of sirolimus-eluting stents in diabetic patients. J Am Coll Cardiol 2007;50(17):1627-34. 92. Sinning JM, Baumgart D, Werner N, Klauss V, Baer FM, Hartmann F, Drexler H, Motz W, Klues H, Voelker W, Pfannebecker T, Stoll HP, Nickenig G, Study S. Five-year results of the Multicenter Randomized Controlled Open-Label Study of the CYPHER Sirolimus-Eluting Stent in the Treatment of Diabetic Patients with De Novo Native Coronary Artery Lesions (SCORPIUS) study: a German multicenter investigation on the effectiveness of sirolimus-eluting stents in diabetic patients. Am Heart J 2012;163(3):446-53, 453 e1. 93. Chechi T, Vittori G, Biondi Zoccai GG, Vecchio S, Falchetti E, Spaziani G, Baldereschi G, Giglioli C, Valente S, Margheri M. Single-center randomized evaluation of paclitaxel-eluting versus conventional stent in acute myocardial infarction (SELECTION). J Interv Cardiol 2007;20(4):282-91. 94. Menichelli M, Parma A, Pucci E, Fiorilli R, De Felice F, Nazzaro M, Giulivi A, Alborino D, Azzellino A, Violini R. Randomized trial of Sirolimus-Eluting Stent Versus Bare-Metal Stent in Acute Myocardial Infarction (SESAMI). J Am Coll Cardiol 2007;49(19):1924-30. 95. Violini R, Musto C, De Felice F, Nazzaro MS, Cifarelli A, Petitti T, Fiorilli R. Maintenance of longterm clinical benefit with sirolimus-eluting stents in patients with ST-segment elevation myocardial infarction 3year results of the SESAMI (sirolimus-eluting stent versus bare-metal stent in acute myocardial infarction) trial. J Am Coll Cardiol 2010;55(8):810-4. 96. Musto C, Fiorilli R, De Felice F, Patti G, Nazzaro MS, Scappaticci M, Bernardi L, Violini R. Longterm outcome of sirolimus-eluting vs bare-metal stent in the setting of acute myocardial infarction: 5-year results of the SESAMI trial. Int J Cardiol 2011. 97. Strozzi M, Ani D. (2007) Comparison of stent graft, sirolimus stent, and bare metal stent implanted in patients with acute coronary syndrome: clinical and angiographic follow-up. Croatian Medical Journal. 98. Lee SW, Park SW, Kim YH, Yun SC, Park DW, Lee CW, Hong MK, Rhee KS, Chae JK, Ko JK, Park JH, Lee JH, Choi SW, Jeong JO, Seong IW, Cho YH, Lee NH, Kim JH, Chun KJ, Kim HS, Park SJ. A randomized comparison of sirolimus- versus Paclitaxel-eluting stent implantation in patients with diabetes mellitus. J Am Coll Cardiol 2008;52(9):727-33. 99. Lee SW, Park SW, Kim YH, Yun SC, Park DW, Lee CW, Hong MK, Rhee KS, Chae JK, Ko JK, Park JH, Lee JH, Choi SW, Jeong JO, Seong IW, Cho YH, Lee NH, Kim JH, Chun KJ, Kim HS, Park SJ. A randomized comparison of sirolimus- versus paclitaxel-eluting stent implantation in patients with diabetes mellitus 2-year clinical outcomes of the DES-DIABETES trial. J Am Coll Cardiol 2009;53(9):812-3. 100. Lee SW, Park SW, Kim YH, Yun SC, Park DW, Lee CW, Kang SJ, Rhee KS, Chae JK, Ko JK, Park JH, Lee JH, Choi SW, Jeong JO, Seong IW, Cho YH, Lee NH, Kim JH, Chun KJ, Kim HS, Park SJ. A randomized comparison of sirolimus- versus paclitaxel-eluting stent implantation in patients with diabetes mellitus: 4-year clinical outcomes of DES-DIABETES (drug-eluting stent in patients with DIABETES mellitus) trial. JACC Cardiovasc Interv 2011;4(3):310-6. 101. Maresta A, Varani E, Balducelli M, Varbella F, Lettieri C, Uguccioni L, Sangiorgio P, Zoccai GB. Comparison of Effectiveness and Safety of Sirolimus-Eluting Stents Versus Bare-Metal Stents in Patients With Diabetes Mellitus (from the Italian Multicenter Randomized DESSERT Study). The American Journal of Cardiology 2008;101(11):1560-1566. 102. Kim MH, Hong SJ, Cha KS, Park HS, Chae SC, Hur SH, Gwon HC, Bae JH, Lim DS. Effect of Paclitaxel-eluting versus sirolimus-eluting stents on coronary restenosis in Korean diabetic patients. J Interv Cardiol 2008;21(3):225-31. 103. Hong SJ, Kim MH, Cha KS, Park HS, Chae SC, Hur SH, Gwon HC, Bae JH, Lim DS. Comparison of three-year clinical outcomes between sirolimus-versus paclitaxel-eluting stents in diabetic patients: prospective randomized multicenter trial. Catheter Cardiovasc Interv 2010;76(7):924-33. 104. Windecker S, Serruys PW, Wandel S, Buszman P, Trznadel S, Linke A, Lenk K, Ischinger T, Klauss V, Eberli F, Corti R, Wijns W, Morice MC, di Mario C, Davies S, van Geuns RJ, Eerdmans P, van Es GA, Meier B, Juni P. Biolimus-eluting stent with biodegradable polymer versus sirolimus-eluting stent with durable polymer for coronary revascularisation (LEADERS): a randomised non-inferiority trial. Lancet 2008;372(9644):1163-73. 105. Garg S, Wykrzykowska J, Serruys PW, de Vries T, Buszman P, Trznadel S, Linke A, Lenk K, Ischinger T, Klauss V, Eberli F, Corti R, Wijns W, Morice MC, di Mario C, Tyczynski P, van Geuns RJ, Eerdmans P, van Es GA, Meier B, Juni P, Windecker S. The outcome of bifurcation lesion stenting using a biolimus-eluting stent with a bio-degradable polymer compared to a sirolimus-eluting stent with a durable polymer. EuroIntervention 2011;6(8):928-35. 106. Klauss V, Serruys PW, Pilgrim T, Buszman P, Linke A, Ischinger T, Eberli F, Corti R, Wijns W, Morice MC, di Mario C, van Geuns RJ, van Es GA, Kalesan B, Wenaweser P, Juni P, Windecker S. 2-year clinical follow-up from the randomized comparison of biolimus-eluting stents with biodegradable polymer and sirolimus-eluting stents with durable polymer in routine clinical practice. JACC Cardiovasc Interv 2011;4(8):887-95. 107. Wykrzykowska J, Serruys P, Buszman P, Linke A, Ischinger T, Klauss V, Eberli F, Corti R, Wijns W, Morice MC, Di Mario C, Van Geuns RJ, Van Es GA, Juni P, Windecker S. The three year follow-up of the randomised "all-comers" trial of a biodegradable polymer biolimus-eluting stent versus permanent polymer sirolimus-eluting stent (LEADERS). EuroIntervention 2011;7(7):789-95. 108. Stefanini GG, Kalesan B, Serruys PW, Heg D, Buszman P, Linke A, Ischinger T, Klauss V, Eberli F, Wijns W, Morice MC, Di Mario C, Corti R, Antoni D, Sohn HY, Eerdmans P, van Es GA, Meier B, Windecker S, Juni P. Long-term clinical outcomes of biodegradable polymer biolimus-eluting stents versus durable polymer sirolimus-eluting stents in patients with coronary artery disease (LEADERS): 4 year follow-up of a randomised non-inferiority trial. Lancet 2011;378(9807):1940-8. 109. Serruys P. LEADERS 5-Year: A Prospective, Randomized Trial of Bioabsorbable Polymer-based Biolimus-Eluting vs. Sirolimus-Eluting Stents. http://www.tctmd.com/show.aspx?id=114397. 110. Li JJ, Qin XW, Yang XC, Li ZC, Zeng HS, Xu B, Gao Z, Wu YJ, Zhang X, Zhang CY. Randomized comparison of early inflammatory response after sirolimus-eluting stent vs bare metal stent implantation in native coronary lesions. Clin Chim Acta 2008;396(1-2):38-42. 111. van der Hoeven BL, Liem SS, Jukema JW, Suraphakdee N, Putter H, Dijkstra J, Atsma DE, Bootsma M, Zeppenfeld K, Oemrawsingh PV, van der Wall EE, Schalij MJ. Sirolimus-eluting stents versus bare-metal stents in patients with ST-segment elevation myocardial infarction: 9-month angiographic and intravascular ultrasound results and 12-month clinical outcome results from the MISSION! Intervention Study. J Am Coll Cardiol 2008;51(6):618-26. 112. Atary JZ, van der Hoeven BL, Liem SS, Jukema JW, van der Bom JG, Atsma DE, Bootsma M, Zeppenfeld K, van der Wall EE, Schalij MJ. Three-year outcome of sirolimus-eluting versus bare-metal stents for the treatment of ST-segment elevation myocardial infarction (from the MISSION! Intervention Study). Am J Cardiol 2010;106(1):4-12. 113. Boden H, van der Hoeven BL, Liem SS, Atary JZ, Cannegieter SC, Atsma DE, Bootsma M, Jukema JW, Zeppenfeld K, Oemrawsingh PV, van der Wall EE, Schalij MJ. Five-year clinical follow-up from the MISSION! Intervention Study: sirolimus-eluting stent versus bare metal stent implantation in patients with STsegment elevation myocardial infarction, a randomised controlled trial. EuroIntervention 2012;7(9):1021-9. 114. Valgimigli M, Campo G, Percoco G, Bolognese L, Vassanelli C, Colangelo S, de Cesare N, Rodriguez AE, Ferrario M, Moreno R, Piva T, Sheiban I, Pasquetto G, Prati F, Nazzaro MS, Parrinello G, Ferrari R, Multicentre Evaluation of Single High-Dose Bolus Tirofiban vs Abciximab With Sirolimus-Eluting Stent or Bare Metal Stent in Acute Myocardial Infarction Study I. Comparison of angioplasty with infusion of tirofiban or abciximab and with implantation of sirolimus-eluting or uncoated stents for acute myocardial infarction: the MULTISTRATEGY randomized trial. JAMA 2008;299(15):1788-99. 115. Valgimigli M, Campo G, Gambetti S, Bolognese L, Ribichini F, Colangelo S, de Cesare N, Rodriguez AE, Russo F, Moreno R, Piva T, Sheiban I, Penzo C, Prati F, Nazzaro MS, Diaz Fernandez JF, Vassanelli C, Parrinello G, Ferrari R, For the MeoSh-dbTvAwsesoBMSiAMIsi. Three-year follow-up of the MULTIcentre evaluation of Single high-dose Bolus TiRofiban versus Abciximab with Sirolimus-eluting STEnt or Bare-Metal Stent in Acute Myocardial Infarction StudY (MULTISTRATEGY). Int J Cardiol 2011. 116. Valgimigli M, Bolognese L, Anselmi M, Campo G, Rodriguez AE, de Cesare N, Cohen DJ, Sheiban I, Colangelo S, Pasquetto G, Hamon M, Vranckx P, Ferrario M, Prati F, Agostoni P, Malagutti P, Arcozzi C, Parrinello G, Vassanelli C, Ferrari R, Percoco G. Two-by-two factorial comparison of high-bolus-dose tirofiban followed by standard infusion versus abciximab and sirolimus-eluting versus bare-metal stent implantation in patients with acute myocardial infarction: design and rationale for the MULTI-STRATEGY trial. Am Heart J 2007;154(1):39-45. 117. Lee JH, Kim HS, Lee SW, Park JH, Choi SW, Jeong JO, Cho Y, Lee N, Rhee KS, Ko JK, Seong IW. Prospective randomized comparison of sirolimus- versus paclitaxel-eluting stents for the treatment of acute STelevation myocardial infarction: pROSIT trial. Catheter Cardiovasc Interv 2008;72(1):25-32. 118. Kim HS, Lee JH, Lee SW, Kim YH, Park JH, Choi SW, Jeong JO, Seong IW, Rhee KS, Ko JK, Jo SH, Choi YJ. Long-term safety and efficacy of sirolimus- vs. paclitaxel-eluting stent implantation for acute STelevation myocardial infarction: 3-year follow-up of the PROSIT trial. Int J Cardiol 2011;147(2):253-7. 119. Galloe AM, Thuesen L, Kelbaek H, Thayssen P, Rasmussen K, Hansen PR, Bligaard N, Saunamaki K, Junker A, Aaroe J, Abildgaard U, Ravkilde J, Engstrom T, Jensen JS, Andersen HR, Botker HE, Galatius S, Kristensen SD, Madsen JK, Krusell LR, Abildstrom SZ, Stephansen GB, Lassen JF, Investigators SOI. Comparison of paclitaxel- and sirolimus-eluting stents in everyday clinical practice: the SORT OUT II randomized trial. JAMA 2008;299(4):409-16. 120. Caixeta A, Lansky AJ, Serruys PW, Hermiller JB, Ruygrok P, Onuma Y, Gordon P, Yaqub M, MiquelHebert K, Veldhof S, Sood P, Su X, Jonnavithula L, Sudhir K, Stone GW, Spirit, II, Investigators III. Clinical follow-up 3 years after everolimus- and paclitaxel-eluting stents: a pooled analysis from the SPIRIT II (A Clinical Evaluation of the XIENCE V Everolimus Eluting Coronary Stent System in the Treatment of Patients With De Novo Native Coronary Artery Lesions) and SPIRIT III (A Clinical Evaluation of the Investigational Device XIENCE V Everolimus Eluting Coronary Stent System [EECSS] in the Treatment of Subjects With De Novo Native Coronary Artery Lesions) randomized trials. JACC Cardiovasc Interv 2010;3(12):1220-8. 121. Stone GW, Midei M, Newman W, Sanz M, Hermiller JB, Williams J, Farhat N, Mahaffey KW, Cutlip DE, Fitzgerald PJ, Sood P, Su X, Lansky AJ, Investigators SI. Comparison of an everolimus-eluting stent and a paclitaxel-eluting stent in patients with coronary artery disease: a randomized trial. JAMA 2008;299(16):190313. 122. Nikolsky E, Lansky AJ, Sudhir K, Doostzadeh J, Cutlip DE, Piana R, Su X, White R, Simonton CA, Stone GW. SPIRIT IV trial design: a large-scale randomized comparison of everolimus-eluting stents and paclitaxel-eluting stents in patients with coronary artery disease. Am Heart J 2009;158(4):520-526 e2. 123. Applegate RJ, Yaqub M, Hermiller JB, Sood P, Yu S, Doostzadeh J, Williams JE, Farhat N, Caputo R, Lansky AJ, Cutlip DE, Sudhir K, Stone GW. Long-term (three-year) safety and efficacy of everolimus-eluting stents compared to paclitaxel-eluting stents (from the SPIRIT III Trial). Am J Cardiol 2011;107(6):833-40. 124. Mehran R, Brodie B, Cox DA, Grines CL, Rutherford B, Bhatt DL, Dangas G, Feit F, Ohman EM, Parise H, Fahy M, Lansky AJ, Stone GW. The Harmonizing Outcomes with RevasculariZatiON and Stents in Acute Myocardial Infarction (HORIZONS-AMI) Trial: study design and rationale. Am Heart J 2008;156(1):4456. 125. Stone GW, Lansky AJ, Pocock SJ, Gersh BJ, Dangas G, Wong SC, Witzenbichler B, Guagliumi G, Peruga JZ, Brodie BR, Dudek D, Mockel M, Ochala A, Kellock A, Parise H, Mehran R, Investigators H-AT. Paclitaxel-eluting stents versus bare-metal stents in acute myocardial infarction. N Engl J Med 2009;360(19):1946-59. 126. Stone GW, Witzenbichler B, Guagliumi G, Peruga JZ, Brodie BR, Dudek D, Kornowski R, Hartmann F, Gersh BJ, Pocock SJ, Dangas G, Wong SC, Fahy M, Parise H, Mehran R, Investigators H-AT. Heparin plus a glycoprotein IIb/IIIa inhibitor versus bivalirudin monotherapy and paclitaxel-eluting stents versus bare-metal stents in acute myocardial infarction (HORIZONS-AMI): final 3-year results from a multicentre, randomised controlled trial. Lancet 2011;377(9784):2193-204. 127. Mehilli J, Kastrati A, Byrne RA, Bruskina O, Iijima R, Schulz S, Pache J, Seyfarth M, Massberg S, Laugwitz KL, Dirschinger J, Schomig A, Stenting L-MI, Angiographic Results: Drug-Eluting Stents for Unprotected Coronary Left Main Lesions Study I. Paclitaxel- versus sirolimus-eluting stents for unprotected left main coronary artery disease. J Am Coll Cardiol 2009;53(19):1760-8. 128. Byrne RA, Mehilli J, Iijima R, Schulz S, Pache J, Seyfarth M, Schomig A, Kastrati A. A polymer-free dual drug-eluting stent in patients with coronary artery disease: a randomized trial vs. polymer-based drugeluting stents. Eur Heart J 2009;30(8):923-31. 129. Byrne RA, Kastrati A, Tiroch K, Schulz S, Pache J, Pinieck S, Massberg S, Seyfarth M, Laugwitz KL, Birkmeier KA, Schomig A, Mehilli J, Investigators I-T-. 2-year clinical and angiographic outcomes from a randomized trial of polymer-free dual drug-eluting stents versus polymer-based Cypher and Endeavor [corrected] drug-eluting stents. J Am Coll Cardiol 2010;55(23):2536-43. 130. Byrne RA, Kastrati A, Kufner S, Massberg S, Birkmeier KA, Laugwitz K-L, Schulz S, Pache J, Fusaro M, Seyfarth M, Schömig A, Mehilli J. Randomized, non-inferiority trial of three limus agent-eluting stents with different polymer coatings: the Intracoronary Stenting and Angiographic Results: Test Efficacy of 3 Limus-Eluting Stents (ISAR-TEST-4) Trial. European Heart Journal 2009;30(20):2441-2449. 131. Byrne RA, Kastrati A, Massberg S, Wieczorek A, Laugwitz KL, Hadamitzky M, Schulz S, Pache J, Fusaro M, Hausleiter J, Schomig A, Mehilli J, Investigators I-T. Biodegradable polymer versus permanent polymer drug-eluting stents and everolimus- versus sirolimus-eluting stents in patients with coronary artery disease: 3-year outcomes from a randomized clinical trial. J Am Coll Cardiol 2011;58(13):1325-31. 132. Juwana YB, Suryapranata H, Ottervanger JP, De Luca G, van't Hof AW, Dambrink JH, de Boer MJ, Gosselink AT, Hoorntje JC. Comparison of rapamycin- and paclitaxel-eluting stents in patients undergoing primary percutaneous coronary intervention for ST-elevation myocardial infarction. Am J Cardiol 2009;104(2):205-9. 133. Li JJ, Yan HB, Xiang XP, Qin XW, Zhang CY. Comparison of changes in early inflammatory markers between sirolimus- and paclitaxel-eluting stent implantation. Cardiovasc Drugs Ther 2009;23(2):137-43. 134. Chevalier B, Silber S, Park SJ, Garcia E, Schuler G, Suryapranata H, Koolen J, Hauptmann KE, Wijns W, Morice MC, Carrie D, van Es GA, Nagai H, Detiege D, Paunovic D, Serruys PW, Investigators NC. Randomized comparison of the Nobori Biolimus A9-eluting coronary stent with the Taxus Liberte paclitaxeleluting coronary stent in patients with stenosis in native coronary arteries: the NOBORI 1 trial--Phase 2. Circ Cardiovasc Interv 2009;2(3):188-95. 135. Di Lorenzo E, De Luca G, Sauro R, Varricchio A, Capasso M, Lanzillo T, Manganelli F, Mariello C, Siano F, Pagliuca MR, Stanco G, Rosato G. The PASEO (PaclitAxel or Sirolimus-Eluting Stent Versus Bare Metal Stent in Primary Angioplasty) Randomized Trial. JACC: Cardiovascular Interventions 2009;2(6):515-523. 136. Di Lorenzo E, Sauro R, Varricchio A, Capasso M, Lanzillo T, Manganelli F, Mariello C, Siano F, Pagliuca MR, Stanco G, Rosato G, De Luca G. Benefits of drug-eluting stents as compared to bare metal stent in ST-segment elevation myocardial infarction: Four year results of the PaclitAxel or Sirolimus-Eluting stent vs bare metal stent in primary angiOplasty (PASEO) randomized trial. American Heart Journal 2009;158(4):e43e50. 137. Brilakis ES, Lichtenwalter C, de Lemos JA, Roesle M, Obel O, Haagen D, Saeed B, Gadiparthi C, Bissett JK, Sachdeva R, Voudris VV, Karyofillis P, Kar B, Rossen J, Fasseas P, Berger P, Banerjee S. A randomized controlled trial of a paclitaxel-eluting stent versus a similar bare-metal stent in saphenous vein graft lesions the SOS (Stenting of Saphenous Vein Grafts) trial. J Am Coll Cardiol 2009;53(11):919-28. 138. Brilakis ES, Lichtenwalter C, Abdel-karim AR, de Lemos JA, Obel O, Addo T, Roesle M, Haagen D, Rangan BV, Saeed B, Bissett JK, Sachdeva R, Voudris VV, Karyofillis P, Kar B, Rossen J, Fasseas P, Berger P, Banerjee S. Continued benefit from paclitaxel-eluting compared with bare-metal stent implantation in saphenous vein graft lesions during long-term follow-up of the SOS (Stenting of Saphenous Vein Grafts) trial. JACC Cardiovasc Interv 2011;4(2):176-82. 139. Claessen BE, Beijk MA, Legrand V, Ruzyllo W, Manari A, Varenne O, Suttorp MJ, Tijssen JG, Miquel-Hebert K, Veldhof S, Henriques JP, Serruys PW, Piek JJ. Two-year clinical, angiographic, and intravascular ultrasound follow-up of the XIENCE V everolimus-eluting stent in the treatment of patients with de novo native coronary artery lesions: the SPIRIT II trial. Circ Cardiovasc Interv 2009;2(4):339-47. 140. Garg S, Serruys P, Onuma Y, Dorange C, Veldhof S, Miquel-Hebert K, Sudhir K, Boland J, Huber K, Garcia E, te Riele JA, Investigators SI. 3-year clinical follow-up of the XIENCE V everolimus-eluting coronary stent system in the treatment of patients with de novo coronary artery lesions: the SPIRIT II trial (Clinical Evaluation of the Xience V Everolimus Eluting Coronary Stent System in the Treatment of Patients with de novo Native Coronary Artery Lesions). JACC Cardiovasc Interv 2009;2(12):1190-8. 141. Garg S, Serruys PW, Miquel-Hebert K, Investigators SI. Four-year clinical follow-up of the XIENCE V everolimus-eluting coronary stent system in the treatment of patients with de novo coronary artery lesions: the SPIRIT II trial. Catheter Cardiovasc Interv 2011;77(7):1012-7. 142. Onuma Y, Miquel-Hebert K, Serruys PW, Investigators SI. Five-year long-term clinical follow-up of the XIENCE V everolimus-eluting coronary stent system in the treatment of patients with de novo coronary artery disease: the SPIRIT II trial. EuroIntervention 2013;8(9):1047-51. 143. Lee CW, Park DW, Lee SH, Kim YH, Hong MK, Kim JJ, Park SW, Yun SC, Seong IW, Lee JH, Lee NH, Cho YH, Cheong SS, Lim DS, Yang JY, Lee SG, Kim KS, Yoon J, Jeong MH, Seung KB, Hong TJ, Park SJ, Investigators Z-A. Comparison of the efficacy and safety of zotarolimus-, sirolimus-, and paclitaxel-eluting stents in patients with ST-elevation myocardial infarction. Am J Cardiol 2009;104(10):1370-6. 144. Pfisterer M, Bertel O, Bonetti PO, Brunner-La Rocca HP, Eberli FR, Erne P, Galatius S, Hornig B, Kiowski W, Pachinger O, Pedrazzini G, Rickli H, De Servi S, Kaiser C. Drug-eluting or bare-metal stents for large coronary vessel stenting? The BASKET-PROVE (PROspective Validation Examination) trial: Study protocol and design. American Heart Journal 2008;155(4):609-614. 145. Kaiser C, Galatius S, Erne P, Eberli F, Alber H, Rickli H, Pedrazzini G, Hornig B, Bertel O, Bonetti P, De Servi S, Brunner-La Rocca HP, Ricard I, Pfisterer M, Group B-PS. Drug-eluting versus bare-metal stents in large coronary arteries. N Engl J Med 2010;363(24):2310-9. 146. Kedhi E, Joesoef KS, McFadden E, Wassing J, van Mieghem C, Goedhart D, Smits PC. Secondgeneration everolimus-eluting and paclitaxel-eluting stents in real-life practice (COMPARE): a randomised trial. Lancet 2010;375(9710):201-9. 147. Smits PC, Kedhi E, Royaards KJ, Joesoef KS, Wassing J, Rademaker-Havinga TA, McFadden E. 2year follow-up of a randomized controlled trial of everolimus- and paclitaxel-eluting stents for coronary revascularization in daily practice. COMPARE (Comparison of the everolimus eluting XIENCE-V stent with the paclitaxel eluting TAXUS LIBERTE stent in all-comers: a randomized open label trial). J Am Coll Cardiol 2011;58(1):11-8. 148. Leon MB, Mauri L, Popma JJ, Cutlip DE, Nikolsky E, O'Shaughnessy C, Overlie PA, McLaurin BT, Solomon SL, Douglas JS, Jr., Ball MW, Caputo RP, Jain A, Tolleson TR, Reen BM, 3rd, Kirtane AJ, Fitzgerald PJ, Thompson K, Kandzari DE, Investigators EI. A randomized comparison of the ENDEAVOR zotarolimuseluting stent versus the TAXUS paclitaxel-eluting stent in de novo native coronary lesions 12-month outcomes from the ENDEAVOR IV trial. J Am Coll Cardiol 2010;55(6):543-54. 149. Leon MB, Kandzari DE, Eisenstein EL, Anstrom KJ, Mauri L, Cutlip DE, Nikolsky E, O'Shaughnessy C, Overlie PA, Kirtane AJ, McLaurin BT, Solomon SL, Douglas Jr JS, Popma JJ. Late Safety, Efficacy, and Cost-Effectiveness of a Zotarolimus-Eluting Stent Compared With a Paclitaxel-Eluting Stent in Patients With De Novo Coronary Lesions: 2-Year Follow-Up From the ENDEAVOR IV Trial (Randomized, Controlled Trial of the Medtronic Endeavor Drug [ABT-578] Eluting Coronary Stent System Versus the Taxus Paclitaxel-Eluting Coronary Stent System in De Novo Native Coronary Artery Lesions). JACC: Cardiovascular Interventions 2009;2(12):1208-1218. 150. Leon MB, Nikolsky E, Cutlip DE, Mauri L, Liberman H, Wilson H, Patterson J, Moses J, Kandzari DE. Improved Late Clinical Safety With Zotarolimus-Eluting Stents Compared With Paclitaxel-Eluting Stents in Patients With De Novo Coronary Lesions: 3-Year Follow-Up From the ENDEAVOR IV (Randomized Comparison of Zotarolimus- and Paclitaxel-Eluting Stents in Patients With Coronary Artery Disease) Trial. JACC: Cardiovascular Interventions 2010;3(10):1043-1050. 151. Rubartelli P, Petronio AS, Guiducci V, Sganzerla P, Bolognese L, Galli M, Sheiban I, Chirillo F, Ramondo A, Bellotti S, Gruppo Italiano di Studio sullo Stent nelle Occlusioni Coronariche IIGI. Comparison of sirolimus-eluting and bare metal stent for treatment of patients with total coronary occlusions: results of the GISSOC II-GISE multicentre randomized trial. Eur Heart J 2010;31(16):2014-20. 152. Sanchez PL, Gimeno F, Ancillo P, Sanz JJ, Alonso-Briales JH, Bosa F, Santos I, Sanchis J, Bethencourt A, Lopez-Messa J, de Prado AP, Alonso JJ, San Roman JA, Fernandez-Aviles F. Role of the paclitaxel-eluting stent and tirofiban in patients with ST-elevation myocardial infarction undergoing postfibrinolysis angioplasty: the GRACIA-3 randomized clinical trial. Circ Cardiovasc Interv 2010;3(4):297307. 153. Mehilli J, Byrne RA, Tiroch K, Pinieck S, Schulz S, Kufner S, Massberg S, Laugwitz KL, Schomig A, Kastrati A, Investigators I-D. Randomized trial of paclitaxel- versus sirolimus-eluting stents for treatment of coronary restenosis in sirolimus-eluting stents: the ISAR-DESIRE 2 (Intracoronary Stenting and Angiographic Results: Drug Eluting Stents for In-Stent Restenosis 2) study. J Am Coll Cardiol 2010;55(24):2710-6. 154. Guagliumi G, Sirbu V, Bezerra H, Biondi-Zoccai G, Fiocca L, Musumeci G, Matiashvili A, Lortkipanidze N, Tahara S, Valsecchi O, Costa M. Strut coverage and vessel wall response to zotarolimuseluting and bare-metal stents implanted in patients with ST-segment elevation myocardial infarction: the OCTAMI (Optical Coherence Tomography in Acute Myocardial Infarction) Study. JACC Cardiovasc Interv 2010;3(6):680-7. 155. Serruys PW, Silber S, Garg S, van Geuns RJ, Richardt G, Buszman PE, Kelbaek H, van Boven AJ, Hofma SH, Linke A, Klauss V, Wijns W, Macaya C, Garot P, DiMario C, Manoharan G, Kornowski R, Ischinger T, Bartorelli A, Ronden J, Bressers M, Gobbens P, Negoita M, van Leeuwen F, Windecker S. Comparison of zotarolimus-eluting and everolimus-eluting coronary stents. N Engl J Med 2010;363(2):136-46. 156. Silber S, Windecker S, Vranckx P, Serruys PW, investigators RAC. Unrestricted randomised use of two new generation drug-eluting coronary stents: 2-year patient-related versus stent-related outcomes from the RESOLUTE All Comers trial. Lancet 2011;377(9773):1241-7. 157. Rasmussen K, Maeng M, Kaltoft A, Thayssen P, Kelbaek H, Tilsted HH, Abildgaard U, Christiansen EH, Engstrom T, Krusell LR, Ravkilde J, Hansen PR, Hansen KN, Abildstrom SZ, Aaroe J, Jensen JS, Kristensen SD, Botker HE, Madsen M, Johnsen SP, Jensen LO, Sorensen HT, Thuesen L, Lassen JF, group SOIs. Efficacy and safety of zotarolimus-eluting and sirolimus-eluting coronary stents in routine clinical care (SORT OUT III): a randomised controlled superiority trial. Lancet 2010;375(9720):1090-9. 158. Maeng M, Tilsted HH, Jensen LO, Kaltoft A, Kelbaek H, Abildgaard U, Villadsen AB, Krusell LR, Ravkilde J, Hansen KN, Christiansen EH, Aaroe J, Jensen JS, Kristensen SD, Botker HE, Madsen M, Thayssen P, Sorensen HT, Thuesen L, Lassen JF. 3-Year clinical outcomes in the randomized SORT OUT III superiority trial comparing zotarolimus- and sirolimus-eluting coronary stents. JACC Cardiovasc Interv 2012;5(8):812-8. 159. Stone GW, Rizvi A, Newman W, Mastali K, Wang JC, Caputo R, Doostzadeh J, Cao S, Simonton CA, Sudhir K, Lansky AJ, Cutlip DE, Kereiakes DJ, Investigators SI. Everolimus-eluting versus paclitaxel-eluting stents in coronary artery disease. N Engl J Med 2010;362(18):1663-74. 160. Stone GW, Rizvi A, Sudhir K, Newman W, Applegate RJ, Cannon LA, Maddux JT, Cutlip DE, Simonton CA, Sood P, Kereiakes DJ, Investigators SI. Randomized comparison of everolimus- and paclitaxeleluting stents. 2-year follow-up from the SPIRIT (Clinical Evaluation of the XIENCE V Everolimus Eluting Coronary Stent System) IV trial. J Am Coll Cardiol 2011;58(1):19-25. 161. Park DW, Kim YH, Yun SC, Kang SJ, Lee SW, Lee CW, Park SW, Seong IW, Lee JH, Tahk SJ, Jeong MH, Jang Y, Cheong SS, Yang JY, Lim DS, Seung KB, Chae JK, Hur SH, Lee SG, Yoon J, Lee NH, Choi YJ, Kim HS, Kim KS, Kim HS, Hong TJ, Park HS, Park SJ. Comparison of zotarolimus-eluting stents with sirolimus- and paclitaxel-eluting stents for coronary revascularization: the ZEST (comparison of the efficacy and safety of zotarolimus-eluting stent with sirolimus-eluting and paclitaxel-eluting stent for coronary lesions) randomized trial. J Am Coll Cardiol 2010;56(15):1187-95. 162. Jang SJ, Park DW, Kim WJ, Kim YH, Yun SC, Kang SJ, Lee SW, Lee CW, Park SW, Park SJ. Differential long-term outcomes of zotarolimus-eluting stents compared with sirolimus-eluting and paclitaxeleluting stents in diabetic and non-diabetic patients: 2-year subgroup analysis of the ZEST randomized trial. Catheter Cardiovasc Interv 2012. 163. Kim WJ, Lee SW, Park SW, Kim YH, Yun SC, Lee JY, Park DW, Kang SJ, Lee CW, Lee JH, Choi SW, Seong IW, Lee BK, Lee NH, Cho YH, Shin WY, Lee SJ, Lee SW, Hyon MS, Bang DW, Park WJ, Kim HS, Chae JK, Lee K, Park HK, Park CB, Lee SG, Kim MK, Park KH, Choi YJ, Cheong SS, Yang TH, Jang JS, Her SH, Park SJ, Investigators E-DS. Randomized comparison of everolimus-eluting stent versus sirolimus-eluting stent implantation for de novo coronary artery disease in patients with diabetes mellitus (ESSENCEDIABETES): results from the ESSENCE-DIABETES trial. Circulation 2011;124(8):886-92. 164. Park KW, Yoon JH, Kim JS, Hahn JY, Cho YS, Chae IH, Gwon HC, Ahn T, Oh BH, Park JE, Shim WH, Shin EK, Jang YS, Kim HS. Efficacy of Xience/promus versus Cypher in rEducing Late Loss after stENTing (EXCELLENT) trial: study design and rationale of a Korean multicenter prospective randomized trial. Am Heart J 2009;157(5):811-817 e1. 165. Park KW, Chae IH, Lim DS, Han KR, Yang HM, Lee HY, Kang HJ, Koo BK, Ahn T, Yoon JH, Jeong MH, Hong TJ, Chung WY, Jo SH, Choi YJ, Hur SH, Kwon HM, Jeon DW, Kim BO, Park SH, Lee NH, Jeon HK, Gwon HC, Jang YS, Kim HS. Everolimus-eluting versus sirolimus-eluting stents in patients undergoing percutaneous coronary intervention: the EXCELLENT (Efficacy of Xience/Promus Versus Cypher to Reduce Late Loss After Stenting) randomized trial. J Am Coll Cardiol 2011;58(18):1844-54. 166. Fukumoto A, Otsuji S, Takiuchi S, Ikushima M, Asano K, Terasoma K, Hasegawa K, Yabuki M, Higashino Y. Comparison of real-world clinical outcomes between Cypher- and Taxus-eluting stents: the GARA–GARA study. Cardiovascular Intervention and Therapeutics 2011;26(3):202-208. 167. Kang WC, Ahn T, Lee K, Han SH, Shin EK, Jeong MH, Yoon JH, Park JS, Bae JH, Hur SH, Rha SW, Oh SK, Kim DI, Jang Y, Choi JW, Kim BO. Comparison of zotarolimus-eluting stents versus sirolimus-eluting stents versus paclitaxel-eluting stents for primary percutaneous coronary intervention in patients with STelevation myocardial infarction: results from the Korean Multicentre Endeavor (KOMER) acute myocardial infarction (AMI) trial. EuroIntervention 2011;7(8):936-43. 168. Park DW, Kim YH, Song HG, Ahn JM, Kim WJ, Lee JY, Kang SJ, Lee SW, Lee CW, Park SW, Yun SC, Seung KB, Yang TH, Lee SG, Lee JH, Seong IW, Cheong SS, Lee BK, Lee NH, Lee SW, Lee SW, Lee K, Kim HS, Jeon DS, Kim MK, Nah DY, Tahk SJ, Park SJ. Comparison of everolimus- and sirolimus-eluting stents in patients with long coronary artery lesions: a randomized LONG-DES-III (Percutaneous Treatment of LONG Native Coronary Lesions With Drug-Eluting Stent-III) Trial. JACC Cardiovasc Interv 2011;4(10):1096-103. 169. Briguori C, Airoldi F, Visconti G, Focaccio A, Caiazzo G, Golia B, Biondi-Zoccai G, Ricciardelli B, Condorelli G. Novel approaches for preventing or limiting events in diabetic patients (Naples-diabetes) trial: a randomized comparison of 3 drug-eluting stents in diabetic patients. Circ Cardiovasc Interv 2011;4(2):121-9. 170. Stone GW, Teirstein PS, Meredith IT, Farah B, Dubois CL, Feldman RL, Dens J, Hagiwara N, Allocco DJ, Dawkins KD, Investigators PT. A prospective, randomized evaluation of a novel everolimus-eluting coronary stent: the PLATINUM (a Prospective, Randomized, Multicenter Trial to Assess an Everolimus-Eluting Coronary Stent System [PROMUS Element] for the Treatment of Up to Two de Novo Coronary Artery Lesions) trial. J Am Coll Cardiol 2011;57(16):1700-8. 171. Kang KW, Ko YG, Shin DH, Kim JS, Kim BK, Choi D, Hong MK, Kang WC, Ahn T, Jeon DW, Yang JY, Jang Y. Impact of positive peri-stent vascular remodeling after sirolimus-eluting and paclitaxel-eluting stent implantation on 5-year clinical outcomes: intravascular ultrasound analysis from the Poststent Optimal Stent Expansion Trial multicenter randomized trial. Circ J 2012;76(5):1102-8. 172. Suttorp MJ, Laarman GJ. A randomized comparison of sirolimus-eluting stent implantation with zotarolimus-eluting stent implantation for the treatment of total coronary occlusions: Rationale and design of the PRImary Stenting of Occluded Native coronary arteries III (PRISON III) study. American Heart Journal 2007;154(3):432-435. 173. Branden BJVd, Koolen JJ, Henriques JP, Tijssen JG, Schaaf RJvd, Vermeersch PH, Suttorp MJ. A Randomized Comparison of Sirolimus-eluting Stent Implantation with Zotarolimus-eluting Stent Implantation for the Treatment of Total Coronary Occlusions: Primary Stenting of Totally Occluded Native Coronary Arteries III (PRISON III trial). http://www.crtonline.org/flash.aspx?PAGE_ID=8659. 174. Tanzilli G, Pelliccia F, Pasceri V, Speciale G, Greco C, Arrivi A, Viceconte N, Mangieri E, Gaudio C. Randomized study on provisional stenting with sirolimus-eluting stent vs. bare metal stent for the treatment of true coronary bifurcations: The PROSUMER (PROvisional with sirolimus-eluting vs. bare metal stents in truE bifuRcations) study. International Journal of Cardiology 2011;146(2):240-241. 175. Burzotta F, Trani C, Todaro D, Mariani L, Talarico GP, Tommasino A, Giammarinaro M, Niccoli G, Porto I, Leone AM, Mongiardo R, Mazzari MA, Schiavoni G, Crea F. Prospective randomized comparison of sirolimus- or everolimus-eluting stent to treat bifurcated lesions by provisional approach. JACC Cardiovasc Interv 2011;4(3):327-35. 176. Park HJ, Kim HY, Lee JM, Choi YS, Park CS, Kim DB, Her SH, Koh YS, Park MW, Kwon BJ, Kim PJ, Chang K, Chung WS, Seung KB. Randomized comparison of the efficacy and safety of zotarolimus-eluting stents vs. sirolimus-eluting stents for percutaneous coronary intervention in chronic total occlusion--CAtholic Total Occlusion Study (CATOS) trial. Circ J 2012;76(4):868-75. 177. Raber L, Kelbaek H, Ostoijc M, Baumbach A, Tuller D, von Birgelen C, Roffi M, Pedrazzini G, Kornowski R, Weber K, Heg D, Matter C, Luscher T, Taniwaki M, Meier B, Juni P, Windecker S. Comparison of biolimus eluted from an erodible stent coating with bare metal stents in acute ST-elevation myocardial infarction (COMFORTABLE AMI trial): rationale and design. EuroIntervention 2012;7(12):1435-43. 178. Raber L, Kelbaek H, Ostojic M, Baumbach A, Heg D, Tuller D, von Birgelen C, Roffi M, Moschovitis A, Khattab AA, Wenaweser P, Bonvini R, Pedrazzini G, Kornowski R, Weber K, Trelle S, Luscher TF, Taniwaki M, Matter CM, Meier B, Juni P, Windecker S, Investigators CAT. Effect of biolimus-eluting stents with biodegradable polymer vs bare-metal stents on cardiovascular events among patients with acute myocardial infarction: the COMFORTABLE AMI randomized trial. JAMA 2012;308(8):777-87. 179. Kim JS, Kim BK, Jang IK, Shin DH, Ko YG, Choi D, Hong MK, Cho YK, Nam CW, Hur SH, Choi JH, Song YB, Hahn JY, Choi SH, Gwon HC, Jang Y. ComparisOn of neointimal coVerage betwEen zotaRolimus-eluting stent and everolimus-eluting stent using Optical Coherence Tomography (COVER OCT). Am Heart J 2012;163(4):601-7. 180. Wijnbergen I, Helmes H, Tijssen J, Brueren G, Peels K, van Dantzig JM, Van' t Veer M, Koolen JJ, Pijls NH, Michels R. Comparison of drug-eluting and bare-metal stents for primary percutaneous coronary intervention with or without abciximab in ST-segment elevation myocardial infarction: DEBATER: the Eindhoven reperfusion study. JACC Cardiovasc Interv 2012;5(3):313-22. 181. Sabate M, Cequier A, Iniguez A, Serra A, Hernandez-Antolin R, Mainar V, Valgimigli M, Tespili M, den Heijer P, Bethencourt A, Vazquez N, Brugaletta S, Backx B, Serruys P. Rationale and design of the EXAMINATION trial: a randomised comparison between everolimus-eluting stents and cobalt-chromium baremetal stents in ST-elevation myocardial infarction. EuroIntervention 2011;7(8):977-84. 182. Sabate M, Cequier A, Iniguez A, Serra A, Hernandez-Antolin R, Mainar V, Valgimigli M, Tespili M, den Heijer P, Bethencourt A, Vazquez N, Gomez-Hospital JA, Baz JA, Martin-Yuste V, van Geuns RJ, Alfonso F, Bordes P, Tebaldi M, Masotti M, Silvestro A, Backx B, Brugaletta S, van Es GA, Serruys PW. Everolimuseluting stent versus bare-metal stent in ST-segment elevation myocardial infarction (EXAMINATION): 1 year results of a randomised controlled trial. Lancet 2012;380(9852):1482-90. 183. Mehilli J. Zotarolimus- vs. Everolimus-Eluting Stents for Treatment of Unprotected Left Main Coronary Artery Lesions : ISAR-LEFT MAIN 2 Randomized Trial. http://www.crtonline.org/flash.aspx?PAGE_ID=10316. 184. Ahn JM, Park DW, Kim YH, Song H, Cho YR, Kim WJ, Lee JY, Kang SJ, Lee SW, Lee CW, Park SW, Yun SC, Han S, Lee SY, Lee BK, Cho JH, Yang TH, Lee NH, Yang JY, Park JS, Shin WY, Kim MH, Bae JH, Kim MK, Yoon J, Park SJ. Comparison of resolute zotarolimus-eluting stents and sirolimus-eluting stents in patients with de novo long coronary artery lesions: a randomized LONG-DES IV trial. Circ Cardiovasc Interv 2012;5(5):633-40. 185. Kadota K, Muramatsu T, Iwabuchi M, Saito S, Hayashi Y, Ikari Y, Nanto S, Fujii K, Inoue N, Namiki A, Kimura T, Mitsudo K. Randomized comparison of the Nobori Biolimus A9-eluting stent with the sirolimuseluting stent in patients with stenosis in native coronary arteries. Catheter Cardiovasc Interv 2012;80(5):789-96. 186. Pan M, Medina A, Suarez de Lezo J, Romero M, Segura J, Martin P, Suarez de Lezo J, Hernandez E, Mazuelos F, Ojeda S. Randomized study comparing everolimus- and sirolimus-eluting stents in patients with bifurcation lesions treated by provisional side-branch stenting. Catheter Cardiovasc Interv 2012;80(7):1165-70. 187. Camenzind E, Wijns W, Mauri L, Boersma E, Parikh K, Kurowski V, Gao R, Bode C, Greenwood JP, Gershlick A, O'Neill W, Serruys PW, Jorissen B, Steg PG, Committee PS, Investigators. Rationale and design of the Patient Related OuTcomes with Endeavor versus Cypher stenting Trial (PROTECT): randomized controlled trial comparing the incidence of stent thrombosis and clinical events after sirolimus or zotarolimus drug-eluting stent implantation. Am Heart J 2009;158(6):902-909 e5. 188. Camenzind E, Wijns W, Mauri L, Kurowski V, Parikh K, Gao R, Bode C, Greenwood JP, Boersma E, Vranckx P, McFadden E, Serruys PW, O'Neil WW, Jorissen B, Van Leeuwen F, Steg PG, Committee PS, Investigators. Stent thrombosis and major clinical events at 3 years after zotarolimus-eluting or sirolimus-eluting coronary stent implantation: a randomised, multicentre, open-label, controlled trial. Lancet 2012;380(9851):1396-405. 189. Kimura T, Morimoto T, Natsuaki M, Shiomi H, Igarashi K, Kadota K, Tanabe K, Morino Y, Akasaka T, Takatsu Y, Nishikawa H, Yamamoto Y, Nakagawa Y, Hayashi Y, Iwabuchi M, Umeda H, Kawai K, Okada H, Kimura K, Simonton CA, Kozuma K, Investigators R. Comparison of everolimus-eluting and sirolimus-eluting coronary stents: 1-year outcomes from the Randomized Evaluation of Sirolimus-eluting Versus Everolimuseluting stent Trial (RESET). Circulation 2012;126(10):1225-36. 190. Sakakibara T, Ishii H, Toriyama T, Aoyama T, Takahashi H, Kamoi D, Kawamura Y, Kawashima K, Yoneda K, Amano T, Tanaka M, Yoshikawa D, Hayashi M, Matsubara T, Murohara T. Sirolimus-eluting stent vs. everolimus-eluting stent for coronary intervention in patients on chronic hemodialysis. Circ J 2012;76(2):351-5. 191. Chung WY, Kang J, Cho YS, Park HJ, Yang HM, Seo JB, Suh JW, Kim KI, Youn TJ, Kim SH, Chae IH, Zo JH, Kim MA, Choi DJ. A randomized, prospective, two-center comparison of sirolimus-eluting stent and zotarolimus-eluting stent in acute ST-elevation myocardial infarction: the SEZE trial. Chin Med J (Engl) 2012;125(19):3373-81. 192. Song H-G, Park D-W, Kim Y-H, Ahn J-M, Kim W-J, Lee J-Y, Kang S-J, Lee S-W, Lee CW, Park S-W, Han S, Seong I-W, Lee N-H, Lee B-K, Lee K, Lee S-W, Nah D-Y, Park S-J. Randomized Trial of Optimal Treatment Strategies for In-Stent Restenosis After Drug-Eluting Stent Implantation. Journal of the American College of Cardiology 2012;59(12):1093-1100. 193. Jensen LO, Thayssen P, Tilsted HH, Ravkilde J, Junker A, Hansen HS, Hansen KN, Pedersen KE, Sorensen HT, Thuesen L, Lassen JF, Scandinavian Organization for Randomized Trials with Clinical Outcome SOUTIVi. Rationale and design of a randomized clinical comparison of everolimus-eluting (Xience v/Promus) and sirolimus-eluting (cypher select+) coronary stents in unselected patients with coronary heart disease. Cardiology 2010;116(2):73-8. 194. Jensen LO, Thayssen P, Hansen HS, Christiansen EH, Tilsted HH, Krusell LR, Villadsen AB, Junker A, Hansen KN, Kaltoft A, Maeng M, Pedersen KE, Kristensen SD, Botker HE, Ravkilde J, Sanchez R, Aaroe J, Madsen M, Sorensen HT, Thuesen L, Lassen JF, Scandinavian Organization for Randomized Trials With Clinical Outcome IVI. Randomized comparison of everolimus-eluting and sirolimus-eluting stents in patients treated with percutaneous coronary intervention: the Scandinavian Organization for Randomized Trials with Clinical Outcome IV (SORT OUT IV). Circulation 2012;125(10):1246-55. 195. Jensen LO, Thayssen P, Christiansen EH, Tilsted HH, Maeng M, Hansen KN, Kaltoft A, Hansen HS, Botker HE, Krusell LR, Ravkilde J, Madsen M, Thuesen L, Lassen JF, Investigators SOI. 2-year patient-related versus stent-related outcomes: the SORT OUT IV (Scandinavian Organization for Randomized Trials With Clinical Outcome IV) Trial. J Am Coll Cardiol 2012;60(13):1140-7. 196. Grube E, Chevalier B, Guagliumi G, Smits PC, Stuteville M, Dorange C, Papeleu P, Kaul U, Dzavik V. The SPIRIT V diabetic study: a randomized clinical evaluation of the XIENCE V everolimus-eluting stent vs the TAXUS Liberte paclitaxel-eluting stent in diabetic patients with de novo coronary artery lesions. Am Heart J 2012;163(5):867-875 e1. 197. Basalus MWZ, Tandjung K, van Houwelingen KG, Stoel MG, de Man FHAF, Louwerenburg JW, Said SAM, Linssen GCM, Kleijne MAWJ, Van der Palen J, Huisman J, Verhorst PMJ, von Birgelen C. Twente study: The real-world endeavor resolute versus xience V drug-eluting stent study in twente: Study design, rationale and objectives. Netherlands Heart Journal 2010;18(7-8):360-364. 198. von Birgelen C, Basalus MW, Tandjung K, van Houwelingen KG, Stoel MG, Louwerenburg JH, Linssen GC, Said SA, Kleijne MA, Sen H, Lowik MM, van der Palen J, Verhorst PM, de Man FH. A randomized controlled trial in second-generation zotarolimus-eluting Resolute stents versus everolimus-eluting Xience V stents in real-world patients: the TWENTE trial. J Am Coll Cardiol 2012;59(15):1350-61. 199. von Birgelen C, Tandjung K, Sen H, Basalus M, Louwerenburg JH, Stoel M, van Houwelingen KG, Linssen G, Saïd S, Nienhuis M, Löwik M, van der Palen J, Verhorst P, de Man F. TCT-47 Two-Year Clinical Outcome of the TWENTE Trial, a Randomized Controlled Trial Comparing Second-Generation ZotarolimusEluting Resolute Stents Versus Everolimus-Eluting Xience V Stents in Real-World Patients. Journal of the American College of Cardiology 2012;60(17, Supplement):B15. 200. Hofma SH, Brouwer J, Velders MA, van't Hof AW, Smits PC, Quere M, de Vries CJ, van Boven AJ. Second-generation everolimus-eluting stents versus first-generation sirolimus-eluting stents in acute myocardial infarction. 1-year results of the randomized XAMI (XienceV Stent vs. Cypher Stent in Primary PCI for Acute Myocardial Infarction) trial. J Am Coll Cardiol 2012;60(5):381-7. 201. Belder Ad. A prospective randomized trial of everolimus-eluting stents vs bare metal stents in octogenarians: XIence or Vision for the Management of Angina in the elderly – The XIMA trial. http://www.crtonline.org/flash.aspx?PAGE_ID=10334. 202. Moreno R, Garcia E, Teles RC, Almeida MS, Carvalho HC, Sabate M, Martin-Reyes R, Rumoroso JR, Galeote G, Goicolea FJ, Moreu J, Mainar V, Mauri J, Ferreira R, Valdes M, Perez de Prado A, Martin-Yuste V, Jimenez-Valero S, Sanchez-Recalde A, Calvo L, Lopez de Sa E, Macaya C, Lopez-Sendon JL. A randomised comparison between everolimus-eluting stent and sirolimus-eluting stent in chronic coronary total occlusions. Rationale and design of the CIBELES (non-acute Coronary occlusion treated by EveroLimus-Eluting Stent) trial. EuroIntervention 2010;6(1):112-6. 203. Moreno R, Garcia E, Teles R, Rumoroso JR, Carvalho HC, Goicolea FJ, Moreu J, Mauri J, Sabate M, Mainar V, Patricio L, Valdes M, Fernandez Vazquez F, Sanchez-Recalde A, Galeote G, Jimenez-Valero S, Almeida M, de Sa EL, Calvo L, Plaza I, Lopez-Sendon JL, Martin JL, Investigators C. Randomized Comparison of Sirolimus-Eluting and Everolimus-Eluting Coronary Stents in the Treatment of Total Coronary Occlusions: Results From the Chronic Coronary Occlusion Treated by Everolimus-eluting Stent Randomized Trial. Circ Cardiovasc Interv 2013;6(1):21-8. 204. Smits PC, Hofma S, Togni M, Vazquez N, Valdes M, Voudris V, Slagboom T, Goy JJ, Vuillomenet A, Serra A, Nouche RT, den Heijer P, van der Ent M. Abluminal biodegradable polymer biolimus-eluting stent versus durable polymer everolimus-eluting stent (COMPARE II): a randomised, controlled, non-inferiority trial. Lancet 2013;381(9867):651-60. 205. Kim S, Kim JS, Shin DH, Kim BK, Ko YG, Choi D, Cho YK, Nam CW, Hur SH, Jang Y, Hong MK. Comparison of early strut coverage between zotarolimus- and everolimus-eluting stents using optical coherence tomography. Am J Cardiol 2013;111(1):1-5. 206. Park KW, Park BE, Kang SH, Park JJ, Lee SP, Cha KS, Rhew JY, Jeon HK, Shin ES, Oh JH, Jeong MH, Kim S, Hwang KK, Yoon JH, Lee SY, Park TH, Moon KW, Kwon HM, Chae IH, Kim HS. The 'Harmonizing Optimal Strategy for Treatment of coronary artery stenosis - sAfety & effectiveneSS of drugelUting stents & antiplatelet REgimen' (HOST-ASSURE) trial: Study protocol for a randomized controlled trial. Trials 2012;13. 207. Kim H-S, Park K-W, Kang S-H, Cha K-S, Park B-E, Rhew J-Y, Chae H-KJ-H. Randomized Comparison of PtCr-EES vs CoCr-ZES in All-Comers Receiving PCI: The HOST-ASSURE Randomized Trial. In; 2013, Presented in San Francisco ACC '13. 208. Natsuaki M, Kozuma K, Morimoto T, Kadota K, Muramatsu T, Nakagawa Y, Akasaka T, Igarashi K, Tanabe K, Morino Y, Ishikawa T, Nishikawa H, Awata M, Abe M, Okada H, Takatsu Y, Ogata N, Kimura K, Urasawa K, Tarutani Y, Shiode N, Kimura T. Biodegradable Polymer Biolimus-eluting Stent versus Durable Polymer Everolimus-eluting Stent: a randomized, controlled, non-inferiority trial. J Am Coll Cardiol 2013. 209. Christiansen EH, Jensen LO, Thayssen P, Tilsted H-H, Krusell LR, Hansen KN, Kaltoft A, Maeng M, Kristensen SD, Bøtker HE, Terkelsen CJ, Villadsen AB, Ravkilde J, Aarøe J, Madsen M, Thuesen L, Lassen JF. Biolimus-eluting biodegradable polymer-coated stent versus durable polymer-coated sirolimus-eluting stent in unselected patients receiving percutaneous coronary intervention (SORT OUT V): a randomised non-inferiority trial. The Lancet;381(9867):661-669.