-
Je něco špatně v tomto záznamu ?
Effect of two-day atorvastatin pretreatment on long-term outcome of patients with stable angina pectoris undergoing elective percutaneous coronary intervention
J. Veselka, D. Zemánek, P. Hájek, M. Malý, R. Adlová, L. Martinkovičová, P. Tomašov, D. Tesař
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, randomizované kontrolované studie, práce podpořená grantem
- MeSH
- angina pectoris farmakoterapie terapie MeSH
- balónková koronární angioplastika MeSH
- dospělí MeSH
- kyseliny heptylové aplikace a dávkování MeSH
- lidé středního věku MeSH
- lidé MeSH
- pyrroly aplikace a dávkování MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- statiny aplikace a dávkování MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
Several randomized studies and meta-analyses have suggested that pretreatment with statins may decrease periprocedural myocardial infarction (MI) in patients undergoing percutaneous coronary intervention (PCI). The purpose of this randomized study was to investigate the effect of a 2-day atorvastatin therapy before PCI on long-term clinical outcome. Two hundred statin-naive patients with stable angina pectoris referred for PCI were enrolled and randomized (ratio 1:1) to 2-day pretreatment with atorvastatin 80 mg/day and subsequent PCI (atorvastatin group), or immediate PCI (control group). The registry group comprised 182 consecutive patients on long-term statin therapy referred for immediate PCI during the same period as randomized patients. We compared the first occurrence of MI or death during long-term follow-up. There were no significant differences in most clinical characteristics and early results among the 3 groups. Median follow-up was 45 months (1 to 59). Incidences of death/MI were 11.4%, 12.9%, and 13.8% in the atorvastatin, control, and registry groups, respectively. In the same groups, age-adjusted estimated 4-year freedom from death/MI was 0.78 versus 0.75 versus 0.80, respectively (p=0.882, log-rank test). In multivariate analysis, only age of patients (odds ratio 1.04, 95% confidence interval 1.02 to 1.07, p<0.001) was identified as a significant predictor of death or MI during follow-up. In conclusion, these results suggest that 2-day therapy with high-dose atorvastatin before PCI did not influence occurrence of periprocedural MI or long-term clinical outcomes.
Cardiology Department Cardiovascular Center University Hospital Motol Prague Czech Republic
Department of Antibody Engineering Genentech 1 DNA Way South San Francisco CA 94080 USA
Department of Cardiology University Hospital Motol 1st Medical Faculty Prague Czech Republic
Department of Cardiology University Hospital Motol Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12027037
- 003
- CZ-PrNML
- 005
- 20160502070511.0
- 007
- ta
- 008
- 120816s2011 xxu f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.amjcard.2010.12.040 $2 doi
- 035 __
- $a (PubMed)21349484
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Veselka, Josef, $d 1965- $7 pna2005261820 $u Department of Cardiology, Cardiovascular Center, University Hospital Motol, 2nd Medical School, Charles University, Prague, Czech Republic. veselka.josef@seznam.cz
- 245 10
- $a Effect of two-day atorvastatin pretreatment on long-term outcome of patients with stable angina pectoris undergoing elective percutaneous coronary intervention / $c J. Veselka, D. Zemánek, P. Hájek, M. Malý, R. Adlová, L. Martinkovičová, P. Tomašov, D. Tesař
- 520 9_
- $a Several randomized studies and meta-analyses have suggested that pretreatment with statins may decrease periprocedural myocardial infarction (MI) in patients undergoing percutaneous coronary intervention (PCI). The purpose of this randomized study was to investigate the effect of a 2-day atorvastatin therapy before PCI on long-term clinical outcome. Two hundred statin-naive patients with stable angina pectoris referred for PCI were enrolled and randomized (ratio 1:1) to 2-day pretreatment with atorvastatin 80 mg/day and subsequent PCI (atorvastatin group), or immediate PCI (control group). The registry group comprised 182 consecutive patients on long-term statin therapy referred for immediate PCI during the same period as randomized patients. We compared the first occurrence of MI or death during long-term follow-up. There were no significant differences in most clinical characteristics and early results among the 3 groups. Median follow-up was 45 months (1 to 59). Incidences of death/MI were 11.4%, 12.9%, and 13.8% in the atorvastatin, control, and registry groups, respectively. In the same groups, age-adjusted estimated 4-year freedom from death/MI was 0.78 versus 0.75 versus 0.80, respectively (p=0.882, log-rank test). In multivariate analysis, only age of patients (odds ratio 1.04, 95% confidence interval 1.02 to 1.07, p<0.001) was identified as a significant predictor of death or MI during follow-up. In conclusion, these results suggest that 2-day therapy with high-dose atorvastatin before PCI did not influence occurrence of periprocedural MI or long-term clinical outcomes.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a senioři nad 80 let $7 D000369
- 650 _2
- $a angina pectoris $x farmakoterapie $x terapie $7 D000787
- 650 _2
- $a balónková koronární angioplastika $7 D015906
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a kyseliny heptylové $x aplikace a dávkování $7 D006538
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a statiny $x aplikace a dávkování $7 D019161
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a pyrroly $x aplikace a dávkování $7 D011758
- 650 _2
- $a výsledek terapie $7 D016896
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a randomizované kontrolované studie $7 D016449
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Zemánek, David, $d 1972- $7 xx0079099 $u Department of Cardiology, University Hospital Motol, Prague, Czech Republic. zejada@seznam.cz
- 700 1_
- $a Hájek, Petr $7 xx0071248 $u Department of Cardiology, Charles University and University Hospital Motol, V Uvalu 84, Prague 5 150 06, Czech Republic. petr.hajek@fnmotol.cz
- 700 1_
- $a Malý, Martin, $d 1966- $7 mzk2004241073 $u Department of Cardiology, University Hospital Motol, 1st Medical Faculty, Prague, Czech Republic. martin.maly@fnmotol.cz
- 700 1_
- $a Adlová, Radka $7 xx0139523
- 700 1#
- $a Martinkovičová, Lucia. $7 _AN033108 $u Department of Cardiology, 2nd Medical School of Charles University and University Hospital Motol, Prague, Czech Republic
- 700 1#
- $a Tomašov, Pavol, $d 1982- $7 xx0243010 $u Cardiology Department, Cardiovascular Center, University Hospital Motol, Prague, Czech Republic
- 700 1_
- $a Tesař, David $7 xx0081874 $u Department of Antibody Engineering, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA
- 773 0_
- $w MED00000236 $t The American journal of cardiology $x 1879-1913 $g Roč. 107, č. 9 (2011), s. 1295-1299
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/21349484 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m $z 0
- 990 __
- $a 20120816 $b ABA008
- 991 __
- $a 20160502070614 $b ABA008
- 999 __
- $a ok $b bmc $g 949079 $s 784383
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 107 $c 9 $d 1295-1299 $e 20110223 $i 1879-1913 $m The American journal of cardiology $n Am J Cardiol $x MED00000236
- LZP __
- $b NLK122 $a Pubmed-20120816/11/02