Рабочая группа по реваскуляризации миокарда Европейского общества кардиологов (esc) и Европейской ассоциации кардиоторакальных хирургов (eActs) Разработаны с участием Европейской ассоциации по чрескожным сердечно-сосудистым вмешательствам (eApcI) Авторы/члены Рабочей группы: stephan Windecker* (Председатель esc) (Швейцария), philippe Kolh* (Председатель eActs) (Бельгия), Fernando Alfonso (Испания), Jean-philippe collet (Франция), Jochen cremer (Германия), Volkmar Falk (Швейцария), Gerasimos Filippatos (Греция), christian Hamm (Германия), stuart J. Head (Нидерланды), peter Jüni (Швейцария), A. pieter Kappetein (Нидерланды), Adnan Kastrati (Германия), Juhani Knuuti (Финляндия), Ulf Landmesser (Швейцария), Günther Laufer (Австрия), Franz-Josef Neumann (Германия), Dimitrios J. Richter (Греция), patrick schauerte (Германия), Miguel sousa Uva (Португалия), Giulio G. stefanini (Швейцария), David paul taggart (Соединённое Королевство), Lucia torracca (Италия), Marco Valgimigli (Италия), William Wijns (Бельгия), and Adam Witkowski (Польша). В подготовке данных рекомендаций приняли участие следующие подразделе-ния esc: Ассоциации esc: Ассоциация специалистов по острой сердечно-сосудистой помощи (Acute cardiovascular care Association; AccA), Европейская ассоциа-ция специалистов по методам визуализации сердечно-сосудистой системы (european Association of cardiovascular Imaging; eAcVI), Европейская ассоциа-ция специалистов по сердечно-сосудистой профилактике и реабилитации (european Association for cardiovascular prevention & Rehabilitation; eAcpR), Европейская ассоциация аритмологов (european Heart Rhythm Association; eHRA), Ассоциация специалистов по сердечной недостаточности (Heart Failure Association; HFA). КомитетРабочие группы esc: Сердечно-сосудистая клеточная электрофизиология, Магнитная резонансная томография сердечно-сосудистой системы, Сер-дечно-сосудистая фармакология и медикаментозная терапия, Сердечно-сосудистая хирургия, Коронарная патофизиология и микроциркуляция, Ядер-ная кардиология и КТ сердца, Периферическая циркуляция, Тромбоз, Коро-нарная болезнь сердца.Советы esc: Кардиологическая практика, Первичная сердечно-сосудистая помощь, Уход за сердечно-сосудистыми больными, Смежные профессии.Содержание данных рекомендаций, подготовленных Европейским Общест-вом Кардиологов (european society of cardiology, esc) опубликовано исклю-чительно для использования в личных и образовательных целях. Не допуска-ется коммерческое использование содержания рекомендаций. Рекомендации esc не могут быть переведены на другие языки либо воспроизведены, полно-стью или частично, без письменного согласия esc. Для получения данного согласия письменная заявка должна быть направлена в oxford University press -организацию, издающую european Heart Journal и официально упол-номоченную esc, рассматривать подобные заявки.Отказ от ответственности. Рекомендации esc отражают взгляды esc и осно-ваны на тщательном анализе научных данных, доступных во время подготовки данных рекомендаций. Медицинским работникам следует придер живаться данных реко...
BackgroundIt is still uncertain whether coronary bifurcations with lesions involving a large side branch (SB) should be treated by stenting the main vessel and provisional stenting of the SB (simple) or by routine two-stent techniques (complex). We aimed to compare clinical outcome after treatment of lesions in large bifurcations by simple or complex stent implantation.MethodsThe study was a randomised, superiority trial. Enrolment required a SB≥2.75 mm, ≥50% diameter stenosis in both vessels, and allowed SB lesion length up to 15 mm. The primary endpoint was a composite of cardiac death, non-procedural myocardial infarction and target lesion revascularisation at 6 months. Two-year clinical follow-up was included in this primary reporting due to lower than expected event rates.ResultsA total of 450 patients were assigned to simple stenting (n=221) or complex stenting (n=229) in 14 Nordic and Baltic centres. Two-year follow-up was available in 218 (98.6%) and 228 (99.5%) patients, respectively. The primary endpoint of major adverse cardiac events (MACE) at 6 months was 5.5% vs 2.2% (risk differences 3.2%, 95% CI −0.2 to 6.8, p=0.07) and at 2 years 12.9% vs 8.4% (HR 0.63, 95% CI 0.35 to 1.13, p=0.12) after simple versus complex treatment. In the subgroup treated by newer generation drug-eluting stents, MACE was 12.0% vs 5.6% (HR 0.45, 95% CI 0.17 to 1.17, p=0.10) after simple versus complex treatment.ConclusionIn the treatment of bifurcation lesions involving a large SB with ostial stenosis, routine two-stent techniques did not improve outcome significantly compared with treatment by the simpler main vessel stenting technique after 2 years.Trial registration numberNCT01496638.
BACKGROUND Guidelines recommend nonstatin lipid-lowering agents in patients at very high risk for major adverse cardiovascular events (MACE) if low-density lipoprotein cholesterol (LDL-C) remains ≥70 mg/dL on maximum tolerated statin treatment. It is uncertain if this approach benefits patients with LDL-C near 70 mg/dL. Lipoprotein(a) levels may influence residual risk. OBJECTIVES In a post hoc analysis of the ODYSSEY Outcomes (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab) trial, the authors evaluated the benefit of adding the proprotein subtilisin/kexin type 9 inhibitor alirocumab to optimized statin treatment in patients with LDL-C levels near 70 mg/dL. Effects were evaluated according to concurrent lipoprotein(a) levels. METHODS ODYSSEY Outcomes compared alirocumab with placebo in 18,924 patients with recent acute coronary syndromes receiving optimized statin treatment. In 4,351 patients (23.0%), screening or randomization LDL-C was <70 mg/dL (median 69.4 mg/dL; interquartile range: 64.3–74.0 mg/dL); in 14,573 patients (77.0%), both determinations were ≥70 mg/dL (median 94.0 mg/dL; interquartile range: 83.2–111.0 mg/dL). RESULTS In the lower LDL-C subgroup, MACE rates were 4.2 and 3.1 per 100 patient-years among placebo-treated patients with baseline lipoprotein(a) greater than or less than or equal to the median (13.7 mg/dL). Corresponding adjusted treatment hazard ratios were 0.68 (95% confidence interval [Cl]: 0.52–0.90) and 1.11 (95% Cl: 0.83–1.49), with treatment-lipoprotein(a) interaction on MACE ( P interaction = 0.017). In the higher LDL-C subgroup, MACE rates were 4.7 and 3.8 per 100 patient-years among placebo-treated patients with lipoprotein(a) >13.7 mg/dL or ≤13.7 mg/dL; corresponding adjusted treatment hazard ratios were 0.82 (95% Cl: 0.72–0.92) and 0.89 (95% Cl: 0.75–1.06), with P interaction = 0.43. CONCLUSIONS In patients with recent acute coronary syndromes and LDL-C near 70 mg/dL on optimized statin therapy, proprotein subtilisin/kexin type 9 inhibition provides incremental clinical benefit only when lipoprotein(a) concentration is at least mildly elevated. (ODYSSEY Outcomes: Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab; NCT01663402 )
We believe that centrally acting sympatholytic agent moxonidine is beneficial in the treatment of postmenopausal women with hypertension by reducing inflammatory cytokine TNFalpha without changing protective adiponectin level.
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