In-hospital Outcome in Octogenarians with Acute Coronary Syndrome Undergoing Emergent Coronary Angiography
スポンサーリンク
概要
- 論文の詳細を見る
Very elderly patients have higher mortality rates than younger patients after acute coronary syndrome (ACS). However, the mechanism by which increasing age contributes to such mortality remains unclear. In addition, the efficacy and safety of invasive coronary procedures for octogenarians with ACS have not been well established. We compared the clinical characteristics and in-hospital outcome of 193 octogenarians (mean age, 83 years) with those of 1,462 younger patients (mean age, 64 years) with ACS who underwent emergent coronary angiography. Octogenarians included a greater number of females, had higher rates of cerebrovascular disease and multivessel disease, a higher Killip class, a higher Forrester class, and lower rates of smoking, diabetes, and hypercholesterolemia than the younger subjects. Interventions, including percutaneous transluminal coronary angioplasty (PTCA) and coronary artery bypass grafting (CABG), were performed less frequently in octogenarians than in younger patients (88.0% versus 90.8%). The procedural success rate in octogenarians did not differ from that in younger patients. However, the in-hospital mortality rate for the octogenarians was about three times higher than for the younger patients (19.2% versus 6.9%). Multivariate analysis revealed that the predictors of in-hospital mortality in the octogenarians were a higher Killip class and a higher Forrester class. Octogenarians with ACS had fewer coronary risk factors and a similar success rate for the intervention, but had more greatly impaired hemodynamics and higher in-hospital mortality than the younger patients. Therefore, impaired myocardial reserve may contribute to a large portion of in-hospital deaths in octogenarians with ACS.
- Japanese Heart Journal Associationの論文
著者
-
Terai Hidenobu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Ino Hidekazu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Hayashi Kenshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Hayashi Tatsumi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Shimizu Masami
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Yamaguchi Masato
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Sakata Kenji
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Inoue Masaru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Mabuchi Hiroshi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Inoue Masaru
石川県立中央病院 循環器内科
-
Ino Hidekazu
金沢大学 医学系研究科循環器内科
-
Kaneda Tomoya
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Kaneda Tomoya
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Oe Kotaro
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Kiyama Masaru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School
-
Shimizu Masami
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Terai Hidenobu
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Hayashi Tatsumi
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Kanazawa Universi
-
Oe Kotaro
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Mabuchi Hiroshi
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Yamaguchi Masato
Molecular Genetics Of Cardiovascular Disorders Division Of Cardiovascular Medicine Graduate School O
-
Kaneda Tomoya
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University
-
Hayashi Tatsumi
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University
-
Terai Hidenobu
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University
-
Yamaguchi Masato
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University
-
Kiyama Masaru
Molecular Genetics of Cardiovascular Disorders, Division of Cardiovascular Medicine, Graduate School of Medical Science, Kanazawa University
関連論文
- Impact of Severe Earthquake on the Occurrence of Acute Coronary Syndrome and Stroke in a Rural Area of Japan : Experience From the Noto Peninsula Earthquake
- Heterogeneity of Clinical Manifestation of Hypertrophic Cardiomyopathy Caused by Deletion of Lysine 183 in Cardiac Troponin I Gene : Insight From Two Autopsy Cases With an Identical Sarcomeric Gene Mutation
- OE-084 Impact of Gene Mutation Regions of HERG Channel, Pore or Nonpore, on Clinical Course of LQTS(Arrhythmia, basic-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- FRS-104 Association between Angiotensin II Receptor Gene Polymorphism and Left Ventricular Systolic Dysfunction in Sarcomere Gene Mutation-induced Hypertrophic Cardiomyopathy(Frontier of Cardiomyopathy Research-2 (M) FRS21,Featured Research Session (Engli
- Brown adipose tissue : Evaluation with ^Tl and ^Tc-sestamibi dual-tracer SPECT
- Left ventricular ejection and filling rate measurement based on the automatic edge detection method of ECG-gated blood pool single-photon emission tomography
- PJ-424 Cardiac Sympathetic Nerve Activity in Patients with Hypertrophic Cardiomyopathy Caused by Thin Filament Gene Mutations(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- PJ-349 The relation between regional myocardial 99m-Tc-MIBI retention increase and coronary flow reserve during coronary vasodilation in human(Nuclear Cardiology 10 (I) : PJ58)(Poster Session (Japanese))
- OJ-242 Feasibility of automatic right ventricular ejection fraction measurement with edge detection program of ECG-gated blood SPET : comparison with first-pass ventriculography(Nuclear Cardiology 6 (I) : OJ28)(Oral Presentation (Japanese))
- Discrepant uptake between fluorine-18 fluorodeoxy glucose and Tc-99m sestamibi in bronchioloalveolar cell carcinoma
- Left Ventricular Systolic and Diastolic Function Measured by ECG-Gated Blood Pool Single-Photon Emission Tomography
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- PJ-643 Prediction of Cardiac Events in Patients with Hypertrophic Cardiomyopathy : Usefulness of MIBG Myocardial Scintigraphy(Cardiomyopathy, basic/clinical-7 (M) PJ108,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- FRS-149 Mutation Site-Specific Differences in Arrhythmic Risk and Sensitivity to Sympathetic Stimulation in Japanese Families with Congenital LQT1 Syndrome(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- 5 Genotype- and Mutation site-Specific Differences in Arrhythmic Risk and Sensitivity to Sympathetic Stimulation in the Long QT Syndrome(APSC/JCS Joint Symposium (APSC) (H) : Emerging Issue in Cardiology for Asian)(Special Program)
- PJ-496 How Effective is Triple Site Pacing and Where is the Ideal Right Ventricular Pacing Site in the Cardiac Resynchronization Therapy?(PJ084,CRT (M),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- Marked Aortic Valve Stenosis Progression After Receiving Long-Term Aggressive Cholesterol-Lowering Therapy Using Low-Density Lipoprotein Apheresis in a Patient With Familial Hypercholesterolemia
- 4 Morphology and Histological Assessment of Vulnerable Plaque Accompanying No-reflow Phenomenon after Intervention in Acute Coronary Syndrome(Symposium 13 (SY-13) (I) Freshscent Forefront in Atherosclerotic Plaque Imagings,Special Program,The 72nd Annual
- PJ-341 Intravascular Ultrasound Virtual Histology Images and Pathological Analysis of Materials Captured by Filter Device in Patients With Acute Coronary Syndrome(Intravascular endoscopy/Intravascular ultrasound(06)(I),Poster Session(Japanese),The 72nd An
- Lispro is superior to regular insulin in transient intensive insulin therapy in type 2 diabetes
- 4 Morphologic Impacts of Angiography and Intravascular Ultrasound on Predicting Prognosis of Acute Coronary Syndrome : Unresolved Issue of No-reflow Phenomenon(New Risk Stratification for Cardiac Events after Acute Myocardial Infarction,Topic 1 (TP-1) (IH
- FRS-077 Genetic Analysis of KCR1 Gene in Japanese LQTS Patients(Arrhythmia (basic), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OE-223 The Long-Term Results for 1554 Bare Metal Stents : Do We Have to Choose Cypher Stent for Large & Short Lesions?(Coronary revascularization, PCI-2 (IHD) OE38,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese
- Abnormal sympathetic innervation of the heart in a patient with Emery-Dreifuss muscular dystrophy
- Differentiation between patients with takotsubo cardiomyopathy and those with anterior acute myocardial infarction
- PE-279 High Incidence of Sudden Cardiac Death with Conduction Disturbances and Atrial Cardiomyopathy Caused by a Mutation in the STA Gene(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- Reduction of hemolysis without reoperation following mitral valve repair
- Identification of two novel missense mutations (p.R1221C and p.R1357W) in the ABCC6 (MRP6) gene in a Japanese patient with pseudoxanthoma elasticum (PXE)
- Type III hyperlipoproteinemia exaggerated by Sheehan's syndrome with advanced systemic atherosclerosis - A 28-year clinical course
- Japan Lipid Intervention Trial (J-LIT) Chart Predicts the Absence of Coronary Artery Disease More Accurately Than Symptom Limited Exercise Stress Electrocardiography
- In-hospital Outcome in Octogenarians with Acute Coronary Syndrome Undergoing Emergent Coronary Angiography
- Gene mutations in adult Japanese patients with dilated cardiomyopathy
- Oxidative Stress Correlates with Left Ventricular Volume after Acute Myocardial Infarction
- PJ-813 Impact of Speckle Tracking Echocardiography on Evaluation of Myocardial Fibrosis in Hypertrophic Cardiomyopathy : Comparison with Study by Cardiovascular Magnetic Resonance(PJ136,Echo/Doppler (Others) 1 (I),Poster Session (Japanese),The 73rd Annual
- Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease
- The Relation between Cell Adhesion Molecules and Late Lumen Loss(Restenosis after Angioplasty, Basic/Clinical 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Difference in the risk factors for coronary, renal and other peripheral arteriosclerosis in heterozygous familial hypercholesterolemia
- FRS-128 Mutations in Phospholamban Gene Cause Hypertrophic and Dilated Cardiomyopathy(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Increased Circulating Matrix Metalloproteinase-2 in Patients with Hypertrophic Cardiomyopathy with Systolic Dysfunction
- Scintigraphic evaluation of regression of abnormal Q waves in myocardial infarction
- PJ-425 Early Development of Dilated Cardiomyopathy in Subjects with Mutations in the Cardiac Troponin Complex Genes(Cardiomyopathy, Clinical 5 (M) : PJ71)(Poster Session (Japanese))
- OJ-511 Missense Mutations in Cardiac Ryanodine Receptor Gene Cause Hypertrophic Cardiomyopathy Associated with Ventricular Arrhythmia or Massive Hypertrophy(Cardiomyopathy, Basic (M) : OJ62)(Oral Presentation (Japanese))
- OJ-229 Atrial Fibrillation in Patients with Hypertrophic Cardiomyopathy with Different Genotypes(Cardiomyopathy, Clinical 1 (M) : OJ26)(Oral Presentation (Japanese))
- OJ-078 Usefulness of Q-T Peak Dispersion for Diagnosis of KCNH2 Gene Mutations in Patients with Long QT Syndrome(Arrhythmia, Basic 1 (A) : OJ10)(Oral Presentation (Japanese))
- FRS-129 Mutations Responsible for Dilated Cardiomyopathy in Japan(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- PJ-596 Exercise-induced Systolic Dysfunction in Patients with Non-obstructive Hypertrophic Cardiomyopathy and Mutations in the Cardiac Troponin Genes(Cardiomyopathy, Clinical 7 (M) : PJ100)(Poster Session (Japanese))
- OJ-335 PRKAR1A Gene Mutation in Patients with Cardiac Myxoma(Valvular Heart Disease/Pericarditis/Cardiac Tumor 2 (M) : OJ40)(Oral Presentation (Japanese))
- Alterations in Echocardiographic Tissue Characterization in Patients with Cardiac Troponin I Gene Mutation a Possible Indicator of Preclinical Hypertrophic Cardiomyopathy
- Cardiac Actin and Alpha-Tropomyosin Genes Are Associated with Neither Hypertrophic Nor Dilated Cardiomyopathy in Patients from Hokuriku District in Japan
- PE-280 Missense Mutations in the MYBPC3 Gene are Responsible for Hypertrophic Cardiomyopathy with Left Ventricular Systolic Dysfunction and Dilatation(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- PE-278 Electrocardiography Shows Preferable Diagnostic Value Even in Carriers of Hypertrophic Cardiomyopathy who do not Manifest Ventricular Wall Hypertrophy on Echocardiography(Cardiomyopathy, Clinical 3 (M) : PE48)(Poster Session (English))
- OJ-237 KCNJ2 Gene Mutation is a Rare Cause of Long QT Syndrome(Arrhythmia, Diagnosis/Pathophysiology/EPS 9 (A) : OJ27)(Oral Presentation (Japanese))
- FRS-132 Phenotypic Discrepancies Between Electrocardiography and Echocardiography for Hypertrophic Cardiomyopathy in Genetically Affected Subjects(Myocardial Disease (M) : FRS16)(Featured Research Session (English))
- Left ventricular dysfunction and dilatation in elderly patients with hypertrophic cardiomyopathy associated with a novel missense mutation in MyBP-C gene
- Relationship between QT Variables and Disproportion of Left Ventricular Wall in Patients with Hypertrophic Cardiomyopathy
- Fluctuation of T-peak to T-end before and after ventricular tachycardia
- Q-T peak dispersion in congenital long QT syndrome ; increased lag of T wave peak as a new marker of HERG
- PJ-466 The Clinical Results of Central Venous Intervention for Hemodialysis Patients in Our Cardiovascular Hospital(PJ079,Peripheral Circulation/Vascular Disease (Therapy) 2 (H),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese
- PE-461 Serial changes of FDG-PET, Tetrofosmin and BMIPP SPECT for anterior acute myocardial infarction(Nuclear cardiology(05)(I),Poster Session(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- OE-057 Genetic Effects of Farnesoid-X-receptor on BMI, HDL-C, LDL-C and Development of Fatty Liver(Lipid disorders-1 (H) OE10,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- Pathophysiological Roles of the Adrenal Renin-Angiotensin System in Patients with Primary Aldosteronism
- Effects of Aldosterone Blockade on Cardiac Renin-Angiotensin-Aldosterone System in Salt-Sensitive Hypertension (Hypertension, Basic 5 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Probucol-Induced Long QT Syndrome Associated with a Novel Missense Mutation M124T in the N Terminus of HERG
- Long QT Syndrome Mutations in Different Sites of HERG Elicit a Variety of Functional Changes
- Double Missense Mutations (D611Y in KCNQ1 and D609G in HERG) in a Japanese Family with Long QT Syndrome
- Characterization of a Novel Missense Mutation E637K in the Pore-S6 Loop of HERG in a Patient with Long QT Syndrome
- Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome
- Crow-Fukase syndrome associated with high-output heart failure
- Acute Inferior Myocardial Infarction and Coronary Spasm in a Patient With an Anomalous Origin of the Right Coronary Artery From the Left Sinus of Valsalva
- Sixteen-slice computed tomography, transthoracic real-time 3-dimensional echocardiography and magnetic resonance imaging assessment of a long-term survivor of rupture of sinus of valsalva aneurysm
- Increased matrix metalloproteinase-2 in patients with hypertrophic cardiomyopathy with systolic dysfunction
- OJ-415 Electrocardiographic Events and Cholesterol Reduction with Pravastatin in Patients with Hypercholesterolemia : Hokuriku Lipid Coronary Heart Disease Study-Pravastatin Atherosclerosis Trial(Preventive Medicine/Epidemiology/Education 3 (H) : OJ50)(Or
- PE-290 Regional Oxidative Metabolism in Complete Left Bundle Branch Block(Heart Failure, Clinical 11 (M) : PE50)(Poster Session (English))
- Changes in myocardial oxidative metabolism after biventricular pacing as evaluated by [^C]acetate positron emission tomography
- PCSK9 Gene Mutation is Less Frequent in Clinically Diagnosed FH Patients without LDLR and ApoB-100 Gene Mutation in Japan(Lipid Disorders 1 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Usefulness of Acoustic Densitometry Method for Detection of Myocardial Changes in Preclinical Patients with Hypertrophic Cardiomyopathy
- Right Ventricular Metastasis From a Primary Cervical Carcinoma
- Difference in Coronary Blood Flow Dynamics between Patients with Hypertension and Those with Hypertrophic Cardiomyopathy
- Q-T peak dispersion in congenital long QT syndrome: Possible marker of mutation of HERG
- Cardiac Manifestations and Long-Term Course in Emery-Dreifuss Muscular Dystrophy Caused by a Nonsense Mutation in the STA Gene
- Effects of gender on the number of diseased vessels and clinical outcome in Japanese patients with acute coronary syndrome
- A novel de novo mutation in the cardiac β - myosin heavy chain gene in patients with dilated cardiomyopathy
- Mitochondrial DNA mutations in hypertrophic cardiomyopathy
- Novel KCNQ1 missense mutation (D611Y) in a Japanese long QT family
- Whole and regional variation of cardiac sympathetic nervous activity in patients with hypertrophic cardiomyopathy with malignant tachyarrthythmias and sudden death
- Association between Single Nucleotide Polymorphisms (SNPs) of Cardiac Potassium Channel Genes and Drug-Induced Long QT Syndrome in Japanese
- A Novel Mutation (lnt21DSG+1A) in the MyBP-C Gene Shows Hypertrophic Cardiomyopathy with a High Degree of Penetrance in Adult Patients
- Diagnostic Values of Abnormal Q Waves for Hypertrophic Cardiomyopathy Based on the Genetic Information
- QT Variables in Preclinical Patients with Hypertrophic Cardiomyopathy
- QT Variables in Various Genotyped Patients with Hypertrophic Cardiomyopathy
- Mitochondrial DNA Mutations in Hypertrophic Cardiomyopathy
- Frequency of Asymmetric Septal Hypertrophy in Patients with Hypertrophic Cardiomyopathy : Difference in Genotypes
- Differences in Diagnostic Values of Abnormal Q Waves between Hypertrophic Cardiomyopathy with a cTnl Gene Mutation and MyBP-C Gene Mutations
- Clinical and Electrophysiological Characteristics of Brugada Syndrome Caused by a Missense Mutation in the S5-pore site of SCN5A(Arrhythmia, Diagnosis/Pathophysiology/EPS 5 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-144 A Novel Missense Mutation of SCN5A Gene Associated with Brugada Syndrome by Bidirectional Effects on Blocking Actions of Antiarrhythmic Drugs(Sudden Cardiac Death (A) : FRS18)(Featured Research Session (English))
- SCN5A Gene Mutations and Clinical Characteristics in Patients With Brugada-Type Electrocardiogram
- Brugada Syndrome With Ventricular Tachycardia and Fibrillation Related to Hypokalemia
- Which DES is the most appropriate for very small target vessels? Experimental study of stent expandable performance with SES, PES, ZES and EES