Risk stratification based on J-ACCESS risk models with myocardial perfusion imaging: Risk versus outcomes of patients with chronic kidney disease

被引:10
|
作者
Nakajima, Kenichi [1 ]
Nakamura, Satoko [2 ,3 ]
Hase, Hiroki [4 ]
Takeishi, Yasuchika [5 ]
Nishimura, Shigeyuki [6 ]
Kawano, Yuhei [2 ,7 ]
Nishimura, Tsunehiko [8 ]
机构
[1] Kanazawa Univ Hosp, Dept Nucl Med, Kanazawa, Ishikawa, Japan
[2] Natl Cerebral & Cardiovasc Ctr, Div Nephrol & Hypertens, Suita, Osaka, Japan
[3] Kansai Univ Welf Sci, Kashihara, Nara, Japan
[4] Toho Univ, Ohashi Med Ctr, Dept Nephrol, Tokyo, Japan
[5] Fukushima Med Univ, Dept Cardiovasc Med, Fukushima, Japan
[6] Saitama Med Univ, Int Med Ctr, Hidaka, Japan
[7] Teikyo Univ, Dept Med Technol, Fukuoka, Japan
[8] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Kyoto, Japan
关键词
Prognosis; cardiac events; multivariable logistic analysis; heart failure; C-reactive protein; EMISSION COMPUTED-TOMOGRAPHY; OPTIMAL MEDICAL THERAPY; PROGNOSTIC VALUE; CARDIAC EVENTS; JAPANESE PATIENTS; PREDICTION; SPECT; REVASCULARIZATION;
D O I
10.1007/s12350-018-1330-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background This study aimed to validate the accuracy of major-event risk models created in the multicenter J-ACCESS prognostic study in a new cohort of patients with chronic kidney disease (CKD). Methods and Results Three multivariable J-ACCESS risk models were created to predict major cardiac events (cardiac death, non-fatal acute coronary syndrome, and severe heart failure requiring hospitalization): Model 1, four variables of age, summed stress score, left ventricular ejection fraction and diabetes; Model 2 with five variables including estimated glomerular filtration rate (eGFR, continuous); and Model 3 with categorical eGFR. The validation data used three-year (3y) cohort of patients with CKD (n = 526, major events 11.2%). Survival analysis of low (< 3%/3y), intermediate (3% to 9%/3y), and high (> 9%/3y)-risk groups showed good stratification by all three models (actual event rates: 3.1%, 9.9%, and 15.9% in the three groups with eGFR >= 15 mL/min/1.73 m(2), P = .0087 (Model 2). However, actual event rates were equally high across all risk groups of patients with eGFR < 15 mL/min/1.73 m(2). Conclusion The J-ACCESS risk models can stratify patients with CKD and eGFR >= 15 mL/min/1.73 m(2), but patients with eGFR < 15 mL/min/1.73 m(2) are potentially at high risk regardless of estimated risk values.
引用
收藏
页码:41 / 50
页数:10
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