Combined assessment of left ventricular perfusion and function by gated single-photon emission computed tomography for the risk stratification of high-risk hypertensive patients
Objective This study was aimed at verifying whether combined information on left ventricular perfusion and function by electrocardiogram-gated single-photon emission computed tomography (SPECT) retains its known prognostic value in patients with systemic hypertension. Methods A total of 415 hypertensive patients underwent rest and stress (exercise in 278 and dipyridamole in 137) gated 99mTc-sestamibi SPECT and prospective follow-up for the composite endpoint of death and acute coronary syndrome. Patients undergoing revascularization were censored. The individual effect of clinical and stress imaging data on outcome was evaluated by Cox regression analysis. Model validation was performed using bootstrap methods adjusted by the degree of optimism in estimates. Survival analysis was performed using the product-limit Kaplan-Meier method. Results During a median follow-up of 24 months, 12 cardiac deaths and 32 acute coronary syndromes occurred. After adjusting for the most significant covariates, age [hazard ratio (HR) 1.62, 95% confidence interval (Cl) 1.02-2.57], diabetes (HR 7.51,95% Cl 1.61-35.2), summed stress score (HR 2.06,95%Cl 1.07-4),and peak end-systolic volume (HR 3.62, 95% CI 1.35-9.69) were multivariable predictors of outcome. The normal perfusion pattern was associated with a low event rate independently of peak end-systolic volume. Conversely, in the case of moderate to severe perfusion abnormalities, a peak end-systolic volume greater than 74 ml was able to identify an increased risk of adverse outcome. Moreover, peak end-systolic volume was significantly higher among patients who died of a cardiac cause compared with those with different outcomes. Conclusion A combined assessment of left ventricular perfusion and function by gated SPECT significantly improves risk stratification in hypertensive patients.
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Duke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Duke Clin Res Inst, Durham, NC USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Piccini, Jonathan P.
Starr, Aijing Z.
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Duke Clin Res Inst, Durham, NC USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Starr, Aijing Z.
Horton, John R.
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Duke Clin Res Inst, Durham, NC USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Horton, John R.
Shaw, Linda K.
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Duke Clin Res Inst, Durham, NC USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Shaw, Linda K.
Lee, Kerry L.
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Duke Clin Res Inst, Durham, NC USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Lee, Kerry L.
Al-Khatib, Sana M.
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Duke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Duke Clin Res Inst, Durham, NC USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Al-Khatib, Sana M.
Iskandrian, Ami E.
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Univ Alabama, Dept Med, Div Cardiovasc Dis, Birmingham, AL 35294 USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Iskandrian, Ami E.
O'Connor, Christopher M.
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Duke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Duke Clin Res Inst, Durham, NC USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
O'Connor, Christopher M.
Borges-Neto, Salvador
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Duke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA
Duke Clin Res Inst, Durham, NC USADuke Univ, Med Ctr, Div Cardiol, Dept Med, Durham, NC 27710 USA