Abstract

Hypokalemia is a common electrolyte disturbance and is related to poor prognosis in patients with cardiovascular disease. However, the role of hypokalemia in patients with vasospastic angina (VSA) has not yet been studied. The present study enrolled 1454 patients diagnosed with VSA according to ergonovine provocation test results and available admission serum potassium data. The primary outcome was a composite of cardiac death, acute coronary syndrome, and new-onset life-threatening arrhythmia. Based on a hypokalemia definition as serum potassium concentration ≤ 3.5 mEq/L, the hypokalaemia group included 70 patients (4.8%). The median potassium levels were 3.4 mEq/L [interquartile range (IQR) 3.3–3.5] in the hypokalemia group and 4.1 mEq/L (IQR 3.9–4.3) in the no-hypokalemia group. The median follow-up duration was 764 days. Primary outcomes occurred in seven patients (10.0%) in the hypokalemia group and 51 patients (3.7%) in the no-hypokalemia group. The Kaplan–Meier analysis showed a higher cumulative incidence of primary outcomes in the hypokalemia group compared to that in the no-hypokalemia group (log-rank P = 0.014). Multivariate Cox regression analysis also showed that hypokalemia was an independent predictor of primary outcomes. In conclusion, hypokalemia at admission was associated with adverse clinical outcomes in VSA.

Highlights

  • MethodsThe Variant Angina Korea (VA-Korea) registry is a nation-wide prospective, observational, and multicentre registry designed to reflect real-world clinical data of Korean patients with VSA

  • Muscle cell proliferation, and arterial ­thrombosis[2]

  • 1454 patients were enrolled in this study, 70 (4.8%) of whom were included in the hypokalemia group according to serum potassium level at admission laboratory test (Fig. 1)

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Summary

Methods

The Variant Angina Korea (VA-Korea) registry is a nation-wide prospective, observational, and multicentre registry designed to reflect real-world clinical data of Korean patients with VSA. A total of 2960 patients with chest pain and suspected VSA who underwent coronary angiography and ergonovine (EG) provocation test at 11 tertiary hospitals in Korea were consecutively enrolled from May 2010 to June 2015. Patients with known malignant or systemic inflammatory disease, end-stage renal disease on dialysis, and catheter-induce spasms at baseline coronary angiography did not include the registry. The study protocol was approved by the institutional review board of each participating hospital including Hallym University Sacred Heart Hospital Institutional Review Board, named ‘HUMC ethics committees & IRB’ (IRB No 2010-I007), and all patients provided written informed consent.

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