Simultaneous presence of atrial arrhythmia and hypocalcemia in dilated cardiomyopathy: A series of two cases

A. Singhi, Sanjeev S Mukherjee, K. Shine Kumar, R. Kumar
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引用次数: 1

Abstract

Dilated cardiomyopathy in young children has varied etiological factors. Some cases have correctable causes such as incessant arrhythmia, correctable metabolic abnormality, and left ventricular obstructive lesions. Two 4-month-old infants presented with severe left ventricular dysfunction and ectopic atrial tachycardia. Biochemical profile of the infants showed low ionic and total calcium, elevated serum phosphate, elevated alkaline phosphatase, and elevated serum lactate. The parathyroid hormone was elevated and 25-hydroxyvitamin D3 was reduced. The patients were treated with beta-blocker, calcium, and Vitamin D supplementation, along with antifailure therapy. The tachycardia resolved over a 12-h period and calcium normalized in the next few days. The left ventricular function returned to normal over a 5–16-month period. In 6–8 years of follow-up, patients were in sinus rhythm doing very well with normal cardiac function with normal calcium-related biochemical parameters. The presence of incessant atrial arrhythmia in a case of hypocalcemic cardiomyopathy is rare and can have link with hypocalcemia-induced electrical changes in the cardiomyocyte in selected cases. Thorough and protocol-based treatment approach helps in correct diagnosis and treatment. Further study and molecular research can shed more light on the complex interaction of hypocalcemia and arrhythmia.
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扩张型心肌病同时存在心房心律失常和低钙血症:一系列两例
幼儿扩张型心肌病有多种病因。一些病例有可纠正的原因,如持续的心律失常,可纠正的代谢异常,左心室梗阻性病变。两个4个月大的婴儿表现出严重的左心室功能障碍和异位房性心动过速。婴儿的生化特征表现为低离子钙和总钙,血清磷酸盐升高,碱性磷酸酶升高,血清乳酸升高。甲状旁腺激素升高,25-羟基维生素D3降低。患者接受受体阻滞剂、钙和维生素D补充剂以及抗衰竭治疗。心动过速在12小时内消退,钙在接下来的几天内恢复正常。5 - 16个月后左心室功能恢复正常。随访6-8年,患者窦性心律良好,心功能正常,钙相关生化指标正常。在低钙血症性心肌病病例中出现持续性心房心律失常是罕见的,在某些病例中可能与低钙血症引起的心肌细胞电变化有关。全面、规范的治疗方法有助于正确诊断和治疗。进一步的研究和分子研究可以进一步揭示低钙血症与心律失常的复杂相互作用。
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