纠正继发性甲状旁腺功能亢进对维持性血液透析患者心脏结构和功能的影响

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目的探讨应用活性维生素D3纠正继发性甲状旁腺功能亢进(SHPT)对维持性血液透析(MHD)患者心脏结构和功能的影响。方法56例MHD患者均符合SHPT诊断标准,采用低钙透析液稳定透析3个月以上,随机分为A组(29例)和B组(27例),测定血钙(Ca)、磷(P)、甲状旁腺素(iPTH)。A组每日午饭中嚼服碳酸钙600mg,B组在此基础上服用活性维生素D3,2~3μg/周,分2~3次于透析后当晚口服,二组连续用药12个月,当Ca>10.2mg/dl或Ca×P≥55mg2/dl2调节药物剂量。分别于实验开始前及6个月、12个月行心脏多普勒超声检查。结果于实验6个月、12个月后,B组iPTH平均值较A组下降明显(P<0.05,P<0.01)。心脏结构和功能比较,治疗前左室肥厚(LVH)、射血分数(EF),舒张早期和舒张晚期二尖瓣口最大血流速度之比(E/A)等指标二组之间差异无统计学意义(P>0.05),治疗6个月、12个月后,A组上述各指标无明显变化(P>0.05,P>0.05),B组随治疗时间的延长上述指标明显好转,差异有统计学意义(P<0.05和P<0.01)。结论活性维生素D3不仅可以减轻MHD患者SHPT,而且有助于改善SHPT患者的心脏结构和功能。 Objective To investigate the effects of active vitamin D3 on cardiac structure and function in patients with maintenance hemodialysis (MHD) after secondary hyperparathyroidism (SHPT). Methods Fifty-six patients with MHD were all eligible for SHPT diagnostic criteria. The patients were divided into group A (n = 29) and group B (n = 27) by dialysis with low calcium dialysis for more than 3 months. Plasma calcium (Ca) ), Parathyroid hormone (iPTH). A group of daily lunch chewing calcium carbonate 600mg, B group on the basis of active vitamin D3, 2 ~ 3μg / week, 2 to 3 times in the evening after dialysis oral administration, two groups of continuous medication for 12 months, when Ca > 10.2 mg / dl or Ca x P> 55 mg2 / dl2. Doppler echocardiography was performed before the start of the experiment and at 6 months and 12 months respectively. Results After 6 months and 12 months, the mean iPTH in group B was significantly lower than that in group A (P <0.05, P <0.01). Comparison of cardiac structure and function, pre-treatment left ventricular hypertrophy (LVH), ejection fraction (EF), early diastolic and mitral valve maximum flow velocity ratio (E / A) and other indicators between the two groups no difference (P> 0.05). After treatment for 6 months and 12 months, there was no significant change in the above indexes in group A (P> 0.05, P> 0.05). The indexes in group B were obviously improved with the prolongation of treatment time, There was statistical significance (P <0.05 and P <0.01). Conclusion Active vitamin D3 can not only reduce the SHPT in MHD patients, but also help to improve the cardiac structure and function of SHPT patients.
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