Severe syncope and sudden death in children with inborn salt-losing hypokalaemic tubulopathies

被引:16
作者
Cortesi, C
Bettinelli, A
Emma, F
Fischbach, M
Bertolani, P
Bianchetti, MG [1 ]
机构
[1] San Giovanni Hosp, Dept Pediat, CH-6500 Bellinzona, Switzerland
[2] Univ Milan, Med Sch, De Marchi Hosp, Pediat Renal Unit, Milan, Italy
[3] Leopoldo Mandic Hosp, Div Pediat, Merate, Italy
[4] Childrens Hosp Bambino Gesu, Div Nephrol, Rome, Italy
[5] Hautepierre Hosp, Div Pediat Nephrol, Strasbourg, France
[6] Univ Modena, Dept Pediat, Modena, Italy
关键词
arrhythmias; Bartter syndrome; Gitelman syndrome; hypokalaemia; sudden death;
D O I
10.1093/ndt/gfh893
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 [基础医学]; 1002 [临床医学]; 100602 [中西医结合临床];
摘要
Background. Potassium deficiency may cause cardiac arrhythmias culminating in syncope or sudden death. Methods. An inquiry performed among physicians caring for a total of 249 patients with inborn salt-losing tubulopathies revealed that acute cardiac complications occurred in seven children. Results. Four patients died suddenly and three had severe syncope. These episodes occurred in the context of severe chronic hypokalaemia (<= 2.5 mmol/l) or were precipitated by acute diseases, which exacerbated hypokalaemia (<= 2.0mmol/l). Conclusions. In conclusion, severe chronic or acute hypokalaemia is hazardous in inborn salt-losing tubulopathies.
引用
收藏
页码:1981 / 1983
页数:3
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