Buck Marcia L
Department of Pharmacy Services, University of Virginia Health System, Box 800674, Charlottesville, VA 22908-0674, USA.
Ann Pharmacother. 2005 May;39(5):823-8. doi: 10.1345/aph.1E618. Epub 2005 Apr 5.
In 2003, the Food and Drug Administration placed spironolactone on its list of drugs needing pediatric studies.
To describe the use of spironolactone in a large group of children and evaluate its safety, focusing on its effects on potassium.
A prospective observational study was conducted. Patient demographic information was collected, as well as dosing regimens, use of other medications, and potassium concentrations. Patients were grouped by diagnosis. Comparisons were made with unpaired t-tests.
One hundred consecutive patients were evaluated. The average age was 20.8 months and weight was 9.5 kg. Sixty-two patients had heart disease (HD), 29 had chronic lung disease (CLD), and 9 had other conditions. The initial dose was 1.8 +/- 0.7 mg/kg/day. Patients with CLD received a higher dose than those with HD (2 +/- 0.8 vs 1.7 +/- 0.5 mg/kg/day; p = 0.04). Sixty-six patients received furosemide and 37 received thiazides (12 received both). The average potassium concentration after initiation was 4.3 +/- 0.8 mEq/L, with higher values in patients with CLD versus HD (4.7 +/- 0.7 vs 4.2 +/- 0.7 mEq/L; p = 0.007). Twenty-six patients required potassium supplementation, including 16 with CLD and 8 with HD; no other adverse effects were noted. Average length of treatment was 16 days, with a length of stay of 38 days. Of the 92 patients surviving to discharge, 66 continued on spironolactone.
This sample demonstrates that spironolactone is a common component of diuretic regimens in pediatric patients. The only adverse effects were alterations in potassium. While hyperkalemia was more common initially, hypokalemia was more frequent with long-term use. Potassium concentrations should be carefully monitored, particularly in children receiving multiple diuretics. Additional research is needed to define the pharmacokinetics and optimal dosing interval of spironolactone, as well as determine its long-term effects on potassium.
2003年,美国食品药品监督管理局将螺内酯列入需要进行儿科研究的药物名单。
描述一大群儿童使用螺内酯的情况,并评估其安全性,重点关注其对钾的影响。
进行了一项前瞻性观察研究。收集了患者的人口统计学信息、给药方案、其他药物的使用情况以及钾浓度。患者按诊断分组。采用不成对t检验进行比较。
对连续100例患者进行了评估。平均年龄为20.8个月,体重为9.5千克。62例患有心脏病(HD),29例患有慢性肺病(CLD),9例患有其他疾病。初始剂量为1.8±0.7毫克/千克/天。CLD患者接受的剂量高于HD患者(2±0.8与1.7±0.5毫克/千克/天;p = 0.04)。66例患者接受了呋塞米,37例接受了噻嗪类药物(12例同时接受了两者)。开始用药后的平均钾浓度为4.3±0.8毫当量/升,CLD患者的值高于HD患者(4.7±0.7与4.2±0.7毫当量/升;p = 0.007)。26例患者需要补充钾,其中16例为CLD患者,8例为HD患者;未观察到其他不良反应。平均治疗时长为16天,住院时长为38天。在92例存活至出院的患者中,66例继续使用螺内酯。
该样本表明螺内酯是儿科患者利尿治疗方案中的常见组成部分。唯一的不良反应是钾的改变。虽然高钾血症最初更常见,但低钾血症在长期使用时更频繁。应仔细监测钾浓度,尤其是在接受多种利尿剂治疗的儿童中。需要进一步研究来确定螺内酯的药代动力学和最佳给药间隔,以及确定其对钾的长期影响。