Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
J Clin Hypertens (Greenwich). 2011 Oct;13(10):758-66. doi: 10.1111/j.1751-7176.2011.00502.x. Epub 2011 Jul 14.
This post hoc analysis assessed the efficacy and tolerability of valsartan for the treatment of hypertension in obese vs non-obese children and adolescents. After a 1-week antihypertensive washout period, 142 obese and 119 non-obese hypertensive children and adolescents aged 6 to 16 years were randomized to 2 weeks of once-daily treatment with valsartan 10 to 20 mg, 40 to 80 mg, or 80 to 160 mg, followed by re-randomization to either valsartan or placebo for an additional 2 weeks. Patients could continue to receive valsartan during an optional 52-week, open-label extension. Valsartan resulted in statistically significant (P<.05) and clinically relevant reductions in mean sitting blood pressure (BP), ranging from approximately 7/4 mm Hg (valsartan 10-20 mg) to 13/9 mm Hg (valsartan 80-160 mg) in both obese and non-obese patients. BP control was achieved in 44% of obese and 56% of non-obese patients. Following re-randomization, non-obese patients experienced an increase in BP during placebo treatment, albeit levels remained below baseline, whereas BP reductions were maintained in valsartan recipients (P<.05). The most frequent adverse events during the open-label phase were headache and fever. Valsartan provides similar antihypertensive efficacy in obese and non-obese hypertensive children and adolescents, with good tolerability in both patient populations.
本事后分析评估了缬沙坦治疗肥胖和非肥胖青少年高血压的疗效和耐受性。在 1 周的降压洗脱期后,142 名肥胖和 119 名非肥胖的 6 至 16 岁高血压儿童和青少年被随机分为两组,分别接受缬沙坦 10 至 20mg、40 至 80mg 或 80 至 160mg ,每日一次,治疗 2 周,然后再重新随机分为缬沙坦或安慰剂治疗 2 周。患者可在可选的 52 周、开放标签扩展期继续接受缬沙坦治疗。缬沙坦治疗可使肥胖和非肥胖患者的坐位血压(BP)均显著(P<.05)和具有临床意义的降低,幅度约为 7/4mmHg(缬沙坦 10-20mg)至 13/9mmHg(缬沙坦 80-160mg)。44%的肥胖患者和 56%的非肥胖患者血压得到控制。重新随机分组后,非肥胖患者在接受安慰剂治疗时血压升高,尽管水平仍低于基线,但缬沙坦组血压降低得以维持(P<.05)。开放标签阶段最常见的不良反应是头痛和发热。缬沙坦在肥胖和非肥胖的青少年高血压患者中提供相似的降压疗效,在这两个患者群体中均具有良好的耐受性。