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普萘洛尔作为婴幼儿血管瘤一线治疗的疗效和安全性。

Efficacy and safety of propranolol as first-line treatment for infantile hemangiomas.

机构信息

Division of Plastic Surgery, University Children's Hospital Zurich, Zurich, Switzerland.

出版信息

Eur J Pediatr. 2011 Apr;170(4):493-501. doi: 10.1007/s00431-010-1324-2. Epub 2010 Oct 9.

Abstract

UNLABELLED

Beta-blockers are a highly promising treatment modality for complicated infantile hemangiomas (IH). However, data on propranolol as first-line treatment, objective outcome measures and impact on hemodynamics in young infants is limited. We retrospectively evaluated a homogenous group of infants with proliferating complicated IH treated with propranolol (2 mg/kg/day). Outcome was assessed by blinded evaluation of clinical photographs by visual analogue scale (VAS), ultrasound examination and ophthalmological review (if appropriate). Tolerance and hemodynamic variables were recorded over time, including a 2-day in-patient observation at the initiation of therapy. Twenty-five infants (median age 3.6 (1.5-9.1) months) were included in the study. The median follow-up-time was 14 (9-20) months and 14 patients completed treatment at a median age of 14.3 (11.4-22.1) months, after a duration of 10.5 (7.5-16) months. In all patients, there was significant fading of colour (with a VAS of -9 (-6 to -9) after 7 months) and significant decrease in size of the IH (with a VAS of -8 (-3 to -10) after 7 months). Median thickness of the lesions assessed by ultrasound at baseline and after 1 month was 14 (7-28) mm and 10 (5-23) mm, respectively (p < 0.01). In children with periocular involvement, astigmatism and amblyopia resolved rapidly within 8 weeks. The overall tolerance of propranolol was good, and no relevant hemodynamic changes were noted.

CONCLUSION

Our report supports the excellent effect and good tolerance of this novel therapy, and we propose the use of propranolol as first-line treatment for IH.

摘要

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β受体阻滞剂是治疗复杂婴幼儿血管瘤(IH)的一种极有前途的治疗方法。然而,关于普萘洛尔作为一线治疗药物、客观疗效评估指标以及对小婴儿血流动力学影响的数据有限。我们回顾性评估了一组接受普萘洛尔(2mg/kg/天)治疗的增殖性复杂 IH 婴儿的同质组。通过视觉模拟量表(VAS)、超声检查和眼科检查(如果需要)对临床照片进行盲法评估来评估结果。随着时间的推移记录了耐受性和血流动力学变量,包括在开始治疗时进行 2 天的住院观察。本研究共纳入 25 例婴儿(中位年龄 3.6(1.5-9.1)个月)。中位随访时间为 14(9-20)个月,14 例患者在中位年龄 14.3(11.4-22.1)个月时完成治疗,治疗持续时间为 10.5(7.5-16)个月。所有患者的颜色均明显消退(7 个月后 VAS 为-9(-6 至-9)),IH 大小明显缩小(7 个月后 VAS 为-8(-3 至-10))。基线和 1 个月时超声评估的病变厚度中位数分别为 14(7-28)mm 和 10(5-23)mm(p <0.01)。在眼周受累的儿童中,8 周内散光和弱视迅速消退。普萘洛尔的总体耐受性良好,未观察到相关的血液动力学变化。

结论

我们的报告支持这种新疗法的卓越疗效和良好耐受性,我们建议将普萘洛尔作为 IH 的一线治疗药物。

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