-受体阻滞剂用于治疗血管瘤。

Pub Date : 2013-01-01 DOI:10.1177/229255031302100103
Vishal K Sharma, Frankie Og Fraulin, Danielle O Dumestre, Lori Walker, A Robertson Harrop
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引用次数: 22

摘要

目的:探讨口服受体阻滞剂治疗疑难血管瘤的适应症、疗效及不良反应。方法:回顾性分析2009年至2011年间在阿尔伯塔儿童医院血管胎记诊所(Calgary, Alberta)就诊的血管瘤患者。对口服β受体阻滞剂治疗的患者亚群进行进一步表征,调查治疗的指征、治疗反应、到指征消退的时间、治疗持续时间、反弹生长的发生和治疗的副作用。结果:2009年至2011年间,新发血管瘤患者311例,其中105例接受口服受体阻滞剂治疗。45名患者完成了β受体阻滞剂治疗,其余患者继续接受治疗。治疗指征为功能问题(68.6%)或毁容(31.4%)。功能问题包括溃疡(29.5%)、眼周定位伴视觉干扰(28.6%)、气道干扰(4.8%)、相位综合征(3.8%)、听觉干扰(0.95%)和内脏定位伴充血性心力衰竭(0.95%)。受体阻滞剂起始时的中位年龄为3.3个月;治疗中位持续时间为10.6个月;最大治疗剂量中位数心得安为1.5 mg/kg/d,阿替洛尔为1.6 mg/kg/d。99名患者(94.3%)对治疗有反应,表现为体积缩小、颜色改变、质地软化和/或溃疡愈合。在23例患者中观察到反弹生长需要额外的疗程。-受体阻滞剂的副作用包括四肢发冷(26.7%)、烦躁(17.1%)、下消化道不适(14.3%)、呕吐(11.4%)、低血压(10.5%)、进食不良(7.6%)、嗜睡(4.8%)、支气管痉挛(0.95%)和皮疹(0.95%)。在任何情况下,副作用都不会导致β受体阻滞剂治疗的完全中断;然而,在某些情况下,它们促使切换到不同的-受体阻滞剂制剂。87例(82.9%)患者的主要适应证得到缓解,中位时间为3个月。结论:口服-受体阻滞剂治疗婴儿血管瘤非常有效且耐受性良好,超过94%的患者对治疗有反应,90%的患者显示治疗的主要功能指征得到解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beta-blockers for the treatment of problematic hemangiomas.

Objective: To examine treatment indications, efficacy and side effects of oral beta-blockers for the treatment of problematic hemangiomas.

Methods: A retrospective review of patients with hemangiomas presenting to the Alberta Children's Hospital Vascular Birthmark Clinic (Calgary, Alberta) between 2009 and 2011 was conducted. The subset of patients treated with oral beta-blockers was further characterized, investigating indication for treatment, response to treatment, time to resolution of indication, duration of treatment, occurrence of rebound growth and side effects of therapy.

Results: Between 2009 and 2011, 311 new patients with hemangiomas were seen, of whom 105 were treated with oral beta-blockers. Forty-five patients completed beta-blocker treatment while the remainder continue to receive therapy. Indications for treatment were either functional concerns (68.6%) or disfigurement (31.4%). Functional concerns included ulceration (29.5%), periocular location with potential for visual interference (28.6%), airway interference (4.8%), PHACES syndrome (3.8%), auditory interference (0.95%) and visceral location with congestive heart failure (0.95%). The median age at beta-blocker initiation was 3.3 months; median duration of therapy was 10.6 months; and median maximal treatment dose was 1.5 mg/kg/day for propranolol and 1.6 mg/kg/day for atenolol. Ninety-nine patients (94.3%) responded to therapy with size reduction, colour changes, softened texture and/or healing of ulceration. Rebound growth requiring an additional course of therapy was observed in 23 patients. Side effects from beta-blockers included cool extremities (26.7%), irritability (17.1%), lower gastrointestinal upset (14.3%), emesis (11.4%), hypotension (10.5%), poor feeding (7.6%), lethargy (4.8%), bronchospasm (0.95%) and rash (0.95%). Side effects did not result in complete discontinuation of beta-blocker treatment in any case; however, they prompted a switch to a different beta-blocker preparation in some cases. Resolution of the primary indication, requiring a median time of three months, occurred in 87 individuals (82.9%).

Conclusions: Treatment of infantile hemangiomas with oral beta-blocker therapy is highly effective and well tolerated, with more than 94% of patients demonstrating a response to treatment and 90% showing resolution of the primary functional indication for treatment.

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