The Role of Medical Therapy in Management of Bicuspid Aortic Valve–Associated Aortopathy in Children

Arif Hussain MD , Louis-Olivier Roy MSc , Nagib Dahdah MD , Tiscar Cavalle-Garrido MD , Hamad Abdulrahman O. Alfuraian MD , Christine Houde MD , Michael Grattan MD, MSc , Andrew Mackie MD , Shreya Moodley MD , Joshua Penslar MD , Derek Wong MD , Santokh S. Dhillon MD, FRCPC, FHRS , Frédéric Dallaire MD, PhD , Canadian Congenital and Pediatric Cardiology Research Network Investigators
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Abstract

Background

Patients with bicuspid aortic valve (BAV) are often treated with medication to slow the rate of aortic dilatation, without established efficacy.

Methods

We conducted a retrospective, multicentre study of 558 children (83 treated and 475 not treated) with BAV and ascending aorta (AscAo) dilatation. The median follow-up was 3.6 years for treated patients and 5.6 years for not treated patients. Longitudinal mixed models assessed the rate of AscAo and sinus of Valsalva (SoV) dilatation expressed as a change in Z score units per year for patients treated and not treated with a β-blocker or an afterload-reducing agent. Secondary outcomes included time to significant AscAo dilatation (Z score ≥6) and proportions of patients achieving Z score stabilization (dilatation rate <0.1 Z/y).

Results

Compared with untreated patients, those treated had a small reduction of AscAo and SoV dilatation rates with an absolute treatment difference of −0.032 Z/y (95% confidence interval [CI]: −0.086 to 0.022) and −0.021 Z/y (95% CI: −0.078 to 0.035), respectively. Patients treated had a small reduction of the time to significant dilatation of AscAo (hazard ratio: 0.83; 95% CI: 0.43-1.61). Patients treated were more likely to achieve Z score stabilization with an increase in the proportion of patients by 4.5% for AscAo (95% CI: −11.3% to 20.2%) and 7% for SoV (95% CI: −9.7% to 22.5%). Overall, the probability of a null effect was high, as the 95% CI for all outcomes between the groups overlapped.

Conclusion

Pharmacologic treatment was not associated with a meaningful reduction of AscAo and SoV dilatation rates in children with BAV.
药物治疗在儿童二尖瓣主动脉瓣相关病变治疗中的作用
背景:患有双尖瓣主动脉瓣(BAV)的患者通常用药物治疗来减缓主动脉扩张的速度,但没有确定的疗效。方法对558例BAV合并升主动脉扩张患儿(83例接受治疗,475例未接受治疗)进行回顾性多中心研究。接受治疗的患者中位随访时间为3.6年,未接受治疗的患者中位随访时间为5.6年。纵向混合模型评估了接受和未接受β受体阻滞剂或后负荷减释剂治疗的患者AscAo和Valsalva窦(SoV)扩张率,以Z评分单位每年的变化表示。次要结局包括AscAo显著扩张的时间(Z评分≥6)和达到Z评分稳定的患者比例(扩张率<;0.1 Z/y)。结果与未经治疗的患者相比,治疗组AscAo和SoV扩张率有小幅下降,绝对治疗差异分别为- 0.032 Z/y(95%可信区间[CI]: - 0.086 ~ 0.022)和- 0.021 Z/y (95% CI: - 0.078 ~ 0.035)。接受治疗的患者出现AscAo显著扩张的时间略有减少(风险比:0.83;95% ci: 0.43-1.61)。接受治疗的患者更有可能实现Z评分稳定,AscAo患者比例增加4.5% (95% CI: - 11.3%至20.2%),SoV患者比例增加7% (95% CI: - 9.7%至22.5%)。总的来说,零效应的概率很高,因为组间所有结果的95% CI重叠。结论药物治疗与BAV患儿AscAo和SoV扩张率的降低无显著相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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