School of Medicine, University of Colorado, Heart Institute, Children's Hospital Colorado, 13123 E. 16Th Ave, Box 100, Aurora, CO, 80045, USA.
Department of Pharmacy, Children's Hospital Colorado, Aurora, CO, USA.
Pediatr Cardiol. 2023 Jun;44(5):1125-1134. doi: 10.1007/s00246-023-03102-3. Epub 2023 Feb 1.
Pulmonary vein stenosis (PVS) is a growing problem for the pediatric congenital heart population. Sirolimus has previously been shown to improve survival and slow down the progression of in-stent stenosis in patients with PVS. We evaluated patients before and after initiation of sirolimus to evaluate its effects on re-intervention and vessel patency utilizing Optical Coherence Tomography (OCT).
We performed a retrospective study, reviewing the charts of patients with PVS, who had been prescribed sirolimus between October 2020 and December 2021. OCT was performed in the pulmonary vein of interest as per our published protocol. Angiographic and OCT imaging was retrospectively reviewed. Statistical analysis was performed using Chi square and Wilcoxon signed-rank test to compare pre-and post-sirolimus data.
Ten patients had been started and followed on sirolimus. Median age at sirolimus initiation was 25 months with median weight of 10.6 kg and average follow-up of 1 year. Median total catheterizations were 7 for patients prior to starting sirolimus and 2 after starting treatment (p = 0.014). Comparing pre- and post-sirolimus, patients were catheterized every 3 months vs every 11 months (p = 0.011), median procedure time was 203 min vs 145 min (p = 0.036) and fluoroscopy time, 80 min vs 57.2 min (p = 0.036). 23 veins had severe in-stent tissue ingrowth prior to SST (luminal diameter < 30% of stent diameter). Post-sirolimus, 23 pulmonary veins had moderate to severe in-stent tissue ingrowth that responded to non-compliant balloon inflation only with stent luminal improvement of > 75%.
Our study suggests that the addition of sirolimus in patients with moderate-severe PVS helps to decrease disease progression with decrease frequency of interventions. Reaching therapeutic levels for sirolimus is critical and medication interactions and side-effects need careful consideration. OCT continues to be important for evaluation and treatment guidance in this patient population.
肺静脉狭窄(PVS)是儿科先天性心脏病患者日益严重的问题。西罗莫司先前已被证明可提高生存率并减缓 PVS 患者支架内狭窄的进展。我们在开始使用西罗莫司前后评估了患者,以利用光学相干断层扫描(OCT)评估其对再介入和血管通畅性的影响。
我们进行了一项回顾性研究,回顾了 2020 年 10 月至 2021 年 12 月期间接受西罗莫司治疗的 PVS 患者的病历。根据我们已发表的方案,在感兴趣的肺静脉中进行 OCT 检查。回顾性分析血管造影和 OCT 成像。使用卡方检验和 Wilcoxon 符号秩检验比较西罗莫司治疗前后的数据。
有 10 名患者开始接受并接受西罗莫司治疗。西罗莫司开始时的中位年龄为 25 个月,中位体重为 10.6kg,平均随访时间为 1 年。在开始治疗之前,患者的中位总导管数为 7 次,而在开始治疗后为 2 次(p=0.014)。与治疗前相比,治疗后患者每 3 个月进行一次导管检查,而每 11 个月进行一次(p=0.011),中位手术时间从 203 分钟减少至 145 分钟(p=0.036),透视时间从 80 分钟减少至 57.2 分钟(p=0.036)。23 条静脉在 SST 前有严重的支架内组织增生(管腔直径<支架直径的 30%)。在使用非顺应性球囊扩张后,23 条肺静脉有中重度支架内组织增生,仅通过支架管腔改善>75%来解决。
我们的研究表明,在中重度 PVS 患者中添加西罗莫司有助于减少疾病进展,减少干预的频率。达到西罗莫司的治疗水平是至关重要的,药物相互作用和副作用需要仔细考虑。OCT 对于该患者人群的评估和治疗指导仍然很重要。