Repair of aortic coarctation in neonates less than two kilograms.

0 CARDIAC & CARDIOVASCULAR SYSTEMS Interdisciplinary cardiovascular and thoracic surgery Pub Date : 2024-12-03 DOI:10.1093/icvts/ivae185
Qiang Chen, Thomas Fleming, Massimo Caputo, Serban Stoica, Andrew Tometzki, Andrew Parry
{"title":"Repair of aortic coarctation in neonates less than two kilograms.","authors":"Qiang Chen, Thomas Fleming, Massimo Caputo, Serban Stoica, Andrew Tometzki, Andrew Parry","doi":"10.1093/icvts/ivae185","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>A significant number of low-birth-weight neonates are born with aortic coarctation. Previous studies of early operation on these patients have shown a high hospital mortality and recurrence at 1 year. We reviewed our data to ascertain whether modern approaches allow better outcomes for these children.</p><p><strong>Methods: </strong>Fourteen patients weighing <2 kg with isolated coarctation between January 2005 and December 2015 were studied by retrospective chart review to ensure >5 years follow-up. All patients underwent extended end-to-side surgical repair. In-hospital and medium-term follow-up data were collected. Data are expressed as median (range).</p><p><strong>Results: </strong>Weight at the time of surgery was 1.8 (1.5-1.9) kg. There were no deaths, in-hospital or during follow-up. In-hospital stay was 11 (4-47) days. At follow-up of 141 (80-207) months echocardiographic velocity across the repair was 1.6 (0.9-3.8) m/s. Two patients required balloon dilatations for recoarctation including 1 with William's syndrome who required balloon coarctoplasty followed by stenting. This patient had grossly abnormal vessels at the time of initial surgery with aortic wall thickness >3 mm. There were no central neurological complications. Other complications included vocal cord dysfunction in 1, development of chylothorax requiring prolonged chest drainage in 2, pneumothorax following chest drain removal in 1 and wound dehiscence in 1 patient.</p><p><strong>Conclusions: </strong>Neonates below 2 kg can undergo coarctation repair safely with low incidence of recurrence. Waiting for growth in this cohort of patients may not therefore be justified.</p>","PeriodicalId":73406,"journal":{"name":"Interdisciplinary cardiovascular and thoracic surgery","volume":"39 6","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11730442/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Interdisciplinary cardiovascular and thoracic surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/icvts/ivae185","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"0","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: A significant number of low-birth-weight neonates are born with aortic coarctation. Previous studies of early operation on these patients have shown a high hospital mortality and recurrence at 1 year. We reviewed our data to ascertain whether modern approaches allow better outcomes for these children.

Methods: Fourteen patients weighing <2 kg with isolated coarctation between January 2005 and December 2015 were studied by retrospective chart review to ensure >5 years follow-up. All patients underwent extended end-to-side surgical repair. In-hospital and medium-term follow-up data were collected. Data are expressed as median (range).

Results: Weight at the time of surgery was 1.8 (1.5-1.9) kg. There were no deaths, in-hospital or during follow-up. In-hospital stay was 11 (4-47) days. At follow-up of 141 (80-207) months echocardiographic velocity across the repair was 1.6 (0.9-3.8) m/s. Two patients required balloon dilatations for recoarctation including 1 with William's syndrome who required balloon coarctoplasty followed by stenting. This patient had grossly abnormal vessels at the time of initial surgery with aortic wall thickness >3 mm. There were no central neurological complications. Other complications included vocal cord dysfunction in 1, development of chylothorax requiring prolonged chest drainage in 2, pneumothorax following chest drain removal in 1 and wound dehiscence in 1 patient.

Conclusions: Neonates below 2 kg can undergo coarctation repair safely with low incidence of recurrence. Waiting for growth in this cohort of patients may not therefore be justified.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
小于2公斤新生儿主动脉缩窄的修复。
目的:大量低出生体重新生儿出生时伴有主动脉缩窄。先前对这些患者进行早期手术的研究表明,1年内的住院死亡率和复发率很高。我们回顾了我们的数据,以确定现代方法是否能给这些孩子带来更好的结果。方法:对14例体重5年的患者进行随访。所有患者均行延长端侧手术修复。收集住院和中期随访资料。数据以中位数(范围)表示。结果:手术时体重1.8 (1.5 ~ 1.9)kg。在医院或随访期间均无死亡病例。住院时间11 (4 ~ 47)d。在随访141(80-207)个月时,超声心动图上的修复速度为1.6 (0.9-3.8)m/s。2例患者需要球囊扩张术进行再狭窄,其中1例患有威廉氏综合征,需要球囊成形术后再进行支架置入。该患者在初次手术时血管严重异常,主动脉壁厚度为30mm。无中枢神经系统并发症。其他并发症包括1例声带功能障碍,2例乳糜胸需要长时间胸腔引流,1例胸腔引流后气胸,1例伤口裂开。结论:2 kg以下新生儿可安全进行缩窄修复,复发率低。因此,等待这批患者的增长可能是不合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Computational fluid dynamics to simulate stenotic lesions in coronary end-to-side anastomosis. Long-term retention of the pedicled thymic flap after bronchial stump coverage. Closure of ventricular septal defect in children with trisomy 18: perioperative events and long-term survival. Intraoperative aortic dissection in a patient with cervical aortic arch. Hyperacute silicosis after bronchoscopy-induced melanoptysis in a lung transplant patient. A first report in literature.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1