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.