Primary Sternal Cleft Repair in First Week of Life.

World J Pediatr Congenit Heart Surg

Division of Cardiac Surgery, 20425Connecticut Children's, Hartford, CT, USA.

Published: September 2021

We present a full-term neonate with a postnatal diagnosis of a sternal cleft. Cardiac evaluation was otherwise remarkable for a patent ductus arteriosus and patent foramen ovale. Computed tomography scan confirmed the absence of a sternum except for a small inferior portion, including the xyphoid process. The patient underwent primary repair at five days of age through a midline incision where an absence of pericardium anteriorly was noted. She was extubated successfully the next day and discharged home on postoperative day 3. On follow-up examination, her sternum has been healing well without any clinical concerns. We advocate early repair of such defects in order to allow primary closure in a tension-free manner.

Download full-text PDF

Source
http://dx.doi.org/10.1177/2150135120975767DOI Listing

Publication Analysis

Top Keywords

sternal cleft
8
primary sternal
4
cleft repair
4
repair week
4
week life
4
life full-term
4
full-term neonate
4
neonate postnatal
4
postnatal diagnosis
4
diagnosis sternal
4

Similar Publications

What is pentalogy of Cantrell?

Cardiol Young

October 2024

Department of Pediatrics, Institute for Health Sciences Education, Georgetown Public Hospital Corporation, Georgetown, Guyana.

Article Synopsis
  • An 8-month-old girl was diagnosed with tetralogy of Fallot, a narrowed aorta (coarctation), and a complete form of pentalogy of Cantrell, which consists of multiple congenital defects.
  • Researchers conducted a meta-analysis of 236 cases of Cantrell's syndrome from existing literature to evaluate and compare their heart-related characteristics.
  • The study highlights the complexity of congenital heart defects and contributes to understanding of the rare pentalogy of Cantrell.
View Article and Find Full Text PDF

The sternal cleft (SC) is a rare congenital anomaly characterized by a complete or partial separation of the sternum, leading to significant clinical concerns, including respiratory and cardiac instability. Due to its rarity, the SC often poses surgical challenges. This case report highlights the management of two neonates with SCs, emphasizing the critical role of early multidisciplinary intervention.

View Article and Find Full Text PDF

Failed midline ventral fusion of sternal bars is the cause of complete sternal cleft, which is a rare congenital anomaly that may cause cardiopulmonary compromise. Very few cases of complete sternal cleft have been reported so far in the literature. Surgical correction is recommended to protect mediastinal structures and to restore respiratory dynamics.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!