Aortopexy Complicated by ST Segment Elevations in a Four-Month-Old Infant
Rita Saynhalath1,2, Rhae Battles1, Sonia D Mehta3
1Anesthesiology and Pain Management, University of Texas Southwestern Medical Center, Dallas, USA.
Cureus
|December 16, 2020
Summary
A rare case of ST segment elevations occurred in an infant during surgery for tracheomalacia. Prompt recognition and workup are crucial for pediatric cardiac events.
Area of Science:
- Pediatric Cardiology
- Thoracic Surgery
- Critical Care Medicine
Background:
- Severe tracheomalacia necessitates surgical intervention, such as thoracoscopic aortopexy, in infants.
- Intraoperative complications, though rare, require vigilant monitoring and rapid response.
- Electrocardiogram (ECG) abnormalities in pediatric patients warrant thorough investigation.
Observation:
- A four-month-old infant undergoing thoracoscopic aortopexy developed significant ST segment elevations on ECG.
- Intraoperative echocardiography did not reveal structural cardiac abnormalities to explain the ECG changes.
- Persistent ST segment elevations were noted for 48 hours post-procedure without hemodynamic compromise.
Findings:
- The infant's ST segment elevations resolved spontaneously with normal troponin levels.
- The patient was discharged without any cardiac sequelae.
- This case highlights a rare occurrence of ST segment elevations in a pediatric patient without congenital heart disease.
Implications:
- Emphasizes the importance of recognizing and managing ST segment elevations in pediatric surgical patients.
- Suggests the need for a systematic workup to determine the etiology of intraoperative ECG changes.
- Underscores potential morbidity and mortality associated with unrecognized ST segment elevations in children.
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