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1.
World J Pediatr Congenit Heart Surg ; 11(6): 802-804, 2020 11.
Article in English | MEDLINE | ID: mdl-32909890

ABSTRACT

We describe a seven-year-old female with acute pericarditis presenting with pericardial tamponade, who screened positive for coronavirus disease 2019 (COVID-19 [SARS-CoV-2]) in the setting of cough, chest pain, and orthopnea. She required emergent pericardiocentesis. Due to continued chest pain and orthopnea, rising inflammatory markers, and worsening pericardial inflammation, she underwent surgical pericardial decortication and pericardiectomy. Her symptoms and pericardial effusion resolved, and she was discharged to home 3 days later on ibuprofen and colchicine with instruction to quarantine at home for 14 days from the date of her positive testing for COVID-19.


Subject(s)
COVID-19/complications , Cardiac Tamponade/etiology , Pericarditis/etiology , SARS-CoV-2/isolation & purification , COVID-19 Testing , Cardiac Tamponade/diagnosis , Chest Pain/etiology , Child , Electrocardiography , Female , Heart/diagnostic imaging , Humans , Pandemics , Pericardial Effusion/diagnostic imaging , Pericardial Effusion/etiology , Pericardiectomy , Pericardiocentesis , Pericarditis/diagnostic imaging , Pericarditis/surgery , Radiography, Thoracic
2.
Ann Thorac Surg ; 98(1): 159-66, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24793683

ABSTRACT

BACKGROUND: Historic outcomes of patients with heterotaxy and pulmonary atresia or pulmonary stenosis (PA/PS) have been poor and in the current era are incompletely described. We reviewed our management of these patients and associated risk factors for death. METHODS: We retrospectively reviewed the records of all patients with heterotaxy and PA/PS treated in our institution from January 1, 2002, to August 31, 2012. Death data were also confirmed with the Social Security Death Index. The log-rank test was done to assess six risk factors for death. RESULTS: We identified 42 patients with heterotaxy and PA/PS. Median age at the first operation was 6.5 days, and median follow-up was 3.5 years. Death data were complete for all patients. Overall mortality was 19% (8 of 42). The 30-day, 1-year, and 5-year mortality estimation was 4.76%, 12.3%, and 19.1% respectively, as determined by the Kaplan-Meier method. The log-rank test showed total anomalous pulmonary venous return (TAPVR) (p<0.05) and obstructed TAPVR requiring an operation at less than 30 days (p=0.001) were significant risk factors for death. CONCLUSIONS: In the current era, surgical treatment of heterotaxy and PA/PS can result in good outcomes. Associated TAPVR and obstructed TAPVR requiring neonatal correction were noted to be risk factors for death.


Subject(s)
Abnormalities, Multiple , Cardiac Surgical Procedures/methods , Heterotaxy Syndrome/surgery , Pulmonary Atresia/surgery , Pulmonary Veins/abnormalities , Pulmonary Veno-Occlusive Disease/surgery , Cardiac Catheterization , Echocardiography , Follow-Up Studies , Heterotaxy Syndrome/diagnosis , Humans , Infant, Newborn , Male , Pulmonary Atresia/diagnosis , Pulmonary Veno-Occlusive Disease/diagnosis , Retrospective Studies , Time Factors , Tomography, X-Ray Computed , Treatment Outcome
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