Device‐detected non‐sustained ventricular tachycardia in adult congenital heart disease without tetralogy of fallot

Author(s):  
Pezad Doctor ◽  
Sanjeev Aggarwal ◽  
David K. Lawrence ◽  
Pooja Gupta ◽  
Gautam K. Singh ◽  
...  
2020 ◽  
Vol 25 (4) ◽  
pp. 583-598 ◽  
Author(s):  
Anna S. Mueller ◽  
Daniel M. McDonald ◽  
Harsimran S. Singh ◽  
Jonathan N. Ginns

Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Audrey Thorp ◽  
Alexander Hajduczok ◽  
Sudhanshu Bhatnagar ◽  
Ravi Shah ◽  
William R Davidson

Introduction: Tetralogy of Fallot (TOF) and Ventricular Septal Defect (VSD) patients have non-diagnostic Q-waves within inferior (II, III, aVF) or septal (V1-V2) leads on ECG, perhaps due to incomplete conduction through septal defects. Non-diagnostic Q-waves tend to either be wide within a single lead, or deep (3-4mm) in contiguous leads, but do not meet diagnostic criteria for infarct. Hypothesis: Non-Adult Congenital Heart Disease (ACHD) physicians may inaccurately characterize non-diagnostic Q-waves as pathologic opposed to expert interpretation by ACHD-trained physicians in VSD and TOF patients. Thus, misinterpreting ECGs to suggest prior infarct and decreasing their positive predictive value (PPV). Methods: With application of pre-specified inclusion and exclusion criteria, we retrospectively reviewed 72 ECGs from TOF or VSD patients at Penn State Hershey Medical Center from 2002-2020 that were separately read by ACHD and non-ACHD specialists. Primary outcomes were ECGs with diagnosed Q-waves in two separate distributions, inferior or septal leads, by both groups using standard criteria for Q-wave infarct. Reported measures were sensitivity, specificity, PPV, and negative predictive value (NPV). Results: The 72 subjects with isolated TOF or VSD had a mean age of 39 years and 63% were male. Total disease prevalence (presence of Q-waves) was 4.6%. Q-wave infarct diagnosed by non-ACHD physicians had a sensitivity and specificity of 33% and 74% respectively. Their PPV was 5.87% and NPV was 95.85%. Conclusions: This retrospective cohort analysis of TOF and VSD patient ECGs showed the low PPV of non-ACHD physician diagnosis of Q-waves in this respective population. Misinterpretation and misdiagnosis of infarct based off ECG, has ramifications for both the patient and medical system as a whole. Sequelae include, but are not limited to, increasing patient risk for unwarranted medical treatment and affecting hospital billing and insurance coverage.


Author(s):  
A. Razinkina ◽  
I. Lebid ◽  
Ye. Segal ◽  
R. Kalashnikova ◽  
Ye. Liebied ◽  
...  

This publication presents case report of primary non-corrected adult congenital heart disease, tetralogy of Fallot, in forty-seven years old female patient. Clinical and anatomic issues were estimated within postoperative follow-up period and literature concerning surgical repair of tetralogy of Fallot in adult with congenital heart disease was reviewed. The aim. There was presentation the case report of adult patient with tetralogy of Fallot after surgical repair carried out at our Institution, as well as literature review concerning grown-up patients with tetralogy of Fallot in early and late postoperative period. Materials and methods. Female patient, forty-seven years old with grown-up congenital heart disease, tetralogy of Fallot with severe comorbidity. Results. Tetralogy of Fallot was radically repaired with high estimated operative risks. In early postoperative period there was increased exudation through both pleural drainages due to the function of major aortopulmonary collateral arteries. The decision was made to perform interventional closure of major aortopulmonary collateral arteries which enabled to discharge patient within 23 days in satisfactory condition. Conclusions. Presented case report and literature review show that the patient`s age is not a contraindication for repair of tetralogy of Fallot in adults with congenital heart disease. Patients with tetralogy of Fallot usually do not survive until adult age without surgical repair. Our presented case report and literature review show that surgery correction of tetralogy of Fallot in grown-up patients above 40 years of age should be performed in specialized centers experienced in pediatric cardiac surgery and in management of adult congenital heart disease regardless of patient age.


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