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1.
World J Pediatr Congenit Heart Surg ; 13(4): 514-516, 2022 07.
Article in English | MEDLINE | ID: mdl-35018849

ABSTRACT

Given the lack of systemic venous return to the heart, palliated single ventricle patients frequently require epicardial pacemaker implantation for management of dysrhythmias including sinus node dysfunction, atrial arrhythmias, and heart block. Repeated device hardware replacement, frequently required due to high lead thresholds or other device failure, is a challenging and significant problem for this population. 3-dimensional imaging can assist in delineating the cardiac anatomy allowing for novel approaches to intervention. We review a patient with extracardiac Fontan circulation who underwent placement of an endocardial atrial pacemaker lead via a transmural approach with a 3D-printed model used for procedural guidance.


Subject(s)
Fontan Procedure , Heart Defects, Congenital , Pacemaker, Artificial , Univentricular Heart , Adult , Arrhythmias, Cardiac , Cardiac Pacing, Artificial/methods , Fontan Procedure/methods , Heart Defects, Congenital/surgery , Humans
2.
Am J Case Rep ; 21: e925602, 2020 Oct 15.
Article in English | MEDLINE | ID: mdl-33056945

ABSTRACT

BACKGROUND Long QT syndrome (LQTS) is an arrhythmogenic heart condition that can be congenital or acquired. Prolonged ventricular repolarizations in individuals with the disorder can cause fatal arrhythmias. Abnormal functioning of cardiac ion channels leads to arrhythmias such as torsades de pointes (TdP) and may be triggered by stress or medications. Many medications used in the perioperative period are triggers for the arrythmia. CASE REPORT A 7-year-old patient with known congenital LQTS type 2 presented for bilateral myringotomy and tube placement. The patient was otherwise healthy and taking propranolol daily. Preoperative midazolam was administered for anxiolysis, and induction of anesthesia was uneventful. He sustained an episode of TdP immediately following general anesthetic induction after failure of an in situ automatic implantable cardioverter-defibrillator (AICD). External defibrillation succeeded, and the patient was stabilized in the Postanesthesia Recovery Unit before transfer to the Pediatric Intensive Care Unit. Interrogation of the AICD revealed several undelivered defibrillation attempts. A chest X-ray showed an area suggestive of an epicardial electrode fracture. The following day, the AICD was replaced with no arrythmias noted. The patient had an uneventful recovery. CONCLUSIONS In patients with a known history of LQTS, preparation and prevention are cornerstones of anesthesia care. Minimizing the use of triggering medications and emotional stress in the perioperative period, combined with ready equipment and medications to respond to arrythmias, are essential. In children, there is a greater chance of lead fracture and resulting device failure. Preoperative history of device function or interrogation of the AICD and possibly a chest X-ray are essential to ensure the integrity of the leads.


Subject(s)
Long QT Syndrome , Torsades de Pointes , Anesthesia, General , Child , Electrocardiography , Humans , Long QT Syndrome/complications , Male , Torsades de Pointes/etiology
3.
Pediatr Cardiol ; 33(4): 659-62, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22290592

ABSTRACT

A 16-year-old Hispanic girl with arrhythmogenic right-ventricle dysplasia (ARVD) presented with angina pectoris and troponin increase on three occasions. There was a family history of sudden cardiac death in a cousin. Her mother was diagnosed with ARVD. The patient herself had a history of nonsustained ventricular tachycardia but did not meet diagnostic criteria for ARVD. Cardiac workup, including serial transthoracic echocardiograms and a coronary angiogram, showed a structurally normal heart without coronary artery stenosis. Results of cardiac magnetic resonance imaging were questionable, but endomyocardial biopsy did not show evidence of viral myocarditis by polymerase chain reaction. Genetic testing confirmed ARVD.


Subject(s)
Angina Pectoris/etiology , Arrhythmogenic Right Ventricular Dysplasia/complications , Troponin/blood , Adolescent , Angina Pectoris/blood , Angina Pectoris/diagnosis , Arrhythmogenic Right Ventricular Dysplasia/blood , Arrhythmogenic Right Ventricular Dysplasia/diagnosis , Biomarkers/blood , Biopsy , Diagnosis, Differential , Disease Progression , Echocardiography , Electrocardiography , Female , Genetic Testing , Humans , Magnetic Resonance Imaging, Cine , Myocardium/pathology
4.
Respir Care ; 52(3): 263-70, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17328824

ABSTRACT

BACKGROUND: The respiratory care department of one campus within our health system evaluated simulation-based medical education for training and competency evaluation of the mini bronchoalveolar lavage (mini-BAL) procedure, with an emphasis on patient safety and procedure performance standards. METHODS: Training and competency evaluation occurred in 4 phases. In phase one, 24 staff respiratory therapists (RTs) were randomly chosen and individually underwent a simulation-based test of their mini-BAL performance, using a patient-simulator mannequin. Their performance on this test reflected the effectiveness of traditional training methods. In phase two, 83 staff RTs were given unlimited access to a Web-based curriculum on mini-BAL, including a video of a mini-BAL. They then took 2 tests: one online Web-based test, then a patient-simulator test. In phase three, the same 83 RTs attended a workshop that used the patient simulator for training and practice, then were re-evaluated with the patient-simulator test. Phase four was another simulator-based re-evaluation, 90 days after phase three, to study skills retention. RESULTS: The mean scores were: phase one 73 +/- 10%, phase two 77 +/- 11%, phase three 95 +/- 5% (p < 0.01), phase four 92 +/- 8%. CONCLUSION: Our results suggest that employing simulation technology within a comprehensive departmental program can enhance staff training.


Subject(s)
Bronchoalveolar Lavage/nursing , Clinical Competence , Health Personnel/education , Inservice Training/methods , Respiratory Care Units , Humans , Pennsylvania
5.
Curr Opin Cardiol ; 19(1): 64-7, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14688637

ABSTRACT

PURPOSE OF REVIEW: Radiofrequency (RF) ablation treatment for tachyarrhythmias has been available only for the past 15 years. The success rates have been excellent with a very low frequency of complications. Because of this efficacy, the use of RF ablation in children has become standard of care even though long-term data are unavailable. In this review, common tachyarrhythmias and their current treatments in children will be discussed. RECENT FINDINGS: Novel electrophysiology technologies such as electroanatomic mapping and sophisticated ablating catheters have improved success rates and decreased complications. The improvement is also due to better understanding of the mechanisms and etiologies of tachyarrhythmias. Both have positively impacted success rates and have made more complicated tachyarrhythmias treatable with ablation. SUMMARY: The technologic advances in ablation and improved understanding of tachyarrhythmias over the past 15 years have greatly improved outcomes in ablative treatment of tachyarrhythmias in children. In most cases this method of treatment is the preferred first-line approach to symptomatic tachyarrhythmias in children.


Subject(s)
Catheter Ablation , Tachycardia/surgery , Catheter Ablation/methods , Child , Humans , Risk Factors , Tachycardia/classification , Tachycardia/physiopathology , Treatment Outcome
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