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1.
J Innov Card Rhythm Manag ; 10(1): 3472-3475, 2019 Jan.
Article in English | MEDLINE | ID: mdl-32494402

ABSTRACT

We report the first case, to our knowledge, of atrial dissociation in a patient who underwent bicaval orthotopic heart transplantation. It was believed that atrioventricular dissociation prompting pacemaker implantation likely represented donor sinus bradycardia/arrest with intact atrioventricular conduction with surgically isolated recipient atrial activity.

2.
J Am Heart Assoc ; 7(15): e008703, 2018 08 07.
Article in English | MEDLINE | ID: mdl-30371253

ABSTRACT

Background Impact of liver disease on development of atrial fibrillation ( AF ) is unclear. The purpose of the study was to evaluate prevalence of AF in the setting of liver disease and whether increasing severity of liver disease, using Model for End-Stage Liver Disease ( MELD ), is independently associated with increased risk of AF . Methods and Results Retrospective data analysis of 1727 patients with liver disease evaluated for liver transplantation between 2006 and 2015 was performed, and patient characteristics were analyzed from billing codes and review of medical records. Multivariable time-dependent Cox proportional hazards model was performed to determine effect of increasing MELD score on risk of developing AF . Prevalence of AF was 11.2%. Incidence of AF at median follow-up time of 1.04 years was 8.5%. Both prevalence and incidence of AF increased with increasing MELD scores. Prevalence of AF was 3.7%, 6.4%, 16.7%, and 20.2% corresponding with MELD quartiles 1 to 10, 11 to 20, 21 to 30, and >30, respectively. Compared with patients with MELD quartile 1 to 10, patients with MELD quartile of 11 to 20 had hazard ratio of 2.73 (confidence interval, 1.47-5.07), those in the MELD quartile of 21 to 30 had a hazard ratio of 5.17 (confidence interval, 2.65-10.09), and those with MELD values >30 had hazard ratio of 9.33 (confidence interval, 3.93-22.14) for development of new-onset AF . Other significant variables associated with new-onset AF were age, sleep apnea, valvular heart disease, hemodynamic instability, and reduced left ventricular ejection fraction <50% (hazard ratio, of 1.06, 2.17, 3.21, 2.00, and 2.44, respectively). Conclusions Prevalence and incidence of AF in patients with liver disease is high. Severity of liver disease, as measured by MELD , is an important predictor of new-onset AF . This novel finding suggests an interaction between inflammatory and neurohormonal changes in liver disease and pathogenesis of AF .


Subject(s)
Atrial Fibrillation/epidemiology , Liver Diseases/epidemiology , Adult , Age Factors , Aged , Carcinoma, Hepatocellular/epidemiology , End Stage Liver Disease , Female , Heart Valve Diseases/epidemiology , Hepatitis C/epidemiology , Humans , Incidence , Liver Diseases, Alcoholic/epidemiology , Liver Neoplasms/epidemiology , Male , Middle Aged , Non-alcoholic Fatty Liver Disease/epidemiology , Prevalence , Proportional Hazards Models , Severity of Illness Index , Sleep Apnea Syndromes/epidemiology
3.
Curr Treat Options Cardiovasc Med ; 20(3): 23, 2018 Mar 06.
Article in English | MEDLINE | ID: mdl-29508149

ABSTRACT

His bundle pacing (HBP) has been shown to be a feasible, beneficial, and safe way to achieve cardiac resynchronization therapy (CRT) with recruitment of the heart's physiological conduction system. HBP should be considered for those with unfavorable coronary sinus (CS) anatomy, and nonresponders to biventricular (BiV) pacing. HBP CRT may also help patients with the nonleft bundle branch block form of conduction delay and heart failure (HF). HBP CRT should be considered strongly in preventing right ventricular (RV) pacing-induced cardiomyopathy, especially after atrioventricular nodal ablation given the discrete nature of the block and the low likelihood of distal block. With increased operator experience and improved lead delivery systems, HBP success rates and safety have improved and are comparable to traditional RV pacing. Battery longevity is also likely comparable to traditional BiV CRT devices. We anticipate the use of HBP CRT growing significantly.

4.
Card Electrophysiol Clin ; 9(4): 665-679, 2017 12.
Article in English | MEDLINE | ID: mdl-29173409

ABSTRACT

Neural remodeling in the autonomic nervous system contributes to sudden cardiac death. The fabric of cardiac excitability and propagation is controlled by autonomic innervation. Heart disease predisposes to malignant ventricular arrhythmias by causing neural remodeling at the level of the myocardium, the intrinsic cardiac ganglia, extracardiac intrathoracic sympathetic ganglia, extrathoracic ganglia, spinal cord, and the brainstem, as well as the higher centers and the cortex. Therapeutic strategies at each of these levels aim to restore the balance between the sympathetic and parasympathetic branches. Understanding this complex neural network will provide important therapeutic insights into the treatment of sudden cardiac death.


Subject(s)
Autonomic Nervous System , Death, Sudden, Cardiac , Heart/innervation , Humans , Tachycardia, Ventricular , Ventricular Fibrillation
5.
Curr Treat Options Cardiovasc Med ; 17(5): 379, 2015 May.
Article in English | MEDLINE | ID: mdl-25894588

ABSTRACT

OPINION STATEMENT: Vagal nerve stimulation (VNS) has shown promise as an adjunctive therapy for management of cardiac arrhythmias by targeting the cardiac parasympathetic nervous system. VNS has been evaluated in the setting of ischemia-driven ventricular arrhythmias and atrial arrhythmias, as well as a treatment option for heart failure. As better understanding of the complexities of the cardiac autonomic nervous system is obtained, vagal nerve stimulation will likely become a powerful tool in the current cardiovascular therapeutic armamentarium.

6.
Clin Vaccine Immunol ; 15(9): 1414-9, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18650400

ABSTRACT

Recombinant Listeria monocytogenes strains induce strong cellular immune responses and may prove useful for antigen delivery for the vaccination of humans. However, the genetic systems currently available for the stable expression of recombinant antigens by L. monocytogenes rely on the use of antibiotic resistance genes. We report on a derivative, pPL2dalGlnA, of the Listeria monocytogenes pPL2 integration vector that completely lacks drug resistance genes. The selectable markers in pPL2dalGlnA are glutamine synthetase (GlnA) and alanine racemase (Dal). This novel vector was stably maintained in auxotropic L. monocytogenes strains that normally require d-alanine. The pPL2dalGlnA vector also partially restored the ability of an L. monocytogenes Deltadal Deltadat strain to colonize the spleens and livers of infected mice. A novel, highly attenuated strain of L. monocytogenes with quadruple deletions was also engineered by deleting the L. monocytogenes actA and plcB virulence genes from a Deltadal Deltadat strain. Infection of mice with recombinants of this mutant strain that express the antigen from pPL2dalGlnA were shown to elicit CD8(+) T-cell responses to human immunodeficiency virus Tat. This vector system is thus useful for stable antigen expression and vaccination studies.


Subject(s)
Bacterial Vaccines/genetics , Gene Expression , Genetic Vectors , Listeria monocytogenes/genetics , Recombinant Proteins/biosynthesis , Recombination, Genetic , Selection, Genetic , AIDS Vaccines/genetics , AIDS Vaccines/immunology , Alanine Racemase/genetics , Alanine Racemase/metabolism , Animals , Bacterial Vaccines/immunology , CD8-Positive T-Lymphocytes/immunology , Female , Gene Deletion , Genes, Bacterial , Genetic Complementation Test , Glutamate-Ammonia Ligase/genetics , Glutamate-Ammonia Ligase/metabolism , Humans , Liver/microbiology , Mice , Mice, Inbred BALB C , Plasmids , Recombinant Proteins/genetics , Spleen/microbiology , Vaccines, Attenuated/genetics , Vaccines, Attenuated/immunology , Virulence
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