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1.
Open Heart ; 8(2)2021 12.
Article in English | MEDLINE | ID: mdl-34949648

ABSTRACT

INTRODUCTION: Pulmonary vein isolation (PVI) is an important treatment for atrial fibrillation (AF). However, many patients need more than one procedure to maintain long-term sinus rhythm. Even after two PVIs some may suffer from AF recurrences. We aimed to identify characteristics of patients who fail after two PVI procedures. METHODS AND RESULTS: We included 557 consecutive patients undergoing a first PVI procedure with a second-generation 28 mm cryoballoon. Follow-up procedures were performed using radiofrequency ablation targeting reconnected PVs only. Recurrent AF was defined as any episode of AF lasting >30 s on ECG or 24 hour Holter monitoring performed at 3, 6 and 12 months post procedure. Mean age was 59.1±10.2 years, 383 (68.8%) were male, 448 (80.4%) had paroxysmal AF and the most common underlying condition was hypertension (36.6%). A total of 140/557 (25.1%) patients underwent redo procedure with PVI only. Of these patients 45 (32.4%) had recurrence of AF. These patients were comparable regarding age and sex to those in sinus rhythm after one or two procedures. Multivariate logistic regression showed that non-paroxysmal AF (OR 1.08 (95% CI 1.01 to 1.15), estimated glomerular filtration rate (OR 0.96, 95% CI 0.94 to 0.99), bundle branch block (OR 4.17, 95% CI 1.38 to 12.58), heart failure (OR 4.17, 95% CI 1.38 to 12.58) and Left Atrium Volume Index (OR 1.04, 95% CI 1.01 to 1.08) were associated with AF recurrence after two PVIs. The area under the curve for the identified risk factors was 0.74. CONCLUSIONS: Using a PVI-only approach, recurrence of AF after two AF ablation procedures is associated with more advanced underlying disease and persistent types of AF.


Subject(s)
Atrial Fibrillation/epidemiology , Catheter Ablation , Electrocardiography, Ambulatory/methods , Pulmonary Veins/surgery , Atrial Fibrillation/physiopathology , Atrial Fibrillation/surgery , Female , Humans , Incidence , Male , Middle Aged , Netherlands/epidemiology , Recurrence , Reoperation , Retrospective Studies , Risk Factors , Time Factors , Treatment Outcome
2.
Histol Histopathol ; 8(4): 699-707, 1993 Oct.
Article in English | MEDLINE | ID: mdl-7508304

ABSTRACT

The anterior horns of the lumbosacral segment of the spinal cord in rats showed an extensive lesion following an intraperitoneal administration of 6-amino-nicotinamide (6-AN). Neuronal chromatolysis was observed in some of the large efferent neurons 1-7 days after the injection of 6-AN. The capability in their uptake of fluorogold and its retrograde transport was comparable to those in the normal rats. Small neurons presumably internuncial cells underwent degeneration. 8 weeks after 6-AN injection, all the surviving neurons appeared normal. 1 day after 6-AN injection microglial cells appeared activated as evidenced by the hypertrophy and expansion of their processes. A large number of macrophages were observed in the lesioned site 7 days after the administration of 6-AN. The activated microglia and macrophages showed intense immunoreactivity with the monoclonal antibody OX-42. The immunoreactivity declined with time so that by 4 weeks after the injection of 6-AN very weak immunoreactivity was seen on some very branched cells. A similar pattern of immunoreactivity was observed with the monoclonal antibodies OX-18 and OX-6. It was concluded from this study that neuronal chromatolysis and neuronal degeneration induced the expression of CR3 receptors (marked by OX-42) and MHC encoded antigens (marked by OX-18 and OX-6) in activated microglia and macrophages. With time the immunoreactivity decreased so that by 4 weeks after the administration of 6-AN only faint immunoreactivity was observed on some branched cells.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
6-Aminonicotinamide/toxicity , Macrophages/drug effects , Microglia/drug effects , Neurons/drug effects , Spinal Cord/drug effects , Animals , Antibodies, Monoclonal , Axonal Transport , Cell Nucleus/ultrastructure , Chromatin/ultrastructure , Endoplasmic Reticulum/ultrastructure , Hypertrophy , Immunohistochemistry , Macrophages/pathology , Macrophages/ultrastructure , Microglia/pathology , Microglia/ultrastructure , Microscopy, Electron , Microscopy, Immunoelectron , Neuromuscular Junction/ultrastructure , Neurons/pathology , Neurons/ultrastructure , Rats , Rats, Wistar , Spinal Cord/pathology , Spinal Cord/ultrastructure
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