Background: Weil's disease is an infection caused by Leptospira bacteria. Leptospirosis may cause arrhythmias, such as atrial fibrillation and ST-T segment changes. We report a rare case of total atrioventricular block induced by leptospirosis. Early diagnosis and prompt management present particular challenges.
Case Report: A 43-year-old Asian woman was referred from internal medicine to cardiology owing to an electrocardiogram abnormality. She complained of worsening chest discomfort 3 days earlier, accompanied by fever, nausea, and intermittent headaches. The patient appeared lethargic and jaundiced; blood pressure was 81/43 mmHg, heart rate was 41 bpm, respiratory rate was 20 times/minute, and temperature was 38.2 °C. The electrocardiogram showed a total atrioventricular block with a junctional escape rhythm of 45 bpm. Laboratory tests revealed increased renal and liver function, thrombocytopenia (98,000/µL), and positive immunoglobulin G and M anti-Leptospira. The patient was diagnosed with Weil's disease (Faine's score 32) and total atrioventricular block. The initial management involved fitting the patient with a transcutaneous pacemaker and giving dopamine 5 mcg/kgBW/minute, titrated to a target systolic blood pressure of > 90 mmHg. The patient was also scheduled to undergo temporary transvenous pacing. However, the patient died of suspected cardiogenic shock due to a deterioration in clinical condition.
Conclusion: Leptospirosis can cause rare but fatal arrhythmias, as seen in this case of fulminant leptospirosis with total atrioventricular block. Clinicians should be vigilant and consider this potential complication in similar cases.
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http://dx.doi.org/10.1186/s13256-024-04970-w | DOI Listing |
Europace
March 2025
Nantes Université, CHU Nantes, Department of Pediatric Cardiology and Pediatric Cardiac Surgery, FHU PreciCare, F-44000 Nantes, France.
Background And Aims: The natural history of congenital or childhood non-immune, isolated atrioventricular block (AVB) is poorly defined. We aimed at clarifying its long-term outcomes.
Methods: We retrospectively studied 385 children with isolated, non-immune AVB diagnosed from in utero or up to 18 years of age, at 29 French medical centers, between 1980 and 2022.
J Thorac Cardiovasc Surg
March 2025
Clinical Operational Research Unit, University College London.
Objectives: We aimed to ascertain rates of completion of essential cardiac procedures and their overall contribution to longer-term mortality in children with congenital heart disease (CHD).
Methods: Cohort study using the United Kingdom National CHD Audit. For 9 sentinel CHDs (hypoplastic left heart syndrome (HLHS), non-HLHS functionally univentricular heart, ventricular septal defect, tetralogy of Fallot, coarctation, aortic stenosis, atrioventricular septal defect, transposition of the great arteries and pulmonary atresia) we described the pathway operations required for treatment that were undertaken at population-level, and the mortality associated with these pathway operations by age 5-years.
J Thorac Cardiovasc Surg
March 2025
Cardiac Surgery Department, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Objectives: Impact of early age on outcomes for repair of complete atrioventricular canal defects (CAVC) remains poorly defined. We evaluated young infants with CAVC, comparing those who underwent primary repair vs. primary pulmonary artery banding (PAB) and results related to left atrioventricular valve (AVV) re-intervention and survival.
View Article and Find Full Text PDFJ Electrocardiol
February 2025
Faculty of Medicine of Bahia, Federal University of Bahia, Bahia, Brazil.
Introduction: Chagas disease (CD) remains a serious public health issue. It can progress from the acute phase to the chronic phase, manifesting as a cardiomyopathy with some typical electrocardiogram abnormality.
Objectives: This systematic review with meta-analysis aims to evaluate the overall prevalence of cardiac arrhythmias in patients with CD and discriminative values to clinical and epidemiological variables for specific arrhythmias.
BMC Cardiovasc Disord
March 2025
Department of Cardiology, The Second Affiliated Hospital, Yuying Children's Hospital of Wenzhou Medical University, No.109 Xueyuan West Road, Lucheng District, Wenzhou, Zhejiang, 325000, PR China.
Aims: To investigate the characteristics of bipolar intracardiac electrograms (bi-EGMs) in target sites of ventricular arrhythmias (VAs) originating from the distal great vein system (DGCVs).
Methods: 169 patients undergoing first-time ablation for VAs originated from DGCVs were enrolled in present study. Successful ablation was achieved in 146 patients.
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