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Background: This case report details the management of a patient who presented with third-degree atrioventricular block and rhabdomyolysis secondary to clozapine intoxication.
Case Summary: The patient was a 55-year-old man who took 100 tablets of clozapine and was transferred to our hospital from a lower-level hospital for treatment. Upon arrival at our hospital, he was in a coma and was assisted with mechanical ventilation. Upon admission, based on the results of toxicological tests and laboratory examination; computed tomography, magnetic resonance imaging, and echocardiography findings, and the patient's clinical manifestations, the diagnosis of third-degree atrioventricular block and rhabdomyolysis due to excessive intake of clozapine was confirmed. The patient received comprehensive treatment, including blood purification, organ protection, nutritional support, and cardiac rate enhancement. The patient was clinically cured and discharged. Clozapine-induced central nervous system inhibition can be dose-dependent, thus leading to coma and organ damage at high doses. Considering that no specific antidotes are available, cases involving clozapine toxicity require careful management. In this instance, beyond the central nervous system and respiratory depression, the patient also exhibited third-degree atrioventricular block and rhabdomyolysis, which warrant significant attention.
Conclusion: Many patients with clozapine poisoning have been admitted to our department. Clozapine poisoning mostly causes symptoms such as accelerated heart rate, but in our patient's case, third-degree atrioventricular block and rhabdomyolysis symptoms occurred unusually. For clozapine poisoning, timely and appropriate management is crucial for the recovery of patients.
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http://dx.doi.org/10.3389/fphar.2025.1572578 | DOI Listing |
Saudi Med J
September 2025
From the Pediatric Cardiology Division (Mashali, Abdelmohsen, Baamer, Elhudairy, Alkhushi, Bahaidarah, Abdelsalam, Elakaby, Maghrabi, Azhar, Zaher, Al Ata, Dohain, Baamer), Department of Pediatrics, King Abdulaziz University, Jeddah, Saudi Arabia, From the Department of Cardiac Surgery (Al-Radi, Jam
Objectives: To assess the surgical outcomes of atrioventricular septal defect associated with Tetralogy of Fallot (AVSD)-TOF repair performed at 2 specialized cardiac centers.
Methods: From May 2012 to December 2024, 20 patients diagnosed with AVSD-TOF who underwent surgical repair were included.
Results: The median age at the time of surgical repair was 13 months, with a median weight of 8.
Cureus
July 2025
Adult Cardiology, Uganda Heart Institute, Kampala, UGA.
Patients with hypertrophic cardiomyopathy (HCM) are commonly affected by ventricular tachyarrhythmias such as ventricular tachycardia, leading to syncope and sudden cardiac death (SCD). Complete atrioventricular (AV) block in patients with HCM is very unusual but may also lead to syncope and SCD. We report a 52-year-old male who presented with recurrent episodes of pre-syncope and effort intolerance.
View Article and Find Full Text PDFEur Heart J Case Rep
August 2025
Board of Director, Thu Duc City Hospital, 29 Phu Chau Street, Tam Binh Ward, Ho Chi Minh City 70000, Vietnam.
Background: The concurrent management of ST-elevation myocardial infarction (STEMI) and acute intracerebral haemorrhage (ICH) poses a significant clinical challenge due to conflicting treatment goals. While the management of STEMI requires coronary reperfusion with antithrombotic agents (anticoagulants and antiplatelets), such treatments are contraindicated in cases of ICH. The coexistence of STEMI and ICH is exceedingly rare in the literature and is associated with high mortality rates.
View Article and Find Full Text PDFAm J Case Rep
August 2025
Jan Mikulicz Radecki University Hospital, Wrocław, Poland.
BACKGROUND Kearns-Sayre syndrome (KSS) is a rare genetic, mitochondrial disorder characterized by a triad of chronic progressive external ophthalmoplegia, pigmentary retina degeneration, and cardiac conduction disorders, with onset before the age of 20 years. The disease can also manifest as several cardiovascular (CV) disorders, such as conduction disorders or dilated cardiomyopathy, along with neuromuscular and endocrinological complications. CASE REPORT A 46-year-old man diagnosed with KSS was admitted to the Institute of Heart Diseases in the qualification process for heart transplantation (Htx).
View Article and Find Full Text PDFFront Med (Lausanne)
July 2025
Department of Endocrinology, Third Hospital of Hebei Medical University, Shijiazhuang, China.
Kearns-Sayre syndrome is a mitochondrial DNA deletion disorder, classically characterized by a triad of onset before the age of 20, pigmentary retinopathy, and chronic progressive external ophthalmoplegia (CPEO). The condition is frequently associated with third-degree atrioventricular block, endocrine dysfunction, and short stature. Here, we report a case of KSS presenting with a progressive clinical course that began at birth with ptosis and later developed type 1 diabetes, hypopituitarism, and third-degree atrioventricular block.
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