This case report presents the first documented instance of vortioxetine-induced syndrome of inappropriate antidiuretic hormone secretion (SIADH) in India. Vortioxetine, a newer antidepressant, was prescribed to an elderly male in his 80s with major depressive disorder, in combination with mirtazapine. Despite initial improvement in mood, he developed hyponatraemia, a rare but serious side effect possibly linked to vortioxetine's serotonergic action. The patient exhibited symptoms such as giddiness and confusion, prompting the discontinuation of vortioxetine and initiation of corrective treatment. His condition improved, with sodium levels returning to normal while he was maintained on mirtazapine alone. This case underscores vortioxetine's potential to induce SIADH, highlighting the need for careful monitoring and the consideration of alternative antidepressants in vulnerable populations.
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http://dx.doi.org/10.1136/bcr-2024-262735 | DOI Listing |
Encephalitis
March 2025
Department of Neurology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Severe fever with thrombocytopenia syndrome (SFTS) is a potentially fatal infectious disease if not diagnosed and treated promptly. Typical clinical features include fever, thrombocytopenia, and lymphadenopathy. However, we encountered a case of SFTS in a 60-year-old male who initially did not exhibit these hallmark symptoms.
View Article and Find Full Text PDFBioelectrochemistry
March 2025
Inner Mongolia Key Laboratory of Solid State Chemistry for Battery, Inner Mongolia Engineering Research Center of Lithium-Sulfur Battery Energy Storage, College of Chemistry and Materials Science, Inner Mongolia Minzu University, Tongliao 028000, People's Republic of China.
The development of highly sensitive methods for detecting infectious diseases is crucial for preventing disease spread. In this study, a novel sensing platform for detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pathogens was developed by combining a magnetic metal-organic framework (FeO@MIL-100) with graphene field-effect transistors (GFET). The FeO@MIL-100 magnetic MOF was functionalized with SARS-CoV-2-specific antibodies, enabling highly selective pathogen capture in a phosphate-buffered solution.
View Article and Find Full Text PDFEndocr Pract
March 2025
Department of Endocrinology & Metabolism, Institute of Post Graduate Medical Education & Research, Kolkata, India.
Objective: Several reports suggested that ACTH level measured by Immulite 1000® may be falsely elevated leading to misdiagnosis of etiology of Cushing syndrome. However, when it comes to fallacies of ACTH measurement in suspected cases of hypocortisolism, evidence is limited. We explored the performance of ACTH assays using Immulite 1000® and Elecsys® Cobas immunoassay platforms in subjects with hypocortisolism.
View Article and Find Full Text PDFJ Ophthalmic Inflamm Infect
March 2025
Medical Retina and Uveitis, Moorfields Eye Hospital, London, UK.
Background: Inadequacies in medicine are manifold including inadequate influence of opinion leaders and consensus groups on terminology, diagnostic criteria and treatment guidelines, obsolete classifications and terms as well as misinterpretations of disease mechanisms. This is no different for uveitis and possibly even more pronounced as these are rare entities.
Purpose: To underline inadequacies in uveitis including inadequate diagnostic criteria and treatment guidelines, misnomers, obsolescence of terminology, misinterpretation of disease processes and inadequate or underuse of investigative modalities in uveitis.
Front Endocrinol (Lausanne)
March 2025
Department of Clinical and Biomedical Science, University of Exeter, Exeter, United Kingdom.
Introduction: Congenital hyperinsulinism (HI) is characterized by inappropriate insulin secretion from the pancreatic beta-cells which causes severe hypoglycemia. Copy number variants (CNVs) encompassing multiple genes (contiguous gene CNVs) can cause syndromic forms of HI although they are not typically screened for during routine genetic testing for this condition. We aimed to assess the prevalence of disease-causing contiguous gene CNVs in a cohort of individuals referred for HI genetic testing.
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