Cardiogenic shock in a woman with a mitochondrial cardiomyopathy: a case report. Issue 4 (18th April 2023)

• Record Type: Journal Article
• Authors: Girard, Andrew; Heindl, Brittain; Clarkson, Stephen; Litovsky, Silvio; Ubogu, Eroboghene; Schwartzlow, Coreen; Tallaj, Jose
• Editors: Safarova, Maya S; Kitai, Takeshi; Nuzzi, Vincenzo; Agarwal, Megha; Salekin, Damien Farhad Nur
• Is Part Of: European heart journal. Volume 7:Issue 4(2023)
• Publication Date: 2023-04-18
• Subjects: Mitochondrial cardiomyopathy -- Mitochondrial DNA disease -- Advanced heart failure -- Mechanical circulatory support device -- Case report; Cardiology -- Periodicals; Cardiology -- Case studies -- Periodicals; Heart -- Diseases -- Periodicals; Heart -- Diseases -- Case studies -- Periodicals; 616.12
• DOI: 10.1093/ehjcr/ytad183
• Languages: English
• ISSNs: 2514-2119

Abstract

Abstract: Background: Mitochondrial cardiomyopathy (MCM) is an alteration in cardiac structure and function caused by gene mutations or deletions affecting components of the mitochondrial respiratory chain. We report a case of MCM presenting as cardiogenic shock, ultimately requiring left ventricular assist device (LVAD) placement. Case summary: A 35-year-old woman with chronic weakness and non-ischaemic cardiomyopathy, on home dobutamine, was referred to our institution for heart transplantation evaluation. She was admitted to the hospital for suspected cardiogenic shock after laboratory tests revealed a lactate level of 5.4 mmol/L (ref: 0.5–2.2 mmol/L). Her hospital course was complicated by persistently undulating lactate levels (0.2–8.6 mmol/L) that increased with exertion and did not correlate with mixed venous oxygen saturation measurements obtained from a pulmonary artery catheter. Electrodiagnostic testing demonstrated a proximal appendicular and axial myopathy. A left deltoid muscle biopsy was performed that demonstrated evidence of a mitochondrial disease on light and electron microscopy. Muscle genetic testing revealed two large-scale mitochondrial deoxyribonucleic acid sequence deletions, confirming the diagnosis of MCM. She subsequently underwent LVAD placement, which was complicated by significant right ventricular failure requiring early mechanical support. She was ultimately discharged home with chronic inotropic support. Discussion: Mitochondrial cardiomyopathy in adults is a diagnostic and therapeutic challenge. Prompt diagnosis should be made in patients with unknown causes of heart failure via skeletal muscle histopathology guided by electrodiagnostic studies, and targeted genetic testing in affected tissue. Outcomes in adult MCM patients who receive an LVAD are unknown and warrant further investigation.