Cargando…
Severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report
BACKGROUND: Cardiac sarcoidosis is found to occur in approximately 5% of patients with sarcoidosis. Its presentation can typically range from complete heart block to ventricular arrhythmias. This condition can rarely present with severe heart failure and cardiogenic shock requiring aggressive and ti...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150484/ https://www.ncbi.nlm.nih.gov/pubmed/37127559 http://dx.doi.org/10.1186/s12872-023-03238-3 |
_version_ | 1785035368773451776 |
---|---|
author | Chakrala, Teja Prakash, Roshni O. Jain, Anshul Vautier, R. Ashton Prasada, Sahil Al-Ani, Mohammed Ahmed, Mustafa M. |
author_facet | Chakrala, Teja Prakash, Roshni O. Jain, Anshul Vautier, R. Ashton Prasada, Sahil Al-Ani, Mohammed Ahmed, Mustafa M. |
author_sort | Chakrala, Teja |
collection | PubMed |
description | BACKGROUND: Cardiac sarcoidosis is found to occur in approximately 5% of patients with sarcoidosis. Its presentation can typically range from complete heart block to ventricular arrhythmias. This condition can rarely present with severe heart failure and cardiogenic shock requiring aggressive and timely management strategies. Advanced imaging techniques are usually required to assist with its diagnosis. CASE PRESENTATION: A 70-year-old woman with a history of pulmonary sarcoidosis presented with non-ST elevation myocardial infarction, congestive hepatopathy, and acute renal failure. Left heart catheterization showed evidence of non-obstructive coronary artery disease, and right heart catheterization revealed severely elevated filling pressures and depressed cardiac index. She underwent aggressive diuresis and placement of an intra-aortic balloon pump in addition to initiation of inotropic and vasopressor support. While in the cardiac intensive care unit, she experienced frequent episodes of ventricular tachycardia and went into cardiac arrest requiring cardiopulmonary resuscitation. High clinical suspicion for cardiac sarcoidosis was confirmed by cardiac magnetic resonance imaging findings. After starting immunosuppressive therapy for cardiac sarcoidosis, she demonstrated clinical improvement. CONCLUSION: Patients with cardiac sarcoidosis may remain asymptomatic or present with conduction abnormalities and arrhythmias. They rarely present with severe biventricular heart failure and cardiogenic shock, and in such cases, they require timely initiation of pharmacologic and device therapies, along with implementation of mechanical circulatory support. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-023-03238-3. |
format | Online Article Text |
id | pubmed-10150484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101504842023-05-02 Severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report Chakrala, Teja Prakash, Roshni O. Jain, Anshul Vautier, R. Ashton Prasada, Sahil Al-Ani, Mohammed Ahmed, Mustafa M. BMC Cardiovasc Disord Case Report BACKGROUND: Cardiac sarcoidosis is found to occur in approximately 5% of patients with sarcoidosis. Its presentation can typically range from complete heart block to ventricular arrhythmias. This condition can rarely present with severe heart failure and cardiogenic shock requiring aggressive and timely management strategies. Advanced imaging techniques are usually required to assist with its diagnosis. CASE PRESENTATION: A 70-year-old woman with a history of pulmonary sarcoidosis presented with non-ST elevation myocardial infarction, congestive hepatopathy, and acute renal failure. Left heart catheterization showed evidence of non-obstructive coronary artery disease, and right heart catheterization revealed severely elevated filling pressures and depressed cardiac index. She underwent aggressive diuresis and placement of an intra-aortic balloon pump in addition to initiation of inotropic and vasopressor support. While in the cardiac intensive care unit, she experienced frequent episodes of ventricular tachycardia and went into cardiac arrest requiring cardiopulmonary resuscitation. High clinical suspicion for cardiac sarcoidosis was confirmed by cardiac magnetic resonance imaging findings. After starting immunosuppressive therapy for cardiac sarcoidosis, she demonstrated clinical improvement. CONCLUSION: Patients with cardiac sarcoidosis may remain asymptomatic or present with conduction abnormalities and arrhythmias. They rarely present with severe biventricular heart failure and cardiogenic shock, and in such cases, they require timely initiation of pharmacologic and device therapies, along with implementation of mechanical circulatory support. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-023-03238-3. BioMed Central 2023-05-01 /pmc/articles/PMC10150484/ /pubmed/37127559 http://dx.doi.org/10.1186/s12872-023-03238-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Chakrala, Teja Prakash, Roshni O. Jain, Anshul Vautier, R. Ashton Prasada, Sahil Al-Ani, Mohammed Ahmed, Mustafa M. Severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report |
title | Severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report |
title_full | Severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report |
title_fullStr | Severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report |
title_full_unstemmed | Severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report |
title_short | Severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report |
title_sort | severe cardiogenic shock and cardiac arrest due to fulminant cardiac sarcoidosis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150484/ https://www.ncbi.nlm.nih.gov/pubmed/37127559 http://dx.doi.org/10.1186/s12872-023-03238-3 |
work_keys_str_mv | AT chakralateja severecardiogenicshockandcardiacarrestduetofulminantcardiacsarcoidosisacasereport AT prakashroshnio severecardiogenicshockandcardiacarrestduetofulminantcardiacsarcoidosisacasereport AT jainanshul severecardiogenicshockandcardiacarrestduetofulminantcardiacsarcoidosisacasereport AT vautierrashton severecardiogenicshockandcardiacarrestduetofulminantcardiacsarcoidosisacasereport AT prasadasahil severecardiogenicshockandcardiacarrestduetofulminantcardiacsarcoidosisacasereport AT alanimohammed severecardiogenicshockandcardiacarrestduetofulminantcardiacsarcoidosisacasereport AT ahmedmustafam severecardiogenicshockandcardiacarrestduetofulminantcardiacsarcoidosisacasereport |