Cargando…

From 13% to 60%: A Rare Case of Multisystem Inflammatory Syndrome in Adults 4 Weeks Following COVID-19 Infection

INTRODUCTION: Multisystem inflammatory syndrome in adults (MIS-A) is a rare but serious entity implicated with COVID-19 infection. Improved diagnosis and treatment of MIS-A may mitigate morbidity and mortality attributed to COVID-19 infection. CASE REPORT: Our patient is a 24-year-old male with no k...

Descripción completa

Detalles Bibliográficos
Autores principales: Habib, E., Baqal, O., LeMond, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988565/
http://dx.doi.org/10.1016/j.healun.2022.01.699
_version_ 1784682989375979520
author Habib, E.
Baqal, O.
LeMond, L.
author_facet Habib, E.
Baqal, O.
LeMond, L.
author_sort Habib, E.
collection PubMed
description INTRODUCTION: Multisystem inflammatory syndrome in adults (MIS-A) is a rare but serious entity implicated with COVID-19 infection. Improved diagnosis and treatment of MIS-A may mitigate morbidity and mortality attributed to COVID-19 infection. CASE REPORT: Our patient is a 24-year-old male with no known past medical history except for COVID-19 infection diagnosed 4 weeks prior. He presented with a 5-day history of intractable nausea, vomiting, and abdominal pain. He was febrile. COVID-19 test was negative. The patient became hypotensive, tachycardic and was aggressively resuscitated (5L crystalloid) with no improvement. He was transferred to ICU, intubated for worsening acute hypoxic respiratory failure, and started on vasopressors. TTE showed EF of 13% with severe global LV hypokinesis and RV enlargement with severe global hypokinesis. He underwent urgent coronary angiogram which showed normal coronaries. His clinical course was consistent with the working definition of MIS-A as specified by the CDC. As the patient was in cardiogenic shock with severe biventricular dysfunction, left femoral Impella CP and right femoral Impella RP were placed. Given his severe hemodynamic compromise leading to persistent shock and multiorgan failure, he was eventually placed on venoarterial ECMO. The patient was being treated with methylprednisolone, IVIg and anakinra. Over the following days, he continued to improve, and his vasopressors were weaned off. His Impella CP was successfully removed with stable LV pulsatility on arterial line. His LV function improved on TTE and the patient was decannulated 5 days after initiation of VA ECMO. TEE done 6 days after initial echocardiogram showed LVEF of 60% and normal RV systolic function. The patient was extubated and continued to improve clinically. SUMMARY: MIS-A is a serious hyperinflammatory condition that presents with multiorgan dysfunction approximately 4 weeks after onset of COVID-19 infection. Aggressive supportive care in the ICU, utilization of advanced heart failure devices, and immunomodulatory therapeutics should be utilized during management. More studies are needed to elaborate on treatment modalities and clinical predictors.
format Online
Article
Text
id pubmed-8988565
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Published by Elsevier Inc.
record_format MEDLINE/PubMed
spelling pubmed-89885652022-04-11 From 13% to 60%: A Rare Case of Multisystem Inflammatory Syndrome in Adults 4 Weeks Following COVID-19 Infection Habib, E. Baqal, O. LeMond, L. J Heart Lung Transplant (678) INTRODUCTION: Multisystem inflammatory syndrome in adults (MIS-A) is a rare but serious entity implicated with COVID-19 infection. Improved diagnosis and treatment of MIS-A may mitigate morbidity and mortality attributed to COVID-19 infection. CASE REPORT: Our patient is a 24-year-old male with no known past medical history except for COVID-19 infection diagnosed 4 weeks prior. He presented with a 5-day history of intractable nausea, vomiting, and abdominal pain. He was febrile. COVID-19 test was negative. The patient became hypotensive, tachycardic and was aggressively resuscitated (5L crystalloid) with no improvement. He was transferred to ICU, intubated for worsening acute hypoxic respiratory failure, and started on vasopressors. TTE showed EF of 13% with severe global LV hypokinesis and RV enlargement with severe global hypokinesis. He underwent urgent coronary angiogram which showed normal coronaries. His clinical course was consistent with the working definition of MIS-A as specified by the CDC. As the patient was in cardiogenic shock with severe biventricular dysfunction, left femoral Impella CP and right femoral Impella RP were placed. Given his severe hemodynamic compromise leading to persistent shock and multiorgan failure, he was eventually placed on venoarterial ECMO. The patient was being treated with methylprednisolone, IVIg and anakinra. Over the following days, he continued to improve, and his vasopressors were weaned off. His Impella CP was successfully removed with stable LV pulsatility on arterial line. His LV function improved on TTE and the patient was decannulated 5 days after initiation of VA ECMO. TEE done 6 days after initial echocardiogram showed LVEF of 60% and normal RV systolic function. The patient was extubated and continued to improve clinically. SUMMARY: MIS-A is a serious hyperinflammatory condition that presents with multiorgan dysfunction approximately 4 weeks after onset of COVID-19 infection. Aggressive supportive care in the ICU, utilization of advanced heart failure devices, and immunomodulatory therapeutics should be utilized during management. More studies are needed to elaborate on treatment modalities and clinical predictors. Published by Elsevier Inc. 2022-04 2022-04-07 /pmc/articles/PMC8988565/ http://dx.doi.org/10.1016/j.healun.2022.01.699 Text en Copyright © 2022 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle (678)
Habib, E.
Baqal, O.
LeMond, L.
From 13% to 60%: A Rare Case of Multisystem Inflammatory Syndrome in Adults 4 Weeks Following COVID-19 Infection
title From 13% to 60%: A Rare Case of Multisystem Inflammatory Syndrome in Adults 4 Weeks Following COVID-19 Infection
title_full From 13% to 60%: A Rare Case of Multisystem Inflammatory Syndrome in Adults 4 Weeks Following COVID-19 Infection
title_fullStr From 13% to 60%: A Rare Case of Multisystem Inflammatory Syndrome in Adults 4 Weeks Following COVID-19 Infection
title_full_unstemmed From 13% to 60%: A Rare Case of Multisystem Inflammatory Syndrome in Adults 4 Weeks Following COVID-19 Infection
title_short From 13% to 60%: A Rare Case of Multisystem Inflammatory Syndrome in Adults 4 Weeks Following COVID-19 Infection
title_sort from 13% to 60%: a rare case of multisystem inflammatory syndrome in adults 4 weeks following covid-19 infection
topic (678)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988565/
http://dx.doi.org/10.1016/j.healun.2022.01.699
work_keys_str_mv AT habibe from13to60ararecaseofmultisysteminflammatorysyndromeinadults4weeksfollowingcovid19infection
AT baqalo from13to60ararecaseofmultisysteminflammatorysyndromeinadults4weeksfollowingcovid19infection
AT lemondl from13to60ararecaseofmultisysteminflammatorysyndromeinadults4weeksfollowingcovid19infection