Management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approach

A phaeochromocytoma (PC) is a rare, catecholamine-secreting neuroendocrine tumour arising from the adrenal medulla. Presenting symptoms of this rare tumour are highly variable but life-threatening multiorgan dysfunction can occur secondary to catecholamine-induced hypertension or hypotension and sub...

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Main Authors: R T Casey, B G Challis, D Pitfield, R M Mahroof, N Jamieson, C J Bhagra, A Vuylsteke, S J Pettit, K C Chatterjee
Format: Article
Language:English
Published: Bioscientifica 2017-11-01
Series:Endocrinology, Diabetes & Metabolism Case Reports
Online Access:https://www.edmcasereports.com/articles/endocrinology-diabetes-and-metabolism-case-reports/10.1530/EDM-17-0122
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spelling doaj-dbec12e896724c188c98f3585e47b14c2020-11-24T21:49:05ZengBioscientificaEndocrinology, Diabetes & Metabolism Case Reports2052-05732052-05732017-11-01111610.1530/EDM-17-0122Management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approachR T Casey0B G Challis1D Pitfield2R M Mahroof3N Jamieson4C J Bhagra5A Vuylsteke6S J Pettit7K C Chatterjee8Department of Endocrinology and Diabetes, Cambridge University NHS Foundation Trust, Cambridge, UKDepartment of Endocrinology and Diabetes, Cambridge University NHS Foundation Trust, Cambridge, UKDepartment of Endocrinology and Diabetes, Cambridge University NHS Foundation Trust, Cambridge, UKDepartment of Anaesthetics, Cambridge University NHS Foundation Trust, Cambridge, UKDepartment of Hepatobiliary and Pancreatic Surgery, Cambridge University NHS Foundation Trust, Cambridge, UKDepartment of Cardiology, Cambridge University NHS Foundation Trust, Cambridge, UKDepartment of Critical Care Unit, Papworth Hospital NHS Foundation Trust, Cambridge, UKDepartment of Advanced Heart Failure Unit, Papworth Hospital NHS Foundation Trust, Cambridge, UKDepartment of Endocrinology and Diabetes, Cambridge University NHS Foundation Trust, Cambridge, UKA phaeochromocytoma (PC) is a rare, catecholamine-secreting neuroendocrine tumour arising from the adrenal medulla. Presenting symptoms of this rare tumour are highly variable but life-threatening multiorgan dysfunction can occur secondary to catecholamine-induced hypertension or hypotension and subsequent cardiovascular collapse. High levels of circulating catecholamines can induce an acute stress cardiomyopathy, also known as Takotsubo cardiomyopathy. Recent studies have focused on early diagnosis and estimation of the prevalence of acute stress cardiomyopathy in patients with PC, but very little is reported about management of these complex cases. Here, we report the case of a 38-year-old lady who presented with an acute Takotsubo or stress cardiomyopathy and catecholamine crisis, caused by an occult left-sided 5 cm PC. The initial presenting crisis manifested with symptoms of severe headache and abdominal pain, triggered by a respiratory tract infection. On admission to hospital, the patient rapidly deteriorated, developing respiratory failure, cardiogenic shock and subsequent cardiovascular collapse due to further exacerbation of the catecholamine crisis caused by a combination of opiates and intravenous corticosteroid. An echocardiogram revealed left ventricular apical hypokinesia and ballooning, with an estimated left ventricular ejection fraction of 10–15%. Herein, we outline the early stabilisation period, preoperative optimisation and intraoperative management, providing anecdotal guidance for the management of this rare life-threatening complication of PC.https://www.edmcasereports.com/articles/endocrinology-diabetes-and-metabolism-case-reports/10.1530/EDM-17-0122
collection DOAJ
language English
format Article
sources DOAJ
author R T Casey
B G Challis
D Pitfield
R M Mahroof
N Jamieson
C J Bhagra
A Vuylsteke
S J Pettit
K C Chatterjee
spellingShingle R T Casey
B G Challis
D Pitfield
R M Mahroof
N Jamieson
C J Bhagra
A Vuylsteke
S J Pettit
K C Chatterjee
Management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approach
Endocrinology, Diabetes & Metabolism Case Reports
author_facet R T Casey
B G Challis
D Pitfield
R M Mahroof
N Jamieson
C J Bhagra
A Vuylsteke
S J Pettit
K C Chatterjee
author_sort R T Casey
title Management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approach
title_short Management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approach
title_full Management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approach
title_fullStr Management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approach
title_full_unstemmed Management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approach
title_sort management of an acute catecholamine-induced cardiomyopathy and circulatory collapse: a multidisciplinary approach
publisher Bioscientifica
series Endocrinology, Diabetes & Metabolism Case Reports
issn 2052-0573
2052-0573
publishDate 2017-11-01
description A phaeochromocytoma (PC) is a rare, catecholamine-secreting neuroendocrine tumour arising from the adrenal medulla. Presenting symptoms of this rare tumour are highly variable but life-threatening multiorgan dysfunction can occur secondary to catecholamine-induced hypertension or hypotension and subsequent cardiovascular collapse. High levels of circulating catecholamines can induce an acute stress cardiomyopathy, also known as Takotsubo cardiomyopathy. Recent studies have focused on early diagnosis and estimation of the prevalence of acute stress cardiomyopathy in patients with PC, but very little is reported about management of these complex cases. Here, we report the case of a 38-year-old lady who presented with an acute Takotsubo or stress cardiomyopathy and catecholamine crisis, caused by an occult left-sided 5 cm PC. The initial presenting crisis manifested with symptoms of severe headache and abdominal pain, triggered by a respiratory tract infection. On admission to hospital, the patient rapidly deteriorated, developing respiratory failure, cardiogenic shock and subsequent cardiovascular collapse due to further exacerbation of the catecholamine crisis caused by a combination of opiates and intravenous corticosteroid. An echocardiogram revealed left ventricular apical hypokinesia and ballooning, with an estimated left ventricular ejection fraction of 10–15%. Herein, we outline the early stabilisation period, preoperative optimisation and intraoperative management, providing anecdotal guidance for the management of this rare life-threatening complication of PC.
url https://www.edmcasereports.com/articles/endocrinology-diabetes-and-metabolism-case-reports/10.1530/EDM-17-0122
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