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Patients with chronic stimulant-induced cardiomyopathy presenting with cardiogenic shock can be stabilized with conventional measures. However, their management post-stabilization has not been well described and poses unique challenges: i less chance of myocardial recovery compared to acute stimulant-induced cardiomyopathy, ii psychosocial barriers to left ventricular assist device LVAD and heart transplantation, and iii concern for use of peripherally inserted central catheter for home inotrope in those with a history of substance abuse. Long-term home inotrope was used as either a bridge to LVAD, reverse remodelling, or stabilization. Home inotrope should be viewed as an option in chronic stimulant-induced cardiomyopathy on a case-by-case basis. It can buy time to allow for myocardial stabilization or recovery through goal-directed medical therapy and stimulant cessation. Home inotrope is an option in stimulant-induced cardiomyopathy on a case-by-case basis. The ability to manage a peripherally inserted central catheter and home inotrope can provide valuable psychosocial information during left ventricular assist device and heart transplant evaluation. The indirect inotropic effect of methamphetamine is an additional source of drug dependence in patients with severe cardiomyopathy. Stimulant use has been reported to cause dilated cardiomyopathy DCM. We present three such cases Table 1. Home inotrope was used as bridge to decision and eventual left ventricular assist device LVAD , as bridge to stabilization, or as bridge to reverse remodelling through stimulant abstinence and guideline-directed medical therapy GDMT. A year-old male had a 2-year history of severe DCM related to prescription dextroamphetamine—amphetamine and non-habitual use of methamphetamine and cocaine. He was on home milrinone since diagnosis and had been deemed ineligible for transplant for psychosocial reasons. He was now admitted with acute worsening of heart failure HF symptoms including dyspnoea with minimal exertion, nausea, and abdominal swelling, despite escalation of outpatient milrinone from 0. On exam, he was ill appearing, had jugular venous distension, bibasilar lung crackles, and significant leg oedema. He progressed to cardiogenic shock requiring mechanical circulatory support MCS with Impella 5. He was deemed eligible for LVAD by a multidisciplinary team based on his improved medical adherence in the months leading up to this admission and the fact that his condition had progressed to MCS dependence. This was facilitated by improved right ventricular afterload and pulmonary artery pressures with left ventricular unloading, improved right ventricular preload by fixing severe functional tricuspid regurgitation, and weeks of peri-operative central venous decongestion. His renal function eventually normalized. He is doing well 8 months after surgery, has had no LVAD complications or readmissions, is adherent to the medical regimen and office visits, and has had multiple negative toxicology screens. A transplant evaluation is currently underway. A year-old male had a year history of DCM related to regular methamphetamine use. His last visit with a cardiologist was 2 years prior to the current admission. At that time, his ejection fraction was severely reduced. He did not follow-up with subsequent office visits and stopped all GDMT. On exam, he had tachypnoea, bilateral lung crackles, and mild leg swelling. He was found to be in a low-output state with acute kidney injury and ischaemic hepatitis. He did not tolerate milrinone due to symptomatic hypotension and was switched to dobutamine. He was weaned off, but 3 days later developed worsening clinical, haemodynamic, and laboratory parameters requiring reinitiation. He had intolerance to afterload reduction. After multidisciplinary discussions, the plan was home dobutamine at the lowest dose that maintained adequate clinical and haemodynamic parameters to provide long-term stability to assess the following:. He agreed to a wearable cardioverter defibrillator WCD. Functional capacity significantly improved. Despite inability to add beta-blocker, his resting heart rate improved to 65—75 b. Blood pressure improved allowing for initiation of GDMT. Given dramatic improvement, he was electively admitted 5 months later for haemodynamic-guided inotrope wean, which he tolerated. Patient 2 echocardiogram. Patient 2 non-invasive haemodynamics. A year-old male had a 3-year history of severe DCM secondary to regular methamphetamine use. On exam, he was in respiratory distress with significant bilateral lung crackles, cool extremities, and mild skin mottling of his feet. He was in cardiogenic shock and new-onset atrial fibrillation with rate of b. He underwent emergent cardioversion but remained unstable, requiring MCS with Impella 5. After improvement of haemodynamic and laboratory parameters, he was weaned off MCS to milrinone with a total of 13 days Impella support and 10 days RVAD support. He failed attempts to wean milrinone despite afterload reduction. After multidisciplinary discussions, the plan was home milrinone with a similar rationale to Patient 2. Despite his advanced HF status, candidacy for advanced therapies had not been excluded, and there remained a possibility of long-term myocardial stabilization with methamphetamine abstinence and preventing tachyarrhythmia. Prior to admission, he was intolerant of beta-blockers developing low-output symptoms including nausea. His heart rate had consistently been sinus — b. After discharge on milrinone and with methamphetamine abstinence, he eventually tolerated quadruple therapy including high-dose beta-blocker. The patient was concerned about the psychosocial aspects of LVAD and transplant and felt a burden even with the peripherally inserted central catheter PICC. Given significant improvement, it was decided to proceed with haemodynamic-guided inotrope wean. He opted to avoid admission and was successfully weaned based on clinical parameters. Four months following milrinone wean, he is NYHA class 1—2, but echocardiogram has yet to demonstrate improvement. Since milrinone wean, adherence with follow-up has been a challenge. Catecholaminergic stimulants include medications such as methylphenidate and dextroamphetamine—amphetamine as well as illicit drugs such as methamphetamine and cocaine. Methamphetamine displaces neurotransmitters into the synapse and inhibits their reuptake. Compared to amphetamine, methamphetamine possesses an extra methyl group contributing to higher lipophilic activity, which enhances central nervous system CNS activity and duration of action. Their potential to cause cardiomyopathy is related to not only indirect adrenergic stimulation but also direct myocardial injury through oxidative stress, apoptosis, altered metabolism, altered gene expression, and abnormal intracellular calcium homeostasis. Addiction to stimulants poses a unique challenge in the setting of severe DCM. In addition to the inherently addictive potential of these substances due to CNS effect, their inotropic effect can palliate debilitating low-output symptoms. This phenomenon was mentioned by Patient 2 when describing the challenges he faced abstaining from methamphetamine. The indirect positive inotropic action of methamphetamine has been demonstrated in a human atrial model and animal studies. Although acute management of MAC has been described in case series, 1 including a subset requiring short-term inotrope or MCS, the use of home inotrope as a bridge to recovery or advanced therapies in those with chronic MAC has not been well described. The potential for reverse remodelling in chronic MAC is unclear. Reassuringly in animal studies, histopathologic cardiac abnormalities induced by daily high-dose injection of methamphetamine for 12 weeks demonstrated pronounced recovery after 8—12 weeks of withdrawal. In those that fail to improve, LVAD and transplant are options. However, LVAD with active substance abuse is associated with negative outcomes. Home milrinone was favoured in our patients, although Patient 2 did not tolerate milrinone due to his initial vasodilatory state. Beyond the phase of acute stabilization, beta-blockers can be combined with home milrinone but not dobutamine due to their competing mechanism of action. This combination was associated with improved survival in two large studies of contemporary home inotropic therapy. An important dilemma exists regarding PICC in those with substance abuse. A literature review for outpatient parenteral antimicrobial therapy in this high-risk population revealed reassuring data on safety, efficacy, mortality, catheter-related adverse events, and misuse of venous catheter. Patients in our series had no PICC-related issues with a duration ranging from 4 to 30 months accounting for a selection bias. Medical adherence improved. In the inpatient setting, patients and family members are provided with education on managing the PICC and pump. Following discharge, they initially have visits from the home health nurse two to three times weekly with the goal of achieving independence. Ability to handle PICC dressing changes, medication bag changes, and pump troubleshooting provides valuable psychosocial information when evaluating for advanced therapies. Interrogation of WCD provides similar information. Patients with stimulant-induced DCM are not a homogenous group. They have a wide psychosocial spectrum related to social support, housing and job situations, adherence, and level of insight. When assessing their candidacy for home inotrope and advanced therapies, a nuanced and personalized approach should be adopted. I am currently a third-year medical student completing my core clerkship rotations. The experiences have given me better insight into the intricacies of medicine while building my knowledge base. Additionally, I am recognizing what my passions are and which path in medicine is best for me. I have been fascinated by cardiology and the complexities of cardiovascular disease processes. My future interests therefore are in internal medicine and cardiology with great interest in preventative care. No new data were generated or analysed in support of this research. All data are present within the manuscript. Clinical characteristics and management of methamphetamine-associated cardiomyopathy: state-of-the-art review. J Am Heart Assoc ; 9 : e Google Scholar. Jafari Giv M. Exposure to amphetamines leads to development of amphetamine type stimulants associated cardiomyopathy ATSAC. Cardiovasc Toxicol ; 17 : 13 — Cardiomyopathy-associated hospital admissions among methamphetamine users. JACC Adv ; 3 : Prevalence and nature of cardiovascular disease in methamphetamine-related death: a national study. Drug Alcohol Depend ; : — Methamphetamine-related cardiovascular diseases. ESC Heart Fail ; 7 : — Methamphetamine increases force of contraction in isolated human atrial preparations through the release of noradrenaline. Toxicol Lett ; : — Ishiguro Y , Morgan JP. Biphasic inotropic effects of methamphetamine and methylphenidate on ferret papillary muscles. J Cardiovasc Pharmacol ; 30 : — Histopathological studies of cardiac lesions after long term administration of methamphetamine in high dosage—part II. Leg Med Tokyo ; 11 : S — S Cardiac magnetic resonance as an alternative to endomyocardial biopsy to predict recoverability of left ventricular function in methamphetamine-associated cardiomyopathy. Substance abuse at the time of left ventricular assist device implantation is associated with increased mortality. J Heart Lung Transplant ; 33 : — Palliative inotropes in advanced heart failure: comparing outcomes between milrinone and dobutamine. J Card Fail ; 28 : — Beta-blockers and ambulatory inotropic therapy. Why has positive inotropy failed in chronic heart failure? Lessons from prior inotrope trials. Eur J Heart Fail ; 21 : — Outpatient parenteral antimicrobial therapy among people who inject drugs: a review of the literature. Open Forum Infect Dis ; 5 : ofy Oxford University Press is a department of the University of Oxford. It furthers the University's objective of excellence in research, scholarship, and education by publishing worldwide. Sign In or Create an Account. Advertisement intended for healthcare professionals. Sign in through your institution. ESC Publications. Advanced Search. Search Menu. Article Navigation. Close mobile search navigation Article Navigation. Volume 8. Article Contents Abstract. Summary figure. Patient 1. Patient 2. Patient 3. Lead author biography. Supplementary material. Data availability. Journal Article. Home inotrope therapy in chronic stimulant-induced cardiomyopathy: a case series. Max Joseph , Max Joseph. Oxford Academic. Sejal Batra. Wali Kamran. Kelsey Barrett. Barbara Ebert. Ahmed Nassar. Timothy Misselbeck. Nael Hawwa. Corresponding author. Conflict of interest: None declared. Revision received:. Corrected and typeset:. Select Format Select format. Permissions Icon Permissions. Abstract Background. Methamphetamine , Cardiogenic shock , Home inotrope , Case report. Learning points. Table 1 Open in new tab. Patient characteristics at baseline and during admission. Open in new tab Download slide. Figure 1. Figure 2. Editor: Matteo Sturla , Matteo Sturla. Alaeldin Addas. Hatem Soliman Aboumarie. Piera Ricci. Download all slides. Supplementary data. Comments 0. Add comment Close comment form modal. I agree to the terms and conditions. You must accept the terms and conditions. Add comment Cancel. Submit a comment. Comment title. You have entered an invalid code. Submit Cancel. Thank you for submitting a comment on this article. Your comment will be reviewed and published at the journal's discretion. Please check for further notifications by email. Views More metrics information. Total Views Email alerts Article activity alert. New issue alert. In progress issue alert. Subject alert. Receive exclusive offers and updates from Oxford Academic. Related articles in PubMed Systemic inflammation is associated with myocardial fibrosis in patients with obstructive hypertrophic cardiomyopathy. Distinguishing hypertensive cardiomyopathy from cardiac amyloidosis in hypertensive patients with heart failure: a CMR study with histological confirmation. The negative effects of long COVID on cardiovascular health and implications for the presurgical examination. The emerging role of clonal haematopoiesis in the pathogenesis of dilated cardiomyopathy. Citing articles via Google Scholar. Most Read Latest Acute myocardial infarction with non-obstructive coronary artery disease due to plaque erosion treated with balloon-occluded thrombolysis. A case report of critical aortic stenosis diagnosed utilizing non-imaging continuous wave Doppler probe. Type A aortic dissection during transoesophageal echocardiography: a case report. Successful use of point-of-care ultrasound for an elderly patient with heart failure in a primary care setting: a case report. 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