Abstract
There have been considerations since the beginning of the Coronavirus pandemic that COVID-19 infection, like any other viral illness, can trigger neurological and metabolic decompensation in patients with mitochondrial diseases. At the time of writing, there were no published reports reviewing experiences and guidelines about management of COVID-19 infection in this patient population. We present a challenging case of an adult patient with a known diagnosis of Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like Episodes (MELAS) complicated by COVID-19 infection. She initially presented with altered mental status and vomiting and went on to develop a stroke-like episode, pancreatitis, and pneumatosis intestinalis. We review salient features of her hospitalization, including initiation of thromboprophylaxis in relation to intravenous arginine therapy, caution regarding medications such as remdesivir, and the incidence of gastrointestinal complications.
Introduction
Management of stroke-like episodes and metabolic decompensation in Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like Episodes (MELAS) with concurrent COVID-19 infection presents a unique set of challenges. There have been no published case reports or management guidelines regarding COVID-19 infection in adult or pediatric patients with MELAS and other mitochondrial disorders. United Mitochondrial Disease Foundation’s Scientific and Medical Advisory Board recently provided some general guidance about the pandemic for the mitochondrial disease patient community [1]. At our institution, we cared for a patient with MELAS who presented with altered mental status and vomiting and was found to have a new stroke-like episode triggered by COVID-19 infection. Considerations related to her care during this admission are reviewed in this report.
Clinical report
The patient was a 27-year-old female with a genetically confirmed diagnosis of MELAS and a history of multiple stroke-like episodes, refractory epilepsy, intellectual disability, and gastrointestinal dysmotility. She presented with a 1-week history of non-bilious, non-bloody emesis and inability to tolerate feeds and medications. She complained of severe generalized abdominal pain and had had a single dark colored stool. She had a breakthrough seizure the day prior to presentation and was described by her parents as not at her mental baseline. On physical examination, she was alert but oriented only to place. She had decreased verbal output and was able to follow simple commands with the exception of those required for visual field testing. Her face was symmetric, her speech was non-dysarthric, and her extra-ocular movements were intact. She had generalized weakness (4/5 strength) in proximal and distal muscles of upper and lower extremities and diminished muscle bulk. She had an ataxic gait and an intention tremor involving the upper extremities. At baseline, she could ambulate independently.
Initial laboratory investigations were significant for lactic acid of 3.6 mmol/L (range 0–2), amylase of 143 units/L (normal < 115), and lipase of 373 units/L (normal 114–286). Basic metabolic panel, complete blood count, and liver function tests were within normal limits. SARS CoV2 PCR from nasopharyngeal swab was positive, and C-reactive protein was elevated at 8.04 mg/dl (normal < 0.50). Given her history of altered mental status raising concern for stroke-like episode, an urgent brain MRI was obtained which demonstrated a new area of diffusion restriction in the left occipital lobe, consistent with acute metabolic injury (Fig. 1). She was administered intravenous (IV) arginine within 5 h of onset of encephalopathy for treatment of the stroke-like episode, and this was continued for 2 days [2]. Vital signs, electrolytes, and acid–base status were carefully monitored. She was continued on her home medications, including her anti-seizure medications (levetiracetam, oxcarbazepine, and lamotrigine) and mitochondrial cocktail (levocarnitine, riboflavin, thiamine, and pyridoxine). Electroencephalogram showed mild generalized slowing with left occipital sharp waves. For anti-coagulation prophylaxis against COVID-19-related thrombosis, heparin was initiated on day 3 of admission after completion of l-arginine therapy. The unfractionated heparin level was noted to be therapeutic at 0.13 units/ml (range 0.1–0.3). She was then transitioned to subcutaneous enoxaparin 40 mg twice a day which was continued until discharge per institutional protocol. Mental status improved slowly, and she was close to her baseline by day 4 of admission. Abdominal ultrasound did not show any evidence of acute appendicitis. Abdominal X-ray demonstrated elongated and stacked appearance of bowel loops and flocculent gas, concerning for pneumatosis intestinalis. Enteral feeds were initially held and slowly advanced while she received total parenteral nutrition (TPN). From a respiratory perspective, she remained stable and did not require intervention.
Discussion
Medical management of this case was complex given the lack of experience in treating stroke-like episode in the setting of COVID-19 infection. We followed our institutional protocol for treatment of stroke-like episode in MELAS; however, the concurrent COVID-19 infection posed unprecedented challenges, requiring close coordination between pediatric intensivists, neurogeneticists, hematologists, and infectious disease specialists. The patient was started on IV arginine given clinical features suggestive of stroke-like episode and confirmation of acute metabolic injury on brain MRI. l-arginine is effective in decreasing the severity and frequency of stroke-like symptoms, as well as in alleviating tissue injury in patients with MELAS [2]. Stroke-like episodes are a cardinal symptom of MELAS caused by defective oxidative phosphorylation in cerebral vessels leading to impaired vasodilation. The mechanism of action of l-arginine involves endothelial-dependent vascular relaxation due to release of nitric oxide [3, 4]. It was considered that not only had the patient suffered from a metabolic stroke but was also at risk for a large vessel occlusion, cerebral venous sinus thrombosis, and other complications from hypercoagulability related to COVID-19 infection [5, 6]. Similar to other centers, our institution follows a standardized protocol to initiate escalated-dose thromboprophylaxis in critically ill adult patients with COVID-19 infection [7]. The decision was made to delay initiation of anti-coagulation in this case because concurrent use of heparin and IV arginine posed a theoretical risk for bleeding. As discussed before, IV arginine causes vasodilation and systemic hypotension via release of nitric oxide and can have an inhibitory effect on hemostasis [8, 9]. After the initial bolus, the infusion was continued for 2 days. It was stopped at 48 h given improved mental status and stable blood lactate levels. The patient began heparin on day 3 of admission after discontinuing IV arginine and subsequently transitioned to subcutaneous enoxaparin. There are no major contraindications to using either anticoagulant in patients with mitochondrial disorders [10, 11].
COVID-19 infection should be considered a catabolic stressor like any other infectious illness and can be associated with worsening lactic acidosis in patients with MELAS. Our patient’s lactic acid levels were at baseline throughout the hospitalization. We supported her with 125% of maintenance caloric needs through TPN as a cautionary measure. Metabolic acidosis can worsen work of breathing in patients with COVID-19 pneumonia. Our patient did not have respiratory symptoms and did not require supplemental oxygen. Dexamethasone and/or remdesivir were not considered appropriate, as recent clinical trials and national consensus guidelines support their use only in persons with severe or critical lower respiratory tract disease [12,13,14]. Additionally, caution should be used when using remdesivir in patients with mitochondrial disorders, especially in those with hepatic dysfunction, as the anti-viral drug can trigger transaminitis [15]. Steroids are typically avoided in patients with mitochondrial disorders as they can promote catabolism and further worsen lactic acidosis [10, 11].
Our patient also had severe abdominal pain and distension and was noted to have pneumatosis intestinalis on abdominal X-ray. Hypothetically, this complication—which has been reported before with COVID-19 infection—might be more common in patients with underlying mitochondrial conditions due to pre-existing gastrointestinal motility issues [16, 17]. Our patient underwent complete bowel rest and was started on TPN. She also had mild elevation in lipase and amylase levels on admission concerning for pancreatitis, which improved throughout the hospital stay. Use of convalescent plasma has been shown to offer clinical benefit, including radiological resolution of lung disease, reduction in viral loads, and improved survival in patients with COVID-19 infection in a limited number of published studies [18]. However, national consensus guidelines did not support its use outside of a clinical trial at the time of treatment for this patient [13, 14].
As the departments of health in each state are determining vaccination strategies for adults with co-morbid conditions, patients with mitochondrial disorders (such as MELAS, Kearns-Sayre syndrome, Leber’s Hereditary Optic Neuropathy, etc.) should be given priority due to risk for severe disease [19]. Our hospital is in the process of identifying vulnerable patients based on ICD-10 codes. We are including patients with mitochondrial diseases including MELAS as tier 1 in our priority list.
Conclusion
This is the first report of COVID-19 infection in a patient with MELAS complicated by stroke-like episode, pneumatosis intestinalis, and pancreatitis. We identified several considerations that impact the treatment of stroke-like episodes/metabolic decompensation with concurrent COVID-19 infection.
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Sen, K., Harrar, D., Hahn, A. et al. Management considerations for stroke-like episodes in MELAS with concurrent COVID-19 infection. J Neurol 268, 3988–3991 (2021). https://doi.org/10.1007/s00415-021-10538-1
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DOI: https://doi.org/10.1007/s00415-021-10538-1