ABSTRACT
Objective: To describe side effects from SARS-Cov-2 vaccination and its effect on underlying neuromuscular disease amongst patients followed at the University of California, Irvine Neuromuscular Center. Background: Extensive data on safety and tolerability of SARS-Cov-2 vaccines exists for healthy individuals. However, patients with neuromuscular conditions and especially those on immune modulatory therapy were not included in the pivotal vaccine trials. It is primarily through expert consensus that vaccination is recommended for this patient population. Design/Methods: Patients were advised to inform the study team about their vaccination status. We collected data during in-person clinic visits or via telehealth encounters using a standardized questionnaire between December 2020 and August 2021. When information was provided about upcoming vaccination dates, patients were contacted within 2 weeks for follow up. Results: Information on 363 administered vaccine doses in 214 patients was recorded, including 199 Pfizer-BioNT, 155 Moderna and 9 Johnson & Johnson doses. Our cohort included 84 patients with myasthenia gravis (MG) and 34 with motor neuron disease (Amyotrophic Lateral Sclerosis, Primary Lateral Sclerosis). The remainder (96 patients) included other immunemediated disorders (idiopathic inflammatory myopathies, Chronic Inflammatory Demyelinating Neuropathy, Guillain-Barre Syndrome and other immune neuropathies) as well as acquired and inherited neuromuscular disorders (Inclusion Body Myositis, muscular dystrophy, inherited and acquired neuropathies). One patient with generalized MG had MG exacerbation, and another experienced impending crisis within one week of vaccine administration;both recovered with appropriate therapy. Detailed analyses of the dataset are being performed and will be presented at the meeting. Conclusions: SARS-Cov-2 vaccinations were well tolerated for the majority of our neuromuscular cohort, similar to what has been reported in healthy individuals. Vaccination did not result in disease exacerbation in the majority of patients with immune-mediated neuromuscular disorders.
ABSTRACT
Background: The transplant patients should be considered a main high-risk population during the COVID-19 outbreak due to the use of immunosuppressive regimens and comorbidities. Objective: This study aimed to evaluate the possibility of COVID-19 transmission by liver transplantation from a donor with a late complication of COVID-19 to the recipients. Methods: This descriptive study was conducted on all the recipients of liver transplantation who had an acute liver failure or were the models for the End-Stage Liver Disease (MELD) higher than 20. Results: In general, 36 liver transplantation was performed during the study period. Out of these patients, only 14 cases (deceased donors) had hemorrhagic cerebrovascular accidents, and other donors died of trauma (n=7) and anoxia (n=15). All patients showed negative results for polymerase chain reaction (PCR) (two negative 24 h PCR), whereas their high-resolution computed tomography (HRCT) test revealed that they had previously lung involvement with COVID-19 as the late complication of the disease. Conclusion: This study supports the safety of continuing donation and transplant process during the outbreak even the transplant donor be infected previously with the COVID-19, which is reinforced by other similar pieces of evidence.
ABSTRACT
Background: Cardiac injury and myocarditis have been described in adults with coronavirus disease 2019 (COVID-19). Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children is typically minimally symptomatic. We report a series of febrile pediatric patients with acute heart failure potentially associated with SARS-CoV-2 infection and the multisystem inflammatory syndrome in children as defined by the US Centers for Disease Control and Prevention. Methods: Over a 2-month period, contemporary with the SARS-CoV-2 pandemic in France and Switzerland, we retrospectively collected clinical, biological, therapeutic, and early outcomes data in children who were admitted to pediatric intensive care units in 14 centers for cardiogenic shock, left ventricular dysfunction, and severe inflammatory state. Results: Thirty-five children were identified and included in the study. Median age at admission was 10 years (range, 2-16 years). Comorbidities were present in 28%, including asthma and overweight. Gastrointestinal symptoms were prominent. Left ventricular ejection fraction was <30% in one-third;80% required inotropic support with 28% treated with extracorporeal membrane oxygenation. Inflammation markers were suggestive of cytokine storm (interleukin-6 median, 135 pg/mL) and macrophage activation (D-dimer median, 5284 ng/mL). Mean BNP (B-type natriuretic peptide) was elevated (5743 pg/mL). Thirty-one of 35 patients (88%) tested positive for SARS-CoV-2 infection by polymerase chain reaction of nasopharyngeal swab or serology. All patients received intravenous immunoglobulin, with adjunctive steroid therapy used in one-third. Left ventricular function was restored in the 25 of 35 of those discharged from the intensive care unit. No patient died, and all patients treated with extracorporeal membrane oxygenation were successfully weaned. Conclusions: Children may experience an acute cardiac decompensation caused by severe inflammatory state after SARS-CoV-2 infection (multisystem inflammatory syndrome in children). Treatment with immunoglobulin appears to be associated with recovery of left ventricular systolic function.