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1.
J Natl Med Assoc ; 113(6): 701-705, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-34521513

RESUMEN

BACKGROUND: Monoclonal antibody therapy (MAT) is recommended in mild to moderate Coronavirus disease 2019 (COVID-19) patients who are at risk of progressing to severe disease. Due to limited data on its outcomes and the logistic challenges in administering the drug, MAT has not been widely used in the United States (US) despite of emergency use authorization (EUA) approval by the Food and Drug Administration (FDA). AIM: We aim to study the outcomes of MAT in patients predominantly from ethnic minority groups and the challenges we experienced in implementing the infusion therapy protocol in an inner-city safety-net-hospital in the South Bronx. METHODS AND RESULTS: We conducted a retrospective observational study of 49 patients who were offered MAT as per EUA protocol of FDA. Patient who met the criteria for MAT and received therapy were included in treatment group (n = 38) and the remaining (n = 11) who declined treatment were included in the control group. A majority of patients (76%) in the study group reported symptomatic improvement, the day after infusion. There was statistically significant reduction in COVID-19 related hospitalizations (7.8 vs 54.5%, P = < 0.001) mortality (0 vs 18.1%, P value = 0.008) in the treatment group. CONCLUSION: MAT reduced both hospitalization and mortality in this predominantly Hispanic patient population with mild to moderate COVID-19 with high risk factors for disease progression.


Asunto(s)
Anticuerpos Monoclonales/uso terapéutico , COVID-19 , COVID-19/terapia , Hispánicos o Latinos , Mortalidad Hospitalaria , Hospitalización , Humanos , Grupos Minoritarios , Ciudad de Nueva York , Estudios Retrospectivos , Proveedores de Redes de Seguridad
2.
Clin Rheumatol ; 32(5): 715-9, 2013 May.
Artículo en Inglés | MEDLINE | ID: mdl-23423441

RESUMEN

Antisynthetase antibody syndrome is a rare autoimmune disease that may present with variable systemic manifestations, mainly polymyositis, interstitial lung disease, skin lesions, and Raynaud's phenomenon. This diagnosis should always come to mind in patients that present with signs of myositis, dermatomyositis, or polymyositis associated with interstitial lung disease. On the following paper, we report the case of a 52-year-old man who presented with a 2-month history of asymmetric polyarthralgia, myalgia, weight loss of 8 kg, and progressive muscle weakness associated with dyspnea, orthopnea, and dysphonia. Further tests revealed myositis, interstitial pneumonia, and elevation of anti-Jo-1 antibodies. A diagnosis of antisynthetase antibody syndrome was made and the patient showed good response to treatment with corticoids and methotrexate. Finally, we present a short review of the literature.


Asunto(s)
Enfermedades Pulmonares Intersticiales/diagnóstico , Miositis/diagnóstico , Anticuerpos Antinucleares/inmunología , Artralgia/diagnóstico , Biopsia , Humanos , Enfermedades Pulmonares Intersticiales/complicaciones , Masculino , Persona de Mediana Edad , Debilidad Muscular/diagnóstico , Músculos/patología , Mialgia/diagnóstico , Miositis/complicaciones , Miositis/terapia , Tomografía Computarizada por Rayos X , Resultado del Tratamiento , Pérdida de Peso
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