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1.
Antimicrob Agents Chemother ; 60(1): 239-44, 2016 01.
Artículo en Inglés | MEDLINE | ID: mdl-26482312

RESUMEN

Gram-positive bacterial infections are an important cause of morbidity and death among cancer patients, despite current therapy. In this case-control study, we evaluated the clinical outcomes and safety of telavancin in cancer patients with uncomplicated Gram-positive bloodstream infections (BSIs). Between March 2011 and May 2013, we enrolled cancer patients with uncomplicated Gram-positive BSIs to receive intravenous telavancin therapy for at least 14 days for Staphylococcus aureus and 7 days for other Gram-positive cocci. Patients with baseline creatinine clearance (CLCR) values of >50 ml/min received 10 mg/kg/day of telavancin, and those with CLCR values between 30 and 49 ml/min received 7.5 mg/kg/day. Patients were compared with a retrospective cohort of 39 historical patients with Gram-positive BSIs, matched for underlying malignancy, infecting organism, and neutropenia status, who had been treated with vancomycin. A total of 78 patients were analyzed, with 39 in each group. The most common pathogen causing BSIs was S. aureus (51%), followed by alpha-hemolytic streptococci (23%), Enterococcus spp. (15%), coagulase-negative staphylococci (8%), and beta-hemolytic streptococci (3%). Sixty-two percent of patients had hematological malignancies, and 38% had solid tumors; 51% of the patients were neutropenic. The overall response rate determined by clinical outcome and microbiological eradication at 72 h following the initiation of therapy, in the absence of relapse, deep-seated infections, and/or infection-related death, was better with telavancin than with vancomycin (86% versus 61%; P = 0.013). Rates of drug-related adverse events were similar in the two groups (telavancin, 31%; vancomycin, 23%; P = 0.79), with similar rates of renal adverse events. Telavancin may provide a useful alternative to standard vancomycin therapy for Gram-positive BSIs in cancer patients. (This study has been registered at ClinicalTrials.gov under registration no. NCT01321879.).


Asunto(s)
Aminoglicósidos/administración & dosificación , Antibacterianos/administración & dosificación , Bacteriemia/tratamiento farmacológico , Infecciones por Bacterias Grampositivas/tratamiento farmacológico , Neoplasias Hematológicas/tratamiento farmacológico , Neutropenia/tratamiento farmacológico , Lesión Renal Aguda/etiología , Lesión Renal Aguda/patología , Adulto , Anciano , Anciano de 80 o más Años , Aminoglicósidos/efectos adversos , Antibacterianos/efectos adversos , Bacteriemia/complicaciones , Bacteriemia/patología , Femenino , Infecciones por Bacterias Grampositivas/complicaciones , Infecciones por Bacterias Grampositivas/patología , Cocos Grampositivos/efectos de los fármacos , Cocos Grampositivos/crecimiento & desarrollo , Neoplasias Hematológicas/complicaciones , Neoplasias Hematológicas/patología , Humanos , Lipoglucopéptidos , Masculino , Pruebas de Sensibilidad Microbiana , Persona de Mediana Edad , Neutropenia/complicaciones , Neutropenia/patología , Proyectos Piloto , Recurrencia , Resultado del Tratamiento , Vancomicina/administración & dosificación , Vancomicina/efectos adversos
2.
Med Clin North Am ; 106(2): 285-298, 2022 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-35227431

RESUMEN

One's total atherosclerotic plaque burden is related to his or her cumulative exposure to low-density lipoprotein cholesterol (LDL-C) and other apoB-containing lipoproteins. Long-term exposure to lower LDL-C levels is associated with a lower risk of cardiovascular events compared with shorter term exposure to lower LDL-C. New lipid-reducing agents have been able to reduce LDL-C to previously unseen levels, showing efficacy in safely decreasing rates of atherosclerotic cardiovascular disease in primary and secondary prevention populations. To date, an LDL-C level less than which there is no clinical benefit has not yet been identified.


Asunto(s)
Aterosclerosis , Enfermedades Cardiovasculares , Aterosclerosis/prevención & control , Enfermedades Cardiovasculares/prevención & control , LDL-Colesterol/uso terapéutico , Femenino , Humanos , Masculino , Factores de Riesgo
3.
Intern Med ; 54(9): 1067-9, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25948349

RESUMEN

Platypnea-orthodeoxia syndrome (POS) is a rare syndrome of severe hypoxemia upon assuming an upright position. It is classically described as shunting from the right atrium to the left atrium usually via a patent foramen ovale (PFO). Alterations in the intrathoracic anatomy after liver resection and regeneration may trigger this condition in patients with clinically silent PFO -a previously unreported cause of POS.


Asunto(s)
Disnea/cirugía , Foramen Oval Permeable/cirugía , Defectos del Tabique Interatrial/cirugía , Hipoxia/cirugía , Hígado/fisiopatología , Anciano , Cateterismo Cardíaco , Disnea/etiología , Foramen Oval Permeable/complicaciones , Defectos del Tabique Interatrial/complicaciones , Humanos , Hipoxia/etiología , Masculino , Postura , Regeneración , Posición Supina , Síndrome
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