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1.
J Med Vasc ; 42(6): 384-387, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29203045

RESUMEN

Echo contrast agents, such as SonoVue®, (Bracco, Milan, Italy) are often used to enhance diagnosis. Although their use is safe, some rare side effects could be severe or even fatal. We are reporting a case of severe systemic allergic reaction after infusion of SonoVue®. After a brief review of the literature, the aim of this paper is to draw attention to this risk and recall the safety instructions coming with the use of ultrasound contrast agents.


Asunto(s)
Anafilaxia/inducido químicamente , Medios de Contraste/efectos adversos , Fosfolípidos/efectos adversos , Hexafluoruro de Azufre/efectos adversos , Ultrasonografía , Humanos , Masculino , Persona de Mediana Edad , Ultrasonografía/métodos
2.
Expert Rev Med Devices ; 13(2): 179-89, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26641026

RESUMEN

The auscultatory technique remains the point of reference for the validation of non-invasive blood pressure measurement devices, although the exact origin of the Korotkoff sounds is still debated and comparison with intra-arterial measurement shows limits and pitfalls. Automatic oscillometric devices are now widely used by nurses, physicians, and patients. However, many available devices have not been duly validated. Moreover, they calculate systolic and diastolic blood pressures using undisclosed algorithms. Therefore, these devices are not interchangeable, and their reliability may be questionable in some clinical situations. Nevertheless, oscillometry is increasingly used, beside NIBP, for the assessment of central blood pressure and systemic arterial wall stiffness. Awareness of its limits and causes of error is all the more necessary.


Asunto(s)
Determinación de la Presión Sanguínea/instrumentación , Presión Sanguínea , Oscilometría/instrumentación , Auscultación , Automatización , Humanos , Reproducibilidad de los Resultados
3.
J Mal Vasc ; 40(1): 37-41, 2015 Feb.
Artículo en Francés | MEDLINE | ID: mdl-25554653

RESUMEN

Neurological disorders are rare complications of foam sclerotherapy. Visual disturbances and headache are the most commonly reported events and are thought to be equivalent to migraine with aura. Exceptionally, strokes have been reported. Papillary fibroelastoma is a rare cardiac tumor, which may embolize in cerebral arteries. We report the case of a patient in whom neurological disorders occurred during a session of foam sclerotherapy, and led to the discovery of a cardiac fibroelastoma.


Asunto(s)
Fibroma/diagnóstico , Neoplasias Cardíacas/diagnóstico , Enfermedades del Sistema Nervioso/etiología , Escleroterapia/efectos adversos , Escleroterapia/métodos , Femenino , Fibroma/cirugía , Neoplasias Cardíacas/cirugía , Humanos , Imagen por Resonancia Magnética , Persona de Mediana Edad
4.
Artículo en Inglés | MEDLINE | ID: mdl-12383491

RESUMEN

A simple reversed-phase liquid chromatographic method has been developed to determine protease inhibitors concentrations in plasma. Plasma samples (250 micro l) containing protease inhibitors were prepared by a simple deproteinization (recovery: 92, 91, 91 and 90.5% for ritonavir, saquinavir, nelfinavir and M8 nelfinavir metabolite, respectively). Chromatography was accomplished using a Hypersil octadecylsilyl column (100 x 4.6 mm I.D.) and a mobile phase composed of acetonitrile, tetrahydrofuran and dihydrogenophosphate buffer (pH 4) (32:10:58, v/v). Ultraviolet detection at 210 nm was used. The limit of detection was 200 ng/ml for ritonavir, saquinavir, nelfinavir and M8 nelfinavir metabolite. Calibration curves were linear up to 20000 ng/ml, with correlation coefficients better than 0.997 for all compounds. Intra- and inter-day coefficients of variation of the assay were

Asunto(s)
Cromatografía Líquida de Alta Presión/métodos , Inhibidores de la Proteasa del VIH/sangre , Nelfinavir/sangre , Ritonavir/sangre , Saquinavir/sangre , Inhibidores de la Proteasa del VIH/farmacocinética , Humanos , Nelfinavir/farmacocinética , Estándares de Referencia , Ritonavir/farmacocinética , Saquinavir/farmacocinética , Sensibilidad y Especificidad
5.
Pathol Biol (Paris) ; 50(4): 227-32, 2002 May.
Artículo en Francés | MEDLINE | ID: mdl-12085667

RESUMEN

UNLABELLED: This study was aimed to compare with previous results (Grillot et al., 1994), the efficacy of amikacin adaptive optimal control in a geriatric hospital. PATIENTS: During six months, 32 patients (aged of 82 +/- 8 years) were included versus 51 during two years (aged of 80 +/- 5). The mean age was not different between the two populations (NS, Student test). They received amikacin initial dosage of 17.7 +/- 5.1 mg/kg/d (vs 13.3 +/- 3.5 for the reference study) and maintenance dosage of 15.1 +/- 4.8 mg/kg/d (vs 11.8 +/- 5.1 for the reference study). METHOD: Two efficacy outcomes (E1 and E2) and 1 toxicity outcome (T) were taken into account: E1 estimated the effect of adaptive control on maximal drug level, E2: overall recovery. Toxicity outcome was used: T the nephrotoxicity (increasing creatininémia over 44 mumol/l). RESULTS: All the results are given versus the reference study. 57.6% versus 29.4% of adaptive strategy were once-a-day. E1: Chi square test show that initial dosage and maintenance dosage are greater our study than the previous one (p < 0.05: 78.8% versus 5.9% for initial dosage, 84.4% versus 13.8% for maintenance dosage). E2: 73.6% overall of recovery versus 77% (NS, Chi square test). T: 94% versus 85% (p < 0.05, Chi square test) of creatininemia variation are lower than 44 mumol/l. Duration of treatment is 9.8 +/- 4.8 versus 15 +/- 9 days (p < 0.5, Student test). CONCLUSIONS: Once-a-day strategy in amikacin therapeutic regimen is no more efficient but decreases toxicity and duration treatment.


Asunto(s)
Amicacina/uso terapéutico , Antibacterianos/uso terapéutico , Anciano , Anciano de 80 o más Años , Amicacina/administración & dosificación , Antibacterianos/administración & dosificación , Esquema de Medicación , Femenino , Humanos , Riñón/efectos de los fármacos , Masculino , Resultado del Tratamiento
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