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1.
Int J Cosmet Sci ; 43(2): 131-135, 2021 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-33038010

RESUMEN

OBJECTIVE: Vitamin C and peptides are widely used in cosmetic products but there is a paucity of clinical studies showing that the formulations are effective in treating signs of facial ageing. These 3 clinical studies evaluated the effectiveness of an anti-ageing formula containing natural vitamin C (10%), biopeptides (rice and lupin), hyaluronic acid, and Vichy volcanic mineralising water, in amber glass ampoules with no preservatives (Peptide-C ampoules). METHODS: Dansyl chloride fluorescence labelling compared cell turnover for Peptide-C ampoules vs untreated skin in 32 female subjects. Study 2, an open clinical study, evaluated the efficacy on wrinkles of Peptide-C ampoules by investigator clinical scoring based on Dynamical Atlas visual assessment (N = 40) and subject self-assessment questionnaires (N = 47). Study 3, an open clinical study, evaluated wrinkles by instrumental quantification with 3D fringe projection analysis (N = 40) and subject questionnaires (N = 51). RESULTS: The mean cell turnover was faster for skin treated with Peptide-C ampoules compared to untreated skin (17.1 days vs. 19.2 days; P < 0.0001). In study 2, after 28 days application of Peptide-C ampoules, clinical grading of crow's-feet wrinkles, forehead wrinkles and nasolabial folds decreased by 9%, 11% and 5%, respectively (all P < 0.05 vs baseline). Of 47 subjects, 77%, 64% and 79% indicated their skin seemed smoothed out, fine lines were less visible, and skin complexion was more radiant, respectively. In study 3, the number of wrinkles decreased by 11.5% after 29 days application of Peptide-C ampoules vs baseline (P < 0.05) and 65% of subjects responded the fine lines were less visible. CONCLUSION: This formulation of a combination of anti-ageing ingredients in ampoules, allowing a minimalist formula, showed significant results on improving facial wrinkles and radiance.


OBJECTIF: La vitamine C et les peptides sont régulièrement utilisés dans les produits dermocosmétiques mais il existe peu d'études cliniques sur l'efficacité des formulations sur les signes du vieillissement cutané du visage. Trois études cliniques ont évalué l'efficacité d'une formule anti-âge contenant de la vitamine C naturelle (10%), des biopeptides (riz et lupin), de l'acide hyaluronique et de l'eau minéralisante volcanique de Vichy, dans un format d'ampoules en verre ambré, sans conservateur (ampoules Peptide-C). MÉTHODES: Une première étude a comparé par la technique de chlorure de Dansyl le renouvellement cellulaire avec la formulation ampoules Peptide-C et la peau non traitée chez 32 sujets féminins. La seconde étude, en ouvert, a évalué l'efficacité clinique sur les rides des ampoules Peptide-C en se reposant sur les Atlas Dynamiques (N=40) et les questionnaires d'auto-évaluation des sujets (N=47). La troisième étude, ouverte, a évalué les rides par quantification instrumentale avec l'analyse de projection de franges 3D (N=40) et les questionnaires d'autoévaluation des sujets (N=51). RÉSULTATS: Le renouvellement cellulaire était plus rapide pour la peau traitée avec des ampoules de Peptide-C comparées à la peau non traitée (17.1 jours contre 19.2 jours ; p<.0001). Dans l'étude 2, après 28 jours d'application des ampoules Peptide-C, l'évaluation clinique des rides de la patte d'oie, du front et des plis naso-labiaux a montré une amélioration de 9 %, 11 % et 5 %, respectivement (tous p<0,05 vs baseline). Sur 47 sujets, 77%, 64% et 79% ont indiqué que leur peau semblait respectivement lissée, que les ridules étaient moins visibles et que le teint de la peau était plus radieux. Dans l'étude 3, le nombre de rides a diminué de 11,5 % après 29 jours d'application des ampoules Peptide-C par rapport à la baseline (p<0,05) et 65 % des sujets ont répondu que les ridules étaient moins visibles. CONCLUSION: Cette combinaison d'ingrédients anti-âge dans un format d'ampoules, et une formulation minimaliste, a montré des résultats significatifs sur l'amélioration des rides faciales et de l'éclat du teint.


Asunto(s)
Ácido Ascórbico/uso terapéutico , Composición de Medicamentos , Péptidos/uso terapéutico , Envejecimiento de la Piel/efectos de los fármacos , Adulto , Ácido Ascórbico/administración & dosificación , Femenino , Humanos , Persona de Mediana Edad , Péptidos/administración & dosificación
2.
Bioprocess Biosyst Eng ; 39(4): 545-54, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-26762940

RESUMEN

The growth rate and desulfurization capacity accumulated by the cells during the growth of Pseudomonas putida KTH2 under different oxygen transfer conditions in a stirred and sparged tank bioreactor have been studied. Hydrodynamic conditions were changed using different agitation conditions. During the culture, several magnitudes associated to growth, such as the specific growth rate, the dissolved oxygen concentration and the carbon source consumption have been measured. Experimental results indicate that cultures are influenced by the fluid dynamic conditions into the bioreactor. An increase in the stirrer speed from 400 to 700 rpm has a positive influence on the cell growth rate. Nevertheless, the increase of agitation from 700 to 2000 rpm hardly has any influence on the growth rate. The effect of fluid dynamics on the cells development of the biodesulfurization (BDS) capacity of the cells during growth is different. The activities of the intracellular enzymes involved in the 4S pathway change with dissolved oxygen concentration. The enzyme activities have been evaluated in cells at several growth time and different hydrodynamic conditions. An increase of the agitation from 100 to 300 rpm has a positive influence on the development of the overall BDS capacity of the cells during growth. This capacity shows a decrease for higher stirrer speeds and the activity of the enzymes monooxygenases DszC and DszA decreases dramatically. The highest value of the activity of DszB enzyme was obtained with cells cultured at 100 rpm, while this activity decreases when the stirrer speed was increased higher than this value.


Asunto(s)
Proteínas Bacterianas/biosíntesis , Reactores Biológicos , Oxigenasas de Función Mixta/biosíntesis , Oxígeno/metabolismo , Pseudomonas putida/crecimiento & desarrollo
3.
Actas Urol Esp (Engl Ed) ; 47(5): 271-278, 2023 06.
Artículo en Inglés, Español | MEDLINE | ID: mdl-36737036

RESUMEN

INTRODUCTION: The expression of PD-L1 in renal cell carcinoma (RCC) is associated with worse survival and prognostic clinical-pathological features. However, they seem to respond better to new therapeutic agents. Knowing the behavior of RCC according to the presence of PD-L1 has implications for medical counseling and therapeutic approaches. OBJECTIVE: To identify the presence of PD-L1 in renal tumor cells and analyze its association with patients' prognostic factors, overall survival (OS) and cancer-specific survival (CSS). METHODOLOGY: Retrospective analysis of RCC tissue samples, obtained between 2018 and 2021. Immunohistochemistry analysis with mouse monoclonal Anti PD-L1, clone 22C3. Definition of PD-L1 "positive" as a Tumor Proportion Score ≥1%. Comparison of prognostic factors according to the presence or absence of PD-L1, and univariate analysis for OS and CSS. RESULTS: 14% (n = 11) of the sample were PD-L1(+). Average age was 59 years. There were no statistically significant differences between PD-L1 status and TNM stages, nuclear grade and histology. PD-L1(+) had worse OS with a HR of 5.27 (CI: 1.1-23.7; P = .03) and CSS showed a unfavorable tendency for PD-L1(+) with a HR of 4.79 (CI: 0.79-28.95; P = .08). CONCLUSION: The prevalence of PD-L1 in RCC is considerable. In this study PD-L1(+) was associated with unfavorable OS and CSS. It seems reasonable to incorporate its routine use in RCC.


Asunto(s)
Carcinoma de Células Renales , Neoplasias Renales , Animales , Ratones , Carcinoma de Células Renales/patología , Pronóstico , Estudios Retrospectivos , Neoplasias Renales/patología
4.
Spectrochim Acta A Mol Biomol Spectrosc ; 292: 122400, 2023 May 05.
Artículo en Inglés | MEDLINE | ID: mdl-36739665

RESUMEN

Here, we studied the interaction between the food colorant tartrazine (TZ) and double stranded DNA (dsDNA), using spectroscopic, electrochemical, and computational methods such as QM/MM combined with TD-DFT. Despite the UV-vis spectroscopy is widely used to study the interaction between molecules, for the case of TZ there are discrepancies in the analyses presented in the literature available, presenting both hyperchromic and hypochromic effects and consequently different rationalizations for their results. Herein we propose the combination of UV-vis experiments with the design of high-level computational models capable of reproducing the experimental behavior to finally define the proper binding mode at the molecular scale together with the rationalization of the experimental optical response due to the complex formation. To complement the UV-vis experiments, we propose the use of electrochemical measurements, to support the results obtained through UV-vis spectroscopy, as it has been successfully used for the determination of interaction modes between small molecules and biomolecules in any condition. Our UV-vis spectroscopy experiments showed only a hypochromic effect of the absorption spectra of TZ after interaction with DNA, indicative of TZ being deeply buried in the DNA structure. The effect of ionic strength in the experimental procedures led to the dissociation of TZ, thus indicating that the interaction mode was groove binding. On the other hand, the electrochemical studies showed an irreversible reduction peak of TZ, which after the interaction with DNA exhibited a positive shift in potential that can be attributed to groove binding. The binding constant for TZ-DNA was calculated as 4.45x104M-1 (UV-vis) and 5.75x104M-1 (electrochemistry), in line with other groove binder azo dyes. Finally, through the QM/MM calculations we found that the minor-groove binding mode interacting in zones rich in adenine and thymine was the model best suited to reproduce the experimental UV-vis response.


Asunto(s)
ADN , Tartrazina , Tartrazina/química , Espectrofotometría Ultravioleta , ADN/química
5.
J Eur Acad Dermatol Venereol ; 24(11): 1278-84, 2010 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-20337830

RESUMEN

BACKGROUND: Azzalure (Galderma SA) is a newly approved European botulinum neurotoxin type A (BoNT-A). It is derived from Dysport (Ipsen Pharma), which has a long history of usages in various applications. Azzalure and Dysport are collectively referred to as BoNT-A (Speywood Unit) and are different from other BoNT-A preparations. OBJECTIVE: To provide consensus recommendations on the treatment of upper face wrinkles with BoNT-A (Speywood Unit). METHODS: The members of the International Board on Botulinum toxin Azzalure (IBBA) convened to develop consensus on the treatment of upper facial wrinkles based on their own extensive experience. RESULTS: The consensus recommendations address the general issues regarding treatment and provide specific guidelines on the anatomy, injection points, dose, injection technique and safety precautions concerning each common upper face indication. The recommended final concentration of BoNT-A (Speywood Unit) is 200 s.U/mL (10 s.U/0.05 mL) after reconstitution. For glabellar lines, the members recommend a total of five injection points with 10 s.U/point. For forehead wrinkles, the members recommend four to six injections into the frontalis with 5-10 s.U/point. For crow's feet, the members recommend three injections per side with 5-10 s.U/point at the lateral part of the orbicularis oculi. For lateral eyebrow lift, the members recommend one point at each eyebrow tail and an additional one in each side of the frontalis with 5-10 s.U/point. CONCLUSION: This guideline provides a framework for physicians who wish to perform safe and efficacious injection of BoNT-A (Speywood Unit).


Asunto(s)
Toxinas Botulínicas Tipo A/uso terapéutico , Técnicas Cosméticas/normas , Frente , Guías de Práctica Clínica como Asunto , Envejecimiento de la Piel/efectos de los fármacos , Humanos , Cooperación Internacional , Neurotoxinas/uso terapéutico
6.
J Eur Acad Dermatol Venereol ; 24(11): 1285-95, 2010 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-20569284

RESUMEN

BACKGROUND: Azzalure® (Galderma SA), a newly approved European botulinum neurotoxin type A (BoNT-A), is derived from Dysport™ (Ipsen Ltd.), which has a 20-year history of product consistency and has been widely used for various aesthetic and therapeutic applications. Azzalure® and Dysport™ are collectively referred to as BoNT-A (Speywood Unit) after the unit of their activity, and are distinct from other commercial BoNT-A preparations. Consensus has been developed for the treatment of upper facial wrinkles with BoNT-A (Speywood Unit). OBJECTIVE: To provide consensus recommendations on the treatment with BoNT-A (Speywood Unit) for wrinkles on the middle and lower face, neck and chest region. METHODS: The members of the International Board on Botulinum toxin Azzalure (IBBA) convened to develop consensus based on their extensive experience. RESULTS: The recommended final concentration of BoNT-A (Speywood Unit) is 200 Speywood Units/ml after reconstitution. The consensus recommendations were provided for nine indications, including lower eyelid wrinkles, bunny lines, drooping nasal tip, perioral wrinkles, masseter hypertrophy, drooping mouth corners, dimpled chin, platysmal bands and décolleté wrinkles. For each indication, anatomy of the region to be treated was discussed, as were potential side-effects. The consensus recommendations included the number and location of the injection points, dose range of each point and the total injection, as well as specific injection technique. CONCLUSION: These recommendations provide a guideline for physicians who wish to perform safe and efficacious treatment with BoNT-A (Speywood Unit) on the less commonly treated middle and lower face, neck and chest region.


Asunto(s)
Toxinas Botulínicas Tipo A/uso terapéutico , Técnicas Cosméticas/normas , Cara , Guías de Práctica Clínica como Asunto , Envejecimiento de la Piel/efectos de los fármacos , Humanos , Cooperación Internacional , Cuello , Neurotoxinas/uso terapéutico , Tórax
7.
Int Arch Occup Environ Health ; 82(5): 603-12, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19034489

RESUMEN

OBJECTIVE: To evaluate the cytological damage and glutathione peroxidase (GPX) content in the nasal epithelium of residents of Southwest Metropolitan Mexico City (SWMMC) along 1 year of ozone and PM(10) exposure. METHOD: Four nasal scrapings were obtained in 20 volunteers from a control low polluted city and SWMMC permanent residents (n = 20) during 1 year. The scrapings were obtained in September and December 2004, and February and May 2005. One part of the scraping was stained by hematoxylin-eosin technique for cytological evaluation and a second part was stained by immunocytochemistry method to evaluate GPX concentration by morphometry. RESULTS: Control subjects: in total, 30% had no cytological alterations and 70% showed only mild or moderate inflammation in four nasal scrapings. All SWMMC residents showed moderate to severe inflammatory processes in some scrapings. Additionally, dysplasia was found once (in 2 cases) or more than on scraping in five cases (25%). GPX concentration in the control group remained highest in median values throughout the study. SWMMC residents with the highest median values of GPX content were found in the May and September scrapings, and the lowest median values were found in December and February when Ozone and PM(10) levels are increased (P < or = 0.05). A lower GPX content was found as the cytological damage increased (P < or = 0.001). CONCLUSION: Cytological evaluation of nasal epithelium and GPX immunodetection are satisfactory methods to evaluate the earliest damage produced by atmospheric pollution in heavily contaminated cities.


Asunto(s)
Contaminantes Atmosféricos/efectos adversos , Glutatión Peroxidasa/metabolismo , Mucosa Nasal/efectos de los fármacos , Oxidantes Fotoquímicos/efectos adversos , Ozono/efectos adversos , Material Particulado/efectos adversos , Adulto , Ciudades , Femenino , Humanos , Inflamación/inducido químicamente , Inflamación/epidemiología , Inflamación/patología , Masculino , México/epidemiología , Mucosa Nasal/enzimología , Mucosa Nasal/patología , Estaciones del Año , Salud Urbana , Población Urbana , Adulto Joven
8.
Rev. Fac. Odontol. (B.Aires) ; 38(88): 65-70, 2023. ilus
Artículo en Español | LILACS | ID: biblio-1552378

RESUMEN

Las pulpectomías en molares primarios están indica-das en casos de diagnóstico de pulpitis irreversible o necrosis y reabsorción radicular mínima o nula. Son tratamientos laboriosos y extensos, que sólo pueden ser llevados a cabo en pacientes colaboradores. En búsqueda de simplificar esta terapéutica y mejorar su eficacia, se propone la mecanización de la pre-paración de los conductos de molares primarios. Diversos autores aseguran que esta técnica opti-miza el tiempo clínico y mejora la calidad del trata-miento, obteniendo gran aceptación en la literatura actual. Se presenta la secuencia de procedimientos, resolución y controles de dos tratamientos de pul-pectomía con instrumentación mecanizada en mola-res primarios (AU)


Pulpectomies in primary molars are indicated in cases of irreversible pulpitis or necrosis with mini-mal or no root resorption. They are laborious and ex-tensive treatments, which only can be carried out in cooperative patients. In order to simplify this therapy and improve its effectiveness, the mechanization of root canal preparation is proposed. Several authors assume that this technique optimizes preparation time and improves the quality of treatment, obtaining great acceptance in the current literature. We report the sequence of procedures, resolution, and controls of two pulpectomies with mechanized instrumenta-tion in primary molars (AU)


Asunto(s)
Humanos , Masculino , Niño , Diente Primario/lesiones , Argentina , Pulpitis/terapia , Facultades de Odontología , Atención Dental para Niños/métodos , Instrumentos Dentales/tendencias
9.
Rev. chil. enferm. respir ; Rev. chil. enferm. respir;39(2): 175-179, 2023. graf, tab
Artículo en Español | LILACS | ID: biblio-1515117

RESUMEN

La incidencia de la tuberculosis (TBC) en Chile se ha ido incrementando en el último quinquenio, excepto al inicio de la pandemia de Covid-19, donde la pesquisa de TBC se redujo en forma importante. El escenario epidemiológico actual dista del objetivo propuesto en la Estrategia Nacional de Salud (ENS) de la década 2011-2020 (un plan nacional de gobierno para enfermedades relevantes en la población) que consistía en alcanzar una tasa de incidencia de todas las formas de TBC menor a 5 / 100.000 habitantes. La nueva ENS para la década 2021-2030 propone reducir la incidencia de la enfermedad mediante el diagnóstico oportuno y precoz focalizando las intervenciones en las poblaciones de riesgo de la enfermedad (grupos vulnerables), a modo de pesquisa activa y no solo como pesquisa por consultas espontáneas de sintomáticos respiratorios, o tamizajes masivos que pueden no seleccionar a la población de riesgo. También propone intervenir en la prevención priorizando el estudio y tratamiento de la población con Infección Tuberculosa Latente (ITL) de mayor riesgo de progresión hacia la enfermedad. Por último, se pretende mejorar la eficiencia del proceso de tratamiento de la TBC, optimizando el acceso y adherencia a las terapias de los casos activos de TBC como medida de incrementar la proporción de curación. Una nueva norma ministerial para el manejo y control de la TBC puede ayudar enormemente a esta propuesta. Esta norma entrada plenamente en vigencia el año 2022 entrega las herramientas operacionales para cumplir el objetivo señalado para la nueva ENS. La norma incorpora actividades tendientes a lograr una mayor cobertura de estudio y tratamiento de la ITL en grupos específicos, donde se incluyen, además de los contactos infantiles, a los contactos adultos y a otros grupos vulnerables. La terapia para esta condición se realizará utilizando la asociación de Isoniazida con Rifapentina de preferencia. Esta terapia se aplica bajo supervisión en una dosis semanal durante 3 meses (12 dosis) y ha demostrado mejor adherencia y menor toxicidad hepática. Para el diagnóstico oportuno de TBC la pesquisa se ha focalizado en los sintomáticos respiratorios (tos con expectoración) de más de 2 semanas en personas que pertenecen a alguno de los grupos vulnerables, o que tienen rasgos clínicos muy sugerentes de la enfermedad (fiebre, sudoración vespertina, hemoptisis, compromiso del estado general). Como herramienta diagnóstica deja de utilizarse la baciloscopía por su baja sensibilidad y es sustituida por pruebas moleculares, siendo la plataforma automatizada de amplificación de ADN del complejo M. tuberculosis más utilizada y disponible en los servicios de salud públicos el GeneXpert MTB/RIF Ultra, que además entrega información de la susceptibilidad a la rifampicina a través de la identificación de una mutación específica del genoma (gen rpoB). Con esta tecnología se agiliza el proceso diagnóstico (puede obtener resultados durante el día de ejecución, habitualmente no demoraría más de 2 horas) y es de alta sensibilidad (sensibilidad muy similar al cultivo). El tratamiento de la TBC sensible a los fármacos del esquema primario (rifampicina = R, isoniazida = H, etambutol = E y pirazinamida = Z) consiste en la administración diaria en la fase inicial (con los 4 fármacos) durante 2 meses y en la fase de continuación (con isoniazida y rifampicina) durante 4 meses, totalmente supervisado. La TBC con resistencia a rifampicina tiene tratamiento con un esquema acortado oral de 9 meses con nuevos fármacos: bedaquilina, linezolid, clofazimina y levofloxacino (6 meses con los 4 fármacos, seguido de 3 meses con clofazimina y levofloxacino). Estas terapias de alta calidad son seguras y prometen mejores resultados de curación. La nueva norma significa una mayor cobertura para la erradicación de los reservorios de la enfermedad y una mayor precisión en el diagnóstico de las fuentes de trasmisión comunitaria de la enfermedad, siendo un aporte significativo hacia la eliminación de la TBC en el país.


The incidence of tuberculosis (TB) in Chile has been increasing in the last five years except at the beginning of the Covid-19 pandemic where TB screening has clearly decreased. The current epidemiological scenario is far from the goal proposed in the National Health Strategy (NHS) of the decade 2011-2020 (a national government plan for relevant diseases in the population) which was to achieve an incidence rate of all forms of TB less than 5/100,000 inhabitants. The new NHS for the decade 2021-2030 proposes to reduce the incidence of the disease through timely and early diagnosis by focusing interventions on populations at risk of the disease (vulnerable groups), as an active screening and not only as screening for spontaneous consultations of respiratory symptomatic or mass screenings that may not select the population at risk. It also proposed to intervene in prevention prioritizing the study and treatment of the population with Latent Tuberculosis Infection (LTI) at higher risk of progression to the disease. Finally, it intends to improve the efficiency of the TB treatment process, optimizing access and adherence to therapies of active TB cases as a measure to increase the cure rate. A new ministerial standard for the management and control of TB can greatly help this proposal. This standard, fully effective in 2022, provides the operational tools to meet the objective set for the new NHS. The standard incorporates activities aimed at achieving greater coverage of study and treatment of LTI in specific groups, which include, in addition to child contacts, adult contacts and other vulnerable groups. Therapy for this condition will be performed using the combination of isoniazid with rifapentine preferably. Therapy is administered under supervision and patients receive therapy once a week for 12 doses for 3 months. This therapy has shown better adherence and lower liver toxicity. For the timely diagnosis of TB, case finding has focused on respiratory symptoms (cough and expectoration) for more than 2 weeks, in individuals that belong to one of the vulnerable groups, or that have additional clinical features very suggestive of the disease (fever, afternoon sweats, hemoptysis, compromise of the general condition). Smear sputum as a diagnostic tool is no longer used due to low sensitivity and it was replaced by molecular tests in automated platform for DNA amplification of the mycobacterium TB complex. The more used and available in public health services is GeneXpert MTB / RIF Ultra, which also provides information on susceptibility to rifampicin through the identification of a specific genome mutation (rpoB gene). With this technology, the diagnostic process is streamlined (you can obtain results during the day of execution, usually it would not take more than 2 hours) and sensitivity is high (sensitivity very similar to culture). Treatment of TB sensitive to first line drugs (rifampicin, isoniazid, ethambutol and pyrazinamide) consists of daily administration in the initial phase (with four drugs) for 2 months and in the continuation phase (with isoniazid and rifampicin) for 4 months, fully supervised. In rifampicin resistant TB, the treatment is a shortened oral regimen of 9 months with new drugs: bedaquiline, linezolid, clofazimine and levofloxacin (six months with four drugs, followed by three months with clofazimine and levofloxacin). These high-quality therapies are safe and promise better healing results. The new national standards mean a greater coverage for the eradication of the reservoirs of the disease and a greater precision in the diagnosis of the sources of community transmission of tuberculosis, being a significant contribution towards the path of control and elimination of TB in the country.


Asunto(s)
Humanos , Tuberculosis/prevención & control , Tuberculosis/diagnóstico , Tuberculosis/terapia , Chile , Congreso
10.
Artículo en Inglés, Español | MEDLINE | ID: mdl-29196226

RESUMEN

INTRODUCTION: Some patients with a hip fracture also present a concomitant upper limb fracture. We want to know whether these patients have a worse functional level and whether they have any differences in various clinical parameters compared with patients with an isolated hip fracture. MATERIAL AND METHODS: We retrospectively reviewed 1061 discharge reports from the Orthogeriatrics Unit. We collected information on several clinical parameters of the fractures. Subsequently, we performed a statistical analysis of the data by comparing the associated fracture group with the isolated fracture group. RESULTS: We detected 44 patients with associated upper limb fracture, 90.9% were women (40) and the average age was 84.45years. Eighty-one point eight percent of the upper limb fractures were distal radius or proximal humerus. Pertrochanteric fractures were the most common (none of them were subtrochanteric fractures). Surgical delay was 2.60days and the average hospital stay was 12.30days. Sixty-four point three percent were nail surgery and 31% arthroplasty. The mean Barthel index score was 84.88 (P=.021). Fifty-two point 5 percent of the patients in the study group were referred to a functional support unit (P=.03). The in-hospital mortality rate was 4.2%, with no differences between groups. CONCLUSIONS: Patients with an associated fracture have a higher previous functional capacity and they are more independent. Nevertheless, after the fracture they need more help from the healthcare system for optimal functional recovery.


Asunto(s)
Fracturas de Cadera/diagnóstico , Húmero/lesiones , Fracturas del Radio/diagnóstico , Anciano , Anciano de 80 o más Años , Femenino , Fijación de Fractura , Anciano Frágil , Fragilidad/complicaciones , Fragilidad/diagnóstico , Estado de Salud , Fracturas de Cadera/complicaciones , Fracturas de Cadera/mortalidad , Fracturas de Cadera/cirugía , Humanos , Húmero/cirugía , Masculino , Pronóstico , Fracturas del Radio/complicaciones , Fracturas del Radio/mortalidad , Fracturas del Radio/cirugía , Recuperación de la Función , Estudios Retrospectivos
11.
Rev. enferm. neurol ; 21(1): 54-79, ene.-abr. 2022. graf, tab
Artículo en Español | LILACS, BDENF - enfermagem (Brasil) | ID: biblio-1397930

RESUMEN

Introducción: la enfermedad vascular cerebral (EVC) es un déficit neurológico súbito causado por alteraciones en la circulación cerebral; considerada por la Organización Mundial de la Salud (OMS) como la segunda causa global de muerte en el mundo, en el 2020 ocupó el séptimo lugar como causa de muerte, en México es un problema de salud pública y una importante causa de discapacidad. Objetivo: realizar un estudio de caso a una persona con EVC hemorrágico a través del proceso de atención de enfermería. Método: plan de cuidados con el modelo de Virginia Henderson; fuentes de información: directa, hoja de enfermería y expediente clínico. Se graficaron signos vitales y presión intracraneal PIC. Análisis de artículos vigentes en PubMed, Redalyc, SciELO, Elsevier. Descripción del caso: masculino hipertenso en descontrol y fumador moderado. En el servicio de urgencias presenta datos de deterioro rostro caudal en fase bulbar, se da manejo avanzado de la vía aérea e ingresa a quirófano para colocación de ventriculostomía. Con probable mortalidad del 97 %. Consideraciones éticas: principios éticos para la investigación en la Escuela Nacional de Enfermería y Obstetricia, ENEO, Código Deontológico de Enfermería, Código de Ética para las Enfermeras y Enfermeros de México y NOM 004 del expediente clínico. Conclusiones: se emplearon cuidados especializados a necesidades alteradas según modelo de Henderson que continúa siendo actual como filosofía adaptativa para valoración integral del ente de nuestros cuidados. Mejoró mi curva de aprendizaje en conocimiento sensible e intelectual con enfoque crítico y neurológico acorde a la enfermería basada en la evidencia. Las EVC son causa de muerte y discapacidad, no deben ser subestimadas sino objeto de atención de instituciones gubernamentales y de salud a nivel mundial pues falta generar cultura de prevención.


Introduction: CVD is a sudden neurological deficit caused by alterations in cerebral circulation; considered by the WHO as the second global cause of death in the world, in 2020 it ranked seventh as a cause of death in Mexico and an important cause of disability. Objective: to carry out a case study of a person with Hemorrhagic CVD through the Nursing Care Process. Method: care plan with the Henderson model; Information sources: direct, Nursing Sheet and Clinical file. Vital signs and ICP were graphed. Analysis of current articles in PubMed, Redalyc, SciELO, ELSEVIER. Case description: patient is uncontrolled hypertensive and a moderate smoker. In the emergency department, he presented data of facial caudal deterioration in the bulbar phase, advanced management of the airway was given, and he entered the operating room for ventriculostomy placement. With Mortality of 97%. Ethical considerations: ethical principles for research in the ENEO, Nursing Code of Ethics, Code of ethics for nurses in Mexico and NOM 004 of the clinical file. Conclusions: specialized care was used for altered needs according to the Henderson model, which continues to be current as an adaptive philosophy for comprehensive assessment of the entity of our care. It improved my learning curve in sensitive and intellectual knowledge with a critical and neurological approach according to evidence-based nursing. CVDs are a cause of death and disability, they should not be underestimated, but rather the object of attention from governmental and health institutions worldwide since it is necessary to generate a culture of prevention.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Accidente Cerebrovascular , Enfermería , Accidente Cerebrovascular Hemorrágico
12.
Rev. chil. enferm. respir ; Rev. chil. enferm. respir;38(3): 194-201, sept. 2022. graf
Artículo en Español | LILACS | ID: biblio-1423701

RESUMEN

La situación epidemiológica y operacional de la tuberculosis en el mundo se vio afectada por la pandemia de COVID-19 durante los años 2020 y 2021. A nivel global, el número de casos de tuberculosis notificados disminuyó en un 18% el año 2020 con respecto al año anterior, y el número de muertes por esta causa mostró un aumento en el mismo año. En Chile, se observó una caída similar en el número de casos diagnosticados el año 2020, en directa relación con una disminución del 70% en el número de muestras procesadas para diagnóstico de tuberculosis pulmonar. El presente trabajo detalla indicadores epidemiológicos y operacionales del control de la tuberculosis en Chile para los años 2020 y 2021, y analiza su relación con el impacto de la pandemia COVID-19 sobre las actividades del Programa Nacional de Tuberculosis.


The COVID-19 pandemic during 2020 and 2021 affected the epidemiological and operational situation of tuberculosis control worldwide. Globally, there was a reduction of 18% in the number of notified cases of tuberculosis in 2020 in comparison to the previous year, and the number of deaths increased in the same year. In Chile, there was a similar fall in the number of notified cases, in direct relation to a decrease of 70% in the number of diagnostic tests performed for pulmonary tuberculosis at a national level. This article details the epidemiological and operational indicators of tuberculosis control in Chile during 2020-2021, and analyzes their relation with the impact of COVID-19 pandemic on the activities of the National Tuberculosis Program.


Asunto(s)
Humanos , Masculino , Femenino , Recién Nacido , Lactante , Preescolar , Niño , Adolescente , Adulto , Persona de Mediana Edad , Anciano , Anciano de 80 o más Años , Adulto Joven , Tuberculosis/epidemiología , COVID-19 , Tuberculosis/mortalidad , Chile/epidemiología , Poblaciones Vulnerables , Pruebas Diagnósticas de Rutina , Distribución por Edad y Sexo , Pandemias
13.
Urol Case Rep ; 13: 48-50, 2017 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-28443242

RESUMEN

We hereby present the case of a 55 years old patient with clinical diagnosis of high-risk prostate cancer T2bN1Mo Gleason 9 (4 + 5) treated with androgen deprivation therapy and external beam radiotherapy. Despite treatment, castration levels were not achieved and clinical progression was evidenced by the appearance of bone metastases and progression of PSA. After several hormonal treatments without any PSA or testosterone response, surgical castration was performed by bilateral orchiectomy. The pathology results showed an incidental Leydig cell tumor in the right testicle.

14.
Rev Chilena Infectol ; 23(1): 73-6, 2006 Mar.
Artículo en Español | MEDLINE | ID: mdl-16462969

RESUMEN

Subdural empyema is a rare complication of sinusitis in children. Its clinical presentation represents a neurosurgical emergency and as a scarcely recognized entity a delayed diagnosis rapidly increases its fatal prognosis. We report the clinical and radiological course of an adolescent with a subdural empyema secondary to sinusitis. Clinical and radiological features, laboratory findings and outcome of this condition are discussed based in a review of previously reported cases.


Asunto(s)
Empiema Subdural/etiología , Sinusitis/complicaciones , Niño , Craneotomía , Empiema Subdural/diagnóstico , Empiema Subdural/cirugía , Humanos , Masculino , Sinusitis/diagnóstico , Sinusitis/cirugía , Tomografía Computarizada por Rayos X
15.
Rev. chil. enferm. respir ; Rev. chil. enferm. respir;37(1): 74-81, mar. 2021. ilus, tab
Artículo en Español | LILACS | ID: biblio-1388134

RESUMEN

Resumen El éxito de los tratamientos acortados de la tuberculosis se debe a la asociación de fármacos bactericidas y esterilizantes, principalmente Rifampicina e Isoniazida. Cuando la Rifampicina no puede ser utilizada por resistencia, los tratamientos son más prolongados y el éxito en la curación se reduce. La resistencia a Rifampicina frecuentemente se acompaña de resistencia a Isoniazida (Multidrogoresistencia o MDR). La OMS informa que en 2019 se diagnosticaron sólo el 44% de los casos estimados de tuberculosis con resistencia a Rifampicina (se proyectaba 465.000 casos) y se trató sólo al 38% de los casos estimados, quedando una gran proporción de casos sin diagnosticar y sin tratar. En Chile la vigilancia de la susceptibilidad a fármacos de primera línea en cepas de Mycobacterium tuberculosis se efectúa mediante biología molecular desde 2014, observándose un progresivo incremento de casos resistentes a Rifampicina desde 1% (23 casos) para ese año hasta 2,2% (65 casos) en 2019. La mayoría de casos de resistencia a Rifampicina corresponden a resistencia inicial. En casos con resistencia a Rifampicina realizamos estudio de susceptibilidad a fármacos de segunda línea en el laboratorio de referencia nacional. La terapia de TB-MDR tradicional tiene baja eficacia, con abandonos frecuentes por su largo tiempo de terapia y toxicidad. Nuevos tratamientos sin inyectables y el uso de Clofazimina, Fluorquinolonas, Linezolid y Bedaquilina tienen una mejor tasa de curación. Recientemente, el Programa de Control de la Tuberculosis de Chile dispone de esta terapia más eficaz y de menor duración por vía oral con estos fármacos.


The high success rate of shortened Tuberculosis (TB) treatments has been achieved by the association of bactericidal and sterilizing drugs. The main drugs are Rifampicin and Isoniazide. When Rifampicin cannot be used by resistance, the treatment is prolonged and success in healing is significantly reduced. Resistance to Rifampicin is often accompanied by resistance to Isoniazide (Multidrug resistance or MDR). WHO reports that only 44% of estimated TB cases with resistance to Rifampicin were diagnosed in 2019 (465,000 cases projected) and only 38% of estimated cases were treated, with a large proportion of cases remaining undiagnosed and untreated. In Chile, monitoring of susceptibility to first-line drugs is conducted in strains of Mycobacterium tuberculosis by molecular biology since 2014, observing a progressive increase in cases with Rifampicin resistance from 1% for that year (23 cases) to 2.2% in 2019 (65 cases). Most cases of resistance to Rifampicin correspond to cases of initial resistance. In cases with resistance to Rifampicin we carry out susceptibility study to second-line drugs in a national reference laboratory. MDR-TB therapy has low efficacy, with frequent abandonments for its long therapy time and toxicity. New non-injectable treatments and use of Clofazimine, Fluorquinolones, Linezolid and Bedaquiline are achieving a better cure rate. Recently, Chile's TB Control Program has this most effective and shorter-lasting oral therapy with these drugs.


Asunto(s)
Humanos , Rifampin/farmacología , Tuberculosis Resistente a Múltiples Medicamentos/tratamiento farmacológico , Tuberculosis Resistente a Múltiples Medicamentos/epidemiología , Antibióticos Antituberculosos/farmacología , Chile/epidemiología
16.
Rev. chil. enferm. respir ; Rev. chil. enferm. respir;37(2): 166-173, jun. 2021.
Artículo en Español | LILACS | ID: biblio-1388146

RESUMEN

Resumen La terapia de la tuberculosis con el esquema primario recomendado por la OMS no logra la curación de todos los casos a nivel mundial, pero en general alcanza un éxito de curación de al menos el 85% de los casos en el año 2018. El mismo año en Chile la eficiencia del tratamiento es solo de 76%, principalmente por la alta proporción de muertes y pérdida de seguimiento durante la terapia. Datos preliminares muestran que la cohorte ingresada en 2019 tuvo un éxito de tratamiento cercano a 74%. En Chile los fracasos de tratamiento son infrecuentes, debido principalmente a la vigilancia nacional de la susceptibilidad a fármacos. Para reducir la letalidad es necesario reforzar las estrategias para el diagnóstico precoz de la tuberculosis, mediante nuevos algoritmos que incorporen la biología molecular y la radiología en casos sospechosos de esta enfermedad, fomentar el adecuado manejo de las comorbilidades, establecer una adecuada red de apoyo social y disponer de centros de hospitalización cuando se requieren. Además, se debe fortalecer la adherencia a la terapia de los pacientes con estrategias de incentivo y facilitación de la asistencia.


Tuberculosis therapy with the primary regimen recommended by the World Health Organization does not cure all cases globally, but it reached success in at least 85% of cases in the year 2018. The same year in Chile, treatment efficiency is achieved in only 76%, mainly due to the high proportion of deaths and loss of follow-up during therapy. Preliminary data show that in the 2019 cohort the success was achieved only in about 74% of new cases. Treatment failures in Chile are rare due to national surveillance of drug susceptibility. To reduce fatality, it is necessary to reinforce the strategies for early diagnosis of tuberculosis through new algorithms. Such strategies should include molecular biology and radiology in suspected TB cases, to promote proper management of comorbidities, establish an adequate social support network and have centers available for prolonged hospitalization when needed. In addition, patient's adherence to therapy should be strengthened with strategies that encourage and facilitate attendance.


Asunto(s)
Humanos , Tuberculosis/tratamiento farmacológico , Pacientes Desistentes del Tratamiento , Tuberculosis/mortalidad , Tuberculosis/epidemiología , Disponibilidad Biológica , Infecciones por VIH/terapia , Infecciones por VIH/epidemiología , Chile/epidemiología , Salud Global , Estudios de Cohortes , Resultado del Tratamiento , Huésped Inmunocomprometido , Farmacorresistencia Bacteriana , Perdida de Seguimiento , Antituberculosos/uso terapéutico
17.
Rev. chil. enferm. respir ; Rev. chil. enferm. respir;37(4): 325-331, dic. 2021. ilus, tab
Artículo en Español | LILACS | ID: biblio-1388160

RESUMEN

La tuberculosis es la principal causa de muerte por un agente infeccioso a nivel mundial y se estima que un 6% de los casos nuevos corresponde a tuberculosis infantil. La presencia de tuberculosis en niños es una señal de la existencia de transmisión del agente en la comunidad. Esta investigación busca describir las características epidemiológicas de la tuberculosis infantil en Chile entre 2011 y 2020. METODOLOGÍA: estudio descriptivo de los casos de tuberculosis infantil registrados en Chile entre los años 2011 y 2020. RESULTADOS: se registraron 544 casos de tuberculosis en menores de 15 años en el período analizado, con una tasa de incidencia anual entre 1,1 y 2,2 casos por 100.000. Se observa un importante aumento de casos en los últimos tres años, especialmente en el grupo de menores de 5 años. 63,2% corresponden a tuberculosis pulmonar, y de ellos 62,3% fueron confirmados por bacteriología. La mayoría de los casos no presenta comorbilidades que impliquen inmunosupresión y la incidencia de meningitis tuberculosa en menores de 5 años es baja. La proporción de contactos es de 29% y la de extranjeros de 17%, ambas variables en aumento en los últimos años. CONCLUSIÓN: La tuberculosis en niños sigue siendo un problema de salud poco frecuente en Chile. Sin embargo, su aumento en los últimos años debe alertar sobre un incremento de la transmisión comunitaria de la enfermedad, por lo que se debe reforzar la detección oportuna de casos contagiantes, la investigación de contactos y el tratamiento preventivo.


Tuberculosis is the leading cause of death from a single infectious agent worldwide and it is estimated that 6% of new cases are children. Childhood tuberculosis reflects ongoing transmission within communities. This study aims to describe the epidemiological characteristics of childhood tuberculosis in Chile between 2011 and 2020. METHODOLOGY: descriptive study of the cases of tuberculosis under 15 years-old registered in Chile from 2011 to 2020. RESULTS: 544 cases were registered in the period analyzed, with an annual incidence rate between 1.1 and 2.2 cases per 100,000. A significant increase in cases is observed in the last three years, especially in the group under 5 years-old. 63.2% correspond to pulmonary tuberculosis, and among them 62.3% are confirmed by bacteriology. Most of the cases do not have comorbidities and the incidence of tuberculous meningitis in children under 5 years is low. Contacts are 29% of the cases and foreigners are 17%, both percentages are increasing in the last years. CONCLUSION: Childhood tuberculosis remains a low frequency health problem in Chile. However, its increase in recent years implies an increase in the community transmission. Active case finding, contact tracing and preventive treatment should be reinforced.


Asunto(s)
Humanos , Masculino , Femenino , Tuberculosis/epidemiología , Migrantes , Tuberculosis/transmisión , Tuberculosis Meníngea/epidemiología , Tuberculosis Pulmonar/epidemiología , Comorbilidad , Chile/epidemiología , Epidemiología Descriptiva , Incidencia , Factores de Riesgo , Trazado de Contacto
18.
Oncogene ; 11(6): 1165-72, 1995 Sep 21.
Artículo en Inglés | MEDLINE | ID: mdl-7566977

RESUMEN

Both the murine and human genomic loci that encode flt3 ligand have been cloned. flt3 ligand is a hematopoietic growth factor that stimulates the proliferation of stem and progenitor cells. The portions of the murine and human flt3 ligand genomic loci encompassing the coding region of the protein are approximately 4.0 kb and 5.9 kb, respectively. The human genomic locus is larger as a result of the presence of repeated sequences within introns I, II, IV, V and VI. The transmembrane isoform of the murine and human flt3 ligand proteins are each encoded within seven exons (1-5 + 7 and 8). Analyses of flt3 ligand cDNA clones show that alternative splicing of a putative sixth exon results in the generation of a soluble form of the flt3 ligand protein. The sizes of each of the exons are well conserved between species. Murine and human flt3 genomic loci have a similar exon: intron structure compared to the genomic loci encoding Steel factor and colony stimulating factor 1. These proteins, which appear to be ancestrally related, are hematopoietic growth factors that stimulate cells via specific and structurally related tyrosine kinase receptors on the cell surface.


Asunto(s)
Mapeo Cromosómico , Factores de Crecimiento de Célula Hematopoyética/genética , Proteínas de la Membrana/genética , Empalme Alternativo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Médula Ósea/metabolismo , Exones , Humanos , Factor Estimulante de Colonias de Macrófagos/genética , Ratones , Ratones Endogámicos C57BL , Datos de Secuencia Molecular , Bazo/metabolismo , Factor de Células Madre/genética
19.
Oncogene ; 10(1): 149-57, 1995 Jan 05.
Artículo en Inglés | MEDLINE | ID: mdl-7824267

RESUMEN

We have recently described a novel hematopoietic growth factor, referred to as the flt3 ligand, that stimulates the proliferation of sub-populations of hematopoietic cells that are enriched for stem and progenitor cells. This factor is a transmembrane protein that undergoes proteolytic cleavage to generate a soluble form of the protein. We have isolated additional flt3 ligand isoforms by PCR that contain an extra exon and encode what are predicted to be either a soluble form of the ligand or a longer version of the transmembrane protein. We have also isolated cDNAs from murine T cell libraries that encode an isoform of the flt3 ligand that has an unusual C-terminus. This isoform results from a failure to splice out an intron during mRNA processing. The protein encoded by this cDNA is expressed on the cell surface, where it is biologically active. However, this novel isoform does not appear to give rise to a soluble form of the protein. Regulation of mRNA splicing is likely to control the generation of cell bound or soluble forms of this hematopoietic growth factor. Genetic mapping studies localize the gene encoding the flt3 ligand to the proximal portion of mouse chromosome 7 and to human chromosome 19q13.3.


Asunto(s)
Empalme Alternativo , Sustancias de Crecimiento/análisis , Proteínas de la Membrana/análisis , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Mapeo Cromosómico , Cromosomas Humanos Par 19 , ADN Complementario , Femenino , Sustancias de Crecimiento/genética , Humanos , Intrones , Masculino , Proteínas de la Membrana/genética , Ratones , Ratones Endogámicos C57BL , Datos de Secuencia Molecular , ARN Mensajero/genética , Solubilidad
20.
Leukemia ; 9(7): 1212-8, 1995 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-7630197

RESUMEN

Expression of the flt3 tyrosine kinase receptor and its ligand were examined on various murine and human hematopoietic cell lines. Surface expression of flt3 receptor and flt3 ligand were detected by flow cytometry using biotinylated human flt3 ligand or biotinylated soluble human flt3 receptor Fc fusion protein (flt3R-Fc), respectively. Flt3 receptor and ligand expression were also examined by Northern blot analysis. Flt3 receptor was expressed on the surface of only two of nine murine cell lines and nine of 15 human cell lines, with positive cells representing the B cell, early myeloid, and monocytic lineages. Staining for surface expression of the flt3 ligand revealed that seven of nine murine cell lines and nine of 15 human cell lines screened were positive by flow cytometry. All murine and human cell lines assayed were positive for flt3 ligand RNA expression by Northern blot analysis, but not all cell lines expressing flt3 ligand mRNA had detectable surface expression. Cells expressing the flt3 ligand were of the myeloid, B cell and T cell lineages at various stages of differentiation. Only the OCI-AML-5, NALM-6, and AML-193 cell lines coexpressed both surface flt3 receptor and ligand. The myeloid leukemic M1 cell terminally differentiate into macrophage-like cells under the influence of leukemia inhibitory factor (LIF). We found that LIF-stimulated M1 cells down-regulated surface expression and mRNA levels of the flt3 receptor, but up-regulated expression of the flt3 ligand. Although we could demonstrate that the flt3 receptor was functional in the M1 cell line, flt3 ligand could not induce the M1 cells to differentiate.


Asunto(s)
Células Madre Hematopoyéticas/metabolismo , Interleucina-6 , Proteínas de la Membrana/metabolismo , Proteínas Proto-Oncogénicas/metabolismo , Proteínas Tirosina Quinasas Receptoras/metabolismo , Receptores de Superficie Celular/metabolismo , Animales , Northern Blotting , Western Blotting , Diferenciación Celular , Regulación hacia Abajo , Citometría de Flujo , Inhibidores de Crecimiento/farmacología , Células Madre Hematopoyéticas/enzimología , Humanos , Factor Inhibidor de Leucemia , Leucemia Mieloide Aguda/patología , Linfocinas/farmacología , Macrófagos/patología , Proteínas de la Membrana/genética , Ratones , Fosforilación , Proteínas Proto-Oncogénicas/genética , ARN Mensajero/metabolismo , Proteínas Tirosina Quinasas Receptoras/genética , Receptores de Superficie Celular/genética , Células Tumorales Cultivadas/patología , Regulación hacia Arriba , Tirosina Quinasa 3 Similar a fms
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