RESUMEN
AIM: To describe the orthogeriatric activity in the elderly with hip fractures in the Hospital Mancha Centro, based on the recommendations of the main guidelines. MATERIAL AND METHOD: Observational prospective study, comprising all patients over 65 years of age admitted to the Traumatology Unit with a hip fracture between April 2015 and December 2015. Patients were admitted under the care of the Traumatology Unit with cross-consultation carried out with the Geriatrics Department, which then carried out a pre-operative geriatric assessment and the post-operative follow-ups. RESULTS: The mean pre-surgery waiting time was 48h and the overall time in hospital was 10.3±8.2 days. Patients who suffered from delirium (42.1%) did not improve as well, and were referred to nursing homes. Blood transfusions were received by 54.7% of the patients, despite 53.5% of them having received intravenous and/or oral iron after the surgery. Treatment with calcium and vitamin D was prescribed in 79% of the patients on discharge. The Rehabilitation Unit assessed 36% of the patients, with 4.8% fully, and 16.7% partially recovering their prior functional status. Upon discharge, 55% of the patients returned to their homes, and 22% were referred to short-term assisted living facilities. DISCUSSION: This article describes how the main clinical problems are handled in the elderly with hip fractures in our hospital, based on recommendations of the main guidelines and publications. CONCLUSIONS: Our hospital follows the recommended guidelines. Aspects for improvement include the management of anaemia during admission and rehabilitation.
Asunto(s)
Fijación de Fractura , Geriatría , Adhesión a Directriz/estadística & datos numéricos , Fracturas de Cadera/cirugía , Comunicación Interdisciplinaria , Pautas de la Práctica en Medicina/estadística & datos numéricos , Traumatología , Anciano , Anciano de 80 o más Años , Femenino , Estudios de Seguimiento , Fijación de Fractura/métodos , Fijación de Fractura/normas , Fijación de Fractura/estadística & datos numéricos , Evaluación Geriátrica , Fracturas de Cadera/diagnóstico , Hospitales Generales , Humanos , Masculino , Atención Perioperativa/métodos , Atención Perioperativa/normas , Guías de Práctica Clínica como Asunto , Estudios Prospectivos , España , Resultado del TratamientoRESUMEN
The aim of this research was to evaluate strategies for the development of a virgin olive oil (VOO) enriched with aqueous extracts of olive leaf and cake to increase the necessary dose in the diet of phenolic compounds with a natural product, as phenolic compounds are involved on the healthy properties of olive oil. Different extraction procedures were evaluated with the aim of increasing the phenol content and antioxidant potential of extracts of olive leaf and cake. As leaves extract presented a higher total phenolic content, it was characterized in order to determine its phenolic profile, and was employed to enrich VOO. Diverse procedures were used to prepare enriched VOO with the leaves extract, and finally the effects of phenol enrichment were evaluated based on the antioxidant potential and oxidative stability of the prepared phenol-enriched virgin olive oils. These enriched VOOs increased significantly the content in phenolic compounds, antioxidant potential and oxidative stability 40, 4 and 1.5 fold more, respectively, than the Control oil. Furthermore, the addition of lecithin had a positive effect both on the phenolic compounds content, and on the antioxidant potential of the oils. Besides, the use of the olive leaves extract, with and without lecithin respectively, supposes a strategy potential for reducing the harmful effects that inflicts long-term preservation of VOOs and its possible deterioration.
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Antioxidantes , Fenoles/análisis , Aceites de Plantas/química , Conservación de Alimentos , Lecitinas , Olea , Aceite de Oliva , Oxidación-Reducción , Extractos Vegetales/química , Hojas de la PlantaRESUMEN
OBJECTIVES: To develop and validate an instrument to measure health-related quality of life (HRQOL) specific to patients with allergic rhinitis (AR) and primarily for use in Spanish and Spanish-speaking populations. METHODS: An initial item pool was generated from literature review, focus groups with AR patients, and consultations with clinical experts. Item reduction was performed using clinimetric and psychometric approaches after administration of the item pool to 400 AR patients. The resulting instrument's internal consistency, test-retest (2-4 weeks) reliability, known groups and convergent validity, and sensitivity to change were tested in a longitudinal, observational, multicenter study in 210 AR patients who also completed the Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ). RESULTS: The new questionnaire took a mean (SD) of 7.1 (5.4) minutes to answer. Floor and ceiling effects were less than 15% on all dimensions. Cronbach's alpha values and intraclass correlation coefficient values for six of the sevendimensions and the overall score exceeded 0.70. Statistically significant differences (P < 0.01) were observed on all ESPRINT-28 dimensions and the overall score between patients with mild (mean overall score 1.97, SD 0.99), moderate (mean overall score 2.78, SD 0.88), and severe AR (mean overall score 3.89, SD 0.87). Patients with persistent AR had worse scores (P < 0.05) on all dimensions than patients with intermittent AR. Correlations between the ESPRINT-28 and the RQLQ were generally as expected. Effect sizes for score changes between the two study visits ranged from 0.96 to 1.76 for individual dimensions and the overall score. CONCLUSIONS: This new, Spanish-developed instrument to measure HRQOL in AR patients has shown good reliability, validity, and sensitivity to change. It has also proved easy to use and administer.
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Estado de Salud , Calidad de Vida , Rinitis Alérgica Perenne , Rinitis Alérgica Estacional , Encuestas y Cuestionarios , Adulto , Femenino , Humanos , Estudios Longitudinales , Masculino , Reproducibilidad de los Resultados , EspañaRESUMEN
Anticonvulsant hypersensitivity syndrome (AHS) is a rare, severe drug hypersensitivity reaction included in the drug-related rash with eosinophilia and systemic symptoms syndrome (DRESS), in which a transient state of immune suppression and reactivation of latent virus infections have been observed. We describe 5 patients who developed neosensitization to different drugs taken during a previous episode of anticonvulsant-related DRESS, in whom skin prick, intradermal and/or patch tests were performed to confirm the diagnosis of drug hypersensitivity. In 1 patient, transient hypogammaglobulinemia was observed during the AHS. Four of the 5 patients developed a delayed skin eruption or a delayed systemic hypersensitivity reaction after intake of a drug that they had also taken during a previous anticonvulsant DRESS which had occurred months or years earlier; in the fifth, a possible reaction was prevented thanks to the allergy workup. The diagnosis of drug allergy was demonstrated by positive delayed reaction to intradermal test with amoxicillin in 2 cases, positive patch tests to paracetamol and amitriptyline in 2 cases, and by clinical evidence of ceftriaxone erythroderma in one. The possibility of neosensitization to drugs administered during anticonvulsant-related DRESS should be considered. A transient state of immunosuppression induced during the anticonvulsant-related DRESS may trigger latent virus reactivation and massive nonspecific immune system response, which may lead to breakdown of tolerance to other drugs present at that time in the organism.
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Anticonvulsivantes/efectos adversos , Hipersensibilidad a las Drogas/etiología , Eosinofilia/inducido químicamente , Exantema/inducido químicamente , Adulto , Anciano , Reacciones Cruzadas , Femenino , Humanos , Masculino , Persona de Mediana Edad , SíndromeRESUMEN
A case showing that soya hull exposure at work causes occupational asthma without flour-related bronchoconstriction.
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Alérgenos/efectos adversos , Asma/etiología , Glycine max/efectos adversos , Enfermedades Profesionales/etiología , Epidermis de la Planta/efectos adversos , Adulto , Pruebas de Provocación Bronquial , Polvo , Humanos , MasculinoRESUMEN
No disponible
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Adulto , Femenino , Humanos , Urticaria/etiología , Amoxicilina/efectos adversos , Reactividad Cruzada , Mariscos/efectos adversos , Tropomiosina/efectos adversos , Pruebas Cutáneas , Inmunoglobulina E/análisisAsunto(s)
Antiinflamatorios no Esteroideos/uso terapéutico , Hipersensibilidad a las Drogas/etiología , Lactonas/uso terapéutico , Adolescente , Adulto , Anciano , Angioedema/inducido químicamente , Angioedema/tratamiento farmacológico , Angioedema/fisiopatología , Antiinflamatorios no Esteroideos/efectos adversos , Asma/inducido químicamente , Asma/tratamiento farmacológico , Asma/fisiopatología , Ensayos Clínicos Controlados como Asunto , Relación Dosis-Respuesta a Droga , Hipersensibilidad a las Drogas/fisiopatología , Tolerancia a Medicamentos , Femenino , Volumen Espiratorio Forzado/fisiología , Humanos , Lactonas/efectos adversos , Lactonas/farmacología , Masculino , Persona de Mediana Edad , Ápice del Flujo Espiratorio/fisiología , Método Simple Ciego , Sulfonas , Urticaria/inducido químicamente , Urticaria/tratamiento farmacológico , Urticaria/fisiopatologíaAsunto(s)
Anestésicos Generales/efectos adversos , Angioedema/inducido químicamente , Quimioterapia Combinada/efectos adversos , Hipotensión/inducido químicamente , Complicaciones Intraoperatorias/inducido químicamente , Enfermedad de Legg-Calve-Perthes/cirugía , Adulto , Combinación Amoxicilina-Clavulanato de Potasio/administración & dosificación , Combinación Amoxicilina-Clavulanato de Potasio/efectos adversos , Anestésicos Generales/administración & dosificación , Angioedema/fisiopatología , Antiinflamatorios no Esteroideos/administración & dosificación , Antiinflamatorios no Esteroideos/efectos adversos , Atracurio/administración & dosificación , Atracurio/efectos adversos , Atropina/administración & dosificación , Atropina/efectos adversos , Diclofenaco/administración & dosificación , Diclofenaco/efectos adversos , Síndrome de Down , Quimioterapia Combinada/administración & dosificación , Cara/fisiopatología , Fentanilo/administración & dosificación , Fentanilo/efectos adversos , Cadera/cirugía , Humanos , Enfermedad de Legg-Calve-Perthes/tratamiento farmacológico , Masculino , Midazolam/administración & dosificación , Midazolam/efectos adversos , Tiopental/administración & dosificación , Tiopental/efectos adversosRESUMEN
BACKGROUND: Hybrid, combined or mixed bariatric surgery is the combination of a degree of 'malabsorption' (as achieved by the intestinal bypass) with a 'restriction' (as achieved by gastric bypass or gastroplasty), thereby simultaneously reducing the absorption of fats in the small bowel and decreasing the intake of food. METHODS: A modification of the bilio-pancreatic diversion (BPD) with a duodenal switch procedure, vertical lineal gastrectomy and preservation of the pylorus, has been used in 23 patients. The antropyloric pump and 4 cm of the duodenum are left intact to preserve physiologic gastric emptying and to prevent anastomotic ulcer. The use of staplers and continuous running sutures reduces surgical risks and operative time. RESULTS: One patient, converted from a vertical gastroplasty, had an intrathoracic esophageal perforation and died of multi-systemic organ failure, a mortality rate of 4.5%. One patient had a partial dehiscence of the laparotomy wound. Three patients developed subcutaneous seromas. Mean weight losses during the first 4 months were 13, 11, 6 and 5 kg, with a loss of 70% of excess weight in patients approaching 1 year. No patient needs treatment for diarrhea. No serious secondary side-effects have been detected. CONCLUSION: This operation appears to result in very satisfactory weight loss, improved quality of life, and a low incidence of complications.
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Royal jelly is the food on which are fed and which causes them to develop into queen bees. It is claimed to have rejuvenating virtues for human beings. This report describes a 15-year-old atopic woman who presented, 15 minutes after the intake of royal jelly, local angioedema, generalised urticaria, dysphonia and bronchospasm. She was given antihistaminics and corticoesteroids and responded well. The ingested product contains royal jelly, lactose and potassium sorbate. No anaphylactic reactions to lactose and sorbates have been described previously. Prick test to common food allergens hymenoptera venoms and pollens were negative. RAST to meletin was also negative. Blood eosinophils were 600 and total IgE 465. Non-commercial prepared specific IgE to royal jelly was positive (0.8 KU/l). Prick by prick was positive to 1/10 dilution, being negative in controls (undiluted). No oral provocation test was performed due to the risk of anaphylaxis. No reported cases of royal jelly allergy were founded in a review of the medical literature. Concluding, it is the first described case of IgE anaphylactic reaction due to royal jelly.
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Anafilaxia/inmunología , Abejas , Ácidos Grasos/efectos adversos , Adolescente , Anafilaxia/diagnóstico , Animales , Femenino , HumanosRESUMEN
Hereditary angioedema (HAE) is due to a deficit of the C1 inhibitor (C1 INH) of a dominant autosomic inheritance. Seven patients are presented from a family with HAE, four of whom with poor prognosis due to the frequency and site of the angioedema. Prophylaxis was obtained with long-term danazol since antifibrinolytic drugs are not efficient in the prevention of outbreaks of angioedema. In three cases a concentrate of C1 INH was administered and in another as short term prophylaxis prior to surgery. C1 INH was more efficient under these indications than fresh plasma or antifibrinolytic drugs.