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1.
Artículo en Inglés, Español | MEDLINE | ID: mdl-34130927

RESUMEN

BACKGROUND AND OBJECTIVE: Most of the studies available in the literature related to the treatment of femoroacetabular impingement (FAA) with surgical hip dislocation (CLD) come from Europe and North America. This study describes the short-term results of the LQC technique for treating PFA in a cohort of Colombian patients. PATIENTS AND METHODS: We retrospectively analysed 42 cases of PFA treated with LQC from 2006 to 2018. The same orthopaedic surgeon performed all surgeries. Clinical outcome was assessed using the Merle d'Aubigné scores, while radiological assessment was performed using the Tönnis score. RESULTS: Fifteen women and 25 men were included in the study, with a mean age of 36.3 years. Two patients had bilateral symptomatic involvement. Of the 42 cases, there were 13 cam type, 11 pincer type and 18 mixed. Preoperatively, 31 hips were classified as poor and moderate, and 11 as good according to the Merle d'Aubigné scale. The preoperative Tönnis radiological classification showed grade 0 in half of the cases. The mean duration of follow-up was 24 months (12 to 37). The final postoperative Merle d'Aubigné scores classified 7 cases as poor or moderate, and 35 as good to excellent (p<0.05). The postoperative Tönnis score showed no significant variation. As complications, one patient had heterotopic ossification, and three had trochanteric nonunion requiring refixation. CONCLUSION: Our results suggest that the LQC technique for the treatment of patients with PFA shows satisfactory short-term results with a low complication rate. To our knowledge, this is the first report of results of the surgical procedure for hip dislocation in our region.

2.
Allergol Immunopathol (Madr) ; 47(3): 282-288, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30595390

RESUMEN

OBJECTIVE: To describe potential regional variations in therapies for severe asthma exacerbations in Chilean children and estimate the associated health expenditures. METHODS: Observational prospective cohort study in 14 hospitals over a one-year period. Children five years of age or older were eligible for inclusion. Days with oxygen supply and pharmacological treatments received were recorded from the clinical chart. A basic asthma hospitalization basket was defined in order to estimate the average hospitalization cost for a single patient. Six months after discharge, new visits to the Emergency Room (ER), use of systemic corticosteroids and adherence to the controller treatment were evaluated. RESULTS: 396 patients were enrolled. Patients from the public health system and from the north zone received significantly more days of oxygen, systemic corticosteroids and antibiotics. Great heterogeneity in antibiotic use among the participating hospitals was found, from 0 to 92.3% (ICC 0.34, 95% CI 0.16-0.52). The use of aminophylline, magnesium sulfate and ketamine varied from 0 to 36.4% between the different Pediatric Intensive Care Units (ICC 0.353, 95% CI 0.010-0.608). The average cost per inpatient was of $1910 USD. 290 patients (73.2%) completed the follow-up six months after discharge. 76 patients (26.2%) were not receiving any controller treatment and nearly a fourth had new ER visits and use of systemic corticosteroids due to new asthma exacerbations. CONCLUSIONS: Considerable practice variation in asthma exacerbations treatment was found among the participating hospitals, highlighting the poor outcome of many patients after hospital discharge, with an important health cost.


Asunto(s)
Corticoesteroides/uso terapéutico , Asma/epidemiología , Costo de Enfermedad , Asma/tratamiento farmacológico , Asma/economía , Niño , Chile/epidemiología , Estudios de Cohortes , Progresión de la Enfermedad , Servicios Médicos de Urgencia , Femenino , Estudios de Seguimiento , Hospitalización , Humanos , Masculino , Estudios Prospectivos , Resultado del Tratamiento
3.
Allergol Immunopathol (Madr) ; 46(6): 533-538, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29720350

RESUMEN

BACKGROUND: Asthma hospitalization rates in Chilean children have increased in the last 14 years, but little is known about the factors associated with this. OBJECTIVE: Describe clinical characteristics of children hospitalized for asthma exacerbation. METHODS: Observational prospective cohort study in 14 hospitals. Over a one-year period, children five years of age or older hospitalized with asthma exacerbation were eligible for inclusion. Parents completed an online questionnaire with questions on demographic information, about asthma, indoor environmental contaminant exposure, comorbidities and beliefs about disease and treatment. Disease control was assessed by the Asthma Control Test. Inhalation technique was observed using a checklist. RESULTS: 396 patients were enrolled. 168 children did not have an established diagnosis of asthma. Only 188 used at least one controller treatment at the time of hospitalization. 208 parents said they believed their child had asthma only when they had an exacerbation and 97 correctly identified inhaled corticosteroids as anti-inflammatory treatment. 342 patients used the wrong spacer and 73 correctly performed all steps of the checklist. CONCLUSIONS: Almost half of the patients were not diagnosed with asthma at the time of hospitalization despite having a medical history suggestive of the disease. In the remaining patients with an established diagnosis of asthma potentially modifiable factors like bad adherence to treatment and poor inhalation technique were found. Implementing a nationwide asthma program including continued medical education for the correct diagnosis and follow up of these patients and asthma education for patients and caregivers is needed to reduce asthma hospitalization rates in Chilean children.


Asunto(s)
Asma/epidemiología , Hospitalización/estadística & datos numéricos , Educación del Paciente como Asunto , Corticoesteroides/uso terapéutico , Asma/terapia , Cuidadores , Niño , Chile/epidemiología , Estudios de Cohortes , Progresión de la Enfermedad , Educación Médica Continua , Femenino , Humanos , Masculino , Cooperación del Paciente , Estudios Prospectivos
5.
Vaccine ; 19(27): 3692-9, 2001 Jun 14.
Artículo en Inglés | MEDLINE | ID: mdl-11395203

RESUMEN

The nasal mucosa may provide a simple, non-invasive route to deliver DNA encoding genes that stimulate a specific immune response. Based on this, a new approach using pCMVbeta-gal plasmid DNA complexed to the Opc meningococcal outer membrane protein was assayed for. Optimal conditions of interaction were established between recombinant Opc protein and pCMVbeta-gal plasmid DNA. Complexes were fully characterized by electrophoresis analysis, DNAse resistance assay and transmission electron microscopy. DNA-protein complexes were also evaluated in in vitro transfection experiments. After the characterisation of complexes, Balb/c mice were intranasal (i.n.) and intramuscularly (i.m.) immunized. The humoral immune response against beta-galactosidase was measured by ELISA. The proliferative response in the spleen lymph nodes was also measured. Complexes administered by i.n. route induced both systemic and mucosal antibody responses. This behavior was not observed with the naked DNA. Finally, a lymphoproliferative response specific to beta-galactosidase induced by DNA-protein complexes was also detected.


Asunto(s)
Antígenos Bacterianos/inmunología , Proteínas de la Membrana Bacteriana Externa/inmunología , Plásmidos/inmunología , Vacunas de ADN/administración & dosificación , Vacunas de ADN/inmunología , Administración Intranasal , Animales , Antígenos Bacterianos/administración & dosificación , Antígenos Bacterianos/genética , Proteínas de la Membrana Bacteriana Externa/administración & dosificación , Proteínas de la Membrana Bacteriana Externa/genética , Células COS , Línea Celular , Esquemas de Inmunización , Ratones , Ratones Endogámicos BALB C , Plásmidos/administración & dosificación , Plásmidos/metabolismo , Plásmidos/ultraestructura , Transfección
6.
Biochem Biophys Res Commun ; 282(2): 442-6, 2001 Mar 30.
Artículo en Inglés | MEDLINE | ID: mdl-11401479

RESUMEN

The immune response against hepatitis B surface and core antigens was evaluated by either coinoculation or independent intramuscular administration of pAEC compact DNA immunization vectors carrying their genes. The pAEC vectors bear just the essential elements for mammalian expression and bacterial amplification. Balb/c mice were immunized with 100 microg of each construct, either alone or in combination. In spite of lacking known immunostimulatory sequences (e.g., AACGTT), significant cellular (proliferative) and humoral immune responses were raised against both antigens. Coadministration of both plasmids maintained the immune response against the two antigens, without interference between them. Modulation of the antigen expression and further immune response, by using the Kozak's translation initiation sequence, was also analyzed. No differences due to its presence or absence were observed.


Asunto(s)
Antígenos del Núcleo de la Hepatitis B/genética , Antígenos del Núcleo de la Hepatitis B/inmunología , Antígenos de Superficie de la Hepatitis B/genética , Antígenos de Superficie de la Hepatitis B/inmunología , Virus de la Hepatitis B/genética , Virus de la Hepatitis B/inmunología , Vacunas de ADN/genética , Vacunas de ADN/farmacología , Animales , Secuencia de Bases , Células COS , Femenino , Vectores Genéticos , Anticuerpos contra la Hepatitis B/biosíntesis , Inmunización , Activación de Linfocitos , Ratones , Ratones Endogámicos BALB C , Plásmidos/genética , Linfocitos T/inmunología , Transfección , Vacunas de ADN/inmunología
7.
Biochem Biophys Res Commun ; 279(2): 548-51, 2000 Dec 20.
Artículo en Inglés | MEDLINE | ID: mdl-11118323

RESUMEN

DNA immunization technology is based on the availability of adequate vectors for cloning and expression of heterologous immunoactive proteins in mammalian cells. We have developed a family of DNA plasmid vectors suitable to manipulate antigen expression and location. Their in vitro and in vivo functionality and application are also reported. The developed immune response, the aspects considered for vector design, and the possible independent manipulation of both blocks for the generation of bicistronic constructs, make of the pAEC family of plasmid vectors a source for DNA vaccine candidate's development for further evaluation in human clinical trials, and for potential use in the gene therapy approach.


Asunto(s)
Vectores Genéticos , Plásmidos , Vacunas de ADN , Animales , Anticuerpos Antivirales/sangre , Formación de Anticuerpos , Antígenos Virales/genética , Clonación Molecular , Citomegalovirus/genética , Ensayo de Inmunoadsorción Enzimática , Eritropoyetina/genética , Escherichia coli/genética , Femenino , Terapia Genética , Humanos , Ratones , Ratones Endogámicos BALB C , Regiones Promotoras Genéticas , Mapeo Restrictivo , Virus 40 de los Simios/genética
8.
Biochem Biophys Res Commun ; 273(2): 557-9, 2000 Jul 05.
Artículo en Inglés | MEDLINE | ID: mdl-10873644

RESUMEN

The HIV-1 gp120 gene with natural signal sequence expressed in eukaryotic expression systems showed extremely low levels of synthesis and secretion. Several expression systems have been used to improve the secretion levels of gp 120. In mammalian cells, the efficient expression of gp120 fused to t-PA signal peptide has been previously reported. Here, the effects of t-PA and EPO signal peptides were compared as secretion sequences for expression of gp120 in COS-7 cells. The EPO's signal peptide is used for the first time as leader sequence for secretion of foreign proteins. Our results indicated that higher amounts of secreted gp 120 were obtained when vectors containing EPO signal peptide were used.


Asunto(s)
Eritropoyetina/genética , Proteína gp120 de Envoltorio del VIH/genética , VIH-1/genética , Señales de Clasificación de Proteína/genética , Secuencia de Aminoácidos , Animales , Células COS , Eritropoyetina/biosíntesis , Expresión Génica , Vectores Genéticos , Proteína gp120 de Envoltorio del VIH/biosíntesis , VIH-1/metabolismo , Humanos , Datos de Secuencia Molecular , Señales de Clasificación de Proteína/biosíntesis , Proteínas Recombinantes de Fusión/biosíntesis , Proteínas Recombinantes de Fusión/genética , Activador de Tejido Plasminógeno/biosíntesis , Activador de Tejido Plasminógeno/genética , Transfección
10.
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