Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Int J Tuberc Lung Dis ; 28(3): 148-153, 2024 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-38454179

RESUMEN

OBJECTIVESDelayed detection in TB due to structural and diagnostic shortcomings is pivotal for disease transmission, morbidity and mortality. We investigated whether an inclusive screening, followed by a structured clinical follow-up (FU) could improve case-finding.METHODSPatients were recruited from health centres in Bissau, Guinea-Bissau, and Gondar, Ethiopia. A routine FU was done at Week 2. If persisting symptoms were found, patients were investigated using chest X-ray (CXR) and Xpert® MTB/RIF, followed by a medical consultation. The main outcome were additional TB patients diagnosed by applying the FU strategy.RESULTSOf 3,571 adults, 3,285 (95%) were examined at Week 2 FU, where 2,491 (72%) were asymptomatic. Screening patients presenting with cough >2 weeks alone contributed to the diagnosis of 93 patients (45% of all patients diagnosed here), whereas a TBscore >3 increased this by 18 (9%); adding a Week 2 FU yielded an additional 94 (46%) patients. Among the 794 (24%) with persisting symptoms, 25 were diagnosed using Xpert and 69 at clinical FU, which constituted 46% (94/205) of the total TB patients diagnosed.CONCLUSIONA Week 2 FU visit, which can be nested into routine healthcare, increased the diagnosis of TB patients by two-fold and avoids diagnostic gaps in the cascade-of-care..


Asunto(s)
Mycobacterium tuberculosis , Tuberculosis , Adulto , Humanos , Tuberculosis/diagnóstico , Tuberculosis/prevención & control , Estudios de Seguimiento , Atención a la Salud , Tos , Etiopía
2.
Int J Tuberc Lung Dis ; 23(11): 1155-1161, 2019 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-31718751

RESUMEN

OBJECTIVE: To investigate how levels of the soluble urokinase plasminogen activator receptor (suPAR) and erythrocyte sedimentation rate (ESR) correlate with disease activity and prognosis in pulmonary tuberculosis (PTB).DESIGN: This was a retrospective analysis of patients with active PTB (n = 500) in Gondar, Ethiopia, for whom the suPAR (n = 301) and ESR (n = 330) were analysed at the start of treatment. Both biomarkers were available for 176 patients. Human immunodeficiency virus (HIV) status, chest X-ray (CXR) findings, classification according to the clinical TBscore and treatment outcome were all recorded.RESULTS: In a multivariable logistic regression analysis adjusted for age, sex and HIV status, surrogate markers of disease activity such as advanced CXR patterns correlated with increased levels of suPAR (adjusted OR [aOR] 8.24, P < 0.001) and of ESR (aOR 1.63, P = 0.030), whereas ESR only correlated significantly with a TBscore >6 points. Increased levels of both suPAR and ESR were associated with unsuccessful treatment outcomes (aOR 2.93, P = 0.013; aOR 2.52, P = 0.025). The highest quartile of suPAR (aOR 13.3, P = 0.029) but not ESR levels correlated independently with increased mortality.CONCLUSION: SuPAR and ESR levels correlate with disease activity in PTB; however, the clinical role of these potentially prognostic biomarkers needs to be verified in prospective studies.


Asunto(s)
Sedimentación Sanguínea , Receptores del Activador de Plasminógeno Tipo Uroquinasa/sangre , Tuberculosis Pulmonar/diagnóstico , Tuberculosis Pulmonar/mortalidad , Adolescente , Adulto , Antituberculosos/uso terapéutico , Biomarcadores/sangre , Etiopía/epidemiología , Femenino , Infecciones por VIH/sangre , Infecciones por VIH/diagnóstico , Humanos , Modelos Logísticos , Masculino , Análisis Multivariante , Pronóstico , Radiografía Torácica , Estudios Retrospectivos , Índice de Severidad de la Enfermedad , Tuberculosis Pulmonar/sangre , Tuberculosis Pulmonar/tratamiento farmacológico , Adulto Joven
3.
Int J Tuberc Lung Dis ; 20(2): 218-22, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-26792474

RESUMEN

BACKGROUND: The incidence of tuberculosis (TB) in sub-Saharan Africa is one of the highest in the world. OBJECTIVE: To evaluate the prevalence of TB, the annual risk of tuberculous infection (ARTI) and associated risk factors in rural Ethiopia. METHODS: A tuberculin skin test was performed among 2743 individuals in a rural community of Ethiopia around Ginci town, west of Addis Ababa, to estimate the prevalence of tuberculin reactivity and to assess factors associated with tuberculous infection. RESULTS: Among 2743 volunteer participants, test results were available for 2640, 691 (26.2%) of whom had an identifiable bacille Calmette-Guérin (BCG) scar; 221 (8.3%) reported household contact with a known TB case. The overall prevalence of TST reactions of ⩾ 10 mm was 29.7%. The ARTI was estimated at 1.7%. Tuberculin reactivity varied with age, sex, income and history of household contact with a TB case. Presence of BCG scar was not related to tuberculin reactivity. CONCLUSIONS: Our findings indicate that despite an effective TB control programme, TB transmission rates are still high in rural Ethiopia. Provision of isoniazid prophylaxis in close contacts of active TB cases among the poorest population groups may reduce TB incidence.


Asunto(s)
Salud Rural , Tuberculosis/epidemiología , Adolescente , Adulto , Factores de Edad , Antituberculosos/uso terapéutico , Etiopía/epidemiología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Prevalencia , Medición de Riesgo , Factores de Riesgo , Factores Socioeconómicos , Factores de Tiempo , Prueba de Tuberculina , Tuberculosis/diagnóstico , Tuberculosis/microbiología , Tuberculosis/prevención & control , Tuberculosis/transmisión , Adulto Joven
4.
Int J Parasitol ; 45(2-3): 133-40, 2015 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-25486494

RESUMEN

Despite several review papers and experimental studies concerning the impact of chronic helminth infection on tuberculosis in recent years, there is a scarcity of data from clinical field studies in highly endemic areas for these diseases. We believe this is the first randomised clinical trial investigating the impact of albendazole treatment on the clinical and immunological outcomes of helminth co-infected tuberculosis patients. A randomised, double-blind, placebo-controlled trial of albendazole (400mg per day for 3 days) in helminth-positive tuberculosis patients was conducted in Gondar, Ethiopia. The primary outcome was clinical improvement (ΔTB score) after 2 months. Among secondary outcomes were changes in the levels of eosinophils, CD4+ T cells, regulatory T cells, IFN-γ, IL-5 and IL-10 after 3 months. A total of 140 helminth co-infected tuberculosis patients were included with an HIV co-infection rate of 22.8%. There was no significant effect on the primary outcome (ΔTB score: 5.6±2.9 for albendazole versus 5.9±2.5 for placebo, P=0.59). The albendazole-treated group showed a decline in eosinophil cells (P=0.001) and IL-10 (P=0.017) after 3 months. In an exploratory analysis after 12 weeks, the albendazole treated group showed a trend towards weight gain compared with the placebo group (11.2±8.5 kg versus 8.2±8.7 kg, P=0.08)). The reductions in eosinophil counts and IL-10 show that asymptomatic helminth infection significantly affects host immunity during tuberculosis and can be effectively reversed by albendazole treatment. The clinical effects of helminth infection on chronic infectious diseases such as tuberculosis merit further characterisation.


Asunto(s)
Albendazol/uso terapéutico , Antihelmínticos/uso terapéutico , Helmintiasis/tratamiento farmacológico , Tuberculosis/complicaciones , Adolescente , Adulto , Peso Corporal , Linfocitos T CD4-Positivos/inmunología , Citocinas/sangre , Método Doble Ciego , Eosinófilos/inmunología , Etiopía , Femenino , Humanos , Masculino , Persona de Mediana Edad , Placebos/administración & dosificación , Linfocitos T Reguladores/inmunología , Resultado del Tratamiento , Adulto Joven
5.
Tuberculosis (Edinb) ; 91(5): 370-7, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21813328

RESUMEN

In tuberculosis (TB), the production of nitric oxide (NO) is confirmed but its importance in host defense is debated. Our aim was to investigate whether a food supplement rich in arginine could enhance clinical improvement in TB patients by increased NO production. Smear positive TB patients from Gondar, Ethiopia (n = 180) were randomized to a food supplementation rich in arginine (peanuts, equivalent to 1 g of arginine/day) or with a low arginine content (wheat crackers, locally called daboqolo) during four weeks. The primary outcome was cure rate according to the WHO classification and secondary outcomes were sputum smear conversion, weight gain, sedimentation rate, reduction of cough and chest X-ray improvement as well as levels of NO in urine (uNO) or exhaled air (eNO) at two months. There was no effect of the intervention on the primary outcome (OR 1.44, 95% CI: 0.69-3.0, p = 0.39) or secondary outcomes. In the subgroup analysis according to HIV status, peanut supplemented HIV+/TB patients showed increased cure rate (83.8% (31/37) vs 53.1% (17/32), p < 0.01). A low baseline eNO (<10 ppb) in HIV+/TB patients was associated with a decreased cure rate. We conclude that nutritional supplementation with a food supplement rich in arginine did not have any overall clinical effect. In the subgroup of HIV positive TB patients, it significantly increased the cure rate and as an additional finding in this subgroup, low initial levels of NO in exhaled air were associated with a poor clinical outcome but this needs to be confirmed in further studies.


Asunto(s)
Antituberculosos , Arginina , Suplementos Dietéticos , Infecciones por VIH/inmunología , Desnutrición/inmunología , Esputo , Tuberculosis Pulmonar/inmunología , Adulto , Antituberculosos/uso terapéutico , Arginina/farmacología , Quimioterapia Adyuvante , Etiopía/epidemiología , Femenino , Infecciones por VIH/complicaciones , Infecciones por VIH/terapia , Humanos , Masculino , Desnutrición/dietoterapia , Óxido Nítrico , Radiografía Torácica , Resultado del Tratamiento , Tuberculosis Pulmonar/complicaciones , Tuberculosis Pulmonar/terapia
6.
Dis Esophagus ; 24(6): 423-9, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21309918

RESUMEN

The necessity of pyloroplasty after esophagectomy and gastric pull-up is debated. Disadvantages of a standard pyloroplasty include the potential for leak, shortening of the length of the graft, and complexity when done during a minimally invasive procedure. The aim of this study is to report our experience with a novel internal pyloroplasty technique using a circular stapler (CS pyloroplasty), which is applicable for both laparoscopic and open esophagectomy. The records of all patients who underwent an esophagectomy with gastric pull-up and pyloroplasty between 2002 and 2007 were reviewed. The CS pyloroplasty was performed through a lesser curve gastrotomy with a 21-mm CS, while the standard pyloroplasty entailed a longitudinal full thickness incision through the pylorus with mucosal closure in the same direction and a Graham patch. A CS pyloroplasty was performed in 144 and a standard pyloroplasty in 133 patients. The median patient age was 66years, and the median follow-up was 17months, and was similar for both types of pyloroplasty. Routine postoperative videoesophagram was significantly more likely to show a delay in contrast transit through the pylorus after standard pyloroplasty (16% standard vs. 8% CS pyloroplasty, P= 0.03). Significantly more patients had postoperative endoscopy after standard pyloroplasty (40% standard vs. 24% CS pyloroplasty, P= 0.004), but the frequency of pyloric dilatation was similar. There were no leaks with either technique. A circular stapled pyloroplasty is as efficacious as a standard pyloroplasty after esophagectomy with gastric pull-up. Potential advantages include the ease and simplicity of the procedure along with virtually no risk of a leak and no graft shortening. The technique is amenable to both open and minimally invasive procedures.


Asunto(s)
Neoplasias Esofágicas/cirugía , Píloro/cirugía , Técnicas de Sutura , Anciano , Trastornos de Deglución/etiología , Esofagectomía/efectos adversos , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Estómago/trasplante , Técnicas de Sutura/efectos adversos , Técnicas de Sutura/instrumentación
8.
J Gastrointest Surg ; 13(8): 1422-9, 2009 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-19421822

RESUMEN

INTRODUCTION: Identifying gastroesophageal reflux disease as the cause of respiratory and laryngeal complaints is difficult and depends largely on the measurements of increased acid exposure in the upper esophagus or ideally the pharynx. The current method of measuring pharyngeal pH environment is inaccurate and problematic due to artifacts. A newly designed pharyngeal pH probe to avoid these artifacts has been introduced. The aim of this study was to use this probe to measure the pharyngeal pH environment in normal subjects and establish pH thresholds to identify abnormality. METHODS: Asymptomatic volunteers were studied to define the normal pharyngeal pH environment. All subjects underwent esophagram, esophageal manometry, upper and lower esophageal pH monitoring with a dual-channel pH catheter and pharyngeal pH monitoring with the new probe. Analyses were performed at 0.5 pH intervals between pH 4 and 6.5 to identify the best discriminating pH threshold and calculate a composite pH score to identify an abnormal pH environment. RESULTS: The study population consisted of 55 normal subjects. The pattern of pharyngeal pH environment was significantly different in the upright and supine periods and required different thresholds. The calculated discriminatory pH threshold was 5.5 for upright and 5.0 for supine periods. The 95th percentile values for the composite score were 9.4 for upright and 6.8 for supine. CONCLUSION: A new pharyngeal pH probe which detects aerosolized and liquid acid overcomes the artifacts that occur in measuring pharyngeal pH with existing catheters. Discriminating pH thresholds were selected and normal values defined to identify patients with an abnormal pharyngeal pH environment.


Asunto(s)
Cateterismo/instrumentación , Monitorización del pH Esofágico/instrumentación , Esófago/metabolismo , Reflujo Gastroesofágico/diagnóstico , Laringe/metabolismo , Adolescente , Adulto , Anciano , Diseño de Equipo , Reflujo Gastroesofágico/metabolismo , Humanos , Concentración de Iones de Hidrógeno , Manometría , Persona de Mediana Edad , Postura/fisiología , Presión , Valores de Referencia , Reproducibilidad de los Resultados , Adulto Joven
9.
Drugs Exp Clin Res ; 30(4): 133-41, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15553659

RESUMEN

The medical and social impact of cough is substantial. Current antitussive agents at effective doses have adverse events such as drowsiness, nausea and constipation that limit their use. There is also recent evidence that standard antitussive agents, such as codeine, may not reduce cough during upper respiratory infections. Therefore, there is a need for more effective and better-tolerated agents. The efficacy of levocloperastine, a novel antitussive, which acts both centrally on the cough center and on peripheral receptors in the tracheobronchial tree in treating chronic cough, was compared with that of other standard antitussive agents (codeine, levodropropizine and DL-cloperastine) in six open clinical trials. The studies enrolled patients of all ages with cough associated with various respiratory disorders including bronchitis, asthma, pneumonia and chronic obstructive pulmonary disease. Levocloperastine significantly improved cough symptoms (intensity and frequency of cough) in all trials, and improvements were observed after the first day of treatment. In children, levocloperastine reduced nighttime awakenings and irritability, and in adults it was effective in treating cough induced by angiotensin-converting enzyme inhibitors. When compared with other antitussive agents, levocloperastine had improved or comparable efficacy, with a more rapid onset of action. Importantly, no evidence of central adverse events was recorded with levocloperastine, whereas drowsiness was reported by a significant number of patients receiving codeine. Levocloperastine is an effective antitussive agent for the treatment of cough in patients of all ages. It has a more rapid onset of action than standard agents with an improved tolerability profile.


Asunto(s)
Antitusígenos/uso terapéutico , Tos/tratamiento farmacológico , Piperidinas/uso terapéutico , Adolescente , Adulto , Anciano , Antitusígenos/clasificación , Antitusígenos/farmacología , Bronquitis/complicaciones , Bronquitis/diagnóstico , Bronquitis/tratamiento farmacológico , Enfermedad Crónica , Ensayos Clínicos como Asunto , Codeína/farmacología , Codeína/uso terapéutico , Tos/etiología , Femenino , Humanos , Enfermedades Pulmonares/clasificación , Enfermedades Pulmonares/complicaciones , Enfermedades Pulmonares/diagnóstico , Enfermedades Pulmonares/tratamiento farmacológico , Masculino , Persona de Mediana Edad , Selección de Paciente , Piperidinas/química , Piperidinas/farmacología , Glicoles de Propileno/farmacología , Glicoles de Propileno/uso terapéutico , Estereoisomerismo , Resultado del Tratamiento
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...