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1.
Neuroepidemiology ; 2024 Mar 12.
Artículo en Inglés | MEDLINE | ID: mdl-38471468

RESUMEN

Background The worldwide incidence of multiple sclerosis (MS) is estimated at 0.5-10 cases per 100,000 person-years and is probably increasing. In 2014, a previous study estimated the incidence of multiple sclerosis in Uruguay at 1.2 cases per 100.000 person-years. Objectives We conducted an observational, prospective, population-based study to determine MS incidence from diagnosis in Uruguay. Methods The population studied included people older than 18 years of age, who were living in Uruguay between July 1, 2019, and June 30, 2021. The diagnosis was based on 2017 McDonald criteria. Multiple data sources were employed including neurologists, magnetic resonance imaging centers, laboratories performing oligoclonal band testing, neurophysiology laboratories, neurorehabilitation centers, the institution Fondo Nacional de Recursos, and the MS Patients' Association of Uruguay (EMUR). The capture-recapture method was used to estimate incidence. Results 155 new MS cases were confirmed after review. The median age was 35 (range 18-62). Thirteen patients (8.38%) were diagnosed with late onset MS. The crude incidence rate was 2.89 cases per 100,000 person-years, 3.95 among female and 1.72 among male patients. The incidence rate estimated using the capture-recapture method was 3.18 (95% CI 3.02-3.34). Conclusions According to the Atlas of MS, Uruguay has a low incidence rate (2.0-3.99), even though it is one of the highest in Latin America. Our country aligns with the global trend of increasing incidence. Age and sex distribution were similar to other studies, with a high incidence of patients with late onset multiple sclerosis. The capture-recapture method confirms the exhaustivity of our investigation.

2.
J Neurol ; 2024 Feb 20.
Artículo en Inglés | MEDLINE | ID: mdl-38378908

RESUMEN

BACKGROUND: Most neurological diseases have no curative treatment; therefore, focusing on prevention is key. Continuous research to uncover the protective and risk factors associated with different neurological diseases is crucial to successfully inform prevention strategies. eHealth has been showing promising advantages in healthcare and public health and may therefore be relevant to facilitate epidemiological studies. OBJECTIVE: In this study, we performed a Delphi consensus exercise to identify the key screening tests to inform the development of a digital neurological examination tool for epidemiological research. METHODS: Twelve panellists (six experts in neurological examination, five experts in data collection-two were also experts in the neurological examination, and three experts in participant experience) of different nationalities joined the Delphi exercise. Experts in the neurological examination provided a selection of items that allow ruling out neurological impairment and can be performed by trained health workers. The items were then rated by them and other experts in terms of their feasibility and acceptability. RESULTS: Ten tests and seven anamnestic questions were included in the final set of screening items for the digital neurological examination. Three tests and five anamnestic questions were excluded from the final selection due to their low ratings on feasibility. CONCLUSION: This work identifies the key feasible and acceptable screening tests and anamnestic questions to build an electronic tool for performing the neurological examination, in the absence of a neurologist.

3.
Artículo en Inglés | MEDLINE | ID: mdl-37865869

RESUMEN

OBJECTIVE: The Latin American Epidemiologic study of ALS (LAENALS) aims to gather data on ALS epidemiology, phenotype, and risk factors in Cuba, Chile, and Uruguay, to understand the impact of genetic and environmental factors on ALS. METHODS: A harmonized data collection protocol was generated, and a Latin-American Spanish language Register was constructed. Patient data were collected in Uruguay in 2018, in Chile from 2017 to 2019, and in Cuba between 2017 and 2018. Statistical analysis was performed using SPSS 25.0.0 software. Crude cumulative incidence, standardized incidence, and prevalence were calculated in the population aged 15 years and older. RESULTS: During 2017-2019, 90 people with ALS from Uruguay (55.6% men), 219 from Chile (54.6% men), and 49 from Cuba (55.1% men) were included. The cumulative crude incidence in 2018 was 1.73/100,000 persons in Uruguay, 1.08 in Chile and 0.195 in Cuba. Crude prevalence in 2018 was 2.19 per 100,000 persons in Uruguay, 1.39 in Chile and 0.55 in Cuba. Mean age at onset was 61.8 ± 11.96 SD years in Uruguay, 61.9 ± 10.4 SD years in Chile, and 60.21 ± 12.45 SD years in Cuba (p = 0.75). Median survival from onset was 32.43 months (21.93 - 42.36) in Uruguay, 24 months (13.5 - 33.5) in Chile, and 29 months (15 - 42.5) in Cuba (p = 0.006). CONCLUSIONS: These preliminary data from LAENALS confirm the lower incidence and prevalence of ALS in counties with admixed populations. The LAENALS database is now open to other Latin American countries for harmonized prospective data collection.


Asunto(s)
Esclerosis Amiotrófica Lateral , Masculino , Humanos , Femenino , América Latina/epidemiología , Esclerosis Amiotrófica Lateral/diagnóstico , Esclerosis Amiotrófica Lateral/epidemiología , Cuba/epidemiología , Uruguay/epidemiología , Prevalencia
4.
Artículo en Inglés | MEDLINE | ID: mdl-35060421

RESUMEN

Background: There is evolving evidence of non-uniform distribution of ALS worldwide, with apparently lower incident and prevalent rates outside populations of European origin. However, the phenotype, survival and environmental risk in populations of mixed ancestral origin have not been well established. Large scale population based studies of incidence, prevalence, phenotype and risk factors in admixed populations are necessary to determine the true demography of ALS, and to test the hypothesis of differential risk and phenotype in populations of mixed ancestry. Methods: The Latin American Epidemiological Network of ALS (LAENALS) has been established to perform a comparative analysis of ALS epidemiology between three different Latin American populations (Cuba, Uruguay and Chile), and to test the hypothesis that the demographics, phenotype and outcome of ALS are influenced by ancestral origin, and that environmental and occupational risk factors differ across different ethnicities due to subtle differences in gene- environmental interactions. Recognition and interrogation of these differences is an important step toward novel therapeutic approaches and personalized medicine for all ALS both in the US, and worldwide. Discussion: This work will enable direct and detailed comparative studies between different ancestral populations with varying degrees of admixture, with facility for comparison with a large European reference dataset for ALS, and will provide a unique and rich dataset of admixed populations for later comparative genomic studies.


Asunto(s)
Esclerosis Amiotrófica Lateral , Esclerosis Amiotrófica Lateral/epidemiología , Esclerosis Amiotrófica Lateral/genética , Etnicidad , Hispánicos o Latinos , Humanos , América Latina/epidemiología , Grupos Raciales
5.
Rev. méd. Urug ; 35(2): 128-136, jun. 2019. tab, fig
Artículo en Español | LILACS | ID: biblio-999612

RESUMEN

Introducción: Uruguay no cuenta con estudios que reporten resultados de alcoholemias en traumatizados y menos aún su asociación con la severidad del trauma. Desde el año 2016 nuestro país cuenta con la llamada ley de tolerancia cero en base al supuesto de que la alcoholemia positiva representa un factor de riesgo para la severidad del trauma. Objetivos: describir el perfil epidemiológico de los traumatizados y estudiar la asociación existente entre el consumo de alcohol y la severidad del trauma. Material y método: estudio transversal; se incluyeron todos los pacientes que presentaron un evento traumático y fueron asistidos en el Departamento de Emergencia del Hospital de Clínicas durante el período 1 de marzo al 31 de agosto de 2017. Los datos se recopilaron prospectivamente y se extrajo muestra de alcoholemia a cada uno de los pacientes. Se consideraron diversas variables relacionadas con los pacientes y la severidad del traumatismo Se analizó la asociación entre las alcoholemias positivas y la severidad del trauma. Resultados: se incluyeron 121 pacientes, 28% presentaron alcoholemia positiva y 27% presentaron trauma severo. La alcoholemia positiva se asoció con la severidad del trauma (p < 0,0001). No se encontró asociación entre el nivel de alcoholemia y la severidad del trauma (p = 0,323). Conclusiones: el consumo de alcohol se asocia significativamente con la severidad del trauma. Nuestro estudio muestra que los traumatismos son severos solo por el hecho de presentar alcoholemias positivas independientemente de su nivel, apoyando la implementación de la ley de tolerancia cero.


Introduction: our country has not conducted studies to report results on blood alcohol levels in traumatized patients or on its association with the severity of the traumatic injury. Objective: to describe the epidemiological profile of trauma patients and to study the relationship between alcohol consumption and the severity of the traumatic injury. Method: transversal study including all patients who suffered a traumatic event and were assisted at the Emergency Department of the Clínicas Hospital between March 1, 2017 and August 31, 2017. Data was prospectively collected and a blood alcohol level sample was taken from each one of the patients. Several patient related variables were considered, as well as the severity of the traumatic injury. Results: 121 patients were included in the study, 28% showed positive blood alcohol levels and 27% presented severe traumatic injuries. Positive blood alcohol levels were associated to severity of the traumatic injury (p < 0.0001). No association was found between blood alcohol levels and the severity of the traumatic injury (p = 0.323). Conclusions: alcohol consumption is significantly associated to the severity of trauma. Our study shows that traumas are severe simply because blood alcohol levels are positive, regardless of the alcohol level, what supports the Zero Tolerance Law.


Introdução: no Uruguai não existem estudos que mostrem não somente os resultados de alcoolemia em traumatizados como também sua associação com a gravidade do trauma. Desde 2016 conta com a Lei de Tolerância 0 baseada no princípio de que a alcoolemia positiva é um fator de risco para a gravidade do trauma. Objetivos: descrever o perfil epidemiológico dos traumatizados e estudar a associação existente entre o consumo de álcool e a gravidade do trauma. Materiais e métodos: estudo transversal que incluiu todos os pacientes que apresentaram um evento traumático e foram atendidos no Departamento de Emergência do Hospital de Clínicas no período 1 de março - 31 de agosto de 2017. Os dados foram levantados prospectivamente e uma amostra de alcoolemia foi coletada a todos os pacientes. Foram incluídas variáveis relacionadas aos pacientes e à gravidade do traumatismo. A associação entre as alcoolemias positivas e a gravidade do trauma foi analisada. Resultados: foram incluídos 121 pacientes; 28% apresentaram alcoolemia positiva e 27% apresentaram trauma severo. As alcoolemias positivas estavam associadas com a gravidade do trauma (p < 0,0001). Os resultados não mostraram associação entre o nível de alcoolemia e a gravidade do trauma (p = 0,323). Conclusões: o consumo de álcool está significativamente associado com a gravidade do trauma. Nosso estudo mostra que os traumatismos são graves somente pela presença de alcoolemias positivas independentemente de seu nível o que respalda a implementação da Lei de Tolerância 0.


Asunto(s)
Humanos , Heridas y Lesiones/epidemiología , Trastornos Inducidos por Alcohol/complicaciones , Trastornos Inducidos por Alcohol/prevención & control , Accidentes de Tránsito/prevención & control , Prevención de Accidentes
6.
J Neurol Neurosurg Psychiatry ; 90(6): 659-665, 2019 06.
Artículo en Inglés | MEDLINE | ID: mdl-30846540

RESUMEN

OBJECTIVES: This study compares the clinical characteristics of patients with amyotrophic lateral sclerosis (ALS) within three clinic-based populations from Cuba, Uruguay and Ireland and determines the impact of known ALS-associated genetic variants on phenotypic manifestations within the Cuban population. METHODS: Demographic and clinical information was collected on 115 Cuban, 220 Uruguayan and 1038 Irish patients with ALS attending national specialist clinics through 1996-2017. All Cuban patients and 676 Irish patients underwent next-generation DNA sequencing and were screened for the pathogenic C9orf72 repeat expansion. RESULTS: The mean age of onset was younger in the Cuban (53.0 years, 95% CI 50.4 to 55.6) and Uruguayan (58.2 years, 95% CI 56.5 to 60.0) populations compared with the Irish population (61.6 years, 95% CI 60.9 to 62.4). No differences in survival between populations were observed. 1.7 % (95% CI 0.6 to 4.1) of Cubans with ALS carried the C9orf72 repeat expansion compared with 9.9% (95% CI 7.8 to 12.0) of Irish patients with ALS (p=0.004). Other known variants identified in the Cuban population included ANG (one patient), CHCHD10 (one patient) and DCTN1 (three patients). CONCLUSIONS AND RELEVANCE: This study is the first to describe the clinical characteristics of ALS in Cuban and Uruguayan populations and report differences between the Cuban and Irish genetic signature in terms of known ALS-associated genetic variants. These novel clinical and genetic data add to our understanding of ALS across different and understudied populations.


Asunto(s)
Esclerosis Amiotrófica Lateral/genética , Edad de Inicio , Esclerosis Amiotrófica Lateral/mortalidad , Esclerosis Amiotrófica Lateral/patología , Cuba , Femenino , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Irlanda , Estimación de Kaplan-Meier , Masculino , Persona de Mediana Edad , Análisis de Supervivencia , Uruguay , Secuenciación Completa del Genoma
7.
Endosc Int Open ; 6(6): E688-E693, 2018 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-29868633

RESUMEN

INTRODUCTION: Despite the widespread use of small-bowel capsule endoscopy (CE), there is still limited data on its utility and effectiveness for the diagnosis and management of patients with iron-deficiency anemia (IDA). AIM: To assess the diagnostic yield of CE and the factors predicting positive findings in patients with IDA. METHODS: Patients with unexplained IDA and negative upper and lower endoscopy were included. A positive diagnostic yield was considered when CE diagnosed one or more lesions that could explain the IDA. Sex, age, NSAID consumption, blood transfusion requirement, and ferritin and hemoglobin levels were recorded. RESULTS: In total, 120 CE were included (mean age 58.5 years; F/M 82:38). Mean hemoglobin levels were 9 g/dL and mean ferritin levels were 15.7 ng/mL. Positive findings were present in 50 % of patients. The most frequent was angiodysplasia (45 %). Despite several baseline variables being significantly associated with positive findings, using a logistic regression model, it was verified that male sex (OR 3.93; 95 %CI 1.57 - 9.86), age (OR 1.03; 95 %CI 1.00 - 1.06), and hemoglobin levels (OR 0.73; 95 %CI 0.57 - 0.94) were the variables having an independent effect on the probability of obtaining positive findings. Age older than 50 years (OR 14.05; 95 %CI 1.69 - 116.23) and male sex (OR 3.63; 95 %CI 1.29 - 10.17) were the variables which increased the risk of diagnosing angiodysplasia. CONCLUSIONS: CE is a useful technique in patients with IDA. To improve its yield, it is necessary to select patients carefully. Male sex, older age, and low hemoglobin levels were associated with a risk of positive finding in this group of patients. The risk of diagnosing angiodysplasia increased with male sex and older age.

8.
Rev. méd. Urug ; 30(1): 37-48, mar. 2014.
Artículo en Español | LILACS | ID: lil-737569

RESUMEN

Introducción: el ataque cerebrovascular (ACV) constituye un problema de salud en Uruguay y en el mundo. Se ha comprobado que la trombolisis intravenosa disminuye la morbimortalidad y las secuelas en los pacientes con ACV isquémicos agudos (nivel de evidencia IA). Objetivos: analizar los casos de ACV isquémico trombolizados en el Hospital de Clínicas y valorar la utilidad de un score de predicción de sangrado intracraneano sintomático en esta población. Material y método: estudio descriptivo, observacional y prospectivo. Población: pacientes trombolizados en el Hospital de Clínicas en el período 2010-2013. Se aplicó score predictivo de hemorragia sintomática a toda la población de trombolizados. Tests estadísticos: test de chi cuadrado, test de student, test de Wilcoxon, se consideraron diferencias estadísticamente significativas aquellas con una p < 0,05. Resultados: treinta y cuatro pacientes trombolizados, promedio de edad 67 años, mayoría mujeres, alto porcentaje de ACV graves, National Institute of Health Stroke Scale (NIHSS) promedio al ingreso: 11, con mejoría estadísticamente significativa al alta. Etiología principal: cardioembolia. Tiempo síntoma aguja promedio: 170 minutos. Hemorragia intracraneana: ocho pacientes (23,5%), fallecieron cuatro de ellos. El puntaje del score de sangrado no predijo el sangrado intracraneano. Conclusiones: en el Hospital de Clínicas, desde la inauguración de la Unidad de ACV, el porcentaje de infartos cerebrales trombolizados ha ido en aumento, siendo actualmente comparable a cifras internacionales. El tiempo síntoma-aguja es menor que en otros estudios. La trombolisis generó un beneficio estadísticamente significativo en la escala de NIHSS. El porcentaje de sangrados fue similar al descrito en la literatura...


Asunto(s)
Accidente Cerebrovascular/terapia , Terapia Trombolítica
9.
Rev. méd. Urug ; 28(1): 35-42, mar. 2012. ilus, graf
Artículo en Español | LILACS | ID: lil-620452

RESUMEN

Introducción: las enfermedades priónicas son enfermedades de carácter degenerativo del sistema nervioso central de curso progresivo y desenlace fatal que presentan largos períodos deincubación antes de manifestarse clínicamente siendo hoy de gran interés científico dado que responden a un modelo autorreplicante proteico sin intervención de ácidos nucleicos. Asimismo tienen un carácter simultáneo de aparición esporádico, hereditario e infectante. La aparición de la encefalopatía bovina espongiforme y su consecuencia en el ser humano, la variante de la enfermedad de Creutzfeldt-Jacob, subrayan la necesidadde un control epidemiológico estricto en la materia.Objetivo: describir la realidad de estas enfermedades en Uruguay en el período que media entre 1984 y 2009 inclusive.Material y método: se realizó una revisión descriptiva y retrospectivade casos clínicos de enfermedades priónicas diagnosticadas en nuestro país.Resultados: se lograron identificar 42 casos de enfermedad de Creutzfeldt-Jakob en Uruguay (8 formas hereditarias y 34 formas esporádicas). La tasa de incidencia estimada globalfue de 0,7 casos por millón de habitantes por año, considerandolas formas probables y definitivas.Conclusiones: en este trabajo se han detectado exclusivamente casos esporádicos y familiares de Creutzfeldt-Jacob, no se han detectado casos vinculados a la variante relacionadacon la encefalopatía espongiforme bovina, ni a otros tipos de enfermedades priónicas que afectan a los seres humanos. Dadas las características de la enfermedad y la distribución de neurólogos en todo el país, es posible realizar un relevamiento y una vigilancia epidemiológica bastante estricta deestas enfermedades en nuestro medio.


Introduction: prion diseases are progressive neurodegenerativedisorders that may result in death and are distinguished by long incubation periods before presenting a clinical manifestation. Today they are scientifically interesting since they follow a protein auto-replicant modelwithout the participation of nucleic acids.These diseases appear sporadically, they are hereditary and infectious as well. The appearance of bovinespongiform encephalopathy and its consequences on human beings and Creutzfeldt-Jacob disease variationsreinforce the need for a strict epidemiological control in the field.Objective: to describe the reality of these diseases in Uruguay from 1984 through 2009.Method: we conducted a retrospective, descriptive review of clinical cases of prion diseases diagnosed in our country.Results: we managed to identify 43 cases of Creutzfeldt-Jacob disease in Uruguay (8 hereditary forms and34 sporadic forms). Global incidence estimated rate was 0.7 cases per million inhabitants, considering both probableand definitive forms.Conclusions: we have exclusively identified sporadic and hereditary cases of Creutzfeldt-Jacob disease, we have not identified variations in connection with bovine spongiform encephalopathy or other kinds of prion diseases affecting human beings. Given the characteristics of the disease and the distribution of neurologists in the country enable a rather strict survey and epidemiological surveillance of thesediseases in our country.


Introdução: as doenças priônicas são enfermidades de caráter degenerativo do sistema nervoso central decurso progressivo y desenlace fatal que apresentam longos períodos de incubação antes de manifestar-seclinicamente sendo hoje de grande interesse científico, pois respondem a um modelo autorreplicante proteicosem intervenção de ácidos nucleicos. Têm ademais um caráter simultâneo de aparição esporádica, hereditária e infectante. O aparecimento da encefalopatia bovina espongiforme, a variante da doença de Creutzfeldt-Jacob e suas consequências nos seres humanos, destacam a necessidade de um controle epidemiológico estrito.Objetivo: descrever a realidade destas doenças no Uruguai no período 1984-2009 inclusive.Material e método: realizou-se uma revisão descritiva y retrospectiva de casos clínicos das doenças priônicasdiagnosticadas no nosso pais.Resultados: identificaram-se 42 casos de doença de Creutzfeldt-Jakob no Uruguai (8 formas hereditárias e34 formas esporádicas).Ataxa de incidência global estimada foi de 0,7 casos por milhão de habitantes por ano,considerando as formas prováveis e definitivas.Conclusões: neste trabalho detectaram-se exclusivamente os casos esporádicos e familiares de Creutzfeldt-Jacob; não se identificaram casos vinculados à variante relacionada com a encefalopatia espongiforme bovina, nem a outros tipos de doenças priônicas que afetam a los seres humanos.Considerando as características desta patologia e a distribuição de neurologistas no país, é possível realizarum relevamento e uma vigilância epidemiológica bastante estrita de estas doenças no nosso meio.


Asunto(s)
Enfermedades por Prión , Síndrome de Creutzfeldt-Jakob , Uruguay
10.
Clín. investig. arterioscler. (Ed. impr.) ; 22(2): 59-69, mar.-abr. 2010. ilus, tab
Artículo en Español | IBECS | ID: ibc-87694

RESUMEN

Introducción El Fondo Nacional de Recursos financia los procedimientos de revascularización miocárdica en Uruguay. Las evaluaciones posteriores a la revascularización mostraron un inadecuado control de los factores de riesgo. Objetivos Describir el control de los factores de riesgo y el uso de fármacos cardioprotectores en los pacientes ingresados en un programa de prevención secundaria así como analizar el impacto de dicho programa en la mortalidad y en la realización de nuevos procedimientos cardiológicos invasivos. Metodología Se estudió una cohorte de pacientes del programa y se comparó la mortalidad y la realización de nuevos procedimientos a los 28 meses con una cohorte histórica de control. Resultados Ingresaron al programa 900 pacientes; en 487 se analizó el alcance de los objetivos terapéuticos a los 6 y 12 meses. Al año se alcanzó el objetivo en el 40,5% para presión arterial (<130/80mmHg), en el 73,2% para cLDL (<100mg/dl) y en el 63,8% para triglicéridos (<150mg/dl), y la prescripción de estatinas, ácido acetilsalicílico, betabloqueantes e inhibidores de la enzima convertidora de la angiotensina fue del 98,2, el 94,5, el 85,2 y el 84,6%, respectivamente. Logró abstinencia mantenida el 60,8% de los fumadores, y el 99% no tuvo recaídas. Al año, el 14,9% bajó de peso más del 5%, y el 49% adhirió al ejercicio físico regular. A los seis meses, el 56,3% de los diabéticos tuvo glucemia preprandial inferior a 130mg/dl. La mortalidad a los 28 meses fue del 1,85 y el 6,2% para el grupo en el programa y el grupo control, respectivamente. La participación en el programa (HR=0,28, p=0,01) y el sexo femenino (HR=0,07, p=0,01) fueron factores protectores para la mortalidad. Conclusiones La implementación del programa mejoró el control de los factores de riesgo, optimizó el uso de fármacos cardioprotectores y probablemente contribuyó a una disminución de la mortalidad (AU)


Introduction Revascularization procedures in Uruguay are financed by the National Resources Fund. Evaluations after revascularization have shown inadequate control of cardiovascular risk factors. Aim To describe control of risk factors and prescription of cardioprotective drugs in patients included in a secondary prevention program and to analyze the impact of the program on mortality and the incidence of new invasive cardiologic procedures. Methodology A cohort of patients admitted to the program was studied and mortality and new cardiologic procedures at 28 weeks were compared with those in a historical control group. Results The program admitted 900 patients. Attainment of therapeutic goals at 6 and 12 months was analyzed in 487 patients. At 1 year, targets were achieved for blood pressure (<130/80mmHg) in 40.5%, low-density lipoprotein-cholesterol (<100mg/dl) in 73.2% and triglycerides (<150mg/dl) in 63.8%; prescription of statins, salicylic acetyl acid, â-blockers and angiotensin-converting enzyme inhibitors was 98.2%, 94.5%, 85.2% and 84.6%, respectively. Among smokers, 60.8% maintained abstinence and 99% did not relapse. At 1 year, 14.9% had a weight loss of at least 5% and 49% performed physical activity regularly. At 6 months, 56.3% of diabetics had preprandial glycemia levels of <130mg/dl. Cumulative mortality at 28 months was 1.85% for the group in the program and was 6.2% for the control group; protective factors against mortality were participation in the program (HR=0.28; p=0.01) and female gender (HR=0.07; p=0.01).Conclusions The implementation of this program improved control of risk factors, optimized pharmacological treatment and probably contributed to a decrease in mortality (AU)


Asunto(s)
Humanos , Enfermedad Coronaria/epidemiología , Enfermedades Cardiovasculares/epidemiología , Enfermedad de la Arteria Coronaria/epidemiología , Factores de Riesgo , Evaluación de Procesos y Resultados en Atención de Salud , Revascularización Miocárdica , Mortalidad
11.
Amyotroph Lateral Scler ; 10(5-6): 355-60, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19922124

RESUMEN

Our objective was to compare clinical features and survival in two groups of ALS patients from countries in opposite hemispheres. The study took place at an ALS referral centre in the Limousin region of France (LIM) and in Uruguay (UY). All consecutive patients diagnosed with ALS between 1 January 2002 and 31 December 2004 were enrolled. Data from a total of 187 ALS patients were analysed: 84 from LIM and 103 from UY. Mean ages at onset and diagnosis were significantly higher in LIM (66 vs. 61 years). UY patients demonstrated more advanced disease at the time of diagnosis. The proportions of definite forms were 82% in UY versus 10% in LIM (p<0.001), and median manual muscle testing (MMT) and ALSFRS scores were significantly lower in LIM. This observed difference was not directly explained by a longer diagnostic delay in UY (10 vs. 9 months). Median survival from time of diagnosis was significantly shorter in UY patients (19 vs. 28 months; log-rank test, p=0.030). In conclusion, survival of ALS patients in UY is nine months shorter than in LIM, probably due to the heterogeneity of medical care and the absence of an ALS referral centre.


Asunto(s)
Esclerosis Amiotrófica Lateral/diagnóstico , Grupos de Población , Edad de Inicio , Anciano , Esclerosis Amiotrófica Lateral/mortalidad , Esclerosis Amiotrófica Lateral/fisiopatología , Femenino , Francia , Humanos , Masculino , Persona de Mediana Edad , Pronóstico , Modelos de Riesgos Proporcionales , Estudios Prospectivos , Derivación y Consulta , Tasa de Supervivencia , Uruguay
12.
Int Psychogeriatr ; 21(4): 622-30, 2009 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-19505354

RESUMEN

BACKGROUND: Dementia is becoming a major public health problem in Latin America (LA), yet epidemiological information on dementia remains scarce in this region. This study analyzes data from epidemiological studies on the prevalence of dementia in LA and compares the prevalence of dementia and its causes across countries in LA and attempts to clarify differences from those of developed regions of the world. METHODS: A database search for population studies on rates of dementia in LA was performed. Abstracts were also included in the search. Authors of the publications were invited to participate in this collaborative study by sharing missing or more recent data analysis with the group. RESULTS: Eight studies from six countries were included. The global prevalence of dementia in the elderly (> or =65 years) was 7.1% (95% CI: 6.8-7.4), mirroring the rates of developed countries. However, prevalence in relatively young subjects (65-69 years) was higher in LA studies The rate of illiteracy among the elderly was 9.3% and the prevalence of dementia in illiterates was two times higher than in literates. Alzheimer's disease was the most common cause of dementia. CONCLUSIONS: Compared with studies from developed countries, the global prevalence of dementia in LA proved similar, although a higher prevalence of dementia in relatively young subjects was evidenced, which may be related to the association between low educational level and lower cognitive reserve, causing earlier emergence of clinical signs of dementia in the LA elderly population.


Asunto(s)
Enfermedad de Alzheimer/epidemiología , Comparación Transcultural , Demencia Vascular/epidemiología , Países en Desarrollo , Factores de Edad , Anciano , Anciano de 80 o más Años , Estudios de Cohortes , Estudios Transversales , Escolaridad , Femenino , Humanos , América Latina , Masculino
13.
Amyotroph Lateral Scler ; 8(4): 224-9, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17653920

RESUMEN

Although several prognostic factors have been identified in ALS, there remains some discordance concerning the prognostic significance of the age and clinical form at onset. In order to clarify these findings, we have analysed already known prognostic factors using a multi-state model. Two hundred and twenty-two sporadic ALS patients were followed. A simple unidirectional three-states model was used to summarize clinical course of ALS. States 1 and 2 reflected the progression of neurological impairment and state 3 represented the end of follow-up (tracheotomy or death). Gender, diagnostic delay, body mass index (BMI) and slow vital capacity (SVC) were also recorded. A time-inhomogeneous Markov model with piecewise constant transition intensities was used to estimate the effect of the covariates in each transition. The bulbar form at onset was only correlated with a more rapid clinical progression between state 1 and state 2. In contrast, an advanced age at diagnosis affected only survival from state 2. This methodological approach suggests that these two factors have a different prognostic significance: age at onset is related to patient's survival and the clinical form at onset predicts the progression of motoneuronal impairment in different regions.


Asunto(s)
Esclerosis Amiotrófica Lateral/epidemiología , Esclerosis Amiotrófica Lateral/mortalidad , Cadenas de Markov , Evaluación de Resultado en la Atención de Salud/métodos , Edad de Inicio , Anciano , Esclerosis Amiotrófica Lateral/diagnóstico , Esclerosis Amiotrófica Lateral/fisiopatología , Análisis de Varianza , Índice de Masa Corporal , Estudios de Cohortes , Progresión de la Enfermedad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Respiración , Estudios Retrospectivos
14.
J Stroke Cerebrovasc Dis ; 11(1): 15-22, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-17903850

RESUMEN

The purpose of this trial was to identify clinical factors and evaluation studies with significant value as mortality predictors in patients suffering an acute stroke. One hundred forty-eight consecutive patients hospitalized at the Hospital de Clínicas, Montevideo, with a clinical diagnosis of stroke were studied: 85 had ischemic strokes and 63 presented with intracerebral hemorrhages. The potentially predictive variables (past medical history, clinical assessment, neuroimaging, biochemical analysis) were evaluated within the first 24 hours of admission; patient follow-up was performed until they left the hospital or died. The modified National Institutes of Health Stoke Scale (NIHSS) was used to assess neurologic impairment. Three variables were identified as early mortality predictors in this population: (1) Glasgow Coma Scale score < or = 11 on admission (R = 0.19); (2) severe mass effect, defined as the presence of ventricular shift across the midline and/or enlargement of contralateral ventricle in early computed tomography (CT) scan (R = 0.26); and (3) modified NIHSS quotient score > or = 0.26 on admission (R = 0.27). We conclude that modified NIHSS was the most consistent instrument for an early identification of patients at high mortality risk, even before confirmatory evidence of the stroke's nature was obtained. A cutoff of 0.26 on NIHSS quotient score on admission was identified as the most significant predictive value.

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