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1.
Rev. parag. reumatol ; 9(2)dic. 2023.
Artigo em Espanhol | LILACS-Express | LILACS | ID: biblio-1536680

RESUMO

Introducción. Las formas clínicas de presentación del lupus eritematoso sistémico (LES) son variadas, así como las recaídas que ocurren en el curso de la enfermedad. Objetivo. Describir las formas de presentación del debut y las recaídas de pacientes con LES. Metodología. Estudio observacional, descriptivo, de corte transversal, de pacientes con LES, que acudieron al Hospital Nacional, durante el periodo 2022 a 2023. Las variables analizadas fueron las variables sociodemográficas, clínicas y de laboratorio, al debut y durante las recaídas. Resultados. Se incluyeron 47 pacientes, entre 14 y 68 años de edad (media: 29,6 ±12 años), 91,5% del sexo femenino, 59,5% del interior del país, con educación secundaria (68,1%) y ocupación ama de casa (55,3%). El tiempo de enfermedad fue en promedio 48,7 ±37.1 meses. La forma más frecuente de debut fue la poli-artralgia (55,3%), seguido de nefritis (27,7%). En la recaída, la nefritis fue más frecuente (44,7%), seguida de dolor poliarticular (40,4%). La causa de recaída más frecuente fue el abandono del tratamiento (34,0%). Conclusión. La mayoría de las pacientes eran mujeres jóvenes que debutaron la enfermedad con artralgias, seguida de la afectación renal. Las recaídas se presentaron con nefritis. La causa principal de las recaídas fue el abandono del tratamiento.


Introduction: The clinical forms of presentation of systemic lupus erythematosus (SLE) are varied, as well are the relapses that occur in the course of the disease. Objective: To describe the onset and relapses in a cohort of patients with SLE. Methodology. Observational, descriptive, cross-sectional study of patients with SLE who attended the National Hospital, during the period 2022 to 2023. The variables analyzed were sociodemographic, forms of onset and relapses. Results: 47 patients between 14 and 68 years of age (mean: 29.6 ±12 years) were included in the study, 91.5% female, 59.5% from the interior of the country, with secondary education (68.1%) and housewife occupation (55.3%). The duration of illness was on average 48.7 ±37.1 months. The most common form of onset was polyarthralgia (55.3%), followed by nephritis (27.7%). In relapse, nephritis was more frequent (44.7%), followed by polyarticular pain (40.4%). The most frequent cause of relapse was treatment abandonment (34.0%). Conclusion: The majority of patients were young women who presented the disease with arthralgia, followed by kidney involvement. Relapses presented with nephritis. The main cause of relapses were treatment abandonment.

2.
Bol. méd. Hosp. Infant. Méx ; 74(5): 349-356, sep.-oct. 2017. tab, graf
Artigo em Espanhol | LILACS | ID: biblio-951271

RESUMO

Resumen: Introducción: La rinitis alérgica (RA) es considerada como un problema de salud pública, por lo tanto, es indispensable poner a prueba estrategias de educación para la salud como la consejería de enfermería (CE) dirigida a grupos poblacionales como niños con rinitis alérgica y sus tutores. Este trabajo tuvo como objetivo medir durante un año los beneficios en la salud de población infantil con esta enfermedad. Métodos: Estudio longitudinal, aleatorio, comparativo, con una muestra de 100 pacientes pediátricos de ambos sexos, con edades de 6 a 12 años, con diagnóstico de rinitis alérgica, con consejería (grupo estudio) y sin consejería (grupo control). En ambos grupos se obtuvo carta de consentimiento informado firmada por ambos tutores, además de cédulas de conocimiento y de valoración; la segunda incluyó escala de sintomatología y de Morisky Green (adherencia al tratamiento). Los niños del grupo estudio recibieron intervención basada en educación personalizada, material didáctico, apoyo del grupo multidisciplinario en caso necesario (médico, dermatólogo y psicólogo). El grupo control recibió atención habitual. En ambos grupos se hizo seguimiento vía telefónica, lo que permitió identi"car el número de recaídas en un año. Resultados: Para la comparación de los resultados se aplicó la prueba de Wilcoxon rank-sum (Mann-Whitney); la presencia de recaídas en el grupo control comparado con el grupo estudio se encontró estadísticamente significativa. Conclusiones: Se encontró que la población infantil que recibe CE, tiene como beneficio mejor control de la sintomatología y disminución de recaídas al año.


Abstract: Background: Allergic rhinitis (AR) is considered to be a public health problem, therefore it is essential to test health education strategies such as nursing counseling (NC) aimed at population groups such as children with allergic rhinitis and their tutors. This study aimed to measure the health benefits of children with this disease for a year. Methods: Longitudinal, randomized, comparative study with a sample of 100 pediatric patients of both sexes, aged 6 to 12 years, with diagnosis of allergic rhinitis, with counseling (study group) and without counseling (control group). In both groups, an informed consent letter signed by both tutors was obtained, in addition to knowledge and assessment papers; the latter included a scale of symptomatology and Morisky Green (adherence to treatment). The children in the study group received intervention based on personalized education, didactic material, support of the multidisciplinary group if necessary (doctor, dermatologist and psychologist). The control group received usual care. In both groups, telephone follow-up was performed, which allowed the number of relapses to be identified in one year. Results: The Wilcoxon rank-sum test (Mann-Whitney) was used to compare the results; the presence of relapses in the control group was statistically significant compared to the study group. Conclusions: It was found that the infant population that receives NC, has as a better benefit the control of the symptomatology and decrease of relapses per year.


Assuntos
Criança , Feminino , Humanos , Masculino , Educação de Pacientes como Assunto/métodos , Aconselhamento/métodos , Rinite Alérgica/enfermagem , Enfermeiras e Enfermeiros/organização & administração , Recidiva , Telefone , Seguimentos , Estudos Longitudinais , Estatísticas não Paramétricas
3.
MedicalExpress (São Paulo, Online) ; 4(2): M170201, Mar.-Apr. 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-841479

RESUMO

PURPOSE: To systematically evaluate whether oral steroids can be used with the same efficacy and safety in comparison with the intravenous regimen for treatment of multiple sclerosis relapses. METHOD: We searched Medline, Embase and Cochrane Library and systematically reviewed articles comparing outcomes of oral versus intravenous steroids for acute relapses in patients with a clinically definite diagnosis of multiple sclerosis. RESULTS: Six articles with 414 participants in total were analyzed. Five of the included trials reported the proportion of patients experiencing improvement in Expanded Disability Status Scale after receiving either oral or intravenous methylprednisolone treatment at four weeks; the pooled results showed that there was no statistically significant difference (OR 0.96; 95% CI 0.60, 1.54; p=0.86) between treatments. Three trials reported the detailed results of adverse events, indicating the two treatments appear to be equally safe. Two trials revealed that there was no significant difference in gadolinium enhancement activity on magnetic resonance imaging. One trial showed that the mean area under the concentration-time curve (AUC) at 24 and 48 hours did not differ between groups. CONCLUSION: No significant differences were found in terms of clinical (benefits and adverse events), radiological and pharmacological outcomes in multiple sclerosis relapses in patients after oral or intravenous steroids treatment. Our meta-analysis provides evidence that oral steroid therapy is not inferior to intravenous steroid therapy. Thus oral administration may be a favorable substitute for intravenous medication of multiple sclerosis relapses.


PROPÓSITO: Avaliar de forma sistemática se esteroides orais podem ser utilizados com a mesma eficácia e segurança em comparação com o regime intravenoso para o tratamento de recaídas da esclerose múltipla (MS). MÉTODO: Foram pesquisados Medline, Embase e Cochrane Library e sistematicamente revistos artigos comparando resultados de esteroides orais versus intravenosos para recaídas agudas em pacientes com diagnóstico de esclerose múltipla clinicamente definida. RESULTADOS: Seis artigos com 414 participantes no total foram analisados. Cinco dos estudos incluídos relataram a proporção de doentes com melhoria através de "Expanded Disability Status Scale" depois de receber um ou outro tratamento: metilprednisolona oral ou intravenosa por quatro semanas. Os resultados combinados mostraram que não houve diferença estatisticamente significativa (OR 0,96; 95% 101 0,60, 1,54 ; p = 0,86). Três estudos mostraram os resultados detalhados de eventos adversos, indicando que os dois tratamentos parecem ser igualmente seguros. Dois ensaios revelaram que não havia nenhuma diferença significativa no aumento de atividade de gadolínio via imagens por ressonância magnética. Um estudo mostrou que a área média sob as curvas de concentração-tempo (AUC) às 24 horas e 48 horas não diferiram entre os grupos. CONCLUSÃO: Não foram encontradas diferenças significativas em termos de clínicos (benefícios e eventos adversos) ou nos resultados radiológicos e farmacológicos em pacientes pós-esteroides por via oral ou intravenosa no tratamento de várias recaídas de esclerose. Nossa metanálise fornece evidências de que a terapia com esteroides por via oral não é inferior à terapia com esteroides por via intravenosa. Assim, a administração oral pode ser um substituto favorável para medicação intravenosa de recidivas da esclerose múltipla.


Assuntos
Humanos , Esteroides/administração & dosagem , Esclerose Múltipla/tratamento farmacológico , Recidiva , Metilprednisolona/administração & dosagem , Administração Oral , Administração Intravenosa
4.
Bol. méd. Hosp. Infant. Méx ; 73(5): 309-317, sep.-oct. 2016. tab, graf
Artigo em Espanhol | LILACS | ID: biblio-951244

RESUMO

Resumen: Introducción: En el síndrome nefrótico cortico-sensible (SNCS), la corticoterapia prolongada podría reducir la frecuencia de recaídas. El objetivo de este trabajo fue la comparación de un esquema corticoide prolongado frente al tratamiento habitual del SNCS primario, evaluando los siguientes parámetros: el número de pacientes con recaídas, el número total de recaídas, el tiempo medio transcurrido al iniciar el tratamiento, hasta la remisión y hasta la primera recaída, la dosis acumulada de corticosteroides y la toxicidad esteroide. Métodos: La población se dividió en dos grupos: el grupo A (27 pacientes) recibió 16-β-metilprednisona durante 12 semanas, reduciendo la dosis hasta la semana 24; y el grupo B (29 pacientes) recibió 16-β-metilprednisona durante 12 semanas, y placebo hasta la semana 24. Resultados: La tasa de incidencia acumulada de recaídas (persona/año) fue en el grupo A 36/100, y en el grupo B 66/100 (p = 0.04). El tiempo medio transcurrido (días) hasta la primera recaída fue de 114 en el grupo A y 75 en el grupo B (p = 0.01). Las diferencias de tiempo transcurrido al iniciar tratamiento y hasta la remisión entre ambos grupos no fueron significativas. El total acumulado de recaídas fue de 9 en el grupo A y 17 en el grupo B (p = 0.04), y el total de pacientes con recaídas fue de 3 (grupo A) y 7 (grupo B) (p = 0.17). La dosis media acumulada (mg/m2) por paciente fue de 5,243 en el grupo A y de 4,306 en el grupo B (p = 0.3), y el cortisol sérico (μg/dl) final fue de 14 en el grupo A y 16 en el grupo B (p = 0.4). La toxicidad esteroide fue similar entre ambos grupos. Conclusiones: La duración del tratamiento disminuyó el número de recaídas, sin incrementar la toxicidad esteroide.


Abstract: Background: In the steroid-sensitive nephrotic syndrome (SSNS) the prolonged treatment with steroids could decrease the frequency of relapses. We conducted a comparative study of prolonged steroid scheme and the usual treatment of primary SSNS to assess: the number of patients with relapses, mean time to treatment initiation, to remission and to first relapse, total number of relapses, total cumulative dose of steroids, and the steroid toxicity. Methods: Patients were divided into two groups: group A (27 patients) received 16-β-methylprednisolone for 12 weeks, reducing the steroid until week 24. Group B (29 patients) received 16-β-methylprednisolone for 12 weeks and placebo until week 24. Results: Cumulative incidence rate of relapse (person/years) for group A was of 36/100 and 66/100 for group B (p = 0.04). Average elapsed time to first relapse was of 114 days for group A and of 75 days to for group B (p = 0.01). The difference in time for initial response to treatment and up to achieve remission between both groups was not significant. Total cumulative relapses were 9 for group A and 17 for group B (p = 0.04). Total patients with relapses were 3 for group A and 7 for group B (p = 0.17). Cumulative average dose per patient was 5,243 mg/m2 for group A and 4,306 mg/m2 for group B (p = 0.3), and serum cortisol was 14 μg/dl for group A and 16 μg/dl for group B (p = 0.4). There were no steroid toxicity differences between groups. Conclusions: The duration of the treatment had an impact on the number of relapses without increasing steroid toxicity.

5.
Cambios rev. méd ; 15(1): 52-55, ene. - 2016. tab
Artigo em Espanhol | LILACS | ID: biblio-1008552

RESUMO

Introducción: El estudio pretende relacionar los niveles séricos de vitamina D, en pacientes con Esclerosis Múltiple (EM), con la severidad y el comportamiento de la enfermedad. Materiales y Métodos: Reclutamos 81 pacientes con EM, de los cuales se obtuvo una muestra de 50 pacientes para compararlos con 50 sujetos sanos, pareados por edad, sexo y color de la piel. La severidad de la enfermedad se evaluó con la escala de Kurtzke, número de recaídas, exposición solar, etc. Resultados: La concentración sérica de vitamina D en pacientes con EM (M=31.9 SD=12.3 ng/ml) fue similar a la de los controles (M=30.3 SD= 8.0 ng/ml; p=0.53). La prevalencia de insuficiencia de vitamina D fue del 42% (n=21) entre los casos y 46% (n=23) entre los controles, p>0.05). Se calculó la relación entre los niveles óptimos de Vitamina D (> 40, ng/ml) con un bajo grado de discapacidad, definida como un valor en la escala de Kurtzke < 3.5 [χ2(1, N=100)= 3.13 p=0.3]. El promedio de vitamina D en los pacientes con más de una recaída fue de 31.0 ng /ml y con menos de una recaída, 32.5 ng/ml fue similar (p=0.66). Discusión: No hubo diferencia significativa en las concentraciones séricas de vitamina D en pacientes con EM y sujetos sanos, pareados por género, edad y color de la piel. No hubo correlación entre el nivel de vitamina D y el grado de discapacidad medido por la escala de Kurtzke ni con el número de recaídas.


Introduction: The study seeks to relate vitamin D serum levels in Multiple Sclerosis (MS) patients with disease severity and its progression. Methods: From eighty one MS patients enrolled, fifty were selected to compare to healthy subjects, paired according to age, gender and skin color. Disease severity was assessed using the Kurtzke severity scale, relapses number, solar exposure. Results: The mean vitamin D serum concentration in MS patients (M= 31.9 SD=12.3 ng/ml) was similar to controls' (M=30.31 SD=8.0 ng/ml; p=0.53). The prevalence of vitamin D insufficiency was 42% (n=22) among cases and 46% (n=23) among controls (p=0.91). The relationship between an optimal vitamin D serum concentration (>40 ng/ml) and a low grade of disability, using a cutoff point in the Kurtzke scale < 3.5, was assessed and a non-significant correlation was found [χ2(1, N=100)= 3.13 p=0.3]. The mean vitamin D level among patients with more than one relapse (M=31.0 ng/ml) was similar to those with less than one relapse (M=32.49, p=0.66). Discusion: There was no difference of vitamin D serum levels between MS patients and the general population. A weak and not significant correlation was found with the degree of disability, measured by the Kurtzke severity scale, and also with the number of relapses.


Assuntos
Humanos , Masculino , Feminino , Adulto , Recidiva , Vitamina D , Índice de Gravidade de Doença , Doenças Neurodegenerativas , América Latina , Esclerose Múltipla , Pele , Doenças Autoimunes , Manifestações Neurológicas
6.
J. bras. patol. med. lab ; 51(6): 359-368, Nov.-Dec. 2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-767692

RESUMO

ABSTRACT Introduction: Multiple myeloma (MM) is an incurable progressive hematological neoplasia characterized by heterogeneous evolution and by relapses after therapy. Objective: Compare the effectiveness of serum immunofixation (SIF) and electrophoresis (SPE) techniques in the detection of relapses in MM patients undergoing treatment at the University Hospital of Santa Maria (HUSM). Material and methods: The study was conducted from January 2012 to July 2014 and included 52 patients from HUSM with confirmed diagnosis of MM. The retrospective monitoring based on laboratory analyses indicated that nine of these patients relapsed, in whom it was possible to compare the effectiveness of SIF and SPE techniques for detecting relapses. Results: For the nine patients, SIF always detected MM relapses earlier than SPE, with a precocity ranging from 2.0 to 18.8 months, for an average of 6.6 months. Discussion and conclusion: The results indicated that SIF was more effective than SPE for the early detection of relapses, regardless of the class and type of M component (mono/biclonal). Therefore, the use of SIF allows for better monitoring of MM patients, especially for the detection of relapses, thereby helping in choosing the most appropriate therapy and resulting in increased duration of survival period free of disease.


RESUMO Introdução: O mieloma múltiplo (MM) é uma neoplasia hematológica progressiva e incurável, caracterizada pela evolução heterogênea e pela ocorrência de recidivas nos pacientes após o tratamento. Objetivo: Comparar as técnicas de imunofixação (IFS) e eletroforese (EFS) séricas quanto à eficácia em detectar precocemente as recidivas em pacientes com MM e em tratamento junto ao Hospital Universitário de Santa Maria (HUSM). Material e métodos: O estudo foi realizado no período de janeiro de 2012 a julho de 2014, sendo incluídos 52 pacientes do HUSM com diagnóstico confirmado de MM. O monitoramento retrospectivo, realizado por meio de análises laboratoriais, indicou que nove desses pacientes recidivaram, nos quais foi possível comparar a eficácia das técnicas de IFS e EFS na detecção de tais recidivas. Resultados: Nos nove pacientes em estudo, a IFS sempre detectou as recidivas do MM antes da EFS, sendo que essa precocidade variou de dois a 18,8 meses, com tempo médio de 6,6 meses. Discussão e conclusão: Os resultados indicaram que a IFS foi mais eficaz do que a EFS em detectar as recidivas, independentemente da classe e do tipo de componente M (mono/biclonal). Portanto, o uso da IFS permite monitorar melhor os pacientes com MM, principalmente na detecção das recidivas, o que pode auxiliar na escolha da terapia mais adequada, além de aumentar o tempo de sobrevida livre da doença.

7.
Dement. neuropsychol ; 9(3): 311-314, July-Sept. 2015. tab
Artigo em Inglês | LILACS | ID: lil-761042

RESUMO

Anti-N-methyl- D-aspartate receptor (NMDAR) encephalitis is a recently discovered autoimmune disorder, in which antibodies target NMDARs in the brain, leading to their removal from synapses. Early in the disease course, patients often present with marked psychosis and mood disturbances (i.e. mania, depression), explaining why most of these patients are first seen by psychiatrists. Hence, autoimmune encephalitis is receiving growing attention from psychiatry, mainly owing to concerns over misdiagnosing immunomediated and potentially curable disorders as primary psychiatric disorders, such as schizophrenia or major depressive disorder. Although anti-NMDAR encephalitis occurs in the context of new-onset psychiatric symptoms, there is a lack of information on differential diagnosis and treatment of this disorder after a long-term diagnostic history of functional psychiatric disorders. We report a case of a patient with a long history of bipolar affective disorder evolving with anti-NMDAR encephalitis, initially misdiagnosed as non-organic psychosis.


A encefalite antirreceptor N-metil-D-aspartato (NMDA) é uma doença autoimmune recentemente descoberta, na qual anticorpos têm como alvo os receptors NMDA no cérebro, levando à sua remoção da sinapse. Os pacientes frequentemente desenvolvem psicose e distúrbios de humor proeminentes nas fases iniciais da doença (i.e: mania e depressão), o que explica o fato de que a maioria destes pacientes seja vista primeiramente por psiquiatras. Consequentemente, as encefalites autoimunes têm recebido atenção crescente pela psiquiatria, principalmente pela preocupação de erroneamente diagnosticar doenças imunomediadas e potencialmente tratáveis como doenças psiquiátricas primárias, como esquizofrenia ou transtorno depressivo maior. Embora a encefalite antirreceptor NMDA ocorra no contexto de sintomas psiquiátricos de início recente, há carência de informações sobre o diagnóstico diferencial e tratamento desta doença após o diagnóstico de doenças psiquiátricas funcionais de longa data. Aqui, nós apresentamos o caso de uma paciente com diagnóstico de transtorno afetivo bipolar de longa data evoluindo com encefalite antirreceptor NMDA, inicialmente diagnosticada erroneamente como uma psicose não-orgânica.


Assuntos
Humanos , Transtornos Psicóticos , Recidiva , Transtorno Bipolar , N-Metilaspartato , Encefalite Antirreceptor de N-Metil-D-Aspartato
8.
Arq. neuropsiquiatr ; 73(7): 593-600, 07/2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-752380

RESUMO

Objective The study aims to investigate the presence of pain amongst multiple sclerosis (MS) patients. Method One hundred MS patients responded to questionnaires evaluating neuropathic and nociceptive pain, depression and anxiety. Statistical analysis was performed using the Mann–Whitney U, Chi-Square and two-tailed Fisher’s exact tests and multivariate logistic regression. Results Women had a statistically higher prevalence of pain (p = 0.037), and chances of having pain after the age of 50 reduced. Women with pain had a statistically significant lower number of relapses (p = 0.003), restricting analysis to those patients with more than one relapse. After the second relapse, each relapse reduced the chance of having pain by 46%. Presence of pain was independent of Expanded Disability Status Scale (EDSS) anxiety, and depression. Conclusion Our findings suggest a strong inverse association between relapses and pain indicating a possible protective role of focal inflammation in the control of pain. .


Objetivo O estudo tem como objetivo investigar a presença de dor entre pacientes com esclerose múltipla (EM). Método Cem pacientes com EM responderam a questionários avaliando dor neuropática e nociceptiva, depressão e ansiedade. A análise estatística foi realizada através dos testes de Mann-Whitney U, Qui-Quadrado, two tailed Fisher exact test e regressão logística multivariada. Resultados As mulheres apresentaram estatisticamente uma maior prevalência de dor (p = 0,037), e as chances de ter dor após a idade de 50 reduziram. As mulheres com dor tinham um número com significância estatística reduzido de surtos (p = 0,003), restringindo a análise aos pacientes com mais de um surto. Após o segundo surto, cada surto reduziu a chance de ter dor em 46%. A presença de dor foi independente da Expanded Disability Status Scale (EDSS) ansiedade e depressão. Conclusão Nossos resultados sugerem uma forte associação inversa entre o surto e a dor, indicando um possível papel protetor da inflamação focal no controle da dor. .


Assuntos
Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Esclerose Múltipla/epidemiologia , Neuralgia/epidemiologia , Dor Nociceptiva/epidemiologia , Distribuição por Idade , Idade de Início , Ansiedade/epidemiologia , Brasil/epidemiologia , Avaliação da Deficiência , Progressão da Doença , Depressão/epidemiologia , Métodos Epidemiológicos , Esclerose Múltipla/fisiopatologia , Neuralgia/fisiopatologia , Dor Nociceptiva/fisiopatologia , Medição da Dor , Recidiva , Distribuição por Sexo , Fatores Sexuais
9.
Indian Pediatr ; 2012 November; 49(11): 881-887
Artigo em Inglês | IMSEAR | ID: sea-169527

RESUMO

Objective: To review the disease course in patients with steroid sensitive nephrotic syndrome (SSNS) and the factors that determine outcome Design: Retrospective, analytical Setting: Pediatric Nephrology Clinic at referral center in North India Participants/patients: All patients with SSNS evaluated between 1990 and 2005 Intervention: None Main outcome measures: Disease course, in patients with at least 1-yr follow up, was categorized as none or infrequent relapses (IFR), frequent relapses or steroid dependence (FR), and late resistance. Details on complications and therapy with alternative agents were recorded. Results: Records of 2603 patients (74.8% boys) were reviewed. The mean age at onset of illness and at evaluation was 49.7±34.6 R E S E A R C H P A P E R INDIAN PEDIATRICS 881 VOLUME 49__NOVEMBER 16, 2012 and 67.5±37.9 months respectively. The disease course at 1-yr (n=1071) was categorized as IFR in 37.4%, FR in 56.8% and late resistance in 5.9%. During follow up, 224 patients had 249 episodes of serious infections. Alternative medications for frequent relapses (n=501; 46.8%) were chiefly cyclophosphamide and levamisole. Compared to IFR, patients with FR were younger (54.9±36.0 vs. 43.3±31.4 months), fewer had received adequate (≥8 weeks) initial treatment (86.8% vs. 81.7%) and had shorter initial remission (7.5±8.6 vs. 3.1±4.8 months) (all P<0.001). At follow up of 56.0±42.6 months, 77.3% patients were in remission or had IFR, and 17.3% had FR. Conclusions: A high proportion of patients with SSNS show frequent relapses, risk factors for which were an early age at onset, inadequate initial therapy and an early relapse.

10.
Rev. Soc. Bras. Med. Trop ; 43(6): 749-750, Nov.-Dec. 2010.
Artigo em Inglês | LILACS | ID: lil-569451

RESUMO

Two cases of malaria by Plasmodium vivax relapsed after treatment with drugs in doses recommended by the Ministry of Health are presented. Both patients were overweight and were followed in the Federal District, an area considered free from vector transmission of the disease. Radical cure was obtained after medication with the same drugs in weight proportional doses.


São apresentados dois casos de pacientes com malária por Plasmodium vivax que apresentaram recaídas após tratamento com medicamentos em doses indicadas pelo Ministério da Saúde. Ambos os pacientes tinham pesos elevados e foram acompanhados no Distrito Federal, área considerada sem transmissão vetorial da doença. A cura radical foi obtida após medicação em dose proporcional ao peso corpóreo dos pacientes.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Antimaláricos/administração & dosagem , Malária Vivax/tratamento farmacológico , Sobrepeso/complicações , Primaquina/administração & dosagem , Malária Vivax/complicações , Recidiva , Falha de Tratamento
11.
Medisan ; 14(8): 1045-1053, 8-oct.-16-nov. 2010.
Artigo em Espanhol | LILACS | ID: lil-585277

RESUMO

Se hizo un estudio descriptivo y transversal de los 36 pacientes con recaídas por tuberculosis en la provincia de Santiago de Cuba desde el 2002 hasta el 2008, para caracterizarles según algunas variables clinicoepidemiológicas. Se observó que las recaídas tuvieron una tendencia ascendente, fundamentalmente en el municipio de Santiago de Cuba, con preponderancia en el sexo masculino, el grupo etario de 60 años y más, las personas solteras y los que tenían nivel escolar primario y condiciones económicas regulares o malas. Se evidenció una inadmisible demora entre la fecha de inicio de los síntomas y la confirmación del diagnóstico, por lo que se recomendó mantener como prioridades la vigilancia y el control del Programa Nacional de Tuberculosis en la comunidad, de manera que permita disminuir la prevalencia de recaída por esta enfermedad en el territorio


A descriptive and cross-sectional study was carried out in 36 patients with relapses due to tuberculosis in Santiago de Cuba province from 2002 to 2008, to characterize them according to some clinical and epidemiological variables. It was observed that relapses had an upward tendency, mainly in Santiago de Cuba municipality, with predominance in male sex, in the age group of 60 years and over, single people and those that had primary school level and middling or bad economic status. An inadmissible delay was evidenced between the date of beginning of the symptoms and the confirmation of the diagnosis, thus recommending to maintain as priorities the surveillance and control of the National Program of Tuberculosis in the community, so that it allows to reduce prevalence of relapses due to this condition in the territory


Assuntos
Humanos , Masculino , Feminino , Programas Nacionais de Saúde , Fatores de Risco , Tuberculose/epidemiologia , Estudos Transversais , Epidemiologia Descritiva , Tuberculose/diagnóstico , Tuberculose/terapia
12.
Acta méd. costarric ; 50(supl.3): 58-59, nov. 2008.
Artigo em Espanhol | LILACS | ID: lil-700671

RESUMO

A pesar del uso universal de la vacuna, la hepatitis B sigue siendo un problema de salud pública en diferentes áreas del mundo. Aún cuando se consiga una supresión eficaz de la replicación viral mediante tratamiento con fármacos, existe la potencial reactivación al suspender el mismo. El enfoque terapéutico para los no respondedores o recaídas post tratamiento, se podría llevar a cabo con combinaciones de medicamentos o el uso de otro tipo de fármaco con mayor potencia.


In spite of the universal use of the vaccine, hepatitis B still is a public health problem in different areas around the world. Eventhough an effective suppression of viral replication by means of treatment with drugs is obtained; there is a potential reactivation when suspending the treatment. The therapeutic approach for non-respondents or relapses post treatment could be carried out with combinations of medicines or use of another type of drug with greater power.


Assuntos
Humanos , Vírus da Hepatite B/efeitos dos fármacos
13.
CES med ; 21(2): 51-60, jul.-dic. 2007. mapas, tab, graf
Artigo em Espanhol | LILACS | ID: lil-561167

RESUMO

La malaria por Plasmodiun vivax es una de las principales causas de morbilidad en centro y sur América. En Colombia es la más prevalente y representa el 75 por ciento de los casos reportados. La primaquina (PQ) es la única droga disponible de uso clínico para eliminar los hipnozoitos y prevenir recaídas en la malaria por P. vivax. Se hizo un ensayo clínico aleatorio controlado sin placebo y no ciego. Se estudió la eficacia antirrecaída de tres esquemas de tratamiento con dosis total de PQ (45, 105 y 210 mg) suministrados en dosis de 15 mg/día, en 210 adultos con diagnóstico de P. vivax en dos municipios de Antioquia (Colombia). Todos los pacientes recibieron una dosis total de 1.500 mg de cloroquina [CQ] en tres días (600 mg el día 1 y 450 mg los días 2 y 3). Los pacientes tuvieron una respuesta clínica adecuada del 100 por ciento al tratamiento CQ+PQ hasta el día 28, en los tres grupos. El porcentaje de recurrencias durante los seis meses de seguimiento fue de 45 por ciento, 36,6 por ciento y 17,6 por ciento para los grupos con 45, 105 y 210 mg de PQ respectivamente. El tratamiento convencional (210 mg) fue un factor de protección para las recurrencias cuando se comparó con los esquemas de 45 y 105 mg respectivamente. El tratamiento convencional sigue siendo el tratamiento más eficaz para prevenir las recaídas en la malaria por P. vivax en una zona endémica...


Plasmodium vivax malaria is an important cause of morbility in Central and South America. In Colombia this is the most prevalent malaria infection representing75 % of the reported cases. To define the efficacy of the chloroquine and primaquine regimen to eliminatehypnozoites and prevent relapses, we a conducted a random controlled clinical trial of three primaquine regimens in an open-label study. We evaluated the anti-relapse efficacy of a total primaquine dose of 45, 105 and 210 mg administered at 15mg/day in 210 adults with P. vivaxinfection from the Northwestern region of Colombia. Cure rates for blood stage vivax malaria by day 28 of followupwere 100 % in all groups. Post-treatment reappearance of parasitaemia during the 6 months of following up was 45 %, 36,6 % and 17,6 % respectively, for each group. When compared to other groups, administration of 210 mg was a significant protection factor for reappearance of parasitaemia in an endemic area.


Assuntos
Adulto , Antimaláricos , Cloroquina/uso terapêutico , Malária Vivax/prevenção & controle , Primaquina/uso terapêutico , Plasmodium
14.
Biomédica (Bogotá) ; 24(2): 133-139, jun. 2004. tab
Artigo em Espanhol | LILACS | ID: lil-635437

RESUMO

La persistencia de bacilos viables y la monoterapia con diamino-difenil-sulfona (DDS) son los principales factores que favorecen las recidivas de la lepra. Presentamos 33 pacientes con lepra lepromatosa (LL) diagnosticada 7 a 48 años antes de la recidiva, que recibieron monoterapia con DDS durante 4 a 38 años. Veintiocho fueron tratados, además, con poliquimioterapia (PQT) irregular, no supervisada, desde 1983. Cinco sólo recibieron DDS. Éstos presentaron la recidiva entre 13 y 20 años después de suspenderla. Las recidivas se diagnosticaron por reaparición de las lesiones clínicas o por la presencia de nuevas zonas anestésicas; todas se confirmaron con la baciloscopia y, en 20 casos, por la biopsia de piel. Cuatro pacientes presentaron en la biopsia de la recidiva, lepra indeterminada (LI) y uno lepra dimorfa tuberculoide (LDT), todos con presencia de bacilos intraneurales; los demás fueron LL. Dos pacientes recidivaron, aun con PQT razonablemente supervisada. Los demás curaron con PQT supervisada. Los factores predisponentes para la recidiva fueron: monoterapia con DDS por varios años; PQT irregular con dosis inadecuadas, sin supervisión del tratamiento; abandono de la PQT, y relación inadecuada entre el paciente y el personal de salud. Las recidivas de la lepra se deben buscar en todos los pacientes colombianos con lepra multibacilar que fueron tratados con DDS solo durante años. La clínica, la baciloscopia y la biopsia individualmente o en conjunto son métodos confiables para establecer las recidivas.


Leprosy relapses are mainly due to bacillary persistence and diamino-diphenyl-sulphone (DDS) monotherapy. Case histories were examined for 33 patients with lepromatous leprosy (LL), diagnosed 7-48 years before the relapse and treated only with DDS during 4 to 38 years. Twenty-eight patients received irregular non-supervised polychemotherapy (PCT) since 1983. Five patients received only DDS, and presented relapses 13-20 years after the treatment was stopped. Relapses were diagnosed by clinical methods, including the reappearance of lesions or presence of new anesthetic areas. All cases were confirmed by bacilloscopy, and a subset of 20 cases by skin biopsy. Four patients presented indeterminate leprosy (IL) and one patient borderline tuberculoid leprosy (BT) in the biopsy. The latter 5 demonstrated presence of intraneural bacilli; the remainder were LL. Two patients relapsed even with PCT treatment. The others were cured with supervised PCT. Predisposing factors for relapses were as follows: DDS monotherapy, irregular PCT with inadequate dosage, unsupervised treatment, treatment uncompliance, and inadequate relationship between the patient and the health staff. Inspections for relapse in leprosy is recommended for in all multibacillary patients that were treated with DDS. The clinical appearance of new lesions or new anesthetic zones, the bacilloscopy and skin biopsy, used together, are effective in establishing the presence of relapses.


Assuntos
Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Hanseníase/tratamento farmacológico , Biópsia , Hanseníase/patologia , Estudos Retrospectivos
15.
Journal of Medical Postgraduates ; (12)2003.
Artigo em Chinês | WPRIM | ID: wpr-587412

RESUMO

Objective: To determine whether mannose-binding lectin(MBL) variant alleles were associated with frequent relapses in childhood nephrotic syndrome(NS). Methods: MBL alleles of codon 54 and promoter region at positions-550 and-221 were genotyped by means of Polymerase Chain Reaction-Restricted Fragment Length Polymorphism(PCR-RFLP)and PCR-Sequence-Specific Primers(PCR-SSP)assay in 32 China Han Nationality children with frequently relapsing NS(FRNS) and 31 with non-frequently relapsing NS(NFRNS),as well as in 32 healthy control subjects. Results: In patients with upper respiratory infections before relapses,the mutant genotype(GGC/GAC and GAC/GAC) frequency of MBL codon 54 was higher in children with FRNS(76.0%) than in children with NFRNS(42.9%).The B allele mutation frequency of MBL codon 54 was higher in children with FRNS than in healthy control subjects(34.4% vs 12.5%,P

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