RESUMEN
This study aimed to analyze the measurement of information quality in the Information System of the Brazilian Hospital in terms of data completeness and consistency. The quality of information is a fundamental factor in evaluating the performance of information systems. Its use is a reasonable condition in the management of the health service and attention to the care of patients. The research had a retrospective, descriptive character exploratory with quantitative analysis of the data. The study had some limitations, we observed incomplete information regarding some studied variables; this is because the primary source of information in the cancer registry is the patient's medical record. Therefore, the patient's medical records are relevant and should contain the entire health history, from birth to death. In addition, they support research, the management of health services.
Asunto(s)
Instituciones Oncológicas , Neoplasias , Brasil/epidemiología , Clero , Hospitales , Humanos , Sistemas de Información , Neoplasias/terapia , Sistema de Registros , Estudios RetrospectivosRESUMEN
Studies on concomitant schistosomiasis and human and experimental malaria have shown a variation in the immunospecific response, as well as an increase in the severity of both parasitoses. In the present study, a murine co-infection model was used to determine the effects of a co-infection with Schistosoma mansoni and Plasmodium berghei on the protective immunity acquired by repeated malarial infections and subsequent curative treatment with chloroquine. Our results have demonstrated that, compared to an infection with P. berghei only, the co-infection increases the malarial parasitaemia and decreases the survival rate. Indeed, mice that were immunized by infection and treatment with drug displayed no mortality whereas co-infected mice showed a reduced protective efficacy of immunization against P. berghei (mortality > 60%). Interestingly, this high mortality rate was not associated with high levels of parasitaemia. Our findings support the idea of a suppressive effect of a Schistosoma co-infection on the anti-malarial protection by immunization. This result reveals a possible drawback of the development of anti-malarial vaccines, especially considering the wide endemic areas for both parasitoses.
Asunto(s)
Antimaláricos/uso terapéutico , Cloroquina/uso terapéutico , Malaria/inmunología , Parasitemia/parasitología , Esquistosomiasis mansoni/inmunología , Animales , Femenino , Malaria/complicaciones , Malaria/tratamiento farmacológico , Ratones , Ratones Endogámicos BALB C , Parasitemia/tratamiento farmacológico , Parasitemia/inmunología , Plasmodium berghei/inmunología , Schistosoma mansoni , Esquistosomiasis mansoni/complicacionesRESUMEN
Studies on concomitant schistosomiasis and human and experimental malaria have shown a variation in the immunospecific response, as well as an increase in the severity of both parasitoses. In the present study, a murine co-infection model was used to determine the effects of a co-infection with Schistosoma mansoni and Plasmodium berghei on the protective immunity acquired by repeated malarial infections and subsequent curative treatment with chloroquine. Our results have demonstrated that, compared to an infection with P. berghei only, the co-infection increases the malarial parasitaemia and decreases the survival rate. Indeed, mice that were immunized by infection and treatment with drug displayed no mortality whereas co-infected mice showed a reduced protective efficacy of immunization against P. berghei (mortality > 60 percent). Interestingly, this high mortality rate was not associated with high levels of parasitaemia. Our findings support the idea of a suppressive effect of a Schistosoma co-infection on the anti-malarial protection by immunization. This result reveals a possible drawback of the development of anti-malarial vaccines, especially considering the wide endemic areas for both parasitoses.