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1.
Community Dent Oral Epidemiol ; 20(5): 292-6, 1992 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-1424551

RESUMEN

The aim of the study was to assess the effect of rheumatoid arthritis (RA) upon dental health. A questionnaire was mailed to all seropositive rheumatoid arthritis (RA) patients aged 44-56 yr in the files of the two main departments of rheumatology in South Eastern Norway. Data were obtained from 125 patients, constituting 91% of the target group. The number of remaining teeth in these patients was not related to disease duration or physical dysfunction, whereas a relationship to prolonged use of medication for pain relief was indicated. Factors known to affect tooth loss in the general population, such as smoking habits, dental attendance, interdental cleaning habits, previous dental disease, and place of residence were found to be important in RA patients as well. The RA patients from Oslo had a mean number of 25 remaining teeth, which is the same as reported for the general Oslo population at this age. Oral dryness was reported by more than 50% of the RA patients, but was not related to the number of teeth. The conclusion is that serious and long lasting rheumatoid arthritis had little influence on the number of remaining teeth in this middle-aged group of Norwegians.


Asunto(s)
Artritis Reumatoide/complicaciones , Pérdida de Diente/epidemiología , Xerostomía/etiología , Acetaminofén/efectos adversos , Adulto , Análisis de Varianza , Codeína/efectos adversos , Índice CPO , Atención Odontológica/estadística & datos numéricos , Caries Dental/epidemiología , Combinación de Medicamentos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Noruega/epidemiología , Higiene Bucal , Enfermedades Periodontales/epidemiología , Factores de Riesgo , Fumar/efectos adversos , Factores Socioeconómicos , Encuestas y Cuestionarios , Pérdida de Diente/etiología
3.
Arthritis Rheum ; 30(1): 88-92, 1987 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-3814200

RESUMEN

Cyclosporine (10 mg/kg/day) and azathioprine (2.5-3 mg/kg/day) were compared for 26 weeks in an open, controlled, randomized study of 24 patients with rheumatoid arthritis. Each treatment group consisted of 12 patients. Those patients who took cyclosporine improved significantly in the 50-foot walk time, circumferences of proximal interphalangeal joints, Ritchie articular index, global assessment by investigator, and grip strength, when compared with baseline findings. In the azathioprine group, there was improvement only in grip strength.


Asunto(s)
Artritis Reumatoide/tratamiento farmacológico , Azatioprina/uso terapéutico , Ciclosporinas/uso terapéutico , Artritis Reumatoide/sangre , Artritis Reumatoide/fisiopatología , Azatioprina/efectos adversos , Ciclosporinas/efectos adversos , Humanos , Proyectos Piloto , Distribución Aleatoria
4.
Kidney Int ; 29(6): 1180-7, 1986 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-3528611

RESUMEN

Cyclosporin A (CyA) and azathioprine (Aza) were compared with respect to renal side effects in an open controlled, randomized study of patients with rheumatoid arthritis. Twelve patients were treated with CyA (mean dose 7.8 +/- 1.2 mg/kg/day) and 12 with azathioprine for 26 weeks. All patients also received prednisolone 5 mg/day. The patients had normal serum creatinine (less than 120 mumoles/liter) and protein-free urine before the trial. CyA increased serum creatinine in nine out of the 11 patients followed for 26 weeks, the mean increase was approximately 50%. Creatinine clearance was reduced by 31%. Mean arterial pressure (MAP) and serum potassium were significantly increased by CyA. Urinary beta 2-microglobulin excretion was significantly increased by CyA, in five of the patients more than ten times. Urinary kallikrein excretion was reduced by more than 50% and urinary albumin excretion was doubled. All these parameters remained normal and unchanged in the azathioprine group. CyA was withdrawn in seven patients after 26 weeks. Urinary beta 2-microglobulin was still increased by 85% nine months after CyA treatment. The other parameters were gradually normalized after three to nine months except for one patient who developed renal failure. Urinary beta 2-microglobulin excretion was a very sensitive parameter for renal tubular damage in this study.


Asunto(s)
Artritis Reumatoide/tratamiento farmacológico , Ciclosporinas/efectos adversos , Enfermedades Renales/inducido químicamente , Albuminuria/inducido químicamente , Aldosterona/sangre , Azatioprina/farmacología , Presión Sanguínea/efectos de los fármacos , Ciclosporinas/sangre , Humanos , Calicreínas/orina , Enfermedades Renales/patología , Enfermedades Renales/fisiopatología , Pruebas de Función Renal , Potasio/sangre , Renina/sangre , Microglobulina beta-2/sangre , Microglobulina beta-2/orina
6.
Scand J Rheumatol ; 15(1): 37-40, 1986.
Artículo en Inglés | MEDLINE | ID: mdl-3515526

RESUMEN

Twenty-nine adult rheumatic patients who were taking 500 mg naproxen at bedtime and had a certain degree of morning stiffness despite this medication took part in a randomized double-blind cross-over study in which the duration of morning stiffness after evening doses of 500 mg enteric-coated naproxen tablets was compared with that after identical doses of plain naproxen tablets. The duration of morning stiffness was significantly shorter after taking enteric-coated tablets (p less than 0.01), and the mean plasma naproxen morning concentration was 34% higher (p = 0.01). Since the results were unambiguous in such a small group of patients, they are judged to be of considerable clinical value.


Asunto(s)
Artritis Reumatoide/fisiopatología , Naproxeno/administración & dosificación , Adulto , Anciano , Artritis Reactiva/fisiopatología , Ritmo Circadiano , Ensayos Clínicos como Asunto , Método Doble Ciego , Elasticidad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Naproxeno/sangre , Cooperación del Paciente , Distribución Aleatoria , Comprimidos , Comprimidos Recubiertos , Tiempo , Factores de Tiempo
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