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1.
Semin Arthritis Rheum ; 50(2): 209-219, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-31521376

RESUMO

OBJECTIVES: To conduct a systematic review and longitudinal meta-analysis of early rheumatoid arthritis (RA) cohorts with long-term data on pain, fatigue or mental well-being. METHODS: Searches using PUBMED, EMBASE and PyscInfo were performed to identify all early RA cohorts with longitudinal measures of pain, fatigue or mental well-being, along with clinical measures. Using longitudinal meta-analyses, the progression of each outcome over the first 60-months was estimated. Cohorts were stratified based on the median recruitment year to investigate secular trends in disease progression. RESULTS: Of 7,319 papers identified, 75 met the inclusion criteria and 46 cohorts from 41 publications provided sufficient data on 18,046 patients for meta-analysis. The Disease Activity Scores (DAS28) and the Short-Form 36 (SF-36) Physical Component Score (PCS) indicated that post-2002 cohorts had statistically significant improvements over the first 60-months compared to pre-2002 cohorts, with standardised mean differences (SMD) of 0.86 (95% Confidence Intervals 0.34 to 1.37) and 0.76 (95% CI 0.25 to 1.27) respectively at month-60. However, post-2002 cohorts indicated statistically non-significant improvements in pain, fatigue, functional disability and SF-36 Mental Component Score (MCS) compared to pre-2002 cohorts, with SMD of 0.24 (95% CI -0.25 to 0.74), 0.38 (95% CI -0.11 to 0.88), 0.34 (95% CI -0.15-0.84) and -0.08 (95% CI -0.41 to 0.58) at month-60 respectively. CONCLUSIONS: Recent cohorts indicate improved levels of disease activity and physical quality of life, however this has not translated into similar improvements in levels of pain, fatigue and functional disability by 60-months.


Assuntos
Artrite Reumatoide/psicologia , Progressão da Doença , Fadiga/etiologia , Artrite Reumatoide/fisiopatologia , Artrite Reumatoide/terapia , Fadiga/psicologia , Feminino , Humanos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Medição da Dor/métodos , Desempenho Físico Funcional , Qualidade de Vida , Índice de Gravidade de Doença , Inquéritos e Questionários
6.
Phytother Res ; 16(1): 80-3, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11807973

RESUMO

Garcinia cambogia extract is a herbal preparation that has been suggested as useful in the treatment of gastrointestinal disorders. In the present study this drug was tested for its antiulcerogenic effect. Oral pretreatment with Garcinia cambogia fruit extract (1 g/kg body wt/day) for 5, 10 or 15 days protected the gastric mucosa against the damage induced by indomethacin (20 mg/kg body wt). The volume and acidity of the gastric juice decreased in the pretreated rats. The glycoprotein levels of the gastric contents which were decreased in the untreated rats, maintained near normal levels in the pretreated rats. Protein which was elevated in the gastric juice of untreated rats, showed near normal levels in the pretreated rats. Garcinia cambogia was able to decrease the acidity and to increase the mucosal defence in the gastric areas, thereby justifying its use as an antiulcerogenic agent.


Assuntos
Antiulcerosos/farmacologia , Garcinia cambogia , Úlcera Péptica/tratamento farmacológico , Fitoterapia , Extratos Vegetais/farmacologia , Animais , Antiulcerosos/uso terapêutico , Frutas/química , Determinação da Acidez Gástrica , Mucosa Gástrica/efeitos dos fármacos , Glicoproteínas/metabolismo , Indometacina/toxicidade , Masculino , Úlcera Péptica/induzido quimicamente , Extratos Vegetais/uso terapêutico , Proteínas/metabolismo , Ratos , Ratos Wistar
7.
Indian J Exp Biol ; 40(1): 58-62, 2002 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12561970

RESUMO

Oral pretreatment of rats with G. cambogia fruit extract (1 g/kg body weight/day at interval of 7 and 15 days) protected gastric mucosa against HCl-ethanol induced damage by decreasing the volume and acidity of gastric juice. Increased lipid peroxidation, decreased activity of antioxidant enzymes, altered levels of protein and glycoproteins in the ulcerated mucosa, and gastric juice were maintained at near normal levels in G. cambogia pretreated rats. The results suggest the anti-ulcer activity of G. cambogia by virtue of its ability to decrease acidity and increase mucosal defense.


Assuntos
Antiulcerosos/uso terapêutico , Frutas/química , Garcinia cambogia , Úlcera Péptica/prevenção & controle , Fitoterapia , Extratos Vegetais/uso terapêutico , Animais , Etanol/toxicidade , Determinação da Acidez Gástrica , Mucosa Gástrica/efeitos dos fármacos , Glicoproteínas/metabolismo , Ácido Clorídrico/toxicidade , Masculino , Úlcera Péptica/induzido quimicamente , Ratos , Ratos Wistar
8.
Indian J Physiol Pharmacol ; 45(3): 345-50, 2001 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11881574

RESUMO

Dexamethasone (10 mg/kg body weight/day, s.c.) administered rats were treated with or without Garcinia cambogia fruit extract (1 g/kg body weight/day, orally) for 8 days. The administration of dexamethasone resulted in marked increase in the levels of triglycerides and cholesterol and free acids in both plasma and liver. The level of phospholipids increased in the plasma but decreased significantly in liver tissue after dexamethasone administration as compared to those in normal rats. The activities of lecithin cholesterol acyl transferase and hepatic lipoprotein lipase were lowered significantly after dexamethasone per se administration. The levels of HDL-triglycerides and HDL-cholesterol remained unchanged, while the LDL and VLDL increased significantly in dexamethasone administered rats. The lipid levels were maintained at near normalcy when co-treated with Garcinia cambogia extract in dexamethasone administered rats. This study reveals the undesirable changes in lipid profile on dexamethasone administration and the hypolipidemic property of Garcinia cambogia extract.


Assuntos
Anti-Inflamatórios/farmacologia , Dexametasona/farmacologia , Garcinia/química , Lipídeos/sangue , Lipoproteínas/sangue , Animais , Peso Corporal/efeitos dos fármacos , Colesterol/sangue , Ácidos Graxos não Esterificados/sangue , Masculino , Tamanho do Órgão/efeitos dos fármacos , Fosfolipídeos/sangue , Extratos Vegetais/farmacologia , Ratos , Triglicerídeos/sangue
9.
Adv Biosci ; 9: 507-13, 1973.
Artigo em Inglês | MEDLINE | ID: mdl-4805861

RESUMO

PIP: This study determines the efficacy of extraamniotic administration of prostaglandins E2 and F2alpha (PGE2 and PGF2alpha) in abortion induction. The method consists of introducing a Foley catheter (14 gauge) through the cervix with the aid of a speculum so that the inflated balloon lies just within the internal os. The balloon volume varies from 30 ml at 12 weeks to 40 ml at 16 weeks gestation and over. Following an initial test dose, a fully effective dose of 200 mcg PGE2 or 750 mcg PGF2alpha is instilled for diffusion into the extraovular space; this dose is repeated at 2 hourly intervals. An automatic pump may also be used to administer the PG. The pattern of uterine contractility with this method is similar to that seen with intravenous therapy. Of 163 consecutive cases analyzed, 144 (88%) achieved abortions within 36 hours, 72% aborted within 24 hours and 94% within 48 hours. Mean abortion time was 22.2 hours. No significant difference was seen in the success rate or abortion time between 21 patients in their 1st trimester of pregnancy and 142 patients in the 2nd trimester. In primigravidas, abortion (within 36 hours) was successful in 87% of the cases; mean abortion time was 24.0 hours. Multigravidas had higher success rate (90%) and shorter mean abortion time (20.4 hours). Comparison of results obtained separately with PGF2alpha and PGE2 shows the superiority of PGE2. Of 93 patients receiving PGF2alpha, 85% aborted within 36 hours (mean abortion time, 24.9 hours). Of 70 PGE2-treated patients, 93% aborted within 36 hours (p=.01) (mean abortion time, 19.4 hours). When parity was considered, PGE2 came out superior again over PGF2alpha. In primigravidas, only 84% of PGF2alpha-treated patients had abortion within 36 hours compared to 90% for PGE2-treated patients. In multigravidas, the success rates at 36 hours were 86% for PGF2alpha and 95% for PGE2. Side effects were minimal. In another trial, intravenous oxytocin was used in addition to extraamniotic PG, resulting in a very substantial decrease in mean abortion time. This method is a simple, effective abortion technique which can be carried out in most cases on a 24-hour basis.^ieng


Assuntos
Aborto Induzido , Ocitocina/uso terapêutico , Prostaglandinas/uso terapêutico , Administração Tópica , Diarreia/induzido quimicamente , Relação Dose-Resposta a Droga , Sinergismo Farmacológico , Feminino , Febre/induzido quimicamente , Humanos , Gravidez , Prostaglandinas/efeitos adversos , Prostaglandinas E/uso terapêutico , Prostaglandinas F/uso terapêutico , Fatores de Tempo , Útero , Vômito/induzido quimicamente
10.
Br Med J ; 3(5819): 146-9, 1972 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-5039777

RESUMO

The use of prostaglandins E(2) and F(2)alpha, administered by extra-amniotic instillation, for the induction of abortion was studied in 94 patients in the first and second trimesters of pregnancy. Abortion was successfully induced in 87% of patients within 36 hours and in 94% within 48 hours. The mean abortion time was 22.4 hours. In 60% of patients abortion was complete.Though the differences were not statistically significant, on average multigravid patients aborted more quickly than primigravidae, while the mean abortion time in PGE(2)-treated patients was less than in those receiving PGF(2)alpha.No serious complications occurred. Some side effects were observed. Occasional vomiting was the commonest symptom but the incidence of side effects was lower than with alternative routes of administration. A leucocytosis was often noted but there were no significant instances of infection.The method has proved a safe and effective means of terminating pregnancies in the second trimester.


Assuntos
Aborto Induzido , Prostaglandinas/uso terapêutico , Líquido Amniótico , Cateterismo , Diarreia/etiologia , Estudos de Avaliação como Assunto , Feminino , Humanos , Leucocitose/induzido quimicamente , Métodos , Paridade , Gravidez , Prostaglandinas/administração & dosagem , Prostaglandinas/efeitos adversos , Fatores de Tempo , Útero/efeitos dos fármacos , Vômito/induzido quimicamente
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