Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
1.
Semin Arthritis Rheum ; 50(2): 209-219, 2020 04.
Article in English | MEDLINE | ID: mdl-31521376

ABSTRACT

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.


Subject(s)
Arthritis, Rheumatoid/psychology , Disease Progression , Fatigue/etiology , Arthritis, Rheumatoid/physiopathology , Arthritis, Rheumatoid/therapy , Fatigue/psychology , Female , Humans , Longitudinal Studies , Male , Middle Aged , Pain Measurement/methods , Physical Functional Performance , Quality of Life , Severity of Illness Index , Surveys and Questionnaires
6.
Phytother Res ; 16(1): 80-3, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11807973

ABSTRACT

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.


Subject(s)
Anti-Ulcer Agents/pharmacology , Garcinia cambogia , Peptic Ulcer/drug therapy , Phytotherapy , Plant Extracts/pharmacology , Animals , Anti-Ulcer Agents/therapeutic use , Fruit/chemistry , Gastric Acidity Determination , Gastric Mucosa/drug effects , Glycoproteins/metabolism , Indomethacin/toxicity , Male , Peptic Ulcer/chemically induced , Plant Extracts/therapeutic use , Proteins/metabolism , Rats , Rats, Wistar
7.
Indian J Exp Biol ; 40(1): 58-62, 2002 Jan.
Article in English | MEDLINE | ID: mdl-12561970

ABSTRACT

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.


Subject(s)
Anti-Ulcer Agents/therapeutic use , Fruit/chemistry , Garcinia cambogia , Peptic Ulcer/prevention & control , Phytotherapy , Plant Extracts/therapeutic use , Animals , Ethanol/toxicity , Gastric Acidity Determination , Gastric Mucosa/drug effects , Glycoproteins/metabolism , Hydrochloric Acid/toxicity , Male , Peptic Ulcer/chemically induced , Rats , Rats, Wistar
8.
Indian J Physiol Pharmacol ; 45(3): 345-50, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11881574

ABSTRACT

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.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Dexamethasone/pharmacology , Garcinia/chemistry , Lipids/blood , Lipoproteins/blood , Animals , Body Weight/drug effects , Cholesterol/blood , Fatty Acids, Nonesterified/blood , Male , Organ Size/drug effects , Phospholipids/blood , Plant Extracts/pharmacology , Rats , Triglycerides/blood
9.
Adv Biosci ; 9: 507-13, 1973.
Article in English | MEDLINE | ID: mdl-4805861

ABSTRACT

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


Subject(s)
Abortion, Induced , Oxytocin/therapeutic use , Prostaglandins/therapeutic use , Administration, Topical , Diarrhea/chemically induced , Dose-Response Relationship, Drug , Drug Synergism , Female , Fever/chemically induced , Humans , Pregnancy , Prostaglandins/adverse effects , Prostaglandins E/therapeutic use , Prostaglandins F/therapeutic use , Time Factors , Uterus , Vomiting/chemically induced
10.
Br Med J ; 3(5819): 146-9, 1972 Jul 15.
Article in English | MEDLINE | ID: mdl-5039777

ABSTRACT

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.


Subject(s)
Abortion, Induced , Prostaglandins/therapeutic use , Amniotic Fluid , Catheterization , Diarrhea/etiology , Evaluation Studies as Topic , Female , Humans , Leukocytosis/chemically induced , Methods , Parity , Pregnancy , Prostaglandins/administration & dosage , Prostaglandins/adverse effects , Time Factors , Uterus/drug effects , Vomiting/chemically induced
SELECTION OF CITATIONS
SEARCH DETAIL
...