Experiment 69636

Details

PropertyValue
Pharmacology
Administration routeORAL
OrganismEphedra sinica (EPHEDRACEAE)
CitationSHEKELLE,PG: HARDY,ML: MORTON,SC: MAGLIONE,M: MOJICA,WA: SUTTORP,MJ: RHODES,SL: JUNGVIG,L: GAGNE,J:. (2003). EFFICACY AND SAFETY OF EPHEDRA AND EPHEDRINE FOR WEIGHT LOSS AND ATHLETIC PERFORMANCE.. 289(12)
Amount utilized
Compound isolated
DiseaseFOR ATHLETIC PERFORMANCE IS INSUFFICIENT. USE OF EPHEDRA OR EPHEDRINE AND CAFFEINE IS ASSOCIATED WITH INCREASED RISK OF PSYCHIATRIC, AUTONOMIC, OR GASTROINTESTINAL SYMPTOMS AND HEART PALPITATIONS. DOCUMENTED TO ALLOW MEANINGFUL ASSESSMENT. EPHEDRINE AND EPHEDRA PROMOTE MODEST SHORT TRM WT. LOSS (APPROX 0.9 KG/MO MORE THAN PLACEBO) IN CLINICAL TRIALS. THERE ARE NO DATA REGARDING LONG TERM WT. LOSS, AND EVIDENCE TO SUPPORT USE OF EPHEDRA OF PSYCHIATRIC, AUTONOMIC, OR GASTROINTESTINAL SYMPTOMS, AND HEART PALPITATIONS. DATA ARE INSUFFICIENT TO DRAW CONCLUSIONS ABOUT ADVERSE EVENTS OCCURING AT A RATE LESS THAN 1.0 PER THOUSAND. THE MAJORITY OF CASE REPORTS ARE INSUFFICIENTLY SUBSTANTIALLY ALTER THE LATTER 3 RESULTS. NO TRIALS OF EPHEDRA AND ATHELITC PERFORMANCE WERE FOUND; 7 TRIALS OF EPHEDRINE WERE TOO HETEROGENEOUS TO SYNTHESIZE. SAFETY DATA FROM 50 TRIALS YIELDED ESTIMATES OF 2.2 TO 3.6 FOLD INCREASES IN ODDS EPHEDRA(N=1), AND EPHEDRA AND HERB CONTAINING CAFFEINE(N=4) YIELDED ESTIMATES OF WT. LOSS (MORE THAN PLACEBO) OF 0.6(95% CONFIDENCE INTERVAL,0.2-1.0),1.0(0.7-1.3), 0.8(0.4-1.2), AND 1.0(0.6-1.3)KG/MO, RESPECTIVELY. SENSITIVITY ANALYSES DID NOT TRIALS AND 65 CASE REPORTS WERE INCLUDED IN THE ADVERSE EVENT ANALYSIS. NO WT. LOSS TRIAL ASSESSED DURATION OF TREATMENT GREATER THAN 6 MONTHS. POOLED RESULTS FOR TRIALS COMPARING PLACEBO WITH EPHEDRINE(N=5), EPHEDRINE AND CAFFEINE(N=12), THAT EPHEDRA OR EPHEDRINE WAS CONSUMED WITHIN 24 HRS PRIOR TO AN ADVERSE EVENT OR THAT EPHEDRINE OR AN ASSOCIATED PRODUCT WAS FOUND IN BLOOD OR URINE, AND THAT OTHER POTENTIAL CAUSES HAD BEEN EXCLUDED. OF THE 530 ARTICLES SCREENED, 52 CONTROLLED AND CASE REPORTS OF ADVERSE EVENTS ASSOCIATED WITH SUCH USE. ELIGIBLE STUDIES FOR WT. LOSS WERE HUMAN STUDIES WITH AT LEAST 8 WKS OF FOLLOW-UP; AND FOR ATHLETIC PERFORMANCE, THOSE HAVING NO MINIMUM FOLLOW-UP. ELIGIBLE CASE REPORTS DOCUMENTED A META-ANALYSIS TO ASSESS THE DATA ON EFFICACY AND SAFETY OF EPHEDRA AND EPHEDRINE USED FOR WT. LOSS AND ENHANCED ATHLETIC PERFORMANCE. ELIGIBLE STUDIES WERE CONTROLLED TRIALS OF EPHEDRA OR EPHEDRINE USED FOR WT. LOSS OR ATHLETIC PERFORMANCE
Dose amountVAR
Number3
Qualitative resultACTIVE
AnimalHUMAN ADULT
Dose expressionDOSE
ExtractTYPE EXT NOT STATED
GenderGIVEN TO BOTH SEXES