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1.
J Am Pharm Assoc (2003) ; 53(3): 297-303, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23699678

RESUMO

OBJECTIVE: To characterize the types of drug and dietary supplement inquiries submitted to the National Center for Drug Free Sport through the Resource Exchange Center (REC). DESIGN: Cross-sectional study. SETTING: United States, from July 2009 through June 2010. PARTICIPANTS: Athletes and athletic personnel associated with the National Collegiate Athletic Association (NCAA). INTERVENTION: Tabulation and classification of drugs and dietary supplement inquiries. MAIN OUTCOME MEASURE: Characteristics and trends of drug and dietary supplement inquiries. RESULTS: Inquiries for prescription medications for albuterol inhalers, methylphenidate, amphetamines, and prednisone were the most common using a drug lookup function. The most common inquiries for over-the-counter medications included pseudoephedrine, loratadine, cetirizine, and caffeine. Among dietary supplements, inquiries for amino acids/metabolites, vitamins and minerals, and herbal products occurred most frequently. One dietary supplement, N.O.-Xplode (Bio-Engineered Supplements and Nutrition, Inc.), accounted for the majority of individual dietary supplement inquiries. Banned substances accounted for 30% of all inquiries submitted to the REC and 18% of medications searched in a drug lookup database. CONCLUSION: Almost 25,000 inquiries were submitted to the REC. Pharmacists can use this information to advise, counsel, and refer NCAA athletes regarding the use of banned and permitted substances. Education programs regarding stimulants, dietary supplements, and the risk of using substances such as animal byproducts are needed, and pharmacists can participate in these programs.


Assuntos
Atletas , Suplementos Nutricionais , Dopagem Esportivo , Preparações Farmacêuticas/administração & dosagem , Estudos Transversais , Bases de Dados Factuais/estatística & dados numéricos , Serviços de Informação sobre Medicamentos/estatística & dados numéricos , Feminino , Humanos , Masculino , Assistência Farmacêutica/organização & administração , Farmacêuticos/organização & administração , Papel Profissional , Estudantes , Estados Unidos , Universidades
2.
Sports Health ; 2(1): 12-8, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23015919

RESUMO

BACKGROUND: In the United States, the National Center for Drug Free Sport manages the drug-testing programs for athletes of the National Collegiate Athletic Association (NCAA). Through its Resource Exchange Center (REC), Drug Free Sport supports athletic staff and athletes with information regarding drugs and dietary supplements. PURPOSE: To characterize the types of drug-related and dietary supplement-related inquiries submitted to Drug Free Sport through the REC. STUDY DESIGN: Cross-sectional study. METHODS: All inquiries submitted to the REC for the period of September 1, 2005, through June 30, 2006, were reviewed. The data were categorized by the method of inquiry submission; the name of the substance in question; the sex, sport, and NCAA division of the athlete involved; the nature of the inquiry; and the response provided by the REC regarding the NCAA's status of the substance in question. RESULTS: Pseudoephedrine, acetaminophen/hydrocodone, and albuterol were the most commonly self-searched medications; stimulants accounted for the majority of banned medications. Dietary supplements accounted for 80% of all inquiries submitted to the REC via the Banned Drug Inquiry Form. Among all dietary supplements, creatine was the most commonly inquired. Banned substances accounted for 29% of all inquiries. CONCLUSIONS: There were more than 10 000 inquiries regarding the status of medications, dietary supplements, and other substances for NCAA athletes during the 2005-2006 academic year. It is helpful for athletes to have resources that help them navigate banned-substance lists and so avoid the inadvertent use of banned substances. CLINICAL RELEVANCE: Educating athletes regarding the stimulant content of various dietary supplements and addressing the lack of clinical trials to support stated claims and safety appear critical.

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