Polypharmacy among anabolic-androgenic steroid users: a descriptive metasynthesis.

Dominic Sagoe, Jim McVeigh, Astrid Bjørnebekk, Marie-Stella Essilfie, Cecilie Schou Andreassen, Ståle Pallesen

Journal: Substance abuse treatment, prevention, and policy 2015;10():12

PMID: 25888931

Abstract

BACKGROUND

As far as we are aware, no previous systematic review and synthesis of the qualitative/descriptive literature on polypharmacy in anabolic-androgenic steroid(s) (AAS) users has been published.

METHOD

We systematically reviewed and synthesized qualitative/descriptive literature gathered from searches in electronic databases and by inspecting reference lists of relevant literature to investigate AAS users' polypharmacy. We adhered to the recommendations of the UK Economic and Social Research Council's qualitative research synthesis manual and the PRISMA guidelines.

RESULTS

A total of 50 studies published between 1985 and 2014 were included in the analysis. Studies originated from 10 countries although most originated from United States (n=22), followed by Sweden (n=7), England only (n=5), and the United Kingdom (n=4). It was evident that prior to their debut, AAS users often used other licit and illicit substances. The main ancillary/supplementary substances used were alcohol, and cannabis/cannabinoids followed by cocaine, growth hormone, and human chorionic gonadotropin (hCG), amphetamine/meth, clenbuterol, ephedra/ephedrine, insulin, and thyroxine. Other popular substance classes were analgesics/opioids, dietary/nutritional supplements, and diuretics. Our classification of the various substances used by AAS users resulted in 13 main groups. These non-AAS substances were used mainly to enhance the effects of AAS, combat the side effects of AAS, and for recreational or relaxation purposes, as well as sexual enhancement.

CONCLUSIONS

Our findings corroborate previous suggestions of associations between AAS use and the use of other licit and illicit substances. Efforts must be intensified to combat the debilitating effects of AAS-associated polypharmacy.

Address: Department of Psychosocial Science, University of Bergen, Christiesgate 12, 5015, Bergen, Norway. [email protected].; Centre for Public Health, Liverpool John Moores University, 15-21 Webster Street, Liverpool, L3 2ET, UK. [email protected].; Department of Physical Medicine and Rehabilitation, Unit of Neuropsychology, Oslo University Hospital, Kirkeveien 166, Ullevål, Norway. [email protected].; Departments of Surgery and Paediatrics, La General Hospital, PMB, Accra, Ghana. [email protected].; Department of Psychosocial Science, University of Bergen, Christiesgate 12, 5015, Bergen, Norway. [email protected].; The Competence Centre, Bergen Clinics Foundation, Vestre Torggate 11, 5015, Bergen, Norway. [email protected].; Department of Psychosocial Science, University of Bergen, Christiesgate 12, 5015, Bergen, Norway. [email protected].
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