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. 2016 Sep;24(9):1955-61.
doi: 10.1002/oby.21533.

Low adoption of weight loss medications: A comparison of prescribing patterns of antiobesity pharmacotherapies and SGLT2s

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Low adoption of weight loss medications: A comparison of prescribing patterns of antiobesity pharmacotherapies and SGLT2s

Catherine E Thomas et al. Obesity (Silver Spring). 2016 Sep.

Abstract

Objective: To characterize the adoption of antiobesity pharmacotherapies, as compared with that of the newest antidiabetes pharmacotherapy, subtype 2 sodium-glucose transport protein inhibitors (SGLT2s), among prescribers in the United States.

Methods: A retrospective analysis of 2012 to 2015 data extracted from the IMS Health National Prescription Audit™ and Xponent™ assessed adoption rates of antiobesity pharmacotherapies and SGLT2s.

Results: The number of dispensed antidiabetes prescriptions was 15 times the number of dispensed antiobesity prescriptions. The antiobesity market share was: 74.0% phentermine, 18.6% new antiobesity pharmacotherapies. The mean increase in prescriptions/month were: 25,259 for SGLT2s, 5,154 for new antiobesity pharmacotherapies, and 2,718 for phentermine. Medical specialties prescribing the majority of the analysis medications were Family Medicine/General Practice and Internal Medicine. Endocrinology had the highest prevalence of prescribers of any subspecialty.

Conclusions: The adoption rate of SGLT2s was nearly exponential, while the adoption rate of new antiobesity pharmacotherapies was linear. Considering the relative prevalence of obesity to diabetes and that obesity is a major cause of diabetes, these results are paradoxical and suggest systematic barriers against the prescribing of antiobesity pharmacotherapies. The under-prescribing of antiobesity pharmacotherapies is widely acknowledged, but this is the first prescription data of these new medications to demonstrate its extent in the United States.

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Figures

Figure 1
Figure 1
Prevalence of obesity and diabetes and pharmacotherapy utilization of antiobesity pharmacotherapies and antidiabetes pharmacotherapies. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com.]
Figure 2
Figure 2
Volumes of dispensed prescriptions of all antiobesity pharmacotherapies, all antidiabetes pharmacotherapies (excluding insulin), and SGLT2s. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com.]
Figure 3
Figure 3
Volumes of dispensed prescriptions of phentermine, new antiobesity pharmacotherapies, and SGLT2s. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com.]

Comment in

References

    1. Ogden CL, Carroll MD, Kit BK, Flegal KM. Prevalence of childhood and adult obesity in the United States, 2011–2012. JAMA. 2014;311:806–814. - PMC - PubMed
    1. Eckel RH, Grundy SM, Zimmet PZ. The metabolic syndrome. Lancet. 2005;365:1415–1428. - PubMed
    1. Samaranayake NR, Ong KL, Leung RY, Cheung BM. Management of obesity in the NHANES, 2007–2008. Ann Epidemiol. 2012;22:349–353. - PubMed
    1. Xia Y, Kelton CM, Guo JJ, Bian B, Heaton PC. Treatment of obesity: Pharmacotherapy trends in the United States from 1999 to 2010. Obesity (Silver Spring) 2015;23:1721–1728. - PubMed
    1. National Center for Health Statistics. Health, United States, 2014. Hyattsville, MD: U.S. Department of Health and Human Services; 2015. p. 165.

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