Kravitz RL. Direct-to-Consumer Advertising of Androgen Replacement Therapy. JAMA. 2017;317(11):1124-1125. Direct-to-Consumer Advertising of Androgen Replacement Therapy
Ads promoting androgen replacement therapy for testosterone deficiency emphasized the high prevalence of subnormal testosterone values in men older than 45 years and implicitly promised better quality of life and improved performance “in the boardroom and the bedroom.”
Until 2012, direct-to-consumer advertising (DTCA) of androgen replacement therapy emphasized nonbranded “disease awareness” spots urging middle-aged men to consult their physicians for common symptoms (eg, fatigue) that might be the result of “low T.” After that time, ads for branded products, such as for Androgel and Axiron, became more common. The industry’s campaign was startlingly effective.
In this issue of JAMA, Layton and colleagues provide evidence that in the period between 2009 and 2013, DTCA of androgen replacement therapy was associated with an increase in new testosterone testing, new testosterone initiation, and, in a departure from existing guidelines, testosterone initiation without prior testing. Direct-to-Consumer Advertising and Testosterone Testing and Initiation
If anything, nonbranded “condition awareness” ads for “low T” were more powerful motivators than ads promoting Androgel and Axiron. By merging data on DTCA exposure (using Nielson ratings in 75 communities) and a large commercial claims database, the authors estimated that 1 additional exposure to an androgen replacement therapy television advertisement was associated with 14 new tests, 5 new initiations, and 2 initiations without testing per 1 million men exposed.
The study used an ecological time-series design, and the results were sensitive to the length of the “lag period” imposed between exposure to androgen replacement therapy–related DTCA at the regional level and testosterone testing and initiation. Nevertheless, the data are consistent with what is known about DTCA in general: patients respond to DTCA and physicians respond to patients.
Whether DTCA improves or worsens the health of the public depends on the balance among 4 factors:
(1) prevalence of the condition in the population targeted by advertising;
(2) diagnostic accuracy in community practice;
(3) prognosis (expected clinical course of the target condition, either with no treatment or with the best available alternative treatment); and
(4) effectiveness and safety of the advertised product.
Ads promoting androgen replacement therapy for testosterone deficiency emphasized the high prevalence of subnormal testosterone values in men older than 45 years and implicitly promised better quality of life and improved performance “in the boardroom and the bedroom.”
Until 2012, direct-to-consumer advertising (DTCA) of androgen replacement therapy emphasized nonbranded “disease awareness” spots urging middle-aged men to consult their physicians for common symptoms (eg, fatigue) that might be the result of “low T.” After that time, ads for branded products, such as for Androgel and Axiron, became more common. The industry’s campaign was startlingly effective.
In this issue of JAMA, Layton and colleagues provide evidence that in the period between 2009 and 2013, DTCA of androgen replacement therapy was associated with an increase in new testosterone testing, new testosterone initiation, and, in a departure from existing guidelines, testosterone initiation without prior testing. Direct-to-Consumer Advertising and Testosterone Testing and Initiation
If anything, nonbranded “condition awareness” ads for “low T” were more powerful motivators than ads promoting Androgel and Axiron. By merging data on DTCA exposure (using Nielson ratings in 75 communities) and a large commercial claims database, the authors estimated that 1 additional exposure to an androgen replacement therapy television advertisement was associated with 14 new tests, 5 new initiations, and 2 initiations without testing per 1 million men exposed.
The study used an ecological time-series design, and the results were sensitive to the length of the “lag period” imposed between exposure to androgen replacement therapy–related DTCA at the regional level and testosterone testing and initiation. Nevertheless, the data are consistent with what is known about DTCA in general: patients respond to DTCA and physicians respond to patients.
Whether DTCA improves or worsens the health of the public depends on the balance among 4 factors:
(1) prevalence of the condition in the population targeted by advertising;
(2) diagnostic accuracy in community practice;
(3) prognosis (expected clinical course of the target condition, either with no treatment or with the best available alternative treatment); and
(4) effectiveness and safety of the advertised product.
