INTRODUCTION
Requests for cosmetic treatment of facial lines have become common in developed countries,1 including the use of minimally invasive therapies such as botulinum
toxin A (BoNT-A). Indeed, BoNT-A treatment has become a mainstay of the modern treatment approach, with applications extending from the smoothing of glabellar lines to a wide range of aesthetic facial treatments.2 However, despite the increasing numbers of patient undergoing BoNT-A treatment, there is currently
no standardized, objective measure available to assess whether treatment is successful and meets with patient expectations;
outcomes are typically measured using subjective patient
satisfaction scores. This has implications for the consent process. For any consent to be valid, a key requirement is that the patient is sufficiently informed as to the potential risks and benefits of treatment.3 Under the current system, patients are not provided with an objective assessment of the likely cosmetic effects
of their treatment, which precludes this criterion being met.
To overcome this shortfall, it could be reasoned that a treatment
goal should be set and agreed to by every patient before treatment, and treatment success should be measured and assessed
against this target. This will not only allow patients to better assess whether they wish to continue with treatment, but also has the potential to provide practitioners with valuable information on how effectively the treatment is working in individual
patients. It may also provide information to allow doses to be tailored accordingly in successive treatments.
The Treat-to-Goal (TTG) approach described in this paper sets objectively defined start points and treatment goals for BoNT-A treatment, utilizing the Merz Aesthetics Scale,4-11 in an attempt to provide a standardized means of establishing patient expectations
and measuring treatment success as an integral part of the consent process. The aim of this study is to evaluate the TTG approach against standard consent procedures to compare
their utility in providing patients with information on the risks and benefits of treatment, the likely outcome of treatment, and overall satisfaction with the consent process.
METHODS
Standard consent and the TTG approach were defined as shown in Table 1. The only difference in the 2 approaches is the incorporation in the TTG approach of a wrinkle severity score before treatment and the definition of the target severity score