INTRODUCTION
Affecting 85-100% of the world’s population at some
time in their lives, acne vulgaris has been treated with
long-term courses of antibiotics since the 1960s.1,2 The
pathogenesis of this extremely common condition consists
of four main processes, including: an androgen-stimulated
increase in sebum production; creation of a microcomedo
through follicular hyperkeratinization; proliferation of propionibacteria
(mainly Propionibacterium acnes [P. acnes]) within
the sebaceous follicle; and inflammation.2 Antibiotics reduce
inflammation as well as target propionibacteria residing in the
hair follicle. When the efficacy of antibiotic treatment for acne
was first established, it was believed that cutaneous propionibacteria
were incapable of becoming resistant, as a resistant
organism could not be detected at that time.1 This belief was
shattered by the first documentation of antibiotic-resistant propionibacteria
in acne patients in 1979. This report indicated that
one in five patients being treated topically with erythromycin or
clindamycin in the United States (U.S.) had antibiotic resistant
strains on their skin.3 Similar reports surfaced globally.4
Over 20 years later, the problem of antibiotic resistance has
grown. Eco-responsible practice encompasses considering the worldwide problem of antibiotic resistance, the impact prescribing
antibiotics can have with every treatment decision and prescribing
the antibiotics only if the benefits outweigh the risks—
including the risk of resistance—and only for the treatment
duration necessary for these benefits. The aim of this study was
to assess the trends in prescribing antibiotics for acne from
1997−2006. Additionally, using current treatment guidelines
and recommendations from the literature for prevention of antimicrobial
resistance, the authors offer suggestions for a more
eco-responsible approach to treating acne vulgaris.
METHODS
The National Ambulatory Medical Care Survey (NAMCS)
database was analyzed for trends in prescriptions for acne
vulgaris from 1997−2006. The NAMCS collects nationwide
outpatient data from U.S. non-federally employed physicians
and uses a multi-stage probability design with the primary
sampling unit consisting of the physician office visit. The
NAMCS uses the term drug “mention†to include medications
that are either discussed by the physician and patient,
currently taken by the patient, administered in office, or prescribed
by the physician. For the purposes of this analyses,
the authors assume that a mention refers to a new prescrip-