`
`Management of acne
`
`CMAJ
`
`Key points
`
`• Effective therapies for acne target one or more pathways
`in the pathogenesis of acne, and combination therapy
`gives better results than monotherapy.
`• Topical therapies are the standard of care for mild to
`moderate acne.
`• Systemic therapies are usually reserved for moderate or
`severe acne, with a response to oral antibiotics taking up
`to six weeks.
`• Hormonal therapies provide effective second-line
`treatment in women with acne, regardless of the presence
`or absence of androgen excess.
`
`ing and follicle-stimulating hormone levels.5 Pelvic ultra-
`sonography may show the presence of polycystic ovaries.5 In
`prepubertal children with acne, signs of hyperandrogenism
`include early-onset accelerated growth, pubic or axillary hair,
`body odour, genital maturation and advanced bone age.
`Treatment for acne vulgaris should aim to reduce severity
`and recurrences of skin lesions as well as to improve appear-
`ance. The approach depends on the severity of the acne, the
`treatment preferences and age of the patient, and adherence and
`response to previous therapy (Table 2).3,6 Various acne treat-
`ments target different steps in the pathogenesis of acne, from
`counteracting androgens and decreasing sebum production to
`preventing follicular occlusion, reducing P. acnes proliferation
`and decreasing inflammation.
`Many research studies on acne therapies are small trials
`comparing the active drug with placebo or larger studies com-
`paring different formulations of the same drug.
`
`How well do topical treatments work?
`
`Topical therapy is the standard of care for mild to moderate
`acne.3 Retinoids and antimicrobials such as benzoyl peroxide
`and antibiotics are the mainstay of topical acne therapy. Such
`treatments are active at application sites, and they can prevent
`new lesions.4 The main side effect is local irritation. Gels,
`pledgets (medication-soaked pads), washes and solutions tend
`to be drying and are helpful for oily skin. Lotions, creams and
`ointments are beneficial for dry, easily irritated skin. Most top-
`ical preparations require at least six to eight weeks before an
`improvement is seen; they may be used for years as needed.6
`
`From the Division of Dermatology, University of Toronto, Toronto, Ont.
`CMAJ 2011. DOI:10.1503/cmaj.090374
`
`John Kraft MD, Anatoli Freiman MD
`
`A cne vulgaris has a substantial impact on a patient’s
`
`quality of life, affecting both self-esteem and psychoso-
`cial development.1 Patients and physicians are faced
`with many over-the-counter and prescription acne treatments,
`and choosing the most effective therapy can be confusing.
`In this article, we outline a practical approach to managing
`acne. We focus on the assessment of acne, use of topical
`treatments and the role of systemic therapy in treating acne.
`Acne is an inflammatory disorder of pilosebaceous units
`and is prevalent in adolescence. The characteristic lesions are
`open (black) and closed (white) comedones, inflammatory
`papules, pustules, nodules and cysts, which may lead to scar-
`ring and pigmentary changes (Figures 1 to 4). The pathogene-
`sis of acne is multifactorial and includes abnormal follicular
`keratinization, increased production of sebum secondary to
`hyperandrogenism, proliferation of Propionibacterium acnes
`and inflammation.2,3
`Lesions occur primarily on the face, neck, upper back and
`chest.4 When assessing the severity of the acne, one needs to
`consider the distribution (back, chest, upper arms), type and
`number of lesions (comedones, papules, pustules, nodules) and
`the presence or absence of scarring (Table 1).2,3
`Different variants of acne exist, including acne conglobata,
`acne fulminans, acne mechanica, excoriated acne, chloracne,
`drug-induced acne (e.g., from anabolic steroids, corticos-
`teroids, isoniazid, lithium, phenytoin), neonatal and infantile
`acne, and occupational acne. These variations have a similar
`clinical and histologic appearance to acne vulgaris, but they
`are distinguishable by clinical setting, severity and associated
`symptoms. The common differential diagnosis of acne
`includes folliculitis, keratosis pilaris, peri oral dermatitis, seb-
`orrheic dermatitis and rosacea.
`
`Is there an underlying cause?
`
`The diagnosis of acne vulgaris is primarily clinical.4 History
`and physical examination can help determine if there is an
`underlying cause of the acne, such as an exacerbating medica-
`tion or endocrinologic abnormality causing hyperandro-
`genism (e.g., polycystic ovarian syndrome). Other dermato-
`logic manifestations of androgen excess include seborrhea,
`hirsutism and androgenetic alopecia. Endocrinologic testing is
`not ordered routinely for women with regular menstrual
`cycles.2,3 Older women, especially those with new-onset acne
`and other signs of androgen excess (e.g., hirsutism, andro-
`genic alopecia, menstrual irregularities, infertility), should be
`tested for androgen excess with measurements of total and
`free serum testosterone, dihydro epi androsterone, and luteiniz-
`
`DOI:10.1503/cmaj.090374
`
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`Antimicrobials
`Topical antimicrobials, including benzoyl peroxide and antibi-
`otics, are effective in treating inflammatory disease.3,4 Benzoyl
`peroxide is a bactericidal agent that prevents the resistance of
`P. acnes to antibiotic therapy9 and has moderate comedolytic
`and anti-inflammatory properties. It is available in various top-
`ical preparations, ranging in strength from 2.5% to 10.0%.
`Any strength can be used initially, although it may be more
`prudent to start with a lower concentration; stronger prepara-
`tions are more irritating and not necessarily more effective.10
`Benzoyl peroxide kills P. acnes by releasing oxygen within
`the follicle. It can be fast-acting, with a response as early as
`five days.4 The main drawback is that it is a potent bleaching
`
`Retinoids
`The main target of acne treatment is the microcomedone. Topi-
`cal retinoid therapy acts on follicular keratinocytes to prevent
`excessive cornification and follicular blockage.4 It may also
`reduce the release of proinflammatory cytokines. Such therapy
`decreases the number of comedones and inflammatory lesions
`by 40% to 70%.2 The most common side effect is irritation with
`erythema and scaling. Patients should be instructed to apply
`very small amounts initially. Optimal response occurs after 12
`weeks.7 Continuous maintenance therapy can prevent flares.3
`The most commonly available topical retinoids are
`tretinoin, adapalene and tazarotene. A meta-analysis of five
`multicentre randomized investigator-blind trials involving
`900 patients showed adapalene 0.1% gel to be as effective as,
`but less irritating than, tretinoin 0.025% gel.8 Different con-
`centrations of retinoids affect tolerability. One commonly
`used approach is to start with the lowest concentration and
`increase as tolerated.
`
`Figure 1: Grade I (mild) acne showing comedones with few
`inflammatory papules and pustules.
`
`Figure 3: Grade III (moderately severe) acne showing numer-
`ous large painful nodules and pustules as well as some
`inflamed nodules.
`
`Figure 2: Grade II (moderate) acne showing papules and pustules.
`
`Figure 4: Grade IV (severe) acne showing many large inflamed
`nodules and pustules as well as scarring.
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`agent.2 Patients should be warned that fabrics that come in
`contact with benzoyl peroxide, including towels, bed sheets
`and clothing, may be bleached.
`Topical erythromycin and clindamycin are generally well-
`tolerated and have been shown to reduce inflammatory lesions
`by 46% to 70% in several randomized controlled trials.2
`Monotherapy with topical antibiotics should not be used rou-
`tinely beause P. acnes may become resistant within one month
`after daily treatment has begun.6 Some argue that this resis-
`tance is not relevant because the antibiotics (e.g., clindamycin,
`tetracyclines, erythromycin) also have intrinsic anti-inflamma-
`tory and antimicrobial effects.11 However, antibiotic-resistant
`Staphylococcus epidermidis and Staphylococcus aureus may
`also develop with monotherapy; resistance can be avoided
`when a topical antibiotic is combined with benzoyl peroxide.12
`
`Combination therapy
`Combination therapy, for example with retinoids and antibi-
`otics, is more effective than either agent used alone.13 However,
`the agents should be applied at separate times, unless they are
`known to be compatible.3 Benzoyl peroxide may oxidize a
`retinoid such as tretinoin if it is applied simultaneously.14 A 12-
`week randomized controlled trial involving 249 patients with
`mild to moderate acne showed treatment with adapalene gel
`0.1% and clindamycin 1.0% to be superior to that with clin-
`damycin 1.0% used alone.15 If inflammatory lesions are present,
`topical antibiotics containing benzoyl peroxide should be com-
`bined with a topical retinoid (e.g., topical antibiotic with ben-
`zoyl peroxide in the morning and retinoid at night). A review of
`three clinical studies with 1259 patients showed that a combi-
`nation of clindamycin 1% and benzoyl peroxide 5% was more
`effective than either drug used alone in reducing lesions and
`suppressing P. acnes.16
`
`Over-the-counter therapy
`Before seeing a physician, patients frequently use over-the-
`counter therapies for their acne. Such treatments may be more
`accessible, cosmetically elegant, less expensive and less irri-
`tating than pres cription therapies.17 However, there is insuffi-
`cient evidence to evaluate and compare the efficacy of over-
`the-counter formulations.2
`The most popular over-the-counter products, such as Proactiv,
`contain benzoyl peroxide but at lower concentrations than most
`prescription-strength products. Proactiv, a system of cleansing
`products in which benzoyl peroxide 2.5% is the active ingredi-
`ent, is claimed to enhance compliance by providing a cosmeti-
`cally elegant product that also minimizes irritation. The makers
`of Proactiv also market Gentle Formula, which replaces benzoyl
`peroxide with salicylic acid for people with allergy or intoler-
`ance. There have been few studies assessing the efficacy of the
`Proactiv system. In one open-label study of 23 patients with mild
`to moderate acne, inflammatory lesions were reduced by 39% in
`patients using a combination of butenifine (an allylamine) and
`benzoyl peroxide compared with 34% in those using Proactiv.18
`Salicylic acid 2% wash is moderately effective but less
`potent than a topical retinoid in acne therapy. Although it has
`been used for many years, well-designed trials of its safety
`and efficacy are lacking. The evidence for the use of topical
`
`zinc, resorcinol, sulfur and aluminum chloride is also either
`limited or negative.
`There is no clear evidence that acne vulgaris is related to
`poor hygiene or that frequent face washing lessens acne.
`Patients should be instructed to wash their face gently with
`warm water and mild soap twice daily; rough scrubbing can
`cause new lesions because of follicular rupture. The only
`antibacterial soaps that may be effective are those containing
`benzoyl peroxide.19
`Patients should ensure that their facial products, includ-
`ing sunscreens, are noncomedogenic. They should also
`avoid oil-based makeup. Some topical acne products contain
`a sunscreen.
`
`When should systemic therapy be started?
`
`Patients with mild acne can be treated with topical therapies;
`however, those with moderate to severe acne will require sys-
`temic therapy. Oral antibiotic treatment, hormonal therapies
`and iso treretinoin are the mainstay systemic therapies for
`acne.
`
`Antibiotics
`When topical agents are insufficient or not tolerated, or in
`cases of moderate to severe acne, especially when the chest,
`back and shoulders are involved, systemic antibiotics are
`often considered the next line of treatment (Table 3).20,21 How-
`ever, regular use of a combination of topical antibiotics and
`benzoyl peroxide may be similarly effective, as shown in a
`randomized controlled trial of five antimicrobial regimens.22
`Response to oral antibiotics is usually seen after at least six
`weeks of therapy.4 If control is maintained for several months,
`the antibiotic may be discontinued gradually and only the top-
`ical therapy continued. Systemic antibiotics should not be
`used to treat mild acne because of the risk of increasing resis-
`tance.23,24 The additional use of nonantibiotic topical agents in
`combination with oral antibiotics should be considered.4 Topi-
`cal retinoids with oral antibiotics may give a faster response
`and be more effective than either drug used alone.3
`Treatment with tetracyclines and erythromycin reduces P.
`acnes within the follicles, thereby inhibiting production of
`bacterial-induced inflammatory cytokines.25 These agents also
`have inherent anti-inflammatory effects, such as suppressing
`
`Table 1: Grading severity of acne2,3
`
`Grade
`
`Severity
`
`Clinical findings
`
`I
`
`II
`
`III
`
`IV
`
`Mild
`
`Moderate
`
`Moderately
`severe
`
`Severe
`
`Open and closed comedones
`with few inflammatory papules
`and pustules
`Papules and pustules, mainly on
`face
`Numerous papules and pustules,
`and occasional inflamed nodules,
`also on chest and back
`Many large, painful nodules and
`pustules
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`leukocyte chemotaxis and bacterial lipase activity. Minocy-
`cline and doxycycline also inhibit cytokines and matrix met-
`alloproteinases that are thought to promote inflammation and
`tissue breakdown.26 Although P. acnes has a resistance rate to
`tetracyclines of 20% to 60%, it is uncertain if this is signifi-
`cant in the treatment of acne.27,28
`Oral antibiotics have been shown to be effective in reducing
`the number of inflammatory lesions (52% to 67% reduction),
`but this is based on limited evidence.3 Higher doses can be tried
`if a patient seeks better control. Doxycycline and minocycline
`are considered more effective than tetracycline.29 Erythromycin
`is reserved for patients in whom tetracyclines are contraindi-
`cated (e.g., pregnant women and children under nine years of
`age), although the development of resistance to erythromycin is
`more common than with the other antibiotics.23
`
`Hormonal therapies
`Hormonal agents provide effective second-line treatment in
`women with acne regardless of underlying hormonal abnor-
`malities.30 It is not necessary to demonstrate androgen excess
`to achieve a benefit from antiandrogen therapy. Clinical
`observation suggests that deep-seated nodules on the lower
`face and neck are especially responsive to hormonal therapy.6
`
`Table 2: Approach to therapy for acne vulgaris3,6
`
`Review
`
`Clinical trials have shown that estrogen-containing oral
`contraceptives can be helpful;31–33 the various formulations are
`thought to decrease levels of free testosterone by increasing
`sex-hormone-binding globulin and are considered equally
`effective. The choice of combined oral contraceptive should
`be based on a patient’s tolerance and potential side effects. It is
`not known whether other estrogen-containing contraceptives
`(e.g., vaginal rings, transdermal patches) are effective. Contra-
`ceptives containing only progesterone may worsen acne.4
`A randomized controlled trial with 128 women showed a
`reduction in acne lesions of 63% with 35 μg ethinylestradiol
`and 3 mg drospirenone and a 59% reduction with 35 μg
`ethinylestradiol and 2 mg cyproterone acetate.34 Antiandrogen
`therapy is usually needed for at least three to six months to see
`significant improvement.
`The oral antiandrogen spironolactone can be added if oral
`contraceptives are not effective.3 Spironolactone is a 5α-reduc-
`tase inhibitor when administered at higher doses.35 Spironolac-
`tone, used alone or as an adjunct at doses of 50–200 mg/d, has
`been shown to be effective in improving acne, but this is based
`on limited evidence.2 However, patients should be warned about
`possible side effects, including hyperkalemia, menstrual irregu-
`larities and feminization of a male fetus. Antiandrogen therapy
`alone may be successful, but in less than
`half of women;36 the acne may recur when
`it is discontinued. Combination therapy
`with topical agents or oral antibiotics pro-
`vides substantially more benefit.37
`
`Treatment options
`
`First line
`
`Second line
`
`Isotretinoin
`Isotretinoin affects all causative mecha-
`nisms of acne — it changes abnormal fol-
`licular keratinization, decreases sebum pro-
`duction by 70%, decreases P. acnes
`colonization and is anti-inflammatory.38
`Indications for isotretinoin include scarring
`disease, severe nodulocystic acne and less
`than 50% improvement with oral antibi-
`otics or hormonal therapies after four
`months.38 Isotretinoin therapy must be
`monitored carefully because adverse
`effects include potent teratogenicity,
`hypertriglyceridemia and pancreatitis,
`hepatoxicity, blood dyscrasias, hyperosto-
`sis, premature epiphyseal closure and night
`blindness. An association with severe skin
`reactions, such as erythema multiforme,
`Stevens–Johnson syndrome and toxic epi-
`dermal necrolysis, has been reported.39
`Although a causal relationship has not
`been shown, patients must be warned
`about depression, suicidal thoughts and
`psychosis, and monitored closely.40
`Before a patient starts oral isotretinoin
`therapy, baseline blood work is recom-
`mended.38 This testing includes serum
`blood lipid measurements, complete
`blood count and differential, liver
`
`Severity;
`clinical findings
`
`Mild
`Comedonal
`
`Papular/pustular
`
`Moderate
`Papular/pustular
`
`Nodular
`
`
`Topical retinoid
`
`Topical retinoid
`Topical antimicrobial
`• benzoyl peroxide
`• clindamycin
`• erythromycin
`Combination products
`
`Oral antibiotics
`• tetracyclines
`• erythromycin
`• trimethoprim–
`sulfamethoxazole
`Topical retinoid
`± benzoyl peroxide
`Oral antibiotic
`Topical retinoid
`± benzoyl peroxide
`
`
`Alternative topical retinoid
`Salicylic acid washes
`Alternative topical retinoid
`plus alternative topical
`antimicrobial
`Salicylic acid washes
`
`
`Alternative oral antibiotic
`Alternative topical retinoid
`Benzoyl peroxide
`
`Oral isotretinoin
`Alternative oral antibiotic
`Alternative topical retinoid
`Benzoyl peroxide
`High-dose oral antibiotic
`Topical retinoid (also
`maintenance therapy)
`Benzoyl peroxide
`
`Severe
`
`Oral isotretinoin
`
`Note: In women with acne, oral contraceptives or androgen receptor blockers (e.g., spironolactone)
`may be used in addition to the above treatment options.
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`enzyme tests and blood glucose levels (and a pregnancy test
`for women of child-bearing age).41 These tests should be
`repeated at monthly intervals during treatment. In women of
`childbearing age, two forms of birth control should be used
`during and for one month after therapy, unless the patient has
`had a hysterectomy or is sexually abstinent.41
`Cutaneous side effects of isotretinoin include dry eyes,
`nose and lips, and dermatitis. Patients should use artificial
`tears, and generous amounts of moisturizer on the nose, lips
`and skin.
`According to a 10-year follow-up study of 88 patients,
`those who had received a cumulative dose of isotreretinoin
`120–150 mg/kg had a substantially lower rate of recurrence
`(30%) than those who received less than 120 mg/kg (82%).42
`An additional course can be prescribed for patients in whom
`the acne recurs after isotretinoin is discontinued.
`
`What about alternative therapies?
`
`Herbal therapies such as tea tree oil, and topical and oral
`ayurvedic compounds seem to be well tolerated; however,
`there are limited data about their efficacy and safety in treat-
`
`Table 3: Oral antibiotic therapy for acne vulgaris20,21
`
`Antibiotic, dose
`
`Tetracycline
`250–500 mg twice
`daily
`
`Minocycline
`50–200 mg daily
`
`Doxycycline
`100–200 mg daily
`
`Erythromycin
`500 mg twice daily
`
`Trimethoprim/
`sulfamethoxazole
`80/400 mg or
`160/800 mg four
`times a day
`
`Notes
`
`• Inexpensive
`• Contraindicated in pregnant women
`or in children under nine years of age
`• Chelated by antacids and milk; to be
`taken on empty stomach
`• Can be taken with food
`• Contraindicated in pregnant women
`or in children under nine years of age
`• Adverse reactions: dizziness, pigment
`changes, hepatitis, lupus-like
`reactions
`• Can be taken with food
`• Acceptable for use in patients with
`renal failure
`• Contraindicated in pregnant women
`or in children under nine years of age
`• Adverse reactions: gastrointestinal
`upset; phototoxicity (greatest of all
`tetracyclines)
`• Safe in pregnant women and
`children
`• Adverse reaction: may cause
`gastrointestinal upset
`• 42% of patients may show resistance
`to Propionibacterium acnes18
`• Useful in patients resistant to other
`antibiotics
`• Adverse reactions: 3%–4% of
`patients experience rash;21 risk of
`serious skin reactions, such as
`Stevens–Johnson syndrome
`
`ing acne.3 One clinical trial showed that topical tea tree oil
`was effective but had a slower onset of action than traditional
`topical agents.43 The Cochrane Collaboration is undertaking a
`systematic review of the effects of treatments in the manage-
`ment of acne that are currently considered complementary or
`alternative.
`
`What physical treatments are available?
`
`Physical treatments for acne include comedone extraction,
`chemical peels and microdermabrasion, intralesion cortico -
`steroid injection for acne cysts, and high-intensity, narrow-
`band blue light photodynamic therapy, as well as injectable
`fillers and laser resurfacing for acne scarring. However, there
`is limited evidence in peer-reviewed literature to support such
`treatments.3,44 The results of small pilot studies have supported
`the use of chemical peels,45 and some evidence suggests that
`cortico steroid injections are helpful for treating large inflam-
`matory lesions.46
`
`How should children and pregnant women
`be treated?
`
`The treatment of acne in children is similar to that in adults.
`Because topical therapies may be more irritating in children, ini-
`tiation with low concentrations is preferred. Systemic treatments
`should be reserved for more extensive cases. Erythromycin is
`preferred over tetracyclines for children under nine years of age,
`because tetracyclines can affect growing cartilage and teeth.
`Although treatment with isotretinoin has numerous poten-
`tial minor side effects in patients of all ages, an uncommon
`complication in young patients is premature epiphyseal clo-
`sure.38 This generally occurs when isotretinoin is administered
`in high doses, thus limiting long-term therapy.
`Selecting appropriate treatment in pregnant women can be
`challenging because many acne therapies are teratogenic; all
`topical and especially oral retinoids should be avoided.38 Oral
`therapies such as tetracyclines and antiandrogens are also
`contraindicated in pregnancy. Topical and oral treatment with
`erythromycin may be considered.
`
`What’s new in treating acne?
`
`Trials are being conducted with currently available therapies,
`in different strengths and combinations. Combining an ally-
`lamine antifungal agent with benzoyl peroxide may prove to
`enhance the effectiveness of benzoyl peroxide in treating acne
`while preventing antibiotic resistance.18 Topical dapsone 5%
`gel is a newer option for treating acne. A large multicentre
`randomized controlled trial in adolescents with acne found
`that when the gel was applied twice daily on the affected
`areas, 40% of the treatment group and 28% of the placebo
`group (p < 0.001) achieved the desired outcome at 12 weeks.47
`The same trial and an additional study found that topical dap-
`sone 5% gel is a safe treatment option in patients with a defi-
`ciency in glucose-6-phosphate dehydrogenase.48
`More studies are needed to resolve the long-standing con-
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`troversy about the role of diet and acne. As well, further direct
`treatment comparison and long-term trials are needed to deter-
`mine the optimal sequence of treatment selection as well as to
`establish the effects on quality of life and long-term efficacy.
`
`This review was solicited and has been peer reviewed.
`Competing interests: None declared.
`
`REFERENCES
`1. Magin P, Adams J, Heading G, et al. Psychological sequelae of acne vulgaris:
`results of a qualitative study. Can Fam Physician 2006;52:978-9.
`2. Haider A, Shaw JC. Treatment of acne vulgaris. JAMA 2004;292:726-35.
`3. Strauss JS, Krowchuk DP, Leyden JJ, et al. Guidelines of care for acne vulgaris
`management. J Am Acad Dermatol 2007;56:651-63.
`James WD. Acne. N Engl J Med 2005;352:1463-72.
`4.
`5. American Association of Clinical Endocrinologists Polycystic Ovary Syndrome
`Writing Committee. American Association of Clinical Endocrinologists position
`statement on metabolic and cardiovascular consequences of polycystic ovary syn-
`drome. Endocr Pract 2005;11:126-34.
`6. Gollnick H, Cunliffe W, Berson D, et al. Management of acne: a report from a global
`alliance to improve outcomes in acne. J Am Acad Dermatol 2003;49(Suppl 1): S1-37.
`7. Webster GF, Guenther L, Poulin YP, et al. A multicenter, double-blind, randomized
`comparison study of the efficacy and tolerability of once daily tazarotene 0.1% gel
`and adapalene 0.1% gel for the treatment of facial acne vulgaris. Cutis 2002; 69
`(Suppl):4-11.
`8. Cunliffe WJ, Poncet M, Loesche C, et al. A comparison of the efficacy and tolera-
`bility of adapalene 0.1% gel vs tretinoin 0.025% gel in patients with acne vulgaris: a
`meta analysis of five randomized trials. Br J Dermatol 1998;139(suppl 52):48-56.
`9. Hughes BR, Norris JF, Cunliffe WJ. A double-blind evaluation of topical
`isotretinoin 0.05%, benzoyl peroxide gel 5% and placebo in patients with acne.
`Clin Exp Dermatol 1992;17:165-8.
`10. Mills OH Jr, Kligman AM, Pochi P, et al. Comparing 2.5%, 5%, and 10% benzoyl
`peroxide on inflammatory acne vulgaris. Int J Dermatol 1986;25:664-7.
`11. Esterly NB, Furey NL, Flanagan LE. The effect of antimicrobial agents on leukocyte
`chemotaxis. J Invest Dermatol 1978;70:51-5.
`12. Cunliffe WJ, Holland KT, Bojar R, et al. A randomized, double-blind comparison
`of a clindamycin phosphate/benzoyl peroxide gel formulation and a matching clin-
`damycin gel with respect to microbiologic activity and clinical efficacy in the topi-
`cal treatment of acne vulgaris. Clin Ther 2002;24:1117-33.
`13. Zouboulis CC, Derumeaux L, Decroix J, et al. A multicentre, single-blind, random-
`ized comparison of a fixed clindamycin phosphate/tretinoin gel formulation (Velac)
`applied once daily and a clindamycin lotion formulation (Dalacin T) applied twice
`daily in the topical treatment of acne vulgaris. Br J Dermatol 2000; 143: 498-505.
`14. Handojo I. The combined use of topical benzoyl peroxide and tretinoin in the treat-
`ment of acne vulgaris. Int J Dermatol 1979;18:489-96.
`15. Wolf JE Jr, Kaplan D, Kraus SJ, et al. Efficacy and tolerability of combined topical
`treatment of acne vulgaris with adapalene and clindamycin: a multicenter, random-
`ized investigator blinded study. J Am Acad Dermatol 2003;49:S211-7.
`16. Ellis CN, Leyden J, Katz HI, et al. Therapeutic studies with a new combination
`benzoyl peroxide/clindamycin topical gel in acne vulgaris. Cutis 2001;67(Suppl
`2): 13-20.
`17. Bowe WP, Shalita AR. Effective over-the-counter acne treatments. Semin Cutan
`Med Surg 2008;27:170-6.
`18. Burkhart CG, Burkhart CN. Treatment of acne vulgaris without antibiotics: tertiary
`amine-benzoyl peroxide combination vs. benzoyl peroxide alone (Proactiv Solu-
`tion). Int J Dermatol 2007;46:89-93.
`19. Magin P, Pond D, Smith W, et al. A systematic review of the evidence for ‘myths and
`misconceptions’ in acne management: diet, face-washing and sunlight. Fam Pract
`2005;22:62-70.
`20. Oprica C, Nord CE. European surveillance study on the antibiotic susceptibility of
`Propionibacterium acnes. Clin Microbiol Infect 2005;11:204-13.
`21. Masters PA, O’Bryan TA, Zurlo J, et al. Trimethoprim–sulfamethoxazole revis-
`ited. Arch Intern Med 2003;163:402-10.
`22. Ozolins M, Eady EA, Avery AJ, et al. Comparison of five antimicrobial regimens
`for treatment of mild to moderate inflammatory facial acne vulgaris in the commu-
`nity: randomized controlled trial. Lancet 2004;364:2188-95.
`
`Review
`
`23. Eady EA, Cove JH, Holland KT, et al. Erythromycin resistant propionibacteria in
`antibiotic treated acne patients: association with treatment failure. Br J Dermatol
`1989; 121:51-7.
`24. Miller YW, Eady EA, Lacey RW, et al. Sequential antibiotic therapy for acne pro-
`motes the carriage of resistant staphylococci on the skin of contacts. J Antimicrob
`Chemother 1996;38:829-37.
`25. Vowels BR, Yang S, Leyden JJ. Induction of proinflammatory cytokines by a solu-
`ble factor of propionibacterium acnes: implications for chronic inflammatory acne.
`Infect Immun 1995;63:3158-65.
`26. Golub LM, Lee HM, Ryan ME, et al. Tetracyclines inhibit connective tissue break-
`down by multiple non-antimicrobial mechanisms. Adv Dent Res 1998;12:12-26.
`27. Ross JI, Snelling AM, Carnegie E, et al. Antibiotic resistant acne: lessons from
`Europe. Br J Dermatol 2003;148:467-78.
`28. Eady AE, Cove JH, Layton AM. Is antibiotic resistance in cutaneous propionibac-
`teria clinically relevant? Implications of resistance for acne patients and pres -
`cribers. Am J Clin Dermatol 2003;4:813-31.
`29. Samuelson JS. An accurate photographic method for grading acne: initial use in a
`double-blind clinical comparison of minocycline and tetracycline. J Am Acad Dermatol
`1985;12:461-7.
`30. Cibula D, Hill M, Vohradnikova O, et al. The role of androgens in determining
`acne severity in adult women. Br J Dermatol 2000;143:399-404.
`31. Worret I, Arp W, Zahradnik HP, et al. Acne resolution rates: results of a single-
`blind, randomized, controlled, parallel phase III trial with EE/CMA (Belara) and
`EE/LNG (Microgynon). Dermatology 2001;203:38-44.
`32. Rosen MP, Breitkopf DM, Nagamani M. A randomized controlled trial of second-
`versus third-generation oral contraceptives in the treatment of acne vulgaris. Am J
`Obstet Gynecol 2003;188:1158-60.
`33. ACOG practice bulletin no.110: noncontraceptive uses of hormonal contracep -
`tives. Obstet Gynecol 2010;115:206-18.
`34. Van Vloten WA, van Haselen CW, van Zuuren EJ, et al. The effect of 2 combined
`oral contraceptives containing either drospirenone or cyproterone acetate on acne
`and seborrhea. Cutis 2002;69(suppl4):2-15.
`35. Goodfellow A, Alaghband-Zadeh J, Carter G, et al. Oral spironolactone improves
`acne vulgaris and reduces sebum excretion. Br J Dermatol 1984;111:209-14.
`36. Miller JA, Wojnarowska FT, Dowd PM, et al. Anti-androgen treatment in women
`with acne: a controlled trial. Br J Dermatol 1986;114:705-16.
`37. Shaw JC, White LE. Long-term safety of spironolactone in acne: results of an 8-
`year follow-up study. J Cutan Med Surg 2002;6:541-5.
`38. Wolverton SE. Comprehensive dermatologic drug therapy. 2nd ed. Philadelphia:
`WB Saunders; 2007.
`39. Health Canada. Health Canada endorsed important safety information on Accutane
`Roche isotretinoin). Available http://hc-sc.gc.ca/dhp-mps/medeff/advisories-
`avis/prof/_2010/accutane_2_hpc-cps-eng.php (accessed 2010 Sep. 7).
`40. Hull PR, D’Arcy C. Isotretinoin use and subsequent depression and suicide. Am J
`Clin Dermatol 2003;4:493-505.
`41. Product monograph. Accutane Roche. Mississauga (ON): Hoffmann-La Roche. 2010.
`42. Layton AM, Knaggs H, Taylor J, et al. Isotretinoin for acne vulgaris—10 years
`later: a safe and successful treatment. Br J Dermatol 1993;129:292-6.
`43. Bassett IB, Pannowitz DL, Barnetson RS. A comparative study of tea-tree oil ver-
`sus benzoyl peroxide in the treatment of acne. Med J Aust 1990;153:455-8.
`Jordan R, Cummins CCL, Burls A, et al. Laser resurfacing for facial acne scars.
`Cochrane Database of Systematic Reviews 2001, Issue 1. Art. No. CD001866.
`DOI:10.1002 /14651858.CD001866.
`45. Grimes PE. The safety and efficacy of salicylic acid chemical peels in darker
`racial-ethnic groups. Dermatol Surg 1999;25:18-22.
`46. Levine RM, Rasmussen JE. Intralesional corticosteroids in the treatment of nod -
`ulocystic acne. Arch Dermatol 1983;119:480-1.
`47. Raimer S, Maloney JM, Bourcier M, et al. United States/Canada Dapsone Gel
`Study Group. Efficacy and safety of dapsone gel 5% for the treatment of acne vul-
`garis in adolescents. Cutis 2008;81:171-8.
`48. Piette WW, Taylor S, Pariser D, et al. Hematologic safety of dapsone gel, 5%, for
`topical treatment of acne vulgaris. Arch Dermatol 2008;144:1564-70.
`
`44.
`
`Correspondence to: Dr. Anatoli Freiman, Division of
`Dermatology, University of Toronto, Women’s College Hospital,
`76 Grenville St., 8th floor, Toronto, ON M5S 1B2;
`anatoli.freiman@gmail.com
`
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