Managing acne in primary care (2024)

General treatment advice for all levels of acne severity

Patients should be advised to wash their face gently with warm water and mild soap or cleanser, twice daily. An un-medicatedface-wash is sufficient, although products containing benzoyl peroxide or salicylic acid can be effective. Rough scrubbingshould be avoided as it causes follicular rupture, increasing the inflammatory response. Patients with sensitive skin,e.g. atopic dermatitis, should avoid soap, and anti-acne cleansers may cause irritation and contact dermatitis.

Acne products should be applied to all areas usually affected by acne, rather than just applied to individual lesions.⁵ Patientsshould also be informed that when using topical products, including prescription products, it may take several monthsbefore significant results are seen.⁴

Patients should ensure that their facial products, including cosmetics and sunscreens, are not contributing to theiracne.

Best Practice Tip: Tell patients to look for cosmetics and skin care productsthat are labelled as “non-comedogenic”.

Mild acne – Topical treatments

First-line treatment for mild acne is a combination of topical benzoyl peroxide and a topical retinoid or a topicalantibiotic.

Benzoyl peroxide is not subsidised and can be purchased over-the-counter.

The topical retinoids adapalene and tretinoin are prescription only and fully subsidised (one tube at a time) for usein patients with acne. Topical isotretinoin gel is available by prescription, but is not subsidised.

Topical erythromycin and clindamycin, and combination products with benzoyl peroxide and adapalene, and benzoyl peroxideand clindamycin are available by prescription, but are not subsidised.

Benzoyl peroxide

Benzoyl peroxide is topical antimicrobial and keratolytic (i.e. softens and removes outer layers of skin).

Benzoyl peroxide is available as a gel, cream or cleanser, and ranges in strength from 2.5% – 10%. The 2.5% strengthis sufficient for most people, and higher concentrations are associated with greater adverse effects. The choice betweengel, cream and wash should be based on patient preference and skin-type, with gels being more suited to oily skin. A rinse-offcleanser is more suitable if irritation occurs and is more convenient for treating acne affecting the trunk.

Washes can be used once or twice daily, and should be applied for thirty seconds before rinsing thoroughly. Topicalbenzoyl peroxide gels and creams should be applied once daily, removing after two hours, for three days, and then, iftolerated, applied once daily, at night, and left on overnight. Some patients may tolerate twice daily applications.

The adverse effects of benzoyl peroxide include skin irritation, dryness and redness. Direct contact with eyes or othermucous membranes will cause severe irritation. Most of the adverse effects can be minimised by reducing the time the productis on the skin before being washed off, or by reducing the concentration used. Advise the patient that if their skin peelsor becomes very dry, an oil-free moisturiser can be used. Benzoyl peroxide will bleach linen, clothing and towels.

Salicylic acid 0.1 – 2% cream is an alternative to benzoyl peroxide, but is generally less effective and may also causeskin dryness.⁶ It works by softening and descaling the skin, thereby reducing comedones.

Topical retinoids

Topical retinoids inhibit keratinocyte differentiation and proliferation. They reduce comedones and have significantanti-inflammatory effects.⁷ They are not suitable for patients with very inflammatory acne and they may notbe tolerated by patients with sensitive skin. Topical retinoids must be applied at night, as UV radiation degrades retinoids.

Adapalene is available as a 0.1% cream and gel. It should be applied thinly, once daily.⁸ Adapalene is usuallybetter tolerated than tretinoin.⁷ The gel is suitable for most people, although those with dry skin may preferthe cream.

Tretinoin is available as a 0.05% cream, and should be applied thinly, once daily. Application should be “built up”to avoid adverse effects: on the first night, apply for five minutes before washing off; on the second night, apply forten minutes; on subsequent nights, increase the application time by 30 minutes until a two-hour application is achieved,at which point the cream can be left on overnight.^{7, 8}

Topical retinoids should be trialled for at least two months before considering another treatment. The initial phaseof treatment may cause a mild acne flare, followed by significantly declining acne severity over one to two months.⁷ Continued,long-term use of retinoids appears to be safe and effective.⁷

Advise patients to continue using the topical retinoid even if acne initially appears slightly worse, but to arrangea review if severe flares develop.

Adverse effects include skin irritation, dryness and erythema. If adverse effects are intolerable, advise patients toreduce the time that the product is on the skin before being washed off, and to apply a mild, oil-free moisturiser ifthere is obvious peeling. Topical retinoids are not associated with the same adverse effects as oral retinoids, such asisotretinoin. However, there is consensus among experts that they should not be used in females that are pregnant or planningpregnancy.

Topical antibiotics

Topical antibiotics work by reducing the number of P. acnes on the surface of the skin and in hair folliclesand sebum ducts. They may also have anti-inflammatory effects.

Topical erythromycin 4% gel or clindamycin 1% solution or lotion should be applied twice daily, with treatment reviewedafter eight to twelve weeks. To limit the development of bacterial resistance they should only be used alongside benzoylperoxide or a topical retinoid.^{2, 4}

Adverse effects of topical antibiotics include skin irritation, contact dermatitis and, rarely, gastrointestinal disturbance.

Moderate acne – oral antibiotics or hormonal contraception

Oral antibiotics may be considered for patients with moderate acne, or mild acne that has not responded to topical treatmentsafter two months. N.B. topical treatment with benzoyl peroxide or retinoid should be continued.

Doxycycline 50 – 100 mg, daily, for four to six months, is the first-line antibiotic choice (N.B. 50 mg tablets arenot fully subsidised).⁶ If effective, the dose can be tapered after four months to alternate day treatment.If the standard dose of doxycycline is ineffective, increase to 100 mg, twice daily, provided it is tolerated. Doxycyclineis contraindicated in children aged under 12 years and women who are pregnant.

Although minocycline is as effective for acne as other tetracyclines, it is associated with a greater risk of lupuserythematosus-like syndrome, hepatitis and pigmentation, and is not fully subsidised.⁹ Erythromycin 400 mg,twice daily, can be used as an alternative to a tetracycline, however, it may be less effective, possibly due to increasing P.acnes resistance.⁶

Adverse effects associated with tetracycline antibiotics include oesophageal irritation, photosensitivity, Candida albicansvulvovaginitis and nausea and vomiting. Oesophageal and gastrointestinal irritation can be reduced by taking doxycyclinewith a glass of water and food, and advising the patient to avoid lying down for one hour after the dose is taken.

Combined oral contraception is an effective treatment for mild to moderate acne in females.¹⁰ In general,oral contraception has fewer adverse effects than long-term antibiotics, and should be considered first for females.

A standard combined oral contraceptive (levonorgestrel + ethinyloestradiol, such as Ava or Microgynon) should be triedinitially.¹⁰ These are fully subsidised and usually well tolerated.

Combined oral contraceptives containing cyproterone, e.g. Ginet (fully subsidised), may be more effective than otheroral contraceptives and are suitable for women with polycystic ovary syndrome.¹⁰ However, cyproterone-containingoral contraceptives slightly raise the risk of venous thromboembolism (approximately 40 cases per 100 000 women treatedfor one year, compared to 20 cases for levonorgestrel-containing contraceptives), and should be used with caution.^11,12

Combined oral contraceptives containing less androgenic progestogens, such as drospirenone + ethinyloestradiol (Yazand Yasmin, not subsidised) or desogetrel + ethinyloestradiol (Mercilon and Marvelon, partly subsidised) may also be suitable.¹⁰ However,these are more expensive to the patient than fully subsidised options, and have a similar risk of venous thromboembolismas cyproterone-containing contraceptives.

Progesterone-only oral contraceptives, depot progesterone and progesterone implants may worsen acne.¹³

Although a reduction in seborrhoea is usually apparent within two to three cycles, it may take up to six cycles afterinitiating the oral contraceptive before an improvement in acne is seen.⁵

Severe acne – isotretinoin

People with severe acne, treatment-resistant acne or older adults with persistent acne may require oral isotretinoin.⁵ Isotretinoinis associated with many adverse effects, is a major teratogen and requires monitoring throughout treatment, thereforemay not be a suitable option for everyone.¹⁴ If isotretinoin is unsuitable or is not tolerated, a higher doseof antibiotic, e.g. doxycycline 100 mg, twice daily, if tolerated and not already trialled, and discussion with, or referralto, a dermatologist is recommended.^{2, 4}

The efficacy of isotretinoin

Isotretinoin has been shown to affect all four pathogenic processes involved in acne formation and results in sebaceousgland apoptosis (cell death) and altered gene expression.^16–18 Isotretinoin is highly effective for clearingacne and reducing recurrence. A single course of isotretinoin will result in significant improvement or complete remissionof acne in nearly all patients. Long-term efficacy depends on individual patient factors and the duration and dose oftreatment.¹⁸ If isotretinoin is ineffective, investigation of a potential endocrine cause for the acne, suchas polycystic ovary syndrome, should be considered.¹⁹

Recurrent acne may be treated with a further course of isotretinoin, and in some cases long-term, low-dose treatmentis appropriate, however, discussion with a Dermatologist is recommended if this is being considered.¹⁸

The adverse effects of isotretinoin

Isotretinoin is associated with a range of serious adverse effects (Table 1). Some, particularly cheilitis, are so commonthat they can be considered indicators of adherence.¹⁷ Isotretinoin may cause an initial worsening of acne,but severe flares are uncommon. It is important to discuss these adverse effects with patients prior to initiation, tooptimise adherence. Most adverse effects are dose-related and starting with a low dose may reduce the incidence and severity.

Females should be aware that isotretinoin is teratogenic and that exposure to it, particularly in the first trimester,is very likely to lead to spontaneous abortion or severe birth deformities.

Both females and males should be advised not to donate blood during treatment with isotretinoin or for one month aftertreatment stops.¹⁴

Initiating isotretinoin

When initiating isotretinoin, it is recommended that an electronic decision support module is used.

Practitioners should discuss with the patient, and then provide in writing, the potential adverse effects, particularlyteratogenicity in females. A suitable patient information brochure is provided with the medicine by the distributor. Baselinelaboratory investigations should be requested. Female patients will require advice on contraceptive options, and wherenecessary, be prescribed contraceptives (some will already be using oral contraceptives for managing acne symptoms). Patients(and parents/caregivers for those under age 16 years) should be asked to sign a consent form, to indicate that they understandthe adverse effects that are possible while taking isotretinoin and, for female patients, the importance of not becomingpregnant during the course of their treatment and a further month after it has been discontinued.

Consent forms for patients are available in the bestpractice Decision Support isotretinoin module.

Dosing isotretinoin

The recommended starting dose of isotretinoin is 0.5 mg/kg/day. Daily doses can be titrated up or down, between 0.1and 1 mg/kg/day, depending on response to treatment and presence of adverse effects. The total dose of isotretinoin overthe course of treatment should be between 120 – 150 mg/kg of body weight.¹⁴ The length of treatment is dictatedby the daily dose. Courses usually last between three to four months but may continue for one year or longer. Total dosesof >150 mg/kg are associated with increased adverse effects.¹⁶ The dose and duration of the course may beadjusted on an individual basis; some patients will wish to reduce the dose or stop isotretinoin when the active acnehas settled.

Isotretinoin should be taken, once daily, after the main meal, which should contain some fat (e.g. milk), to help increaseabsorption.

While isotretinoin is available in 5, 10, 20 and 30 mg capsules, only the 10 and 20 mg capsules are fully subsidised.Doses calculated by body weight may need to be rounded to suit the subsidised options.

Contraception is essential for females taking isotretinoin

Isotretinoin is a major teratogen, and will cause significant birth defects or spontaneous abortion in approximatelyhalf of all pregnant women taking the medicine.^{21, 22} Practitioners should obtain an up-to-date and reliablesexual history from the patient and ensure that all females of reproductive age are: ¹⁷

• Not pregnant prior to beginning treatment
• Given strong advice against becoming pregnant during or within one month of completion of a course of isotretinoin
• Using two forms of reliable contraception, ideally hormonal contraception* and a barrier method
• Prescribed, or know how to access, emergency contraception, and know how and when to use it

* Combined oral contraceptives are generally recommended as progesterone-only contraceptives may be less effective ina person taking isotretinoin and can worsen acne.

Monitoring patients taking isotretinoin

Isotretinoin can have significant adverse effects, including liver enzyme abnormalities, hyperlipidaemia, hypertriglyceridaemiaand cytopaenias (a reduction in one or more types of blood cell), and monitoring is recommended throughout the courseof treatment.¹⁷ Due to a long history of use in New Zealand and internationally, there has been a trend amongDermatologists toward reduced testing for patients taking low doses of isotretinoin, however, the recommendation for regulartesting remains as best practice.

Triglyceride levels can be elevated due to isotretinoin treatment.¹⁷ Several reasons for this have been proposed,including down-regulation of lipases and changes in gene expression leading to increased antagonism of triglyceride metabolism.²³ Trigylceridelevels > 9 mmol/L are associated with pancreatitis. A reduction in dose or cessation of treatment should be consideredif triglyceride levels rise above 6 mmol/L. Isotretinoin must be stopped if pancreatitis occurs.¹⁷

Transient increases in liver enzymes can occur in people taking isotretinoin.¹⁷ These increases are usuallymild and benign and will resolve upon cessation of isotretinoin. If liver transaminases are > 2.5 times the upper limitof normal, investigation of possible causes of liver dysfunction (e.g. viral hepatitis, alcoholism) is required and itis recommended that isotretinoin is stopped. Patients should be advised of the risk of drinking alcohol in excess whiletaking isotretinoin.

Rarely, isotretinoin causes reversible cytopaenias, therefore it is recommended to monitor full blood count.¹⁷

People with severe liver or kidney dysfunction, hyperlipidaemia, hypercholesterolaemia or diabetes may be at an increasedrisk of these adverse effects and discussion with or referral to a dermatologist should be considered before prescribingisotretinoin.

Adverse psychological issues have been associated with isotretinoin, particularly depression and suicidality, but causalityhas not been established. Depression may be present before treatment or can occur for unrelated reasons.¹⁷ Abrief psychological assessment for depression and suicidal tendency should be performed prior to prescribing isotretinoin,and then briefly whenever the patient is seen during and after treatment.

Baseline investigations should occur prior to prescribing isotretinoin and repeated at least once during thecourse of treatment, and should include:^{6, 14, 21}

• Lipid levels
• Liver function tests
• Full blood count

Pregnancy testing with serum hCG is also required at baseline, monthly during treatment, and againfive weeks post-treatment.

Access to subsidised oral isotretinoin for severe acne, was widened on 1 March, 2009, to allow vocationally registeredGeneral Practitioners and Nurse Practitioners working in an appropriate field to prescribe the medicine, fully subsidised,subject to Special Authority criteria.¹⁵

The widening of access created significant debate among Dermatologists and General Practitioners. Dermatologists wereparticularly concerned that:

The medicine is difficult to use and General Practitioners would not have the training or experience to use it safely

Widening access would increase prenatal exposure to teratogens and therefore increase pregnancy terminations and birthdefects

For further information see: “The isotretinoindebate; should we be arguing about who is prescribing isotretinoin or is the real issue how it is being prescribed?”,BPJ 20 (April, 2009).

Is general practice prescribing isotretinoin correctly?

General Practitioners are now significant prescribers of isotretinoin. From July, 2011 – June, 2012 there were a totalof 46 531 dispensed prescriptions for isotretinoin, of which 58% originated from a General Practitioner.²⁴

Since 2009 the number of prescriptions dispensed per patient prescribed isotretinoin has decreased by approximately15%.²⁴ The reason for this is unclear, but may be due to larger doses per prescription, lower overall dosesof isotretinoin or increased rates of medicine cessation.

There has also been an important methodological improvement in isotretinoin prescribing. Recording of patient NHI numberson prescriptions has improved markedly since access to isotretinoin was widened to include General Practitioner prescribing.From July, 2011 – June, 2012 NHI numbers were recorded in 91% of all isotretinoin dispensings compared to only 60% prior.²⁵ Recordingof NHI numbers allows analysis of medicine use to occur.

There has been no change in the number of serious adverse effects reported to Centre for Adverse Reactions Monitoring(CARM) since the widened access to prescribing. However, the impact of General Practitioner prescribing of isotretinoinon abortion rates due to teratogen exposure is not able to be monitored due to differences in the way that prescriptionmedicines are coded between primary and secondary care.

Have the prescribing disparities of isotretinoin been reduced?

An unintended effect of limiting access to isotretinoin was an increase in health disparities due to the limited accessto publicly funded and private Dermatologists in New Zealand.²⁵ The result was that a person living in theleast deprived socioeconomic area was 2.5 times more likely to be prescribed isotretinoin than a person living in themost deprived area, and that Māori and Pacific peoples were five times less likely to be prescribed isotretinoin thanpeople in other ethnic groups, largely New Zealand Europeans.²⁵ This is despite the fact that there is no significantevidence of an association between the incidence of acne and deprivation level or ethnicity.^{25, 26} One of theprimary reasons for widening access to isotretinoin was to reduce this disparity.

However, the most up-to-date data shows no obvious changes in prescribing behaviour between the highest and lowest decilesocioeconomic areas, and between ethnicities (Figure 1 and 2).²⁵ This is despite increased access to isotretinoinvia general practice. This may suggest that the actual or perceived severity of acne is lower in these groups, and thereforetreatment is not sought.