2.4 Viral skin infections

ANTIVIRALS › NUCLEOSIDE ANALOGUES

Aciclovir

(Acyclovir)

l INDICATIONS AND DOSE

Herpes simplex infection (local treatment)

▶ TO THE SKIN

▶ Child: Apply 5 times a day for 5–10 days, to be applied

to lesions approximately every 4 hours, starting at first

sign of attack

▶ Adult: Apply 5 times a day for 5–10 days, to be applied

to lesions approximately every 4 hours, starting at first

sign of attack

l UNLICENSED USE

▶ In children Cream licensed for use in children (age range

not specified by manufacturer).

l CAUTIONS Avoid cream coming in to contact with eyes and

mucous membranes

l INTERACTIONS → Appendix 1: aciclovir

l SIDE-EFFECTS

▶ Uncommon Skin reactions

l PREGNANCY Limited absorption from topical aciclovir

preparations.

l PATIENT AND CARER ADVICE

Medicines for Children leaflet: Aciclovir cream for herpes

www.medicinesforchildren.org.uk/aciclovir-cream-herpes-0

l PROFESSION SPECIFIC INFORMATION

Dental practitioners’ formulary

Aciclovir Cream may be prescribed.

l EXCEPTIONS TO LEGAL CATEGORY A 2-g tube and a pump

pack are on sale to the public for the treatment of cold

sores.

l MEDICINAL FORMS There can be variation in the licensing of

different medicines containing the same drug.

Cream

EXCIPIENTS: May contain Cetostearyl alcohol (including cetyl and

stearyl alcohol), propylene glycol

▶ Aciclovir (Non-proprietary)

Aciclovir 50 mg per 1 gram Aciclovir 5% cream | 2 gram P £1.09 DT = £1.09 | 10 gram P £5.45 DT = £5.45

▶ Zovirax (GlaxoSmithKline Consumer Healthcare, GlaxoSmithKline UK

Ltd)

Aciclovir 50 mg per 1 gram Zovirax 5% cream | 2 gram P £4.63

DT = £1.09 | 10 gram P £13.96 DT = £5.45

3 Inflammatory skin

conditions

3.1 Eczema and psoriasis

Eczema

Types and management

Eczema (dermatitis) has several causes, which may influence

treatment. The main types of eczema are irritant, allergic

contact, atopic, venous and discoid; different types may coexist. Lichenification, due to scratching and rubbing, may

complicate any chronic eczema. Atopic eczema is the most

common type and it usually involves dry skin as well as

infection and lichenification.

Management of eczema involves the removal or treatment of

contributory factors including occupational and domestic

irritants. Known or suspected contact allergens should be

avoided. Rarely, ingredients in topical medicinal products

may sensitise the skin; the BNF lists active ingredients

together with excipients that have been associated with skin

sensitisation.

Skin dryness and the consequent irritant eczema requires

emollients applied regularly (at least twice daily) and

liberally to the affected area; this can be supplemented with

bath or shower emollients. The use of emollients should

continue even if the eczema improves or if other treatment is

being used.

Topical corticosteroids are also required in the

management of eczema; the potency of the corticosteroid

should be appropriate to the severity and site of the

condition. Mild corticosteroids are generally used on the face

and on flexures; potent corticosteroids are generally

required for use on adults with discoid or lichenified eczema

or with eczema on the scalp, limbs, and trunk. Treatment

should be reviewed regularly, especially if a potent

corticosteroid is required. In patients with frequent flares

(2–3 per month), a topical corticosteroid can be applied on

2 consecutive days each week to prevent further flares.

Bandages (including those containing ichthammol with

zinc oxide p. 1253) are sometimes applied over topical

corticosteroids or emollients to treat eczema of the limbs.

Dry-wrap dressings can be used to provide a physical barrier

to help prevent scratching and improve retention of

emollients. See Wound management products and elasticated

garments for details of elasticated viscose stockinette tubular

bandages and garments, and silk clothing.

See Eczema and psoriasis, drugs affecting the immune

response p. 1240 for the role of topical pimecrolimus p. 1255

and tacrolimus p. 1256 in atopic eczema.

Infection

Bacterial infection (commonly with Staphylococcus aureus

and occasionally with Streptococcus pyogenes) can exacerbate

eczema and requires treatment with topical or systemic

antibacterial drugs. Antibacterial drugs should be used in

short courses (typically 1 week) to reduce the risk of drug

resistance or skin sensitisation. Associated eczema is treated

simultaneously with a topical corticosteroid which can be

combined with a topical antimicrobial.

Eczema involving widespread or recurrent infection

requires the use of a systemic antibacterial that is active

against the infecting organism. Products that combine an

antiseptic with an emollient application and with a bath

emollient can also be used; antiseptic shampoos can be used

on the scalp.

Intertriginous eczema commonly involves candida and

bacteria; it is best treated with a mild or moderately potent

topical corticosteroid and a suitable antimicrobial drug.

Widespread herpes simplex infection may complicate

atopic eczema and treatment with a systemic antiviral drug

is indicated.

Management of other features of eczema

Lichenification, which results from repeated scratching is

treated initially with a potent corticosteroid. Bandages

containing ichthammol paste p. 1252 (to reduce pruritus)

and other substances such as zinc oxide can be applied over

the corticosteroid or emollient. Coal tar and ichthammol

can be useful in some cases of chronic eczema.

A non-sedating antihistamine may be of some value in

relieving severe itching or urticaria associated with eczema.

A sedating antihistamine can be used if itching causes sleep

disturbance.

Exudative (‘weeping’) eczema requires a potent

corticosteroid initially; infection may also be present and

require specific treatment. Potassium permanganate

solution (1 in 10,000) p. 1276 can be used in exudating

1238 Inflammatory skin conditions BNF 78

Skin

13

eczema for its antiseptic and astringent effects; treatment

should be stopped when exudation stops.

Severe refractory eczema

Severe refractory eczema is best managed under specialist

supervision; it may require phototherapy or drugs that act on

the immune system. Alitretinoin p. 1262 is licensed for the

treatment of severe chronic hand eczema refractory to

potent topical corticosteroids; patients with hyperkeratotic

features are more likely to respond to alitretinoin than those

with pompholyx.

Seborrhoeic dermatitis

Seborrhoeic dermatitis (seborrhoeic eczema) is associated with

species of the yeast Malassezia and affects the scalp,

paranasal areas, and eyebrows. Shampoos active against the

yeast (including those containing ketoconazole p. 1233 or

coal tar p. 1253) and combinations of mild corticosteroids

with suitable antimicrobials are used.

Psoriasis

Management

Psoriasis is characterised by epidermal thickening and

scaling. It commonly affects extensor surfaces and the scalp.

Occasionally, psoriasis is provoked or exacerbated by

drugs such as lithium, chloroquine and hydroxychloroquine,

beta-blockers, non-steroidal anti-inflammatory drugs, and

ACE inhibitors. Psoriasis may not be seen until the drug has

been taken for weeks or months.

Emollients, in addition to their effects on dryness, scaling

and cracking, may have an anti-proliferative effect in

psoriasis, and may be the only treatment necessary for mild

psoriasis. They are particularly useful in inflammatory

psoriasis and in plaque psoriasis of palms and soles, in which

irritant factors can perpetuate the condition. Emollients are

useful adjuncts to other more specific treatment.

More specific topical treatment for chronic stable plaque

psoriasis on extensor surfaces of trunk and limbs involves the

use of vitamin D analogues, coal tar p. 1253, dithranol

p. 1253, and the retinoid tazarotene p. 1262. However, they

can irritate the skin and they are not suitable for the more

inflammatory forms of psoriasis; their use should be

suspended during an inflammatory phase of psoriasis. The

efficacy and the irritancy of each substance varies between

patients. If a substance irritates significantly, it should be

stopped or the concentration reduced; if it is tolerated, its

effects should be assessed after 4 to 6 weeks and treatment

continued if it is effective.

Scalp psoriasis is usually scaly, and the scale may be thick

and adherent; this will require softening with an emollient

cream, ointment, or oil. A tar-based shampoo is first-line

treatment for scalp psoriasis; a keratolytic, such as salicylic

acid, should also be used if there is significant scaling, to

allow other treatments to work.

Some preparations prescribed for psoriasis affecting the

scalp, combine salicylic acid with coal tar or sulfur. The

product should be applied generously, and an adequate

quantity should be prescribed. It should be left on for at least

an hour, often more conveniently overnight, before washing

off. The use of scalp preparations containing a potent

corticosteroid or a vitamin D analogue, either alone or in

combination, can also be helpful.

Facial, flexural and genital psoriasis can be managed with

short-term use of a mild or moderate potency topical

corticosteroid (a mild potency topical corticosteroid is

preferred for the initial treatment of facial psoriasis).

Calcitriol p. 1263 or tacalcitol p. 1264 can be used for longerterm treatment, or if the response to mild or moderate

potency topical corticosteroids is inadequate; calcipotriol

p. 1263 is more likely to cause irritation. Low strength tar

preparations can also be used. Pimecrolimus p. 1255 or

tacrolimus p. 1256 by topical application [unlicensed

indication] can be used short-term, under specialist

supervision, in patients whose condition has not responded

adequately to other treatments, or who are intolerant of

them.

Widespread unstable psoriasis of erythrodermic or

generalised pustular type requires urgent specialist

assessment. Initial topical treatment should be limited to

using emollients frequently and generously; emollients

should be prescribed in quantities of 1 kg or more. More

localised acute or subacute inflammatory psoriasis with hot,

spreading or itchy lesions, should be treated topically with

emollients or with a corticosteroid of moderate potency.

Calcipotriol and tacalcitol are analogues of vitamin D that

affect cell division and differentiation. Calcitriol is an active

form of vitamin D. Vitamin D and its analogues are used

first-line for the long-term treatment of plaque psoriasis;

they do not smell or stain and they may be more acceptable

than tar or dithranol products. Of the vitamin D analogues,

tacalcitol and calcitriol are less likely to irritate.

Coal tar has anti-inflammatory properties that are useful

in chronic plaque psoriasis; it also has antiscaling properties.

Crude coal tar (coal tar, BP) is the most effective form,

typically in a concentration of 1 to 10% in a soft paraffin

base, but few outpatients tolerate the smell and mess.

Cleaner extracts of coal tar included in proprietary

preparations, are more practicable for home use but they are

less effective and improvement takes longer. Contact of coal

tar products with normal skin is not normally harmful and

they can be used for widespread small lesions; however,

irritation, contact allergy, and sterile folliculitis can occur.

The milder tar extracts can be used on the face and flexures.

Tar baths and tar shampoos are also helpful.

Dithranol is effective for chronic plaque psoriasis. Its

major disadvantages are irritation (for which individual

susceptibility varies) and staining of skin and of clothing.

Dithranol is not generally suitable for widespread small

lesions nor should it be used in the flexures or on the face.

Proprietary preparations are more suitable for home use;

they are usually washed off after 5 to 60 minutes (‘short

contact’). Specialist nurses may apply intensive treatment

with dithranol paste which is covered by stockinette

dressings and usually retained overnight. Dithranol should

be discontinued if even a low concentration causes acute

inflammation; continued use can result in the psoriasis

becoming unstable.

Tazarotene, a retinoid, has a similar efficacy to vitamin D

and its analogues, but is associated with a greater incidence

of irritation. Although irritation is common, it is minimised

by applying tazarotene sparingly to the plaques and avoiding

normal skin; application to the face and in flexures should

also be avoided. Tazarotene does not stain and is odourless.

A topical corticosteroid is not generally suitable for longterm use or as the sole treatment of extensive chronic plaque

psoriasis; any early improvement is not usually maintained

and there is a risk of the condition deteriorating or of

precipitating an unstable form of psoriasis (e.g.

erythrodermic psoriasis or generalised pustular psoriasis) on

withdrawal. Topical use of potent corticosteroids on

widespread psoriasis can also lead to systemic as well as local

side-effects. However, topical corticosteroids used shortterm may be appropriate to treat psoriasis in specific sites

such as the face or flexures (with a mild or moderate

corticosteroid), and psoriasis of the scalp, palms, and soles

(with a potent corticosteroid). Very potent corticosteroids

should only be used under specialist supervision.

Combining the use of a corticosteroid with another specific

topical treatment may be beneficial in chronic plaque

psoriasis; the drugs may be used separately at different times

of the day or used together in a single formulation. Eczema

co-existing with psoriasis may be treated with a

corticosteroid, or coal tar, or both.

BNF 78 Eczema and psoriasis 1239

Skin

13

Phototherapy

Phototherapy is available in specialist centres under the

supervision of a dermatologist. Ultraviolet B (UVB)

radiation is usually effective for chronic stable psoriasis and

for guttate psoriasis. It may be considered for patients with

moderately severe psoriasis in whom topical treatment has

failed, but it may irritate inflammatory psoriasis.

Photochemotherapy combining long-wave ultraviolet A

radiation with a psoralen (PUVA) is available in specialist

centres under the supervision of a dermatologist. The

psoralen, which enhances the effect of irradiation, is

administered either by mouth or topically. PUVA is effective

in most forms of psoriasis, including localised palmoplantar

pustular psoriasis. Early adverse effects include phototoxicity

and pruritus. Higher cumulative doses exaggerate skin

ageing, increase the risk of dysplastic and neoplastic skin

lesions, especially squamous cancer, and pose a theoretical

risk of cataracts.

Phototherapy combined with coal tar, dithranol,

tazarotene, topical vitamin D or vitamin D analogues, or oral

acitretin, allows reduction of the cumulative dose of

phototherapy required to treat psoriasis.

Systemic treatment

Systemic treatment is required for severe, resistant,

unstable or complicated forms of psoriasis, and it should be

initiated only under specialist supervision. Systemic drugs

for psoriasis include acitretin and drugs that affect the

immune response (such as ciclosporin p. 838 and

methotrexate p. 913).

Systemic corticosteroids should be used only rarely in

psoriasis because rebound deterioration may occur on

reducing the dose.

Acitretin p. 1261, a metabolite of etretinate, is a retinoid

(vitamin A derivative); it is prescribed by specialists. The

main indication for acitretin is psoriasis, but it is also used in

disorders of keratinisation such as severe Darier’s disease

(keratosis follicularis), and some forms of ichthyosis.

Although a minority of cases of psoriasis respond well to

acitretin alone, it is only moderately effective in many cases

and it is combined with other treatments. A therapeutic

effect occurs after 2 to 4 weeks and the maximum benefit

after 4 months. Consideration should be given to stopping

acitretin if the response is inadequate after 4 months at the

optimum dose. The manufacturers of acitretin do not

recommend continuous treatment for longer than 6 months.

However, some patients may benefit from longer treatment,

provided that the lowest effective dose is used, patients are

monitored carefully for adverse effects, and the need for

treatment is reviewed regularly.

Apart from teratogenicity, which remains a risk for 3 years

after stopping, acitretin is the least toxic systemic treatment

for psoriasis; in women with a potential for child-bearing,

the possibility of pregnancy must be excluded before

treatment and effective contraception must be used during

treatment and for at least 3 years afterwards (oral

progestogen-only contraceptives not considered effective).

Topical treatment

The vitamin D and analogues, calcipotriol p. 1263, calcitriol

p. 1263, and tacalcitol p. 1264 are used for the management

of plaque psoriasis. They should be avoided by those with

calcium metabolism disorders, and used with caution in

generalised pustular or erythrodermic exfoliative psoriasis

(enhanced risk of hypercalcaemia).

Eczema and psoriasis, drugs

affecting the immune response

Overview

Drugs affecting the immune response are used for eczema or

psoriasis. Systemic drugs acting on the immune system are

used under specialist supervision.

Pimecrolimus p. 1255 by topical application is licensed for

mild to moderate atopic eczema. Tacrolimus p. 1256 is

licensed for topical use in moderate to severe atopic eczema.

Both are drugs whose long-term safety is still being

evaluated and they should not usually be considered firstline treatments unless there is a specific reason to avoid or

reduce the use of topical corticosteroids. Treatment of atopic

eczema with topical pimecrolimus or topical tacrolimus

should be initiated only by prescribers experienced in

managing the condition. Topical tacrolimus and

pimecrolimus have a role in the treatment of psoriasis.

A short course of a systemic corticosteroid can be given for

eczema flares that have not improved despite appropriate

topical treatment.

Ciclosporin p. 838 by mouth can be used for severe

psoriasis and for severe eczema. Azathioprine p. 836 or

mycophenolate mofetil p. 846 are used for severe refractory

eczema [unlicensed indication]. Dupilumab p. 1257 is

licensed for the treatment of moderate to severe atopic

eczema in patients requiring systemic therapy. Dimethyl

fumarate p. 853 is licensed for the treatment of moderate to

severe plaque psoriasis.

Methotrexate p. 913 can be used for severe psoriasis, the

dose being adjusted according to severity of the condition

and haematological and biochemical measurements. Folic

acid p. 1025 should be given to reduce the possibility of sideeffects associated with methotrexate. Folic acid can be given

once weekly [unlicensed indication], on a different day from

the methotrexate; alternative regimens of folic acid may be

used in some settings.

Etanercept p. 1113, adalimumab p. 1108, and infliximab

p. 1116 inhibit the activity of tumour necrosis factor (TNFa).

They are used for severe plaque psoriasis either refractory to

at least 2 standard systemic treatments and

photochemotherapy, or when standard treatments cannot be

used because of intolerance or contra-indications; while

either etanercept or adalimumab is considered to be the first

choice in stable disease, infliximab or adalimumab may be

useful when rapid disease control is required. Secukinumab

p. 1100 and ixekizumab p. 1259 inhibit the activity of

interleukin-17A, brodalumab p. 1257 inhibits the activity of

interleukin-17RA and guselkumab p. 1258 inhibits the

activity of interleukin-23. They are used for moderate to

severe plaque psoriasis in patients who are candidates for

systemic therapy. Secukinumab is also licensed for psoriatic

arthritis and ankylosing spondylitis. Ustekinumab p. 1103 (a

monoclonal antibody that inhibits interleukins 12 and 23)

can be used for severe plaque psoriasis that has not responded

to at least 2 standard systemic treatments and

photochemotherapy, or when these treatments cannot be

used because of intolerance or contra-indications.

Adalimumab is also licensed for the treatment of active

moderate to severe hidradenitis suppurativa (acne inversa)

in patients who have had inadequate response to

conventional systemic therapy. Adalimumab, etanercept,

infliximab, ixekizumab and ustekinumab are also licensed

for psoriatic arthritis.

Other drugs used for Eczema and psoriasis Apremilast,

p. 1119 . Certolizumab pegol, p. 1111

1240 Inflammatory skin conditions BNF 78

Skin

13

CORTICOSTEROIDS

Topical corticosteroids

Overview

Topical corticosteroids are used for the treatment of

inflammatory conditions of the skin (other than those

arising from an infection), in particular eczema, contact

dermatitis, insect stings, and eczema of scabies.

Corticosteroids suppress the inflammatory reaction during

use; they are not curative and on discontinuation a rebound

exacerbation of the condition may occur. They are generally

used to relieve symptoms and suppress signs of the disorder

when other measures such as emollients are ineffective.

Topical corticosteroids are not recommended in the

routine treatment of urticaria; treatment should only be

initiated and supervised by a specialist. They should not be

used indiscriminately in pruritus (where they will only

benefit if inflammation is causing the itch) and are not

recommended for acne vulgaris.

Systemic or very potent topical corticosteroids should be

avoided or given only under specialist supervision in

psoriasis because, although they may suppress the psoriasis

in the short term, relapse or vigorous rebound occurs on

withdrawal (sometimes precipitating severe pustular

psoriasis). See the role of topical corticosteroids in the

treatment of psoriasis.

In general, the most potent topical corticosteroids should

be reserved for recalcitrant dermatoses such as chronic

discoid lupus erythematosus, lichen simplex chronicus,

hypertrophic lichen planus, and palmoplantar pustulosis.

Potent corticosteroids should generally be avoided on the

face and skin flexures, but specialists occasionally prescribe

them for use on these areas in certain circumstances.

When topical treatment has failed, intralesional

corticosteroid injections may be used. These are more

effective than the very potent topical corticosteroid

preparations and should be reserved for severe cases where

there are localised lesions such as keloid scars, hypertrophic

lichen planus, or localised alopecia areata.

Perioral lesions

Hydrocortisone cream 1% p. 1247 can be used for up to

7 days to treat uninfected inflammatory lesions on the lips.

Hydrocortisone with miconazole cream or ointment p. 1252

is useful where infection by susceptible organisms and

inflammation co-exist, particularly for initial treatment (up

to 7 days) e.g. in angular cheilitis. Organisms susceptible to

miconazole include Candida spp. and many Gram-positive

bacteria including streptococci and staphylococci.

Choice of formulation

Water-miscible corticosteroid creams are suitable for moist

or weeping lesions whereas ointments are generally chosen

for dry, lichenified or scaly lesions or where a more occlusive

effect is required. Lotions may be useful when minimal

application to a large or hair-bearing area is required or for

the treatment of exudative lesions. Occlusive polythene or

hydrocolloid dressings increase absorption, but also increase

the risk of side effects; they are therefore used only under

supervision on a short-term basis for areas of very thick skin

(such as the palms and soles). The inclusion of urea or

salicylic acid also increases the penetration of the

corticosteroid.

In the BNF publications topical corticosteroids for the skin

are categorised as ‘mild’, ‘moderately potent’, ‘potent’ or

‘very potent’; the least potent preparation which is effective

should be chosen but dilution should be avoided whenever

possible.

Absorption through the skin

Mild and moderately potent topical corticosteroids are

associated with few side-effects but care is required in the

use of potent and very potent corticosteroids. Absorption

through the skin can rarely cause adrenal suppression and

even Cushing’s syndrome, depending on the area of the body

being treated and the duration of treatment. Absorption is

greatest where the skin is thin or raw, and from

intertriginous areas; it is increased by occlusion.

Suitable quantities of corticosteroid

preparations to be prescribed for specific areas

of the body

Area of body Creams and Ointments

Face and neck 15 to 30 g

Both hands 15 to 30 g

Scalp 15 to 30 g

Both arms 30 to 60g

Both legs 100 g

Trunk 100 g

Groins and genitalia 15 to 30 g

These amounts are usually suitable for an adult for a single daily

application for 2 weeks

Compound preparations

The advantages of including other substances (such as

antibacterials or antifungals) with corticosteroids in topical

preparations are uncertain, but such combinations may have

a place where inflammatory skin conditions are associated

with bacterial or fungal infection, such as infected eczema.

In these cases the antimicrobial drug should be chosen

according to the sensitivity of the infecting organism and

used regularly for a short period (typically twice daily for

1 week). Longer use increases the likelihood of resistance

and of sensitisation.

The keratolytic effect of salicylic acid p. 1286 facilitates the

absorption of topical corticosteroids; however, excessive and

prolonged use of topical preparations containing salicylic

acid may cause salicylism.

Topical corticosteroid preparation potencies

Potency of a topical corticosteroid preparation is a result of

the formulation as well as the corticosteroid. Therefore,

proprietary names are shown.

Mild

. Hydrocortisone 0.1–2.5%

. Dioderm

. Mildison

. Synalar 1 in 10 dilution

Mild with antimicrobials

. Canesten HC

. Daktacort

. Econacort

. Fucidin H

. Nystaform-HC

. Terra-Cortril

. Timodine

Moderate

. Betnovate-RD

. Eumovate

. Haelan

. Modrasone

. Synalar 1 in 4 Dilution

. Ultralanum Plain

Moderate with antimicrobials

. Trimovate

Moderate with urea:

. Alphaderm

BNF 78 Eczema and psoriasis 1241

Skin

13

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