Pruritus: an overview. What drives people to scratch an itch?

Pruritus is a common complaint associated with many conditions. It negatively impacts sleep, quality of life, and mortality. Itch is transmitted along both histaminergic and non-histaminergic pathways with a complex interplay between keratinocytes, immune cells and cutaneous neurons. Individuals who present with pruritus should undergo a thorough assessment, especially those over 65 years old, to exclude underlying malignancy. Treatment no longer consists of antihistamines alone. Physicians now have an array of therapies in their armamentarium, to help alleviate this distressing symptom.

INTRODUCTION

Pruritus is a common complaint with many aetiologies. It is defined as a sensation that drives the urge to scratch.[1] It can be acute (less than 6 weeks) or chronic (greater than 6 weeks). Pruritus severely impacts upon quality of life affecting activities of daily living and sleep.[2] It is important when assessing patients to take a detailed history, perform a focused physical examination, form a structured differential diagnosis and request appropriate investigations.

CASE REPORT

A 45-year-old woman presents to clinic with generalised itch, which has been present for 1 year but has increased in severity over the last few weeks. It is worse at night. On questioning, she states that while she is itchy everywhere it is worse on the palms and soles. She also complains of fatigue and nausea. Family have commented that recently her skin has turned yellow. She has a past history of hypothyroidism, controlled with thyroxine and she has not been started on any new medications.

On general inspection there is evidence of jaundice and scleral icterus. On full skin examination there are excoriations and lichenification, pronounced on her hands and feet. There is no evidence of a primary skin rash and she is clinically euthyroid.

What is the diagnosis and what would be the management plan for this patient? (Answer at the end of this review)

PATHOPHYSIOLOGY

Pruritus originates in the epidermis and dermo-epidermal junction. There is a complex interplay between activated un-myelinated C nerve fibers, immune cells and keratinocytes. There is release of several pruritogens, including proteases, cytokines, prostaglandins, neuropeptides, nerve growth factor and histamine. There is also activation of several pruritic receptors including protease-activated receptors and ion channel receptors. (TRPV1, TRPV3, TRPA1, TRPM8) Opioids and the different receptors are known to be involved in pruritus. Activation of the μ opioid receptor (e.g with morphine) causes pruritus. Conversely, antagonism of the κ-opioid receptor is pruritogenic.

The pruritic nerve impulse is propagated along C nerve fibers to the dorsal root ganglion at the spinal cord. Here the nerve impulse crosses to the contralateral spinothalamic tract, where the impulse then ascends to the laminar nuclei of the thalamus.[3, 4] It is interesting to note that the histamine dependent and histamine independent pathways have separate projections in the spinothalamic tracts. Scratching activity has been shown to inhibit activation of spinothalamic tract neuronal activity in primate models and experimental evidence suggests that scratching activates inhibitory interneurons to release glycine and gamma-aminobutyric acid (GABA) and inhibit itch neurons.[5, 6]

NEUROBIOLOGY OF ITCH

From the thalamus, the pruritic nerve impulse is transmitted to different regions of the brain. Functional neuroimaging studies have identified many different subcortical and cortical areas involved in itch.[7-10] These areas relate to the sensory perception of itch, evaluation of the sensation, motivation, attention, emotion, and motor functions, such as motor planning.[7-9]

In addition, the precuneus, involved in memory, visual-spatial awareness and consciousness, is activated after acute itch stimulation.[11] In contrast, no activation of the precuneus was identified, after application of an acute painful stimulus.[12]

Once scratching begins, imaging shows activation of the reward system due to the feeling of pleasure.[10]

In one study, the cerebellum, which is involved in the coordination of motor-related activity, showed no activation during both itch-induced scratching and scratching alone, in chronic itch subjects; however in healthy subjects, cerebellar activation was observed.[9] This suggests decreased control of motor-related activity in patients suffering from chronic pruritus.

This pattern of neuronal network activation is different from that of pain perception, although there is significant overlap. Early studies have shown that when patients experience itch, activation of the ipsilateral motor areas, which plan the scratching response, occurs. (e.g, allowing the right hand to scratch the left forearm) This is in contrast to a painful stimulus where there is activation of the contralateral motor areas, in order to withdraw the limb from the painful stimulus.[8]

Two mechanisms have been postulated that contribute to chronic itch, namely peripheral and central sensitisation.[7] In peripheral sensitisation there is a reduced threshold at which itch sensation is perceived along with a higher basal activity of pruritogenic receptors and nerve fibres. Central sensitisation results from the effects of neural plasticity, whereby non-itch stimuli exacerbate and are perceived as an itch sensation.

There is also a complex interplay between itch and sleep mechanisms.[2] Pruritus may be experienced throughout the sleep cycle, with a predilection for the lightest stages. There is a complex interaction between circadian factors, and inflammatory mediators as well as psychological factors that can exacerbate nocturnal itch. This is a neglected area, which has already been shown to have a huge impact on mortality in patients with hemodialysis dependent renal failure.[13]

CAUSES

A myriad of conditions can cause chronic pruritus. Table 1 outlines a short list of different dermatologic and non-dermatologic causes.[14-16]

Table 1

Common causes of pruritus.

Common causes of itch
Dermatological	Non-dermatological
Atopic dermatitis	Cholestasis Intra-hepatic Extra-hepatic Drug-induced
Seborrheic dermatitis	Kidney End-stage renal disease
Contact dermatitis	Neurological CNS	Multiple sclerosis Brain neoplasm Cerebrovascular accident
	PNS	Brachio-radial pruritus Notalgia paresthetica Post-herpetic neuralgia Small fiber neuropathy
Psoriasis	Hematopoietic disease Lymphoma Multiple myeloma Myeloproliferative disorders (e.g polycythemia vera, essential thrombocytosis, 1°myelofibrosis) Iron-deficiency anemia Myelodysplastic disorders
Urticaria	Endocrine Thyroid disease Diabetes mellitus; diabetic neuropathy Anorexia nervosa Parathyroid disease
Infestations Scabies Bed bugs Pediculosis Pinworms	Connective tissue disorders Dermatomyositis Scleroderma Sjögrens syndrome
Dermatophytosis Tinea corporis Tinea cruris Tinea pedis	Psychological Depression Delusion of parasitosis Obsessive compulsive disorder Stress Fibromyalgia
Bullous disorders Bullous pemphigoid Dermatitis herpetiformis Pregnancy associated Drug eruption	Medications (some examples) Opioids Anti-hypertensives (ACE inhibitors, ARB’s, beta-adrenergic blockers, diuretics, calcium channel blockers) Antibiotics Biguanides; Sulphonylurea derivatives Chloroquine Hydroxyethyl starch (artificial colloid intravenous fluid) Statins
Lichen planus; lichen sclerosus	Neoplasia/Paraneoplastic phenomenon
Lichen simplex chronicus	HIV
Cutaneous T-cell lymphoma	Advanced age (senile)
Xerosis	Pregnancy associated cutaneous disorders
Stasis dermatitis (venous eczema)	Post transplant
Mastocytosis (cutaneous & systemic)	Hypereosinophilic syndrome

Abbreviations: CNS = central nervous system. PNS = peripheral nervous system. ACE = angiotensin converting enzyme. ARB = angiotensin II receptor blocker (antagonist). HIV = human immunodeficiency virus

DERMATOLOGICAL DISORDERS

Numerous dermatological disorders are associated with chronic itch. Some important examples are provided below.

ATOPIC DERMATITIS

Pruritus is the hallmark of atopic dermatitis (AD) and has a significant impact on sleep and quality of life.[2, 17] Atopic dermatitis is an immune-mediated inflammatory skin disease with damage to the skin barrier. Epidermal barrier dysfunction has been associated with both decreased expression of filaggrin (an important protein involved in epidermal structure) and a reduced amount of epidermal lipids such as ceramides, aiding the entry of different pruritogens.[18] Repetitive scratching may also disrupt the epidermal barrier, and further contribute to the resultant immune response. Activation of T-lymphocytes results in the release of several cytokines, such as the Th2 cytokines IL-31, IL-4 and IL-13. Targeting these cytokines is revolutionising the treatment of atopic dermatitis.[19] Alloknesis, a phenomenon in which a normally innocuous stimulus induces itch, such as changes in temperature or contact with clothing, is a prominent feature in atopic eczema.

Finally, patients with atopic dermatitis have an altered microbiome favouring growth of staphylococcus aureus. These organisms release molecules which further contribute to the resultant inflammation and pruritus.(

There are many cutaneous findings in patients with AD – e.g. predominant flexural cutaneous involvement, hyperlinearity of the skin on the palms and soles and Dennie-Morgan folds (creases on the skin below the eyelashes).[21] In addition, an infra-auricular fissure (fissure present on the posterior aspect of the ear lobe) may be present, the severity of which correlates with AD severity.[22]

PSORIASIS

Psoriasis is a chronic immune-mediated inflammatory disorder, occurring in genetically predisposed individuals, with different environmental factors attributed to the disease and its flares. (e.g infections, medications, stress) Pruritus is reported in approximately 60-90% of psoriatic patients[23, 24] and has only recently been recognized as a major symptom in this chronic disease that affects 2-3% of the population.[25] In psoriasis, a dysregulated immune system is related to the overproduction of pro-inflammatory cytokines, including TNF-α, IL-12, IL-17, IL-23, which have a pruritic effect. In addition, the neural system is activated, with release of multiple substances, (in particular nerve growth factor (NGF) and Substance P), along with abnormal psoriatic skin innervation, imbalance in kappa- and mu-opioid pathways and increased levels of gamma-aminobutyric acid (GABA) and its receptor (GABAA).[24] These have all been shown to contribute to pruritus in psoriatic patients.

INFESTATIONS

Patients suffering from scabies infestation often complain of severe (predominantly nocturnal) itch. The pruritus occurs through the release of proteases excreted in the mite’s faeces. The release of pruritic cytokines, from the activation of T-helper 2 lymphocytes, is also attributed to the pruritus in scabies, pediculosis (lice) and pinworm infestations. The movement of enterobius vermicularis (the causative agent in pinworm infestations) on the skin, as well as the release of eggs, commonly causes intense peri-anal pruritus. Subsequent scratching deposits these eggs under the fingernails and the pinworm may therefore re-enter the oral cavity and gastrointestinal tract, if patients exhibit poor hand hygiene.[26, 27] Finally bed bugs are attracted to carbon dioxide and heat, and commonly feed on humans while they are sleeping at night.[28]

ADVANCED AGE PRURITUS

Pruritus is a common symptom in the elderly. A detailed history, examination and appropriate investigations must be performed, but often, no cause is identified. Patients exhibit xerosis (dry skin) with epidermal barrier dysfunction (with increased trans-epidermal water loss), alterations in pH, release of molecules (e.g proteases) and decreased estrogen levels. In addition there is immunosenescence (dampening of the immune system during the aging process) and neural degeneration comprising neuropathic itch (e.g. post herpetic neuralgia) and nerve compression (radiculopathy)[29]

CHRONIC URTICARIA

Urticaria is a disorder associated with mast cell degranulation releasing substances including histamine, leukotrienes and prostaglandins. It has a prevalence of 0.5-1%.[30] Clinically, this manifests with wheals, angioedema or both, and usually lasts less than 24 hours. Urticaria is divided into acute (duration <6 weeks) or chronic (duration >6 weeks). New classification subdivides chronic urticaria into chronic inducible urticaria (CINDU) and chronic spontaneous urticaria (CSU).[31] There are many different triggers for CINDU including cold, sunlight, contact and aqueous. In many cases, a specific cause may not be identified.

The arms, back and legs are commonly affected. The accompanying pruritus is described as stinging, tickling or burning.[32]

Second generation, non-sedating antihistamines are currently recommended as first-line therapy for chronic urticaria.[33]. Other treatments include doxepin, leukotriene antagonists, histamine-2 antagonists, ciclosporin and mycophenolate mofetil. Omalizumab, a monoclonal antibody that targets and neutralizes free IgE, is a useful alternative antipruritic medication in unresponsive patients.[34] Its use is restricted to physicians with experience in prescribing this medication.

NON-DERMATOLOGICAL DISORDERS CHOLESTATIC ITCH

Cholestatic pruritus may be subdivided into intra-hepatic, (e.g chronic hepatitis, carcinoma, primary biliary cirrhosis, intrahepatic cholestasis of pregnancy, Alagille syndrome) extra-hepatic (e.g cholelithiasis/choledocholithiasis, primary sclerosing cholangitis, bile duct stricture, cholangiocarcinoma, pancreatic carcinoma) and drug-induced. (e.g macrolides, chlorpromazine)[35] Patients classically complain of itch affecting the palms and soles of the feet.

The exact pathophysiology is not fully known, however cholestatic pruritus has been associated with accumulation of bile salts, bile acids as well as increased levels of bilirubin and endogenous opioids. Elevated levels of a phospholipid (lysophosphatidic acid) and autotaxin, the enzyme that forms LPA, have been found in this cohort. Autotaxin has been shown to be a biomarker for cholestatic pruritus.[36]

Therapies such as bile acid sequestrants, mu-opioid antagonists, sertraline and rifampicin have been shown to improve cholestatic pruritus.[36, 37]

CKD ASSOCIATED PRURITUS

End stage renal disease patients, particularly those requiring haemodialysis, may suffer from chronic pruritus. The Dialysis Outcomes and Practice Patterns study (DOPPS) showed an increased mortality risk of 17% among 18,801 pruritic haemodialysis patients. This was in part attributed to a decreased quality of sleep.[13] Around 50-90% of patients on dialysis suffer from pruritus.[38] The pathophysiology is uncertain. There are several hypotheses, including abnormal calcium, phosphate and parathyroid levels, an imbalance among opioids, central neuropathy and a pro-inflammatory state.[39] Pruritus is usually only observed in patients with chronic (rarely acute) kidney disease.[40]

Itching commonly involves the back, but the head, neck and torso may also be affected.[4, 40–42] Treatment involves adequate skin hydration and optimization of renal status. Antihistamines tend not to be effective. Gabapentin has been shown to improve CKD itch,43 but care should be taken in monitoring renal function. Nalfurafine, a kappa opioid agonist, has also shown to improve CKD pruritus but is currently unlicensed for this indication.19,44 Ultraviolet light therapy is another modality that may be employed. 39 Other opioid therapies are undergoing trials for this condition.45-47

HAEMATOLOGICAL

Itch may be a prominent feature in haematological disorders e.g Hodgkin’s lymphoma, chronic lymphocytic leukemia, multiple myeloma, cutaneous T-cell lymphoma (CTCL) and polycythemia vera. Pruritus is present in around 19% of patients with Hodgkin’s lymphoma[48] and approximately 15% of patients with non-Hodgkin’s lymphoma.[49] The pruritus in Hodgkin’s lymphoma is usually associated with disease activity.[14] IL-31 has been shown to be significantly increased in the epidermis and dermis of patients with CTCL.[50] There have been reports of patients who have chronic pruritus with no cutaneous manifestations, but with underlying mycosis fungoides.[51-53] This highlights the necessity to constantly review the diagnosis in patients with chronic pruritus. Finally, while water may also aggravate pruritus in patients with urticaria, aquagenic pruritus warrants investigation for evidence of polycythemia vera.

NEUROPATHIC ITCH

Neurological disorders may also display pruritus. Neuropathic itch has been defined as “an itch initiated or caused by a primary lesion or dysfunction at any point along the afferent pathway of the nervous system.”[54] Brachioradial pruritus (BRP) usually presents with itch affecting dermatomes C4-C7. Compression of nerve fibers from cervical disc degeneration, spinal stenosis or malignancy may be the underlying cause. Notalgia paresthetica is another form of radiculopathy that may present with unilateral localized pruritus in the mid back, following a T2-T6 distribution. It may be associated with a sensory neuropathy and burning pain.[54]

Post-herpetic neuralgia can cause significant pruritus in up to 48% of patients. The itch commonly involves the face and neck.[55, 56]

Topical capsaicin, which decreases Substance P release from C-nerve fibers, and GABAergic medications, may help.[57]

Central nervous system (CNS) disorders causing itch are usually due to brainstem or subcortical lesions.[7] Unilateral itch has been reported following cerebral infarction, as well as in patients with a cortical stroke.[7] Pruritus associated with multiple sclerosis is rare, occurring in only 4.5% of patients.[58]

INVESTIGATIONS

If pruritus is acute (< 6 weeks) one should determine if any new medications have been prescribed and check for any associated rash – e.g. urticaria causes itch and an erythematous rash but generally does not persist for >24 hours.

If the pruritus is chronic (> 6 weeks), then a comprehensive review is required. In the elderly, it is important to consider underlying malignancy. The presence of a rash may be pivotal in determining the diagnosis; however not every patient will have a rash and often there may just be excoriations or lichenification. Figure 2 outlines a flowchart for the management of patients who present with chronic pruritus.

Fig 2

Chronic pruritus algorithm

highlights these activated brain regions.

TREATMENT

Before commencing treatment, it is important to determine if the patient has acute or chronic pruritus, and then investigate for the cause and evidence of any underlying malignancy; however, while results are awaited, therapy may be initiated.

Treatment can be divided into topical or oral therapy. Antihistamines are generally not effective in chronic pruritus. Topical therapies such as moisturizers, low pH cleansers, short-term use of topical corticosteroids, menthol, capsaicin, strontium and topical anesthetic agents may be employed. Oral medications, such as low dose mirtazapine and gabaergic agents (gabapentin, pregabalin) have been shown to be beneficial. Therapies to treat the underlying condition are also important.

Major pharmacological treatment modalities, both topical and systemic, are discussed below and summarized in Table 3 and 4.

Table 3

Examples of systemic therapies to treat chronic pruritus

Systemic medications	Mode of action	Dose
Sedating antihistamines e.g. Chlorphenamine Diphenhydramine Hydroxyzine	H1 antagonist	4-16 mg 5-200 mg 25-100 mg
Non-sedating antihistamines e.g. Cetirizine Fexofenadine Levocetirizine Loratadine	H1 antagonist	10-20 mg 180-360 mg 5-10 mg 10-20 mg
Mirtazapine	SNRI, SSRI	7.5-15 mg
GabapentinPregabalin	Modulate GABA	300-3600 mg 150-450 mg
Opioids Naltrexone	μ-opioid receptor antagonist	25–50 mg
Butorphanol Nalfurafine	κ-opioid receptor agonist	1–4 mg 2.5-5 μg

Abbreviations: H1 = histamine 1. SNRI = serotonin noradrenaline re-uptake inhibitor. SSRI = selective serotonin re-uptake inhibitor. GABA = gamma-aminobutyric acid

Topical

An array of medications is available to treat pruritus. Basic skin care management cannot be over-emphasised. Simple treatment with moisturisers can have a huge impact upon the intensity of pruritus by improving skin barrier dysfunction and reducing the entry of pruritogens. Patients should use moisturisers liberally. For convenience, creams are usually applied during the day and greasier ointments at night. If patients are required to apply topical steroid creams, these should be applied before moisturisers. Wet pyjama therapy, whereby the patient applies a topical moisturiser with a corticosteroid and then dons ‘wet’ pyjamas (pyjamas that have been rinsed in water and then wrung out) has been shown to improve pruritus.[59] Explanation of the efficacy of this treatment is recommended due to the lack of willingness to adopt this approach.

It now recognized that high skin pH results in the release of proteases and activation of proteinase activating receptors. (PAR-2) This leads to inflammation, an impaired skin barrier and decreased stratum corneum cohesion. As such, syndet (synthetic detergent) products, which have a lower pH, (4.5-6.0) should be favored.[60, 61]

Ion channels, such as TRPV1 and TRPM8 are known to be involved in the pathophysiology of chronic pruritus. Capsaicin, an ingredient of hot chili peppers, initially activates but over time desensitizes TRPV1 ion channels.[62] It may be used to treat patients with notalgia paresthetica, CKD and prurigo nodularis.[63, 64] The burning sensation that may occur after application of capsaicin may be reduced with pre-treatment with local anaesthetic cream.[65] An 8% patch has also shown efficacy in patients with neuropathic pruritus.[62, 66] Menthol, a TRPM8 agonist, evokes a cooling sensation and promotes repair of the skin barrier. [19] It may reduce pruritus in conditions such as lichen sclerosus and lichen amyloidosis.[67]

Other topical agents that are useful in reducing pruritus include pramoxine, strontrium and the compounded formulation of ketamine, amitriptyline and lidocaine. Pramoxine is a local anesthetic agent that reduces neuropathic, anogenital and CKD-associated pruritus.[68, 69] It may also be combined with corticosteroids to reduce both inflammation and pruritus. Topical strontium 4% hydrogel (a calcimimetic) has been shown to reduce both histaminergic and non-histaminergic induced pruritus.[70, 71]

The compounded formulation of ketamine, amitriptyline and lidocaine, (KAL) in various dosing percentages, has been successfully used to treat localised neuropathic itch. (unpublished data, Yosipovitch)

Finally Crisaborole (a topical phosphodiesterase-4 inhibitor) has shown promise in early trials by reducing pruritus associated with AD.[72]

Oral

Traditionally, antihistamines have been used to treat pruritus. These can be helpful in treating urticaria, cutaneous mastocytosis and drug-induced pruritus.[15] Antihistamines work by antagonizing the histamine-1 receptor and can have indirect effects on the TRPV1 ion channel.[16] They can be divided into sedating (e.g chlorphenamine, diphenhydramine, hydroxyzine) and non-sedating (e.g cetirizine, levocetirizine, fexofenadine). Sedating antihistamines cause drowsiness and as such are generally taken at night. These medications can still exert adverse daytime effects and may lead to daytime somnolence and increased risk of accidents. Improvement of nocturnal pruritus is likely due to this sedating effect. Guidelines recommend use of non-sedating antihistamines if these agents are to be employed to treat pruritus associated with urticaria.[33] There is a lack of data however on the efficacy of antihistamines to treat chronic pruritus. Given that the histaminergic pathway is not the main pathway involved in chronic pruritus, novel therapies have been sought.

Gabaergics, such as gabapentin and pregabalin, which are structural analogs of gamma-aminobutyric acid, have shown efficacy in treating pruritus in CKD patients[43] as well as in patients with neuropathic itch. [3] They may also be effective in other causes of chronic pruritus. Side-effects include drowsiness, increased appetite, and lower limb edema.

Mirtazapine has been shown to improve nocturnal pruritus. It is an antagonist of alpha-2 noradrenergic receptors, as well as H1, 5HT-2 and 5HT-3 cutaneous receptors. It has been used successfully to treat pruritus associated with malignant cholestasis, uremia, lymphoma, atopic dermatitis, urticaria and carcinoma en cuirasse.[73-75] Mirtazapine has a favorable safety profile. Side-effects include drowsiness, increased appetite and dry mouth. While patients may be hesitant to commence this medication due to fear of weight gain and drowsiness, these side-effects are also associated with sedating anti-histamines.

As noted above, there is a complex interaction between pain and itch – e.g. when patients scratch an itch it initially incites a pleasurable sensation. Medications, such as morphine, a μ-opioid receptor agonist, are known to cause pruritus. Conversely κ-opioid receptor antagonists will cause pruritus. It is therefore intuitive to prescribe patients either antagonists or agonists of the μ-/κ-opioid receptor, respectively. Naltrexone, a μ-opioid receptor antagonist, has been shown to reduce cholestatic pruritus and refractory itch in burn patients.[76, 77] Its efficacy in CKD-associated pruritus has not always been reproduced.[78, 79] Nalfurafine, a selective κ-opioid receptor agonist, has been shown to reduce CKD itch, however it is currently not licensed in the USA or Europe.[44] Butorphanol, a partial μ receptor antagonist and κ receptor agonist, has been used for intractable chronic pruritus.[80] It is an intranasal spray with 1 puff representing 1mg. Up to 4mg may be used over 24 hours if necessary. A recent study revealed that butorphanol deactivates areas of the brain that were initially activated during itch processing.[81]

Other

Immunosuppressants such as methotrexate, cyclosporine, azathioprine, mycophenolate mofetil have been used for inflammatory pruritic skin diseases.[82-84]

Novel medications that target specific pruritic cytokines and neurotrophins, are undergoing clinical trials, with promising results. Dupilumab, a monoclonal antibody that targets IL-4 and IL-13 has been shown to reduce pruritus in patients with moderate to severe atopic dermatitis. It has been assigned breakthrough status by the FDA.[85] Monoclonal antibodies targeting the pruritic IL-31 cytokine have shown quantitative reduction in pruritus in early trials.[19] Ustekinumab (IL-12 and IL-23 receptor antagonist) is currently licensed for use in psoriasis and psoriatic arthritis and has been shown to improve psoriatic pruritus. It is currently undergoing clinical trial evaluation in patients with atopic dermatitis.[86] Secukinumab and Ixekizumab (targeting IL-17A) have shown significant anti-pruritic effect in psoriatic patients.[87, 88] The oral phosphodiesterase-4 inhibitor, apremilast, has also shown an anti-pruritic effect in psoriasis.[89]

Non-pharmacological therapy

Non-pharmacological management of pruritus may also be employed. Psychological interventions such as progressive muscle relaxation and habit-reversal therapy may improve chronic pruritus.[90] We have found at our institution (MJL, GY) that progressive muscle relaxation, subjectively improves pruritus.

Diet is a major concern for patients with chronic pruritus, especially those suffering with atopic dermatitis. While these patients often have associated food allergies, strict dietary practice is not advocated.[18] The American Academy of Dermatology has recently produced guidelines on the management of atopic dermatitis, including dietary recommendations.[91] These include avoidance of foods that cause a true IgE-mediated allergy; however it does not recommend eliminating foods, based on allergy tests alone.

CONCLUSION

Research has increased our understanding of the pathophysiology of pruritus. It is imperative that physicians investigate for underlying systemic disease and malignancy, especially in the elderly.

There is now awareness of the different brain pathways that are activated and further research into how this knowledge can be incorporated into treatments is warranted.

In addition, knowledge of the different pathways (histamine and non-histamine) and mediators involved in itch has changed the pharmacological management of pruritus. Histamine is no longer the only known mediator associated with pruritus, and therefore antihistamines used alone, may not be effective. Novel targeted therapies which not only reduce the severity of the disease, but also reduce pruritus have ushered in a new era. The aim of treatment for both patients and physicians is to reduce itch intensity. Completely curing the pruritus is unlikely and patients should recognise this.

Table 2

Examples of topical therapies to treat chronic pruritus

Topical Medications	Mode of action	Dose
Emollients	Improve barrier function	Apply as needed
Oat meal extracts	Anti-inflammatoryAnti-oxidant	Apply as needed
Corticosteroid	Anti-inflammatory	As prescribed Short-term use advocated
TacrolimusPimecrolimus	Calcineurin inhibitor	0.03%; 0.1% ointment1% cream
Menthol	TRPM8 agonist	1-2% cream
Capsaicin	TRPV1 agonistReduces Substance P release from C-nerve fibers	0.025% - 0.1%Transdermal patch 8%
Pramoxine(with hydrocortisone)	Ion channel blocker(anti-inflammatory)	1% cream(2.5%)
Strontium 4%	Calcimimetic	4% hydrogel
Ketamine/Amitriptyline/Lidocaine	Ion channel blocker	Ketamine 5-10%,Amitriptyline 2-5%Lidocaine 2.5-5%Apply during pruritic episode
Doxepin	H1 and H2 antagonistTricyclic antidepressant	5% cream

Abbreviation: TRPM8 = Transient receptor potential subfamily M member 8. TRPV1 – Transient receptor potential subfamily V member 1. H1 = histamine 1. H2= histamine 2