Chronic Intractable Pruritus in Chronic Kidney Disease Patients: Prevalence, Impact, and Management Challenges — A Narrative Review

Abstract

Chronic kidney disease (CKD) is recognized as a leading public health problem and causes numerous health complications. One of the most common and burdensome dermatological symptoms affecting patients undergoing dialysis is CKD-associated pruritus (CKD-aP). This condition not only has a negative impact on sleep, mood, daily activities, and quality of life but also increases the mortality risk of hemodialyzed patients. Despite that, this condition is greatly underestimated in clinical practice. Due to the complex and still not fully understood etiopathogenesis of CKD-aP, the choice of an effective therapy remains a challenge for clinicians. Most common therapeutic algorithms use topical treatment, phototherapy, and various systemic approaches. This review aimed to summarize most recent theories about the pathogenesis, clinical features, and treatment of CKD-aP.

Introduction

Chronic itch (CI) is an uncomfortable sensation that causes a desire to scratch and lasts >6 weeks. In contrast to acute itch, which is regarded as a defense mechanism, CI occurs in many skin conditions and systemic diseases. The International Forum for the Study of Itch (IFSI) expert group created the classification of CI, basing it on the etiology of pruritus. They distinguished causes of CI as cutaneous (I), systemic (II), neurological (III), psychogenic (IV), mixed (V), and other (VI).1 Over the whole range of systemic disorders occurring with itch, special attention should be paid to chronic kidney disease (CKD). This condition was defined in 2002 by the National Kidney Foundation as an abnormality of kidney structure or function presenting at least for 3 months and having implications for patients’ health.2 The prevalence of CKD is about 13%, and it is recognized as a leading public health problem.3,4 CKD has a broad spectrum of complications, of which cutaneous manifestations play a great role. Changes in skin color, elastosis, ecchymoses, xerosis, and uremic frost, as well as perforating disorders, metastatic calcification, or bullous dermatosis, are often observed in end-stage renal disease (ESRD).5 One of the most common and burdensome dermatological symptoms affecting patients undergoing dialysis, described for the first time in 1932, is CKD-associated pruritus (CKD-aP). The nomenclature of this condition has changed over the years. Originally “uremic pruritus” was a common definition for itch associated with CKD. However, due to a lack of dependence between uremia and this sensation, CKD-aP or “CKD-associated itch” are more suitable.6 This condition not only has a negative impact on sleep, mood, daily activities, and quality of life (QoL) but also increases the mortality risk of hemodialysis (HD) patients.7,8 Despite this, the condition is often underestimated in clinical practice.9 Due to the etiopathogenesis of CKD-aP not being fully understood, therapy for this condition remains a challenge for dermatologists and nephrologists.

Prevalence

Over the years, studies on CKD-aP have shown variable prevalence of this condition. From the beginning of dialysis therapy, scientists reported that even 85% of the patients with ESRD may suffer from CI.10 This number decreased with the development and accessibility of renal replacement therapy. It is difficult to specify a clear cause of this phenomenon, although possible explanations could be revealed through more precisely performed dialysis based on Kt/V or creatinine-clearance measurements.

The usage of more modern and biocompatible dialyzers can also bring about this positive effect.11 Additionally, by learning about other new factors that may cause uremic pruritus, it is possible to control them. One of the possible explanations is better control of calcium and phosphate metabolism in CKD patients. Pisoni et al12 in 2006 presented the results of the large international Dialysis Outcomes and Practice Patterns Study (DOPPS). The research assessed CI in 18,801 HD patients from 12 countries for 1996–2004. The first phase of the study focused on 1996–2001 (DOPPS I) and the second 2002–2004 (DOPPS II). Those perceiving moderate–extreme itch came to 45% and 42%, respectively, which confirmed a decreasing tendency of CKD-aP prevalence. A follow-up (2012–2015, DOPPS V), which involved 6,256 patients from 17 countries, showed that the proportion of patients with moderate or severe itch had declined to 37%.13 Rayner et al13 also emphasized how strongly underestimated CKD-aP is among nephrologists. Of HD patients in their study, 17% with CI did not report their symptoms to any health-care provider and 18% were not receiving any therapy. Similar results were observed for dialysis outcomes and practice patterns in Japan, where moderate–xtreme pruritus was noted by 44% of HD patients between 1999 and 2004.14 A German cross-sectional study investigated 860 HD patients and revealed CI prevalence of 25% and 12-month prevalence 27.2%. Approximately 35% of subjects had suffered from CI at least once in their lifetime.15 A meta-analysis of 42 cross-sectional studies showed that the prevalence of CKD-aP ranged between 18% and 97.8% and the overall prevalence of CKD-aP reached 55%. The analysis did not find any difference in prevalence the sexes. Pooled prevalence in male and female patients was 55%. CI occurred comparably often in patients undergoing peritoneal dialysis (PD) and HD patients (56% and 55%, respectively).16 However, a South Korean study assessed pruritus in 648 patients with ESRD and showed that not only prevalence (62.5% vs 48.3%) but also intensity of itch measured by a visual analogue scale (VAS) was significantly higher in PD patients than HD patients.17 On the other hand, Wu et al18 showed the opposite results. VAS scores were significantly higher in HD patients than PD patients. This notwithstanding, another study showed a lack of significant difference in severity of itching and similar prevalence of CI in HD and PD patients (61.8% and 61.5%, respectively).19 The research also investigated pruritus in a group of patients with stage 4 or 5 CKD without dialysis therapy, where the prevalence of CI was 43.2%. Another cross-sectional study determined the prevalence of CI in a group of 3,780 non-dialysis patients with CKD stages 3–5. The results showed that the prevalence of moderate–extreme pruritus was 24% and was more likely in older patients, women, and those with stage 5 CKD, lung disease, diabetes, and physician-diagnosed depression.20 Similar prevalence was found in a cross-sectional study of 402 stage 2–5 CKD patients. On the contrary, the prevalence of CKD-aP did not correlate with CKD stage and reached 18.9%.21

CI has been well investigated not only in adult populations but also among pediatric patients. CKD-aP in children occurs less commonly and with a more benign course than in adults.22 Data from German pediatric dialysis centers showed that only 9.1% of 199 children perceived itch. Reported intensity of pruritus was not severe.23 A multicenter Polish study found that pruritus affected 20.8% of children with CKD in stages 3–5.24 This was 18.4% in a group of predialysis patients and 23.5% on dialysis (HD or PD). The severity, duration, and location of pruritus did not statistically vary by method of applied therapy.

Underestimation

Despite the prevalence of CKD-aP — approximately 40% in HD patients — the problem appears to be markedly underestimated by clinicians. In phase V of DOPPS, 65% of medical directors estimated that <5% of their patients had severe pruritus, and overall they underestimated the prevalence of pruritus in 69% of facilities. Furthermore, as mentioned before, patients tend not to report CI to health-care providers. This varied from 8% in Italy and 12% in Gulf countries to 21% in Sweden and 33% in the US.13 This may be due to patients’ fear of numerous medical tests and extension of the diagnostic process, which can be burdensome for them. Years after reporting the CKD-aP and not receiving effective therapy, patients may feel resigned. A German cross-sectional survey completed by 204 nephrologists showed that most respondents estimated the prevalence of CI in HD patients to be <30%. This figure is inadequate to compare with international CKD-aP prevalence. The authors of that study presumed that clinicians neglecting this problem may be due to a lack of knowledge of effective therapy for CKD-aP.25 It is important to emphasize that lack of reporting this burdensome problem very often may be caused by a lack of interest and questions from nephrologists. A lack of available gold-standard therapy that could help patients intensifies this trend.

Pathogenesis

Scientists have developed several hypotheses regarding the development of pruritus in chronic renal failure, but the precise etiopathogenesis of this phenomenon remains elusive. False assumptions about the pathophysiological mechanisms of CKD-aP slow the discovery of better therapy in clinical practice; therefore, deeper research is necessary for breakthroughs in this area. This paper presents the most popular and proven theories as follow.

Xerosis

Characterized by rough and scaly skin, xerosis is a common complication in HD patients, with prevalence of 50%–85% and occurring with greater frequency in PD patients than HD patients.26 Evaluation of this skin condition among children with CKD was first performed by Wojtowicz-Prus et al.27 Approximately 68% of children undergoing dialysis presented xerosis. Based on published studies, it can be concluded that xerosis is a risk factor associated with CKD-aP.28,29 Research has shown that xerosis has an impact on the severity of itch.30 Morton et al31 demonstrated not only a correlation between itch and reduced stratum corneum hydration but also the efficacy of emollients in relieving the pruritus. However, not all studies in this area have confirmed these findings. Yosipovitch et al32 did not find a correlation between xerosis and itch. Similarly, in another cross-sectional study, there was no significant difference in xerosis prevalence between pruritic and nonpruritic patients.33 Despite these discrepancies, regular use of emollients is widely recommended for patients with CKD-aP and may improve not only dryness of the skin but also itch severity and patients’ QoL.34–36

CKD-aP as an Inflammatory Disease

Results of a multicenter study showed that inflammation and dysregulation of the immune system play a great role in the pathogenesis of CKD-aP. In research on 13 HD patients with CKD-aP and 13 without CKD-aP serum levels of inflammatory markers, IL6 and C-reactive protein were significantly elevated in patients with pruritus versus those without. This may be explained by augmented T_h1 lymphocyte differentiation in patients suffering from CKD-aP.36 Fallahzadeh et al37 supported the theory of T_h1 overactivity, showing significantly increased levels of the proinflammatory cytokine IL2 in HD patients with itch versus those without it. Two studies confirmed an important role of IL31 in CKD-aP pathophysiology, which may cause itch by stimulating peripheral nerve endings. Serum levels of IL31 were higher in patients reporting uremic itch.38,39 Despite this fact, a randomized double-blind placebo-controlled study with nemolizumab, a monoclonal antibody against IL31RA, did not find statistically significant reductions of VAS scores in CKD-aP patients.40 However, further investigation with a bigger, more representative group is required.

Uremic Toxins

CKD prevents proper elimination of various substances resulting from metabolic processes and predispose to its accumulation in the organism. These compounds, which interact negatively with various biological functions, are known as uremic toxins (UTs) and can be distinguished into three subgroups: small solutes, middle molecules, and protein-bound toxins. In 2021, the European Uremic Toxin (EUTox) database41 listed 130 substances. Low–molecular weight molecules can be readily removed during the process of dialysis. One of the substances belonging to this group — uric acid — not only has an impact on CKD progression and mortality risk but can also cause CKD-aP.42 According to a study performed by Wang et al43 on 320 patients with CKD, pruritus was associated with higher levels of uric acid. However, the outcomes of two other studies were contrary to this.21,44 The aforementioned research also estimated the role of protein-bound UTs (PBUTs), ie, indoxyl sulfate (IS) and p-cresyl sulfate (PCS), in the pathogenesis of pruritus. PBUTs are predominantly excreted by renal tubular secretion, which cannot be replaced by conventional dialysis. Thereby, they are barely eliminated in patients undergoing HD or PD.45 Patients with CKD-aP have higher total levels of IS and PCS than patients without itch. Total PCS concentration is significantly associated with pruritus severity.43 Another study investigated the effect of IS, PCS, and uremic sera from CKD patients on PAR2 expression in normal human epidermal keratinocytes. Both PBUTs and CKD induced PAR2 expression and upregulated PAR2 expression in skin samples taken from human and mouse CKD subjects compared to healthy controls.46 Similarly, Moon et al47 found significantly higher epidermal PAR2 expression in ESRD patients then in controls. In addition, a positive correlation between PAR2 expression and VAS pruritus scores was found. All these findings and the implication that PAR2 is a histamine-independent pruritic mediator confirmed the possible role of this receptor in CKD-aP etiopathogenesis.48 Wu et al49 performed metabolic profiling on 200 uremic patients to find metabolites associated with CKD-aP. They found nine markers likely to play a role in the pathogenesis of CKD-aP. Metabolites associated with severe CKD-aP were LysoPE (20:3[5Z,8Z,11Z]/0:0), p-cresol glucuronide, LysoPC (20:2[11Z,14Z]), hypotaurine, 4-aminohippuric acid, LysoPC (16:0), phenylacetic acid, kynurenic acid, and androstenedione. It must be noted, however, that it is difficult to draw any direct causal relationship between elevated serum levels of these compounds and CKD-aP occurrence. On the contrary, in their metabolomic analysis of plasma of HD patients with severe pruritus versus mild/no pruritus, Bolanos et al50 did not find any solutes associated with pruritus.

Calcium and Phosphorus Metabolism in CKD

CKD leads to imbalances in calcium, phosphorus, and vitamin D metabolism. An initial theory of CKD-aP mechanism also included calcium phosphate skin deposits, which arise as a result of imbalance between calcium and phosphorus in HD patients’ blood and are able to activate local nerve fibers.51,52 In 1985 Blachley et al53 suggested that an increased number of divalent ions found in skin biopsies obtained from patients with CKD-aP may lead to microprecipitation of calcium or magnesium phosphate and be the cause of pruritus. Momose et al54 found higher deposition of calcium ions in the basal layer of the epidermis in patients with moderate–severe itch versus patients without. Hyperphosphatemia, hypocalcemia, and decreased calcitriol production can all increase parathyroid hormone (PTH) production and consequently cause secondary hyperparathyroidism.55 PTH has been proposed by some authors as a pruritogenic factor. This conclusion was made based on studies that confirmed reductions in CKD-aP after parathyroidectomy.56,57 Makhlough et al58 found a significant difference in CKD-aP intensity between patients with and without hyperparathyroidism (5.71±5.39 and 4.93±2.93 points, respectively; P=0.005). PTH levels correlated with severity of pruritus in HD patients.58 However, other studies did not support the role of PTH as a mediator of CKD-aP.33,59,60 Intradermal injections of PTH analogues did not induce pruritus or any other cutaneous reaction in dialysis patients or control groups. This hormone was not detected in skin biopsies of HD patients either.61 Additionally, research performed by Duque et al62 on 105 HD patients excluded the role of PTH and serum phosphorus in presence or intensity of itch, but demonstrated a positive correlation between CKD-aP and calcium serum concentration. This interdependence was confirmed by several other studies, including DOPPS, which identified other factors associated with pruritus as well: longer period of dialysis, male sex, Kt/V_urea (ratio representing fractional urea clearance) <1.5, and lower serum levels of albumin, ferritin, and hemoglobin.12,55,63

Mast Cells

Histamine is well known as a classical itch mediator released from mast cells. However, it plays a key role only in certain pruritic diseases, such as mastocytosis or urticaria. Initially, the significance of this potential pruritogen was thoroughly tested in terms of CKD-aP. Various studies showed a positive correlation between serum levels of histamine and CKD-aP,64,65 whereas others disproved this theory.66,67 Additionally, according to different reports, mast cells occur in increased numbers, are diffusely spread, and more often degranulated in the skin of patients suffering from CKD-aP than in healthy controls.68–71 Nonetheless, Mettang et al72 did not confirm that histamine plasma levels and number of mast cells in the skin correlated with the presence of CKD-aP. Another pruritogenic mediator released from mast cells is tryptase. Dugas-Breit et al73 demonstrated a significant correlation between tryptase serum levels and itch severity. Likewise, serum levels of serotonin were higher in patients with CKD-aP than the control group.74 With the therapeutic use of a 5HT₃-receptor inhibitor, ondansetron, significant reduction in the severity of pruritus has been observed.75 Despite these contradictory findings, personal clinical experience affirms a lack of antihistamine effectiveness in CKD-aP therapy.

Opioid System

The opioid system is one of the several components involved in the etiopathogenesis of CKD-aP. Exogenous opioids, eg, morphine, are enabled to induce itch as a side effect. The incidence of opioid-induced pruritus depends on the route of administration and occurs in 10%–50% of intravenous administrations and 20%–100% of neuraxial administrations.76 This fact inspired scientists to examine if opioid receptors were somehow associated with chronic pruritus. Bergasa et al77 supported the hypothesis that cholestatic pruritus is modulated by endogenous opioids. They proved the effectiveness of opiate antagonists in alleviating this itch. Thus far, published reports have suggested that activation of µ-opioid receptors can trigger the itch and agonists of κ-opioid receptors are able to reduce the itch by inhibiting histamine and substance P.78,79 Studies utilizing mouse models have revealed that the activation of central κ-opioid receptors antagonize the central µ-opioid receptor, thereby reducing itch sensation.80 Wieczorek et al81 assessed the expression of µ- and κ-opioid receptors in the skin of HD patients with and without uremic pruritus, and concluded that changes in the peripheral opioid system may play an important role in CKD-aP pathogenesis. This study demonstrated a negative correlation between skin expression of κ-opioid receptors and the intensity of CKD-aP. All these observations prompted scientists to experimentally implement opioid agonists and antagonists in the treatment of CKD-aP, which brought diverse outcomes (reviewed in subsequent sections).

Neuropathy

Dysfunction of the central or peripheral nervous system is considered another etiopathogenetic mechanism in CKD-aP. Itch can be caused by centrally acting mediators, defects in the peripheral sensory pathway, cortical hypersensitivity, decreased cortical inhibitory mechanisms, or a defective spinal cord inhibition.35 A positive correlation between itch severity and occurrence of paresthesia in HD patients has been found. Most pruritic patients also develop peripheral sensorimotor neuropathy and dysautonomia.82 Johansson et al83 found altered cutaneous innervation in 12 CKD patients in whom nerve fibers sprouted through the epidermis, in contrast to healthy controls. Another study found a reduction in total number of skin nerve terminals in uremic patients.84 Additionally, central brain neuropathy has been confirmed in functional magnetic resonance imaging of the brain in 13 patients undergoing HD and suffering from pruritus.85 Sorour et al86 aimed to evaluate serum levels of two neurotrophins — BDNF and NT4 — in 60 uremic patients with pruritus, 60 nonpruritic uremic patients, and 60 healthy subjects. The results showed not only significantly increased serum levels of NT4 in uremic patients with pruritus but also revealed a positive correlation between concentrations of NT4 and the severity of CKD-aP. Serum BDNF levels were higher in uremic patients than controls, but the presence of pruritus did not significantly influence the concentration of this neurotrophin. Natriuretic polypeptide B, also known as brain natriuretic peptide (BNP), has been described as a neuropeptide enabled to activate pruriceptive neurons in mice.87 In a cross-sectional study, serum levels of BNP were found to be frequently elevated in HD patients. As such, the authors suggested BNP as one of many possible causes of daytime CKD-aP.88

Other Risk Factors of CKD-aP

According to DOPPS, patients on HD with coexisting hepatitis C infection are 1.29 times more likely to perceive CKD-aP.12 This viral infection predisposes to development of CI, due to cholestasis, induction of interferon-stimulated gene,s and elevated production of cytokines (eg, IL8) and chemokines (eg, CCL2, CXCL1, and CXCL5).22,35 Interestingly, hepatitis B does not show a significant association with pruritus, and this has raised the question of whether the pathogenesis of pruritus differs between these two diseases.de Kroes and Smeenk found elevated serum levels of vitamin A in all 35 CKD patients included in their research. However, there was no correlation between vitamin A concentration and the presence of CKD-aP. Two other studies have reported that increased serum levels of aluminum correlate significantly with the occurrence and intensity of CKD-aP.89,22

Clinical Presentation

Clinical presentation of CKD-aP assessed in studies has varied among studied populations. In general, the sensation of the itch affects large, discontinuous regions of the skin and shows bilateral symmetry. It is very often unceasing, recurrent, and the intensity seems to be worse during the night.90 Clinically, excoriations, erosions, ulcerations, nodules, or dyspigmentation can be observed, mostly as secondary lesions caused by scratching. Certain factors are known to exacerbate or reduce itching, including heat, dialysis, stress, cold, physical activity, or showering.91 CKD-aP can be localized or generalized. Weiss at al92 observed that the most common location of CKD-aP is the legs, back, and scalp. The results were similar to a study conducted by Heisig et al.93 Overall, 38% of respondents reported a single location of the itch — mostly the back, lower extremities, scalp, upper extremities, and abdomen — and bilateral symmetry was predominant. Generalized itch presented in 26.6% of the patients. On the other hand, a cross-sectional study on Iranian HD patients showed generalized pruritus in 70% of respondents.33 Ozen et al94 estimated entire-body pruritus to be present in 35.3% of patients. Another important aspect that is constantly assessed by researchers is the intensity of CI. In a large German study, mean severity of itch measured with a VAS was 4.1±1.7 points, while severity at the time of investigation amounted to 4.2±2.6 points and the worst severity within the last 6 weeks was 6.5±2.5 points.92 Mathur et al90 showed that mean worst itching intensity for enrolled patients was 59.9 mm using the 100 mm VAS. Scores were significantly higher for the 12-hour nighttime period than for the 12-hour daytime period, which corresponds with the research on patients undergoing PD conducted by Minato et al.95 Additionally, in DOPPS, a third of patients were most bothered by itch at night.13

Apart from the time of day, there are many other factors that can affect the course of itch. A study on 130 HD patients conducted at our center revealed that the frequency of itching can positively correlate with xerosis. Itch appeared more often (56.2%) in patients with very rough skin than patients with rough (34.5%) or slightly dry skin (27%).96 According to Ozen et al,94 dry skin is a risk factor of CKD-aP. In other research skin dryness just after rest was the second–most common exacerbating factor of chronic pruritus in patients undergoing dialysis.97 Heat, sweat, wool clothing, and stress were aggravating factors, while activity, sleep, hot/cold showers, and cold temperatures were considered ameliorating factors. Surprisingly, dialysis had no significant influence on itch severity.97 Other studies have revealed a connection between the dialysis process and itching. About 29% of patients in a Polish study reported itch to be the most severe during, at the end, or immediately after dialysis.93 Rayner et al13 found that 15% of the patients admitted that the worst itch was perceived during the dialysis session and 9% indicated the period soon after the session. However, for 14%, the itch was the most intense on days without dialysis. Some authors have emphasized the influence of the dialysis membrane on pruritus and hypothesized that some pruritogenic cytokines or substances may be activated after blood contact with membranes. This thesis needs more precise evaluation. A positive significant correlation has been found between HD period and total pruritus score.96 Interestingly, Rad et al98 proved that the severity of pruritus was significantly reduced in patients receiving a cool dialysis solution (35.5°C) during three consecutive dialysis sessions.

CKD-aP Assessment

CI should be characterized multidimensionally. Questionnaires, surveys, and similar tools are the best way to evaluate this subjective sensation. The IFSI recommends estimating not only the severity of itch but also its clinical course and consequences.99 Several scales are widely used to rate the intensity of CI. Numeric rating scales (NRSs) are the most commonly used tool for self-reported pruritus intensity. Visual analogue and verbal rating scales are equally helpful instruments. These quick and undemanding tools should be used together with at least one multidimensional questionnaire assessing frequency, duration, and distribution of the itch, as well as impact on daily activities, sleep, and psychosocial life. Such an extensive assessment of CKD-aP may be of help in evaluation of the effects of applied itch therapy and comparability of studies.100 Examples of such instruments are the 5-D Itch Scale, four-item Itch Questionnaire, Patient Benefit Index for Pruritus, Skindex 10, and Brief Itching Inventory. Due to the enormous impact of CKD-aP on QoL, assessment of this aspect in patients with CI is significant. The Dermatology Life Quality Index (DLQI) is a popular tool to evaluate QoL in patients with various dermatological diseases. However, ItchyQoL, an instrument dedicated to estimating the influence of CI on QoL, appears to be the best choice. Despite various instruments describing itch in use, only recently has a specific instrument for CKD-aP — Uremic Pruritus in Dialysis Patients — questionnaire been created.101 It evaluates three dimensions of UP in patients on dialysis: signs and symptoms, sleep, and psychosocial burden during the last 2 weeks. Besides the original version, only Chinese and Polish versions of this questionnaire have been created and validated.102,103

Clinical Outcomes

CKD-aP not only has a negative impact on patients’ QoL but also consequently leads to impairment of various patient-oriented outcomes and increased mortality risk. In the first and second part of DOPPS,12 patients suffering from moderate–extreme pruritus had 2.3–5.2 the odds of feeling drained and 1.3–1.7 times the odds of physician-diagnosed depression than patients not affected by pruritus. uring the QoL results showed that patients strongly bothered by itchy skin had mental and physical composite scores 3.1–8.6 points lower than patients with no or mild pruritus (P<0.0001). Likewise, poor sleep quality associated with waking up at night was mentioned by approximately 45% of patients with moderate–severe pruritus. In a group with mild/no pruritus, this amounted to only 29%. A correlation between severity of perceptible itch and mortality risk was also found. Patients with moderate–extreme pruritus had a 17% higher mortality risk than patients not bothered by pruritus.12 The Japanese DOPPS confirmed these findings: researchers found a 22% higher mortality rate for patients with moderate or extreme pruritus. This condition also induces 1.9–3.7 times the probability of impaired quality of sleep.14 Interestingly, in an Italian study, pruritus was associated with 8.4 times the adjusted odds of poor sleep.104 Mathur et al90 found that intensity of itch measured by VAS was significantly associated with lower health-related QoL in such domains as sleep, mood, and social relationships. Similarly, Szepietowski et al,9 using a short form scale (SF12) and the DLQI, concluded that not only CKD-aP but also uremic xerosis had a negative impact on patients’ QoL and were unfortunately underestimated in clinical practice. Ibrahim et al105 assessed the QoL of 200 HD patients using the WHOQOL-Bref questionnaire. QoL was impaired markedly in all four domains — physical health, psychological health, social relationships, and environmental health — in a group of patients with CI compared to a control group with no pruritus. All these papers highlight how strongly CKD-aP affects miscellaneous aspects of life and can lead to poor clinical outcomes.

Treatment of CKD-aP

The etiopathogenesis of CKD-aP is particularly complex, and numerous aspects remain to be explored and explained in more detail. As such, successful therapy for this condition often remains a demanding challenge for nephrologists or dermatologists. Considering common comorbidities in this group of patients, every single case ought to be considered individually, and applied therapy must be planned properly. The age of the patient, preexisting diseases, medications, and the quality and intensity of CI should be examined. Most of all, avoiding all exacerbating factors, such as allergenic and irritant substances, stress, hot drinks, alcohol, or hot and spicy food, is crucial.97 Fundamental antipruritic therapy must include reducing xerosis by moisturizing the skin.

Topical Therapy

Topical therapy is a treatment of first choice in numerous dermatological conditions. Emollients are capable of restoring the skin barrier and retaining water in the stratum corneum, which is crucial in reducing xerosis and thus can be of help in alleviating the itch.106 To achieve therapeutic effect, an appropriate amount of product and high frequency of application are essential.22 There are specific ingredients of emollients with proven antipruritic effects. In a randomized, multicenter study performed on 99 patients with uremic xerosis, 15% glycerol and 10% paraffin emulsion, high efficiency was found.107 The satisfactory treatment response concerned 73% of the patients compared with 44% of patients who responded to a comparator. By day 56 of that trial, patients reported significant relief from the itch (mean VAS score 10.66±2.14 mm vs 40.64±3.36 mm at the beginning of the trial). At the end of the study, a significant improvement in patients’ QoL, which was measured by the DLQI and SF12 questionnaire, was revealed. In other studies, the application of 10% urea plus dexpanthenol lotion or γ-linolenic acid cream turned out to be effective in alleviating CKD-aP.108,109 Topical capsaicin has also found the interest of scientists in local therapy. Studies have proved its safety and ability to reduce HD-induced pruritus.110–112 In Makhlough et al’s112 study on 17 patients with CKD-aP, 0.03% capsaicin was applied for 4 weeks, while 17 patients from control study group received placebo. During the therapy, decrease in pruritus severity was greater in the study group than the placebo group (P<0.001). However, it should be noted that in contrast to emollients, capsaicin may cause irritation of the skin. Therefore, this therapy should be used with great caution, especially in children, where emollients are considered the preferred approach in topical therapy.22 A prospective Polish study on 21 HD patients using a topical cream containing structured physiological lipids and endogenous cannabinoids twice a day for 3 weeks was conducted. A marked reduction in itch severity was observed after the trial in 38.1% of the patients.113 This was probably related to the inhibition of mast-cell degranulation and histamine release, as well as the moisturizing effect of the preparation. Studies using calcineurin inhibitors in the treatment of CKD-aP have not shown conclusive results. According to Kuypers et al,114 treatment with 0.1% and 0.3% tacrolimus ointment for 6 weeks significantly reduced the severity of CKD-aP. This finding was confirmed by Pauli-Magnus et al.115 On the other hand, in a study carried out by Duque et al,116 these conclusions were refuted. Likewise, a larger, randomized, double-blind, placebo-controlled study using 1% pimecrolimus demonstrated a lack of efficacy of calcineurin inhibitors for the treatment of HD-related pruritus.117 Based on clinical experience, good tolerance of topical therapy, and rarity of adverse effects, it is recommended that it be used as a preliminary treatment, especially in patients presenting xerosis.

Phototherapy

Ultraviolet (UV) radiation is widely used in the treatment of various dermatoses. The effectiveness of phototherapy is related to a range of mechanisms, including inhibition of Langerhans cells, decreasing levels of proinflammatory cytokines, strengthening the skin barrier, increasing serum levels of 25-hydroxyvitamin D₃, or stimulating the apoptosis of mastocytes.22 The use of phototherapy in CKD-aP was first mentioned in the 1970s. Since then, numerous studies have reported beneficial effects after implementation of broadband UVB (290–320 nm wavelength) radiation. Additionally, several studies have proved the effectiveness of narrow-band UVB (NB-UVB) radiation, both in HD and PD patients with CI.118–121 However, a study comparing NB-UVB (treatment group) and long-wave UVA radiation (control group) in patients with CKD-aP did not show significant differences concerning pruritus intensity between these two groups.122 A systematic review on this topic defined heliotherapy as a beneficial, efficacious, efficient, safe method of CKD-aP treatment. IT emphasized also that broadband BB-UVB compared to other subtypes is the most effective phototherapy in this condition.123 NB-UVB may also be considered in children aged >4 years bothered by recurrent CKD-aP thatdoes not respond to topical therapy, although there is still no literature available regarding its potential effectiveness and safety in this particular population.22 Finally, it must be noted that despite the established role of phototherapy in managing CKD-aP, this method can be troublesome, due to the limited availability and the necessity of frequent irradiation, mostly three to four times a week.

Antihistamines and Mast-Cell Stabilizers

Antihistamines are often the first-line therapy in CI, primarily when it comes to the use of over-the-counter drugs. According to DOPPS data, antihistamines were very widely prescribed for pruritus by doctors who were not skin specialists: 57% of medical directors chose oral antihistamines as an “appropriate” therapy dedicated to CKD-aP.13 This tendency is not substantiated in light of the research and expert opinions, which emphasize poor or moderate antipruritic effects of histamine-receptor antagonists in CKD-aP.91,124–129 Additionally, some reviews have suggested that the relief perceived after administration of the antihistamines may be a result of a sedative effect, rather than an antipruritic mechanism. On account of its limited value and risk of oversedation in elderly populations, this group of drugs should be avoided for this condition.91 Antihistamines are not a recommended modality in CKD-aP, and it is crucial to suppress their overuse in the subtype of CI. On the other hand, several recent studies have proved that the use of mast-cell stabilizers, which preclude histamine release, brings satisfactory effects in the treatment of CKD-aP.130 Both ketotifen and cromolyn sodium have proved to be effective in reducing itch severity.67,131 Furthermore, a trial on 60 HD patients in which cromolyn sodium cream 4% was applied twice a day for 4 weeks revealed significantly reduced pruritus severity compared to a placebo.132

Antiepileptic Drugs

Gabapentin is an anticonvulsant medication, an analogue of γ-aminobutyric acid, that is widely used in therapy for focal seizures and neuropathic pain. The mechanism of action of gabapentin in the treatment of CKD-aP is not fully known, but due to binding to α₂δ subunits of calcium channels and suppressing the influx of calcium into nerves, this drug is able to discontinue itch. A systematic review of randomized controlled trials using gabapentin as a treatment for pruritus in patients undergoing HD established that gabapentin significantly alleviated CKD-aP and was a safe choice. A pooled analysis of seven studies showed reduced VAS scores among HD patients. Furthermore, side effects associated with the therapy were well tolerateds.133 Another systematic review emphasized that effectiveness of gabapentin in CKD-aP has been evidenced in the greatest number of trials compared to other interventions.134 Pregabalin, which is another antiepileptic drug with similar mechanism of action to gabapentin, is also advantageous in CKD-aP management and may be effective in patients unable to tolerate the latter.135 Ravindran et al136 concluded that pregabalin was associated with fewer side effects than gabapentin. Proven effectiveness of these two antiepileptics makes them the main choice in CKD-aP oral therapy.136,137

Opioid-Receptor Agonists and Antagonists

Difelikefalin, a highly selective peripheral agonist of the κ-opioid receptor, can be seen as a new and revolutionary treatment for pruritus in patients undergoing HD.138 It is the first and only therapy approved by the US Food and Drug Administration for treatment of moderate–severe CKD-aP in adults undergoing HD. Injections of difelikefalin are a real breakthrough in CKD-aP treatment and should be considered as a first-line therapy. In one study, ifelikefalin 0.5, 1.0, or 1.5 μg/kg was administered intravenously three times a week for 8 weeks to HD patients with moderate–severe pruritus. A significant reduction from baseline in itch intensity scores at week 8 favored all difelikefalin doses combined versus placebo (P=0.002). At the end of the trial, 59% of patients receiving difelikefaline reported more than 3-point improvements in mean weekly Worst Itch Intensity NRS (WI-NRS) scores compared to 29% in the placebo group. The study also demonstrated that difelikefalin improved patients’ sleep, mood, and social functioning. A significantly larger reduction from baseline in mean Skindex-10 total score in a study group over the control group was observed (−16.4 and −8.2, respectively; P<0.001). Sleep disturbance measured by the Medical Outcomes Study scale in all difelikefalin combined groups had decreased after 8 weeks’ therapy (P≤0.006).139 Similarly, in a double-blind, placebo-controlled, phase III trial, more patients reported at least 3 points of improvement in itch severity measured by the WI-NRS than patients without treatment (49.1% vs 27.9%, P<0.001). The most common adverse events associated with difelikefalin were diarrhea, dizziness, and vomiting. The severity of side effects was generally mild–moderate, and they resolved without evident clinical consequence.140

In a systematic review and meta-analysis conducted by Jaiswal et al,78 nalfurafine, a selective κ-opioid agonist, was mentioned as a potentially effective treatment for CKD-aP. Two studies showed reductions in itch severity in HD patients after 2 weeks of orally applied nalfurafine. In a study on 86 patients who received 5 µg/day nalfurafine and 58 who received placebo, a 50% decrease from initial “worst itching” score assessed by VAS was reported by 36% of patients included in therapy and by only 14% of respondents in the control group.141 Similarly, in a prospective randomized, placebo-controlled study, Kumagai et al142 showed that decreases in VAS scores were markedly larger in a group receiving treatment than a placebo group. The most frequent adverse reaction to nalfurafine was insomnia. Four of six patients with this side effect discontinued the therapy. Wikström et al141 also mentioned headache, vertigo, nausea, and vomiting as common side effects. Both studies emphasized that adverse events were transient and easily resolved, which makes nalfurafine a safe agent for patients who are undergoing routine HD and suffering from CKD-aP.141,142 However, both studies that evaluated the effectiveness of κ-opioid agonists showed quite high percentages of placebo effectiveness. In a study evaluating difelikefalin, a placebo decreased the intensity of CKD-aP by at least 3 points in WI-NRS score in 27.9% of patients.140 Wikström et al141 found that 14% of patients in a placebo group reported a 50% decrease from baseline in “worst itching” VAS scores. According to the authors, subjective improvement in this chronic and burdensome condition can arise from increased attention given to the patients and their confidence in receiving the right therapy. The effectiveness of the μ-receptor antagonist naltrexone in CKD-aP varied between the studies. Naltrexone 50 mg/day received orally for 7 days significantly reduced CKD-aP in a group of 15 HD patients.143 Notwithstanding, Pauli-Magnus et al144 established that antipruritic therapy of CKD-aP with naltrexone was ineffective and the frequency of side effects high. Another opioid mediator applied in patients with moderate or severe CKD-aP with a satisfactory effect was nalbuphine. It is a mixed κ-agonist/µ-antagonist opioid modulator. In a large, multicenter, randomized, double-blind, placebo-controlled trial, 373 HD patients received extended-release nalbuphine tablets (60 or 120 mg) or placebo for 8 weeks. Theere was a significant reduction in itch severity in the group receiving 120 mg in comparison to placebo group. In contrast to placebo, this dose significantly improved sleep disturbances caused by itch.145

Toxin Removal

Several studies have examined dialysis efficiency in the context of CKD-aP. Interestingly, researchers found discrepant results concerning the relationship between Kt/V values and the presence of itch in HD patients. Hiroshige et al146 were the first to reveal that higher dialysis efficacy leads to reductions in prevalence and intensity of pruritus in HD patients. A prospective cohort study of patients receiving maintenance PD147 found that weekly total Kt/V <1.88 was associated with higher itch intensity. Similarly Ko et al,148 found Kt/V ≥1.5 and use of a high-flux dialyzer to be factors that may alleviate CKD-aP. Not all results in this topic are equivocal. Duque et al62 pointed out that increasing the number of months on dialysis, skin dryness, and surprisingly higher Kt/V positively correlated with the intensity of CKD-aP. Even when dialysis is properly optimized, the retention of middle molecules and PBUTs is inevitable However, the removal of IS and PCS may improve health, inhibit CKD progression, and most importantly decrease pruritus.149

Originally used to inhibit poison absorption in the intestine, activated charcoal seems to be a promising solution in removing UTs. This alternative to conventional HD and hemodiafiltration was first described by Pederson et al.150 However, bigger and better-designed studies are necessary to prove this theory. This study showed that 6 g activated charcoal applied once a day for 8 weeks significantly reduced itching compared to placebo and an economical and safe therapy for CKD-aP. Another oral charcoal adsorbent, AST120, has induced reduction in PBUTs. Levels of IS, PCS, and phenyl sulfate were significantly reduced after 2 weeks’ usage of 6 g per day in a study group of 20 HD patients.151 However, this study did not assess the severity of pruritus in patients. On the other hand, cholestyramine, a synthetic resin thatprevents bile reabsorption in the gastrointestinal tract, noticeably improved pruritus in patients undergoing chronic HD.152 However, study was performed on a very small number of patients, and adverse effects of constipation and nausea were noted. Cupisti et al149 also emphasized the importance of hemoperfusion and dialysis membranes with activated carbon in itch therapy.

Other Modalities

Parathyroidectomy in patients with ESRD who develop secondary hyperparathyroidism is effective in alleviating CKD-aP.56,57,153 However, as mentioned before, not all studies have confirmed the pruritogenic nature of PTH. Additionally, hyperparathyroidism is not present in all patients with CKD-aP. Therefore, parathyroidectomy cannot be considered a form of CKD-aP therapy, except in the case of concurrent hyperparathyroidism.35 In some reports, reduction of itch prevalence after successful renal transplantation has been highlighted.154,155 The biggest published study on this topic thus far, conducted on 197 renal transplant recipients, showed that in 73.7% of patients the itch disappeared completely after transplantation, while in 23.7% itch had lower intensity and only 2.6% patients did not report any improvement. Nevertheless, 21.3% patients suffered from itch after transplantation, among which in 52.4% cases the itch appeared after renal transplantation.156 The supplementation of ₃ fatty acids is not only relevant in the range of diseases coexisting with chronic renal failure but also, according to three studies, can be of help in decreasing itch in comparison to ₆, ₉, and placebo supplementation.157 Nonpharmacological methods taken from alternative medicine have also attracted the attention of researchers in this area. Acupuncture and acupressure have been found to be beneficial in CKD-aP, although some authors underline the high risk of bias in such studies.158–161 In addition, aromatherapy, stress-reduction techniques, psychotherapy, and physical exercises can be considered support strategies.162 It is vital to emphasize that in no way can these alternative methods be currently regarded as the basic or only antipruritic modality in the CDK-aP population.

Conclusion

CKD-aP is a pervasive but very often underestimated condition in patients undergoing HD or suffering from CKD, impairs QoL and increases the risk of mortality. Due to its complex etiopathogenesis, the choice of an effective therapy remains a challenge for clinicians. Future research looking for new factors responsible for CKD-aP can help in the development of novel drugs, specifically targeting particular molecules. Despite continuous research and considerable interest from scientists in understanding the full etiopathogenesis of CKD-aP, the results of many studies have been contradictory. The current situation requires continued research in this area and reevaluation of certain theories that may have a significant impact on the therapeutic management of patients with CKD-aP. Dspite many unknowns, we possess proven therapeutic methods. The proper algorithm in CKD-aP should consist of topical therapy, phototherapy, and systemic therapy. Among the latter, difelikefalin is the first and only therapy to be approved by the US Food and Drug Administration as treatment for moderate–severe CKD-aP. This may result in wide use of this substance as first-line therapy in the near future. Other group of systemic drugs with good effectiveness in this condition are gabapentinoids. Reasonable use of methods with proven effectiveness definitely contributes to improvements in patients’ QoL and is crucial in this troublesome condition. It is necessary to underline the recent extensive interest in the role of UTs in CKD-aP. It is hoped that further research in this area will provide more effective and innovative management options in HD patients with CKD-aP.

Author Contributions

All authors made significant contributions to conception and study design, acquisition of data, or analysis and interpretation of data, took part in drafting, revising, and critically reviewing the article, agreed to submit to the current journal, gave final approval to the version to be published, and agree to be accountable for all aspects of the work.

Disclosure

Jacek Szepietowski reports personal fees from AbbVie, Leo Pharma, Menlo Therapeutics, Novartis, Pierre-Fabre, Sandoz Sanofi-Genzyme, Trevi, and Viofor, personal fees from AbbVie, Bauch, Eli-Lilly, Leo-Pharma, Novartis, and Sanofi-Genzyme, and personal fees from AbbVie, Amgen, Behringer Ingelheim, Galapagos, Incyte, InflaRx, Janssen-Cilag, Leo Pharma, Menlo Therapeutics, Merck, Novartis, Pfizer, Regeneron, Trevi, and UCB, outside the submitted work. The authors declare no other conflicts of interest in this work.