Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 -- 2245 2022-05-24 05:56:59 |
2 format correct Meta information modification 2245 2022-05-25 07:44:21 |

Video Upload Options

Do you have a full video?


Are you sure to Delete?
If you have any further questions, please contact Encyclopedia Editorial Office.
Wong, L.S. Treatments for Uremic Pruritus. Encyclopedia. Available online: (accessed on 25 April 2024).
Wong LS. Treatments for Uremic Pruritus. Encyclopedia. Available at: Accessed April 25, 2024.
Wong, Lai San. "Treatments for Uremic Pruritus" Encyclopedia, (accessed April 25, 2024).
Wong, L.S. (2022, May 24). Treatments for Uremic Pruritus. In Encyclopedia.
Wong, Lai San. "Treatments for Uremic Pruritus." Encyclopedia. Web. 24 May, 2022.
Treatments for Uremic Pruritus

Conventional treatments for uremic pruritus including emollient, topical agents, antihistamine, dialysis modification, phototherapy, and serotonin receptor antagonists.

uremic pruritus chronic kidney disease associated pruritus chronic pruritus

1. Moisturizers

Xerosis is found in 50–85% of patients with uremic pruritus and is an aggravating factor of pruritus [1]. Multiple trials using different emollients including glycerol and paraffin, 10% urea and dexpanthenol, physiological lipids, and baby oil decrease xerosis and pruritus in patients with uremic pruritus [2][3][4][5][6]. Emollient is suggested as first-line therapy in patients with uremic pruritus, especially for those with less severity [7].

2. Topical Calcineurin Inhibitor (Tacrolimus, Pimecrolimus)

Tacrolimus, a calcineurin inhibitor, is used for its anti-inflammatory effects in atopic dermatitis and vitiligo [8][9]. A case study reported that 0.03% tacrolimus ointment reduced pruritus intensity in three cases with severe uremic pruritus [10]. However, a randomized, double-blind, vehicle-controlled study demonstrated that 0.1% tacrolimus applied twice daily for 4 weeks was not more efficacious than the vehicle [11]. Another 8-week, randomized, double-blind study of 1% pimecrolimus also revealed a lack of efficacy compared to the placebo group [12].

3. Other Topical Agents

Capsaicin, a compound found in chili pepper and transient receptor potential vanilloid member 1 (TRPV1) agonist, was used to relieve pain and neuropathy [13]. Three randomized controlled trials of capsaicin cream for uremic pruritus showed limited efficacy [14]. Pramoxine is a topical anesthetic with antipruritic effects. A randomized, double-blind, controlled comparative trial with 28 patients using 1% pramoxine lotion showed a 61% decrease in pruritus intensity compared to 12% in the placebo group [15].

4. High Quality of Dialysis

Since uremic toxins are suggested as potential pruritogens, increasing the efficiency of dialysis and modification of hemodialysis prescription is a potential strategy for the treatment of uremic pruritus. One randomized trial found that increased dialysis efficiency with mean Kt/V up to 1.28 resulted in pruritus improvement compared to mean Kt/V of around 1.09 [16]. Dialysis modification to remove more middle molecules also showed improvement in pruritus intensity. Hemodialysis modifications including high-flux hemodialysis [17], hemodiafiltration with hemodialysis [18], and high-permeability hemodialysis [19] have shown significant decreases in pruritus intensity. Therefore, increasing dialysis efficiency as well as modulating dialysis parameters are suggested as first-line treatments in patients with uremic pruritus [20].

5. Phototherapy

Phototherapy has been widely used in inflammatory skin diseases such as psoriasis, atopic dermatitis, and vitiligo [8][9][21] by modulating Th1 and Th2 lymphocyte differentiation and attenuating Th1-mediated responses [22][23]. Broadband ultraviolet B phototherapy was found to be effective in patients with uremic pruritus compared to ultraviolet A phototherapy [24]. One single-blind, randomized, controlled trial of 21 patients with uremic pruritus showed a significant improvement in pruritus by narrowband ultraviolet B phototherapy and long-wave ultraviolet A phototherapy compared to the non-treated group [22]. A recent controlled trial of narrowband ultraviolet B phototherapy revealed a significant reduction in visual analog scale (VAS) from 9.1 to 1.9 compared to treatment with antihistamine and emollients. In addition, the effect was sustained for up to 6 months in most of the study group [25]. Due to its wide adoption in pruritic dermatoses, narrowband ultraviolet B is considered an efficacious treatment in uremic pruritus.

6. Antihistamine

Antihistamine, mainly targeting histamine H1 receptor, has been widely used for anti-pruritus. It has been reported that over half of physicians prescribed an oral anti-histamine and one-fourth of them prescribed a topical anti-histamine as first-line therapy for uremic pruritus; however, anti-histamines were generally unsatisfactory for the treatment of uremic pruritus [7][26][27]. In addition, side effects of anti-histamines such as dizziness, sedation, and urine retention are concerns in patients with CKD [7].

7. Gabapentin, Pregabalin

Both pregabalin and gabapentin, analogs of gamma-aminobutyric acid, are modulators of neurotransmitters, acting possibly by decreasing neurotransmitter release [28]. The neuropathic role was implicated in the pathogenesis of various pruritic disorders such as brachioradial pruritus and pruritus in patients with diabetic neuropathic pain [29]. Several clinical trials of gabapentin and pregabalin have shown them to be statistically significant in the reduction in pruritus intensity in patients with uremic pruritus [30][31][32][33]. One recent systematic review showed decreased severity of pruritus after treatment with gabapentin in four out of seven studies (n = 171). Incidences of adverse effects with gabapentin including dizziness, drowsiness, and somnolence were higher but not significant in a pooled analysis (n = 290) [34]. Another clinical trial demonstrated that pruritus was relieved in 85% of 71 patients by gabapentin or pregabalin and that patients intolerant to gabapentin might tolerate pregabalin [35]. One study comparing the effects of gabapentin after each dialysis session and pregabalin daily showed a significant improvement in the reduction in pruritus and neuropathic pain in both groups [33]. A systematic review concluded that gabapentin is the most reliable and effective treatment as an off-label treatment for uremic pruritus [36].

8. Opioid Receptor Agonist/Antagonist

8.1. Naloxone

Intravenous injection of naloxone, a mu-receptor antagonist, was firstly reported to be efficacious in treating uremic pruritus in 1984 [37]. However, inconsistent results were found in subsequent large studies of oral naltrexone for uremic pruritus. In addition, some studies revealed frequent adverse effects such as nausea and sleep disturbance [38][39][40].

8.2. Nalfurafine

Nalfurafine, a selective kappa agonist, was found to be effective in uremic pruritus in a multicenter, randomized, double-blind, placebo-controlled clinical study [41]. A phase III randomized, double-blind, placebo-controlled study of 337 patients also revealed that nalfurafine significantly reduce the itch severity in intractable uremic pruritus [42]. Nalfurafine was officially approved for clinical use for uremic pruritus in Japan.

8.3. Difelikefalin

Recently, difelikefalin, a peripheral restricted and selective kappa opioid receptor agonist, proved its efficacy in the treatment of uremic pruritus in a large double-blind, placebo-controlled, multicenter phase III trial [43]. A total of 378 hemodialysis patients with moderate to severe pruritus were randomly treated with intravenous difelikefalin at the dose of 0.5 μg per kilogram or placebo for 12 weeks. Difelikefalin significantly decreased the intensity of pruritus (at least 3 points from baseline according to a 24-h worst itching intensity numerical rating scale) in 51.9% of patients compared to 30.9% of patients in the placebo group. Itch-related quality of life also improved significantly compared to the placebo group. Common adverse events include diarrhea, dizziness, and vomiting, but no adverse events of dysphoria, hallucination, euphoria, or discontinuation-related discomfort were reported in the difelikefalin group. Based on the successful results of the phase III trial, difelikefalin was approved by the FDA in the United States in 2021. A regulatory review is ongoing in Europe and a phase III trial is in progress in Japan. Oral difelikefalin is under investigation [44].

8.4. Nalbuphine

Nalbuphine, a combination of kappa-opioid receptor antagonist and mu-opioid receptor agonist, has been reported to be beneficial for morphine-related itch [45]. In addition, nalbuphine also decreased the intensity of uremic pruritus [46]. A multicenter, randomized, double-blind, placebo-controlled trial of 373 hemodialysis patients with moderate to severe pruritus demonstrated that the group receiving nalbuphine 120 mg twice daily for 8 weeks reported significantly decreased pruritus. However, there was no significant difference between nalbuphine at the dose of 60 mg twice daily and the placebo group.

9. Mast Cell Stabilizer

Mast cell stabilizers, which prevent degranulation of inflammatory mediators from mast cells, have been shown to be effective in uremic pruritus, and include topical cromolyn sodium [47], oral cromolyn sodium [48], ketotifen [31], and zinc sulfate [49]. One double-blind, randomized clinical trial of 52 patients revealed similar efficacy in decreasing pruritus severity and no significant difference in adverse effect with gabapentin and ketotifen [31]. However, one randomized control trial of 36 patients with 4-week duration of zinc sulfate showed non-significant reduction in pruritus in hemodialysis patients [50]. Mast cell stabilizer is safe and potentially efficacious in uremic pruritus, but more studies are needed.

10. Montelukast

Leukotriene B4, primarily released by macrophage and leukocytes, is involved in itch and may induce scratching [51][52]. Montelukast, a leukotriene receptor antagonist, is used in atopic dermatitis, asthma, allergic rhinitis, and idiopathic urticaria. One randomized double-blind controlled trial of 80 hemodialysis patients receiving 10 mg montelukast daily for 30 days revealed that montelukast significantly decreased pruritus compared to the placebo group. The authors concluded that montelukast might serve as an add-on treatment in intractable uremic pruritus [53].

11. Serotonin Receptor Antagonist: Ondansetron

5-HT3 receptor antagonists have been studied for their treatment efficacy in uremic pruritus. Ondansetron, a selective 5-HT3 receptor antagonist, had an insignificant effect on uremic pruritus in two randomized controlled trials [54][55].

12. Nemolizumab

Due to the higher concentration of IL-31 in hemodialysis patients with uremic pruritus, the role of nemolizumab, an IL-31 receptor alpha antibody, in the treatment of uremic pruritus is suggested [56]. A randomized, double-blind, placebo-controlled phase IIB trial of a single dose of nemolizumab was conducted in 69 patients with uremic pruritus but failed to meet the primary efficacy endpoint [57].

13. Dupilumab

As the possible involvement of IL-31 was implicated in uremic pruritus, the role of T-helper 2, which is the upstream regulator of IL-31, in uremic pruritus has been suggested. Dupilumab, an IL-4 receptor alpha-blocker, was reported to successfully treat cases with intractable uremic pruritus [58][59]. More studies are necessary.

14. Acupuncture, Acupressure

Acupuncture, defined by acupuncture needle insertion into specific points of the skin as treatment, has long been used for a variety of symptoms, such as acute or chronic pain, sleep disturbance, and poor quality of life in East Asia [60]. Acupuncture was believed to act through modulating the endogenous opioid system [61], which accounts for the hypothesis of it treating uremic treatment. Similarly, acupressure stimulates the acupuncture points with body parts of practitioners or designed equipment. A systematic review including six trials showed that acupuncture and acupressure were effective for uremic pruritus [62]. Recent studies comparing Zolpidem and acupressure revealed that both improved sleep quality and quality of life in patients with uremic pruritus-associated sleep disturbance [63][64]. However, more evidence is needed to affirm this as a recommended treatment for uremic pruritus.

15. Charcoal

Given the hypothesis of non-dialyzable uremic toxins as possible pruritogens, the adequate removal of potential toxins by charcoal is a reasonable therapeutic option. Activated charcoal, a non-selective absorbent, is usually used for detoxication in certain kinds of poisoning. An 11-patient, placebo-controlled, double-blind, crossover study showed that a daily dose of 6 g of activated charcoal for 8 weeks decreased pruritus in most patients with uremic pruritus [65]. In addition, coated charcoal in extracorporeal techniques showed decreased levels of parathyroid hormone and pruritus in a study of 12 patients [66]. Although evidence with large case numbers and well-designed studies are lacking, a recent review showed a promising role of charcoal in uremic pruritus [67].

16. Other Treatment

Early studies have proposed the association of uremic pruritus with hyperthyroidism, calcium, and phosphate. It is reported that the level of calcium multiplied by phosphate is correlated with the extent of pruritus after parathyroidectomy, and intractable pruritus improved after parathyroidectomy in some cases [68][69].
Thalidomide, an immunomodulator and neuromodulator, was initially observed to reduce pruritus in dialysis patients with leprosy [70]. One early randomized, crossover study with 29 patients found a statistically significant decrease in pruritus in the thalidomide group [71].
Gamma-linolenic acid (GLA), an essential acid, is thought to modulate T lymphocytes and lymphokines. In one small-sized, randomized control trial, GLA-enriched cream significantly improved the pruritus severity in dialysis patients [72].
Cannabinoids act on the endocannabinoid system to modulate pruritus and shed light on the treatment of chronic and refractory pruritus with legalized medical marijuana [73]. In a study of 21 patients applying topical cream containing structured physiological lipids, anandamide, and palmitoylethanoamine twice daily for 3 weeks, 8 out of 21 patients with uremic pruritus were completely free from pruritus [3]. However, randomized trials for cannabinoids are lacking [74].
Kidney transplantation, a kidney replacement therapy, largely decreased or cured chronic pruritus in patients with uremic pruritus [20][75][76]. Other medical considerations remain issues due to the shortage of human kidneys.
Catabolism of exogenous protein may lead to the retention of protein-bound molecules. Therefore, protein-restrictive diets and probiotics may serve as a potential treatments for uremic pruritus [67]. Omega-3 supplements were found to be effective to decrease pruritus in a cross-randomized trial [77].
Table 1. Summary of studies of interventions for uremic pruritus.


  1. Szepietowski, J.C.; Reich, A.; Schwartz, R.A. Uraemic xerosis. Nephrol. Dial. Transpl. 2004, 19, 2709–2712.
  2. Balaskas, E.; Szepietowski, J.C.; Bessis, D.; Ioannides, D.; Ponticelli, C.; Ghienne, C.; Taberly, A.; Dupuy, P. Randomized, double-blind study with glycerol and paraffin in uremic xerosis. Clin. J. Am. Soc. Nephrol. 2011, 6, 748–752.
  3. Szepietowski, J.C.; Szepietowski, T.; Reich, A. Efficacy and tolerance of the cream containing structured physiological lipids with endocannabinoids in the treatment of uremic pruritus: A preliminary study. Acta Dermatovenerol. Croat. 2005, 13, 97–103.
  4. Okada, K.; Matsumoto, K. Effect of skin care with an emollient containing a high water content on mild uremic pruritus. Ther. Apher. Dial. 2004, 8, 419–422.
  5. Morton, C.A.; Lafferty, M.; Hau, C.; Henderson, I.; Jones, M.; Lowe, J.G. Pruritus and skin hydration during dialysis. Nephrol. Dial. Transpl. 1996, 11, 2031–2036.
  6. Singh, V.S.; Vinayadev, V. Effectiveness of Baby Oil Therapy for Uremic Pruritus in Hemodialysis Patients. Saudi J. Kidney Dis. Transpl. 2021, 32, 163–169.
  7. Verduzco, H.A.; Shirazian, S. CKD-Associated Pruritus: New Insights into Diagnosis, Pathogenesis, and Management. Kidney Int. Rep. 2020, 5, 1387–1402.
  8. Rodrigues, M.; Ezzedine, K.; Hamzavi, I.; Pandya, A.G.; Harris, J.E. Current and emerging treatments for vitiligo. J. Am. Acad Dermatol. 2017, 77, 17–29.
  9. Langan, S.M.; Irvine, A.D.; Weidinger, S. Atopic dermatitis. Lancet 2020, 396, 345–360.
  10. Pauli-Magnus, C.; Klumpp, S.; Alscher, D.M.; Kuhlmann, U.; Mettang, T. Short-term efficacy of tacrolimus ointment in severe uremic pruritus. Perit. Dial. Int. 2000, 20, 802–803.
  11. Duque, M.I.; Yosipovitch, G.; Fleischer, A.B., Jr.; Willard, J.; Freedman, B.I. Lack of efficacy of tacrolimus ointment 0.1% for treatment of hemodialysis-related pruritus: A randomized, double-blind, vehicle-controlled study. J. Am. Acad. Dermatol. 2005, 52, 519–521.
  12. Ghorbani, A.R.; Feily, A.; Khalili, A.; Dormanesh, B. Lack of efficacy of topical calcineurin inhibitor pimecrolimus 1% on pruritus of severely uremic patients: A randomized double-blind study in 60 patients. Dermatitis 2011, 22, 167–168.
  13. Blair, H.A. Capsaicin 8% Dermal Patch: A Review in Peripheral Neuropathic Pain. Drugs 2018, 78, 1489–1500.
  14. Gooding, S.M.; Canter, P.H.; Coelho, H.F.; Boddy, K.; Ernst, E. Systematic review of topical capsaicin in the treatment of pruritus. Int. J. Dermatol. 2010, 49, 858–865.
  15. Young, T.A.; Patel, T.S.; Camacho, F.; Clark, A.; Freedman, B.I.; Kaur, M.; Fountain, J.; Williams, L.L.; Yosipovitch, G.; Fleischer, A.B., Jr. A pramoxine-based anti-itch lotion is more effective than a control lotion for the treatment of uremic pruritus in adult hemodialysis patients. J. Dermatol. Treat. 2009, 20, 76–81.
  16. Hiroshige, K.; Kabashima, N.; Takasugi, M.; Kuroiwa, A. Optimal dialysis improves uremic pruritus. Am. J. Kidney Dis. 1995, 25, 413–419.
  17. Jiang, X.; Ji, F.; Chen, Z.W.; Huang, Q.L. Comparison of high-flux hemodialysis with hemodialysis filtration in treatment of uraemic pruritus: A randomized controlled trial. Int. Urol. Nephrol. 2016, 48, 1533–1541.
  18. Zhang, J.; Yuan, Y.; An, X.; Ouyang, C.; Ren, H.; Yang, G.; Yu, X.; Lv, X.; Zhang, B.; Wang, N.; et al. Comparison of combined blood purification techniques in treatment of dialysis patients with uraemic pruritus. Int. J. Clin. Exp. Med. 2016, 9, 8563–8568.
  19. Chen, Z.J.; Cao, G.; Tang, W.X.; Lv, X.Y.; Huang, S.M.; Qin, W.; Ping, F.; Ye, T. A randomized controlled trial of high-permeability haemodialysis against conventional haemodialysis in the treatment of uraemic pruritus. Clin. Exp. Dermatol. 2009, 34, 679–683.
  20. Mettang, T.; Kremer, A.E. Uremic pruritus. Kidney Int. 2015, 87, 685–691.
  21. Armstrong, A.W.; Read, C. Pathophysiology, Clinical Presentation, and Treatment of Psoriasis: A Review. JAMA 2020, 323, 1945–1960.
  22. Ko, M.J.; Yang, J.Y.; Wu, H.Y.; Hu, F.C.; Chen, S.I.; Tsai, P.J.; Jee, S.H.; Chiu, H.C. Narrowband ultraviolet B phototherapy for patients with refractory uraemic pruritus: A randomized controlled trial. Br. J. Dermatol. 2011, 165, 633–639.
  23. Garssen, J.; Vandebriel, R.J.; De Gruijl, F.R.; Wolvers, D.A.; Van Dijk, M.; Fluitman, A.; Van Loveren, H. UVB exposure-induced systemic modulation of Th1- and Th2-mediated immune responses. Immunology 1999, 97, 506–514.
  24. Gilchrest, B.A.; Rowe, J.W.; Brown, R.S.; Steinman, T.I.; Arndt, K.A. Relief of uremic pruritus with ultraviolet phototherapy. N. Engl. J. Med. 1977, 297, 136–138.
  25. Sherjeena, P.B.; Binitha, M.P.; Rajan, U.; Sreelatha, M.; Sarita, S.; Nirmal, C.; Deepthi, N.S. A controlled trial of narrowband ultraviolet B phototherapy for the treatment of uremic pruritus. Indian J. Dermatol. Venereol. Leprol. 2017, 83, 247–249.
  26. Rayner, H.C.; Larkina, M.; Wang, M.; Graham-Brown, M.; van der Veer, S.N.; Ecder, T.; Hasegawa, T.; Kleophas, W.; Bieber, B.A.; Tentori, F.; et al. International Comparisons of Prevalence, Awareness, and Treatment of Pruritus in People on Hemodialysis. Clin. J. Am. Soc. Nephrol. 2017, 12, 2000–2007.
  27. Weisshaar, E.; Dunker, N.; Röhl, F.W.; Gollnick, H. Antipruritic effects of two different 5-HT3 receptor antagonists and an antihistamine in haemodialysis patients. Exp. Dermatol. 2004, 13, 298–304.
  28. Robertson, K.; Marshman, L.A.G.; Plummer, D.; Downs, E. Effect of Gabapentin vs Pregabalin on Pain Intensity in Adults With Chronic Sciatica: A Randomized Clinical Trial. JAMA Neurol. 2019, 76, 28–34.
  29. Gunal, A.I.; Ozalp, G.; Yoldas, T.K.; Gunal, S.Y.; Kirciman, E.; Celiker, H. Gabapentin therapy for pruritus in haemodialysis patients: A randomized, placebo-controlled, double-blind trial. Nephrol. Dial. Transpl. 2004, 19, 3137–3139.
  30. Foroutan, N.; Etminan, A.; Nikvarz, N.; Shojai Shahrokh Abadi, M. Comparison of pregabalin with doxepin in the management of uremic pruritus: A randomized single blind clinical trial. Hemodial. Int. 2017, 21, 63–71.
  31. Amirkhanlou, S.; Rashedi, A.; Taherian, J.; Hafezi, A.A.; Parsaei, S. Comparison of Gabapentin and Ketotifen in Treatment of Uremic Pruritus in Hemodialysis Patients. Pak. J. Med. Sci. 2016, 32, 22–26.
  32. Nofal, E.; Farag, F.; Nofal, A.; Eldesouky, F.; Alkot, R.; Abdelkhalik, Z. Gabapentin: A promising therapy for uremic pruritus in hemodialysis patients: A randomized-controlled trial and review of literature. J. Dermatol. Treat. 2016, 27, 515–519.
  33. Solak, Y.; Biyik, Z.; Atalay, H.; Gaipov, A.; Guney, F.; Turk, S.; Covic, A.; Goldsmith, D.; Kanbay, M. Pregabalin versus gabapentin in the treatment of neuropathic pruritus in maintenance haemodialysis patients: A prospective, crossover study. Nephrology 2012, 17, 710–717.
  34. Eusebio-Alpapara, K.M.V.; Castillo, R.L.; Dofitas, B.L. Gabapentin for uremic pruritus: A systematic review of randomized controlled trials. Int. J. Dermatol. 2020, 59, 412–422.
  35. Rayner, H.; Baharani, J.; Smith, S.; Suresh, V.; Dasgupta, I. Uraemic pruritus: Relief of itching by gabapentin and pregabalin. Nephron Clin. Pract. 2012, 122, 75–79.
  36. Simonsen, E.; Komenda, P.; Lerner, B.; Askin, N.; Bohm, C.; Shaw, J.; Tangri, N.; Rigatto, C. Treatment of Uremic Pruritus: A Systematic Review. Am. J. Kidney Dis. 2017, 70, 638–655.
  37. Andersen, L.W.; Friedberg, M.; Lokkegaard, N. Naloxone in the treatment of uremic pruritus: A case history. Clin. Nephrol. 1984, 21, 355–356.
  38. Peer, G.; Kivity, S.; Agami, O.; Fireman, E.; Silverberg, D.; Blum, M.; Laina, A. Randomised crossover trial of naltrexone in uraemic pruritus. Lancet 1996, 348, 1552–1554.
  39. Pauli-Magnus, C.; Mikus, G.; Alscher, D.M.; Kirschner, T.; Nagel, W.; Gugeler, N.; Risler, T.; Berger, E.D.; Kuhlmann, U.; Mettang, T. Naltrexone Does Not Relieve Uremic Pruritus: Results of a randomized, double-blind, placebo-control crossover study. J. Am. Soc. Nephrol. 2000, 11, 514–519.
  40. Legroux-Crespel, E.; Clèdes, J.; Misery, L. A comparative study on the effects of naltrexone and loratadine on uremic pruritus. Dermatology 2004, 208, 326–330.
  41. Wikström, B.; Gellert, R.; Ladefoged, S.D.; Danda, Y.; Akai, M.; Ide, K.; Ogasawara, M.; Kawashima, Y.; Ueno, K.; Mori, A.; et al. Kappa-opioid system in uremic pruritus: Multicenter, randomized, double-blind, placebo-controlled clinical studies. J. Am. Soc. Nephrol. 2005, 16, 3742–3747.
  42. Kumagai, H.; Ebata, T.; Takamori, K.; Muramatsu, T.; Nakamoto, H.; Suzuki, H. Effect of a novel kappa-receptor agonist, nalfurafine hydrochloride, on severe itch in 337 haemodialysis patients: A Phase III, randomized, double-blind, placebo-controlled study. Nephrol. Dial. Transpl. 2009, 25, 1251–1257.
  43. Fishbane, S.; Jamal, A.; Munera, C.; Wen, W.; Menzaghi, F. A Phase 3 Trial of Difelikefalin in Hemodialysis Patients with Pruritus. N. Engl. J. Med. 2020, 382, 222–232.
  44. Deeks, E.D. Difelikefalin: First Approval. Drugs 2021, 81, 1937–1944.
  45. Liao, C.C.; Chang, C.S.; Tseng, C.H.; Sheen, M.J.; Tsai, S.C.; Chang, Y.L.; Wong, S.Y. Efficacy of intramuscular nalbuphine versus diphenhydramine for the prevention of epidural morphine-induced pruritus after cesarean delivery. Chang. Gung Med. J. 2011, 34, 172–178.
  46. Mathur, V.S.; Kumar, J.; Crawford, P.W.; Hait, H.; Sciascia, T. A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial of Nalbuphine ER Tablets for Uremic Pruritus. Am. J. Nephrol. 2017, 46, 450–458.
  47. Feily, A.; Dormanesh, B.; Ghorbani, A.R.; Moosavi, Z.; Kouchak, M.; Cheraghian, B.; Mousavi, S.S.; Mehrabian, A.; Ranjbari, N. Efficacy of topical cromolyn sodium 4% on pruritus in uremic nephrogenic patients: A randomized double-blind study in 60 patients. Int. J. Clin. Pharmacol. Ther. 2012, 50, 510–513.
  48. Rosner, M.H. Cromolyn sodium: A potential therapy for uremic pruritus? Hemodial. Int. 2006, 10, 189–192.
  49. Najafabadi, M.M.; Faghihi, G.; Emami, A.; Monghad, M.; Moeenzadeh, F.; Sharif, N.; Davarpanah Jazi, A.H. Zinc sulfate for relief of pruritus in patients on maintenance hemodialysis. Ther. Apher. Dial. 2012, 16, 142–145.
  50. Mapar, M.A.; Pazyar, N.; Siahpoosh, A.; Latifi, S.M.; Beladi Mousavi, S.S.; Khazanee, A. Comparison of the efficacy and safety of zinc sulfate vs. placebo in the treatment of pruritus of hemodialytic patients: A pilot randomized, triple-blind study. G. Ital. Dermatol. Venereol. 2015, 150, 351–355.
  51. Kremer, A.E.; Feramisco, J.; Reeh, P.W.; Beuers, U.; Oude Elferink, R.P. Receptors, cells and circuits involved in pruritus of systemic disorders. Biochim. Biophys. Acta 2014, 1842, 869–892.
  52. Toyama, S.; Tominaga, M.; Takamori, K. Connections between Immune-Derived Mediators and Sensory Nerves for Itch Sensation. Int. J. Mol. Sci. 2021, 22, 2365.
  53. Mahmudpour, M.; Roozbeh, J.; Raiss Jalali, G.A.; Pakfetrat, M.; Ezzat Zadegan, S.; Sagheb, M.M. Therapeutic Effect of Montelukast for Treatment of Uremic Pruritus in Hemodialysis Patients. Iran J. Kidney Dis. 2017, 11, 50–55.
  54. Wang, W.; Zhou, L.; Sun, L. Ondansetron for neuraxial morphine-induced pruritus: A meta-analysis of randomized controlled trials. J. Clin. Pharm. Ther. 2017, 42, 383–393.
  55. To, T.H.; Clark, K.; Lam, L.; Shelby-James, T.; Currow, D.C. The role of ondansetron in the management of cholestatic or uremic pruritus—A systematic review. J. Pain Symptom Manag. 2012, 44, 725–730.
  56. Oweis, A.O.; Al-Qarqaz, F.; Bodoor, K.; Heis, L.; Alfaqih, M.A.; Almomani, R.; Obeidat, M.A.; Alshelleh, S.A. Elevated interleukin 31 serum levels in hemodialysis patients are associated with uremic pruritus. Cytokine 2021, 138, 155369.
  57. Kinugasa, E.; Igawa, K.; Shimada, H.; Kondo, M.; Funakoshi, S.; Imada, N.; Itami, N.; Fukazawa, N.; Takubo, R.; Kawata, Y.; et al. Anti-pruritic effect of nemolizumab in hemodialysis patients with uremic pruritus: A phase II, randomized, double-blind, placebo-controlled clinical study. Clin. Exp. Nephrol. 2021, 25, 875–884.
  58. Silverberg, J.I.; Brieva, J. A successful case of dupilumab treatment for severe uremic pruritus. JAAD Case Rep. 2019, 5, 339–341.
  59. Zhai, L.L.; Savage, K.T.; Qiu, C.C.; Jin, A.; Valdes-Rodriguez, R.; Mollanazar, N.K. Chronic Pruritus Responding to Dupilumab-A Case Series. Medicines 2019, 6, 72.
  60. Kim, K.H.; Lee, M.S.; Choi, S.M. Acupuncture for treating uremic pruritus in patients with end-stage renal disease: A systematic review. J. Pain Symptom Manag. 2010, 40, 117–125.
  61. Chen, T.; Zhang, W.W.; Chu, Y.X.; Wang, Y.Q. Acupuncture for Pain Management: Molecular Mechanisms of Action. Am. J. Chin. Med. 2020, 48, 793–811.
  62. Badiee Aval, S.; Ravanshad, Y.; Azarfar, A.; Mehrad-Majd, H.; Torabi, S.; Ravanshad, S. A Systematic Review and Meta-analysis of Using Acupuncture and Acupressure for Uremic Pruritus. Iran J. Kidney Dis. 2018, 12, 78–83.
  63. Rehman, I.U.; Wu, D.B.; Ahmed, R.; Khan, N.A.; Rahman, A.U.; Munib, S.; Lee, L.H.; Chan, K.G.; Khan, T.M. A randomized controlled trial for effectiveness of zolpidem versus acupressure on sleep in hemodialysis patients having chronic kidney disease-associated pruritus. Medicine 2018, 97, e10764.
  64. Rehman, I.U.; Ahmed, R.; Rahman, A.U.; Wu, D.B.C.; Munib, S.; Shah, Y.; Khan, N.A.; Rehman, A.U.; Lee, L.H.; Chan, K.G.; et al. Effectiveness and safety profiling of zolpidem and acupressure in CKD associated pruritus: An interventional study. Medicine 2021, 100, e25995.
  65. Pederson, J.A.; Matter, B.J.; Czerwinski, A.W.; Llach, F. Relief of idiopathic generalized pruritus in dialysis patients treated with activated oral charcoal. Ann. Intern. Med. 1980, 93, 446–448.
  66. Morachiello, P.; Landini, S.; Fracasso, A.; Righetto, F.; Scanferla, F.; Toffoletto, P.; Genchi, R.; Bazzato, G. Combined hemodialysis-hemoperfusion in the treatment of secondary hyperparathyroidism of uremic patients. Blood Purif. 1991, 9, 148–152.
  67. Cupisti, A.; Piccoli, G.B.; Gallieni, M. Charcoal for the management of pruritus and uremic toxins in patients with chronic kidney disease. Curr. Opin. Nephrol. Hypertens. 2020, 29, 71–79.
  68. Massry, S.G.; Popovtzer, M.M.; Coburn, J.W.; Makoff, D.L.; Maxwell, M.H.; Kleeman, C.R. Intractable pruritus as a manifestation of secondary hyperparathyroidism in uremia. Disappearance of itching after subtotal parathyroidectomy. N. Engl. J. Med. 1968, 279, 697–700.
  69. Chou, F.F.; Ho, J.C.; Huang, S.C.; Sheen-Chen, S.M. A study on pruritus after parathyroidectomy for secondary hyperparathyroidism. J. Am. Coll. Surg. 2000, 190, 65–70.
  70. Sharma, D.; Kwatra, S.G. Thalidomide for the treatment of chronic refractory pruritus. J. Am. Acad. Dermatol. 2016, 74, 363–369.
  71. Silva, S.R.; Viana, P.C.; Lugon, N.V.; Hoette, M.; Ruzany, F.; Lugon, J.R. Thalidomide for the treatment of uremic pruritus: A crossover randomized double-blind trial. Nephron 1994, 67, 270–273.
  72. Chen, Y.C.; Chiu, W.T.; Wu, M.S. Therapeutic effect of topical gamma-linolenic acid on refractory uremic pruritus. Am. J. Kidney Dis. 2006, 48, 69–76.
  73. Avila, C.; Massick, S.; Kaffenberger, B.H.; Kwatra, S.G.; Bechtel, M. Cannabinoids for the treatment of chronic pruritus: A review. J. Am. Acad. Dermatol. 2020, 82, 1205–1212.
  74. Rein, J.L.; Wyatt, C.M. Marijuana and Cannabinoids in ESRD and Earlier Stages of CKD. Am. J. Kidney Dis. 2018, 71, 267–274.
  75. Krajewski, P.K.; Olczyk, P.; Krajewska, M.; Krajewski, W.; Szepietowski, J.C. Clinical Characteristics of Itch in Renal Transplant Recipients. Front. Med. 2021, 7, 615334.
  76. Mettang, T. Uremic Itch Management. Curr. Probl. Dermatol. 2016, 50, 133–141.
  77. Forouhari, A.; Moghtaderi, M.; Raeisi, S.; Shahidi, S.; Parin Hedayati, Z.; Zaboliyan, J.; Ani, S.; Moeinzadeh, F.; Mortazavi, M. Pruritus-reducing effects of omega-3 fatty acids in hemodialysis patients: A cross-over randomized clinical trial. Hemodial. Int. 2022. online ahead of print.
Subjects: Dermatology
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to :
View Times: 343
Revisions: 2 times (View History)
Update Date: 25 May 2022