Kidney

Newsletter

Keeping you up to date with the latest exciting advances and discussions in nephrology

Clinical challenges in kidney disease management

The following irregularities contribute to the multifactorial nature of the pathophysiology of CKD-associated pruritus (CKD-aP):

Upregulated
inflammatory state1–6

Dysregulated endogenous
opioid system1–5

Peripheral
neuropathy1,3,5,7

Uremic
abnormalities1–5

CKD-aP is a debilitating condition characterized
by a chronic, systemic itch8,9
The images are not of real patients

CKD-aP is common in patients on dialysis (up to 69%)10

Of which

37% experience moderate-to-severe pruritus10

Pruritus distribution is highly variable from patient to patient11

Severe itching is typically bilateral, symmetrical, persistent and generalized11

Studies in dialysis patients have shown that CKD-aP:

Disrupts sleep10,12
Is associated with an increased
likelihood of being diagnosed
with depression compared
with patients on hemodialysis
without CKD-aP11,12
May impair ability to
work
or maintain an
active social life10

Severe CKD-aP is also an independent predictor of mortality and hospitalization, related to an increased susceptibility to cardiovascular, infection and skin-related complications8,9,13

Mortality
Hospitalization
Infection

What are the barriers to optimizing
clinical care across the ckd continuum?

Data suggest that CKD-aP is significantly under-recognized

of nephrologists underestimated the prevalence of CKD-aP in their dialysis facility10
1 in 4 patients “bothered
by itchy skin” did not
report their symptoms
to an HCP
10

Clinical management of CKD-aP is challenging as guidance is mostly restricted to broad dermatology guidelines and expert reviews14,15

There is an unmet medical need as there are currently no widely-approved therapies specifically for CKD-aP16:
  • Antihistamines are the most commonly used systemic antipruritic drugs in dermatology, but are not recommended as a treatment option in CKD-aP due to a lack of proven efficacy15
  • Off-label treatments have limited supporting evidence and adverse effects may limit their use in patients with CKD-aP16
References and footnotes

FOOTNOTES

CKD-aP, chronic kidney disease-associated pruritus; HCP, healthcare professional.

 

 

REFERENCES

  1. Shirazian S, et al. Int J Nephrol Renovasc Dis 2017;10:11–6;
  2. Mettang T, Kremer A. Kidney Int 2015;87:685–91;
  3. Wang H, Yosipovitch G. Int J Dermatol 2010;49:1–11;
  4. Kuypers D. Nat Clin Pract Nephrol 2009;5:157–70;
  5. Patel T, et al. Am J Kidney Dis 2007;50:11–20;
  6. Kimmel M, et al. Nephrol Dial Transplant 2006;21:749–55;
  7. Zakrzewska-Pniewska B, et al. Neurophysiol Clin 2001;31:181–93;
  8. Narrita I, et al. Kidney Int 2006;69:1626–32;
  9. Ramakrishnan K, et al. Int J Nephrol Renovasc Dis 2014;7:1–12;
  10. Rayner H, et al. Clin J Am Soc Nephrol 2017;12:2000–17;
  11. Mathur V, et al. Clin J Am Soc Nephrol 2010;5:1410–9;
  12. Pisoni R, et al. Nephrol Dial Transplant 2006;21:3495–505;
  13. Sukul N, et al. Kidney Med 2020;3:42–53;
  14. Combs S, et al. Semin Nephrol 2015;35:383–91;
  15. Weisshaar E, et al. Acta Derm Venereol 2019;99:469–506;
  16. Verduzco H, Shirazian S. Kidney Int Rep 2020;5:1387–402.