It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Objective
To explore the prevalence and influencing factors of Chronic Kidney Disease-associated Pruritus (CKD-aP) among maintenance hemodialysis (MHD) patients in China through a meta-analysis.
Methods
A systematic computerized search was conducted across ten databases, including CNKI, VIP, Wanfang, PubMed, Web of Science, and The Cochrane Library, to identify studies on the prevalence and influencing factors of pruritus among Chinese hemodialysis patients up to January 2025. Two independent graduate students conducted literature screening, data extraction, and bias risk assessment for the included studies. Data analysis was performed using Stata 17.0 software.
Results
A comprehensive meta-analysis of 27 studies involving 10,346 participants identified 5,968 cases of CKD-ap among hemodialysis patients, examining 30 potential influencing factors. The meta-analysis revealed that the prevalence of CKD-ap in China was 52%, with 26% of patients experiencing mild CKD-ap, 22% moderate CKD-ap, and 8% severe CKD-ap. Factors associated with an increased risk of CKD-ap included duration of dialysis treatment (OR = 1.51, 95% CI: 1.15–1.88), primary disease (OR = 1.43, 95% CI: 0.87–1.99), dry skin disease (OR = 2.46, 95% CI: 1.74–3.19), phosphorus (OR = 1.18, 95% CI: 0.55–1.81), Ca - P product (OR = 2.18, 95% CI: 1.14–3.22), C - reactive protein (CRP) (OR = 1.14, 95% CI: 0.78–1.51), iPTH (OR = 2.45, 95% CI: 0.81–4.09), β2 - MG(OR = 2.24, 95% CI: 0.94–3.53), and SCr (OR = 1, 95% CI: 1.001–1.005). Conversely, factors including blood calcium levels (OR = 0.33, 95% CI: 0.31–0.35), dialysis modality (OR = 0.54, 95% CI: 0.23–0.85), and Kt/V (OR = 0.60, 95% CI: 0.24–0.96) were associated with a reduced risk of CKD-ap.
Conclusion
This meta-analysis demonstrates a high prevalence of CKD-ap among Chinese MHD patients, underscoring the urgent need for improved awareness, preventive interventions, and management strategies in clinical practice.
Clinical trial number
Not applicable.
Trial number
The study was registered in PROSPERO: No. CRD42024562865.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer