Barely Significant
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Safety of Roxadustat in Chronic Kidney Disease Patients: An Updated Systematic Review and Meta-Analysis.

Pharmaceuticals (Basel) · 2025 · PMC12567109 · PMID 41155680

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borderline significantno p-value reported
In long-term treatment, the risk of SAEs, hypertension, and diarrhea was notable, while the risk of hyperkalemia remained borderline significant. 5.

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near-significantno p-value reported
Notably, the subgroup of patients without dialysis and with treatment > 30 weeks had a near-significant increased risk of hyperkalemia compared to placebo (pooled OR = 1.28; 95% CI: 0.99–1.65; I 2 = 0.0%) but not compared to ESAs ( Figure 13 c).

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Similarly, when we analyzed the data according to the duration of Roxadustat treatment, an increased risk was observed with both longer and shorter treatments than 30 weeks, but this increase did not reach statistical significance in either case ( Figure 13 a,b).

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marginally non-significantno p-value reported
Subgroup analysis by dialysis or non-dialysis status indicated that the risk of SAEs was statistically significant in the anemic CKD patient group not receiving dialysis (pooled OR = 1.15; 95% CI: 1.01–1.30; I 2 = 0.0%) ( Figure 4 a), while it was marginally non-significant in the dialysis patient group (pooled OR = 1.12; 95% CI: 0.99–1.26; I 2 = 0.0%) ( Figure 4 a).

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