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. Author manuscript; available in PMC: 2012 Mar 24.
Published in final edited form as: Kidney Int. 2011 Aug 17;80(9):992–999. doi: 10.1038/ki.2011.247

Table 3.

Association of variant hemoglobin and higher-dose ESAa

Univariate analysis
Multivariate analysisb
Simplified analysisc
OR (95% CI) P-value OR (95% CI) P-value OR (95% CI) P-value
Logistic regression
 Variant Hgb 2.05 (0.92–4.56) 0.08 3.31 (1.20–9.11) 0.02 3.02 (1.26–7.25) 0.01
IRR (95% CI)
P-value
IRR (95% CI)
P-value
IRR (95% CI)
P-value
Poisson regression
 Variant Hgb 1.60 (0.98–2.64) 0.06 1.94 (1.16–3.25) 0.01 2.03 (1.24–3.31) 0.005

Abbreviations: CI, confidence interval; ESA, erythropoiesis-stimulating agent; HbAS, hemoglobin S trait; OR, odds ratio.

a

Hemoglobin variants included sickle cell trait (HbAS) and hemoglobin C trait. Higher-dose erythropoiesis-stimulating agent defined as ≥6500 U/treatment (≥19,500 U/week). Poisson regression used to more closely approximate risk ratio as odds ratio as determined by logistic regression likely overstates effect estimate, as outcome was common (29.9%).

b

Multivariate analysis from fully adjusted model—adjusted for percent of missed treatments, albumin, dialysis access, dialysis vintage, Kt/V, ferritin, iron saturation, intact parathyroid hormone, dialysis unit, history of gastrointestinal bleeding, and iron dose per treatment.

c

Simplified analysis or ‘final model’ derived from full model with removal of covariates by backward elimination via change in estimate testing—adjusted for percent of missed treatments, albumin, and dialysis access.