TY - JOUR
T1 - Do differences in dialysis prescription impact on KDOQI bone mineral targets? The Pan Thames Renal Audit
AU - Davenport, A.
AU - Gardner, C.
AU - Delaney, M.
N1 - Original article can be found at : http://content.karger.com/ Copyright Karger [Full text of this article is not available in the UHRA]
PY - 2010
Y1 - 2010
N2 - Background and Objectives: Patients achieving the Kidney Disease Outcomes Quality Initiative (KDOQI) bone mineral clinical practice guidelines have been reported to have improved survival. Many factors affecting calcium and phosphate control are not modifiable; however, we wished to determine whether differences in dialysis treatment could affect achievement of KDOQI clinical guideline targets. Methods: We audited pre-mid-week session calcium and phosphate levels in 5,324 adult patients receiving thrice weekly dialysis in the 14 Pan Thames centres: 60% male, mean age 62 ± 16 years, median dialysis vintage 29 months (14–58), 84% treated by haemodialysis, 16% by online haemodiafiltration, median session time 4.0 h (3.5–4.0). Results: Patients achieving the KDOQI guidelines varied between the centres: 23.4–60% for calcium, 31.7–56.7% for phosphate, 60–87.3% for calcium-phosphate product, 17.1–46.8% for parathyroid hormone (PTH) and 1.8–10.8% for all 4 targets. Those centres which used the highest dialysate calcium concentrations (1.5 mmol/l, 3 mEq/l) had more patients above the KDOQI serum calcium and more below the PTH target, than those centres using the lowest calcium dialysates (1 mmol/l, 2 mEq/l), with χ2 = 85.1 and χ2 = 52.4, p < 0.001, respectively. On logistic regression analysis, serum phosphate was negatively associated with duration of dialysis session time (F = 21.4, p = 0.000) and haemodiafiltration (F = 9.6, p = 0.000), respectively. Conclusions: Although many of the factors determining calcium and phosphate control in haemodialysis patients are unmodifiable, dialysate calcium concentration, the duration of the dialysis session and haemodiafiltration all had an impact on calcium, phosphate and PTH.
AB - Background and Objectives: Patients achieving the Kidney Disease Outcomes Quality Initiative (KDOQI) bone mineral clinical practice guidelines have been reported to have improved survival. Many factors affecting calcium and phosphate control are not modifiable; however, we wished to determine whether differences in dialysis treatment could affect achievement of KDOQI clinical guideline targets. Methods: We audited pre-mid-week session calcium and phosphate levels in 5,324 adult patients receiving thrice weekly dialysis in the 14 Pan Thames centres: 60% male, mean age 62 ± 16 years, median dialysis vintage 29 months (14–58), 84% treated by haemodialysis, 16% by online haemodiafiltration, median session time 4.0 h (3.5–4.0). Results: Patients achieving the KDOQI guidelines varied between the centres: 23.4–60% for calcium, 31.7–56.7% for phosphate, 60–87.3% for calcium-phosphate product, 17.1–46.8% for parathyroid hormone (PTH) and 1.8–10.8% for all 4 targets. Those centres which used the highest dialysate calcium concentrations (1.5 mmol/l, 3 mEq/l) had more patients above the KDOQI serum calcium and more below the PTH target, than those centres using the lowest calcium dialysates (1 mmol/l, 2 mEq/l), with χ2 = 85.1 and χ2 = 52.4, p < 0.001, respectively. On logistic regression analysis, serum phosphate was negatively associated with duration of dialysis session time (F = 21.4, p = 0.000) and haemodiafiltration (F = 9.6, p = 0.000), respectively. Conclusions: Although many of the factors determining calcium and phosphate control in haemodialysis patients are unmodifiable, dialysate calcium concentration, the duration of the dialysis session and haemodiafiltration all had an impact on calcium, phosphate and PTH.
KW - haemodialysis
KW - kidney disease outcomes quality initiative
KW - calcium
KW - phosphate
KW - parathyroid hormone
KW - clinical targets
U2 - 10.1159/000319954
DO - 10.1159/000319954
M3 - Article
SN - 0253-5068
VL - 30
SP - 111
EP - 117
JO - Blood Purification
JF - Blood Purification
IS - 2
ER -