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Volume 19, Issue 4, Pages 321-333 (July 2009)


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Effect of Aggressive Osteodystrophy Management on Clinical Outcomes in Stage 5 Chronic Kidney Disease

Laura Byham-Gray, PhD, RDCorresponding Author Informationemail address, Tammy Drasher, RD, LDN, Karen Deckman, MA, RD, LDN, Diane Graham, MS, RD, LDN§, Carol Liftman, MS, RD, LDN, Linda Roberto, MA, RD, LDN∗∗, Phyllis Peiffer, MBA, RD, LDN††, Robert Denmark, PhD§§

published online 25 May 2009.

Objective

The study investigated whether the type of bone disease management (aggressive versus conventional) had an impact on clinical outcomes, namely bone health measures (e.g., biointact parathyroid hormone [BiPTH], serum corrected calcium [cCa] level, serum phosphorus [phos] level, and corrected calcium-phosphorus product [cCaPO4]).

Design and Setting

Retrospective chart review of 173 closed medical records of maintenance hemodialysis patients on thrice-weekly therapy from January 1, 2005, through December 31, 2005. Two Conventional Management (i.e., control group) and three Aggressive Management (i.e., treatment group) dialysis facilities were enrolled.

Results

There was a significant interaction for group assignment and BiPTH levels (F = 4.12, P = .01), with the Aggressive Group trending toward lower BiPTH levels than the Conventional Group. The Conventional Group experienced a significantly lower mean annualized serum cCa level (F = 8.85, P = .003), and used non–calcium-based binders significantly more (P < .0005) than the Aggressive Group. In terms of serum phos level, the Aggressive Group had a significantly lower (F = 2.73, P = .05) value than the Conventional Group. No significant differences were reported for cCaPO4 product (F = 1.87, P = .17). The percentage of the total sample that achieved target range for all bone health measures included 29.8% (n = 50).

Conclusions

The study demonstrated that aggressive bone disease management appears to be as effective as traditional interventions in the treatment of mineral and bone metabolism disorders in chronic kidney disease.

 Department of Nutritional Sciences, University of Medicine and Dentistry of New Jersey, School of Health-Related Professions, Stratford, NJ

 Dialysis Clinic, Inc., North Billerica, MA

 Dialysis Corporation of America (formerly), Vineland, NJ

§ Hershey Medical Center-Dialysis Unit, Hershey, PA

 Franklin Dialysis Center/DaVita, Philadelphia, PA

∗∗ Fresenius Medical Care-Mount Airy, Philadelphia, PA

†† Wellspan Dialysis, York, PA

§§ University of Medicine and Dentistry of New Jersey, School of Health-Related Professions, Newark, NJ

Corresponding Author InformationAddress reprint requests to Laura Byham-Gray, PhD, RD, Department of Nutritional Sciences, University of Medicine and Dentistry of New Jersey, School of Health-Related Professions, University Educational Center, Room 2111, 40 East Laurel Road, Stratford, NJ 08084.

 This work was supported by a Council on Renal Nutrition Research Grant of the National Kidney Foundation.

PII: S1051-2276(09)00040-5

doi:10.1053/j.jrn.2009.01.018


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