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THE JOHN F. MAHER AWARD RECIPIENT LECTURES 2006 |
Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, and David Geffen School of Medicine at UCLA, Los Angeles, California, USA
Correspondence to: R. Mehrotra, 1124 W. Carson Street, Torrance, California
90502
USA.
rmehrotra{at}labiomed.org
End-stage renal disease (ESRD) patients undergoing renal replacement
therapy have a high mortality rate and suffer from considerable morbidity.
Degree of nutritional decline, disordered mineral metabolism, and vascular
calcification are some of the abnormalities that predict an adverse outcome
for ESRD patients. All these abnormalities begin early during the course of
chronic kidney disease (CKD), long before the need for maintenance dialysis.
Thus, CKD represents a continuum of metabolic and vascular abnormalities.
Treatment of these abnormalities early during the course of CKD and a timely
initiation of dialysis have the potential of improving patient outcomes.
However, the thesis that successful management of these abnormalities will
favorably modify the outcomes of dialysis patients remains untested.
The proportion of incident USA ESRD patients starting chronic peritoneal
dialysis (CPD) has historically been low. Limited physician training and
inadequate predialysis patient education appear to underlie the low CPD
take-on in the USA. Furthermore, two key changes have occurred in the USA:
steep decline in CPD take-on and progressive increase in the use of automated
peritoneal dialysis. The decline in CPD take-on has afflicted virtually every
subgroup examined and has occurred, paradoxically, when the CPD outcomes in
the country have improved. Understanding the reasons for historically low CPD
take-on and recent steep declines in utilization may allow the development of
plans to reverse these trends.
KEY WORDS: KEY WORDS:; End-stage renal disease; chronic kidney disease; chronic peritoneal dialysis; hemodialysis; initiation of dialysis; mineral metabolism; vascular calcification; nutrition; dietary protein intake; dialysate protein losses.
Received 18 December 2006; accepted 2 January 2007.
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