NKF-KDOQI Clinical Practice Guidelines and Clinical Practice
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clinical practice guidelines, chronic kidney disease, kidney disease, national kidney foundation, kdoqi guidelines, disease outcomes, quality initiative, dialysis patients, renal failure, practice guidelines, kidney function, hemodialysis patients, patients with chronic, end-stage kidney disease, guideline development
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NKF-KDOQI Clinical Practice
Guidelines and Clinical Practice
Recommendations for Anemia in
Chronic Kidney Disease
UPDATE OF HEMOGLOBIN TARGET
Am.J.Kidney.Dis. 50 (3):471-530, 2007.
KDOQI Anemia
Organization
Evidence Review Team
Tufts New England Medical Center
Work Group
9 Adult Nephrologists
2 Pediatric Nephrologists
2 Hematologists
1 Nurse Practitioner
1 Dietician
CPR and CPG 2.1: Hb Target
Introduction
The Hb target is the
intended aim of ESA
therapy for the individual
CKD patient. In clinical
practice, achieved Hb
results vary considerably
from the Hb target.
CPR 2.1.1
Considerations
In the opinion of the work group, selection
of the Hb target and selection of the Hb
level at which ESA therapy is initiated in
the individual patient should include
consideration of potential benefits
(including improvement in quality of life
and avoidance of transfusion) and potential
harms (including the risk of life-
threatening adverse events). (Clinical
Practice RECOMMENDATION)
CPR 2.1.2
Selection of the Hb target
In the opinion of the work group,
in dialysis and non-dialysis CKD
patients receiving ESA therapy, the
selected Hb target should generally
be in the range of 11.0 to 12.0
g/dL. (Clinical Practice
RECOMMENDATION)
CPG 2.1.3
Hb targets to avoid
In dialysis and non-dialysis
CKD patients receiving ESA
therapy, the Hb target should
not be above 13.0 g/dL.
(Clinical Practice
GUIDELINE -
MODERATELY STRONG
EVIDENCE)
Rationale: 2.1.2
Rationale: 2.1.2
Distinguishing Target Hb from
Achieved Hb
Target Hb is the aim of ESA therapy
Achieved Hb is the result of ESA
therapy
Achieved Hb results vary considerably
from the Hb target
Safety of achieved Hb relative to 11-12
g/dL target Hb or Hb > 11 g/dL
threshold is well-established
Rationale: 2.1.3
The Hb target should not be above 13.0 g/dL
(Moderately Strong Recommendation)
Evidence from RCTs
Considered all trials that compared Hb
target > 13.0 g/dL to lower target
All these RCTs tested the hypothesis that
the higher target would prevent adverse
cardiovascular events or mortality, or all
cause mortality
None showed a benefit on those outcomes
Meta-Analysis
Performed by Evidence Review Team
RCTs with ≥ 6 months follow-up, no
restriction on study size
Statistical model: random effects
Separated dialysis from non-dialysis CKD
trials
Combined all cardiovascular disease events for
analysis of cardiovascular adverse event risk
Rationale: 2.1.3
Relative mortality risk for assignment to
higher treatment targets: Non-Dialysis-CKD
Higher
Hb Target
11.7
11.0-11.7
13.0
12.0-14.0
13.0-15.0
13.0-15.0
13.5
11.0
Relative Risk: 1.02, 95% CI 0.63-1.61
Rationale: 2.1.3
Relative risk of cardiovascular events for
assignment to higher targets: Non-dialysis CKD
Higher
Hb Target
11.7
12.0-14.0
13.0-15.0
13.0-15.0
13.5
13.0-15.0
Relative Risk: 1.24, 95% CI 1.02-1.51
Rationale: 2.1.3
Relative mortality risk for assignment to
higher treatment targets: Dialysis CKD
Higher
Hb Target
14.0
13.0-14.0
13.5-16.0
13.5-14.5
Relative Risk: 1.12, 95% CI 0.91-1.37
Rationale: 2.1.3
Relative risk of cardiovascular events for
assignment to higher targets: Dialysis CKD
Higher
Hb Target
14.0
13.0-14.0
13.5-14.5
Relative Risk: 1.14, 95% CI 0.79-1.64
Rationale: 2.1.3
The Statement:
Hb Target should not be above 13 g/dL
Reflects Work Group judgment
The possibility to cause harm weighs more
heavily than the potential to improve
quality of life and reduce the likelihood of
transfusions
Moderately strong, evidence-based, clinical
practice guideline
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