This document discusses recurrent anemia in patients with end-stage renal disease (ESRD) undergoing hemodialysis. It provides details of a patient's medical history and medications. It then reviews causes of anemia in chronic kidney disease, including decreased dietary intake, inflammation, blood tests, and dialysis treatments. The document discusses evaluation of anemia and guidelines for iron supplementation. It also examines erythropoietin use and disadvantages, as well as FDA labeling and KDIGO anemia guideline recommendations regarding hemoglobin targets and use of erythropoiesis-stimulating agents.
This document discusses recurrent anemia in patients with end-stage renal disease (ESRD) undergoing hemodialysis. It provides details of a patient's medical history and medications. It then reviews causes of anemia in chronic kidney disease, including decreased dietary intake, inflammation, blood tests, and dialysis treatments. The document discusses evaluation of anemia and guidelines for iron supplementation. It also examines erythropoietin use and disadvantages, as well as FDA labeling and KDIGO anemia guideline recommendations regarding hemoglobin targets and use of erythropoiesis-stimulating agents.
This document discusses recurrent anemia in patients with end-stage renal disease (ESRD) undergoing hemodialysis. It provides details of a patient's medical history and medications. It then reviews causes of anemia in chronic kidney disease, including decreased dietary intake, inflammation, blood tests, and dialysis treatments. The document discusses evaluation of anemia and guidelines for iron supplementation. It also examines erythropoietin use and disadvantages, as well as FDA labeling and KDIGO anemia guideline recommendations regarding hemoglobin targets and use of erythropoiesis-stimulating agents.
IIUM • HD 1, 3 , 5 since 2011 • Via Left BCF • Qb 350. IDWG 2.5-3.0 kg • TDW achieved • kT/V 1.93 • Medications : • Felodipine 10mg ON • Recormon 6000 U/ week • BCO / Folate • CaCO3 2gm tds • 1-alfacalcidol 2mcg EOD • January 2015 – OGDS and Colonoscopy Anemia - in CKD 5D Case Reports Lower Gastrointestinal Bleeding in Chronic Hemodialysis Patients Anaemia – Initial evaluation
• Anaemia of CKD – hypoproliferative,
normochromic and normocytic
• Macrocytosis : folate, B12 deficiencies,
alcohol
• Hypochromic / microcytic: iron deficiency,
haemoglobinopathies , chronic blood loss Anaemia evaluation
• Ferritin and TSAT
• Percentage of hypochromic red cells • CHr ( Retics Hb content ) monitoring
• Other test: hs‐CRP
ERBP position statement on the KDIGO anaemia guideline
• Different cut‐off for ferritin and TSAT
• No previous iron treatment:
• Ferritin < 300 ng/ml • TSAT < 25%
• Post Iron treatment:
• Ferritin 500 ng/ml and TSAT 30% should not be intentionally exceeded NDT (2013) 28: 1346‐1359 IDA in CKD - causes • Decreased dietary intake • • Decreased GI absorption • • Increased inflammation • • Frequent blood testing • • Use of phosphate binders • • Procedures done & haemodialysis Rx itself • • Treatments with ESAs (?) Erythropoietin EPO Disadvantages Erythropoietin abuse What Does the guidelines say ? The New US FDA ESA label: 12/11 For patients with CKD not on dialysis:
• • Consider initiating ESA treatment only when the
hemoglobin level is less than 10 g/dL and the following considerations apply: • The rate of hemoglobin decline indicates the likelihood of requiring a red blood cell transfusion; and • Reducing the risk of alloimmunization and/or other red blood cell transfusion-related risks is a goal. • If the hemoglobin level exceeds 10 g/dL, reduce or interrupt the dose of ESA and use the lowest dose of ESA sufficient to reduce the need for red blood cell transfusions. • The New KDIGO Anemia Guidelines (KI supplement Aug 2012) :
• 3.1: Address all correctable causes of anemia (including iron deficiency
and inflammatory states) prior to initiation of ESA therapy. (Not Graded) • 3.2: In initiating and maintaining ESA therapy, we recommend balancing the potential benefits of reducing blood transfusions and anemia-related symptoms against the risks of harm in individual patients (e.g., stroke, vascular access loss, hypertension). (1B) • We recommend using ESA therapy with great caution, if at all, in CKD patients with active malignancy—in particular when cure is the anticipated outcome—(1B), a history of stroke (1B), or a history of malignancy (2C).
• 3.4.1: For adult CKD ND patients with Hb concentration >10.0 g/dl
• (> 100 g/l), we suggest that ESA therapy not be initiated. (2D) • 3.4.2: For adult CKD ND patients with Hb concentration 10.0 g/dl (100 g/l) we suggest that the decision whether to initiate ESA therapy be individualized based on the rate of fall of Hb concentration, prior response to iron therapy, the risk of needing a transfusion, the risks related to ESA therapy and the presence of symptoms attributable to anemia. (2C)
• 3.4.3: For adult CKD 5D patients, we suggest that ESA
therapy be used to avoid having the Hb concentration fall below 9.0 g/dl (90 g/l) by starting ESA therapy when the hemoglobin is between 9.0– 10.0 g/dl (90–100 g/l). (2B) • 3.4.4: Individualization of therapy is reasonable as some patients may have improvements in quality of life at higher Hb concentration and ESA therapy may be started above 10.0 g/dl (100 g/l). (Not Graded) • What is the target Hb ?? Hb targets Relatively Newer Agents