Anemia

1. Anemia Robb Friedman, MD Modified by Sean Hesselbacher, MD, Eyal Oren, MD, David Antonetti, MD and Cathy Okuliar, MD

2. What is Anemia? • ANEMIA IS NEVER NORMAL • Reduction below normal in the mass of red blood cells in the circulation • Hemoglobin concentration, hematocrit, RBC count • Men: HGB < 14 or HCT < 41% • Women: HGB < 12.0 or HCT < 36%

3. Anemia and Volume Status • HGB and HCT are CONCENTRATIONS • Therefore dependent upon plasma volume • Acute bleeds not reflected for 24-36 hrs • Due to volume deficit being slowly repaired via movement of fluid from extravascular space to intravascular • Anemic patients who are dehydrated will not appear anemic • Pregnant women expand RBCs 25% but plasma volume increases 50%, producing “physiologic anemia”

4. Anemia: Special Cases • Erythrocytosis • People who live at high altitude have greater RBC volume • Smokers have increased HCT – impairs the ability of the RBCs to deliver O2 • African-American HGBs are 0.5 to 1.0g/dL lower than Caucasians • Athletes (increased plasma volume, Fe deficiency, hemolysis, polycythemia, use of performance enhancing agents)

5. Anemia and the Elderly • Multiple studies show that the elderly do not have a “lower normal range” • Anemia, while common in the elderly, is still abnormal • HGB < 13 in males and < 12 in females associated with an increased relative risk of mortality (1.6 and 2.3 respectively)

6. Anemia: History • Is the patient bleeding? • NSAIDs, ASA • Menstrual history, if applicable (include older women) • Prior intestinal surgery? • Hx of hemorrhoids, hematochezia, or melena? • Past medical history of anemia? Family history? • Alcohol, nutritional questions • Liver, renal diseases • Ethnicity • Environmental/work toxins (ie lead)

7. Symptoms of Anemia • Decreased O2 delivery • Hypovolemia if acute loss • Exertional dyspnea, fatigue, palpitations, lightheadedness • Severe: heart failure, angina • “Pica”– craving for clay or paper products • Pagophagia– craving for ice

8. Signs of Anemia • Tachycardia, tachypnea, orthostasis • Pallor • Jaundice • Murmur • Koilonychia or “Spoon nails” • Splenomegaly, lymphadenopathy • Petechiae, ecchymoses • Atrophy of tongue papillae • Heme + stool

9. The Four Causes of Anemia • Decreased red blood cell production • Increased red blood cell destruction • Red blood cell loss • Red blood cell sequestration * Underlying disorder is abnormal production vs. premature loss

10. Decreased RBC production • Deficiency of iron, B12, folate • Marrow is dysfunctional from myelodysplasia, tumor infiltration, aplastic anemia, etc. • Bone marrow is suppressed by chemotherapy or radiation • Low levels of erythropoeitin, thyroid hormone, or androgens

11. Increased RBC destruction • RBCs live about 100 days • Acquired: autoimmune hemolytic anemia, TTP-HUS, DIC, malaria • Inherited: spherocytosis, sickle cell, thalassemia

12. RBC Loss • Bleeding! • Obvious vs occult • Iatrogenic: venesection e.g. daily CBC, surgical, hemodialysis • Retroperitoneal

13. CBC Reticulocyte count MCV RI > 2% RI < 2% Underproduction Increased destruction or loss MCV Further work up Based on history, Physical, other MCV 81 – 99 Normocytic MCV > 100 Macrocytic MCV < 80 Microcytic Approach to Anemia

14. Approach to Anemia • LOOK AT THE SMEAR!!!! • Convenient to separate into three classes based on the size of the RBC • MCV and RDW • Microcytosis: < 80 fL • Normocytosis: 80-100 fL • Macrocytosis: >100 fL • CBC, reticulocyte count, Fe, Ferritin, TIBC, folate, B12, LDH, CMP, ESR…

15. Reticulocytes • Nucleated RBCs – form in marrow where they mature for 3 days and then spend 1 day in circulation (before maturing to RBC) • Given avg life span of RBC of 100 days, 1% of RBCs are destroyed each day • Retics form 1% of circulating RBCs qd • Nl RBC count is 5 million/uL so marrow makes 50,000 reticulocytes/uL blood qd • With epo, can increase to 250,000 retics/uL blood qd (given nl marrow and replete iron, folate, b12)

16. Reticulocyte Count • Assess adequacy of bone marrow response to anemia • Must adjust for the degree of anemia, use Reticulocyte Production Index • RI = (measured retic) x (Hct/45) / (Correction Factor) • CF: Hct 41-50 (1); 30-40 (1.5); 20-29 (2); 10-19 (2.5) • Reflects increased circulating time for retics as Epo pushes them out of the marrow earlier • RI < 1.0 is abnormally low and indicates inadequate marrow response

17. Microcytic Anemia • Iron Deficiency Anemia • Thallasemia • Anemia of chronic disease • Sideroblastic anemia

18. Iron Deficiency Anemia • The definitive test is serum ferritin • Low serum ferritin (<12 ug/L)is diagnostic of iron deficiency • Although ferritin is an acute phase reactant, it will still be low in iron deficiency • Also, high TIBC • Fe saturation = Fe/TIBC < 10% in Fe deficiency • If ferritin is indeterminate • Low serum Fe is not in itself diagnostic, neither is marrow staining • Anisocytosis (heterogeneous in shape) and poikilocytosis (abnormal shape) • Reactive thrombocytosis

19. Iron deficiency

20. Thalassemia • Decreased production of either α-globin or β-globin chains • Abnormal hemoglobin electrophoresis • Polychromasia (dark staining retics), target cells, basophilic stippling • Normal/increased RBC mass • Mentzer index: MCV/RBC ct < 13

21. Alpha-Thalassemia • Alpha-Thalassemia: 4 genes • 1/4: silent carrier • 2/4: Alpha-Thalassemia trait, microcytosis and mild anemia • 3/4: excess Beta-chains form tetramers, results in severe anemia and microcytosis • 4/4: hydrops fetalis • Most common in SE Asian populations

22. Basophilic stippling

23. Beta-Thalassemia • 2 genes • 1/2 mutation: Beta-Thal trait, increased Hgb A2, rarely anemic, mild microcytosis • 2/2 mutation: Beta-Thalassemia disease, Hgb F, microcytosis, anemia • Usually found in people of African or Mediterranean descent but has world-wide distribution

24. Beta - Thalassemia

25. Sideroblastic Anemia • Failure of synthesis of porphyrin ring • Hereditary • Acquired (INH, EtOH, B6 deficiency, Lead) • Smear: sideroblasts and basophilic stippling

26. Macrocytic Anemia (MCV>100) • Drug Induced (hydroxyurea, AZT, MTX, chemotherapy, anticonvulsants) • B12 / folate deficiency • Myelodysplastic syndrome • Liver disease • Alcohol abuse • Reticulocytes • Hypothyroidism

27. Folate and B12 • Serum folate usually sufficient, but if folate level is normal but folate deficiency is suspected, check serum homocysteine (elevated because of impaired folate dependent conversion of homocysteine to methionine) or RBC-folate. • B12 can be spuriously low– a more sensitive and specific test is serum methylmalonic acid level, will be increased if B12 is low. • Classically check Schilling Test for B12 deficiency (parietal cell antibody or Intrinsic Factor antibody)

29. B12 and Folate Deficiency

30. Myelodysplastic Syndrome • Primary bone marrow disorder, often found in elderly • Macrocytosis, anemia • Pseudo-Pelger-Huet abnormality– the bilobed nucleus

31. Normocytic Anemia • Large and complicated group of disorders! • Hemolytic anemias • Anemia of chronic disease • Bone marrow disorder • Nutritional (early Fe, B12, folate deficiency) • Renal insufficiency

32. Nutritional Anemias • Iron deficiency and B12/folate deficiency can present with normocytic anemia– esp. if both deficiencies are concurrent. • Check iron studies and B12, folate levels.

33. Anemia of Renal Insufficiency • Unremarkable peripheral blood smear • Inappropriately normal erythropoietin level • Anemia usually severe and symptomatic when Cr > 3.0 • Mild to moderate anemia found in Cr 1.5-3.0 • Tx: Epogen or similar, Fe (oral, IV) if iron stores are found to be low

34. Hemolytic Anemias

35. Evaluation of Hemolysis • LDH: increases • Indirect bilirubin increases (increased Hgb catabolism) • Haptoglobin decreases • Reticulocyte count increases • Urine hemosiderin test = present in intravascular, absent in extravascular hemolysis! • Coombs test: • (+) = autoimmune hemolytic anemia • (-) consider PNH (abnormal GPI protein, send flow for CD55 and CD59)

36. Hemolytic Anemia: Intrinsic causesSpherocytosis, Sickle Cell

37. More hemolytic anemias

38. Anemia of Chronic Disease • Thought to be a cytokine mediated process which inhibits red blood cell production or interferes with action of erythropoietin • Therefore, the disease needs to be inflammatory • Decreased iron utilization/mobilization • Seen with rheumatologic diseases, chronic infections, malignancy • Indices: Low Fe, Low TIBC, Nl/increased Ferritin • May be seen in conjunction with Fe-deficiency

39. Anemia due to Primary Bone Marrow Disorder • Myelodysplastic syndrome • Bone marrow infiltration: nucleated red blood cells found in circulation • Might see “rouleaux” formation in multiple myeloma • WBC, plts often abnormal • Bone marrow biopsy

40. Anemia: Treatments • “Transfusion triggers” • CAD: Hgb > 10 • All pts: Hgb > 7.0 • Iron supplementation • Erythropoietin analogs • B12, folate

41. What in the world is a Howell-Jolly Body?

42. Acanthocytes vs Echinocytes • Acanthocytes: “spur cells” found in liver disease • Echinocytes: “burr cells” found in renal disease

43. Helmet vs. Teardrop Cells

44. Anemia: Summary • ANEMIA IS NEVER NORMAL • Determine if ACUTE or CHRONIC • CONSIDER THE FOUR CAUSES • CALCULATE the RETIC INDEX • LOOK AT THE SMEAR • CONSIDER THE ETIOLOGY BASED ON RBC MORPHOLOGY AND LABORATORY STUDIES • TREAT APPROPRIATELY

45. MKSAP Questions

46. An 80-year-old man who had a hemicolectomy for colon cancer is evaluated because of a 4-month history of diarrhea, anorexia, and fatigue. He had a remote history of alcoholism. • On physical examination, he is cachectic and mildly confused. His pulse rate is 70/min, and blood pressure is 140/85 mm Hg. His tongue is smooth. The abdomen is soft; there are no palpable masses or hepatosplenomegaly. A stool specimen is negative for occult blood. Neurologic examination shows loss of position sense in the feet. He has a wide-based gait. The Romberg test is positive. His hemoglobin is 9.4 g/dL, reticulocyte count is 2.5%, mean corpuscular volume is 125 fL, and serum lactate dehydrogenase is 400 U/L. • Which of the following is the most likely cause for his symptoms? • ( A ) Alcoholic cerebellar degeneration( B ) Vitamin B12 deficiency( C ) Brain metastases( D ) Folate deficiency( E ) Liver metastases

47. Critique (Correct Answer = B) • The patient most likely has vitamin B12 deficiency, based on the degree of macrocytosis and neurologic findings. An elevated serum lactate dehydrogenase level, due to intramarrow cell death from ineffective erythropoiesis, is consistent with this diagnosis. • Severe macrocytosis (mean corpuscular volume > 120 fL) is often associated with vitamin B12 deficiency or folate deficiency (megaloblastic anemia), usually seen in conjunction with “oval” macrocytes. The presence of frequent hypersegmented neutrophils (> 5 segments) is strongly suggestive of vitamin B12 or folate deficiency. • Bone marrow morphology in patients with vitamin B12 or folate deficiency is referred to as “megaloblastic” and is characterized by the presence of large cells with immature nuclear chromatin but maturing erythrocyte cytoplasm (nuclear-cytoplasmic dissociation). Anemia accompanies this process; hence the term “ineffective erythropoiesis.” The intramarrow death of megaloblastic cells causes the serum lactate dehydrogenase level to rise. If a patient has a low serum vitamin B12 or folate level, a bone marrow examination is probably unnecessary. However, the physician should determine the cause of the deficiency. If a patient has a normal serum vitamin B12 or folate level, a bone marrow examination is frequently helpful to exclude myelodysplastic syndromes or other infiltrative marrow disorders. • Folate deficiency can induce megaloblastosis within weeks to months, whereas vitamin B12 deficiency requires years to cause megaloblastosis since stores of vitamin B12 persist for years in the liver and other tissues. In patients with vitamin B12 or folate deficiency, parenteral or oral repletion of vitamin B12 or folate reverses some morphologic abnormalities within hours. Serum folate levels fluctuate quickly with changes in dietary consumption. Low erythrocyte folate levels often reflect prior nutritional depletion. In patients who are hospitalized and are begun on regular diets, the erythrocyte folate test may provide a better assessment of tissue folate levels than determination of the serum folate level. The erythrocyte folate test often requires a special laboratory, and results often are not quickly available. • In patients with megaloblastic anemias, erythrocyte production is diminished and a “corrected” reticulocyte count is inappropriately low for the degree of anemia. This patient had a corrected reticulocyte count of 1% (inappropriately low for a hemoglobin level of 9.4 g/dL). • In addition to changes in the blood, the epithelial cells in patients with megaloblastic anemias may become atrophic and cause a smooth tongue and cheilosis. Posterior column dysfunction, particularly in patients with vitamin B12 deficiency, may lead to changes in vibratory or position sense, causing ataxia. Signs of dementia may appear. However, neurologic dysfunction is very uncommon in adults with folate deficiency. • Alcoholic cerebellar degeneration results in ataxia but not position loss. Although liver metastases are possible in a patient with a history of colon cancer, their presence would not account for the neurological findings in this patient. Brain metastases would most likely produce focal neurological findings and also would not account for the blood findings.

48. A 26-year-old man is evaluated because of progressive fatigue, dyspnea on exertion, and orthostatic dizziness for the past 2 to 3 weeks. He takes no medications. Physical examination is normal except for pallor. • Laboratory Studies: Hematocrit 13%Leukocyte count 8300/μL; normal differential. Reticulocyte count: 0, Platelet count 320,000/μL. A routine biochemical profile, including liver function tests, is normal. A chest radiograph shows normal lung fields and a widened mediastinum, suggestive of an anterior mediastinal mass. Bone marrow biopsy shows absent erythrocyte precursors, normal megakaryocytes, and normal leukocyte numbers and maturation. • Which of the following is the most likely cause of the mediastinal mass and anemia? • ( A ) Hodgkin’s disease( B ) Non-Hodgkin’s lymphoma( C ) Thyroid carcinoma( D ) Thymoma( E ) Germ cell carcinoma

49. Critique (Correct Answer = D) • Each of the listed neoplasms may present as an anterior mediastinal mass and may be associated with anemia of chronic disease. However, pure red cell aplasia (which this patient has) is often associated with a benign or invasive thymoma. Approximately 5% to 15% of thymomas occur in patients with pure red cell aplasia. Other thymoma-associated autoimmune disorders include myasthenia gravis, systemic lupus erythematosus, thrombocytopenia, and, rarely, malabsorption states. A careful search by CT or MRI is always warranted in patients with newly diagnosed or relapsing red cell aplasia or myasthenia. • The other listed entities are also included in the differential diagnosis for an anterior mediastinal mass. Germ cell tumors have not been associated with pure red cell aplasia, and Hodgkin’s disease, non-Hodgkin’s lymphoma, and thyroid carcinoma are rarely associated with this disorder. Chronic lymphocytic leukemia is also commonly associated with red cell aplasia and may present with variable degrees of lymphadenopathy but not with an isolated anterior mediastinal mass, as in the patient discussed here.

50. A 36-year-old black man with known sickle cell anemia is evaluated because of a 2-week history of fever, a macular rash on his trunk, and arthralgias. Subsequently, he developed weakness and dyspnea on exertion. Several of his children had febrile illnesses with associated rashes and fatigue over the past month. These illnesses resolved spontaneously without sequelae. On physical examination, his temperature is 38.8 °C (101.8 °F), pulse rate is 100/min, and blood pressure is 160/70 mm Hg. A maculopapular, truncal rash is noted. There is conjunctival pallor. The remainder of his examination is unremarkable. Laboratory StudiesHemoglobin 5.2 g/dLLeukocyte count 5000/μLReticulocyte count 0%Platelet count 130,000/μLSerum lactate dehydrogenase 622 U/LWhich of the following is the most likely diagnosis? ( A ) Paroxysmal nocturnal hemoglobinuria( B ) Parvovirus infection( C ) Glucose-6-phosphate dehydrogenase deficiency( D ) Aplastic anemia