Home

helps physicians and healthcare professionals

Erectile Dysfunction

helps physicians and healthcare professionals

Doctor123.org

helps physicians and healthcare professionals

Anemia, Emergency Medicine


Basics


Description


  • Reduction below normal in the mass of RBCs
  • Measured by 1 or more of the major RBC components:
    • Hemoglobin (Hgb): Concentration of the major oxygen-carrying component in whole blood
    • Hematocrit (Hct): Percent volume of whole blood occupied by intact RBCs
    • RBC count: RBCs contained in a volume of whole blood
  • Adult female: Hgb <12 g/dL or Hct <37%
  • Adult male: Hgb <14 g/dL or Hct <42%
  • Normal blood count values depend on age:
    • Birth: Hgb 16.5, Hct 51
    • 1 yr: Hgb 12, Hct 36
    • 6 yr: Hgb 12.5, Hct 37
    • Adult male: Hgb 14, Hct 42
    • Adult female: Hgb 12, Hct 37
  • Hgb/Hct depend on oxygen pressure:
    • Increased in neonates and people living above 4,000 ft
  • Hgb, Hct, and RBC count are concentrations:
    • Dependent on RBC mass and plasma volume
    • Values decrease if RBC mass decreases or plasma volume increases.
  • Anemia is an indication of an underlying disorder or deficiency.

Etiology


  • Never a normal variant:
    • May be the first manifestation of a systemic disorder
    • Always seek a cause.
  • Excessive blood loss (most common cause):
    • Trauma
    • GI bleed
    • Menstruation
  • Hemolysis (increased RBC destruction, RBC lifespan <100 days):
    • Hypersplenism
    • Autoimmune hemolytic anemia
    • Mechanical trauma (prosthetic heart valves, vasculitis, thrombotic thrombocytopenic purpura [TTP], hemolytic uremic syndrome [HUS], or disseminated intravascular coagulation [DIC])
    • Toxins
    • Infections (malaria, babesiosis)
    • Membrane abnormalities
    • Intracellular RBC abnormalities (G6PD, sickle cell anemia, or thalassemia)
  • Decreased RBC synthesis:
    • Classified by measurement of RBC size
    • Hypochromic/microcytic:
      • Iron deficiency
      • Thalassemia
      • Sideroblastic
      • Chronic disease
    • Normochromic/macrocytic:
      • Hypothyroidism
      • Folate deficiency
      • Vitamin B12 deficiency
      • Liver disease
      • Myelodysplasia
      • Certain leukemias
    • Normochromic/normocytic:
      • Aplastic anemia
      • Chronic renal failure
      • Malignancy
      • Adrenal insufficiency
      • Hyperparathyroidism
      • Alcohol abuse
      • Acute blood loss

Diagnosis


Signs and Symptoms


Depends on: á
  • Rapidity of onset:
    • Hypovolemia if acute
    • Asymptomatic if mild and chronic

History
  • Underlying disease
  • Severity and type of anemia
  • Fatigue
  • Decreased exercise intolerance
  • Shortness of breath
  • Dyspnea on exertion
  • Chest pain/angina
  • Syncope
  • Blood in stool/tarry black stools
  • Irregular or heavy menses
  • Easy bruising or history of excessive bleeding

Physical Exam
  • Cardiovascular:
    • Tachycardia, cardiomegaly, or murmurs
    • Postural hypotension
  • Dermatologic:
    • Skin:
      • Cool
      • Pallor
      • Jaundice
      • Purpura
      • Telangiectasia
      • Petechiae
      • Ecchymosis
    • Spoon-shaped nails (koilonychia)
  • Neurologic:
    • Neuropathy
    • Altered mental status
  • Bone (especially sternal) or joint pain (sickle cell disease)
  • Hepatomegaly, splenomegaly
  • Lymphadenopathy
  • Findings reflect underlying disease

Essential Workup


  • CBC
  • Vital signs/orthostatics
  • Determine if:
    • Bleeding
    • Increased RBC destruction
    • Bone marrow suppression
    • Iron deficient

Diagnosis Tests & Interpretation


Lab
  • Type and crossmatch or type and screen
    • Depends on severity
  • CBC
    • RBC indices:
      • Mean corpuscular volume (MCV; normal: 80-100 ╬╝m3)
      • Mean corpuscular hemoglobin (MCH; normal: 27-34 pg/cell)
      • Mean corpuscular hemoglobin concentration (MCHC; normal: 33-36%)
    • Platelet count
      • Thrombocytosis suggests:
        • Iron deficiency
        • Myeloproliferative disorders
        • Inflammation
        • Infection
        • Neoplasm
      • Thrombocytopenia suggests:
        • Bone marrow malignancy
        • Hypersplenism
        • Sepsis
        • Vitamin B12 or folate deficiency
        • Autoimmune disorders
  • Reticulocyte (retic) count:
    • Normal 0.5-1.5% (retics/1,000 RBCs)
    • Increased retic count: Increased erythropoietic response to continued blood loss or hemolysis
    • Stable anemia with low retic count: Impaired RBC production
    • Active hemolysis or blood loss with low retic count: Concurrent disorder
    • Low retic count with pancytopenia: Aplastic anemia
    • Low retic count with normal WBC and platelets: Pure RBC aplasia
  • Reticulocyte index (RI): Retic count (%) Ś (patient Hct/normal Hct):
    • RI <2% implies inadequate RBC production.
    • RI >2% implies increased RBC production with excessive RBC destruction or loss.
  • WBC with differential and peripheral smear:
    • Leukopenia with anemia suggests bone marrow suppression, hypersplenism, or deficient vitamin B12/folate
  • Stool for occult blood
  • Electrolytes, BUN, creatinine, glucose:
    • Chronic renal failure
  • Urinalysis:
    • Hematuria
    • Hemoglobinuria in hemolytic anemia
  • Workup strategy:
    • Hypochromic/microcytic anemias:
      • Iron
      • Total iron-binding capacity
      • Transferrin saturation
      • Ferritin
    • Macrocytic anemias:
      • Folate
      • Vitamin B12
      • LFT
      • Thyroid function tests
    • Hemolytic anemia:
      • Rapid fall in Hgb
      • Reticulocytosis
      • Fragmented RBCs
      • Increased LDH
      • Increased indirect bilirubin
      • Decreased serum haptoglobin
      • Coombs positive
  • Special tests:
    • Peripheral smear:
      • Helmet cells/schistocytes-microangiopathic hemolysis
      • Teardrop cells-myelofibrosis
      • Spherocytes-autoimmune hemolysis
      • Leukoerythroblastic pattern-bone marrow replacement
      • Bite cells-oxidative hemolysis
      • RBC parasites-malaria or babesiosis
      • Target cells-liver disease
      • Burr cells-uremia
      • Sideroblasts-alcoholism or myelodysplasia
      • Howell-Jolly bodies-asplenia
    • Hgb electrophoresis for sickle cell/thalassemia
    • Iron, iron-binding capacity, transferrin saturation, ferritin:
      • Iron deficiency
      • Iron-decreased
      • Iron-binding capacity-increased
      • Transferrin saturation-decreased
      • Ferritin-decreased
    • Chronic disease:
      • Iron-decreased
      • Iron-binding capacity-decreased
      • Transferrin saturation-decreased/normal
      • Ferritin-normal/increased
    • Thalassemia:
      • Iron-normal
      • Iron-binding capacity-normal
      • Ferritin-normal
    • Sideroblastic anemia:
      • Iron-increased
      • Iron-binding capacity-normal
      • Ferritin-increased

Diagnostic Procedures/Surgery
Bone marrow biopsy evaluates: á
  • Aplastic anemia
  • Myelodysplasia
  • Bone marrow malignancy
  • Myeloproliferative disorders

Differential Diagnosis


  • Acquired versus inherited anemia
  • Anemia of chronic disease
  • Blood loss
  • CHF
  • Dilutional anemia
  • Hemolysis
  • Malignancy
  • Nutritional deficiency/malabsorption
  • Toxic bone marrow suppression

  • Hemolytic anemia of the newborn:
  • Rh antibody crosses placenta when Rh-negative mother has Rh-positive child.

  • Physiologic or dilutional anemia in 3rd-trimester pregnancy:
  • 25% increase of RBC mass and 50% increase in plasma volume

  • Values for Hgb/Hct in healthy elderly are generally lower than in younger adults.
  • This lower "normal"Ł must be a diagnosis of exclusion.

Treatment


Pre-Hospital


Ongoing blood loss requires close assessment and rapid transport: á
  • Control bleeding to include wound packing and use of tourniquets if needed.
  • Two large-bore IVs

Initial Stabilization/Therapy


  • Airway, breathing, circulation (ABCs)
  • Oxygen
  • IV fluid resuscitation with 0.9% NS if ongoing loss/hypotension

Ed Treatment/Procedures


  • Depends on severity of anemia and acuteness of onset
  • Transfusion for hemorrhage with unstable vital signs not responding to crystalloid resuscitation.
  • Most anemias seen in ED are chronic and do not require immediate intervention.
  • Therapy for specific anemia:
    • Iron deficiency:
      • FeSO4: 300 mg PO TID
      • Investigate underlying cause.
      • Increased Hgb expected in 2-3 wk
    • Renal failure:
      • Endogenous erythropoietin is diminished.
      • Replace with recombinant erythropoietin
    • Autoimmune hemolytic anemia:
      • Corticosteroids (prednisone 60 mg/day until response)
      • Immunosuppressive agents
      • Plasmapheresis
      • Splenectomy if splenic sequestration
    • Drug-induced hemolytic anemia: Stop offending agent.
    • Anemia of chronic disease: Treat underlying disease.
    • Vitamin B12 deficiency:
      • Vitamin B12: 1,000 ╬╝g IM daily for 1 wk, then weekly for 1 mo, then monthly
      • Hematologic parameters normalize within 2 mo.
      • Neurologic symptoms present >6 mo may be permanent.
    • Folate deficiency:
      • Folic acid: 1 mg PO daily
    • Aplastic anemia
    • Antithymocyte globulin
    • Bone marrow transplantation:
      • Sickle cell anemia
      • Supportive care with oxygen, rehydration, analgesia
      • Treat precipitating cause.
    • Leukemia:
      • Bone marrow replacement

Medication


  • Iron supplements
  • Erythropoietin for renal failure
  • Corticosteroids for autoimmune
  • Vitamin B12
  • Folic acid (B9)

Follow-Up


Disposition


Admission Criteria
  • Unstable vital signs
  • Ongoing blood loss
  • Symptomatic anemia-angina/dyspnea/syncope/neurologic symptoms
  • Need for transfusion
  • Need for aggressive evaluation
  • Severe anemia
    • Initial, unexplained Hgb <8 g/dL
    • Major difficulty in obtaining outpatient care for patients whose Hgb are significantly low or when comorbidity is present

Discharge Criteria
Discharge vast majority of stable patients for outpatient workup. á

Followup Recommendations


Newly diagnosed anemic patients need to be worked up: á
  • If stable for discharge from the ED, provide follow-up options for workup

Pearls and Pitfalls


  • Anemia is an indication of an underlying disorder or deficiency.
  • Severe or life-threatening cases require immediate correction via blood transfusion.
  • Most cases seen in the ED are chronic and do not require immediate intervention.

Additional Reading


  • Bryan áL, Zakai áN. Why is my patient anemic? Hematol Oncol Clin N.  2012;26:205-230.
  • Bunn áHF. Goldman: Goldmans Cecil Medicine. 24th ed. Philadelphia, PA: Saunders, an imprint of Elsevier Inc.; 2011.
  • Hoffman áR, Benz áEJ Jr, Silberstein áLE, et al. Hematology: Basic Principles and Practice. 6th ed. Philadelphia, PA: Saunders, an imprint of Elsevier Inc.; 2012.
  • Recht áM. Thrombocytopenia and anemia in infants and children. Emerg Med Clin North Am.  2009;27:505-523.
  • Rizack áT. Special hematologic issues in the pregnant patient. Hematol Oncol Clin N.  2012;26:409-432.

See Also (Topic, Algorithm, Electronic Media Element)


  • GI Bleeding
  • Renal Failure
  • Sickle Cell Disease

Codes


ICD9


  • 280.0 Iron deficiency anemia secondary to blood loss (chronic)
  • 285.1 Acute posthemorrhagic anemia
  • 285.9 Anemia, unspecified
  • 283.9 Acquired hemolytic anemia, unspecified
  • 285.29 Anemia of other chronic disease

ICD10


  • D50.0 Iron deficiency anemia secondary to blood loss (chronic)
  • D62 Acute posthemorrhagic anemia
  • D64.9 Anemia, unspecified
  • D58.9 Hereditary hemolytic anemia, unspecified
  • D63.8 Anemia in other chronic diseases classified elsewhere

SNOMED


  • 271737000 Anemia (disorder)
  • 267530009 Acute posthemorrhagic anemia (disorder)
  • 413533008 anemia due to chronic blood loss (disorder)
  • 61261009 Hemolytic anemia (disorder)
  • 234347009 Anemia of chronic disorder (disorder)
Copyright © 2016 - 2017
Doctor123.org | Disclaimer