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    ANEMIASANEMIAS

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    Anemia is defined as a reduction in the oxygen-carrying capacity of the bloodAnemia is defined as a reduction in the oxygen-carrying capacity of the blood

    and usually is related to a decrease in number of circulating red blood cells (RBC)and usually is related to a decrease in number of circulating red blood cells (RBC)

    or to an abnormality in the hemoglobin (Hb) contained within the RBCsor to an abnormality in the hemoglobin (Hb) contained within the RBCs

    AnemiaAnemia

    Decreased production of RBCsDecreased production of RBCs

    Blood lossBlood loss Usually chronic blood lossUsually chronic blood loss

    Increased rate of destruction of RBCsIncreased rate of destruction of RBCs Hemolytic anemiaHemolytic anemia

    Iron deficiencyIron deficiency

    Pernicious anemia (vit BPernicious anemia (vit B1212 ))

    Folate deficiencyFolate deficiency

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    Represents the % of packed RBCs inRepresents the % of packed RBCs inwhole bloodwhole blood

    41-50 36-45

    MF

    Some important conceptsSome important concepts

    Normal Values:Normal Values:

    Men 41.5-50.4%Men 41.5-50.4%

    Women 35.9-44.6%Women 35.9-44.6%

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    Classification ofClassification ofanemiaanemia by pathogenesisby pathogenesis

    SpleenSpleen PeripheralPeripheralFactoryFactory

    MaterialsMaterials

    FormulaFormula

    Hypoproliferative anemiasHypoproliferative anemias

    Disorders of HemoglobinDisorders of Hemoglobin

    Hemolytic anemiasHemolytic anemiasBlood Loss AnemiasBlood Loss Anemias

    Bone MarrowBone Marrow

    Destruction of RBCsDestruction of RBCs ChronicChronic

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    Classification ofClassification ofanemiaanemia by pathogenesisby pathogenesis

    Blood loss anemiaBlood loss anemia

    Hemolytic anemiasHemolytic anemias

    Disorders of hemoglobinDisorders of hemoglobin

    Hypoproliferative anemiasHypoproliferative anemias

    Iron deficiency anemiaIron deficiency anemia

    Plummer-Vinson SyndromePlummer-Vinson Syndrome

    Glucose 6 phosphate dehydrogenaseGlucose 6 phosphate dehydrogenase

    Deficiency (G-6-PD deficiency)Deficiency (G-6-PD deficiency)Drug InducedDrug Induced

    Immune mediatedImmune mediated

    Sickle cell anemiaSickle cell anemia

    ThalassemiaThalassemia

    Vitamin B12 DeficiencyVitamin B12 Deficiency

    Pernicious anemiaPernicious anemia

    Folic acid deficiencyFolic acid deficiency

    Aplastic anemiaAplastic anemia

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    Blood loss anemiasBlood loss anemias

    Iron deficiencyIron deficiencyanemiaanemia

    -Most common of all anemiasMost common of all anemias

    -30% of the world population30% of the world population

    -In U.S. 5-11% of women and 2% of menIn U.S. 5-11% of women and 2% of men

    -Southeast AsiaSoutheast Asia High prevalence: Cultural backgroundHigh prevalence: Cultural background

    -Causes:Causes:Chronic blood lossChronic blood loss

    Malabsorption syndromeMalabsorption syndrome PicaPica

    Celiac diseaseCeliac disease

    Helicobacter PyloriHelicobacter Pylori

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    Blood loss anemiasBlood loss anemias

    Iron deficiencyIron deficiency

    anemiaanemia

    Diagnosis:Diagnosis:

    Low hemoglobin levelLow hemoglobin levelMicrocytic hypochromic cells in a peripheral blood smearMicrocytic hypochromic cells in a peripheral blood smearDecrease mean corpuscular value (hemoglobin)Decrease mean corpuscular value (hemoglobin)

    Low serum iron levelLow serum iron levelMarkedly reduced serum ferritin levelMarkedly reduced serum ferritin levelHigh serum iron-binding capacityHigh serum iron-binding capacity

    GOLD STANDARDGOLD STANDARD Iron stores in bone marrowIron stores in bone marrow

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    Blood loss anemiasBlood loss anemias

    Iron deficiencyIron deficiencyanemiaanemia

    Low number of RBCs, pale and small in sizeLow number of RBCs, pale and small in size

    peripheral blood smearperipheral blood smear

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    FoodFood Liver, meat, green vegetables, legumes,Liver, meat, green vegetables, legumes,

    nuts, egg yolk whole grain or enrichednuts, egg yolk whole grain or enrichedbreads, cerealsbreads, cereals

    SupplementsSupplements

    VitaminsVitamins Elemental iron in iron supplementsElemental iron in iron supplements Ferrous fumarateFerrous fumarate 33%33%

    Ferrous gluconateFerrous gluconate 11.6%11.6%

    Ferrous SOFerrous SO44

    20%20%

    Ferrous sulfate, dessicated 30%Ferrous sulfate, dessicated 30%

    Iron interferes with absorption of: tetracyclines, quinolones, levothyroxine, pencillamine, levodopa. Wait 2 hrsIron interferes with absorption of: tetracyclines, quinolones, levothyroxine, pencillamine, levodopa. Wait 2 hrs

    between drugs.between drugs.

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    G6 PD deficiency anemia

    Due to a deficiency of an enzyme in the hexosemonophosphate shunt pathway

    Found in 400 M persons worldwide 11% of African Americans (has an association with SCA) Very prominent in persons of Mediterranean origin

    Blockage of this pathway allows accumulation ofoxidants in the RBCs with altered cell

    membranes and resulting hemolysis Hemolytic episodes can be triggered by infection,drugs and foods (fava beans) Aspirin, dapsone, ascorbic acid, vitamin K

    Hemolytic anemiasHemolytic anemias

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    SCA falls under a broad entity of diseases known as hemoglobinopathiesSCA falls under a broad entity of diseases known as hemoglobinopathies

    Main Problem: Abnormal hemoglobinMain Problem: Abnormal hemoglobin

    SCA: autosomal recessive disorder and is characterized by an abnormality inSCA: autosomal recessive disorder and is characterized by an abnormality inthe B-chain of the hemoglobin and an abnormal RBC (trait vs disease)the B-chain of the hemoglobin and an abnormal RBC (trait vs disease)

    Mainly affects persons of African or Afro-Caribbean descentMainly affects persons of African or Afro-Caribbean descent

    When the red blood cell is subjected to a low oxygen tension the hemoglobin willWhen the red blood cell is subjected to a low oxygen tension the hemoglobin will

    form a sickle-shaped crystal within the erythrocyteform a sickle-shaped crystal within the erythrocyte

    Sickling may also be precipitated by infection, dehydration, hypoxia, acidosisSickling may also be precipitated by infection, dehydration, hypoxia, acidosis

    and results in painful crises due to infarcts caused by stasis of blood flowand results in painful crises due to infarcts caused by stasis of blood flow

    (spleen, bones, joints, brian, kidneys, lungs, eyes and skin)(spleen, bones, joints, brian, kidneys, lungs, eyes and skin)

    Disorders of the hemoglobinDisorders of the hemoglobin

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    When the red blood cell is subjected to aWhen the red blood cell is subjected to a

    low oxygen tensionlow oxygen tension the hemoglobin willthe hemoglobin will

    form a sickle-shaped crystal within theform a sickle-shaped crystal within the

    erythrocyteerythrocyte

    Disorders of the hemoglobinDisorders of the hemoglobin

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    Sickle cell traitSickle cell trait

    Normal adult hemoglobin molecule is made of 2 alpha and 2 beta chains:Normal adult hemoglobin molecule is made of 2 alpha and 2 beta chains:

    Hemoglobin AHemoglobin A

    In patients with SCA the normal molecule is substituted for 75-100% hemoglobin SIn patients with SCA the normal molecule is substituted for 75-100% hemoglobin S

    (substitution of the a.a.)(substitution of the a.a.)

    In patients with the sickle cell traitIn patients with the sickle cell trait 20-35% of the hemoglobin is S, the rest20-35% of the hemoglobin is S, the rest

    is normalis normal hemoglobin Ahemoglobin A

    Patients with the trait: usually have aPatients with the trait: usually have a normal life with mild symptoms,normal life with mild symptoms,

    except under ABNORMAL low oxygen conditionsexcept under ABNORMAL low oxygen conditions

    Disorders of the hemoglobinDisorders of the hemoglobin

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    Thalassemias Due to a genetic defect in either the - or

    -globin chain of hemoglobin resulting indiminished survival of RBCs Common in persons of Mediterranean,

    African and Southeast Asian ancestry

    -thalassemia treated with bloodtransfusion, folic acid supplement andascorbic acid, and possibly splenectomy

    Disorders of hemoglobinDisorders of hemoglobin

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    Vitamin B12 deficiencyVitamin B12 deficiency

    Vitamin B12 deficiency along with folic acid deficiency falls under theVitamin B12 deficiency along with folic acid deficiency falls under the

    group: MEGALOBLASTIC ANEMIASgroup: MEGALOBLASTIC ANEMIAS

    Foods of animal origin are the primary dietary sources of Vitamin B12Foods of animal origin are the primary dietary sources of Vitamin B12

    Vitamin B12 deficiency takes 2 to 5 years to developVitamin B12 deficiency takes 2 to 5 years to develop storagestorage

    Cobalamin is necessary for DNA synthesis and a deficiency preventsCobalamin is necessary for DNA synthesis and a deficiency prevents

    the normal cell duplication in the bone marrowthe normal cell duplication in the bone marrow

    Production of large erythrocytesProduction of large erythrocytes

    Vitamin B12 deficiencyVitamin B12 deficiency seen inseen in MalabsorptionMalabsorption

    Strict vegetarians.Strict vegetarians.

    Hypoproliferative anemiasHypoproliferative anemias

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    -Pernicious Anemia (PA) is the most common cause of Vitamin BPernicious Anemia (PA) is the most common cause of Vitamin B1212

    deficiency and is associated with chronic atrophic gastritis.deficiency and is associated with chronic atrophic gastritis.

    -Other conditions than can lead to vitamin BOther conditions than can lead to vitamin B1212 deficiency: gastrectomydeficiency: gastrectomy

    -PA develops because atrophic changes in the gastric mucosa resultsPA develops because atrophic changes in the gastric mucosa results

    in lack ofin lack of intrinsic factorintrinsic factorproduction, which is necessary for the absorptionproduction, which is necessary for the absorption

    of Vitamin Bof Vitamin B1212 from the gutfrom the gut

    Hypoproliferative anemiasHypoproliferative anemias

    PerniciousPernicious AnemiaAnemia

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    -In 85% of the patients serum antibodies to the gastric parietal cells areIn 85% of the patients serum antibodies to the gastric parietal cells are

    notednoted

    -Additionally in 50% of patients, serum antibodies to intrinsic factorAdditionally in 50% of patients, serum antibodies to intrinsic factor

    have been notedhave been noted

    -Other autoimmune conditions: Graves, Hashimoto, AddisonOther autoimmune conditions: Graves, Hashimoto, Addison

    -Diagnosis: Shilling test: small amount of radioactive Vitamin B12 orallyDiagnosis: Shilling test: small amount of radioactive Vitamin B12 orally

    after 24 hours: amount of radioactive Vit. B12 in the urine (7-30%)after 24 hours: amount of radioactive Vit. B12 in the urine (7-30%)

    Hypoproliferative anemiasHypoproliferative anemias

    PerniciousPernicious AnemiaAnemia

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    Physical and Oral ManifestationsPhysical and Oral Manifestations

    Iron deficiencyIron deficiency anemiaanemia

    PallorPallor

    - Oral mucosa: Soft palate, tongue and sublingual tissues- Oral mucosa: Soft palate, tongue and sublingual tissues

    - Conjunctiva- Conjunctiva

    Jaundice is usually not evidentJaundice is usually not evident

    Spoon-shaped fingernailsSpoon-shaped fingernails KoilonychiaKoilonychia

    Atrophic tongueAtrophic tongue

    GlossodyniaGlossodynia

    Burning Mouth DisordersBurning Mouth Disorders

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    Physical and Oral ManifestationsPhysical and Oral Manifestations

    Plummer-Vinson SyndromePlummer-Vinson Syndrome

    Type of Iron deficiency characterized by dysphagia and microcytic hypochromic anemiaType of Iron deficiency characterized by dysphagia and microcytic hypochromic anemia

    Sore depapillated tongueSore depapillated tongue

    XerostomiaXerostomia

    Angular stomatitisAngular stomatitis

    KoilonychiaKoilonychia

    Atrophic changes are not limited to the oral cavityAtrophic changes are not limited to the oral cavity pharynx, upper GIpharynx, upper GI

    Pallor fatigue, dyspneaPallor fatigue, dyspnea

    DYSPHAGIADYSPHAGIA Muscular degeneration of the esophagusMuscular degeneration of the esophagus

    Important: Increased prevalence of oral and pharyngeal carcinomaImportant: Increased prevalence of oral and pharyngeal carcinoma

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    Physical and Oral ManifestationsPhysical and Oral Manifestations

    Glucose 6-phosphate dehydrogenase deficiencyGlucose 6-phosphate dehydrogenase deficiency

    Most common manifestation : JAUNDICEMost common manifestation : JAUNDICE

    Jaundice: sclera,Jaundice: sclera, palate and floor of the mouthpalate and floor of the mouth

    Radiographic changes: Increase in the trabeculation of the bone (more radiolucent)Radiographic changes: Increase in the trabeculation of the bone (more radiolucent)

    Hyperplasia of the erythroid elements of the bone marrowHyperplasia of the erythroid elements of the bone marrow

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    Physical and Oral ManifestationsPhysical and Oral Manifestations

    Sickle cellSickle cell anemiaanemia

    Marked underdevelopmentMarked underdevelopment

    Majority of the patients die before 40 years of ageMajority of the patients die before 40 years of age

    Hemolytic anemiaHemolytic anemia PallorPallor

    JaundiceJaundiceCongestive Heart FailureCongestive Heart Failure

    StrokesStrokes

    Pain crisisPain crisis

    Small InfarctsSmall Infarcts

    Increased risk for developing infections with:Increased risk for developing infections with:

    -- S. pneumoniaeS. pneumoniae- H. influenza- H. influenza

    - Salmonella- Salmonella

    -- E. ColiE. Coli

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    Physical and Oral ManifestationsPhysical and Oral Manifestations

    Sickle cell anemiaSickle cell anemia

    Hypoplasia of the dentitionHypoplasia of the dentition

    Delayed eruptionDelayed eruption

    Increased bone trabeculationIncreased bone trabeculation

    Dense lamina duraDense lamina dura

    Skull film: thick cortexSkull film: thick cortex classical appearance hair on endclassical appearance hair on end

    Areas of bone sclerosis in periapical filmsAreas of bone sclerosis in periapical films

    Sometimes paresthesia of mental nerveSometimes paresthesia of mental nerve

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    Physical and Oral ManifestationsPhysical and Oral Manifestations

    ThalassemiaThalassemia

    Bone marrow expansionBone marrow expansion Ineffective erythropoiesisIneffective erythropoiesis

    Bimaxillary protrusionBimaxillary protrusion

    Spacing of the teethSpacing of the teeth

    Marked open biteMarked open bite

    Prominent malar bonesProminent malar bones

    Thin cortical boneThin cortical bone

    Discoloration of the teethDiscoloration of the teeth Iron depositIron deposit

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    Physical and Oral ManifestationsPhysical and Oral Manifestations

    Folic Acid deficiency anemiaFolic Acid deficiency anemia

    -PharyngitisPharyngitis

    -Ulcerative StomatitisUlcerative Stomatitis

    -Angular cheilitisAngular cheilitis

    -Difference with pernicious anemia: No neurological symptomsDifference with pernicious anemia: No neurological symptoms

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    Physical and Oral ManifestationsPhysical and Oral Manifestations

    Vitamin B12 deficiency / pernicious anemiaVitamin B12 deficiency / pernicious anemia

    In children Vitamin B12 deficiency often presents with non-specific symptomsIn children Vitamin B12 deficiency often presents with non-specific symptoms

    Neurological symptoms: paresthesia, sensory deficit, loss of reflexes, hypotoniaNeurological symptoms: paresthesia, sensory deficit, loss of reflexes, hypotonia

    seizures, dementiaseizures, dementia

    Abnormal skin pigmentationAbnormal skin pigmentation

    Systolic murmursSystolic murmurs

    GlossodyniaGlossodynia

    Atrophic tongueAtrophic tongue

    Tongue hypotonic (advance stage)Tongue hypotonic (advance stage)

    Erythema and macular lesions in the dorsum of the tongueErythema and macular lesions in the dorsum of the tongue

    Dysphagia and taste aberrationsDysphagia and taste aberrations

    BMD: Burning mouth DisorderBMD: Burning mouth Disorder

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    Dental Management of Patients withDental Management of Patients with

    AnemiaAnemia

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    Dental Management of Patients with AnemiaDental Management of Patients with Anemia

    1.1. CBC with differential in who patient presents with sign and symptomsCBC with differential in who patient presents with sign and symptomsof anemiaof anemia

    1.1. Consultation with primary MD if low hematocrit or hemoglobin is foundConsultation with primary MD if low hematocrit or hemoglobin is found

    2.2. Assessment of the severity of the anemia in conjunction with the patient MDAssessment of the severity of the anemia in conjunction with the patient MD

    3.3. Possible blood transfusion prior to treatment if anemia is severePossible blood transfusion prior to treatment if anemia is severe

    4.4. Avoidance of elective treatment in patient who are in crisisAvoidance of elective treatment in patient who are in crisis

    General issues:General issues:

    Patients with severe anemia may not tolerate blood loss or hypoxiaPatients with severe anemia may not tolerate blood loss or hypoxia

    Patients with anemia may not tolerate certain drugsPatients with anemia may not tolerate certain drugs

    Patients with anemia may not handle infection wellPatients with anemia may not handle infection well

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    Dental Management of Patients with AnemiaDental Management of Patients with Anemia

    Sickle cell anemiaSickle cell anemia

    Cautious use of nitrous oxide analgesia in patient with sickle cell anemia;Cautious use of nitrous oxide analgesia in patient with sickle cell anemia;

    ensure good oxygenation at all timesensure good oxygenation at all times

    Avoid respiratory depressantsAvoid respiratory depressants

    Avoid aspirin in large doses (to avoid acidosis); acetaminophen or codeineAvoid aspirin in large doses (to avoid acidosis); acetaminophen or codeineare better choicesare better choices

    Consider prophylactic antibiotics for surgical proceduresConsider prophylactic antibiotics for surgical procedures

    Aggressive management of infectionsAggressive management of infections

    G-6-PD DeficiencyG-6-PD Deficiency

    Avoid the use of aspirinAvoid the use of aspirin

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    The endThe end