Heme II Important Values

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Last updated 4:58 PM on 9/17/26
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90 Terms

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Factor I Name

fibrinogen

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Factor I, II V, have what PT/aPTT

increased PT

Increased aPTT

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Factor II Name

prothrombin

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Factor III Name

thromboplastin

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Factor IV Name

calcium

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Factor V Name

Labile factor

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Factor VII name

Stable factor

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Factor VIII name

Antihemophilic factor A

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Facor IX name

Christmas Factor

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Factor X name

Stuart Prower

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Factor XI name

Plasma thromboplastin antecedent

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Factor XII name

Hageman

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Factor XIII name

fibrin stabalizing factor

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Factors VIII, IX, XI and XII have what PT/aPTT

normal PT

increased aPTT

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Factor VII has what PT/aPTT

increased PT

normal aPTT

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Factor XIII has what PT/aPTT

normal PT

normal aPTT

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Stage 1 IDA

decreased ferritin

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Granulocytic myeloblast

first

<p>first</p>
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Granulocyte progranulocyte

second

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Neutrophilic myelocyte

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Basophilic myelocyte

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Eosinophilic myelocyte

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Abnormal GPIb

Bernard soulier

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Polychromasia

RBCs with increased bluish-gray staining due to residual RNA

<p><span>RBCs with increased bluish-gray staining due to residual RNA</span></p>
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Coagulation studies PT/aPTT tube color

Light blue

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Microcytic

MCV < 80

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Normocytic

MCV 80-100

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Macrocytic

MCV > 100

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Normal MCHC

32-36 g/dL

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Spherocytosis/dehydration

MCHC >36 g/dL

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Hypochromic

MCHC <32 g/dL

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Normal MCH

27-33 pg

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Hyperchromic

MCH >33 pg

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Hypochromic

MCH <27 pg

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Spherocyte

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Plasminogen → Plasmin

tPA Breaks down fibrin/clot

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Fibrinogen → Fibrin

Thrombin (Factor IIa) Builds the clot

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Prothrombin → Thrombin

Prothrombinase complex (Xa + Va)

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Fibrin → fibrin degradation products

Plasmin Breaks down the clot

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Coagulation phase 1

initiation

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Initiation

Coagulation starts at the site of injury

Tissue factor + VII → Xa → small amount of thrombin

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Coagulation phase 2

Amplification

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Amplification

Prepares platelets and coagulation factors

Thrombin activates platelets, V, VIII, XI

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Coagulation phase 3

Propagation

Xa + Va = prothrombinase → LOTS of thrombin

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Propagation

Big thrombin production

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Coagulation phase 4

Stabilization

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Stabilization

Strong, stable clot forms

Thrombin → fibrinogen → fibrin; XIII cross-links fibrin

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Schistocyte

Helmet cell

<p>Helmet cell</p>
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Stomatocyte

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Ovalocyte

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Acanthocyte

Spur cell

<p>Spur cell</p>
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Echinocyte

Burr cell

<p>Burr cell</p>
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Teardrop cell / Dacrocyte

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Aplastic anemia

Hypocellular marrow

No major abnormal cells/blasts

pancytopenia

Retics ↓

Usually normocytic/normochromic

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Acute leukemia

Maybe pancytopenia

Retics can be ↓

Blasts in peripheral blood/BM

BM is packed with abnormal cells

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Iron deficiency anemia

RBC ↓

Microcytic

Hypochromic

Retics ↓

WBC/platelets usually aren't all decreased

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B12/folate deficiency

Anemia

Macrocytic

Hypersegmented neutrophils

Retics ↓

Can cause pancytopenia

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Fanconi anemia

inherited aplastic

physical abnormalities

breakage with DNA crosslinking agents (mitomycin C)

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hereditary elliptocytosis

defective spectrin

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sideroblastic anemia

increased iron

decreased ferritin

normal TIBC

ring sideroblasts

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Metamyelocyte

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Promyelocyte

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Myeloblast

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Segmented neutrophil

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Prorubricyte

first recognizable erythroid precursor

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Mixing test correcting means?

Factor deficiency

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Mixing test not correcting means?

inhibitor

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Which test for extrinsic/common pathways?

PT

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Which test for intrinsic pathway?

aPTT

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P. malariae

Infects older RBCs

40–72 hr fever cycle, band forms

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P. vivax

Young RBCs (reticulocytes)

Enlarged RBCs, Schüffner dots

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P. ovale

Young RBCs (reticulocytes)

Enlarged, oval/fimbriated RBCs

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P. falciparum

RBCs of all ages

Most severe; multiple rings/RBC, banana-shaped gametocytes

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warfarin affects what factors

II, VII, IX, X

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Factor V Leiden

Factor V resistance to activated protein C

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Mature neutrophil

segmented nucleus

<p><span>segmented nucleus</span></p>
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INR equation

(Patient PT/Control PT)^ISI

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Enterocyte

iron absorption from small intestine

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rubriblast

Earliest recognizable erythroid precursor in bone marrow

starts RBC production

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Sideroblast

Immature RBC precursor that incorporates iron → heme

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Hepatocyte

Stores iron as ferritin/hemosiderin

produces hepcidin

Controls iron availability

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GPIb

binds vWF

Platelet adhesion

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GPIIb/IIIa

Fibrinogen

Platelet aggregation

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87
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Purple tube

CBC

EDTA

binds calcium strongly

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Blue tube

coagulation

sodium citrate

binds calcium reversibly

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Green tube

chemistry

heparin inhibits thrombin no clots

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Gray tube

glucose (glycolysis inhibitor)

fluoride