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GY59 Gynaecology Toronto Notes 2023

References

Agency lor Healthcare Research and Quality.Clinical Guidelines andRecommendations [Internet].Rockville (MD): U.S.Department olHealth and HumanServices:2020Sep [updated 2018 Jut:cited 2020 Jun 22].

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FIBRISTAL (ulipristalacetate tablets.5 mg|

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GY60 Gynaecology TorontoNotes 2023

Reid R.SOGC ClinicalPractice Guidelines:Oral contraceptives and the risk of venous thromboembolism:An update.JObstet Gynaecol Can 2010:32:1192-1197.

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Hematology

Reid Gallant, Syed Shahan Haider, and Nathan Kuehnc, chapter editors

Karolina Gaebe and Alyssa Li, associate editors

Wei Hang Dai and Camilla Giovino, EB\1 editors

Dr. Matthew Cheung, Dr. Lisa Chodirker, Dr. Helena Dhamko, Dr. Zachary Liedcrman, Dr. Michael

Scott, and Dr. Martina Trinkaus, staff editors

Hematology

Acronyms

Basics of Hematology.

CompleteBlood Count

Blood Film Interpretation

Bone Marrow Aspiration and Biopsy

Common Presenting Problems

Anemia

Erythrocytosis

Thrombocytopenia

Thrombocytosis

Pancytopenia

Neutrophilia

Neutropenia

Lymphocytosis

Lymphopenia

Eosinophilia

Agranulocytosis

Leukemoid Reaction

Approach to Lymphadenopathy.

Approach to Splenomegaly

Microcytic Anemia

Iron Metabolism

Iron Deficiency Anemia

Anemia of Chronic Disease

Sideroblastic Anemia

Lead Poisoning

Normocytic Anemia

Aplastic Anemia

Hemolytic Anemia

Thalassemia

p-Thalassemia Minor (Thalassemia Trait)

P-Thalassemia Major

P-Thalassemia Intermedia

a-Thalassemia

Sickle Cell Disease

Autoimmune Hemolytic Anemia

Microangiopathic Hemolytic Anemia/Thrombotic

Microangiopathy

Hereditary Spherocytosis

Hereditary Elliptocytosis

Glucose-6-Phosphate Dehydrogenase Deficiency

Macrocytic Anemia

Vitamin B12 Deficiency

Folate Deficiency

Hemostasis.

Stages of Hemostasis

Disorders of Primary Hemostasis

Immune Thrombocytopenia

Thrombotic Thrombocytopenic Purpura and Hemolytic Uremic

Syndrome

von Willebrand Disease

Disorders of Secondary Hemostasis

Hemophilia A (Factor VIII Deficiency)

Hemophilia B (Factor IX Deficiency)

Factor XI Deficiency

Liver Disease

Vitamin K Deficiency

Disseminated Intravascular Coagulation

HI Hypercoagulable Disorders

Venous Thromboembolism

Approach to Treatment of Venous Thromboembolism

Hematologic Malignancies and Related Disorders.

Myeloid Malignancies

Acute Myeloid Leukemia

Myelodysplastic Syndromes

Myeloproliferative Neoplasms

Chronic Myeloid Leukemia

Polycythemia Vera

Idiopathic Myelofibrosis

Essential Thrombocythemia

Lymphoid Malignancies

Acute Lymphoblastic Leukemia

Lymphomas

Hodgkin Lymphoma

Non-Hodgkin Lymphoma

Malignant Clonal Proliferations of Mature B-Cells.

Chronic Lymphocytic Leukemia

Multiple Myeloma

Monoclonal Gammopathyof Unknown Significance

Lymphoplasmacytic Lymphoma

Complications of Hematologic Malignancies

Hyperviscosity Syndrome

Tumour Lysis Syndrome

Blood Products and Transfusions

Blood Products

Red Blood Cells

Platelets

Coagulation Factors

Acute Blood Transfusion Reactions

Delayed Blood Transfusion Reactions

Common Medications

Antiplatelet Therapy

Anticoagulant Therapy

Chemotherapeutic and Biologic Agents Used in Oncology

Landmark Hematology Trials

References

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H2 ,H36

H2

,H39

,H39

H6

H42

H46

H47

H50 H12

H13

H14

H53

H54

H17

H18

H58

H61

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H28

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HI Hematology Toronto Notes 2023

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H2 Hematology Toronto Notes 2023

Acronyms

antibody

atrial fibrillation

DVT deep vein thrombosis

Epstcin- Barr virus

ethylenediamlnetetraacetic add IIP

erythropoietin

erythropoiesis-stimulating agent

erythrocyte sedimentation rate

essential thrombocythemia

fibrin degradation products

fine needle aspiration

frozen plasma

granulocyte-colony stimulating

factor

reduced glutathione

genitourinary

graft versus host disease

hemolytic anemia

hemoglobin

hepatitis B virus

hematocrit

hepatitis C virus

hemolysis,elevated liver enzymes, OCP

and low platelet count

heparin- induced thrombocytopenia PE

Hodgkin lymphoma

high molecular weight kininogen Ph

hemolytic uremic syndrome

inflammatory bowel disease

idiopathic myelofibrosis

immunomodulatory drugs

internationalnormalized ratio

intermittent pneumatic compression Pf

IPSS international prognostic scoring

system

immune thrombocytopenia

Janus kinase 2

PIT partial thromboplastin time

PUD peptic ulcer disease

PV polycythemia vera

RCMD refractory cytopenia with

multilineage dysplasia

RCMD RS refractory cytopenia with

multilineage dysplasia and ringed

Ab

AFrb EBV

AFLP acute fatty liver of pregnancy

atypical hemolytic uremic syndrome EPO

autoimmune hemolytic anemia ESA

acute lymphoblastic leukemia ESR

acute myeloid leukemia

absolute neutrophil count

activated protein C

acute promyelocytic leukemia FP

antiphospholipid antibodies

antiphospholipid antibody

EDTA

aHUS JAK:

LAD lymphadenopathy

LMWH low molecular weight heparin

MAHA/ microangiopathic hemolytic

TMA anemia/thrombotic microangiopathy sideroblasts

MCH mean corpuscular Hb

MCHC mean corpuscular Hb concentration SCD

MCV mean cotpuscularvolume

MDS myelodysplastic syndromes

myelofibrosis

MGUS monoclonal gammopathy of

unknown significance

multiple myeloma

MPN myeloproliferative neoplasm

MPV mean platelet volume

MUGA multi-gated acquisition

non-Hodgkin lymphoma

oral contraceptive pill

PCC prothrombin complex concentrates TIP

pulmonary embolism

progression-free survival

Philadelphia chromosome

proteasome inhibitors

prekalliktein

PMN polymorphonuclear neutrophil

paroxysmal nocturnal

AIHA

All

AML El

ANC FDP

APC FNA lit

'

,', RBC distribution width

sickle celldisease

stem cell transplantation

serum protein electrophoresis

soluble transferrin receptor

T-cell lymphoma

total iron binding capacity

tyrosine kinase inhibitor

T -cell large granular lymphocyte

tumour lysis syndrome

tissue plasminogen activator

thrombopoietin

thrombin time

thrombotic thrombocytopenic

API

APIA G-CSF SCT

APS SPEP

syndrome GSH MF sTfR

aPTT activated partial thromboplastin GU TCI

time GVHD TIBC

ARDS acute respiratory distress syndrome HA

ATIII antithrombin III

ATRA all-trans retinoic acid

bone marrow

CALR calreticulin

chimeric antigen receptor

Cll chronic lymphocytic leukemia

CMl chronic myeloid leukemia

CMV cytomegalovirus

CRP C-reactive protein

DAT direct antiglobulin test

ODAVP - desmopressin

DIC disseminated intravascular

coagulation

DLBCl diffuse large 8-cell lymphoma

DOAC direct oral anticoagulant

MV TKI

Hb T-lGl

HBV as

BM Hct tPA

HCV NHL TPO

CAR HELLP TT

HIT purpura

HL UFH unfractionated heparin

urine protein electrophoresis

venous thromboembolism

von Willebrand disease

von Willebrand factor

World Health Organization

radiation therapy

HMWK UPEP

HUS PI VIE

IBD PK VWD

IMF VWF

IMID PNH WHO

INR hemoglobinuria XRT

IPC prothrombin lime

Basics of Hematology

Hematopoietic Stem Cell

Erythrocyte:carries oxygen from lungs

to peripheral tissues

Reticulocyte:immature erythrocyte

Hb: protein contained in erythrocytes

which binds oxygen

Neutrophil: granulocyte integral in

innate immunity;main cell in acute

inflammation

Eosinophil:granulocyte involved

in response to parasites (especially

helminths) and allergic response

Basophil:granulocyte mainly involved in

allergy and parasitic infection

Lymphocyte:integral cell in adaptive

Immunity

Monocyte:involved in innate immunity:

can differentiate into macrophage or

dendritic cell

Platelet:mediator of primary hemostasis

Plasma:acellular,fluid component of

blood containing water and proteins

(including coagulation factors and

Immunoglobulins)

Serum:equivalent to plasma minus

coagulation factors

Myeloid piecursor Lymphoid precursor

Megakaryocyte/erythrocyte precursor

I I

Myeloblast Lymphoblast

Megakaryoblast Proerythroblast Monoblast

: Progranulocyte

Megakaryocyte Polychromatic

erythroblast

Monocyte

2

1

S

Basophil Eosinophil Neutrophil :

I

Erythrocyte Macrophage .1CJl

Platelets

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S

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Granulocytes 0 r t

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Figure 1. Hematopoiesis

• over 101

'

blood cells arc produced daily

• sites ofhematopoiesis in adults: pelvis,sternum, vertebral bodies, and cranium

• lifespan of mature cells in blood

erythrocytes (90-120 d), neutrophils (~1 d), platelets (7-10 d),lymphocytes (varies- memory cells

pe rsist for years)

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H3 Hematology Toronto Notes 2023

• role of lymphoid organs

spleen: part of reticuloendothelial system, sequesters aged RBCs, removes opsonized cells, and

site of Ab production

thymus:site of T-cell maturation and involutes with age

• lymph nodes: sites of B- and T-cell activation (adaptive immune response)

Complete Blood Count

Table 1. Common Terms Found in the CBC

Test Definition Normal Values'

RBCCount Number of RBCs per volume of blood 3.5-5.0 x10l7L (female)

4.0-5.5 x 10RI (male)

115-155 9/1 (female)

125-170 g/L (male)

37-46% (female)

38-50% (male)

80100 ft

27-34 pg

315-355g/L

11.5-15.5%

23-90 x 1CP /L (0.5-1.5%)

<20 mm/h (female)

<10 mm/h (male)

3.5-10.5 X 103A

2 71 lOv.'

l

<0.7 x 1011

<0.10 *

1CP /L

<0.5x 109/1

1.0-4.0 x 101/1

0.1-1.0*

109 /1

130 380 x 109 /1

9.0-14.0 fl

Hb Amount olHbm the blood

Percentage of a given volume of whole blood occupied by packed

RBCs

Average RBC site

Average amount of Hb per RBCs

Average concentration of Hb inside RBCs

Percentage of variance in RBC size

Humber of reticulocytes per volume of blood

Rate at which RBCsseparate from the serum, becoming sediment in

the bottom of the test tube

Humber of WBCs per volume of blood

Segmented neutrophils

Band neutrophils

Basophils

Eosinophils

Lymphocytes

Monocytes

Humber of platelets pet volume of blood

Mean Platelet Volume (MPV ) Measurement ol plateletsize

Hct

MCV

MCH

MCHC

ROW

Reticulocyte Count

ESR

WBC Count

WBC Differential

Platelet Count

“All values apply to adults. Reference standards do not apply to all ethnic groups.

Approach to Interpreting a CBC

1 . consider values in the context of an individual'

s baseline:

up to 5% of population without disease may have values outside “normal" range

• an individual may display a clinically significant change from their baseline without violating

“normal"

reference range

2. is one cell line affected or are several?

• if all lines are low: pancytopenia (see Pancytopenia, HS )

if RBCs and platelets are low: consider a MAHA/TMA (see Microangiopathic Hemolytic Anemia/

thrombotic Microangiopathy, H23 ) or an autoimmune process (Evan’

s Syndrome)

• if single cell line affected: see Common Presenting Problems, H6

To estimate Hb based on the Hct,

multiply by 3

Clinical UseofRDW

. To distinguish the etiologies of

microcytosis:

• Iron deficiency:increased RDW

(anisocytosis) as cells are of varying

sizes in iron deficiency

• 3-thalassemia minor:normal RDV7

(also expect a high RBC count) as

cells are of similarsize because

the red cell abnormality is not

progressive

Blood Film Interpretation

RED BLOOD CELLS

Size

• microcytic (MCV <80 fL), normocvtic (MCV = 80-100 fL), macrocytic (MCV >100 fL)

• anisocytosis: RBCs with increased variability in size (increased RDW )

• iron deficiency anemia, HAs, Ml'

, blood transfusion, and MDS

Colour

• hypochromic: increase in size of central pallor (normal = less than 1/3 of RBC diameter)

iron deficiency anemia, anemia of chronic disease, and sideroblastic anemia

• polychromasia: suggests increased reticulocytes (pinkish-blue cells)

• increased RBC production by BM

Shape

• poikilocytosis: increased proportion of RBCs of abnormal shape

• iron deficiency anemia, hemoglobinopathies, ME, severe Bi:deficiency, MDS, and burns

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