Unit 2 - Hematology Part I Flashcards

1
Q

blood pressure

A

change in pressure = P1-P2

change in P = flow (Q) x vessel resistance (R)

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2
Q

circulatory shock (5 types)

A
  • septic
  • neurogenic
  • obstructive
  • cardiogenic
  • hypovolemic
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3
Q

edema

A

accumulation of excessive fluid with the interstitial tissues or within body cavities

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4
Q

congestion

A

implies accumulation of excessive blood within the vessels of an organ or tissue

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5
Q

thrombus and embolus

A

thrombus: blood clot that has formed either in a blood vessel or in the heart that has remained stationary
embolus: blood clot that has been broken off from its original location and has moved through a vessel to lodge at a distant site

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6
Q

infarction

A

cell death and tissue necrosis that is caused by a disruption in the blood supply

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7
Q

lymphedema

A

chronic swelling of an area due to accumulation of interstitial fluid secondary to obstruction of lymphatic vessels/nodes

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8
Q

shock

A

BP falls so low that perfusion of the organs cannot occur

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9
Q

anemia

A

RBC count falls significantly, thus resulting in reduction in hemoglobin and the ability of the blood to carry o2 to the organs and the tissues

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10
Q

polycythemia

A

too many RBCs cause viscosity increase of the blood and congestion

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11
Q

leukocytopenia

A

significant reduction in the total WBC count

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12
Q

leukocytosis

A

blood disorder in which immature WBCs accumulate

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13
Q

aging and the hematopoietic system: decrease in… (3 things)

A
  • intestinal absorption of iron
  • iron-binding capacity
  • iron storage capacity
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14
Q

destination

A

bone marrow

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15
Q

decreases result in…

A
  • decreased RBC’s (iron deficiency anemia)

- increased RBC fragility

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16
Q

decreased vitamin B12 GI absorption results in

A

decrease in red bone marrow production of RBCs

disease outcome - pernicious anemia

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17
Q

decreased number/size of lymph nodes and cellular immunity/t-cell function outcome

A

reduced immunity

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18
Q

blood composition - plasma

A

55% of blood volume
Water-90+%
Solids-<10% (electrolytes, proteins)

19
Q

blood composition - cells

A

45% of blood volume
Red blood cells (Erythrocytes)
White blood cells (Leukocytes)
Platelets (Thrombocytes)

20
Q

blood transfusions

A

Necessary following prolonged surgery or accident

Elective surgery-autologous transfusions

21
Q

blood transfusion complication

A
ABO Incompatibility (Type II Hyperimmune reaction)
Signs of complications
Chills and Fever
Rash
Jaundice
Blood stained urine
Adult Respiratory Distress                                                                      Syndrome
Hepatitis B or C infection
HIV infection
Air embolism
Circulatory overload
Delayed reaction
22
Q

erythroprotein

A

active form of renal erthyropoietic factor, which is produced by the kidneys

when activated, it stimulates bone marrow, thus promoting hematopoiesis

23
Q

Hemochromatosis

A

genetic disorder

  • too much iron absorbed from the GI tract
  • too much iron deposited in organs and various tissues
  • “rusty” colored skin
24
Q

Hemochromatosis etiology

A
Men: Women=8:1
Peak age: 50’s and 60’s
Autosomal Recessive 
Defect in the HFE Gene
(High Fe gene)
25
Hemochromatosis - iron accumulates causing
``` Iron induced Arthropathy Iron Induced Cirrhosis and Hepatocellular Cancer Iron induced Cardiomyopathy Fe induced Emphysema-Lungs Fe induced Diabetes Mellitus-pancreas Fe induced Sterility-Reproductive organs ```
26
Porphyria
Accumulation of porphyrins Porphyrins form “Heme” portion of Hemoglobin Accumulate in tissues and organs, i.e. CNS Seizures, cognitive changes, behavioral changes Polyneuropathy with Polyneuritis Spill over as “Port wine urine” Porphyrins are a purple pigment
27
cutaneous porphyria
photodermatitis
28
complete blood count
``` Total rbc count (4.2-6.1 million cells/mcL) Total wbc count (4.5-9.5 thousand cells/mcL) Total platelet count (150, 000-400,00 cells/mcL) Hemoglobin (grams/100 ml) Hematocrit (%) Leukocyte differential count: Granulocytes - 50-75% Neutrophils (PMN’s) - 1-2% Eosinophils - 0.5-1% Basophils Agranulocytes - 25-33% Lymphocytes - 6% Monocytes ``` ``` Reticulocyte count (1% immature RBC’s) RBC indices MCV (~87 cubic microns) MCHC (~30%) MCH (~30 picograms)* ```
29
everything included in a CBC
``` Red Blood Cell count + indices White Blood Cell count + differential Platelet Count Hemoglobin and Hematocrit Reticulocyte Count ```
30
Hemoglobinopathies-Sickle Cell Disease
Abnormal, “sickle cell” shaped erythrocyte in Sickle cell disease Autosomal recessive trait: sickle cell disease (HbSS) Heterozygote: sickle cell trait” (HbAS) Commonly in people from parts of tropical and sub-tropical areas where malaria is common, or their descendants .. .
31
sickle cell disease clinical issues
Poor Affinity for O2 Vascular Occlusive Crisis Hemolytic Crisis
32
Vascular Occlusive Crisis
``` Stroke Heart Attack Venous thrombus Thromboembolism Auto-splenectomy Acute chest syndrome ```
33
Hemolytic Crisis
``` Creates “sludge” and vascular occlusion Stroke Heart Attack Venous thrombus Thromboembolism Auto-splenectomy Acute chest syndrome ```
34
the anemias - CDC
“Hemoglobin < 14 gms/100 ml (males)” | “Hemoglobin < 12 gms/100 ml (females"
35
Anemia s/s
``` Pallor Resting Tachycardia Cardiac Murmurs >100 bpm Angina Dyspnea Anorexia Constipation/Diarrhea Headaches -Dizziness Syncope (fainting) Tinnitus Stomatitis Pica fatigue ```
36
causes of anemia
Excessive Blood Loss Increased Destruction of Erythrocytes Decreased Production of Erythrocytes
37
anemia caused by excessive blood loss
- most common - from cancer, long term use of aspirin/other drugs, menstruation - also known as Normocytic, normochromic - RBC Indices (MCV, MCHC, MCH) all normal
38
anemias caused by destruction of RBCs
- may be congenital or acquired - congenital: sickle cell - acquired: autoimmune, malaria
39
anemia caused by destruction of erythrocytes - type 1
macrocytic, normochronic: - RBCs are enlarged but hemoglobin concentration is normal - when DNA synthesis has been interfered with, b12 deficiency (pernicious anemia)
40
anemia caused by destruction of erythrocytes - type 2
microcytic, hypochromic: - RBCs are smaller than normal, and hemoglobin concentration per RBC is below normal - iron deficiency
41
aplastic anemia
life threatening illness bone marrow is suppressed, resulting in an insufficient number of production of all blood cells - congenital, idiopathic, or acquired - may survive long term on supportive therapy or death by internal bleeding
42
polycythemia
- myeloproliferative disorder (too many RBCs) | - increased blood volume and viscosity
43
primary polycythemia (vera)
- bone marrow overproduces blood cells - older men, progressive Rust colored skin Blood-shot eyes Headache, “fullness” in the head Dizziness Fatigue Pruritus (itchy”) deep venous thrombus - Budd Chiari syndrome
44
secondary polycythemia
- aquired 1) circulating volume of plasma decreases (dehydration) 2) RBCs increase from external causes - smoking high altitude