The document discusses hematology and provides information on blood components, blood disorders, and their management in the prehospital setting. It covers red blood cell disorders like anemia and sickle cell disease. White blood cell and platelet disorders are also reviewed. Physical exam findings and treatment focus on maintaining ABCs, oxygenation, volume replacement, and transporting appropriately.
3. Hematology
The Study of Blood and Blood-Forming Organs
Includes study of blood disorders.
Red blood cell disorders
White blood cell disorders
Platelet disorders
Coagulation problems
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8. Components of Blood
Red Blood Cells
Hemoglobin
Oxygen transport
Bohr effect
2,3 DPG
Oxygen–hemoglobin
dissociation curve
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9. Red Blood Cells
Average life-span of Red Blood Cells ~120 days
Due to wear and tear on plasma membranes as they squeeze
through capillaries.
A healthy male has about 5.4 million RBC’s/mm3
A healthy female has about 4.8 million/mm3.
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10. Red Blood Cells
Red blood cell production
Erythropoiesis
Hemolysis
Sequestration
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16. White Blood Cells
Immunity
Subpopulation of lymphocytes known as T cells and
B cells
T cells develop cellular immunity.
B cells produce humoral immunity.
Autoimmune disease
Alterations in the immune process
Inflammatory process
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23. Blood Products and
Blood Typing
Blood Types
Antigens
A, B, AB, O
Universal donors
Rh factor
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24. Transfusion Reactions
Donor’s RBC and Recipient’s Plasma
Recipient
Type A
Donor - RBC A antigens
B antibodies
Type B
B antigens
A antibodies
Type A
A antigens
B antibodies
Type B
B antigens
A antibodies
Type AB
A+B antigens
O antibodies
Type O
O antigens
A+B
antibodies
No reaction
Major
reaction
Major
reaction
No reaction
Minor
reaction
Major
reaction
Major
reaction
Major
reaction
No reaction
Major
reaction
Minor
reaction
Minor
reaction
Minor
reaction
No reaction
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Type AB
Type O
A+B antigens O antigens
O antibodies A+B
antibodies
Minor
Major
reaction
reaction
26. Transfusion Reactions
Hemolytic Reactions
Signs & Symptoms
Facial flushing, hyperventilation, tachycardia, hives,
chest pain, wheezing, fever, chills, and cyanosis
Treatment
Stop transfusion, change all IV tubing, and initiate IV
therapy with normal saline or lactated Ringer’s.
Consider furosemide, dopamine, and diphenhydramine.
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27. Transfusion Reactions
Febrile Nonhemolytic Reactions
Signs & Symptoms
Headache, fever, and chills
Treatment
Stop transfusion, change all IV tubing, and initiate IV
therapy with normal saline or lactated Ringer’s.
Consider diphenhydramine and an antipyretic.
Observe closely to ensure reaction is nonhemolytic.
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28. General Assessment
and Management
Scene Size-up
Initial Assessment
Focused History and Physical Exam
SAMPLE history
Hematological disorders are rarely the chief
complaint.
Physical exam
Evaluate nervous system function.
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34. Managing Specific
Patient Problems
Diseases of the Red Blood Cells
Diseases of the White Blood Cells
Diseases of the Platelets/Blood Clotting
Abnormalities
Other Hematopoietic Disorders
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36. Anemias
Pathophysiology
Morbidity/ mortality
Can be self-limiting disease
Must be confirmed by laboratory diagnosis
Precipitating causes
Blood loss (acute or chronic)
Decreased production of erythrocytes
Increased destruction of erythrocytes
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37. Anemias
Pathophysiology cont.
Hemolytic
Hereditary
Sickle cell
Thalassemia
Glucose-6-phosphate dehydrogenase deficiency
Acquired
Immune
Drug
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38. Anemias
Signs and symptoms may not be present until
the body is stressed.
Treat signs and symptoms.
Maximize oxygenation and limit blood loss.
Establish IV therapy if indicated.
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39. Anemias
Initial assessment findings
Airway/ breathing
Labored breathing may or may not be present
Circulation
Peripheral pulses
Quality
Rhythm
Changes in skin
Color
Temperature
Moisture
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41. Anemias
Focused History Complaints
Complaints secondary to leukopenia
Infections
Fevers
Complaints secondary to thrombocytopenia
Cutaneous bleeding
Bleeding from mucous membranes
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42. Anemias
Management
Airway and ventilation
Circulatory support
Pharmacological
Analgesics
Fluid volume replacement
Control of bleeding
Non-pharmacological
Position of comfort
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43. Anemias
Transport considerations
Appropriate mode
Indications for rapid transport
Significant changes in LOC
Hypotension/ hypoperfusion
Appropriate facility
Support and communication strategies
Explanation for patient, family, significant others
Communications and transfer of data to the physician
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46. Sickle Cell Disease
Epidemiology
Highest incidence in blacks, Puerto Ricans and
persons of Spanish, French, Italian, Greek and
Turkish origin
Pathophysiology
A congenital hemolytic anemia
A chemical defect within the hemoglobin of red
blood cells
Morbidity/ mortality
Sepsis
Shock
Death
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47. Sickle Cell Disease
Initial assessment findings
Levels of consciousness
Airway/ breathing
Circulation
Peripheral pulses
Changes in skin
Pallor, Cool, Clammy
Hypotension/ hypoperfusion
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48. Sickle Cell Disease
Focused history
Chief complaint
Sudden onset develops into a condition called
“crisis”
Thrombotic crisis (painful)
Aplastic
Hemolytic
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49. Sickle Cell Disease
Detailed physical exam
Airway / Breath sounds
Circulation
Skin
As above
Temperature may vary
ECG findings
Tachycardia
Ectopy
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50. Sickle Cell Disease
Detailed physical exam continued
Increased weakness
Aching
Chest pain
Sudden, severe abdominal pain
Bony deformities
Icteric sclera
Abdominal pain
Fever
Arthralgia
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51. Sickle Cell Disease
Management
Position of comfort
Pharmacological
Analgesia
Fluid volume replacement
Transport for reperfusion
Indications for no transport
Refusal
Support and communication strategies
Explanation for patient, family, significant others
Communications and transfer of data to the physician
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52. Polycythemia
Epidemiology
Overabundant production of red blood cells, white
blood cells and platelets
Rare disorder seen in persons over 50 years of age
Pathophysiology
Thrombosis
Death from thrombosis
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53. Polycythemia
Initial assessment findings
Levels of consciousness
Airway/ breathing
Labored breathing is common
Circulation
Peripheral pulses
Quality
Tachycardia
Changes in skin
Color - red-purple complexion
Red hands and feet
Pruritic
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54. Polycythemia
Focused history
Dyspnea
Generalized pruritus
Detailed physical exam
Airway / Breath sounds
Circulation
Skin
As above
Temperature may vary
ECG findings
Tachycardia
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56. Polycythemia
Transport
Indications for no transport
Refusal
Referral
Support and communication strategies
Explanation for patient, family, significant others
Communications and transfer of data to the
physician
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57. Diseases of the White
Blood Cells
Leukopenia/Neutropenia
Too few white blood cells or neutrophils.
Follow general treatment guidelines and provide
supportive care.
Leukocytosis
An increase in the number of circulating white
blood cells, often due to infection.
Leukemoid reaction
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59. Leukemia
Initial assessment findings
Levels of consciousness
Airway/ breathing
Labored breathing may or may not be present
Circulation
Peripheral pulses
Quality
Tachycardia
Changes in skin
Color
Temperature
Moisture
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60. Leukemia
Focused history
Complaints
Fatigue, bone pain, diaphoresis
Elevated body temperature
Sternal tenderness
Heat intolerance
Abdominal fullness
Bleeding
Contributing history
Recurrent bleeding
Increasing frequency and/ or duration
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62. Leukemia
Management
Position of comfort
Pharmacological
Analgesia
Increase or decrease heart rate
Fluid volume replacement
Electrical
Constant ECG monitoring
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63. Leukemia
Transport
Criteria for rapid transport
No relief with medications
Hypotension/ hypoperfusion
Significant changes in ECG
Indications for no transport
Refusal
Referral
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64. Lymphomas
Epidemiology
Hyperplasia of the lymphoreticular system
Pathophysiology
Morbidity/ mortality
Blood loss
Pain
Death
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65. Lymphomas
Initial assessment findings
Levels of consciousness
Airway/ Breathing
Circulation
Focused history
Complaints
Fever
Night sweats
Generalized pruritus
Anorexia
Weight loss
Fatigue, bone pain, diaphoresis
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66. Lymphomas
Detailed physical exam
Airway / Breath sounds
May be clear to auscultation
Congestion in bases may be present
Circulation
Skin
Pallor during the episode
Temperature may vary
Diaphoresis is usually present
Blood pressure may low
ECG findings
Tachycardia
Ectopy
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67. Lymphomas
Management
Position of comfort
Pharmacological
Analgesia
Increase or decrease heart rate
Fluid volume replacement
Electrical
Constant ECG monitoring
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68. Lymphomas
Transport
Criteria for rapid transport
No relief with medications
Hypotension/ hypoperfusion
Significant changes in ECG
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69. Diseases of the Platelets
Thrombocytosis and Thrombocytopenia
Thrombocytosis
Thrombocytopenia
An abnormal increase in the number of platelets
An abnormal decrease in the number of platelets
Management
Provide supportive care and follow general treatment
guidelines.
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70. Hemophilia
Epidemiology
A hereditary disorder transmitted by the female to
the male
In true hemophilia A factor VIII is nearly absent
In hemophilia B there is a deficiency in factor IX
The ability to produce thrombin is severely impaired
by deficiency or absence of these factors
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72. Hemophilia
Initial assessment findings
Levels of consciousness
Airway/ breathing
Labored breathing is common
Circulation
Peripheral pulses
Weak and thready
Tachycardia
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73. Hemophilia
Changes in skin
Pallor, Cool, clammy
Bleeding
From body orifices
Knees, Wrists, Elbows
Hematuria
Epistaxis
Hemoptysis
Hematemesis
Melena
Hypotension/ hypoperfusion
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74. Hemophilia
Focused history
Dyspnea
Bleeding
Detailed physical exam
Airway / Breath sounds
May be clear to auscultation
Congestion in bases may be present
Circulation
ECG findings
Tachycardia
Ectopy
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75. Hemophilia
Management
Position of comfort
Pharmacological
Analgesia
Fluid volume replacement
Transport for reperfusion
Indications for no transport
Refusal
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76. Blood Clotting Abnormalities
Von Willebrand’s Disease
Deficient component of factor VIII
Generally results in excessive bleeding.
Generally is not serious; provide supportive care.
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78. Disseminated Intravascular
Coagulopathy
Epidemiology
A complication of severe injury, trauma or disease;
acute bleeding disorder resulting from defibrination
First phase characterized by free thrombin in the
blood, fibrin deposits and aggregation of platelets
Phase two is hemorrhage caused by depletion of
clotting factors
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82. Disseminated Intravascular
Coagulopathy
Detailed physical exam
Airway / Breath sounds
May be clear to auscultation
Congestion in bases may be present
Circulation
Skin
As above
Temperature may vary
ECG findings
Tachycardia
Ectopy
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83. Disseminated Intravascular
Coagulopathy
Management
Position of comfort
Pharmacological
Analgesia
Increase or decrease heart rate
Fluid volume replacement
Support and communication strategies
Explanation for patient, family, significant others
Communications and transfer of data to the physician
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84. Multiple Myeloma
Epidemiology
A plasma cell dyscrasia characterized by neoplastic
cells that infiltrate bone marrow
Eventually plasma cells become malignant leading to
tumor formation within the bone
Pathophysiology
Morbidity/ mortality
Fractures
Bleeding
Shock
Death
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85. Multiple Myeloma
Initial assessment findings
Levels of consciousness
Airway/ breathing
Labored breathing is common
Circulation
Peripheral pulses
Weak and thready
Tachycardia
Changes in skin
Pallor, Cool, clammy
Bleeding
Hypotension/ hypoperfusion
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88. Multiple Myeloma
Management
Position of comfort
Pharmacological
Analgesia
Fluid volume replacement
Transport for reperfusion
Indications for no transport
Refusal
Support and communication strategies
Explanation for patient, family, significant others
Communications and transfer of data to the physician
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