Cardiovascular system, Lecture notes of Physiology

Anderson cardiovascular system for nclex

Typology: Lecture notes

2025/2026

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Integrated Basic Science
Review
Cardiovascular System-C
Dr. Paul S. Anderson
Copyright Medical Board Review Services
WHITE CELL DYSCRASIAS
Multiple Myeloma:
Lytic lesions / Bone pain
Plasma cells overproduce Ig’s
Monoclonal overproduction
Hypercalcemia
Bence-Jones proteins in urine
Hairy Cell Leukemia:
B cells with hair-like projections
virus related, pancytopenia
Middle aged men most common
Most survive > 10 yrs
WHITE CELL DYSCRASIAS
Acute Lymphoblastic Leukemia: “ALL”
Most common Leukemia & Cancer in children, peak age 4 yrs,
(assoc. with virus, Down’s, radiation exposure)
Remission or cure with tx. Fever / Bone pain,
Hepatosplenomegaly.
Acute Myeloblastic Leukemia: (AKA: Acute Nonlymphocytic
Leukemia/8 types)
Most common leukemia in adults 15-39,
poorly differentiated, live 1 yr with chemotherapy, cure 10 15%.
Auer Rods.
Chronic Myelogenous Leukemia:
well-differentiated granulocytic, Philadelphia chromosome,
25-60, slow for 3 yrs, then blast crisis when 85% die (accelerated
phase).
May include any cell line. Hepatosplenomegaly, Generalized LA.
Chronic Lymphocytic Leukemia:
Most common overall Leukemia, and most common after 60.
well-differ entiat ed B-Cell lymphocytic.
More males / Never Asian. Few sx., survive 4-6 yrs.
Acute state RARE unlike CML.
CLOTTING PATHWAYS
Measured by:
PTT
Drugs: Heparin
Measured by
PT/INR
Drugs: Warfarin, ASA,
Vitamin-E, EFA’s
Factors
2-7-9-10
PROTHROMBIN ACTIVATOR
made up of V&X: Started by X alone and V
becomes active with + feedback
Extrinsic Pathway:
Damage outside of
blood vessels.
Intrinsic Pathway:
Blood trauma (turbulence and viscosity) or
collagen and blood contact.
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Integrated Basic Science

Review

Cardiovascular System-C

Dr. Paul S. Anderson

Copyright – Medical Board Review Services

WHITE CELL DYSCRASIAS

  • Multiple Myeloma:
    • Lytic lesions / Bone pain
    • Plasma cells overproduce Ig’s
      • Monoclonal overproduction
    • Hypercalcemia
    • Bence-Jones proteins in urine
  • Hairy Cell Leukemia:
    • B cells with hair-like projections
    • virus related, pancytopenia
    • Middle aged men most common
    • Most survive > 10 yrs

WHITE CELL DYSCRASIAS

  • Acute Lymphoblastic Leukemia: “ALL”
    • Most common Leukemia & Cancer in children, peak age 4 yrs,
    • (assoc. with virus, Down’s, radiation exposure)
    • Remission or cure with tx. Fever / Bone pain, Hepatosplenomegaly.
  • Acute Myeloblastic Leukemia: (AKA: Acute Nonlymphocytic Leukemia/8 types) - Most common leukemia in adults 15- 39 , - poorly differentiated, live 1 yr with chemotherapy, cure 10 – 15%. - Auer Rods.
  • Chronic Myelogenous Leukemia:
    • well-differentiated granulocytic, Philadelphia chromosome ,
    • 25 - 60, slow for 3 yrs, then blast crisis when 85% die (accelerated phase).
    • May include any cell line. Hepatosplenomegaly, Generalized LA.
  • Chronic Lymphocytic Leukemia:
    • Most common overall Leukemia, and most common after 60.
    • well-differentiated B-Cell lymphocytic.
    • More males / Never Asian. Few sx., survive 4-6 yrs.
    • Acute state RARE unlike CML.

CLOTTING PATHWAYS

Measured by: PTT Drugs: Heparin Measured by PT/INR Drugs: Warfarin, ASA, Vitamin-E, EFA’s Factors 2 - 7 - 9 - 10 PROTHROMBIN ACTIVATOR made up of V&X: Started by X alone and V becomes active with + feedback Extrinsic Pathway: Damage outside of blood vessels. Intrinsic Pathway: Blood trauma (turbulence and viscosity) or collagen and blood contact.

Poiseuille’s Equation

  • About resistance in the blood vessels
  • The thicker the blood the greater the

resistance

CLOTTING DISORDERS

  • Hemophilia A: factor VIII def., sex-linked recessive, males (female carrier), spontaneous bleeding into joints
  • Hemophilia B/Christmas Dz: factor IX def., Male only (female carrier)
  • Von Willebrand’s: autosomal dominant, VWF needed for platelet clumping, needed for factor VIII activity, spontaneous bleeding from mucus membranes, prolonged bleeding time, prolonged PTT, normal platelet numbers
  • Vit K def: needed for factors II, VII, IX, X & protein C, def= hypoprothrombinemia & bleeding
  • Thrombocytopenia : aka. Too few platelets. Typically significant below 70,000 (normal 150,000 to 400,000). - Increased destruction: Immunologic destruction - Decreased production: Congenital or Acquired (ie. drug) - Increased consumption: - Disseminated Intravascular Coagulation (DIC)

HEMORRHAGE – SYSTEMIC RESPONSE

HYDROSTATIC

HEMODYNAMICS

  • Hemorrhage:
    • Etiology: rupture of a blood vessel due to

some form of injury (e.g. trauma,

atherosclerosis; inflammation causing erosion

of vessel wall; neoplasm causing erosion)

  • Clinical Significance:
  • Depends on volume, rate & site of blood loss.

If greater than 20% of blood volume is lost can

produce hemorrhagic (hypovolemic) shock.

LYMPH NODE DISORDERS

  • Burkitt’s Lymphoma:
    • B lymphocyte tumor,
    • maxilla or mandible,
    • EBV / Malaria, Africa
  • Hodgkin’s Lymphoma:
    • Young adults - OR - 60 yo ages,
    • curable, familial, prognosis depends on stage,
    • intermittent spiking fever. Single / asymptomatic node, then spreads.
    • Reed-Sternberg cell
  • Non-Hodgkin’s Lymphoma:
    • Most common Lymphoma.
    • More deadly (prognosis based on grade),
    • Assoc. with Burkitt’s and Immunoblastic Lymphomas.

CARDIAC CYCLE

FRANK-STARLING

  • Intrinsic ability of the Heart to adapt to

changing blood flow volumes.

  • Basic idea: The greater the Heart is filled

during diastole (PRELOAD) the greater

the volume of blood that will be pumped

into the Aorta.

  • Within normal limits, changes in arterial

pressure (after load) have little effect on

the rate of pumping by the heart.

CARDIAC OUTPUT

• Cardiac output = Heart Rate X Stroke

Volume

• OR: CO = HR X SV

• STROKE-WORK: Principle that as

ventricular pressure increases the

stroke work output increases (up to

physiologic limits).

CHF

• Right-Side CHF:

– emphysema, mitral stenosis, left

ventricular failure,

– left to right shunt; jugular venous

distension,

– enlarged spleen & liver, dependent

edema,

– pleural effusion, ascites

CHF

• Left CHF:

– ischemic heart dz, systemic

hypertension,

– aortic or mitral valve dz; exertional

dyspnea,

– PND, tachycardia, cardiac asthma,

– crackles, cough, cyanosis