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  Thursday 16 October 2025 / 01:43 PM

 

HA Medicine I & Gynecology

Unit 2: Hematological & Cardiovascular Conditions

Second Year Health Science (PCL) | Syllabus-Based Notes

Introduction & Importance

Hematological and cardiovascular conditions form the cornerstone of clinical medicine, affecting millions globally. Understanding the pathophysiology, clinical features, and management of these disorders is crucial for any health science professional. This unit covers essential topics from anemia and coagulation disorders to heart failure and hypertension, integrating theoretical knowledge with clinical application.

Mastery of this unit enables accurate diagnosis, effective intervention, and improved patient outcomes in diverse healthcare settings.

2.1 Anemia

Definition: A condition characterized by a decrease in the number of red blood cells (RBCs) or hemoglobin concentration, leading to reduced oxygen-carrying capacity.

Coagulation Cascade & Hemostasis

Hemostasis is the process to prevent and stop bleeding, involving:

  1. Vascular spasm: Immediate vasoconstriction.
  2. Primary hemostasis: Platelet adhesion and formation of a temporary plug.
  3. Secondary hemostasis: Coagulation cascade (intrinsic/extrinsic pathways → common pathway → thrombin → fibrin).
  4. Clot retraction and repair.
  5. Fibrinolysis: Clot breakdown.

Key concept: Balance between procoagulant and anticoagulant factors.

Signs & Symptoms

  • Fatigue, weakness, pallor
  • Shortness of breath, palpitations
  • Headache, dizziness
  • Pica (craving for non-food items in iron deficiency)

Classification

Based on RBC Morphology Based on Etiology
Microcytic Hypochromic (e.g., Iron deficiency) Blood loss
Normocytic Normochromic (e.g., Aplastic) Decreased production
Macrocytic (e.g., Megaloblastic) Increased destruction (Hemolytic)

Clinical Features of Different Anemias

Type Key Features Cause
Iron Deficiency Koilonychia, glossitis, pica Chronic blood loss, poor intake
Megaloblastic Jaundice, neurological symptoms (B12 deficiency) B12/Folate deficiency
Aplastic Pancytopenia, infections, bleeding Bone marrow failure
Sickle Cell Pain crises, dactylitis, susceptibility to infections HbS mutation (autosomal recessive)
Hemophilia A/B Prolonged bleeding, hemarthrosis Factor VIII/IX deficiency (X-linked)

📌 Clinical Tip: Anemia Investigations

Basic workup includes: CBC, Peripheral smear, Reticulocyte count, Iron studies (ferritin, TIBC, serum iron), B12/Folate levels, LDH/Bilirubin (if hemolytic). Always consider the clinical context when interpreting results.

Management & Prevention

  • Iron deficiency: Oral/IV iron, treat underlying cause.
  • Megaloblastic: B12/Folate supplementation.
  • Prevention: Balanced diet, parasite control, genetic counseling for hereditary anemias.

2.2 Polycythemia & Leukocytosis | 2.3 Leukemia & Lymphoma

Polycythemia: Increased RBC mass; can be primary (Polycythemia Vera) or secondary (hypoxia).

Leukocytosis: Increased WBC count; often reactive (infection).

Leukemia: Definition & Classification

Definition: Malignant proliferation of hematopoietic cells in bone marrow.

  • Acute vs. Chronic (based on onset and cell maturity).
  • Lymphoid vs. Myeloid (based on cell line).

🧠 Memory Aid: Leukemia Types

“ALL is common in Children, AML in Adults, CLL in Elderly”
ALL: Acute Lymphoblastic Leukemia
AML: Acute Myeloid Leukemia
CLL: Chronic Lymphocytic Leukemia
CML: Chronic Myeloid Leukemia (Philadelphia chromosome t(9;22))

Clinical Features & Management

Features: Fatigue, recurrent infections, bleeding/bruising, bone pain, lymphadenopathy.

Management: Chemotherapy, targeted therapy (e.g., imatinib for CML), stem cell transplant, supportive care.

2.4 Hemostatic & Atherosclerotic Disorders

Common disorders: Deep Vein Thrombosis (DVT), Pulmonary Embolism (PE), Atherosclerosis (CAD, PVD, stroke).

Risk Factors (Atherosclerosis)

  • Non-modifiable: Age, male sex, family history
  • Modifiable: Hypertension, Diabetes, Smoking, Dyslipidemia, Obesity

Pathophysiology

Key steps: Endothelial injury → LDL accumulation → Foam cell formation → Plaque growth → Rupture → Thrombosis.

Management & Prevention

  • Lifestyle: Diet, exercise, smoking cessation.
  • Pharmacological: Statins, antiplatelets (aspirin), anticoagulants.
  • Surgical: Angioplasty, bypass grafting.

2.5 Cardiac Disorders

Angina: Chest pain due to myocardial ischemia.

MI: Necrosis due to prolonged ischemia.

Emergency management of MI: MONA + PCI.

MONA Mnemonic for MI:
Morphine, Oxygen, Nitrates, Aspirin.

2.6 Hypertension

Definition: BP ≥140/90 mmHg.

Classification: Primary (essential) 90-95%, Secondary (renal, endocrine).

Hypertensive Emergency: Severe BP with end-organ damage (requires IV meds in ICU).

Management: Lifestyle + Antihypertensives (ACEi, ARBs, CCB, Diuretics).

2.7 Congestive Cardiac Failure

Definition: Heart’s inability to pump sufficient blood.

Etiology: CAD, Hypertension, Cardiomyopathy.

Pathophysiology: Compensatory mechanisms (RAAS activation) → fluid overload.

Management: Diuretics, ACEi, Beta-blockers, Digoxin.

📊 Anemia Diagnostic Flowchart (Simplified)

Low Hb → Check MCV
Low MCV (Microcytic)
→ Check Ferritin
↓ Low: Iron Deficiency
↓ Normal/High: Thalassemia/ACD
High MCV (Macrocytic)
→ Check B12/Folate
↓ Low: Megaloblastic
↓ Normal: Liver/EtOH
Normal MCV (Normocytic)
→ Check Reticulocyte
↓ High: Hemolytic
↓ Low: Aplastic/ACD

🧪 Quick Self-Assessment

Question: A 30-year-old female presents with fatigue, pallor, and pica. CBC shows microcytic hypochromic anemia. What is the most likely cause?



📝 Summary & Key Points

  • Anemia is classified by morphology (MCV) and etiology; management is cause-specific.
  • Coagulation cascade involves intrinsic, extrinsic, and common pathways.
  • Leukemia is acute/chronic, lymphoid/myeloid; treatment includes chemo/targeted therapy.
  • Atherosclerosis underlies most cardiovascular diseases; manage risk factors.
  • Hypertension is a silent killer; treat to prevent complications.
  • Heart failure management focuses on reducing preload/afterload and improving contractility.

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🏷️ Related Tags

Anemia
Coagulation Cascade
Leukemia
Lymphoma
Atherosclerosis
Hypertension
Myocardial Infarction
Heart Failure
Hemostasis
Thalassemia
Sickle Cell
Polycythemia
Angina
Arrhythmia
Valvular Disease
Cardiology
Hematology
PCL Nursing
Medical Notes
CTEVT Syllabus

 

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