Cardiology

On this page 9 sections
One Liners
- Essential = Hyaline Arteriolosclerosis
- Malignant = Fibrinoid Necrosis
- Libmann Sack endocarditis valve = Mitral and aortic
Heart Anatomy
| Coronary Artery | Main Regions Supplied | Key Branches |
| Left Anterior Descending (LAD) | Heart apex, anterior 2/3 of interventricular septum, anterior LV wall | Diagonal branches, Septal perforators |
| Left Circumflex (LCX) | Lateral and posterior LV walls, left atrium | Obtuse Marginal branches |
| Right Coronary Artery (RCA) | Right atrium, right ventricle, SA node (~60%), AV node (~90%) | SA Nodal branch, Right Marginal artery |
| Posterior Descending (PDA) | Inferior LV wall, posterior 1/3 of septum, posterior RV wall | Arises from RCA (85%) or LCX (8%) |
Valvular Diseases
| Valve | Opens between |
|---|---|
| Mitral | LA → LV |
| Tricuspid | RA → RV |
| Aortic | LV → Aorta |
| Pulmonary | RV → Pulmonary artery |
| Lesion | Timing | Character | Location | Radiation |
|---|---|---|---|---|
| Aortic stenosis | Systolic | Crescendo-decrescendo | RUSB | Carotids |
| Aortic regurgitation | Diastolic | Early diastolic blowing | LSB | — |
| Mitral stenosis | Diastolic | Rumbling + opening snap | Apex | — |
| Mitral regurgitation | Systolic | Holosystolic | Apex | Axilla |
| Tricuspid regurgitation | Systolic | Holosystolic | LLSB | — |
| Tricuspid stenosis | Diastolic | Rumbling | LLSB | — |
| Pulmonary stenosis | Systolic | Ejection | LUSB | — |
| Pulmonary regurgitation | Diastolic | Blowing | LUSB | — |
| Disease | Overload | Chamber affected |
|---|---|---|
| Aortic stenosis | Pressure | LV |
| Aortic regurgitation | Volume | LV |
| Mitral stenosis | Pressure | LA → pulmonary circulation → RV |
| Mitral regurgitation | Volume | LA + LV |
| Pulmonary stenosis | Pressure | RV |
| Pulmonary regurgitation | Volume | RV |
| Tricuspid stenosis | Pressure | RA |
| Tricuspid regurgitation | Volume | RA/RV |
Heart Sound Auscultation Landmarks
Mitral Valve (Apex): 5th left intercostal space in the midclavicular line.
Aortic Valve: 2nd right intercostal space at the sternal border.
Pulmonic Valve: 2nd left intercostal space at the sternal border.
Tricuspid Valve: 4th or 5th left intercostal space at the lower left sternal border.
Murmur hint
Aortic valve
Should be OPEN during systole
→ Aortic stenosis = systolic
Should be CLOSED during diastole
→ Aortic regurgitation = diastolic
Mitral valve
Should be OPEN during diastole
→ Mitral stenosis = diastolic
Should be CLOSED during systole
→ Mitral regurgitation = systolic
MI
| Biomarker | Initial Rise | Peak Level | Normalization / Duration Raised | Clinical Utility & High-Yield Notes |
| Myoglobin | 1–3 hours | 6–9 hours | 24 hours | Earliest to rise; good for ruling out early MI, but low specificity (found in skeletal muscle). |
| Troponin I (cTnI) | 3–4 hours | 18–24 hours | 7–10 days | Gold Standard; highly cardiac-specific. |
| Troponin T (cTnT) | 3–4 hours | 18–24 hours | 10–14 days | Stays elevated slightly longer than cTnI. |
| CK-MB | 4–6 hours | 12–24 hours | 2–3 days (48–72 hrs) | Best marker for detecting re-infarction due to its quick return to baseline. |
| AST / SGOT | 12–24 hours | 24–48 hours | 3–4 days | Historical marker; rarely used today due to low cardiac specificity. |
| LDH (LDH-1) | 24–48 hours | 48–72 hours | 7–14 days | Used for late-presenting MIs prior to modern troponin assays. |
Four major causes of oedema
| Mechanism | Examples | Why oedema occurs |
|---|---|---|
| Increased capillary hydrostatic pressure | Heart failure, venous obstruction, fluid overload | More fluid is pushed out of capillaries |
| Decreased plasma oncotic pressure | Nephrotic syndrome, cirrhosis, severe malnutrition | Reduced plasma protein osmotic pull |
| Increased capillary permeability | Inflammation, burns, allergic reactions | Fluid and proteins escape more readily |
| Lymphatic obstruction | Lymph node dissection, lymphatic damage, filariasis | Interstitial fluid and protein clearance is impaired |
FCPS pearl: Oedema can result from increased filtration, reduced plasma oncotic pressure, increased permeability, or inadequate lymphatic drainage.