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VASCULAR SURGERY
Dr. D.S. Kucey and Dr. C.M. Peniston
Alex Kulik and Ted Rapanos, chapter editors
Neety Panu, associate editor
PREOPERATIVE ASSESSMENT . . . . . . . . . . . . 2
History and Physical Exam
Consent
Preadmission Tests and Orders
Preoperative Medications
CARDIAC TRANSPLANTATION . . . . . . . . . . . . . 17
CONGENITAL HEART SURGERY . . . . . . . . . . . . 18
Palliative Procedures
Pure Obstructive Lesions
Simple Left-to-Right Shunts
Right-to-Left Shunts
Complex Cyanotic Defects
SURGERY
COMMON POSTOPERATIVE . . . . . . . . . . . . . . . 4
COMPLICATIONS
Arrhythmias
Bleeding
Renal Failure
Respiratory Failure
Low Cardiac Output (CO) and
Intra-aortic Balloon Pump (IABP)
Cardiac Tamponade
Perioperative Myocardial Infarction
Hypertension
Postoperative Fever
CNS Complications
. . . . . . . 3
VASCULAR - ARTERIAL DISEASES . . . . . . . . . 22
Acute Arterial Occlusion/Insufficiency
Chronic Aterial Occlusion/Insufficiency
Critical Ischemia
Abdominal Aortic Aneurysm (AAA)
Abdominal Aortic Dissection
Ruptured Abdominal Aortic Aneurysm
Cartoid Surgery
VASCULAR - VENOUS DISEASES . . . . . . . . . . . 27
Anatomy
Deep Venous Thrombosis (DVT) (Acute)
Superficial Thrombophlebitis
Varicose Veins
Chronic Deep Venous Insufficiency (post phlebitic
Syndrome, Ambulatory Venous Hypertension)
Lymphatic Obstruction/Lymphangitis
CARDIAC ANESTHESIA . . . . . . . . . . . . . . . . . . . 7
Preoperative
Intraoperative Anesthesia
Intraoperative Monitoring
Postoperative
PRINCIPLES OF CARDIOPULMONARY . . . . . 8
BYPASS (CPB)
VASCULAR - TRAUMA . . . . . . . . . . . . . . . . . . . . . 31
Penetrating (Laceration)
Blunt (Contusion, Spasm, Compression)
REFERENCES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
MYOCARDIAL PROTECTION AND . . . . . . . . . 10
CARDIOPLEGIA
CORONARY ARTERY BYPASS GRAFT . . . . . .11
SURGERY
VALVE REPLACEMENT AND REPAIR . . . . . .13
Aortic Stenosis (AS)
Aortic Regurgitation (AR)
Choice of Aortic Valve Prosthesis
Mitral Stenosis (MS)
Mitral Regurgitation (MR)
Choice of Mitral Valve Prosthesis
AORTA REPLACEMENT AND REPAIR . . . . . .16
Thoracic Aortic Dissection
Thoracic Aorta Aneurysm
Traumatic Aortic Disruption
MCCQE 2006 Review Notes
Cardiac and Vascular Surgery – CVS1
CARDIAC AND
ASSESSING RISK AND BENEFIT OF
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PREOPERATIVE ASSESSMENT
HISTORY AND PHYSICAL EXAM
history of present illness
• inquire about symptoms of cardiac disease i.e. chest pain, dyspnea, fatigue, hemoptysis, syncope,
palpitations, peripheral edema, cyanosis
• determine the degree of physical disability caused by cardiac symptoms
(angina, shortness of breath (SOB), undue fatigue, palpitations) using the
New York Heart Association (NYHA) functional classification (see Table 2 Cardiology Chapter)
• determine severity of angina pectoris using the Canadian Cardiovascular
Society classification (see Table 1 Cardiology Chapter)
past medical history
• cardiac risk factors: smoking, family history, elevated cholesterol,
diabetes mellitus (DM), hypertension (HTN), +/– elevated homocysteine levels
• previous operations: thoracotomy, saphenous vein stripping/ligation, peripheral vascular surgery,
carotid endarterectomy
• allergies, medications i.e. anticoagulants, antiarrhythmics,
antiplatelet agents, ACE inhibitors, diuretics, etc.
family and social history
• family history of coronary artery disease (CAD), congenital heart disease, Marfan syndrome,
malignant hyperthermia and other hereditary disorders should be noted
• consider marital status and living conditions in discharge planning
review of symptoms
• cardiovascular: past cardiac procedures, and investigations
• CNS: previous transient ischemic attack (TIA) or stroke (requires full neurologic work-up)
• respiratory: if chronic obstructive pulmonary disease (COPD) is suspected, obtain spirometry,
pulse oximetry and ABG pre-op
• endocrine: DM and its complications should be noted
• hematologic: bleeding disorders, sickle cell screening if African heritage
• renal: impaired renal function and renal dialysis increase the risk of perioperative complications;
renal transplant patients should be followed by renal transplant service
perioperatively to manage medications
• gastrointestinal (GI): active peptic ulcer disease, active hepatitis, cirrhosis,
and other GI problems can seriously affect the outcome of cardiac surgery
• peripheral vascular: venous and arterial disease should be noted; intra-aortic balloon pump insertion
through a femoral artery may be difficult with aorta-iliac occlusive disease
• genitourinary (GU): prostate problems may impair Foley catheter insertion
• musculoskeletal (MSK): major skeletal deformities or active arthritic conditions may interfere
with airway management, ambulating, and recovery
physical examination
• height, weight, and vital signs
• examine mouth, airway, neck, chest and abdomen
• assess all peripheral pulses and auscultate the carotid and subclavian arteries for bruits
• examine saphenous veins
• perform Allen's test on both hands in case a radial artery is used as a bypass conduit
for coronary artery bypass
• infection following cardiac surgery can be disastrous, therefore rule
out skin infections and dental caries (especially prior to valve surgery)
CONSENT
risks and benefits of surgery should be clearly outlined to the patient and his/her family
(with patient's permission)
serious complications should be explained, such as death, stroke, myocardial infarction (MI), infection, etc.
PREADMISSION TESTS AND ORDERS
CBC, PTT, INR, electrolytes, glucose, BUN, creatinine, and other special blood tests as needed
urinalysis
PA and lateral CXR (+/– CT chest, especially in re-operations to determine relation
of sternum to heart and ascending aorta)
ECG to diagnose heart rhythm abnormalities and myocardial ischemia
cross and type for 2 units PRBCs
NPO after midnight
Dulcolax suppository preop
ancef 1 g IV to be given in OR (vancomycin 1 g IV or clindamycin 600 mg IV if penicillin allergic)
CVS2 – Cardiac and Vascular Surgery
MCCQE 2006 Review Notes
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PREOPERATIVE ASSESSMENT . . . CONT.
PREOPERATIVE MEDICATIONS
All regular cardiac medications should be continued to the morning of surgery (including nitro patch), except:
• amiodarone - should be stopped 4 weeks preop to avoid potential intraoperative problems
(resistant bradycardia, hypotension, etc.)
• ACE inhibitors - small risk of hypotension perioperatively with these drugs,
therefore stop 24 hours preop (controversial)
anticoagulants
• warfarin - stop 4-5 days prior to surgery; admit and start on IV heparin if high risk of thrombosis
large left atrium, atrial fibrillation (A fib), mitral valve prosthesis
• heparin - IV heparin should be stopped 2-3 hours preop
(unless on intra-aortic balloon pump (IABP) support)
• ASA/Ticlodipine/NSAIDs - stop 7-10 days preop if possible
psychotropic drugs
• MAO inhibitors - discontinue 3 weeks preop if long acting, 1 week if short acting
others
• steroids and anti-rejection drugs (transplant patients) must be continued
ASSESSING RISK AND BENEFIT OF SURGERY
ventricular function
• the most important determinant of outcome of all heart diseases
• patients with severe left ventricular (LV) dysfunction usually have a poor prognosis,
but surgery can sometimes dramatically improve LV function
• patients with severe LV dysfunction but good arteries to bypass usually do very well from the
operative risk viewpoint, but those with bad ventricles and marginally graftable coronary arteries
are usually poor surgical candidates
• to assess viability of non-functioning myocardial segments, use thallium and
sestamibi myocardial imaging, PET scanning or MRI (see Cardiology chapter)
• surgically correcting volume overloading conditions such as aortic or mitral regurgitation (AR/MR)
may not change the prognosis (due to irreversibly damaged myocardium)
but symptomatology can be improved
• depressed ventricular function caused by aortic stenosis almost always improves
following relief of obstruction
coronary artery disease (CAD)
• isolated proximal disease in large coronary arteries (>1.0 - 1.5 mm) is ideal for bypass surgery
• small, diffusely diseased coronary arteries are not suitable for bypass surgery
• see Cardiology Chapter for discussion of PTCA vs. surgery
heart valve disease
• repair of heart valves is preferable to replacement because the ideal artificial valve
has not yet been developed
• repair is not feasible in all patients with heart valve disease, therefore valve replacement is necessary
numerous risk factors for CABG mortality have been identified in several major studies
(in decreasing order of significance)
• urgency of surgery (emergent or urgent)
• reoperation
• older age
• poor ventricular function
• female gender
• left main disease
• others include catastrophic conditions (cardiogenic shock, ventricular septal rupture, ongoing CPR),
dialysis-dependent renal failure, end-stage COPD, diabetes, cerebrovascular disease,
and peripheral vascular disease
commonly identified factors found to increase CABG post-operative morbidity or length of stay
(in decreasing order of significance):
• reoperation
• emergent procedure
• preoperative usage of intra-aortic balloon pump (IABP)
• congestive heart failure (CHF)
• CABG-valve surgery
• older age
• renal dysfunction
• COPD
• DM
• Cerebrovascular disease (CVD)
see Table 1 - Cleveland Clinic Clinical Severity Scoring System
MCCQE 2006 Review Notes
Cardiac and Vascular Surgery – CVS3
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ASSESSING RISK AND BENEFIT OF SURGERY . . . CONT.
Table 1. Cleveland Clinic Clinical Severity Scoring System
Preoperative Factor
Score
Added Score
Morbidity*
Mortality
Emergency Case
6
0-2
4-7%
0-2%
Creatinine 141-167 umol/L
1
3-5
10%
2-4%
Creatinine >168 umol/L
4
6
18%
5%
Severe LV dysfunction
3
7-9
23%
7%
Reoperation
3
10+
> 50%
> 25%
Mitral Regurgitation
3
Age 65-74
1
Age 75+
2
Prior vascular surgery
2
Hematocrit <34%
2
Aortic stenosis
1
Diabetes
1
Cerebrovascular disease
1
*Morbidity defined as myocardial infarction requiring use of IABP, mechanical ventilation for 3+ days, neurological deficit, oliguric or anuric renal
failure, or serious infection.
Adapted from Higgins et al. Stratification of morbidity and mortality outcome by preoperative risk factors in coronary artery bypass patients. JAMA. 1992:267:234-8.
COMMON POSTOPERATIVE COMPLICATIONS
ARRHYTHMIAS
ventricular ectopy most common
• premature ventricular contractions (PVC's) are usually benign, but may reflect marginal coronary
perfusion and ongoing myocardial ischemia
• if frequent (> 6-10/min) or multifocal PVCs, check serum electrolytes,
repeat 12 lead ECG and assess hemodynamics
• treatment
• Lidocaine 100 mg IV bolus (may repeat 50 mg IV bolus), followed by drip at 1-4 mg/min
• Magnesium sulfate 2-4 g IV, may repeat
• Amiodarone 150 mg IV slowly over 15-30 minutes,
then 900-1,200 mg (in 250 cc D5W) over 24-48 h
• cardioversion needed if progresses to symptomatic ventricular tachycardia (VT)
or if patient develops ventricular fibrillation (V fib)
• atrial or atrioventricular pacing at a slightly higher rate may suppress ectopy
nodal or junctional rhythm
• treatment may not be necessary (assure no hypotension)
• rule out digoxin toxicity, make certain serum K + > 4.5, rule out hypomagnesemia
• may require A-V sequential pacing if loss of atrial kick has significant hemodynamic sequelae
supraventricular tachycardia (SVT) - includes atrial fibrillation (A fib) and flutter
• onset may be heralded by multiple premature atrial contractions (PAC's)
• atrial ECG using atrial pacing leads often helpful in distinguishing fibrillation from
flutter during rapid rates
• treatment of A fib
• digoxin used to control rate - 0.5 mg IV once, then 0.25 mg q6h x 2,
then 0.125-0.375 mg PO daily depending on body weight and renal function
• if no asthma/COPD: metoprolol 5 mg IV q15min x 3, then 25-50 mg PO bid
• if asthma/COPD: diltiazem 0.25 mg/kg IV bolus (further 0.35 mg/kg bolus if
inadequate response), then switch to amiodarone 400 mg PO tid x 3-5 days,
then 200 mg PO od after loading dose
• if unstable or Grade IV LV: consider amiodarone 150 mg IV bolus (can repeat),
then 900 mg IV over 24 h, then switch to PO amiodarone as above
• treatment of atrial flutter
• rapid atrial pacing > 400 bpm
• digitalization followed by IV beta blocker
• IV verapamil followed by digitalization (calcium channel blockers must be used judiciously
as wide complex SVT can mimic VT)
• in both instances, the arrhythmia should be treated with synchronous direct current (DC) cardioversion
at 25-50 joules should there be a significant drop in blood pressure (BP) or cardiac output (CO)
• never give IV CCB and B blocker together
• adenosine can be used as a diagnostic and therapeutic intervention
(transient bradycardia/asystole to allow interpretation of rhythm, may be therapeutic)
CVS4 – Cardiac and Vascular Surgery
MCCQE 2006 Review Notes
COPD
2
Weight <65 kg
1
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COMMON POSTOPERATIVE COMPLICATIONS . . . CONT.
outcome
• mortality rates 0.3-23% depending on the degree of azotemia
• if dialysis is required, mortality ranges from 27-53%
RESPIRATORY FAILURE
mechanical - mucous plugging, malpositioned endotracheal tube, pneumothorax,
pre-existing COPD, bronchospasm
intrinsic - volume overload, pulmonary edema, atelectasis, pnemonia, pulmonary embolus
(uncommon), acute respiratory distress symptom (ARDS)
management
• examine patient and evaluate CXR for correctable causes
• if intubated: add positive end-expiratory pressure (PEEP) (7.5-10 cm H 2 O),
increase % oxygen inspired (FiO 2 ), diuresis, consider bronchoscopy with lavage for sputum,
bronchodilators
• if extubated: pain control, chest physio, diuresis, increase FiO 2 ,
facial continuous positive air pressure (CPAP), bronchodilators
• if pneumonia: sputum culture and gram stain, bronchoscopy,
consider antibiotics early if prosthetic materials in heart
LOW CARDIAC OUTPUT (CO)
cardiac index < 2.0 L/min/m 2
signs - decreased urine output, acidosis, hypothermia, altered sensorium, cool clammy skin
assessment - heart rate and rhythm (ECG: possible acute MI), preload and afterload states
(Swan-Ganz catheter readings), measurement of CO
treatment
• stabilize rate and rhythm
• optimize volume status, systemic vascular resistance (SVR)
• consider ECHO to rule out tamponade
• give calcium chloride 1 g IV until more definitive diagnosis reached
• correct acidosis, hypoxemia if present (CXR for pneumothorax)
• inotropic agents if necessary - see Table 4
• Dopamine: increases SVR, protects renal function (increases renal blood flow,
GFR and sodium excretion), produces tachycardia only in high doses
• Dobutamine: increases CO, decreases LV pressure, decreases SVR
• Epinephrine: increases heart rate, contractility and stroke volume (SV), decreases urine flow
• Norepinephrine: increases mean arterial pressure (MAP) with less increase in HR
compared to epinephrine
• Milrinone: improves cardiac output and myocardial contractility, decreases systemic
and pulmonary vascular resistance without increasing HR, used for right ventricle (RV)
failure or high pulmonary artery (PA) pressure
• Amrinone: similar to milrinone but more prone to cause arrhythmias in high doses
• persistent low cardiac output despite inotropic support requires placement of IABP
MCCQE 2006 Review Notes
Cardiac and Vascular Surgery – CVS5
BLEEDING
causes include medications, clotting deficits, prolonged operation, emergency surgery,
technical factors, deep hypothermia, renal impairment, and transfusion reactions
patients at high risk for bleeding complications: endocarditis, aortic dissection, redo cases
treatment
• assure normothermia
• measure clotting factors stat: INR, PTT, fibrinogen, platelet count, activated clotting time
• tranexamic acid bolus (50 mg/kg) occasionally given if > 150 cc/h chest tube output
• correct with fresh frozen plasma, cryoprecipitate, platelets, DDAVP,
protamine for continued heparinization
• transfusion reaction protocol if suspected
indications for surgical exploration of post-operative hemorrhage
• mediastinal tube output > 300 cc/h despite correction of clotting factors
• 1.5% rate for CABG, 4% rate for valve surgery
• technical factors found as cause > 50% of time
RENAL FAILURE
incidence is 0.3-1%
diagnosis - prerenal vs. renal vs. postrenal
management
• optimize volume status and cardiac output
• discontinue nephrotoxic drugs (indomethacin, aminoglycosides, ACE inhibitors)
• maintain urine output > 40 cc/h using low-dose dopamine (1-3 ug/kg/h),
furosemide 10-300 mg IV bolus +/– 10-20 mg/h drip, or ethacrynic acid (50-100 mg IV bolus) as indicated
• furosemide/mannitol drips if persistent oliguria
• dialysis
• continuous arterial-venous hemodialysis (CAVHD) or continuous venous-venous (CVVHD)
approach are most suitable for hemodynamically unstable patients
• for hemodynamically stable patients, consider intermittent hemodialysis or peritoneal dialysis
(peritoneal cavity may communicate with mediastinum and be ineffective)
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