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Approximately 70% of patients who develop perioperative pulmonary edema do so in the first hour after surgery, and the greatest onset occurs during the first 30 minutes. Causes include the following:
Volume overload
Cessation of positive-pressure ventilation with subsequent increase in preload
Anesthetic -induced myocardial depression
Postoperative hypertension
Arrhythmias and conduction abnormalities
Incidence
Up to 84% of patients who undergo surgery exhibit abnormalities of cardiac rate or rhythm in the perioperative period. Only 5% of these abnormalities are clinically significant.
The incidence of arrhythmias is highest during surgery that lasts longer than 3 hours, during neurosurgical or thoracic surgery, and during endotracheal intubation.
Metabolic abnormalities are the most common cause of arrhythmia (i.e., hypoxia, hypercarbia, hypokalemia, hyperkalemia). Therapy is aimed at reversal of these abnormalities.
Electrocautery used during surgery can affect the performance of cardiac pacemakers and implanted cardiac defibrillators (AICD)
The electromagnetic interference generated by electrocautery may be “sensed” by a pacemaker as intrinsic cardiac electrical activity and inhibit cardiac pacemaker activity. This inhibition may be prevented by temporarily programming the pacemaker to a fixed rate mode. In the operating room, placing a pacemaker magnet on the pacemaker during the surgical procedure will make the pacemaker operate in a fixed rate mode.
An AICD may interpret the electromagnetic interference of electrocautery as ventricular tachycardia or ventricular fibrillation, which would trigger the AICD to deliver a
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defibrillating shock. This may be prevented by turning off the AICD immediately prior to surgery and turning on the AICD on completion of the surgical procedure.
Valvular heart disease
Critical aortic stenosis is associated with an increased risk of perioperative cardiac complications.
These patients typically cannot increase cardiac output because an outflow obstruction is present at the site of the aortic valve.
Therefore, any hemodynamic changes that could result in a need for increased cardiac output (e.g., vasodilatation) should be avoided.
Aortic or mitral regurgitation. Operative risk is related to the status of left ventricular function rather than to the degree of valvular regurgitation.
Mitral stenosis. Volume status and heart rate are key factors in the perioperative period.
Tachycardia decreases diastolic filling time and may result in pulmonary edema.
Small fluid shifts may result in marked hemodynamic abnormalities.
Prosthetic heart valves. Patients with prosthetic heart valves are at risk for valve thrombosis and thromboembolic complications if anticoagulants are withheld for an excessive period preoperatively.
For most patients, anticoagulants can be discontinued up to 3 days before surgery and restarted 2–3 days after surgery without thromboembolic complications.
Patients with caged-disk prosthetic mitral valves have a high risk of valve thrombosis when they are not receiving anticoagulation.
For these patients, warfarin anticoagulation should be stopped 3 days before surgery and replaced with full -dose intravenous heparin, which is stopped 12 hours before surgery.
Once hemostasis is stable after surgery (usually at 12–24 hours postoperatively), heparin therapy is resumed. Warfarin therapy is started again once oral intake is begun.
Hypertrophic cardiomyopathy. Patients with hypertrophic cardiomyopathy with left ventricular outflow tract obstruction are at risk for worsening of left ventricular outflow tract obstruction in the perioperative period. Factors that may lead to worsening of the left ventricular outflow tract gradient include excessive preload or afterload reduction, which may occur with volume depletion or vasodilator therapy. Perioperative catecholamine release may directly act on the left ventricular outflow tract to increase myocardial contractility and increase the outflow tract gradient.
D Approaches to reduction of perioperative cardiac risk
Perioperative beta blocker therapy
Data from small clinical trials suggest that beta blockers decrease the risk of cardiac complications in the perioperative period.
An observational study has found that perioperative beta blockers have their greatest benefit in preventing cardiac complications in patients at increased cardiac risk, i.e., those having three or more of the following clinical features: (a) ischemic heart disease, (b) cerebrovascular disease, (c) renal insuficiency, (d)diabetes mellitus, (e) undergoing high-risk surgery.
The American College of Cardiology/American Heart Association 2006 Update on Perioperative Beta Blocker Therapy recommends that beta blockers be continued in patients already receiving beta blockers and initiated in patients undergoing vascular surgery who are estimated to be at high cardiac risk as determined by the presence of ischemia on preoperative testing. This guideline states that beta blockers are probably recommended for patients who undergo vascular surgery with a history of coronary artery disease or who have multiple coronary artery disease risk factors and for patients with multiple cardiac risk factors who undergo intermediate -risk or high-risk surgical procedures. Beta blockers may be considered for patients who undergo intermediate -risk or highrisk surgical procedures who have a single clinical cardiac risk factor and may also be considered for patients who undergo vascular surgery who have no cardiac risk factors.
Beta blocker therapy should be titrated to achieve a heart rate of 60–70 beats per minute in the perioperative period.
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For the patient who requires perioperative beta blocker therapy but does not have indications for the long-term use of beta blockers, we typically continue beta blockers for 30 days following surgery.
Perioperative alpha adrenergic agonists (clonidine, mivazerol) have been demonstrated to decrease perioperative ischemia and mortality following vascular surgery. This approach is not commonly used in the United States.
Anesthetic agents
Meta-analyses suggest that neuraxial anesthetic techniques (epidural, spinal anesthesia) is associated with a lower risk of pulmonary or thrombotic complications compared with general anesthesia. While these techniques were initially thought to also lower the risk of perioperative cardiac complications, recent meta-analysis has not confirmed that finding.
Prophylactic coronary artery revascularization
There is no evidence that coronary artery revascularization is indicated “just to get the patient through a noncardiac surgical procedure.” Coronary artery revascularization should be done prior to noncardiac surgery following the same guidelines and indications that would be followed if the patient were not undergoing noncardiac surgery.
Maintenance of normothemia in the postoperative period has been shown to decrease cardiac complications in patients at increased cardiac risk. This impact is primarily related to a reduction in postoperative ventricular arrhythmias.
HMG-CoA reductase inhibitors in observational studies have been shown to be associated with a reduced incidence of postoperative cardiac complications. Data from prospective studies is necessary before these agents can be recommended to reduce perioperative cardiac risk.
E
The patient who has had coronary artery angioplasty with placement of a coronary artery stent needs attention placed to the antiplatelet regimen utilized with stent placement.
A drug -eluting stent is the most commonly used coronary artery stent in the United States. It is essential that the patient's antiplatelet regimen (apirin and clopidogrel) be continued for at least 3 months following placement of a sirolimus -coated stent and for at least 6 months following placement of a paclitaxol -coated stent. Premature discontinuation of this antiplatelet regimen may result in acute stent thrombosis with subsequent MI.
If surgery cannot be performed in the presence of aspirin and clopidogrel, delay elective surgery until the patient's antiplatelet course is completed.
If emergency surgery is required and the patient has not completed a poststent placement antiplatelet regimen, consider each case on an individual basis. For most patients, proceed to surgery, and utilize platelet transfusions in the event that excessive bleeding occurs.
If a patient presents for coronary artery angioplasty and it is known that he or she is to have subsequent noncardiac surgery in less than 3 months, consider the use of a bare -metal stent, which requires 1 month of antiplatelet therapy (aspirin and clopidogrel).
F Invasive hemodynamic monitoring
No well-designed, randomized, prospective study has been undertaken on the impact of invasive hemodynamic monitoring in the perioperative period. Examples of intuitive indications for invasive hemodynamic monitoring include the following:
Anticipation of fluid shifts in the patient with left ventricular dysfunction or fixed cardiac output
Major vascular surgery in the patient with left ventricular dysfunction Surgery in the patient with a recent MI or unstable angina
G
Bacterial endocarditis prophylaxis (Tables 3-4, 3-5, 3-6, 3-7, 3-8) is indicated for procedures associated with bacteremia for patients with
Prosthetic heart valves
Rheumatic or other acquired valvular abnormalities
Mitral valve prolapse with mitral regurgitation
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TABLE 3-4 Cardiac Conditions Associated with Endocarditis
Endocarditis prophylaxis recommended
High-risk category
Prosthetic cardiac valves, including bioprosthetic and homograft valves Previous bacterial endocarditis
Complex cyanotic congenital heart disease (e.g., single ventricle states, transposition of the great
arteries, tetralogy of Fallot)
Surgically constructed systemic pulmonary shunts or conduits
Moderate-risk category
Most other congenital cardiac malformations (other than above and below) Acquired valvar dysfunction (e.g., rheumatic heart disease)
Hypertrophic cardiomyopathy
Mitral valve prolapse with valvar regurgitation or thickened leaflets
Endocarditis prophylaxis not recommended
Negligible-risk category (no greater risk than the general population)
Isolated secundum atrial septal defect
Surgical repair of atrial septal, ventricular septal defect, or patent ductus arteriosus (without residua beyond 6 months)
Previous coronary artery bypass graft surgery Mitral valve prolapse without valvar regurgitation Physiologic, functional, or innocent heart murmurs
Previous Kawasaki disease without valvar dysfunction Previous rheumatic fever without valvar dysfunction
Cardiac pacemakers (intravascular and epicardial) and implanted defibrillators
From Dajani AS, Taubert K, Wilson W, et al. Prevention of bacterial endocarditis: recommendations by the American Heart Association. JAMA. 1997;277:1794–1801.
TABLE 3-5 Dental Procedures and Endocarditis Prophylaxis
Endocarditis prophylaxis recommended*
Dental extractions
Periodontal procedures including surgery, scaling and root planing, probing, and recall maintenance
Dental implant placement and reimplantation of avulsed teeth
Endodontic (root canal) instrumentation or surgery only beyond the apex Subgingival placement of antibiotic fibers or strips
Initial placement of orthodontic bands but not brackets Intraligamentary local anesthetic injections
Prophylactic cleaning of teeth or implants where bleeding is anticipated
Endocarditis prophylaxis not recommended
Restorative dentistry (operative and prosthodontic) with or without retraction cord‡ Local anesthetic injections (nonintraligamentary)
Intracanal endodontic treatment; postplacement and buildup Placement of rubber dams
Postoperative suture removal
Placement of removable prosthodontic or orthodontic appliances Taking of oral impressions
Fluoride treatments Taking of oral radiographs
Orthodontic appliance adjustment Shedding of primary teeth
*Prophylaxis is recommended for patients with highand moderate-risk cardiac conditions.
This includes restoration of decayed teeth (filling cavities) and replacement of missing teeth.
‡Clinical judgment may indicate antibiotic use in selected circumstances that may create significant bleeding.
From Dajani AS, Taubert K, Wilson W, et al. Prevention of bacterial endocarditis: recommendations by the American Heart Association. JAMA. 1997;277:1794–1801.
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TABLE 3-6 Other Procedures and Endocarditis Prophylaxis
Endocarditis prophylaxis recommended
Respiratory tract
Tonsillectomy or adenoidectomy
Surgical operations that involve respiratory mucosa
Bronchoscopy with a rigid bronchoscope
Gastrointestinal tract*
Sclerotherapy for esophageal varices
Esophageal stricture dilation
Endoscopic retrograde cholangiography with biliary obstruction
Biliary tract surgery
Surgical operations that involve intestinal mucosa
Genitourinary tract
Prostatic surgery
Cystoscopy
Urethral dilatation
Endocarditis prophylaxis not recommended
Respiratory tract
Endotracheal intubation
Bronchoscopy with a flexible bronchoscope, with or without biopsy
Tympanostomy tube insertion
Gastrointestinal tract
Transesophageal echocardiography
Endoscopy with or without gastrointestinal biopsy
Genitourinary tract
Vaginal hysterectomy
Vaginal delivery
Cesarean section
In uninfected tissue:
Urethral catheterization
Uterine dilatation and curettage
Therapeutic abortion
Sterilization procedures
Insertion or removal of intrauterine devices
Other
Cardiac catheterization, including balloon angioplasty
Implanted cardiac pacemakers, implanted defibrillators, and coronary stents
Incision or biopsy of surgically scrubbed skin
Circumcision
*Prophylaxis is recommended for high-risk patients; it is optional for medium-risk patients.
Prophylaxis is optional for high-risk patients.
From Dajani AS, Taubert K, Wilson W, et al. Prevention of bacterial endocarditis: recommendations by the American Heart Association. JAMA. 1997;277:1794–1801.
Most congenital cardiac defects
Surgically constructed systemic-pulmonary shunts
Hypertrophic obstructive cardiomyopathy
Prior history of bacterial endocarditis
III The Surgical Patient with Chronic Lung Disease
Chronic lung disease is common and affects surgical patients of all ages and diagnoses. It has multiple causes and, when severe, increases the risk of surgery. The disease may be symptomatic (in the form of dyspnea) or totally asymptomatic. In addition, an acute infectious process may be superimposed on a chronic disorder. P.74
TABLE 3-7 Prophylactic Regimens for Dental, Oral, Respiratory Tract, or Esophageal Procedures
Situation |
Agent |
Regimen |
Standard general prophylaxis |
Amoxicillin |
Adults: 2 g; children: 50 mg/kg orally 1 hour |
|
|
before procedure |
Unable to take oral |
Ampicillin |
Adults: 2 g IM or IV; children: 50 mg/kg IM |
medications |
|
or IV within 30 minutes before procedure |
Allergic to penicillin |
Clindamycin or |
Adults: 600 mg; children: 20 mg/kg orally 1 |
|
|
hour before procedure |
|
Cephalexin |
Adults: 2 g; children; 50 mg/kg orally 1 hour |
|
or cefadroxil |
before procedure |
|
or |
|
|
Azithromycin |
Adults: 500 mg; children: 15 mg/kg orally 1 |
|
or |
hour before procedure |
|
clarithromycin |
|
|
|
|
Allergic to penicillin and |
Clindamycin or |
Adults: 600 mg; children: 20 mg/kg IV within |
unable to take oral |
|
30 minutes before procedure |
medications |
|
|
|
Cefazolin |
Adults 1 g; children: 25 mg/kg IM or IV |
|
|
|
|
|
within 30 minutes before procedure |
IM, intramuscularly; IV, intravenously.
*Total child's dose should not exceed the adult dose.
Cephalosporins should not be used in individuals with an immediate-type hypersensitivity reaction (urticaria, angioedema, or anaphylaxis) to penicillins.
From Dajani AS, Taubert K, Wilson W, et al. Prevention of bacterial endocarditis: recommendations by the American Heart Association. JAMA. 1997;277:1794–1801.
A Assessment of pulmonary risk
History
A history of pulmonary symptoms and disorders should alert the physician that further intervention and evaluation may be necessary.
Dyspnea
Sputum production
Chronic cough
Exercise intolerance
Prior medical conditions
Recurrent bronchitis or pneumonia
Chronic obstructive pulmonary disease (COPD)
Emphysema
Systemic disease with potential pulmonary involvement
Previous lung surgery
Exposure to environmental toxins
Cigarette smoking , the most common cause of chronic lung disease, is toxic to the respiratory epithelium and cilia and results in impaired transport of mucus, with consequent impaired resistance
to infection.
Physical examination. Abnormal findings follow.
Anatomic abnormalities (e.g., scoliosis or chest wall abnormalities)
Findings on auscultation of the chest (e.g., decreased breath sounds, wheezing, and rhonchi or rales)
Signs of inadequate oxygenation (e.g., cyanosis, finger clubbing, and use of accessory muscles for breathing)
Chest radiograph. Abnormal findings include blebs, pneumonitis, consolidation, pleural effusion, and hyperaeration with flattening of the diaphragm.
Laboratory studies
Arterial blood gases provide information on the adequacy of ventilation and oxygenation. Abnormal laboratory values include hypoxemia and hypercarbia.
Secondary polycythemia may also be seen in patients with chronic hypoxia.
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TABLE 3-8 Prophylactic Regimens for Genitourinary/Gastrointestinal (Excluding Esophageal) Procedures
Situation |
Agent* |
Regimen |
High-risk patients |
Ampicillin |
Adults: ampicillin 2 g IM or IV plus |
|
plus |
gentamicin 1.5 mg/kg (not to exceed 120 |
|
gentamicin |
mg) within 30 minutes of starting the |
|
|
procedure; 6 hours later, ampicillin 1 g |
|
|
IM/IV or amoxicillin 1 g orally |
|
|
Children: ampicillin 50 mg/kg IM or IV |
|
|
(not to exceed 2 g) plus gentamicin 1.5 |
|
|
mg/kgwithin 30 minutes of starting the |
|
|
procedure; 6 hours later, ampicillin 25 |
|
|
mg/kg IM/IV or amoxicillin 25 mg/kg |
|
|
orally |
High-risk patients |
Vancomycin |
Adults: vancomycin 1 g IV over 1–2 |
allergic to |
plus |
hours plus gentamicin 1.5 mg/kg IV/IM |
ampicillin/amoxicillin |
gentamicin |
(not to exceed 120 mg); complete |
|
|
injection/infusion within 30 minutes of |
|
|
starting the procedure |
|
|
Children: vancomycin 20 mg/kg IV over |
|
|
1–2 hours plus gentamicin 1.5 mg/kg |
|
|
IV/IM; complete injection/infusion within |
|
|
30 minutes of starting the procedure |
Moderate-risk |
Amoxicillin |
Adults: amoxicillin 2 g orally 1 hour |
patients |
or |
before the procedure, or ampicillin 2 g |
|
ampicillin |
IM/IV within 30 minutes of starting the |
|
|
procedure |
|
|
Children: amoxicillin 50 mg/kg orally 1 |
|
|
hour before the procedure, or ampicillin |
|
|
50 mg/kg IM/IV within 30 minutes of |
|
|
starting the procedure |
|
|
|
Moderate-risk |
Vancomycin |
Adults: vancomycin 1 g IV over 1–2 |
patients allergic to |
|
hours; complete infusion within 30 |
ampicillin/amoxicillin |
|
minutes of starting the procedure |
|
|
Children: vancomycin 20 mg/kg IV over |
|
|
1–2 hours; complete infusion within 30 |
|
|
minutes of starting the procedure |
IM, intramuscularly; IV, intravenously.
*Total child's dose should not exceed the adult dose.
No second dose of vancomycin or gentamicin is recommended.
From Dajani AS, Taubert K, Wilson W, et al. Prevention of bacterial endocarditis: recommendations by the American Heart Association. JAMA. 1997;277:1794–1801.
Pulmonary function tests. The correlation between preoperative pulmonary function tests and postoperative complication rates is controversial. No single pulmonary function test absolutely contraindicates an operation; however, abnormal results on several pulmonary function tests are thought to be associated with an increased probability of postoperative pulmonary complications.
In the absence of symptoms or significant history, routine preoperative spirometry is not indicated in extrathoracic surgery.
Preoperative spirometry and arterial blood gases may be considered in patients with
Planned thoracic procedures , with or without pulmonary resection
Productive cough and dyspnea
A history or physical findings of cardiopulmonary disease
A history of more than 20 pack -years of cigarette smoking
Abnormal chest radiograph findings
Morbid obesity
The ASA risk classification , when greater than class I or II, in combination with other risk factors, may predict the occurrence of pulmonary complications.
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For patients with planned thoracic surgery ,
Specific criteria have been published for the minimum pulmonary function necessary to tolerate varying degrees of pulmonary resection (Table 3-9).
Pulmonary function tests may be repeated after bronchodilator therapy to assess improvement after