Chapter 4 Preoperative Pitfalls
PREOPERATIVE EVALUATION
Neurologic Evaluation and Assessment of Pain Susceptibility
Failure to Recognize Carotid Disease
• Consequence
• Intervention
• Prevention
This recommendation would be concordant with that applied to patients with carotid disease and requiring coronary artery revascularization (CABG). Debate still exists as to the timing of CEA versus CABG, but in the setting of asymptomatic coronary artery disease (CAD), the carotid is addressed first to decrease the rate of CVA at the time of CABG (10%–5.3%). Conversely, risks of comorbid cardiac disease must be considered in the context of asymptomatic carotid disease, because delay of coronary revascularization to allow recovery from CEA leads to an increase in overall mortality (9.4%) despite low rates of stroke.4 The possibility of concurrent CEA and CABG has been explored, but its role is controversial.
Failure to Recognize Low Pain Threshold
• Consequence
• Intervention
Drug | Contraindications/Side Effects |
---|---|
Nonsteroidal anti-inflammatory drugs (e.g., ketorolac) | Renal dysfunction/acute renal failure |
Dextromethorphan | Seizure, arrhythmia, brain damage |
Cyclo-oxygenase 2 inhibitors | Cardiovascular disease, renal dysfunction/acute renal failure, gastrointestinal bleeding |
Acetaminophen | Hepatic dysfunction |
Neurontin | Somnolence, dizziness, fatigue |
Local anesthetic | Seizure, arrhythmia |
Ketamine | Psychotropic effects |
Peripheral nerve block | Seizure, arrhythmia |
Epidural anesthesia | Seizure, arrhythmia, hypotension |
• Prevention
Adjuvant therapies such as those outlined in Table 4-1 have been shown to reduce postoperative opioid requirements in patients with chronic pain. Of note, epidurals should utilize lipophilic narcotics because these are more effective in patients with chronic pain and should not replace IV narcotics because such management could result in withdrawal. Partial opioid agonists such as buprenorphine or nalbuphine should also be avoided because they too may cause withdrawal.5
Transition to an oral regimen provides another challenge for patient and clinician. The equivalent to the daily postoperative narcotic requirement can be calculated (Table 4-2) and prescribed in part (generally one half the requirement) as long-acting oral opioids such as oxycodone or methadone. Intermittent breakthrough doses of short-acting medications can be prescribed to fulfill the remainder of the daily requirement and can be slowly tapered to return the patient to his or her baseline narcotic regimen over a 2- to 4-week period.5
Drug | Oral Dose | Intravenous Dose |
---|---|---|
Hydrocodone | 30 mg q3h | — |
Hydromorphone | 7.5 mg q3h | 1.5 mg q3h |
Fentanyl | — | 0.1 mg q1h |
Meperidine | 300 mg q3h | 100 mg q3h |
Morphine | 30 mg q3h | 10 mg q3h |
Oxycodone | 30 mg q3h | — |
Failure to Recognize Alcohol Dependence
• Consequence
• Intervention
Box 4-1 Sedation Scales
Adapted from Ramsey MAE, Savege TM, Simpson BRJ, et al. Controlled sedation with alphaxalanoe-alphadolone. BMJ 1974;2:656–659; and from Sessler C, Gosnell M, Grap MJ, et al. The Richmond agitation-sedation scale. Validity and reliability in adult intensive care patients. Am J Respir Crit Care Med 2002;166:1338.
Richmond Agitation-Sedation Scale (RASS)
+4 Combative | Overtly combative or violent, immediate danger to staff |
+3 Very agitated | Pulls on or removes tubes or catheters, aggressive behavior toward staff |
+2 Agitated | Frequent nonpurposeful movement or patient-ventilator dyssynchrony |
+1 Restless | Anxious or apprehensive but movements not aggressive or vigorous |
0 Alert and calm | |
− 1 Drowsy | Not fully alert, sustained (>10 sec) awakening, eye contact to voice |
− 2 Light sedation | Briefly (<10 sec) awakens with eye contact to voice |
− 3 Moderate sedation | Any movement (but no eye contact) to voice |
− 4 Deep sedation | No response to voice, any movement to physical stimulation |
− 5 Unarousable | No response to voice or physical stimulation |
Prescription of clonidine, haldol, or propofol for persistant symptoms can be beneficial as an adjunct to benzodiazepenes, but these drugs have not been shown to prevent seizure when given as monotherapy.8,9 Supplementation of IV fluids with magnesium, thiamine, and folate can correct deficiencies seen in many patients with alcohol dependence.
• Prevention (Fig. 4-2)
Box 4-2 CAGE Questions
Adapted from Ewing JA. Detecting alcoholism: the CAGE Questionnaire. JAMA 1984;252:1905–1907. Copyright © 1984, American Medical Association. All rights reserved.
Standard dosing regimens for prophylaxis include regular administration of diazepam or lorazepam. Again, haldol and clonidine can be employed for breakthrough symptoms, and patients should be monitored for signs of psychomotor agitation, hemodynamic instability, and cognitive changes.8
Cardiac Risk Assessment and Preoperative Optimization
Failure to Recognize or Medically Optimize the Patient with Ischemic Heart Disease or Congestive Heart Failure
• Consequence
• Intervention
• Prevention
Table 4-3 Preoperative Cardiac Risk Stratification
Rights were not granted to include this table in electronic media. Please refer to the printed book.
Adapted from recommendations in Eagle KA, Berger PB, Calkins H, et al. ACC/AHA Guideline Update for Perioperative Cardiovascular Evaluation for Noncardiac Surgery—executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Update the 1996 Guidelines on Perioperative Cardiovascular Evaluation for Noncardiac Surgery). Circulation 2002;105:1257–1267.
Table 4-4 Preoperative Evaluation for Ischemic Heart Disease
Rights were not granted to include this table in electronic media. Please refer to the printed book.
Adapted from recommendations in Eagle KA, Berger PB, Calkins H, et al. ACC/AHA Guideline Update for Perioperative Cardiovascular Evaluation for Noncardiac Surgery—executive summary: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Update the 1996 Guidelines on Perioperative Cardiovascular Evaluation for Noncardiac Surgery). Circulation 2002;105:1257–1267.
β-Blockade has become the mainstay of pharmacotherapy for prevention of postoperative MI. In randomized, prospective studies, patients at risk for cardiac events were given β-blockers in the perioperative period and had reduced incidences of ischemic events and mortality.17–19 This has been borne out in a recent meta-analysis.20 When patients are stratified according to the Revised Cardiac Risk Index (Box 4-3), those with three risk factors clearly benefit from preoperative β-blockade in conjunction with high-risk procedures; those with no risk factors do not require the drug.21,22 Intermediate-risk patients are likely helped and, in the absence of clear contraindications, should be prescribed the drugs. In the context of widespread prescription of β-blockers, risks of perioperative cardiac complications have significantly decreased. In fact, a contemporary study suggested that preoperative stress tests may no longer benefit patients at intermediate risk because revascularization does not improve outcomes after high-risk surgery in certain populations but simply delays the timing of the procedure.23 In a manner similar to that of β-blockers, recent evaluation of α2-agonists suggests that these medications may prevent perioperative cardiac events.20
Box 4-3 Revised Cardiac Risk Index (Indications for Preoperative β-Blockers)
Rights were not granted to include this box in electronic media. Please refer to the printed book.
Adapted from Lee TH, Marcantanio ER, Mangione CM, et al. Derivations and prospective validation of a simple index for prediction of cardiac risk of major noncardiac surgery. Circulation 1999;100:1043–1049.
Failure to Recognize Risk of Atrial Fibrillation
• Consequence
• Intervention
Cardioversion is more often accomplished using antiarrhythmics such as amiodorone. Electrical cardioversion may be necessary in the hemodynamically unstable patient. No clear difference in long-term outcomes has been demonstrated between rate control and antiarrhythmic therapies.24 However, contraindications to the drugs may dictate therapy. β-Blockers are inappropriate in advanced chronic obstructive pulmonary disease (COPD), and amiodorone can cause severe pulmonary toxicity when administered intravenously after lung resection.25
Additional roles have been identified for drugs such as adenosine that can slow the heart rate, at least transiently, to define the underlying rhythm. Potassium and magnesium should be administered to maintain serum levels greater than 4 mEq/L and 2 mEq/L, respectively, stabilizing myocardial muscle fibers. Anticoagulation should be considered after 48 hours of atrial fibrillation to reduce the risk of thromboembolic events.25
• Prevention
Pulmonary Risk Assessment and Preoperative Optimization
Failure to Recognize Obstructive Sleep Apnea
• Consequence
• Intervention
• Prevention
Patients with OSA should not be prescribed benzodiazepenes because resultant muscle relaxation further compromises the airway. Opioids blunt patient response to hypercarbia and hypoxia, resulting in a tendency toward apnea, and their use should be minimized. Those adjuvant drugs listed in Table 4-1 can be used to decrease narcotic requirements. Continuous pulse oximetry suffices for monitoring OSA patients in cases in which multiple comorbidities, high narcotic requirements, or hypertensive volatility are not noted. If these issues are of concern, ICU monitoring may be warranted in the OSA patient (Fig. 4-3).
As noted previously, patients with known or suspected diagnosis of sleep apnea should be prescribed CPAP in the pre- and postoperative periods. Patients with observed episodes of apnea should also be considered for treatment. No level-one data have shown clear benefit with use of short-term CPAP, although small studies suggest that patients with OSA on preoperative CPAP may have better blood pressure control and fewer postoperative complications.29