Patient preparation and principles of sedation in gastrointestinal endoscopy

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28 Patient preparation and principles of sedation in gastrointestinal endoscopy

Case

A 67-year-old male with a past history of mitral valve stenosis and insulin-dependent diabetes mellitis with moderate renal impairment requests his primary care physician to organise colon cancer screening. An open-access colonoscopy is arranged.

The patient presents for the procedure with moderate dehydration following preparation with three sachets of sodium phosphate solution. The patient is noted to be hypoglycaemic, having taken his usual dose of insulin that morning. He requests antibiotic prophylaxis for the procedure (as he has been told always to request this prior to invasive procedures). He is angry when this is refused and becomes more agitated when the consultant acquiesces and asks the nurse to prepare 1 g of ampicillin.

He is sedated with midazolam and fentanyl. During the procedure he receives oxygen supplementation but no capnography or pulse oximetry. He is uncomfortable during the procedure and complains that he is not ‘asleep’. He is given three further doses of midazolam, initially becoming more agitated, but eventually settling. After several minutes the nurse notes that he does not appear to be breathing. The medical emergency team is called but takes 5 minutes to respond. He is given flumazenil and becomes extremely agitated and tremulous. It is then noted that he takes valium for anxiety and temazepam at night.

This patient, although an extreme example, illustrates some of issues of appropriate preparation for an endoscopic procedure. The patient was given inappropriate bowel preparation, no instruction on the management of his insulin and no information about what to expect during the procedure. The proceduralist was correct not to recommend antibiotics, but his reasoning should have been explained and discussed rather than simply agreeing with the request and ordering penicillin without discussion. He had not had a chance to adequately discuss his history with the proceduralist, who did not know that he was allergic to penicillin, nor that he was on regular benzodiazepines. He was subsequently over-sedated for the procedure and had inadequate non-invasive monitoring.

‘Open access’ endoscopic services are relatively common, but if this type of service is to utilised it is paramount that the proceduralist have effective measures in place in order to obtain appropriate informed consent and identify patients for whom special issues regarding preparation are required. In short, the patient must understand the procedure and the proceduralist must understand the patient.

Preparing Patients for Endoscopy

Bowel preparation for colonoscopy

The quality of the bowel preparation prior to colonoscopy is critical in order to provide good views during endoscopy, and thus minimise the risk of missed lesions due to poor endoscopic views. The importance of this is illustrated by the fact that adequate bowel preparation is often included as a quality indicator in colonoscopy. The preparation is often regarded as unpleasant, and many patients are more concerned about the preparation than the actual procedure. As such, detailed explanation both verbally and written is important in order for this to be performed correctly and safely. If the bowel preparation is inadequate, the procedure may need to be deferred. It is important for patients to be informed that they should drink clear fluids only on the day prior to the procedure in addition to the bowel preparation in order to prevent dehydration, and to improve the effectiveness of the bowel cleansing. In addition, mobilising during the preparation may improve the effectiveness of the preparation, especially in the elderly.

The two main constituents widely used for bowel preparation are non-absorbed, isotonic solutions such as polyethylene glycol and low volume hypertonic solutions such as sodium phosphate and sodium picosulfate. Polyethylene glycol is an osmotic laxative that contains electrolytes in order to balance electrolyte shifts; as such it can be regarded as isoosmotic. It is mixed in a large quantity of water; for example the patient may need to drink a total of 3–4 L of fluid. This is usually taken the day prior to the procedure, but if a morning procedure it should be given as a ‘split’ preparation, where part of the preparation is given on the morning of the procedure. This may improve the effectiveness and tolerability of the preparation; however, it needs to be taken at least 4 hours prior to the procedure in order for the stomach to be empty, to reduce the risk of gastric aspiration.

Sodium phosphate (NaP)-based solutions work via a hyperosmotic mode of action, and can be given in much smaller volumes of water. As such, NaP is often tolerated better by patients. It can be combined with a polyethylene glycol-based regimen in order to improve tolerability and reduce volume. The NaP-based solutions do have some risks, including sudden fluid shifts within the body and precipitating acute phosphate nephropathy. Therefore, it should be avoided in the elderly and in patients with congestive heart failure or renal failure. In addition, caution is required if patients have an increased risk of electrolyte disturbance such as those with cirrhosis, small or large bowel dysmotility or other preexisting electrolyte imbalances.

The sodium picosulfate (Picoprep) preparation has no risk of phosphate nephropathy. Patients should be encouraged to drink fluids liberally during hypertonic-based bowel preparation. Patients with known or suspected inflammatory bowel disease may not be suitable for NaP-based preparations, due to an increased risk of causing preparation-related colonic inflammation compared to polyethylene glycol-based solutions.

Endoscopic retrograde cholangiopancreatography

Patients undergoing ERCP will be exposed to ionising radiation. Therefore women of childbearing age should have pelvic shielding during the procedure. If there is any possibility of pregnancy a serum or urinary β-human chorionic gonadotropin should be checked. Contrast medium in the bowel lumen can obstruct views of the biliary system, so patients who have recently had a CT scan with contrast or a barium study should have a plain abdominal x-ray to ensure the biliary system is not obscured. As iodinated contrast is used to inject into the biliary system, a history of iodine allergy or hyperthyroidism should be elicited, though history of a contrast allergy is not an absolute contraindication as the risk of an allergic reaction during ERCP is extremely low. Patients with biliary obstruction should receive prophylactic antibiotics prior to the procedure. Due to the risk of bleeding with sphincterotomy of the ampulla of Vater, elective patients on clopidogrel should ideally withhold this medication for 7–10 days if feasible. The risk is lower with aspirin (all therapeutic endoscopy can be performed on aspirin). Discussion with the patient’s cardiologist is prudent if there is uncertainty whether it is safe to withhold these medications. Coagulopathy should be reversed if present; patients on warfarin may need to change to low-molecular-weight heparin prior to the procedure depending upon the indication. The decision when to reinstitute anticoagulant therapy following therapeutic procedures such as ERCP and colonic polypectomy is a difficult one and should be individualised in consultation with the patient’s cardiologist.

Antibiotic prophylaxis

Advice regarding antibiotic prophylaxis prior to endoscopic procedures was significantly updated in American Society for Gastrointestinal Endoscopy guidelines (2008) based on the recognition from the American Heart Association that bacterial endocarditis from endoscopic procedures was exceedingly rare. For the majority of patients undergoing endoscopic procedures, including those with prosthetic heart valves or congenital cardiac abnormalities, antibiotic prophylaxis to prevent bacterial seeding was no longer recommended. There are however, certain situations in which the risk of infective complications (which may be local rather than systemic) is increased and antibiotics are warranted; these are listed in Box 28.1.

All patients with cholangitis require antibiotics; patients with biliary obstruction without cholangitis undergoing ERCP require antibiotics only if incomplete drainage is anticipated. Similarly, patients with diffuse sclerosing cholangitis should receive periprocedural antibiotics. There is insufficient evidence to recommend antibiotic prophylaxis for endoscopic ultrasound-guided aspiration of solid lesions, though it is warranted for cystic lesions or pseudocyst drainage.

Disease-specific issues

Patients can take their normal medications several hours prior to the procedure with a sip of water. The management of patients taking antiplatelet agents or anticoagulants is a complex issue, and should be in accordance with published guidelines. These guidelines take into account whether the procedure is elective or an emergency procedure, the indication for the antiplatelet agent or anticoagulant, and the bleeding risk related to the procedure. A suggested algorithm for management of patients requiring anticoagulation is outlined in Figure 28.1.

The management of patients with diabetes mellitus will depend upon whether they have type 1 or type 2 diabetes, and on whether they are diet-controlled or on diabetic medications or insulin. Patients with type 2 diabetes are more easily managed as they can generally withhold their medications or insulin on the morning of the procedure. If undertaking bowel preparation on the previous day, similar withholding or reduction in dosage is appropriate. For type 1 diabetes the management is more complicated as some maintenance insulin is required in order to avoid the risk of precipitating ketoacidosis. Involvement of the patient’s diabetic specialist may be useful, and in some situations admission to hospital early on the day of the procedure or even the night before the procedure for an insulin/dextrose infusion may be appropriate. Diabetic patients should be first on elective morning endoscopy lists in order to minimise fasting and disruption of glycaemic control.

Principles of Anaesthesia for Endoscopy

Introduction

The anaesthetic management of a patient undergoing an endoscopic procedure should take into account a number of factors including the type of procedure, the patient characteristics and their wishes, and the expertise and preferences of the proceduralist and staff members.

Patients may have comorbidities that increase the risk of sedation, especially in the older age group. Gastroenterologists need to be comfortable assessing patients for their anaesthetic requirements prior to a procedure in addition to managing their primary gastroenterological problem. Depending upon the facility in which procedures are performed, the anaesthetic (which may also be referred to as ‘sedation’ with the exception of general anaesthesia) may be given by the proceduralist with the assistance of nursing staff, a nurse anaesthetist or by a dedicated anaesthetist. There is wide variation between different countries regarding sedation management; it is a reflection of cultural expectations, health insurance structure and workforce training (e.g. nurse anaesthetists are common in some countries but not others).

The aim of anaesthesia is to provide a comfortable experience for the patient during the procedure, and to keep the patient still to enable the procedure to be performed. Sedation can be divided into different categories according to the depth of sedation. The American Society of Anaesthesiologists provides the following categorisation (see Table 28.1). The term ‘moderate sedation’ is being increasingly used instead of the potentially confusing term ‘conscious sedation’. Note that patients can move between different sedation states quickly, and proceduralists targeting a level of sedation should be competent at managing patients who enter the next deeper level of sedation. Assessment of the depth of sedation can be difficult as there is no widely accepted objective measure of the depth of sedation. A study of 80 patients sedated for endoscopy with the view to moderate sedation with midazolam and meperidine (pethidine) showed that 68% of patients entered a period of deep sedation at some point during their procedure.

Table 28.1 Clinical states of sedation (American Society of Anaesthesiologists)

Sedation level Characteristics
Minimal sedation Normal response to verbal stimulation.
Moderate sedation Purposeful response to verbal or tactile stimulation. Spontaneous ventilation is adequate and no airway intervention is required.
Deep sedation Purposeful response only after repeated or painful stimulation. Spontaneous ventilation may be inadequate, and airway intervention may be required.
General anaesthesia Unrousable, even with painful stimuli. Airway intervention is often required and spontaneous breathing is usually inadequate. Cardiovascular compromise may occur.

Patient assessment

The assessment of a patient initially comprises a thorough history of comorbidities, exercise tolerance and medications (including over-the-counter remedies and allergies). History of tobacco, alcohol and illicit drugs should be elicited, as should difficulties related to previous anaesthetics. A focused cardiorespiratory examination should be performed for all patients, especially to detect occult valvular disease. Of particular interest is the use of potent thienopyridine antiplatelet agents such as clopidogrel and prasugrel, and anticoagulants such as warfarin.

A useful guide for assessing anaesthetic risk has been developed by the American Society for Anaesthesiology (Table 28.2). Patients with an ASA status greater than III should be managed by an anaesthetist.

Table 28.2 American Society of Anaesthesiologists (ASA) classification of anaesthetic risk

Class  
I The patient is normal and healthy
II Mild systemic disease that does not limit activity (e.g. controlled hypertension)
III Moderate or severe systemic disease that does not limit activity (e.g. stable angina, diabetes mellitus with systemic sequelae)
IV Severe systemic disease that is a ‘constant threat to life’ (e.g. end-stage renal failure, severe cardiac failure)
V Patient is morbid and at substantial risk of death within 24 hours (whether the procedure is performed or not)
E Emergency status: add this as a suffix for emergency cases (e.g. IIIE)

For some patients with significant comorbidities, liaison with the patient’s treating specialist may be useful. For example, if a patient with reduced exercise tolerance due to emphysema has not been reviewed by a respiratory physician for a long period of time, it would be reasonable for the respiratory physician to review the patient in order to optimise his or her periprocedural status and to help stratify the anaesthetic risk.

Monitoring of patients

All patients should be monitored during sedation in order to detect complications of sedation and allow early management of these problems. The most common adverse event during endoscopy is the development of respiratory depression and hypoxia due to the administration of sedative agents. In addition to respiratory effects, sedation can cause cardiovascular depression so blood pressure and heart rate should be monitored as well.

Medications used in sedation

Drugs used for sedation have a number of common properties. These drugs are often synergistic when used together rather than being cumulative, and as such care should be taken when drugs are coadministered. A given dose of a sedative can have a wide variation in sedative effect in different patients, so careful titration of dosages is important to avoid oversedation—there is no such thing as a ‘standard dose’. In addition, the peak effect of a medication may be delayed, and over-frequent administration of doses can also lead to oversedation, especially in the recovery room. It should be remembered that the key end point of sedation is patient comfort rather than complete unconsciousness, and in some situations it is perfectly reasonable for the patient to be awake during the procedure. Patient expectation is essential here—patients often complain of awareness during endoscopic procedures because they had the misconception that they would undergo general anaesthesia.

Propofol

Propofol is an anaesthetic agent that acts by causing the release of gamma amino butyric acid in the brain. It is increasingly used in endoscopy due to its attractive properties such as rapid onset and offset, shortened recovery time, and fewer effects on neuropsychiatric functioning postprocedure. The half-life is 1–4 minutes, and the onset of sedation is within 30–60 seconds. Propofol is regarded as having a ‘narrow therapeutic window’ that can result in rapid depression to deep sedation or even general anaesthesia. In addition, hypotension can occur due to decreased systemic vascular resistance and negative cardiac inotropy. It has been approved by the US Food and Drug Administration for use by anaesthetists, but it is commonly used ‘off label’ by endoscopists for sedation. A meta-analysis of randomised controlled trials comparing propofol use during endoscopy to combined midazolam and opiates suggested that there were no differences in hypoxaemia, hypotension, the proportion of patients reporting pain or physician satisfaction, though patient satisfaction was higher in the propofol group. Furthermore, in contrast to benzodiazepines and narcotics there is no reversal agent. This means that a practitioner using propofol must be prepared to artificially ventilate an apnoeic patient for up to several minutes if necessary.

Generally propofol should not be used as a single agent as its analgesic effects are minimal, and it combines well with use of a small dose of opiate with or without a benzodiazepine at the beginning of the procedure.

Management of oversedation

Oversedation as manifested by reduced conscious state and respiratory depression or apnoea may initially manifest as a drop in oxygen saturation, though ideally it should be detected earlier by the clinical assessment of responsiveness (if conscious sedation is used), respiration or capnography. Initial management depends upon the degree of respiratory depression. This includes increasing supplemental oxygen (which may be administered via a Hudson mask rather than via nasal prongs), patient stimulation, airway management with the use of a ‘jaw thrust’ manoeuvre, and possibly withdrawal of the endoscope if gastroscopy is being performed. If these measures fail to resolve the situation, bag-and-mask ventilation should be performed and reversal medication such as flumazenil (for benzodiazepines) or naloxone (for opiates) should be administered. It should be noted that the half-life of these reversal agents is shorter than the active drugs, leading to the possibility that patients can slip back into deep sedation after the procedure. In practice this is a rare phenomenon. If the situation is deteriorating or additional help is required urgently, early notification of a medical emergency team is appropriate.

Key Points

Further reading

[Anonymous]. Practice guidelines for sedation and analgesia by non-anesthesiologists. Anesthesiology. 2002;96(4):1004-1017.

Australia and New Zealand College of Anaesthetists, Gastroenterology Society of Australia and Royal Australian College of Surgeons. PS9: guidelines on sedation and/or analgesia for diagnostic and interventional medical or surgical procedures, February 2008. Online.

Banerjee S., Shen B., Baron T.H., et al. Antibiotic prophylaxis for GI endoscopy. Gastrointest Endosc. 2008;67(6):791-798.

Burton J.H., Harrah J.D., Germann C.A., et al. Does end-tidal carbon dioxide monitoring detect respiratory events prior to current sedation monitoring practices? Academic Emergency Medicine. 2006;13(5):500-504.

Carbonell N., Pauwels A., Serfaty L., et al. Erythromycin infusion prior to endoscopy for acute upper gastrointestinal bleeding: a randomized, controlled, double-blind trial. Am J Gastroenterol. 2006;101(6):1211-1215.

Cohen L.B., DeLegge M.H., Aisenberg J., et al. AGA Institute review of endoscopic sedation. Gastroenterology. 2007;133(2):675-701.

Eisen G.M., Baron T.H., Dominitz J.A., et al. Guideline on the management of anticoagulation and antiplatelet therapy for endoscopic procedures. Gastrointest Endosc. 2002;55(7):775-779.

Evans L.T., Saberi S., Kim H.M., et al. Pharyngeal anesthesia during sedated EGDs: is ‘the spray’ beneficial? A meta-analysis and systematic review. Gastrointest Endosc. 2006;63(6):761-766.

Ladas S.D., Aabakken L., Rey J.F., et al. Use of sedation for routine diagnostic upper gastrointestinal endoscopy: a European Society of Gastrointestinal Endoscopy survey of McQuaid KR, Laine L. A systematic review and meta-analysis of randomized, controlled trials of moderate sedation for routine endoscopic procedures. Gastrointestinal endoscopy. 2008;67(6):910-923.

National Endoscopy Society members. Digestion. 2006;74(2):69-77.

Patel S., Vargo J.J., Khandwala F., et al. Deep sedation occurs frequently during elective endoscopy with meperidine and midazolam. Am J Gastroenterol. 2005;100(12):2689-2695.

Rex D.K. Review article: moderate sedation for endoscopy: sedation regimens for non-anaesthesiologists. Alimentary Pharmacology & Therapeutics. 2006;24(2):163-171.

Robin C., Trieger N. Paradoxical reactions to benzodiazepines in intravenous sedation: a report of 2 cases and review of the literature. Anesth Prog. 2002;49(4):128-132.

Sorbi D., Gostout C.J., Henry J., et al. Unsedated small-caliber esophagogastroduodenoscopy (EGD) versus conventional EGD: a comparative study. Gastroenterology. 1999;117(6):1301-1307.

Vargo J.J., Zuccaro G.Jr., Dumot J.A., et al. Automated graphic assessment of respiratory activity is superior to pulse oximetry and visual assessment for the detection of early respiratory depression during therapeutic upper endoscopy. Gastrointest Endosc. 2002;55(7):826-831.

Veitch A.M., Baglin T.P., Gershlick A.H., et al. Guidelines for the management of anticoagulant and antiplatelet therapy in patients undergoing endoscopic procedures. Gut. 2008;57(9):1322-1329.