Designing safe procedural sedation: adopting a resilient culture


Glossary of terms

AGA

American Gastroenterological Association

ANZCA

Australian and New Zealand College of Anaesthetists

ASA

American Society of Anesthesiologists

ASGE

American Society for Gastrointestinal Endoscopy

BIS

Bispectral Index

BMI

Body mass index

BPS

Balanced propofol sedation

CAD

Coronary artery disease

CO

Carbon monoxide

CO 2

Carbon dioxide

COPD

Chronic obstructive pulmonary disease

DM

Diabetes mellitus

ECG

Electrocardiogram

ED

Emergency department

EDNAPS

Endoscopist-directed, nurses-administered propofol sedation

EDP

Endoscopist-directed propofol

ERCP

Endoscopic retrograde cholangiopancreatography

ESA

European Society of Anaesthesiologists

ESRD

End-stage renal disease

EtCO 2

End-tidal carbon dioxide

EUS

Endoscopic ultrasound

GABA

γ-Aminobutyric acid

GERD

Gastroesophageal reflux disease

HR

Heart rate

HTN

Hypertension

ICU

Intensive care unit

ISAS

Iowa Satisfaction with Anesthesia Scale

IV

Intravenous

MAC

Monitored anesthesia care

MET

Metabolic equivalent for task

MI

Myocardial infarction

NAAP

Nonanesthetist-administered propofol

NAPS

Nurse-administered propofol sedation

PROSAS

Procedural sedation assessment survey

QoR

Quality of Recovery

RCRI

Revised Cardiac Risk Index

RHSMD

Ratio of height to sternomental distance

RHTMD

Ratio of height to thyromental distance

RR

Respiratory rate

SCOPE

Stratifying Clinical Outcomes Prior to Endoscopy

SMD

Sternomental distance

TIA

Transient ischemic attack

TMD

Thyromental distance

ULBT

Upper lip bite test

Introduction

While millions of patients receive sedation every day, high-profile cases have brought medical errors in sedation to the public's attention. Alleviating pain and anxiety is a key component of the care provided to hospitalized and ambulatory patients. While reassurance, distraction, and behavioral strategies may offer relief, pharmacologic interventions are often required, especially in acute care settings. Sedation in the operating room and increasingly outside the operating rooms has been a growing industry due to the increase in the volume and types of procedures outside the operating room, an increase in the demand for special conditions to produce better image and results (i.e., MRI and dentistry), and an increase in the complexity of cases due to an increase in survival rates with complex pathology.

Sedation for gastrointestinal endoscopy has revolutionized the diagnosis, treatment, and prognosis of gastrointestinal tract diseases. Worldwide, a growing number of endoscopies (of increasing complexity and duration) for gastroenterology are performed each year, of which a large part requires sedation or anesthesia. The goal of sedation is to guard the patient's safety, provide comfort, control behavior, and minimize its impact on normal physiology. The practice of (endoscopic) sedation requires a thorough understanding of preprocedural assessment and preparation, sedation pharmacology, practical airway training, monitoring, adverse event management, and postprocedural care. The purpose of sedation is to relieve the patient's discomfort and anxiety while simultaneously reducing disruptive movements so that an adequate examination may be performed. Patient safety needs to be ensured while procedural efficacy is maintained.

A clinical microsystem is a group of clinicians and staff working together with a shared clinical purpose to provide care for a population of patients. The clinical purpose and setting define the microsystem's essential components, which include the clinicians and support staff, information and technology, the specific care processes, and the behaviors required to provide care to its patients. Examples of clinical microsystems include a cardiovascular surgical care team, a community-based outpatient care center, neonatal intensive care, and a pediatric sedation service. The clinical microsystem provides a conceptual and practical framework for approaching organizational learning and delivery of safe sedation care. To understand the functioning of these healthcare microsystems, and to improve their perioperative patient safety, it is necessary to study the components that make up the system—humans, technologies, and their complex interactions. In healthcare, the premium placed on practitioner autonomy, the drive for productivity, and the economics of the system may lead to severe safety constraints and adverse medical events.

The focus on the actions of individuals, without addressing the underlying microsystem, as the sole cause of adverse events, inevitably results in continued system failures and the resultant injuries and deaths of patients. Strategies to make sedation care more resilient and even safer might include the adoption of reliability engineering principles; setting up robust near-miss reporting systems ; applying critical event analysis tools such as trigger tools and failure mode and effects analysis (FMEA) when adverse incidents occur ; wide adoption of simulation and sedation team training; adopting checklists ; deploying standardized medication—doses, concentration, sets, implementing robust handoff protocols, and patient identification checklists ; and adherence to safe sedation practice standards.

Adequate pain control and sedation ensures the patient's comfort and cooperation, can influence the procedure's success, and can affect future attitudes toward healthcare providers and medical care. This chapter will describe key developments in sedation safety, safety research, risk and reliability management approaches, the role of human factors, and organizational practice models.

Preprocedural assessment

Sedation preparation involves performing an adequate risk assessment and determining when to enlist the assistance of anesthesia professionals. This should be done congruently with other pre-endoscopic evaluations, such as the need for antibiotic prophylaxis and bleeding tendency. The person administering sedation needs to assess for a previous adverse reaction to sedatives, symptoms of obstructive sleep apnea, and a history of alcohol overuse or drug abuse. These risk factors are associated with sedation complications. The physical examination should focus on vital signs, mental status, and the presence of pathologic anatomic features associated with a greater risk of airway obstruction and sedation difficulties.

Several distinct examinations must be performed based on an initial medical and surgical history review: firstly, a general exam to identify any underlying undiagnosed pathology present, looking closely for any obvious cardiovascular, respiratory, or abdominal signs; secondly, a thorough airway examination to predict the difficulty of airway management; and thirdly, detailed investigations may be required depending on comorbidities, age, and the nature of the procedure. Finally, there are standardized and validated score cards or tools available that can be used to document the assessment findings effectively, which not only facilitates day-of procedural review but also allows for benchmarking and quality improvements.

There is a well documented large variability in the: (1) level of experience and the scope of practice of clinical providers administering sedation and/or general anesthesia, i.e., gastrointestinal specialists, endoscopy-trained nurses, nurse anesthetists, physician assistants, and anesthesiologists and each has to know their limitations; (2) drugs administered during the procedure (sedatives, pain killers, anesthetic drugs); (3) airway techniques used (there is an extensive range of devices available for airway management requiring different levels of skills); (4) level of monitoring (including cardiovascular and respiratory monitoring); (5) duration and difficulty level of the procedure; (6) depth of sedation/anesthesia; (7) hospital (major teaching hospital vs. rural hospital) and the number of procedures performed, and (8) patients, each with their risk factors (e.g., obesity, hypoventilation, obstructive sleep apnea).

Medical history

A full past medical history review is important to obtain good insights into the patient's risk factors for procedural sedation. Previous surgical operations, medical procedures or diagnosis and anesthesia experiences, and allergies should be reviewed. Screening questions may also elucidate undiagnosed disease and prompt further investigation.

Respiratory diseases can limit the patient from lying flat for an extended period, or the patient can suffer from a chronic cough or snoring. An assessment of the cardiovascular status is necessary to establish the overall exercise tolerance (cardiovascular fitness), hypertension, exertional chest pain, syncopal episodes, or orthopnea. For patients with renal, liver, endocrine, and gastrointestinal diseases, baseline functions and management need to be assessed, especially as they can interfere with sedation medication usage and airway management, e.g., active gastroesophageal reflux disease (GERD) has a high aspiration risk.

While most hereditary conditions relating to anesthesia are extremely rare, such as malignant hyperthermia, it is vital to ask about any known family history of problems with anesthesia. Also, issues like postoperative nausea and vomiting, delirium, and awareness must be addressed.

Medication usage

The use of medications prescribed and nonprescribed, herbal medicine, and vitamin and mineral supplements need to be reviewed in detail, including what, indication, when, dosage, and effect (including side effects). Asking the patient about social factors like smoking history, alcohol intake, and any recreational drug use can have their influence on the sedative medication choice and dosaging. Other critical social factors to take note of include language spoken and the need for an interpreter. This is especially important if the patient will undergo a procedure under conscious sedation as they must be able to communicate clearly with the healthcare team. The personal living situation of patients can impact the hospitalization process as the patient may require additional support before or after the sedation.

Deconditioning

The level of deconditioning of a patient before undergoing a procedure refers to the changes in the body that occur during a period of inactivity. The changes happen in the heart, lungs, and muscles and cause tiredness and fatigue. The three stages of deconditioning include mild deconditioning with changes in the ability to do the usual exercise activities, moderate deconditioning with changes in the ability to do everyday activities, and severe deconditioning when the patient is no longer able to do a minimal activity or usual self-care. Deconditioning symptoms include weakness and tiredness, shortness of breath with minor physical effort (exertion), a faster heart rate than normal, pain or discomfort with activity, decreased strength, endurance, and balance. People at high risk for deconditioning are older adults; hospitalized or bedridden patients; patients who have cancer, obesity, or poor nutrition; and those patients with an illness or injury that affects movement and activity.

Frailty

Frailty is another indication of high risk for postprocedural sedation complications. It is not an inevitable part of aging. Frailty is associated with poor mobility, increased falls, hospitalizations, admission to residential care and mortality, poor quality of life, depression, cognitive decline, and reported loneliness. Different validated frailty score cards are available, and they all help document a person's physical performance, nutritional status, cognition, mental health, and health supports.

Assessing the metabolic equivalent for task level ( Table 10.1 )

One way of determining patients' activity levels is using the metabolic equivalent for task (MET) level score. The MET is a unit that estimates the amount of energy used by the body during physical activity as compared to resting metabolism. The MET is the oxygen used by a person in milliliters per minute per kilogram body mass divided by 3.5. One metabolic equivalent (MET) is the amount of oxygen consumed while sitting at rest, equal to 3.5 mL O 2 per kg body weight × min. The MET level is an easy way to describe the physical activity tolerance of a patient. Wahid et al. performed a systematic review of physical activity and major chronic diseases. They found that 150 minutes of moderate-intensity aerobic activity per week compared to inactivity resulted in a 23% lower risk of mortality (related to cardiovascular disease), 17% lower incidence of cardiovascular diseases, and 26% lower incidence of type 2 diabetes mellitus.

Table 10.1
Metabolic equivalents for tasks (METs).
MET Activity Perioperative cardiac risk
1–3 MET Taking care of yourself, eating, drinking, desk work, walking one or two blocks High
4–9 MET Climb stairs, walk briskly, running short distances, moderate sports Intermediate to low
10 ≤ MET Vigorous active sports Low

Revised cardiac risk index

Lee Goldman published the Goldman Risk Index (GRI) in 1977, which was updated in 1999 and published as the Revised Cardiac Risk Index (RCRI) to estimate a patient's risk of perioperative cardiac complications in noncardiac surgery. If a patient scores positive for two or more out of the six factors, a patient is defined as “high-risk.” The first factor “high-risk surgery (intraperitoneal, intrathoracic, or suprainguinal vascular procedures)” is irrelevant for our patient undergoing sedation. The other five factors are: history of ischemic disease, congestive heart failure or cerebrovascular disease, perioperative treatment with insulin or preoperative serum creatinine levels >2.0 mg/dL.

ASA classification ( Table 10.2 )

The American Society of Anesthesiologists (ASA) physical status classification system is a widely accepted and validated risk stratification system for assessing the fitness of patients before surgery. It was developed in the 1940s and is used to assess and communicate a patient's pre-surgical medical comorbidities.

Table 10.2
ASA classification levels.
Definition Adult examples, including, but not limited to:
ASA I A normal healthy patient Healthy, non-smoking, no or minimal alcohol use
ASA II A patient with mild (systemic) disease, without substantive functional limitations Current smoker, social alcohol drinker, pregnancy, obesity (30 < BMI < 40), well-controlled DM or HTN, mild lung disease
ASA III A patient with severe systemic disease, substantive functional limitations, or one or more moderate to severe diseases Poorly controlled DM or HTN, COPD, morbid obesity (BMI ≥ 40), active hepatitis, alcohol dependence or abuse, implanted pacemaker, moderate reduction of ejection fraction, ESRD undergoing regularly scheduled dialysis, history (>3 months) of MI, CVA, TIA, or CAD/stents
ASA IV A patient with severe systemic disease that is a constant threat to life Recent (<3 months) MI, CVA, TIA, or CAD/stents, ongoing cardiac ischemia or severe valve dysfunction, severe reduction of ejection fraction, shock, sepsis, disseminated intravascular coagulation, ascites reinfusion dialysis, or ESRD not undergoing regularly scheduled dialysis
ASA V A moribund patient who is not expected to survive without the operation Ruptured abdominal/thoracic aneurysm, massive trauma, intracranial bleed with mass effect, ischemic bowel in the face of significant cardiac pathology, or multiple organ/system dysfunction
ASA VI A declared brain-dead patient whose organs are being removed for donor purposes

Smoking

Smoking habits can have an important impact on risks of sedation care. Patients should be instructed to stop smoking at least 3–4 weeks before the procedure. Smoking increases airway reactiveness, inhibits ciliary motility to remove secretions, causes poor wound healing, and increases the rate of complications after surgery. The maximal beneficial effects occur if smoking is stopped for at least 8 weeks prior to surgery. However, carboxyhemoglobin (carbon monoxide—CO) levels decrease in the first 12–24 hours after quitting smoking (improves oxygenation). Both nicotine and CO have negative effects on the heart (increased oxygen demand, decreased contractility). It should be noted that in some patients, airway reactiveness and secretions might increase paradoxically for about a week after smoking cessation.

Fasting guidelines

Fasting guidelines for sedation are similar to general anesthesia. Although each country has its own fasting guidelines for elective interventions, there is consensus about fasting for adults: 2 hours is enough for clear fluids, but 6 hours is required for solid food or cow's milk. The Canadian and American anesthesiologist's societies differentiate between 6 hours for a light meal and 8 hours for heavy meal with meat, fried, or fatty foods. Chewing gum is often considered similar to the risk of having clear fluids.

In conclusion, nowadays most reviews take place via video, phone call, or online self-assessment tools. After a complete review of all data, the person performing the sedation must develop and communicate a plan with the patient and obtain their consent for the sedation. This plan should entail management of medications, smoking or drug use, fasting guidelines, potential complications, and the admission process. Also, a preliminary airway management plan can be included but a complete airway assessment is only possible during a direct face-to-face contact. On the day of the sedation, a quick review of the assessment is advisable as conditions may have changed and a final ASA classification is made after evaluating the patient. Increased ASA scores and especially class III or higher positively correlate with a higher rate of sedation complications and a requirement for high recovery e strategies.

Preprocedural airway assessment

This section will concentrate on how best to predict difficulties in maintaining adequate oxygenation either with face-mask ventilation or with advanced airway management during (gastrointestinal) endoscopic procedures under sedation, whereby the patient's ventilation should be continuously observed by clinical assessment and monitoring of oxygen saturation (measured by pulse oximetry), and ventilation (with end-tidal carbon dioxide through noninvasive waveform capnography).

Airway management remains one of the most important responsibilities of the clinician administering sedation. Complications can occur even during conscious sedation procedures. Prediction of a difficult airway allows a management plan to be developed, time for proper patient selection, and proper selection of equipment, devices and techniques and support from others.

Difficult airway management remains a significant cause of morbidity and mortality and is generally encountered during unexpected clinical conditions. It is usually defined as difficulties with either performing adequate bag-mask ventilation, problems with visualizing the glottis with a direct laryngoscope (failed laryngoscopy), or difficulties with the insertion of a supraglottic airway device or the endotracheal tube leading to challenges or even failed endotracheal intubation. Furthermore, even a good view of the glottis does not necessarily translate into easy control of the airway.

Correctly predicting difficulties during airway management (i.e., difficulties with a facemask, OPAs, NPAs, SADs, ETTs) contributes to safer airway management. Therefore, a preoperative assessment of every patient's airway is recommended. Many countries have produced their own guidelines for preoperative airway assessment, although there does not exist a specific overall recommendation about what exactly needs to be evaluated, nor what is the most optimal selection of metrics that provide an accurate identification for predictors of difficult airways. No single test has shown to be an accurate predictor of difficult airway management, and none of the current tests are both highly sensitive and highly specific. Yet there is a clear need for a more accurate, simple, and clinically applicable airway assessment tools for predicting difficulties. Several predictive scores for difficult airway use different anthropometric features as simple preprocedural bedside tests ; Honarmand 2014, , ( Table 10.3 ).

Table 10.3
Predictors of Airway difficulties.
Management predictor High-risk score Definition and measurement
Mallampati classification Grades 3 and 4 Identifies potential obstructive sleep apnea and predicts difficulty with any endotracheal intubation. This classification is based on the structures visualized with maximal mouth opening and tongue protrusion in the sitting position.
Class 1: Soft palate, fauces, uvula, anterior and posterior pillars visible
Class 2: Soft palate, fauces, uvula visible
Class 3: Soft palate, base of uvula visible
Class 4: Soft palate not visible at all
Interincisor gap <3 cm Rigid ruler, measuring in the midline
Upper lip bite test (ULBT) Classes 2 and 3 Place bottom teeth in front of upper teeth. Move mandibular – incisors—as high on the upper lip as possible.
Class 1: Lower incisor can bite upper lip above vermilion line
Class 2: Incisor can bite upper lip below vermilion line
Class 3: Cannot bite upper lip
Thyromental distance (TMD) <6 cm Rigid ruler from lower border of thyroid notch to bony point of mentum with patient's head extended and mouth closed.
Ratio of height to thyromental distance (RHTMD) >23.5 Predictor for difficult laryngoscopy.
RHTMD = height in cm/TMD in cm
Sternomental distance (SMD) <13.5 cm Indicator of head and neck mobility.
The straight distance between the upper border of the manubrium sterni and the bony point of the mentum with the head in full extension and the mouth closed.
Ratio of height to sternomental distance (RHSMD) >12.5 Predictor for difficult laryngoscopy.
RHSMD = height in cm/SMD in cm
Neck mobility <90° Normal >90°
Neck circumference >43 cm
BMI >30 kg/m 2

Other criteria that may cause a difficult airway are buck teeth, snoring/CPAP, oral infections, abscesses or tumors, posterior neck fat pad, cervical spine mobility, and loose or missing teeth. Patients with bushy beards can be difficult to manually ventilate via bag mask ventilation.

Combinations of these tests result in better prediction scores of anatomically difficult airways as reported by Wilson and El Ganzouri. Other factors can contribute to difficulties in airway management, i.e., obesity, protruding incisors, single canines. However, numerous studies have demonstrated the limited ability to reliably and accurately predict a difficult airway. Alessandri et al. showed the relationship between ultrasound assessment of the anterior soft tissues of the neck, difficult laryngoscopy, and difficult mask ventilation. Ultrasound neck screening provides quick, relatively easy, and accurate information, with diagnostic and therapeutic relevance. Longer skin-to-larynx distances appears predictive for both difficult mask ventilation and difficult laryngoscopy.

The prediction of airway difficulties remains a challenging task, and the results of all studies underline the importance of being constantly prepared for unexpected challenges. None of the airway screening tests seems to perform well alone, and different combinations are suggested to improve accuracy and higher predictability. The STOP-BANG acronym (for Snoring, Tiredness, Observed aPnea, hypertension, high Body mass index, Age, Neck circumference, and Gender) questionnaire is an instrumental screening tool and a good predictor for airway complications in patients with undiagnosed obstructive sleep apnea. The choice of assessment is ultimately at the discretion of the individual sedation provider. Even large cohort studies, including hundreds of thousands of patients in Denmark, showed that the accuracy of clinical prediction of a difficult airway is poor. However, the recommended preoperative airway assessment is the way forward using a combination of presurgery metrics. These researchers demonstrate an overall prevalence of difficult/impossible facemask ventilation of 1.1%, which may be particularly important in conscious sedation.

Routine physical evaluation of the airway is generally done by the healthcare professional responsible for the sedation. However, during the COVID-19 pandemic, to reduce unnecessary exposure of healthcare professionals, virtual airway assessment was done via remote telemedicine, as part of the preprocedural evaluation of the patient, providing a valid alternative to direct physical consultation. Simple tests are: Can you fit three fingers in your mouth when fully opened? Can you place your lower teeth in front of your upper teeth? Can you fit three fingers between your chin and your Adam's apple? Do you have any problems with neck movements? What is your neck circumference? These are some of the questions that can easily provide valuable information even from a remote distance.

It's key is to focus on unanticipated airway compromise and obstruction by preprocedural airway assessment and preparation. The inability to maintain an open airway and adequate oxygenation is one of the most feared complications during deep sedation, such as gastrointestinal endoscopic procedures, which can result in catastrophic outcomes, such as anoxic brain injury and death.

Levels of sedation

Procedural sedation is a drug-induced depression of consciousness. Depending on the level of sedation, patients will be able to respond purposefully to verbal or tactile stimuli and may lack memory. Although we may aim for a certain level of sedation, sedation is a continuum of consciousness states, ranging from near awake to deep sedation, and can be obtained by using a variety of drugs and administration routes.

The level of sedation required to perform the procedure successfully and with high patient satisfaction depends on several factors. The healthcare professionals consenting and providing sedation need to consider the level of the patient's anxiety, gender, age, pain tolerance, existing pain, bowel sensitivity, and the use of medication and illicit drugs. Procedural considerations may be the complexity of the procedure and the therapeutic maneuvers necessary to reach the optimal therapeutic result and also strongly depends on the endoscopist's technical expertise, patience, and speed. After considering all factors, it is essential to discuss the most suitable level of sedation and to bring these in line with the patient's expectations. The clinician providing sedation should not be distracted by other responsibilities and is responsible for safe sedation and monitoring.

Different definitions were used to describe varying sedation levels, and they may differ for patients in the ICU, ED, and general anesthesia. In anesthesia, the most commonly used definitions for sedation were originally developed by the ASA in 1999 and was last updated in 2019 ( Table 10.4 ).

Table 10.4
ASA sedation levels.
Minimal sedation anxiolysis Moderate sedation (conscious sedation) Deep sedation General anesthesia
Responsiveness Normal response to verbal stimulation Purposeful response to verbal or tactile stimulation Purposeful response following repeated or painful stimulation Unrousable even with painful stimulus
Airway Unaffected No intervention required Intervention may be required Intervention often required
Spontaneous ventilation Unaffected Adequate May be inadequate Frequently inadequate
Cardiovascular function Unaffected Adequate May be inadequate May be impaired

Minimal and moderate sedation can still leave the patient with the ability to respond purposefully to actions and commands while cardiovascular and ventilation functions are still preserved. Deep and general sedation represents a continuum in which patients may require assistance with maintaining the airway or cardiovascular function or full ventilation support.

The Ramsay sedation scale was developed to promote adequate sedation in the intensive care unit (ICU), and it was slightly modified for anesthesia ( Table 10.5 ).

Table 10.5
Ramsay sedation scale.
Response Level
Fully awake 1
Drowsy 2
Apparently asleep but rousable by normal speech 3
Apparently asleep but responding to standardized physical stimuli (e.g., glabellar tap) 4
Asleep, but not responding to strong physical stimuli (comatose) 5

The Modified Observer's Assessment of Alertness/Sedation (MOAA/S) scale is directed at determining the degree of suppression of consciousness and is widely used in the anesthesia research literature for quantifying the hypnotic effects of drugs ( Table 10.6 ).

Table 10.6
MOAA/S scale.
Response Score
Agitated 6
Responds readily to name spoken in normal tone (alert) 5
Lethargic response to name spoken in normal tone 4
Responds only after name is called loudly and/or repeatedly 3
Responds only after mild prodding or shaking 2
Does not respond to mild prodding or shaking 1
Does not respond to a deep stimulus 0

Healthcare professionals providing sedation need to recognize the different sedation levels and be alert to changes with deepening sedation levels and be able to rescue a patient in respiratory failure from a deep level of sedation or even unconsciousness. Deep sedation and general anesthesia should strictly be overseen by anesthesia specialists who can maintain adequate respiration and cardiovascular function.

Quality measurements

Clinicians are mainly concerned about the safety of the sedation and levels of comfort. Leffler et al. developed a procedural sedation assessment survey (PROSAS) measuring the quality of moderate sedation. Procedural sedation quality was defined as the absence of any sedation-related adverse event, and patient satisfaction was within the predetermined threshold. Patient satisfaction is directly influenced by the side effects of the sedation, control over the sedation level, level of comfort, and adverse events of the sedation.

The Iowa Satisfaction with Anesthesia Scale (ISAS) is a similar tool as the PROSAS, but the ISAS measures patient satisfaction after deep sedation ( Table 10.7 ). The items in the survey tool are very similar but do not include the experience of adverse events during the procedure, as patients will not be aware of them during deep sedation. The PROSAS can often be completed during the first phase of recovery whereas the ISAS tool needs to be completed during the second stage recovery—such as the day after the procedure (via phone call). The items are rated on a positive to negative scale: agree very much – disagree very much ( Table 10.8 ). Post anesthesia satisfaction studies done days after the procedure reveal as much as 6% of patients report minor events such as postoperative nausea and vomiting, significant sore throat, and hoarseness, and are significantly associated with patient dissatisfaction.

Table 10.7
Iowa satisfaction with anesthesia survey (ISAS).
I threw up or felt like throwing up
I would want to have the same anesthetic again
I itched
I felt relaxed
I felt pain
I felt safe
I was too cold or too hot
I was satisfied with my anesthetic care
I felt pain during the procedure
I felt good
I hurt

Table 10.8
Procedural Sedation Assessment survey (PROSAS) a .
Patient
How much discomfort did you experience during the procedure? Scale 0–10: None – slight discomfort – moderate discomfort – significant discomfort – sever pain
If having this procedure again in the future, how much sedation would you prefer to have? Scale −5–0 +5: Markedly less sedation – somewhat less sedation – same amount of sedation – somewhat more sedation – markedly more sedation
On a scale of 0–10, how much pain were you feeling before the procedure? Scale 0–10: None – slightly pain – moderate pain – significant pain – severe pain
On a scale of 0–10, how much pain are you feeling now? Scale 0-10: None – slightly pain – moderate pain – significant pain – severe pain
Do you have any nausea now? Yes - No
Do you have any dizziness now? Yes - No
Do you have any fatigue/tiredness now? Yes - No
Clinician administering sedation
Any episodes of O 2 desaturation <90% or leading to intervention? Yes - No
Any problematic changes in heart rate or blood pressure during intervention? (Systolic blood pressure <90 mm hg, >160 mm hg; heart rate <50 bpm, >120 bpm) Yes - No
Any hemodynamic or respiratory conditions that interrupted the procedure? Yes - No
What level of sedation best describes the case overall? Scale -5 – 0 + 5: Markedly undersedated – somewhat undersedated – appropriate sedation – somewhat oversedated – markedly oversedated
How much discomfort did the patient experience during the procedure? Scale 0–10: None – slight discomfort – moderate discomfort – significant discomfort – sever pain
Please rate the patient's cooperation during the procedure:
  • procedure aborted due to lack of cooperation

  • procedure delayed/interrupted due to lack of cooperation

  • adequately cooperative

Endoscopist
Was the exam interrupted in any way due to patient discomfort? Yes – No
Recovery nurse
How did procedural sedation impact patient recovery? Scale -5–0 + 5: Persistent pain due to undersedation – minor discomfort due to undersedation – optimal recovery - slightly sedated: Slow and minor difficulty in attaining awareness and consciousness - sedated: Difficulty in attaining awareness and consciousness
Did the patient report any pain during recovery? Yes - No
Did the patient complain of any nausea during recovery? Yes - No

a , .

Patient selection and screening

The selection of appropriate patients for minimal and moderate sedation is crucial to the safety and success of sedation. Minimal and moderate sedation can be provided by nonanesthetists depending on the healthcare professional training and competency levels and on local legal requirements.

Important criteria to consider in patients that will likely require anesthesia support include:

  • Younger than 18 years old

  • Gravidity

  • ASA class III of cardiac cause or higher

  • Advanced therapeutic endoscopy (e.g., ERCP, balloon dilatation)

  • Morbid obesity (BMI >35 kg/m 2 )

  • Severe sleep apnea (based on clinical diagnosis)

  • Difficult airway

  • Previously experienced anesthesia issues

  • Allergy to propofol or soy oil

  • Interventions requiring (intermittent) deep sedation

  • Anticipated intolerance to standard sedatives and opioids

  • Chronic use of significant amounts of pain medication

  • Patients with previous high sedation needs

In 2014, Braunstein et al. developed a scoring system to risk-stratify patients for high sedation needs during gastroscopy and colonoscopy who could benefit from anesthesia support. Based on the patient's characteristics, a SCOPE score was established, which correlates well with the patient's estimated risk for high sedation needs ( Tables 10.9 and 10.10 ).

Table 10.9
Stratifying Clinical Outcomes Prior to Endoscopy (SCOPE) scoring system.
Gastroduodenoscopy Colonoscopy
Characteristics Points Characteristics Points
Ages 18–29 10 Ages 18–29 10
Ages 30–39 9 Ages 30–39 10
Ages 40–49 7 Ages 40–49 6
Ages 50–59 3 Ages 50–59 2
Ages 60–69 0 Ages 60–69 0
Indication for reflux a 2 Diagnostic indication 3
Indication not for reflux a or abdominal pain 1 Female gender 3
Male gender 1 BMI <25 2
Psychiatric history 1 Tobacco use 1
Benzodiazepine use 2 Benzodiazepine use 6
Opioid use 2 Opioid use 4
Fellow present 1 Other psychoactive medication use 1

a Includes GERD, esophagitis, and Barrett's esophagus.

Table 10.10
Estimate a patient's risk of high sedation needs based on their SCOPE score.
Gastroscopy Colonoscopy
SCOPE score Risk % SCOPE score Risk %
I 10 I 10
II 20 II 15
III 25 III 20
IV 30 IV 30
V 50 V 75

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