Complications of three deep sedation methods for magnetic resonance imaging

Abstract

Introduction

Propofol, pentobarbital, dexmedetomidine, and other agents are commonly used to induce deep sedation (DS) in children undergoing magnetic resonance imaging (MRI) scanning to minimize motion artifacts. Studies have shown that propofol's rapid distribution and plasma clearance increase the need for repeated boluses and continuous infusion to maintain the level of sedation. Use of propofol for sedation has been associated with respiratory depression that may lead to hypoxia.[1–3] Nonetheless, a study of 49,836 propofol sedation/anesthesia cases found that the technique is unlikely to result in serious adverse outcomes in institutions with organized sedation services.[4] Propofol also permits faster onset and recovery and has comparable efficacy to a pentobarbital/midazolam/fentanyl regimen.[5] Pentobarbital has also been shown to be safe and effective when used with midazolam or fentanyl for sedation during pediatric diagnostic imaging.[6,7] Dexmedetomidine sedation was associated with a 16% incidence of bradycardia; however, mean arterial blood pressures and oxygen saturations were reported to be within normal limits for these patients.[8]

At Oregon Health and Science University (OHSU), children are sedated for diagnostic imaging with intravenous (IV) propofol (PROP) or mixed pentobarbital/propofol (PENT) regimens. Patients sedated with the PENT regimen but then required supplemental sedation, defined as an additional dose of pentobarbital and/or propofol by bolus or infusion more than 20 min after the initial dose of pentobarbital, were categorized under a third sedation method called the PENT SUPP group. In addition, airway devices such as laryngeal mask airways (LMAs) or endotracheal tubes (ETTs) are very rarely used. It was not known whether these different types of sedation are associated with different incidence of complications. Therefore, the aim of this study was to compare the safety among the PROP, PENT, and PENT SUPP regimens in patients receiving noncardiac MRI. We hypothesized that the type of sedation is a significant predictor of complications.

Materials and Methods

This case-control study used data on pediatric patients deeply sedated by attending pediatric anesthesiologists between 1998 and 2008 for noncardiac MRI scanning and recorded in our institution's Sedation Quality Improvement (SQI) database to compare the safety of propofol and pentobarbital regimens. The study protocol was approved by the OHSU Institutional Review Board.

The SQI database is administered by the Department of Anesthesiology and Peri-operative Medicine at our institution and populated by sedation nurses based on information recorded on a paper pediatric sedation form by attending anesthesiologists performing the DSs. The SQI database includes data on demographics, procedural details, sedation techniques, and outcomes including side effects and complications. In addition to data collection from the SQI database, one of the authors manually searched through original paper sedation charts for corroboration of data with the SQI database and to obtain data missing from the SQI database, when available. Data collected from both the SQI database and/or the paper sedation charts were populated in a Microsoft Excel^® spreadsheet for further analysis.

The sedation form also includes specific check boxes for each of the predefined major and minor complications. In particular, major complications were defined as aborted procedure, aspiration, cardiac arrest, dysrhythmia, hypotension with more than a 30% decrease from baseline, unplanned admission to ICU, unplanned admission to ward, and unplanned intubation. Minor complications were defined as airway obstruction without intervention, airway obstruction with intervention, apnea without intervention, apnea with intervention, coughing, desaturation (oxygen saturation below 92%) with or without intervention, drug error, inadequate sedation, IV infiltration, multiple IV sticks (>3 tries), nausea and/or vomiting, poststudy agitation (paradoxical reaction), excessive secretions complicating airway management, and unplanned admission to PACU. In addition, the form includes specific inquires on whether an unplanned admission to PACU, Ward or PICU, or an aborted procedure occurred.

Patients who received MRI that was not cardiac MRI were categorized as noncardiac patients, and only noncardiac MRI pediatric patients who were deeply sedated between 1998 and 2008 for MRI scanning were eligible to be considered in this analysis. Patients who received cardiac MRI were excluded from this study due to cardiovascular compromise that creates potential for increased problems with DS. In addition, we excluded all patients of one of the attending anesthesiologists who utilized a unique loading dose of propofol (LDP) method of sedation (large propofol bolus over 10–15 min and no infusion). The LDP method may have significantly different physiological effects that would invalidate any comparison with patients sedated with propofol using the “usual” method (typical induction bolus followed by infusion). Patients who received chloral hydrate were also excluded from the study. Patients who were administered either midazolam and/or ketamine premedication were included in the study. During DS, ketamine is administered as a synergistic agent prior to administration of either propofol or pentobarbital; it also has minimal respiratory depressant effects at low doses. Ketamine is widely used in pediatric sedation in emergency departments, burns units, and pediatric sedation units.

The SQI database had a total of 7,839 pediatric patients deeply sedated for MRI from 1998 to 2008 including cardiac, noncardiac, and LDP patients. We reviewed data from the SQI database and identified 619 eligible noncardiac patients who experienced one or more complications as cases. We matched each case with an eligible noncardiac MRI patient without complication (control) from the SQI database based on American Society of Anesthesiologists (ASA) Physical Status Classification, weight, and age. The patient with the same ASA classification, and weight and age within 20% of the corresponding case patient was selected as the control. For each case and control, additional data were collected from original paper sedation charts and scanned paper records stored on the Electronic Health Record (Epic, Epic Systems Corporation), including gender, additional complications, the type and doses of premedication and sedation used, sedation duration, recovery time, airway interventions used, anesthesiologist, and patient diagnoses, when available.

The type of DS was the primary predictor variable. In addition to type of DS, other potential confounding variables considered in the multiple conditional logistic regression model included premedication, anesthesiologist, and gender.

Results

Results of demographic characteristics, ASA Physical Status Classification, sedation regimen, and sedation times for both the case and control group are presented in Table 1. Cases and controls were matched well on ASA classification, and weight and age, and similar in gender distribution.

Table 1

Demographic and clinical characteristics

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Complications occurred in 794 (10.1%) of all 7,839 DSs performed for MRI in the database. The distribution of the type of MRI performed for the 619 eligible noncardiac cases and controls is reported in Table 2. The distribution was similar, with 86.1% of cases and 83.4% of controls completing MRI of the brain and/or spine; and with 8.2% of cases and 7.1% of controls completing MRI of the chest/abdomen/pelvis. Among the 619 eligible noncardiac cases with complications, 595 (96.1%) experienced minor complications, and 24(3.9%) had major complications. The vast majority of the minor complications were airway obstruction requiring intervention and transient oxygen de-saturation requiring [Table 3]. The major complications included 15 (62.5%) aborted procedures, 4 (16.6%) unplanned intubations, 2 (8.3%) episodes of hypotension, and 1 (4.1%) instance each of pulmonary aspiration, dysrhythmia, and unplanned ward admission. The overall distribution of major and minor complications and the distribution for each regimen are presented in Table 3. There were no instances of cardiac arrest or unplanned ICU admission. Of the aborted procedures, seven were due to airway obstruction, oxygen desaturation, and/or difficulty maintaining airway; five were due to coughing and secretions complicating airway management; one was due to persistently blurred images secondary to motion artifacts; one was due to patient movement; and one was due to inability to accommodate resedation.

Table 2

Region of magnetic resonance imaging scan for deep sedations performed^*

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Table 3

Complications of Noncardiac MRI group^*

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In the multivariate model, premedication, anesthesiologist, and gender were not significant predictors for the occurrence of complications [Table 4]. After adjusting for other variables in the model, the type of sedation was a significant predictor for the occurrence of complications (P = 0.0002). The PENT regimen was significantly associated with a lower risk of complications when compared to the PROP regimen (OR 0.68; 95% CI 0.46, 0.98; P = 0.040), and compared to the PENT SUPP group (OR 0.60; 95% CI 0.31, 0.89; P < 0.0001). There was no significant difference in association with complications when comparing the PROP regimen to the PENT SUPP group (P = 0.300).

Table 4

Association between predictors and complications from the multivariable model

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Discussion

In our study, complications occurred in 794 (10.1%) of all 7,839 DSs performed for MRI in the database. A study by Hoffman et al. indicated an adverse event rate of 9.2% associated with DS, though with a much smaller sample size of only 65.[11] A study of 30,037 pediatric sedation patients reported a 5.3% incidence of complications but included all levels of sedation including anxiolysis and moderate sedation, as opposed to DS only, which is likely to explain the difference in incidence.[12]

The PENT regimen was associated with a significantly lower risk of complications than the PROP regimen in noncardiac MRI patients. Several studies have shown that short-acting barbiturates are safe and effective for sedation during pediatric diagnostic imaging.[6,7,13–15] One study showed that although oral pentobarbital and oral chloral hydrate are equally effective, the incidence of adverse events with oral pentobarbital sedation (0.5%) was significantly lower in infants younger than 2 years during MRI and CT than with chloral hydrate sedation (2.7%) (P < 0.001).[6] Propofol has also been associated with a significantly greater incidence of adverse respiratory events and more frequent physiologic changes than pentobarbital during pediatric diagnostic imaging procedures.[16,17]

Propofol has significant advantages as well. The study by Zgleszewski et al. showed that patients in the propofol group had a faster recovery than patients in the pentobarbital group (34 min +/- 17 vs. 100 min +/- 30, P < 0.001).[15] Pershad et al. reported that a pentobarbital regimen was associated with prolonged sedation in six patients (20%), emergence agitation in two patients (6.7%), and one episode of delayed agitation after discharge from the hospital.[5] Pentobarbital has been associated with undesirable side effects in some children, including prolonged recovery, nausea, vomiting, ataxia, agitation, and unplanned admission.[15,17–19]

Mallory et al. also described the spectrum of complications with pentobarbital for diagnostic imaging which are typically different from those of propofol, such as inadequate sedation, prolonged recovery, allergic complications, unplanned admission, and vomiting.[17] Unlike their study, we did not find the use of pentobarbital was associated with inadequate sedation, probably as a result of our practice of using a small bolus of propofol in association with pentobarbital to alleviate the excitement that often accompanies pentobarbital administration.

Respiratory complications such as apnea can be life-threatening, and few studies have attempted to elucidate the effects of anesthetics on upper airway muscles.[20–22] During deep anesthesia, increasing doses of pentobarbital have been shown to increase the phasic genioglossus electromyogram, which theoretically increases the size of the airway and decreases collapsibility.[20] Our study did find that apnea with intervention occurred at a lower incidence in the pentobarbital group than in the propofol group. Eikermann et al. also showed that genioglossus activity is maintained at the same levels that are observed during natural non-REM sleep, and in fact exceeds the activity level observed during REM sleep.[20] Further study is necessary to elucidate whether pentobarbital's effect on the genioglossus activity could contribute to a more stable airway in a clinically meaningful way, such as when DS is required for patients with a compromised airway. Sedation with a mixed pentobarbital technique may be associated with less physiological derangement as demonstrated in our study by the decreased odds of complications when this technique is used instead of a propofol-based technique.

The regression analysis also indicates that the PENT SUPP group was associated with a significantly increased risk of complications than the PENT group. The PENT SUPP group includes patients who were sedated for MRI with the mixed pentobarbital regimen, but then required a resedation known as “supplemental” sedation 20 min or more after the initial sedation. The increased risk of complications in this group may be a result of the need for additional sedative agents (propofol or pentobarbital) on top of existing residual effects of barbiturate and benzodiazepine, with resultant synergy that could result in adverse physiologic effects such as airway obstruction, apnea, and hypoxia.

Sanborn et al. concluded that the use of multidrug sedation regimens should be avoided, as their study found that all patients who require airway resuscitation had undergone a multidrug sedation regimen.[23] It is important to note that Sanborn's study included chloral hydrate, fentanyl, pentobarbital, and midazolam, but did not include propofol. A landmark study in 2000 found that adverse events were commonly associated with drug interactions and synergistic effects.[24] Similarly, patients in the PENT SUPP group received some combination of pentobarbital and low-dose propofol, followed by supplemental sedation with propofol, and sometimes pentobarbital as well. Our results indicate that for longer scans, avoiding multiple drugs and using a single-drug regimen such as propofol alone may result in improved outcomes since the favorable recovery profile of propofol compared to pentobarbital is likely to result in fewer side effects such as nausea, vomiting, dizziness, and prolonged somnolence following sedation.

Despite prospective data collection, the retrospective analysis has inherent limitations. We had to rely on the accuracy of written record and there is potential reporting bias and missing or incomplete documentation. Not all confounding variables were captured in the database and data abstraction and there was always the potential for residual confounding. However, we excluded patients who received cardiac MRI, and patients who received a unique LDP method of sedation, and matched cases and controls based on three clinically relevant variables to minimize confounders. In addition, gender was also evenly distributed for the case and control groups. The finding that the anesthesiologist was not a significant predictor variable helped adjust for minor variations in practice between anesthesiologists. Data from this study came from one site with a highly experienced sedation service, thus generalizability of the study may be limited.

To conclude, in our study, the use of a pentobarbital technique was found to be associated with a lower incidence of complications during sedation in noncardiac MRI patients compared to a propofol technique or a pentobarbital technique requiring supplemental sedation. The vast majority of complications in our study were airway obstruction and transient oxygen desaturation.

Footnotes

References