Comparison of ketamine-propofol mixture (ketofol) and midazolam-meperidine in endoscopic retrograde cholangiopancretography (ERCP) for oldest old patients.

Background and aim: Endoscopic retrograde cholangiopancreatography (ERCP) requires moderate-to-deep conscious sedation. Combinations of ketamine and propofol (ketofol) and of midazolam and meperidine were analyzed using the bispectral index (BIS). There is no research on the use of ketofol on very elderly patients. The aim of this study is to use BIS and offer insight into the use and safety of ketofol sedation for oldest old patients undergoing ERCP. Materials and methods: For the ERCP procedure, 168 patients aged 85+ years were enrolled in a 2-year retrospective single center study. Seventy-five patients received midazolam-meperidine (MM) sedation in 2016, while 75 patients received ketofol (KP) sedation in 2018. The two groups were compared for patient data, procedure duration, Ramsay Sedation Score (RSS), heart rate (HR), blood pressure (BP), and pulse oximetry (SpO2), BIS, facial pain score (FPS), time to achieve BIS, recovery time, and complications. The total amount of rescue medication was recorded.
Results: The two groups did not differ by patient data or procedure duration (p>0.05). Group KP had significantly higher systolic and diastolic BP, HR, and SpO2 values and lower BIS scores than Group MM (p=0.0001). The two groups did not differ by time to achieve BIS scores (p>0.05). Group KP had significantly fewer complications and a shorter recovery time than Group MM (p<0.001).
Conclusion: Ketofol induced sedation results in more stable vital signs and fewer complications than the midazolam-meperidine sedation regimen during ERCP in oldest old patients, indicating that ketofol can be an alternative to midazolam-meperidine.

Introduction

Endoscopic retrograde cholangiopancreatography (ERCP) is a gold standard treatment of biliary tract diseases that require moderate-to-deep sedation.1

A distinction should be made between moderate and deep sedation needs. In moderate sedation, patients can respond to verbal commands and/or tactile stimulations while maintaining adequate spontaneous ventilation and cardiovascular functions. However, in deep sedation, patients respond to repeated and/or painful stimuli but have all protective reflexes intact with spontaneous respiration, require assistance to maintain the airway, and cardiovascular functions may be compromised.2,3

The percentage of deep sedation episodes was 26% for ERCP, and the percentage of patients experiencing at least one episode of deep sedation was 85% in the very elderly.4 ERCP is an invasive procedure during which patients with poor general health secondary to old age and multiple associated diseases are more vulnerable to potential complications mainly caused by respiratory and cardiovascular conditions such as hypertension, hypotension, bradycardia, oxygen desaturation, abdominal discomfort, and dizziness, which may occur during operation.5,6

Anesthesiologists use different doses and anesthetic agents depending on factors such as age, comorbidities, American Society of Anesthesiologists (ASA) score, reason for ERCP procedure, and time for procedure completion. Protective reflexes are not compromised, and cardiac functions are little affected by low doses of anesthetics. However, the procedure is interrupted or terminated due to patient agitation in some clinical situations. Deeper sedation is generally considered safe, unless the patient has underlying comorbidities which may increase the risk of aspiration.7–9 Ketamine and propofol were mixed in different concentrations in the same syringe (ketofol) for procedural sedation.10–14

The administration of benzodiazepines such as midazolam, which contains an opioid like meperidine, requires the titration of doses of sedative agents.15–17 Bispectral index (BIS) is a non-invasive technology that provides valuable data used to assess the level of sedation and BIS values that have good correlation with Ramsay Sedation Score (RSS).18,19 There is limited data on the use of BIS in very elderly patients during sedation.20

We hypothesized that a subdissociative dose of ketamine is safer than the combination of midazolam and meperidine for sedation during ERCP. We aimed to use BIS to show that ketofol sedation is safe to use for oldest old patients undergoing ERCP.

To this end, we compared the patient data, procedure duration, heart rate (HR), blood pressure (BP), and pulse oximetry (SpO2), BIS, Ramsay Sedation Score (RSS), facial pain score (FPS), recovery time, and complications of Group MM (75 patients), who received midazolam-meperidine sedation in 2016, and Group KP (75 patients), who received ketofol sedation in 2018.

Methods

The initial sample consisted of 168 patients aged 85+ years. However, 14 patients did not meet the inclusion criteria and four patients had missing data. Therefore, the final sample consisted of 150 patients. The study was approved by the Ethics Committee of Ümraniye Training and Research Hospital (B. 10.1.TKH.4.34.H. GP.0.01), and written informed consent was obtained from participants according to the guidelines presented in the Declaration of Helsinki.

The records of Groups MM and KP were compared. The exclusion criteria were as follows: 1) ASA V, 2) younger than 85 years of age, 3) presence of epilepsy, arterial aneurysm, or intracranial mass, 4) history of drug allergy, and 5) presence of hemodynamical instability such as peripheral oxygen saturation <90%, systolic blood pressure (SBP) <60 mmHg and HR ≤40 bpm.

Two experienced anesthesiologists administered sedation to patients. Groups MM and KP did not differ by the duration of the procedure conducted by two endoscopists who had over 5 years of experience in ERCP.

Patients were referred to the endoscopy unit. Twenty-gauge intravenous catheters were inserted, and 10 mL/kg/h of isotonic infusion was administered. Patients were laterally positioned and monitored for HR, SBP, diastolic blood pressure (DBP), peripheral oxygen saturation (SPO2), and bispectral index (BIS). Data were recorded at pre-induction (t0), at (t1) following induction and at (t2) 10 minutes and (t3) 30 minutes. Supplemental oxygen was administered using a nasal cannula at the beginning of the procedure. FPS (0–10) was used to evaluate pain at (t1), (t2), and (t3) (Figure 1). Time to achieve RSS scores ≥4 was recorded (Figure 2). Procedure duration was defined as the time between the insertion of the endoscope and the end of the procedure. Drug infusion was discontinued at the end of the procedure. Recovery time was defined as the time from the termination of drug infusion until the achievement of a Modified Aldrete Score (MAS) (9–10). SPO2<90% for more than 10 seconds was defined as respiratory depression. Apnea was defined as the cessation of airflow for at least 20 seconds. Hypotension was recorded at SBP <70 mmHg, and bradycardia was taken into account when HR <50 bpm.

Figure 1

Distribution of BIS scores of each groups. The y-axis presents BIS level and the x-axis presents the number of patients.

Abbreviation: BIS, bispectral index.

Figure 2

Facial pain score.

Bolus was administered to Group KP. They received 0.5 mg/kg ketamine and 0.5 mg/kg propofol intravenously. Afterwards, ketofol (1:1) consisting of 2 mL ketamine (50 mg/mL) and 10 mL propofol (10 mg/mL), while 8 mL normal saline containing 5 mg ketamine and 5 mg propofol for each milliliter was titrated to maintain a BIS ranging from 60–80 and RSS ≥4. Midazolam (2.5 mg) and meperidine (0.5 mg/kg) were administered as intravenous bolus doses to Group MM for induction. They intravenously received single injections of 1 mg midazolam depending on RSS level of sedation and BIS monitorization ranging from 60–80 throughout the procedure. No continuous anesthetic infusion was used in Group MM. When the RSS score reached 4, the procedure was started with the insertion of the endoscope by the endoscopist. We monitored BIS and RSS values for dose adjustment of anesthetics during the procedure.

In cases where the endoscopist or patient felt uncomfortable or the patient needed to cough, gag, or needed restraint or FPS>5, participants were injected with another dose (ie, increment dose of 10 mg) of rescue sedation (propofol), the total amount of which was recorded. Post-ERCP recovery was based on MAS. Patients with a MAS ≥9 were discharged. The anesthesiologist monitored postoperative MAS for 1 minute and every 5 minutes during the follow-up period. Hypotension, respiratory depression, bradycardia, nausea, vomiting, and emergence reactions such as delirium and excitement were recorded during the recovery period. Ephedrine (5 mg) or atropine (0.5 mg) were administered if SBP <70 mmHg and/or HR <50 bpm.

The primary outcomes were: 1) the amount of propofol used as a rescue medication; and 2) time of reaching RSS ≥4. The secondary outcomes were: 1) the duration of postoperative recovery based on MAS ≥9; and 2) the prevalence of respiratory depression, laryngospasm, and nausea/vomiting, and the incidence of other side-effects such as bradyarrhythmia and/or change in circulatory dynamics. Groups MM and KP were compared in terms of these outcomes. Head tilt/chin lift maneuver or mask ventilation technique were used when needed.

Statistical methods

Frequencies were calculated for nominal and ordinal data, which were analyzed using chi-square and chi-square with Linear Likelihood ratios. Mean and standard deviation (SD) were presented for scale parameters. The Kolmogorov-Smirnov test was used to determine whether the data met the assumptions for parametric tests. Independent-samples t-tests (for normally distributed data) and Mann Whitney-U analysis (for non-normally distributed data) were used to determine group differences. Data were analyzed using SPSS 17 for Windows (Statistical Package for the Social Sciences) at a significance level of 0.05.

Results

Table 1 shows the demographic characteristics of the participants and duration of the procedures. Groups KP and MM did not significantly differ by age, gender, Body Mass Index (BMI), ASA scores, duration of each group, and ERCP difficulties which were classified by ASGE criteria (Table 1) and types of indications for ERCP (Table 2) (p>0.05).

Table 1

Demographic characteristics and duration of the procedures

	Group KP (n=75)	Group MM (n=75)	p-value
Age (years)	88.15±3.11	87.99±2.62	0.510a
Female, n (%)	47 (62.7)	34 (45.3)	0.033c
Male, n (%)	28 (37.3)	41 (54.7)	0.033c
BMI	24.16±2.50	24.20±2.28	0.930b
ASA, n (%)
III	43 (57.3)	41 (54.7)	0.742c
IV	32 (42.7)	34 (45.3)
Duration of procedures	41.52±13.19	49.15±13.12	0.0001a
Grade of ERCP procedures
Grade I, n (%)	19 (25.3)	13 (17.3)	0.433c
Grade II, n (%)	50 (66.7)	57 (76.0)
Grade III, n (%)	6 (8.0)	5 (6.7)

Notes: aMann Whitney U-test, bIndependent samples t-test, cchi-square test.

Abbreviations: ASA, American Society of Anesthesiologists; BMI, body mass index; ERCP, endoscopic retrograde cholangiopancreatography

Table 2

Diagnosis of the patients

	Group KP (n=75)	Group MM (n=75)	p-value
Indication type
Choledoc stone, n (%)	40 (53.3)	43 (57.3)	0.425a
Cholangitis, n (%)	21 (28.0)	15 (20.0)
Pancreatitis*, n (%)	6 (8.0)	6 (8.0)
Malignancy, n (%)	5 (6.7)	10 (13.3)
Sepsis, without biliary pathologyn (%)
Cholangitis	3 (4.0)	1 (1.3)
Malignancy seconder	3 (4.0)	5 (6.0)	>0.05
Calculi and sludge	18 (24.0)	10 (13)

Note: achi-square test.

The groups did not significantly differ by SBP at T0. However, Group KP had significantly higher DBP at T0, T1, T2, and T3 and higher SBP, SPO2, and HR (Table 3) at T1, T2, and T3 than Group MM (P=0.0001).

Table 3

Time-dependent changes in circulatory dynamics, Categorical BIS scores, distribution, and differences between patient groups*

	Group KP (n=75)	Group MM (n=75)	p-value
SBP
T0	148.33±18.83	141.77±22.69	0.056a
T1	139.96±19.73	114.00±19.73	0.0002a
T2	136.04±20.45	116.36±20.93	0.0001a
T3	132.44±19.92	116.31±17.26	0.0001a
DBP
T0	71.19±12.68	64.21±12.60	0.001b
T1	62.28±9.55	54.25±11.01	0.0001b
T2	60.51±7.85	54.11±8.34	0.0001b
T3	59.91±9.51	52.80±6.03	0.0001b
HR
T0	70.39±11.10	70.03±11.61	0.846a
T1	65.49±11.15	70.19±9.14	0.005a
T2	63.60±8.47	69.59±7.22	0.0001a
T3	70.36±6.74	74.21±5.04	0.0001a
SPO2
T0	93.40±2.49	93.00±2.75	0.267b
T1	92.29±2.09	88.93±2.86	0.0001b
T2	91.95±1.99	89.60±2.66	0.0001b
T3	91.79±2.00	90.09±1.66	0.0001b
T0 BIS score, n (%)
<60	—	4 (5.3)
60–80	73 (97.3)	71 (94.7)	0.015c
>80	2 (2.7)	—
T1 BIS score, n (%)
<60	5 (6.7)	—
60–80	70 (93.3)	63 (84.0)	0.0001c
>80	—	12 (16.0)
T2 BIS score, n (%)
<60	5 (6.7)	-
60–80	69 (92.0)	61 (81.3)	0.0001c
>80	1 (1.3)	14 (18.7)
T3 BIS Score, n (%)
<60	2 (2.7)	—
60–80	72 (96.0)	72 (96.0)	0.148c
>80	1 (1.3)	3 (4.0)

Notes: aIndependent samples t-test, bMann Whitney U-test, cchi-square with linear likelihood ratio. *Since parameters were compared separately, Bonferroni Correction was not usable.

Abbreviations: BIS, Bispectral index; DBP, Diastolic blood pressure; SBP, Systolic blood pressure.

Although Group KP had higher BIS scores at T0 than Group MM, the latter had significantly higher BIS scores at T1, T2, and T3 than the former (p<0.0001) (Figure 1). Table 3 shows the categorical BIS scores and depression distribution and differences between the two groups.

Table 6 presents the comparison of the primary outcomes of the two groups. The results show that Group MM had a higher time to achieve RSS scores ≥4 (p<0.001) (Table 4) and MAS scores ≥9 (Table 5), and total dose of propofol as rescue sedation than Group MM (p<0.001).

Table 6

Sedation related complications during the procedure and the recovery

	Group KP (n=75)	Group MM (n=75)	p-value
Bradycardia, n (%)	2 (2.7)	17 (22.7)	<0.05a
Apnea, n (%)	3 (4.0)	22 (29.3)	<0.05a
Hypotension, n (%)	1 (1.3)	3 (4.0)	0.300a
Desaturation n (%)	9 (12.0)	13 (17.3)	0.356a
Coughs, n (%)	2 (2.7)	3 (4.0)	0.648
Gagging, n (%)	0 (0.0)	2 (2.7)	0.094
Restraint, n (%)	2 (2.7)	4 (5.3)	0.400
During recovery
Respiratory depression, n (%)	0	0	N/A
Hypotension	3 (4.0)	4 (5.3)	0.698
Bradycardia	1 (1.3)	3 (4.0)	0.300
PONV	4 (5.3)	6 (8.0)	0.513
Apnea	0	0	N/A
Agitation/delirium	3 (4.0)	0	N/A

Note: achi-square test.

Table 4

Ramsay sedation scale

Ramsay sedation scale
1	Patient is anxious and agitated or restless, or both
2	Patient is co-operative, oriented, and tranquil
3	Patient responds to commands only
4	Patient exhibits a brisk response to light glabellar tap or loud auditory stimulus
5	Patient exhibits a sluggish response to light glabellar tap or loud auditory stimulus
6	Patient exhibits no response

Note: Group MM had significantly higher FPS than Group KP (P<0.0001) (Figures 2 and 3).

Abbreviation: FPS, facial pain score.

Table 5

Time to achieve RSS, MAS, and total dose of rescue medication

Variable	Group KP	Group MM	p-value
Time to RSS 4 (min)	3.21±0.41	5.41±0.49	<0.001
Time to MAS (min)	10.93±0.25	11.11±0.31	<0.001
Total dose of propofol as rescue sedation	10.32±0.62	12.15±0.56	<0.001

Abbreviations: MAS, Modified Aldrete Score; RSS, Ramsay Sedation Score.

Figure 3

Distribution of facial pain scores of each group.

In Group KP, two patients (2.7%) had cough and two patients (2.7%) needed restraint. In Group MM, three patients (4%) had cough, two patients (2.7%) had gag reflex, and four patients (5.3%) needed restraint, indicating no statistically significant difference between the two groups (p>0.05). During recovery, three patients had hypotension, one bradycardia, four PONV and three agitation/delirium in Group KP. On the other hand, four had hypotension, three bradycardia, and six PONV in Group MM during recovery (p>0.05) (Table 6).

Discussion

Ketamine is a derivate of phencyclidine, which is a non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist binding to opioid and sigma receptors. Ketamine, with its rapid onset and short duration, leads to a condition referred to as “dissociative anesthesia”, resulting in amnesia and analgesia with little or no cardio-respiratory depression. The use of ketamine alone as a sedative agent has been limited due to its propensity to cause frightening and vivid irrelevant emergence reactions and nausea-vomiting and its sympathomimetic effects.8,9 Ketamine is water-soluble and lipophilic. The onset of action of intravenously administered ketamine is rapid, ranging from 15–30 minutes. The recommended sedation dose of ketamine is 0.5–1 mg/kg.

Prepared in a 10% lipid emulsion, propofol is a lipophilic alkyl phenol derivative, which is a short-acting sedative (~ 10 minutes, depending on dose) with a rapid onset of action (<1 minute). Its clearance is not affected by renal or hepatic dysfunction, as it has no active metabolites. Propofol can be used as a short-term sedative agent starting from a dose of 1 mg/kg and then titrated to effect with incremental doses of 0.5 mg/kg in adults. Propofol has respiratory and cardiovascular depressant effects.12–15

Propofol is a strong anesthetic with no property of internal analgesia that reduces respiratory depression and blood pressure in patients. Using opioid with propofol increases the frequency of respiratory depression and reduces the amount of propofol required. Ketamine is a safe sedative analgesic agent that can be used with propofol. It causes no respiratory depression and increases blood pressure and heartbeat thanks to its sympathetic effects.13–15 This is the reason why we used ketamine to decrease the unwanted side-effects of propofol. We found that ketofol reduced the incidence of sedation-related complications and maintained hemodynamic stability with an adequate level of sedation in very elderly patients undergoing ERCP.

Many studies have shown that the combination of propofol and ketamine in low doses can be used to maintain hemodynamic stability and to avoid side-effects that may occur when either of them is individually administered in large doses.13–15,21–23 There are numerous studies investigating the ideal dose of the combination of propofol and ketamine for deep sedation. There are, however, no studies that investigate the best combination dose for elderly patients.

Participants in Group KP, who received a 1:1 combination of ketamine and propofol (ketofol), had better hemodynamical stability in SBP, DBP, HR, and SPO2 and higher BIS scores than those in Group MM. This result indicates that ketamine was effective in counteracting the hemodynamic depression of propofol in high-risk (ASA III and IV) oldest old patients.

Our results are consistent with those of several studies that used ketofol in conjunction with regional anesthesia. Throughout our study, 1,337 patients under the age of 85 years underwent ERCP in our institution. We used ketofol anesthesia in 1,207 of them and observed no major anesthesia-related complications. Rapeport et al24 reported that ketofol infusion (1:1) is a safe and effective sedative and analgesic agent that can be used to achieve adequate sedation under regional anesthesia in high risk patients. Micdadqy et al25 administered the same dose of ketofol (1:1) in conjunction with regional anesthesia, and reported no episode of cardiovascular and respiratory failure. Andolfatto and Willman26 used ketofol (1:1) and found adequate sedation in emergency procedural sedation. Eberl et al28 suggested that ketamine and propofol be used together to reduce the total amount of propofol.

Olson et al29 compared ketofol (0.75 mg/kg) and propofol (1,5 mg/kg) in general anesthesia at induction and reported less myocardial depression and vasodilation in the ketofol group. Lemoel et al30 also reported better hemodynamic results with respiratory stability in the ketofol group.

Benzodiazepines have frequently been used in endoscopic procedures in recent years. However, studies report adverse effects such as respiratory depression, especially in very elderly patients with comorbidities. Paradoxical excitement is a serious adverse effect observed in up to 10–15% of elderly patients.16,17

Midazolam, which is a benzodiazepine, is widely used alone or in combination with an opiate such as meperidine, due to its quick onset of action and relatively short duration of effect. Nevertheless, using a combination of midazolam and an opiate extends their effects, increases the likelihood of respiratory depression, and prolongs the recovery period.23,24

Following infusion, propofol is characterized by rapid distribution and elimination without any cumulative effect. It is, however, much narrower than midazolam, and, therefore, should be more closely monitored to differentiate sedation levels. Propofol used25–29 in ERCP has been reported to provide more cooperation, a shorter recovery period, and a better sedation quality than midazolam

We observed apnea in 22 patients in Group MM at the beginning of the procedure. The head-tilt/chin-lift maneuver was used to open the airway of 17 of them. Mask ventilation was used in five of them. Atropine was administered to 17 of them, due to apnea accompanied by bradycardia. In three patients in Group KP, we observed respiratory depression and apnea that were resolved after the aspiration of the secretions. No cardiac arrest was observed, and no patients were admitted to the intensive care unit.

ERCP is an invasive procedure in which papillary balloon expansion and dilation can be painful. FPS was used for pain assessment during the procedure because all our patients were older than 85 years old and difficult to communicate with due to impaired cognitive functions. We, therefore, relied on facial expressions during the procedure and recovery period. Group MM had a higher FPS scores at T1 and T3, which might be due to the fact that we used a low dose of meperidine to prevent respiratory depression. The low FPS scores of Group KP might be due to the analgesic properties of ketamine. Our results are consistent with those of Hassan et al, who reported that ketofol sedation (1:1) was adequate and painless. Tosun also reported that ketofol provided effective sedation and analgesia.

Nejati et al27 conducted a randomized prospective study in an emergency department for the reduction of bone fractures and compared ketofol (1:1) with a combination of midazolam and fentanyl (MF). They reported that Group KP, with adequate sedation, had significantly lower pain scores than Group MF.27

Based on change in the level of alertness, BIS is a non-invasive technology that provides valuable information that can be used to assess the level of sedation. A numeric scale ranging from 0–100 has been has developed. In recent years, numerous studies have reported a good correlation between BIS values and clinical scores of sedation (ie, RSS) in outpatient procedures.18,19 There are some studies reporting no correlation BIS and unconsciousness when ketamine is used alone or in combination with propofol. There are no data, up to date, on the use of BIS on oldest old patients.10–12,20 In our study, BIS was used to assess the depth of sedation. Patients in Group KP had lower BIS scores at T1, T2, and T3, indicating that they achieved an adequate depth of sedation to end the procedure successfully.

Propofol was administered as rescue medication to reduce movements, cough, and restraints. Group KP was given significantly less rescue medication.

Group KP achieved MAS scores faster than Group MM. The longer recovery time in Group MM can be explained by the slower clearance meperidine.

Group MM had higher rates of nausea and vomiting. Propofol is an efficient anti-emetic agent which reduces the emetic properties of ketamine. Higher rates of hypotension in Group MM might, therefore, be associated with increased incidence of nausea and vomiting.13–15

Ketofol (1:1) provided adequate analgesia and sedation for ERCP and resulted in less oxygen desaturation than did the combination of midazolam meperidine in the very elderly patients. Adverse effects can occur in sedation procedures, and, therefore, close monitoring and cardiorespiratory support should be ready during ERCP.

Conclusion

Ketofol is more effective and safer than the combination of midazolam and meperidine in order to achieve adequate sedation in ERCP patients in a shorter period of time with lower doses. Ketofol provides better hemodynamic stability and results in lower rates of nausea/vomiting and respiratory complications than does midazolam-meperidine. We believe that ketofol is a better choice than the combination of midazolam and meperidine for patients who need a shorter period of induction at the onset of sedation. Ketofol is a safe alternative to conventional sedation regimens during ERCP for oldest old patients.