A Randomized Controlled Trial On Procedural Sedation Among Adult Patients At Emergency Department Hospital
Universiti Sains Malaysia: Comparing Fentanyl With Midazolam Versus Fentanyl With Propofol
12TH. INTERNATIONAL CONFERENCE ON EMERGENCY MEDICINE
SAN FRANCISCO, USA3RD - 6TH APRIL 2008
Nik HNA Rahman1 (MBChB, MMed), R Ahmad2 (MD, MMed)
A Hashim3 (MBBS, MMed)
(Emergency Physicians)
1 Head of Department of Emergency Medicine, Hospital Universiti Sains Malaysia2Lecturer in Emergency Medicine, Hospital Universiti Sains Malaysia
3 Head of Accident & Emergency Department, Queen Elizabeth Hospital, SabahHospital Universiti Sains Malaysia, Kubang Kerian, 16150, Malaysia.
Tel: 00609-766 3000, Fax: 00609-765 3370Email: [email protected]
INTRODUCTIONINTRODUCTION Patients attended the emergency department for any forms of trauma and critically ill conditions frequently presented with physical or mental pain and agitation.
Some of them will require extra acute painful procedure in the ED as a form of treatment i.e fracture reduction, wound management, cardioversion.
In HUSM, we conducted in average approximately 35 cases per month in 2007. (65% orthopedic procedures, 30 % surgical/wound management, 5% medical cases)
INTRODUCTIONINTRODUCTION Such patients would be subjected to some forms of chemical induction to facilitate the procedure planned to either save their lives or salvage the remaining functioning organs or limbs.
The procedure known as “Procedural Sedation” would involve a collective decision to choose the most appropriate form of chemical induction for the purpose of analgesia or sedation
This procedure is not without risk i.e effects of drugs, insufficient sedation etc
Typically in HUSM we use a combination of analgesics & sedatives (fentanyl, morphine, midazolam, ketamine etc)
INTRODUCTIONINTRODUCTION The choice of drugs depends on the general medical conditions of patients, potential adverse events, efficacy/potency, duration of action etc.
The main goals of procedural sedation and analgesia are to give patients some relief from both pain and anxiety during the procedure while the patient maintains his/her own airway with minimal or NO adverse events
In addition to that this technique must be effective in reducing the stress response and improves patient’s compliance to undergo a procedure.
INTRODUCTIONINTRODUCTION Potential & well known adverse events: deep sedation, hypotension, respiratory depression/desaturation, allergies, prolong sedation.
Statistically in HUSM in 2007: adverse events in all procedural sedation 55% respiratory depression, 25% hypotension, 8% airway obstruction, 3% Arrhythmias, 9% others
Commonly associated drugs with adverse events: midazolam, morphine, ketamine
Therefore the procedure must be done in a controlled environment by experience staff
INTRODUCTIONINTRODUCTION In this study we explored the use of IV propofol & fentanyl compare with midazolam & fentanyl.
Propofol is a short/rapid acting hypnotic agent which when given via intravenous route the effect is almost immediate.
Sedative, analgesic, bronchodilating, antiemetic, reduce cerberal oxygen consumption
However it causes: apnoea, hypercapnia, hypotension, pain at injection site Basset et al (2002) and Guenther et al (2000) have showed that with a bolus dose of 1mg/kg followed by 0.5 mg/kg (titration) may reduce both the hypoxia and apnea
STUDY OBJECTIVESSTUDY OBJECTIVESAim of the Study
To initiate the creation of a standard or comparable protocol for procedural sedation delivered at the Emergency Department setting in Hospital Universiti Sains Malaysia.
To evaluate the importance of using capnography routinely when procedural sedation is given at the Emergency Department setting.
STUDY OBJECTIVESSTUDY OBJECTIVESGeneral Objective
To compare the safety and efficacy between combination of fentanyl and propofol with combination of fentanyl and midazolam in procedural sedation. (Side effects)
Specific Objectives
To compare the outcomes between combination of fentanyl and propofol with fentanyl and midazolam on subjects during and after a procedural sedation. (MAP, Oxygen saturation, ETCO2, time to recovery)
METHODOLOGYMETHODOLOGY Null Hypothesis
The use of combined fentanyl and propofol has no difference over fentanyl and midazolam for procedural sedation
Population Adult patients who full fill the criteria for the procedural sedation
InterventionAdministration of either fentanyl with midazolam or fentanyl with propofol
METHODOLOGYMETHODOLOGY Randomized control trial study which was carried out at the Emergency Department, University Hospital over a period of 12 months commencing from December 2006 until May 2007.
The proposal of this study was presented to the Department Board Review and Hospital Ethical Committee. Short term grant was awarded for the research by the University. (USMKK/PPSP®/JK P&E 2006)
70 patients were recruited and randomized using computer generated random permuted blocks of four patients and were divided equally into two groups (n=35 each group)
Single patient blinded to the drugs used
METHODOLOGYMETHODOLOGY Drugs were supplied by the HUSM pharmacy and were wrapped individually and placed in sealed envelope labeled accordingly as drug A or drug B
The research operators were the on-call emergency physician and the senior trainee in EM
All identified patients for procedural sedation were placed in procedural room well equipped with resus. Equipments
Both verbal and written consent were obtained as required by the University Research Ethical Committee
METHODOLOGYMETHODOLOGY Standard monitoring of systolic and diastolic BP, HR, RR,
O2 saturation & ETCO2 were carried out to each patient selected into the study
Patients were randomly allocated to one of the two groups:
a. Group A - Subjects received IV Fentanyl 1 mcg/kg as a bolus dose and Propofol 1mg/kg followed by Propofol 0.5mg/kg if needed.
b. Group B - Subjects received IV Fentanyl 1 mcg/kg as a bolus dose and a bolus dose of Midazolam 0.1mg/kg and 0.1mg/kg if needed.
METHODOLOGYMETHODOLOGY Titrating dose of sedatives were used until the patients
achieved either Ramsay Sedation Score of 3 or 4Modified Ramsay Scale
Ref: Modified Ramsay Scale: 1974
State of patient Score
Anxious, agitated, restless 1
Awake, cooperative, orientated, tranquil 2
Semi-asleep but responds to commands 3
Asleep but responds briskly to glabellar tap or loud auditory stimulus 4
Asleep with sluggish or decreased response to glabellar tap or loud
auditory stimulus
5
No response can be elicited 6
METHODOLOGYMETHODOLOGY Vital signs were monitored/recorded for every 5 minutes
including the adverse events
The time of regaining full consciousness in each subject was charted upon the completion of the procedure.
Upon regaining full consciousness subjects would be reviewed by attending medical officer before decision is made for the disposal
The data was analyzed using SPSS program version 12.0(vital signs, time to discharge, adverse events)
RESULTS
1 0 2 0 3 0 4 0 5 0 6 0 7 0 8 0
p a t i e n t a g e
0
2
4
6
8
1 0
Frequency
F i g u r e 5 . 2 : A g e d i s t r i b u t i o n
The youngest subject that has been recruited in this trial was 13 years of age while the oldest being 78 years old with the mean age of 37.8 years
M a l e
7 7 %
F e m a l e
2 3 %
M a l e F e m a l e
In subjects receiving propofol, the mean age was 39.52 ± 17.64 while for midazolam the mean age of subjects was 37.00 ± 15.58 (p>0.05)
RESULTS
Var iables propofol propofol midazolam midazolam Mean Median Mean Median
MAP
Pre procedure 94.45 (9.88) 94.50
94.66 (10.31) 93.30
Intra procedure
82.00 (8.70) 81.65
83.84 (12.27) 85.00
Post procedure
87.76 (9.41) 86.70
87.73 (12.44) 86.70
MAP dropped for both drugsBUT p>0.05MAP improved post proceduresPrior to discharge
Respiratory rate increased slightlyIntraprocedure and normalizedpost procedure (Both drugs)(P=0.106)
RESULTS
Var iables propofol propofol midazolam midazolam
Mean Median Mean Median
O2 Saturation
Pre procedure 99.90 100.00
99.85
100.00
Intra procedure 99.80 100.00
99.05
100.00
Post procedure 99.90 100.00
99.80
100.00
Var iables propofol propofol midazolam midazolam
Mean Median Mean Median
ETCO2
Pre procedure 36.05
38.50
34.45
36.00
Intra procedure 37.80
38.00
35.05
39.50
Post procedure 36.75
38.00
36.70
39.00
No significant dropped in O2 Saturationfor both drugs
No significant change in ETCO2
RESULTS Median (iqr)
kruska-wallis ( chi-square) P- value
Systolic Pre-procedure 130 (120,140) 0.172 0.679
Intra procedure 120 (110,120) 0.746 0.388 Post procedure 120 (110,130) 0.263 0.608
Diastolic Pre-procedure 75 (70,80) 0.118 0.731
Intra procedure 65 (60,70) 0.028 0.868
Post procedure 70 (60, 78.75) 0.001 0.989 MAP Pre-procedure 93.3 (87.1,100.0) 0.089 0.765
Intra procedure 84.1 (76.7,89.2) 0.106 0.744
Post procedure 86.7 (80.0,92.7) 0.116 0.733 Heart rate Pre-procedure 80.0 (75.0,99.25) 0.156 0.693
Intra procedure 80.0 (65.0,88.75) 0.067 0.795
Post procedure 80.0 (65.0,85.0) 0.982 0.322
Median (iqr) kruska-wallis ( chi-square) P- value
Oxygen saturation Pre-procedure 100.0 (100,100) 0.317 0.574
Intra procedure 100.0 (100,100) 3.034 0.082 Post procedure 100.0 (100,100) 0.351 0.554
Resp. rate Pre-procedure 18.5 (16.0,22.0) 1.466 0.226
Intra procedure 20.0 (16.0,24.0) 2.608 0.106
Post procedure 20.0 (16.0,22.0) 1.537 0.215 EtCO2 Pre-procedure 37.5 (33.25,39.75) 0.343 0.558
Intra procedure 38.5 (34.0,40.75) 0.081 0.775
Post procedure 38.5 (35.0,40.0) 0.267 0.606
Decreased
Decreased
Decreased
Unchanged
Unchanged
Unchanged
Unchanged
BUT P>0.05
RESULTS
P r o p o f o l M i d a z o l a m
0 . 0 0
2 0 . 0 0
4 0 . 0 0
6 0 . 0 0
8 0 . 0 0
Mean duration regain full consciousness
P < 0 . 0 0 1
For the duration of regain full consciousness, the mean (sd) in propofol
was 29.25(11.03) while in midazolam, it was 71.75(60.64) with p value
<0.001.
DISCUSSIONDISCUSSION This study aimed to evaluate the safety profile and effectiveness between the two sedative-hynotics namely the propofol and midazolam which have been commonly used in patients undergoing procedural sedation
This trial which took 6 months to complete involved seventy (n=70) subjects who had fully consented to participate. There was no drop-out
This study was dominated by male subjects that make almost 80% of the sample. This follows the general trend: victims of trauma/soft tissue injury which predominates in male group
DISCUSSIONDISCUSSION As a whole this study did not show remarkable differences between the two drugs used namely propofol and midazolam (MAP, Respiratory rate, O2 sat.)
Both drugs did not cause any serious adverse side effects throughout the study such as hypoventilation, hypotension, apnea, hypoxia or allergy reaction
These findings were consistent and supported the study done by Gabopoulou et al. (2005) on procedural sedation using intravenous propofol for 48 patients undergoing elective orthopaedic surgery under regional blockade
Cheol H.P et al (2006) who conducted a randomized double blind comparative study using propofol alone and combined propofol and midazolam in colonoscopy have found that both propofol alone and combined propofol and midazolam are safe and effective
DISCUSSIONDISCUSSION This study has shown beyond any doubt that propofol is much more superior than midazolam in term of duration taken for patients to regain full consciousness after procedural sedation has been delivered
The shorter time taken to reverse a patient undergoing procedural sedation after a procedure had been completed may offer excellent indication to use propofol in the emergency setting (twice longer in midazolam group)
Based on RCT involving 96 patients, Riphau et al found that the mean recovery time was significantly better in patients who received propofol sedation than midazolam with the time taken to recover was reported to be 14 minutes versus 25 minutes with p value < 0.01
DISCUSSIONDISCUSSION This study utilized ETCO2 monitoring for early detection of respiratory/cardiovascular compromise state
In this study, the ETCO2 in propofol group did not show much variation between the pre and intra procedural readings
Similar finding for the midazolam group was noted
This is due to the fact the dose of both drugs used were safe to cause sedation without complications
Crespo AS. 1997, pointed out that capnography is capable of providing important data regarding cardiorespiratory & metabolic status & could replace the need to analyze ABG in the non invasive manner
DISCUSSIONDISCUSSION Dang K. (1998) has stressed the significance of unrecognized respiratory difficulty and hypoxeamia as a major factor to contribute morbidity and mortality among patients with procedural sedation in the ambulatory setting
Dang strongly recommended the use of capnography which has the ability to monitor and detect any evidence of respiratory compromise early with combined use of pulse oxymetry (Dang K. 1998).
CONCLUSIONCONCLUSION
This study has proven the null hypothesis, where there were no difference in the complications between the study drugs midazolam and proporfol during procedural sedation
Both propofol and midazolam given at the recommended doses are equally safe and effective in procedural sedation that is performed at the emergency department setting
Propofol has been found to shorten the recovery process after procedural sedation at the emergency department setting and is a drug of choice over midazolam
CONCLUSIONCONCLUSION Propofol could be recommended to be used in the emergency department for any procedural sedation if the emergency physicians are trained and familiar with the use of the drug
Capnography is a very important mean of monitoring and detecting End tidal carbon dioxide during procedural sedation
The procedural sedation should be carried out in a controlled environment i.e with the presence of monitoring and resuscitation equipment.
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