Pain Management & Medicine
Pain Management & Medicine
Pain Management & Medicine
Me
Journa
dicine
Pain Management & Medicine
Research Article OMICS International
Abstract
Background: Major upper gastrointestinal cancer surgeries induce postoperative pain, that if not controlled may
cause various organ dysfunctions and prolonged hospital and ICU stay. Thus an appropriate pain therapy to those
patients must be applicated.
Objective: To compares the effects of continuous perioperative thoracic epidural Fentanyl-bupivacaine infusion
versus continuous perioperative Fentanyl intravenous infusion in patients undergoing major upper gastrointestinal
cancer surgery.
Methods: 60 patients (ASA II) of either sex were scheduled for elective upper gastrointestinal cancer surgeries.
Patients were allocated randomly into two groups (30 patients each) to receive: continuous peri-operative epidural
infusion with bupivacaine 0.132 and fentanyl (TEA group), or continuous peri-operative intravenous infusion with
fentanyl (control group). Postoperative pain was assessed over 72 h using visual analogue scale (VAS). The intra
and post-operative haemodynamic, sedation score and overall patient fentanyl consumption were recorded. Any
concomitant events like nausea; vomiting, pruritus or respiratory complications were recorded postoperatively.
Results: There was a significant decrease in pain sensation in TEA group during first day postoperative. Patient
haemodynamics was significantly decreased in TEA group. As regard sedation scale, patients of the TEA group were
significantly less sedated than control group at immediate postoperative only.
Conclusion: Continuous perioperative thoracic epidural Fentanyl-bupivacaine infusion was much better in
pain relief, less sedating effect and shorter duration of hospital and ICU stay than continuous perioperative fentanyl
intravenous infusion in patients undergoing major upper gastrointestinal cancer surgery.
Keywords: Thoracic epidural analgesia; Major Upper gastrointestinal However, TEA is occasionally contra indicated and may also lead
cancer surgeries; Postoperative pain; VAS scale to serious risks as, high incidence of failure rate, premature catheter
dislodgement, motor block involving lower limbs preventing early
Introduction mobilization of patient and hypotension with risk of hypervolemia
or prolonged use of vasopressors [7]. Also TEA may cause rare but
Recent estimates indicate that millions of major surgical procedures
serious a neurologic complications (hematoma, abscess and paraplegia)
are performed worldwide each year and patients undergoing
[8]. This study compares the effects of continuous perioperative
gastrointestinal surgery for malignancy are typical representatives of
thoracic epidural Fentanyl-bupivacaine infusion versus continuous
such high-risk patients [1]. Major abdominal surgeries induce neuro-
perioperative Fentanyl intravenous infusion in patients undergoing
hormonal changes responsible for postoperative pain, various organ major upper gastrointestinal cancer surgery.
dysfunctions and prolonged hospitalization. Inadequate pain control is
harmful and costly thus an appropriate pain therapy must be used to Patients and Methods
those patients (Table 1) [2]. Some of the main complications of under
This prospective randomized study was approved by the local ethics
controlled postoperative pain are cardio-circulatory complications like
committee of the South Egypt Cancer Institute, Assiut University,
tachycardia, hypertension, increase of cardiac output, increase of heart
work and dysrhythmias, increasing the risk of ischemia or myocardial
infarction in the postoperative period [3]. The presence of high-quality
*Corresponding author: Elzohry AAM, Department of Anesthesia, ICU and Pain
analgesia in the postoperative period is very important, to relieve post- Relief, South Egypt Cancer Institute, Assiut University, Egypt, Tel: 20 0106190556;
surgical pain and improve well-being, and also because inadequate pain E-mail: [email protected]
control may increase morbidity, lead to prolonged hospital stays, and Received February 15, 2018; Accepted February 19, 2018; Published February
increase medical costs [4]. 23, 2018
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10 to 30 breaths/min, PaO2/IFO2 ≥ 80/0.4, PaCO2, 30 to 45 mmHg). mixture with lockout interval of 20 min. The analgesic regimen was
Intra operative analgesia in control group: Intra operative analgesia: By adjusted to achieve a visual analog scale score ˂3.
continuous intravenous fentanyl infusion 1 μg g/kg/hr intra operatively
Intra operative data collection includes (MAP, HR, and duration of
along with a bolus dose of fentanyl 0.5 μg/kg to maintain heart rate (HR)
anaesthesia and surgery) (Figures 3 and 4).
and blood pressure within 20% of the basal value. Rescue analgesia of
0.5 μg/g/kg was given. Fentanyl infusion was continued until shifting Post-operative all patients were admitted to surgical ICU and beside
the patient to ICU (Figure 2). routine follow up, the following were recorded:
Intra operative analgesia in TEA group: By slowly injection of • Sedation was assessed one day postoperatively by 5 points
epidural bolus dose of 0.1 ml/kg of 0.125% bupivacaine/Fentanyl 10 µg/ Sedation score (at the same time intervals of VAS) as follows
ml. After a negative response to test dose-was administered, epidural 0=aware, 1=drowsy, 2=asleep/easily respond to verbal command,
were considered to be adequately working if there is decreased pin prick 3=asleep/difficulty responding to verbal command, 4=asleep/no
sensation at the expected dermatomal level, decreased blood pressure respond to verbal command (Table 3).
from its basal level and absence of stress response to surgical incision.
• HR, MAP and were recorded every one hour in ICU.
Then, the bolus dose is followed by continuous infusion of 0.1 ml/kg of
0.125% bupivacaine/Fentanyl 8 µg/ml until the end of surgery guided • Any concomitant events like nausea; vomiting, pruritus or
by patient hemodynamic. All patients were transmitted post-operative respiratory depression (decrease oxygen saturation ≥ 90%) were
ICU. recorded postoperatively
Thoracic epidural catheter • Duration of hospital and ICU (Table 4).
Under strict aseptic precautions thoracic epidural was performed • Visual analogue scale- every 4 hours for 3 days-for pain
using a 16 gauge Tuhy epidural needle by a paramedian approach. T7- measurement. And total doses of Fentanyl consumption (both
T8 or T8-T9 interspace was chosen for the injection (with air) after skin intra and post-operative) were calculated (Table 5).
wheal of lidocaine local anesthetic 2%. The catheter was introduced
approximately 4 cm into the epidural space. The epidural space was 100
identified by the loss of resistance technique. A 3 ml test dose of 2% p value of mean HR=0.247
Lidocaine with 1: 200,000 Adrenaline was given after the placement of 90
the epidural catheter.
Patient-controlled I.V analgesia 80
Mean+SD
Control
Using Fentanyl 10 μg/ml solutions through PCA device that 70
TEA
programmed to give a bolus dose 2 ml/dose with a minimal lockout
interval of 10 min with no background infusion. The analgesic regimen 60
was adjusted to achieve a visual analog scale score ˂3.
Patient-controlled epidural analgesia 50
Day1 Day2 Day3
In the PCEA group, postoperative pain treatment was achieved by Post-operative MAP
background epidural infusion of 0.1 ml/kg/h of the mixture 1.25 mg/ Figure 3: Post-operative MAP.
ml bupivacaine plus 5 μg/ml Fentanyl, and 3 ml as top up dose of this Data are expressed as mean ± SD, TEA: Thoracic Epidural Analgesia Group,
MAP: Mean Arterial Pressure. P. value<0.05 considered statistically significant.
Between two groups there was no significant difference regarding patient's
post-operative MAP.
120
p value of mean HR=0.016*
100 90
p value of mean HR=0.148
80 85
Mean+SD
80
60
Mean+SD
Control
TEA 75
Control
40
70 TEA
20
65
0 60
0h 1h 2h 3h 4h 5h Mean Day1 Day2 Day3
Intraoperative HR Post-operative HR
Figure 2: Intraoperative Heart Rate. Figure 4: Post-operative HR.
Data are expressed as mean ± SD, TEA: Thoracic Epidural Analgesia Group; Data are expressed as mean ± SD, TEA: Thoracic Epidural Analgesia Group,
H.R.: Heart Rate. P. value <0.05 considered statistically significant. Between H.R: Heart Rate. P. value <0.05 considered statistically significant. Between
two groups there was significant difference regarding patient's Intraoperative two groups there was significant difference regarding patient's post-operative
H.R. H.R.
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Post-operative Control (n=30) TEA (n=30) P analgesia was better and sedation scores were significantly decreased
sedation score Range Mean ± SD Range Mean ± SD value especially at immediate postoperative period in patients of the TEA
0h (2–1) 2 (1–1) 1 0.00* group in comparison to control group. We believe in the concept of
4h (2–1) 2 (1–1) 1 0.00* preemptive analgesia which is to prevent altered sensory processing.
8h (2–1) 2 (1–1) 1 0.956 Therefore we started our pain control strategy in intraoperative period;
12 h (1–1) 1 (1–1) 1 0.943 preemptive may not simply mean “before incision” An insufficient
16 h (1–1) 1 (1–1) 1 0.948 afferent blockade cannot be preemptive, even if it is administered before
20 h (1–1) 1 (1–1) 1 0.943 the incision [10]. PCA is considered one of best methods in controlling
24 h (1–1) 1 (1–1) 1 0.956 pain and can be used either intravenously or epidural. Advantages
Table 3: Post-operative sedation score.
of PCA over conventional pain management are that the therapy is
Data are expressed as mean ± SD, TEA: Thoracic Epidural Analgesia Group, P individualized to the patient. Patients are the best to assess their pain
value<0.05 considered statistically significant. and they can get medication as and when required by pressing a button of
PCA pump. Thus it reduces overdose and also reduces nursing aid [11].
Control (n=30) TEA (n=30) P. value
No complication 17(56.7%) 24(80%) 0.319 We used in this study PCEA using both bupivacaine and fentanyl
Vomiting 3 (10%) 0(0%) 0.383 because Epidural LA drugs administered alone have never become
Pruritus 2 (6.6%) 0(0%) 0.059 widely used for routine postoperative analgesia because of the
Respiratory depression 4 (13%) 1(3.3%) 0.798 significant failure rate resulting from regression of the sensory block and
Bradycardia 4 (13%) 5(16.7%) 0.178 the unacceptable incidence of motor blockade and hypotension [12].
Table 4: Post-operative complication. Consistent with us, Mann et al, who compared the effectiveness
Data are expressed as mean ± SD, TEA: Thoracic Epidural Analgesia Group, P. on postoperative pain and safety of PCEA and intravenous PCA after
value<0.05 considered statistically significant. There was no significant difference
between two groups. major abdominal surgery, they found pain relief was better at rest and
after coughing in the PCEA group during the five postoperative days
Control (n=30) TEA (n=30) P. [13]. And in the study done by Behera et al, the number of patients with
Range Mean ± SD Range Mean ± SD value analgesic failure was significantly less in PCEA group as compared to IV
ICU STAY 03-Nov 7.47 ± 2.16 03-Aug 5.6 ± 1.57 0.000* PCA group [14]. Moreover a study performed on patients undergoing
Hospital stay Mar-31 22.13 ± 7.62 Oct-25 18.13 ± 4.12 0.014* upper abdominal surgery; despite the infusion of bupivacaine 37.5
Post op. ± 50 mg/h via a thoracic epidural 30% of patient's required opioid
Fentanyl 753.33 ± supplementation for inadequate analgesia and 80% had significant
1200-2000 1646.67 ± 234.5 600-1000 0.000*
(mic/72h) 122.43
consumption hypotension [15]. So, opioids must be added either morphine or
Intra op. fentanyl and our choice of fentanyl based on the higher lipophilicity of
Fentanyl fentanyl that makes it shorter duration of action, lower incidence of side
280-480 384.8 ± 92.5 65.6-120 80.9 ± 22 0.000*
(mic/72h) effects, and reduced risk of respiratory depression [16].
consumption
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