The study is randomized, controlled, double blinded trial and conducted in Cairo
university hospital after approval of departmental and institutional research ethics
committee. Written informed consent will be obtained from all participants. Randomization
will be achieved using a computer-generated sequence. Concealment will be achieved using
opaque envelopes.
On arrival of the patients to operating room, patients will be secured with 20 gauge
intravenous cannula. Monitoring will include ECG, non-invasive arterial blood pressure
(NIBP), and pulse oximetry (SpO2). Before receiving general anesthesia, patients will be
randomly assigned into one of the two study groups; EOI block Group and ESPB Group.
Induction of general anesthesia will be induced with patients in ramped position and
after adequate preoxygenation using 1 µg/kg fentanyl (based on lean body weight), 2 mg/kg
propofol (based on total body weight), and 0.5 mg/kg atracurium (based on the ideal body
weight), in addition to 8mg IV dexamethasone for prevention of postoperative nausea &
vomiting. Endotracheal intubation will be established. Anesthesia will be maintained by
1.2% MAC of isoflurane with oxygen (50%) in air and 0.1 mg/kg of atracurium will be
administered every 20 minutes as maintenance anesthetic drugs. Volume-controlled
ventilation will be maintained with a tidal volume of 6 mL/kg of ideal body weight and
the respiratory rate will be adapted to maintain ET CO2 between 30 and 40 mmHg, and a 10
cmH2O positive end-expiratory pressure (PEEP) will be applied in all patients. Monitoring
through ECG, NIBP, pulse oximetry and capnography (ETCO2) continued throughout the
surgeries.
US (Siemens ACUSON X300 Ultrasound System) guided blocks will be administered immediately
after the induction of anesthesia and prior to surgical incision by consultant
anesthesiologists who had experience in regional anesthesia and were familiar with the
EOI and ESPB blocks.
EOI block Group (n=25): this group will receive bilateral ultrasound-guided external
oblique intercostal block.
The technique of ultrasound-guided EOI block will be performed with the patient in supine
position. A linear ultrasound probe (4-12MHz) will be placed paramedian sagittal
orientation between the midclavicular and anterior axillary lines at the level of sixth
rib, visualizing the external oblique and intercostal muscles. Local anesthetics inject
the under the external oblique muscle.
A 22-gauge needle will be advanced in-plane superomedial-to-inferolateral direction, into
the fascial plane between the external oblique and intercostal muscles at the caudal end
of the sixth rib and between the sixth and seventh ribs. The location of the needle tip
will be confirmed by hydrodissection of inter-fascial planes by 3 ml of normal saline.
After negative aspiration, a total of 20 mL bupivacaine 0.25% will be injected in the
fascial plane incrementally, aspirating every 5 ml and the block will be repeated on the
other side.
ESPB Group (n=25): this group will receive bilateral ultrasound-guided erector spinae
plane block The technique of ultrasound-guided ESPB will be performed with the patient in
lateral position. A curvilinear ultrasound probe (5-7 MHz) will be placed transversely to
identify tip of T9 transverse process 2.5-3 cm from midline then it will be rotated
longitudinally to get a parasagittal view visualizing the transverse process as a
hyperechoic curvilinear structure with prominent finger-like acoustic shadowing beneath
(the trident sign), with lamina (sawtooth pattern), spinous process, and costochondral
junction medially and laterally. The erector spinae muscles are identified superficial to
the tip of the T9 transverse process. A 22-gauge needle will be advanced in-plane
craniocaudally into the fascial plane deep to erector spinae muscle. The location of the
needle tip will be confirmed by hydrodissection of erector spinae muscle from tip of
transverse process by 3 ml of normal saline. After negative aspiration, a total of 20 mL
bupivacaine 0.25% will be injected under the fascial plane incrementally, aspirating
every 5 ml and the block will be repeated on the other side.
To achieve double blinding, patients will receive the block with 40 mL bupivacaine
(0.25%) by the anesthetist. Another doctor not involved in the block procedure will
evaluate the patients intraoperative and postoperative.
Intraoperative inadequate analgesia, indicated by increase of HR or MAP more than 20%
above preinduction baseline values, will be managed using incremental 50 microgram doses
of fentanyl. Intraoperative fentanyl consumption will be calculated. All patients will
receive 10 minutes before the end of surgery 1 mg granisetron or 4 mg ondansetron IV for
antiemetic prophylaxis and ketorolac 30mg IV and paracetamol 1g for postoperative
analgesia. At the end of surgery, muscle relaxant will be reversed using neostigmine 0.05
mg/kg and atropine 0.02 mg/kg. Awake extubation will be established after adequate
reversal of neuromuscular block.
Patients will be transported to PACU and placed in the semi-sitting position, and oxygen
will be given via a nonrebreathing facemask with a reservoir bag. Postoperative pain will
be assessed using VAS (where 0 corresponds to no pain and 100 mm to the worst pain) at 2,
4, 6, 12, 18, and 24 hours postoperatively.
Postoperatively, all patients will receive 1 g paracetamol every 6 h, 30 mg ketorolac
every 12 h.
IV morphine titration will be carried out at patient wake-up to achieve pain control (VAS
≤ 30mm) by an attending anesthesiologist blinded to group allocation. Patients with a VAS
score of ≥ 40mm and patients who will request rescue analgesia will be treated with IV
morphine in 2 mg increments every 5 minutes with no upper limit for the total
administered dose and total morphine consumption will be recorded. If the patient
appeared sedated (Ramsay sedation scale > 2), and/or severe morphine-related side effects
are encountered including respiratory depression (Spo2 < 95% and/or respiratory rate < 12
breaths/min), allergic reaction, hypotension, or severe pruritus, morphine titration will
be stopped and the patient will be excluded from the study.