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The aim of this study is to compare the analgesic effect and safety of Modified Pectoral Nerve Block and Transverse thoracic plane block versus Erector Supine plane Block in cases undergoing modified radical mastectomy (MRM).
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The aim of this study is to compare the analgesic effect and safety of Modified Pectoral Nerve Block and Transverse thoracic plane block versus Erector Supine plane Block in cases undergoing modified radical mastectomy (MRM).
Primary outcome: The Nalbuphine consumption in the first 24 hours post-operative.
Secondary outcome Severity of pain will be recorded through the Visual Analogue Scale (VAS) on arrival to PACU (T0) then at 4, 8, 12, 16, 20, and 24hr postoperatively.
• Study Population: Adult female patients,aged 25-65 years undergoing modified radical mastectomy will be assigned into two equal groups using simple randomization computer generated method.
Inclusion Criteria:
Exclusion Criteria:
Sampling Method:
Simple randomization computer guaranteed. Patients will be divided into 2 groups via sealed envelopes randomly distributed to them and will be enrolled into group A, group B.
-Sample Size: After reviewing previous study results (Abedalmohsen and Bakri, 2024) showing that among patients underwent modified radical mastectomy, the morphine consumption (mg) in postoperative follow up period was lower in patients received erector spinae plane block than in patients received erector spinae plane block (0.93 + 0.63 versus 2.13 + 0.42 respectively); a sample size of at least 40 adult female patients undergoing modified radical mastectomy divided randomly into 2 groups (20 patients in each group) will achieve 100% power, at significance level 0.05, by using Power Analysis and Sample Size Software (PASS 15) (Version 15.0.10) for sample size calculation.
Preoperative settings:
After history taking and clinical examination, routine preoperative investigations will be done to all patients including:
Intraoperative settings:
After completion of surgery and before extubation:
Group A:
All blocks will be performed by an experienced anesthetist.
US-guided PECSII block will be done on the same side of surgery with the patient lying in the supine position and the ipsilateral arm will be abducted and externally rotated, and the elbow flexed 90°.(Sonosite turbo M, Bothell, Washington, USA) and linear ultrasound probe(2.5-7.5MHZ) Transduser will be put in the ipsilateral para median sagittal plane in order to identify the coracoid process. Then the transducer is rotated slightly to allow an in-plane needle trajectory from the proximal and medial side toward the lateral side (ie, the caudal border of the transducer is moved laterally, while the proximal border remains unchanged). This rotation helps image the pectoral branch of the thoracoacromial artery.
After identification of the Pectoralis major muscle, Pectoralis minor muscle, Serratus anterior muscle and the planes in between, the 1st injection will be in the plane between the Pectoralis minor muscle and the serratus anterior muscle. The needle (disposable spinal needle, K-3 point type LUER-Lock HUB 22G) will be advanced in an in-plane technique. Two mL of normal saline will be injected to confirm the location, produce hydro-dissection, and improve needle visualization. Afterward, 20 mL of bupivacaine, 0.25%, will be injected. During the withdrawal of the needle a 2nd injection will be done in the plane between the Pectoralis major muscle and the Pectoralis minor muscle. 2ml of normal saline will be injected to produce hydro-dissection and confirm the location. 10ml of Bupivicaine 0.25% will be injected (Bakeer et al., 2020).The TTPB, 10 ml bupivacaine 0.25% was injected between the deep transversus thoracic and the superficial internal inter-costal muscles para-sternal between the third and fourth left ribs under US guidance (Abedalmohsen, 2023).
GroupB:
The ESP block will be performed positioning the patient in the lateral decubitus position with probe placement in cranio cephalad orientation by identifying the spinous process in the upper thoracic area and subsequently transverse process by moving the probe laterally as an oval hyperechoic sonographic structure. In total, 20 ml of 0.25% bupivacaine will be deposited between the erector spinae muscle and transverse process using a Sono Plex Stim cannula (21G X 100 mm, Pajunk, Germany) with the in plane technique after hydro dissection and negative aspiration. The patient will be turned supine after block placement 1gm of paracetamol, 30mg of ketorolac and 1mg Granitryl will be given to all patients. The patient will then be transferred to recovery room for follow up.(Bakeer et al., 2020).
Postoperative settings:
In the first postoperative 24 hours, VAS score will be assessed at 0, 2 ,4, 8, 12, 16 and 24 hours postoperatively.
A dose of 5 mg Naluphin will be given if VAS score exceeded 3, to maintain a score less than 3, not to exceed 20 mg per dose. IV boluses of naluphin will be given as a rescue analgesia to maintain VAS ≤ 3,
. Paracetamol 1 gm IV infusion will be given every 8 hours and ketorolac 30 mg every 12 hours postoperatively (Stormholt et al., 2021).
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40 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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