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Erector Spina Plane Block Versus Deep Serratus Anterior Plane Block for Post Mastectomy Analgesia

Només els usuaris registrats poden traduir articles
Inicieu sessió / registreu-vos
L'enllaç es desa al porta-retalls
EstatCompletat
Patrocinadors
King Saud University

Paraules clau

Resum

Breast cancer surgery like Mastectomy and modified radical mastectomy are associated with significant postoperative pain, and management depends largely on patient controlled analgesia with intravenous Morphine or other opioids equivalents. Respiratory depression, Ileus, sedation, nausea and vomiting are some of the potential side effect of opioid treatment which prolonged hospital length of stay and increase the coast. Recent advance in ultrasound guided regional anesthesia has led to the development of two novel regional anesthesia techniques specific to chest wall analgesia; Erector spina plain block and Serratus anterior plain block, with its potential to reduce or eliminate the need for opioids to manage post-operative pain.

Descripció

Experimental: erector spinae plain block After giving general anesthesia, patient is positioned in lateral decubitus with the surgical side up, and prepping para-spinous area with antiseptic solution. Ultrasound high frequency linear transducer is positioned in a para-sagittal plane at the level of fifth thoracic vertebra. Scanning of interested structures from superficial to deep planes, Trapezius muscle, Rhomboid major muscle, Erector spina muscle and transverse process of fifth thoracic vertebra.

Comparator: serratus anterior plane block After giving general anesthesia, patient is positioned in lateral decubitus, with the surgical side up. The upper arm is abducted and elevated above the head level. Under sterile aseptic technique, a linear ultrasound transducer (6-15 MHz) is placed in a sagittal oblique plane over the fourth and fifth ribs at the mid-axillary line. The following muscles are identified overlying the fourth/ fifth rib: the latissimus dorsi (superficial) and serratus anterior muscle (deep) overlying the ribs.

Dates

Darrera verificació: 01/31/2020
Primer enviat: 07/06/2019
Inscripció estimada enviada: 09/26/2019
Publicat per primera vegada: 09/29/2019
Última actualització enviada: 02/28/2020
Publicació de l'última actualització: 03/02/2020
Data d'inici de l'estudi real: 07/06/2019
Data estimada de finalització primària: 02/01/2020
Data estimada de finalització de l’estudi: 02/25/2020

Condició o malaltia

MASTECTOMY

Intervenció / tractament

Procedure: ESPB GROUP

Procedure: SAPB group

Fase

-

Grups de braços

BraçIntervenció / tractament
Active Comparator: ESPB GROUP
Erector spina plane block group
Procedure: ESPB GROUP
After giving general anesthesia, patient is positioned in lateral decubitus with the surgical side up, An erector Spina plain block is performed with inserting block needle (Pajunk, Geisingen, Germany) in-plane under ultrasound control until needle tip hits the transverse process, a volume of 0.3 ml/kg of bupivacaine 0.25% (Marcaine, Astra Zeneca Pharmaceuticals) is injected. Pain management assessment and analgesic consumption will be provided through patient-controlled analgesia (PCA) for 24 hours. The PCA pump is programmed to deliver 1 mg morphine bolus per press with a lockout interval of 10 min. Pain scores will be measured using eleven points numerical rating scale NRS (0 to 10) and opioids consumption will be documented at 0, 1, 4, 8 and 24 hours. Time of admission to post-anesthesia care unit PACU is considered 0 hours. Any opioid equivalents given during the first 24 hours to manage breakthrough pain will be documented
Active Comparator: SAPB group
Deep Serratus anterior plane block group
Procedure: SAPB group
After giving general anesthesia, the patient is positioned in lateral decubitus, with the surgical side up. The upper arm is abducted and elevated above the head level. A block needle is introduced in-plane, targeting the plane deep to the serratus anterior muscle, and a bolus of 0.3 ml/kg bupivacaine 0.25% is injected through ultrasound guidance. Pain management assessment and analgesic consumption will be provided through patient-controlled analgesia PCA for 24 hours. The PCA pump is programmed to deliver 1 mg morphine bolus per press with a lockout interval of 10 min. Pain scores will be measured using eleven points numerical rating scale NRS (0 to 10), and opioids consumption will be documented at 0, 1, 4, 8 and 24 hours. Time of admission to PACU is considered 0 hours. Any opioid equivalents given during the first 24 hours to manage breakthrough pain will be documented

Criteris d'elegibilitat

Edats elegibles per estudiar 18 Years Per a 18 Years
Sexes elegibles per estudiarFemale
Accepta voluntaris saludables
Criteris

Inclusion Criteria:

- ASA I-III patients age 18 to 75 years undergoing unilateral breast surgery

Exclusion Criteria:

- Patients refusal

- History of amide local anesthetics allergy

- Alcohol or drug abuse

- Chronic opioid intake

- Language barriers

- Patient with psychiatric disorders

- Contraindications for regional anesthesia

- BMI > 40 Kg/m2

- Obstructive sleep apnea that preclude PCA opioids

Resultat

Mesures de resultats primaris

1. Cumulative Opioid consumption in the first 24 hours. [0 hours post- operative( 0 time is considered time to admission to post anesthesia care unit)]

Post- operative morphine consumption measured from patient controlled analgesia pump (PCA machine)

2. Cumulative Opioid consumption in the first 24 hours. [1 hour post-operative]

Post- operative morphine consumption measured from patient controlled analgesia pump (PCA machine)

3. Cumulative Opioid consumption in the first 24 hours. [4 hours post-operative]

Post- operative morphine consumption measured from patient controlled analgesia pump (PCA machine)

4. Cumulative Opioid consumption in the first 24 hours. [8 hours post-operative]

Post- operative morphine consumption measured from patient controlled analgesia pump (PCA machine)

5. Cumulative Opioid consumption in the first 24 hours. [24 hours post-operative]

Post- operative morphine consumption measured from patient controlled analgesia pump (PCA machine)

6. Post-operative pain intensity [pain at 0 hour, 0 time is considered time to admission to post anesthesia care unit]

pain intensity is measured by ( 11 point numerical scale from 0 to 10), where 0 is considered no pain, 10 is the worst pain

7. Post-operative pain intensity [pain at 1 hour post operative]

pain intensity is measured by ( 11 point numerical scale from 0 to 10), where 0 is considered no pain, 10 is the worst pain

8. Post-operative pain intensity [pain at 4 hours post operative]

pain intensity is measured by ( 11 point numerical scale from 0 to 10), where 0 is considered no pain, 10 is the worst pain

9. Post-operative pain intensity [pain at 8 hours post operative]

pain intensity is measured by ( 11 point numerical scale from 0 to 10), where 0 is considered no pain, 10 is the worst pain

10. Post-operative pain intensity [pain at 24 hours post operative]

pain intensity is measured by ( 11 point numerical scale from 0 to 10), where 0 is considered no pain, 10 is the worst pain

Mesures de resultats secundaris

1. Time to patient mobilization [First 24 hours post operative( 0 time is considered time to admission to post anesthesia care unit)]

Recording first time patient is able to mobilize without assistance

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