Distant Extrafascial Injection vs Subfascial Injection for Interscalene Block: Acute Pain Outcomes and Rates of Complications

Postoperative Analgesia Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02074397
• Other study ID #: CHUV-465/13
• Status: Completed
• Phase: N/A
• Start date: February 2014
• Est. completion date: April 2015

Study information

• Verified date: February 2020
• Source: Centre Hospitalier Universitaire Vaudois
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this randomized controlled trial is to compare the analgesic efficacy and the safety profile between two techniques of injection for the interscalene block. The interscalene block consists of injecting local anesthetic around the cervical roots of the brachial plexus and allows analgesia after shoulder surgery.

Stated differently, the dual objective of that study is:

1. to confirm that an injection at a distance of 4 mm away from the lateral sheath of the plexus (distal injection) provides similar analgesia as a classical injection within the plexus (subfascial injection);

2. to demonstrate that a distant extrafascial injection produces less respiratory complications than a subfascial injection, defined as hemidiaphragmatic paresis.

Description:

This is a prospective randomized controlled double-blinded trial on patients undergoing shoulder surgery (shoulder arthroscopy or open shoulder surgery), aged between 18 and 85 years old.

The exclusion criteria will be contraindications to brachial plexus block (e.g., allergy to local anesthetics, coagulopathy, malignancy or infection in the area); existing neurological deficit in the area to be blocked; severe respiratory disease; inability to understand the informed consent and patient refusal.

Prior to the procedure, all patients will be fully informed about the risks and benefits of participating in the study and written informed consent will be obtained.

Interscalene brachial plexus block will be performed with the patient lying lateral on the non-operative side, following our routine clinical practice, with twenty milliliters of local anesthetic containing bupivacaine 0.5% with 1:200,000 epinephrine. For patients in the subfascial injection group, the needle tip will be positioned lateral to the brachial plexus at a distance of 4 mm, measured with a caliper.

Block assessment and definition of a successful block Evaluation of sensory and motor blockades will be performed by a blinded research assistant every 5 min, for a total of 30 min, after local anesthetic (LA) injection. Sensory block and motor blockades will be tested in the C4, C5, C6, C7, and C8 dermatomes using a blunt tip needle pinprick test and muscular testing. A successful block will be defined as complete sensory and motor blockade in the distribution of the C5 and C6 nerve roots within 30 minutes of performing the ISB. In cases of a failed block, the ISB will be repeated at the discretion of the attending anesthesiologist and these patients will be excluded from the intraoperative and postoperative secondary outcome analyses.

Definition of hemidiaphragmatic paresis Diaphragmatic movement will be assessed by real-time M-mode ultrasonography on each side using a curvilinear 2 - 5 MHz US probe, following previous published descriptions [16]. Patients will be examined in the lying position. The presence of paradoxical cephalad movement will represent a hemidiaphragmatic paresis.

Assessment of the ventilatory function (pulmonary function tests) A bedside spirometer (EasyOneTM Spirometer; ndd Medical Technologies, Andover, UK) will be used to assess ventilatory function. After instructions, the full vital capacity (VC) in supine and sitting upright positions will be measured. The percent fall of vital capacity from sitting to supine position will be considered as an index of diaphragmatic dysfunction.

Intraoperative and postoperative procedure After application of routine monitors in the operating theatre, patients will receive a standardized general anesthetic. Following surgery, pain (Numeric rating scale [NRS] ≥ 4 or patient request for analgesia) will be treated with morphine 2 mg every 10 min as needed, in the postanesthetic recovery unit. On the ward, patients will receive oxycodone 5-10 mg per os every 2 hours as needed and acetaminophen 1000 mg per os every 6 h for pain. All these managements represent the current standard of care at Centre Hospitalier Universitaire Vaudois.

Outcomes

The dual primary outcomes will be:

• The rate of successful block defined as above;

• The rate of hemidiaphragmatic paresis 30 minutes after completion of the block.

Secondary outcomes will include presence of paresthesia during the procedure; pain scores (NRS out of 10) upon arrival in PACU, and at 2 hours postoperatively; postoperative morphine consumption in PACU; duration of analgesia; and total consumption of oxycodone during the first 24 postoperative hours.

Finally, the blinded research assistant will contact the patients on day 7 by telephone to record post block complications such as persistent paresthesia and limb weakness.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: April 2015
• Est. primary completion date: April 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

• ASA (American Society of Anesthesiology) physical status I-II

• 18 - 85 years of age

• surgery less than 3 hours

Exclusion Criteria:

• indication for continuous interscalene block (catheters)

• contraindications for brachial plexus block (eg allergy to local anesthetics, coagulopathy, malignancy or infection in the area)

• existing neurological deficit in the area to be blocked

• history of neck surgery or radiotherapy

Related Conditions & MeSH terms

• Interscalene Block
• Postoperative Analgesia
• Respiratory Function
• Shoulder Surgery
• Ultrasound-guided Regional Anesthesia

Intervention

Procedure:
• Distant extrafascial injection

• Subfascial injection

Locations

Country	Name	City	State
Switzerland	CHUV (Centre Hospitalier Universitaire Vaudois)	Lausanne	Vaud

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire Vaudois

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of success block defined as complete motor and sensory block on C5-C6 territories		30 minutes after block procedure
Primary	Rate of hemidiaphragmatic paresis, assessed with the ultrasound		30 minutes after block procedure