Erector Spinae Plane (ESP) Versus Paravertebral Nerve (PVB) Blockade for Acute Unilateral Rib Fracture Pain

NCT ID: NCT03540095

Last Updated: 2019-05-16

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 7 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-07-23
• Study Completion Date: 2019-05-07

Brief Summary

Continuous paravertebral analgesia and erector spinae plane blockade (ESP) are accepted techniques at University of Pittsburgh Medical Center (UPMC) for the management of thoracic pain following surgery and trauma. Recently, an increasing number of erector spinae plane blocks are being performed as it has been demonstrated in our institution and via case reports that they provide clinical effectiveness, but may have a better side-effect profile than the paravertebral nerve block. However, the relative efficacy of ESP and continuous paravertebral analgesia for patients with rib fractures remains to be established. This study will include 60 consecutive patients presenting to the UPMC Presbyterian Acute Interventional Perioperative Pain Service suffering from unilateral rib fractures and will be randomized to receive either nerve blocks via continuous paravertebral infusion or via erector spinae plane infusion. In addition, to treat breakthrough pain, the patients in both arms will receive multimodal adjunctive therapy per routine. Bupivicaine and ropivicaine are FDA approved for use in nerve block catheters. The primary outcome will be total opioid consumption in the first 3 days of nerve block. Secondary outcomes include highest visual analog pain score (VAS) with deep breathing and at rest, adverse events, and total number of nerve blocks. Other data points include time to readiness for discharge, and length of hospital stay.

Detailed Description

All interventions regarding the placement and management of ESP and paravertebral blocks in this study are consistent with existing standard of care practices at UPMC and utilize protocols that are already in use. In addition, by nature of being included in a research study, patients are likely to receive closer monitoring for side-effects.

Screening and enrollment: After approval by the institutional review board, all (American Society of Anesthesiology) ASA I-IV patients aged 18-85 years, weighing between 50 and 120 kg with unilateral rib fractures will be screened for enrollment. Sixty patients will be enrolled in this randomized prospective study with equal numbers in each arm of the trial. This study design is unblinded as we cannot blind patients nor observers as to the type of block performed (slightly different location). This is an accepted limitation of the study. No advertising will be used and no monetary compensation will be offered. The nature of the study, planned interventions, risks, benefits, and alternatives will be discussed in detail with the patients at the time of enrollment and prior to the patients' signing of a written consent form.

Randomization: Patients will be enrolled into one of the study groups on the day of consultation in an alternating fashion. The study groups are defined as: Group I: Erector Spinae Plane Block (ESP) 30 patients Group II: Paravertebral Block (PVB) 30 patients.

Day of Block: After written informed consent is confirmed, a research assistant will introduce the scoring system used for pain assessment (VAS), and demonstrate proper use of the incentive spirometer.

All nerve blocks will be performed by an experienced member of UPMC's pain management service. Both nerve blocks can take between 10-60 minutes to perform. They will either occur in the ICU or on a monitored medicine floor.

Paravertebral nerve block catheter placement and activation (PVB group only): Paravertebral catheters will be placed according to UPMC standard of care practices as outlined below: After an intravenous catheter has been established and standard monitors and oxygen applied, the patient will be placed in the sitting position. The patient will be administered appropriate sedation based on the discretion of the provider if needed to safely perform the procedure.

Paravertebral technique: With the patient in a sitting position, the point of needle entry will be marked on the skin corresponding to paravertebral catheter placement. The thoracic spine level will be at the anatomic level corresponding to the ribs fractured. The needle entry sites will be 2.5 cm lateral to the midpoint of the spinous process of the corresponding thoracic vertebrae. The area will be prepped and draped in a sterile fashion, and 1% lidocaine infiltrated subcutaneously at each point of anticipated needle entry. For each of the catheter placement, a sterile gauge Tuohy needle will be introduced with ultrasound guidance towards the paravertebral space. After final needle placement, a hanging drop technique will be used to assess for interpleural placement while the patient inhales and exhales deeply. Next 5 mL of ropivicaine 0.5% will be injected incrementally through each needle after negative aspiration under ultrasound visualization, followed by insertion of the nerve block catheter to a depth 5 cm beyond the tip of the needle. An additional 20 mL of ropivicaine 0.5% will then be injected in 5 mL increments with negative aspiration in between, through each catheter yielding a total activation dose of 25 ml of ropivicaine 0.5% via each catheter. The catheters will be secured with Steri-strips and a transparent occlusive dressing. Vital signs will be monitored at regular intervals until the procedure is complete.

Erector spinae catheter placement and activation (ESP group only): An erector spinae plane catheter will be placed according UPMC standard of care practices as outlined below: After an intravenous infusion has been established and standard monitors and oxygen applied, the patient will be placed in the sitting position. The patient will be administered appropriate sedation based on the discretion of the provider if needed to safely perform the procedure.

ESP technique: With the patient in a sitting position, the point of needle entry will be marked on the skin corresponding to the appropriate vertebral level relative to the rib fractures. The area will be prepared and draped in a sterile fashion, and 1% lidocaine infiltrated subcutaneously at the point of anticipated needle entry. A sterile Tuohy needle will be introduced and advanced towards the corresponding transverse process. Hydrodissection will ensure that the proper plane is located. Once the erector spinae musculature is separated from the rib, 25ml of ropivicaine 0.5% will be introduced into the plane under ultrasound guidance. A catheter will be placed to a depth 5 cm beyond the tip of the needle. The catheter will be secured with Steri-strips and a transparent occlusive dressing. Vital signs will be monitored at regular intervals until the procedure is completed.

Paravertebral infusions of Bupivicaine 0.0625% will be titrated to 12 ml/hr maximum for the patients in the paravertebral catheter group (Group PVB). Patients in the ESP group (ESP) will start a continuous infusion of Bupivicaine 0.0625% and titrate to 12 mL/hr maximum as needed for pain. The patients in both groups will also be given access to acetaminophen 1000 mg every 6 hours IV or PO if there is no contraindication. Other adjuncts such as gabapentin, celebrex, ketamine, and opioid analgesics may be adjusted by the physicians involved based on the patients clinical condition. A PCA may be required for opioid pain medication administration initially, and will be continued until the patient is able to tolerate oral pain medication. Additional pain relief is available via nurse-administered 3 mL boluses of 0.0625% bupivacaine via the catheter pumps.

Post nerve block anesthesia protocol: Once on the floors, additional pain relief is available via nurse-administered 3 mL boluses of Bupivicaine via the catheter pumps given no more than hourly. All patients will be assessed daily by members of the acute interventional perioperative pain service. The infusion rates via the paravertebral and ESP catheters may be adjusted at the discretion of the pain service up to a rate of 12 mL/hr on each side (standard infusion rate used at UPMC-Presbyterian). All paravertebral ESP catheters will be stopped and removed as tolerated by the patient or post-procedure day #5, whichever occurs first. Additional pain medication will be available to all patients per standard of care.

ICU (Intensive Care Unit): Patients will be admitted to an intensive care unit at the discretion of the emergency department. Patients who are intubated and sedated, and who are unable to participate medical decision making will not be accepted for this study. If a patient fits the inclusion criteria and is in the ICU, the nerve block will be placed and managed in the ICU as above for all other situations.

Data will be collected daily from the patients until the nerve block is removed or 5 days post-procedure, whichever comes first.

Discharge: The readiness for discharge will be determined by the primary team: This decision will likely include (1) return of respiratory function, (2) hemodynamic stability, (3) normothermia, (4) no clinical evidence of DVT/PE (Deep Vein Thrombosis/Pulmonary Embolism) which is untreated, (5) pain controlled by oral agents. In addition, actual length of hospital stay will be recorded. Nerve block will be performed and the catheters will be removed according to the ASRA (American Society of Regional Anesthesia and Pain Medicine) guidelines for regional anesthesia catheter placement and removal available on the ASRA website.

Conditions

Rib Fractures; Pain, Acute; Thoracic Injuries; Neuropathic Pain; Neuromuscular Blockade; Anesthesia, Local

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Erector Spinae Plane Block

The patients randomized to the Erector Spinae Plane Block arm will receive this nerve block at the level corresponding to the rib fractures. Ropivicaine 0.5% 25 mL will be used during the procedure for initiation of pain control. Bupivicaine 0.0625% will be used for continuous infusion of local anesthetic. It will be titrated to effect, at maximum 12 mL/hr. Bupivicaine 0.0625% 3mL will be given every hour as a bolus additionally.

Group Type: EXPERIMENTAL

Erector Spinae Plane Block

Intervention Type: DRUG

See arm description

Paravertebral Nerve Block

The patients randomized to the Paravertebral Nerve Block arm will receive this nerve block at the level corresponding to the rib fractures. Ropivicaine 0.5% 25 mL will be used during the procedure for initiation of pain control. Bupivicaine 0.0625% will be used for continuous infusion of local anesthetic. It will be titrated to effect, at maximum 12 mL/hr. Bupivicaine 0.0625% 3mL will be given every hour as a bolus additionally.

Group Type: EXPERIMENTAL

Paravertebral Nerve Block

Intervention Type: DRUG

See arm description

Interventions

Erector Spinae Plane Block

See arm description

Intervention Type: DRUG

Paravertebral Nerve Block

See arm description

Intervention Type: DRUG

Other Intervention Names

Ropivicaine 0.5%; Bupivicaine 0.0625%; Braun 18 Ga x 3.5 in TUOHY Epidural Needle; Braun 20 Ga CLOSED TIP CATHETER; Sonosite X-Porte portable ultrasound machine; Ropivicaine 0.5%; Bupivicaine 0.0625%; Braun 18 Ga x 3.5 in TUOHY Epidural Needle; Braun 20 Ga CLOSED TIP CATHETER; Sonosite X-Porte portable ultrasound machine

Eligibility Criteria

Inclusion Criteria

• Age between 18-85 years
• no contraindications to the placement of a paravertebral catheter or erector spinae plane catheter
• American Society of Anesthesiologists physical status between I-IV
• no chronic opioid use
• patients who are not expected to be on therapeutic anticoagulants post-procedurally
• no clopidogrel in last 48 hours
• no known allergies to any of the drugs/agents used study protocol
• no personal or family history of malignant hyperthermia
• not pregnant
• not having an altered mental status (oriented to place, person, or time)
• no comorbid condition(s) that in the judgment of the anesthesiologist, would preclude the patient from any aspect of the study. Comorbid conditions include bleeding disorders, thrombocytopenia, localized infection, sepsis, possibly abnormalities of the thoracic spine or paravertebral anatomy neoplastic mass occupying the paravertebral space, empyema, allergy to local anesthestic drug, increased intracranial pressure, severe uncorrected hypovolemia, fixed cardiac output states.

Exclusion Criteria

• Age younger than 18 years or older than 85 years
• any contraindication to the placement of a paravertebral or erector spinae catheters
• American Society of Anesthesiologists physical status V or greater
• chronic opioid use
• coagulation abnormalities or patients who are expected to be on therapeutic anticoagulants postprocedurally
• clopidogrel use within 48 hours
• allergy to any of the drugs/agents used study protocol
• personal or family history of malignant hyperthermia
• pregnancy
• having an altered mental status (not oriented to place, person, or time), (11) any comorbid condition that in the judgment of the anesthesiologist would preclude the patient from any aspect of the study
• patient refusal. Comorbid conditions include bleeding disorders, thrombocytopenia, localized infection, sepsis, possibly abnormalities of the thoracic spine or paravertebral anatomy neoplastic mass occupying the paravertebral space, empyema, allergy to local anesthetic drug, increased intracranial pressure, severe uncorrected hypovolemia, fixed cardiac output states.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Pittsburgh

OTHER

Sponsor Role: lead

Responsible Party

Samuel Goldstein

Anesthesia Resident

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Samuel Goldstein, MD

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

Locations

University of Pittsburgh Medical Center - Presbyterian Hospital

Pittsburgh, Pennsylvania, United States

Countries

United States

Other Identifiers

PRO18040578

Identifier Type: -

Identifier Source: org_study_id