Overview

The "promise" was that video-assisted thoracoscopic surgery (VATS) would be associated with less severe pulmonary impairment and less acute post-operative pain compared to open thoracotomy. However, VATS can cause moderate to severe post-operative pain in a significant number of patients and the reason for this is not well understood. In addition it has been found that post-surgical pain can be a strong predictor for the development of chronic pain. Inadequate control of acute pain not only causes serious discomfort and significant respiratory problems, but it may place this population of patients at greater risk of chronic pain and prescription opioid dependence.

Current protocols to manage and/or reduce VATS associated pain include combining the use of regional anesthesia techniques with opioid and non-opioid analgesics. Recent studies have investigated the efficacy of intercostal blocks using liposomal bupivacaine after thoracic surgery. However, these studies lacked an active comparator population of patients.

The study is designed as a prospective randomized study evaluating intercostal blocks using liposomal bupivacaine. The control population of patients will be treated with a paravertebral block using plain bupivacaine.

Principal investigator

Eligibility criteria

Inclusion Criteria:
*  Age over 18 years and less than 80 years
*  Undergoing video-assisted thoracoscopic surgery (VATS) procedure
*  BMI less than 40

Exclusion Criteria:
*  Unable to provide informed consent
*  Non-English speaking
*  Pregnant
*  BMI greater than 40
*  Video-assisted thoracoscopic surgery pleurodesis subjects
*  Patients with pre-existing chronic pain
*  Opioid tolerance
*  Pain syndromes including fibromyalgia, regional pain syndrome or post therapeutic neuralgia in a thoracic distribution
*  Allergy to the study medication
*  Patients with infectious disease
*  Patients with impaired coagulation
*  Severe hepatic disease
*  Incarcerated
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For Referring Providers

Do you have a patient you think would be a good candidate for this trial? Learn more about enrolling your patient.

Contact the study coordinator

Nada Sadek
Not currently recruiting, contact if interested.