Study of Opioid Use After Lumbar and Cervical Spine Surgery

Not Applicable

Completed

Brief Summary: The purpose of this project is to assess the impact of an educational video on the use of prescription opioid medication during a 6-month period following spine surgery. Subjects will be recruited from the pool of patients coming in for the pre-operative appointment prior to spine surgery. Patients that consent and enroll will be randomized to receive either a brief educational video at this appointment or usual care. Patients will be followed after surgery weekly for the first month, and then again at 6 months to determine their prescription opioid medication utilization patterns. Prescription data will also be pulled from electronic medical records.

Detailed Description: After consenting, meeting inclusion criteria, and enrollment, all participants will complete several standard self-report questionnaires related to medical history, social demographic, and psychosocial variables that are related to low back pain, and often used in clinics that manage patients with low back pain. They will then be randomized to either receive the education, or only usual care (which is the typical information the surgeon provides the patient verbally during the pre-operative appointment). All patients will receive the usual care education from their surgeon.

Education Group:

The educational video is a white board style patient-centric video. The content of the education focus on providing a historical perspective for opioid prescription from the time when the risk of dependence was highly underestimated. The video discusses the current evidence for the effect of opioid medications in non-cancer on-acute pain. It also discusses some of the dangers of long-term opioid usage.

All Subjects:

All subjects will receive the usual care education that is typically given by their surgeon. That will be left up to the discretion of each surgeon.

All patients will proceed with the surgical procedure as planned. Each week during the 1-month period after the surgery, patients will be contacted, and then again at 6 months to ask history of prescription opioid utilization.

Recruitment & Eligibility

Inclusion Criteria

Currently scheduled for a pre-operative appointment with an orthopaedic spine surgeon or neurosurgeon specifically for a lumbar surgery.
Surgery is taking place for a condition that has been ongoing for 6 months or longer (chronic)
Between the age of 18 - 65 years
Read and speak English well enough to understand the education, provide informed consent and follow study instructions

Exclusion Criteria

a. Known aversion or allergy that would prevent the patient from taking any opioid based pain medication

Arm && Interventions

Group	Intervention	Description
Educational Video	Educational Video	Evidence-based video: Best Advice for People Taking Opioid Medication

Primary Outcome Measures

Name	Time	Method
Number of Opioid Medication Prescriptions	12 months	Number of prescriptions within 12 months after surgery

Secondary Outcome Measures

Name	Time	Method
Numeric Pain Rating Scale (NPRS)	6 months	A 0-10 numeric pain rating scale ('0' indicating no pain, and '10' worst imaginable pain) will be used to assess pain intensity.
Modified Oswestry Disability Index (ODI) or Neck Disability Index (NDI)	6 months	The ODI and NDI are 10-item scales with higher numbers indicating greater disability. Each item has 6 possible questions (0-5), which are then summed and multiplied to provide a % score out of 100%. The ODI focused on low back pain and the NDI on neck pain. As values are on the same scale, they were entered as one outcome since we included both neck and low back pain patients. Patients undergoing cervical spine surgery filled out the NDI (Neck Disability Index) and patients undergoing lumbar spine surgery filled out the ODI (Oswestry Disability Index)