EBQ:SPACE Trial: Difference between revisions

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==Population Studied==
==Population Studied==
===Inclusion Criteria===
===Inclusion Criteria===
Eligible patients had chronic back pain or hip or knee osteoarthritis pain that was moderate to severe despite analgesic use. Chronic pain was defined as pain nearly every day for 6 months or more. Moderate or greater severity was defined by a score of 5 or more on the 3-item pain intensity, interference with enjoyment of life, and interference with general activity (PEG) scale (range, 0-10).
*Back pain or knee or hip pain associated with osteoarthritis
*Pain occurring almost every day for ≥6 months despite non-opioid analgesic use
*Brief Pain Inventory (BPI) scale average pain ≥5 and BPI interference score ≥5
===Exclusion Criteria===
===Exclusion Criteria===
Patients on long-term opioid therapy were excluded. Other reasons for exclusion included contraindications to all drug classes in either group, including class-level opioid contraindications (eg, active substance use disorder), and conditions that could interfere with outcome assessment (eg, life expectancy <12 months). Patients with severe depression or posttraumatic stress disorder symptoms were not excluded because these patients often receive opioids in practice.
*Severe mental illnesses
*Moderate severe cognitive function
*Planned surgery to address pain in the next year
*Long term opioid treatment
*Contraindications to study medications
*Life expectancy <12 months
===Baseline Characteristics===
===Baseline Characteristics===
*Demographics: Mean age 57 years, 13% female, 88% white, 6% black, 6% other ethnicity, higher education 24%
*Employment: Employed 42%, self-employed 6%, retired 36%
*Pain eligibility: Back pain 65%, Hip/knee osteoarthritis pain 35%
*Smoker 21%, hazardous alcohol use (AUDIT Score ≥8) 3%, illicit drug use in prior year 7%
*Mental Health: Moderate depression 23%, Moderate anxiety 9%, PTSD 21%
==Interventions==
==Interventions==
Participants were randomized to a group in and received stepwise approach to management of pain:
*Opioid Group - Titrated to maximum of 100 morphine-equivalent mg:
*#Morphine IR, hydrocodone/acetaminophen, oxycodone IR
*#Morphine sustained release, oxycodone sustained release
*#Transdermal fentanyl
*Non-opioid
*#Acetaminophen and NSAIDs
*#Adjuvant oral medications (nortriptyline, amitriptyline, gabapentin), topical analgesics (capsaicin, lidocaine)
*#Drugs requiring pre-authorization in VA system (pregabalin, duloxetine, tramadol)
==Outcomes/Results==
==Outcomes/Results==
===Primary Outcomes===
===Primary Outcomes===
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*The reported adverse events may not represent the highly concerning ones.
*The reported adverse events may not represent the highly concerning ones.
==Funding==
==Funding==
*Merit Review Award from the US Department of Veterans Affairs Health Services Research and Development Service
==See Also==
==See Also==
*[[Opioid Deprescribing]]
*[[Opioid Deprescribing]]


[[Category:EBQ]]
[[Category:EBQ]]

Revision as of 19:07, 26 April 2021

Krebs et al.. Effect of Opioid vs Nonopioid Medications on Pain-Related Function in Patients With Chronic Back Pain or Hip or Knee Osteoarthritis Pain: The SPACE Randomized Clinical Trial. JAMA 2018. 319:872-882. PMID: 29509867. DOI. Full Text.

Clinical Question

To compare opioid vs nonopioid medications over 12 months on pain-related function, pain intensity, and adverse effects in patients with moderate to severe chronic back or osteoarthritic hip/knee pain.

Bottom Line

In patients with severe back or hip/knee pain that weren't currently receiving opioid treatment, there was no difference between opioid vs. non-opioid treatment over 12 months with an escalating treatment-to-target approach. There may be more adverse events with opioid therapy.

Study Design

  • Pragmatic, single-centre, open label, randomized trial
  • N=240
    • Opioid (n=120)
    • Non-opioid (n=120)
  • Setting: 62 American primary care clinicians affiliated with the Veterans Affairs
  • Enrolment: June 2013 to December 2015
  • Mean follow-up: 12 months
  • Analysis: Intention-to-treat, masked outcome assessment.
  • Primary Outcome: Improvement in pain-related function assessed with the Brief Pain Inventory (BPI)

Population Studied

Inclusion Criteria

  • Back pain or knee or hip pain associated with osteoarthritis
  • Pain occurring almost every day for ≥6 months despite non-opioid analgesic use
  • Brief Pain Inventory (BPI) scale average pain ≥5 and BPI interference score ≥5

Exclusion Criteria

  • Severe mental illnesses
  • Moderate severe cognitive function
  • Planned surgery to address pain in the next year
  • Long term opioid treatment
  • Contraindications to study medications
  • Life expectancy <12 months

Baseline Characteristics

  • Demographics: Mean age 57 years, 13% female, 88% white, 6% black, 6% other ethnicity, higher education 24%
  • Employment: Employed 42%, self-employed 6%, retired 36%
  • Pain eligibility: Back pain 65%, Hip/knee osteoarthritis pain 35%
  • Smoker 21%, hazardous alcohol use (AUDIT Score ≥8) 3%, illicit drug use in prior year 7%
  • Mental Health: Moderate depression 23%, Moderate anxiety 9%, PTSD 21%

Interventions

Participants were randomized to a group in and received stepwise approach to management of pain:

  • Opioid Group - Titrated to maximum of 100 morphine-equivalent mg:
    1. Morphine IR, hydrocodone/acetaminophen, oxycodone IR
    2. Morphine sustained release, oxycodone sustained release
    3. Transdermal fentanyl
  • Non-opioid
    1. Acetaminophen and NSAIDs
    2. Adjuvant oral medications (nortriptyline, amitriptyline, gabapentin), topical analgesics (capsaicin, lidocaine)
    3. Drugs requiring pre-authorization in VA system (pregabalin, duloxetine, tramadol)

Outcomes/Results

Primary Outcomes

Secondary Outcomes

Adverse events

Discussion

This is a landmark study published in 2018 by Krebs et al - the SPACE study. It was a pragmatic randomised controlled trial comparing opioid versus non opioid analgesics for 12 months in primary care. Participants were 240 VA patients with moderate to severe chronic back pain or knee/hip OA, and not on opioids. The mean pain intensity initially was 5.4 in both arms. Pain scores at 1 year was worse in the opioid arm (4.0) than non opioid (3.5) (P=0.034). There was no difference in pain interference, and adverse effects were worse in opioid group (P=0.03).

Criticism

  • Unblinded
  • Patient self-reporting is an area of bias
  • The patients were veterans, and so this might limit the external validity
  • Patients using opioids already were excluded
  • The reported adverse events may not represent the highly concerning ones.

Funding

  • Merit Review Award from the US Department of Veterans Affairs Health Services Research and Development Service

See Also