Chronic Pain
Study register · detail Fallserie (prospektives Register) · Chronic Pain · 2022

UK Medical Cannabis registry: an analysis of clinical outcomes of medicinal cannabis therapy for chronic pain conditions

Clear benefit GRADE Very low 41 citations
Samplen = 190 Pat.
Duration1, 3 and 6 months from baseline
EndpointBPI
Blindingn.a.
DesignFallserie (prospektives Register)
Cannabinoidkombination
Max. dose22.0 mg
Key finding

CBMPs were associated with significant improvements in pain intensity and health-related quality of life over 6 months.

Summary

UK Medical Cannabis Registry, n=190 patients with chronic pain; significant improvements in BPI, SF-MPQ-2, VAS pain, GAD-7, SQS and EQ-5D-5L at all measurement time points (1, 3, 6 months; p<0,050); adverse events in 39,47% (mild 19,47%, moderate 12,11%, severe 7,37%); most common AE nausea (n=11; 5,8%).

P
PopulationAdults with chronic pain conditions, n=190, from the UK Medical Cannabis Registry
I
InterventionCannabis-based medicinal products (CBMPs), median THC 2,0 mg/day, median CBD 20,0 mg/day, oral/inhaled (registry data)
O
OutcomeSignificant improvements in BPI, SF-MPQ-2, VAS, GAD-7, SQS and EQ-5D-5L at all measurement time points (1, 3, 6 months; each p<0,050); 75 adverse events (39,47%), mostly mild to moderate
Confidence in the evidence
Very low

The lowest GRADE level, the effect estimate remains uncertain.

Quality profile
Sample size
Blinding
Effect size Clear benefit
Citations / year
Authors
Harris M, Erridge S, Ergisi M et al.
DOI 10.1080/17512433.2022.2017771
Design: Fallserie (prospektives Register)
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Abstract
<h4>Objectives</h4>To explore pain-specific, general health-related quality of life (HRQoL), and safety outcomes of chronic pain patients prescribed cannabis-based medicinal products (CBMPs).<h4>Methods</h4>A case series was performed using patients with chronic pain from the UK Medical Cannabis Registry. Primary outcomes were changes in Brief Pain Inventory short-form (BPI), Short-form McGill Pain Questionnaire-2 (SF-MPQ-2), Visual Analogue Scale-Pain (VAS), General Anxiety Disorder-7 (GAD-7), Sleep Quality Scale (SQS), and EQ-5D-5L, at 1, 3, and 6 months from baseline. Statistical significance was defined at p-value<0.050.<h4>Results</h4>190 patients were included. Median initial Δ<sup>9</sup>-tetrahydrocannabinol and cannabidiol daily doses were 2.0mg (range:0.0-442.0mg) and 20.0mg (range:0.0-188.0mg) respectively. Significant improvements were observed within BPI, SF-MPQ-2, GAD-7, SQS, EQ-5D-5 L index, and VAS measures at all timepoints (p<0.050). Seventy-five adverse events (39.47%) were reported, of which 37 (19.47%) were rated as mild, 23 (12.11%) as moderate, and 14 (7.37%) as severe. Nausea (n=11; 5.8%) was the most frequent adverse event.<h4>Conclusion</h4>An association was identified between patients with chronic pain prescribed CBMPs and improvements in pain-specific and general HRQoL outcomes. Most adverse events were mild to moderate in severity, indicating CBMPs were well tolerated. Inherent limitations of study design limit its overall applicability.

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