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UK Medical Cannabis registry: an analysis of clinical outcomes of medicinal cannabis therapy for chronic pain conditions.
Harris, Michael; Erridge, Simon; Ergisi, Mehmet; Nimalan, Devaki; Kawka, Michal; Salazar, Oliver; Ali, Rayyan; Loupasaki, Katerina; Holvey, Carl; Coomber, Ross; Usmani, Azfer; Sajad, Mohammed; Hoare, Jonathan; Rucker, James J; Platt, Michael; Sodergren, Mikael H.
Afiliación
  • Harris M; Imperial College London, London, UK.
  • Erridge S; Imperial College London, London, UK.
  • Ergisi M; Sapphire Medical Clinics, London, UK.
  • Nimalan D; Imperial College London, London, UK.
  • Kawka M; Imperial College London, London, UK.
  • Salazar O; Imperial College London, London, UK.
  • Ali R; Imperial College London, London, UK.
  • Loupasaki K; Imperial College London, London, UK.
  • Holvey C; Imperial College London, London, UK.
  • Coomber R; Sapphire Medical Clinics, London, UK.
  • Usmani A; Sapphire Medical Clinics, London, UK.
  • Sajad M; St. George's Hospital NHS Trust, London, UK.
  • Hoare J; Sapphire Medical Clinics, London, UK.
  • Rucker JJ; Dartford and Gravesham Nhs Trust, Kent, UK.
  • Platt M; Sapphire Medical Clinics, London, UK.
  • Sodergren MH; Dudley Group of Hospitals Nhs Trust, West Midlands, UK.
Expert Rev Clin Pharmacol ; 15(4): 473-485, 2022 Apr.
Article en En | MEDLINE | ID: mdl-34937477
ABSTRACT

OBJECTIVES:

To explore pain-specific, general health-related quality of life (HRQoL), and safety outcomes of chronic pain patients prescribed cannabis-based medicinal products (CBMPs).

METHODS:

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.

RESULTS:

190 patients were included. Median initial Δ9-tetrahydrocannabinol and cannabidiol daily doses were 2.0mg (range0.0-442.0mg) and 20.0mg (range0.0-188.0mg) 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.

CONCLUSION:

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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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Dolor Crónico / Marihuana Medicinal Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Expert Rev Clin Pharmacol Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Dolor Crónico / Marihuana Medicinal Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Expert Rev Clin Pharmacol Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido