Sativex Patients and Caregivers Reported Improved Daily Function and Reduced Need for Other Medications

A survey of 124 patients prescribed Sativex (mostly for MS spasticity and pain) found the majority reported improvements in daily functional activities, with reduced use of other anti-spasticity medications and healthcare resources.

Notcutt, William G·Primary health care research & development·2013·Preliminary EvidenceObservational
RTHC-00711ObservationalPreliminary Evidence2013RETHINKTHC RESEARCH DATABASErethinkthc.com/research

Quick Facts

Study Type
Observational
Evidence
Preliminary Evidence
Sample
Not reported

What This Study Found

One hundred twenty-four patients who had received repeat Sativex prescriptions completed a questionnaire survey (57% response rate). Most patients had multiple sclerosis, using Sativex primarily for spasticity and pain. The majority of both patients and their caregivers reported improvements across a range of daily functional activities.

Notably, patients reported reduced use of concomitant anti-spasticity medications and reduced use of other healthcare resources after starting Sativex. Caregiver responses corroborated patient reports. The findings complemented RCT evidence by providing a real-world effectiveness perspective.

Key Numbers

124 questionnaires returned (57% response rate). Most patients had MS. Primary indications: spasticity and pain. Majority reported improved daily function. Reduced anti-spasticity medication use. Reduced healthcare resource use.

How They Did This

Questionnaire survey with mostly multiple-choice questions and some free-text. Distributed through UK prescribers to patients who had received repeat Sativex prescriptions within the previous 16 weeks. Developed in consultation with a patient organization. No control group. 57% response rate (124 returned).

Why This Research Matters

Clinical trial results do not always translate to real-world effectiveness. This survey provides evidence that Sativex produces patient-perceived benefits in daily life, reduces polypharmacy (fewer other medications needed), and reduces healthcare utilization, supporting its practical value beyond trial settings.

The Bigger Picture

This real-world evidence complements the controlled trial data for Sativex by showing that the benefits observed in trials translate to patient-perceived improvements in daily life. The reduction in other medication use and healthcare visits has economic as well as clinical implications.

What This Study Doesn't Tell Us

No control group. Only patients with repeat prescriptions were surveyed, creating selection bias (those who stopped would not be included). Self-reported outcomes are subject to bias. 43% non-response may reflect dissatisfied patients. UK-specific prescribing patterns may not generalize.

Questions This Raises

  • ?Why did 43% not respond, and were non-responders less satisfied?
  • ?What specific daily activities improved most?
  • ?Is the reduction in other medications clinically appropriate or does it leave symptoms under-treated?
  • ?What is the long-term satisfaction rate?

Trust & Context

Key Stat:
Majority reported improved daily function and reduced need for other medications
Evidence Grade:
Uncontrolled questionnaire survey; preliminary real-world evidence complementing RCT findings.
Study Age:
Published in 2013. Sativex has gained further regulatory approvals and real-world usage data since.
Original Title:
A questionnaire survey of patients and carers of patients prescribed Sativex as an unlicensed medicine.
Published In:
Primary health care research & development, 14(2), 192-9 (2013)
Database ID:
RTHC-00711

Evidence Hierarchy

Meta-Analysis / Systematic Review
Randomized Controlled Trial
Cohort / Case-Control
Cross-Sectional / ObservationalSnapshot without intervening
This study
Case Report / Animal Study

Watches what happens naturally without intervening.

What do these levels mean? →

Frequently Asked Questions

What do patients actually think of Sativex?

In this survey, the majority of patients on repeat Sativex prescriptions reported improvements in daily functional activities, and their caregivers agreed. Patients also reported needing fewer other medications and fewer healthcare visits. However, this only captures the views of patients who continued using Sativex, and those who stopped (possibly due to lack of benefit or side effects) were not surveyed.

Does Sativex reduce the need for other medications?

According to patient reports in this survey, yes. Many patients reduced their use of other anti-spasticity medications after starting Sativex. This has both clinical implications (fewer medication side effects) and economic implications (reduced healthcare costs). However, without a control group, it is difficult to attribute this entirely to Sativex.

Read More on RethinkTHC

Cite This Study

RTHC-00711·https://rethinkthc.com/research/RTHC-00711

APA

Notcutt, William G. (2013). A questionnaire survey of patients and carers of patients prescribed Sativex as an unlicensed medicine.. Primary health care research & development, 14(2), 192-9. https://doi.org/10.1017/S1463423612000333

MLA

Notcutt, William G. "A questionnaire survey of patients and carers of patients prescribed Sativex as an unlicensed medicine.." Primary health care research & development, 2013. https://doi.org/10.1017/S1463423612000333

RethinkTHC

RethinkTHC Research Database. "A questionnaire survey of patients and carers of patients pr..." RTHC-00711. Retrieved from https://rethinkthc.com/research/notcutt-2013-a-questionnaire-survey-of

Access the Original Study

Study data sourced from PubMed, a service of the U.S. National Library of Medicine, National Institutes of Health.

This study breakdown was produced by the RethinkTHC research team. We analyze and report published research findings without making health recommendations. All interpretations are based solely on the published abstract and study data.