Background:
Conducting a systematic review for the first time involves a substantial amount of work for a team. The incremental effort to update or to conduct more reviews in the same topic decreases, since many components of the protocol are reutilised, and there might be gains derived from parallelisation of tasks.
Objectives:
To demonstrate a model of parallel production of multiple living systematic reviews in the same topic.
Methods:
We developed a common protocol for a suite of reviews about medical use of cannabis and cannabinoids, and a map of all the possible PICO questions on that topic based on existing systematic reviews available at Epistemonikos database and other documents.
We run monthly searches in MEDLINE, Cochrane Central Register of Controlled Trials (CENTRAL) and Embase, and search in other sources. Deduplicated records are screened in duplicate for a team of researchers using an online tool developed by our team. Full texts of potentially eligible studies are evaluated in duplicate as well. Discrepancies are solved by a third reviewer.
All of the included trials (i.e. randomised trials on medical use of cannabis and cannabinoids) are allocated to the specific reviews, and then managed by independent teams for each review.
Results:
Based on the revision of 151 existing systematic reviews that include 528 primary studies overall, we developed a map of 82 PICO questions in this topic, namely different conditions or symptoms that might be treated with the intervention.
We have screened 20,118 records, and identified 40 new trials not included in existing reviews. A team of 27 people, composed of methods and content experts is now extracting data for all the reviews in parallel. The completion of all the reviews and submission for publication is expected to be August 2018. All of the reviews will be maintained as living systematic reviews, that is they will be updated as new evidence emerge.
Conclusions:
A production model of multiple living systematic reviews in the same topic is feasible if a large team of researchers is centrally co-ordinated, and the appropriate technological tools to streamline and manage the process are available.
Patient or healthcare consumer involvement:
None.