2016
DOI: 10.1186/s12913-016-1816-5
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Adding non-randomised studies to a Cochrane review brings complementary information for healthcare stakeholders: an augmented systematic review and meta-analysis

Abstract: BackgroundTo reduce the burden of asthma, chronic disease management (CDM) programmes have been widely implemented and evaluated. Reviews including randomised controlled trials (RCTs) suggest that CDM programmes for asthma are effective. Other study designs are however often used for pragmatic reasons, but excluded from these reviews because of their design. We aimed to examine what complementary information could be retrieved from the addition of non-randomised studies to the studies included in a published C… Show more

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Cited by 59 publications
(42 citation statements)
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“…Reviews with few or no randomised controlled trials are still valuable for inclusion within systematic reviews as they provide information regarding the feasibility of an intervention [ 73 ]. They can also prove to be of high value and of high interest to patients, healthcare professionals and stakeholders [ 74 , 75 ]. The sample sizes within the studies were also relatively small, in one case with only one eligible participant.…”
Section: Discussionmentioning
confidence: 99%
“…Reviews with few or no randomised controlled trials are still valuable for inclusion within systematic reviews as they provide information regarding the feasibility of an intervention [ 73 ]. They can also prove to be of high value and of high interest to patients, healthcare professionals and stakeholders [ 74 , 75 ]. The sample sizes within the studies were also relatively small, in one case with only one eligible participant.…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, observational studies might provide insight into a variety of populations and long term effects compared with the usually highly selected patient populations in RCTs. 12 13 Both RCTs and observational studies are increasingly used in orthopaedic trauma meta-analyses for the evaluation of treatment effects. 14 15 16 17 …”
Section: Introductionmentioning
confidence: 99%
“…Eligible study designs will be randomized controlled trials (including parallel-group, cluster, cross-over and factorial trials), cohort studies (both prospective and retrospective), case-control studies, and other non-randomized intervention studies (including quasi-randomized controlled trials, controlled before-after studies and interrupted time series studies). We included a broader set of observational study designs than is commonly included, because a recent augmented Cochrane Review of complex interventions identified valuable additional studies using such a broader set of study designs 60 . As we have an interest in quantifying risk and not in qualitative assessment of hazard 61 , we will exclude all other study designs (e.g.…”
Section: Types Of Studiesmentioning
confidence: 99%