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A research study Writing a Systematic Review in Clinical Research – Pubrica
A Research Study
Writing a
Systematic Review
in Clinical
Research
An Academic presentation by
Dr. Nancy Agnes, Head, Technical
Operations, Pubrica Group:
www.pubrica.com
Email: [email protected]
TODAY'S
DISCUSSION
In Brief
Introduction
A systematic review involves a series of distinct steps
About Pubrica
IN
BRIEF
A systematic review summarises the findings of
precisely organized healthcare research (controlled
trials) and gives a high degree of evidence on the
efficacy of healthcare interventions.
The evidence may be used to make decisions and
guide healthcare recommendations.
These analyses are complex and rely heavily on the
available clinical trials, how they were conducted
(trial quality), and the assessed health outcomes.
Contd...
Meta-analyses are a standard method used by review authors to pool numerical data regarding
treatment outcomes.
Next,theauthorsevaluatetheevidenceforanyadvantagesorrisksassociatedwithsuch therapies.
Systematic Review Writing might summarise the existing clinical research on a topic in this way.
INTRODUC
TION
The most dependable source of evidence to guide
clinical practice is a high-quality systematic review.
A systematic review aims to provide a detailed overview
of all available primary research in answer to a
specific research issue.
Asystematicreview,often knownassecondary
research, usesallavailable research(researchon
research).
Contd.
..
They are commonly used in guideline creation
and are typically needed by research funders to
establish the status of current knowledge.
The results of systematic reviews are frequently
employed in the healthcare field, but they can
also be used elsewhere.
The process used in C onducting a Systematic
Review is detailed and precise to reduce bias and
increase the reliability of the results reached.
A systematic review has the following
characteristics
Contd...
explicit objectives with predetermined study eligibility and relevance criteria;
transparent, repeatable methodology; thorough search to
find all suitable studies; a systematic performance
and synthesis of the included research,
as well as an assessment of the validity of the conclusions of the included
studies
A SYSTEMATIC REVIEW
INVOLVES A SERIES OF
DISTINCT STEPS
Establish a research question: A well-defined
review question is the backbone of the
Clinical T rial Systematic Review Services
systematic
review, similar to a precise specific goal in a
clinical study.
A good review question is clinically relevant, not
too broad but targeted, and usually identifies the
population, the intervention or exposure, and the
desired outcome(s).
Contd...
Clearly define the criteria for inclusion and exclusion:
Eligibility requirements are derived mainly from the study q
uestion.
PICO
(population, intervention, comparator, outcomes) is an abbr
eviation that helps identify which patient population,
treatments or exposures
in the treatment and control groups and outcome(s) researc
h must report being eligible for
inclusion.
Other criteria, such as research design,
publication date, or language, might be used to include or e
xclude Contd.
people. ..
Conductathoroughliteraturesearch:BibliographicdatabaseslikePubMed,
WebofKnowledge,Scopus,andEMBASEarecommonlyusedto conduct
literature searches.
Thestudyselectioncriteriamustbemappedontosensiblesearchphrases, which
must then be combined coherently using Boolean operators.
Extra search strategies, such as reviewing reference lists, conference
proceedings, or trial registries, might help you find unpublished research or
additional references.
Contd...
Selectstudies:Titlesandabstractsarefirst evaluated
for inclusion and exclusion criteria.
Full-texts of possibly suitable references are
retrieved to determine which publications to add
further depth.
Two or more researchers should independently
pick studies, extract data, and assess quality, with
the search and selection approach outcomes
shown in a flow diagram.
Contd.
..
Extractdata:Thekindandamountofdata
extracted depends on the review’s goal and scope,
but typically these data include study design
type(s), patient characteristics, and outcome data.
A well-designed d ata extraction procedure and
form facilitates consistent and thorough data
extraction.
Assess the quality of the studies included:
There is a range of quality evaluation techniques for
different research types (e.g., Cochrane risk of bias
tool; Grading of Recommendations Assessment,
Development, and Evaluation [GRADE]; Newcastle-
Ottawa scale).
Contd...
The quality evaluation findings are critical for readers to determine if the research provided
trustworthy and generalizable information.
To prevent a “garbage in, garbage out” impact, authors occasionally remove low-quality
papers altogether.
Analyze the data, display it, and analyze it: A meta-analysis is frequently employed to c
ombine quantitative data, although not always.
However, a meta-analysis should not be undertaken if the included studies are not sufficiently
comparable to allow for significant data synthesis.
For example, here found a lot of clinical and methodological variability (e.g., different chronic
pain conditions, treatment and follow-up durations, and magnesium formulations). Therefore
they did a qualitative analysis and presented the findings descriptively.
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