Keywords
Data Extraction, Natural Language Processing, Reproducibility, Systematic reviews, Text mining
This article is included in the Living Evidence collection.
Data Extraction, Natural Language Processing, Reproducibility, Systematic reviews, Text mining
In the second version we incorporated changes based on the first two peer reviews. These changes included a clarification that the scope of data extraction that we are interested in goes beyond PICOs, we elaborated on the rationale of looking at data extraction specifically, we clarified the objectives and added some more recent related literature.W e also clarified the proposed schedule for updating the review in living mode. We have also added a new author James Thomas.
See the authors' detailed response to the review by Matt Carter
See the authors' detailed response to the review by Emma McFarlane
Research on systematic review (semi)automation sits at the interface between evidence-based medicine and data science. The capacity of computers for supporting humans increases, along with the development of processing power and storage space. Data extraction for systematic reviewing is a repetitive task. This opens opportunities for support through intelligent software. Tools and methods in this domain frequently focused on automatic processing of information related to the PICO framework (Population, Intervention, Comparator, Outcome). A 2017 analysis of 195 systematic reviews investigated the workload associated with authoring a review. On average, the analysed reviews took 67 weeks to write and publish. Although review size and the number of authors varied between the analysed reviews, the authors concluded that supporting the reviewing process with technological means is important in order to save thousands of personal working hours of trained and specialised staff1. The potential workload for systematic reviewers is increasing, because the evidence base of clinical studies that can be reviewed is growing rapidly (Figure 1). This entails not only a need to publish new reviews, but also to commit to them and to continually keep the evidence up to date.
Language processing toolkits and machine learning libraries are well documented and available to use free of charge. At the same time, freely available training data make it easy to train classic machine-learning classifiers such as support vector machines, or even complex, deep neural networks such as long short-term memory (LSTM) neural networks. These are reasons why health data science, much like the rest of computer science and natural language processing, is a rapidly developing field. There is a need for fast publication, because trends and state-of-the-art methods are changing at a fast pace. Preprint repositories, such as the arXiv, are offering near rapid publication after a short moderation process rather than full peer review. Consequently, publishing research is becoming easier.
An easily updatable review of available methods and tools is needed to inform systematic reviewers, data scientists or their funders on the status quo of (semi)automated data extraction methodology. For data scientists, it contributes to reducing waste and duplication in research. For reviewers, it contributes to highlighting the current possibilities for data extraction and empowering them to choose the right tools for their task. Currently, data extraction represents one of the most time consuming1 and error-prone (Jones, Remmington, Williamson, Ashby, & Smyth, 2005) elements of the systematic review process, particularly if a large number of primary studies meet the inclusion criteria. Data mining, paralleled by automatic data extraction of relevant data for any specific systematic review project, has the potential to disrupt the traditional systematic reviewing process. This systematic review workflow usually follows the steps of searching, screening, and extracting data. If high-quality and curated data mining results are available then the searching and screening process is likely to change in the future. This review will provide constant surveillance of emerging data extraction tools.
Many systematic reviewers are free to use any tool that is available to them and need sufficient information to make informed decisions about which tools are to be preferred. Our proposed continuous analysis of the available tools will include the final performance metrics that a model achieves, and will also assess dimensions such as transparency of methods, reproducibility, and how these items are reported. Reported pitfalls of applying health data science methods to systematic reviewing tasks will be summarised to highlight risks that current, as well as future, systems are facing. Reviewing the available literature on systematic review automation is one of many small steps towards supporting evidence synthesis of all available medical research data. If the evidence arising from a study is never reviewed, and as a result never noticed by policy makers and providers of care, then it counts towards waste in research.
This review aims to:
1. Review published methods and tools aimed at automating or semi-automating the process of data extraction in the context of a systematic review of medical research studies.
2. Review this evidence in the scope of a living review, keeping information up to date and relevant to the challenges faced by systematic reviewers at any time.
Our objectives are three-fold. First we want to examine the methods and tools from the data science perspective, seeking to reduce duplicate efforts, summarise current knowledge, and encourage comparability of published methods. Second, we seek to highlight contributions of methods and tools from the perspective of systematic reviewers who wish to use (semi)automation for data extraction: what is the extent of automation?; is it reliable?; and can we identify important caveats discussed in the literature, as well as factors that facilitate the adoption of tools in practice?
We have identified three previous reviews of tools and methods, two documents providing overviews and guidelines relevant to our topic, and an ongoing effort to characterise published tools for different parts of the systematic reviewing process with respect to interoperability and workflow integration. In 2014, Tsafnat et al. provided a broad overview on automation technologies for different stages of authoring a systematic review2. O'Mara-Eves et al. published a systematic review focusing on text-mining approaches in 2015. It includes a summary of methods for the evaluation of systems (such as recall, F1 and related scores). The reviewers focused on tasks related to PICO classification and supporting the screening process3. In the same year, Jonnalagadda et al. described methods for data extraction, focusing on PICOs and related fields4.
These reviews present an overview of classical machine learning and NLP methods applied to tasks such as data mining in the field of evidence-based medicine. At the time of publication of these documents, methods such as topic modelling (Latent Dirichlet Allocation) and support vector machines constituted the state-of-the art for language models. The age of these documents means that the latest static or contextual embedding-based and neural methods are not included. These modern methods, however, are used in contemporary systematic review automation software5.
Marshall and Wallace (2019)6 present a more recent overview of automation technologies, with a focus on availability of tools and adoption into practice. They conclude that tools facilitating screening are widely accessible and usable, while data extraction tools are sill at piloting stages or require higher amounts of human input.
Beller et al.7 present a brief overview of tools for systematic review automation. They discuss principles for systematic review automation from a meeting of the International Collaboration for the Automation of Systematic Reviews (ICASR). They highlight that low levels of funding, as well as the complexity of integrating tools for different systematic reviewing tasks have led to many small and isolated pieces of software. A working group formed at the ICASR 2019 Hackathon is compiling an overview of tools published on the Systematic Review Toolbox website8. This ongoing work is focused on assessing maintenance status, accessibility and supported reviewing tasks of 120 tools that can be used in any part of the systematic reviewing process as of November 2019.
We registered this protocol via OSF (https://doi.org/10.17605/OSF.IO/ECB3T). PROSPERO was initially considered as platform for registration, but it is limited to reviews with health related outcomes.
The challenges highlighted in the previous section create several problems. A large variety of approaches and different means of expressing results creates uncertainty in the existing evidence. At the same time, new evidence is being published constantly. Rapid means of publications necessitate a structured, but at the same time easily updatable review of published methods and tools in the field. We therefore chose a living review approach as the updating strategy for this review.
For literature searches and updates we follow the living review recommendations published by Elliott et al.9 and Brooker et al.10, as well as F1000Research guidelines for projects that are included in their living evidence collection. We plan to run searches for new studies every second month. This will also include screening abstracts of the newly retrieved reports. The bi-monthly interval for screening was chosen because we expect no sudden rise in relevant publications that could justify daily, weekly or monthly screening. The review itself will be updated every six months, providing that a sufficient quantity of new records are identified for inclusion. As a threshold for updating, we plan to use 10 new records, but we will consider updating the review earlier if new impactful evidence is published. We define impactful evidence as, for example, the publication of a tool that is immediately accessible to systematic reviewers and offers substantial automation of the data extraction process, or a tool that aims to change the traditional SR workflow. Figure 2 describes the anticipated reviewing process in more detail.
Our Medline search strategy was developed with the help of an information specialist. Due to the interdisciplinary topic of this review, we plan to search bibliographic databases related to both medicine and computer science. These include Medline via Ovid and Web of Science Core Collection, as well as the computer science arXiv and the DBLP computer science bibliography. We aim to retrieve publications related to two clusters of search terms. The first cluster includes computational aspects such as data mining, while the second cluster identifies publication related to systematic reviews. The Medline search strategy is provided as Extended data11. We aim to adapt this search strategy for conducting searches in all mentioned databases. Previous reviews of data mining in systematic reviewing contexts identified the earliest text mining application in 20053,4. We therefore plan to search all databases from this year on. In a preliminary test our search strategy was able to identify 4320 Medline records, including all Medline-indexed records included by O’Mara-Eves et al.3. We plan to search the Systematic Review Toolbox website for further information on any published or unpublished tools8.
All titles and abstracts will be screened independently by two reviewers. Any differences in judgement will be discussed, and resolved with the help of a third reviewer if necessary. The process for assessing full texts will be the same. Data extraction will be carried out by single reviewers, and random 10% samples from each reviewer will be checked independently. If needed, we plan to contact the authors of reports for clarification or further information. In the base review, as well as in every published update, we will present a cross-sectional analysis of the evidence from our searches. This analysis will include the characteristics of each reviewed method or tool, as well as a summary of our findings. In addition, we will assess the quality of reporting at publication level. This assessment will focus on transparency, reproducibility and both internal and external validity of the described data extraction algorithms. If we at any point deviate from this protocol, we will discuss this in the final publication.
All search results will be de-duplicated and managed with EndNote. The screening and data extraction process will be managed with the help of Abstrackr12 and customised data extraction forms in Excel. All data, including bi-monthly screening results, will be continuously available on our Open Science Framework (OSF) repository, as discussed in the Data availability section.
Tsafnat et al.2 categorised sub-tasks in the systematic reviewing process that contained published tools and methods for automation. In our overview, we follow this categorisation and focus on tasks related to data retrieval. More specifically, we will focus on software architectures that receive as input a set of full texts or abstracts of clinical trial reports. Report types of interest are randomised controlled trials, cohort, or case-control studies. As output, the tools of interest should produce structured data representing features or findings from the study described. A comprehensive list with data fields of interest can be found in the supplementary material for this protocol.
Eligible papers
We will include full text publications that describe an original natural language processing approach to extract data related to systematic reviewing tasks. Data fields of interest are adapted from the Cochrane Handbook for Systematic Reviews of Interventions13, and defined in the Extended data11. We will include the full range of natural language processing (NLP) methods, including for example regular expressions, rule-based systems, machine learning, and deep neural networks.
Papers must describe a full cycle of implementation and evaluation of a method.
We will include reports published from 2005 until the present day, similar to O’Mara-Eves et al.3 and Jonnalagadda et al.4. We will translate non-English reports where feasible.
The data that that included papers use for mining must be texts from randomised controlled trials, comparative cohort studies or case control studies in the form of abstracts, conference proceedings, full texts or part of the text body.
Ineligible papers
We will exclude papers reporting:
methods and tools related solely to image processing and importing biomedical data from PDF files without any NLP approach, including data extraction from graphs;
any research that focuses exclusively on protocol preparation, synthesis of already extracted data, write-up, pre-processing of text and dissemination will be excluded;
methods or tools that provide no natural language processing approach and offer only organisational interfaces, document management, databases or version control; or
any publications related to electronic health reports or mining genetic data will be excluded.
Primary:
1. Machine learning approaches used
2. Reported performance metrics used for evaluation
3. Type of data
Scope: Abstract, conference proceeding, or full text
Target design: Randomised controlled trial, cohort, case-control
Type of input: The input data format, for example data imported as structured result of literature search (e.g. RIS), APIs, from PDF or text files.
Type of output: In which format are data exported after the extraction, for example as text file.
Secondary:
1. Granularity of data mining: Does the system extract specific entities, sentences, or larger parts of text?
2. Other reported metrics, such as impacts on systematic review processes (e.g. time saved during data extraction).
Assessment of the quality of reporting: We will extract information related to the quality of reporting and reproducibility of methods in text mining14. The domains of interest, adapted for our reviewing task, are listed in the following.
1. Reproducibility:
2. Transparency of methods:
3. Testing:
4. Availability of the final model or tool:
5. Internal and external validity of the model:
Does the dataset or assessment measure provide a possibility to compare to other tools in same domain?
Are explanations for the influence of both visible and hidden variables in the dataset given?
Is the process of avoiding over- or underfitting described?
Is the process of splitting training from validation data described?
Is the model’s adaptability to different formats and/or environments beyond training and testing data described?
6. Other:
We plan to publish the finished review, along with future updates, via F1000Research.
All data will be available via a project on Open Science Framework (OSF): https://osf.io/4sgfz/ (see Data availability).
Open Science Framework: Data Extraction Methods for Systematic Review (semi)Automation: A Living Review / Protocol. https://doi.org/10.17605/OSF.IO/ECB3T11
This project contains the following extended data:
Open Science Framework: Data Extraction Methods for Systematic Review (semi)Automation: A Living Review / Protocol. https://doi.org/10.17605/OSF.IO/ECB3T11
Data are available under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) data waiver.
We thank Sarah Dawson for developing and evaluating the search strategy, and providing advice on databases to search for this review. Many thanks also to Alexandra McAleenan and Vincent Cheng for providing valuable feedback on this protocol.
Views | Downloads | |
---|---|---|
F1000Research | - | - |
PubMed Central
Data from PMC are received and updated monthly.
|
- | - |
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Automation of Systematic Reviews
Is the rationale for, and objectives of, the study clearly described?
Yes
Is the study design appropriate for the research question?
Yes
Are sufficient details of the methods provided to allow replication by others?
Yes
Are the datasets clearly presented in a useable and accessible format?
No
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Automation of Systematic Reviews
Is the rationale for, and objectives of, the study clearly described?
Yes
Is the study design appropriate for the research question?
Yes
Are sufficient details of the methods provided to allow replication by others?
Yes
Are the datasets clearly presented in a useable and accessible format?
Not applicable
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: I am currently conducting a systematic review of automation in systematic reviewing or guideline development. I am also working on a research project on machine learning within the context of guideline recommendations.
Alongside their report, reviewers assign a status to the article:
Invited Reviewers | ||
---|---|---|
1 | 2 | |
Version 2 (revision) 08 Jun 20 |
read | |
Version 1 25 Mar 20 |
read | read |
Provide sufficient details of any financial or non-financial competing interests to enable users to assess whether your comments might lead a reasonable person to question your impartiality. Consider the following examples, but note that this is not an exhaustive list:
Sign up for content alerts and receive a weekly or monthly email with all newly published articles
Already registered? Sign in
The email address should be the one you originally registered with F1000.
You registered with F1000 via Google, so we cannot reset your password.
To sign in, please click here.
If you still need help with your Google account password, please click here.
You registered with F1000 via Facebook, so we cannot reset your password.
To sign in, please click here.
If you still need help with your Facebook account password, please click here.
If your email address is registered with us, we will email you instructions to reset your password.
If you think you should have received this email but it has not arrived, please check your spam filters and/or contact for further assistance.
Comments on this article Comments (0)