This study was based exclusively on the review and synthesis of previously published evidence and did not involve the recruitment of participants, collection of individual patient data, or implementation of clinical interventions. As no human subjects were directly involved, approval from an institutional ethics committee and informed consent were not required. Protocol registration was not undertaken because the study aimed to develop a best-evidence summary and clinical assessment workflow using published and pre-appraised evidence rather than to conduct a conventional systematic review evaluating intervention effectiveness. All the tools used for this study are listed in the Table of Materials.
Literature search
A comprehensive literature search was conducted using the 6S evidence hierarchy framework, which prioritizes pre-appraised evidence before primary research studies. The search covered the following electronic databases and evidence resources: Chinese National Knowledge Infrastructure (CNKI), Wanfang Data, SinoMed, CINAHL, Embase, MEDLINE, Joanna Briggs Institute (JBI), Cochrane Library, BMJ Best Practice, UpToDate, DynaMed, National Comprehensive Cancer Network (NCCN), National Institute for Health and Care Excellence (NICE), Scottish Intercollegiate Guidelines Network (SIGN), and Guidelines International Network (GIN).
The search period extended from March 2019 to March 2024. This timeframe was selected to capture the most recent and valid evidence because guidelines, evidence summaries, and clinical decision-support resources in palliative care are updated regularly. Earlier publications were retained only when they provided important background information, validated assessment tools, or conceptual support identified through reference-list screening. Search strategies were developed using a combination of controlled vocabulary terms, including Medical Subject Headings (MeSH) where applicable, and free-text keywords. The main search terms included “life-sustaining treatment,” “life support treatment,” “do not resuscitate,” “DNR,” “advance directives,” and “advance care planning.” Boolean operators (AND and OR) were applied to adapt the search strategy to the indexing structure of each database. Searches were limited to studies published in English or Chinese. Detailed search strategies, database-specific terms, date restrictions, and search procedures are presented in Supplementary Table 1.
All retrieved records were exported to reference-management software for organization and duplicate removal. To ensure a comprehensive search and minimize the risk of missing relevant evidence, additional manual searches were performed by reviewing the reference lists of included documents and examining related guidelines, evidence summaries, and clinical decision-support resources available on the source websites. Controlled vocabulary and free-text terms were combined according to the indexing requirements of each database, and supplementary reference checking was conducted to identify any additional eligible evidence.
Screen and select eligible studies
Following the removal of duplicate records, all remaining citations were independently screened by two reviewers. Title and abstract screening were performed to exclude publications that were clearly unrelated to the assessment of life-sustaining treatment decision-making in patients with advanced cancer. Full-text articles were subsequently obtained for all potentially relevant records and assessed for eligibility. Studies were considered eligible if they involved hospitalized adults aged 18 years or older with advanced cancer and an estimated life expectancy of six months or less. Evidence addressing the assessment of life-sustaining treatments (LSTs) in inpatient settings caring for patients with advanced cancer was included. Eligible evidence sources comprised clinical practice guidelines, expert consensus statements, evidence summaries, clinical decision-support resources, systematic reviews, and meta-analyses. Only publications available in English or Chinese and published within the previous five years were considered. Evidence sources were excluded if they represented updated or duplicate versions of previously published guidelines or recommendations. Publications with incomplete information, insufficient methodological details, or unavailable full-text articles were also excluded. Any disagreements regarding study eligibility were resolved through discussion and consensus between the reviewers.
Appraise the quality of included evidence
The methodological quality of the included evidence was evaluated using appraisal instruments appropriate to each evidence source. Clinical practice guidelines were assessed using the Appraisal of Guidelines for Research and Evaluation II (AGREE II) instrument. For evidence summaries, the original supporting studies were traced and critically appraised using the assessment tool corresponding to their study design. Systematic reviews were evaluated using the Joanna Briggs Institute (JBI) critical appraisal checklist for systematic reviews, whereas clinical decision-support resources were assessed using the Critical Appraisal for Summaries of Evidence (CASE) tool. All quality assessments were performed independently by two reviewers who were trained in evidence appraisal methods. The reviewers examined each evidence source according to predefined criteria and documented their assessments separately. Any differences in appraisal results were resolved through discussion and consensus. When necessary, additional review and clarification were undertaken to ensure consistency and accuracy in the final quality ratings.
Define the criteria for considering studies
The scope of the evidence search was defined using the PIPOST framework, which considers Population, Intervention, Professionals, Outcomes, Setting, and Type of evidence. This framework was used to formulate the clinical questions and establish clear eligibility criteria for identifying evidence related to the assessment of life-sustaining treatment (LST) decision-making in hospitalized adults with advanced cancer. The PIPOST elements also guided the screening process and ensured consistency in study selection. Evidence sources were considered eligible if they involved hospitalized patients aged 18 years or older with advanced cancer and an estimated life expectancy of six months or less. Studies focusing on the assessment of life-sustaining treatments within inpatient settings caring for patients with advanced cancer were included. Eligible evidence types comprised clinical practice guidelines, expert consensus statements, evidence summaries, clinical decision-support resources, systematic reviews, and meta-analyses. Only articles published in English or Chinese during the previous five years were considered for inclusion. Evidence sources were excluded if they represented duplicate, superseded, or updated versions of previously published recommendations or guidelines. Publications with incomplete information, insufficient methodological details, or inaccessible full-text articles were also excluded from the final evidence synthesis.
Study selection, data extraction, and quality assessment
Study selection, quality appraisal, and data extraction were conducted independently by two reviewers according to predefined eligibility criteria. Following title and abstract screening, full-text articles were retrieved and assessed for inclusion. Final eligibility decisions were made independently by both reviewers. Any disagreements were resolved through discussion and consensus, and unresolved issues were referred to a senior member of the evidence-based research team for adjudication. The methodological quality of the included evidence was evaluated using appraisal tools appropriate for each evidence type. Clinical practice guidelines were assessed using the Appraisal of Guidelines for Research and Evaluation II (AGREE II) instrument. Evidence summaries were appraised by tracing their original evidence sources and applying the corresponding appraisal tools. Systematic reviews were evaluated using the Joanna Briggs Institute (JBI) critical appraisal checklist for systematic reviews, whereas clinical decision-support resources were assessed using the Critical Appraisal for Summaries of Evidence (CASE) tool. Relevant data were extracted independently by the same two reviewers using a standardized extraction form. Evidence published in languages other than English was translated prior to synthesis. The synthesis process prioritized recommendations supported by methodologically robust and internally consistent evidence. Complementary findings from different sources were integrated based on their conceptual and clinical relevance, while conflicting recommendations were resolved by giving preference to higher-quality evidence. Finally, all included evidence was classified according to the 2014 Joanna Briggs Institute evidence pre-grading system, with evidence levels ranging from Level 1 (highest quality) to Level 5 (lowest quality).