| Literature DB >> 33092602 |
Jing Si1, Rong Guo2, Xiang Lu3, Chao Han3, Li Xue3, Dan Xing3, Caiping Chen4.
Abstract
BACKGROUND: Breast cancer is a worldwide health concern. For early stage breast cancer patients, choosing the surgical method after diagnosis is always a dilemma. Decision aids designed for use by patients are tools which may help with surgical decision making for these patients. <br> METHODS: We screened through MEDLINE, EMBASE, PubMed and Web of Science using the inclusion criteria which included (1) newly diagnosed patients with early stage breast cancer, (2) outcomes/results involving surgical options including breast conserving surgery. The search strategy used these key words or the combination of these words: "breast cancer", "decision aid", "decision making", "decision support", "breast conserving surgery", "breast conserving therapy". <br> RESULTS: A total of 621 studies were identified, but only seven studies were included. Results were synthesized into narrative format. Various patterns of decision aids designed for use by patients were implemented. Mostly were educational materials via booklet, video or CDROM with or without assistance from surgeons. After decision aids, four studies showed that patients were more likely to change their original choices into mastectomy or modified radical instead of sticking to breast conserving surgery. Other results such as knowledge of breast cancer and treatments, decisional conflict and satisfaction, psychological changes after surgery and quality of life were all showed with a better trend in patients with decision aids in most studies. <br> CONCLUSION: Decision aids on breast conserving surgery made it easier for patient involvement in surgical decision making and improved decision-related outcomes in most early stage breast cancer patients. With more attention, improving procedures, and better interdisciplinary cooperation, more research is necessary for the improvement of decision aids. And we believe decision aids with agreed objective information are needed.Entities:
Keywords: Breast cancer; Breast conserving surgery; Breast conserving therapy; Decision aids; Decision making; Decision support
Mesh:
Year: 2020 PMID: 33092602 PMCID: PMC7583180 DOI: 10.1186/s12911-020-01295-8
Source DB: PubMed Journal: BMC Med Inform Decis Mak ISSN: 1472-6947 Impact factor: 2.796
Search strategies and records for databases (Searched in January 2019)
| Database | Search strategies | Limits | Records |
|---|---|---|---|
| Medline | (Breast cancer and (decision aid or decision making or decision support) and (breast conserving surgery or breast conserving therapy)).mp.[mp = title, abstract, original title, name of substance word, subject heading word, keyword heading word, protocol supplementary concept word, rare disease supplementary concept word, unique identifier, synonyms] | Full text | 166 |
| English language | |||
| Human | |||
| Embase | (Breast cancer and (decision aid or decision making or decision support) and (breast conserving surgery or breast conserving therapy)).mp.[mp = title, abstract, original title, name of substance word, subject heading word, keyword heading word, protocol supplementary concept word, rare disease supplementary concept word, unique identifier, synonyms] | Full text | 152 |
| English language | |||
| Human | |||
| PubMed | ("Breast Neoplasms"[Mesh] AND (decision aid[Title/Abstract] OR decision making[Title/Abstract] OR decision support[Title/Abstract]) AND (breast conserving surgery[Title/Abstract] OR breast conserving therapy[Title/Abstract]) | Full text | 153 |
| English language | |||
| Human | |||
| Web of science | TS = (breast cancer) AND TS = ((decision aid OR decision making) OR decision support) AND TS = (breast conserving surgery OR breast conserving therapy) | Full text | 170 |
| English language |
Fig. 1Systematic review flow diagram
PRISMA diagram checklist
| Section/topic | # | Checklist item | Reported on page # |
|---|---|---|---|
| Title | |||
| Title | 1 | Identify the report as a systematic review, meta-analysis, or both | Title |
| Abstract | |||
| Structured summary | 2 | Provide a structured summary including, as applicable: background; objectives; data sources; study eligibility criteria, participants, and interventions; study appraisal and synthesis methods; results; limitations; conclusions and implications of key findings; systematic review registration number | Abstract and key words |
| Introduction | |||
| Rationale | 3 | Describe the rationale for the review in the context of what is already known | Background, paragraph 1–3 |
| Objectives | 4 | Provide an explicit statement of questions being addressed with reference to participants, interventions, comparisons, outcomes, and study design (PICOS) | Background, paragraph 4 |
| Methods | |||
| Protocol and registration | 5 | Indicate if a review protocol exists, if and where it can be accessed (e.g., Web address), and, if available, provide registration information including registration number | N/A |
| Eligibility criteria | 6 | Specify study characteristics (e.g., PICOS, length of follow-up) and report characteristics (e.g., years considered, language, publication status) used as criteria for eligibility, giving rationale | Methods, paragraph 1 |
| Information sources | 7 | Describe all information sources (e.g., databases with dates of coverage, contact with study authors to identify additional studies) in the search and date last searched | Methods, paragraph 1 and Table |
| Search | 8 | Present full electronic search strategy for at least one database, including any limits used, such that it could be repeated | Methods, paragraph 1 and Table |
| Study selection | 9 | State the process for selecting studies (i.e., screening, eligibility, included in systematic review, and, if applicable, included in the meta-analysis) | Methods, paragraph 2 and Fig. |
| Data collection process | 10 | Describe method of data extraction from reports (e.g., piloted forms, independently, in duplicate) and any processes for obtaining and confirming data from investigators | Methods, paragraph 2 and Fig. |
| Data items | 11 | List and define all variables for which data were sought (e.g., PICOS, funding sources) and any assumptions and simplifications made | Methods, paragraph 2 and Table |
| Risk of bias in individual studies | 12 | Describe methods used for assessing risk of bias of individual studies (including specification of whether this was done at the study or outcome level), and how this information is to be used in any data synthesis | Methods, paragraph 2 and Table |
| Summary measures | 13 | State the principal summary measures (e.g., risk ratio, difference in means) | N/A |
| Synthesis of results | 14 | Describe the methods of handling data and combining results of studies, if done, including measures of consistency (e.g., I2) for each meta-analysis | N/A |
| Risk of bias across studies | 15 | Specify any assessment of risk of bias that may affect the cumulative evidence (e.g., publication bias, selective reporting within studies) | Methods, paragraph 2 and Table |
| Additional analyses | 16 | Describe methods of additional analyses (e.g., sensitivity or subgroup analyses, meta-regression), if done, indicating which were pre-specified | N/A |
| Results | |||
| Study selection | 17 | Give numbers of studies screened, assessed for eligibility, and included in the review, with reasons for exclusions at each stage, ideally with a flow diagram | Methods, paragraph 2, Results, paragraph 1 and Fig. |
| Study characteristics | 18 | For each study, present characteristics for which data were extracted (e.g., study size, PICOS, follow-up period) and provide the citations | Results and Table |
| Risk of bias within studies | 19 | Present data on risk of bias of each study and, if available, any outcome level assessment (see item 12) | Table |
| Results of individual studies | 20 | For all outcomes considered (benefits or harms), present, for each study: (a) simple summary data for each intervention group (b) effect estimates and confidence intervals, ideally with a forest plot | Results, outcomes and Table |
| Synthesis of results | 21 | Present results of each meta-analysis done, including confidence intervals and measures of consistency | N/A |
| Risk of bias across studies | 22 | Present results of any assessment of risk of bias across studies (see Item 15) | Table |
| Additional analysis | 23 | Give results of additional analyses, if done (e.g., sensitivity or subgroup analyses, meta-regression [see Item 16]) | N/A |
| Discussion | |||
| Summary of evidence | 24 | Summarize the main findings including the strength of evidence for each main outcome; consider their relevance to key groups (e.g., healthcare providers, users, and policy makers) | Discussion, paragraph 1 |
| Limitations | 25 | Discuss limitations at study and outcome level (e.g., risk of bias), and at review-level (e.g., incomplete retrieval of identified research, reporting bias) | Discussion, paragraph 5 |
| Conclusions | 26 | Provide a general interpretation of the results in the context of other evidence, and implications for future research | Conclusion |
| Funding | |||
| Funding | 27 | Describe sources of funding for the systematic review and other support (e.g., supply of data); role of funders for the systematic review | Declarations |
From: Moher et al. [25]
For more information, visit: www.prisma-statement.org
QualSyst scores of studies included in the review
| References | 1. Question sufficiently described | 2. Design evident and appropriate | 3. Subject selection method | 4. Subject characteristics described | 5. If randomized, was procedure reported | 6. If blinded to investigators, was it reported | 7. If blinded to subjects, was it reported | 8. Outcome well defined and robust to measurement/misclassification bias | 9. Sample size appropriate | 10. Analysis described and appropriate | 11. Some estimate of variance reported | 12. Controlled for confounding | 13. Results reported in sufficient detail | 14. Results support conclusions | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| [ | 2 | 2 | 1 | 2 | 2 | 2 | 0 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 0.89 |
| [ | 1 | 2 | 1 | 1 | 2 | 0 | 0 | 1 | 2 | 2 | 0 | 1 | 2 | 1 | 0.57 |
| [ | 1 | 2 | 2 | 1 | 2 | 0 | 0 | 2 | 2 | 2 | 2 | 1 | 2 | 2 | 0.75 |
| [ | 2 | 2 | 2 | 2 | 1 | 0 | 0 | 2 | 1 | 1 | 0 | 0 | 2 | 2 | 0.61 |
| [ | 2 | 1 | 2 | 1 | N/A | N/A | N/A | 1 | 2 | 2 | 2 | 1 | 2 | 2 | 0.82 |
| [ | 2 | 1 | 2 | 2 | N/A | N/A | N/A | 1 | 2 | 2 | 2 | 1 | 2 | 2 | 0.86 |
| [ | 2 | 1 | 2 | 1 | N/A | N/A | N/A | 0 | 2 | 2 | 0 | 1 | 1 | 2 | 0.64 |
Overview of the articles
| Authors | Year | Country | Design | Sample | Intervention | Control | Measurement tools | Outcomes | Qualsyst |
|---|---|---|---|---|---|---|---|---|---|
| Lam [ | 2013 | China | Randomized control trial | 276 patients with early stage BC DA: 138 patients Control: 138 patients | Take-home booklet | The standard information booklet | Treatment decision-making difficulties and decisional conflict scale, knowledge scale, decision regret, Hospital Anxiety and Depression Scale (HADS)-Anxiety subscale and HADS-Depression subscale, decision regret | Choice of surgery did not differ between the DA and control arms. (BCS, MRM or MRM + BR/MRM or MRM + BR) The DA group had lower decisional conflict scores 1 week after consultation ( | 0.89 |
| Jibaja-Weiss [ | 2011 | USA | Randomized control trial | 76 patients with early stage BC (I–IIIA) DA: 40 patients Control: 36 patients | An entertainment-based decision aid for breast cancer treatment along with usual care | Usual care only | A questionnaire for evaluating breast cancer knowledge, Satisfaction with Decision Scale (SWD), Satisfaction with the Process of Making a Treatment Decision scale (SWDMP), low-literacy version of the Decisional Conflict Scale | Patients in DA group prefer to MRM (59.5% vs. 39.5%, DA group showed a significant improvement in knowledge at the pre-surgery assessment ( | 0.57 |
| Whelan [ | 2004 | Canada | Randomized control trial | 201 patients with stage I or II BC and 20 surgeons DA: 94 patients and 10 surgeons Control: 107 patients and 10 surgeons | Decision board (written and visual information) Takes 20 min | Usual consultation style without using the decision board | A 44-item questionnaire for patient knowledge, decisional conflict scale, effective decision-making subscale of the decisional conflict scale, the Spielberger State Anxiety Inventory and the Centre for Epidemiologic Studies Depression scale | Patients in DA group were more likely to choose BCS (94% vs. 76%, The DA group had higher knowledge scores about their treatment options (66.9 vs. 58.7; | 0.75 |
| Street [ | 1995 | USA | Randomized control trial | 60 patients with stage I or II BC DA: 30 patients Control: 30 patients | Multimedia program (including text, graphic display, audio narration, music, and audio–video clips) Takes 30–45 min | An 8-page brochure, Care of Patients with Early Breast Cancer Takes 15–20 min | An 11-item, multiple choice test for knowledge about BC treatment, an 8-item instrument for patients’ optimism, behavioral and self-report measures for patient involvement and physician communication, modified Perceived Involvement in Care Scale (PICS), modified Perceived Decision Control (PDC), 5-item doctor facilitation subscale of PICS | More patients educated with the computer chose BCS (76%) than did those reading the brochure (58%). (BCS or MT) Patients using the computer program scored higher in the knowledge test (mean, 82.6%; SD, 11.58%) after the intervention than did patients reading the brochure (mean, 76.4%; SD, 13.77%). The only variable predicting a patient’s optimism was knowledge (r = 0.31, | 0.61 |
| Wilkins [ | 2006 | USA | Nonrandomized trial with concurrent control | 101 patients with stage I or II BC DA: 52 patients Control: 49 patients | Educational video Takes 60 min | Written educational materials | Autonomy and Information-Seeking Preferences, Self-Efficacy to Communicate with Physician/Manage Disease, Knowledge about Breast Cancer, State-Trait Anxiety Inventory, Perceived Involvement in Care, Satisfaction with Decision | 25% of people who saw the video chose mastectomy compared to 14% of those who did not see the video ( No statistically significant differences between the 2 groups measured with all the scales | 0.82 |
| Molenaar [ | 2001 | the Netherlands | Nonrandomized trial with concurrent control | 180 patients with stage I or II BC DA: 92 patients Control: 88 patients | Interactive Breast Cancer CDROM Takes 70 min | Standard care including oral information and brochures | A 4-item scale for satisfaction with the decision-making process, 3 out of 4 items of the “effective decision-making” subscale of the DCS for satisfaction with the decision, the MOS20 and the EORTC QLQ-BR23 | No difference between the CDROM and standard care condition in the treatment decision made. Most patients in both conditions selected BCS (CDROM: 75%; standard care 68%). (BCS or MT) CDROM patients expressed more satisfaction with information, the decision-making process, and communication. CDROM patients reported better physical functioning, less pain and fewer arm symptoms | 0.86 |
| Whelan [ | 1999 | Canada | Nonrandomized trial with historical control | patients with clinical stage I or II BC and 7 surgeons DA: 175 patients and 7 surgeons Control: 194 patients | The surgical Decision Board Takes 20 min | Before DA | A 6-point Likert scale for patient preference, questionnaire for general acceptability of the decision aid, a 14-statement response for patient comprehension, a 5-point Likert scale for patient satisfaction with information and decision-making | The rate of breast-conserving surgery decreased when the Decision Board was introduced (88% vs. 73%, 98% patients using the Decision Board reported that the Decision Board was easy to understand, and 81% indicated that it helped them make decisions. Surgeons found the Decision Board to be helpful in presenting information to patients in 91% of consultations | 0.64 |
BC breast cancer, DA decision aids, BCS breast-conserving surgery, MRM modified radical mastectomy, BR breast reconstruction, MT mastectomy