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. 2018 Oct 25;105(13):1721–1730. doi: 10.1002/bjs.11009

Systematic review of shared decision‐making in surgery

S M L de Mik 1, F E Stubenrouch 1, R Balm 1, D T Ubbink 1,
PMCID: PMC6282808  PMID: 30357815

Abstract

Background

Multiple treatment options are generally available for most diseases. Shared decision‐making (SDM) helps patients and physicians choose the treatment option that best fits a patient's preferences. This review aimed to assess the extent to which SDM is applied during surgical consultations, and the metrics used to measure SDM and SDM‐related outcomes.

Methods

This was a systematic review of observational studies and clinical trials that measured SDM during consultations in which surgery was a treatment option. Embase, MEDLINE and CENTRAL were searched. Study selection, quality assessment and data extraction were conducted by two investigators independently.

Results

Thirty‐two articles were included. SDM was measured using nine different metrics. Thirty‐six per cent of 13 176 patients and surgeons perceived their consultation as SDM, as opposed to patient‐ or surgeon‐driven. Surgeons more often perceived the decision‐making process as SDM than patients (43·6 versus 29·3 per cent respectively). SDM levels scored objectively using the OPTION and Decision Analysis System for Oncology instruments ranged from 7 to 39 per cent. Subjective SDM levels as perceived by surgeons and patients ranged from 54 to 93 per cent. Patients experienced a higher level of SDM during consultations than surgeons (93 versus 84 per cent). Twenty‐five different SDM‐related outcomes were reported.

Conclusion

At present, SDM in surgery is still in its infancy, although surgeons and patients both think of it favourably. Future studies should evaluate the effect of new interventions to improve SDM during surgical consultations, and its assessment using available standardized and validated metrics.

Short abstract

Heterogeneous data

Introduction

More than one treatment option is usually available to treat a patient's disease. If none of these treatments is superior when weighing the benefits and possible harms, a treatment dilemma exists. In this case the best treatment option is the one that best fits the patient's preferences1.

Shared decision‐making (SDM) is a process that, on the one hand, helps patients to consider and share their preferences regarding the pros and cons of the treatment options. On the other hand, SDM helps physicians explicitly to evoke these preferences and incorporate them into the final decision2, 3. SDM has been shown to improve patient satisfaction and adherence to therapy, and may also reduce undesired care4, 5, 6, 7. Therefore, it is important to involve patients in the decision‐making process. This is particularly relevant within surgical practice, when decisions have to be made between different types of surgery or surgery versus no surgery8. Surgical interventions are typically irreversible and patients have to deal with potential harmful consequences. Moreover, surgical complications do not resolve as easily as side‐effects from some medications.

Because of the importance and increasing recognition of SDM in improving quality of (surgical) care8, the extent to which it has currently been implemented in surgeon–patient encounters and the metrics used to measure SDM were reviewed systematically. This review aimed to answer the following questions: what are the objective and subjective measurements of SDM during surgeon–patient encounters; and which metrics are used to measure SDM and SDM‐related outcomes?

Methods

Protocol and registration

This systematic review is reported in accordance with the guidelines of the PRISMA statement9. The review protocol was registered in PROSPERO, the international prospective register of systematic reviews database (http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=CRD42017073406).

Eligibility criteria

Studies were eligible if they reported on SDM during the consultation between patient and physician in which a treatment decision was made. Surgery had to be at least one of the possible treatment options. In addition, studies needed to measure and report the extent to which SDM was applied with any type of metric. The following specialties were included: vascular surgery, trauma surgery, gastrointestinal surgery, hepatopancreatobiliary surgery, orthopaedic surgery, urological surgery, plastic surgery and cardiothoracic surgery. Cross‐sectional studies and RCTs were eligible. Cross‐referencing was performed to identify additional eligible studies.

Studies were excluded if not written in English or Dutch, if the study evaluated the effectiveness of decision‐making support tools, and if the study focused only on informed decision‐making. The publication interval was not restricted.

Search

The Embase, MEDLINE and CENTRAL electronic databases were searched. The final search was undertaken on 14 June 2017. The Population, Intervention, Comparison and Outcome (PICO) framework was used to construct the search strategy with the assistance of a clinical librarian. The full search strategy is shown in AppendixS1 (supporting information).

Study selection

Titles and abstracts of the studies identified by the search strategy were screened independently for eligibility by two review authors. Eligibility was based on the aforementioned inclusion and exclusion criteria. Full‐text screening was also performed independently. Disagreements were resolved by discussion. If necessary, a third review author acted as arbitrator.

Data collection

Data extraction was carried out independently and in duplicate by two review authors using a predefined data extraction form. Disagreements, if any, were once again resolved by discussion.

The following study characteristics were extracted: first author, publication year, country or countries in which the study was performed, study design, number of participating patients and/or surgeons, patient diagnosis and available treatment options.

Recorded outcomes were the extent to which SDM was applied, irrespective of the metric used. SDM can be scored subjectively by patients and/or physicians10, 11, 12, 13, or objectively by independent observers using checklists14, 15.

In addition, information was collected about other questionnaires or instruments that measured outcomes associated with SDM, for example quality of life16 or decisional conflict17.

Risk of bias in individual studies

Risk of bias was evaluated independently by two investigators using checklists. Cross‐sectional studies were evaluated using the critical appraisal tool for analytical cross‐sectional studies from the Joanna Briggs Institute18. RCTs were evaluated by means of the critical appraisal checklist issued by the Dutch Cochrane collaboration19.

Summary measures

SDM and SDM‐related outcomes were expressed in the metrics used by the authors.

Synthesis of results

Meta‐analysis was performed if the metric used to measure SDM was reported in more than two studies using a similar questionnaire or instrument. If statistical heterogeneity was limited (I 2 value 50 per cent or less), a fixed‐effect model was used. If statistical heterogeneity was present (I 2 value over 50 per cent), a random‐effects model was used.

Additional analyses

SDM measured among patients was compared with that measured among surgeons in studies that provided data from both groups. In addition, SDM scored subjectively (by patients or physicians) was compared with SDM scored objectively, if these were measured in the same study.

Results

Study selection

A total of 2365 articles was identified. After removing duplicates, 1814 articles were screened based on title and abstract. Full‐text screening of 174 articles was undertaken. Cross‐referencing did not provide any additional eligible articles. Sixty‐eight articles were excluded as they did not measure SDM. Thirty‐two articles were included for data extraction and 22 articles were eligible for meta‐analysis (Fig. 1).

Figure 1.

BJS-11009-FIG-0001-c

PRISMA diagram showing selection of articles for review. SDM, shared decision‐making

Study characteristics

All 32 included publications20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51 had a cross‐sectional study design, 11 of which derived their patient population from previous cohort studies, or from the control group of a randomized trial33. Twenty of the 32 studies were published after 2010, 11 between 2000 and 2010, and one in 198938.

These 32 studies had a median of 130 participants (range 20–4825). Participants were studied across North America, Europe, Asia and Australia. Twenty‐six studies scored SDM from the patient's perspective, three from the surgeon's perspective, and another three scored both perspectives. Seventeen studies focused on treatment decisions in women with breast cancer. Colorectal cancer and lung cancer were each studied three times and carpal tunnel syndrome twice. Four studies included patients with various diagnoses who needed to decide between surgery or no surgery (Table1).

Table 1.

Characteristics of included studies

Reference Country Diagnosis Treatment options No. of participants
Agrawal et al.20 India Breast cancer Breast‐conserving surgery Mastectomy 47
Ananian et al.21 France Breast cancer Direct breast reconstruction Delayed breast reconstruction No breast reconstruction 181
Ankuda et al.22 USA Various Surgery No surgery 1034
Aravind et al.23 USA Severe lower leg trauma Primary amputation Reconstruction 20
Bleicher et al.24 USA Breast cancer Breast‐conserving surgery Mastectomy 1131
Budden et al.25 Australia Breast cancer Breast‐conserving surgery Mastectomy 104
Burton et al.26 UK Breast cancer Surgery + endocrine therapy Endocrine therapy alone 93
Cyran et al.27 USA Breast cancer Breast‐conserving surgery Mastectomy 198
Garcia‐Retamero et al.28 Switzerland Various Surgery No surgery 292*
Gong et al.29 South Korea Carpal tunnel syndrome One‐sided surgery Two‐sided surgery No surgery 78
Hawley et al.30 USA Breast cancer Breast‐conserving surgery + radiation Mastectomy 925
Hawley et al.31 USA Breast cancer Breast‐conserving surgery + radiation Mastectomy 1038
Hou et al.32 China Colorectal cancer Defunctioning stoma No defunctioning stoma 113
Janz et al.33 USA Breast cancer Breast‐conserving surgery 99
Mastectomy 8*
Katz et al.34 USA Breast cancer Breast‐conserving surgery Mastectomy 1422
Keating et al.35 USA Breast cancer Breast‐conserving surgery Mastectomy 1081
Kehl et al.36 USA Colorectal cancer and lung cancer Surgery Chemotherapy Radiation 4825
Lam et al.37 Hong Kong Breast cancer Breast‐conserving surgery Mastectomy 283
Larsson et al.38 Sweden Various Surgery No surgery 666
Mandelblatt et al.39 USA Breast cancer Breast‐conserving surgery Mastectomy 613
Mokhles et al.40 Netherlands Lung cancer Surgery Radiation 46*
Morgan et al.41 UK Breast cancer Surgery Endocrine therapy 729
Nam et al.42 South Korea Carpal tunnel syndrome Surgery Orthosis Corticosteroid injections 85
Nguyen et al.43 Canada and France Breast cancer Breast‐conserving surgery Mastectomy 121
O'Connor et al.44 Canada Various Surgery No surgery 122
Orom et al.45 USA Prostate cancer Active surveillance Cryotherapy Brachytherapy External beam radiation Surgery 120
Santema et al.46 Netherlands Abdominal aortic aneurysm and peripheral artery disease Conservative treatment 54
Endovascular surgery 12*
Open surgery
Seror et al.47 France Breast cancer Breast‐conserving surgery Mastectomy 415
Snijders et al.48 Netherlands Colorectal cancer Anastomosis – defunctioning stoma Anastomosis + defunctioning stoma End colostomy 32*
Vogel et al.49 Germany Breast cancer Breast‐conserving surgery Mastectomy Neoadjuvant treatment 137
Winner et al.50 USA Gastrointestinal and lung cancer Surgery 106
No surgery 10*
Woltz et al.51 Netherlands Mid‐shaft clavicle fracture Sling Open reduction and plate fixation 50
*

Surgeons.

Risk of bias in included studies

Overall, the methodological quality of the included studies was good. Inclusion criteria were defined clearly in 31 studies. The validity of the measures used was unclear in 15 of the 32 studies. Thirty studies described at least two of three items: demographics, location and time interval. Eight studies did not include participants based on a specified diagnosis or definition. Twenty‐four studies identified confounders and all but one of these studies stated how they dealt with them. Sixteen studies reported the use of at least one validated questionnaire to study outcomes. Thirty‐one studies stated the statistical analysis used clearly (Table  S1, supporting information).

Results of individual studies

Shared decision‐making scored by patients and/or surgeons (subjectively)

Table2 provides an overview of the metrics used to measure SDM and their results. The Control Perception Scale (CPS) questionnaire13 uses a five‐item Likert scale to measure whether the decision‐making process was perceived as more patient‐driven, shared or physician‐driven. The CPS questionnaire, or adapted versions, were used in 22 studies to study the number of patients and/or surgeons who perceived the decision‐making process as SDM. The adapted versions either used a three‐item rather than a five‐item Likert scale, or asked the same question without actually calling it the CPS questionnaire, or without referring to the original publication of this questionnaire. Two other questionnaires were also used to measure whether the decision‐making process was perceived as SDM. This was accomplished by deciding between four decision‐making strategies (paternalistic; some shared accepting or declining suggested treatment; shared; informed) and by asking which strategy best matched the consultation35, 43. Overall, between 10 and 37 per cent of patients and surgeons perceived the decision‐making process as SDM.

Table 2.

Overview of questionnaires or instruments to measure shared decision‐making and their results

Use of SDM
Shared decision‐making scored by patients and/or surgeons (subjectively)
Control Perception Scale questionnaire Meta‐analysis: 36 (95% c.i. 32 to 40, range 0–100)%20–24,26–34,36,41,42,44,47,49–51
Description of 4 decision‐making strategies 33·0% of patients (357 of 1081) matched with SDM (range 0–100%)35
9·8% of patients (18 of 184) matched with SDM (range 0–100%)43
23% of surgeons (16 of 70) matched with SDM (range 0–100%)43
Asking surgeons if they always use SDM 36·9% of surgeons (38 of 103) always use SDM (range 0–100%)48
SDM‐Q‐9 questionnaire 93 (i.q.r. 79–100, range 0–100)%46
74 (s.d. 23, range 0–100)%51
Perceived Involvement in Care Scale Patients aged 67–74 years: 62 (s.d. 25·0, range 0–100)%39
Patients aged >75 years: 54% (s.d. 27·4, range 0–100)%39
SDM‐Q‐Doc questionnaire 84 (i.q.r. 73–92, range 0–100)%46
Physicians' participatory decision‐making style 65 (s.d. 29·89, range 0–100)%45
Shared decision‐making scored by independent observers (objectively)
12‐item OPTION instrument 31 (s.d. 11, range 0–100)%46
7 (range 0–100)%48
Decision Analysis System for Oncology 39 (s.d. 6·4, range 0–100)%37

SDM, shared decision‐making.

Other metrics used to measure SDM subjectively were questionnaires that ask patients or physicians to score several statements related to the (shared) decision‐making process. For example, ‘My doctor and I thoroughly weighed the different treatment options’ is one of nine statements used in the SDM‐Q‐9 questionnaire. This questionnaire was used in two studies46, 51. Other questionnaires used, in which statements related to the decision‐making process are scored, were the SDM‐Q‐Doc questionnaire46, the Perceived Involvement in Care Scale (PICS) questionnaire39 and the physicians' participatory decision‐making style questionnaire45. Each of these three instruments was used in a single study. The SDM‐Q‐9 and PICS questionnaires are to be used by patients. The SDM‐Q‐Doc and physicians' participatory decision‐making style questionnaires are meant for physicians. Overall, levels of SDM as measured by the different metrics ranged from 54 to 93 per cent (Table2).

Shared decision‐making scored by independent observers (objectively)

SDM was measured objectively in two studies46, 48 using the 12‐item OPTION instrument and in one study37 using the Decision Analysis System for Oncology (DAS‐O). The 12‐item OPTION and DAS‐O instruments are scored by two observers independently using audio and audiovisual recordings respectively. Overall, SDM levels as measured by these two metrics ranged from 7 to 39 per cent (Table2).

Outcomes related to shared decision‐making

The 32 included studies reported on 25 different outcomes, which are summarized in Table3. Meta‐analysis was not possible owing to clinical heterogeneity. Nine of 25 SDM‐related outcomes were measured using validated questionnaires. The disabilities of the arm, shoulder and hand questionnaire was used and the effect of SDM on the treatment decision was measured in multiple studies. Six studies presented SDM‐related outcomes as the combined effect of SDM and patient‐driven decision‐making compared with the effect of surgeon‐driven decision‐making.

Table 3.

Overview of additional outcomes associated with shared decision‐making

Effect of SDM
Decisional conflict Decisional Conflict Scale =37
Quality of life WHO Quality of Life short form =47 *
Impact of breast cancer on life ↑39
Treatment decision Breast‐conserving surgery > mastectomy20, 26
Breast‐conserving surgery < mastectomy24 * ,34 *
Breast‐conserving surgery = mastectomy39,47 *
Mastectomy < mastectomy + breast reconstruction21
Surgery ↓ versus surgeon‐driven and ↑ versus patient‐driven41
Endocrine therapy ↓ versus patient‐driven and ↓ versus surgeon‐driven41
Depression Center for Epidemiologic Studies – Depression Scale =47 *
Brief Symptom Inventory‐18 ↓25 *
Anxiety or distress Brief Symptom Inventory‐18 ↓25 *
Global Severity Index ↓25 *
Unsure about surgery ↓22 *
Decision regret Decision regret scale ↑ (SDM framework present)37
Decision regret scale ↓ (SDM clear unbiased information present)37
Satisfaction with Amount of discussion ↑22 *
Amount of information ↑ versus surgeon‐driven and ↓ versus patient‐driven35
Information provided ↑47 *
Treatment decision process ↓25 *
Decision Scale ↑33 *
Treatment choice =35
Quality of care ↑ versus surgeon‐driven and = versus patient‐driven36
Communication ↑ versus surgeon‐driven and = versus patient‐driven36
Medical consultation ↑ (SDM framework present)37
Medical consultation ↓ (SDM clear unbiased information present)37
Overall breast cancer surgery ↑39
Decision‐making process =49
Functional outcome measures Disabilities of the arm, shoulder and hand questionnaire =29, 42
Effect on treatment Adhering to active surveillance ↑45
Antidepressant consumption ↑47 *
Tranquilizer/sedative consumption = * 47
Effect on consultation Duration =33 *

Increase (↑), decrease (↓) or no effect (=) resulting from shared decision‐making (SDM).

*

Combined effect of SDM and patient‐driven decision versus surgeon‐driven decision.

Synthesis of results

Data from the CPS questionnaire reported in 22 studies (patients and surgeons) were pooled to estimate the overall proportion of patients and surgeons who perceived the decision‐making process as SDM. Nineteen of these studies reported patient data alone, one reported only surgeon data, and two studies reported data from both patients and surgeons. A random‐effects model was used for meta‐analysis as the I 2 value was 94 per cent. Some 36 (95 per cent c.i. 32 to 40) per cent of 13 176 patients and surgeons perceived their consultations as SDM, 34 (30 to 38) per cent as patient‐driven and 25 (19 to 31) per cent as surgeon‐driven.

Additional analyses

Two studies33, 50 compared SDM among patients and among surgeons using the CPS questionnaire. Eighty‐nine of 204 surgeons (43·6 per cent) perceived the decision‐making process as SDM. In comparison, 60 of 205 patients (29·3 per cent) perceived the decision‐making process as SDM.

In addition, one study46 compared the 12‐item OPTION instrument with the SDM‐Q‐9 and SDM‐Q‐DOC questionnaires, showing that the level of SDM scored objectively was much lower (31 per cent) than that scored subjectively by patients (93 per cent) and surgeons (84 per cent).

Discussion

A substantial number of studies have addressed SDM in surgeon–patient encounters, indicating growing interest in SDM in surgery. Despite this interest, the present review shows that use of SDM within surgical practice, interpreted subjectively by patients and surgeons as well as the objectively scored level, is infrequent. Subjectively, however, patients and surgeons appear to have a more optimistic view than the objective measurements show. Surgeons report using SDM more often than their patients, whereas patients report a higher level of SDM during the consultation than surgeons. The large number of metrics used to measure SDM and SDM‐related outcomes makes comparison between studies difficult.

Based on the overall results of the CPS questionnaire, the decision‐making process scored subjectively during surgeon–patient encounters was most commonly perceived as shared or patient‐driven. The prevalence of SDM among surgeon–patient encounters reviewed here is slightly higher than in the usual‐care group in the review on decision aids by Stacey and colleagues7. They also reported a high level of patient‐driven decision‐making. This may be related to the predominance of studies on breast cancer, an area in which patient‐driven decision‐making has become common. Another explanation may be that patients perceived the decision‐making process as patient‐driven, just because they were asked whether they agreed with the proposed treatment (gave informed consent)46. Nevertheless, the CPS questionnaire appears useful for comparing the preferred decision‐making approach before the encounter with the perceived level of involvement in the treatment decision after the encounter.

Other subjective metrics, such as the SDM‐Q‐9 and SDM‐Q‐Doc questionnaires, showed slightly higher levels of SDM in surgery than in other medical specialties. For example, Doherr and co‐workers52 reported mean total SDM‐Q‐9 and SDM‐Q‐Doc scores ranging from 42 to 75 per cent. These high subjective SDM levels in surgical studies may also be caused by a misinterpretation of the informed consent procedure for SDM.

Data obtained using the objective instruments OPTION and DAS‐O showed low SDM levels in surgical settings. Similar scores were seen in patient encounters with other medical specialties14, showing an overall mean(s.d.) of 23 (14) per cent using the OPTION instrument.

The large difference between objective and subjective SDM scores has been explained previously by the inability of the OPTION instrument to account for non‐verbal communication53. However, the DAS‐O instrument, as used by Lam and colleagues37, was adjusted to include non‐verbal communication using audiovisual recordings. These audiovisual recordings also showed low SDM scores, but this instrument was not compared with subjective questionnaires.

This difference between objectively and subjectively scored SDM levels may be due to insufficient knowledge of what SDM really means. This was confirmed in a recent study among trauma surgeons51. Under these circumstances, the subjectively scored metrics suffer from a ceiling effect when users express their satisfaction with the consultation or informed consent procedure, rather than the level of SDM if unaware of what SDM entails.

The use and scoring of SDM may be improved by educating both surgeons and patients about it54. Programmes have been initiated to make physicians aware of the benefits of SDM, and to make patients mindful that they are allowed and even encouraged to give their opinion. These initiatives comprise, for instance, national campaigns, training sessions and the development of decision support tools55.

Nevertheless, it remains unclear whether the focus should be on improving objectively scored SDM levels. Perhaps subjective high SDM scores by patients might also bring forth beneficial SDM‐related outcomes. Unfortunately, none of the included studies evaluated the correlation of both objective instruments and subjective questionnaires with SDM‐related outcomes.

In addition to the wide range of instruments and questionnaires available to study the level of SDM, the list of metrics used to measure outcomes associated with SDM was also extensive. None of these outcomes could be compared with each other, because the questionnaires used were either non‐validated, used in only one study, disease‐specific, combined SDM and patient‐driven decision‐making, or provided outcomes for different subscales of SDM. In addition, very few studies reported absolute data, making comparison with other studies even more difficult.

As advised by both the Core Outcome Measures in Effectiveness Trial (COMET) initiative56 and the International Consortium for Health Outcomes Measurement (ICHOM)57, the use of standard instruments or questionnaires is particularly valuable as it permits pooling of results to determine, for instance, the effectiveness of new interventions to improve SDM, such as the development of decision support tools. In addition, being able to compare levels of SDM and SDM‐related outcomes may provide insight into which medical specialties are SDM frontrunners, or, in contrast, which low‐performing specialties require additional support.

From the perspective of SDM, the authors advocate the use of currently available standardized, validated and preferably generic instruments and questionnaires. To measure the level of SDM in a surgeon–patients encounter in which treatment decisions are made, the CPS questionnaire, the OPTION instrument, and SDM‐Q‐9 and SDM‐Q‐DOC questionnaires are recommended. More research is needed on whether subjectively or objectively scored metrics for SDM correlate best with SDM‐related outcomes, such as decisional conflict and satisfaction with treatment. In addition, studies should find out which SDM metrics can be used to evaluate new interventions for improving SDM.

Limitations of this study include the heterogeneity of the outcome measures used. This made it difficult to compare studies and to perform meta‐analyses. Despite this heterogeneity, a decision was made to continue pooling the CPS questionnaire data, to provide an overall sense of the extent to which patients and surgeons currently perceive SDM. Exploring this heterogeneity by selecting only articles that used the CPS questionnaire with the five‐item Likert scales, articles published since 2010, or articles focusing on breast cancer or no breast cancer, did not yield valuable information. Furthermore, all studies were observational. Although SDM can effectively be measured outside a trial setting, there may have been some limitations owing to the observational design. It was often unclear how much time had passed between the consultation and the moment patients and surgeons were asked to evaluate the consultation. Perhaps, over time, patients and surgeons may not exactly remember how the decision was made. The observational design also makes it difficult to know the extent to which patients and surgeons were informed about SDM before both the consultation and the evaluation. Finally, only three studies compared the level of SDM between patients and surgeons in the same investigation, using two different questionnaires. Thus, no clear statements could be made about whether there is a true difference between patients and surgeons in how they view the decision‐making process.

The difference between the present systematic review and other reviews regarding SDM in surgery is that previous studies focused mostly on the availability or effectiveness of tools developed to improve SDM58, 59. This review concludes that, before focusing on ways to improve SDM, it is first necessary to evaluate the current use of SDM and, even more importantly, how to measure SDM uniformly.

Supporting information

Appendix S1 Search strategy

Table S1 Risk of bias analysis

Acknowledgements

The authors thank F. S. van Etten‐Jamaludin, clinical librarian and medical information specialist, for assistance in preparing the literature search. This paper reports the results of a preregistered systematic review (http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=CRD42017073406). This study was funded by the AMC Foundation, which was not involved in the study design, data analysis or interpretation of results.

Disclosure: The authors declare no conflict of interest.

References

  • 1. Barry MJ, Edgman‐Levitan S. Shared decision making – pinnacle of patient‐centered care. N Engl J Med 2012; 366: 780–781. [DOI] [PubMed] [Google Scholar]
  • 2. Stiggelbout AM, Pieterse AH, De Haes JC. Shared decision making: concepts, evidence, and practice. Patient Educ Couns 2015; 98: 1172–1179. [DOI] [PubMed] [Google Scholar]
  • 3. Elwyn G, Durand MA, Song J, Aarts J, Barr PJ, Berger Z et al A three‐talk model for shared decision making: multistage consultation process. BMJ 2017; 359: j4891. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Knops AM, Legemate DA, Goossens A, Bossuyt PM, Ubbink DT. Decision aids for patients facing a surgical treatment decision: a systematic review and meta‐analysis. Ann Surg 2013; 257: 860–866. [DOI] [PubMed] [Google Scholar]
  • 5. Mulley AG, Trimble C, Elwyn G. Stop the silent misdiagnosis: patients' preferences matter. BMJ 2012; 345: e6572. [DOI] [PubMed] [Google Scholar]
  • 6. Oshima Lee E, Emanuel EJ. Shared decision making to improve care and reduce costs. N Engl J Med 2013; 368: 6–8. [DOI] [PubMed] [Google Scholar]
  • 7. Stacey D, Legare F, Lewis K, Barry MJ, Bennett CL, Eden KB et al Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev 2017; (4)CD001431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Ubbink DT, Hageman MG, Legemate DA. Shared decision‐making in surgery. Surg Technol Int 2015; 26: 31–36. [PubMed] [Google Scholar]
  • 9. Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group . Preferred reporting items for systematic reviews and meta‐analyses: the PRISMA statement. Int J Surg 2010; 8: 336–341. [DOI] [PubMed] [Google Scholar]
  • 10. Barr PJ, Thompson R, Walsh T, Grande SW, Ozanne EM, Elwyn G. The psychometric properties of collaborate: a fast and frugal patient‐reported measure of the shared decision‐making process. J Med Internet Res 2014; 16: e2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Kriston L, Scholl I, Hölzel L, Simon D, Loh A, Härter M. The 9‐item shared decision making questionnaire (SDM‐Q‐9). Development and psychometric properties in a primary care sample. Patient Educ Couns 2010; 80: 94–99. [DOI] [PubMed] [Google Scholar]
  • 12. Scholl I, Kriston L, Dirmaier J, Buchholz A, Härter M. Development and psychometric properties of the Shared Decision Making Questionnaire – physician version (SDM‐Q‐DOC). Patient Educ Couns 2012; 88: 284–290. [DOI] [PubMed] [Google Scholar]
  • 13. Degner LF, Kristjanson LJ, Bowman D, Sloan JA, Carriere KC, O'Neil J et al Information needs and decisional preferences in women with breast cancer. JAMA 1997; 277: 1485–1492. [PubMed] [Google Scholar]
  • 14. Couët N, Desroches S, Robitaille H, Vaillancourt H, Leblanc A, Turcotte S et al Assessments of the extent to which health‐care providers involve patients in decision making: a systematic review of studies using the OPTION instrument. Health Expect 2015; 18: 542–561. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Stubenrouch FE, Pieterse AH, Falkenberg R, Santema TK, Stiggelbout AM, van der Weijden T et al Option(5) versus option(12) instruments to appreciate the extent to which healthcare providers involve patients in decision‐making. Patient Educ Couns 2016; 99: 1062–1068. [DOI] [PubMed] [Google Scholar]
  • 16. Ware J Jr, Kosinski M, Keller SD. A 12‐item short‐form health survey: construction of scales and preliminary tests of reliability and validity. Med Care 1996; 34: 220–233. [DOI] [PubMed] [Google Scholar]
  • 17. O'Connor AM. Validation of a decisional conflict scale. Med Decis Making 1995; 15: 25–30. [DOI] [PubMed] [Google Scholar]
  • 18. Moola S, Munn Z, Tufanaru C, Aromataris E, Sears K, Sfetcu R et al In Joanna Briggs Institute Reviewer's Manual, Aromataris E, Munn Z. (eds). The Joanna Briggs Institute: Adelaide, 2017. [Google Scholar]
  • 19. Higgins JPT, Green S. (eds). Cochrane Handbook for Systematic Reviews of Interventions. The Cochrane Collaboration: London, 2011. [Google Scholar]
  • 20. Agrawal S, Goel AK, Lal P. Participation in decision making regarding type of surgery and treatment‐related satisfaction in North Indian women with early breast cancer. J Cancer Res Ther 2012; 8: 222–225. [DOI] [PubMed] [Google Scholar]
  • 21. Ananian P, Houvenaeghel G, Protière C, Rouanet P, Arnaud S, Moatti JP et al Determinants of patients' choice of reconstruction with mastectomy for primary breast cancer. Ann Surg Oncol 2004; 11: 762–771. [DOI] [PubMed] [Google Scholar]
  • 22. Ankuda CK, Block SD, Cooper Z, Correll DJ, Hepner DL, Lasic M et al Measuring critical deficits in shared decision making before elective surgery. Patient Educ Couns 2014; 94: 328–333. [DOI] [PubMed] [Google Scholar]
  • 23. Aravind M, Shauver MJ, Chung KC. A qualitative analysis of the decision‐making process for patients with severe lower leg trauma. Plast Reconstr Surg 2010; 126: 2019–2029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Bleicher RJ, Abrahamse P, Hawley ST, Katz SJ, Morrow M. The influence of age on the breast surgery decision‐making process. Ann Surg Oncol 2008; 15: 854–862. [DOI] [PubMed] [Google Scholar]
  • 25. Budden LM, Hayes BA, Buettner PG. Women's decision satisfaction and psychological distress following early breast cancer treatment: a treatment decision support role for nurses. Int J Nurs Pract 2014; 20: 8–16. [DOI] [PubMed] [Google Scholar]
  • 26. Burton M, Kilner K, Wyld L, Lifford KJ, Gordon F, Allison A et al Information needs and decision‐making preferences of older women offered a choice between surgery and primary endocrine therapy for early breast cancer. Psychooncology 2017; 26: 2094–2100. [DOI] [PubMed] [Google Scholar]
  • 27. Cyran EM, Crane LA, Palmer L. Physician sex and other factors associated with type of breast cancer surgery in older women. Arch Surg 2001; 136: 185–191. [DOI] [PubMed] [Google Scholar]
  • 28. Garcia‐Retamero R, Wicki B, Cokely ET, Hanson B. Factors predicting surgeons' preferred and actual roles in interactions with their patients. Health Psychol 2014; 33: 920–928. [DOI] [PubMed] [Google Scholar]
  • 29. Gong HS, Huh JK, Lee JH, Kim MB, Chung MS, Baek GH. Patients' preferred and retrospectively perceived levels of involvement during decision‐making regarding carpal tunnel release. J Bone Joint Surg Am 2011; 93: 1527–1533. [DOI] [PubMed] [Google Scholar]
  • 30. Hawley ST, Janz NK, Hamilton A, Griggs JJ, Alderman AK, Mujahid M et al Latina patient perspectives about informed treatment decision making for breast cancer. Patient Educ Couns 2008; 73: 363–370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Hawley ST, Lantz PM, Janz NK, Salem B, Morrow M, Schwartz K et al Factors associated with patient involvement in surgical treatment decision making for breast cancer. Patient Educ Couns 2007; 65: 387–395. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Hou XT, Pang D, Lu Q, Xu Z, Zhou YJ. Preferred and actual participation roles in operation treatment decision making of patients with colorectal cancer. Int J Nurs Sci 2014; 1: 376–380. [Google Scholar]
  • 33. Janz NK, Wren PA, Copeland LA, Lowery JC, Goldfarb SL, Wilkins EG. Patient‐physician concordance: preferences, perceptions, and factors influencing the breast cancer surgical decision. J Clin Oncol 2004; 22: 3091–3098. [DOI] [PubMed] [Google Scholar]
  • 34. Katz SJ, Lantz PM, Janz NK, Fagerlin A, Schwartz K, Liu L et al Patient involvement in surgery treatment decisions for breast cancer. J Clin Oncol 2005; 23: 5526–5533. [DOI] [PubMed] [Google Scholar]
  • 35. Keating NL, Guadagnoli E, Landrum MB, Borbas C, Weeks JC. Treatment decision making in early‐stage breast cancer: should surgeons match patients' desired level of involvement? J Clin Oncol 2002; 20: 1473–1479. [DOI] [PubMed] [Google Scholar]
  • 36. Kehl KL, Landrum MB, Arora NK, Ganz PA, van Ryn M, Mack JW et al Association of actual and preferred decision roles with patient‐reported quality of care: shared decision making in cancer care. JAMA Oncol 2015; 1: 50–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Lam WW, Kwok M, Chan M, Hung WK, Ying M, Or A et al Does the use of shared decision‐making consultation behaviors increase treatment decision‐making satisfaction among Chinese women facing decision for breast cancer surgery? Patient Educ Couns 2014; 94: 243–249. [DOI] [PubMed] [Google Scholar]
  • 38. Larsson US, Svärdsudd K, Wedel H, Säljö R. Patient involvement in decision‐making in surgical and orthopaedic practice: the Project Perioperative Risk. Soc Sci Med 1989; 28: 829–835. [DOI] [PubMed] [Google Scholar]
  • 39. Mandelblatt J, Kreling B, Figeuriedo M, Feng S. What is the impact of shared decision making on treatment and outcomes for older women with breast cancer? J Clin Oncol 2006; 24: 4908–4913. [DOI] [PubMed] [Google Scholar]
  • 40. Mokhles S, Maat APWM, Aerts JGJV, Nuyttens JJME, Bogers AJJC, Takkenberg JJM. Opinions of lung cancer clinicians on shared decision making in early‐stage non‐small‐cell lung cancer. Interact Cardiovasc Thorac Surg 2017; 25: 278–284. [DOI] [PubMed] [Google Scholar]
  • 41. Morgan JL, Burton M, Collins K, Lifford KJ, Robinson TG, Cheung KL et al; Bridging the Age Gap Trial Management Team . The balance of clinician and patient input into treatment decision‐making in older women with operable breast cancer. Psychooncology 2015; 24: 1761–1766. [DOI] [PubMed] [Google Scholar]
  • 42. Nam KP, Gong HS, Bae KJ, Rhee SH, Lee HJ, Baek GH. The effect of patient involvement in surgical decision making for carpal tunnel release on patient‐reported outcome. J Hand Surg Am 2014; 39: 493–498. [DOI] [PubMed] [Google Scholar]
  • 43. Nguyen F, Moumjid N, Charles C, Gafni A, Whelan T, Carrère MO. Treatment decision‐making in the medical encounter: comparing the attitudes of French surgeons and their patients in breast cancer care. Patient Educ Couns 2014; 94: 230–237. [DOI] [PubMed] [Google Scholar]
  • 44. O'Connor AM, Drake ER, Wells GA, Tugwell P, Laupacis A, Elmslie T. A survey of the decision‐making needs of Canadians faced with complex health decisions. Health Expect 2003; 6: 97–109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45. Orom H, Homish DL, Homish GG, Underwood W III. Quality of physician–patient relationships is associated with the influence of physician treatment recommendations among patients with prostate cancer who chose active surveillance. Urol Oncol 2014; 32: 396–402. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Santema TB, Stubenrouch FE, Koelemay MJ, Vahl AC, Vermeulen CF, Visser MJ et al Shared decision making in vascular surgery: an exploratory study. Eur J Vasc Endovasc Surg 2016; 51: 587–593. [DOI] [PubMed] [Google Scholar]
  • 47. Seror V, Cortaredona S, Bouhnik AD, Meresse M, Cluze C, Viens P et al Young breast cancer patients' involvement in treatment decisions: the major role played by decision‐making about surgery. Psychooncology 2013; 22: 2546–2556. [DOI] [PubMed] [Google Scholar]
  • 48. Snijders HS, Kunneman M, Bonsing BA, de Vries AC, Tollenaar RA, Pieterse AH et al Preoperative risk information and patient involvement in surgical treatment for rectal and sigmoid cancer. Colorectal Dis 2014; 16: O43–O49. [DOI] [PubMed] [Google Scholar]
  • 49. Vogel BA, Helmes AW, Hasenburg A. Concordance between patients' desired and actual decision‐making roles in breast cancer care. Psychooncology 2008; 17: 182–189. [DOI] [PubMed] [Google Scholar]
  • 50. Winner M, Wilson A, Yahanda A, Kim Y, Pawlik TM. A cross‐sectional study of patient and provider perception of ‘cure’ as a goal of cancer surgery. J Surg Oncol 2016; 114: 677–683. [DOI] [PubMed] [Google Scholar]
  • 51. Woltz S, Krijnen P, Meylaerts SAG, Pieterse AH, Schipper IB. Shared decision making in the management of midshaft clavicular fractures: nonoperative treatment or plate fixation. Injury 2017; 48: 920–924. [DOI] [PubMed] [Google Scholar]
  • 52. Doherr H, Christalle E, Kriston L, Härter M, Scholl I. Use of the 9‐item Shared Decision Making Questionnaire (SDM‐Q‐9 and SDM‐Q‐DOC) in intervention studies – a systematic review. PLoS One 2017; 12: e0173904. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53. Kasper J, Heesen C, Köpke S, Fulcher G, Geiger F. Patients' and observers' perceptions of involvement differ. Validation study on inter‐relating measures for shared decision making. PLoS One 2011; 6: e26255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54. Légaré F, Labrecque M, Cauchon M, Castel J, Turcotte S, Grimshaw J. Training family physicians in shared decision‐making to reduce the overuse of antibiotics in acute respiratory infections: a cluster randomized trial. CMAJ 2012; 184: E726–E734. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55. van der Weijden T, Post H, Brand PLP, van Veenendaal H, Drenthen T, van Mierlo LA et al Shared decision making, a buzz‐word in The Netherlands, the pace quickens towards nationwide implementation. Z Evid Fortbild Qual Gesundhwes 2017; 123‐124: 69–74. [DOI] [PubMed] [Google Scholar]
  • 56. Kryworuchko J, Stacey D, Bennett C, Graham ID. Appraisal of primary outcome measures used in trials of patient decision support. Patient Educ Couns 2008; 73: 497–503. [DOI] [PubMed] [Google Scholar]
  • 57. Ong WL, Schouwenburg MG, van Bommel ACM, Stowell C, Allison KH, Benn KE et al A standard set of value‐based patient‐centered outcomes for breast cancer: the International Consortium For Health Outcomes Measurement (ICHOM) initiative. JAMA Oncol 2017; 3: 677–685. [DOI] [PubMed] [Google Scholar]
  • 58. Fowler GE, Baker DM, Lee MJ, Brown SR. A systematic review of online resources to support patient decision‐making for full‐thickness rectal prolapse surgery. Tech Coloproctol 2017; 21: 853–862. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59. Zdenkowski N, Butow P, Tesson S, Boyle F. A systematic review of decision aids for patients making a decision about treatment for early breast cancer. Breast 2016; 26: 31–45. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Appendix S1 Search strategy

Table S1 Risk of bias analysis


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