Abstract
Objectives.
Lung cancer screening is a complex and individualized decision. To understand how best to support patients in this decision, we must understand how shared decision-making is associated with both decisional and behavioral outcomes.
Methods.
Observational cohort study combining patient survey data with electronic health record data of lung screening-eligible patients who recently engaged in a shared decision-making discussion about screening with a primary care clinician.
Results.
Using multivariable analysis (n=529), factors associated with higher lung cancer screening decisional quality include higher knowledge (OR=1.33, p<.0001), lower perceived benefits (OR=0.90, p=.0004), higher perceived barriers (OR=1.07, p<.0001), higher self-efficacy (OR=1.13, p<.0001), and higher levels of perceiving the discussion was shared (OR=1.04, p<.0001). Factors associated with the patient’s decision to screen include older age (OR=1.12, p=.0050) and higher self-efficacy (OR=1.11, p=.0407). Factors associated with screening completion included older age (OR=1.05, p=.0050), higher knowledge (OR=1.24, p=.0045), and higher self-efficacy (OR= 1.12, p=.0003).
Conclusions.
Shared decision-making in lung cancer screening is a dyadic process between patient and clinician. As we continue to strive for high quality patient-centered care, patient decision quality may be enhanced by targeting key factors such as high-quality knowledge, self-efficacy, and fostering a shared discussion to support patient engagement in lung cancer screening decisions.
Keywords: lung cancer screening, shared decision-making, decision quality
1. Introduction
In the U.S., annual lung cancer screening (LCS) with chest low-dose computed tomography (LDCT) is recommended for individuals aged 50 to 80 years with a 20 pack-year smoking history who either currently smoke cigarettes or quit within the past 15 years.1 However, LCS is a complex and individualized decision where the benefits and risks must be weighed against personal risk factors, comorbidities that may preclude surgical treatment, and available treatment options as well as personal tolerance for uncertainty.2,3 To date, patient awareness about LCS remains exceptionally low with less than 30% of the screening-eligible patient population aware that screening exists.4 Educating eligible patients about the option to screen for lung cancer is critically important if the public health benefit of screening and early detection, which is improved survival in the wake of an earlier lung cancer diagnosis, is to be realized. A key reimbursement requirement of the Center for Medicare and Medicaid Services National Coverage Determination for lung cancer screening is that the decision occur as a result of shared decision making between an individual and an informed clinician.2 To understand how best to support patients in the decision to screen, or not, for lung cancer, we must determine how shared decision making (SDM) is associated with patient decisional and behavioral (i.e., screening) outcomes.
In 2015, Medicare made an unprecedented move in mandating documentation of a SDM discussion for LCS reimbursement.2 SDM is viewed as the pinnacle of patient-centered care and resonates with the ethical imperative of respect for patient autonomy and engagement.5 This unique health policy change created a need for optimal strategies that support patients and clinicians in making shared decisions to screen, or not, for lung cancer. The purposes of this study were to: 1) identify factors associated with a patient’s: a) perception of LCS decisional quality; b) decision to screen; and c) screening completion among those who decided to screen; and 2) determine if, and how, decisional quality is related to the decision to screen and screening completion.
2. Methods
2.1. Study Design
This was an observational cohort study guided by the patient-focused Conceptual Model for Lung Cancer Screening Participation.6 We surveyed patients from the Kaiser Permanente Washington (KPWA) health system who underwent SDM for LCS and linked them with patient electronic health record (EHR) data. We used the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement checklist to guide reporting of results.7
2.2. Study Setting
Patients who had recently engaged in a SDM discussion about LCS with a primary care clinician were recruited from KPWA health system located in Washington State. KPWA developed smart-sets in 2015 that were integrated into the electronic health record for clinicians to use with potentially eligible patients to confirm eligibility, document the SDM process, and document the patient’s initial decision (opt-in, opt-out, or undecided about screening).8 This process allowed the study programmer to rapidly identify patients who had an SDM visit with a clinician about LCS. Institutional review board (IRB) approval was received from the Kaiser Permanente Washington IRB.
Beginning in 2019, the study programmer used KPWA EHR data to identify patients who met USPSTF LCS guideline eligibility criteria and had recently engaged in an SDM conversation with a primary care clinician. In September 2019, USPSTF LCS guidelines included individuals aged 55 to 80 years with a 30 pack-year or greater smoking history who currently smoked or quit within the past 15 years. In response to new scientific evidence, the USPSTF LCS guideline was updated in March 2021 to reduce the minimum screening-eligible age to 50 years and smoking history to 20 pack-years.1 Study inclusion criteria were therefore updated in April 2021 in response to these revised criteria.
The study programmer ran code daily to identify patients who had an SDM discussion with a primary care clinician documented in the EHR on the prior business day. Each individual was mailed a study invitation letter and information sheet within one week of being identified. Study participation was outlined in the written invitation and included the information sheet. Participants were offered the choice to complete the 30-minute survey online or by telephone. The informed consent form included permission to use relevant data from the participant’s EHR. The information sheet from the recruitment packet was considered part of the informed consent process and provided information about potential risks and benefits of study participation, privacy protection, voluntary participation that would not impact their care, study incentive information, and a phone number to call with questions.
2.3. Study Measures
2.3.1. Study Outcomes
The study outcomes were patient perception of LCS decisional quality, decision to screen, and screening completion. Decisional Quality of the LCS decision was measured using the well-established, multidimensional Decisional Conflict Scale (DCS).9 The DCS is a 16-item Likert-response scale that was modified by the investigators for the LCS context,9 and has been validated in many health decision contexts, including mammography.10–13 Despite its name, the DCS measures more than decisional conflict; it encompasses personal perceptions of decision-making quality including: 1) uncertainty in choosing options, modifiable factors contributing to uncertainty (such as feeling uninformed or unclear about personal values and unsupported in decision making), 2) effective decision making including feeling the choice is informed, values-based, and likely to be implemented, and 3) decisional satisfaction. Each item is assessed on a 5-point Likert scale that spans from 0 (strongly agree) to 4 (strongly disagree), resulting in a total score ranging from 0 to 64. This total score is commonly transformed into a standardized score that falls within a 0 to 100 range.9,12 Decisional quality measured on this numeric scale from which lower scores represent lower decisional conflict and, therefore, higher decisional quality. Scores below 25 have been associated with low decisional conflict. We use this cut-off score to dichotomize this variable in our analysis.9 The Decision to Screen was captured categorically in the EHR through smart-sets that clinicians use to confirm screening eligibility, document the SDM discussion, use of a PDA, and the patient’s screening decision. Lung Cancer Screening Completion was assessed prospectively via EHR and coded as “yes” or “no” at six months after the initial SDM conversation.
Antecedent Variables.
Shared Decision-Making. Patients’ perceptions that the screening decision was shared was measured using the validated 9-item Shared Decision-Making Questionnaire (SDM-Q-9).14 The SDM-Q-9 is a theory-driven instrument that measures the extent to which patients are involved in the process of decision-making from the perspective of the individual making the decision.14 Lower scores indicate the patient perceived the SDM discussion with the clinician to be minimally shared.14 Knowledge. Knowledge of lung cancer screening was measured using a 7-item investigator-developed scale used in our prior studies.15–18 Items with a multiple-choice response format were used to assess knowledge of lung cancer, risk factors, and screening. Correct responses were coded as 1 and incorrect responses as 0 and were summed to indicate the total number of correct responses. Lung Cancer Screening Health Beliefs. Perceived risk of lung cancer, benefits of, barriers to, and self-efficacy for lung cancer screening were measured using four psychometrically validated Likert-response option scales.15 Perceived Smoking-related Stigma was measured using the 5-item smoking-related subscale of the Cataldo Lung Cancer Stigma Scale,19 with higher scores indicating higher levels of perceived stigma. Medical Mistrust was measured using the 5-item theoretically-driven psychometrically validated Patient Trust in the Medical Profession Scale with higher scores indicative of higher levels of trust in the clinician.19,20 Sociodemographic and Health Status Characteristics. Patient age and gender were collected from the EHR. Patient race, ethnicity, education, perceived financial adequacy, general health status, and family history of lung cancer were collected via survey. Patient smoking status was collected from the EHR and verified via survey.
2.4. Data Analysis
We used a complete case analysis (Figure 1). Descriptive statistics were reported using frequency (percentage) and mean (SD), respectively, for categorical and continuous variables. Bivariable tests of association between predictors and dependent variables were modeled using general linear models when the outcomes were continuous, yielding estimates of regression parameters (i.e., coefficients) or least square means for continuous and categorical independent variables, respectively, and using logistic regression models when the outcomes were dichotomous, providing odds ratios (OR) with 95% confidence intervals. Multivariable analyses were performed using those variables that had p-values <0.20 in the bivariable analyses, to determine which independent variables were independently associated with the outcomes of interest. All analytic assumptions were verified and collinearity was assessed. Analyses were performed using SAS v9.4 (SAS Institute, Cary, NC).
Figure 1.

CONSORT Flow Diagram for DECIDE Study: Patient Participants
3. Results
3.1. Participants
A flow diagram of participant inclusion is shown in Figure 1. Overall, the study participation rate (defined as the total number of participants who completed the survey divided by the total number of individuals identified as eligible for the study) was 35.2% and the response rate (defined as the total number of participants who completed the survey divided by the number of participants in the sample that enrolled in the study) was 71%. A total of 529 patients were included in the analyses. The majority of participants (81.1%, n=429) completed the survey after their SDM discussion with a clinician and before completing the screening LDCT of the chest. The mean(+SD) age of participants was 66.4 years(+5.9), 44.4% were women, 87.5% were White , 2.3% were Hispanic, and 34.4% had completed college (Table 1).
Table 1.
Participant Demographic Characteristics (N=529)
| Characteristic | n (%) | 
|---|---|
| Age; mean (std) | 66.4 (5.9) | 
| Sex | |
| Female | 235 (44.4) | 
| Race | |
| White | 463 (87.5) | 
| Ethnicity | |
| Hispanic | 12 (2.3) | 
| Education | |
| Less than high school | 20 (3.8) | 
| High school graduate or equivalent | 94 (17.8) | 
| Some college | 233 (44.0) | 
| College graduate or higher | 182 (34.4) | 
| Perceived Financial Adequacy | |
| Enough money for special things after paying bills | 288 (54.4) | 
| Enough money to pay bills, but little else | 177 (33.5) | 
| Enough money to pay bills, but have to cut back | 48 (9.1) | 
| Difficulty paying bills | 16 (3.0) | 
| General Health | |
| Excellent | 13 (2.5) | 
| Very good | 124 (23.4) | 
| Good | 237 (44.8) | 
| Fair | 127 (24.0) | 
| Poor | 26 (4.9) | 
| Don’t Know | 2 (0.4) | 
| Family History of Lung Cancer | |
| Yes | 143 (27.0) | 
| Smoking Status | |
| Currently Smokes | 233 (44.0) | 
We examined all variables in the overall sample, and by screening completion outcome (Table 2). Descriptively, the overall sample had moderate knowledge levels about lung cancer risk and screening (total mean score 4.7, SD 1.4; possible range 0-7), high self-efficacy for LCS (total mean score 32.1, SD 4.3; possible range 16-36), fairly high perceived barriers to LCS (total mean score 57.2, SD 8.3; possible range 34–68), low perceived benefits of LCS (total mean score 11.1, SD 3.1; possible range 6–24), moderate perceived risk of lung cancer (total mean score 7.8, SD 1.8; range 3–12), fairly low medical trust (total mean score 10.7, SD 2.8; possible range 5–20), moderate perceived stigma (total mean score 11.0, SD 2.5; possible range 5–20), and moderately high perceptions that the LCS decision was a shared decision (total mean score 65.8, SD 29.9; possible range 0–100). When compared by screening outcome using bivariable tests, there were significant differences in knowledge, self-efficacy, perceived barriers, and perception that the LCS decision was shared. Patients who screened had higher knowledge scores and higher self-efficacy scores compared to those who did not screen (Table 2). Those who screened also had higher perceived barriers to screening and lower perceptions that the decision was shared (Table 2). Decisional quality scores were significantly lower in those who decided to screen and completed screening compared with those who decided not to screen or were undecided; mean=20.2 (SD 14.2) vs. 25.4 (SD 18.3) (p=.0038), respectively (Table 2). We focus on multivariable results, described next in the text. It should be noted that we conducted a sensitivity analysis in which linear models were used with the decisional quality scores (i.e., continuous DCS total scale scores) initially and where we found similar results to the dichotomized DCS scale scores. We are reporting the dichotomous DCS scale score models, given that odds ratios are more intuitively interpreted by clinicians compared to linear regression coefficients.
Table 2.
Health Beliefs, Psychological Characteristics, Decisional Quality, & Perception of Shared Lung Cancer Screening decision
| Overall | Screened | Not screened | p | ||
|---|---|---|---|---|---|
| Construct | n (%) | Mean (SD), Range | Mean (SD) | Mean (SD) | |
| Knowledge: Lung Cancer Risk and Screening | 529 | 4.7 (1.4); 0 – 7 | 4.8 (1.4) | 4.3 (1.5) | .0002 | 
| Self-Efficacy for Lung Cancer Screening | 529 | 32.1 (4.3); 16 – 36 | 32.6 (4.0) | 30.6 (4.9) | <.0001 | 
| Perceived Barriers to Lung Cancer Screening | 528 | 57.2 (8.3); 34 – 68 | 57.7 (8.4) | 55.9 (7.6) | .0331 | 
| Perceived Benefits of Lung Cancer Screening | 524 | 11.1 (3.1); 6 – 24 | 11.0 (3.0) | 11.5 (3.3) | .0734 | 
| Perceived Risk of Lung Cancer | 500 | 7.8 (1.8); 3 – 12 | 7.8 (1.8) | 8.0 (1.8) | .2790 | 
| Medical Trust | 521 | 10.7 (2.8); 5 – 20 | 10.6 (2.7) | 10.8 (3.0) | .4256 | 
| Perceived Stigma | 525 | 11.0 (2.5); 5 – 20 | 11.0 (2.5) | 11.0 (2.6) | .8265 | 
| Decisional Quality | 529 | 21.5 (15.5); 0 – 75 | 20.2 (14.2) | 25.4 (18.3) | .0038 | 
| Perception that Lung Cancer Screening Decision was Shared | 511 | 65.8 (29.9); 0 – 100 | 57.4 (29.2) | 60.9 (31.5) | .0341 | 
3.2. Factors Associated with Lung Cancer Screening Decisional Quality
Overall, patients reported moderate decisional quality (total mean score 21.5, SD 15.5; possible range 0–75). As shown in Table 3, patient factors associated with higher decisional quality in multivariable analysis included higher total knowledge scores (OR=1.33, p<0001), lower perceived benefits of LCS (OR=0.91, p=.0016), higher perceived barriers to LCS (OR=1.07, p<0001), higher self-efficacy for LCS (OR=1.12, p<.0001), and greater perceptions that the screening decision was shared (OR=1.04, p<0001) The odds ratio (OR) for continuous predictors is per a 1-point increase. (Table 3).
Table 3:
Factors Associated with Patient-Perceived Lung Cancer Screening Decisional Quality (N=529)
| Variable | Bivariable Model | Multivariable Modela | 
|---|---|---|
| 
 | ||
| Gender | ||
| Female (n=235) | 0.91 (0.65, 1.29); p=.6043 | |
| Male (n=294) | Reference | |
| 
 | ||
| Race | ||
| White (n=463) | 1.42 (0.85, 2.38); p=.1817 | 1.25 (0.77, 2.04); p=.3607 | 
| Non-White (n=66) | Reference | Reference | 
| 
 | ||
| Education | ||
| Less than high school (n=20) | 0.31 (0.12, 0.81); p=.0574 | |
| High school graduate or equivalent (n=94) | 0.70 (0.42, 1.17); p=.4551 | |
| Some college (n=233) | 0.63 (0.42, 0.93); p=.8508 | |
| College graduate or higher (n=182) | Reference | |
| 
 | ||
| Perceived Financial Adequacy | ||
| Have enough for special things (n=288) | 1.38 (0.97, 1.94); p=.0701 | 1.23 (0.89, 1.70); p=.2204 | 
| Barely or Not Enough (n=241) | Reference | Reference | 
| 
 | ||
| Family History of Lung Cancer | ||
| Yes (n=143) | 1.30 (0.88, 1.93); p=.1858 | |
| No (n=386) | Reference | |
| 
 | ||
| Smoking Status | ||
| Currently Smokes (n=233) | 1.14 (0.81, 1.61); p=.4602 | |
| Used to Smoke (n=296) | Reference | |
| 
 | ||
| Age | 1.02 (0.99, 1.05); p=.1308 | 1.01 (0.98, 1.04); p=.5384 | 
| 
 | ||
| Knowledge: Lung Cancer Risk & Screening | 1.43 (1.26, 1.63); p<.0001 | 1.33 (1.18, 1.49); p<.0001 | 
| 
 | ||
| Lung Cancer Screening Health Beliefs | ||
| 
 | ||
| Perceived Risk of Lung Cancer | 0.89 (0.80, 0.98); p=.0180 | 0.94 (0.86, 1.03); p=.2045 | 
| 
 | ||
| Perceived Benefits of Lung Cancer Screening | 0.82 (0.77, 0.88); p<.0001 | 0.90 (0.85, 0.96); p=.0004 | 
| 
 | ||
| Perceived Barriers to Lung Cancer Screening | 1.10 (1.07, 1.12); p<.0001 | 1.07 (1.04, 1.09); p<.0001 | 
| 
 | ||
| Self-Efficacy for Lung Cancer Screening | 1.27 (1.21, 1.34); p<.0001 | 1.13 (1.07, 1.18); p<.0001 | 
| 
 | ||
| Psychological Characteristics | ||
| 
 | ||
| Stigma | 0.96 (0.90, 1.03); p=.2702 | |
| 
 | ||
| Mistrust (Trust) | 0.84 (0.79, 0.90); p<.0001 | 0.98 (0.92, 1.05); p=.5612 | 
| 
 | ||
| Perception that Lung Cancer Screening Decision was Shared | 1.03 (1.03, 1.04); p<.0001 | 1.04 (1.03, 1.04); p<.0001 | 
Multivariable model includes independent variables that had p<.20 from bivariate models.
Values are OR (95% CI) from logistic regression models of having low decision conflict (DCS <25 group, n=297, 56.1%) versus higher decision conflict (DCS ≥25, n=232, 43.9%). The odds ratio (OR) for continuous predictors is per a 1-point increase.
3.3. Factors Associated with the Patient’s Decision to Screen for Lung Cancer
At SDM discussion with their clinician, 95.3% (n=504 out of 529 total) of patients decided to screen (opted-in), and 4.7% (n=25 out of 529 total) were undecided or decided not to screen (data not shown in tables). In multivariable modelling, older age (OR=1.12, p=.0050) and higher self-efficacy scores (OR=1.11, p=.0407) were associated with opting into LCS; the OR for continuous predictors is per a 1-point increase (data not shown in tables).
3.4. Factors Associated with Lung Cancer Screening Completion
Screening completion rates were high. Among the total sample of participants, 399 (75.4%) participants completed screening; 99% completed screening among those who reported deciding to screen; and screening completion was 0.93% among those who reported they were undecided (data not shown in tables). Multivariable analyses showed that older age (OR=1.05, p=.0050), higher knowledge scores (OR=1.24, p=.0045), and higher self-efficacy scores (OR=1.12, p=.0003) were associated with screening completion; the OR for continuous predictors is per a 1-point increase. (Table 4).
Table 4.
Patient Factors Associated with Screening Completion (N=529)
| Variable | Bivariable Model | Multivariable Modela | 
|---|---|---|
| 
 | ||
| Age | 1.05 (1.01, 1.08); p=.0064 | 1.05 (1.02, 1.09); p=.0050 | 
| 
 | ||
| Gender | ||
| Female (n=235) | 1.17 (0.78, 1.74); p=.4461 | |
| Male (n=294) | Reference | |
| 
 | ||
| Race | ||
| White (n=463) | 1.40 (0.79, 2.46); p=.2495 | |
| Non-White (n=66) | Reference | |
| 
 | ||
| Education | ||
| Less than high school (n=20) | 1.31 (0.42, 4.13); p=.6407 | |
| High school graduate or equivalent (n=94) | 1.01 (0.57, 1.80); p=.9625 | |
| Some college (n=233) | 0.99 (0.63, 1.55); p=.9687 | |
| College graduate or higher (n=182) | Reference | |
| 
 | ||
| Perceived Financial Adequacy | ||
| Have enough for special things (=288) | 0.84 (0.56, 1.25); p=.3919 | |
| Barely or Not Enough (n=241) | Reference | |
| 
 | ||
| Family History of Lung Cancer | ||
| Yes (n=143) | 1.48 (0.92, 2.36); p=.1057 | 1.39 (0.84, 2.31); p=.2044 | 
| No (n=386) | Reference | Reference | 
| 
 | ||
| Smoking Status | ||
| Currently smokes (n=233) | 1.01 (0.68, 1.51); p=.9580 | |
| Used to smoke (n=296) | Reference | |
| 
 | ||
| Knowledge: Lung Cancer Risk & Screening | 1.04 (1.00, 1.09); p=.0323 | 1.24 (1.07, 1.44); p=.0045 | 
| 
 | ||
| Lung Cancer Screening Health Beliefs | ||
| 
 | ||
| Perceived Risk of Lung Cancer | 0.94 (0.84, 1.05); p=.2787 | |
| 
 | ||
| Perceived Benefits of Lung Cancer Screening | 0.94 (0.88, 1.01); p=.0741 | 1.00 (0.93, 1.08); p=.9850 | 
| 
 | ||
| Perceived Barriers to Lung Cancer Screening | 1.03 (1.00, 1.05); p=.0338 | 0.99 (0.96, 1.02); p=.4650 | 
| 
 | ||
| Self-Efficacy for Lung Cancer Screening | 1.11 (1.06, 1.16); p<.0001 | 1.12 (1.05, 1.19); p=.0003 | 
| 
 | ||
| Psychological Characteristics | ||
| 
 | ||
| Stigma | 0.99 (0.92, 1.07);p=.8262 | |
| 
 | ||
| Mistrust (Trust) | 0.97 (0.90, 1.04); p=.4250 | |
| 
 | ||
| Perception that Lung Cancer Screening Decision was Shared | 1.01 (1.00, 1.01)); p=.0348 | 1.00 (1.00, 1.01); p=.5333 | 
Multivariable model includes independent variables that had p<.20 from bivariate models.
Values are OR (95% CI) from logistic regression models of screening completion (n=399, 75.4%) versus non-completion (n=130, 24.6%).
The odds ratio (OR) for continuous predictors is per a 1-point increase.
3.5. Decisional Quality and the Decision to Screen and Screening Completion
For those who decided to screen, participants who then followed through and completed a lung scan reported significantly (p=.0038) better decisional quality (mean=20.21, SD=14.20) compared to those who did not follow through and complete a lung scan (mean=25.36, SD=18.36) (data not shown in tables).
4. Discussion and Conclusion
4.1. Discussion
Consistent with Rennert et al. (2020), an overwhelming majority of study participants who engaged in a SDM discussion with a clinician decided to screen after that discussion and most of those followed through by completing a lung scan,21 highlighting the importance of the patient-clinician discussion in complex cancer screening decisions. Findings from this study offer insights into the role of SDM in the patient-clinician encounter related to LCS as to which patient factors are associated with decisional quality, the decision to screen, screening completion, and the relationship between patient decisional quality and screening decision and completion. To date, understanding SDM in LCS has been limited by the use of a proxy for the patient’s decision to screen through the use of EHR data to confirm the presence, or not, of LDCT scan results for the patient. However, SDM in LCS is a process that involves a patient-clinician discussion resulting in a patient decision (i.e., to screen, not to screen, undecided) and a patient behavior (i.e., screening, not screening). The early adoption by the health system to create an EHR-based prompt for clinicians to engage in SDM regarding LCS with their eligible patients and to document the outcome of that conversation allowed the study team a unique real-world laboratory within which to study patients’ perceptions about SDM and the factors associated with the actual decision to screen and the completion of LCS.
Our findings support decisional quality as an important variable in SDM in LCS as higher decisional quality scores were associated with both the decision to get screened and screening completion in this study. As healthcare systems have increased a focus on patient-centered care, decisional quality has emerged as an important component of healthcare. In other studies, decisional quality has also been associated with less decisional anxiety and greater patient satisfaction with their medical care,10,22 further supporting the importance of patient engagement in healthcare decisions. Ultimately, the individual patient is usually tasked with following through with a healthcare decision (particularly in the context of cancer screening). Because higher decisional quality has the potential to lead to a more satisfying patient engagement experience from the perspective of the individual making the decision, it also has the potential to support recommended cancer screening receipt.
Results of this study have potential to inform tailored intervention development, specifically which variables should be used to tailor messages. It may also be beneficial to tailor messages into patient decision aids to support improvements in decisional quality as a component of an effective patient decision aid. Future research is needed to test this hypothesis. Knowledge, self-efficacy, and perceiving the decision to be shared were associated with higher decisional quality, giving insight into the most salient variables on which to tailor interventions that would support both patients and clinicians in SDM for LCS. For example, tailored interventions delivered prior to the clinical encounter that increase LCS knowledge and empower a patient’s self-efficacy may positively impact the SDM discussion between the patient and their clinician. Equally, clinician targeted interventions that support empathic communication that is perceived by the patient as a “shared” discussion may also lead to higher decisional quality and subsequent screening completion. Unexpectedly, higher decisional quality was associated with decreased perceived benefits of and increased perceived barriers to LCS which is inconsistent with our prior work testing the Conceptual Model for Lung Cancer Screening Participation6 where both perceived benefits of and perceived barriers to LCS were associated with LCS behavior in the hypothesized directions. It is possible that benefits and barriers to LCS may be perceived differently among patients who are insured and receive care in an integrated health system as they may not experience similar barriers that individuals outside an integrated health system experience.
Prior studies have also noted the importance of an individuals’ perception of risk as a motivator to screen for multiple cancers, including lung. However, results from this study did not support an association between perceived risk of getting lung cancer and the decision to screen or screening completion. This finding raises the question of how important it may be to address perceived risk as a potentially modifiable intervention target for LCS uptake. This is consistent with our prior findings testing the Conceptual Model for Lung Cancer Screening Participation which did not support a significant association between an individuals’ perception of risk and LCS behavior. While it may be logical to assume that higher perceived risk would be associated with LCS behavior, perceived risk may be moderated by other key variables such as fatalism, worry, or fear. This may also be in part related to the role that stigma may play in this unique patient population.
Trust in the clinician was not associated in this study with LCS completion in contrast with results of our prior qualitative work conducted in the KPWA health system with patients (n=20) who had completed LCS.23 That study revealed that trust in the referring clinician was one of four key themes that were primary motivators to screen.23 As noted in our prior work testing the Conceptual Model on Lung Cancer Screening Participation,6 both quantitative and qualitative data are critical to understanding the complex phenomenon of LCS behavior more robustly. In this prior work, trust was not significantly associated with screening behavior in the quantitative data but qualitative interviews with screening-eligible participants revealed trust/mistrust as an important variable related to both an individuals’ decision to screen and screening behavior.6 Additional research is needed to better understand the concept of trust and how it interacts with SDM.
Lung cancer screening has been recommended by the USPSTF for the past decade, however, screening uptake nationally remains extremely low compared to other types of cancer screening at this same historical stage of implementation (see for example, Chao et al., 2019, Knudsen et al., 2021, Nisbet et al., 2019).24–26 Results from this study demonstrate that SDM may promote LCS by providing an opportunity to learn about the option to screen from an informed clinician, discussing the benefits and barriers to screening, receiving a personalized recommendation from one’s clinician, and receiving a referral for screening if desired.
4.2. Limitations
Several limitations should be considered when interpreting our study results. The sample was insured, predominantly White and highly educated; similar results may not be seen in more diverse populations. Also, the integrated health system setting may be unique in several ways. KPWA provides health insurance and care to more than 600,000 members.8 In addition, KPWA’s lung cancer screening program was established in 2015 and included continuing education to all clinicians and staff which may limit generalizability given the high screening completion rate of our study participants when compared nationally. Although it is important to note that the screening rate in our study reflects those who underwent SDM who were eligible to screen as the denominator, and ultimately decided to screen as the numerator. Other studies estimate the national screening rate in the U.S. is <10-15% among those who screen (numerator) by those who are eligible for lung cancer screening (denominator). We did not directly calculate this rate to be comparable to national data, as we did not capture the entire sample of eligible patients in this study.
Other components of the KPWA program included integration of modules to guide and document SDM discussions and the patient’s decision about whether or not to screen into the EHR. For patients who decide to screen after a SDM discussion with their clinician, the EHR prompts clinicians to order a screening LDCT. In other health systems that do not have LCS integrated into the EHR, or that serve more diverse populations, outcomes may be different. Further, because SDM mandates may alter who receives SDM and how SDM occurs, care should be taken when generalizing findings to other clinical contexts. Additionally, we did not conduct mixed-effects models accounting for clustering of patients within clinicians because only 353 of the 529 patients could be linked to clinician IDs; and the average number of patients per clinician was small (353/106 = 3.33); however, and importantly, the intraclass correlation coefficient (ICC) for the decisional quality scores, estimated in the 353 subset using a mixed-effects model with clinician class specified as a random effect, was slightly less than zero (−0.0238), indicating that the true ICC is near zero and that two patient participants chosen randomly from any same clinician vary as much on decisional quality scores as any two randomly chosen patient participants of the whole population. This suggests that results presented here would have changed negligibly if clinician clustering had been accounted. Finally, the descriptive study design imposes limitations on conclusions that can be drawn regarding causality.
5. Conclusion
Shared decision making in LCS is a dyadic process involving communication between a patient and an informed clinician followed by enactment of a behavior on the part of the patient to follow-through on the decision. As we continue to strive for high quality patient-centered care, decisional quality can support or hinder patient engagement in the healthcare decision-making process. Key factors such as sufficient knowledge secondary to education support, enhancing self-efficacy, and fostering a SDM discussion may contribute to the environmental milieu that leads to improved patient engagement in LCS decisions.
5.1. Practice Implications
Decisional quality is an important variable in patient-clinician discussions about the option to screen, or not, for lung cancer. Because higher levels of decisional quality have the potential to lead to a more satisfying patient engagement experience from the perspective of the individual making the decision, it also has the potential to support recommended lung cancer screening receipt. Higher decisional quality is associated with both the decision to get screened and screening completion, and findings from this study support knowledge of lung cancer risk and screening, self-efficacy for lung cancer screening, and perceiving the decision to be shared were associated with higher levels of patient-perceived decisional quality, giving insight into the most salient variables on which to tailor patient and clinician-facing interventions.
Table 5.
Factors Associated with Decision to Screen for Lung Cancer (N=529)
| Variable | Bivariable Model | Multivariable Modela | 
|---|---|---|
| 
 | ||
| Age | 1.13 (1.05, 1.22); p=.0009 | 1.12 (1.04, 1.22);p=.0050 | 
| 
 | ||
| Gender | ||
| Female (n=235) | 0.73 (0.33, 1.62); p=.4364 | |
| Male (n=294) | Reference | |
| 
 | ||
| Race | ||
| White (n=463) | 1.36 (0.45, 4.09); p=.5863 | |
| Non-White (n=66) | Reference | |
| 
 | ||
| Education | ||
| Less than high school (n=20) | >99 (<0.1, >999); p=.9998 | |
| High school graduate or equivalent (n=94) | 0.59 (0.19,1.80); p=.3507 | |
| Some college (n=233) | 0.74 (0.28, 1.91); p=.5297 | |
| College graduate or higher (n=182) | reference | |
| 
 | ||
| Perceived Financial Adequacy | ||
| Enough for special things (n=288) | 0.79 (0.35, 1.79); p=.5684 | |
| Barely or Not Enough (n=241) | Reference | |
| 
 | ||
| Family History of Lung Cancer | ||
| Yes (n=143) | 0.64 (0.28, 1.49); p=.3044 | |
| No (n=386) | Reference | |
| 
 | ||
| Smoking Status | ||
| Currently Smokes (n=233) | 1.00 (0.45, 2.25); p=.9963 | |
| Used to Smoke (n=296) | reference | |
| 
 | ||
| Knowledge: Lung Cancer Risk & Screening | 0.97 (0.63, 1.51); p=.9092 | |
| 
 | ||
| Lung Cancer Screening Health Beliefs | ||
| 
 | ||
| Perceived Risk of Lung Cancer | 0.82 (0.64, 1.05); p=.1099 | 0.93 (0.69, 1.25); p=.6146 | 
| 
 | ||
| Perceived Benefits of Lung Cancer Screening | 0.80 (0.71, 0.92); p=.0011 | 0.87 (0.74, 1.02); p=.0787 | 
| 
 | ||
| Perceived Barriers to Lung Cancer Screening | 1.07 (1.02, 1.12); p=.0068 | 1.02 (0.95, 1.09); p=.5594 | 
| 
 | ||
| Self-Efficacy for Lung Cancer Screening | 1.14 (1.06, 1.23); p=.0008 | 1.11 (1.00, 1.23); p=.0407 | 
| 
 | ||
| Psychological Characteristics | ||
| 
 | ||
| Stigma | 0.89 (0.76, 1.04); p=.1464 | 0.91 (0.76, 1.08); p=.2677 | 
| 
 | ||
| Mistrust (Trust) | 0.93 (0.81, 1.07); p=.2953 | |
| 
 | ||
| Perception that Lung Cancer Screening Decision was Shared | 1.00 (0.99, 1.01); p=.8695 | |
Multivariable model includes independent variables that had p<.20 from bivariate models.
Values are OR (95% CI) from logistic regression models of decision to opt-in (n=504, 95.3%) versus deciding to not opt-in (n=25, 4.7%).
The odds ratio (OR) for continuous predictors is per a 1-point increase.
Highlights.
Decisional quality is an important variable associated with higher decisional quality associated with the decision to get screened and subsequent screening completion.
Because higher levels of decisional quality have the potential to lead to a more satisfying patient engagement experience from the patient’s perspective, it also has the potential to support recommended lung cancer screening receipt.
Results give insight into the most salient variables – knowledge of lung cancer risk and screening, self-efficacy for lung cancer screening, and perceiving the decision to be shared – on which to tailor patient and clinician-facing interventions.
Acknowledgements:
The authors would like to acknowledge and thank Dr. Diana S. Buist for her valuable contributions to the study. They would also like to express gratitude to the patients and healthcare professionals for taking part in the study.
Funding
This work was supported by funding from the National Cancer Institute (R01CA222090). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Footnotes
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Ethics Approval and Consent to Participate
This submission is the authors’ own original work, which has not been previously published elsewhere. This paper is not currently being considered for publication elsewhere. The paper reflects the authors’ own research and analysis in a truthful and complete manner. The paper properly credits the meaningful contributions of co-authors and co-researchers. The results are appropriately placed in the context of prior and existing research. All sources used are properly disclosed. All authors have been personally and actively involved in substantial work leading to the paper and will take public responsibility for its content. In addition, this study was reviewed and approved by the Institutional Review Board of Kaiser Permanente Washington Health Research Institute prior to any research activities commencing.
Competing Interests
There are no financial or non-financial competing interests for any of the authors.
Availability of Data and Materials
The quantitative datasets generated and analyzed during the current study are available from the corresponding author on reasonable request.
References
- 1.Recommendation: Lung Cancer: Screening | United States Preventive Services Taskforce. Accessed June 15, 2023.https://uspreventiveservicestaskforce.org/uspstf/recommendation/lung-cancer-screening
 - 2.NCA - Screening for Lung Cancer with Low Dose Computed Tomography (LDCT) (CAG-00439N) - Decision Memo. Accessed June 15, 2023. https://www.cms.gov/medicare-coverage-database/view/ncacal-decision-memo.aspx?proposed=N&NCAId=274
 - 3.Final Recommendation Statement: Lung Cancer: Screening | United States Preventive Services Taskforce. Accessed June 15, 2023. https://www.uspreventiveservicestaskforce.org/uspstf/document/RecommendationStatementFinal/lung-cancer-screening [Google Scholar]
 - 4.Lung Health Barometer Media Summary 2022.
 - 5.Institute of Medicine (US) Committee on Quality of Health Care in America. Crossing the Quality Chasm: A New Health System for the 21st Century. National Academies Press; (US: ); 2001. Accessed June 15, 2023. http://www.ncbi.nlm.nih.gov/books/NBK222274/ [PubMed] [Google Scholar]
 - 6.Carter-Harris L, Davis LL, Rawl SM. Lung Cancer Screening Participation: Developing a Conceptual Model to Guide Research. Res Theory Nurs Pract. 2016;30(4):333–352. doi: 10.1891/1541-6577.30.4.333 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 7.von Elm E, Altman DG, Egger M, et al. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. J Clin Epidemiol. 2008;61(4):344–349. doi: 10.1016/j.jclinepi.2007.11.008 [DOI] [PubMed] [Google Scholar]
 - 8.Wernli KJ, Tuzzio L, Brush S, et al. Understanding Patient and Clinical Stakeholder Perspectives to Improve Adherence to Lung Cancer Screening. Perm J. 2021;25(3):1–1. doi: 10.7812/TPP/20.295 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 9.O’Connor AM. Validation of a decisional conflict scale. Med Decis Mak Int J Soc Med Decis Mak. 1995;15(1):25–30. doi: 10.1177/0272989X9501500105 [DOI] [PubMed] [Google Scholar]
 - 10.Song MK, Sereika SM. An evaluation of the Decisional Conflict Scale for measuring the quality of end-of-life decision making. Patient Educ Couns. 2006;61(3):397–404. doi: 10.1016/j.pec.2005.05.003 [DOI] [PubMed] [Google Scholar]
 - 11.Garvelink MM, Boland L, Klein K, et al. Decisional Conflict Scale Use over 20 Years: The Anniversary Review. Med Decis Making. 2019;39(4):301–314. doi: 10.1177/0272989X19851345 [DOI] [PubMed] [Google Scholar]
 - 12.Garvelink MM, Boland L, Klein K, et al. Decisional Conflict Scale Findings among Patients and Surrogates Making Health Decisions: Part II of an Anniversary Review. Med Decis Making. 2019;39(4):316–327. doi: 10.1177/0272989X19851346 [DOI] [PubMed] [Google Scholar]
 - 13.Pozzar RA, Berry DL, Hong F. Item response theory analysis and properties of decisional conflict scales: findings from two multi-site trials of men with localized prostate cancer. BMC Med Inform Decis Mak. 2019;19(1):124. doi: 10.1186/s12911-019-0853-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 14.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(1):94–99. doi: 10.1016/j.pec.2009.09.034 [DOI] [PubMed] [Google Scholar]
 - 15.Carter-Harris L, Slaven JE, Monohan P, Rawl SM. Development and Psychometric Evaluation of the Lung Cancer Screening Health Belief Scales. Cancer Nurs. 2017;40(3):237–244. doi: 10.1097/NCC.0000000000000386 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 16.Carter-Harris L, Slaven JE, Monahan PO, Shedd-Steele R, Hanna N, Rawl SM. Understanding lung cancer screening behavior: Racial, gender, and geographic differences among Indiana long-term smokers. Prev Med Rep. 2018;10:49–54. doi: 10.1016/j.pmedr.2018.01.018 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 17.Carter-Harris L, Slaven JE, Monahan PO, Draucker CB, Vode E, Rawl SM. Understanding lung cancer screening behaviour using path analysis. J Med Screen. 2020;27(2):105–112. doi: 10.1177/0969141319876961 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 18.Carter-Harris L, Comer RS, Slaven Ii JE, et al. Computer-Tailored Decision Support Tool for Lung Cancer Screening: Community-Based Pilot Randomized Controlled Trial. J Med Internet Res. 2020;22(11):e17050. doi: 10.2196/17050 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 19.Cataldo JK, Slaughter R, Jahan TM, Pongquan VL, Hwang WJ. Measuring stigma in people with lung cancer: psychometric testing of the cataldo lung cancer stigma scale. Oncol Nurs Forum. 2011;38(1):E46–54. doi: 10.1188/11.ONF.E46-E54 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 20.Carter-Harris L, Hermann CP, Schreiber J, Weaver MT, Rawl SM. Lung Cancer Stigma Predicts Timing of Medical Help-Seeking Behavior. Oncol Nurs Forum. 2014;41(3):E203–E210. doi: 10.1188/14.ONF.E203-E210 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 21.Rennert L, Zhang L, Lumsden B, et al. Factors influencing lung cancer screening completion following participation in shared decision-making: A retrospective study in a U.S. academic health system. Cancer Treat Res Commun. 2020;24:100198. doi: 10.1016/j.ctarc.2020.100198 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 22.Lam WWT, Kwok M, Liao Q, et al. Psychometric assessment of the Chinese version of the decisional conflict scale in Chinese women making decision for breast cancer surgery. Health Expect. 2015;18(2):210–220. doi: 10.1111/hex.12021 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 23.Roth JA, Carter-Harris L, Brandzel S, Buist DSM, Wernli KJ. A qualitative study exploring patient motivations for screening for lung cancer. Guo NL, ed. PLOS ONE. 2018;13(7):e0196758. doi: 10.1371/journal.pone.0196758 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 24.Nisbet AP, Borthwick-Clarke A, Scott N, Goulding H, Jane H. Effectiveness of a small breast screening programme: 25 year evaluation (25 year breast screening evaluation). BJR Open. 2019;1(1):20180018. doi: 10.1259/bjro.20180018 [DOI] [PMC free article] [PubMed] [Google Scholar]
 - 25.Knudsen AB, Rutter CM, Peterse EFP, et al. Colorectal Cancer Screening: An Updated Decision Analysis for the U.S. Preventive Services Task Force. Agency for Healthcare Research and Quality (US); 2021. Accessed June 25, 2023. http://www.ncbi.nlm.nih.gov/books/NBK570833/ [PubMed] [Google Scholar]
 - 26.Chao CR, Xu L, Lonky NM. Adherence to Cervical Cancer Screening Guidelines Among Women Aged 66-68 Years in a Large Community-Based Practice. Am J Prev Med. 2019;57(6):757–764. doi: 10.1016/j.amepre.2019.08.011 [DOI] [PubMed] [Google Scholar]
 
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The quantitative datasets generated and analyzed during the current study are available from the corresponding author on reasonable request.
