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PLOS One logoLink to PLOS One
. 2022 Feb 3;17(2):e0262592. doi: 10.1371/journal.pone.0262592

Costs, benefits, and cost-benefit of Collaborative Assessment and Management of Suicidality versus enhanced treatment as usual

Phoebe K McCutchan 1,*, Brian T Yates 1, David A Jobes 2, Amanda H Kerbrat 3, Katherine Anne Comtois 3
Editor: Isabelle Durand-Zaleski4
PMCID: PMC8812929  PMID: 35113921

Abstract

Suicide rates have been steadily increasing in both the U.S. general population and military, with significant psychological and economic consequences. The purpose of the current study was to examine the economic costs and cost-benefit of the suicide-focused Collaborative Assessment and Management of Suicidality (CAMS) intervention versus enhanced treatment as usual (ETAU) in an active duty military sample using data from a recent randomized controlled trial of CAMS versus ETAU. The full intent-to-treat sample included 148 participants (mean age 26.8 years ± 5.9 SD years, 80% male, 53% White). Using a micro-costing approach, the cost of each condition was calculated at the individual level from a healthcare system perspective. Benefits were estimated at the individual level as cost savings in past-year healthcare expenditures based on direct care reimbursement rates. Cost-benefit was examined in the form of cost-benefit ratios and net benefit. Total costs, benefits, cost-benefit ratios, and net benefit were calculated and analyzed using general linear mixed modeling on multiply imputed datasets. Results indicated that treatment costs did not differ significantly between conditions; however, CAMS was found to produce significantly greater benefit in the form of decreased healthcare expenditures at 6-month follow-up. CAMS also demonstrated significantly greater cost-benefit ratios (i.e., benefit per dollar spent on treatment) and net-benefit (i.e., total benefit less the cost of treatment) at 12-month follow-up. The current study suggests that beyond its clinical effectiveness, CAMS may also convey potential economic advantages over usual care for the treatment of suicidal active duty service members. Our findings demonstrate cost savings in the form of reduced healthcare expenditures, which theoretically represent resources that can be reallocated toward other healthcare system needs, and thus lend support toward the overall value of CAMS.

Introduction

Amid unprecedented increases in active duty military suicide rates in recent years, the U.S. Department of Defense (DoD) has recognized suicide prevention to be a top military priority [1,2]. Active duty service members have demonstrated continuously rising suicide rates across all branches of service. In 2019, the suicide mortality rate for the Active Component (i.e., full-time service members) across all services was 25.9 per 100,000, representing a per-year rate ratio of 1.04 from calendar years 2011 through 2019 [3]. These trends are particularly alarming in that they represent the first time in recorded history that the U.S. military suicide rate has equaled or exceeded that of comparable U.S. general population cohorts, beginning in 2008 and continuing to date. Indeed, the 2019 suicide mortality rate for the Active Component was statistically indistinguishable from the 2018 U.S. population rate after adjusting for age and gender [4]. Although the exact causes of the increase in military suicides are uncertain, the most consistently reported factor appears to be increasing co-occurrence of mental health conditions such as posttraumatic stress disorder (PTSD), depression, and substance use [59].

In response to this alarming increase in military suicide rates, the DoD has collaborated with other government and private agencies to make considerable investments in research geared toward determining the risk factors and correlates of suicidality and developing effective prevention and management strategies [10]. New interventions aimed specifically at managing suicidality are emerging, but additional research is needed to carefully evaluate the effectiveness of these interventions in rigorous, well-powered studies in order to inform clinical practice guidelines and facilitate integration into routine clinical care.

One promising suicide-focused approach is the Collaborative Assessment and Management of Suicidality (CAMS) [1113], a therapeutic framework that aims to identify and address patient-articulated “suicidal drivers.” To date, CAMS has amassed a substantial evidence base demonstrating its effectiveness in reducing suicidal ideation, overall symptom distress, depression, and hopelessness, including several correlational and quasi-experimental studies [1421] and five randomized controlled trials (RCTs) across a variety of settings [2226]. A recent systematic review of CAMS reported it to be a promising approach to managing suicide risk and deliberate self-harm in adults [27], although it noted a high degree of heterogeneity and attrition across existing studies and emphasized the need for additional high-quality studies, particularly RCTs and meta-analyses. Further, a more recent meta-analysis reported that CAMS treatment resulted in significantly lower suicidal ideation and general distress compared to alternative interventions, concluding that it is a well-supported intervention for suicidal ideation according to Center of Disease Control and Prevention criteria [28].

In addition to its clinical effectiveness, another important factor requiring further examination is the cost of the CAMS intervention, particularly in comparison to alternatives. As with any health intervention, understanding the costs of delivering CAMS in relation to both clinical and monetary outcomes produced can be seen as an essential component of informed decision-making by policymakers, healthcare administrators, and even clinicians. The economic reality, especially in a population-based system such as the Military Health System (MHS), is that resources allocated to one intervention are then no longer available for other needed services [29,30]. Therefore, it could be helpful to examine the value of an intervention (i.e., costs relative to outcomes) compared to that of other possible alternatives in order to “provide the best to the most for the least” [31].

Preliminary analyses using archival data in one retrospective non-randomized controlled comparison study of CAMS vs. treatment as usual at two U.S. Air Force outpatient clinics found that costs of the treatment conditions did not differ [16]. However, CAMS patients utilized significantly fewer medical services (e.g., emergency room visits, medical appointments, and minutes spent in these settings) after initiating suicide-related mental health treatment, indicating relative cost savings in the form of reduced healthcare expenditures. Extrapolating the observed utilization rates to the anticipated number of suicidal patients presenting to the clinics over the next fiscal year (n = 75), the authors estimated a potential cost savings of approximately $32,500 ($434.25 per patient on average; 2004 dollars). Extrapolating across the total 80 Air Force clinics worldwide, cost savings estimates approached $2 million per year [16]. Still, the significant methodological limitations of the study must be noted, including a small and unequally distributed sample size (N = 55; n = 25 for CAMS and n = 30 for treatment as usual), lack of random assignment, and lack of fidelity measures. Consequently, it is premature to definitively conclude based on these analyses that CAMS is associated with economic advantages compared to treatment alternatives.

Although these preliminary findings were encouraging, additional examinations using more robust study designs, detailed costing methods, and systematic evaluation of treatment benefits are warranted. The purpose of the current study was to extend previous analyses by examining the costs, benefits, and cost-benefit of CAMS compared to enhanced treatment as usual (ETAU) for the treatment of suicidality in active duty Soldiers using data from a recent clinical effectiveness RCT. Results of the primary RCT indicated that CAMS treatment was associated with significant postbaseline improvements in suicidal ideation and suicide attempt behaviors across one year of follow-up. However, the ETAU condition evidenced comparable improvements, with the exception of a significantly greater reduction in probability of suicidal ideation at 3-month follow-up observed in the CAMS condition [24]. Examination of treatment costs and benefits become especially useful in such scenarios where two treatment alternatives appear similarly effective, to select the intervention which maximizes return on investment.

In the current secondary cost analysis, treatment costs (i.e., the value of resources required to implement the intervention) were determined using micro-costing and gross-costing techniques. Benefits of the intervention (i.e., the value of resources generated or saved as a result of the intervention) were assessed as potential cost savings based on healthcare expenditures across multiple categories of services. Finally, cost-benefit (i.e., the relationship between the value of resources used and the value of resources saved by an intervention) was examined using cost-benefit ratio and net benefit metrics [32].

Previous analyses found no significant differences in direct costs (i.e., resource use directly attributable to the intervention) for CAMS compared to usual care [16]. Although CAMS as delivered in the current study required more resources to support the training and consultation activities performed over and above that of the usual care condition, the costs associated with these activities were anticipated to be relatively minimal at the individual level; therefore, it was hypothesized that CAMS would be no more costly than ETAU at each follow-up timepoint (Hypothesis 1).

With regard to benefits, evidence suggests that suicidality is associated with increased health service utilization in active duty Soldiers [3335]. Because CAMS was anticipated to lead to greater and more rapid clinical improvement in suicidality than ETAU, we predicted that health service utilization would decrease correspondingly. Indeed, usual-care patients have been found to attend significantly more medical appointments compared to CAMS patients over a one-year period [16]. Consequently, it was hypothesized that CAMS would evidence greater benefit (i.e., cost savings) in the form of lower between-group cumulative healthcare expenditures at each follow-up timepoint (Hypothesis 2) and greater reduction in within-subjects past-year healthcare expenditures at 12-month follow-up (Hypothesis 3). Because CAMS was predicted to be less costly and more beneficial than ETAU, we further anticipated that CAMS would be associated with greater cost-benefit than ETAU, as evidenced by significantly greater cost-benefit ratios (Hypothesis 4) and significantly greater net benefit (Hypothesis 5) at 12-month follow-up.

Materials and methods

Trial design

The current study was a secondary data analysis of the DoD-funded “Operation Worth Living” (OWL) study, an RCT of CAMS versus ETAU for suicidal Soldiers. The trial was conducted in the Department of Behavioral Health at an Army Medical Center on an infantry military installation in the Southern United States. Participants were randomly assigned to either CAMS or ETAU matched on histories of suicide attempts, medication class, severity of physical injury or disability, and current enrollment in outpatient behavioral health treatment (i.e., psychiatric, clinical psychology, or social work services). Participants were assessed on clinical variables and service utilization measures at baseline and 1-month, 3-month, 6-month, and 12-month timepoints after baseline. Details about the trial design, including study procedures and power analysis, are described elsewhere [24]. All study procedures were approved by The Catholic University of America, University of Washington, and Eisenhower Army Medical Center Institutional Review Boards. The current archival study was approved by the American University Institutional Review Board (IRB-2017-75).

Participants

Soldier participants in the study were 148 active duty U.S. infantry Soldiers with current suicidal ideation recruited via provider referral from the community behavioral health clinic, emergency department, and inpatient psychiatric unit. Soldiers were eligible to participate if they were over 18 years old, English-speaking, and had significant suicidal ideation (i.e., a score of ≥ 13 on the Scale for Suicidal Ideation-Current) [36]. Soldiers were excluded if they were a member of the Warriors in Transition unit (a unit providing support to soldiers being treated for chronic and/or severe injuries who cannot yet return to work), pregnant, exhibiting significant psychosis or cognitive or physical impairment, judicially ordered to treatment, or ineligible for behavioral health care at the military installation.

On-site clinicians were also consented participants in the study as they completed routine assessments. Eligible clinicians were assigned to either the CAMS or ETAU condition based on their relative self-reported allegiance to treatment models for managing suicidal patients; clinicians reporting weaker preference for a specific treatment were assigned to the CAMS condition to ensure high adherence of ETAU clinicians to their existing approach. The final sample of study therapists participating in the intent-to-treat phase of the trial (n = 4 per treatment condition) consisted of seven licensed clinical social workers and one masters-level mental health counselor. Mean years of practice experience since professional degree were 5.0 (SD = 4.7) for ETAU therapists and 13.25 (SD = 7.4) for CAMS therapists.

Treatments

CAMS is best described as a therapeutic framework that accommodates a wide range of theoretical orientations and techniques. A core tenet of CAMS therapy is an empathetic and collaborative therapeutic relationship geared toward developing a shared understanding of the patient’s suicidality. Guided by the Suicide Status Form (SSF), the fundamental goal is to engage the patient in identifying and addressing the causes (“drivers”) that compel him or her to consider suicide using appropriate driver-focused interventions, subsequently reducing suicidal ideation and behaviors as coping mechanisms are increased [11,13]. In the current study, the CAMS intervention consisted of approximately 4 to 11 weekly individual sessions (after the initial session, CAMS concludes after three consecutive sessions with resolved suicidality) following the suicide-specific CAMS framework [13].

In ETAU, clinicians provided typical care in as many sessions as appropriate to their treatment approach and theoretical orientation without constraint by the study, reflecting the real-world conditions examined within an effectiveness framework to maximize generalizability. This treatment condition was considered “enhanced” treatment as usual in that it specified a minimum number of four treatment sessions, providers had access to consultation and supervision as needed, and Soldiers were routinely engaged and evaluated at the study assessment intervals [24].

Measures

The Scale for Suicide Ideation-Current (SSI-C) [36], a 19-item interviewer-rated measure assessing suicidal ideation at its highest intensity over the past two weeks, was used to assess suicidal ideation severity (total score of 0–38) and resolution (i.e., a total score of zero). The SSI-C has demonstrated good convergent and criterion validity in previous research in psychiatric patients [36] and evidenced high internal consistency in the current study (α = .88).

Medical and behavioral health service utilization was assessed using the Treatment History Interview-Military version (THI-M), adapted from the Treatment History Interview (THI) [37] for use in the military healthcare system. The THI-M is an interviewer-administered measure that captures the history (e.g., service frequency, duration, and provider type) of outpatient psychotherapy and counseling visits, crisis medical services, medical provider visits, and medication use. The THI has been found to have high convergent validity with medical records (r = .99). Pilot studies found no significant differences between THI self-report and therapist records for number of psychotherapy hours [37]. In the current study, THI-M responses were validated against available administrative data sources (i.e., electronic health records). In the baseline assessment, the THI-M measured service utilization over the past year; in follow-up assessments, the THI-M measured service utilization since the previous assessment.

Cost assessment

The cost of each treatment condition was calculated from a healthcare system perspective, given that the MHS is the sole payor and primary decision-maker with regard to implementation of these suicide prevention services. Total treatment costs were comprised of two categories: training and implementation activity costs and treatment delivery costs.

Training and implementation activity costs

Micro-costing was applied to determine the cost of training and implementation activities beyond standard clinical practice [31,38,39]. Costs related to these activities only applied to the CAMS condition in the current analyses as ETAU therapists did not receive any additional training or require preparatory activities for the provision of treatment. Further, although ETAU therapists were offered additional supervision and consultation as needed, key informant interviews indicated that they elected not to participate in these activities during the course of the study. This may reflect stronger allegiance to a specific treatment approach for managing suicidality. Consequently, there were no additional costs beyond those captured in the provision of clinical services, as described in a later section. For costs related to training and implementation activities, micro-costing entailed the following steps:

Itemization of activities. An inventory was developed listing all major non-clinical activities that occur for each treatment condition at the individual level, including training and other preparatory activities that must take place prior to implementing the intervention. Activities performed were identified by study protocols, intervention manuals, administrative data systems maintained by research personnel, and qualitative interviews with research personnel and study therapists as feasible and appropriate.

Estimating resource inputs and unit costs. The resources used to perform each activity were identified and then the amounts of each resource used were estimated. Resources included personnel time, travel, and materials.

Costs for personnel time were measured in hourly units based on 2018 annual salary plus fringe benefits, divided by 2080 hours (an assumed 40 hours per week). Annual base salaries for CAMS trainers and consultants were estimated using the Bureau of Labor Statistics Occupational Employment Statistics Query System based on geographical area and occupation classification. Study investigators’ salaries were included to reflect the real-world cost of CAMS training delivered directly by the developers of the intervention. Study therapists were clinical social workers assumed to be GS-12 paygrade based on key informant interviews; annual base salaries were estimated based on the 2018 General Schedule Base Pay Scale [40] and adjusted for locality. A fringe benefit rate of 29.1% was applied to annual base salaries for study investigators and therapists based on the 2018 national average for private industry workers in the South Atlantic region [41]. Annual base salaries and fringe rates for four pre-doctoral graduate student assistants who contributed to fidelity assessment were estimated based on typical grant-funding allowances reported by The Catholic University of America Office of Sponsored Programs.

Travel costs reflect resources needed for personnel to attend on-site trainings of CAMS study therapists. Two on-site trainings were conducted at the military installation as part of the OWL study; however, the current cost analyses assumed that only one on-site training would be required to better approximate real-world implementation not constrained by research conditions. Costing of on-site training assumed attendance by two CAMS study investigators and four study therapists. Because the OWL study was funded through a federal grant, travel costs were assumed to be consistent with General Services Administration allowable rates. Cost of airfare was estimated using the 2018 maximum allowable airfare rate determined by the General Services Administration City Pair Program [42]. Cost of lodging was estimated based on 2018 hotel rates negotiated by the federal government by locality [43]. Cost of meals and incidental expenses was estimated based on 2018 government allowable per diem rates by locality [44]. Traveling personnel shared one rental car at a cost estimated based on 2018 daily government rental car rates by locality (www.FedTravel.com).

The on-site training required facility space large enough to host all attendees in the same room. The size of the room was estimated to be approximately 300 square feet. Facility costs were estimated based on the current median cost for office space in the closest available locality [45], adjusted to reflect 2018 dollars. Specifically, the median annual cost per square foot was multiplied by 300 square feet and then divided by 2,080 hours (the total number of hours the room could be used annually). Hourly costs of electricity were estimated using 2018 commercial electricity costs in the region per the Department of Energy [46].

Costs for materials (for example, training or psychoeducational materials) were estimated per item based on study receipts, treatment protocols, and/or information obtained in key informant interviews.

Calculating total costs. The total cost per activity was calculated by multiplying resource inputs by per-unit costs. Costs were then summed to determine the total cost for training and non-clinical implementation activities across the CAMS condition. Because training and implementation costs were incurred at the treatment condition-level, a fixed, per-individual cost was calculated by dividing total cost of activities by the total number of individuals a trained CAMS therapist might ultimately treat with the CAMS intervention during his/her career as an MHS provider based on rates of suicidal ideation in military populations [7,33,4750] and estimated typical caseload size and length of career for MHS behavioral health providers [51,52]. These estimates also assume a relatively high degree of adherence to CAMS across the provider’s MHS career, as supported by the absence of drift reported in the primary trial [24] and a community survey of mental health practitioners reporting generally high levels of adherence to the CAMS therapeutic approach and practice [53]. The fixed cost of non-clinical implementation activities was then added to each CAMS participant’s study treatment delivery costs to estimate the overall per-individual cost of the intervention.

Treatment delivery costs

The cost of delivering each intervention was estimated at the individual level based on the number of treatment visits attended as documented in THI-M assessments and validated by administrative study records. Each visit was assigned an appropriate Current Procedural Terminology (CPT) [54] and costed using corresponding 2018 TRICARE/CHAMPUS Maximum Allowable Charges based on facility, non-physician provider, and appropriate locality rates. TRICARE (formerly known as CHAMPUS) is a DoD health insurance program, and its Maximum Allowable Charges rates reflect costs directly related to provision of the service (i.e., provider time used in the visit), practice expenses such as facilities and administrative staff, and malpractice insurance. This same procedure was applied to missed treatment visits (i.e., no-shows) to reflect the missed opportunity to deliver services and collect payment for dedicated provider time [55]. Out-of-session contacts that occurred as part of treatment (e.g., phone calls) were assigned a CPT code based on the purpose and duration of the communication and costed accordingly.

Benefits assessment

Benefits, in the form of cost savings, were then estimated based on healthcare expenditures for behavioral health services, medical services, crisis services, and certain medications using the THI-M. Each visit was assigned an appropriate CPT code(s) and direct care costs for these services were estimated based on the TRICARE Reimbursement Manual and CHAMPUS Maximum Allowable Charge rates. Of note, because the nature of available data did not allow for determination of exact timing of service delivery, all non-study-treatment services were captured in the assessment of benefits rather than treatment costs, including those delivered during windows with active study treatment.

Analyses

Outcome analysis used an intent-to-treat approach that included all participants who completed a baseline assessment. Multiple imputation using chained equations with predictive mean matching was used to minimize uncertainty related to the replacement of missing data for health services utilization [56]. Treatment cost data did not require imputation as data were available for all participants. Participants who did not complete at least one follow-up assessment (n = 6) were excluded from imputation and subsequent analyses. Fifteen imputed datasets were created to adequately address the observed proportion of missing data [57,58]. Planned statistical analyses were carried out on each imputed dataset, producing separate summary statistics (e.g., means or regression coefficients) with corresponding standard errors. For regression analyses, Rubin’s rules [59] were applied to derive pooled coefficients and standard errors [60]. For nonparametric tests, observed and imputed datasets were analyzed and reported separately.

Descriptive analyses were conducted to examine unadjusted costs per individual, major category of activity, and treatment condition at each follow-up timepoint. General linear mixed models (LMMs) were used to assess group differences in intervention costs at each follow-up timepoint with a random intercept and slope for participant. Wilcoxon rank-sum tests were conducted to examine differences in median costs, a useful measure of the most typical cost per individual.

Benefits were examined both between-participant (i.e., ETAU versus CAMS) and within-participant (i.e., pre- versus post-intervention). LMMs were used to assess group differences across time in total healthcare expenditures and by categories of expenditure (i.e., behavioral health, medical providers, crisis services, and medications). Linear regression was used to assess within-subjects change in pre- versus post-intervention past-year healthcare expenditures at 12-month follow-up. Cost-benefit ratios (CBRs; derived as the cumulative monetary benefit of treatment divided by the cumulative cost) and net benefit (derived as the cumulative benefit minus the cumulative cost of treatment) were calculated at the individual level. Linear regression was used to examine group differences in cost-benefit and net benefit at 12-month follow-up, as these outcomes reflect pre-intervention versus post-intervention change in past-year expenditures [61].

For all regression models of repeated-measures outcomes, treatment condition, time, and an interaction term were entered as fixed effects, with a random intercept for participants and random slope for participants by time. Nesting of participants within study therapists was examined but did not significantly improve model fit and was therefore not used in analyses. A stepwise procedure was used to identify appropriate demographic and clinical covariates as fixed effects terms, and likelihood ratio tests were used to examine random parameters. All statistical analyses were conducted using Stata v.16.0.

Results

Sample at baseline

Of the 148 individuals enrolled in the study, 73 were randomized to the CAMS condition and 75 were randomized to ETAU. The full study sample (N = 148) was predominantly male (80%), White (53%), and married (51%), with a mean age of 26.8 (SD = 5.9). Participants mostly held the rank of junior enlisted (E1-E4; 70%). The mean total SSI-C score at baseline was 20 (SD = 5.3), and half of participants reported a lifetime history of at least one suicide attempt, with 27% reporting multiple attempts. There were no statistically significant differences between the CAMS and ETAU conditions with regard to patient participants’ sociodemographic or baseline clinical characteristics.

Missing data

Study retention rates in the intent-to-treat sample were 96%, 89%, 79%, and 78% for CAMS and 90%, 83%, 79%, and 77% for ETAU at 1-, 3-, 6-, and 12-month follow-ups, respectively, with an overall missing data rate of 13% for primary outcomes. Separate mixed effect logistic regression models revealed no statistically significant differences in rates of missing data across time based on age, gender, ethnicity, marital status, education level, rank, number of lifetime suicide attempts, treatment condition, or primary study therapist.

Costs

The total cost of CAMS training and consultation activities was $7,960.32; assuming each of the four CAMS clinicians could treat 160 individuals over the course of an MHS career, this amounted to a cost of $12.44 per participant. Table 1 displays the results of micro-costing procedures for these activities [31].

Table 1. Resource x activity table for CAMS training and consultation activities.

Resource Unit Measure Units Required Total Resource Cost
Review CAMS Manual
    Time
        Cliniciansa 1 hour 13 $592.02
    Materials 1 manual 4 $152.04
Attend On-site Training
    Time
        Cliniciansa 1 hour 48 $2,185.92
        Study Investigators 1 hour 24 $1,888.32
    Facilities
        Office Space 1 hour 12 $23.37
        Electricity 1 kW hour 12 $1.14
    Materials 1 page 80 $16.00
    Travel
        Airfare 1 roundtrip ticket 2 $944.00
        Lodging 1 room/night 4 $372.00
        Rental Car 1 day 2 $130.00
        Meals & Incidental Expenses Per Diem 1 day 6 $255.00
Case Consultation b
    Time
        Cliniciansa 1 hour 16 $728.64
        Study Investigators 1 hour 12 $671.88
TOTAL $7,960.32

a Costs reflect training and consultation activities for four CAMS clinicians.

bAssumes a total of four hourly group consultation calls, as is typical in real-world CAMS implementation training.

CAMS−Collaborative Assessment and Management of Suicidality; kW−kilowatt.

Table 2 shows descriptive statistics for cumulative costs of treatment over time by treatment condition. Mean total study treatment cost at 12-month follow-up was $434.82 (SD = $209.66) for ETAU and $433.38 (SD = $248.29) for CAMS; LMM results indicated that treatment conditions did not differ significantly in treatment costs across time. Wilcoxon rank-sum tests examining group differences in median total study treatment costs were consistent with linear mixed modeling (p = .57 to .80). The average number of active study treatment sessions attended at 12 months was comparable between treatment conditions (M = 6.40 [SD = 3.53] for ETAU, M = 6.20 [SD = 3.89] for CAMS; Z = 0.69, p = .49), as was the average number of out-of-session contacts (M = 0.56 [SD = 1.27] for ETAU, M = 0.59 [SD = 1.67] for CAMS; Z = -0.37, p = .71) and average number of missed visits (M = 0.55 [SD = 1.33] for ETAU, M = 0.81 [SD = 2.20] for CAMS; Z = -0.97, p = .33).

Table 2. Descriptive statistics for total cumulative study treatment costs.

Mean (SD) Median (95% CI)
Timepoint ETAU CAMS ETAU CAMS
1-month $282.64 ($86.46) $273.55 ($75.17) $247.92 ($247.92-$309.9) $260.35 ($260.35-$322.33)
3-months $404.53 ($168.94) $393.58 ($138.74) $371.88 ($309.90-$433.86) $384.31 ($322.33-$384.31)
6-months $434.82 ($209.66) $427.84 ($221.70) $371.88 ($309.90-$448.55) $384.31 ($322.33-$384.31)
12-months $434.82 ($209.66) $433.38 ($248.38) $371.88 ($309.90-$448.55) $384.31 ($322.33-$384.31)

SD−standard deviation; CI−confidence interval; ETAU−enhanced treatment as usual; CAMS−Collaborative Assessment and Management of Suicidality.

Benefits

Due to a few extreme outliers, crisis services and total healthcare expenditure variables were separately Winsorized at the 1st and 99th percentiles to better approximate a normal distribution [62]. Table 3 presents descriptive statistics for cumulative healthcare expenditures for each treatment condition by category of service and timepoint. At baseline, mean past year total healthcare expenditures were comparable between the two treatment conditions after controlling for gender and race (p = .17). Multivariate LMMs of cumulative total healthcare expenditures across follow-up timepoints revealed a significant interaction of treatment condition x time at 6-months (β = -2,480.34, SE = 1,198.95; p = .04), indicating a decreased rate of healthcare expenditure for the CAMS condition at this timepoint.

Table 3. Descriptive statistics for cumulative healthcare expenditures.

Timepoint Behavioral Health M(SD) Medical Providers M(SD) Crisis Services M(SD) Medications M(SD) Total M(SD)
1-month
    ETAU $344.56 ($733.37) $445.57 ($339.55) $828.19 ($2,397.55) $58.35 ($68.60) $1,676.68 ($2,535.78)
    CAMS $394.28 ($409.52) $373.07 ($312.23) $1,567.83 ($3,588.47) $48.15 ($56.80) $2,385.66 ($3,881.25)
3-months
    ETAU $846.53 ($1,960.07) $866.41 ($650.71) $2,319.58 ($4,584.65) $157.11 ($183.43) $4,035.30 ($5,228.14)
    CAMS $739.42 ($630.30) $923.15 ($689.72) $2,686.91 ($5,071.78) $122.11 ($143.79) $4,471.59 ($5,835.28)
6-months
    ETAU $1,587.44 ($3,005.15) $1,445.01 ($974.37) $4,882.80 ($7,167.52) $307.61 ($339.82) $8,433.70 ($9,730.96)
    CAMS $1,412.42 ($2,508.25) $1,530.42 ($1,148.55) $3,879.50 ($6,241.34) $232.08 ($310.09) $7,054.42 ($7,660.61)
12-months
    ETAU $2,693.53 ($5,425.58) $2,384.50 ($1,589.13) $7,386.36 ($9,223.68) $608.02 ($641.90) $13,256.40 ($14,094.71)
    CAMS $2,569.90 ($5,226.55) $2,395.66 ($1,929.21) $5,576.90 ($7,286.21) $446.07 ($566.48) $11,004.54 ($10,388.93)

M−mean; SD−standard deviation; ETAU−enhanced treatment as usual; CAMS−Collaborative Assessment and Management of Suicidality.

In models of cumulative healthcare expenditures by category of services, there were no significant differences by treatment condition with respect to behavioral health services, medical provider services, or medications. However, for crisis services, a significant interaction of treatment condition x time was found at 6-month (β = -2,036.12, SE = 793.38; p = .01) and 12-month (β = -2,743.24, SE = 1,300.88; p = .04) follow-ups, indicating a decreased rate of crisis services expenditures for the CAMS condition.

In examining within-subject effects, mean changes in pre- versus post-intervention total past-year healthcare expenditures suggested a slight reduction in past-year expenditures for CAMS participants at 12-month follow-up (M = -$14.21, SD = $13,075.90), whereas past-year expenditures increased for ETAU participants (M = $3,304.72, SD = $14,756.44). Aggregated across participants by treatment condition, this represents a pre- versus post-intervention increase in total past-year healthcare expenditures of $234,637.59 for ETAU compared to a decrease of $1,009.42 for CAMS. Still, linear regression indicated that within-subject changes in pre- to post-intervention expenditures were not significantly different by treatment condition, likely due to substantial variability among observations.

Cost-benefit

Mean CBRs at 12-month follow up were -13.26 (SD = 55.10) for ETAU and 1.68 (SD = 40.53) for CAMS. Linear regression revealed that CAMS participants had significantly greater CBRs (i.e., more benefit per dollar spent) compared to ETAU condition after controlling for race and gender (β = 21.67, SE = 8.17; p < .01). Mean within-subject net benefit at 12-months was -$3,739.54 (SD = $14,755.23) for ETAU and -$419.13 (SD = $12,941.40) for CAMS, indicating that descriptively neither treatment paid for itself through reduced healthcare expenditures. However, across all datasets, one-sample Wilcoxon signed-rank tests showed that median net benefits were significantly less than zero for ETAU whereas they were not significantly different from zero for CAMS. Further, linear regression revealed that CAMS was associated with significantly greater net benefit compared to ETAU after controlling for gender and race (β = -5,167.93, SE = 2,271.79; p = .03).

Discussion

This study examined the costs, benefits, and cost-benefit of CAMS versus ETAU for the treatment of suicidality in active duty service members from a healthcare perspective. Consistent with a preliminary cost analysis [16], there were no significant differences in costs of treatment between CAMS and ETAU. As anticipated, the CAMS intervention did require training and consultation activities over and above that of usual care; however, the costs of these activities were relatively minimal when spread across the entire population of beneficiaries.

With regard to benefits at the group level, CAMS was associated with significantly reduced total cumulative healthcare expenditure compared to ETAU at 6-month follow-up, likely driven by significantly lower crisis services expenditures. However, ETAU eventually matched CAMS in total cumulative healthcare expenditures at 12-month follow-up timepoints, although crisis services expenditures remained significantly lower for CAMS. The data suggest that participants in the CAMS condition may use more crisis services than ETAU in the first month of treatment but use significantly fewer crisis services by 6- and 12-month follow-ups. The early uptick in crisis service utilization may be explained by CAMS’s suicide-specific focus which promotes accessing such services in an acute crisis, whereas the decreased utilization by six months likely reflects findings from the primary trial that CAMS participants had a lower probability of having suicidal ideation at 3-month follow-up [24]. In examining within-subject pre- versus post-intervention past-year healthcare expenditures, no significant differences were found between CAMS and ETAU participants for any category of healthcare expenditures.

CBRs were significantly greater for CAMS participants at 12-month follow-up, indicating greater benefit per dollar spent compared to ETAU. On average, CAMS participants reduced their past-year total healthcare expenditures by $0.68 for each dollar spent on treatment, whereas ETAU participants increased spending by $13.26 for each dollar spent on treatment. Neither treatment condition evidenced positive net benefit; that is, neither treatment paid for itself through reduced healthcare expenditures. Still, net benefit was significantly greater in the CAMS condition compared to ETAU by approximately $3,320 per individual, on average.

Limitations and future directions

This study had several limitations. With regard to estimating intervention costs, our micro-costing approach likely resulted in inflated estimates of CAMS costs. Micro-costing was used in the current study to maximize precision in cost estimates; however, a known limitation of micro-costing is a potential lack of generalizability beyond the specific setting or population being studied [63]. Because the current analyses were based on data from a randomized controlled trial designed to ensure internal validity, greater resources were required to provide CAMS than would be observed in real-world settings. We attempted to mitigate potential overestimation of costs related to research procedures through application of some real-world practice assumptions to enhance external validity. Still, costs of real-world CAMS delivery may be substantially lower in some settings owing to the availability of less expensive training formats (e.g., online video courses; www.CAMS-care.com) and delivery formats (e.g., group therapy) [64], as well as its suitability for use by diverse types of providers (e.g., paraprofessionals) [13]. Conversely, costs may be greater in settings where outpatient mental health services are typically delivered by doctoral-level therapists. Additional cost-inclusive evaluations of CAMS across these various implementation approaches are needed to inform wider dissemination of the framework.

A second limitation of the current study is that is solely reflects the MHS perspective. While our findings may inform decision-making that maximizes impact for the payer, it is important to consider that such a narrow scope likely undermines the true benefit of an intervention [65]. Future cost-inclusive analyses of CAMS should consider adopting a broader range of perspectives, particularly a societal perspective in which all costs and outcomes associated with an intervention are taken into consideration regardless of whom experiences them directly [66,67]. For example, it is possible that effective treatment of suicidality may also produce improvements related to productivity, employment, crime, incarceration, and consumption that further enhance societal welfare [68]. Similar improvements may also extend to others impacted by the individual’s suicidality (e.g., family members, friends, colleagues, and clinicians). Indeed, one study found that indirect costs represented 97.1% of the $58.4 billion total U.S. economic costs of reported suicide-related acts in 2013 [69]. In light of research indicating that Soldiers may be more likely to attempt suicide if there has been a past-year suicide attempt within their unit [70], it is conceivable that effective treatment of suicidality might even have a multiplicative effect within a military population. Incorporating these broader societal considerations into future cost-inclusive evaluations of suicide interventions may enhance our understanding of their true value.

Third, in the original trial, study clinicians were assigned to their respective treatment conditions based on their preferred approach for managing suicidal patients. Although this approach maximized fidelity to study treatment, it should be noted that CAMS therapists inadvertently had more than twice the years of practice experience since professional degree than ETAU therapists. This finding is consistent with research suggesting that less-experienced therapists may be more inclined to adhere to a specific treatment protocol or newly learned therapy whereas more seasoned providers may be more open to a variety of approaches [7173]. Previous research suggests that years of practice experience is not necessarily correlated with therapist effectiveness [74,75] and statistical modeling in the current study did not suggest any therapist effects on clinical outcomes. Further, differences in practice experience did not impact treatment costs between treatment conditions as all study therapists were classified as “non-physician” under TRICARE reimbursement procedures [76]. Still, some studies indicate that greater suicide-specific practice experience is associated with enhanced suicide intervention competence and skills [77,78], and thus future CAMS investigations would be strengthened by ensuring comparable practice experience among providers to remove this potential confounding.

Finally, due to limitations in the available data, the current study was unable to determine the exact temporal sequence of healthcare services delivered to participants within each follow-up window. It is therefore possible that some non-study-related services classified as outcomes (i.e., benefit) were actually delivered concurrently with active study treatment rather than post-treatment, as the designation of outcome would imply. Although this approach allowed for the greatest use of service utilization data while avoiding conflation with study treatment costs, future cost-inclusive evaluations would benefit from greater precision in the assessment of benefits.

Conclusions

Suicide prevention represents a top force health and readiness priority for the DoD. The CAMS framework has been increasingly recognized as a promising approach for the treatment of suicidal risk. Although CAMS has amassed a robust evidence base supporting its clinical effectiveness, the current study provides evidence that CAMS may also be associated with greater benefit and cost-benefit compared to treatment as usual. Although the differences observed in our study were small, the potential impact grows appreciably once extrapolated across the population of 1.38 million active duty service members (and 9.5 million beneficiaries total) served by the MHS [79]. These economic advantages may become more pronounced as CAMS’s more cost-effective training and delivery formats become more widely adopted. Ideally, such cost savings could allow limited financial resources to be re-allocated toward meeting other healthcare system needs. Although additional evaluations are necessary to enhance the generalizability of our findings, the current study provides a valuable insight into the costs and benefits of CAMS within the context of the MHS. These findings may inform more robust cost-inclusive analyses in future trials and ultimately facilitate decision-making among the policymakers, healthcare administrators, and clinicians tasked with selecting mental health programs that will provide the biggest ‘bang for the buck’ amidst constrained resources.

Data Availability

Public sharing of data used in this study is prohibited under the protocol approved by the U.S. Army Medical Research and Development Command Office of Research Protections as well as Institutional Review Boards at Dwight D. Eisenhower Army Medical Center, The Catholic University of America, and the University of Washington. Additional restrictions apply to the availability of these data in order to protect participants’ privacy. Requests for access from interested researchers may nevertheless be considered, subject to the terms and conditions of the request and in compliance with the applicable regulations. Requests may be directed to the Office of Sponsored Programs and Research Services, The Catholic University of America, 213 McMahon Hall, 620 Michigan Ave., NE, Washington, DC 20064; Phone: 202-319-5218; Fax: 202-319-4495; Email: CUA-OSP@cua.edu.

Funding Statement

The current study represents an unfunded secondary analysis of a randomized-controlled trial; the primary trial was supported by the Department of the Army through federal grant W81XWH-11-1-0164, awarded and administered by the Military Operational Medicine Research Program (MOMRP). The authors received no specific funding for the present work.

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Decision Letter 0

Isabelle Durand-Zaleski

11 Jun 2021

PONE-D-21-12016

Costs, Benefits, and Cost-Benefit of Collaborative Assessment and Management of Suicidality versus Enhanced Treatment as Usual

PLOS ONE

Dear Dr. McCutchan,

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"I have read the journal's policy and the authors of this manuscript have the following competing interests: David Jobes has conflicts to disclose related to grant funding from the National Institute of Mental Health; he receives book royalties from the American Psychological  Association Press and Guilford Press; and he is the founder of CAMS-care, LLC (a professional training and consultation company). Phoebe McCutchan, Brian Yates, Amanda Kerbrat, and Katherine Comtois have declared that no competing interests exist."

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

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Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

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Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Article well written and well presented. I have only a few remarks to propose.

This article is focused on a medico-economic analysis of a prevention program (CAMS) on suicidal behaviors in suicidal soldiers of the US army. This intervention is delivered by social workers, and is compared to an Enhanced version of Treatment As Usual ETAU).

I would be interested if some items could be further discussed:

1) Social workers are not randomized and in CAMS program are far more experienced. It is only discussed in the limitations part saying it has no influence. Some articles emphasize that experience might be important. (For instance: Suicide intervention skills and related factors in community and health professionals Suicide Life Threat Behav . 2010 Apr;40(2):115-24. doi: 10.1521/suli.2010.40.2.115.)

2) CAMS protocol stops if 3 consultations in a row are without suicidal ideas, as ETAU does not. This might have direct economic implications.

3) It seems that Crisis Services use is different in the 2 programs and seems more important in CAMS program in the 1st month, and less at 6 months and 12 months. This seems very interesting and should be further discussed.

Reviewer #2: Thank you for the opportunity to review this interesting paper. Similarly to reviewer 2, I was not among the initial reviewers and carried out a first blind review of the manuscript before considering the authors’ responses to the initial review and revising my recommendations based on things that had already been addressed or discussed (which contributes to the reduced number of comments I have). Overall, I believe that this article is of research and policy interest, rigorous, well-written and clear. I, however, still have a couple of comments to improve the latest version of the manuscript but want to stress that in my view the comments of previous reviewers have been appropriately addressed overall.

1/ I believe that, for non-US readers, some parts could be made clearer or more specific. In particular, behavioral health is a concept which is very specific to the US and which would be worth defining once. The involvement of social workers in mental care is also very specific to your national context and could require some additional information to justify why you used social workers wages in your economic evaluation. In the introduction, it would be interesting to provide more specific figures on the unprecedented rate of increase in suicides among the military workforce in the US over time since such figures appear to be available. Also briefly mention what is TRICARE and CHAMPUS. Minor additional precisions needed: “Active component”: clarify for readers what this refers to; “condition”: maybe replace everywhere by “treatment condition” as you do once, that way it is less confusing for non-native English speakers (as conditions can refer to diseases); “modeling on multiply imputed datasets” (abstract): multiple?, “member of the Warriors in Transition unit”: explain what it is very briefly?

2/ I think the discussion or conclusion could stress more the policy implications of the research for the military health system (make it more explicit maybe).

3/ I am surprised that none of the ETAU clinicians, when provided with potential supervision upon request, asked for it. Maybe discuss potential hypotheses about why this happened (while it seems to be less the case with CAMS while it is carried out by providers with more years of experience).

4/ At some point you mention the time required for transit between the patient’s place of residence and the place of care and justify that you did not include it in your economic evaluation because you were not able to access confidential information regarding the place of residence of patients. I wonder if anyway this cost should be included in an evaluation adopting the military health services perspective? Would not those costs lie on the patients anyway or be more related to loss of productivity for the military?

5/ I read your answer to a previous comment on the pre-doctoral graduate students included in the cost assessment. I am still not fully convinced they should be included in an evaluation which aims to accurately fit real-world settings. “We presume these cost rates are comparable to those of staff who might conduct administrative activities in real-world settings.”: This should be more justified to be convincing.

6/ Some reorganization might be necessary: “In the current secondary analysis, treatment costs […] were determined using micro-costing” and subsequent paragraph of the introduction: this would be better suited in the method section; “Multiple imputation using chained equations with predictive mean matching was used to minimize uncertainty…”: this would be better suited in the method section of the paper as well.

7/ For the ethical approvals that you mention in the first paragraph of the method section, it would better (more transparent and traceable) to also provide the identification number of the approval received.

8/ Measures section: “were validated against available administrative data sources (e.g., electronic health records”: it would be better to be exhaustive and more specific here; and the comma after e.g. (or sometimes i.e. in the text) seems misplaced. Similarly, in the ‘Training and implementation activity costs’ paragraph: “Activities performed were identified by intervention manuals, administrative data systems, and qualitative interviews as feasible and appropriate”: it would be better to be more precise here.

9/ “There were no statistically significant differences between the CAMS and ETAU conditions with regard to sociodemographic or baseline clinical characteristics”: maybe specify that you are talking about patients’ characteristics.

10/ I must admit I am a bit concerned about the involvement of the founder of a company called CAMS-care in a research which strongly supports the overall value of CAMS.

**********

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Reviewer #1: No

Reviewer #2: No

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PLoS One. 2022 Feb 3;17(2):e0262592. doi: 10.1371/journal.pone.0262592.r003

Author response to Decision Letter 0


26 Jul 2021

Dear Dr. Robinson, Dr. Sisask, Dr. Kõlves, Dr. Oquendo, Dr. Heber, and Reviewers,

Thank you for your review of our manuscript entitled, “Costs, Benefits, and Cost-Benefit of Collaborative Assessment and Management of Suicidality versus Enhanced Treatment as Usual” (PONE-D-20-33804). We are pleased to respond to each Journal and Reviewer comment below.

-------------------------------------------------------

Journal requirements: When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

We have reviewed the style requirements and believe our submission to be consistent with the guidance provided.

2. Thank you for stating the following in the Competing Interest Section:

"I have read the journal's policy and the authors of this manuscript have the following competing interests: David Jobes has conflicts to disclose related to grant funding from the National Institute of Mental Health and the American Foundation for Suicide Prevention; he receives book royalties from the American Psychological Association Press and Guilford Press; and he is the founder of CAMS-care, LLC (a professional training and consultation company). Phoebe McCutchan and Brian Yates have declared that no competing interests exist."

2.1. We note that you have provided funding information that is not currently declared in your Funding Statement. Currently, your Funding Statement reads as follows:

"The author(s) received no specific funding for this work."

Please include your amended statements within your cover letter; we will change the online submission form on your behalf.

The current study represents an unfunded secondary analysis of a randomized-controlled trial. The primary trial was supported by the Department of the Army through federal grant W81XWH-11-1-0164, awarded and administered by the Military Operational Medicine Research Program (MOMRP). We have added this information to the cover letter for clarity. Funding described in Dr. Jobes’ conflicts of interest disclosure did not apply to the current study.

2.2. Please confirm that this ("he receives book royalties from the American Psychological Association Press and Guilford Press; and he is the founder of CAMS-care, LLC (a professional training and consultation company)") does not alter your adherence to all PLOS ONE policies on sharing data and materials, by including the following statement: "This does not alter our adherence to PLOS ONE policies on sharing data and materials.” (As detailed online in our guide for authors http://journals.plos.org/plosone/s/competing-interests). If there are restrictions on sharing of data and/or materials, please state these. Please note that we cannot proceed with consideration of your article until this information has been declared.

Please include your updated Competing Interests statement in your cover letter; we will change the online submission form on your behalf.

Please know it is PLOS ONE policy for corresponding authors to declare, on behalf of all authors, all potential competing interests for the purposes of transparency. PLOS defines a competing interest as anything that interferes with, or could reasonably be perceived as interfering with, the full and objective presentation, peer review, editorial decision-making, or publication of research or non-research articles submitted to one of the journals. Competing interests can be financial or non-financial, professional, or personal. Competing interests can arise in relationship to an organization or another person. Please follow this link to our website for more details on competing interests: http://journals.plos.org/plosone/s/competing-interests

The authors confirm that Dr. Jobes’s competing interests do not alter our adherence to all PLOS ONE policies on sharing data and materials. We have included the statement, “This does not alter our adherence to PLOS ONE policies on sharing data and materials” in our revised cover letter.

Please note that we have made an additional change was made to the Competing Interests statement in the cover letter. Dr. Jobes no longer receives grant funding from the American Foundation for Suicide Prevention; the statement has been updated accordingly.

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The dataset uploaded as a Supporting Information file in our original submission has been deleted to ensure compliance with IRB requirements. We have added a Data Availability Statement detailing the restrictions and providing contact information for the institutional body to which data requests may be sent. Because no Supporting Information files are included as part of the current submission, no captions were added to the revised manuscript.

Reviewer #1 comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Partly

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The authors examined the economic cost-benefit ratio of CAMS versus enhanced treatment-as-usual (TAU) in a sample of 148 active duty military with current suicidal ideation. The study involved a secondary analysis of data from a randomized clinical trial of CAMS versus TAU for soldiers with current suicidal ideation who obtained services at outpatient mental health clinics. The study addresses a topic of substantial importance. The suicide rate is rising, and we have limited information available about the costs of treatment, which are critical to decision making and actual implementation. The study and manuscript also have several strengths, particularly in the description of treatment training and implementation costs, and in the description of data analyses. However, in some areas the manuscript is somewhat vague and the presentation of background information, findings, and their interpretation would benefit from being more balanced (critical) and scholarly. A clear statement of hypotheses and primary outcomes would also be helpful.

The following suggestions may enable the authors to improve their manuscript.

1. Abstract: It is recommended that the statement be removed that CAMS is “one of the most empirically-supported suicide-focused interventions to date” and has “demonstrated clinical effectiveness across a number of clinical trials.” This seems too broad sweeping for this abstract, particularly as it’s noted in Introduction that the need for studies with more robust designs has been emphasized.

These statements have been removed from the Abstract.

The phrase “to examine the economic costs, benefits, and cost-benefit” is confusing as used in the Abstract and throughout the manuscript. Is there a way to put this more succinctly and define the term(s) in Introduction? It seems to be a “cost analysis” that considers financial costs and Also, the differential meanings of “cost-benefit” and “net benefit” are unclear in the Abstract.

We appreciate the Reviewer highlighting that these economic terms may be confusing for readers. The overarching aim of the study was, as stated, to examine the economic costs, benefits, and cost-benefit of the interventions (that is, the costs of delivering treatment, the value of resources generated or saved as a result of the intervention, and measures of costs relative to resources gained). We view these as three distinct economic constructs and have respectfully opted not to revise this statement in the Abstract; however, the Introduction was revised to operationalize these terms and provide greater clarity on their distinctions as primary outcomes.

We also recognize that the distinction between ‘cost-benefit’ and ‘net-benefit’ is unclear in the Abstract. We have revised the Abstract to reflect that the construct of ‘cost-benefit’ was assessed using two distinct indices common in economic evaluation, cost-benefit ratios (i.e., ratios of benefits divided by costs) and net benefit (i.e., benefits minus costs): “Cost-benefit was examined in the form of cost-benefit ratios and net benefit.” We have also revised the Introduction to include clarification of these as outcome variables.

It would be helpful to include the sample size and a brief statement of demographics.

The Abstract was revised to include the following statement, “The full intent-to-treat sample included 148 participants (mean age 26.8 years± 5.9 SD years, 80% male, 53% White).”

2. Introduction: As the suicide rate has increased in all age groups in recent years, it would be helpful to state the 2018 rate for the age and gender-adjusted U.S. general population. This will enable readers to have a sense of how different it is from the rate for active military.

To provide greater clarity to this statement, we have revised it to read, “These trends are particularly alarming in that they represent the first time in recorded history that the U.S. military suicide rate has equaled or exceeded that of comparable U.S. general population cohorts, beginning in 2008 and continuing to date. According to the most recent publication of the DoD Annual Suicide Report, in 2019 the suicide mortality rate for the Active Component was statistically indistinguishable from the 2018 U.S. population rate after adjusting for age and gender [4].”

In the second paragraph, the last sentence could also include that research is needed to carefully evaluate the effectiveness of these interventions in rigorous studies that are powered to examine key outcomes.

The paragraph has been revised to read, “New interventions aimed specifically at managing suicidality are emerging, but additional research is needed to carefully evaluate the effectiveness of these interventions in rigorous, well-powered studies in order to inform clinical practice guidelines and facilitate integration into routine clinical care.”

Related to this, in the third paragraph, it is noted that CAMS has amassed a substantial evidence base for its effectiveness; however, information is not included about 1) the results of the “parent” RCT study (from same data set);

The “parent” RCT study is listed as part of the citation related to the RCT evidence-base, but we appreciate how it could be more clearly referenced. Additional detail has been added to paragraph 6 of the Introduction: “The purpose of the current study was to extend previous analyses by examining the costs, benefits, and cost-benefit of CAMS compared to enhanced treatment as usual (ETAU) for the treatment of suicidality in active duty Soldiers using data from a recent clinical effectiveness RCT. Results of the primary RCT indicated that CAMS treatment was associated with significant postbaseline improvements in suicidal ideation and suicide attempt behaviors across one year of follow-up. However, the ETAU condition evidenced comparable improvements, with the exception of a significantly greater reduction in probability of suicidal ideation at 3-month follow-up observed in the CAMS condition [24]. Examination of treatment costs and benefits becomes especially useful in such scenarios where two treatment alternatives appear similarly effective, to select the intervention which maximizes return on investment.”

and 2) the limitations of research to date on CAMS and why more “robust” or rigorous studies have been recommended. These are both critical gaps in the Introduction.

The paragraph in question has been revised to read, “Further, recent systematic review of CAMS reported it to be a promising approach to managing suicide risk and deliberate self-harm in adults [27], although it noted a high degree of heterogeneity and attrition across existing studies and emphasized the need for additional high-quality studies, particularly randomized-controlled trials (RCTs) and meta-analyses.”

Additionally, we have added a citation for a forthcoming meta-analysis indicating that CAMS is a well-supported intervention for suicidal ideation: “Further, a more recent meta-analysis reported that CAMS treatment resulted in significantly lower suicidal ideation and general distress compared to alternative interventions, concluding that it is a well-supported intervention for suicidal ideation according to Center of Disease Control and Prevention criteria [28].”

The next paragraph (first full paragraph on second page of the Introduction) includes the statement, “…what remains to be studied is the cost of the intervention.” This is contrary to the earlier statement that more robust studies of effectiveness are still needed.

This statement has been revised to read, “In addition to its clinical effectiveness, another important factor requiring further examination is the cost of the CAMS intervention, particularly in comparison to alternatives.”

The paragraph that begins “Preliminary analyses using archival data…” seems to go too far in extrapolating from the data given that this was not a RCT and was a small study. It’s important to add a statement such as “This study involved XXX patients (XX/group) and there may have been biases in assignment to groups such that we cannot conclude that CAMS resulted in a cost savings…”

The following statement has been added, “Still, the significant methodological limitations of the study must be noted, including a small and unequally distributed sample size (N = 55; n = 25 for CAMS and n = 30 for treatment as usual), lack of random assignment, and lack of fidelity measures. Consequently, it is premature to definitively conclude based on these analyses that CAMS is associated with economic advantages compared to treatment alternatives.”

As noted above regarding the Abstract, the phrase “…the costs, benefits, and cost-benefit” would benefit from simplification and an operational definition of the one or two constructs that are primary to (related to the hypotheses of) this study.

Again, we appreciate the Reviewer’s feedback regarding the clarity of these terms for readers. The paragraph has been revised to include operationalization of each primary construct (cost, benefit, and cost-benefit): “In these analyses, treatment costs (i.e., the value of resources required to implement the intervention) were determined using micro-costing and gross-costing techniques. Benefits of the intervention (i.e., the value of resources generated or saved as a result of the intervention) were assessed as potential cost savings based on healthcare expenditures across multiple categories of services. Finally, cost-benefit (i.e., the relationship between the value of resources used and the value of resources saved by an intervention) was examined using cost-benefit ratio and net benefit metrics [31].”

Please add a clear statement of hypotheses and the study’s primary outcome(s).

The final two paragraphs of the Introduction have been revised to specifically label the five study hypotheses.

3. Materials and Methods.

How was TAU enhanced?

Paragraph 2 under Methods/Treatments states, “This condition was considered ‘enhanced’ treatment as usual in that it specified a minimum number of four treatment sessions, providers had access to consultation and supervision as needed, and Soldiers were routinely engaged and evaluated at the study assessment intervals.” We have added a citation for the primary aims manuscript (Jobes et al., 2017) which also defines the ETAU condition, and are happy to provide further clarification if necessary.

In the Measures section, it would be helpful to provide a 1-2 sentence description of the Scale for Suicidal Ideation-Current and to provide more information about the THI-M (e.g., number of items). How were follow-up assessments combined when some were missing?

A brief description of the SSI-C was added to the Measures section: “The Scale for Suicide Ideation-Current (SSI-C) [36], a 19-item interviewer-rated measure assessing suicidal ideation at its highest intensity over the past two weeks, was used to assess suicidal ideation severity (total score of 0-38) and resolution (i.e., a total score of zero). The SSI-C has demonstrated good convergent and criterion validity in previous research in psychiatric patients [36] and evidenced high internal consistency in the current study (α = .88).”

Additionally, the following details were added to the description of the THI-M: “The THI-M is an interviewer-administered measure that captures the history (e.g., service frequency, duration, and provider type) of outpatient psychotherapy and counseling visits, crisis medical services, medical provider visits, and medication use.”

Missing data in follow-up assessments were handled using multiple imputation, as described in the Results/Missing Data Section: “Multiple imputation using chained equations with predictive mean matching was used to minimize uncertainty related to the replacement of missing data for health services utilization [55]. Treatment cost data did not require imputation as data were available for all participants. Participants who did not complete at least one follow-up assessment (n = 6) were excluded from imputation and subsequent analyses. Fifteen imputed datasets were created to adequately address the observed proportion of missing data [56, 57]. Planned statistical analyses were carried out on each imputed dataset, producing separate summary statistics (e.g., means or regression coefficients) with corresponding standard errors. For regression analyses, Rubin’s rules [58] were applied to derive pooled coefficients and standard errors [59]. For nonparametric tests, observed and imputed datasets were analyzed and reported separately.” We are happy to provide further detail if necessary.

Regarding clinicians, what was the extent of booster sessions, consultation, or feedback sessions for CAMS? For ETAU? Were these figured in?

In the effectiveness trial, CAMS therapists engaged in regular study-related consultation calls.

Although these activities may have impacted CAMS therapists’ practice, these calls were more reflective of research procedure than real-world clinical practice. Subsequently, in an effort to represent the potential impact of these activities while avoiding unnecessarily inflating CAMS costs, we assumed that CAMS providers attended a total of four one-hour group consultation calls, as is typical in real-world CAMS-Care training. These consultation calls were factored into the costs of Training/Implementation activities, as noted in Table 1. No other booster or feedback sessions were utilized by these therapists.

ETAU therapists were offered additional supervision/consultation by study investigators but declined usage of such resources. As stated in the Methods/Cost Assessment/Training and implementation activity costs section, “Further, although ETAU therapists were offered additional supervision and consultation as needed, key informant interviews indicated that they elected not to participate in these activities during the course of the study. Consequently, there were no additional costs beyond those captured in the provision of clinical services.”

It would be helpful to read, more specifically, about why the authors think their CAMS group was more experienced – what was pathway to becoming a CAMS therapist?

Eligible clinicians were licensed behavioral health clinicians employed by the FSGA Soldier Resiliency Center who were willing and able to consent to see randomized client participants using the treatment to which they are assigned and to consent to confidential digital recordings of treatment sessions and completion of therapist assessments. Clinicians were excluded if they were expected to leave the FSGA Soldier Resiliency Center in less than 12 months or were determined by FSGA Soldier Resiliency Center leadership to be inappropriate to participate in the study. As described in the revised Methods/Participants section, “Eligible clinicians were assigned to either the CAMS or ETAU condition based on their relative self-reported allegiance to treatment models for managing suicidal patients; clinicians reporting weaker preference for a specific treatment were assigned to the CAMS condition to ensure high adherence of ETAU clinicians to their existing approach.”

We note in the Discussion section the observed discrepancy in practice experience as a study limitation and have revised the Discussion/Limitations section to offer the following explanation: “Third, in the original trial, study clinicians were assigned to their respective treatment conditions based on their allegiance to a specific approach for managing suicidal patients. Although this approach maximized fidelity to study treatment, it should be noted that CAMS therapists inadvertently had more than twice the years of practice experience since than ETAU therapists. This finding is consistent with research suggesting that less-experienced therapists may be more inclined to adhere to a specific treatment protocol or newly learned therapy whereas more seasoned providers may be more open to a variety of approaches [71-73]."

4. Cost Assessment

In some areas the authors argue for using more realistic costs (e.g., onsite training); however, this is not consistent. An example is using the salary and fringe rates for pre-doctoral graduate students who would probably not be the clinicians if this was not a research study.

We acknowledge some inconsistency in the use of micro-costing techniques versus applying real-world assumptions. As noted as a limitation in the Discussion section, strict micro-costing procedures may exaggerate the costs of the CAMS condition owing to research activities performed for scientific rigor, above and beyond typical CAMS practice. Therefore, in some instances we applied assumptions that better reflect the costs of implementing CAMS in real-world settings. These assumptions are noted in the manuscript. A statement has been added to the Discussion section to emphasize this point: “We attempted to mitigate potential overestimation of costs related to research procedures through application of some real-world practice assumptions to enhance external validity.”

With regard to the pre-doctoral graduate students included in the cost assessment, the role of these individuals was limited to participating in consultation calls where feedback was provided related to treatment adherence; they did not serve as study clinicians. [As described in the Methods/Cost Assessment section, “Study therapists were clinical social workers assumed to be GS-12 paygrade based on key informant interviews.” To clarify this distinction, the section was revised to read “Annual base salaries and fringe rates for four pre-doctoral graduate student assistants who contributed to fidelity assessment were estimated based on typical grant-funding allowances reported by The Catholic University of America Office of Sponsored Programs.”]. We chose to micro-cost these activities based on the actual salary and fringe rates of pre-doctoral graduate students because (1) it represented a relatively small proportion of training and implementation costs (approximately 4 person hours total) and (2) we presume these cost rates are comparable to those of staff who might conduct administrative activities in real-world settings.

What were primary hypotheses and primary study outcomes? Findings are presented for 6 months and 12 months, and for different cost outcomes and different cost variables. It is recommended that the primary outcome(s) be included in the Introduction, with a more specific statement of study hypotheses regarding the cost analysis variable(s) and outcome time point. Then, it would be helpful to organize the Results in keeping with this, presenting the primary outcomes first followed by any follow-up analyses.

As noted in an earlier response to the Reviewer, we have revised the Introduction section to specifically label the five study hypotheses, including the specific timepoints at which they were assessed. The Reviewer is correct that variables were analyzed at different timepoints; repeated measures, between-subjects variables were assessed at each follow-up timepoint (1-, 3-, 6-, and 12-month), whereas variables representing a within-subjects outcome were assessed only at 12-month follow-up. The latter was necessary because baseline (i.e., pre-intervention) healthcare expenditures were assessed on the THI-M over a “past year” timeframe, and therefore follow-up (post-intervention) healthcare utilization was only comparable after an equivalent 12-month period. These differences in assessment timeframes on the THI-M at baseline versus follow-ups are described in the Methods/Measures section, and we have specifically labeled the outcome as change in past-year expenditures. In addition, the following text was added to the Methods/Analyses section to provide clarification: “Linear regression was used to examine group differences in cost-benefit and net benefit at 12-month follow-up, as these outcomes reflect pre-intervention versus post-intervention change in past-year expenditures [54].” We are happy to include further clarification in the manuscript regarding outcome timepoints if deemed necessary.

We further made minor revisions to the Results section to be better organized in accordance with our primary outcomes.

5. Discussion and Conclusions. It is recommended that these focus on primary hypotheses and associated results and include as balanced as possible a presentation of findings.

The Discussion section has been reviewed to ensure focus on the results of primary hypotheses. Additionally, minor revisions to language have been made to present findings in a more neutral and balanced manner (e.g., expanding the implications and future directions of our work to suicide prevention more broadly).

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

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Reviewer #1: No

Reviewer #2 Comments

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #2: (No Response)

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2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #2: Yes

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3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #2: I Don't Know

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4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #2: Yes

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5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #2: Yes

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6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #2: Thank you for the opportunity to review the revised manuscript, “Costs, Benefits, and Cost-Benefit of Collaborative Assessment and Management of Suicidality versus Enhanced Treatment as Usual.” I was not among the initial reviewers from the first submission, and so did a ‘clean’ review of the new manuscript first, before examining the previous requests/responses to the initial review and revising my recommendations based on things that had already been addressed/discussed. Overall, the manuscript is well-written and more research is certainly needed regarding cost and cost-benefits of suicide-focused interventions, such as CAMS. I have outlined my specific recommendations and feedback below:

1) I was a bit confused when first reading the abstract, particularly the results reported on lines 34-38. They seem to indicate that CAMS had a significantly greater cost-benefit, but that this wasn’t significant when factoring in the intervention cost—wouldn’t intervention cost be factored into the cost-benefit? This part of the abstract may need to be reworded to clarify differences that are statistically significant. I also ran into this problem in the main manuscript where it was at times unclear whether a finding was suggesting a statistically significant difference between E-TAU and CAMS, or just trending in a particular direction.

We agree that these lines in the Abstract are a bit confusing. As originally worded, it is not clear how the cost-benefit metrics used (i.e., CBRs and net benefit) reflect different relationships between cost and benefit. To clarify, we have revised the Abstract to read, “CAMS also demonstrated significantly greater cost-benefit ratios (i.e., benefit per dollar spent on treatment) and net-benefit (i.e., total benefit less the cost of treatment) at 12-month follow-up.” Additionally, Reviewer #2 is correct that the term “significant” was misapplied on line 37. We have removed this statement and revised the Results and Discussion sections of the manuscript to clarify findings that were descriptive rather than statistically significant.

2) It was stated that the E-TAU group required a minimum of 4 sessions, and that CAMS consists of “approximately” 4-11 sessions. Was there a requirement of at least 4 sessions for the CAMS group? If not, this might present a conflict in the costs (given that ETAU needed 4 to be included). If the use of approximately meant that 4 and 11 represented the minimum and maximum range in the study, I would recommend making this explicit.

A minimum of 4 sessions was required in both treatments. The CAMS intervention requires a minimum of 4 sessions (initial plus three consecutive sessions without suicidality); thus, in the trial, ETAU was augmented with the same minimum for attention control. We have revised the Methods section of the manuscript to clarify that CAMS entailed a minimum of 4 sessions: “In the current study, the CAMS intervention consisted of approximately 4 to 11 weekly individual sessions (after the initial session, CAMS concludes after three consecutive sessions with resolved suicidality) following the suicide-specific CAMS framework [11].”

3) I was initially a bit surprised by the report that the cost of the CAMS intervention was not significantly different from E-TAU (given that there is a clear cost to CAMS, and not for E-TAU), and I’m a bit skeptical of the denominator used (160) for the number of patients treated with CAMS for each provider trained. It was described as being derived from suicidal ideation rates in the military population, the typical caseload size of a clinician, and the typical length of career for MHS behavioral health providers. Does this then assume that a clinician would be utilizing CAMS for every case of SI, with full fidelity? Many conditions (e.g., depression, PTSD) might have co-occurring SI where treating the SI may not be the primary treatment target. And with regard to the estimated career length, is this accounting for years already ‘served’ by the study therapists, or was this calculated as though training occurred for a new hire out of school? There are certainly differences in fidelity and adherence when in a consultation phase of an active RCT versus standard practice over a career, and I’d hesitate to extend the CAMS delivery with fidelity beyond a few years from the training. If there is existing evidence from CAMS or other EBPs regarding longevity of fidelity that supports the current estimates, please do cite and include. Otherwise, I would recommend revising down the current estimate of 160 patients being provided with fidelity-level CAMS, as it seems likely to be an overestimate that has significant implications for the rest of the cost equation.

The current analysis assumes that CAMS could be administered to nearly all patients presenting with suicidal ideation and the rate of appropriate patients was informed by both empirical evidence and key informant interviews with local providers. Treatment for co-occurring mental health conditions does not preclude concurrent treatment with CAMS, and in fact, CAMS is still indicated given empirical evidence suggesting that effective treatment of suicidal behaviors requires a suicide-specific focus (versus treatment focused on targeting a mental disorder with the reduction of suicidality as a secondary effect; see reviews by Wenzel, Brown, & Beck, 2008; Tarrier, Taylor, & Gooding, 2008). Thus, our analysis considered each suicidal patient as a potential candidate for CAMS regardless of the possibility that co-occurring conditions were the primary presenting concern.

The analysis further assumes CAMS will be provided with an acceptable degree of fidelity. Reviewer #2 makes an excellent point that adherence may vary between an active RCT and standard practice. However, we anticipated that CAMS providers would remain generally adherent given (a) the lack of therapeutic drift in the primary RCT (see Jobes et al., 2017); (b) previous research from an online survey of practitioners trained in CAMS that indicated generally high levels of adherence to CAMS therapeutic approach and practice (Crowley, 2015); (c) the flexibility and adaptability of the CAMS framework to accommodate different suicidal patients and presentations; and (d) the relatively short Military Health System career span (estimated to be ~five years, conservatively). With regard to the estimated career length, our analyses assume that training would be provided at the beginning of the provider’s career such that it might be implemented for the full five years, which we believe to be a very conservative estimate of typical career length across both military and civilian providers.

Per Reviewer #2’s comment, we have added a statement regarding our assumption of maintained adherence to CAMS: “These estimates also assume a relatively high degree of adherence to CAMS across the provider’s MHS career, as supported by the absence of drift reported in the primary trial [24] and a community survey of mental health practitioners reporting generally high levels of adherence to the CAMS therapeutic approach and practice [53].”

4) I would recommend adding a quick note to the ‘cost’ section that the numbers also include 4 clinicians per training when arriving at the $12.44.

The Results/Cost section and Table 1 have been revised to specify that four clinicians were included in costing estimates for CAMS training and consultation activities.

5) Was there any data on whether these active duty soldiers were medically or otherwise discharged during this one-year period? If they were, would this have precluded them from receiving services that could have been captured by the cost analysis? If discharge rates differed between groups, and services would have been obtained outside of the DoD, this might look like cost savings, when in actuality, represents a more severe (and costly) outcome.

The Treatment History Interview (Military Version) captured all healthcare services within an assessment window regardless of where services were received; thus, the cost analysis reflects all services received, even if a participant separated from the military during follow-up. For reference, separation rates were comparable between conditions (53% separated from military services, 37.3% remained on active duty, and 9.3% status unknown in the ETAU condition versus (47.9% separated from military services, 43.8% remained on active duty, and 8.2% status unknown in the CAMS condition).

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Reviewer #2: No

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REVIEWS RECEIVED 6/11/2021

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We have reviewed our reference list and believe it to be complete and correct. Two citations in the Introduction section have been replaced with more appropriate citations in the revised manuscript; both instances are marked with a comment in the ‘track changes’ version of the manuscript. Additionally, several new citations have been added to support revisions requested by reviewers; these instances are marked in red font.

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REVIEWERS' COMMENTS:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: I Don't Know

Reviewer #2: Yes

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

4. Is the manuscript presented in an intelligible fashion and written in standard English?

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Reviewer #2: Yes

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1:

Article well written and well presented. I have only a few remarks to propose. This article is focused on a medico-economic analysis of a prevention program (CAMS) on suicidal behaviors in suicidal soldiers of the US army. This intervention is delivered by social workers, and is compared to an Enhanced version of Treatment As Usual ETAU). I would be interested if some items could be further discussed:

1) Social workers are not randomized and in CAMS program are far more experienced. It is only discussed in the limitations part saying it has no influence. Some articles emphasize that experience might be important. (For instance: Suicide intervention skills and related factors in community and health professionals Suicide Life Threat Behav . 2010 Apr;40(2):115-24. doi: 10.1521/suli.2010.40.2.115.)

We appreciate the reviewer’s comment and agree that this limitation could be presented in a more balanced manner given research suggesting that suicide-specific practice experience (although not necessarily general practice experience) is associated with greater suicide prevention skills. We have revised this paragraph of the Limitations section to read, “Still, some studies indicate that greater suicide-specific practice experience is associated with enhanced suicide intervention competence and skills [77, 78], and thus future CAMS investigations would be strengthened by ensuring comparable years of practice experience among providers to remove this potential confounding.”

2) CAMS protocol stops if 3 consultations in a row are without suicidal ideas, as ETAU does not. This might have direct economic implications.

The randomized controlled trial which provided data for the current study was designed to examine real-world effectiveness. The CAMS protocol in the current study was delivered in accordance with the standardized treatment manual typically used in CAMS implementation (i.e., the criteria for treatment termination were not specific to this study). ETAU clinicians concluded study treatment when the suicidal risk for which they were referred resolved, as defined by their and the clinic’s standard practices. Once study treatment concluded, they could continue to see or refer the participant for other treatment issues or discharge the participant from treatment. This ‘real world’ comparison control condition was intentionally chosen to maximize the external validity and generalizability of the study, to include the estimation of treatment costs for comparison. The purpose of the current study was to examine the economic implications of providing each of these treatment interventions under real world conditions.

Interestingly, as described in the manuscript, there were no significant differences in the number of study treatment sessions between CAMS and ETAU, indicating that treatment length was comparable between groups and likely not impacted by discrepant treatment termination protocols.

3) It seems that Crisis Services use is different in the 2 programs and seems more important in CAMS program in the 1st month, and less at 6 months and 12 months. This seems very interesting and should be further discussed.

We have revised the Discussion section to read, “With regard to benefits at the group level, CAMS was associated with significantly reduced total cumulative healthcare expenditure compared to ETAU at 6-month follow-up, likely driven by significantly lower crisis services expenditures. However, ETAU eventually matched CAMS in total cumulative healthcare expenditures at 12-month follow-up timepoints, although crisis services expenditures remained significantly lower for CAMS. The data suggest that participants in the CAMS condition may use more crisis services than ETAU in the first month of treatment but use significantly fewer crisis services by 6- and 12-month follow-ups. The early uptick in crisis service utilization may be explained by CAMS's suicide-specific focus which promotes accessing such services in an acute crisis, whereas the decreased utilization by six months likely reflects findings from the primary trial that CAMS participants had a lower probability of having suicidal ideation at 3-month follow-up [24].”

Reviewer #2:

Thank you for the opportunity to review this interesting paper. Similarly to reviewer 2, I was not among the initial reviewers and carried out a first blind review of the manuscript before considering the authors’ responses to the initial review and revising my recommendations based on things that had already been addressed or discussed (which contributes to the reduced number of comments I have). Overall, I believe that this article is of research and policy interest, rigorous, well-written and clear. I, however, still have a couple of comments to improve the latest version of the manuscript but want to stress that in my view the comments of previous reviewers have been appropriately addressed overall.

1/ I believe that, for non-US readers, some parts could be made clearer or more specific. In particular, behavioral health is a concept which is very specific to the US and which would be worth defining once.

We have revised the manuscript to define ‘behavioral health’ the first time it appears in the text: “Participants were randomly assigned to either CAMS or ETAU matched on histories of suicide attempts, medication class, severity of physical injury or disability, and current enrollment in outpatient behavioral health treatment (i.e., psychiatric, clinical psychology, or social work services).”

The involvement of social workers in mental care is also very specific to your national context and could require some additional information to justify why you used social workers wages in your economic evaluation.

Social worker wages were used in this economic evaluation to reflect the actual wages received by the therapists employed in the study, in line with our micro-costing approach. The credentials of the providers are described under the Methods/Participants section and the Cost Assessment/Training and implementation activity costs/Estimating resource inputs and unit costs section.

We acknowledge that our cost estimates may not generalize to all healthcare contexts and have noted this as a limitation in the Discussion section. In response to the reviewer’s comment, we have added an additional sentence emphasizing that costs may be influenced by therapists’ credentials: “Still, costs of real-world CAMS delivery may be substantially lower in some settings owing to the availability of less expensive training formats (e.g., online video courses; www.CAMS-care.com) and delivery formats (e.g., group therapy) [64], as well as its suitability for use by diverse types of providers (e.g., paraprofessionals) [13]. Conversely, costs may be greater in settings where outpatient mental health services are typically delivered by doctoral-level therapists. Additional cost-inclusive evaluations of CAMS across these various implementation approaches are needed to inform wider dissemination of the framework.”

In the introduction, it would be interesting to provide more specific figures on the unprecedented rate of increase in suicides among the military workforce in the US over time since such figures appear to be available.

We have added the rate of increase to the manuscript, in addition to updating the suicide mortality rate to reflect estimates published since the initial submission of this manuscript: “Active duty service members have demonstrated continuously rising suicide rates across all branches of service. In 2019, the suicide mortality rate across all active duty services combined was 25.9 per 100,000, representing a per-year rate ratio of 1.04 from calendar years 2011 through 2019 [3].”

Also briefly mention what is TRICARE and CHAMPUS.

We have revised the manuscript to read, “Each visit was assigned an appropriate Current Procedural Terminology (CPT) [54] and costed using corresponding 2018 TRICARE/CHAMPUS Maximum Allowable Charges based on facility, non-physician provider, and appropriate locality rates. TRICARE (formerly known as CHAMPUS) is a DoD health insurance program, and its Maximum Allowable Charges rates reflect costs directly related to provision of the service (i.e., provider time used in the visit), practice expenses such as facilities and administrative staff, and malpractice insurance.”

Minor additional precisions needed:

“Active component”: clarify for readers what this refers to;

We have revised the first mention of this term in the manuscript to read, “In 2019, the suicide mortality rate for the Active Component (i.e., full-time service members) across all services was 25.9…”

“condition”: maybe replace everywhere by “treatment condition” as you do once, that way it is less confusing for non-native English speakers (as conditions can refer to diseases);

The manuscript has been revised to replace “condition” with “treatment condition” except in instances where the treatment condition is specified (i.e., CAMS condition or ETAU condition).

“modeling on multiply imputed datasets” (abstract): multiple?,

We believe “multiply” to be the appropriate term; specifically, the analytic procedure of ‘multiple imputation’ produces ‘multiply imputed’ data.

“member of the Warriors in Transition unit”: explain what it is very briefly?

We have added the following description to the manuscript, “Warrior Transition Unit (a unit providing support to soldiers being treated for chronic and/or severe injuries who cannot yet return to work)”

2/ I think the discussion or conclusion could stress more the policy implications of the research for the military health system (make it more explicit maybe).

We have added to the Conclusions section, “These findings may inform more robust cost-inclusive analyses in future trials and ultimately facilitate decision-making among the policymakers, healthcare administrators, and clinicians tasked with selecting mental health programs that will provide the biggest ‘bang for the buck’ amidst constrained resources.”

3/ I am surprised that none of the ETAU clinicians, when provided with potential supervision upon request, asked for it. Maybe discuss potential hypotheses about why this happened (while it seems to be less the case with CAMS while it is carried out by providers with more years of experience).

We have added the following hypothesis to the Methods/Cost Assessment/Training and implementation activity costs section: “Further, although ETAU therapists were offered additional supervision and consultation as needed, key informant interviews indicated that they elected not to participate in these activities during the course of the study. This may reflect stronger allegiance to a specific treatment approach for managing suicidality.”

4/ At some point you mention the time required for transit between the patient’s place of residence and the place of care and justify that you did not include it in your economic evaluation because you were not able to access confidential information regarding the place of residence of patients. I wonder if anyway this cost should be included in an evaluation adopting the military health services perspective? Would not those costs lie on the patients anyway or be more related to loss of productivity for the military?

The reviewer is correct that participant time/travel costs are not pertinent to an economic analysis from a healthcare payer perspective (such as the current study). We have removed this text from the manuscript to avoid confusion.

5/ I read your answer to a previous comment on the pre-doctoral graduate students included in the cost assessment. I am still not fully convinced they should be included in an evaluation which aims to accurately fit real-world settings. “We presume these cost rates are comparable to those of staff who might conduct administrative activities in real-world settings.”: This should be more justified to be convincing.

We appreciate the concern that inclusion of the pre-doctoral graduate student activities may not entirely reflect real-world settings. However, we felt the need to include these activities as part of our micro-costing procedures because the attention to fidelity may have had an impact on the overall effectiveness (and thus economic outcomes) associated with CAMS treatment. We also maintain that such fidelity monitoring activities may be performed as part of real-world CAMS implementation, for example as part of training new hires. In such instances, it is reasonable to assume that such activities may be performed by supervisory staff using the CAMS Rating Scale. Additionally, while the individual cost rates used in the study may not entirely represent real-world settings, we believe that the aggregate of Dr. Jobes’ estimated salary rate (most expensive) and graduate students’ estimated salary rate (less expensive) likely captures a cost rate comparable to a typical supervisor’s time.

6/ Some reorganization might be necessary: “In the current secondary analysis, treatment costs […] were determined using micro-costing” and subsequent paragraph of the introduction: this would be better suited in the method section;

We believe that including a brief methodological description in the Introduction allows for definition of key concepts which may be unfamiliar to readers unacquainted with economic assessment and provide context for the hypotheses presented.

“Multiple imputation using chained equations with predictive mean matching was used to minimize uncertainty…”: this would be better suited in the method section of the paper as well.

Our description of multiple imputation procedures has been moved to Materials and methods/Analyses section.

7/ For the ethical approvals that you mention in the first paragraph of the method section, it would better (more transparent and traceable) to also provide the identification number of the approval received.

We have added the ID number of the current archival study reviewed by the American University IRB.

8/ Measures section: “were validated against available administrative data sources (e.g., electronic health records”: it would be better to be exhaustive and more specific here;

We have replaced “e.g.,” in this instance with “i.e.,”.

and the comma after e.g. (or sometimes i.e. in the text) seems misplaced.

We respectfully maintain that the commas in “e.g.,” and “i.e.,” are consistent with the PLOS ONE style but are happy to revise upon the editorial board’s request.

Similarly, in the ‘Training and implementation activity costs’ paragraph: “Activities performed were identified by intervention manuals, administrative data systems, and qualitative interviews as feasible and appropriate”: it would be better to be more precise here.

We have revised this description to read, “Activities performed were identified by study protocols, intervention manuals, administrative data systems maintained by research personnel, and qualitative interviews with research personnel and study therapists as feasible and appropriate.”

9/ “There were no statistically significant differences between the CAMS and ETAU conditions with regard to sociodemographic or baseline clinical characteristics”: maybe specify that you are talking about patients’ characteristics.

We have revised this sentence to read, “There were no statistically significant differences between the CAMS and ETAU conditions with regard to patient participants’ sociodemographic or baseline clinical characteristics.”

10/ I must admit I am a bit concerned about the involvement of the founder of a company called CAMS-care in a research which strongly supports the overall value of CAMS.

Dr. Jobes, the pioneer of the CAMS intervention, has plainly and clearly disclosed his competing interests in accordance with PLOS ONE policy. We also refer the Reviewer to a recent meta-analysis finding little to no publication or allegiance bias in the broader evidence base supporting CAMS as a treatment for suicidal ideation (Swift JK, Trusty WT, Penix EA. The effectiveness of the Collaborative Assessment and Management of Suicidality (CAMS) compared to alternative treatment conditions: A meta-analysis. Suicide Life Threat Behav. 2021. Epub 2021/05/18).

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Reviewer #1: No

Reviewer #2: No

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Attachment

Submitted filename: Response to Reviewers.docx

Decision Letter 1

Isabelle Durand-Zaleski

30 Dec 2021

Costs, Benefits, and Cost-Benefit of Collaborative Assessment and Management of Suicidality versus Enhanced Treatment as Usual

PONE-D-21-12016R1

Dear Dr. McCutchan,

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Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

Isabelle Durand-Zaleski

25 Jan 2022

PONE-D-21-12016R1

Costs, Benefits, and Cost-Benefit of Collaborative Assessment and Management of Suicidality versus Enhanced Treatment as Usual

Dear Dr. McCutchan:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

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Kind regards,

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on behalf of

Dr. Isabelle Durand-Zaleski

Academic Editor

PLOS ONE

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    Attachment

    Submitted filename: Response to Reviewers.docx

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    Submitted filename: Response to Reviewers.docx

    Data Availability Statement

    Public sharing of data used in this study is prohibited under the protocol approved by the U.S. Army Medical Research and Development Command Office of Research Protections as well as Institutional Review Boards at Dwight D. Eisenhower Army Medical Center, The Catholic University of America, and the University of Washington. Additional restrictions apply to the availability of these data in order to protect participants’ privacy. Requests for access from interested researchers may nevertheless be considered, subject to the terms and conditions of the request and in compliance with the applicable regulations. Requests may be directed to the Office of Sponsored Programs and Research Services, The Catholic University of America, 213 McMahon Hall, 620 Michigan Ave., NE, Washington, DC 20064; Phone: 202-319-5218; Fax: 202-319-4495; Email: CUA-OSP@cua.edu.


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