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1 Department of Family Medicine, University of Colorado Health Sciences Center, Aurora, Colo
2 Center for Research Strategies, Denver, Colo
3 Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pa
4 RAND - University of Pittsburgh Health Institute, Pittsburgh, Pa
CORRESPONDING AUTHOR: L. Miriam Dickinson, PhD, Department of Family Medicine, UCHSC at Fitzsimons, PO Box 6508, Mail Stop F496, Aurora, CO 80045-0508, Miriam.Dickinson{at}UCHSC.edu
| ABSTRACT |
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METHODS We undertook a group-randomized controlled trial (RCT) of depression comparing intervention with usual care in 12 primary care practices. Intervention practices encouraged depressed patients to engage in active treatment, using nurses to provide regularly scheduled care management for 24 months. The study sample included 200 adults beginning a new depression treatment episode where patient presentation style could be identified. Outpatient costs were defined as intervention plus outpatient treatment costs for the 2 years. Cost-offset analysis used general linear mixed models, 2-part models, and bootstrapping to test hypotheses regarding a differential intervention effect by patients style, and to obtain 95% confidence intervals for costs.
RESULTS Intervention effects on outpatient costs over time differed by patient style (P <.05), resulting in a $980 cost decrease for depressed patients who complain of psychological symptoms and a $1,378 cost increase for depressed patients who complain of physical symptoms only.
CONCLUSIONS Depression intervention for a 2-year period produced observable clinical benefit with decreased outpatient costs for depressed patients who complain of psychological symptoms. It produced limited clinical benefit with increased costs, however, for depressed patients who complain exclusively of physical symptoms, suggesting the need for developing new intervention approaches for this group.
Key Words: Cost-benefit analysis depression somatoform disorders primary health care
| INTRODUCTION |
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| METHODS |
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5 major depression symptoms in the past 2 weeks,5 not currently receiving treatment with antidepressant medication, and having no specialty care in previous 6 months). Patients were excluded if they could not complete written screening questionnaires because of literacy problems; had no access to a telephone; did not intend to receive ongoing care in the clinic during the next year; had a life-threatening physical illness; were cognitively impaired; were pregnant, breastfeeding, or postpartum; or met study criteria for bereavement, mania, or alcohol dependence.
Intervention
Prior to patient enrollment, the research team provided brief training to participating physicians and nurse care managers in enhanced care practices. The goal was to encourage enhanced care practices to provide high-quality acute care6 supplemented by systematic monitoring for 2 years. During the acute stage, care managers notified physicians that patients were depressed, educated patients about treatment options, and evaluated patients response to treatment, alerting physicians when patients needed treatment adjustment. During systematic monitoring, care managers assessed each patients depression symptoms during brief telephone calls encouraging continued treatment adherence or adjustment, and summarized relevant information to physicians in monthly written reports. Care managers reached 93.7% of 111 patients in enhanced care practices during the 24 months, for an average of 11.8 contacts (SD = 5.9) per patient. Usual care practices were not given any training in depression management, nor were they systematically informed about which patients were participating in the study.
Data Collection
Of 11,006 eligible patients, 653 had positive screening results for depression on the 2-stage screening questionnaire. Of these patients, 73.4% participated in further evaluation, and 44.0% met criteria for beginning a new treatment episode for major depression (Figure 1
). Complete medical records with primary care physician documentation of symptoms at the index visit were available for 200 patients. After screening, data were collected from participating patients during structured telephone interviews by an interviewer blinded to intervention status, except for 3 patients whose practices were contacted to get updated location information. Concordant with an intent-to-treat design, patients who left the practice were interviewed again even though they could not participate in ongoing intervention. The 6-, 12-, 18-, and 24-month follow-up interviews conducted between October 1996 and September 1999 achieved response rates of 89.0%, 82.0%, 70.0%, and 68.0%, respectively. A total of 181 patients (90.0%) completed at least 1 follow-up interview and are included in longitudinal analyses.
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Data Analysis
We conducted analyses in SAS 8.2 (SAS Institute, Cary, NC), log-transforming cost data before analysis to normalize distributions.1315 General linear mixed models,1620 adjusted for clustering of patients within practice, were used to test whether there were differences between enhanced care and usual care patients on outpatient costs, and whether there was a differential intervention effect on costs by patient style.4 For component costs with sufficient sample size (primary care, medication, and emergency department visit costs), we used 2-part models7,2124 to estimate costs when more than 10% of patients had $0 costs. In 2-part models the probability of any cost is estimated using logistic regression, then costs are estimated for patients with costs of less than $0, and finally the 2 parts are combined to yield overall estimates. To enhance model stability, we totaled costs for each year and used repeated measures models. Patients who failed to complete a wave during the second half of year 1 or year 2 were considered to have $0 costs for that wave. Although dropout was minimal and similar across treatment groups and patient styles, we performed a sensitivity analysis using last-value-carried-forward methods to replace missing values. To obtain less biased confidence intervals, we calculated outpatient costs for each of 1,000 bootstrap samples15,25,26 in the same manner, producing a distribution of outpatient cost estimates.8,21 Sensitivity analysis was performed to assess whether reclassification of the 9 patients (5 in enhanced care and 4 in usual care) whose styles were difficult to classify affected our findings.
| RESULTS |
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At the index visit, 66.0% of patients complained of physical symptoms only, and 34.0% complained of psychological symptoms only or mixed psychological-physical symptoms. The percentage of patients complaining of physical symptoms was similar for enhanced and usual care patients (63% vs 70%, respectively, P = .28). As previously reported,1,3 enhanced care resulted in improvement in depression treatment (eg, use of antidepressant medication) compared with usual care for patients who complained of both psychological and physical symptoms. There was modest (and very similar) clinical improvement during the first 6 months in usual care and enhanced care patients complaining of physical symptoms and usual care patients complaining of psychological symptoms. Enhanced care patients complaining of psychological symptoms, however, experienced significantly greater improvement in depression severity than all other groups.3
Effect of Intervention and Patient Style on Costs
In the entire sample, the intervention increased outpatient costs for the 2 years (P <.01), but the 3-way interaction term indicates that there were differential intervention effects by patient style (intervention*presentation style*time, P = .04). As shown in Figure 2
, outpatient costs for enhanced care patients decreased with time, whereas outpatient costs for usual care patients who had psychological complaints increased considerably during year 2, and there was little change in outpatient costs for usual care patients who had physical complaints (Figure 2
). During the 2 years, ongoing enhanced care for patients who had a psychological complaint at the beginning of a new depression treatment episode reduced outpatient costs by $980 (Table 2
). In contrast, ongoing enhanced care for patients who complained exclusively of physical symptoms at the beginning of a new depression treatment episode increased outpatient costs by $1,378 for the 2 years. Results from sensitivity analysis with missing waves replaced by last value carried forward were similar ($782 reduction vs $1,027 increase). Sensitivity analysis with reclassification of patients difficult to classify yielded similar results (available from authors on request), as did unadjusted analyses. When examining cost offset (enhanced care outpatient plus intervention costs the same or lower than usual care), we observed a potential cost offset 929 of 1,000 times among patients with psychological complaints compared with 2 of 1,000 times among patients with physical complaints in bootstrap replications.
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| DISCUSSION |
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Using ongoing depression intervention to improve clinical outcomes with no increase to outpatient costs has recently been reported in efforts to improve primary care panic management.28 Acute intervention to improve primary care depression management improves clinical outcomes but increases outpatient costs by $256 to $1,008 for 1 year.2,22 We suspect that long-term care management is better able to achieve cost offset because of greater sustained improvement in physical functioning,1,7,29 reducing patient demand for health care in the second year.
For patients who complain of psychological symptoms, ongoing intervention reduced outpatient costs during year 2 in contrast to increasing costs for usual care. Increasing costs in usual care patients who complain of psychological symptoms suggest that health plans undertaking systematic depression screening without providing other components of ongoing intervention may inadvertently stimulate patients who recognize they are depressed to seek escalating amounts of outpatient care. Although further study is needed to confirm and expand our findings, these results have potentially important implications for comparing strategies for improving primary care depression management. Health plan administrators may wish to consider the possibility that (1) paying for screening alone may fail to improve outcomes30,31 while increasing health plan costs for patients who recognize they are depressed, (2) paying for screening plus acute intervention may improve outcomes while increasing health plan costs,7,8,13,23 and (3) paying for screening plus ongoing intervention may improve outcomes for a select group of depressed patients while reducing health plan costs.
For depressed patients who complain of physical problems at the beginning of a new treatment episode, ongoing intervention increased costs with no additional clinical benefits from the added health care expenditures associated with improved depression management. We suspect that patients who had physical problems exclusively after acknowledging an average of 6 depression symptoms might also be suffering from somatization or somatic fixation, which often occurs with depression in primary care patients.32 This explanation is congruent with research showing that, in patients with somatization, outpatient medical utilization increases after mental health treatment.33 It is possible that comorbid somatization diminishes clinical gains and cost savings of improved depression management because patients have greater concern about physical problems even though physical disease is similar.33
Current primary care depression interventions do not target physician or patient beliefs about frequently co-occurring somatic symptoms. Thus, when depressed patients complain of physical problems, physicians who do not recognize that the symptoms might represent somatized depression or a somatization disorder are put in the uncomfortable position of choosing to address the physical problems for which the patient is seeking help or the emotional problem identified by the screening questionnaire.34 Additionally, the patients belief that physical symptoms represent physical disease may reduce confidence in antidepressant medication treatment.3537 Alternative explanations include treatment induction failure, early termination of antidepressant medications, chronic physical pain that prolongs the depressive state,38 or early-stage physical disease that would affect the subsequent course of depressive symptoms, general medical condition, and costs. Finally, despite meeting the study criteria for major depression, these patients may not actually have depression, or they may have a variant not captured in the current classification system, ie, a mixed somatization-depressive disorder, that has different prognostic and treatment implications.
Further research is needed to develop and test intervention strategies for depressed patients who have physical complaints. Cognitive behavioral therapy appears to be a particularly promising treatment for patients with somatic symptoms, a treatment that was not available to most patients in our study.39,40
Internal validity of our results is strengthened by use of a group-randomized design in the original study. Intent-to-treat analysis evaluates the impact of the intervention even in enhanced care patients who did not participate. Because enhanced care physicians were trained to improve depression management for patients participating in the study, they may have elicited and recorded chief complaints that were different from those recorded by usual care physicians; however, we could find no evidence that the intervention affected physician recording of patient complaints at the index visit.3 Although we were forced to rely on patient-reported health care utilization, we expect that any error this method introduced would bias our findings counter to our hypothesis, because of the potential for enhanced care patients to report care manager telephone contacts as outpatient visits. Although the cost offset we observed for the 2 years in patients with psychological complaints was robust across a number of modeling assumptions, we were unable to determine conclusively what types of utilization were reduced, because there was an insufficient number of patients who were using a particular service during the multiple waves of the study.24,41
External validity is enhanced because we tested the intervention in a clinically and socioeconomically heterogeneous patient population under natural conditions in which physicians and patients were free to select the treatments they preferred. The study was designed to be generalizable to primary care practices with diverse organizational and financing structures, as the intervention was tested in 12 geographically diverse, mixed-model practices caring for patients insured through numerous health plans. Although we were not able to follow up every patient for 2 years, we attempted to reduce the impact of sample loss by using modeling techniques based on all available data. Our findings cannot be generalized to primary care patients who are depressed despite recent treatment, because we could not reliably determine patient style at the index visit. We do not anticipate that the intervention will achieve a cost offset in this group because of the increased occurrence in this cohort of treatment-resistant depression, which requires more extensive intervention to achieve clinical benefit.42
This study contributes to observational studies supporting the potential for cost offset4346 for mental health treatment by providing evidence from a randomized trial that outpatient costs for ongoing management of primary care depression for 2 years in targeted depressed populations offset the added health care expenditures associated with improved depression management. This finding suggests that interventions for targeted depressed patients could be implemented within the primary care practice without increasing overall health care costs and would allow health plans to adopt these interventions for targeted depressed populations without increasing health care premiums. The results suggest the need to examine whether other interventions can achieve cost offset in populations that can be identified at baseline as likely to benefit clinically. Finally, the study provides evidence that health services researchers, clinicians, and mental health professionals need to focus on an intensive effort to develop interventions to improve clinical and cost outcomes in patients whose depression may be complicated by somatization.
| ACKNOWLEDGMENTS |
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| FOOTNOTES |
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Funding support: This research was supported by National Institute of Mental Health grant R01 MH54444, Health Resources and Services Administration National Research Service Award 5T32 HP10006-10 and by a grant from the John D. and Catherine T. MacArthur Foundation. Dr. Rost is also supported by NIMH K02 Independent Scientist Award MH63651.
Received for publication December 22, 2003. Revision received May 7, 2004. Accepted for publication May 24, 2004.
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