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Published Online: 28 August 2015

Isn’t It About Time to Employ Measurement-Based Care in Practice?

Measurement-based care is by no means novel. In fact, for decades the regular measurement of both symptoms and side effects has been an integral component of all randomized controlled trials that establish the efficacy of antidepressant medications. Research clinicians, blind to treatment type, use both symptom and side effect measures to adjust and tailor the dosage to each patient, attempting to maximize the dosage and therapeutic effects, side effects permitting.
In the early 1990s, the Agency for Healthcare Policy and Research commissioned the development of clinical practice guidelines for the diagnosis and treatment of depression in primary care. These guidelines recommended the regular measurement of symptoms and side effects to manage depression because the evidence that supported the efficacy of both medications and psychotherapy was based on controlled trials that used these processes. These procedures, the authors reasoned, would serve to tailor the dosage to each patient, avoiding underdosing and severe side effects while maximizing individual benefit (1).
Both the Texas Medication Algorithm Project (TMAP) (psychiatric outpatients) (2, 3) and the German Algorithm Project (GAP) (psychiatric inpatients) (4, 5) required clinicians to regularly assess symptoms and side effects and to consider dosage and medication changes at specified times during treatment based on these measurements. Both studies, however, combined these measurement-based care procedures with medication algorithms that included a varying range of medication options. These two-part interventions (measurement-based care procedures and the algorithms) were more effective than treatment as usual in both studies (6, 7). Whether the benefit was due to the measurement-based care procedures per se, to medication differences, or to both was unknown.
The cleverly designed, blind-rater, 24-week, randomized, controlled, single-site trial that Dr. Guo and colleagues report in this issue (8) was able to isolate the effect of measurement-based care processes alone by requiring clinicians in both the measurement-based care and standard treatment groups to use the same two medications within the same dosage ranges. This design allowed between-group differences to be attributed to the use (or not) of measurement-based care.
The results reveal a wide range of clinically meaningful benefits that seem largely attributable to more aggressive—albeit patient-tailored—dosing without increasing side effects, number of clinic visits, or attrition compared with usual care procedures.
Patients in the measurement-based care group responded or remitted about twice as fast as those in the standard treatment group. Furthermore, the response and remission rate differences between the groups were substantial, equaling or exceeding differences between medication and placebo, based on the numbers needed to treat. Thus, how a medication is delivered may be as important as which medication is chosen.
Importantly, measurement-based care did not increase the number of visits, but medication adjustments were twice as frequent in the measurement-based care visits compared with standard treatment visits. Tailored but higher medication dosages in measurement-based care likely led to a greater proportion of responders actually achieving remission in the measurement-based care group. Suboptimal dosing seems a major cause of response that falls short of remission, which in turn is associated with a greater risk of relapse (9).
The study’s research staff provided immediate feedback to measurement-based care clinicians on their adherence to the recommended dosing schedule. Such staffing is not sustainable in real-world practice. However, computerized reminder systems have been developed and can become part of the electronic medical record as a sustainable alternative (10, 11). Such prompts are likely very helpful and contribute to the greater dosing observed in measurement-based care.
What are the implications of this study for patients, practitioners, and payers? By providing patients with the tools and experience of monitoring their symptoms and side effects, measurement-based care seemingly better prepares them to participate in shared decision making and their own longer-term care.
Despite the absence of controlled-trial evidence, one might speculate that regular measurements provide a level of precision that facilitates cross-coverage between physicians, the acquisition of reliable second opinions, and enhanced efficiency of telemedicine visits by using patient-based metrics to assess outcome even at a distance.
Results with measurement-based care (with its individualized dosage adjustments) reveal that higher dosages were associated with higher remission rates compared with usual care. The Sequenced Treatment Alternatives to Relieve Depression study also found that higher dosages were typical when a measurement-based care approach was used (12). Despite fixed-dosage studies that have often not found between-dosage differences, within the therapeutic dosage range, modestly greater dosages seem to produce far better outcomes. Measurement-based care processes seem to help make these adjustments.
Most clinical practice guidelines for depression (1316) recommend the regular assessment of symptoms. However, they do not typically recommend specific tools, visit frequencies, dosage adjustment schedules, the routine measurement of side effects, or when to change treatments—all of which tailor treatment to individual patients. The randomized blinded trial design in the Guo et al. study makes a reasonably strong case for augmenting the clinical guidance with more specific recommendations.
While no economic analyses were conducted in this study, the results suggest that measurement-based care seems likely to be close to cost-neutral yet has substantial clinical benefit by increasing remission rates. Measurement-based care combined with treatment algorithms in inpatients seems to provide cost savings (17).
If measurement-based care procedures offer at least some of these benefits, why are they not more widely used in practice? The Guo et al. study addresses the objection that the controlled-trial evidence is too scant. However, some may believe that global clinical judgment is sufficiently precise, so we don’t need itemized measures. The present study results (more frequent dosage adjustments in measurement-based care visits), some clinical experience, and logic would argue against this objection. A more precise metric to monitor symptoms should make the ascertainment of remission as well as the detection of worsening more reliable and time efficient. In addition, measurement-based care provides patients with the ability to monitor themselves, without having to rely entirely on the clinician’s judgment.
Some object that measurement-based care requires clinician-completed measures that are time consuming. In nonpsychotic patients, a variety of self-reports perform as adequately as so-called clinician ratings (18, 19), most of which are interviewer-elicited self-reports anyway. These self-reports are likely to save time, once patients gain experience and understanding with them.
Finally, some argue that clinical variation across patients is just too great to allow for a single protocol to recommend the times and clinical states at which dosage changes should be considered. However, these recommendations are typically written with some flexibility as to the timing of and indicators for the dosage changes. This flexibility allows, for example, a more gradual approach in the more medically fragile patients. Furthermore, these are recommendations, not requirements. They are prompts that focus the clinician’s attention on opportune times at which changes might be considered. Clinician judgment still prevails.
Measurement-based care seems to benefit patient care without adding staff or extra visits (assuming computer prompts can be implemented). Whether this innovation is cost saving for care systems that serve mood and other major psychiatric conditions deserves study.

Acknowledgments

The author gratefully acknowledges the editorial support of Jon Kilner, M.S., M.A.

References

1.
Depression Guideline Panel: Depression in Primary Care, vol 2, Treatment of Major Depression (Clinical Practice Guideline Number 5, AHCPR Publication 93-0551). Rockville, Md, Agency for Healthcare Policy and Research, April 1993
2.
Rush AJ, Rago WV, Crismon ML, et al: Medication treatment for the severely and persistently mentally ill: the Texas Medication Algorithm Project. J Clin Psychiatry 1999; 60:284–291
3.
Rush AJ, Crismon ML, Kashner TM, et al: Texas Medication Algorithm Project, phase 3 (TMAP-3): rationale and study design. J Clin Psychiatry 2003; 64:357–369
4.
Adli M, Wiethoff K, Baghai TC, et al: Evaluating algorithm-guided treatment for depression: the German Algorithm Project (GAP). Pharmacopsychiatry 2005; 38:A002
5.
Wiethoff K, Bauer M, Baghai TC, et al: Prevalence and treatment outcome in anxious versus nonanxious depression: results from the German Algorithm Project. J Clin Psychiatry 2010; 71:1047–1054
6.
Trivedi MH, Rush AJ, Crismon ML, et al: Clinical results for patients with major depressive disorder in the Texas Medication Algorithm Project. Arch Gen Psychiatry 2004; 61:669–680
7.
Adli M, Bauer M, Rush AJ: Algorithms and collaborative-care systems for depression: are they effective and why? A systematic review. Biol Psychiatry 2006; 59:1029–1038
8.
Guo T, Xiang YT, Xiao L, et al: Measurement-based care versus standard care for major depression: a randomized controlled trial with blind raters. Am J Psychiatry 2015; 172:1004–1013
9.
McIntyre RS, O’Donovan C: The human cost of not achieving full remission in depression. Can J Psychiatry 2004; 49(suppl 1):10S–16S
10.
Trivedi MH, Kern JK, Grannemann BD, et al: A computerized clinical decision support system as a means of implementing depression guidelines. Psychiatr Serv 2004; 55:879–885
11.
Kurian BT, Trivedi MH, Grannemann BD, et al: A computerized decision support system for depression in primary care. Prim Care Companion J Clin Psychiatry 2009; 11:140–146
12.
Trivedi MH, Rush AJ, Wisniewski SR, et al: Evaluation of outcomes with citalopram for depression using measurement-based care in STAR*D: implications for clinical practice. Am J Psychiatry 2006; 163:28–40
13.
American Psychiatric Association: Practice Guideline for the Treatment of Patients With Major Depressive Disorder, 3rd ed. Am J Psychiatry 2010;167(Oct suppl)
14.
National Institute for Health and Clinical Excellence (NICE): Depression in Adults: The Treatment and Management of Depression in Adults (NICE Clinical Guideline 90). London, NICE, Oct 2009. www.guidance.NICE.org.uk/cg90
15.
Cleare A, Pariante CM, Young AH, et al: Evidence-based guidelines for treating depressive disorders with antidepressants: a revision of the 2008 British Association for Psychopharmacology guidelines. J Psychopharmacol 2015; 29:459–525
16.
Bauer M, Pfennig A, Severus E, et al: World Federation of Societies of Biological Psychiatry (WFSBP) guidelines for biological treatment of unipolar depressive disorders, part 1: update 2013 on the acute and continuation treatment of unipolar depressive disorders. World J Biol Psychiatry 2013; 14:334–385
17.
Ricken R, Wiethoff K, Reinhold T, et al: Algorithm-guided treatment of depression reduces treatment costs: results from the randomized controlled German Algorithm Project (GAPII). J Affect Disord 2011; 134:249–256
18.
Carmody TJ, Rush AJ, Bernstein IH, et al: Making clinicians’ lives easier: guidance on use of the QIDS self-report in place of the MADRS. J Affect Disord 2006; 95:115–118
19.
Rush AJ, Trivedi MH, Carmody TJ, et al: Self-reported depressive symptom measures: sensitivity to detecting change in a randomized, controlled trial of chronically depressed, nonpsychotic outpatients. Neuropsychopharmacology 2005; 30:405–416

Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 934 - 936
PubMed: 26315984

History

Accepted: July 2015
Published online: 28 August 2015
Published in print: October 01, 2015

Authors

Details

A. John Rush, M.D.
From the Duke–National University of Singapore Graduate Medical School, Singapore.

Notes

Address correspondence to Dr. Rush ([email protected]).

Funding Information

Dr. Rush has received consulting fees from Brain Resource, Eli Lilly, Emmes Corporation, Lundbeck A/S, MedAvante, NIDA, Santium, Stanford University, Takeda; speaking fees from the University of California at San Diego, Hershey Penn State Medical Center, New York State Psychiatric Institute, and the American Society for Clinical Psychopharmacology; royalties from Guilford Publications and the University of Texas Southwestern Medical Center; a travel grant from CINP; and research support from Duke–National University of Singapore. Through the University of Texas Southwestern Medical Center, he has a potential financial interest in the Inventory of Depressive Symptomatology and several variations of it. Dr. Freedman has reviewed this editorial and found no evidence of influence from these relationships.

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