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USPSTF: Screen all adults for depression

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Use a flexible approach in depression diagnosis and treatment

The new USPSTF recommendations carry a B grade, reflecting both the heterogeneous nature of the diagnosis of depression and the many areas of uncertainty in screening and treatment of the disorder. Major depressive disorder (MDD) is a varied condition that may respond to a variety of treatments, including medication and various forms of therapy. The clinical spectrum of MDD may range from a mild, self-limited course to disabling depression that interferes with daily function and that may persist for long periods of time.

Even the nine-item depression scale of the Patient Health Questionnaire (PHQ-9), considered the first choice of many in primary care, only has a positive predictive value of about 50%, and will miss about one in five cases of true depression. This means that screening must be followed by clinically appropriate evaluation to assure accurate diagnosis of MDD.

Dr. Michael E. Thase

No biomarker has been identified that will predict which treatment will work for which patient with depression, and first-line antidepressants will only help about 50% of an intent-to-treat population.

Against that backdrop, clinicians should take patient preference into account, especially for patients with more severe depression, for whom preference may matter more. Individuals with more severe illness may require multiple adjustments to their pharmacologic and therapeutic regimen, so care systems should be built to anticipate this need.

Early warning systems that use technology to assess patient adherence and response may help effective tailoring of a therapeutic approach: Patients could complete online symptom diaries to assess early response to therapies, and a missed prescription refill – or failure to fill an initial prescription – could trigger prompt intervention by the care team.

Dr. Michael E. Thase is professor of psychiatry and chief of the mood and anxiety disorders treatment and research program at the University of Pennsylvania, Philadelphia. The comments above were summarized from Dr. Thase’s editorial accompanying the USPSTF depression screening recommendation (JAMA. 2016 Jan 26;315[4]:349-50).


 

FROM JAMA

References

All adults, including pregnant and postpartum women, should be screened for depression, according to new recommendations of the U.S. Preventive Services Task Force.

The recommendation also calls for screening to be coupled with “adequate systems” to ensure diagnosis, treatment, and follow-up (JAMA. 2016 Jan 26;315[4]:380-7).

Dr. Albert L. Siu

Dr. Albert L. Siu

The depression screening recommendation, authored by Dr. Albert L. Siu and the other members of the USPSTF, is a level B recommendation, meaning that it has either high certainty of moderate net benefit, or moderate certainty of moderate to substantial net benefit.

The new guidance in screening for depression helps address a disorder that is “the leading cause of disability among adults in high-income countries,” said Dr. Siu and his coauthors. Lost productivity attributable to depression cost $23 billion in the United States in 2011, and $22.8 billion was spent on treatments for depression in 2009, the last year for which figures are available.

Dr. Siu, chair of geriatrics and palliative medicine at Icahn School of Medicine at Mount Sinai, New York, and his coauthors cited “convincing evidence that screening improves the accurate identification of adult patients with depression in primary care settings, including pregnant and postpartum women.”

In addition, the task force found convincing evidence that for older adults as well as the general adult population, treatment of “depression identified through screening in primary care settings with antidepressants, psychotherapy, or both decreases clinical morbidity.”

For pregnant and postpartum women with depression, Dr. Siu and his coauthors found “adequate” evidence that cognitive behavioral therapy (CBT) improves outcomes.

The recommendation does not identify optimal timing and intervals for depression screening, citing a need for more research in this area. However, “a pragmatic approach might include screening all adults who have not been screened previously and using clinical judgment in consideration of risk factors, comorbid conditions, and life events to determine if additional screening of high-risk patients is warranted,” explained Dr. Siu and his coauthors.

The new depression screening recommendation from USPSTF updates the 2009 recommendation, which recommended universal screening if “staff-assisted depression care supports” were in place, and targeted screening based on clinical judgment and patient preference if such support were unavailable.

The rationale for the current recommendation of universal screening for those 18 years and older is the “recognition that such support is now much more widely available and accepted as part of mental health care,” the task force members said.

Any potential harms of screening, said Dr. Siu and his coauthors, were minimal to nonexistent.

Overall, the USPSTF assigned a small to moderate risk to the use of medication in depression. However, the use of “second-generation” antidepressants – mostly SSRIs – was associated with some harms, including increased risk of suicidal behavior in young adults and of gastrointestinal bleeding in older adults, as well as potential fetal harms in pregnant women taking antidepressants.

Using CBT to treat depression in pregnant and postpartum women was also associated with minimal to no harm.

The USPSTF screening recommendation is aligned with the American Academy of Family Physicians’ recommendation to screen the general adult population for depression, and with the American Academy of Pediatrics’ recommendation that pediatricians screen mothers for depression at their babies’ 1-, 2-, and 4-month office visits.

Released in draft form in July 2015, the depression screening recommendation was available for public comment for a period of 4 weeks. In response to public input, the final recommendation’s implementation section clarifies and characterizes an “adequate system” of screening, and gives more resources for evidence-based depression screening and treatment.

The Agency for Healthcare Research and Quality supports the operations of the USPSTF, but the task force’s recommendations are independent of the federal government. Dr. Siu and the other task force members reported no conflicts of interest.

koakes@frontlinemedcom.com

On Twitter @karioakes

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