You are leaving Medscape Education
Cancel Continue
Log in to save activities Your saved activities will show here so that you can easily access them whenever you're ready. Log in here CME & Education Log in to keep track of your credits.
 

CME / ABIM MOC / CE

Sleep Disorders and Depression: Could Electroacupuncture Be the Answer?

  • Authors: News Author: Batya Swift Yasgur, MA, LSW; CME Author: Laurie Barclay, MD
  • CME / ABIM MOC / CE Released: 9/2/2022
  • Valid for credit through: 9/2/2023
Start Activity

  • Credits Available

    Physicians - maximum of 0.25 AMA PRA Category 1 Credit(s)™

    ABIM Diplomates - maximum of 0.25 ABIM MOC points

    Nurses - 0.25 ANCC Contact Hour(s) (0 contact hours are in the area of pharmacology)

    Physician Assistant - 0.25 AAPA hour(s) of Category I credit

    IPCE - 0.25 Interprofessional Continuing Education (IPCE) credit

    You Are Eligible For

    • Letter of Completion
    • ABIM MOC points

Target Audience and Goal Statement

This activity is intended for psychiatrists, family medicine and primary care clinicians, internists, physician assistants, nurses, nurse practitioners, neurologists, sleep medicine clinicians, geriatricians, and other members of the health care team who treat and manage patients with sleep disorders and depression.

The goal of this activity is for learners to be better able to describe the efficacy and safety of electroacupuncture plus standard care.

Upon completion of this activity, participants will:

  • Assess the efficacy and safety of electroacupuncture plus standard care compared with sham acupuncture treatment and standard care, or standard care only as control, as an alternative therapy in improving sleep quality and mental state for patients with insomnia and depression, based on a randomized, sham-controlled clinical trial
  • Evaluate the clinical implications of the efficacy and safety of electroacupuncture plus standard care compared with sham acupuncture treatment and standard care, or standard care only as control, as an alternative therapy in improving sleep quality and mental state for patients with insomnia and depression, based on a randomized, sham-controlled clinical trial
  • Outline implications for the healthcare team


Disclosures

Medscape, LLC requires every individual in a position to control educational content to disclose all financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.

All relevant financial relationships for anyone with the ability to control the content of this educational activity are listed below and have been mitigated. Others involved in the planning of this activity have no relevant financial relationships.


News Author

  • Batya Swift Yasgur, MA, LSW

    Freelance writer, Medscape

    Disclosures

    Batya Swift Yasgur, MA, LSW, has no relevant financial relationships.

CME Author

  • Laurie Barclay, MD

    Freelance writer and reviewer
    Medscape, LLC

    Disclosures

    Laurie Barclay, MD, has the following relevant financial relationships:
    Formerly owned stocks in: AbbVie

Editor/Nurse Planner

  • Stephanie Corder, ND, RN, CHCP

    Associate Director, Accreditation and Compliance, Medscape, LLC

    Disclosures

    Stephanie Corder, ND, RN, CHCP, has no relevant financial relationships.

Compliance Reviewer

  • Yaisanet Oyola, MD

    Associate Director, Accreditation and Compliance, Medscape, LLC

    Disclosures

    Yaisanet Oyola, MD, has no relevant financial relationships.

Peer Reviewer

This activity has been peer reviewed and the reviewer has no relevant financial relationships.


Accreditation Statements



In support of improving patient care, Medscape, LLC is jointly accredited with commendation by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.

This activity was planned by and for the healthcare team, and learners will receive 0.25 Interprofessional Continuing Education (IPCE) credit for learning and change.

    For Physicians

  • Medscape, LLC designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credit(s)™ . Physicians should claim only the credit commensurate with the extent of their participation in the activity.

    Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 0.25 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit.

    Contact This Provider

    For Nurses

  • Awarded 0.25 contact hour(s) of nursing continuing professional development for RNs and APNs; 0.00 contact hours are in the area of pharmacology.

    Contact This Provider

  • For Physician Assistants

    Medscape, LLC has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit for activities planned in accordance with AAPA CME Criteria. This activity is designated for 0.25 AAPA Category 1 CME credits. Approval is valid until 9/2/2023 PAs should only claim credit commensurate with the extent of their participation.

For questions regarding the content of this activity, contact the accredited provider for this CME/CE activity noted above. For technical assistance, contact [email protected]


Instructions for Participation and Credit

There are no fees for participating in or receiving credit for this online educational activity. For information on applicability and acceptance of continuing education credit for this activity, please consult your professional licensing board.

This activity is designed to be completed within the time designated on the title page; physicians should claim only those credits that reflect the time actually spent in the activity. To successfully earn credit, participants must complete the activity online during the valid credit period that is noted on the title page. To receive AMA PRA Category 1 Credit™, you must receive a minimum score of 75% on the post-test.

Follow these steps to earn CME/CE credit*:

  1. Read the target audience, learning objectives, and author disclosures.
  2. Study the educational content online or printed out.
  3. Online, choose the best answer to each test question. To receive a certificate, you must receive a passing score as designated at the top of the test. We encourage you to complete the Activity Evaluation to provide feedback for future programming.

You may now view or print the certificate from your CME/CE Tracker. You may print the certificate but you cannot alter it. Credits will be tallied in your CME/CE Tracker and archived for 6 years; at any point within this time period you can print out the tally as well as the certificates from the CME/CE Tracker.

*The credit that you receive is based on your user profile.

CME / ABIM MOC / CE

Sleep Disorders and Depression: Could Electroacupuncture Be the Answer?

Authors: News Author: Batya Swift Yasgur, MA, LSW; CME Author: Laurie Barclay, MDFaculty and Disclosures

CME / ABIM MOC / CE Released: 9/2/2022

Valid for credit through: 9/2/2023

processing....

Clinical Context

Depressive disorders affect more than 264 million people worldwide and more than 50 million in China. Sleep disturbance is a leading symptom in depression.

Depression and sleep issues have a bidirectional relationship. Poor sleep quality contributes to development of depression, which increases risk for insomnia. Patients with both conditions have increased risk for suicide, severe social functioning impairment, and relapse.

Study Synopsis and Perspective

Electroacupuncture (EA) may significantly improve sleep quality in patients with depression who also have insomnia, new research suggests.

In a study of almost 300 adults with depression and comorbid insomnia, change from baseline to week 8 on the Pittsburgh Sleep Quality Index (PSQI) was 3 points greater in the group receiving EA vs a group receiving sham acupuncture (SA) plus standard care, and 5 points greater vs a control group receiving standard care only. The improvements were sustained during a 24-week postintervention follow-up.

The EA group also showed significant improvement in depression, insomnia, self-rated anxiety, and total sleep time, all of which were not found in the SA or control groups.

"Based on the results of our trial, we recommend patients with depression and insomnia seek the treatment of EA as an alternative and complementary therapy for better results," study investigator Shifen Xu, PhD, from Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, China, told Medscape Medical News.

The findings were published online July 7 in JAMA Network Open.[1]

Bidirectional Relationship

"Sleep disturbance is the prominent symptom in patients with depression," the investigators note. Depression and sleep issues have a bidirectional relationship, in that "poor sleep quality contributes to the development of depression, and having depression makes a person more likely to develop sleep issues," they write.

Patients with co-occurring depression and sleep disorders are more difficult to treat and have a greater risk for relapse and recurrence of depression, they add.

Acupuncture may be an "effective drug-free approach for helping to treat mental illness and sleep disorders," the researchers note. A previous study suggested that acupuncture may improve sleep efficacy and prolong total sleep in patients with primary insomnia.

"EA is the combination of traditional Chinese acupuncture with electric-impulse stimulation, and it can enhance the therapeutic effect of the acupoints throughout the needle retention time," Dr Xu said.

A previous pilot study of EA for depression-related insomnia showed significant improvements in sleep quality after EA treatment, but the sample size was small.

The current researchers, therefore, undertook the present study, which had a larger sample size and comparison with SA and standard care. They divided 270 adults (mean age, 50.3 years; 71.9% women) at 3 tertiary hospitals in Shanghai into 3 groups, each consisting of 90 participants.

The EA plus standard care group and the SA plus standard care group received 30-minute treatments 3 times per week for 8 weeks. The control group received standard care only.

All participants had Diagnostic and Statistical Manual of Mental Disorders (Fifth Edition) (DSM-5)-diagnosed depression; baseline PSQI scores greater than 7, with higher scores indicating worse sleep quality and a greater number or sleep disorders; and Hamilton Depression Rating Scales (HDRS-17) scores of 20 to 35, with higher scores indicating higher depression levels.

Patients with secondary depressive disorders attributable to other conditions, medication, or psychotic disorders were excluded, as were patients with a history of alcohol abuse or drug dependence or those who had received acupuncture within the previous year.

Of the patients who completed the 8-week intervention, 83 were in the EA group, 81 in the SA group, and 83 in the control group. Almost all participants (91.5%) completed all outcome measurements by the end of the 24-week follow-up period (also known as week 32).

Calm Mind, Balanced Mood

At the 8-week posttreatment assessment, which was the primary endpoint, the EA group had a mean reduction from baseline of 6.2 points (95% confidence interval [CI], −6.9 to −5.6) in PSQI score.

There was a significant difference in PSQI score between the EA group and the SA group (−3.6 points; 95% CI, −4.4 to −2.8; P<.001) and vs the control group (−5.1 points; −6.0 to −4.2; P<.001).

The efficacy of EA in treating insomnia was sustained during the postintervention follow-up period, when the EA group had a significantly greater reduction in PSQI score compared with the SA group (−4.7; 95% CI, −5.4 to −3.9; P<.001) and the control group (−5.0; 95% CI, −5.8 to −4.1; P<.001).

Patients receiving EA also experienced significant (all Ps<.001) improvement from baseline on secondary outcomes, including:

  • Scores on the HDRS (−10.7; 95% CI, −11.8 to −9.7),
  • Scores on the Insomnia Severity Index (−7.6; 95% CI, −8.5 to −6.7),
  • Scores on the Self-rated Anxiety Scale (−2.9; 95% CI, −4.1 to −1.7), and
  • Total sleep time, as recorded by sleep actigraphy (29.1 minutes; 95% CI, 21.5-36.7).

In addition, the EA group showed significant improvement in depression scores compared with the SA and control groups at both 8 and 32 weeks (all Ps<.001).

Outcome

EA vs SA (95% CI)

EA vs control (95% CI)

HDRS

8 weeks: −5.5 (−6.8 to −4.3)

32 weeks: −5.8 (−6.8 to −4.7)

8 weeks: −8.8 (−10.1 to −7.4)

32 weeks: −5.8 (−7.1 to −4.5)

Participants in the EA group also had a 4.2% (95% CI, 2.6%-5.8%) higher sleep efficiency score at week 8 compared with those in the SA group (P<.001).

In addition, they had lower scores on the Insomnia Severity Index and the Self-rated Anxiety Scale and longer total sleep time compared with the control group at week 8. None of the participants reported any serious adverse events.

"Our findings constitute subjective and objective evidence of the efficacy and safety of EA with standard care in treating comorbid depression and insomnia compared with SA with standard care or standard care alone," the investigators write.

"The acupoints we used in this trial mainly act on calming mind, relieving negative mood, and balancing the yin-yang," Dr Xu added.

Viable Adjunctive Treatment

Commenting for Medscape Medical News, Albert Yeung, MD, ScD, associated director of the Mass General Depression and Clinical Research Program and associate professor of psychiatry, Harvard Medical School, Boston, Massachusetts, said that with the evidence from this study, "acupuncture and/or electroacupuncture could be a viable adjunctive treatment for depressed patients who suffer from insomnia."

Dr Yeung, who was not involved with the study, is the co-author of an accompanying editorial.[2]

"More well-designed studies are warranted to provide evidence for integrating holistic treatment in medicine," he said.

The study was funded by grants from the National Natural Science Foundation of China, and Shanghai Municipal Health. The investigators have reported no relevant financial relationships. Although Dr Yeung also reports no relevant financial relationships, his coauthor's disclosures are listed in the original editorial.

JAMA Netw Open. Published online June 7, 2022.

Study Highlights

  • This 32-week (8-week intervention; 24-week follow-up), patient- and assessor-blinded, sham-controlled randomized, sham-controlled clinical trial took place from September 1, 2016, to July 30, 2019, at 3 tertiary hospitals in Shanghai, China.
  • Patients (n=270; 71.9% women; mean age, 50.3±14.2; range, 18-70 years) had insomnia and met DSM-5 criteria for depression.
  • Patients were randomly assigned to EA plus psychiatrist-guided standard care, SA plus standard care, or standard care only (control); 91.5% completed the 32-week trial.
  • EA and SA consisted of 24 sessions (3 sessions/week for 8 weeks).
  • Mean difference in PSQI from baseline to week 8 (primary outcome) was −6.2 (95% CI, −6.9 to −5.6) in the EA group (difference, −3.6; 95% CI, −4.4 to −2.8; P<.001) vs SA and −5.1 (95% CI, −6.0 to −4.2; P<.001) vs controls.
  • During the 8-week intervention, the EA group had significant (P<.001) improvements in HDRS-17 (−10.7; 95% CI, −11.8 to −9.7), Insomnia Severity Index (−7.6; 95% CI, −8.5 to −6.7), and Self-rating Anxiety Scale (−2.9; 95% CI, −4.1 to −1.7) scores and total actigraphy sleep time (29.1 minutes; 95% CI, 21.5-36.7 minutes).
  • The groups did not differ in frequency of sleep awakenings.
  • Acupuncture-related adverse events occurred in 7.8% of the EA group (mostly hematoma and local pain) and 4.4% of the SA group.
  • There were no serious adverse events.
  • EA efficacy for insomnia was sustained during follow-up, with significantly greater reduction in PSQI in the EA vs SA group (−4.7; 95% CI, −5.4 to −3.9; P<.001) and controls (−5.0; 95% CI, −5.8 to −4.1; P<.001).
  • The EA group had significant improvement in depression scores vs SA and control groups at both 8 and 32 weeks (all P<.001) and 4.2% (95% CI, 2.6%-5.8%) higher sleep efficiency score at week 8 than those in the SA group (P<.001).
  • The investigators concluded that quality of sleep in patients with insomnia and depression improved significantly with EA vs SA or control at week 8 and was clinically meaningful and sustained at week 32, suggesting subjective and objective evidence that 8 weeks of EA is effective and safe for treating insomnia in patients with depression.
  • Patients in the EA group also had a greater reduction of severity of insomnia, sleep awakenings, depressive mood, and anxiety symptoms at the end of the intervention, and significant improvements in sleep efficiency and total sleep time.
  • Future research should examine longer treatment and precise objective outcomes.
  • Depression and sleep issues have a bidirectional relationship.
  • Patients with both conditions have a higher risk for suicide and severe impairment in social functioning and are difficult to treat, with greater risk for relapse and recurrence of depression.
  • Cognitive behavioral therapy is effective for chronic insomnia, but cultural differences and limited medical resources hinder widespread use in China.
  • Some antidepressants with activating effects may worsen sleep in the short-term; sedating antidepressants rapidly improve sleep but may cause oversedation and worse long-term outcomes.
  • Study limitations include lack of acupuncturist blinding and only 1- to 2-night actigraphy assessment, which might inaccurately reflect long-term sleep state.
  • An accompanying commentary noted that EA could be a viable adjunctive treatment for depressed patients with insomnia. More well-designed studies are needed to provide evidence for integrating holistic treatment into medicine.

Clinical Implications

  • Sleep quality in patients with insomnia and depression improved significantly with EA vs SA or control at week 8 and week 32.
  • EA may be a viable adjunctive treatment for depressed patients with insomnia, but more well-designed studies are needed.
  • Implications for the Health Care Team: For the complex management of sleep disorders, members of the healthcare team should employ a patient-centered approach and present both pharmacologic and adjunctive non-pharmacologic options for care.

 

Earn Credit

  • Print