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Database of Abstracts of Reviews of Effects (DARE): Quality-assessed Reviews [Internet]. York (UK): Centre for Reviews and Dissemination (UK); 1995-.

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Database of Abstracts of Reviews of Effects (DARE): Quality-assessed Reviews [Internet].

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Treating depression during pregnancy and the postpartum: a preliminary meta-analysis

and .

Review published: .

CRD summary

The authors concluded that the largest effects in women with non-psychotic depression during pregnancy, or postpartum, were seen with medication, alone or with cognitive-behavioural therapy (CBT); group therapy with CBT, educational and transactional analysis components; interpersonal psychotherapy; and CBT. Several limitations mean that these results should be interpreted with caution.

Authors' objectives

To determine the efficacy of current treatment interventions for non-psychotic major depression in pregnancy and the postpartum period. A secondary aim was to the compare the efficacy of the different interventions, while a tertiary aim was to determine the effect of timing during pregnancy or postpartum on the efficacy of these interventions.

Searching

The Cochrane CENTRAL Register, MEDLINE, PsycLIT and Social Work Abstracts were searched for studies published within the previous 15 years (no dates provided); the search terms were reported. The references of all selected papers were also checked, while letters were sent to experts in an attempt to locate any additional relevant studies.

Study selection

Study designs of evaluations included in the review

Randomised controlled trials (RCTs) and before-and-after studies were eligible for inclusion.

Specific interventions included in the review

Studies of any intervention targeting women with non-psychotic major depression during pregnancy or the postpartum were eligible for inclusion. The interventions included medication (fluoxetine), medication (fluoxetine) plus cognitive-behavioural therapy (CBT), CBT, counselling, psychodynamic therapy, interpersonal psychotherapy (IPT), educational intervention, and group therapy with CBT, educational and transactional analysis components. The duration of the treatment varied between the included studies, ranging from 5 to 16 weeks.

Participants included in the review

Studies of women diagnosed with non-psychotic major depression during pregnancy or the postpartum were eligible for inclusion. The studies included women with depression up to 13 weeks postpartum.

Outcomes assessed in the review

Studies using a standardised measure of depressive symptomatology were eligible for inclusion. Such measures included: the Revised Clinical Schedule, Edinburgh Postnatal Depression Scale (EPDS), the Hamilton Rating Scale, Structured Clinical Interview for DSM-III-R/IV, Beck Depression Inventory, Profile of Mood States (POMS), Goldberg's Standardized Psychiatric Interview, and the Clinical Global Impression. Most of the studies used more than one outcome measure. The EPDS was selected as the primary outcome measure for the meta-analysis; the Hamilton Rating Scale and POMS were used for studies that did not use the EPDS.

How were decisions on the relevance of primary studies made?

Two reviewers selected papers for inclusion in the review.

Assessment of study quality

The quality of the primary studies was evaluated based on the following criteria: presence of randomisation, presence of a control group, number of participants and year of publication. The studies were given a quality rating of high, medium or low.

Data extraction

One reviewer extracted the data. In addition to standard data, information on the types and timing of the intervention were extracted. The data were reported as presented in the original studies.

Methods of synthesis

How were the studies combined?

An overall effect size of treatment was calculated (primarily from the EPDS); the authors stated that a meta-analysis was used but did not provide any further details. Studies were also combined by intervention type or timing (pregnancy or postpartum). All estimates were presented as effect sizes.

How were differences between studies investigated?

The authors did not report whether statistical heterogeneity was assessed.

Results of the review

Eleven studies, describing 16 interventions, were included in the review: 7 RCTs (n=703), 3 open-label before-and-after studies (n=36) and 1 open-label trial (n=6).

Six studies were considered high quality, 4 studies medium quality and 1 study low quality.

The overall effect size of treatment was 0.673 (p<0.01); 14 interventions had a positive effect size.

When different intervention types were compared, a statistically significant effect size was found for medication (3.485, p<0.001; 2 studies, n=45), medication plus CBT (3.871, p<0.001; 1 study, n=30), group therapy (2.046, p<0.001; 1 study, n=30), IPT (1.260, p<0.001; 4 studies, n=181) and CBT (0.642, p<0.001; 3 studies, n=172). Medication, alone or in combination with CBT, was found to have the largest effect size. Psychodynamic therapy (1 study, n=95), counselling (2 studies, n=147) and education did not demonstrate statistically significant effect sizes of treatment: 0.53 (p=0.14), 0.418 (p=0.14) and 0.100 (p=0.457), respectively.

A statistically significant effect size was found for interventions implemented in the postpartum period (0.837, p<0.001; 8 studies, n=837). A small reduction in the effect size was seen when interventions with medication were removed from the analysis. A statistically significant effect size was found for interventions implemented during pregnancy (0.377, p=0.002; 5 studies, n=304).

Authors' conclusions

Preliminary findings suggested that medication (alone or in combination with CBT), group therapy with CBT, educational and transactional analysis components, IPT and CBT produce the greatest effect sizes for women with non-psychotic depression during pregnancy or the postpartum, although further research is needed to validate the results of this review.

CRD commentary

The review question was supported by fairly broad inclusion criteria. Several electronic databases were searched for relevant studies. Although two reviewers were involved in selecting the primary studies, it was unclear whether this process was conducted independently. The methods reported for the data extraction were unlikely to have minimised the possibility of reviewer error or bias. The authors did not report how many reviewers assessed study quality. The authors also did not report sufficient information to assess whether the analysis conducted was appropriate or not, or whether differences between the studies were formally assessed. Few details of the participants were provided, which makes it more difficult for the reader to interpret the results. In addition, the conclusions were based on a small number of studies with small datasets; the authors themselves suggested that these results should be interpreted with caution.

Implications of the review for practice and research

Practice: The authors did not indicate any implications for practice.

Research: The authors stated that future research should consider other available measures of depression; examine other variables such as occupational and social functioning, social support and the cost-effectiveness of the interventions; and continue to address the safety of pharmacological treatment for major depression during pregnancy and the postpartum. They also suggested that research into non-pharmacological treatments for major depression in the perinatal period is needed, and that culturally relevant treatments should be explored.

Funding

National Institute of Mental Health, grant numbers 5T32MH014623-24 and K23 MH67595.

Bibliographic details

Bledsoe S E, Grote N K. Treating depression during pregnancy and the postpartum: a preliminary meta-analysis. Research on Social Work Practice 2006; 16(2): 109-120.

Indexing Status

Subject indexing assigned by CRD

MeSH

Adult; Anxiety Disorders /prevention & control; Depression, Postpartum /prevention & control; Depressive Disorder /prevention & control; Female; Pregnancy; Pregnancy Complications /prevention & control; Prenatal Care /methods

AccessionNumber

12006006053

Database entry date

31/10/2007

Record Status

This is a critical abstract of a systematic review that meets the criteria for inclusion on DARE. Each critical abstract contains a brief summary of the review methods, results and conclusions followed by a detailed critical assessment on the reliability of the review and the conclusions drawn.

Copyright © 2014 University of York.
Bookshelf ID: NBK73095

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