Abstract
Introduction
The differentiation between postnatal depression and other types of depression is often unclear, but there are treatment issues in nursing mothers that do not apply in other situations. Overall, the prevalence of depression in postpartum women is the same as the prevalence in women generally, at about 12–13%. Suicide is a major cause of maternal mortality in resource-rich countries, but rates are lower in women postpartum than in women who have not had a baby.
Methods and outcomes
We conducted a systematic review and aimed to answer the following clinical questions: What are the effects of drug treatments, and of non-drug treatments, for postnatal depression? We searched: Medline, Embase, The Cochrane Library, and other important databases up to May 2008 (Clinical Evidence reviews are updated periodically, please check our website for the most up-to-date version of this review). We included harms alerts from relevant organisations such as the US Food and Drug Administration (FDA) and the UK Medicines and Healthcare products Regulatory Agency (MHRA).
Results
We found 34 systematic reviews, RCTs, or observational studies that met our inclusion criteria. We performed a GRADE evaluation of the quality of evidence for interventions.
Conclusions
In this systematic review we present information relating to the effectiveness and safety of the following interventions: group cognitive behavioural therapy, hormones, individual cognitive behavioural therapy (CBT), infant massage by mother, interpersonal psychotherapy, light therapy, mother–infant interaction coaching, non-directive counselling, other antidepressants, physical exercise, psychodynamic therapy, psychoeducation with partner, selective serotonin reuptake inhibitors (SSRIs), St John’s Wort, telephone-based peer support.
Key Points
The differentiation between postnatal depression and other types of depression is often unclear, but there are treatment issues in nursing mothers that do not apply in other situations.
Overall, the prevalence of depression in postpartum women is the same as the prevalence in women generally, at about 12–13%.
Suicide is a major cause of maternal mortality in resource-rich countries, but rates are lower in women postpartum than in women who have not had a baby.
Most episodes resolve spontaneously within 3–6 months, but a quarter of depressed mothers still have symptoms at 1 year. Depression can interfere with the mother–infant relationship.
SSRIs may improve symptoms of postnatal depression, but we found few studies evaluating their effect specifically in postpartum women.
We don't know whether other types of antidepressant are effective compared with placebo or psychological treatments.
We don't know whether oestrogen treatment or St John's Wort improve symptoms compared with placebo.
Psychological treatments such as individual CBT, non-directive counselling, interpersonal psychotherapy, and psychodynamic therapy are likely to improve symptoms compared with routine care, but long-term benefits are unclear.
We don't know whether light therapy, group CBT, psychoeducation with the partner, mother–infant interaction coaching, telephone-based peer support, infant massage, or physical exercise improve symptoms of postnatal depression as we found few studies.
About this condition
Definition
Postnatal depression (PND) has been variously defined as non-psychotic depression occurring during the first 6 months, the first 4 weeks, and the first 3 months postpartum; but recently 3 months postpartum was suggested in the UK as a useful clinical definition.[1] Puerperal mental disorders have only recently been categorised separately in psychiatric classifications, but both the ICD-10[2] and the DSM-IV (see table 1 ) require certain qualifications to be met that limit their use: ICD-10 categorises mental disorders that occur postpartum as puerperal, but only if they cannot otherwise be classified, and DSM-IV allows “postpartum onset” to be specified for mood disorders starting within 4 weeks postpartum.[3] In clinical practice and research, the broader definition above is often used, because whether or not PND is truly distinct from depression in general, depression in the postpartum period raises treatment issues for the nursing mother and has implications for the developing infant (see prognosis below). However, there is increased recognition that the depression often starts during pregnancy.[4] [5] The symptoms are similar to symptoms of depression at other times of life, but in addition to low mood, sleep disturbance, change in appetite, diurnal variation in mood, poor concentration, and irritability, women with PND also experience guilt about their inability to look after their new baby. In many countries, health visitors screen for PND using the Edinburgh Postnatal Depression Scale,[6] [7] which identifies depressive symptoms, but does not include somatic symptoms such as appetite changes, which can be difficult to assess in most women in the postnatal period.
Table 1.
Psychiatric classification | Criteria for postnatal depression |
ICD-10, WHO | Depressed mood for most of the day Loss of interest or pleasure in normally pleasurable activities such as playing with the baby Tiredness, decreased energy, and fatigue Additionally, any four of the following should be present: Loss of confidence and self-esteem Feelings of guilt and blaming oneself Recurrent thoughts of suicide or death, including that of the child Difficulty in concentration Agitation or lethargy Sleep disturbance Appetite disturbance |
DSM-IV – Postpartum onset specifier | Onset of depressive episode must be within 4 weeks postpartumSymptoms do not differ from symptoms in non-postpartum mood episodes and may include: Fluctuations in mood Preoccupation with infant wellbeing Severe anxiety Panic attacks Fearfulness of being alone with infant |
Incidence/ Prevalence
The prevalence of depression in women postpartum is similar to that found in women generally. However, the incidence of depression in the first month after childbirth is three times the average monthly incidence in non-childbearing women.[8] A meta-analysis of studies mainly based in resource-rich countries found the incidence of PND to be 12–13%,[9] with higher incidence in resource-poor countries.[10] [11]
Aetiology/ Risk factors
Four systematic reviews have identified the following risk factors for PND: history of any psychopathology (including history of previous PND), low social support, poor marital relationship, and recent life events.[9] [12] [13] [14]There is also an increased risk of PND amongst immigrant populations.[15]Recent studies from India also suggest that spousal disappointment with the sex of the newborn child, particularly if the child is a girl, is associated with the development of PND.[10] [16]
Prognosis
Most episodes of PND resolve spontaneously within 3–6 months,[17] but about one in four affected mothers are still depressed at the child's first birthday.[18]In resource-rich countries, suicide remains a leading cause of maternal deaths in the first year postpartum, although the postpartum suicide rate is lower than the rate in age-matched, non-postpartum women.[19] [20] PND is also associated with negative effects in the infant, including reduced likelihood of secure attachment,[21] deficits in maternal–infant interactions,[22] and impaired cognitive and emotional development of the child, particularly in boys living in areas of socioeconomic deprivation.[23] [24] These associations remain significant even after controlling for subsequent episodes of depression in the mother. However, there is also evidence to suggest that later effects on the child are related to chronic or recurrent maternal depression, rather than postpartum depression per se.[25] Women whose depression persists beyond 6 months postpartum have been found to have fewer positive interactions with their infants than women who were depressed but whose depressive symptoms ended before 6 months,[26] suggesting that the timing of depression is an important factor in determining its effect on the mother–infant relationship.
Aims of intervention
To improve symptoms, quality of life, mother–infant interaction, with minimal adverse effects on mother and child.
Outcomes
Symptom scores (e.g. the Edinburgh Postnatal Depression Scale[6] [7]) and other scales used in studies of depression at other times in life (e.g. the Hamilton Depression Rating Scale [27]) (see review on depression in adults: drug and other physical treatments), quality of life, mother–infant interaction (rated using questionnaires or observer rated videos), effect on marital/family relationship (rated using questionnaires), rates of suicide, and adverse effects.
Methods
Clinical Evidence search and appraisal May 2008. The following databases were used to identify studies for this review: Medline 1966 to May 2008, Embase 1980 to May 2008, and The Cochrane Database of Systematic Reviews and Cochrane Central Register of Controlled Clinical Trials 2008, Issue 2. Additional searches were carried out using these websites: NHS Centre for Reviews and Dissemination (CRD) — for Database of Abstracts of Reviews of Effects (DARE) and Health Technology Assessment (HTA), Turning Research into Practice (TRIP), and NICE. Abstracts of the studies retrieved were assessed independently by two information specialists using pre-determined criteria to identify relevant studies. Study design criteria for inclusion in this review were: published systematic reviews and RCTs in any language, at least single blinded, and containing more than 20 individuals of whom more than 80% were followed up. The minimum length of follow-up required to include studies was 6 weeks. We excluded all studies described as “open”, “open label”, or not blinded unless blinding was impossible: for example, for psychological interventions. We use a regular surveillance protocol to capture harms alerts from organisations such as the FDA and the UK Medicines and Healthcare products Regulatory Agency (MHRA), which are added to the review as required. We have performed a GRADE evaluation of the quality of evidence for interventions included in this review (see table ). To aid readability of the numerical data in our reviews, we round many percentages to the nearest whole number. Readers should be aware of this when relating percentages to summary statistics such as RRs and ORs.
Table 1.
Important outcomes | Depression score, quality of life, suicide, adverse effects | ||||||||
Number of studies (participants) | Outcome | Comparison | Type of evidence | Quality | Consistency | Directness | Effect size | GRADE | Comment |
What are the effects of drug treatments for postnatal depression? | |||||||||
1 (87) [31] | Depression scores | Fluoxetine plus CBT v placebo plus CBT | 4 | –2 | 0 | –1 | 0 | Very low | Quality points deducted for sparse data and poor follow-up. Directness point deducted for recruitment issues |
1 (109) [35] | Depression score | Sertraline v nortriptyline | 4 | –2 | 0 | –1 | 0 | Very low | Quality points deducted for sparse data and poor follow-up. Directness point deducted for recruitment issues |
1 (61) [39] | Depression score | Oestrogen v placebo | 4 | –1 | 0 | –1 | 0 | Low | Quality point deducted for sparse data. Directness point deducted for narrow inclusion criteria |
What are the effects of non-drug treatments for postnatal depression? | |||||||||
1 (37)[41] | Depression score | Individual CBT v ideal standard care | 4 | –2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and incomplete reporting of results |
1 (92) [42] | Depression score | Individual CBT v routine primary care | 4 | –1 | –1 | 0 | 0 | Low | Quality point deducted for sparse data. Consistency point deducted for conflicting results at different end points |
1 (84)[42] | Depression score | Individual CBT v non-directive counselling | 4 | –4 | 0 | 0 | 0 | Very low | Quality points deducted for poor follow-up, incomplete reporting of results, sparse data, and other methodological flaws |
1 (192)[52] | Depression score | Group CBT v non-directive counselling | 4 | –2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and poor follow-up |
1 (193) [43] | Proportion free of depression | Individual CBT v psychodynamic therapy | 4 | –2 | –1 | 0 | 0 | Very low | Quality points deducted for sparse data and incomplete reporting of results. Consistency point deducted for conflicting results at different end points |
1 (35)[45] | Depression score | Paroxetine plus CBT v paroxetine alone | 4 | –1 | 0 | –1 | 0 | Low | Quality points deducted for sparse data. Directness point deducted for exclusion of suicidal women |
1 (120)[47] | Proportion free of depression | Interpersonal therapy v waiting list | 4 | –1 | 0 | –1 | 0 | Low | Quality point deducted for sparse data. Directness point deducted for recruitment issues |
3 (293)[50] [51] [42] | Proportion free of depression | Non-directive counselling v routine primary care | 4 | –2 | –1 | 0 | 0 | Very low | Quality points deducted for baseline differences and statistical flaws. Consistency point deducted for conflicting results |
1 (193) [43] | Depression score | Non-directive counselling v routine primary care | 4 | –3 | 0 | 0 | 0 | Very low | Quality points deducted for sparse data, baseline differences, and statistical flaws. |
1 (193) [43] | Proportion free of depression | Non-directive counselling v psychodynamic therapy | 4 | –3 | 0 | 0 | 0 | Very low | Quality points deducted for sparse data, baseline differences, statistical flaws, and incomplete reporting of results |
1 (192)[52] | Depression score | Individual non-directive counselling v group counselling | 4 | –2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and poor follow-up |
1 (45)[46] | Depression score | Group CBT v routine primary care | 4 | –2 | 0 | 0 | 0 | Low | Quality point deducted for sparse data and issues about definition of response |
1 (1220)[57] | Depression score | Interaction coaching v usual care | 4 | –1 | 0 | 0 | 0 | Moderate | Quality point deducted for sparse data |
1 (20) [59] | Depression score | Exercise plus social support v control | 4 | –2 | 0 | –1 | 0 | Very low | Quality point deducted for sparse data and issues about baseline differences. Directness point deducted for use of combined social and exercise interventions |
1 (193) [43] | Depression score | Psychodynamic therapy v routine primary care | 4 | –3 | 0 | 0 | 0 | Very low | Quality points deducted for sparse data, baseline differences, and statistical flaws |
1 (29)[60] | Depression score | Psychoeducation with partner v psychoeducation without partner | 4 | –2 | 0 | 0 | 0 | Low | Quality points deducted for sparse data and uncertainty about baseline differences |
1 (42) [61] | Depression score | Telephone-based peer support v usual care | 4 | –1 | 0 | –1 | 0 | Low | Quality point deducted for sparse data. Directness point deducted for recruitment issues |
Type of evidence: 4 = RCT; 2 = Observational; 1 = Non-analytical/expert opinion. Consistency: similarity of results across studies. Directness: generalisability of population or outcomes.Effect size: based on relative risk or odds ratio.
Glossary
- Ainsworth Strange Situation Procedure
is a laboratory procedure used to assess infant attachment style. The procedure consists of prespecified episodes of parental separation and return. The infant's behaviour upon the parent's return is the basis for classifying the infant into attachment categories (e.g. secure and insecure).
- Beck Depression Inventory
Standardised scale to assess depression. This instrument consists of 21 items to assess the intensity of depression. Each item is a list of 4 statements (rated 0, 1, 2, or 3), arranged in increasing severity, about a particular symptom of depression. The range of scores possible are 0 = least severe depression to 63 = most severe depression. It is recommended for people aged 13 to 80 years. Scores of more than 12 or 13 indicate the presence of depression.
- Behavioural Screening Questionnaire
is a maternal interview that examines infant difficulties, such as sleep disturbance, feeding problems, separation problems, and excessive temper tantrums. It has been found to distinguish between infants of mothers with and without depression.
- Clinical Global Impression Scale
A one-item, observer-rated scale for measuring the severity of a condition. It has been investigated for validity and reliability. The scale is scored from 0 (not ill at all) to 7 (severely ill).
- Clinical Global Impressions Scale
is a clinician rated scale of severity of illness.
- Clinical Interview Schedule-Revised (CIS-R)
is a semistructured interview covering non-psychotic symptoms particularly those associated with depression and anxiety.
- Cognitive behavioural therapy (CBT)
A form of psychological therapy that uses a range of techniques including examination and challenging of unhelpful thoughts, help with changing behaviours, and examination of underlying dysfunctional assumptions.
- Dyadic Adjustment Scale
is a specific self-report measure of adjustment in relationship with partner. The four subscales are Dyadic Satisfaction, Dyadic Consensus, Dyadic Cohesion, and Affectional Expression.
- Dyadic Mutuality Code (DMC) Scores
are based on live or videotaped observations of face-to-face interactions between mother and infant. The DMC shows the level of responsiveness in the maternal–infant relationship where responsiveness is defined as the mother's ability to accommodate to her infant's behaviour and to give it meaning through regulation of her own behavioural responses. The DMC contains six key components of responsive interactions: mutual attention, positive affect, turn-taking, maternal pauses, infant clarity of cues, and maternal sensitivity.
- Edinburgh Postnatal Depression Scale (EPDS)
was designed as a screening questionnaire to identify possible depression in a clinical or research setting. The EPDS has a high sensitivity (95%) and specificity (93%) for postnatal depression, and is used by many health visitors and in many clinical research studies of postnatal depression. The EPDS consists of 10 questions, with responses scored on a 4-point scale according to increased severity of the symptom. Total scores range from 0 to 30 with a score 12 or greater indicating probable depression.
- Group cognitive behavioural therapy
In the trial described here it consisted of weekly meetings run by health visitors in primary care. It included education, provision of information on postnatal depression, strategies for coping with difficult childcare situations and eliciting social support, use of cognitive behavioural techniques to tackle women's erroneous cognitions about motherhood, and strategies for coping with anxiety, such as the use of relaxation.
- Hamilton Depression Rating Scale
a measure of depressive symptoms using 17 items, with total scores from 0 to 54 (higher scores indicate increased severity of depression).
- Interaction coaching
for at-risk parents and their infants is a six-key-element intervention strategy designed to strengthen the early parent–infant relationship. This includes teaching the mother to identify the infant's behavioural cues and to tailor responses to match the infant's preferences by showing ways to modulate the use of pauses; imitation; sequences; and combinations of facial expressions, voice, and touch.
- Interpersonal psychotherapy
places the depression in an interpersonal context, reviews the person's current and past interpersonal relationships, and relates problematic aspects of these relationships to the person's depression.
- Low-quality evidence
Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
- McCarthy Scales of Children's Abilities
is a general measure of children's cognitive development.
- Mental Development Index of the Bayley Scales of Infant Development
provides information about the child's language development and problem solving skills.
- Moderate-quality evidence
Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
- Non-directive counselling
provides women with the opportunity to air their feelings about any current concerns, such as marital problems or financial difficulties, as well as problems they might raise about their infant.
- Postpartum Adjustment Questionnaire
is a specific self-report measure of postpartum adjustment, with subscales measuring work in the home, relationship with spouse, relationships with children other than the baby, relationships with friends, work outside of the home, relationships with other family members, and relationship with the new baby.
- Preschool Behaviour Checklist
is a questionnaire completed by preschool and reception class teachers to identify significant child behaviour problems.
- Psychodynamic therapy
is therapy in which an understanding of the mother's representation of her infant and her relationship with her infant is promoted by exploring aspects of the mother's own early attachment history.
- Psychoeducation
consists of education about the psychological disorder the person is suffering from, in addition to monitoring and treatment of the person's mental disorder.
- Rutter A2 Scale
is a reliable and well validated questionnaire completed by the mother, which identifies clinically significant child behaviour problems at 5 years.
- Social Adjustment Scale-Self Report (SAS-SR)
is a questionnaire with subscales measuring work in the home, work outside of the home, relationship with spouse, relationship with children older than 2 years, relationship with immediate family, and relationships with friends.
- Structured Clinical Interview for Diagnostic and Statistical Manual (DSM)-III-R (SCID)
is a structured interview to generate an operationalised diagnosis that would fulfil DSM-III-R criteria.
- Very low-quality evidence
Any estimate of effect is very uncertain.
Depression in adults: drug and other physical treatments.
Disclaimer
The information contained in this publication is intended for medical professionals. Categories presented in Clinical Evidence indicate a judgement about the strength of the evidence available to our contributors prior to publication and the relevant importance of benefit and harms. We rely on our contributors to confirm the accuracy of the information presented and to adhere to describe accepted practices. Readers should be aware that professionals in the field may have different opinions. Because of this and regular advances in medical research we strongly recommend that readers' independently verify specified treatments and drugs including manufacturers' guidance. Also, the categories do not indicate whether a particular treatment is generally appropriate or whether it is suitable for a particular individual. Ultimately it is the readers' responsibility to make their own professional judgements, so to appropriately advise and treat their patients. To the fullest extent permitted by law, BMJ Publishing Group Limited and its editors are not responsible for any losses, injury or damage caused to any person or property (including under contract, by negligence, products liability or otherwise) whether they be direct or indirect, special, incidental or consequential, resulting from the application of the information in this publication.
Contributor Information
Michael Craig, Institute of Psychiatry, London, UK.
Louise Michele Howard, Health Service and Population Research Department, Institute of Psychiatry, London, UK.
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