| ICD-116E20 | MENTAL OR BEHAVIOURAL DISORDERS ASSOCIATED WITH PREGNANCY, CHILDBIRTH OR THE PUERPERIUM, WITHOUT PSYCHOTIC SYMPTOMSMental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms |
| ICD-10F53.0 | Mild mental and behavioural disorders associated with the puerperium, not elsewhere classified |
| DSM-5-TR— | Peripartum onset specifier (no separate DSM-5-TR category) |
1. Definition and nosology
Postnatal Depression (ICD-11: 6E20 Mental and Behavioural Disorders Associated with Pregnancy, Childbirth or the Puerperium; DSM-5-TR: F32.x / F33.x Major Depressive Disorder with peripartum onset specifier) — a major depressive episode developing after childbirth (typically first 6 months; some guidelines up to 1 year). Affects 10–15% of women.
2. History
- Marcé L.V. (1858) — first clinical description of postpartum psychosis and depression.
- EPDS — Cox J.L. et al. (1987) — Edinburgh Postnatal Depression Scale.
- NICE CG192 (2014, 2018) — antenatal and postnatal mental health.
- FDA — brexanolone (2019), zuranolone (2023) — first specifically approved drugs for postpartum depression.
3. Epidemiology
- Prevalence: 10–15% (high-income countries), 20–30% (low- and middle-income countries).
- “Baby blues” — milder, short-term (1–2 weeks) — occurs in 50–80% of women; does not require clinical intervention.
- Comorbidity: anxiety, OCD, panic.
- Risk factors: previous depression, family history, depression during pregnancy, lack of partner support, socio-economic stress.
4. Aetiology and pathogenesis
- Hormonal — sharp drop in estrogen and progesterone after childbirth; allopregnanolone dysregulation.
- Sleep disturbance with newborn care.
- Psychosocial stress, relationships, social support.
- Genetic and prior history of affective disorder.
5. Clinical features
- Major depressive episode symptoms (sleep disturbance, appetite loss, anhedonia, worthlessness, suicidal thoughts).
- Specific characteristics: affective distancing towards the infant, difficulties in infant bonding, belief in inability to fulfill the maternal role, intrusive thoughts regarding harming the infant (ego-dystonic — similar to OCD; distinct from postpartum psychosis).
- Suicide risk and, in rare cases, infanticide (higher in postnatal psychosis).
6. Diagnosis
6.1 Unified diagnostic criteria
Major depressive episode criteria (DSM-5-TR 5+ symptoms for 2 weeks; ICD-11) + peripartum onset specifier (DSM-5-TR — during pregnancy or within 4 weeks postpartum; ICD-11 — broader, up to 6 months-1 year).
6.2 Source-specific clarifications
- NICE CG192 (2014, 2018) — diagnosis and treatment.
- ACOG Committee Opinion 757 (2018) — perinatal depression screening.
- USPSTF — screening in pregnant and postpartum women.
6.3 Diagnostic algorithm
- EPDS (Edinburgh Postnatal Depression Scale, 10 items) — gold standard screening; cut-off ≥ 10 — possible depression (sensitive screening threshold), ≥ 13 — probable major depression.
- Clinical interview (assessment of the need for hospitalisation and of suicide risk).
- Postnatal psychosis differential — urgent hospitalization if psychotic symptoms present.
- Medical evaluation — thyroid (postpartum thyroiditis), anemia.
- Comorbid anxiety, OCD screening.
6.4 Differential diagnosis
| Condition | Distinguishing feature |
|---|---|
| “Baby blues” | ≤ 2 weeks, mild, does not require clinical intervention. |
| Postnatal psychosis (6E21) | Psychotic symptoms; urgent hospitalization. |
| Bipolar depressive episode | History of manic/hypomanic episode. |
| Postpartum thyroiditis | TSH. |
| Anemia | Hemoglobin. |
| Postnatal OCD | Ego-dystonic intrusions of harm to infant; comorbid postnatal depression. |
7. Examination and assessment
- EPDS, PHQ-9.
- C-SSRS — suicide and risk of harm to infant.
- TSH, hemoglobin.
8. Treatment
8.1 General principles (NICE CG192 · ACOG · APA)
- Mild-moderate: Psychotherapy is first-line — CBT, IPT (particularly adapted to the perinatal context).
- Moderate-severe: psychotherapy + SSRI. In breastfeeding context:
- Sertraline (least excreted into milk) and paroxetine — first-line;
- Fluoxetine — long half-life, use with caution;
- Citalopram, escitalopram — appropriate.
- Refractory severe PPD:
- Brexanolone (Zulresso) — IV 60-hour infusion; FDA 2019 approval; monitored in clinic under REMS program; rapid effect.
- Zuranolone (Zurzuvae) — oral 14 days; FDA 2023 approval; more convenient.
- ECT — psychotic depression, severe suicide risk, impaired food intake, also safe during pregnancy.
- Family support, peer support (e.g., PND helpline).
- Social service and mother-infant bonding support.
- Sleep hygiene and involvement of family members in night care.
8.2 Source-specific clarifications
- NICE CG192 — sertraline and paroxetine first-line in breastfeeding.
- Louik C. et al. NEJM 2007 · Huybrechts K.F. et al. NEJM 2014 — SSRI in pregnancy cardiac malformations (paroxetine cautiously).
- Meltzer-Brody S. et al. Lancet 2018 — brexanolone RCT.
Treatment methods
- Perinatal Interpersonal Therapy (IPT) — Stuart (Stuart S.), Robertson (Robertson M.) — Major role transitions, partner relationships, social support system.
- CBT Perinatal Adapted — Cognitive disturbances, behavioral activation.
- Brexanolone (Zulresso) — IV 60-hour; REMS program; clinic monitoring.
- Zuranolone (Zurzuvae) — Oral 50 mg × 14 days; FDA 2023.
- Edinburgh Postnatal Depression Scale (EPDS) — 10-item self-assessment.
- ECT — Safe in pregnancy and lactation; in severe refractory cases.
9. Prognosis
- 70-80% remission with adequate treatment.
- Risk of recurrence in subsequent pregnancies (~25%).
- Without treatment, chronicity and comorbidity.
10. Myths and misconceptions
Myth 1: “PPD is just ordinary ‘baby blues’, transient”
Evidence: baby blues ≤ 2 weeks, mild; PPD clinical depressive episode, requires intervention; can be prolonged.
Myth 2: “Antidepressants are dangerous during breastfeeding”
Evidence: sertraline and paroxetine are acceptable during breastfeeding; milk transfer minimal; clinical counseling.
Myth 3: “Mother is weak, she should ‘fix herself’”
Evidence: PPD is a clinical condition; risk of suicide and infanticide exists; intervention is required.
Myth 4: “Brexanolone cures PPD”
Evidence: Rapid effect, but cost and need for clinic monitoring significant; standard approach SSRI + psychotherapy.
Myth 5: “PPD does not affect the infant”
Evidence: PPD affects mother-infant bonding and impacts the child's cognitive and emotional development; early intervention is crucial.
Myth 6: “Intrusive thoughts (harming a baby) are always a sign of psychosis”
Evidence: In postpartum OCD, intrusive thoughts are ego-dystonic — the patient suffers from them and avoids them; in postpartum psychosis they are ego-syntonic and can lead to behavior — different intervention.
11. Sources
- WHO. ICD-11. 6E20 Mental and behavioural disorders associated with pregnancy, childbirth and the puerperium. 2024.
- APA. DSM-5-TR. 2022.
- NICE CG192. Antenatal and postnatal mental health. 2014, 2018 update.
- ACOG Committee Opinion No. 757: Screening for Perinatal Depression. 2018.
- Cox J.L., Holden J.M., Sagovsky R. Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale. Br J Psychiatry 1987;150:782–786.
- Meltzer-Brody S. et al. Brexanolone injection in post-partum depression. Lancet 2018;392(10152):1058–1070.
- Deligiannidis K.M. et al. Effect of zuranolone vs placebo in postpartum depression. JAMA Psychiatry 2021;78(9):951–959.
- Louik C., Lin A.E., Werler M.M., Hernández-Díaz S., Mitchell A.A. First-trimester use of selective serotonin-reuptake inhibitors and the risk of birth defects. N Engl J Med 2007;356(26):2675–2683.
- Huybrechts K.F., Palmsten K., Avorn J. et al. Antidepressant use in pregnancy and the risk of cardiac defects. N Engl J Med 2014;370(25):2397–2407.
- Stuart S., Robertson M. Interpersonal Psychotherapy: A Clinician’s Guide. 2nd ed. London: Hodder Arnold, 2012.