ICD-116E20

MENTAL OR BEHAVIOURAL DISORDERS ASSOCIATED WITH PREGNANCY, CHILDBIRTH OR THE PUERPERIUM, WITHOUT PSYCHOTIC SYMPTOMS

Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms
ICD-10F53.0Mild mental and behavioural disorders associated with the puerperium, not elsewhere classified
DSM-5-TRPeripartum 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

  1. EPDS (Edinburgh Postnatal Depression Scale, 10 items) — gold standard screening; cut-off ≥ 10 — possible depression (sensitive screening threshold), ≥ 13 — probable major depression.
  2. Clinical interview (assessment of the need for hospitalisation and of suicide risk).
  3. Postnatal psychosis differential — urgent hospitalization if psychotic symptoms present.
  4. Medical evaluation — thyroid (postpartum thyroiditis), anemia.
  5. Comorbid anxiety, OCD screening.

6.4 Differential diagnosis

ConditionDistinguishing feature
“Baby blues”≤ 2 weeks, mild, does not require clinical intervention.
Postnatal psychosis (6E21)Psychotic symptoms; urgent hospitalization.
Bipolar depressive episodeHistory of manic/hypomanic episode.
Postpartum thyroiditisTSH.
AnemiaHemoglobin.
Postnatal OCDEgo-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)

  1. Mild-moderate: Psychotherapy is first-line — CBT, IPT (particularly adapted to the perinatal context).
  2. 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.
  3. 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.
  4. ECT — psychotic depression, severe suicide risk, impaired food intake, also safe during pregnancy.
  5. Family support, peer support (e.g., PND helpline).
  6. Social service and mother-infant bonding support.
  7. 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

  1. Perinatal Interpersonal Therapy (IPT) — Stuart (Stuart S.), Robertson (Robertson M.) — Major role transitions, partner relationships, social support system.
  2. CBT Perinatal Adapted — Cognitive disturbances, behavioral activation.
  3. Brexanolone (Zulresso) — IV 60-hour; REMS program; clinic monitoring.
  4. Zuranolone (Zurzuvae) — Oral 50 mg × 14 days; FDA 2023.
  5. Edinburgh Postnatal Depression Scale (EPDS) — 10-item self-assessment.
  6. 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

  1. WHO. ICD-11. 6E20 Mental and behavioural disorders associated with pregnancy, childbirth and the puerperium. 2024.
  2. APA. DSM-5-TR. 2022.
  3. NICE CG192. Antenatal and postnatal mental health. 2014, 2018 update.
  4. ACOG Committee Opinion No. 757: Screening for Perinatal Depression. 2018.
  5. 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.
  6. Meltzer-Brody S. et al. Brexanolone injection in post-partum depression. Lancet 2018;392(10152):1058–1070.
  7. Deligiannidis K.M. et al. Effect of zuranolone vs placebo in postpartum depression. JAMA Psychiatry 2021;78(9):951–959.
  8. 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.
  9. 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.
  10. Stuart S., Robertson M. Interpersonal Psychotherapy: A Clinician’s Guide. 2nd ed. London: Hodder Arnold, 2012.

Order the book

The book is being prepared for print publication. If you would like to be among the first readers, leave your details — we will contact you as soon as it is published.