Postpartum Complications: Sepsis, hematoma, Mastitis, UTI, DVT, Psychological
- Park's Textbook of Preventive and Social Medicine
- Jawetz Melnick & Adelberg's Medical Microbiology 28E


- Tintinalli's Emergency Medicine
- Park's Textbook of Preventive and Social Medicine
| Factor | Postpartum Change |
|---|---|
| Stasis | Immobility, bed rest, prolonged labor |
| Hypercoagulability | Elevated clotting factors, decreased protein S, increased fibrinogen |
| Endothelial injury | Pelvic/perineal trauma, C-section |
- Park's Textbook of Preventive and Social Medicine
- Adams & Victor's Principles of Neurology, 12th Ed
- Rosen's Emergency Medicine
| Complication | Timing | Key Feature | First-line Management |
|---|---|---|---|
| Puerperal Sepsis | Within 3 weeks | Foul lochia, fever, uterine tenderness | IV broad-spectrum antibiotics |
| Hematoma | First 24 hours | Tense painful vulval/perineal swelling | Incision & evacuation if large |
| Mastitis | Week 2 postpartum | Unilateral red, tender breast with fever | Antistaphylococcal antibiotics + continue feeding |
| UTI/Pyelonephritis | Any time | Dysuria/loin pain; predisposed by catheterization | Antibiotics per culture |
| DVT/Thrombophlebitis | First 6 weeks (highest: weeks 1-2) | Swollen, tender, pale leg | LMWH anticoagulation |
| Postpartum Blues | Days 3-5 | Tearfulness, transient | Reassurance and support |
| Postpartum Depression | Within 4 weeks - months | Persistent low mood, poor bonding | SSRI + psychotherapy |
| Postpartum Psychosis | 48-72 hours | Confusion, rejection of infant, infanticidal risk | Emergency psychiatric admission |
More detail onto he case as a medical syudent
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The puerperium = the period from delivery of the placenta to 6 weeks postpartum. Normal physiological changes (involution, lochia, hormonal shifts) create a backdrop against which complications must be recognized.
| Category | Factors |
|---|---|
| Labor-related | Prolonged rupture of membranes (PROM), prolonged Stage 2 labor, frequent vaginal examinations |
| Delivery-related | Operative/instrumental delivery, cesarean section, intrauterine monitoring |
| Patient-related | Poor nutritional status, anemia, lack of prenatal care, immunosuppression, diabetes |
| Finding | Significance |
|---|---|
| Uterine subinvolution | Infected uterus fails to shrink normally |
| Uterine tenderness on palpation | Endometritis |
| Adnexal mass | Parametritis / tubo-ovarian abscess |
| Peritonism (guarding, rigors) | Peritonitis - progression |
| Wound erythema/discharge | Coexistent wound infection (common with C-section) |
PELVIC FLOOR
________________|________________
| |
BELOW pelvic floor ABOVE pelvic floor
Vulval hematoma Paravaginal hematoma
(most common) Broad ligament hematoma
(most dangerous - can be massive)
| Type | Site | Notes |
|---|---|---|
| Vulval | Below levator ani, in ischioanal fossa | Most common; visible as perineal swelling |
| Paravaginal | Above levator ani, lateral to vaginal wall | May track into retroperitoneum |
| Broad ligament / Retroperitoneal | Above pelvic floor, extends along broad ligament | Potentially life-threatening |
| Sign | Significance |
|---|---|
| Tense, fluctuant, bluish-purple perineal swelling | Classic vulval hematoma |
| Visible swelling lateral to vaginal wall | Paravaginal hematoma |
| Uterus deviated to one side | Suggests broad ligament hematoma |
| Shock (tachycardia, hypotension) | Large blood loss - internal hemorrhage |
| Falling Hb without visible bleeding | Internal hematoma - always consider this postpartum |
| Organism | Notes |
|---|---|
| Staphylococcus aureus | 40% of cases; most common; consider MRSA |
| E. coli | 2nd most common |
| Streptococcus spp. | Groups A, B |
| CA-MRSA | Community-acquired MRSA - increasing; suspect if no response to standard antibiotics |
Milk stasis (poor latch, missed feeds, engorgement)
↓
Milk accumulates → creates inflammatory response
↓
Skin bacteria (S. aureus) enter via nipple crack/fissure
↓
Retrograde infection into lactiferous ducts and parenchyma
↓
MASTITIS → (if untreated) → ABSCESS
| Finding | Mastitis | Abscess |
|---|---|---|
| Warmth, redness, swelling | Diffuse, one segment | Localised, fluctuant area |
| Tenderness | Generalised in segment | Point tenderness |
| Fluctuance | Absent | Present |
| Fever | Common | High fever |


| Step | Action |
|---|---|
| 1. Continue breastfeeding | Most important - do NOT stop; continued emptying is therapeutic |
| 2. Breast emptying | Frequent feeds + pumping to clear stasis |
| 3. Analgesia | NSAIDs (ibuprofen - also anti-inflammatory), paracetamol |
| 4. Antibiotics | 10-14 day course |
| Factor | Mechanism |
|---|---|
| Bladder hypotonia/atony | Overdistension during labor; neurological effects of epidural |
| Incomplete bladder emptying | Large residual urine = stagnant culture medium |
| Urethral trauma | Edema, bruising from delivery |
| Urinary catheterization | Introduces organisms directly; catheter-associated UTI (CAUTI) |
| Perineal contamination | Proximity of urethral meatus to perineal wound |
| Urinary stasis | Vesicoureteric reflux worsened; diuresis of pregnancy reverses |
Asymptomatic Bacteriuria
↓ (if untreated, ~30-40% progress)
Cystitis (lower UTI)
↓ (ascending infection via ureters)
Pyelonephritis (upper UTI) ← serious; causes ~10-15% of postpartum fever
↓ (if severe/untreated)
Urosepsis
| Test | Finding |
|---|---|
| Urinalysis (dipstick) | Nitrites +ve (bacteria), leukocyte esterase +ve (WBCs), blood ± protein |
| Microscopy | WBCs >10/hpf = pyuria; bacteria present |
| Urine culture (MSU) | Gold standard; >10⁵ colony-forming units/mL = significant bacteriuria |
| FBC | Raised WBC (neutrophilia) - more prominent in pyelonephritis |
| Blood cultures | If pyelonephritis/urosepsis - sepsis workup |
| Renal ultrasound | If obstruction suspected or no response to treatment |
| Virchow's Factor | Postpartum Mechanism |
|---|---|
| Stasis | Immobility, bed rest, prolonged labor, compression of pelvic veins by gravid uterus |
| Hypercoagulability | ↑ Clotting factors (I, VII, VIII, X), ↑ fibrinogen, ↓ Protein S, ↓ fibrinolytic activity, resistance to activated Protein C |
| Endothelial injury | Pelvic/perineal trauma, cesarean section, instrumental delivery |
| Feature | Superficial | DVT |
|---|---|---|
| Vessel affected | Superficial veins (varicosities) | Deep veins (femoral, popliteal, iliac) |
| Clinical features | Tender, red, cord-like superficial vein | Swollen, pale, tender, warm leg |
| PE risk | Very low | High |
| Management | NSAIDs, compression, warm compress | Anticoagulation |
| Association | Varicose veins | Any DVT risk factor |
| Criterion | Points |
|---|---|
| Active malignancy | +1 |
| Paralysis, paresis, or recent plaster immobilization | +1 |
| Recently bedridden >3 days or major surgery within 4 weeks | +1 |
| Localized tenderness along deep vein distribution | +1 |
| Entire lower limb swollen | +1 |
| Calf swelling >3 cm vs. asymptomatic leg | +1 |
| Strong family history of DVT (≥2 first-degree relatives) | +1 |
| Alternative diagnosis at least as likely | -2 |
Fuster and Hurst's The Heart, 15th Ed
| Test | Notes |
|---|---|
| D-dimer | High sensitivity, low specificity; very high postpartum physiologically - use with caution; adjusted thresholds being studied |
| Compression Duplex Ultrasound | First-line imaging; sensitivity 96.5% for proximal DVT; 71% for distal (calf) DVT; specificity 94% |
| CT Pulmonary Angiogram (CTPA) | Gold standard for PE |
| MR Venography | For pelvic vein DVT (inadequate on US) |
| Catheter venography | Gold standard for direct visualisation; reserved for surgical/interventional cases |
| Thrombophilia screen | After anticoagulation complete (not acute phase) - Protein C, S, antithrombin, Factor V Leiden, antiphospholipid antibodies |
| Drug | Details |
|---|---|
| LMWH (e.g., enoxaparin) | Drug of choice in postpartum; therapeutic dose twice daily; safe in breastfeeding |
| Unfractionated heparin (UFH) | Used if rapid reversal needed (renal failure, delivery imminent) |
| Warfarin | Can use postpartum; safe in breastfeeding; target INR 2-3; needs INR monitoring |
| DOACs (rivaroxaban, apixaban) | Generally avoided in breastfeeding (insufficient safety data) |
| Risk Level | Prophylaxis |
|---|---|
| Low risk (vaginal delivery, no risk factors) | Early mobilization, hydration |
| Intermediate (obesity, C-section, ≥2 risk factors) | LMWH for 10 days post-C-section |
| High risk (prior VTE, thrombophilia, antiphospholipid syndrome) | LMWH for 6 weeks postpartum |
POSTPARTUM BLUES ←――――――――――――――――――――→ POSTPARTUM PSYCHOSIS
(Mild, transient) (PPD - moderate) (Severe, emergency)
65% of mothers 3-6% of mothers 1-2 per 1,000
Days 3-5 Weeks to months 48-72 hours
Self-limiting Needs treatment Psychiatric emergency
| Category | Specific Risk Factors |
|---|---|
| Strongest predictor | Past history of PPD or depression |
| Psychiatric | Bipolar disorder, anxiety disorders, previous major depression |
| Social | Lack of partner/social support, financial stress, domestic violence |
| Obstetric | Unplanned pregnancy, difficult delivery, NICU admission, poor infant health |
| Physiological | Thyroid dysfunction (check TSH in all cases), sleep deprivation |
| Family history | First-degree relative with PPD or bipolar disorder |
| Severity | Treatment |
|---|---|
| Mild | Psychoeducation, peer support, self-help resources, watchful waiting |
| Mild-Moderate | CBT (Cognitive Behavioural Therapy) or Interpersonal Therapy (IPT) - first-line non-pharmacological |
| Moderate-Severe | SSRIs (first-line pharmacotherapy) + psychotherapy |
| Severe/psychotic features | Inpatient psychiatric admission; antipsychotics ± mood stabilisers |
| Drug | Breastfeeding Safety |
|---|---|
| Sertraline | Preferred - minimal transfer into breast milk; undetectable in most infant sera |
| Paroxetine | Also low transfer; acceptable |
| Fluoxetine | Higher transfer; active metabolite norfluoxetine accumulates in infants - less preferred |
| Feature | Detail |
|---|---|
| Alternating hyperactivity and mutism | Patient swings between frantic activity and silence/stupor |
| Disorientation and confusion | Unable to think clearly; disorientation to time and place |
| Delusions | Often about the baby; may believe baby is not hers, is possessed, is in danger |
| Hallucinations | Command hallucinations (auditory) may instruct her to harm the baby |
| Infanticide risk | Baby may be rejected; instances of infanticide documented |
| Suicidal ideation | Most dangerous aspect alongside infanticidal thoughts |
| Differential | Clinical clue |
|---|---|
| Eclampsia | Hypertension, proteinuria, seizures |
| Sheehan's syndrome (pituitary infarction) | PPH, failure to lactate, haemodynamic instability |
| Cerebral venous sinus thrombosis (CVST) | Headache, seizures, focal neurology, papilloedema |
| Ergot-induced psychosis | History of ergot administration |
| Hypoxic-ischemic cerebral injury | Prolonged hypotension/haemorrhage in labor |
| Thyroid storm | Tachycardia, tremor, fever |
| Priority | Action |
|---|---|
| 1. Safety | Immediate psychiatric admission; mother-and-baby unit (MBU) if available - maintain attachment while ensuring safety |
| 2. Risk assessment | Formal assessment of infanticidal and suicidal risk; do NOT leave mother alone with baby until assessed |
| 3. Antipsychotics | Olanzapine, haloperidol, quetiapine - for psychotic symptoms |
| 4. Mood stabilisers | Lithium - highly effective; caution with breastfeeding (monitor infant lithium levels); valproate (avoid if reproductive age) |
| 5. Benzodiazepines | Lorazepam for acute agitation, sleep, and seizure prophylaxis |
| 6. ECT | For severe, refractory cases; effective and safe postpartum |
| 7. Neuro-steroid therapies | Under investigation; unclear role in psychosis vs. depression |
| Complication | Timing | Pathogen/Cause | Key Sign/Symptom | First-Line Tx |
|---|---|---|---|---|
| Puerperal Sepsis (Endometritis) | Day 2-3 | Group A Strep, E. coli, anaerobes | Foul lochia + uterine tenderness + fever | Clindamycin + Gentamicin IV |
| Hematoma | First 24 hrs | Vessel injury without laceration | Perineal pain + tense bluish swelling | Conservative (small) / Incision & drainage (large) |
| Mastitis | Week 2 | S. aureus (40%); MRSA possible | Unilateral red painful breast + fever | Flucloxacillin/Cefalexin + continue breastfeeding |
| Breast Abscess | Any | S. aureus / MRSA | Fluctuant tender mass + failed mastitis treatment | US-guided aspiration; IV vancomycin if septic |
| UTI/Cystitis | Any | E. coli (80%) | Dysuria, frequency, no fever | Cefalexin or nitrofurantoin orally |
| Pyelonephritis | Any | E. coli, Klebsiella | Fever + loin pain + CVA tenderness | IV ceftriaxone; 14-day total course |
| DVT | Weeks 1-2 (peak) | Virchow's triad | Unilateral swollen tender leg | Therapeutic LMWH (enoxaparin) |
| Pulmonary Embolism | Any | DVT extension | Sudden dyspnoea + tachycardia + hypoxia | CTPA + therapeutic LMWH ± thrombolysis |
| Postpartum Blues | Day 3-5 | Hormonal withdrawal | Tearfulness + mood lability (self-limiting) | Reassurance + support |
| PPD | Weeks to months | Multifactorial | Persistent low mood + poor bonding | Sertraline + CBT; screen with EPDS |
| Postpartum Psychosis | 48-72 hrs | Hormonal/genetic | Confusion + delusions + infanticide risk | Emergency admission + antipsychotics + lithium |
Sources: Rosen's Emergency Medicine; Tintinalli's Emergency Medicine; Adams & Victor's Principles of Neurology 12th Ed; Park's Textbook of Preventive and Social Medicine; Fuster and Hurst's The Heart 15th Ed; Creasy & Resnik's Maternal-Fetal Medicine
Make table diff the 3 psychological problem
| Feature | 🟡 Postpartum Blues | 🟠 Postpartum Depression (PPD) | 🔴 Postpartum Psychosis |
|---|---|---|---|
| Incidence | 50-65% of mothers | 3-15% of mothers | 1-2 per 1,000 deliveries |
| Onset | Day 3-5 postpartum | 2 weeks to 3 months postpartum (DSM-5: within 4 weeks; clinically up to 12 months) | 48-72 hours postpartum (can be within first 2 weeks) |
| Duration | < 2 weeks (self-limiting) | Weeks to months if untreated | Days to months (requires active treatment) |
| Severity | Mild | Moderate to severe | Severe - psychiatric emergency |
| Mood | Labile - swings between happy and tearful | Persistently low, flat affect | Extremely labile - euphoria/mania OR deep depression |
| Tearfulness | Yes - prominent, episodic | Yes - persistent | May be present |
| Anhedonia | No | Yes - loss of pleasure in all activities | Variable |
| Anxiety | Mild | Often prominent | Present, with agitation |
| Cognitive function | Normal | Poor concentration, indecisiveness | Severely impaired - confusion, disorientation |
| Sleep disturbance | Mild | Insomnia (even when baby sleeps) | Severe - often sleepless, exhausted |
| Contact with reality | Intact | Intact | LOST - delusions, hallucinations |
| Delusions | None | None | Yes - often about the baby (e.g., baby is not hers, baby is evil/possessed) |
| Hallucinations | None | None | Yes - auditory command hallucinations common (may be instructed to harm baby) |
| Thought disorder | None | None | Yes - disorganised, illogical thinking |
| Psychomotor changes | None | Retardation or agitation | Alternating hyperactivity and mutism/stupor |
| Mother-infant bonding | Normal | Impaired - reduced responsiveness, guilt about not feeling love | Severely disrupted - may reject baby, believe baby is not hers |
| Infant care ability | Maintained | Reduced - may neglect feeds/care | Cannot safely care for infant |
| Infanticide risk | None | Very low (passive ideation only) | HIGH - command hallucinations, delusional beliefs about baby |
| Suicide risk | None | Moderate (passive ideation, "they'd be better without me") | HIGH - active suicidal ideation |
| Guilt/worthlessness | Absent | Prominent ("I'm a bad mother") | May be delusional in nature |
| Appetite | Normal | Usually reduced | Variable; self-neglect |
| Physical symptoms | Mild fatigue | Fatigue, somatic complaints | Autonomic instability, agitation |
| Precipitants | Hormonal withdrawal (oestrogen/progesterone drop) | Multifactorial - biological, psychological, social | Genetic/bipolar diathesis + hormonal shift + sleep deprivation |
| Prior psychiatric history | None required | Past depression/anxiety common | Often first presentation of bipolar disorder |
| Family history | Not significant | Depression in family | Bipolar disorder in family (strong association) |
| Recurrence in next pregnancy | Common (blues recur) | ~50% recurrence | Up to 50% recurrence (very high) |
| Screening tool | None needed (universal, self-limiting) | EPDS (Edinburgh Postnatal Depression Scale); score ≥10 = likely PPD | Clinical diagnosis - no scale; urgency over scoring |
| Investigations | None | TSH (thyroid), FBC (anaemia), drug screen | Neurological workup to exclude - eclampsia, CVST, Sheehan's, ergot toxicity |
| Management | Reassurance + support | CBT/IPT (mild-mod) + SSRIs (sertraline - preferred in breastfeeding) + Brexanolone (FDA-approved) | Immediate psychiatric admission + antipsychotics + lithium ± ECT |
| Hospital admission needed? | No | Usually No (unless severe/suicidal) | YES - emergency |
| Mother-baby unit? | No | Only if severe | Yes - maintains infant attachment under supervision |
| Breastfeeding | Can continue | Can continue (sertraline, paroxetine safe) | Case-by-case (lithium requires infant monitoring) |
| Prognosis | Excellent - resolves spontaneously | Good with treatment; risk of recurrence and later depressive episodes | Recovers with treatment; linked to long-term bipolar disorder diagnosis |
"Blues vs PPD vs Psychosis - ask 3 questions:"
- When did it start? Blues = day 3-5; PPD = weeks later; Psychosis = 48-72 hrs
- Is reality intact? Blues/PPD = YES; Psychosis = NO
- Is the baby safe? Blues = yes; PPD = maybe (neglect risk); Psychosis = immediate danger
| Blues | PPD | Psychosis | |
|---|---|---|---|
| Touch with reality | ✅ Normal | ✅ Normal | ❌ Lost |
| Infant safety concern | ❌ None | ⚠️ Mild-moderate | 🚨 Severe |
| Admission needed | ❌ No | ❌ Usually no | ✅ Emergency |
| Pharmacotherapy | ❌ No | ✅ SSRIs | ✅ Antipsychotics + Lithium |
Definition of psychological type in postpartum
A transient, self-limiting period of emotional lability occurring in the first days after delivery, characterised by tearfulness, mood swings, irritability, and mild anxiety, with no impairment of the mother's ability to care for her infant and no loss of contact with reality.
"Usually this lasts for only a few days, being quelled by the return home, responsibility for the infant, and nursing." - Adams & Victor's Principles of Neurology, 12th Ed
A major depressive episode with onset during pregnancy or within 4 weeks of delivery (DSM-5 specifier: "with peripartum onset"), characterised by persistent low mood, anhedonia, impaired bonding with the infant, and significant functional impairment, lasting weeks to months if untreated.
"With peripartum onset" - applied when onset of a major depressive episode occurs during pregnancy or within 4 weeks following delivery
A severe and acute psychiatric emergency arising within days of delivery, characterised by the abrupt onset of psychotic symptoms - including delusions, hallucinations, disorganised thinking, and gross disorientation - representing a complete break from reality, with significant risk of infanticide and suicide.
"The patient alternates between periods of noisy hyperactivity and of mutism and inactivity. She is disoriented and incapable of thinking clearly. The baby is sometimes rejected as not belonging to her." - Adams & Victor's Principles of Neurology, 12th Ed
| Postpartum Blues | Postpartum Depression | Postpartum Psychosis | |
|---|---|---|---|
| DSM-5 category | Not a diagnosis (normal variant) | MDD with peripartum onset specifier | Brief psychotic disorder / Bipolar I with peripartum onset |
| Defining word | Transient emotional lability | Persistent depressive episode | Psychotic break - loss of reality |
| Core requirement | Mood lability + tearfulness | ≥5 depressive symptoms for ≥2 weeks | Delusions/hallucinations + disorganisation |
| Reality testing | Intact | Intact | Absent |
| Onset | Day 3-5 | Weeks to months | 48-72 hours |
| Duration | < 2 weeks | Weeks to months | Days to months |
| Diagnosis requires | Nothing (clinical observation) | ≥5 DSM-5 MDD criteria | Active psychotic symptoms |
| Clinical boundary | Becomes PPD if > 2 weeks | Becomes psychosis if delusions/hallucinations appear | Medical emergency from the outset |