Maternal Sepsis
Clinical detail
Additional detail checked 2026-10-17 against the linked sources. This check covers the section below; the rest of the module retains its displayed verification status.
Maternal sepsis assessment must recognise physiological changes of pregnancy and the possibility of rapid deterioration. Source assessment, antimicrobial treatment, haemodynamic care and escalation should proceed together.
Assessment & interpretation
- Use the pregnancy-specific risk-assessment pathway and review observations, mental state, oxygenation, urine output and lactate.
- Obtain appropriate blood and microbiological samples before antimicrobials when this does not delay urgent treatment. Look for an obstetric, urinary, respiratory, wound or other source.
Decisions that change management
- NICE’s high-risk pregnancy pathway requires immediate senior assessment and broad-spectrum antimicrobial treatment within 1 hour of identifying high-risk criteria.
- Assess fluid response and the need for critical-care support; persistent circulatory or respiratory compromise needs prompt escalation.
- Source control may require obstetric or surgical intervention as well as antibiotics.
Follow-up & safety-netting
- Record repeated observations, treatment response and the next reassessment time. A non-response requires a new management decision.
- Coordinate obstetric, critical-care and neonatal involvement as appropriate, and communicate the infection and treatment plan at handover.
Clinical pitfalls
- An isolated lactate value does not replace the full assessment. Do not apply a general-adult scoring pathway without checking its suitability in pregnancy and the recent postnatal period.
Admission & discharge
Admission/discharge guidance checked 2026-10-18 against the linked sources. This is a clinical checklist for an individual decision, not an automatic discharge order.
When admission or continued hospital care is needed
- Admit suspected sepsis, hypotension, respiratory compromise, altered mental state, oliguria or inability to maintain intake. Arrange urgent source control and appropriate organ support.
When clinic, day care or home care may be suitable
- Suspected maternal sepsis with systemic illness is not a routine outpatient antibiotic prescription. A localised infection without sepsis may follow its own outpatient pathway after assessment.
Before going home
- The source has been controlled or has a definitive plan; haemodynamics/respiratory function and organ trends support care outside hospital.
- No unresolved vasopressor/acute organ-support need; an effective oral regimen or a formally supported outpatient IV service is arranged if antibiotics remain necessary. Persistent fever or deterioration needs reassessment.
Discharge medicines and treatment changes
- Reconcile cultures with the actual infection diagnosis; give the selected antibiotic’s dose, route, remaining duration and stop/review date. Do not prescribe every sepsis example combination together.
Tests, pending results and their reviewer
- Assign a named reviewer and action plan for pending cultures, susceptibilities, pathology and abnormal renal/liver/blood results; ensure a patient callback route.
Home care and counselling
- Explain the source, treatment, risk of recurrence and post-sepsis physical/emotional effects. Provide written warning symptoms, 24-hour access and support for infant care if relevant.
Follow-up: when and what to review
| When | Action / responsible service |
|---|---|
Before discharge | Book the early clinical/antimicrobial review required by the source and organ injury, with the responsible team. |
At the documented postnatal/post-sepsis review | Review recovery, medicines, outstanding results and any specialist rehabilitation needs. |
Return urgently
- Recurrent fever/rigors, confusion, faintness, breathlessness, reduced urine, worsening abdominal/wound pain or offensive lochia requires immediate reassessment.
Treatment
① Immediate stabilization — first minutes
- Measure lactate, obtain appropriate cultures and bloods BEFORE antibiotics only if doing so causes no substantial delay. Give empiric broad-spectrum IV antibiotics ideally within 1 h for septic shock/high-likelihood sepsis.
- Select treatment for the suspected source, allergies, renal function and local resistance. The complete cards below show named obstetric-infection combinations, not a claim that one antibiotic treats every maternal sepsis source: chorioamnionitis uses ampicillin PLUS gentamicin; postpartum endometritis may use clindamycin PLUS gentamicin; septic miscarriage needs broad anaerobic cover and evacuation.
- For hypotension/hypoperfusion, give balanced crystalloid with frequent response/tolerance checks. SMFM recommends 1–2 L in the first 3 h; NICE NG255 uses 500 mL boluses over <15 min with reassessment and consultant review if two boluses fail. Do not apply an automatic unmonitored 30 mL/kg prescription in pregnancy.
- If shock persists or fluids are poorly tolerated, start norepinephrine with critical-care supervision, using the explicit salt/concentration/pump calculation below. Catheterise and track hourly urine output; assess oxygenation and perfusion continuously.
② Assessment & investigations
Never delay antibiotics >45-60 min for results.
③ First-line treatment & drug regimens
Use the indication-specific antimicrobial and vasopressor cards below with the source-control assessment. Regimens are labelled by source and syndrome; do not use one combination for every sepsis presentation.
④ Drug treatment detail (5 agents)
- Indication: Intra-amniotic infection, in combination with gentamicin; add anaerobic cover for caesarean according to the chosen guideline
- This is not GBS prophylaxis and is not ampicillin monotherapy. The postpartum duration differs between guidelines; record the local choice explicitly.
- Temperature, pulse, BP, uterine tenderness, fetal heart rate, cultures and renal function
- Indication: Combination therapy for chorioamnionitis, postpartum endometritis or septic miscarriage
- Renal / hepatic: Adjust interval/dose to renal function and measured levels; do not keep automatic daily dosing in AKI
- Baseline and serial creatinine/urine output; drug-level monitoring using the hospital once-daily schedule
- Ask about tinnitus, hearing change or vertigo; stop and review suspected ototoxicity
- Indication: Combination treatment of selected septic miscarriage/endometritis or caesarean chorioamnionitis
- Renal / hepatic: In severe hepatic impairment the cited MSF monograph reduces the daily dose to one third
- Clinical response, LFTs in prolonged treatment, interacting anticoagulants and neuropathy with prolonged exposure
- Indication: Postpartum endometritis, in combination with gentamicin when appropriate
- Temperature, uterine tenderness, renal function/gentamicin levels for the partner drug; diarrhoea/C. difficile risk
- Indication: Persistent shock while fluid responsiveness/source control are addressed; first-line vasopressor in maternal septic shock
- Continuous ECG, frequent BP (arterial when possible), perfusion and urine output; inspect peripheral site frequently for extravasation
- Clearly label SALT versus BASE: this MSF tartrate dose is twice the numerical BASE dose; NEVER copy its pump rate into a base-labelled concentration
Definitive treatment
- Rapidly remove/control the source: evacuate infected retained tissue, drain an abscess, debride an infected wound or relieve urinary obstruction when indicated.
- If the uterus is the suspected/confirmed source, prompt delivery/evacuation may be needed regardless of gestation (SMFM); sepsis alone from another source is not an automatic indication for delivery.
- Review antibiotics when microbiology and the clinical response are available, usually within 24–48 h: narrow, adjust renal dosing, stop unnecessary partners and record the total course for the actual infection. Persistent fever/shock requires a search for uncontrolled source or resistant organisms.
Monitoring
| Parameter | Frequency until improving |
|---|---|
Obs/qSOFA elements | Hourly |
Urine output | Hourly (>0.5 mL/kg/h) |
Lactate repeat | At 2-4 h if initially raised |
Antibiotic review | 48-72 h culture-guided de-escalation |
Response assessment
- Lactate falling, vasopressor-free stability, afebrile trajectory, organ recovery
Treatment failure
Persistent hypotension, escalating vasopressor need, respiratory failure, altered consciousness, rising lactate or organ dysfunction: ICU immediately.
Assess need for ventilation, renal support and obstetric surgery without waiting for a complete test panel.
Second-line treatment
- Meropenem-class escalation per microbiology; antifungal consideration prolonged ICU
Rescue treatment
Necrotising infection: emergency wide debridement theatre; toxic-shock physiology: clindamycin+immunoglobulin discussion.
Procedure / surgery
MVA/EVAC under antibiotics COVER (not after "cure") when products retained.
Escalation
- HDU/ICU criteria: vasopressors, ventilation, dialysis
- Peripheral centre: start bundle THEN transfer with escort
⑮ Complications & their management
DIC
Component therapy; treat trigger
AKI
Fluid stewardship; dialysis indications
Sheehan (late pituitary insult)
Endocrine follow-up if prolonged shock
Post-treatment care
- Complete antibiotic course per source; wound care
- Debrief + documentation
- Contraception/breastfeeding continuity planning
Diagnosis & assessment
- Temp >38 or <36 · HR>110 · RR>25 · SBP<90 · SpO2<94%
- Confusion/sluggishness post-birth ("just tired")
- Foul-smelling liquor/discharge + uterine tenderness
- Rigors + loin pain (pyelonephritis)
- Retained products + fever = surgical emergency combo
Definition: Life-threatening organ dysfunction from infection in pregnancy/puerperium (qSOFA/news-style screening plus obstetric context).
Initial assessment
- RECOGNISE: obs-triggered screening each shift
- CALL senior + declare sepsis; note time
- SEPSIS SIX within the hour: O2 if hypoxic · IV access x2 + bloods incl. lactate+cultures · balanced crystalloid with frequent reassessment (SMFM initial 1–2 L over 3 h; avoid fluid overload) · IV broad-spectrum antibiotics · catheter+hourly urine · reassess
- SOURCE hunt: PV exam, US for RPOC/collections, wound inspection
Investigations
| Test | Looking for |
|---|---|
Lactate | >2 raised; >=4 high-risk |
Blood cultures x2 BEFORE antibiotics (never delaying them) | Organism guidance |
CBC, CRP, U&E, LFT, coags | Organ dysfunction/DIC |
US pelvis | Retained products/collections driving source control |
Differential diagnosis
| Condition | Clue |
|---|---|
Chorioamnionitis | Intrapartum fever+foul liquor |
Endometritis | Post-CS/post-evacuation uterine tenderness |
Septic abortion | Unsafe-MTP context; retained products |
Pyelonephritis | Loin pain+urine findings |
Necrotising fasciitis (perineal/wound) | Pain out of proportion+skin changes |
Algorithm
Principles & follow-up
Management principles
Sources (11)
19 November 2025 · checked 2026-10-18 · verified-live
Open source ↗
Scope: additional clinical-detail explanation for maternal-sepsis. Checked the assessment, management-decision and follow-up statements in that section against this source. This does not certify all pre-existing regimens, calculations or recommendations in the module. Additional admission/discharge …
· checked 2026-10-18 · verified-live
Open source ↗
Sepsis without obligatory fever, cultures without antibiotic delay, early broad-spectrum treatment, 1–2 L balanced crystalloid in 3 hours with response-guided reassessment, norepinephrine and uterine source control. Additional admission/discharge check 18 October 2026 (limited to the following): Pro…
· checked 2026-10-18 · verified-live
Open source ↗
Source-specific combinations and durations for chorioamnionitis, endometritis and septic miscarriage; GBS ampicillin 2 g then 1 g every 4 h until delivery. Regional guidance is labelled; local resistance and culture review remain required. Additional admission/discharge check 18 October 2026 (limite…
· checked 2026-10-17 · verified-live
Open source ↗
Adult 5–6 mg/kg daily, 40 mg/mL presentation, 100 mL adult infusion over 30 minutes and renal/ototoxicity/compatibility precautions; obstetric combination choice from the national infection guideline.
· checked 2026-10-17 · verified-live
Open source ↗
500 mg/100 mL over 30 minutes, every-8-hour adult dosing, switch to oral, severe hepatic reduction and interactions. Syndrome duration supplied separately by the infection guideline.
· checked 2026-10-17 · verified-live
Open source ↗
MSF peripheral TARTRATE-based 0.1 microgram/kg/min starting dose, dilution to 100 micrograms TARTRATE/mL, pump formula, titration/ceiling and salt-versus-base distinction; SMFM supplies maternal-sepsis vasopressor choice.
· checked 2026-10-18 · verified-live
Open source ↗
Full primary recommendations read, focusing on critical-care-to-ward transfer: structured written handover, shared plan, monitoring, rehabilitation and receiving-team capability. Step-down is distinct from home discharge; no universal organ-support discharge cutoff is asserted.
· checked 2026-10-18 · verified-live
Open source ↗
Maternal/newborn transfer assessment, first void and effective feeding, handover, support/safeguarding, first midwife visit within 36 hours after transfer, postnatal danger symptoms. Full recommendations page read.
· checked 2026-10-18 · verified-live
Open source ↗
Normal-delivery discharge not less than 48 hours: full primary SOP PDF normal-delivery/discharge passages read. Corroborated by NHM CEmONC 2024 Part 1, chapter 8. This does not define a universal post-caesarean or complicated-case stay.
· checked 2026-10-18 · verified-live
Open source ↗
Official WHO summary read: at least 24-hour facility care after birth; additional contacts at 48–72 hours, 7–14 days and week 6; individual assessment/support. Summary facts only, not a claim that the full 242-page PDF was reviewed.
· checked 2026-10-18 · verified-live
Open source ↗
Full primary patient recovery page read: pain control, wounds, activity/VTE, urinary/bowel and infection warning signs, adult support and no driving/important decisions during the first 24 hours after general anaesthesia. Used as general recovery/handover principles, not operation-specific discharge…