Infection in pregnancy Flashcards

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1
Q

Discuss BV in pregnancy
-Impact to pregnancy
-When to treat
-Impact of treatment

A
  1. Impact to pregnancy
    -PPROM, PTB
  2. When to treat
    -Treat if symptoms as would outside of pregnancy
    -Treat in early pregnancy up to 20/40. May be beneficial for some women with previous PTB
  3. Impact of treatment
    -Cochrane reviews finds no improvement in outcomes with treatment
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2
Q

Discuss bacterial sepsis in pregnancy
-Incidence
-Mortality rate
-Definition of sepsis
-Definition of septic shock
-Definition of puerperal sepsis

A
  1. Incidence
    -11.4% of maternal deaths in Australia
  2. Mortality rate
    -0.8/100,000
    -20-40% if bacterial sepsis
    -60% if bacterial septic shock
  3. Definition of sepsis
    -Life threatening organ dysfunction caused by dysregulated host response to infection
    -Infection + systemic manifestation of sepsis
  4. Septic shock
    -Underlying circulatory and metabolic abnormalities associated with increased mortality indicated by hypotension with MAP ,65 or lactate >2.0 despite fluid resus
  5. Definition of puerperal sepsis
    -Development of sepsis after birth and until 6 weeks PP (Different from WHO def)
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3
Q

Discuss scoring systems for sepsis in obstetrics
-omqSOFA
-omSOFA

A
  1. omqSOFA = obstetric modified quick SOFA
    -Use for screening
    -Based on SBP <90, RR>25 and altered mentation
    -A score >2 is considered sepsis
  2. omSOFA = obstetric modified SOFA
    -Use if + for sepsis by omqSOFA
    -A score of 2 or change in score of 2 or more is significant
    -Based on PaO2, plt levels, bilirubin, MAP, mental state, Cr
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4
Q

Discuss fever in pregnancy
-Impact in early pregnancy
-In late pregnancy
-Neurodevelopmental outcomes

A
  1. Impact in early pregnancy
    -Organogenesis related to height and duration of fever
    -Most strongly associated with neurological defects (neural tube, microcephaly, micropthalmia)
    -Associated with oral clefts and congenital heart anomalies
  2. Late pregnancy
    -PTB
  3. Neurodevelopment
    -Possible association with autism and developmental delay
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5
Q

What are the common bacterial pathogens which cause maternal sepsis and which is the most common cause of maternal death from sepsis.

A

-E.coli - most common cause of infection
-GAS (Strep pyogenes) - most common cause of maternal death from sepsis
-GBS (Step agalactiae)

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6
Q

Discuss GAS in pregnancy (7 points)

A
  1. GAS = streptococcus pyogenes
  2. Usually asx carriage on skin or throat
  3. Causes 50% of maternal septic deaths in NZ and 25% in AUs
  4. 20 x increased risk in pregnancy
  5. 1:10 GAS infections healthcare related
  6. Treat in isolated room
  7. Treat Healthcare workers
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7
Q

Discuss management of maternal sepsis (5)

A
  1. Recognise - omqSOFA and omSOFA
  2. Resuscitate
    -Maintain airway and oxygenate if required
    -IV access
    -Blood tests and cultures from blood + other sites
    -IVF - crystalloid
  3. Respond
    -ABX (cef, Met, Gent or clinda and gent if allergy) within 60mins. DO NOT DELAY
    -Consider IVIG in GAS to neutrolise exotoxins
  4. Re-assess
    -Look for deterioration (change in omSOFA)
    -Assess fetal wellbeing depending on gestation
    -Step up to ICU if required
  5. Consider VTE prophylaxis with dose adjustment if renal impairment
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8
Q

Discuss timing and mode of delivery for maternal bacterial sepsis
-Intrauterine infection (5 points)
-Extrauterine infection (2 points)
-If goes into premature labour (1 point)
-Perimortem CS (3 points)

A
  1. Intrauterine infection
    -Consider delivery regardless of gestation
    -If previable can consider IOL to manage source control
    -Consider mode of delivery based on cervical favourability, chance of neonatal survival, expectation of rapid delivery
    -Consider steroids but don’t delay delivery for this.
    -Risk of cerebral palsy and encephalopathy - 2.4 in intrauterine infection
  2. Extrauterine infection
    -Aim to treat maternal sepsis and prolong gestation
    -Consider delivery in term pregnancies if pregnancy is impacting maternal response to infection
  3. Premature labour
    -Consider tocolytics for steroids unless intrauterine infection
  4. Perimortem CS
    -Perform in event of maternal cardiopulmonary arrest >20 weeks or if uterus palpable above umbilicus
    -Commence immediately. Don’t wait 4 mins, Better outcomes with shorter intervals
    -Associated with better neonatal outcomes
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9
Q

What are the risk factors for maternal sepsis (11)

A

-Obesity
-Impaired glucose tolerance
-Immunosupression
-Anaemia
-Vaginal discharge
-History of pelvic infection
-Hx of GBS infection
-Cervical cerclage
-Invasive procedures (Amnio)
-PROM
-GAS in close family or contacts

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