Lecture 37 - Clinical infections - childhood and pregnancy Flashcards
Infections during pregnancy may cause
miscarriage congenital anomalies Fetal hydrops Fetal death preterm delivery preterm rupture of the membranes
-Maternal antibodies cross the placenta and give passive immunity to the foetus
Route of acquisition of cytomegalovirus
respiratory droplet. secretions
Route of acquisition of Parvovirus B19
respiratory droplet. secretions
Route of acquisition of Toxoplasmosis
Ingestion of oocytes
Route of acquisition of Syphilis (blood)
Sexual
Route of acquisition of Varicella Zoster Virus
respiratory droplet/secretions
Route of acquisition of rubella
Nasopharyngeal secretions
Route of acquisition of Zika virus
Mosquito bite
Neonatal infections acquired during passage through birth canal
Group B Streptococcus Herpes simplex virus (HSV) Gonorrhoea Chlamydia HIV Hep B
NICE CG62
Antenatal care for uncomplicated pregnancies
Women should be offered routine screening for asymptomatic bacteriuria by midstream urine culture early in pregnancy.
Identification and treatment of asymptomatic bacteriuria reduces the risk of pyelonephritis.
Asymptomatic bacteriuria in pregnancy
Symptomatic UTI in pregnancy is frequently preceded by asymptomatic bacteriuria
Prevalence is around 5%
Untreated, at least 30% of women with ASB will develop acute pyelonephritis
Screening for ASB is considered to be a cost effective approach to preventing pyelonephritis
Why is Screening for Group B Streptococci not recommended in UK
Until it is clear that antenatal screening for GBS carriage does more good than harm and that the benefits are cost-effective, the National Screening Committee does not recommend routine screening in the UK
Prevention of Early-onset Neonatal Group B Streptococcal Disease
Intrapartum antibiotic prophylaxis (IAP) offered to:
Women with a previous baby with neonatal GBS disease
Women with GBS in current pregnancy
Women who are pyrexial in labour should be offered broad-spectrum antibiotics including an antibiotic for prevention of neonatal EOGBS disease
UTI during pregnancy
Screening for bacteriuria is indicated in pregnancy
Asymptomatic bacteriuria - no symptoms of UTI and 2 samples containing > 105 same organisms
Bacteriuria can develop into symptomatic UTI if untreated
Continuing bacteriuria is associated with premature delivery and increased perinatal mortality
Antimicrobial prescribing in pregnancy and puerperium
The potential to cause harm to the embryo/foetus/neonate must be considered
All antimicrobials cross the placenta to some extent
Virtually all antimicrobials appear in breast milk if given in therapeutic amounts to breast feeding women
Safe antimicrobials in pregnancy
Penicillins Cephalosporins
Some antimicrobials considered unsafe in pregnancy
Chloramphenicol Tetracycline Fluoroquinolones (e.g. ciprofloxacin) Trimethoprim-sulphamethoxazole
Intra-amniotic infections
Affects 1-2% term pregnancies
Affects 20-25% pregnancies with pre-term labour
major cause of perinatal morbidity and mortality
“chorioamnionitis” refers to inflammation of umbilical cord, amniotic membranes, placenta
Risk factors for intra-amniotic infections
Most common after prolonged rupture of membranes
Other risk factors include:amniocentesis, cordocentesis, cervical cerclage multiple vaginal examinations, ?BV
Pathogenesis of intra-amniotic infections
Bacteria present in the vagina cause infection by ascending through the cervix
Haematogenous (via blood ) infection is rare e.g. Listeria monocytogenes
Causative organisms of intra-amniotic infections
Group B Streptococcus
enterococci
Escherichia coli
Management of intra-amniotic infections
antimicrobials and delivery of the foetus
antimicrobials should be administered at the time of diagnosis (not after delivery)
Puerperal endometritis
infection of the womb during puerperium affects ~5% of pregnancies
puerperal sepsis remains a major cause of maternal death
Risk factors for puerperal endometritis
caesarean section, prolonged labour, prolonged rupture of membranes, multiple vaginal examinations
Clinical features of puerperal endometritis
fever (38.5oC in first 24 h post delivery or >38.0o for 4 hours, 24 h+ after delivery) uterine tenderness purulent, foul-smelling lochia increased white cell count general malaise, abdominal pain
puerperal endometritis causative organisms
Escherichia coli
Beta-haemolytic streptococci
Anaerobes
Diagnosis of puerperal endometritis
the role of transvaginal endometrial swabs is controversial
Treatment for puerperal endometritis
Broad-spectrum intravenous antimicrobials - continued until the patient has been apyrexial for 48 hours.