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بسم الله الرحمن الرحيم
PROLONGED RUPTURE OF MEMBRANES AND NEONATAL INFECTION Ayman Abou Mehrem, MD, CABP Staff Physician Department of Pediatrics King Abdulaziz National Guard Hospital
Pathogenesis of Ascending Bacterial Infection
In most cases  the fetus or neonate is not exposed to potentially pathogenic bacteria until the membranes rupture and the infant passes through the birth canal and/or enters the extra uterine environment
The   human birth canal is colonized with aerobic and anaerobic organisms that may result in ascending amniotic infection and/or colonization of the infant at birth
VERTICAL TRANSMISSION  of bacterial agents that infect the amniotic fluid and/or vaginal canal may occur in utero or  more commonly  during labor and/or delivery
CHORIOAMNIONITIS   results from microbial invasion of amniotic fluid as a result of prolonged rupture of the chorioamniotic membrane
On occasion ,  amniotic infection occurs with apparently intact membranes or with a relatively brief duration of membrane rupture
Amniotic fluid infection may be asymptomatic or may produce maternal fever with or without local or systemic signs of chorioamnionitis
THE DURATION OF MEMBRANE RUPTURE  is directly correlated with the development of chorioamnionitis LONGER THAN 18 HOURS   is the current cut off for increased risk of neonatal infection
OTHER FACTORS  that associated with increased frequency of  NEONATAL INFECTION ,[object Object],[object Object],[object Object],[object Object]
In most cases ,  bacterial colonization of the newborn  does not  result in disease
What are the factors influencing which colonized infant will develop disease? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Aspiration  or  ingestion  of bacteria in amniotic fluid may lead to congenital pneumonia or systemic infection, with manifestations become apparent before delivery or after a latent period of a few hours. Aspiration or ingestion of bacteria during the birth process may lead to infection after an interval of 1-2 days.
Prematurity and Infection
Preterm infants have 3- to 10-fold higher incidence of infection than full term, normal birth weight infants do
is considered to be an important cause of preterm labor with an increased risk of vertical transmission to the newborn   Maternal genital tract infection
gestational age The frequency of intra-amniotic infection is inversely related to
immune dysfunction Premature infants have documented
Premature infants often require prolonged intravenous access, endotracheal intubation or other invasive procedures that provide a portal of entry or impair clearance mechanisms
The most common bacterial organisms causing neonatal infection are: ,[object Object],[object Object],[object Object],[object Object],[object Object]
Group B Streptococcus GBS
[object Object],[object Object]
Approaches for GBS Prevention in the Newborn ,[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object]
2002 Revised IAP Guidelines
[object Object]
[object Object],[object Object]
Patients recommended for IAP
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Patients not recommended for IAP
[object Object],[object Object],[object Object],The use of broad spectrum intrapartum antibiotics for the treatment of presumed chorioamnionitis in febrile women in labor is left to the discretion of the obstetrician
IAP  regimens ,[object Object],[object Object],[object Object]
[object Object],[object Object]
IAP is continued from hospital admission through delivery The greatest efficacy is achieved if penicillin G, ampicillin, or theoretically cefazolin is administered ≥4 hours before delivery
Approach to Threatened Preterm Delivery ,[object Object],[object Object],[object Object],GBS + GBS - Penicillin IV for >=48 hrs (during tocolysis) Obtain vaginal and rectal GBS culture and initiate IV penicillin No GBS prophylaxis IAP at delivery Stop penicillin GBS + No growth at 48 hrs
Management of the infant whose mother has received IAP
Any gestational age If the infant is ill-appearing or sepsis is otherwise strongly suspected, a full diagnostic evaluation including a CBC with differential, a blood culture, and a lumbar puncture (unless the clinical status dictates otherwise) should be done and empiric antibiotic treatment initiated using ampicillin and gentamicin until laboratory results are known. A chest radiograph should be obtained if respiratory symptoms are present
Infants born at <35 wks of gestation ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Infants born at ≥35 wks of gestation ,[object Object],[object Object],[object Object],[object Object]
[object Object]
Maternal IAP for GBS? Maternal antibiotics for suspected chorioamnionitis? Limited evaluation Observe ≥48hrs If sepsis is suspected, full diagnostic evaluation and empiric therapy Full diagnostic evaluation Empiric therapy Signs of neonatal sepsis? GA <35 weeks? No evaluation No therapy Observe ≥48 hrs Duration of IAP before delivery <4 hrs? Yes Yes Yes Yes Yes No No No Management of the infant whose mother has received IAP
Management of the infant whose mother has prolonged rupture of membranes Rupture of Membranes ≥ 18 hrs Mother has Chorioamnionitis? Sings of Neonatal Sepsis? GBS Screening at 35-37 wks gestation Negative No Evaluation No Therapy Observe ≥ 48 hrs Positive or Unknown Mother received IAP ≥ 4 hrs prior to delivery GA < 35 wks Limited Evaluation (CBC with differential, and blood culture) Observe ≥ 48 hrs Full Septic Screen and Start I.V. Antibiotics if:  1- Change in clinical status 2- Blood culture yields GBS GA < 35 wks Full Septic Screen:  CBC with differential, blood culture, LP, and chest X-ray (if indicated). Start I.V. Antibiotics Yes Yes Yes Yes Yes No No No No No Prepared by: Dr. Ayman Abu Mehrem Approved by: Dr. Hesham Al-Girim Reference:
 
 
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Prolonged Rupture Of Membranes

  • 2. PROLONGED RUPTURE OF MEMBRANES AND NEONATAL INFECTION Ayman Abou Mehrem, MD, CABP Staff Physician Department of Pediatrics King Abdulaziz National Guard Hospital
  • 3. Pathogenesis of Ascending Bacterial Infection
  • 4. In most cases the fetus or neonate is not exposed to potentially pathogenic bacteria until the membranes rupture and the infant passes through the birth canal and/or enters the extra uterine environment
  • 5. The human birth canal is colonized with aerobic and anaerobic organisms that may result in ascending amniotic infection and/or colonization of the infant at birth
  • 6. VERTICAL TRANSMISSION of bacterial agents that infect the amniotic fluid and/or vaginal canal may occur in utero or more commonly during labor and/or delivery
  • 7. CHORIOAMNIONITIS results from microbial invasion of amniotic fluid as a result of prolonged rupture of the chorioamniotic membrane
  • 8. On occasion , amniotic infection occurs with apparently intact membranes or with a relatively brief duration of membrane rupture
  • 9. Amniotic fluid infection may be asymptomatic or may produce maternal fever with or without local or systemic signs of chorioamnionitis
  • 10. THE DURATION OF MEMBRANE RUPTURE is directly correlated with the development of chorioamnionitis LONGER THAN 18 HOURS is the current cut off for increased risk of neonatal infection
  • 11.
  • 12. In most cases , bacterial colonization of the newborn does not result in disease
  • 13.
  • 14. Aspiration or ingestion of bacteria in amniotic fluid may lead to congenital pneumonia or systemic infection, with manifestations become apparent before delivery or after a latent period of a few hours. Aspiration or ingestion of bacteria during the birth process may lead to infection after an interval of 1-2 days.
  • 16. Preterm infants have 3- to 10-fold higher incidence of infection than full term, normal birth weight infants do
  • 17. is considered to be an important cause of preterm labor with an increased risk of vertical transmission to the newborn Maternal genital tract infection
  • 18. gestational age The frequency of intra-amniotic infection is inversely related to
  • 19. immune dysfunction Premature infants have documented
  • 20. Premature infants often require prolonged intravenous access, endotracheal intubation or other invasive procedures that provide a portal of entry or impair clearance mechanisms
  • 21.
  • 23.
  • 24.
  • 25.
  • 26. 2002 Revised IAP Guidelines
  • 27.
  • 28.
  • 30.
  • 32.
  • 33.
  • 34.
  • 35. IAP is continued from hospital admission through delivery The greatest efficacy is achieved if penicillin G, ampicillin, or theoretically cefazolin is administered ≥4 hours before delivery
  • 36.
  • 37. Management of the infant whose mother has received IAP
  • 38. Any gestational age If the infant is ill-appearing or sepsis is otherwise strongly suspected, a full diagnostic evaluation including a CBC with differential, a blood culture, and a lumbar puncture (unless the clinical status dictates otherwise) should be done and empiric antibiotic treatment initiated using ampicillin and gentamicin until laboratory results are known. A chest radiograph should be obtained if respiratory symptoms are present
  • 39.
  • 40.
  • 41.
  • 42. Maternal IAP for GBS? Maternal antibiotics for suspected chorioamnionitis? Limited evaluation Observe ≥48hrs If sepsis is suspected, full diagnostic evaluation and empiric therapy Full diagnostic evaluation Empiric therapy Signs of neonatal sepsis? GA <35 weeks? No evaluation No therapy Observe ≥48 hrs Duration of IAP before delivery <4 hrs? Yes Yes Yes Yes Yes No No No Management of the infant whose mother has received IAP
  • 43. Management of the infant whose mother has prolonged rupture of membranes Rupture of Membranes ≥ 18 hrs Mother has Chorioamnionitis? Sings of Neonatal Sepsis? GBS Screening at 35-37 wks gestation Negative No Evaluation No Therapy Observe ≥ 48 hrs Positive or Unknown Mother received IAP ≥ 4 hrs prior to delivery GA < 35 wks Limited Evaluation (CBC with differential, and blood culture) Observe ≥ 48 hrs Full Septic Screen and Start I.V. Antibiotics if: 1- Change in clinical status 2- Blood culture yields GBS GA < 35 wks Full Septic Screen: CBC with differential, blood culture, LP, and chest X-ray (if indicated). Start I.V. Antibiotics Yes Yes Yes Yes Yes No No No No No Prepared by: Dr. Ayman Abu Mehrem Approved by: Dr. Hesham Al-Girim Reference:
  • 44.  
  • 45.  

Editor's Notes

  1. 4 Endotracheal intubation, Umbilical venous catheter
  2. Possible explanations for the increased incidence of infection in preterm infants