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| Chorioamnionitis | |
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| Micrograph showing acute chorioamnionitis, with neutrophils in the chorion. Also seen are fibrin thrombi, which indicate a severe fetal inflammatory response.[1]H&E stain. | |
| Specialty | Obstetrics and gynaecology  |
Chorioamnionitis, also known asamnionitis andintra-amniotic infection (IAI), isinflammation of thefetal membranes (amnion andchorion), usually due tobacterialinfection.[1] In 2015, a National Institute of Child Health and Human Development Workshop expert panel recommended use of the term "triple I" to address the heterogeneity of this disorder. The term triple I refers to intrauterine infection or inflammation or both and is defined by strict diagnostic criteria, but this terminology has not been commonly adopted although the criteria are used.[2]
Chorioamnionitis results from an infection caused by bacteria ascending from the vagina into the uterus and is associated with premature or prolongedlabor.[3] It triggers an inflammatory response to release various inflammatory signaling molecules, leading to increasedprostaglandin andmetalloproteinase release. These substances promote uterine contractions and cervical ripening, causations ofpremature birth.[4] The risk of developing chorioamnionitis increases with number ofvaginal examinations performed in the final month of pregnancy, including labor.[5][6] Tobacco and alcohol use also puts mothers at risk for chorioamnionitis development.[7]
Chorioamnionitis is caught early by looking at signs and symptoms such as fever, abdominal pain, or abnormal vaginal excretion.[8] Administration of antibiotics if the amniotic sac bursts prematurely can prevent chorioamnionitis occurrence.[9]
The signs and symptoms of clinical chorioamnionitis include fever,leukocytosis (>15,000 cells/mm3), maternal (>100 bpm)[10] or fetal (>160 bpm)tachycardia, uterine tenderness and preterm rupture of membranes.[2]
Causes of chorioamnionitis stem from bacterial infection as well as obstetric and other related factors.[3][7]
Bacterial,viral, and evenfungal infections can cause chorioamnionitis. Most commonly fromUreaplasma,Fusobacterium, andStreptococcus bacteria species. Less commonly,Gardnerella,Mycoplasma, andBacteroides bacteria species. Sexually transmitted infections,chlamydia andgonorrhea, can cause development of the condition as well.[7] Studies are continuing to identify other microorganism classes and species as infection sources.[11]
Birthing-related events, lifestyle, and ethnic background have been linked to an increase in the risk of developing chorioamnionitis apart from bacterial causation.[11] Premature deliveries, ruptures of theamniotic sac membranes, prolonged labor, and primigravida childbirth are associated with this condition.[12] At term mothers who experience a combination of pre-labor membrane ruptures and multiple invasive vaginal examinations, prolonged labor, or havemeconium appear in the amniotic fluid are at higher risk than at term mothers experiencing just one of those events.[11] In other studies, smoking, alcohol use and drug use are noted as risk factors. Those of African American ethnicity are noted to be at higher risk.[7][12]
Theamniotic sac consists of two parts:
Chorioamnionitis is diagnosed from ahistologic (tissue) examination of the fetal membranes.[12] Confirmed histologic chorioamnionitis without any clinical symptoms is termed subclinical chorioamnionitis and is more common than symptomatic clinical chorioamnionitis.[2]
Infiltration of the chorionic plate byneutrophils is diagnostic of (mild) chorioamnionitis. More severe chorioamnionitis involves subamniotic tissue and may have fetal membranenecrosis and/orabscess formation.[1]
Severe chorioamnionitis may be accompanied byvasculitis of theumbilical blood vessels due to the fetus' inflammatory cells. If very severe,funisitis, inflammation of the umbilical cord connective tissue, occurs.[12]
The presence of fever between 38.0°C and 39.0°C alone is insufficient to indicate chorioamnionitis and is termedisolated maternal fever. Isolated maternal fever may not have an infectious cause and does not require antibiotic treatment.[2]
When intrapartum (during delivery) fever is higher than 39.0°C, suspected diagnosis of chorioamnionitis can be made. Alternatively, if intrapartum fever is between 38.0°C and 39.0°C, an additional risk factor must be present to make a presumptive diagnosis of chorioamnionitis. Additional risk factors include:[14]
Diagnosis is typically not confirmed until after delivery. However, people with confirmed diagnosis and suspected diagnosis have the same post-delivery treatment regardless of diagnostic status. Diagnosis can be confirmed histologically or through amniotic fluid tests such as gram staining, glucose levels, or other culture results consistent with infection.[14]
If the amniotic sac breaks early into pregnancy, the potential of introducing bacteria in the amniotic fluid can increase. Administering antibiotics maternally can potentially prevent chorioamnionitis and allow for a longer pregnancy.[9] In addition, it has been shown that it is not necessary to deliver the fetus quickly after chorioamnionitis is diagnosed, so a C-section is not necessary unless maternal health concern is present.[12] However, research has found that beginning labor early at approximately 34 weeks can lessen the likelihood of fetal death, and reduce the potential for excessive infection within the mother.[12]
In addition, providers should interview people suspected to have chorioamnionitis about whether they are experiencing signs and symptoms at scheduled obstetrics visits during pregnancy, including whether the individual has experienced excretion vaginally, febrile, or abdominal pain.[8]
The American College of Obstetricians and Gynecologists' Committee Opinion proposes the use of antibiotic treatment in intrapartum mothers with suspected or confirmed chorioamnionitis and maternal fever without an identifiable cause.[14]
Intrapartum antibiotic treatment consists of:[2]
However, there is not enough evidence to support the most efficient antimicrobial regimen.[16] Starting the treatment during the intrapartum period is more effective than starting it postpartum; it shortens the hospital stay for the mother and the neonate.[17] There is currently not enough evidence to dictate how long antibiotic therapy should last. Completion of treatment/cure is only considered after delivery.[2]
Acetaminophen is often used for treating fevers and may be beneficial for fetal tachycardia. There can be increased likelihood for neonatal encephalopathy when mothers have intrapartum fever.[12]
Chorioamnionitis has possible associations with numerous neonatal conditions. Intrapartum (during labor) chorioamnionitis may be associated with neonatalpneumonia,meningitis,sepsis, and death. Long-term infant complications likebronchopulmonary dysplasia,cerebral palsy, andWilson-Mikity syndrome have been associated to the bacterial infection.[14] Furthermore, histological chorioamnionitis may increase the likelihood of newbornnecrotizing enterocolitis, where one or more sections of the bowel die. This occurs when the fetal gut barrier becomes compromised and is more susceptible to conditions like infection and sepsis.[18] In addition, chorioamnionitis can act as a risk factor for premature birth andperiventricular leukomalacia.[19]
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For mother and fetus, chorioamnionitis may lead to short-term and long-term issues when microbes move to different areas or trigger inflammatory responses due to infection.[12]
Mothers with chorioamnionitis who undergo a C-section may be more likely to develop pelvic abscesses, septic pelvic thrombophlebitis, and infections at the surgical site.[11]
In the long-term, infants may be more likely to experiencecerebral palsy or neurodevelopmental disabilities. Disability development is related to the activation of the fetal inflammatory response syndrome (FIRS) when the fetus is exposed to infected amniotic fluid or other foreign entities.[4][12] This systemic response results in neutrophil and cytokine release that can impair the fetal brain and other vital organs.[4][9] Compared to infants with clinical chorioamnionitis, it appears cerebral palsy may occur at a higher rate for those with histologic chorioamnionitis. However, more research needs to be done to examine this association.[22] There is also concern about the impact of FIRS on infant immunity as this is a critical time for growth and development. For instance, it may be linked to chronic inflammatory disorders, such as asthma.[23]
Chorioamnionitis is approximated to occur in about 4%[8] of births in the United States. However, many other factors can increase the risk of chorioamnionitis. For example, in births with premature rupture of membranes (PROM), between 40 and 70% involve chorioamnionitis. Furthermore, clinical chorioamnionitis is implicated in 12% of all cesarean deliveries. Some studies have shown that the risk of chorioamnionitis is higher in those of African American ethnicity, those with immunosuppression, and those who smoke, use alcohol, or abuse drugs.[12]
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