Chorioamnionitis

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Continuing Education Activity

Chorioamnionitis is an infection that can occur before labor, during labor, or after delivery. It can be acute, subacute, or chronic. Chorioamnionitis is associated with chronic lung disease in the infant. Chronic chorioamnionitis is associated with retinopathy of prematurity, very low birth weight, and impaired brain development in the premature infant. Chronic chorioamnionitis is common. Most commonly, chorioamnionitis is associated with preterm labor, prolonged rupture of membranes, prolonged labor, tobacco use, nulliparous pregnancy, meconium-stained fluid, multiple vaginal exams post rupture of membranes, and in women with known bacterial or viral infections. However, it can occur at term and in women without prior infections. Chorioamnionitis can lead to morbidity and mortality for the mother and neonate if left untreated. Antibiotic therapy has been shown to reduce the incidence and severity of the infection in both the mother and neonate. This activity describes the clinical evaluation of chorioamnionitis and explains the health professional team's role in coordinating the care of patients with this condition.

Objectives:

  • Outline the cause of chorioamnionitis.
  • Describe the presentation of chorioamnionitis.
  • Summarize the treatment of chorioamnionitis.
  • Outline the clinical evaluation of chorioamnionitis and explain the role of the health professional team in coordinating the care of patients with this condition.

Introduction

Chorioamnionitis is an infection that can occur before labor, during labor, or after delivery. It can be acute, subacute, or chronic. Chorioamnionitis is associated with chronic lung disease in the infant.[1] Chronic chorioamnionitis is associated with retinopathy of prematurity, very low birth weight, and impaired brain development in the premature infant. Chronic chorioamnionitis is common.[2][3][4] This terminology refers to histologic chorioamnionitis. Histologic chorioamnionitis at term is rarely infectious.

In general, the clinical presentation of chorioamnionitis is defined as acute chorioamnionitis. The Greek etymology of the words chorion and amnion mean fetal membrane, and itis means inflammation. Further description denotes chorioamnionitis includes the amniotic fluid. Chorioamnionitis may be identified either postdelivery or postmortem on a pathological review of the placenta and cord. In histologic chorioamnionitis, symptoms may be absent, and the placenta or cultures may not show evidence of chorioamnionitis.

Most commonly, chorioamnionitis is associated with preterm labor, prolonged rupture of membranes, prolonged labor, tobacco use, nulliparous pregnancy, meconium-stained fluid, multiple vaginal exams post rupture of membranes, and in women with known bacterial or viral infections. However, it can occur at term and in women without prior infections. Chorioamnionitis can lead to morbidity and mortality for the mother and neonate if left untreated. Neonatal morbidity and mortality increase in severity and occurrence with earlier gestations. Antibiotic therapy has been shown to reduce the incidence and severity of the infection in both the mother and neonate. 

Etiology

The literature defines chorioamnionitis as an inflammatory and infectious process. Inflammation in utero is linked to preterm birth, brain abnormalities, and retinopathy.[5][6][7] Infection can be due to bacterial, fungal, or viral agents. Bacterial agents in chorioamnionitis can vary depending on the geographic location and population. Common bacterial agents found in chorioamnionitis include group B streptococcus, Mycoplasma pneumoniae[8], Ureaplasma, Gardnerella vaginalis, Escherichia coli, and Bacteroides. Candida species are identified as risk factors for chorioamnionitis, leading to preterm birth and adverse fetal outcomes.[9][10] In adolescents with sexually transmitted infections, studies show that trichomoniasis is a risk factor for the development of chorioamnionitis. Although chorioamnionitis is a risk factor for vertical transmission in pregnancy, the maternal HIV status is not a risk factor for chorioamnionitis. In one study of 298 women with similar risk factors and demographics, both groups of women had a high incidence of chorioamnionitis. The higher incidence for each group was strongly associated with the number of vaginal exams during labor.[11]

Epidemiology

Chorioamnionitis occurs in about 4% of deliveries at term but occurs more frequently in preterm deliveries and premature rupture of membranes. In evaluating women with symptoms of chorioamnionitis, studies show a strong correlation between histologic chorioamnionitis and the key clinical symptoms of fever, uterine tenderness, meconium aspiration syndrome, and foul-smelling vaginal discharge.[12][13] Histologic chorioamnionitis with vasculitis is associated with a higher incidence of premature rupture of membranes and preterm delivery.[5]

In deliveries between 21 and 24 weeks gestation, histological chorioamnionitis can be found in more than 94% of cases.[14] Term deliveries of mothers with chorioamnionitis are associated with failure to progress. Chorioamnionitis in preterm labor is likely to end in preterm delivery. Studies show that the placenta or chorioamnionitis inflammation can be found in approximately 8% to 50% of preterm deliveries.[15][16] In the term pregnancy, chorioamnionitis is most likely associated with labor and a history of prolonged ruptured membranes.

Pathophysiology

Chorioamnionitis is an ascending infection, originating in the lower genitourinary tract and migrating to the amniotic cavity. The infection usually originates from the cervical and vaginal area. Vertical transmission has been documented in bacterial and viral infections transmitted to the fetus.[8]

Histopathology

Chorioamnionitis is an inflammatory process that ranges from mild to severe. Histopathologic findings consistent with inflammation also can be present in the placentas of women with normal pregnancy.[17]

In chorioamnionitis, the membranes may appear normal or show evidence of infection. Fluid can be clear or cloudy. There is neutrophilic infiltration into the decidua on histologic examination, and in more severe cases, microabscesses are present. A recent study suggests that neutrophils in the amniotic cavity are mostly of fetal origin. In extreme prematurity, maternal and fetal neutrophils are more likely to be present in the amniotic cavity with chorioamnionitis.[18]

History and Physical

The initial history should include maternal age, gestational age, parity, highlights of the pregnancy including any complications, whether membranes are ruptured or intact, the presence of meconium, presence of or history of sexually transmitted infections, urinary tract infections, and recent illness. The physical exam must be thorough and include vitals and complete physical evaluation, including the abdomen, vagina, and uterus.Chorioamnionitis presents as a febrile illness associated with an elevated white blood cell (WBC) count, uterine tenderness, abdominal pain, foul-smelling vaginal discharge, and fetal and maternal tachycardia. Diagnosing clinical chorioamnionitis includes fever of at least 39 C (102.2 F) or between 38 C (100.4 F) and 39 C (102.2 F) within 30 minutes and one of the clinical symptoms. The majority of women presenting with chorioamnionitis are in labor or have ruptured membranes.

Evaluation

Initial evaluation for chorioamnionitis includes a thorough clinical assessment of the mother and fetus. Although the maternal WBC count is a routine test done when there is suspicion of an infection, recent studies show that the WBC count does not identify the presence of microbial invasion or inflammation in the amniotic cavity for women with premature rupture of membranes on admission.[19]The WBC count also has low sensitivity and specificity. Bacterial cultures taken from the cervix are not indicated and do not correlate with infection secondary to chorioamnionitis.[20]

Treatment / Management

The primary management of chorioamnionitis is antibiotic therapy. The most common antibiotics used are ampicillin and gentamicin. Alternative antibiotics include clindamycin, cefazolin, and vancomycin in women allergic to penicillin. After delivery, the current recommendation is to administer one additional dose with a cesarean section but no additional antibiotics for vaginal deliveries. Additional broad-spectrum antibiotics may be required, depending on the clinical status.[21]

Differential Diagnosis

Abdominal pain and uterine tenderness associated with fever are nonspecific signs. Women with fever, pain, and tenderness during labor must be evaluated for other common infections such as appendicitis, urinary tract infection, pyelonephritis, and pneumonia. Additional ancillary testing and examination must be thoroughly reviewed before making a final diagnosis.

Prognosis

Chorioamnionitis is a risk factor for both maternal and neonatal sequelae. Endometritis can occur in up to one-third of women treated for chorioamnionitis who undergo a cesarean section. The rate of endometritis is the same in vaginal deliveries and cesarean deliveries following chorioamnionitis. Recent studies show that management with postpartum antibiotics does not decrease the risk of endometritis following chorioamnionitis.[22]

The majority of women with chorioamnionitis will recover and not require further antibiotics after delivery.

Complications

Neonatal complications of chorioamnionitis include premature birth, cerebral palsy, retinopathy of prematurity, neurologic abnormalities, respiratory distress syndrome, bronchopulmonary dysplasia in premature infants, neonatal sepsis, and neonatal death. Neonatal sepsis is suspected as a complication of chorioamnionitis; however, in more than 99% of cases, cultures are negative. Perinatal listeriosis is associated with high morbidity. Current antibiotic regimens may not cover listeriosis in chorioamnionitis.

Maternal complications of chorioamnionitis include severe pelvic infections, subcutaneous wound infections, preterm delivery, postpartum hemorrhage, operative delivery, and maternal sepsis.

Chorioamnionitis is associated with vertical transmission of HIV in pregnancy.[23][24]

Deterrence and Patient Education

Patients who are pregnant should receive routine counseling at each prenatal visit. Education should include reporting rupture of membranes, vaginal discharge, fever, and abdominal pain to their obstetrical provider. Every woman should receive information on risk factors and signs and symptoms of infection during the prenatal period.

Enhancing Healthcare Team Outcomes

Women presenting with abdominal pain, uterine tenderness, and fever during labor must be evaluated for other causes. In women with premature rupture of membranes, the interprofessional team must consider the risk of multiple examinations and avoid multiple digital exams. Nursing and physician communication is important to assure the initial examination is done with a sterile speculum. Clear communication is also required between team members to ensure the physician is alerted to any changes in pain, fever, or clinical status. Obstetrical nurses administer care, monitor patients, and provide feedback to the team.When choosing antibiotics, medical records should be reviewed thoroughly, giving special attention to the history of allergies and any previous reactions to penicillin or any other antibiotics. This information must be reported to the pharmacy when ordering medication and reviewed by the team. Pharmacists review medications prescribed, check for drug-drug interactions, and may participate in patient education.If the patient requires a cesarean section, these items must be reviewed again during the time out in the operating room. [Level 5]


Details

Editor:

Leslie V. Simon

Updated:

9/4/2023 6:15:42 PM

References


[1]

Ohyama M, Itani Y, Yamanaka M, Goto A, Kato K, Ijiri R, Tanaka Y. Re-evaluation of chorioamnionitis and funisitis with a special reference to subacute chorioamnionitis. Human pathology. 2002 Feb:33(2):183-90     [PubMed PMID: 11957143]


[2]

Bennet L, Dhillon S, Lear CA, van den Heuij L, King V, Dean JM, Wassink G, Davidson JO, Gunn AJ. Chronic inflammation and impaired development of the preterm brain. Journal of reproductive immunology. 2018 Feb:125():45-55. doi: 10.1016/j.jri.2017.11.003. Epub 2017 Nov 26     [PubMed PMID: 29253793]


[3]

Miyano A, Miyamichi T, Nakayama M, Kitajima H, Shimizu A. Differences among acute, subacute, and chronic chorioamnionitis based on levels of inflammation-associated proteins in cord blood. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 1998 Nov-Dec:1(6):513-21     [PubMed PMID: 9724338]


[4]

Kim CY, Jung E, Kim EN, Kim CJ, Lee JY, Hwang JH, Song WS, Lee BS, Kim EA, Kim KS. Chronic Placental Inflammation as a Risk Factor of Severe Retinopathy of Prematurity. Journal of pathology and translational medicine. 2018 Sep:52(5):290-297. doi: 10.4132/jptm.2018.07.09. Epub 2018 Jul 16     [PubMed PMID: 30008195]


[5]

Palmsten K, Nelson KK, Laurent LC, Park S, Chambers CD, Parast MM. Subclinical and clinical chorioamnionitis, fetal vasculitis, and risk for preterm birth: A cohort study. Placenta. 2018 Jul:67():54-60. doi: 10.1016/j.placenta.2018.06.001. Epub 2018 Jun 6     [PubMed PMID: 29941174]


[6]

Bierstone D, Wagenaar N, Gano DL, Guo T, Georgio G, Groenendaal F, de Vries LS, Varghese J, Glass HC, Chung C, Terry J, Rijpert M, Grunau RE, Synnes A, Barkovich AJ, Ferriero DM, Benders M, Chau V, Miller SP. Association of Histologic Chorioamnionitis With Perinatal Brain Injury and Early Childhood Neurodevelopmental Outcomes Among Preterm Neonates. JAMA pediatrics. 2018 Jun 1:172(6):534-541. doi: 10.1001/jamapediatrics.2018.0102. Epub     [PubMed PMID: 29610829]


[7]

Garcia-Flores V, Romero R, Miller D, Xu Y, Done B, Veerapaneni C, Leng Y, Arenas-Hernandez M, Khan N, Panaitescu B, Hassan SS, Alvarez-Salas LM, Gomez-Lopez N. Inflammation-Induced Adverse Pregnancy and Neonatal Outcomes Can Be Improved by the Immunomodulatory Peptide Exendin-4. Frontiers in immunology. 2018:9():1291. doi: 10.3389/fimmu.2018.01291. Epub 2018 Jun 18     [PubMed PMID: 29967606]


[8]

Huber BM, Meyer Sauteur PM, Unger WWJ, Hasters P, Eugster MR, Brandt S, Bloemberg GV, Natalucci G, Berger C. Vertical Transmission of Mycoplasma pneumoniae Infection. Neonatology. 2018:114(4):332-336. doi: 10.1159/000490610. Epub 2018 Aug 8     [PubMed PMID: 30089291]


[9]

Rivasi F, Gasser B, Bagni A, Ficarra G, Negro RM, Philippe E. Placental candidiasis: report of four cases, one with villitis. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica. 1998 Dec:106(12):1165-9     [PubMed PMID: 10052725]

Level 3 (low-level) evidence

[10]

Maki Y, Fujisaki M, Sato Y, Sameshima H. Candida Chorioamnionitis Leads to Preterm Birth and Adverse Fetal-Neonatal Outcome. Infectious diseases in obstetrics and gynecology. 2017:2017():9060138. doi: 10.1155/2017/9060138. Epub 2017 Oct 17     [PubMed PMID: 29180840]


[11]

Newman T, Cafardi JM, Warshak CR. Human immunodeficiency virus-associated pulmonary arterial hypertension diagnosed postpartum. Obstetrics and gynecology. 2015 Jan:125(1):193-195. doi: 10.1097/AOG.0000000000000504. Epub     [PubMed PMID: 25560124]


[12]

Suzuki S. Association between clinical chorioamnionitis and histological funisitis at term. Journal of neonatal-perinatal medicine. 2019:12(1):37-40. doi: 10.3233/NPM-17155. Epub     [PubMed PMID: 30040750]


[13]

Kim B, Oh SY, Kim JS. Placental Lesions in Meconium Aspiration Syndrome. Journal of pathology and translational medicine. 2017 Sep:51(5):488-498. doi: 10.4132/jptm.2017.07.20. Epub 2017 Aug 9     [PubMed PMID: 28793392]


[14]

Kim CJ, Romero R, Chaemsaithong P, Chaiyasit N, Yoon BH, Kim YM. Acute chorioamnionitis and funisitis: definition, pathologic features, and clinical significance. American journal of obstetrics and gynecology. 2015 Oct:213(4 Suppl):S29-52. doi: 10.1016/j.ajog.2015.08.040. Epub     [PubMed PMID: 26428501]


[15]

Perkins RP, Zhou SM, Butler C, Skipper BJ. Histologic chorioamnionitis in pregnancies of various gestational ages: implications in preterm rupture of membranes. Obstetrics and gynecology. 1987 Dec:70(6):856-60     [PubMed PMID: 3684120]


[16]

Conti N, Torricelli M, Voltolini C, Vannuccini S, Clifton VL, Bloise E, Petraglia F. Term histologic chorioamnionitis: a heterogeneous condition. European journal of obstetrics, gynecology, and reproductive biology. 2015 May:188():34-8. doi: 10.1016/j.ejogrb.2015.02.034. Epub 2015 Feb 26     [PubMed PMID: 25770845]


[17]

Romero R, Kim YM, Pacora P, Kim CJ, Benshalom-Tirosh N, Jaiman S, Bhatti G, Kim JS, Qureshi F, Jacques SM, Jung EJ, Yeo L, Panaitescu B, Maymon E, Hassan SS, Hsu CD, Erez O. The frequency and type of placental histologic lesions in term pregnancies with normal outcome. Journal of perinatal medicine. 2018 Aug 28:46(6):613-630. doi: 10.1515/jpm-2018-0055. Epub     [PubMed PMID: 30044764]


[18]

Gomez-Lopez N, Romero R, Xu Y, Leng Y, Garcia-Flores V, Miller D, Jacques SM, Hassan SS, Faro J, Alsamsam A, Alhousseini A, Gomez-Roberts H, Panaitescu B, Yeo L, Maymon E. Are amniotic fluid neutrophils in women with intraamniotic infection and/or inflammation of fetal or maternal origin? American journal of obstetrics and gynecology. 2017 Dec:217(6):693.e1-693.e16. doi: 10.1016/j.ajog.2017.09.013. Epub 2017 Sep 28     [PubMed PMID: 28964823]


[19]

Musilova I, Pliskova L, Gerychova R, Janku P, Simetka O, Matlak P, Jacobsson B, Kacerovsky M. Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes. PloS one. 2017:12(12):e0189394. doi: 10.1371/journal.pone.0189394. Epub 2017 Dec 12     [PubMed PMID: 29232399]


[20]

Saghafi N, Pourali L, Ghazvini K, Maleki A, Ghavidel M, Karbalaeizadeh Babaki M. Cervical bacterial colonization in women with preterm premature rupture of membrane and pregnancy outcomes: A cohort study. International journal of reproductive biomedicine. 2018 May:16(5):341-348     [PubMed PMID: 30027150]


[21]

. Committee Opinion No. 712: Intrapartum Management of Intraamniotic Infection. Obstetrics and gynecology. 2017 Aug:130(2):e95-e101. doi: 10.1097/AOG.0000000000002236. Epub     [PubMed PMID: 28742677]

Level 3 (low-level) evidence

[22]

Shanks AL, Mehra S, Gross G, Colvin R, Harper LM, Tuuli MG. Treatment Utility of Postpartum Antibiotics in Chorioamnionitis Study. American journal of perinatology. 2016 Jul:33(8):732-7. doi: 10.1055/s-0036-1571327. Epub 2016 Feb 18     [PubMed PMID: 26890440]


[23]

Chi BH, Mudenda V, Levy J, Sinkala M, Goldenberg RL, Stringer JS. Acute and chronic chorioamnionitis and the risk of perinatal human immunodeficiency virus-1 transmission. American journal of obstetrics and gynecology. 2006 Jan:194(1):174-81     [PubMed PMID: 16389028]


[24]

Ocheke AN, Agaba PA, Imade GE, Silas OA, Ajetunmobi OI, Echejoh G, Ekere C, Sendht A, Bitrus J, Agaba EI, Sagay AS. Chorioamnionitis in pregnancy: a comparative study of HIV-positive and HIV-negative parturients. International journal of STD & AIDS. 2016 Mar:27(4):296-304. doi: 10.1177/0956462415580887. Epub 2015 Apr 16     [PubMed PMID: 25887063]

Level 2 (mid-level) evidence