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Temporal Trends in Chorioamnionitis by Maternal Race/Ethnicity and Gestational Age (1995–2010)

DOI: 10.1155/2013/906467

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Abstract:

Objective. To characterize trends in chorioamnionitis (CAM) by maternal race/ethnicity and gestational age. Study Design. We examined trends in CAM from 1995–2010 among singleton births in all Kaiser Permanente Southern California hospitals ( ). Data were extracted from Perinatal Service System and clinical utilization records. Gestational age- and race/ethnicity-specific biannual diagnosis rates were estimated using the Poisson regression after adjusting for potential confounding factors. Results. Overall diagnosis rates of CAM increased from 2.7% in 1995-1996 to 6.0% in 2009-2010 with a relative increase of 126% (95% confidence intervals [CI] 113%–149%). From 1995-1996 to 2009-2010, CAM increased among the Whites (1.8% to 4.3%, -value for trend <.001), Blacks (2.2% to 3.7%, -value for trend <.001), Hispanics (2.4% to 5.8%, -value for trend <.001), and Asian/Pacific Islanders (3.6% to 9.0%, -value for trend <.001). The adjusted relative percentage change in CAM from 1995-1996 to 2009-2010 was for Whites [preterm 21% (9%–78%), term 138% (108%–173%)], for Blacks [preterm 24% (?9%–81%), term 62% (30%–101%)], for Hispanics [preterm 31% (3%–66%), term 135% (114%–159%)], and for Asian/Pacific Islanders [preterm 44% (9%–127%), term 145% (109%–188%)]. Conclusion. The findings suggest that CAM diagnosis rate has increased for all race/ethnic groups. This increase is primarily due to increased diagnosis at term gestation. 1. Introduction Chorioamnionitis, an infection and inflammation of the maternal and fetal interface, is arguably the most important cause of preterm birth and infant morbidity. Despite advancements in diagnosis and treatment, chorioamnionitis and its complications remain major public health concern in the United States. It has been estimated that about 10 percent of all pregnancies are complicated by chorioamnionitis [1, 2]. Documented immediate and long-term sequelae of chorioamnionitis include fetal mortality [3], preterm premature rupture of membranes [4], neonatal intensive care admission [5], bronchopulmonary dysplasia [6, 7], and cerebral palsy [8]. Most importantly, chorioamnionitis is responsible for approximately half of all preterm births [9–11]. Prevalence varies with race/ethnicity and is higher in non-Whites than Whites [12]. The most common route of infection is ascending microbial invasion of the amniotic cavity from upper genital tract [13, 14]. Inflammatory processes at sites remote from the female genital tracts are also described as important sources of infection [15, 16]. There is a gap in knowledge about the recent trends

References

[1]  R. S. Gibbs and P. Duff, “Progress in pathogenesis and management of clinical intraamniotic infection,” American Journal of Obstetrics and Gynecology, vol. 164, no. 5, pp. 1317–1326, 1991.
[2]  D. Getahun, D. Strickland, R. S. Zeiger et al., “Effect of chorioamnionitis on early childhood asthma,” Archives of Pediatrics & Adolescent Medicine, vol. 164, no. 2, pp. 187–192, 2010.
[3]  D. Getahun, C. V. Ananth, and W. L. Kinzler, “Risk factors for antepartum and intrapartum stillbirth: a population-based study,” American Journal of Obstetrics and Gynecology, vol. 196, no. 6, pp. 499–507, 2007.
[4]  Y. Tasci, B. Dilbaz, B. Uzmez Onal et al., “The value of cord blood interleukin-6 levels for predicting chorioamnionitis, funisitis and neonatal infection in term premature rupture of membranes,” European Journal of Obstetrics, Gynecology, and Reproductive Biology, vol. 128, pp. 34–39, 2006.
[5]  S. Marret, P. Y. Ancel, L. Marpeau et al., “Neonatal and 5-year outcomes after birth at 30-34 weeks of gestation,” Obstetrics and Gynecology, vol. 110, no. 1, pp. 72–80, 2007.
[6]  P. Groneck, B. Gotze-Speer, M. Oppermann, H. Eiffert, and C. P. Speer, “Association of pulmonary inflammation and increased microvascular permeability during the development of bronchopulmonary dysplasia: a sequential analysis of inflammatory mediators in respiratory fluids of high- risk preterm neonates,” Pediatrics, vol. 93, no. 5, pp. 712–718, 1994.
[7]  C. P. Speer, “Inflammation and bronchopulmonary dysplasia,” Seminars in Neonatology, vol. 8, no. 1, pp. 29–38, 2003.
[8]  Y. W. Wu, G. J. Escobar, J. K. Grether, L. A. Croen, J. D. Greene, and T. B. Newman, “Chorioamnionitis and cerebral palsy in term and near-term infants,” Journal of the American Medical Association, vol. 290, no. 20, pp. 2677–2684, 2003.
[9]  R. L. Goldenberg, J. C. Hauth, and W. W. Andrews, “Intrauterine infection and preterm delivery,” The New England Journal of Medicine, vol. 342, no. 20, pp. 1500–1507, 2000.
[10]  R. S. Gibbs, R. Romero, S. L. Hillier, D. A. Eschenbach, and R. L. Sweet, “A review of premature birth and subclinical infection,” American Journal of Obstetrics and Gynecology, vol. 166, no. 5, pp. 1515–1528, 1992.
[11]  R. L. Goldenberg and D. J. Rouse, “Prevention of premature birth,” The New England Journal of Medicine, vol. 339, no. 5, pp. 313–320, 1998.
[12]  C. Holzman, X. Lin, P. Senagore, and H. Chung, “Histologic chorioamnionitis and preterm delivery,” American Journal of Epidemiology, vol. 166, no. 7, pp. 786–794, 2007.
[13]  M. A. Krohn, S. L. Hillier, R. P. Nugent et al., “The genital flora of women with intraamniotic infection,” Journal of Infectious Diseases, vol. 171, no. 6, pp. 1475–1480, 1995.
[14]  M. Abele-Horn, M. Scholz, C. Wolff, and M. Kolben, “High-density vaginal ureaplasma urealyticum colonization as a risk factor for chorioamnionitis and preterm delivery,” Acta Obstetricia et Gynecologica Scandinavica, vol. 79, no. 11, pp. 973–978, 2000.
[15]  S. Offenbacher, S. Lieff, K. A. Boggess et al., “Maternal periodontitis and prematurity. Part I: obstetric outcome of prematurity and growth restriction,” Annals of Periodontology, vol. 6, no. 1, pp. 164–174, 2001.
[16]  P. N. Madianos, S. Lieff, A. P. Murtha et al., “Maternal periodontitis and prematurity. Part II: maternal infection and fetal exposure,” Annals of Periodontology, vol. 6, no. 1, pp. 175–182, 2001.
[17]  American College of Obstetrics and Gynecology (ACOG), “ACOG practice bulletin no. 107: induction of labor,” Obstetrics & Gynecology, vol. 114, pp. 386–397, 2009.
[18]  E. R. Newton, T. J. Prihoda, and R. S. Gibbs, “Logistic regression analysis of risk factors for intra-amniotic infection,” Obstetrics and Gynecology, vol. 73, no. 4, pp. 571–575, 1989.
[19]  D. E. Soper, C. G. Mayhall, and H. P. Dalton, “Risk factors for intraamniotic infection: a prospective epidemiologic study,” American Journal of Obstetrics and Gynecology, vol. 161, no. 3, pp. 562–568, 1989.
[20]  M. B. Greenberg, Y. W. Cheng, L. M. Hopkins, N. E. Stotland, A. S. Bryant, and A. B. Caughey, “Are there ethnic differences in the length of labor?” American Journal of Obstetrics and Gynecology, vol. 195, no. 3, pp. 743–748, 2006.
[21]  A. Ohlsson and V. S. Shah, “Intrapartum antibiotics for known maternal Group B streptococcal colonization,” Cochrane Database of Systematic Reviews, no. 3, Article ID CD007467, 2009.
[22]  J. M. Alexander, D. M. McIntire, and K. J. Leveno, “Chorioamnionitis and the prognosis for term infants,” Obstetrics and Gynecology, vol. 94, no. 2, pp. 274–278, 1999.
[23]  D. J. Rouse, M. Landon, K. J. Leveno et al., “The maternal-fetal medicine units cesarean registry: chorioamnionitis at term and its duration—relationship to outcomes,” American Journal of Obstetrics and Gynecology, vol. 191, no. 1, pp. 211–216, 2004.

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