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16 June 2017: Articles  USA

Premature Labor and Neonatal Septicemia Caused by Capnocytophaga Ochracea

Challenging differential diagnosis, Diagnostic / therapeutic accidents, Management of emergency care, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)

Abdullah A. Alhifany ABDEF 1*, Thamer A. Almangour ABDEF 2, Deanne E. Tabb ABDEF 3, David H. Levine D 3

DOI: 10.12659/AJCR.903824

Am J Case Rep 2017; 18:674-676

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Abstract

BACKGROUND: Capnocytophaga ochracea is a gram-negative anaerobic organism commonly found in human oral flora. It is characteristically sensitive to beta-lactams and resistant to aminoglycosides.

CASE REPORT: A 23-year-old woman presented with lower abdominal pain and was admitted for premature labor at 24-weeks of gestation. At presentation, the cervix was closed and the membrane was intact; however, contractions continued, the membrane subsequently ruptured before receiving any steroids or magnesium, and the mother gave birth to a 540-gram female baby. At birth, Apgar scores were 1 at 5 minutes, 1 at 10 minutes, and 2 at 15 minutes. On the fifth day of life, the blood culture grew Capnocytophaga species. Consequently, Cefotaxime was started and ampicillin continued for a total of 14 days; however, on the 6th day, the head ultrasound showed grade 4 intraventricular hemorrhage and a Do Not Resuscitate (DNR) order was placed in the chart. The patient’s health continued to deteriorate, having multiple episodes of bradycardia and desaturation until cardiac arrest on the 17th day.

CONCLUSIONS: Capnocytophaga ochracea was isolated from the blood culture of a preterm neonate. It was thought to be the cause of the premature labor and subsequent neonatal septicemia. This case report suggests that the prevalence of Capnocytophaga infections is most likely underestimated and that additional premature labors and abortions could have been caused by Capnocytophaga infections that were never detected. Hence, more studies are needed to investigate the route of transmission.

Keywords: Bacteremia, Capnocytophaga, Infant, Newborn, Obstetric Labor, Premature, Sepsis

Background

The genus Capnocytophaga consists of gram-negative fastidious anaerobic organisms [1,2]. The genus consists of 8 species that are usually isolated from the oral cavity; however, these organisms are opportunistic pathogens and have been described in 5 major types of infections: septicemia, central nervous system (CNS) infections, eye infections, illnesses associated with pregnancy, and infections of bone and tissue [1,2]. These infections mainly occur in immunocompromised patients, but may also occur in immunocompetent hosts. Even though this genus is rarely isolated from the female genital tract, several case reports attribute intrauterine, intra-amniotic, and perinatal organism invasion to both uncomplicated and complicated infections. Generally, these infections are often polymicrobial in origin and the role of Capnocytophaga in their pathogenesis remains unclear [1,2]. Organism identification is challenging; they grow very slowly and are identified using classic biochemical methods and molecular techniques [2].

Capnocytophaga ochracea and 2 other species, Capnocytophaga sputigena and Capnocytophaga gingivalis were formerly known as Bacteroides ochracea [2]. These 3 organisms are characterized as fastidious, fusiform, non-spore forming, gliding, gram-negative bacilli. They are usually found in the oral cavity of humans, contribute to early plaque formation, and have been associated with periodontal diseases [2,3]. Capnocytophaga ochracea is known to cause sepsis, purpura fulminans, and gangrene in immunocompromised patients [2]. The mortality rate is 14–43%. Additionally, intrauterine infections, endocarditis, and septic arthritis can also occur in immunocompetent patients [2]. Capnocytophaga ochracea has the capacity to form biofilms, which play a role in the coaggregation of other bacteria and plaque formation, and could also play a role in the degree of virulence and resistance [2]. The present case is considered the third confirmed case of Capnocytophaga ochracea of proven early neonatal septicemia, based on the evidence of positive cultures of Capnocytophaga ochracea from neonatal blood samples [4,5].

Case Report

A 23-year-old primigravida (gravida 1, para 0) presented with lower abdominal pain and was admitted for premature labor at 24 weeks of gestation. She had received prenatal care; however, the pregnancy was complicated with maternal hypertension and a chlamydia infection that was treated. The cervix was closed and the membrane was intact at presentation; however, the blood leukocyte count was 21.89×109/L, contractions continued, the membrane subsequently ruptured, and the mother gave birth via vaginal delivery to a female baby within 6 hours of admission. The mother did not receive any steroids, antibiotics, or magnesium prior to delivery.

The baby weighed 540 grams at birth and Apgar scores were 1 at 5 minutes, 1 at 10 minutes, and 2 at 15 minutes. The baby’s heart rate was less than 100 without any respiration. The baby was then transferred to NICU and intubated successfully within 15 minutes of life and was given a dose of surfactant. Ampicillin and gentamicin were started to rule out early-onset sepsis of the newborn. Fluconazole prophylaxis was also initiated. On the fifth day of life, the blood culture grew Capnocytophaga species. The isolate was sent to a reference laboratory for further speciation. Gentamicin was changed to cefotaxime and ampicillin to be continued for a total of 14 days. On the 6th day, the head ultrasound showed grade 4 intraventricular hemorrhage and a DNR order was placed in the chart. The baby’s health continued to deteriorate, having multiple episodes of bradycardia and desaturation until cardiac arrest on the 17th day.

Discussion

Only 2 previous case reports have reported perinatal infection caused by Capnocytophaga ochracea (Table 1) [4,5]. The first case of Capnocytophaga ochracea, reported by Paerregaard et al., was isolated from a blood sample of a mother that had given birth to a preterm infant after 28 weeks of gestation [4]. Capnocytophaga was not isolated from the baby because ampicillin and gentamicin were initiated immediately after birth to rule out sepsis before microbiological samples were obtained. Capnocytophaga is sensitive to ampicillin and could have caused a false-negative culture [4]. In the second case of Capnocytophaga ochracea, reported by Mayatebek et al., the sample was isolated from the mother’s endometrium and the preterm infant’s blood and gastric aspirate [5]. The infant was born after only 24 weeks of gestation and had also developed grade III intracranial hemorrhage, similar to our reported case, yet the baby survived [5]. Reports suggest that the prevalence of Capnocytophaga infections is most likely underestimated and that additional premature labors and abortions could have been caused by Capnocytophaga infections that were never detected [6–8]. Several studies have investigated the route of transmission, and 2 theories have been proposed; one suggested that maternal periodontal disease could increase the risk of premature labor. However, 2 randomized controlled trials enrolled 922 pregnant women found that treatment of maternal periodontal disease did not significantly alter the rate of preterm birth [9,10]. Three case reports suggested that oral sex during the third trimester could cause Capnocytophaga ochracea to ascend to the amniotic fluid, especially after isolating Capnocytophaga spp. from partners with periodontal infections [11–13]. However, more studies are needed to confirm any association between oral sex in the third trimester, premature labor, and neonatal septicemia.

Conclusions

Capnocytophaga ochracea was isolated from the blood culture of a preterm neonate. It was thought to be the cause of the premature labor and subsequent neonatal septicemia. This case report suggests that the prevalence of Capnocytophaga infections is likely underestimated and that additional premature labors and abortions could have been caused by Capnocytophaga infections that were never detected. Hence, more studies are needed to investigate the route of transmission.

References:

1.. Frandsen EVG, Poulsen K, Könönen E: J Syst Evol Microbiol, 2008; 58; 324-36

2.. Bonatti H, Rossboth DW, Nachbaur D: Clin Microbiol Infect, 2003; 9(5); 380-87, pmid: 12848750

3.. Peterson SN, Snesrud E, Liu J, The dental plaque microbiome in health and disease: PLoS One, 2013; 8(3); e58487, pmid: 23520516

4.. Paerregaard A, Gutschik E: Eur J Clin Microbiol, 1987; 6(5); 580-81, pmid: 3436319

5.. Mayatepek E, Zilow E, Pohl S: Biol Neonate, 1991; 60(3–4); 184-86, pmid: 1797120

6.. Offenbacher S, Maternal periodontal infections, prematurity, and growth restriction: Clin Obstet Gynecol, 2004; 47(4); 808-21, pmid: 15596935 discussion 881–82

7.. Michalowicz BS, Hodges JS, DiAngelis AJ, Treatment of periodontal disease and the risk of preterm birth: N Engl J Med, 2006; 355(18); 1885-94, pmid: 17079762

8.. Goepfert AR, Jeffcoat MK, Andrews WW, Periodontal disease and upper genital tract inflammation in early spontaneous preterm birth: Obstet Gynecol, 2004; 104(4); 777-83, pmid: 15458901

9.. Michalowicz BS, Hodges JS, DiAngelis AJ, Treatment of periodontal disease and the risk of preterm birth: N Engl J Med, 2006; 355(18); 1885-94, pmid: 17079762

10.. Pirie M, Linden G, Irwin C, Intrapregnancy non-surgical periodontal treatment and pregnancy outcome: A randomized controlled trial: J Periodontol, 2013; 84(10); 1391-400, pmid: 23237583

11.. Hansen LM, Dorsey TA, Batzer FA, Donnenfeld AE: Obstet Gynecol, 1996; 88(4 Pt 2); 731, pmid: 8841277

12.. Edwards C, Yi CH, Currie JL: Am J Obstet Gynecol, 1995; 173(1); 244-45, pmid: 7631698

13.. Dixon NG, Ebright D, Defiancessco MA, Hawkins RE, Orogenital contact: A cause of chorioamnionitis?: Obstet Gynecol, 1994; 84(4 Pt 2); 654-55, pmid: 9205437

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923