Home            Past Issues            About IP            About IAP           Author Information            Subscription            Advertisement              Search  

   
research brief

Indian Pediatr 2011;48: 723-725

Outbreak of Sphingomonas paucimobilis Septicemia in a Neonatal Intensive Care Unit


Mehmet Mutlu, *Gülçin Bayramoglu, Gürdal Yilmaz, Berna Saygin and Yakup Aslan

From the Departments of Pediatrics, *Microbiology and Clinical Microbiology, and Infection Diseases, Karadeniz Technical University, Trabzon, Turkey.

Correspondence to: Dr Mehmet Mutlu, Kalkinma Mah. Farabi Hastanesi, Department of Pediatrics, Karadeniz Technical University, Trabzon, Turkey.
Email: [email protected]

Received: October 25, 2010;
Initial review: December 2, 2010;
Accepted: December 22, 2010.

PII:S09747559INPE1000369-2
 

Abstract

We describe an outbreak of Sphingomonas paucimobilis in 13 newborn infants with septicemia and septic shock. Fifteen available isolates were obtained from patients and distilled water. Pulsed-field gel electrophoresis showed that there was a cross-transmission of S. paucimobilis in eleven patients but these types were not the same the isolate obtained from the distilled water. The outbreak was terminated by taking appropriate control measures for infection and change of source of distilled water.

Key words: Neonate, Outbreak, Sepsis, Sphingomonas paucimobilis, Turkey.

 


Sphingomonas paucimobilis
is an aerobic, weakly oxidase-positive, catalase-positive, motile, glucose non-fermenting and gram-negative rod. This microorganism has been isolated from the hospital water systems, mechanical ventilators, soil, and different clinical specimens [1]. S. paucimobilis can cause nosocomial and community-acquired infections [1,2]. Although nosocomial outbreaks of S. paucimobilis bacteremia have been reported in pediatric wards [3], it has rarely been reported in neonatal intensive care unit (NICU) [4].
We report an outbreak of septicemia caused by S. paucimobilis in 13 neonates in a NICU.

Methods

Medical charts of all the newborns having a blood culture positive for S. paucimobilis were reviewed for the following factors: birthweight; gestational age; delivery type; gender; postnatal age at time of admission to the NICU; sepsis related death; exposure to antimicrobial agents; receiving total parental nutrition (TPN); histamine 2-blockers and steroids; staying in incubator; invasive and procedures such as mechanical ventilation, central catheterization and operation. Newborns with S. paucimobilis infection were included if they had spent at least 48 hours in NICU before their positive cultures and fulfilled the criteria for having sepsis and septic shock [5].

Cultures were obtained from the hands of healthcare workers and environment of NICU to identify the source. All the isolates were analyzed by pulsed-field gel electrophoresis (PFGE) using XbaI endonuclease. PFGE patterns were compared accor-ding to the criteria established by Tenover, et al. [6].

To determine the potential risk factors for S. paucimobilis septicemia, a matched case-control study was performed by comparing each case of S. paucimobilis to two uninfected controls and one case of extended-spectrum beta-lactamase-producing Klebsiella pneumoniae blood stream infection. Controls were infants who (a) were hospitalized in the NICU during the same period and their cultures negative for epidemic strain, (b) had been in the NICU for at least 48 hours during the outbreak, and (c) had a primary diagnosis that was similar of the infants with S. paucimobilis infections. We compared S. paucimobilis infections with K. pneumoniae infection, because K. pneumoniae is the most common GNR causative agent for nosocomial sepsis in our unit.

Results

Fifteen isolates of S. paucimobilis were identified between October 7, 2008 and November 15, 2008. Two of them (13.3%) were isolated from the distilled water, and 13 (86.7%) from the blood sample of the newborn babies. Twelve neonates had sepsis and one premature newborn had septic shock.

TABLE I Characteristics and Potential Risk Factors in Culture Postive and Uninfected Controls
Characteristic Culture positive for Controls
S. paucimobilis (n=13) K. pneumoniae (n=13)  (n=26)
Birthweight (g) 2172±1003 2303±1112 2302±658
Gestational age (wks) 33.7±4.9 34.6±4.4 34.1±2.5
Preterm labor, n (%) 7 (54) 7 (54) 21 (81)
Males, n 8 9 17
Vaginal delivery, n (%) 5 (38) 6 (46) 9 (35)
Prolonged rupture of membranes, n (%) 3 (23) 2 (15) 1 (4)
Day of life positive culture 32.8±30.4 25.2±17.7 -
Duration of receiving  antibiotics* (d) 9.9±8.7 8.9±5.6 -
Central venous cathetar, n (%) 5 (38) 8 (62)a 3 (12)b
Duration of stay in incubator (d) 32.8±30.4c 11.8±11.5d 5.8±10.5e
Exposure to postnatal steroids 3 (23) 3 (23) 2 (8)
Duration of indwelling central line* (d) 5.5±8.7f 6.2±6.1g 0.8±2.2h
Duration of mechanical ventilation (d) 15.6±23.9ý 6.5±10.4i 0.5±1.7j
Surgery, n (%) 2 (15) 1 (8) 1 (4)
Duration of TPN (d) 18.8±26.4k 14.8±11.2l 2.4±5.7m
Treatment with H2-blokers, n (%) 6 (46) 10 (77)n 5 (19)o
Death, n (%) 1 (8) 4 (31)ö 0 (0)p
* Prior to onset of infection; P<0.05: c-d, ý-j, i-j; P<0.005: a-b, f-h, g-h, k-m, l-m, ö-p;  P<0.001: c-e, n-o.

Patients with S. paucimobilis infections had a longer stay in incubator (P=0.0001), were receiving TPN (P=0.002), received mechanical ventilation (P=0.006), and had more number of days with indwelling central line (P=0.035) than controls. Patients with S. paucimobilis infection had longer stay in incubator than patients with K. pneumoniae infection (P<0.036).

We detected three major PFGE patterns (A-C) out of the 15 isolates tested. Nine of the thirteen patients’ isolates (pattern A) were indistinguishable by PFGE while the two differed by two bands (pattern A1). One other patient’s isolates were considered epidemiologically unrelated to the outbreak (pattern B). Two patterns (pattern C) were shared by the isolates from distilled water. One patient’s blood isolate had identical antibiotype as outbreak isolates was not available for PFGE testing. Molecular typing proved that there was a cross-transmission of S. paucimobilis in eleven patients, but these types were not the same the isolates from the distilled water. Healthcare worker hand cultures were negative for this organism. S. paucimobilis strains of the one dead patient were type A in PFGE pattern. She died due to septic shock. No further cases were found during a 20-month period.

Discussion

We report an outbreak caused by S. paucimobilis during a 6-week period in a neonatal intensive care unit. Various infections caused by S. paucimobilis include bacteremia, septic shock, osteomyelitis, septic arthritis, endophthalmitis, myositis, peritonitis, intravascular catheter-related bacteremia, biliary tract infection, wound infection, urinary tract infection, ventilator-associated pneumonia, pyoderma, neutropenic fever and gastrointestinal infection have been reported previously [2,3,7-12]. In this study, we observed nosocomial sepsis in twelve patients and septic shock in one patient. All neonates with positive blood culture for S. paucimobilis infections had clinical sepsis. Thus, growing of these micro-organisms in the blood cultures were not accepted as contaminant.

Distilled water is used for the humidifying of incubators and mechanical ventilators. It can be hypothesized that this bacterium from distilled water may be a major source for S. paucimobilis outbreaks. But S. paucimobilis types obtained from distilled water were different from the types obtained from patients. Major limitation of this study is source of the outbreak is not certain. The outbreak was terminated within 3 months by intensified infection-control measures.

Contributors: All authors contributed to concept and design of the study. All authors were involved in drafting of the manuscript and approved the final version.

Funding: Research Fund of Karadeniz Technical University (Project number: 2007.114.001.8).

Competing interests: None stated.


What This Study Adds?

• S. paucimobilis can cause sepsis and septic shock in newborns, and outbreaks in NICU.
 

References

1. Morrison AJ Jr, Shulman JA. Community-acquired bloodstream infection caused by Pseudomonas paucimobilis: case report and review of the literature. J Clin Microbiol. 1986;24:853-5.

2. Cheong HS, Wi YM, Moon SY, Kang CI, Son JS, Ko KS, et al. Clinical features and treatment outcomes of infections caused by Sphingomonas paucimobilis. Infect Control Hosp Epidemiol. 2008;29:990-2.

3. Kilic A, Senses Z, Kurekci AE, Aydogan H, Sener K, Kismet E, et al. Nosocomial outbreak of Sphingomonas paucimobilis bacteremia in a hemato/oncology unit. Jpn J Infect Dis. 2007;60:394-6.

4. Lemaitre D, Elaichouni A, Hundhausen M, Claeys G, Vanhaesebrouck P, Vaneechoutte M, et al. Tracheal colonization with Sphingomonas paucimobilis in mechanically ventilated neonates due to contaminated ventilator temperature probes. J Hosp Infect. 1996;32:199-206.

5. Goldstein B, Giroir B, Randolph A. International Pediatric Sepsis Consensus Conference: definitions for sepsis and organ dysfunction in pediatrics. Pediatr Crit Care Med. 2005;6:2-8.

6. Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, et al. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol. 1995;33:2233-9.

7. Dervisoglu E, Meric M, Kalender B, Sengul E. Sphingomonas paucimobilis peritonitis: a case report and literature review. Perit Dial Int. 2008;28:547-50.

8. Al-Anazi KA, Abu Jafar S, Al-Jasser AM, Al-Shangeeti A, Chaudri NA, Al Jurf MD, et al. Septic shock caused by Sphingomonas paucimobilis bacteremia in a patient with hematopoietic stem cell transplantation. Transpl Infect Dis. 2008;10:142-4.

9. Charity RM, Foukas AF. Osteomyelitis and secondary septic arthritis caused by Sphingomonas paucimobilis. Infection. 2005;33:93-5.

10. Adams WE, Habib M, Berrington A, Koerner R, Steel DH. Postoperative endophthalmitis caused by Sphingomonas paucimobilis. J Cataract Refract Surg. 2006;32:1238-40.

11. Pegoraro E, Borsato C, Dal Bello F, Stramare R, Fanin M, Palu G, et al. Sphingomonas paucimobilis associated with localised calf myositis. J Neurol Neurosurg Psychiatry. 2008;79:1194-5.

12. Hsueh PR, Teng LJ, Yang PC, Chen YC, Pan HJ, Ho SW, et al. Nosocomial infections caused by Sphingomonas paucimobilis: Clinical features and microbiological characteristics. Clin Infect Dis. 1998;26:676-81.
 

 

Copyright© 1999 by the Indian Pediatrics (Disclaimer)