Clinical aspects of an outbreak of Serratia marcescens infections in neonates

신생아 중환자실에서 Serratia marcescens에 의한 집단 감염 발생에 대한 고찰

  • Sung, Min-Jung (Department of Pediatrics, College of Medicine, Pusan National University) ;
  • Chang, Chul-Hun (Department of Laboratory Medicine, College of Medicine, Pusan National University) ;
  • Yoon, Yeon-Kyong (Department of Infection Control Team, College of Medicine, Pusan National University) ;
  • Park, Su-Eun (Department of Pediatrics, College of Medicine, Pusan National University)
  • 성민정 (부산대학교 의과대학 소아과학교실) ;
  • 장철훈 (부산대학교 의과대학 진단검사의학교실) ;
  • 윤연경 (부산대학교병원 감염관리실) ;
  • 박수은 (부산대학교 의과대학 소아과학교실)
  • Received : 2005.12.29
  • Accepted : 2006.02.24
  • Published : 2006.05.15

Abstract

Purpose : We evaluated an outbreak of Serratia marcescens infections in 24 neonates in a neonatal intensive care unit(NICU). Methods : From January to August, 2004 a nosocomial outbreak of S. marcescens occurred in our NICU. We describe the clinical characteristics of the outbreak and analyse the risk factors for infections with S. marcescens. After the outbreak stopped, 7 isolates from blood were typed using rapid amplified polymorphic DNA analysis(RAPD). Results : S. marcescens was isolated from 24 neonates, 19 infected and 5 colonized. Seven out of nineteen neonates had bacteremia, 4 had ventilator associated pneumonia, 4 had purulent conjunctivitis, 2 had UTI, 1 had meningitis and 1 had a wound infection. Three neonates died due to S. marcescens infection, 2 of 3 had ventilator associated pneumonia, 1 had meningitis complicated with abscess. The mortality rate of S. marcescens infection was 15.8%. Factors associated with S. marcescens infections were previous antibiotic therapy, indwelling catheter and use of ventilators. The isolated strains were resistant to most antibiotics, but frequently sensitive to imipenem, bactrim and amikacin. RAPD typing results show that at least 3 epidemic strains were related with this outbreak. But one genotype was predominant type in this outbreak. The control measures were instituted and the outbreak stopped within 2 months. Conclusion : S. marcescens can cause rapidly spreading outbreaks associated with fatal infections in neonates. If S. marcescens is isolated from clinical specimens, meticulous infection control measures and epidemiologic investigations should be done at an early stage of the outbreak.

목 적 : 신생아 중환자실에서 일어났던 S. marcescens의 대유행의 임상적 양상과 위험 요소에 대해 알아보고자 하였다. 방 법 : 2004년 1월부터 8월까지 8개월간 부산대학교병원 신생아 중환자실에 입원해 있던 환아 중 S. marcescens이 분리되었던 24명을 환아군으로 하고, 같은 기간에 신생아 중환자실에 입원해 있었지만 균이 배양되지 않았던 21명을 대조군으로 하며, 균이 배양되었던 24명 중 감염을 일으킨 19명을 감염군으로 감염의 증거가 없던 5명을 보균군으로 나누어 각 군의 임상적 양상, 위험 요소의 비교 및 분리된 균주에 대한 항생제 감수성을 검사하였다. 동시에 환경 배양 검사를 하여 유행의 원인을 조사하였다. 결 과 : 환아군과 대조군, 감염군과 보균군 사이에 성별, 제태 연령, 출생시 체중, 분만 방법, 산모의 감염 여부, 입원 기간에는 유의한 차이점이 없었다. 환아들이 가진 기저질환으로는 신생아 호흡 곤란 증후군, 선천성 심질환, 괴사성 장염의 순으로 나타났다. 환자군이 대조군에 비해 카테터의 사용, 수술의 과거력, 항생제 사용, 인공 호흡기 사용, 비위관 삽입의 빈도가 많았다. 감염군에서 균이 배양되었던 검체는 혈액이 7명, 기도내에서 검출된 환아는 4명, 결막 삼출물은 4명, 소변에서 균이 검출된 환아는 2명, 뇌척수액에서 검출된 환아는 1명이었고, 이 중 S. marcescens의 감염으로 인해 사망한 환아는 3명으로 15.8%의 사망률을 나타내었다. 감염군 19명에서 배출된 균의 항생제 감수성은 ampicillin, cefotaxime, ceftazidime, gentamicin에 저항성을 imipenem, bactrim, amikacin에 감수성을 나타내었다. 분자학적 방법으로 분석한 결과 6월의 유행 당시 모두 같은 균종으로 나왔다. 철저한 소독과 격리를 한 뒤 더 이상 균이 발견되지 않고 있다. 결 론 : S. marcescens는 신생아와 같이 면역이 저하된 환자에게 빠르게 전파하여 폭발적인 유행을 일으킬 수 있으며 사망률도 높다. 임상 검체에서 S. marcescens가 분리되면 유행적 발생의 위험성을 빨리 인지하여 처음부터 적절한 감염 관리를 실시하여야 한다.

Keywords

References

  1. Davis JT, Foltz E, Blakemore WS. Serratia marcescens. A pathogen of increasing clinical importance. JAMA 1970;214: 2190-2 https://doi.org/10.1001/jama.214.12.2190
  2. Vigeant P, Loo VG, Bertrand C, Dixon C, Hollis R, Pfaller MA, et al. An outbreak of Serratia marcescens infections related to contaminated chlorhexidine. Infect Control Hosp Epidemiol 1998;19:791-4 https://doi.org/10.1086/647728
  3. Kappstein I, Schneider CM, Grundmann H, Scholz R, Janknecht P. Long-lasting contamination of a vitrectomy apparatus with Serratia marcescens. Infect Control Hosp Epidemiol 1999;20:192-5 https://doi.org/10.1086/501610
  4. Sartor C, Jacomo V, Duvivier C, Tissot-Dupont H, Sambuc R, Drancourt M. Nosocomial Serratia marcescens infections associated with extrinsic contamination of a liquid nonmedicated soap. Infect Control Hosp Epidemiol 2000;21:196-9 https://doi.org/10.1086/501743
  5. Newport MT, John JF, Michel YM, Levkoff AH. Endemic Serratia marcescens infection in a neonatal intensive care nursery associated with gastrointestinal colonization. Pediatr Infect Dis 1985;4:160-7 https://doi.org/10.1097/00006454-198503000-00010
  6. Zaidi M, Sifuentes J, Bobadilla M, Moncada D, Ponce de Leon S. Epidemic of Serratia marcescens bacteremia and meningitis in a neonatal unit in Mexico City. Infect Control Hosp Epidemiol 1989;10:14-20 https://doi.org/10.1086/645909
  7. Bollmann R, Halle E, Sokolowska-Kohler W, Grauel EL, Buchholz P, Klare I, et al. Nosocomial infections due to Serratia marcescens--clinical findings, antibiotic susceptibility patterns and fine typing. Infection 1989;17:294-300 https://doi.org/10.1007/BF01650711
  8. Campbell JR, Diacovo T, Baker CJ. Serratia marcescens meningitis in neonates. Pediatr Infect Dis J 1992;11:881-6 https://doi.org/10.1097/00006454-199210000-00015
  9. van Ogtrop ML, van Zoeren-Grobben D, Verbakel-Salomons EM, van Boven CP. Serratia marcescens infections in neonatal departments : description of an outbreak and review of the literature. J Hosp Infect 1997;36:95-103 https://doi.org/10.1016/S0195-6701(97)90115-8
  10. Gargallo-Viola D. Enzyme polymorphism, prodigiosin production, and plasmid fingerprints in clinical and naturally occurring isolates of Serratia marcescens. J Clin Microbiol 1989;27:860-8
  11. Sarvikivi E, Lyytikainen O, Salmenlinna S, Vuopio-Varkila J, Luukkainen P, Tarkka E, et al. Clustering of Serratia marcescens infections in a neonatal intensive care unit. Infect Control Hosp Epidemiol 2004;25:723-9 https://doi.org/10.1086/502467
  12. Khan EA, Wafelman LS, Garcia-Prats JA, Taber LH. Serratia marcescens pneumonia, empyema and pneumatocele in a preterm neonate. Pediatr Infect Dis J 1997;16:1003-5 https://doi.org/10.1097/00006454-199710000-00021
  13. Kimpen JL, Brus F, Arends JP, de Vries-Hospers HG. Successful medical treatment of multiple Serratia marcescens brain abscesses in a neonate. Eur J Pediatr 1996;155: 916
  14. Lam AH, Berry A, deSilva M, Williams G. Intracranial Serratia infection in preterm newborn infants. AJNR Am J Neuroradiol 1984;5:447-51
  15. Messerschmidt A, Prayer D, Olischar M, Pollak A, Birnbacher R. Brain abscesses after Serratia marcescens infection on a neonatal intensive care unit : differences on serial imaging. Neuroradiology 2004;46:148-52 https://doi.org/10.1007/s00234-003-1140-8
  16. Acar JF. Serratia marcescens infections. Infect Control 1986;7:273-8 https://doi.org/10.1017/S0195941700064201
  17. Gaynes RP, Edwards JR, Jarvis WR, Culver DH, Tolson JS, Martone WJ. Nosocomial infections among neonates in high-risk nurseries in the United States. National Nosocomial Infections Surveillance System. Pediatrics 1996;98: 357-61
  18. Braver DJ, Hauser GJ, Berns L, Siegman-Igra Y, Muhlbauer B. Control of a Serratia marcescens outbreak in a maternity hospital. J Hosp Infect 1987;10:129-37 https://doi.org/10.1016/0195-6701(87)90138-1
  19. Berthelot P, Grattard F, Amerger C, Frery MC, Lucht F, Pozzetto B, et al. Investigation of a nosocomial outbreak due to Serratia marcescens in a maternity hospital. Infect Control Hosp Epidemiol 1999;20:233-6 https://doi.org/10.1086/501617
  20. Steppberger K, Walter S, Claros MC, Spencker FB, Kiess W, Rodloff AC, et al. Nosocomial neonatal outbreak of Serratia marcescens--analysis of pathogens by pulsed field gel electrophoresis and polymerase chain reaction. Infection 2002;30:277-81 https://doi.org/10.1007/s15010-002-2141-y
  21. Lai KK, Baker SP, Fontecchio SA. Rapid eradication of a cluster of Serratia marcescens in a neonatal intensive care unit : use of epidemiologic chromosome profiling by pulsedfield gel electrophoresis. Infect Control Hosp Epidemiol 2004;25:730-4 https://doi.org/10.1086/502468
  22. Bando SY, do Valle GR, Martinez MB, Trabulsi LR, Moreira- Filho CA. Characterization of enteroinvasive Escherichia coli and Shigella strains by RAPD analysis. FEMS Microbiol Lett 1998;165:159-65 https://doi.org/10.1111/j.1574-6968.1998.tb13141.x
  23. Polyzou A, Sofianou D, Pournaras S, Tsakris A. RAPDfingerprinting of Serratia marcescens after formaldehyde inactivation of DNase activity. Lett Appl Microbiol 2000;30: 419-21 https://doi.org/10.1046/j.1472-765x.2000.00743.x
  24. Gransden WR, Webster M, French GL, Phillips I. An outbreak of Serratia marcescens transmitted by contaminated breast pumps in a special care baby unit. J Hosp Infect 1986;7:149-54 https://doi.org/10.1016/0195-6701(86)90057-5
  25. Moloney AC, Quoraishi AH, Parry P, Hall V. A bacteriological examination of breast pumps. J Hosp Infect 1987;9: 169-74 https://doi.org/10.1016/0195-6701(87)90056-9
  26. Wake C, Lees H, Cull AB. The emergence of Serratia marcescens as a pathogen in a newborn unit. Aust Paediatr J 1986;22:323-6
  27. Christensen GD, Korones SB, Reed L, Bulley R, McLaughlin B, Bisno AL. Epidemic Serratia marcescens in a neonatal intensive care unit : importance of the gastrointestinal tract as a reservoir. Infect Control 1982;3:127-33 https://doi.org/10.1017/S0195941700055909
  28. Miranda-Novales G, Leanos-Miranda B, Diaz-Ramos R, Gonzalez-Tejeda L, Peregrino-Bejarano L, Villegas-Silva R, et al. An outbreak due to Serratia marcescens in a neonatal intensive care unit typed by 2-day pulsed field gel electrophoresis protocol. Arch Med Res 2003;34:237-41 https://doi.org/10.1016/S0188-4409(03)00026-2
  29. Gong J, Hogman CF, Hambraeus A, Johansson CS, Eriksson L. Transfusion-associated Serratia marcescens infection : studies of the mechanism of action. Transfusion 1993; 33:802-8 https://doi.org/10.1046/j.1537-2995.1993.331094054615.x
  30. Sleigh JD. Antibiotic resistance in Serratia marcescens. Br Med J 1983;287:1651-2 https://doi.org/10.1136/bmj.287.6406.1651
  31. Cook LN, Davis RS, Stover BH. Outbreak of amikacinresistant Enterobacteriaceae in an intensive care nursery. Pediatrics 1980;65:264-8
  32. Lewis DA, Hawkey PM, Bennett PM. Antibiotic resistance in Serratia marcescens. Br Med J 1984;288:148-9 https://doi.org/10.1136/bmj.288.6411.148-b
  33. Casewell MW, Ronan P. Infection with netilmicin resistant Serratia marcescens. Br Med J 1984;288:487