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Clinical value of procalcitonin for suspected nosocomial bloodstream infection

  • Cha, Joo Kyoung (Department of Internal Medicine, Dongguk University Ilsan Hospital) ;
  • Kwon, Ki Hwan (Department of Internal Medicine, Dongguk University Ilsan Hospital) ;
  • Byun, Seung Joo (Department of Internal Medicine, Dongguk University Ilsan Hospital) ;
  • Ryoo, Soo Ryeong (Department of Internal Medicine, Dongguk University Ilsan Hospital) ;
  • Lee, Jeong Hyeon (Department of Internal Medicine, Dongguk University Ilsan Hospital) ;
  • Chung, Jae-Woo (Department of Laboratory Medicine, Dongguk University Ilsan Hospital) ;
  • Huh, Hee Jin (Department of Laboratory Medicine, Dongguk University Ilsan Hospital) ;
  • Chae, Seok Lae (Department of Laboratory Medicine, Dongguk University Ilsan Hospital) ;
  • Park, Seong Yeon (Department of Internal Medicine, Dongguk University Ilsan Hospital)
  • Received : 2016.04.18
  • Accepted : 2016.09.13
  • Published : 2018.01.01

Abstract

Background/Aims: Procalcitonin (PCT) may prove to be a useful marker to exclude or predict bloodstream infection (BSI). However, the ability of PCT levels to differentiate BSI from non-BSI episodes has not been evaluated in nosocomial BSI. Methods: We retrospectively reviewed the medical records of patients ${\geq}18$ years of age with suspected BSI that developed more than 48 hours after admission. Results: Of the 785 included patients, 105 (13.4%) had BSI episodes and 680 (86.6%) had non-BSI episodes. The median serum PCT level was elevated in patients with BSI as compared with those without BSI (0.65 ng/mL vs. 0.22 ng/mL, p = 0.001). The optimal PCT cut-off value of BSI was 0.27 ng/mL, with a corresponding sensitivity of 74.6% (95% confidence interval [CI], 66.4% to 81.7%) and a specificity of 56.5% (95% CI, 52.7% to 60.2%). The area under curve of PCT (0.692) was significantly larger than that of C-reactive protein (CRP; 0.526) or white blood cell (WBC) count (0.518). However, at the optimal cut-off value, PCT failed to predict BSI in 28 of 105 cases (26.7%). The PCT level was significantly higher in patients with an eGFR < $60 mL/min/1.73m^2$ than in those with an eGFR ${\geq}60mL/min/1.73m^2$ (0.68 vs. 0.17, p = 0.01). Conclusions: PCT was more useful for predicting nosocomial BSI than CRP or WBC count. However, the diagnostic accuracy of predicting BSI remains inadequate. Thus, PCT is not recommended as a single diagnostic tool to avoid taking blood cultures in the nosocomial setting.

Keywords

References

  1. Pittet D, Wenzel RP. Nosocomial bloodstream infections: secular trends in rates, mortality, and contribution to total hospital deaths. Arch Intern Med 1995;155:1177-1184. https://doi.org/10.1001/archinte.1995.00430110089009
  2. Parrillo JE. Pathogenetic mechanisms of septic shock. N Engl J Med 1993;328:1471-1477. https://doi.org/10.1056/NEJM199305203282008
  3. Nakamura A, Wada H, Ikejiri M, et al. Efficacy of procalcitonin in the early diagnosis of bacterial infections in a critical care unit. Shock 2009;31:586-591.
  4. Hoenigl M, Wagner J, Raggam RB, et al. Characteristics of hospital-acquired and community-onset blood stream infections, South-East Austria. PLoS One 2014;9:e104702. https://doi.org/10.1371/journal.pone.0104702
  5. Diekema DJ, Beekmann SE, Chapin KC, Morel KA, Munson E, Doern GV. Epidemiology and outcome of nosocomial and community-onset bloodstream infection. J Clin Microbiol 2003;41:3655-3660. https://doi.org/10.1128/JCM.41.8.3655-3660.2003
  6. Kollef MH, Zilberberg MD, Shorr AF, et al. Epidemiology, microbiology and outcomes of healthcare-associated and community-acquired bacteremia: a multicenter cohort study. J Infect 2011;62:130-135. https://doi.org/10.1016/j.jinf.2010.12.009
  7. Leibovici L, Shraga I, Drucker M, Konigsberger H, Samra Z, Pitlik SD. The benefit of appropriate empirical antibiotic treatment in patients with bloodstream infection. J Intern Med 1998;244:379-386. https://doi.org/10.1046/j.1365-2796.1998.00379.x
  8. Goncalves-Pereira J, Povoa PR, Lobo C, Carneiro AH. Bloodstream infections as a marker of community-acquired sepsis severity: results from the Portuguese community-acquired sepsis study (SACiUCI study). Clin Microbiol Infect 2013;19:242-248. https://doi.org/10.1111/j.1469-0691.2012.03776.x
  9. Jensen JU, Heslet L, Jensen TH, Espersen K, Steffensen P, Tvede M. Procalcitonin increase in early identification of critically ill patients at high risk of mortality. Crit Care Med 2006;34:2596-2602. https://doi.org/10.1097/01.CCM.0000239116.01855.61
  10. Mitaka C. Clinical laboratory differentiation of infectious versus non-infectious systemic inflammatory response syndrome. Clin Chim Acta 2005;351:17-29. https://doi.org/10.1016/j.cccn.2004.08.018
  11. Bates DW, Sands K, Miller E, et al. Predicting bacteremia in patients with sepsis syndrome: Academic Medical Center Consortium Sepsis Project Working Group. J Infect Dis 1997;176:1538-1551. https://doi.org/10.1086/514153
  12. Jaimes F, Arango C, Ruiz G, et al. Predicting bacteremia at the bedside. Clin Infect Dis 2004;38:357-362. https://doi.org/10.1086/380967
  13. Clyne B, Olshaker JS. The C-reactive protein. J Emerg Med 1999;17:1019-1025. https://doi.org/10.1016/S0736-4679(99)00135-3
  14. Assicot M, Gendrel D, Carsin H, Raymond J, Guilbaud J, Bohuon C. High serum procalcitonin concentrations in patients with sepsis and infection. Lancet 1993;341:515-518. https://doi.org/10.1016/0140-6736(93)90277-N
  15. Riedel S, Melendez JH, An AT, Rosenbaum JE, Zenilman JM. Procalcitonin as a marker for the detection of bacteremia and sepsis in the emergency department. Am J Clin Pathol 2011;135:182-189. https://doi.org/10.1309/AJCP1MFYINQLECV2
  16. Hattori T, Nishiyama H, Kato H, et al. Clinical value of procalcitonin for patients with suspected bloodstream infection. Am J Clin Pathol 2014;141:43-51. https://doi.org/10.1309/AJCP4GV7ZFDTANGC
  17. Levy MM, Fink MP, Marshall JC, et al. 2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference. Crit Care Med 2003;31:1250-1256. https://doi.org/10.1097/01.CCM.0000050454.01978.3B
  18. Stevens LA, Coresh J, Greene T, Levey AS. Assessing kidney function: measured and estimated glomerular filtration rate. N Engl J Med 2006;354:2473-2483. https://doi.org/10.1056/NEJMra054415
  19. Liaudat S, Dayer E, Praz G, Bille J, Troillet N. Usefulness of procalcitonin serum level for the diagnosis of bacteremia. Eur J Clin Microbiol Infect Dis 2001;20:524-527. https://doi.org/10.1007/s100960100548
  20. Chirouze C, Schuhmacher H, Rabaud C, et al. Low serum procalcitonin level accurately predicts the absence of bacteremia in adult patients with acute fever. Clin Infect Dis 2002;35:156-161. https://doi.org/10.1086/341023
  21. Hoenigl M, Raggam RB, Wagner J, et al. Procalcitonin fails to predict bacteremia in SIRS patients: a cohort study. Int J Clin Pract 2014;68:1278-1281. https://doi.org/10.1111/ijcp.12474
  22. Groeneveld AB, Hack CE. The role of the innate immune response in hospital- versus community-acquired infection in febrile medical patients. Int J Infect Dis 2008;12:660-670. https://doi.org/10.1016/j.ijid.2008.03.009
  23. Laupland KB, Kibsey PC, Galbraith JC. Community-onset bloodstream infection during the 'after hours' is not associated with an increased risk for death. Can J Infect Dis Med Microbiol 2012;23:170-172.
  24. Hoeboer SH, van der Geest PJ, Nieboer D, Groeneveld AB. The diagnostic accuracy of procalcitonin for bacteraemia: a systematic review and meta-analysis. Clin Microbiol Infect 2015;21:474-481. https://doi.org/10.1016/j.cmi.2014.12.026
  25. Oussalah A, Ferrand J, Filhine-Tresarrieu P, et al. Diagnostic accuracy of procalcitonin for predicting blood culture results in patients with suspected bloodstream infection: an observational study of 35,343 consecutive patients (a STROBE-compliant article). Medicine (Baltimore) 2015;94:e1774. https://doi.org/10.1097/MD.0000000000001774
  26. Brechot N, Hekimian G, Chastre J, Luyt CE. Procalcitonin to guide antibiotic therapy in the ICU. Int J Antimicrob Agents 2015;46 Suppl 1:S19-S24. https://doi.org/10.1016/j.ijantimicag.2015.10.012
  27. Meisner M, Brunkhorst FM, Reith HB, Schmidt J, Lestin HG, Reinhart K. Clinical experiences with a new semiquantitative solid phase immunoassay for rapid measurement of procalcitonin. Clin Chem Lab Med 2000;38:989-995.
  28. Wagner KE, Martinez JM, Vath SD, et al. Early immunoneutralization of calcitonin precursors attenuates the adverse physiologic response to sepsis in pigs. Crit Care Med 2002;30:2313-2321. https://doi.org/10.1097/00003246-200210000-00021
  29. Mimoz O, Benoist JF, Edouard AR, Assicot M, Bohuon C, Samii K. Procalcitonin and C-reactive protein during the early posttraumatic systemic inflammatory response syndrome. Intensive Care Med 1998;24:185-188. https://doi.org/10.1007/s001340050543
  30. Carsin H, Assicot M, Feger F, et al. Evolution and significance of circulating procalcitonin levels compared with IL-6, TNF alpha and endotoxin levels early after thermal injury. Burns 1997;23:218-224. https://doi.org/10.1016/S0305-4179(96)00124-6
  31. Kylanpaa-Back ML, Takala A, Kemppainen EA, et al. Procalcitonin, soluble interleukin-2 receptor, and soluble E-selectin in predicting the severity of acute pancreatitis. Crit Care Med 2001;29:63-69. https://doi.org/10.1097/00003246-200101000-00016
  32. Meisner M, Tschaikowsky K, Hutzler A, Schick C, Schuttler J. Postoperative plasma concentrations of procalcitonin after different types of surgery. Intensive Care Med 1998;24:680-684. https://doi.org/10.1007/s001340050644
  33. Charles PE, Ladoire S, Aho S, et al. Serum procalcitonin elevation in critically ill patients at the onset of bacteremia caused by either gram negative or gram positive bacteria. BMC Infect Dis 2008;8:38. https://doi.org/10.1186/1471-2334-8-38
  34. Kumar S, Ingle H, Prasad DV, Kumar H. Recognition of bacterial infection by innate immune sensors. Crit Rev Microbiol 2013;39:229-246. https://doi.org/10.3109/1040841X.2012.706249
  35. Echchannaoui H, Frei K, Schnell C, Leib SL, Zimmerli W, Landmann R. Toll-like receptor 2-deficient mice are highly susceptible to Streptococcus pneumoniae meningitis because of reduced bacterial clearing and enhanced inflammation. J Infect Dis 2002;186:798-806. https://doi.org/10.1086/342845
  36. Takeuchi O, Hoshino K, Kawai T, et al. Differential roles of TLR2 and TLR4 in recognition of gram-negative and gram-positive bacterial cell wall components. Immunity 1999;11:443-451. https://doi.org/10.1016/S1074-7613(00)80119-3
  37. Poltorak A, He X, Smirnova I, et al. Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. Science 1998;282:2085-2088. https://doi.org/10.1126/science.282.5396.2085
  38. Meisner M, Lohs T, Huettemann E, Schmidt J, Hueller M, Reinhart K. The plasma elimination rate and urinary secretion of procalcitonin in patients with normal and impaired renal function. Eur J Anaesthesiol 2001;18:79-87.
  39. Amour J, Birenbaum A, Langeron O, et al. Influence of renal dysfunction on the accuracy of procalcitonin for the diagnosis of postoperative infection after vascular surgery. Crit Care Med 2008;36:1147-1154. https://doi.org/10.1097/CCM.0b013e3181692966
  40. Dahaba AA, Rehak PH, List WF. Procalcitonin and C-reactive protein plasma concentrations in nonseptic uremic patients undergoing hemodialysis. Intensive Care Med 2003;29:579-583. https://doi.org/10.1007/s00134-003-1664-8
  41. Park JH, Kim DH, Jang HR, et al. Clinical relevance of procalcitonin and C-reactive protein as infection markers in renal impairment: a cross-sectional study. Crit Care 2014;18:640. https://doi.org/10.1186/s13054-014-0640-8
  42. Herget-Rosenthal S, Klein T, Marggraf G, et al. Modulation and source of procalcitonin in reduced renal function and renal replacement therapy. Scand J Immunol 2005;61:180-186. https://doi.org/10.1111/j.0300-9475.2005.01545.x
  43. Sitter T, Schmidt M, Schneider S, Schiffl H. Differential diagnosis of bacterial infection and inflammatory response in kidney diseases using procalcitonin. J Nephrol 2002;15:297-301.
  44. Marra AR, Edmond MB, Forbes BA, Wenzel RP, Bearman GM. Time to blood culture positivity as a predictor of clinical outcome of Staphylococcus aureus bloodstream infection. J Clin Microbiol 2006;44:1342-1346. https://doi.org/10.1128/JCM.44.4.1342-1346.2006

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