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Listeriosis natural history, complications and prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2]

Overview

Following transmission, the majority of healthy patients do not develop clinical manifestations or may develop a mild, transient bacteremia. Early clinical manifestations (usually fever) typically develop early within 24 hours of transmission. If left untreated, patients typically progress within 1-90 days to develop Listeria-associated complications, including bacteremia, abscess formation, pneumonia, ARDS, acute kidney injury, and CNS impairment. Among healthy children and young adults, the prognosis of listeriosis is generally good. Prognosis is poorer among high-risk populations, who are more likely to develop complications and death even with prompt management.

Natural History

  • Following transmission, the majority of healthy patients do not develop clinical manifestations or may develop a mild, transient bacteremia.[1]
  • The median incubation period for listeriosis-associated gastroenteritis is approximately 24 hours (range from 6 hours to 10 days).
  • Systemic manifestations of listeriosis may be slow-occurring, and the duration from transmission to development of systemic manifestations widely varies between 1 day to 90 days following transmission.[2][3][4]

Febrile Gastroenteritis

Infection in Pregnancy

Neonates

CNS Infection

Endocarditis

Listerial endocarditis may affect either native or prosthetic valves.

Complications

Prognosis

The prognosis of listeriosis depends on the health status of the host:[12]

  • Healthy children and young adults have a good prognosis and are at low-risk of developing Listeria-associated complications and long-term sequelae.
  • High-risk populations, including pregnant women, neonates, elderly, and immunosuppressed individuals, have a poorer prognosis with a high death rate (even when treatment is administered promptly).

References

  1. 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 Mandell, Gerald L.; Bennett, John E. (John Eugene); Dolin, Raphael. (2010). Mandell, Douglas, and Bennett’s principles and practice of infectious disease. Philadelphia, PA: Churchill Livingstone/Elsevier. ISBN 0-443-06839-9.
  2. Ooi ST, Lorber B (2005). “Gastroenteritis due to Listeria monocytogenes”. Clin Infect Dis. 40 (9): 1327–32. doi:10.1086/429324. PMID 15825036.
  3. Dalton CB, Austin CC, Sobel J, Hayes PS, Bibb WF, Graves LM; et al. (1997). “An outbreak of gastroenteritis and fever due to Listeria monocytogenes in milk”. N Engl J Med. 336 (2): 100–5. doi:10.1056/NEJM199701093360204. PMID 8988887.
  4. Linnan MJ, Mascola L, Lou XD, Goulet V, May S, Salminen C; et al. (1988). “Epidemic listeriosis associated with Mexican-style cheese”. N Engl J Med. 319 (13): 823–8. doi:10.1056/NEJM198809293191303. PMID 3137471.
  5. Lorber, B. (1997). “Listeriosis”. Clin Infect Dis. 24 (1): 1–9, quiz 10-1. PMID 8994747. Unknown parameter |month= ignored (help)
  6. “Listeriosis”.
  7. 7.0 7.1 Gray, M. L., and A. H. Killinger. 1966. Listeria monocytogenes and listeric infection. Bacteriol. Rev. 30:309-382.
  8. Armstrong, R. W., and P. C. Fung. 1993. Brainstem encephalitis (Rhombencephalitis) due to Listeria monocytogenes: case report and review. Clin. Infect. Dis. 16:689-702.
  9. Holland, S., E. Alfonso, H. Gelender, D. Heidemann, A. Mendelsohn, S. Ullman, and D. Miller. 1987. Corneal ulcer due to Listeria monocytogenes. Cornea 6:144-146.
  10. Whitelock-Jones, L., J. Carswell, and K. C. Rassmussen. 1989. Listeria pneumonia. A case report. South African Medical Journal 75:188-189.
  11. Maertens de Noordhout C, Devleesschauwer B, Angulo FJ, Verbeke G, Haagsma J, Kirk M, Havelaar A, Speybroeck N (2014). “The global burden of listeriosis: a systematic review and meta-analysis”. Lancet Infect Dis. 14 (11): 1073–82. doi:10.1016/S1473-3099(14)70870-9. PMC 4369580. PMID 25241232.
  12. “Listeria”.


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