Listeriosis natural history, complications and prognosis: Difference between revisions
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===Febrile Gastroenteritis=== | ===Febrile Gastroenteritis=== | ||
*''[[Listeria monocytogenes|Listeria]]''-associated | *''[[Listeria monocytogenes|Listeria]]''-associated [[gastroenteritis]] typically occurs 24 hours following [[ingestion]] of contaminated food. | ||
*Patients typically manifest with [[fever]], [[nausea]], [[vomiting]], and [[watery diarrhea]]. | *Patients typically manifest with [[fever]], [[nausea]], [[vomiting]], and [[watery diarrhea]]. | ||
*''[[Listeria monocytogenes|Listeria]]''-associated [[gastroenteritis]] is usually self-limited and lasts for a mean of 2 days among healthy individuals. | *''[[Listeria monocytogenes|Listeria]]''-associated [[gastroenteritis]] is usually self-limited and lasts for a mean of 2 days among healthy individuals. | ||
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*Pregnant women typically first present with mild [[flu]]-like [[symptoms]], such as [[fever]] and [[chills]], that are difficult to diagnose. | *Pregnant women typically first present with mild [[flu]]-like [[symptoms]], such as [[fever]] and [[chills]], that are difficult to diagnose. | ||
*As the disease progresses, [[pregnant]] women typically develop ''[[Listeria monocytogenes|Listeria]]''-associated [[bacteremia]] (typically without [[CNS]] involvement) | *As the disease progresses, [[pregnant]] women typically develop ''[[Listeria monocytogenes|Listeria]]''-associated [[bacteremia]] (typically without [[CNS]] involvement) | ||
*If left untreated, [[listeriosis]] among [[pregnant]] women typically results in fetal sequelae, including [[fetal death]], [[premature birth]], or [[neonatal sepsis]].<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. | title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref> | *If left untreated, [[listeriosis]] among [[pregnant]] women typically results in [[fetal]] sequelae, including [[fetal death]], [[premature birth]], or [[neonatal sepsis]].<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. | title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref> | ||
===Neonates=== | ===Neonates=== | ||
*[[Neonates]] may be infected either in-utero infection, which manifests with [[neonatal sepsis]] or during [[delivery]], which manifests with [[neonatal]] [[meningitis]]. | *[[Neonates]] may be infected either in-utero [[infection]], which manifests with [[neonatal sepsis]] or during [[delivery]], which manifests with [[neonatal]] [[meningitis]]. | ||
*Both [[infections]] are usually rapid-occurring, and infected [[neonates]] appear sick-looking with greyish-bluish discoloration at birth. | *Both [[infections]] are usually rapid-occurring, and [[infected]] [[neonates]] appear sick-looking with greyish-bluish discoloration at birth. | ||
*If left untreated, [[neonates]] may develop granulomatosis infantiseptica, a severe in-utero [[infection]], and death.<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. | title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref> | *If left untreated, [[neonates]] may develop [[granulomatosis]] infantiseptica, a severe in-utero [[infection]], and death.<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. | title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref> | ||
===CNS Infection=== | ===CNS Infection=== | ||
*''[[Listeria monocytogenes|L. monocytogenes]]'' has tropism for the [[brain stem]] and [[meninges]]. | *''[[Listeria monocytogenes|L. monocytogenes]]'' has [[tropism]] for the [[brain stem]] and [[meninges]]. | ||
*Patients with ''[[Listeria monocytogenes|Listeria]]''-associated [[CNS]] [[infection]] typically develop [[fever]] followed by [[altered mental status]], [[seizures]], [[cranial nerve palsy]], [[hemiplegia]], and [[ataxia]].<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. |title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref> | *Patients with ''[[Listeria monocytogenes|Listeria]]''-associated [[CNS]] [[infection]] typically develop [[fever]] followed by [[altered mental status]], [[seizures]], [[cranial nerve palsy]], [[hemiplegia]], and [[ataxia]].<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. |title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref> | ||
*Patients may either develop rhombencephalitis, [[cerebritis]], [[spinal cord]] [[infection]], [[meningitis]] alone, [[encephalitis]] alone, or both ([[meningoencephalitis]]). | *Patients may either develop rhombencephalitis, [[cerebritis]], [[spinal cord]] [[infection]], [[meningitis]] alone, [[encephalitis]] alone, or both ([[meningoencephalitis]]). | ||
*Patients with ''[[Listeria monocytogenes|Listeria]]''-associated rhombencephalitis typically experience a bi-phasic course. First, patients develop worsening [[headache]], [[fever]], [[vomiting]] for a 3-5 days, followed by an abrupt-onset of neurological impairment ([[cranial nerve palsy]], [[ataxia]], [[altered mental status]], [[seizures]]).<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. |title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref> | *Patients with ''[[Listeria monocytogenes|Listeria]]''-associated rhombencephalitis typically experience a bi-phasic course. First, patients develop worsening [[headache]], [[fever]], [[vomiting]] for a 3-5 days, followed by an abrupt-onset of [[Neurological disorders|neurological impairment]] ([[cranial nerve palsy]], [[ataxia]], [[altered mental status]], [[seizures]]).<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. |title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref> | ||
*If left untreated, [[brain abscesses]] may develop. The location of the [[brain abscesses]] is typically in the [[thalamus]], [[pons]], and/or [[medulla]]. | *If left untreated, [[brain abscesses]] may develop. The location of the [[brain abscesses]] is typically in the [[thalamus]], [[pons]], and/or [[medulla]]. | ||
*The majority of patients with advanced [[CNS disease]] develop long-term sequelae. | *The majority of patients with advanced [[CNS disease]] develop long-term sequelae. | ||
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==Complications== | ==Complications== | ||
*Compared with the general population, high-risk patients are more likely to develop invasive disease and ''[[Listeria monocytogenes|Listeria]]''-associated complications.<ref name="Lorber-1997">{{Cite journal | last1 = Lorber | first1 = B. | title = Listeriosis. | journal = Clin Infect Dis | volume = 24 | issue = 1 | pages = 1-9; quiz 10-1 | month = Jan | year = 1997 | doi = | PMID = 8994747 }}</ref> | *Compared with the general population, high-risk patients are more likely to develop invasive [[disease]] and ''[[Listeria monocytogenes|Listeria]]''-associated complications.<ref name="Lorber-1997">{{Cite journal | last1 = Lorber | first1 = B. | title = Listeriosis. | journal = Clin Infect Dis | volume = 24 | issue = 1 | pages = 1-9; quiz 10-1 | month = Jan | year = 1997 | doi = | PMID = 8994747 }}</ref> | ||
*Complications of invasive disease include the following:<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. | title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref><ref name=WHO>{{cite web | title = Listeriosis | url = http://www.who.int/ith/diseases/listeriosis/en/ }}</ref> | *Complications of invasive disease include the following:<ref name=Mandell>{{Cite book | last1 = Mandell | first1 = Gerald L. | last2 = Bennett | first2 = John E. (John Eugene) | last3 = Dolin | first3 = Raphael. | title = Mandell, Douglas, and Bennett's principles and practice of infectious disease | date = 2010 | publisher = Churchill Livingstone/Elsevier | location = Philadelphia, PA | isbn = 0-443-06839-9 | pages = }}</ref><ref name=WHO>{{cite web | title = Listeriosis | url = http://www.who.int/ith/diseases/listeriosis/en/ }}</ref> | ||
* [[Disseminated intravascular coagulation]] | * [[Disseminated intravascular coagulation]] | ||
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* [[Corneal ulcer]]<ref name=Holland_1987>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.</ref> | * [[Corneal ulcer]]<ref name=Holland_1987>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.</ref> | ||
* [[Pneumonia]]<ref name=whitelock_1989>Whitelock-Jones, L., J. Carswell, and K. C. Rassmussen. 1989. Listeria pneumonia. A case report. South African Medical Journal 75:188-189.</ref> | * [[Pneumonia]]<ref name=whitelock_1989>Whitelock-Jones, L., J. Carswell, and K. C. Rassmussen. 1989. Listeria pneumonia. A case report. South African Medical Journal 75:188-189.</ref> | ||
* [[uterus|Intrauterine]] or [[cervix|cervical]] infection in pregnant women, may result in:<ref name="pmid25241232">{{cite journal |vauthors=Maertens de Noordhout C, Devleesschauwer B, Angulo FJ, Verbeke G, Haagsma J, Kirk M, Havelaar A, Speybroeck N |title=The global burden of listeriosis: a systematic review and meta-analysis |journal=Lancet Infect Dis |volume=14 |issue=11 |pages=1073–82 |year=2014 |pmid=25241232 |pmc=4369580 |doi=10.1016/S1473-3099(14)70870-9 |url=}}</ref> | * [[uterus|Intrauterine]] or [[cervix|cervical]] [[infection]] in pregnant women, may result in:<ref name="pmid25241232">{{cite journal |vauthors=Maertens de Noordhout C, Devleesschauwer B, Angulo FJ, Verbeke G, Haagsma J, Kirk M, Havelaar A, Speybroeck N |title=The global burden of listeriosis: a systematic review and meta-analysis |journal=Lancet Infect Dis |volume=14 |issue=11 |pages=1073–82 |year=2014 |pmid=25241232 |pmc=4369580 |doi=10.1016/S1473-3099(14)70870-9 |url=}}</ref> | ||
:* [[miscarriage|Spontaneous abortion]] (2nd/3rd trimester) | :* [[miscarriage|Spontaneous abortion]] (2nd/3rd trimester) | ||
:* [[Stillbirth]] | :* [[Stillbirth]] |
Latest revision as of 15:56, 5 April 2017
Listeriosis Microchapters |
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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
- Listeria-associated gastroenteritis typically occurs 24 hours following ingestion of contaminated food.
- Patients typically manifest with fever, nausea, vomiting, and watery diarrhea.
- Listeria-associated gastroenteritis is usually self-limited and lasts for a mean of 2 days among healthy individuals.
- In high-risk patients, systemic manifestations of Listeria may occur, and patients are at higher risk of developing Listeria-associated complications.[1]
Infection in Pregnancy
- Among pregnant women, listeriosis typically manifests during the third trimester of gestation.[1]
- Pregnant women typically first present with mild flu-like symptoms, such as fever and chills, that are difficult to diagnose.
- As the disease progresses, pregnant women typically develop Listeria-associated bacteremia (typically without CNS involvement)
- If left untreated, listeriosis among pregnant women typically results in fetal sequelae, including fetal death, premature birth, or neonatal sepsis.[1]
Neonates
- Neonates may be infected either in-utero infection, which manifests with neonatal sepsis or during delivery, which manifests with neonatal meningitis.
- Both infections are usually rapid-occurring, and infected neonates appear sick-looking with greyish-bluish discoloration at birth.
- If left untreated, neonates may develop granulomatosis infantiseptica, a severe in-utero infection, and death.[1]
CNS Infection
- L. monocytogenes has tropism for the brain stem and meninges.
- Patients with Listeria-associated CNS infection typically develop fever followed by altered mental status, seizures, cranial nerve palsy, hemiplegia, and ataxia.[1]
- Patients may either develop rhombencephalitis, cerebritis, spinal cord infection, meningitis alone, encephalitis alone, or both (meningoencephalitis).
- Patients with Listeria-associated rhombencephalitis typically experience a bi-phasic course. First, patients develop worsening headache, fever, vomiting for a 3-5 days, followed by an abrupt-onset of neurological impairment (cranial nerve palsy, ataxia, altered mental status, seizures).[1]
- If left untreated, brain abscesses may develop. The location of the brain abscesses is typically in the thalamus, pons, and/or medulla.
- The majority of patients with advanced CNS disease develop long-term sequelae.
Endocarditis
Listerial endocarditis may affect either native or prosthetic valves.
- If left untreated, the majority of patients with Listeria-associated endocarditis progress to develop bacteremia.[1]
Complications
- Compared with the general population, high-risk patients are more likely to develop invasive disease and Listeria-associated complications.[5]
- Complications of invasive disease include the following:[1][6]
- Disseminated intravascular coagulation
- ARDS
- Rhabdomyolysis
- Acute kidney injury
- Septicemia[7]
- Meningitis[7]
- Encephalitis[8]
- Corneal ulcer[9]
- Pneumonia[10]
- Intrauterine or cervical infection in pregnant women, may result in:[11]
- Spontaneous abortion (2nd/3rd trimester)
- Stillbirth
- Preterm birth
- Granulomatosis infantiseptica: pyogenic granulomas distributed over the whole body, and the newborn may suffer from physical retardation
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
- ↑ 1.0 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.
- ↑ Ooi ST, Lorber B (2005). "Gastroenteritis due to Listeria monocytogenes". Clin Infect Dis. 40 (9): 1327–32. doi:10.1086/429324. PMID 15825036.
- ↑ 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.
- ↑ 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.
- ↑ Lorber, B. (1997). "Listeriosis". Clin Infect Dis. 24 (1): 1–9, quiz 10-1. PMID 8994747. Unknown parameter
|month=
ignored (help) - ↑ "Listeriosis".
- ↑ 7.0 7.1 Gray, M. L., and A. H. Killinger. 1966. Listeria monocytogenes and listeric infection. Bacteriol. Rev. 30:309-382.
- ↑ 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.
- ↑ 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.
- ↑ Whitelock-Jones, L., J. Carswell, and K. C. Rassmussen. 1989. Listeria pneumonia. A case report. South African Medical Journal 75:188-189.
- ↑ 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.
- ↑ "Listeria".