Listeriosis natural history, complications and prognosis: Difference between revisions
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===Bacteremia=== | ===Bacteremia=== | ||
After the [[neonatal]] period, the most common manifestation of [[listeriosis]] is [[bacteremia]] without and evident focus of [[infection]]. The clinical manifestations may include fever, myalgias and nausea. | |||
Often times, healthy individuals who experience these manifestations do not have [[blood culture]]s, they have higher probability of transient [[bacteremias]] going undetected.<ref>{{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=== |
Revision as of 03:33, 23 July 2014
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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
Natural History
The majority of cases of listeriosis are sporadic. ALthough the source is usually unknown, contaminated food is the most common vehicle of transmission. Some patients may be transitory carriers of the bacteria, without having the disease. Once the bacteria penetrate the gastrointestinal lining, it will travel through the blood to otherwise aseptic sites, such as the CNS, the uterus, and sometimes the heart, being responsible for diseases such as:
- Febrile gastroenteritis
- Infection in pregnancy
- Sepsis of unknown origin
- Bacteremia
- CNS Infection
- Endocarditis
- Focal infections
The mean incubation period for febrile gastroenteritis following listeriosis is 24h, however, these may range from 6h up to 10 days. In the case of the remaining invasive diseases, the mean incubation period is 35 days, ranging from 1 up to 91 days.[1][2][3]
Febrile Gastroenteritis
Febrilegastroenteritis accounts for less than 1% of reported bacterial food-born infections occurring usually after ingestion of a large inoculum of bacteria from contaminated foods. Illness typically occurs 24 hours after ingestion of contaminated food, presenting with symptoms such as fever, nausea, vomiting and watery diarrhea.
It generally lasts for 2 days and the patient experiences complete recovery from the symptoms. Some patients may be asymptomatic for the disease, while others, immunocompromised, pregnant women and elder patients, in rare cases, present with invasive infection. L. monocytogenes infection should be considered when outbreaks of foodborne gastroenteritis surge and stool cultures fail to identify the pathogen[4].
Infection in Pregnancy
Pregnant women have greater risk of contracting listeriosis since during pregnancy there is a slight impairment of cell-mediated immunity. Lysteria is also able to proliferate in the placenta, in hard-to-reach areas for the immune system. Infection occurs more frequently during the third trimester of gestation, with an estimated 17 fold increase[5], presenting most commonly with flu-like symptoms, such as fever and chills.
The infection may be mild and the diagnosis missed when blood cultures are not obtained. Since bacteremia with no CNS involvement is common rule in pregnant women with listeriosis, blood cultures should always be obtained in pregnant women who present with fever, with no other possible cause, such as UTI or pharyngitis. Because cell-to-cell transmission facilitates maternal-fetal transmission[6], listeriosis in pregnant women, can result in fetal death, premature birth, or infected newborns.
Among pregnant women with listeriosis, 2/3 of the surviving infants develop clinical neonatal listeriosis.[7]. The newborn also has great risk of developing granulomatosis infantiseptica, a severe in utero infection resulting from transplacental transmission, in which infants may present with:
- disseminated abscesses
- granulomas in multiple internal organs (brain, lungs, liver, spleen and kidneys)
- papular or ulcerative skin lesions.
- most infants with this disease are stillborn or die soon after birth.
L. monocytogenes is one of the three major causes of neonatal meningitis, worldwide. The early diagnosis and treatment of pregnant women infected with Listeria may lead to the birth of a normal healthy child.[8]
Sepsis of Unknown Origin
Occurs in patients of all ages. Neonates usually tend to acquire the infection during or after birth. When this occurs during the first week of life, it usually manifests as sepsis, while after this first week, it tends to have more variable manifestations, such as meningitis.
Early onset of sepsis is associated with higher neonatal mortality. In this case, L. monocitogenes can be isolated from conjunctivae, amniotic fluid, meconium, placental blood, with higher concentrations of bacteria being found in the neonatal lung and gut, which suggests that infection is acquired in uterus, by inhalation of infected amniotic fluid.[9]
- Listerial meningoencephalitis is more common in neonates after 3 days of age, as well as in immunocompromised and elderly adults.
- Adults presenting Listerial sepsis, are most commonly immunocompromised or elderly, and typically present with fever and chills. Septic shock can occur with brain and/or meningeal involvement, leading to meningoencephalitis or cerebritis.
Bacteremia
After the neonatal period, the most common manifestation of listeriosis is bacteremia without and evident focus of infection. The clinical manifestations may include fever, myalgias and nausea.
Often times, healthy individuals who experience these manifestations do not have blood cultures, they have higher probability of transient bacteremias going undetected.[10]
CNS Infection
Endocarditis
Focal Infections
Complications
Invasive disease might complicate into:[11][12]
- Disseminated intravascular coagulation
- ARDS
- Rhabdomyolysis
- Acute Renal Failure
- Septicemia[13], meningitis (or meningoencephalitis)[13]
- Encephalitis[14]
- Corneal ulcer[15]
- Pneumonia[16]
- Intrauterine or cervical infection in pregnant women, may result in:
- Spontaneous abortion (2nd/3rd trimester)
- Stillbirth
- Surviving neonates of Fetomaternal Listeriosis may suffer from:
- Granulomatosis infantiseptica - pyogenic granulomas distributed over the whole body, and may suffer from physical retardation
- Influenza-like symptoms, including persistent fever usually precede the onset of the aforementioned disorders.
- Reinfection (rare)
Prognosis
The prognosis of Listeriosis depends on the health status of the host:[17]
- Healthy older children and adults have a lower death rate.
- Listeriosis in a fetus or infant results in a poor outcome with a high death rate.
- Even with prompt treatment, some listeriosis cases result in death. This is particularly likely in older adults and in persons with other medical conditions.
References
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ "Listeriosis".
- ↑ 13.0 13.1 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.
- ↑ "Listeria".