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{{Strongyloidiasis}}
{{Strongyloidiasis}}
{{CMG}} : {{AE}} {{ADG}}
{{CMG}}; {{AE}} {{ADG}}
==Overview==
==Overview==
The gold standard for the diagnosis of [[Strongyloidiasis|strongyloides]] is serial [[stool examination]]. Duodenal aspirate is more [[Sensitivity (tests)|sensitive]] than [[stool examination]], and duodenal biopsy may reveal [[parasites]] in the gastric crypts, in the [[duodenal glands]], or [[eosinophilic]] infiltration in the [[lamina propria]]. In disseminated cases of [[strongyloidiasis]], larvae can be detected in [[sputum]] by simple wet-mount in fluid from a [[bronchoalveolar lavage]] ([[BAL]]). [[Immunodiagnostics|Immunodiagnostic tests]] for [[strongyloidiasis]] are indicated when the infection is suspected and the organism cannot be demonstrated by duodenal aspiration, string tests, or by repeated examinations of stool. [[Enzyme immunoassay]] ([[EIA]]) is currently recommended because of its greater [[sensitivity]] (90%). Cross-reactions in patients with [[filariasis]] and some other [[nematode]] infections can occur. Antibody test results cannot be used to differentiate between the past and current infection.<ref name="pmid28210503">{{cite journal |vauthors=Mendes T, Minori K, Ueta M, Miguel DC, Allegretti SM |title=Strongyloidiasis Current Status with Emphasis in Diagnosis and Drug Research |journal=J Parasitol Res |volume=2017 |issue= |pages=5056314 |year=2017 |pmid=28210503 |pmc=5292188 |doi=10.1155/2017/5056314 |url=}}</ref><ref name="pmid27213420">{{cite journal |vauthors=Beknazarova M, Whiley H, Ross K |title=Strongyloidiasis: A Disease of Socioeconomic Disadvantage |journal=Int J Environ Res Public Health |volume=13 |issue=5 |pages= |year=2016 |pmid=27213420 |pmc=4881142 |doi=10.3390/ijerph13050517 |url=}}</ref><ref name="pmid11528578">{{cite journal |vauthors=Siddiqui AA, Berk SL |title=Diagnosis of Strongyloides stercoralis infection |journal=Clin. Infect. Dis. |volume=33 |issue=7 |pages=1040–7 |year=2001 |pmid=11528578 |doi=10.1086/322707 |url=}}</ref>
The diagnosis of strongyloidiasis is made by presence of clinical signs and symptoms, [[eosinophilia]], and positive serological findings. Definitive diagnosis of strongyloidiasis is generally made by the [[Stool examination|detection of larvae in the stool]]. [[Sputum culture|Sputum examination]] may rarely be used to identify organisms in cases of hyperinfection. [[Agar]] tracking (detection of larval tracks on [[Agar|agar culture]] plates) has been shown to be more [[Sensitivity (tests)|sensitive]] than the conventional [[stool examination]]. However, [[agar]] tracking is usually unavailable on a routine basis in clinical microbiology laboratories. [[Immunodiagnostics|Immunodiagnostic tests]] for [[strongyloidiasis]] are indicated when the [[infection]] is suspected and the organism cannot be demonstrated by repeated examinations of [[stool]]. [[Enzyme immunoassay]] ([[EIA]]) is currently recommended because of its greater [[sensitivity]] (90%). [[Antibody]] test results cannot be used to differentiate between the past and current infection. In disseminated cases of [[strongyloidiasis]], larvae can be detected in [[sputum]] by simple wet-mount in fluid from a [[bronchoalveolar lavage]] ([[BAL]]).


==Laboratory Findings==
==Laboratory Findings==
===Eosinophilia===
===Eosinophilia===
Blood [[eosinophilia]] is generally present during the acute and chronic stages, but may be absent with dissemination.
[[Eosinophilia]] is generally present during the acute and [[chronic]] stages but may be absent with dissemination.


=== Stool Samples ===  
===Microscopic Stool Examination===  
*The gold standard for the diagnosis of strongyloides is serial [[stool examination]].
*The gold standard for the diagnosis of strongyloidiasis is serial [[stool examination]].<ref name="pmid10405376">{{cite journal |vauthors=Cartwright CP |title=Utility of multiple-stool-specimen ova and parasite examinations in a high-prevalence setting |journal=J. Clin. Microbiol. |volume=37 |issue=8 |pages=2408–11 |year=1999 |pmid=10405376 |pmc=85240 |doi= |url=}}</ref><ref name="pmid28210503">{{cite journal |vauthors=Mendes T, Minori K, Ueta M, Miguel DC, Allegretti SM |title=Strongyloidiasis Current Status with Emphasis in Diagnosis and Drug Research |journal=J Parasitol Res |volume=2017 |issue= |pages=5056314 |year=2017 |pmid=28210503 |pmc=5292188 |doi=10.1155/2017/5056314 |url=}}</ref><ref name="pmid27213420">{{cite journal |vauthors=Beknazarova M, Whiley H, Ross K |title=Strongyloidiasis: A Disease of Socioeconomic Disadvantage |journal=Int J Environ Res Public Health |volume=13 |issue=5 |pages= |year=2016 |pmid=27213420 |pmc=4881142 |doi=10.3390/ijerph13050517 |url=}}</ref><ref name="pmid11528578">{{cite journal |vauthors=Siddiqui AA, Berk SL |title=Diagnosis of Strongyloides stercoralis infection |journal=Clin. Infect. Dis. |volume=33 |issue=7 |pages=1040–7 |year=2001 |pmid=11528578 |doi=10.1086/322707 |url=}}</ref>
*The diagnosis rests on the [[microscopic]] identification of larvae (rhabditiform and occasionally filariform) in the stool or [[duodenal]] fluid.  
*The diagnosis rests on the [[microscopic]] identification of larvae (rhabditiform and occasionally filariform) in the [[stool]].  
*[[Duodenal]] aspirate is more sensitive than [[stool examination]], and duodenal biopsy may reveal [[parasites]] in the [[gastric]] crypts, in the [[duodenal]] glands, or [[eosinophilic]] infiltration in the [[lamina propria]].
*Single ova and parasite examination can have negative results in up to 70% of cases.
*Specialized stool examinations include Baermann concentration, Horadi-Mori filter paper culture, quantitative acetate concentration technique, and nutrient [[agar plate]] cultures.
*Repeated examinations of stool specimens increase the chances of detecting larvae.
*The stool can be examined in wet mounts:
*The diagnostic sensitivity increases to 50% with three stool examinations and can approach 100% if seven serial stool samples are examined
**Directly
*Specialized [[Stool examination|stool examinations]] techniques include Baermann concentration, Horadi-Mori filter paper culture, quantitative [[acetate]] concentration technique, and nutrient [[agar plate]] cultures.
**After concentration (formalin-ethyl acetate)
*Diagnostic characteristics:
**After recovery of the larvae by the Baermann funnel technique
**length 200 to 250 µm (up to 380 µm)
**After culture by the Harada-Mori filter paper technique
**Short [[buccal cavity]]
**After culturing in [[Agar plate|agar plates]]
**Prominent genital primordium.
*The duodenal fluid can be examined using techniques such as the Enterotest string or duodenal aspiration.
*In disseminated cases of strongyloidiasis, larvae can be detected in sputum by simple wet-mount in fluid from a [[bronchoalveolar lavage]] (BAL).
*Diagnostic characteristics: length 200 to 250 µm (up to 380 µm); buccal cavity short, and prominent genital primordium.


[[Image:Strongyl larva1 DPDx.jpg|center|thumb|300px|A: Strongyloides stercoralis]]
[[Image:Strongyl larva1 DPDx.jpg|center|thumb|300px|Strongyloides stercoralis:The prominent genital primordium in the mid-section of the larva (black arrow) is readily evident. Note also the Entamoeba coli cyst (white arrow) near the posterior end of the larva. Source:<nowiki>https://commons.wikimedia.org/w/index.php?curid=219824</nowiki>]]
 
'''A:''' The prominent genital primordium in the mid-section of the larva (black arrow) is readily evident. Note also the Entamoeba coli cyst (white arrow) near the posterior end of the larva.


===Antibody Detection===
===Antibody Detection===
*[[Immunodiagnostics|Immunodiagnostic]] tests for strongyloidiasis are indicated when the infection is suspected and the organism cannot be demonstrated by duodenal aspiration, string tests, or by repeated examinations of stool.  
*[[Immunodiagnostics|Immunodiagnostic]] tests for strongyloidiasis are indicated when the [[infection]] is suspected and the organism cannot be demonstrated by [[duodenal]] aspiration, string tests, or by repeated examinations of [[stool]].  
* [[Antibody]] detection tests should use [[antigens]] derived from Strongyloides stercoralis filariform larvae for the highest sensitivity and specificity.  
* [[Antibody]] detection tests should use [[antigens]] derived from [[Strongyloides stercoralis|''Strongyloides stercoralis'']] filariform larvae for the highest sensitivity and specificity.  
* Although indirect [[fluorescent antibody]] (IFA) and indirect [[hemagglutination]] (IHA) tests have been used,   
* Although indirect [[fluorescent antibody]] (IFA) and indirect [[hemagglutination]] (IHA) tests have been used,   
* [[Immunocompromised]] persons with disseminated strongyloidiasis usually have detectable [[IgG]] antibodies despite their [[immunosuppression]].   
* [[Immunocompromised]] persons with disseminated strongyloidiasis usually have detectable [[IgG]] antibodies despite their [[immunosuppression]].   
* Cross-reactions in patients with [[filariasis]] and some other [[nematode]] infections can occur.  
* Cross-reactions in patients with [[filariasis]] and other [[nematode]] infections can occur.  
* [[Antibody]] test results cannot be used to differentiate between the past and current infection.
* [[Antibody]] test results cannot be used to differentiate between the past and current infection.
* A positive test warrants continuing efforts to establish a parasitological diagnosis followed by [[antihelminthic]] treatment.  
* A positive test warrants continuing efforts to establish a parasitological diagnosis followed by [[antihelminthic]] treatment.  
* [[Serologic]] monitoring may be useful in the follow-up of [[immunocompetent]] treated patients: antibody levels decrease markedly within 6 months after successful [[chemotherapy]]. <ref>http://www.dpd.cdc.gov/dpdx/HTML/Strongyloidiasis.htm</ref>
* [[Serologic]] monitoring may be useful in the follow-up of [[immunocompetent]] treated patients: [[antibody]] levels decrease markedly within 6 months after successful [[chemotherapy]].<ref>http://www.dpd.cdc.gov/dpdx/HTML/Strongyloidiasis.htm</ref>
* More sensitive and specific serologic tests using [[recombinant]] [[antigens]] have been, and are being developed, and are available at specific laboratories.  
* More sensitive and specific serologic tests using [[recombinant]] [[antigens]] have been and are being developed, and are available at specific laboratories.  
*An additional advantage to these serologic tests is that there is typically a significant drop in titer by 6 months after [[Parasites|parasite]] eradication, which may make it possible to use these tests as a "test of cure."
*An additional advantage of these serologic tests is that there is typically a significant drop in [[titer]] by 6 months after [[Parasites|parasite]] eradication, which may make it possible to use these tests as a check the response to medical therapy.


{{#ev:youtube|TSwN602mcn4}}
{{#ev:youtube|TSwN602mcn4}}
===Enzyme-linked immunosorbent assay===
*Serology can be useful but is not commonly available and can give false-negative results.
*Results for ELISA should be used in conjunction with clinical history and geographical data


==References==
==References==


{{Reflist|2}}
{{Reflist|2}}
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Latest revision as of 00:19, 30 July 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aditya Ganti M.B.B.S. [2]

Overview

The diagnosis of strongyloidiasis is made by presence of clinical signs and symptoms, eosinophilia, and positive serological findings. Definitive diagnosis of strongyloidiasis is generally made by the detection of larvae in the stool. Sputum examination may rarely be used to identify organisms in cases of hyperinfection. Agar tracking (detection of larval tracks on agar culture plates) has been shown to be more sensitive than the conventional stool examination. However, agar tracking is usually unavailable on a routine basis in clinical microbiology laboratories. Immunodiagnostic tests for strongyloidiasis are indicated when the infection is suspected and the organism cannot be demonstrated by repeated examinations of stool. Enzyme immunoassay (EIA) is currently recommended because of its greater sensitivity (90%). Antibody test results cannot be used to differentiate between the past and current infection. In disseminated cases of strongyloidiasis, larvae can be detected in sputum by simple wet-mount in fluid from a bronchoalveolar lavage (BAL).

Laboratory Findings

Eosinophilia

Eosinophilia is generally present during the acute and chronic stages but may be absent with dissemination.

Microscopic Stool Examination

  • The gold standard for the diagnosis of strongyloidiasis is serial stool examination.[1][2][3][4]
  • The diagnosis rests on the microscopic identification of larvae (rhabditiform and occasionally filariform) in the stool.
  • Single ova and parasite examination can have negative results in up to 70% of cases.
  • Repeated examinations of stool specimens increase the chances of detecting larvae.
  • The diagnostic sensitivity increases to 50% with three stool examinations and can approach 100% if seven serial stool samples are examined
  • Specialized stool examinations techniques include Baermann concentration, Horadi-Mori filter paper culture, quantitative acetate concentration technique, and nutrient agar plate cultures.
  • Diagnostic characteristics:
    • length 200 to 250 µm (up to 380 µm)
    • Short buccal cavity
    • Prominent genital primordium.
Strongyloides stercoralis:The prominent genital primordium in the mid-section of the larva (black arrow) is readily evident. Note also the Entamoeba coli cyst (white arrow) near the posterior end of the larva. Source:https://commons.wikimedia.org/w/index.php?curid=219824

Antibody Detection

  • Immunodiagnostic tests for strongyloidiasis are indicated when the infection is suspected and the organism cannot be demonstrated by duodenal aspiration, string tests, or by repeated examinations of stool.
  • Antibody detection tests should use antigens derived from Strongyloides stercoralis filariform larvae for the highest sensitivity and specificity.
  • Although indirect fluorescent antibody (IFA) and indirect hemagglutination (IHA) tests have been used,
  • Immunocompromised persons with disseminated strongyloidiasis usually have detectable IgG antibodies despite their immunosuppression.
  • Cross-reactions in patients with filariasis and other nematode infections can occur.
  • Antibody test results cannot be used to differentiate between the past and current infection.
  • A positive test warrants continuing efforts to establish a parasitological diagnosis followed by antihelminthic treatment.
  • Serologic monitoring may be useful in the follow-up of immunocompetent treated patients: antibody levels decrease markedly within 6 months after successful chemotherapy.[5]
  • More sensitive and specific serologic tests using recombinant antigens have been and are being developed, and are available at specific laboratories.
  • An additional advantage of these serologic tests is that there is typically a significant drop in titer by 6 months after parasite eradication, which may make it possible to use these tests as a check the response to medical therapy.

{{#ev:youtube|TSwN602mcn4}}

Enzyme-linked immunosorbent assay

  • Serology can be useful but is not commonly available and can give false-negative results.
  • Results for ELISA should be used in conjunction with clinical history and geographical data

References

  1. Cartwright CP (1999). "Utility of multiple-stool-specimen ova and parasite examinations in a high-prevalence setting". J. Clin. Microbiol. 37 (8): 2408–11. PMC 85240. PMID 10405376.
  2. Mendes T, Minori K, Ueta M, Miguel DC, Allegretti SM (2017). "Strongyloidiasis Current Status with Emphasis in Diagnosis and Drug Research". J Parasitol Res. 2017: 5056314. doi:10.1155/2017/5056314. PMC 5292188. PMID 28210503.
  3. Beknazarova M, Whiley H, Ross K (2016). "Strongyloidiasis: A Disease of Socioeconomic Disadvantage". Int J Environ Res Public Health. 13 (5). doi:10.3390/ijerph13050517. PMC 4881142. PMID 27213420.
  4. Siddiqui AA, Berk SL (2001). "Diagnosis of Strongyloides stercoralis infection". Clin. Infect. Dis. 33 (7): 1040–7. doi:10.1086/322707. PMID 11528578.
  5. http://www.dpd.cdc.gov/dpdx/HTML/Strongyloidiasis.htm

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