2018
DOI: 10.1016/j.actatropica.2018.02.019
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Molecular diagnosis of Trypanosoma cruzi

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Cited by 80 publications
(64 citation statements)
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References 107 publications
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“…Similar rates of positivity have been previously reported for untreated CD chronic patients outside of endemic areas [20][21]. Moreover, PCR sensitivity reported in several studies performed in Latin America achieved results higher than 60% in chronic patients [22]. The use of different PCR protocols; the likelihood of re-infection episodes; or parasitological factors such as heterogeneous distribution of different strains could explain this difference.…”
Section: Discussionsupporting
confidence: 82%
“…Similar rates of positivity have been previously reported for untreated CD chronic patients outside of endemic areas [20][21]. Moreover, PCR sensitivity reported in several studies performed in Latin America achieved results higher than 60% in chronic patients [22]. The use of different PCR protocols; the likelihood of re-infection episodes; or parasitological factors such as heterogeneous distribution of different strains could explain this difference.…”
Section: Discussionsupporting
confidence: 82%
“…This may account in part for the estimation that one in two of all congenital infections with CD are missed [76]. New molecular diagnostic tools such as PCR, which is used in the United States for the diagnosis of congenital CD, may eventually facilitate less cumbersome diagnosis of such cases if they can be successfully adapted to clinical settings [ In patients who are immunosuppressed, detection of the parasite by a direct parasitological test or exponential increase of parasitic load on quantitative PCR must be considered a reactivation, and the affected individual should receive anti-parasitic treatment immediately to avoid severe morbidity and/or mortality [81,82].…”
Section: Diagnosis Of T Cruzi In Special Populationsmentioning
confidence: 99%
“…Real-time PCR have been developed with greater sensitivity than previous methods. For the design of primers, the variable region of the minicircle kinetoplast DNA (kDNA), a repeat tandem sequence of nuclear DNA (stDNA), ribosomal RNA (rRNA) or the paraflagellar rod (PFR) genes have been used [103,104].…”
Section: Lamp In Diagnosis Of American Try-panosomiasis (T Cruzi)mentioning
confidence: 99%