Likely False-Positive Pneumococcal Antigen Test BinaxNOW Due to Parvimonas micra

CHEST Journal ◽  
2018 ◽  
Vol 153 (4) ◽  
pp. e71-e73 ◽  
Author(s):  
Marie-Caroline Ploton ◽  
Marion Caseris ◽  
Christelle Jost ◽  
Yoann Picard ◽  
Jean Gaschignard ◽  
...  
The Lancet ◽  
2001 ◽  
Vol 358 (9289) ◽  
pp. 1273-1274 ◽  
Author(s):  
Carles Alonso-Tarrées ◽  
Cristina Cortés-Lletget ◽  
Teresa Casanova ◽  
Anna Domènech

2013 ◽  
Vol 43 (11-12) ◽  
pp. 483-485 ◽  
Author(s):  
A.S. Daubié ◽  
J. Mayaux ◽  
L. Epelboin ◽  
C. de Tymowski ◽  
A. Mbadi ◽  
...  

2004 ◽  
Vol 39 (2) ◽  
pp. 289-290 ◽  
Author(s):  
J. Maertens ◽  
K. Theunissen ◽  
G. Verhoef ◽  
J. Van Eldere

2020 ◽  
Vol 13 (1) ◽  
Author(s):  
Viktor Szatmári ◽  
Martin Willem van Leeuwen ◽  
Christine Jantine Piek ◽  
Luigi Venco

Abstract Background Dirofilaria immitis is responsible for heartworm disease in dogs in endemic areas worldwide. Screening for this infection is done by blood tests. Antigen testing is the most sensitive method to detect an infection with adult (female) worms. Microscopic examination of a blood smear or Knott’s test can be used to detect circulating microfilariae, the infective larvae. To increase the sensitivity of the antigen test by decreasing the false negative test results, heating of the blood sample has been recommended in recent guidelines. Heating is believed to remove blocking immune-complexes. Circulating microfilariae are not specific findings for heartworm infection, as other nematodes (among others, Acanthocheilonema dracunculoides) can also result in microfilaremia. Although the type of microfilariae cannot be determined by microscopy alone, real-time PCR can reliably identify the infecting nematode species. Correct identification of the parasite is of major importance, as an infection with D. immitis requires antiparasitic therapy, whereas A. dracunculoides is thought to be a clinically irrelevant coincidental finding. The present case report describes a microfilaremic dog where the initial antigen test for D. immitis turned positive after heat treatment, whereas real-time PCR revealed that the microfilariae were A. dracunculoides (syn. Dipetalonema dracunculoides). Results A circa 5-year old, asymptomatic Spanish mastiff dog was referred for heartworm therapy because microfilariae were found via a screening blood test. The dog was recently imported to the Netherlands from Spain, where it had been a stray dog. Antigen tests on a plasma sample for D. immitis were performed with three different test kits, which all turned out to be negative. However, heat treatment of two of these samples were carried out and both of them led to a positive antigen test result. Real-time PCR showed that the circulating microfilariae belonged to A. dracunculoides species. Three administrations of moxidectin spot-on at monthly intervals resulted in a negative antigen and a negative Knott’s tests one month after the last treatment. Conclusions We conclude that heat treatment of initially negative blood samples for D. immitis could lead to false positive antigen test results if the dog is infected with A. dracunculoides.


2000 ◽  
Vol 19 (11) ◽  
pp. 1114-1115 ◽  
Author(s):  
Suzanne Schroeder ◽  
Gary W. Procop
Keyword(s):  

2020 ◽  
Vol 26 (2) ◽  
Author(s):  
Yohanes Firmansyah ◽  
Jessica Elizabeth ◽  
Hendsun Hendsun ◽  
Darren Gosal

Abstract: Early diagnosis of dengue fever and COVID-19 is made very easy due to technological advancements. The  non-structural protein 1 antigen test strips are widely used in various regions; however, false-positive events have begun to be reported in the dengue-endemic areas with the COVID-19 pandemic, even though statistically non-structural protein 1 antigens are very specific to dengue infection. We reported a case of the false-positive non-structural protein 1 test in a patient with COVID-19 infection.


2021 ◽  
Author(s):  
Zannat Kawser ◽  
Mohabbat Hossain ◽  
Sara Suliman ◽  
Shahin Lockman ◽  
Jesse Gitaka ◽  
...  

Early detection of SARS-CoV-2 infection is crucial to prevent the spread of the virus. In this study, we evaluated the performance of a commercial rapid antigen detection test, BD Veritor, and compared this (and another rapid test, Standard Q) against a gold-standard of nasopharyngeal (NP) swab tested by reverse transcription-polymerase chain reaction (RT-PCR) in prospectively recruited adults in Dhaka, Bangladesh. We compared the sensitivity and specificity of the two rapid antigen tests against RT-PCR results in 130 symptomatic and 130 asymptomatic adults. In addition, we evaluated the suitability and ease-of-use of the BD Veritor test in a subsample of study participants (n=42) and implementers (n=5). The sensitivity of the BD Veritor rapid antigen 66 test was 70% in symptomatic (95% confidence interval [CI]: 51-85%) and 87% (95% CI: 69-96%) in asymptomatic individuals with positive SARSCoV-2 RT-PCR, for overall sensitivity of 78% (95% CI: 66-88%). The sensitivity of the Standard Q rapid antigen test was 63% (95% CI: 44-69 80%) in symptomatic and 73% (95% CI: 54-87%) in asymptomatic individuals. One false positive in BD Veritor test (specificity 99.5) and no false positive in Standard Q tests were observed (specificity 100%). The BD Veritor rapid antigen test was 78% sensitive when compared with RT-PCR irrespective of the cycle threshold (Ct) levels in this evaluation in Bangladesh. The implementation evaluation data showed good acceptability in the field settings. This warrants large field evaluation as well as use of the rapid antigen test for quick assessment of SARS-CoV-2 for containment of epidemics in the country.


2017 ◽  
Vol 55 (8) ◽  
pp. 2294-2297 ◽  
Author(s):  
Kristle L. Haberichter ◽  
Paul C. Johnson ◽  
Paul J. Chittick ◽  
Peter Millward ◽  
Barbara Robinson-Dunn ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document