Comparative Evaluation of Three Rapid Influenza Diagnostic Tests for Detection of Influenza A and B Viruses Using RT‐PCR as Reference Method
ABSTRACT To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT‐PCR. A total of 291 subjects with acute respiratory infections were enrolled. Respiratory specimens were collected and tested for influenza A and B viruses us...
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Published in | Journal of medical virology Vol. 97; no. 1; pp. e70162 - n/a |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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01.01.2025
John Wiley and Sons Inc |
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Abstract | ABSTRACT
To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT‐PCR. A total of 291 subjects with acute respiratory infections were enrolled. Respiratory specimens were collected and tested for influenza A and B viruses using three RIDTs. The results were compared with those obtained using an RT‐PCR assay from Shanghai Berger Medical Technology Co. Ltd. as the reference method. Among the 291 subjects, 119 (40.9%) tested positive for influenza A virus and 38 (13.1%) for influenza B virus by RT‐PCR. The sensitivities of the three RIDTs for influenza A virus were 92.4%, 89.1%, and 79.8%, respectively, while their specificities were 98.8%, 98.8%, and 100%, respectively. For influenza B virus, the sensitivities of the three RIDTs were 92.1%, 92.1%, and 73.7%, respectively, and their specificities were 100%, 100%, and 100%, respectively. The positive predictive values (PPVs) for influenza A virus were 98.2%, 98.1%, and 100%, respectively, while the negative predictive values (NPVs) were 94.5%, 92.4%, and 86.9%, respectively. For influenza B virus, the PPVs were all 100%, and the NPVs were 99.2%, 99.2%, and 97.7%, respectively. The three evaluated RIDTs demonstrated high specificity but varied sensitivity for detecting influenza A and B viruses. Negative results from RIDTs should be confirmed by RT‐PCR, especially during peak influenza seasons. The high PPVs suggest that positive RIDT results are reliable for influenza diagnosis, while the high NPVs indicate that negative results are more likely to be true negatives. |
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AbstractList | ABSTRACT
To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT‐PCR. A total of 291 subjects with acute respiratory infections were enrolled. Respiratory specimens were collected and tested for influenza A and B viruses using three RIDTs. The results were compared with those obtained using an RT‐PCR assay from Shanghai Berger Medical Technology Co. Ltd. as the reference method. Among the 291 subjects, 119 (40.9%) tested positive for influenza A virus and 38 (13.1%) for influenza B virus by RT‐PCR. The sensitivities of the three RIDTs for influenza A virus were 92.4%, 89.1%, and 79.8%, respectively, while their specificities were 98.8%, 98.8%, and 100%, respectively. For influenza B virus, the sensitivities of the three RIDTs were 92.1%, 92.1%, and 73.7%, respectively, and their specificities were 100%, 100%, and 100%, respectively. The positive predictive values (PPVs) for influenza A virus were 98.2%, 98.1%, and 100%, respectively, while the negative predictive values (NPVs) were 94.5%, 92.4%, and 86.9%, respectively. For influenza B virus, the PPVs were all 100%, and the NPVs were 99.2%, 99.2%, and 97.7%, respectively. The three evaluated RIDTs demonstrated high specificity but varied sensitivity for detecting influenza A and B viruses. Negative results from RIDTs should be confirmed by RT‐PCR, especially during peak influenza seasons. The high PPVs suggest that positive RIDT results are reliable for influenza diagnosis, while the high NPVs indicate that negative results are more likely to be true negatives. To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT‐PCR. A total of 291 subjects with acute respiratory infections were enrolled. Respiratory specimens were collected and tested for influenza A and B viruses using three RIDTs. The results were compared with those obtained using an RT‐PCR assay from Shanghai Berger Medical Technology Co. Ltd. as the reference method. Among the 291 subjects, 119 (40.9%) tested positive for influenza A virus and 38 (13.1%) for influenza B virus by RT‐PCR. The sensitivities of the three RIDTs for influenza A virus were 92.4%, 89.1%, and 79.8%, respectively, while their specificities were 98.8%, 98.8%, and 100%, respectively. For influenza B virus, the sensitivities of the three RIDTs were 92.1%, 92.1%, and 73.7%, respectively, and their specificities were 100%, 100%, and 100%, respectively. The positive predictive values (PPVs) for influenza A virus were 98.2%, 98.1%, and 100%, respectively, while the negative predictive values (NPVs) were 94.5%, 92.4%, and 86.9%, respectively. For influenza B virus, the PPVs were all 100%, and the NPVs were 99.2%, 99.2%, and 97.7%, respectively. The three evaluated RIDTs demonstrated high specificity but varied sensitivity for detecting influenza A and B viruses. Negative results from RIDTs should be confirmed by RT‐PCR, especially during peak influenza seasons. The high PPVs suggest that positive RIDT results are reliable for influenza diagnosis, while the high NPVs indicate that negative results are more likely to be true negatives. To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT-PCR. A total of 291 subjects with acute respiratory infections were enrolled. Respiratory specimens were collected and tested for influenza A and B viruses using three RIDTs. The results were compared with those obtained using an RT-PCR assay from Shanghai Berger Medical Technology Co. Ltd. as the reference method. Among the 291 subjects, 119 (40.9%) tested positive for influenza A virus and 38 (13.1%) for influenza B virus by RT-PCR. The sensitivities of the three RIDTs for influenza A virus were 92.4%, 89.1%, and 79.8%, respectively, while their specificities were 98.8%, 98.8%, and 100%, respectively. For influenza B virus, the sensitivities of the three RIDTs were 92.1%, 92.1%, and 73.7%, respectively, and their specificities were 100%, 100%, and 100%, respectively. The positive predictive values (PPVs) for influenza A virus were 98.2%, 98.1%, and 100%, respectively, while the negative predictive values (NPVs) were 94.5%, 92.4%, and 86.9%, respectively. For influenza B virus, the PPVs were all 100%, and the NPVs were 99.2%, 99.2%, and 97.7%, respectively. The three evaluated RIDTs demonstrated high specificity but varied sensitivity for detecting influenza A and B viruses. Negative results from RIDTs should be confirmed by RT-PCR, especially during peak influenza seasons. The high PPVs suggest that positive RIDT results are reliable for influenza diagnosis, while the high NPVs indicate that negative results are more likely to be true negatives.To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT-PCR. A total of 291 subjects with acute respiratory infections were enrolled. Respiratory specimens were collected and tested for influenza A and B viruses using three RIDTs. The results were compared with those obtained using an RT-PCR assay from Shanghai Berger Medical Technology Co. Ltd. as the reference method. Among the 291 subjects, 119 (40.9%) tested positive for influenza A virus and 38 (13.1%) for influenza B virus by RT-PCR. The sensitivities of the three RIDTs for influenza A virus were 92.4%, 89.1%, and 79.8%, respectively, while their specificities were 98.8%, 98.8%, and 100%, respectively. For influenza B virus, the sensitivities of the three RIDTs were 92.1%, 92.1%, and 73.7%, respectively, and their specificities were 100%, 100%, and 100%, respectively. The positive predictive values (PPVs) for influenza A virus were 98.2%, 98.1%, and 100%, respectively, while the negative predictive values (NPVs) were 94.5%, 92.4%, and 86.9%, respectively. For influenza B virus, the PPVs were all 100%, and the NPVs were 99.2%, 99.2%, and 97.7%, respectively. The three evaluated RIDTs demonstrated high specificity but varied sensitivity for detecting influenza A and B viruses. Negative results from RIDTs should be confirmed by RT-PCR, especially during peak influenza seasons. The high PPVs suggest that positive RIDT results are reliable for influenza diagnosis, while the high NPVs indicate that negative results are more likely to be true negatives. |
Author | Kou, Hanlin Sun, Yuzhen Yin, Hailun Lv, Yuyang Wu, Wenjuan |
AuthorAffiliation | 2 Department of Respiratory Medicine Tianjin Fifth Central Hospital Tianjin China 1 Department of clinical laboratory Tianjin Fifth Central Hospital Tianjin China 3 Radiology department Tianjin Fifth Central Hospital Tianjin China |
AuthorAffiliation_xml | – name: 2 Department of Respiratory Medicine Tianjin Fifth Central Hospital Tianjin China – name: 3 Radiology department Tianjin Fifth Central Hospital Tianjin China – name: 1 Department of clinical laboratory Tianjin Fifth Central Hospital Tianjin China |
Author_xml | – sequence: 1 givenname: Hailun surname: Yin fullname: Yin, Hailun organization: Tianjin Fifth Central Hospital – sequence: 2 givenname: Wenjuan surname: Wu fullname: Wu, Wenjuan organization: Tianjin Fifth Central Hospital – sequence: 3 givenname: Yuyang surname: Lv fullname: Lv, Yuyang organization: Tianjin Fifth Central Hospital – sequence: 4 givenname: Hanlin surname: Kou fullname: Kou, Hanlin organization: Tianjin Fifth Central Hospital – sequence: 5 givenname: Yuzhen surname: Sun fullname: Sun, Yuzhen email: sunyuzhen2024@163.com organization: Tianjin Fifth Central Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39812072$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.5713/ab.24.0117 10.1093/infdis/jis548 10.1016/j.jcv.2014.01.009 10.3346/jkms.2022.37.e3 10.1161/CIRCOUTCOMES.124.011496 10.3389/fimmu.2024.1385362 10.1016/S0140-6736(20)30251-8 10.1016/j.jcv.2016.11.008 10.1515/jom-2022-0065 10.1093/cid/ciy866 10.1111/irv.13141 10.3390/v8040096 10.7326/0003-4819-156-7-201204030-00403 10.1128/JCM.00711-18 10.1128/JCM.02184-10 10.1016/j.jacc.2024.08.048 10.1086/600383 10.1038/s41598-024-71349-8 10.1016/j.jemermed.2009.11.031 10.1016/S0140-6736(17)33293-2 10.7326/M17-0848 10.1016/j.amjmed.2007.10.040 10.1002/jcla.22234 10.2217/fvl-2023-0091 |
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Keywords | reverse transcription‐polymerase chain reaction (RT‐PCR) rapid influenza diagnostic tests (RIDTs) influenza A and B viruses |
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To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT‐PCR. A total of... To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT‐PCR. A total of 291... To evaluate the performance of three rapid influenza diagnostic tests (RIDTs) for detecting influenza A and B viruses compared to RT-PCR. A total of 291... |
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SubjectTerms | Adolescent Adult Aged Aged, 80 and over Child Child, Preschool China Diagnostic systems Diagnostic tests Diagnostic Tests, Routine - methods Female Humans Infant Influenza Influenza A influenza A and B viruses Influenza A virus - genetics Influenza A virus - isolation & purification Influenza B Influenza B virus - genetics Influenza B virus - isolation & purification Influenza, Human - diagnosis Influenza, Human - virology Male Medical technology Middle Aged Performance evaluation Polymerase chain reaction Predictive Value of Tests rapid influenza diagnostic tests (RIDTs) Respiratory tract infection Reverse Transcriptase Polymerase Chain Reaction - methods reverse transcription‐polymerase chain reaction (RT‐PCR) Sensitivity analysis Sensitivity and Specificity Viruses Young Adult |
Title | Comparative Evaluation of Three Rapid Influenza Diagnostic Tests for Detection of Influenza A and B Viruses Using RT‐PCR as Reference Method |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmv.70162 https://www.ncbi.nlm.nih.gov/pubmed/39812072 https://www.proquest.com/docview/3158702761 https://www.proquest.com/docview/3155721055 https://pubmed.ncbi.nlm.nih.gov/PMC11733857 |
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