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Auditec Inc frequency pattern test (fpt) auditec version
Frequency Pattern Test (Fpt) Auditec Version, supplied by Auditec Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/test+sequence/pitch+pattern+sequence+test/pm33237189-101-1-5
Average 90 stars, based on 1 article reviews
frequency pattern test (fpt) auditec version - by Bioz Stars, 2026-10
90/100 stars

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Article Title: Performance of public and private school students in auditory processing, receptive vocabulary, and reading comprehension.
Article Snippet: The auditory skills of figure-ground, association between auditory and visual stimuli, figure-ground for linguistic sounds, binaural integration, temporal ordering, and temporal resolution were assessed using the following auditory behavioral instruments: Pediatric Speech Intelligibility (PSI) test, Dichotic Digits Test (DDT), Auditec® Frequency Pattern Test (FPT), and Gaps-in-Noise (GIN) test.

Article Title: Referral and Diagnosis of Developmental Auditory Processing Disorder in a Large, United States Hospital-Based Audiology Service.
Article Snippet: Background: Children referred to audiology services with otherwise unexplained academic, listening, attention, language, or other difficulties are often found to be audiometrically normal.. Some of these children receive further evaluation for auditory processing disorder (APD), a controversial construct that assumes neural processing problems within the central auditory nervous system.. This study focuses on the evaluation of APD and how it relates to diagnosis in one large pediatric audiology facility.

Article Title: DPOAE growth function in schoolchildren with impaired temporal ordering skills
Article Snippet: Subsequent to the compliance with the inclusion criteria, the participants performed the following temporal processing assessments (children's version, Auditec Saint Louis ( ) ): Frequency Pattern Test (FPT) and Duration Pattern Test (DPT).

Article Title: Performance of public and private school students in auditory processing, receptive vocabulary, and reading comprehension.
Article Snippet: The Frequency Pattern Test (FPT) (Auditec® version) (1997)(23) was used to evaluate the temporal ordering ability.

Article Title: Age-Related Listening Performance Changes Across Adulthood
Article Snippet: Design: We assessed 80 participants with normal hearing, at least 10 years of education, and normal global cognition.. The participants completed various auditory tests, including speech-in-noise, dichotic digits, duration, pitch pattern sequence, gap in noise, and masking level difference.. In addition, we conducted working memory assessments and administered a questionnaire on self-perceived hearing difficulties.

Article Title: Auditory processing abilities in prematurely born children.
Article Snippet: Aim To compare the performance in temporal auditory ordering and resolution tests and the latency and amplitude in the records of middle latency auditory evoked potential and P3 of prematurely born children with the performance of full-term children undergoing the same assessment protocol.. Study design: Cross-sectional observational study.. Subjects: Fifty-two children, aged 8 to 10 years, participated in the study and were divided into two groups: study group: 16 prematurely born children, and control group: 36 born full-term, at low risk for developmental alteration and without scholastic or hearing difficulties.

Article Title: Temporal Ordering and Auditory Resolution in Individuals with Sensorineural Hearing Loss
Article Snippet: The tests were a frequency pattern test (FPT), a duration pattern test (DPT), and an RGDT (standard and expanded versions), all commercialized by Auditec, Inc. (Saint Louis, MO, US).

Labeling:

Article Title: Masking Level Difference: Performance of School Children Aged 7–12 Years
Article Snippet: .. Data were collected in the following order: 1) Signing of the Informed Consent Form (ICF) and anamnesis with parents and/or guardians, 2) Otoscopy, 3) Peripheral hearing assessment, 4) MLD, 5) Dichotic digits test (DDT) in the stage of binaural integration, with a list of 80 digits, two presented in each ear simultaneously [ ], 6) Pediatric speech intelligibility (PSI) test or synthetic sentence identification (SSI) [ ], with ipsilateral competing message at -15 dB signal /noise ratio, 7) Random interval detection test (RGDT) for detecting the temporal acuity threshold [ ], 8) Noise speech test (NST) which consists of 25 monosyllabic words with white noise, presented monoaurally, and 9) Frequency pattern test (FPT), presented for the labeling task, using the Auditec ® (Auditec, Inc., St. Louis, MO, USA) [ ] version for children aged 7 and 8, and the Musiek version (available from https://auditec.com/price/ ; Auditec, Inc., St. Louis, MO, USA) for children over 9 years old [ ]. ..



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Summary of enrolled plasma mcfDNA-sequencing studies published from 1st January 2015 to 28th February 2025. USA*: Refer to. , , , , China*: Refer to. , Germany*:Refer to.

Journal: Infection and Drug Resistance

Article Title: Refining the Clinical Utility of Plasma Microbial Cell-Free DNA Sequencing in High-Risk Population of Infection: A Narrative Review

doi: 10.2147/IDR.S562107

Figure Lengend Snippet: Summary of enrolled plasma mcfDNA-sequencing studies published from 1st January 2015 to 28th February 2025. USA*: Refer to. , , , , China*: Refer to. , Germany*:Refer to.

Article Snippet: Christians et al developed a workflow that enriches ultrashort and rare mcfDNA fragments prior to Karius test sequencing, enabling the identification of key AMR genes, such as SCCmec, mecA, mecC, vanA, vanB, blaCTX-M , and blaKPC , with diagnostic yields ranging from 56.8% to 83.3%.

Techniques: Clinical Proteomics, Sequencing

The refinement strategy of clinical utility of plasma mcfDNA sequencing and prospective. *Co-mNGS Integration (Plasma + Blood Cell DNA): Cost-effectiveness should be further investigated, particularly in resource-limited settings.

Journal: Infection and Drug Resistance

Article Title: Refining the Clinical Utility of Plasma Microbial Cell-Free DNA Sequencing in High-Risk Population of Infection: A Narrative Review

doi: 10.2147/IDR.S562107

Figure Lengend Snippet: The refinement strategy of clinical utility of plasma mcfDNA sequencing and prospective. *Co-mNGS Integration (Plasma + Blood Cell DNA): Cost-effectiveness should be further investigated, particularly in resource-limited settings.

Article Snippet: Christians et al developed a workflow that enriches ultrashort and rare mcfDNA fragments prior to Karius test sequencing, enabling the identification of key AMR genes, such as SCCmec, mecA, mecC, vanA, vanB, blaCTX-M , and blaKPC , with diagnostic yields ranging from 56.8% to 83.3%.

Techniques: Clinical Proteomics, Sequencing

Flow diagram depicting patient and sample selection for the comparison of BAL fluid mcfDNA sequencing with the Karius® test and standard of care testing.

Journal: medRxiv

Article Title: Microbial cell-free DNA sequencing of bronchoalveolar lavage fluid improves diagnostic yield and may add clinical utility in immunocompromised patients with severe pneumonia

doi: 10.1101/2025.11.05.25339543

Figure Lengend Snippet: Flow diagram depicting patient and sample selection for the comparison of BAL fluid mcfDNA sequencing with the Karius® test and standard of care testing.

Article Snippet: For each sample, the BAL fluid mcfDNA sequencing test report included the name of each identified organism, the number of microbial reads found for the organism, and the Karius® designation for the pathogenicity of the organism (see Definitions).

Techniques: Selection, Comparison, Sequencing

Additive diagnostic value of BAL fluid mcfDNA sequencing with the Karius® test (KT-BAL) compared to standard of care (SOC) testing in immunocompromised patients with pneumonia. A) Number of organisms across all samples identified by either SOC alone, KT-BAL alone, or both techniques, split by KT-BAL category. B) Organisms identified exclusively by KT-BAL across all samples, split by KT-BAL category.

Journal: medRxiv

Article Title: Microbial cell-free DNA sequencing of bronchoalveolar lavage fluid improves diagnostic yield and may add clinical utility in immunocompromised patients with severe pneumonia

doi: 10.1101/2025.11.05.25339543

Figure Lengend Snippet: Additive diagnostic value of BAL fluid mcfDNA sequencing with the Karius® test (KT-BAL) compared to standard of care (SOC) testing in immunocompromised patients with pneumonia. A) Number of organisms across all samples identified by either SOC alone, KT-BAL alone, or both techniques, split by KT-BAL category. B) Organisms identified exclusively by KT-BAL across all samples, split by KT-BAL category.

Article Snippet: For each sample, the BAL fluid mcfDNA sequencing test report included the name of each identified organism, the number of microbial reads found for the organism, and the Karius® designation for the pathogenicity of the organism (see Definitions).

Techniques: Diagnostic Assay, Sequencing

Patients for whom BAL fluid mcfDNA testing with the Karius® test (KT-BAL) identified Category One or Two organisms missed by standard of care (SOC) had significantly more cumulative intubation days compared to patients where KT-BAL and SOC were concordant for all Category One or Two organisms. Hospital length of stay, ICU length of stay, and ICU mortality were worse in the KT-BAL only group, but these differences were not significant (Mann-Whitney U test for continuous variables, Fisher’s exact test for mortality).

Journal: medRxiv

Article Title: Microbial cell-free DNA sequencing of bronchoalveolar lavage fluid improves diagnostic yield and may add clinical utility in immunocompromised patients with severe pneumonia

doi: 10.1101/2025.11.05.25339543

Figure Lengend Snippet: Patients for whom BAL fluid mcfDNA testing with the Karius® test (KT-BAL) identified Category One or Two organisms missed by standard of care (SOC) had significantly more cumulative intubation days compared to patients where KT-BAL and SOC were concordant for all Category One or Two organisms. Hospital length of stay, ICU length of stay, and ICU mortality were worse in the KT-BAL only group, but these differences were not significant (Mann-Whitney U test for continuous variables, Fisher’s exact test for mortality).

Article Snippet: For each sample, the BAL fluid mcfDNA sequencing test report included the name of each identified organism, the number of microbial reads found for the organism, and the Karius® designation for the pathogenicity of the organism (see Definitions).

Techniques: MANN-WHITNEY