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pediatric upper extremity function computer adaptive test ue  (ProMIS Neurosciences)

 
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    ProMIS Neurosciences pediatric upper extremity function computer adaptive test ue
    Pediatric Upper Extremity Function Computer Adaptive Test Ue, supplied by ProMIS Neurosciences, 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/adaptative/upper+extremity+computer+adaptive+test/nct05131685-56-2-10
    Average 90 stars, based on 1 article reviews
    pediatric upper extremity function computer adaptive test ue - by Bioz Stars, 2026-11
    90/100 stars

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    Article Title: Addition of PROMIS Pain Instruments to PROMIS Upper Extremity Physical Function Improves the Responsiveness of PROMIS scores compared to Legacy scores in patients undergoing Total Shoulder Arthroplasty: A Prospective Study.
    Article Snippet: Please cite this article as: Romeo PV, Alben MG, Papalia AG, Chowdhury T, Cecora AJ, Ragland D, Kwon YW, Zuckerman JD, Virk MS, Addition of PROMIS Pain Instruments to PROMIS Upper Extremity Physical Function Improves the Responsiveness of PROMIS scores compared to Legacy scores in patients undergoing Total Shoulder Arthroplasty: A Prospective Study, Journal of Shoulder and Elbow Surgery (2025), doi: https://doi.org/10.1016/j.jse.2024.11.012.

    Article Title: Does the Addition of PROMIS Pain Instruments Improve the Sensitivity of PROMIS Upper Extremity Scores Following Arthroscopic Rotator Cuff Repair?
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

    Article Title: Reduction and Nonreduction Treatment of Displaced Pediatric Distal Radius Fractures (Peds-DRIFT Trial - Distal Radius Interventions for Fracture Treatment)
    Article Snippet: Measure Description: pediatric upper extremity function PROMIS computer adaptive test (PROMIS UE CAT).

    Article Title: The Use of Patient-Reported Outcomes in Clinical Practice: A National Survey of Hand Surgeons
    Article Snippet: PROMIS upper-extremity computer adaptive testing and Quick DASH have been found to demonstrate large ceiling effects in high-functioning individuals., However, studies have found the computer adaptive testing technique PROMIS physical function upper-extremity computer adaptive testing to be an efficient, useful, and less burdensome alternative to the Quick DASH with fewer floor or ceiling effects.

    Article Title: PROMIS-9 UE physical function demonstrates moderate responsiveness for patients following upper limb prosthesis intervention
    Article Snippet: Previous work with the PROMIS Upper Extremity Computer Adaptive Test (PROMIS-UE CAT) demonstrated high responsiveness to change in a population of patients with hand or upper extremity injury [ ].

    Article Title: Establishing the Patient Acceptable Symptoms State for the Boston Carpal Tunnel Questionnaire in a Postoperative Carpal Tunnel Surgery Population.
    Article Snippet: Methods Adults ( 18 years) from a single, tertiary-care academic institution were contacted 12 1 months after carpal tunnel release.. The Boston Carpal Tunnel Questionnaire and two PASS anchor questions were administered via REDCap—one queried acceptability of their current symptoms, and the other queried function.. Participants were classified as being in an acceptable symptom state (“PASS(þ)”) if they answered “very satisfied” or “somewhat satisfied,” whereas those responding “neither satisfied nor dissatisfied,” “somewhat dissatisfied,” or “very dissatisfied” were classified as “PASS( ).” Threshold values were calculated using three methods: (1) the mean score for PASS(þ) participants, (2) the 75th percentile score for PASS(þ) patients, and (3) the Youden Index determined using receiver operating curve (ROC) analysis to maximize sensitivity and specificity.

    Article Title: Clinical outcomes of open Latarjet-Patte procedures performed for recurrent anterior shoulder instability with primary bone loss versus failed arthroscopic Bankart repair.
    Article Snippet: Metrics acquired included baseline patient demographics, shoulder range of motion (ROM), radiological imaging (radiographs, magnetic resonance imaging [MRI], computed tomography [CT] scans), and pre-operative clinical outcome scores in the form of patient-reported outcomes measurement information system (PROMIS) upper extremity (UE) computer adaptive test version 2.0, pain intensity, and pain interference.

    Chloramphenicol Acetyltransferase Assay:

    Article Title: PROMIS-9 UE physical function demonstrates moderate responsiveness for patients following upper limb prosthesis intervention.
    Article Snippet: One methodology that was created to produce high-quality instruments to quantify various domains of health and wellness, including physical function, was the Patient- Reported Outcomes Measurement Information System (PROMIS) [2, 22]. .. Previous work with the PROMIS Upper Extremity Computer Adaptive Test (PROMIS-UE CAT) demonstrated high responsiveness to change in a population of patients with hand or upper extremity injury [9]. ..



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    FPD response as a function of PIFR for the 26 runs. (A) The runs in red are counted in the desired FPD range (600 ± 200 μg) and (B) the runs in red are counted in the constant FPD region (750 ± 200 μg) for the low resistance RS01 DPI. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Journal: International Journal of Pharmaceutics: X

    Article Title: Determination of the optimal resistance in RS01 for robust aerosol performance of inhaled controlled-release budesonide powder for chronic obstructive inflammatory respiratory diseases patients

    doi: 10.1016/j.ijpx.2026.100581

    Figure Lengend Snippet: FPD response as a function of PIFR for the 26 runs. (A) The runs in red are counted in the desired FPD range (600 ± 200 μg) and (B) the runs in red are counted in the constant FPD region (750 ± 200 μg) for the low resistance RS01 DPI. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Article Snippet: An impaction test is performed using three size 3 HPMC capsules filled with 20 ± 0.5 mg of the blend, inserted into the RS01 inhaler connected onto the AIT using an RS01 adapter (Copley Scientific).

    Techniques:

    FPD response as a function of PIFR for 23 runs. (A) The runs in red are counted in the desired robust FPD region (600 ± 200 μg) and (B) The runs in red are counted in the constant FPD region (650 ± 200 μg) for the low-medium resistance RS01 DPI. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

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    Article Title: Determination of the optimal resistance in RS01 for robust aerosol performance of inhaled controlled-release budesonide powder for chronic obstructive inflammatory respiratory diseases patients

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    Figure Lengend Snippet: FPD response as a function of PIFR for 23 runs. (A) The runs in red are counted in the desired robust FPD region (600 ± 200 μg) and (B) The runs in red are counted in the constant FPD region (650 ± 200 μg) for the low-medium resistance RS01 DPI. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

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