Wednesday, October 23, 2019 4:17:13 PM
https://ignsconference.com/36-study-to-evaluate-patient-centered-outcomes-and-infusion-parameters-using-the-rms-highflo-super-26-needle-set-vs-rms-standard-highflo-26gauge-needle-set-in-patients-with-primary-immunodeficiency/
The Super 26 needle is FDA-cleared but has yet to be released for commercial or clinical use on a larger scale. Patient-completed surveys captured infusion parameters, satisfaction scores, and incidental (minor) adverse events at each of 8 infusions (4 infusions with standard 26g needles vs. 4 infusions with Super 26g needles). Each subject will serve as his/her own control. Paired analysis of variance will be used to assess for differences in continuous variables and chi squared tests will be used to assess dichotomous variables. Results: Study is currently ongoing and results will be available at the time of conference presentation. Discussion: Study is currently ongoing and discussion will be available at the time of conference presentation. Conclusions: Study is currently ongoing and conclusion will be available at the time of conference presentation.[color=red][/color]
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