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A large prospective study assessing injection site reactions, quality of life and preference in patients using the Biojector vs standard needles for enfuvirtide administration.

A large prospective study assessing injection site reactions, quality of life and preference in patients using the Biojector vs standard needles for enfuvirtide administration. Research Abstract Details 

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  • A large prospective study assessing injection site reactions, quality of life and preference in patients using the Biojector vs standard needles for enfuvirtide administration. Abstract Text:

    m r loutfyM R Loutfy,m harrisM Harris,j m raboudJ M Raboud,t antoniouT Antoniou,c kovacsC Kovacs,s shenS Shen,s dufresneS Dufresne,f smaillF Smaill,d rouleauD Rouleau,a rachlisA Rachlis,k goughK Gough,r lalondeR Lalonde,c tsoukasC Tsoukas,b trottierB Trottier,s l walmsleyS L Walmsley,j s g montanerJ S G Montaner,

    OBJECTIVES: To determine the severity of injection site reactions (ISRs), patient quality of life (QoL) and preference when enfuvirtide is administered by the Biojector (Bioject, Medical Technologies, Inc., Tualatin, OR, USA) relative to standard needles. METHODS: A total of 201 HIV-positive patients on stable enfuvirtide-based therapy (n=184) or initiating such therapy (n=17) were evaluated prospectively after switching from standard needles to the Biojector system. Patients used needles for a minimum of 2 weeks prior to switching to the Biojector. Questionnaires to assess the incidence and severity of ISRs (31-item score) and QoL [Medical Outcomes Study HIV Health Survey (MOS-HIV)] were administered at baseline and following a minimum of 14 days of Biojector use. RESULTS: The median changes in ISR score and number of ISRs following a median of 1.0 month [interquartile range (IQR) 0.9, 1.3] of Biojector use were -3 (IQR -7, 1) and -1 (IQR -3, 1), respectively. The severity of pain (P<0.0001), induration (P<0.0001), pruritus (P<0.0001), nodules (P<0.0001) and erythema (P<0.0001) all decreased with the Biojector. Administration of enfuvirtide with the Biojector was associated with an improved patient QoL (P<0.0001), and was preferred by 72% of patients. CONCLUSIONS: Compared with needles, the Biojector was associated with a decreased severity of ISRs and improved QoL in patients taking enfuvirtide.

    A large prospective study assessing injection site reactions, quality of life and preference in patients using the Biojector vs standard needles for enfuvirtide administration. Publishing Authors By Initials

    mr loutfyMR Loutfy,m harrisM Harris,jm raboudJM Raboud,t antoniouT Antoniou,c kovacsC Kovacs,s shenS Shen,s dufresneS Dufresne,f smaillF Smaill,d rouleauD Rouleau,a rachlisA Rachlis,k goughK Gough,r lalondeR Lalonde,c tsoukasC Tsoukas,b trottierB Trottier,sl walmsleySL Walmsley,js montanerJS Montaner,

    For similar abstracts research abstracts see: abstracts research

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    A large prospective study assessing injection site reactions, quality of life and preference in patients using the Biojector vs standard needles for enfuvirtide administration. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: HIV medicine

    VOLUME: 8

    Page Numbers: 427-32

    Journal Abbreviation: HIV Med.

    ISSN: 1464-2662

    DAY: 31

    MONTH: Oct

    YEAR: 2007

    A large prospective study assessing injection site reactions, quality of life and preference in patients using the Biojector vs standard needles for enfuvirtide administration. Information

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    LANGUAGE: eng

    NlmUniqueID: 100897392

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    Grant and Affiliation Information for A large prospective study assessing injection site reactions, quality of life and preference in patients using the Biojector vs standard needles for enfuvirtide administration.

    AFFILIATION: Department of Medicine, University of Toronto, Maple Leaf Medical Clinic, and Department of Family and Community Medicine, St Michael's Hospital, Toronto, Ontario, Canada. Mona.Loutfy@wchospital.ca

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: HIV Med

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