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Long-term efficacy and safety of polyalkylimide gel for the treatment of HIV-associated lipoatrophy

Bibliographic Data

ID21111727
AuthorsTony Antoniou (0000-0002-6984-8953, Canadian Institutes of Health Research, corresponding author), Janet Raboud (University Health Network), Janet M Raboud (b Division of Infectious Diseases , University Health Network, University of Toronto , Canada), Colin Kovacs (0000-0003-3932-6545, Maple Leaf Medical Clinic), Christina Diong (University Health Network), Jason Brunetta (0000-0002-0506-8616, Canadian Institutes of Health Research), Graham Smith (0000-0002-8537-4241, Canadian Institutes of Health Research), Roberta Halpenny (Canadian Institutes of Health Research), Francis Beninger (University of Toronto), Mona Loutfy (0000-0001-7887-8997, Women's College Hospital), Mona R Loutfy (f Canadian Immunodeficiency Research Collaborative, Women's College Hospital , University of Toronto , Canada)
Year2009
Volume21
Issue10
Pages1247-1252
Publication date2009-10-01
Peer ReviewedYes
Open AccessNo
TypeARTICLE
VenueAIDS Care (JOURNAL)
Journal identifiersISSN: 0954-0121 • E-ISSN: 1360-0451
PublisherInforma UK Limited (PUBLISHER • GB)
DOI10.1080/09540120902814379
PMID20024700
OpenAlexW2024038220
LanguageEN
References cited15

The long-term safety and efficacy of products used in the correction of HIV-associated facial lipoatrophy (FLA) are largely unknown. The purpose of this study was to describe the long-term efficacy and safety of polyalkylimide gel (PAIG) in the treatment of HIV-associated FLA. In this open-label, randomized, single-center study, 31 HIV-positive individuals (median age 48 years (interquartile ranges (IQR) 45, 55, 97% male) with FLA were randomized to immediate (week 0 and six) or delayed (week 12 and 18) PAIG injections. Week 96 endpoints included change in FLA severity scores (FLSS) (five-point scale), proportion of patients with adverse events, and changes in quality of life, depression and anxiety using validated surveys. Results at week 96 were available for 28 patients. Adverse events, including swelling, redness, bruising and pain, were mild, and resolved after a median of three days following the injection. At week 96, median changes in physician and patient FLSS scores were -2 (IQR -3, -1; p<0.001 vs. baseline) and -2 (IQR -2, -1; p<0.001 vs. baseline), respectively. Physician and patient FLSS scores were not significantly different between the groups at week 96. Significant improvements in patient's anxiety (p<0.001), depression (p<0.001) and mental health (p=0.01) were observed from baseline to week 96. In conclusion, treatment with PAIG was associated with sustained improvements in both the physical and psychological components of FLA through 96 weeks of follow-up

Adverse effect · Antiretroviral therapy · Anxiety · Interquartile range · Lipoatrophy · Physical therapy · Psychiatry · Randomized controlled trial · Viral load · Dermatological and COVID-19 studies · Herpesvirus Infections and Treatments · Medicine · Systemic Lupus Erythematosus Research · Internal Medicine

  • Evidence for reliability, validity and usefulness of the Medical Outcomes Study HIV Health Survey (MOS-HIV)

    Open Access•A W Wu, D A Revicki et al.•Quality of Life Research•1997

Citation velocityhistorical
Highly citedNo

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