PATIENT PERSPECTIVES

KEEPING LONG-TERM HEALTH IN MIND STARTS WITH VIROLOGICAL SUPPRESSION, BUT PLHIV ARE LOOKING FOR MORE FROM THEIR TREATMENT

Based on Insights From Positive Perspectives, a Global Study of 2,389 PLHIV Currently Receiving ART, Many Participants Were Not Optimally Served by Their Current Regimens[1,2]

long term
long term

In the Positive Perspectives study, participants self-rated their overall health, treatment satisfaction and virological control. Current and past treatments were not reported. The study expanded from 2,112 participants in 24 countries to 2.389 participants in 25 countries following the first publication. Among the 2,112 original participants, 1,550 had ever switched ART since starting treatment.[1,2]

*Willingness to switch was predicated on the understanding that they would remain virologically suppressed.[2]

IS POLYPHARMACY* LINKED TO POORER HEALTH OUTCOMES? 

People With Polypharmacy Report Significantly Poorer Health Outcomes Compared With Those Without Polypharmacy, Independent of Existing Comorbidities (N=2,112)[2]

Survey results from patients with and without polypharmacy present.
Survey results from patients with and without polypharmacy present.

*Polypharmacy was defined as taking 5 or more pills per day for HIV or non-HIV conditions, or taking medicines currently for 5 or more conditions, including HIV. All differences between people with a report of polypharmacy compared with those not reporting polypharmacy were significant at P<0.05.[2]

PLHIV REPORTED SIGNIFICANT IMPROVEMENTS IN TREATMENT SATISFACTION AFTER SWITCHING TO DOVATO

Greater Patient Satisfaction with Dovato vs. Continued Current Regimens

Top Five Factors Driving Improvements vs. Baseline Through 48 Weeks[3

  • Improvements vs baseline also seen across all other factors measured, including convenience, flexibility, satisfaction with treatment demands and satisfaction with current treatment*
Survey results that show patient satisfaction
Survey results that show patient satisfaction

Patient-reported outcomes were assessed using the HIV Treatment Satisfaction Questionnaire, stats version and the symptom distress module at baseline and Weeks 24 and 48. Percentages reflect the percentage change from baseline in proportion of participants with a 6 out of 6 score for each treatment satisfaction individual item through Week 48 where 0=very dissatisfied, poorly controlled, inconvenient and inflexible; 3=neutral response; and 6=very satisfied, convenient and flexible.
*Improvements vs continued current regimens in 9 of 10 factors, and the same improvement with continued current regimens in 1 of 10.

Durable and robust[4,5]

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Beyond viral suppression

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References:

  1. Okoli C, Brough G, Allan B, et al. Putting the heart back into HAART: greater HCP-patient engagement is associated with better health outcomes among persons living with HIV (PLHIV) on treatment. Presented at: 23rd International AIDS Conference; July 6-10, 2020; Virtual. Poster PED0808.
  2. Okoli C, de los Rios P, Eremin A, Brough G, Young B, Short D. Relationship between polypharmacy and quality of life among people in 24 countries living with HIV. Prev Chronic Dis. 2020;17:E22. doi:10.5888/pcd17.190359 
  3. Kumar PN, Clarke AE, Jonsson-Oldenbüttel C, et al. Patient-reported outcomes after switching to a 2-drug regimen of fixed-dose combination dolutegravir/lamivudine (DTG/3TC): 48-week results from the SALSA study. ViiV Healthcare. 2022. Poster P07.
  4. Cahn P, Sierra Madero J, Arribas JR, et al. Three-year durable efficacy of dolutegravir plus lamivudine in antiretroviral therapy-naïve adults with HIV-1 infection. AIDS. 2022;36(1):39-48. doi:10.1097/QAD.0000000000003070
  5. Osiyemi O, De Wit S, Ajana F, et al. Efficacy and safety of switching to dolutegravir/lamivudine (DTG/3TC) versus continuing a tenofovir alafenamide-based 3- or 4-drug regimen for maintenance of virologic suppression in adults living with HIV-1: results through week 144 from the phase 3, non-inferiority TANGO randomized trial. Clin Infect Dis. 2022;ciac036 and suppl 1-18. doi:10.1093/cid/ciac036

October 2022 PM-GB-DLL-WCNT-220006

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