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Comparative Effectiveness of First Antiretroviral Regimens in Clinical Practice Using a Causal Approach
- Source :
- Medicine, Medicine, Lippincott, Williams & Wilkins, 2015, 94 (39), pp.e1668, Medicine, 2015, 94 (39), pp.e1668. ⟨10.1097/MD.0000000000001668⟩, Medicine, Lippincott, Williams & Wilkins, 2015, 94 (39), pp.e1668. ⟨10.1097/MD.0000000000001668⟩
- Publication Year :
- 2015
- Publisher :
- HAL CCSD, 2015.
-
Abstract
- International audience; The objective of this study was to estimate the cumulative incidences of failure by months 12 (M12) and 24 (M24) for the most prescribed first-line anti-retroviral regimens (ART). It is retrospective analysis of a prospectively collected database. All patients who initiated their first ART with the most prescribed regimens between 1st January 2004 and 30th June 2013 in 12 large HIV reference centers in France were included. The outcome was treatment failure--defined by any treatment modification for virological or tolerability reasons--and comparisons between regimens were carried out at M12 and M24. Adjusted and weighted methods via the propensity score (PS) were used to compare the effectiveness of the first antiretroviral regimens. Potential confounders of the treatment-outcome association were used to estimate PS with multinomial logistic regression. Overall, 3128 and 2690 patients were included in the M12 and M24 analyses, respectively. Patients received 5 different regimens (ABC/3TC with ATV/r or DRV/r, TDF/FTC with ATV/r, DRV/r, or EFV). Failure was reported in 25% and 42% at M12 and M24, respectively. Patients who received TDF/FTC/EFV had a significantly higher proportion of failure at M12 by comparison with TDF/FTC with DRV/r (reference), but not at M24. Patients in the 3 other groups had a trend toward a higher proportion of failure at M12 although not statistically significant. No difference was found at M24. Using data from a large prospective cohort, we found that boosted atazanavir and darunavir had comparable effectiveness, whatever the associated NRTIs, whereas efavirenz-based regimens were relatively less performing on the short term.
- Subjects :
- Male
Time Factors
MESH : Retrospective Studies
MESH: Treatment Failure
HIV Infections
MESH : Viral Load
MESH: Logistic Models
Cohort Studies
chemistry.chemical_compound
[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases
MESH : Female
Treatment Failure
Prospective cohort study
MESH: Cohort Studies
MESH: Middle Aged
General Medicine
MESH: HIV Infections
Middle Aged
Viral Load
MESH : Adult
3. Good health
[ SDV.MHEP.MI ] Life Sciences [q-bio]/Human health and pathology/Infectious diseases
Anti-Retroviral Agents
Tolerability
[SDV.MHEP.MI] Life Sciences [q-bio]/Human health and pathology/Infectious diseases
Drug Therapy, Combination
Female
France
MESH: Viral Load
Research Article
medicine.drug
Cohort study
MESH : Time Factors
Adult
medicine.medical_specialty
Efavirenz
MESH : Male
Observational Study
MESH : Cohort Studies
MESH: Anti-Retroviral Agents
MESH : Treatment Failure
Internal medicine
medicine
MESH : HIV Infections
Humans
MESH : Anti-Retroviral Agents
MESH : Middle Aged
MESH : France
Darunavir
Retrospective Studies
MESH: Humans
business.industry
MESH : Drug Therapy, Combination
MESH : Humans
MESH: Time Factors
Retrospective cohort study
MESH: Adult
MESH: Retrospective Studies
MESH: Male
Surgery
Atazanavir
MESH: France
MESH: Drug Therapy, Combination
Logistic Models
chemistry
Propensity score matching
business
MESH: Female
MESH : Logistic Models
Subjects
Details
- Language :
- English
- ISSN :
- 00257974 and 15365964
- Database :
- OpenAIRE
- Journal :
- Medicine, Medicine, Lippincott, Williams & Wilkins, 2015, 94 (39), pp.e1668, Medicine, 2015, 94 (39), pp.e1668. ⟨10.1097/MD.0000000000001668⟩, Medicine, Lippincott, Williams & Wilkins, 2015, 94 (39), pp.e1668. ⟨10.1097/MD.0000000000001668⟩
- Accession number :
- edsair.doi.dedup.....c25cf6c7df49a2f1e27a72b617fd94bc