# Healthcare Resource Consumption and Related Costs of People Living with HIV and Antiviral Treatment: A Retrospective Observational Study in Italy

**Authors:** Luca Degli Esposti, Stefania Mazzoni, Maria Cappuccilli, Franco Maggiolo, Sergio Lo Caputo, Silvia Nozza, Lucia Taramasso, Anna Marra, Mario Pittorru

PMC · DOI: 10.3390/diseases14030110 · 2026-03-18

## TL;DR

This study found that a new HIV treatment called B/F/TAF improves patient adherence and reduces healthcare costs in Italy.

## Contribution

The study provides real-world evidence on the cost-effectiveness and adherence benefits of B/F/TAF in HIV treatment.

## Key findings

- Patients on B/F/TAF had lower risk of treatment discontinuation and higher adherence compared to other ART regimens.
- B/F/TAF users had fewer non-HIV hospitalizations and lower total healthcare costs over 12 months.
- The study confirms B/F/TAF's effectiveness in improving treatment continuity and reducing costs.

## Abstract

Background/Objectives: Among the antiretroviral therapies (ARTs) recently introduced for people living with HIV (PLWH), the fixed-dose combination of bictegravir, emtricitabine and tenofovir alafenamide (B/F/TAF) became reimbursable in Italy in June 2019. Methods: This study evaluated drug utilization, healthcare resource consumption and direct costs among ART-naïve adults initiating B/F/TAF or other non-bictegravir-based regimens, identified from June 2019 to September 2022 within administrative databases of healthcare entities covering approximately nine million citizens. Baseline clinical characteristics at first ART prescription were compared across B/F/TAF-treated patients, those receiving other ART regimens, and non-HIV controls, while treatment outcomes during follow-up were evaluated among PLWH receiving B/F/TAF or other ARTs; healthcare consumption and costs were assessed after propensity score matching within the PLWH cohorts only. Results: Overall, 374 individuals initiated B/F/TAF and 5576 other ARTs. Patients treated with B/F/TAF showed greater adherence and persistence, with multivariate analyses confirming a lower risk of discontinuation or switching (HR = 0.66, 95% CI 0.57–0.76, p < 0.001) and a higher likelihood of adherence (HR = 2.40, 95% CI 1.58–3.64, p < 0.001). After matching, the B/F/TAF group exhibited lower 12-month consumption of non-HIV medications, fewer non-HIV hospitalizations, and reduced total healthcare costs, particularly for non-HIV drug prescriptions compared to other ART users. Conclusions: Overall, B/F/TAF was associated with better treatment continuity and meaningful cost savings.

## Linked entities

- **Chemicals:** bictegravir (PubChem CID 90311989), emtricitabine (PubChem CID 60877), tenofovir alafenamide (PubChem CID 461543)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** PLWH (MESH:C000719191), cardiovascular disease (MESH:D002318), osteoporosis (MESH:D010024), hypertension (MESH:D006973), respiratory disease (MESH:D012140), alcohol/drugs abuse (MESH:D019966), diabetes (MESH:D003920), -9- (MESH:C557826), renal failure (MESH:D051437), dyslipidemia (MESH:D050171), HIV (MESH:D015658), injury to (MESH:D014947), HBV/HCV infection (MESH:D006509), CCI (MESH:C566784), death (MESH:D003643), cancer (MESH:D009369), depression (MESH:D003866)
- **Chemicals:** tenofovir (MESH:D000068698), nucleoside (MESH:D009705), tenofovir alafenamide (MESH:C442442), ART (-), bictegravir (MESH:C000620396)
- **Species:** Homo sapiens (human, species) [taxon 9606], hepatitis C virus [taxon 11103], Hepatitis B virus (no rank) [taxon 10407], Human immunodeficiency virus (species) [taxon 12721], Human immunodeficiency virus 1 (no rank) [taxon 11676]
- **Mutations:** N06A

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13024942/full.md

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Source: https://tomesphere.com/paper/PMC13024942