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The Ambulatory Medical Assistance (AMA) programme during active‐phase treatment in patients with haematological malignancies: A cost‐effectiveness analysis

CONTEXT: The need for patient navigator is growing, and there is a lack of cost evaluation, especially during survivorship. OBJECTIVE: The objective of this study is to evaluate the cost‐effectiveness of an Ambulatory Medical Assistance (AMA) programme in patients with haematological malignancies (H...

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Detalles Bibliográficos
Autores principales: Michallet, Anne‐Sophie, Malartre, Stephanie, Vignaud, Elodie, Bocquet, Alexiane, Sontag, Pascale, Galvez, Christelle, Blay, Jean‐Yves, Heudel, Pierre, Vimont, Alexandre, Blachier, Martin, Ferrua, Marie, Minvielle, Etienne, Mir, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786720/
https://www.ncbi.nlm.nih.gov/pubmed/36168105
http://dx.doi.org/10.1111/ecc.13709
Descripción
Sumario:CONTEXT: The need for patient navigator is growing, and there is a lack of cost evaluation, especially during survivorship. OBJECTIVE: The objective of this study is to evaluate the cost‐effectiveness of an Ambulatory Medical Assistance (AMA) programme in patients with haematological malignancies (HM). DESIGN: A cost‐effectiveness analysis of the AMA programme was performed compared to a simulated control arm. SETTING: An interventional, single‐arm and prospective study was conducted in a French reference haematology–oncology centre between 2016 and 2020. PARTICIPANTS: Adult patients were enrolled with histologically documented malignant haematology, during their active therapy phase, and treated either by intravenous chemotherapy or oral therapy. METHODS: An extrapolation of the effectiveness was derived from a similar nurse monitoring programme (CAPRI study). Cost effectiveness of the programme was evaluated through adverse events of Grade 3 or 4 avoided in different populations. RESULTS: Included patient (n = 797) from the AMA programme were followed during 125 days (IQR: 0–181), and adverse events (Grade 3/4) were observed in 10.1% of patients versus 13.4% in the simulated control arm. The overall cost of AE avoided was estimated to €81,113, leading to an ICER of €864. CONCLUSION: The AMA programme was shown to be cost‐effective compared to a simulated control arm with no intervention.