Evidence map›Paper›PMID 38634483›Full record

SynthesisHealth technology assessment (Winchester, England)2024

Bisphosphonate alternative regimens for the prevention of osteoporotic fragility fractures: BLAST-OFF, a mixed-methods study.

Opinder Sahota, Melanie Narayanasamy, Anastasios Bastounis, Zoe Paskins, Simon Bishop, Tessa Langley, Neil Gittoes, Sarah Davis, Ann Baily, Moira Holmes and 1 more

Open access · diamondAbstract readSystematic Review
In one paragraph

Synthesis in Health technology assessment (Winchester, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 1 country.

Opinder SahotaDepartment of Health Care for Older People, Nottingham University Hospitals NHS Trust, Nottingham, UK.ORCID 0000-0003-0055-7637
Melanie NarayanasamyBusiness School, University of Nottingham, Nottingham, UK.ORCID 0000-0003-3483-0777
Anastasios BastounisSchool of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0001-5861-9373
Zoe PaskinsSchool of Medicine, Keele University and Haywood Academic Rheumatology Centre, Stoke-on-Trent, UK.ORCID 0000-0002-7783-2986
Simon BishopBusiness School, University of Nottingham, Nottingham, UK.ORCID 0000-0001-8527-7081
Tessa LangleySchool of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0001-9560-1148
Neil GittoesCentre for Endocrinology Diabetes and Metabolism, University of Birmingham, Birmingham, UK.ORCID 0000-0001-5963-214X
Sarah DavisSchool of Health and Related Research, University of Sheffield, Sheffield, UK.ORCID 0000-0002-6609-4287
Ann BailyLay Member, Nottingham Osteoporosis Society Patient Support group, Nottingham, UK.
Moira HolmesLay Member, Nottingham Osteoporosis Society Patient Support group, Nottingham, UK.
Jo Leonardi-BeeSchool of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0003-0893-6068
University of Nottingham · GBRoyal Osteoporosis Society · GBKeele University · GBNottingham University Hospitals NHS Trust · GBUniversity of Birmingham · GBUniversity of Sheffield · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bisphosphonates are a class of medication commonly used to treat osteoporosis. Alendronate is recommended as the first-line treatment; however, long-term adherence (both treatment compliance and persistence) is poor. Alternative bisphosphonates are available, which can be given intravenously and have been shown to improve long-term adherence. However, the most clinically effective and cost-effective alternative bisphosphonate regimen remains unclear. What is the most cost-effective bisphosphonate in clinical trials may not be the most cost-effective or acceptable to patients in everyday clinical practice. Objectives: 1. Explore patient, clinician and stakeholder views, experiences and preferences of alendronate compared to alternative bisphosphonates. 2. Update and refine the 2016 systematic review and cost-effectiveness analysis of bisphosphonates, and estimate the value of further research into their benefits. 3. Undertake stakeholder/consensus engagement to identify important research questions and further rank research priorities. Methods: The study was conducted in two stages, stages 1A and 1B in parallel, followed by stage 2: • Stage 1A - we elicited patient and healthcare experiences to understand their preferences of bisphosphonates for the treatment of osteoporosis. This was undertaken by performing a systematic review and framework synthesis of qualitative studies, followed by semistructured qualitative interviews with participants. • Stage 1B - we updated and expanded the existing Health Technology Assessment systematic review and clinical and cost-effectiveness model, incorporating a more comprehensive review of treatment efficacy, safety, side effects, compliance and long-term persistence. • Stage 2 - we identified and ranked further research questions that need to be answered about the effectiveness and acceptability of bisphosphonates. Results: Patients and healthcare professionals identified a number of challenges in adhering to bisphosphonate medication, balancing the potential for long-term risk reduction against the work involved in adhering to oral alendronate. Intravenous zoledronate treatment was generally more acceptable, with such regimens perceived to be more straightforward to engage in, although a portion of patients taking alendronate were satisfied with their current treatment. Intravenous zoledronate was found to be the most effective, with higher adherence rates compared to the other bisphosphonates, for reducing the risk of fragility fracture. However, oral bisphosphonates are more cost-effective than intravenous zoledronate due to the high cost of zoledronate administration in hospital. The importance of including patients and healthcare professionals when setting research priorities is recognised. Important areas for research were related to patient factors influencing treatment selection and effectiveness, how to optimise long-term care and the cost-effectiveness of delivering zoledronate in an alternative, non-hospital setting. Conclusions: Intravenous zoledronate treatment was generally more acceptable to patients and found to be the most effective bisphosphonate and with greater adherence; however, the cost-effectiveness relative to oral alendronate is limited by its higher zoledronate hospital administration costs. Future work: Further research is needed to support people to make decisions influencing treatment selection, effectiveness and optimal long-term care, together with the clinical and cost-effectiveness of intravenous zoledronate administered in a non-hospital (community) setting. Limitations: Lack of clarity and limitations in the many studies included in the systematic review may have under-interpreted some of the findings relating to effects of bisphosphonates. Trial registration: This trial is registered as ISRCTN10491361. Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme (NIHR award ref: NIHR127550) and is published in full in

Indexed as

AlendronateBone Density Conservation AgentsCost-Benefit AnalysisDiphosphonatesOsteoporotic FracturesAgedFemaleHumansMaleMedication AdherenceMiddle AgedOsteoporosisQualitative ResearchQuality-Adjusted Life YearsTechnology Assessment, BiomedicalZoledronic AcidAlendronateBone Density Conservation AgentsDiphosphonatesZoledronic AcidADHERENCEALENDRONATEBISPHOSPHONATECOMPLIANCEHEALTH-ECONOMICSIBANDRONATEINTRAVENOUSMIXED METHODSOSTEOPOROSISPERSISTENCEQUALITATIVERISEDRONATEZOLEDRONATE

Identifiers

PMID38634483
PMCPMC11056815
OpenAlexW4394921418

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.