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Obesity Surgery

, Volume 29, Issue 2, pp 474–484 | Cite as

Multi-Centre Micro-Costing of Roux-En-Y Gastric Bypass, Sleeve Gastrectomy and Adjustable Gastric Banding Procedures for the Treatment of Severe, Complex Obesity

  • Brett DobleEmail author
  • Richard Welbourn
  • Nicholas Carter
  • James Byrne
  • Chris A. Rogers
  • Jane M. Blazeby
  • Sarah Wordsworth
  • On behalf of the By-Band-Sleeve Trial Management Group
Original Contributions
  • 140 Downloads

Abstract

Background

There is a growing interest in comparing the effectiveness and costs of alternative forms of bariatric surgery. We aimed to examine the per-patient, procedural costs of Roux-en-Y gastric bypass (RYGB), sleeve gastrectomy (SG) and adjustable gastric banding (AGB) in the United Kingdom.

Methods

Multi-centre (two National Health Service; NHS and one private hospital) micro-costing, using a time-and-motion study. Prospective collection of surgery times, staff quantities, equipment, instruments and consumables for 12 patients (four RYGB, five SG, three AGB) from patients’ first surgeon interaction on the day of surgery to departure from the theatre recovery area. Costs were attached to quantities and mean costs compared. Sensitivity and scenario analyses assessed the impact of varying surgery inputs and consideration of additional plausible factors respectively on total costs.

Results

Mean procedural costs were £5002 for RYGB, £4306 for SG and £2527 for AGB. Varying staff seniority or altering procedure times had small impacts on costs (± 4–6%). Reducing prices of consumables by 20% reduced costs by 10–13%. Accounting for differences in surgical technique by altering the number of staple reloads used impacted costs by ± 7–10%. Adjusted total costs from scenario analyses were similar to NHS tariffs for RYGB and SG (difference of £51 and -£119 respectively) but were much lower for AGB (difference of £1982).

Conclusions

These detailed costs will allow for more precise reimbursement of bariatric surgery and support comprehensive assessments of cost-effectiveness. Additional work to investigate costs of post-surgical care, re-operations and life-long support received by patients following surgery is required.

Keywords

Bariatric surgery Bottom-up costing Costs Cost analysis Economics Micro-costing Reimbursement Tariffs Time-in-motion study 

Notes

Acknowledgements

By-Band-Sleeve Trial Management Group: Jane Blazeby (Chief Investigator), University of Bristol; Richard Welbourn (Surgical Lead), Musgrove Park Hospital; James Byrne (Surgical Expertise), Southampton University Hospitals NHS Trust; Jenny Donovan (Qualitative Research Lead), University of Bristol; Barnaby C. Reeves (Methodologist Lead), University of Bristol; Sarah Wordsworth (Health Economics Lead), University of Oxford; Robert C. Andrews (Endocrinology Lead), University of Exeter; Janice L. Thompson (Nutritional Lead), University of Birmingham; Graziella Mazza (Trial Manager), University of Bristol; Chris A. Rogers (Trials Unit and Statistical Lead), University of Bristol.

Funding

This study is funded by The National Institute for Health Research Health Technology Assessment (NIHR HTA) programme (project number 09/127/53) for which Richard Welbourn, Nicholas Carter, James Byrne, Chris A. Rogers, Jane M. Blazeby and Sarah Wordsworth are investigators. The views and opinions expressed are those of the authors and do not necessarily reflect those of the HTA programme, NIHR, the UK National Health Service, or the Department of Health. Jane M. Blazeby is an NIHR Senior Investigator.

Compliance with Ethical Standards

Conflict of Interest

Author 2 declares receiving support from Ethicon Endo-Surgery for attending conferences and funding a Bariatric Clinical Fellow as well as receiving honoraria from Novo Nordisk. Author 5 received salary funding from the British Heart Foundation. All the other authors have no conflict of interests to declare, except support from a government grant detailed in the acknowledgements.

Ethical Approval

The National Research Ethics Committee South West – Frenchay approved the micro-costing on 6th December 2011 as part of the BBS study protocol. All procedures performed in studies involving human participants were in accordance with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed Consent

Informed consent was obtained from all individual participants included in the BBS study.

Supplementary material

11695_2018_3553_MOESM1_ESM.docx (77 kb)
ESM 1 (DOCX 77 kb)

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  • Brett Doble
    • 1
    Email author
  • Richard Welbourn
    • 2
  • Nicholas Carter
    • 3
  • James Byrne
    • 4
  • Chris A. Rogers
    • 5
  • Jane M. Blazeby
    • 6
  • Sarah Wordsworth
    • 1
  • On behalf of the By-Band-Sleeve Trial Management Group
  1. 1.Health Economics Research Centre, Nuffield Department of Population HealthUniversity of OxfordOxfordUK
  2. 2.Department of Upper Gastrointestinal and Bariatric SurgeryMusgrove Park HospitalTauntonUK
  3. 3.Bariatric and Metabolic Surgery Department, Queen Alexandra HospitalPortsmouth Hospitals NHS TrustPortsmouthUK
  4. 4.Southampton University Hospitals NHS TrustSouthamptonUK
  5. 5.Clinical Trials and Evaluation Unit, Bristol Medical SchoolUniversity of BristolBristolUK
  6. 6.Bristol Centre for Surgical Research, Bristol Medical SchoolUniversity of BristolBristolUK

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