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Abstract Number: 2667

Fast-Track Pathway In Giant Cell Arteritis: A Cost-Effectivenss Analysis

Katerina Achilleos1, Pravin Patil1, Win Win Maw1, Laura Bown2, David Halsall2, Charles Dobson2, Christian Dejaco3, Frances Borg1, Sunil Gupta4 and Bhaskar Dasgupta1, 1Rheumatology, Southend University Hospital, Westcliff-on-sea, United Kingdom, 2Department Of Health, National Health Service England, Leeds, United Kingdom, 3Rheumatology and Immunology, Medical University Graz, Graz, Austria, 4Castlepoint and Rochford, Clinical Commissioning Group, Southend-on-sea, United Kingdom

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: giant cell arteritis

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Session Information

Title: Health Services Research, Quality Measures and Quality of Care - Innovations in Health Care Delivery

Session Type: Abstract Submissions (ACR)

Background/Purpose:   With incidence of 2.2 per 10,000 patient years, it is estimated that 12,000 new cases of Giant Cell Arteritis (GCA) are diagnosed every year in the UK of whom 20% lose sight permanently. This has significant implications on personal, social care and socioeconomic costs. A fast-track GCA pathway was introduced in 2012 aimed at reducing multiple referral routes, delayed review and treatment and improving outcomes. We report the cost effectiveness of this pathway.

 Methods: A retrospective data analysis of 138 patients investigated for GCA (Jan 2009-Dec 2012), comparing costs of fast-track pathway (57 patients; Jan – Dec 2012) with the conventional referral route (81 patients; pre 2012) using the incremental cost effectiveness ratio (ICER).  Data was collected from patient records, general practice and pathology databases along with telephone questionnaires. Direct costs included: GP appointments, investigations such as blood tests, scans and biopsies, outpatient appointments (Rheumatology, Eye Clinic and Neurology), A&E attendances, Inpatient stays, readmissions, drugs for treatment of GCA. Costing data for treatment and diagnosis costs was gathered from Reference Costs 2011/12, Prescription Cost Analysis 2012, and Unit Costs of Health and Social Care 2012. QOL was measured in 66 patients using the EQ5D. Health gains from diagnosis and treatment of GCA were quantified using Quality Adjusted Life Years (QALY’s).

Results: The fast-track pathway has seen a reduction in number of GP appointments and cost of diagnosis and treatment.  The difference in QALYs between patients with and without sight loss due to GCA was 0.2. Each patient that didn’t lose vision gained on average 2.6 QALY’s.  The average cost of diagnosing and treating a patient with suspected GCA in the conventional pathway was £2,600, whilst in the fast-track; this was £1,675, a difference of £925 per patient.  The ICER of implementing the fast-track pathway is –£1,950 per QALY. Thus, there is an average cost saving to the NHS of £925 for each patient treated for suspected GCA.

Table1 Patients with sight loss and the costs of treatment/diagnosis in the conventional and fast-track pathway

 

Total number of patients suspected of having  GCA

Total number of patients diagnosed with  GCA

Number of patients with Sight loss

Average cost of diagnosis and treatment

Conventional pathway

81

46

17 (37%)

£2,600

Fast-track pathway

57

33

3 (9%)

£1,675

Conclusion: The fact-track pathway leads to a reduction in irreversible sight loss and is associated with reduced diagnosis and treatment costs. It results in 2.6 QALY’s gained for each patient that does not suffer sight loss, suggesting that the fast-track pathway is more cost effective than the conventional pathway for management of early GCA. The ICER of implementing the fast-track pathway is –£1,950 per QALY with an average cost saving to the NHS of £925 for each patient. Our results do not include the small educational/refresher costs and are preliminary but indicate that the Fast track GCA pathway should be ‘rolled out’ globally.


Disclosure:

K. Achilleos,
None;

P. Patil,
None;

W. W. Maw,
None;

L. Bown,
None;

D. Halsall,
None;

C. Dobson,
None;

C. Dejaco,
None;

F. Borg,
None;

S. Gupta,
None;

B. Dasgupta,
None.

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