# The impact of time to diagnosis on health service use, cost, and quality of life for patients with juvenile idiopathic arthritis: a cost-utility analysis

**Authors:** Amy Von Huben, Diana M. Bond, Samantha Lain, Davinder Singh-Grewal, Ruth Colagiuri, Stephen Colagiuri, Natasha Nassar

PMC · DOI: 10.1186/s12969-026-01195-7 · Pediatric Rheumatology · 2026-02-24

## TL;DR

Delays in diagnosing juvenile arthritis increase healthcare costs and reduce quality of life, but timely diagnosis saves money and improves outcomes.

## Contribution

This study quantifies the economic and quality-of-life benefits of timely diagnosis of juvenile idiopathic arthritis.

## Key findings

- Timely diagnosis within 6 months reduces healthcare costs by over $10,000 annually per child.
- Early diagnosis improves health-related quality of life by 0.14 utility units.
- Lifetime cost savings from timely diagnosis reach $208,458 per child.

## Abstract

Timely referral and diagnosis of Juvenile Idiopathic Arthritis (JIA) by a pediatric rheumatologist ensures early intervention to minimize long-term joint damage and disability. This study aimed to quantify the impact of delays in diagnosis on health service use, health-related quality of life (HRQoL) and associated costs to the health system.

A cost-utility analysis was conducted over a lifetime horizon from a health funder perspective in 2023 Australian dollars, comparing time from actively seeking treatment to formal diagnosis (< 6 months, 6 + months). Time to diagnosis, healthcare use, including medical investigations, health professional visits, hospitalizations and medications, was determined using The IMPACT Survey. Incremental costs were estimated by applying Australian government subsidy item costs (medications), schedule fees (medical services), and National Efficient Prices (hospitalizations). HRQoL was measured using Child Health Utility Instrument (CHU9D). Incremental Quality Adjusted Life Years (QALYs) were estimated using participants’ CHU9D utility values based on Australian preference weights and life expectancy. Costs and QALYs were present valued at 5% per annum. Sensitivity analyses were conducted for robustness.

Over one-third (n = 61/163) of children were diagnosed 6 + months from actively seeking treatment. Compared with 6 + months, diagnosis within 6 months was associated with a lower use of health services, resulting in a mean annual decrease in costs for the healthcare funder of more than $10,000 per child. The majority of the cost savings were due to reductions in hospitalizations for pain, inflammation, and investigative procedures. There were also significant increases in HRQoL; 0.14 (95%CI 0.05, 0.23) utility value. The differences in health service use and HRQoL from timely diagnosis persisted over 20 years from diagnosis. Over a lifetime, the present value of healthcare cost savings was $208,458 (95%CI $45,388, $371,528) and the increase in HRQoL resulted in an additional 2.82 (95%CI 1.03, 4.61) QALYs per child. At a willingness to pay of $50,000 per QALY, the estimated net benefit to the health funder was $349,520 (95%CI $139,630, $559,411) per child.

Interventions to improve the time to diagnosis of JIA within six months are likely cost-effective and can significantly improve HRQoL for people living with JIA.

Not applicable.

The online version contains supplementary material available at 10.1186/s12969-026-01195-7.

## Linked entities

- **Diseases:** Juvenile Idiopathic Arthritis (MONDO:0011429), JIA (MONDO:0011429)

## Full-text entities

- **Genes:** PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}
- **Diseases:** diabetes (MESH:D003920), autism (MESH:D001321), joint damage (MESH:D007592), JIA (MESH:D001171), joint pain (MESH:D018771), ventricular dysfunction (MESH:D018754), CHU9D (MESH:C562515), swelling (MESH:D004487), Rheumatic Diseases (MESH:D012216), Pericarditis (MESH:D010493), Arthritis (MESH:D001168), inflammation (MESH:D007249), disease (MESH:D004194), epilepsy (MESH:D004827), vision loss (MESH:D014786), pain (MESH:D010146), physical disability (MESH:D059445), Chronic pain (MESH:D059350), endocarditis (MESH:D004696), uveitis (MESH:D014605), myocarditis (MESH:D009205), Type 1 diabetes (MESH:D003922)
- **Chemicals:** Tofacitinib (MESH:C479163), Leflunomide (MESH:D000077339), ORAL corticosteriods (-), Hydroxychloroquine (MESH:D006886), Tocilizumab (MESH:C502936), Upadacitinib (MESH:C000613732), Baricitinib (MESH:C000596027), Secukinumab (MESH:C555450), Infliximab (MESH:D000069285), Prednisone (MESH:D011241), Adalimumab (MESH:D000068879), Methotrexate (MESH:D008727)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937577/full.md

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Source: https://tomesphere.com/paper/PMC12937577