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. 2020 Dec 8:7:589794.
doi: 10.3389/fmed.2020.589794. eCollection 2020.

Fast-Track Ultrasound Clinic for the Diagnosis of Giant Cell Arteritis Changes the Prognosis of the Disease but Not the Risk of Future Relapse

Affiliations

Fast-Track Ultrasound Clinic for the Diagnosis of Giant Cell Arteritis Changes the Prognosis of the Disease but Not the Risk of Future Relapse

Sara Monti et al. Front Med (Lausanne). .

Abstract

Background: Color Duplex sonography (CDS) of temporal arteries and large vessels (LV) is a recently validated diagnostic methodology for Giant Cell Arteritis (GCA). CDS combined with a fast-track approach (FTA) has improved the early diagnosis of the disease. Objectives: To assess FTA effects on the prevention of permanent visual loss (PVL), relapse and late complications of GCA compared to conventional practice. To assess the impact of COVID-19 pandemic on outcomes of GCA patients assessed with FTA. Methods: GCA patients diagnosed up to June 2020 at the Rheumatology Department, University of Pavia, were included. FTA was implemented since October 2016. FTA consists in the referral within 1 working day of a suspected GCA case to an expert rheumatologist who performs clinical evaluation and CDS. Results: One hundred sixty patients were recruited [female 120 (75%), mean age 72.4 ± 8.2 years]. Sixty-three (39.4%) evaluated with FTA, 97 (60.6%) with conventional approach. FTA patients were older (75.1 ± 7.6 vs. 70.6 ± 8.2 years old; p < 0.001). Median follow-up duration was shorter in the FTA group compared to the conventional one (0.9 vs. 5.0 years; p < 0.001). There was no difference between the two cohorts regarding major vessel district involvement (LV-GCA 17.5% vs. 22.7%; p = 0.4). PVL occurred in 8 (12.7%) FTA patients and 26 (26.8%) conventional ones (p = 0.03). The relative risk of blindness in the conventional group was 2.11 (95% C.I. 1.02-4.36; P = 0.04) as compared to FTA. Median symptom latency of patients experiencing PVL was higher in the conventional group (23 days IQR 12-96 vs. 7 days IQR 4-10, p = 0.02). During COVID-19 there was a significant increase in the occurrence of PVL (40%) including bilateral blindness despite a regularly operating FTA clinic. Cumulative incidence of relapses and time to first relapse did not change after FTA introduction (P = 0.2). No difference in late complications (stenosis/aneurysms) was detected. Conclusions: FTA including CDS evaluation contributed to a substantial reduction of PVL in GCA by shortening the time to diagnosis and treatment initiation. Relapse rate did not change upon FTA introduction, highlighting the need for better disease activity monitoring and treatment strategies optimization based on risk stratification that would predict the occurrence of relapse during glucocorticoid de-escalation.

Keywords: fast-track; giant cell arteritis; large vessel vasculitis; permanent visual loss; sonography; ultrasoud.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
CDS findings of patients evaluated with the FTA. Number of patients according to number of sites with halos (0–8 sites including the different branches of the temporal artery and the axillary arteries).
Figure 2
Figure 2
CDS findings distribution and intima-media thickness of patients evaluated with the FTA. Number of patients with positive CDS in each vascular district, the average halo thickness (± S.D., range) is reported below. C-GCA, cranial giant cell arteritis; LV-GCA, large-vessel giant cell arteritis.
Figure 3
Figure 3
Time to first relapse before and after FTA introduction.
Figure 4
Figure 4
Cumulative incidence of LV complications among LV-GCA compared to C-GCA. LV complications include thoracic/abdominal aortic aneurysm or dissection and stenosis, aneurysm or ectasia of other large arteries.
Figure 5
Figure 5
Comparison of the fast-track clinic activity amongst different periods of 2020, including the lockdown months due to COVID-19 pandemic (March-April). GCA, giant cell arteritis; PVL, permanent visual loss.

References

    1. Jennette JC, Falk RJ, Bacon PA, Basu N, Cid MC, Ferrario F, et al. 2012 Revised international chapel hill consensus conference nomenclature of vasculitides. Arthritis Rheum. (2013) 65:1–11. 10.1002/art.37715 - DOI - PubMed
    1. Salvarani C, Boiardi L. Polymyalgia rheumatica and giant-cell arteritis. N Engl J Med. (2002) 347:261–71. 10.1056/NEJMra011913 - DOI - PubMed
    1. Salvarani C, Cantini F, Hunder GG. Polymyalgia rheumatica and giant-cell arteritis. Lancet. (2008) 372:234–45. 10.1016/S0140-6736(08)61077-6 - DOI - PubMed
    1. Nuenninghoff DM, Hunder GG, Christianson TJH, McClelland RL, Matteson EL. Incidence and predictors of large-artery complication (aortic aneurysm, aortic dissection, and/or large-artery stenosis) in patients with giant cell arteritis: a population-based study over 50 years. Arthritis Rheum. (2003) 48:3522–31. 10.1002/art.11353 - DOI - PubMed
    1. Patil P, Williams M, Maw WW, Achilleos K, Elsideeg S, Dejaco C, et al. Fast track pathway reduces sight loss in giant cell arteritis: results of a longitudinal observational cohort study. Clin Exp Rheumatol. (2015) 33(2 Suppl. 89):S103–6. - PubMed