Comparison of temporal artery ultrasound versus biopsy in the diagnosis of giant cell arteritis.


Journal

Eye (London, England)
ISSN: 1476-5454
Titre abrégé: Eye (Lond)
Pays: England
ID NLM: 8703986

Informations de publication

Date de publication:
02 2023
Historique:
received: 12 03 2021
accepted: 17 01 2022
revised: 13 01 2022
pmc-release: 01 02 2024
pubmed: 31 1 2022
medline: 27 1 2023
entrez: 30 1 2022
Statut: ppublish

Résumé

Giant cell arteritis (GCA) is a medical and ophthalmological emergency due to risk of stroke and sudden irreversible loss of vision. Fast and accurate diagnosis is important to prevent complications and long-term high dose glucocorticoids toxicity. Temporal artery biopsy is gold standard for diagnosing GCA. However, temporal artery ultrasound is a fast and non-invasive procedure which may provide a supplement or an alternative to biopsy. This study assesses the diagnostic performance of ultrasound and biopsy in the diagnosis of GCA. Examination results of patients suspected of having GCA in the period from August 2018 to June 2019 were reviewed. Patients underwent clinical examination and blood tests. Within a few days of starting glucocorticoid treatment, temporal ultrasound and unilateral biopsy were performed. Experienced physicians established the final clinical diagnosis at 6-months follow-up. Seventy-eight patients underwent both ultrasound and biopsy. Thirty-five (45%) received the final clinical diagnosis of GCA. Compared with the final clinical diagnosis, biopsy had a sensitivity of 69% (51-83%) and a specificity of 100% (92-100%), and ultrasound a sensitivity of 63% (45-79%) and a specificity of 79% (64-94%). Area under the receiver operating characteristics curves were 0.84 and 0.71 for biopsy and ultrasound respectively (p = 0.048). False negative rate of ultrasound was 4 out of 78 (5%). Sensitivity of ultrasound is almost on par with that of biopsy although the overall diagnostic accuracy of ultrasound was slightly lower. We find that ultrasound is a reliable tool for first line diagnosis of GCA.

Sections du résumé

BACKGROUND/OBJECTIVES
Giant cell arteritis (GCA) is a medical and ophthalmological emergency due to risk of stroke and sudden irreversible loss of vision. Fast and accurate diagnosis is important to prevent complications and long-term high dose glucocorticoids toxicity. Temporal artery biopsy is gold standard for diagnosing GCA. However, temporal artery ultrasound is a fast and non-invasive procedure which may provide a supplement or an alternative to biopsy. This study assesses the diagnostic performance of ultrasound and biopsy in the diagnosis of GCA.
SUBJECTS/METHODS
Examination results of patients suspected of having GCA in the period from August 2018 to June 2019 were reviewed. Patients underwent clinical examination and blood tests. Within a few days of starting glucocorticoid treatment, temporal ultrasound and unilateral biopsy were performed. Experienced physicians established the final clinical diagnosis at 6-months follow-up.
RESULTS
Seventy-eight patients underwent both ultrasound and biopsy. Thirty-five (45%) received the final clinical diagnosis of GCA. Compared with the final clinical diagnosis, biopsy had a sensitivity of 69% (51-83%) and a specificity of 100% (92-100%), and ultrasound a sensitivity of 63% (45-79%) and a specificity of 79% (64-94%). Area under the receiver operating characteristics curves were 0.84 and 0.71 for biopsy and ultrasound respectively (p = 0.048). False negative rate of ultrasound was 4 out of 78 (5%).
CONCLUSION
Sensitivity of ultrasound is almost on par with that of biopsy although the overall diagnostic accuracy of ultrasound was slightly lower. We find that ultrasound is a reliable tool for first line diagnosis of GCA.

Identifiants

pubmed: 35094027
doi: 10.1038/s41433-022-01947-1
pii: 10.1038/s41433-022-01947-1
pmc: PMC9873813
doi:

Substances chimiques

Glucocorticoids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

344-349

Informations de copyright

© 2022. The Author(s), under exclusive licence to The Royal College of Ophthalmologists.

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Auteurs

Michael Stormly Hansen (MS)

Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark. michael.stormly.hansen@regionh.dk.

Lene Terslev (L)

Center for Rheumatology and Spine Diseases, Rigshospitalet, Copenhagen, Denmark.

Mads Radmer Jensen (MR)

Department of Clinical Physiology and Nuclear Medicine, Bispebjerg & Frederiksberg Hospital, Copenhagen, Denmark.

Jane Maestri Brittain (JM)

Department of Clinical Physiology, Nuclear Medicine and PET, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Uffe Møller Døhn (UM)

Center for Rheumatology and Spine Diseases, Rigshospitalet, Copenhagen, Denmark.

Carsten Faber (C)

Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Steffen Heegaard (S)

Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Eye Pathology Section, Department of Pathology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Oliver Niels Klefter (ON)

Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Elisabeth Bay Kønig (EB)

Eye Pathology Section, Department of Pathology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Yousif Subhi (Y)

Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Anne Katrine Wiencke (AK)

Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Steffen Hamann (S)

Department of Ophthalmology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

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