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Meta-analysis of [18F]FDG-PET/CT in pulmonary sarcoidosis.
Donnelly, Ryan; McDermott, Michael; McManus, Gerry; Franciosi, Alessandro N; Keane, Michael P; McGrath, Emmet E; McCarthy, Cormac; Murphy, David J.
Afiliação
  • Donnelly R; St. Vincent's University Hospital, Elm Park, Dublin, 4, Ireland. ryandonnellymd@gmail.com.
  • McDermott M; University College Dublin, Belfield, Dublin, 4, Ireland. ryandonnellymd@gmail.com.
  • McManus G; St. Vincent's University Hospital, Elm Park, Dublin, 4, Ireland.
  • Franciosi AN; St. Vincent's University Hospital, Elm Park, Dublin, 4, Ireland.
  • Keane MP; St. Vincent's University Hospital, Elm Park, Dublin, 4, Ireland.
  • McGrath EE; University College Dublin, Belfield, Dublin, 4, Ireland.
  • McCarthy C; St. Vincent's University Hospital, Elm Park, Dublin, 4, Ireland.
  • Murphy DJ; University College Dublin, Belfield, Dublin, 4, Ireland.
Eur Radiol ; 2024 Jul 23.
Article em En | MEDLINE | ID: mdl-39044038
ABSTRACT

BACKGROUND:

18F-Fluorodeoxyglucose (FDG) PET/CT is emerging as a tool in the diagnosis and evaluation of pulmonary sarcoidosis, however, there is limited consensus regarding its diagnostic performance and prognostic value.

METHOD:

A meta-analysis was conducted with PubMed, Science Direct, MEDLINE, Scopus, and CENTRAL databases searched up to and including September 2023. 1355 studies were screened, with seventeen (n = 708 patients) suitable based on their assessment of the diagnostic performance or prognostic value of FDG-PET/CT. Study quality was assessed using the QUADAS-2 tool. Forest plots of pooled sensitivity and specificity were generated to assess diagnostic performance. Pooled changes in SUVmax were correlated with changes in pulmonary function tests (PFT).

RESULTS:

FDG-PET/CT in diagnosing suspected pulmonary sarcoidosis (six studies, n = 400) had a pooled sensitivity of 0.971 (95%CI 0.909-1.000, p = < 0.001) and specificity of 0.873 (95%CI 0.845-0.920)(one study, n = 169). Eleven studies for prognostic analysis (n = 308) indicated a pooled reduction in pulmonary SUVmax of 4.538 (95%CI 5.653-3.453, p = < 0.001) post-treatment. PFTs displayed improvement post-treatment with a percentage increase in predicted forced vital capacity (FVC) and diffusion capacity of the lung for carbon monoxide (DLCO) of 7.346% (95%CI 2.257-12.436, p = 0.005) and 3.464% (95%CI -0.205-7.132, p = 0.064), respectively. Reduction in SUVmax correlated significantly with FVC (r = 0.644, p < 0.001) and DLCO (r = 0.582, p < 0.001) improvement.

CONCLUSION:

In cases of suspected pulmonary sarcoidosis, FDG-PET/CT demonstrated good diagnostic performance and correlated with functional health scores. FDG-PET/CT may help to guide immunosuppression in cases of complex sarcoidosis or where treatment rationalisation is needed. CLINICAL RELEVANCE STATEMENT FDG-PET/CT has demonstrated a high diagnostic performance in the evaluation of suspected pulmonary sarcoidosis with radiologically assessed disease activity correlating strongly with clinically derived pulmonary function tests. KEY POINTS In diagnosing pulmonary sarcoidosis, FDG-PET/CT had a sensitivity and specificity of 0.971 and 0.873, respectively. Disease activity, as determined by SUVmax, reduced following treatment in all the included studies. Reduction in SUVmax correlated with an improvement in functional vital capacity, Diffusion Capacity of the Lungs for Carbon Monoxide, and subjective health scoring systems.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Eur Radiol Assunto da revista: RADIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Irlanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Eur Radiol Assunto da revista: RADIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Irlanda