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Optic Nerve Sheath Ultrasound for the Detection and Monitoring of Raised Intracranial Pressure in Tuberculous Meningitis.
Donovan, Joseph; Oanh, Pham Kieu Nguyet; Dobbs, Nicholas; Phu, Nguyen Hoan; Nghia, Ho Dang Trung; Summers, David; Thuong, Nguyen Thuy Thuong; Thwaites, Guy E.
Afiliação
  • Donovan J; Oxford University Clinical Research Unit, Centre for Tropical Medicine, Ho Chi Minh City, Vietnam.
  • Oanh PKN; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Dobbs N; Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
  • Phu NH; Department of Clinical Neuroscience, Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
  • Nghia HDT; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Summers D; Vietnam National University School of Medicine, Ho Chi Minh City, Vietnam.
  • Thuong NTT; Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
  • Thwaites GE; Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Vietnam.
Clin Infect Dis ; 73(9): e3536-e3544, 2021 11 02.
Article em En | MEDLINE | ID: mdl-33283229
BACKGROUND: Neurological complications of tuberculous meningitis (TBM) often lead to raised intracranial pressure (ICP) resulting in high morbidity and mortality. Measurement of optic nerve sheath diameter (ONSD) by point-of-care ultrasound may aid in the identification of raised ICP in TBM. METHODS: From June 2017 to December 2019, 107 Vietnamese adults with TBM, enrolled in the ACT HIV or LAST ACT trials (NCT03092817, NCT03100786), underwent ONSD ultrasound at ≥1 of days 0, 3, 7, 14, 21, and day ±30 after enrollment. Demographic data, TBM severity grade, HIV coinfection status, and clinical endpoints by 3 months were recorded. ONSD values were correlated with disease severity, baseline brain imaging, cerebrospinal fluid parameters, and clinical endpoints. RESULTS: 267 ONSD ultrasound scans were performed in 107 participants over the first 30 days of treatment, with measurements from 0.38-0.74 cm. Paired baseline ONSD and brain imaging were performed in 63 participants. Higher baseline ONSD was associated with more severe disease and abnormal brain imaging (abnormal imaging 0.55 cm vs 0.50 cm normal imaging, P = .01). Baseline median ONSD was significantly higher in participants who died by 3 months (0.56 cm [15/72]) versus participants who survived by 3 months (0.52 cm [57/72]) (P = .02). Median ONSD was higher at all follow-up times in participants who died by 3 months. CONCLUSIONS: Higher ONSD was associated with increased disease severity, brain imaging abnormalities, and increased death by 3 months. ONSD ultrasound has a potential role as a noninvasive, affordable bedside tool for predicting brain pathology and death in TBM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article