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Objectives: In 2023/24, England had its largest measles outbreak in a decade. Lags from symptom onset to test results made laboratory-confirmed case data inherently retrospective rather than real-time. Reporting lags varied by measles prevalence and testing purpose. Nowcasting models can predict future backfilling of reported cases and estimate recent trends.
Methods: We developed a generalised additive model accounting for reporting delays, location, and day-of-week effects in line-list data by symptom onset date. The model was re-fit weekly providing real-time nowcasts and directional trends for national and regional users. Retrospectively, we tested alternative specifications to optimise structure and confirm predictive performance, evaluating with log weighted interval score (WIS) and ranked probability score (RPS).
Results: For national case estimates, the operational and retrospective models outperformed the baseline model, reducing daily log WIS by 42% and 41%, respectively. For four-week trends, the operational and retrospective models provided better national estimates than the baseline, reducing RPS by 69% and 6%, respectively. An alternative model indexed by report date sometimes outperformed others for trend direction but lagged trend changes.
Conclusions: Our work highlights the value of real-time nowcasting during outbreaks to inform fast-evolving trends, and early access to accurate reporting delay data for effective modelling.
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http://dx.doi.org/10.1016/j.jinf.2025.106569 | DOI Listing |
J Med Genet
September 2025
Department of Pediatrics, Danish Epilepsy Center, Dianalund, Denmark
Rare variants in , the gene encoding the GluA3 subunit of amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type glutamate receptors (AMPARs), are associated with defects in early brain development. Disease-causing variants are generally categorised as either loss of function (LoF) or gain of function (GoF) that appear to be linked to different symptoms. Here, we reported a de novo variant (N651D) that has mixed LoF and GoF in a female patient with a devastating developmental and epileptic encephalopathy, parkinsonism and cortical malformation.
View Article and Find Full Text PDFBr J Ophthalmol
September 2025
Apgujeong St. Mary's Eye Center, Seoul, Korea (the Republic of).
Background/aims: In cytomegalovirus-induced anterior uveitis (CMV-AU), frequent recurrences are the primary cause of glaucomatous damage and corneal endothelial cell loss, yet factors influencing such recurrences remain unclear. Our study aims to investigate the impact of glaucoma surgery (GS) on recurrence rate in patients with CMV-AU.
Methods: This retrospective study included 149 immunocompetent patients with CMV-AU treated with antiviral medication following PCR confirmation.
Ren Fail
December 2025
Department of Critical Care Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, China.
This study aimed to develop a predictive model and construct a graded nomogram to estimate the risk of severe acute kidney injury (AKI) in patients without preexisting kidney dysfunction undergoing liver transplantation (LT). Patients undergoing LT between January 2022 and June 2023 were prospectively screened. Severe AKI was defined as Kidney Disease: Improving Global Outcomes stage 3.
View Article and Find Full Text PDFAm J Geriatr Psychiatry
August 2025
Department of Psychiatry (MLO, SEC, JZ, KS), Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, The Netherlands; Neuroimmunology Research Group (KS), Netherlands Institute for Neuroscience, Amsterdam, The Netherlands; Psychiatric Program of the Netherlands Brain Bank (KS), Ne
Parkinson's disease (PD) is characterized by two neurobiological markers: pathological α-synuclein and/or a dopaminergic deficit. Depression is common in PD, and may precede motor signs, particularly in late-onset depression (LOD). We conducted two systematic reviews and a meta-analysis to examine the relationship between depression and PD development.
View Article and Find Full Text PDFIntern Med
September 2025
Department of Hematology and Oncology, University of Fukui Hospital, Japan.
Symptoms of bleeding caused by vitamin K-dependent coagulation factor deficiency (VKCFD) are rare in adults. We present two Japanese cases of adult-onset VKCFD, in which the cause of vitamin K deficiency remains unknown despite comprehensive evaluation. Both patients showed markedly decreased levels of coagulation factors (F) VII, FIX, FX, FII, protein C (PC), and protein S (PS), along with elevated levels of protein induced by vitamin K absence/antagonist II (PIVKA-II).
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