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AnteayerBMJ Open

Hospital services utilisation of patients with vestibular disease in France: a retrospective nationwide study using electronic hospital health records

Por: Sanchez · S. · Bouazzi · L. · Chabbert · C. · Darrouzet · V. · Dubernard · X. · Grill · E.
Objectives

While most acute vestibular disorders do not require a hospital stay, admission to inpatient care because of acute vertigo, dizziness and balance problems (VDB) seems to be more frequent than necessary. The aim of this study was to analyse the frequency and regional distribution of hospital admissions for acute VDB and to estimate the associated healthcare costs.

Setting

We used the complete database of inpatient stays from the French healthcare system between January 2014 and December 2022.

Participants

Patients were included if they had a typical diagnosis code and at least one of the diagnostic or therapeutic procedures for vestibular diseases. Information on regional deprivation and physician density at a regional level is included in our analyses.

Primary and secondary outcome measures

Inpatient stay for acute VDB.

Results

Out of 277 409 765 hospitalisations, a total of 482 578 inpatient stays could be directly attributed to VDB as a primary diagnosis. Patients were predominantly female (range 63.0%–64.3%) and older (from 2014 to 2022, mean age 52.8 to 56.0 years). Total costs per year ranged from 61.3 million euros in 2020 to 72.8 million in 2021 with an average cost per case ranging between 1237 and 1394 euros. There was a positive association between age, general practitioner density, neurologist density and a high hospitalisation rate of the respective area with β=0.01 (95% CI 0.003 to 0.02; p=0.0005), β=0.13 (95% CI 0.12 to 0.14; p

Conclusions

High social deprivation was independently associated with higher hospitalisation rates. We show considerable regional variations of hospital admissions for VDB in France. Awareness and training efforts for VDB must be increased.

Pragmatic, open-label, multicentre, randomised controlled trial to guide initial therapy for immune checkpoint inhibitor-induced inflammatory arthritis comparing standard of care (prednisolone) to adalimumab without glucocorticoids: REACT trial protocol

Por: Fisher · B. A. · Rowe · A. · Hodson · C. · Wilkhu · M. · Williams · E. · Turner · E. · Allard · A. · Blake · T. · Bombardieri · M. · Cope · A. P. · Dubey · S. · Mankia · K. · Malley · T. · Moore · O. · Payne · M. · Plummer · R. · Tilby · M. · Tillett · T. · Wong · E. · Wu · Y. · Filer · A. · Pra
Introduction

Immune checkpoint inhibitors (ICIs) have revolutionised cancer treatment through targeted disruption of the physiological pathways that maintain tissue tolerance, but which are co-opted by cancers to evade immunosurveillance. Thus, the resultant T-cell activity often causes immune-related adverse events including immune checkpoint inhibitor-induced inflammatory arthritis (ICI-IA). ICI-IA results in functional impairment that frequently persists, even after ICI discontinuation, with substantial quality-of-life impacts for cancer survivors.

A high-quality body of evidence to guide ICI-IA management remains an unmet need. Pharmacological treatment may be prolonged, typically begins with non-specific immunosuppression, including systemic steroids, and is usually only rationalised to more targeted therapy in resistant cases. Moreover, retrospective data suggest the high dose glucocorticoids sometimes used in new-onset ICI-IA may be associated with worse cancer outcomes.

Tumour necrosis factor (TNF) inhibition strategies are well established with excellent efficacy and safety profiles in ‘spontaneous’ inflammatory arthritides including rheumatoid and psoriatic arthritis. Mechanistic evidence from ex vivo and murine studies also supports the utility of anti-TNF therapy for steroid-refractory cases of ICI-IA. Although good clinical responses have been reported in this setting, the REACT trial (REmission induction of Arthritis caused by Cancer ImmunoTherapy) aims to provide randomised and robust clinical evidence for deploying targeted therapy earlier in ICI-IA management. It will test whether up-front anti-TNF therapy can more effectively and quickly control symptoms, reduce glucocorticoid exposure, prevent early ICI discontinuation and increase the frequency of drug-free ICI-IA remission.

Methods and analysis

REACT is a prospective, multicentre, open-label, superiority, two-arm, randomised controlled clinical trial to guide initial therapy for patients with ICI-IA. The trial will compare the current standard of care (initial prednisolone; Arm A) with the anti-TNF drug, adalimumab without glucocorticoids (Arm B).

The primary outcome is glucocorticoid-free arthritis remission rate at 24 weeks where remission is defined as: (i) No use of systemic or intra-articular glucocorticoids (except when used for adrenal insufficiency) within 4 weeks prior to assessment at 24 weeks; and (ii) absence of synovitis on clinical examination.

Ethics and dissemination

The protocol was approved by East Midlands—Leicester South Research Ethics Committee on 31-Oct-2024 (Ref: 24/EM/0202). Participants are required to provide written informed consent. The results of this trial will be disseminated through national and international presentations and peer-reviewed publications.

Trial registration number

ISRCTN18217497.

Gut microbiome profile among children and adolescents living with sickle cell disease: a protocol for systematic review and meta-analysis

Por: Salako · A. O. · Ogbeh · J. I. · Adekola · H. A. · Odubela · O. · Akinsolu · F. · Jimoh · R. · Musari-Martins · T. E. · Luka · S. · Oba · A. · Ayegbeso · D. · Odubela · O. O. · Gbaja-Biamila · T. A. · Musa · A. Z. · Salako · B. L.
Introduction

This systematic review aims to synthesise current evidence on gut microbiome profiles among children with sickle cell disease (SCD), assess the influence of analgesic and antibiotic use, and explore the contributions of environmental factors on their gut microbiota diversity. Through identification of consistent microbial patterns and gaps in the existing literature, this review will provide vital insight into potential microbiome-targeted strategies for improving health outcomes in paediatric SCD care.

Methods and analysis

Studies describing the gut microbiota among paediatric SCD human subjects (

Ethics and dissemination

Ethical approval will not be required as this is a systematic review of published data. The findings will be disseminated through publications in peer-reviewed journals and presentations at relevant scientific conferences.

PROSPERO registration number

CRD420251102736.

What factors influence nutrition-related information-seeking behaviour among pregnant women attending antenatal care at public hospitals in Bahir Dar City, northwest Ethiopia: a cross-sectional study

Por: Bitacha · G. K. · Asemahagn · M. A. · Mekonnen · Z. A. · Chekol · T. M. · Ahmed · M. H. · Meshesha · N. A. · Guadie · H. A. · Dube · G. N.
Objective

This study aimed to assess the proportion of nutrition-related information-seeking behaviour and its associated factors among pregnant women attending antenatal care at public hospitals in Bahir Dar City, northwest Ethiopia, 2023.

Method

A cross-sectional quantitative supplemented with qualitative study design was conducted from March to April 2023 among 406 pregnant women. Pre-tested structured interviewer-administered and semistructured open-ended questionnaires were used to collect quantitative and qualitative data, respectively. Data were collected using the Kobo toolbox, and SPSS V.25 was used for analysis. Descriptive statistics were used to describe study subjects, and multivariate logistic regression analysis was employed to investigate the associated factors. The strength of associations was described using the OR with the corresponding 95% CI.

Result

The study included 406 pregnant mothers with a median age of 28 with an IQR of 8 and 212 (52.2%) from rural settings. Of the total respondents, 173 (42.6%; 95% CI 37.7 to 47.6) of pregnant mothers were nutrition-related information seekers. Educational status, residence, monthly income and nutrition information literacy were significantly associated with nutrition-related information-seeking behaviour.

Conclusion

The proportion of nutrition information seeking among pregnant mothers in Bahir Dar City public hospitals was low. Lower educational status, low nutrition information literacy level, being from a rural residence and low monthly income are significantly associated factors.

Recommendation

Awareness creation for pregnant mothers from rural areas and with low educational status and improving nutrition information literacy of pregnant mothers are important activities to improve their nutrition information-seeking behaviour.

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