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Evaluation of an ambulatory care pathway for patients with nitrous oxide-induced myeloneuropathy.
Zaloum, Safiya A; Paris, Alvar; Mair, Devan; Gutteridge, Charles; Ayling, Ruth M; Onen, Barbara L; Walton, Joseph; Workman, Anna; Villanueva, Nelia; Noyce, Alastair J.
Affiliation
  • Zaloum SA; Centre for Preventive Neurology, Wolfson Institute of Preventive Medicine, Queen Mary University of London, London, UK.
  • Paris A; Centre for Preventive Neurology, Wolfson Institute of Preventive Medicine, Queen Mary University of London, London, UK.
  • Mair D; University of Cambridge, Cambridge, UK.
  • Gutteridge C; Centre for Preventive Neurology, Wolfson Institute of Preventive Medicine, Queen Mary University of London, London, UK.
  • Ayling RM; Barts Health NHS Trust, London, UK.
  • Onen BL; Barts Health NHS Trust, London, UK.
  • Walton J; Barts Health NHS Trust, London, UK.
  • Workman A; Barts Health NHS Trust, London, UK.
  • Villanueva N; Barts Health NHS Trust, London, UK.
  • Noyce AJ; Barts Health NHS Trust, London, UK.
BMJ Neurol Open ; 6(1): e000737, 2024.
Article in En | MEDLINE | ID: mdl-38835539
ABSTRACT

Introduction:

Cases of nitrous oxide (N2O)-induced myeloneuropathy are increasing at UK hospitals. At our centre, a dedicated ambulatory care pathway, endorsed nationally, was established to treat and monitor patients with N2O-myeloneuropathy in 2021 and refined through three audit cycles. We analysed the outcomes of patients on this pathway to better understand factors associated with non-engagement. Alongside, a novel approach using WhatsApp for questionnaire delivery was trialled in an attempt to improve engagement with treatment.

Methods:

Patients on the N2O ambulatory care pathway were identified from MDT meeting lists from 9 September 2022 to 25 April 2023. Clinical data were collected via electronic clinical records, including the most recent neurological examination and reason for discharge from the pathway. Patients identified from MDT lists from 27 January 2023 to 14 March 2023 were approached to participate in weekly 12-item surveys, delivered via WhatsApp. This was approved as a service development project with approval for WhatsApp use given by the chief clinical information officer.

Results:

35/56 (62.5%) patients were discharged from ambulatory care due to non-attendance and 17/56 (30.4%) completed their treatment course. The median time from initial presentation to discharge was 49 days. 24/40 (60.0%) of patients with a final neurological examination documented had a residual deficit, with objective sensory deficits most common. 12 patients were approached to receive weekly questionnaires via WhatsApp. 5/8 who expressed interest returned a consent form. All participants were withdrawn due to non-response or participant choice. 1/5 returned more than two surveys.

Conclusion:

Despite poor participation in surveys delivered via WhatsApp, novel approaches are needed to improve engagement with patients on the N2O ambulatory care pathway.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BMJ Neurol Open Year: 2024 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BMJ Neurol Open Year: 2024 Document type: Article Affiliation country: United kingdom