Safely reducing haemodialysis frequency during the COVID-19 pandemic.


Journal

BMC nephrology
ISSN: 1471-2369
Titre abrégé: BMC Nephrol
Pays: England
ID NLM: 100967793

Informations de publication

Date de publication:
07 12 2020
Historique:
received: 14 07 2020
accepted: 17 11 2020
entrez: 8 12 2020
pubmed: 9 12 2020
medline: 19 12 2020
Statut: epublish

Résumé

Patients undergoing haemodialysis (HD) are at higher risk of developing worse outcomes if they contract COVID-19. In our renal service we reduced HD frequency from thrice to twice-weekly in selected patients with the primary aim of reducing COVID 19 exposure and transmission between HD patients. Dialysis unit nephrologists identified 166 suitable patients (38.4% of our HD population) to temporarily convert to twice-weekly haemodialysis immediately prior to the peak of the COVID-19 pandemic in our area. Changes in pre-dialysis weight, systolic blood pressure (SBP) and biochemistry were recorded weekly throughout the 4-week project. Hyperkalaemic patients (serum potassium > 6.0 mmol/L) were treated with a potassium binder, sodium bicarbonate and received responsive dietary advice. There were 12 deaths (5 due to COVID-19) in the HD population, 6 of which were in the twice weekly HD group; no deaths were definitively associated with change of dialysis protocol. A further 19 patients were either hospitalised and/or developed COVID-19 and thus transferred back to thrice weekly dialysis as per protocol. 113 (68.1%) were still receiving twice-weekly HD by the end of the 4-week project. Indications for transfer back to thrice weekly were; fluid overload (19), persistent hyperkalaemia (4), patient request (4) and compliance (1). There were statistically significant increases in SBP and pre-dialysis potassium during the project. Short term conversion of a large but selected HD population to twice-weekly dialysis sessions was possible and safe. This approach could help mitigate COVID-19 transmission amongst dialysis patients in centres with similar organisational pressures.

Sections du résumé

BACKGROUND
Patients undergoing haemodialysis (HD) are at higher risk of developing worse outcomes if they contract COVID-19. In our renal service we reduced HD frequency from thrice to twice-weekly in selected patients with the primary aim of reducing COVID 19 exposure and transmission between HD patients.
METHODS
Dialysis unit nephrologists identified 166 suitable patients (38.4% of our HD population) to temporarily convert to twice-weekly haemodialysis immediately prior to the peak of the COVID-19 pandemic in our area. Changes in pre-dialysis weight, systolic blood pressure (SBP) and biochemistry were recorded weekly throughout the 4-week project. Hyperkalaemic patients (serum potassium > 6.0 mmol/L) were treated with a potassium binder, sodium bicarbonate and received responsive dietary advice.
RESULTS
There were 12 deaths (5 due to COVID-19) in the HD population, 6 of which were in the twice weekly HD group; no deaths were definitively associated with change of dialysis protocol. A further 19 patients were either hospitalised and/or developed COVID-19 and thus transferred back to thrice weekly dialysis as per protocol. 113 (68.1%) were still receiving twice-weekly HD by the end of the 4-week project. Indications for transfer back to thrice weekly were; fluid overload (19), persistent hyperkalaemia (4), patient request (4) and compliance (1). There were statistically significant increases in SBP and pre-dialysis potassium during the project.
CONCLUSIONS
Short term conversion of a large but selected HD population to twice-weekly dialysis sessions was possible and safe. This approach could help mitigate COVID-19 transmission amongst dialysis patients in centres with similar organisational pressures.

Identifiants

pubmed: 33287730
doi: 10.1186/s12882-020-02172-2
pii: 10.1186/s12882-020-02172-2
pmc: PMC7720264
doi:

Substances chimiques

Potassium RWP5GA015D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

532

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Auteurs

Michelle Da Silva Lodge (MDS)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Thilini Abeygunaratne (T)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Helen Alderson (H)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Ibrahim Ali (I)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Nina Brown (N)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Constantina Chrysochou (C)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Rosie Donne (R)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Ibi Erekosima (I)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Philip Evans (P)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Emma Flanagan (E)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Simon Gray (S)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Darren Green (D)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Janet Hegarty (J)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Audrey Hyde (A)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Philip A Kalra (PA)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Elizabeth Lamerton (E)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

David Lewis (D)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Rachel Middleton (R)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

David New (D)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Robert Nipah (R)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Donal O'Donoghue (D)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Edmond O'Riordan (E)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Dimitrios Poulikakos (D)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Francesco Rainone (F)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Maharajan Raman (M)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

James Ritchie (J)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Smeeta Sinha (S)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

Grahame Wood (G)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK.

J Tollitt (J)

Department of Renal Medicine, Salford Royal NHS Trust, Stott Lane, Salford, M68HD, UK. James.Tollitt@srft.nhs.uk.

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