Evidence map›Paper›PMID 42854181›Full record

Observational studyNeurology. Clinical practice2026

Infection Risk During Rituximab Therapy in Multiple Sclerosis: Effect of Dosing Interval and Age.

Gorm Pihl-Jensen, Maria Lie Selle, Jan Harald Aarseth, Kjell-Morten Myhr, Øivind Torkildsen, Ola Nakken, Trygve Holmøy

Abstract readObservational Study
In one paragraph

Observational study in Neurology. Clinical practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Gorm Pihl-JensenDepartment of Neurology, Akershus University Hospital, Norway.ORCID 0009-0005-4448-4419
Maria Lie SelleHealth Services Research Unit, Akershus University Hospital, Lørenskog, Norway.ORCID 0009-0000-2630-5740
Jan Harald AarsethNorwegian MS Registry and Biobank, Departtment of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0009-0004-8443-2261
Kjell-Morten MyhrDepartment of Neurology, Neuro-SysMed, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-0980-510X
Øivind TorkildsenDepartment of Neurology, Neuro-SysMed, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0001-5294-2866
Ola NakkenDepartment of Neurology, Akershus University Hospital, Norway.ORCID 0000-0003-4765-0636
Trygve HolmøyDepartment of Neurology, Akershus University Hospital, Norway.ORCID 0000-0002-2529-5664

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesRituximab is the most frequently used disease-modifying therapy in multiple sclerosis (MS) in Norway. Extended dosing intervals beyond 6 months may offer the same efficacy, but the impact on infection risk is unclear. We examined how dosing frequency and age affect infection risk in rituximab-treated patients with MS.

methodsWe conducted a nation-wide observational study linking compulsory Norwegian health registries with the Norwegian MS registry. Registry data captured hospital-treated infections and further infections requiring prescription treatment and/or physician contact with primary practice. Data were analyzed using the Prentice, Williams, and Peterson model with clustering on subject to account for longitudinal design, recurrent rituximab infusions and recurrent infection events while adjusting for relevant explanatory variables. Rituximab interval length was modelled as the number of rituximab infusions within 2 years. Age was grouped into 5-year intervals.

resultsAmong 3,410 patients (13,811 treatment episodes between 2010 and June 2022), 13,774 infections occurred, including 971 hospital-treated events. Compared with 4 infusions over 2 years (6-month intervals), extended dosing was associated with a lower risk of any infection (hazard ratio [HR] 0.90 [95% CI 0.82-0.99]) for 2 infusions; (HR 0.78 [95% CI 0.69-0.88] for 1 infusion). A reduced risk of hospital-treated infections was observed only for 1 infusion per 2 years relative to 4, and this was not robust in sensitivity analyses and not present for the subgroup of infections associated with overnight hospital stay. Patients ≥60 years had a significantly higher risk of hospital-treated infections (HR 1.36 [95% CI 1.07-1.71]). DISCUSSION: Extended rituximab intervals are associated with reduced overall infection risk, but the benefit for hospital-treated infections is limited. Age ≥60 years independently increases the risk of hospital-treated infections. These findings support cautious interval extension and careful risk-benefit assessment in older patients.

Indexed as

Immunologic FactorsInfectionsMultiple SclerosisRituximabAdultAge FactorsDrug Administration ScheduleFemaleHumansMaleMiddle AgedNorwayRegistriesImmunologic FactorsRituximab

Identifiers

PMID42854181
PMCPMC13676286

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.