Evidence map›Paper›PMID 39666070›Full record

ArticleJournal of neurology2024

Medical costs of treating myasthenia gravis in patients who need intravenous immunoglobulin (IVIg) - a register-based study.

Christoffer Bugge, Ingrid Engebretsen, Ivar Sønbø Kristiansen, Erik Magnus Sæther, Ingrid Lindberg-Schager, Fredrik Arneberg, Nils Erik Gilhus

Abstract read
In one paragraph

Article in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 pooled it
–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

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
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.

Christoffer BuggeOslo Economics, Oslo, Norway.ORCID http://orcid.org/0000-0002-0766-2870
Ingrid EngebretsenOslo Economics, Oslo, Norway. ien@osloeconomics.no.ORCID http://orcid.org/0000-0001-9608-6731
Ivar Sønbø KristiansenDepartment of Health Management and Health Economics, Institute of Health and Society, University of Oslo, Forskningsveien 3A, 0373, Oslo, Norway.ORCID http://orcid.org/0000-0002-5389-6010
Erik Magnus SætherOslo Economics, Oslo, Norway.
Ingrid Lindberg-SchagerUCB, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-6549-6065
Fredrik ArnebergUCB, Oslo, Norway.
Nils Erik GilhusDepartment of Clinical Medicine, University of Bergen, Bergen, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral innovative treatments are expected for myasthenia gravis (MG) in the coming years. Healthcare payers usually require cost-effectiveness analyses before reimbursement. We aimed to investigate resource utilization and direct medical costs for patients with MG treated with intravenous immunoglobulin (IVIg) to inform such analyses.

methodsWe identified patients with MG in the Norwegian Patient Registry based on at least two hospital encounters with an MG diagnosis (ICD-10 G70.0) from 1 Jan 2010 to 31 Dec 2021. IVIg treatment was identified by medical procedure and Anatomical Therapeutic Chemical (ATC) codes (RPGM05 and J06BA02). Using Diagnosis-Related Group (DRG) cost weights, we estimated direct medical costs for each year following the first MG diagnosis.

resultsOver the study period, 1083 patients were diagnosed with MG in Norway, of whom 155 (14.3%) were treated with IVIg. No significant differences in age or sex were observed between IVIg and non-IVIg patients. Compared with non-IVIg patients, IVIg-patients had 2.3 times higher direct medical costs during the first year after MG diagnosis (EUR 35,714 vs. EUR 15,457) and 3.1 times higher costs during the second year (EUR 19,119 vs. EUR 6256). In the fifth year after diagnosis, IVIg-patients still had higher costs and resource utilization than non-IVIg patients (EUR 9953 vs. EUR 5634).

conclusionIVIg treatment represents an important marker for high direct medical costs among patients with MG. The costs continue to be high during the first five years after MG diagnosis.

Indexed as

Health Care CostsImmunoglobulins, IntravenousMyasthenia GravisRegistriesAdultAgedAged, 80 and overFemaleHumansImmunologic FactorsMaleMiddle AgedNorwayYoung AdultImmunoglobulins, IntravenousImmunologic FactorsCost of illnessHealthcare costsIntravenous immunoglobulinMyasthenia gravisRegistry data

Identifiers

PMID39666070
PMCPMC11638270

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Registered trials

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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.