Evidence map›Paper›PMID 39885983›Full record

ArticleFrontiers in immunology2024

Intravenous immunoglobulin for mortality and inflammatory status in patients with sepsis: a retrospective database study.

Hayabusa Takano, Naoki Kanda, Yuji Wakimoto, Hiroyuki Ohbe, Kensuke Nakamura

Abstract read
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Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hayabusa TakanoDepartment of Emergency and Critical Care Medicine, Hitachi General Hospital, Ibaraki, Japan.
Naoki KandaDepartment of Emergency and Critical Care Medicine, Hitachi General Hospital, Ibaraki, Japan.
Yuji WakimotoDepartment of Emergency and Critical Care Medicine, Hitachi General Hospital, Ibaraki, Japan.
Hiroyuki OhbeDepartment of Emergency and Critical Care Medicine, Tohoku University Hospital, Sendai, Japan.
Kensuke NakamuraDepartment of Emergency and Critical Care Medicine, Hitachi General Hospital, Ibaraki, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sepsis is a life-threatening condition caused by severe infection. The efficacy of intravenous immunoglobulin (IVIG) as adjunctive therapy on mortality remains controversial. Moreover, IVIG may favorably affect sepsis-induced immunosuppression like persistent inflammation, immunosuppression, and catabolism syndrome (PICS). Methods: This study was a retrospective cohort study using inpatient claims database provided by Medical Data Vision, which included approximately 190,000 episodes of intensive care unit admissions in Japanese acute care hospitals between April 2008 and September 2021. We used a propensity score-matched analysis to compare outcomes between the IVIG and control groups. Primary outcomes were 28-day mortality, while secondary outcomes included in-hospital mortality, the Barthel Index at discharge, length of hospital stay and laboratory data (albumin, C-reactive protein (CRP), and lymphocyte count) on days 14 and 28. Results: Of the 17,626 patients enrolled, 15,159 (786 in the IVIG group and 14,373 in the control group) were included in the analysis. Propensity score matching generated 758 matched pairs. Before matching, 28-day mortality and in-hospital mortality were lower in the control group; however, in the matched cohort, 28-day mortality was significantly lower in the IVIG group than in the control group (90/758 [11.9%] vs 124/758 [16.4%]; risk difference [95% confidence intervals (CI)], -4.5% [-8.0% to -1.0%]; P = 0.015). In-hospital mortality in the matched cohort was also significantly more favorable in the IVIG group (137/758 [18.1%] vs 177/758 [23.4%]; risk difference [95%CI], -5.3% [-9.3% to -1.2%]; P = 0.013). Favorable outcomes in terms of albumin on days14 and 28 and CRP levels on day 28 were observed in the IVIG group. Conclusions: The administration of IVIG was associated with a reduction in sepsis mortality and favorable outcomes in laboratory parameters and the functional status. These results will contribute to the ongoing debate on the efficacy of IVIG for sepsis. The results obtained herein suggest the benefit of IVIG, particularly in mitigating PICS. Further research, including prospective studies, is warranted to confirm these results and examine long-term outcomes.

Indexed as

Immunoglobulins, IntravenousInflammationSepsisAgedAged, 80 and overDatabases, FactualFemaleHospital MortalityHumansMaleMiddle AgedPropensity ScoreRetrospective StudiesTreatment OutcomeImmunoglobulins, Intravenousintravenous immunoglobulinIVIGPICSpropensity score matchingretrospectivesepsis

Identifiers

PMID39885983
PMCPMC11779611

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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.