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Prognostic factors for liver, blood and kidney adverse events from glucocorticoid sparing immune-suppressing drugs in immune-mediated inflammatory diseases: a prognostic systematic review.
Leaviss, Joanna; Carroll, Christopher; Essat, Munira; van der Windt, Danielle; Grainge, Matthew J; Card, Tim; Riley, Richard; Abhishek, Abhishek.
Affiliation
  • Leaviss J; SCHARR, The University of Sheffield, Sheffield, Yorkshire, UK J.leaviss@sheffield.ac.uk.
  • Carroll C; SCHARR, The University of Sheffield, Sheffield, Yorkshire, UK.
  • Essat M; SCHARR, The University of Sheffield, Sheffield, Yorkshire, UK.
  • van der Windt D; School of Medicine, Keele University, Keele, UK.
  • Grainge MJ; Academic Unit of Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, UK.
  • Card T; Division of Epidemiology and Public Health, University of Nottingham, Nottingham, UK.
  • Riley R; Institute of Applied Health Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
  • Abhishek A; National Institute for Health and Care Research (NIHR) Birmingham Biomedical Research Centre, Birmingham, UK.
RMD Open ; 10(1)2024 Jan 10.
Article de En | MEDLINE | ID: mdl-38199851
ABSTRACT

BACKGROUND:

Immune-suppressing drugs can cause liver, kidney or blood toxicity. Prognostic factors for these adverse-events are poorly understood.

PURPOSE:

To ascertain prognostic factors associated with liver, blood or kidney adverse-events in people receiving immune-suppressing drugs. DATA SOURCES MEDLINE, Web of Science, EMBASE and the Cochrane library (01 January 1995 to 05 January 2023), and supplementary sources. DATA EXTRACTION AND

SYNTHESIS:

Data were extracted by one reviewer using a modified CHARMS-PF checklist and validated by another. Two independent reviewers assessed risk of bias using Quality in Prognostic factor Studies tool and assessed the quality of evidence using a Grading of Recommendations Assessment, Development and Evaluation-informed framework.

RESULTS:

Fifty-six studies from 58 papers were included. High-quality evidence of the following associations was identified elevated liver enzymes (6 studies) and folate non-supplementation (3 studies) are prognostic factors for hepatotoxicity in those treated with methotrexate; that mercaptopurine (vs azathioprine) (3 studies) was a prognostic factor for hepatotoxicity in those treated with thiopurines; that mercaptopurine (vs azathioprine) (3 studies) and poor-metaboliser status (4 studies) were prognostic factors for cytopenia in those treated with thiopurines; and that baseline elevated liver enzymes (3 studies) are a prognostic factor for hepatotoxicity in those treated with anti-tumour necrosis factors. Moderate and low quality evidence for several other demographic, lifestyle, comorbidities, baseline bloods/serologic or treatment-related prognostic factors were also identified.

LIMITATIONS:

Studies published before 1995, those with less than 200 participants and not published in English were excluded. Heterogeneity between studies included different cut-offs for prognostic factors, use of different outcome definitions and different adjustment factors.

CONCLUSIONS:

Prognostic factors for target-organ damage were identified which may be further investigated for their potential role in targeted (risk-stratified) monitoring. PROSPERO REGISTRATION NUMBER CRD42020208049.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Lésions hépatiques dues aux substances / Glucocorticoïdes Type d'étude: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Systematic_reviews Limites: Humans Langue: En Journal: RMD Open Année: 2024 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Lésions hépatiques dues aux substances / Glucocorticoïdes Type d'étude: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Systematic_reviews Limites: Humans Langue: En Journal: RMD Open Année: 2024 Type de document: Article Pays d'affiliation: Royaume-Uni
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