Plasma Exchange versus Intravenous Immunoglobulin in Worsening Myasthenia Gravis: A Systematic Review and Meta-Analysis with Special Attention to Faster Relapse Control

Author:

Pavlekovics Mark12ORCID,Engh Marie Anne1ORCID,Lugosi Katalin13,Szabo Laszlo1,Hegyi Peter145,Terebessy Tamas16,Csukly Gabor17,Molnar Zsolt18ORCID,Illes Zsolt910ORCID,Lovas Gabor12

Affiliation:

1. Center for Translational Medicine, Semmelweis University, Üllöi út 26, 1085 Budapest, Hungary

2. Department of Neurology, Jahn Ferenc Teaching Hospital, Köves út 1, 1204 Budapest, Hungary

3. Department of Neurology, Bajcsy-Zsilinszky Hospital, Maglódi út 89–91, 1106 Budapest, Hungary

4. Institute of Pancreatic Diseases, Semmelweis University, Baross utca 22–24, 1085 Budapest, Hungary

5. Institute for Translational Medicine, Medical School, University of Pécs, 12 Szigeti Street, 7623 Pécs, Hungary

6. Department of Orthopedics, Semmelweis University, Üllői út 78/b, 1082 Budapest, Hungary

7. Department of Psychiatry and Psychotherapy, Semmelweis University, Balassa utca 6, 1083 Budapest, Hungary

8. Department of Anesthesiology and Intensive Therapy, Semmelweis University, 78 Üllöi St, 1085 Budapest, Hungary

9. Department of Neurology, Odense University Hospital, Winslows Vej 4, 5000 Odense, Denmark

10. Institute of Clinical Research, University of Southern Denmark, Campusvej 55, 5230 Odense, Denmark

Abstract

Currently used rescue interventions to prevent rapid myasthenic deterioration are plasma exchange (PLEX) and intravenous immunoglobulin (IVIG). We investigated the evidence to determine whether the two methods were interchangeable or whether one was superior to the other. This review was registered on PROSPERO (CRD42021285985). Only randomized controlled trials (RCTs) comparing the efficacy and safety of PLEX and IVIG in patients with moderate-to-severe myasthenia gravis (MG) were included. Five major databases were systematically searched (PubMed, CENTRAL, Embase, Scopus, and Web of Science). Odds ratios (OR) with 95% confidence intervals (CI) were calculated for adverse events and mean differences (MD) for changes in quantitative myasthenia gravis scores (QMG). Three RCTs met the inclusion criteria. Two investigating 114 patients in total were eligible for meta-analysis to analyze efficacy and safety. For the change in QMG score, the MD was −2.8 (95% CI: −5.614–0.113), with PLEX performing better. For adverse events, an OR of 1.04 was found (95% CI: 0.25–4.27). This study demonstrated a low risk of bias in evaluating treatment efficacy but indicated a high risk of bias in assessing procedural safety outcomes. Although the results did not show any significant difference, there was a tendency indicating faster efficacy of PLEX in the first two weeks of treatment. In such a critical clinical condition, this tendency may be clinically meaningful, but further studies should clarify this benefit.

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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