PMID- 27902746 OWN - NLM STAT- MEDLINE DCOM- 20170918 LR - 20220317 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 11 IP - 11 DP - 2016 TI - The Effect of Intravenous Immunoglobulin Combined with Corticosteroid on the Progression of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: A Meta-Analysis. PG - e0167120 LID - 10.1371/journal.pone.0167120 [doi] LID - e0167120 AB - BACKGROUND: Intravenous immunoglobulin (IVIG) treatment is commonly used to treat Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) with controversial therapeutic effect. METHODS: We conducted a comprehensive meta-analysis through combining the published eligible studies to evaluate the effectiveness of IVIG on SJS and TEN treatment. RESULTS: A total of 26 studies were selected from public available databases. The combination of IVIG and corticosteroid markedly reduced the recovery time (by 1.63 days, 95% CI: 0.83-2.43, P < 0.001), compared with solo corticosteroid group. The favorable effects were greater in Asian (2.19, 95% CI: 1.41-2.97, P < 0.001), TEN (2.56, 95% CI: 0.35-4.77, P = 0.023) and high-dose IVIG treated individuals (1.78, 95% CI: 0.42-3.14, P = 0.010). The hospitalization length reduced by 3.19 days (95% CI: 0.08-6.30, P = 0.045), though the outcome was proven to be unstable. We found heterogeneities, which sources were probably regional factors. Besides, IVIG was inclined to decrease SJS/TEN mortality (SMR: 0.84, 95% CI: 0.66-1.08, P = 0.178). This impact was possibly more profound when patients were treated with high dose IVIG (SMR: 0.74, 95% CI: 0.50-1.08, P = 0.116), or when patients were diagnosed as TEN (SMR: 0.68, 95% CI: 0.45-1.01, P = 0.058). CONCLUSIONS: Our current meta-analysis suggests that IVIG combined with corticosteroid could reduce recovery time for SJS and TEN. This effect is greater among Asian patients. Whereas, its impact on reducing mortality is not significant. FAU - Ye, Liang-Ping AU - Ye LP AD - Institute of Dermatology and Department of Dermatology at No.1 Hospital, Anhui Medical University, Hefei, Anhui, China. AD - Physical Examination Centre, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China. FAU - Zhang, Cheng AU - Zhang C AD - Department of Occupational and Environmental Health, School of Public Health, Anhui Medical University, Hefei, Anhui, China. FAU - Zhu, Qi-Xing AU - Zhu QX AD - Institute of Dermatology and Department of Dermatology at No.1 Hospital, Anhui Medical University, Hefei, Anhui, China. AD - Department of Occupational and Environmental Health, School of Public Health, Anhui Medical University, Hefei, Anhui, China. LA - eng PT - Journal Article PT - Meta-Analysis DEP - 20161130 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Adrenal Cortex Hormones) RN - 0 (Immunoglobulins, Intravenous) SB - IM MH - Adrenal Cortex Hormones/*pharmacology/therapeutic use MH - *Disease Progression MH - Drug Interactions MH - Humans MH - Immunoglobulins, Intravenous/*pharmacology/therapeutic use MH - Stevens-Johnson Syndrome/*drug therapy PMC - PMC5130247 COIS- This article does not have any actual or potential conflict of interest including financial, personal or other relationships with other people or organizations. EDAT- 2016/12/03 06:00 MHDA- 2017/09/19 06:00 PMCR- 2016/11/30 CRDT- 2016/12/01 06:00 PHST- 2016/02/21 00:00 [received] PHST- 2016/11/09 00:00 [accepted] PHST- 2016/12/01 06:00 [entrez] PHST- 2016/12/03 06:00 [pubmed] PHST- 2017/09/19 06:00 [medline] PHST- 2016/11/30 00:00 [pmc-release] AID - PONE-D-16-04334 [pii] AID - 10.1371/journal.pone.0167120 [doi] PST - epublish SO - PLoS One. 2016 Nov 30;11(11):e0167120. doi: 10.1371/journal.pone.0167120. eCollection 2016.