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The objective of this study was to summarize existing evidence on the probability of sequelae following confirmed CE.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>All studies included in previous reviews and meta\u2010analyses on this topic were retrieved and assessed for eligibility; a systematic literature search was conducted to collect more recent reports. For each sequela, random effects meta\u2010analyses were performed; the risk of bias and the quality of evidence were evaluated.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>In total, 50 reports of observational studies were included; between 110,765 and 175,839 CE cases were considered for each sequela. The pooled proportion of CE cases that developed a sequela was 1.72% (95% CI 0.81\u20133.61; prediction interval [PI]: 0.03\u201347.65) for REA, 0.07% (0.03\u20130.16; PI: 0.003\u20131.59) for GBS, 0.22% (0.06\u20130.73; PI: 0.002\u201320.69) for Crohn's disease (CD), 0.35% (0.11\u20131.15; PI: 0.003\u201328.16) for ulcerative colitis (UC), and 4.48% (1.92\u201310.08; PI: 0.09\u201370.62) for IBS. The high between\u2010study heterogeneity could partially be explained by study size and design, the method of assessing sequelae, and the period between CE and sequelae onset. The quality of evidence was rated as moderate for GBS and UC, and low for REA, CD, and IBS.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Updated estimates of the probability to develop sequelae after CE are provided, for CD and UC for the first time. 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