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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Clinical characteristics and prognosis of Chinese patients with hereditary transthyretin amyloid cardiomyopathy

Fig. 2

Kaplan-Meier survival curves for patients grouped by EF% at diagnosis. Survival was better in patients with EF ≥ 50% than in those with EF < 50% at diagnosis [log Rank (Mantel-Cox), χ2 = 4.03, P = 0.045]. The median survival time of EF ≥ 50% was 46.0 (95CI: 15.5–76.5) months. The median survival time of EF < 50% was 23.0 (95CI: 20.8–25.1) months. HFrEF indicates the poor prognosis in ATTR-CM

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172