# Experience in emergency management of first-episode immune thrombotic thrombocytopenic purpura over the past 21 years: a single-center retrospective study

**Authors:** Liqian Zhang, Wenfeng Huang, Fengtao Yang, Lingjie Cao, Maojing Shi, Weibo Gao, Yuanyuan Pei, Jihong Zhu

PMC · DOI: 10.3389/fimmu.2025.1645558 · Frontiers in Immunology · 2026-01-14

## TL;DR

This study examines emergency treatment of a rare blood disorder called iTTP and finds that early use of rituximab and corticosteroids improves survival.

## Contribution

The study provides real-world insights into emergency management of first-episode iTTP and identifies risk factors and effective therapies.

## Key findings

- Rituximab administration increased over time and was associated with improved survival in first-episode iTTP patients.
- Corticosteroid pulse therapy was an independent predictor of clinical response in emergency treatment.
- Age over 45, pentad symptoms, and elevated lactate dehydrogenase were independent predictors of mortality.

## Abstract

Immune thrombotic thrombocytopenic purpura (iTTP) is a rare but fatal hematologic disorder characterized by thrombocytopenia, microangiopathic hemolytic anemia, and multiorgan dysfunction. Early diagnosis and prompt treatment, including plasma exchange (PE), corticosteroids, and rituximab (RTX), are critical for improving outcomes. However, real-world emergency management experiences for first-episode iTTP remain understudied.

This single-center retrospective study analyzed 96 patients with first-episode iTTP admitted to the emergency department of Peking University People’s Hospital between 2004 and 2024. Baseline characteristics, clinical features, treatment modalities, and outcomes were evaluated. Logistic and Cox regression analyses were conducted to identify predictors of clinical response and mortality.

Among the enrolled patients, the median age was 45 years and 54.2% were female. The comorbidities included rheumatologic and antoimmune diseases (28.1%) and cancer (11.5%). The mortality rate was 38.5% whereas the relapse rate was 13.6% in survival group. RTX administration increased over time (0% in 2004–2010 vs. 51.9% in 2018-2024) and was associated with improved survival (HR = 0.27, 95% CI: 0.11-0.66). Corticosteroid pulse therapy was an independent predictor of clinical response (OR = 2.8, 95% CI: 1.1-7.6). Independent predictors for mortality included age over 45 years (HR = 5.5, 95% CI: 2.1-14.3), pentad symptoms (HR = 3.5, 95% CI: 1.5-8.4), and lactate dehydrogenase over 1500 U/L (HR = 2.7, 95% CI: 1.2-5.8).

This study highlighted the importance of early RTX and corticosteroid pulse therapy in the emergency management of first-episode iTTP. We also provide a risk stratification framework for emergency clinicians, guiding more prompt and effective management as well as personalized therapy.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Diseases:** hematologic disorder (MESH:D006402), microangiopathic hemolytic anemia (MESH:D000743), pentad symptoms (MESH:D012816), multiorgan dysfunction (MESH:D009102), cancer (MESH:D009369), thrombocytopenia (MESH:D013921), rheumatologic and antoimmune diseases (MESH:D012216), Immune thrombotic thrombocytopenic purpura (MESH:D011697)
- **Chemicals:** RTX (MESH:D000069283)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12847437/full.md

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Source: https://tomesphere.com/paper/PMC12847437