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The efficacy and safety of anticoagulant therapy for hepatic sinus occlusive syndrome caused by pyrrolidine: a multicenter retrospective cohort study

The efficacy and safety of anticoagulant therapy for hepatic sinus occlusive syndrome caused by pyrrolidine: a multicenter retrospective cohort study.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017775
Enrollment
Unknown
Registered
2018-08-14
Start date
2018-12-01
Completion date
Unknown
Last updated
2018-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hepatic sinus occlusive syndrome caused by pyrrolidine

Interventions

Anticoagulant therapy group:low molecular heparin and/or warfarin
Routine basic treatment group:protecting liver function,improving microcirculation and diuresis

Sponsors

Nanjing Drum Tower Hospital The Affiliated Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years old; 2. Patients diagnosised with acute stage PA-HSOS From January 2012 to December 2017, diagnostic criteria of PA-HSOS: Patients with a clear tacking history of pyrrolidine alkaloid plants ,three of the following situations occur: (1) abdominal distension, ascites, and Upper abdominal pain; (2) serum total bilirubin >17.1 umol/L; (3) pyrrole Protein compounds can be decteted in peripheral blood; (4) typical ultrasonography and CT manifestations (portal vein blood flow velocity <25cm/s, "flower spot" uneven enhancement can be seen in CT balanced period, etc.); (5) in liver biopsy pathology ,Small blood vessels and hepatic sinus have extensive hematopoiesis expansion which mainly occurs in III region of Liver acinus can be seen;

Exclusion criteria

Exclusion criteria: 1. combined with liver cancer or malignant tumor of other organs; 2. during the period of pregnancy or lactation; 3. most of the clinical data is missing.

Design outcomes

Primary

MeasureTime frame
Curative effect index;

Countries

China

Contacts

Public ContactYuZheng Zhuge

Gulou Hospital Affiliated to Nanjing University Medical College

yuzheng9111963@aliyun.com+86 15996289206

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026