Effect of LSD on Lipid Profiles in Cirrhosis Patients With Portal Hypertension Bleeding (2-Year Follow-Up)

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorNorthern Jiangsu People's Hospital

About this trial

Patients with liver cirrhosis frequently exhibit dyslipidemia due to impaired hepatic lipid synthesis, altered bile acid metabolism, and portal hypertension. Laparoscopic Splenectomy and Azygoportal Disconnection (LSD) is commonly used to treat Cirrhosis with Portal Hypertension Bleeding in these patients, but its impact on lipid profiles over 2 years remains poorly characterized. This study will follow patients undergoing LSD to measure changes in serum lipid parameters before and after surgery, identify risk factors for lipid profile deterioration or improvement, and determine whether LSD can ameliorate dyslipidemia in the long term, thereby informing metabolic management strategies in cirrhotic patients.

Eligibility criteria

Qualifiers

Age 18-80 years, male or female

Confirmed diagnosis of liver cirrhosis (clinical, laboratory, imaging)

Splenomegaly and hypersplenism

History of portal hypertension bleeding (esophageal and gastric variceal bleeding )

Disqualifiers

Child-Pugh Class C liver cirrhosis

Previous abdominal surgery precluding safe laparoscopic splenectomy and azygoportal disconnection

Severe cardiac, pulmonary, cerebrovascular dysfunction; malignant tumors; primary hematological disorders

Metabolic/endocrine diseases: Familial hyperlipidemia; uncontrolled severe diabetes mellitus, thyroid dysfunction, nephrotic syndrome; use of lipid-lowering drugs, hormones, or other drugs affecting blood lipids within 1 month before surgery.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed