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Patients with liver cirrhosis frequently exhibit dyslipidemia due to impaired hepatic lipid synthesis, altered bile acid metabolism, and portal hypertension. Laparoscopic splenectomy is commonly used to treat splenomegaly and hypersplenism in these patients, but its impact on lipid profiles over 2 years remains poorly characterized. This study will follow patients undergoing laparoscopic splenectomy to measure changes in serum lipid parameters before and after surgery, identify risk factors for lipid profile deterioration or improvement, and determine whether laparoscopic splenectomy can ameliorate dyslipidemia in the long term, thereby informing metabolic management strategies in cirrhotic patients.
Rationale: Liver cirrhosis disrupts hepatic lipid homeostasis through multiple mechanisms, including decreased apolipoprotein synthesis, impaired cholesterol esterification, and altered very-low-density lipoprotein (VLDL) secretion, resulting in characteristic lipid abnormalities such as hypocholesterolemia and low high-density lipoprotein cholesterol (HDL-C). Hypersplenism further complicates this metabolic profile through increased lipid peroxidation and inflammatory cytokine-mediated dysregulation of lipid metabolism. Laparoscopic splenectomy (LS) reduces splenic sequestration and inflammatory burden, potentially improving hepatic lipid synthetic capacity and peripheral lipid clearance. However, perioperative stress responses, anesthetic effects, and abrupt hemodynamic changes may transiently worsen lipid profiles. Current evidence lacks prospective, 2-year data on lipid profile dynamics after LS in this population, particularly regarding the trajectory of total cholesterol, triglycerides, LDL-C, HDL-C. This study aims to fill this gap to guide perioperative metabolic monitoring and long-term dyslipidemia management.
Study Design: Prospective, single-center, observational cohort study with a total duration of 24 months (2 years). Patients with cirrhosis, splenomegaly and hypersplenism scheduled for elective laparoscopic splenectomy will be enrolled and followed for 2 years to assess lipid profile dynamics and identify risk factors for metabolic deterioration or improvement.
Study Timeline:
Months 1-6: Patient screening, enrollment, baseline lipid assessment Months 1-18: Laparoscopic splenectomy and perioperative short-term lipid monitoring Months 7-24: Long-term follow-up at 3, 6, 9,12, 24 months postoperatively Month 24: Data analysis and study completion
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| Measure | Description | Time Frame |
|---|---|---|
| Total cholesterol (TC) level | Change in total cholesterol (TC) level | at preoperative baseline, postoperative month 1, month 3, month 6, month 12, month 18, month 24 |
| Total triglycerides (TG) level | Change in total triglycerides (TG) level | at preoperative baseline, postoperative month 1, month 3, month 6, month 12, month 18, month 24 |
| High-density lipoprotein cholesterol (HDL-C) level | Change in high-density lipoprotein cholesterol (HDL-C) | at preoperative baseline, postoperative month 1, month 3, month 6, month 12, month 18, month 24 |
| Low-density lipoprotein cholesterol (LDL-C) level | Change in low-density lipoprotein cholesterol (LDL-C) | at preoperative baseline, postoperative month 1, month 3, month 6, month 12, month 18, month 24 |
| Measure | Description | Time Frame |
|---|---|---|
| Intraoperative variables | operation time, intraoperative blood loss, fluid infusion, mean arterial pressure | During the procedure of operation |
| Postoperative complications | postoperative complications (bleeding, infection, hepatic encephalopathy, ascites) |
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Inclusion Criteria:
Exclusion Criteria:
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A 24-month (2-year) prospective, single-center, observational cohort study. Patients with liver cirrhosis and hypersplenism scheduled for elective laparoscopic splenectomy will be recruited and followed up for 2 years to evaluate dynamic changes in lipid profiles.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Guo-Qing Jiang, MD | Contact | +8651487373272 | jgqing2003@hotmail.com | |
| Dou-Sheng Bai, MD | Contact | +8651487373372 | bdsno1@hotmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Guo-Qing Jiang, MD | Clinical Medical College of Yangzhou University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Clinical Medical College of Yangzhou University | Yangzhou | Jiangsu | 225001 | China |
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| ID | Term |
|---|---|
| D005355 | Fibrosis |
| D006971 | Hypersplenism |
| D006975 | Hypertension, Portal |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D013158 | Splenic Diseases |
| D008206 | Lymphatic Diseases |
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| at preoperative baseline, postoperative month 1, month 3, month 6, month 12, month 18, month 24 |
| Albumin, bilirubin | Changes in albumin, bilirubin | at preoperative baseline, postoperative month 1, month 3, month 6, month 12, month 18, month 24 |
| Child-Pugh grade | Changes in Child-Pugh grade The Child-Pugh score is calculated based on five parameters, each assigned 1, 2, or 3 points.
Total score and corresponding grade
| at preoperative baseline, postoperative month 1, month 3, month 6, month 12, month 18, month 24 |
| D006425 | Hemic and Lymphatic Diseases |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |