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Association Between Preoperative HALP and Immediate Postoperative Outcomes

Mortality Clinical Trial

Official title:
Association Between Preoperative HALP and Immediate Postoperative Outcomes in Patients Undergoing Pancreaticoduodenectomy

Clinical Trial Summary

Multiple inflammation-based prognostic scores have been developed for the prediction of perioperative morbidity and mortality following pancreaticoduodenectomy (PD). Preoperative "Hemoglobin, Albumin, Lymphocytes and Platelets index (HALP)" is one of the promising inflammatory markers that has emerged as a predictor of postoperative survival. To date, no study has been done with preoperative HALP to predict 30days morbidity and mortality. Is there any association between Preoperative HALP (hemoglobin, albumin, lymphocyte, and platelet) and 30 days post operative morbidity and mortality in patients undergoing Pancreaticoduodenectomy?

Clinical Trial Description

General Objective: To assess the association between preoperative HALP and immediate postoperative outcome among patients undergoing PD. Specific Objectives: 1. To identify the magnitude of immediate post-operative morbidity and mortality in patients undergoing PD. 2. To evaluate the descriptive measurement of preoperative Hemoglobin, Albumin, Lymphocytes, Platelets and HALP among patients undergoing PD. 3. To compare the preoperative HALP with morbidity and mortality among patients undergoing PD. Operational Definition: 1. Immediate postoperative time - was taken as 30days following surgery. 2. Morbidity- was defined by Clavién-Dindo20 grading for the surgical complication and DGE,21 POPF,22 and PPH23 -according to International Study Group of Pancreatic Surgery (ISGPS) grading. 3. Mortality- survival within 30days. 4. Level of preoperative HALP- normality test was done via SPSS and data of HALP followed normal Gaussian distribution. So, mean was used for the calculation of cut off value as 35.83. And, patients were divided into low HALP (≤35.83) group and high HALP (>35.83) group respectively ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05506748
Study type Observational
Source Chitwan Medical College
Contact
Status Completed
Phase
Start date April 20, 2021
Completion date April 20, 2022
View Details
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