Major Surgery as a Risk of Gall Stone Disease?

September 27, 2022 updated by: Nabin Pokharel, Nepal Medical College and Teaching Hospital

History of Abdominal Surgery Can be a Risk Factor of Gall Stone Disease? A Case Control Study

Gall stone disease is one of the most common diseases occurring in the world as well as in our country, Nepal. This disease is problematic to a lot of patients and poses a huge economic burden to the country. Gall stone disease is usually diagnosed by abdominal ultrasonography as echogenic foci that cast an acoustic shadow. The risk factors for the development of gall stones are multiple; age, sex, genetic susceptibility, pregnancy, dyslipidemia, obesity, rapid weight loss, prolonged fasting and parenteral nutrition, spinal cord injury, cirrhosis, hyperbilirubinemia, and Crohn's disease. In cases of prolonged fasting, total parenteral nutrition, and spinal cord injury; biliary stasis due to lack of enteral stimulation is thought to contribute for the development of gall stones.8 Biliary stasis leads to the formation of sludge which consists of mucus, calcium bilirubinate, and cholesterol crystals. It has been established that several drugs viz.fibrates, ceftriaxone, somatostatin analogues and oral contraceptive pill can promote gall stone formation.

The elective surgeries are performed after preoperative fasting >6 hrs. as recommended by different society of anesthesiology. Moreover, fasting continues throughout surgery and few post-operative hours which usually lasts more than 12 hours. Also group of people after major abdominal surgeries frequently develop post-operative hyperbilirubinemia.

All these factors after any major surgeries may pose a risk for the development of Gall stones.

The major goal of this study is to look if the history of major surgery in the past is one of the etiological factors for the development of gall stone disease. It is a case-control study carried out in the Department of Surgery. It will also help us analyze other multiple epidemiological factors like age, sex, BMI, drugs, lipid profile, family history lifestyle, and dietary factors associated with the disease. The epidemiological data from this study can also help us analyze other confounding and determining factors.

Study Overview

Detailed Description

The risk factors for the development of gall stones are multiple which a reason for its high prevalence. Past history of major surgeries does carry some of the biological causations of the gall stones like prolonged fasting during the perioperative period and post-operative hyperbilirubinemia, effects of stress in the gall bladder, and bile flow. However, there have not been recent studies to redefine the etiology of gall stone and history of major surgery. Meanwhile, some of the studies are found be of a great value for the background of this study.

A study published by J M Little and J Ivramovic in 1991 showed that the major abdominal surgery had a statistically significant difference in a cumulative prevalence of the gall stone compared to those who did not undergo any surgery. However, the exact mechanism behind the formation of the stone was not revealed but the sludge formation during fasting was assumed to be the common pathways. L Bolondi, S Gaiani have ultrasonographically assessed the prevalence of sludge in a group of 48 fasting patients after gastrointestinal tract surgery with a period of fasting lasting for 7 to 10 days. It showed the presence of gall stones with different ultrasonographic patterns in three sludge positive patients after the end of six months. They concluded in the early postoperative period there is a high risk for sludge development and that in some cases sludge may subsequently evolve into gall stones.

Another cross-sectional study by A F Attili,E Scafato showed that Prevalence of gallstone was higher among subjects who had an overnight fasting period of over 12 hours than subjects with that of less than 12 hours. H M Bloch et al studied the effects of fasting and composition of gall bladder, where the mean cholesterol saturation index was significantly greater after a 15 hour fast (1.35+0.08) than after a 10 hour fast (105+0.10). The cholesterol saturation index is the ratio of the cholesterol of the sample to the maximum soluble cholesterol of that sample. In the study, it was determined by using the criteria of Hegardt and Dam. The saturation index of greater than 1 represents the cholesterol is supersaturated and forms gall stones. Henceforth, the findings suggested that fasting for between 10 to 20 hours increases the risk for gallstones formation. Another study by Lee et al where they followed the 94 patients with biliary sludge for the mean of 37.8 months. It was found that 8.3% developed asymptomatic gall stones and 6.3% underwent cholecystectomy.

Another prospective study by Christine Evans et al followed 180 patients following major operations found an incidence of 3.7% severe jaundice and 16.5% mild jaundice (serum bilirubin 1.5-4 mg/dl) and a study by Stefan Stenderet al followed 61,212 patients for 34 years, which showed that the risk for gall stone disease is significantly higher in population with bilirubin level in 10th decile (geometric mean 1.34 gm/dl). Though the previous studies have examined the relationship between fasting and the formation of gallstones, none of them examined the direct relationship between any major surgeries and the incidence of gallstones. They also did not study the other factors like the effects of stress, drugs during surgeries and anesthesia on the gall bladder, and the bile flow. However, they have given enough background to establish a hypothesis that any major surgery can be a significant risk factor for the development of gallstones. However, there is no widely accepted consensus on the grading of surgery so by major surgery we mean all surgeries done under general or regional anesthesia and involves procedures in abdominal cavity.

With our observation of the evidence, it indicates that any major surgery may itself is an important determinant of the gallstone formation soon after the surgery and so a study can address this gap of the knowledge. A case-control study can help us assess the past history of major surgery as a significant risk factor for gallstone disease. Any significant findings will warrant other higher studies like cohort study for a detailed assessment of the cause. It has been evident that prolonged fasting or fasting over 10-12 hours imposes a risk factor for gallstone disease. It has also been established that major gastrointestinal surgery, hyperbilirubinemia is also a risk factor for gallstone disease. However, there is a clear gap of knowledge whether any major surgery with similar biological causation imposes a risk factor for gallstone disease or not. The rationale of the study is to look over this lack of knowledge.

The gall stone disease is itself a major economic burden to a lot of patients and the development of symptomatic gallstone in patients who have undergone major surgery in the past few years would be distressing to the patients and relatives. Even if few people after major surgery develop gall stones in future, and those at such risks could be identified, then we could institute surveillance ultrasonography or medical prophylactic measures like ursodeoxycholic acid.

Study Type

Observational

Enrollment (Actual)

755

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Bagmati
      • Bharatpur, Bagmati, Nepal, 44200
        • Chitwan Medical college and teaching hospital
      • Kathmandu, Bagmati, Nepal, 44600
        • Nepal Medical College and Teaching Hospital
    • Lumbini
      • Palpa, Lumbini, Nepal, 32500
        • Lumbini Medical College and teaching hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients above 18 years in the department of surgery in Nepal medical college and teaching hospital, Lumbini Medical College and teaching hospital and Chitwan medical college and teaching hospital

Description

Inclusion Criteria:

  • Must be above 18 years of age.

Exclusion Criteria:

  • Liver Cirrhosis
  • Hepatobiliary and pancreatic malignancy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Case
Cases will be patients in the department of surgery above 18 years with ultrasound findings of gall stone disease.
Any surgery performed under general or regional anesthesia and procedures involving abdominal cavity is considered major abdominal surgery and those who have undergone any major abdominal surgery before 6 months from the date of ultrasound findings confirming the presence or absence of gall stone will be considered exposed.
Control
Controls will be patients in the department of surgery above 18 years with ultrasound findings showing evidence of no gallstones
Any surgery performed under general or regional anesthesia and procedures involving abdominal cavity is considered major abdominal surgery and those who have undergone any major abdominal surgery before 6 months from the date of ultrasound findings confirming the presence or absence of gall stone will be considered exposed.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Odds ratio
Time Frame: 2 months
Ratio of the odds for gall stone disease among patient with past history of major abdominal surgery to patient without history of major abdominal surgery and it its significance.
2 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gaurav Dr Katwal, MS, Chitwan Medical college and teaching hospital, Nepal
  • Principal Investigator: Neeraj Dr. Thapa, MS, Lumbini Medical college and teaching hospital, Nepal
  • Study Chair: Sunil Prof. Dr. Shrestha, MS, Nepal medical college and teaching hospital, Nepal
  • Study Chair: Harish C Prof. Dr. Neupane, MS, Chitwan Medical college and teaching hospital, Nepal
  • Study Chair: Kishor K Prof. Dr. Tamrakar, MS, Chitwan Medical colllege and teaching hospital, Nepal
  • Principal Investigator: Nabin Dr. Pokharel, MCh, Nepal medical college and teaching hospital, Nepal
  • Study Chair: Biplov Dr. Adhikari, MBBS, Nepal medical college and teaching hospital, Nepal

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

October 22, 2020

Primary Completion (ACTUAL)

November 20, 2021

Study Completion (ACTUAL)

April 1, 2022

Study Registration Dates

First Submitted

December 4, 2020

First Submitted That Met QC Criteria

December 15, 2020

First Posted (ACTUAL)

December 19, 2020

Study Record Updates

Last Update Posted (ACTUAL)

September 28, 2022

Last Update Submitted That Met QC Criteria

September 27, 2022

Last Verified

September 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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