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Diagnostic Value of Hyperbilirubinaemia as a Predictive Factor for Appendiceal Perforation in Acute Appendicitis
This study has been completed.
Sponsored by: Ruhr University of Bochum
Information provided by: Ruhr University of Bochum
ClinicalTrials.gov Identifier: NCT00677417
  Purpose

The values of laboratory examinations which are useful for the diagnoses of appendicitis are white blood cell count (WBC), C-reactive protein (CRP) and erythrocyte blood sedimentation rate (ESR). However up to date there is no laboratory marker for the pre-operative diagnosis of appendiceal perforation in acute appendicitis. Recently hyperbilirubinaemia has been associated with appendiceal perforation. Aim of this retrospective study is therefore to investigate if hyperbilirubinaemia has a diagnostic value for the pre-operative diagnosis of appendiceal perforation in patients with appendicitis.


Condition
Perforated Appendicitis

MedlinePlus related topics: Appendicitis Jaundice
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Retrospective
Official Title: A Retrospective Study Investigating the Diagnostic Value of Hyperbilirubinaemia as a Predictive Factor for Appendiceal Perforation in Acute Appendicitis

Further study details as provided by Ruhr University of Bochum:

Biospecimen Retention:   None Retained

Biospecimen Description:

Enrollment: 538
Study Start Date: May 2008
Study Completion Date: May 2008
Primary Completion Date: May 2008 (Final data collection date for primary outcome measure)
Detailed Description:

We identified 538 patients with histologically proved acute appendicitis who underwent laparoscopic or conventional appendicectomy between January, 2004 and December, 2007 in a surgical department of an academic teaching hospital. A retrospective multiple chart review of the medical records including laboratory values (bilirubin, CRP, white blood count) and histological results was conducted.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients who are appendectomied and who received preoperative Liver function test (bilirubin, liver transaminases GOT and GPT)

Criteria

Inclusion Criteria:

  • Appendicitis and a preoperative laboratory workup with Leukocytes, C-reactive Protein, Bilirubin and liver transaminases GOT and GPT

Exclusion Criteria:

  • Alcoholism
  • A history of viral hepatitis
  • Gilbert's disease
  • Dubin Johnson syndrome
  • BRIC (benign recurrent intra-hepatic cholestasis) and other documented biliary
  • Hemolytic or liver diseases associated with hyperbilirubinaemia.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00677417

Sponsors and Collaborators
Ruhr University of Bochum
Investigators
Principal Investigator: Benno Mann, PD Dr. med. Department of General and Visceral Surgery, Augusta Krankenanstalt, Academic Teaching Hospital of the Ruhr-University Bochum, Germany
Principal Investigator: Michael Sand, Dr. med. Department of General and Visceral Surgery, Augusta Krankenanstalt, Academic Teaching Hospital of the Ruhr-University Bochum, Germany
  More Information

Responsible Party: Department of General and Visceral Surgery, Augusta Krankenanstalt, Academic Teaching Hospital of the Ruhr-University Bochum, Germany ( Dr. med. Michael Sand )
Study ID Numbers: 001
Study First Received: May 12, 2008
Last Updated: August 4, 2008
ClinicalTrials.gov Identifier: NCT00677417  
Health Authority: Germany: Ethics Commission

Study placed in the following topic categories:
Digestive System Diseases
Gastrointestinal Diseases
Hyperbilirubinemia
Appendicitis
Intestinal Diseases
Gastroenteritis

Additional relevant MeSH terms:
Pathologic Processes
Cecal Diseases

ClinicalTrials.gov processed this record on January 14, 2009