Table. 1.

Summary of Helicobacter pylori detection techniques

Technique Description Advantage Disadvantage Sensitivity (%) Specificity (%)
Polymerase chain reaction Primers of common conserved genes used to detect H. pylori are the urease A [18], urease C [19], 16S rRNA [20], Hsp60 gene [21] High sensitivity and specificity Susceptible to false positives 63–100 [21] 28–100 [21]
Serology Utilizes enzyme-linked immunosorbent assay to detect serum H. pylori–specific immunoglobulin antibodies Inexpensive and easily performed
Able to detect H. pylori even in cases with low bacterial density
Cross reacts with antigens of other Helicobacter species and Campylobacter organisms
Not specific for H. pylori infection of the gallbladder
80– 90 [17] 80– 90 [17]
Histology Several stains used are the modified Giemsa, Warthin–Starry, Gimenez, Genta, and immunohistochemical H. pylori antibody stains Able to directly demonstrate the presence of H. pylori in the gallbladder Sensitivity is affected by factors such as site and pattern of colonization 69– 93 [23] 87–100 [23]
Microbial culture Culture of H. pylori taken from bile or mucosal scrapings Definitive method for demonstrating the presence of H. pylori infection in the gallbladder Hard to culture due to type of specimens used and fastidious nature of H. pylori virus
Affected by prior antibiotic usage
44 [22] 67 [22]
Ann Hepatobiliary Pancreat Surg 2023;27:241-50 https://doi.org/10.14701/ahbps.22-056
© 2023 Ann Hepatobiliary Pancreat Surg