eWe surveyed national Helicobacter pylori diagnostic testing practices and diagnoses using commercial and Medicare medical claims data from Optum Labs (Cambridge, MA). Serologic testing for antibodies to H. pylori remains the most commonly ordered diagnostic test despite recent expert recommendations. Changes in reimbursement for serologic testing will likely drive future provider ordering practices.
Helicobacter pylori remains among the most common bacterial infections worldwide. It is estimated that globally one in every two individuals is infected. Local prevalence rates vary, however, with approximately 20 to 40% of individuals in the United States exposed to H. pylori by adulthood (1-5). Despite these infection rates, most individuals remain asymptomatic. A number of welldefined clinical syndromes have been associated with infection, however, including dyspepsia, peptic ulcer disease, gastric adenocarcinoma, and mucosa-associated lymphoid tissue (MALT) lymphoma, with the latter two collectively occurring in Ͻ1% of individuals (3). Eradication of H. pylori through appropriate antibiotic regimens leads to a significant reduction of ulcer recurrence and long-term remission of MALT lymphoma for the majority of afflicted patients (6-8). Therefore, accurate and prompt diagnosis of H. pylori infection is essential.Three noninvasive testing methods are available to detect H. pylori, including serologic assays to measure anti-H. pylori IgM, IgA, and IgG antibodies, H. pylori stool antigen tests (SATs), and urea breath test (UBTs) (9-11). Choosing among these methods requires a thorough understanding of each assay's clinical utility. Serologic testing shows poor sensitivity (74% to 85%) and specificity (79% to 90%) for active infection, although such testing is not affected by prior intake of protein pump inhibitors (PPIs), bismuth compounds, or antibiotics. Additionally, serologic testing should not be used to document H. pylori eradication due to demonstrable antibody levels for years following the initial exposure (10). Finally, most serologic assays, aside from certain IgG tests, lack Food and Drug Administration (FDA) clearance. Conversely, detection of H. pylori antigen by the SAT or urease activity by the UBT is indicative of active H. pylori infection, and either assay can be applied to confirm H. pylori clearance following completion of antibiotic therapy (9-11). Both methods also have commercially available, FDA-cleared assays that offer high sensitivities and specificities for H. pylori infection (both Ͼ95% in pretreatment conditions). Certain drawbacks exist for these two assays, including the generally higher cost compared to that of serologic testing, although this cost is offset by the improved diagnostic accuracy and typically higher reimbursement rates for UBTs and SATs (11, 12). Additionally, due to the specimen collection requirements and assay complexity, UBT availability may be limited to larger hospitals and reference laboratories. Finally, PPIs, bismuth compounds, and antibiotics need to be dis...