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Helicobacter pylori Screening

(Download  Helicobacter pylori Screening.pdf)

Background

It is estimated that 10% of the population are afflicted by peptic ulcer disease. The Helicobacter pylori (HP) bacterium is thought to be the cause of most peptic ulcers. Helicobacter seroprevalence rates rise with age and lower socio-economic status, with rates of >50% in Australians aged over 50 years.

Rationale of Testing

Patients with peptic ulcers in whom HP infection is documented will in most cases have their symptoms and ulceration cured by combination antimicrobial therapy that eradicates the organism. The various approaches that have been used to diagnose HP infection are listed in the following table, indicating the best-published figures for sensitivity and specificity for each test.

Methods for Diagnosis HP Infection

Method

Sensitivity (%)

Specificity (%)

Comments

Invasive Methods

Histology of gastric biopsy

95-99

95-99

Sampling site errors do occur; detects coccoidal forms of HP only

Culture gastric biopsy

70-90

100

Sampling site errors do occur; provides antibiotic sensitivity

Rapid urease test

90-95

95-98

Rapid result; sampling errors do occur

Gastric biopsy PCR

95

100

Very sensitive; false-positives can occur

Non-Invasive Methods

Serology

95

95

Unable to confirm eradication

C13-urea breath test

95-98

95-98

Expensive; requires mass spectroscopy; confirms eradication

C14-urea breath test

95-98

95-98

Radioactive contra-indicated in pregnancy and children; requires gamma counter; confirms eradication

Stool culture

30-50

100

Technically difficult; can provide antibiotic sensitivity

Stool EIA

89-94

91-95

Technical sampling errors; less sensitive

 

Based upon an extensive literature review and an assessment of available methodologies by HAPS, we offer the following recommendations for diagnosing and monitoring HP infection.

Diagnosing HP Infection

Serological testing, measuring IgG antibodies to HP, represents the most sensitive assessment for HP infection. It is not prone to the sampling error problems seen with more direct approaches such as histology and Clotest assessment, and avoids the inconvenience of medication cessation associated with breath testing.

We do not recommend faecal HP antigen testing for HP diagnosis as this method is less sensitive than serology and has technical sampling errors.

Confirming Eradication of HP after Antibiotic Therapy

We recommend that HP eradication after appropriate antibiotic therapy be confirmed with C14-urea breath testing (C14-UBT).

Recommendations for C14-UBT testing:

  • Wait for at least 6 weeks after eradication therapy completed
  • Cease acid-suppressing agents for 1 week before C14-UBT
  • Fast overnight before test

While faecal HP antigen testing has been advocated as a replacement for the C14-UBT to confirm eradication, there is sufficient controversy surrounding the sensitivity and specificity of the faecal test to recommend against its diagnostic use at this time.

References

  1. Leong VK, Sung JJ. Diagnosis of Helicobacter pylori infection. J. Int. Fed. Clin. Chem. 1996, 8(4):161-166
  2. Makristathis A, Pasching E, Schutze K, et al. Detection of Helicobacter pylori in stool specimens by PCR and antigen enzyme immunoassay. J. Clin. Microbiol. 1998, 36(9):2772-2774
  3. Vaira D. et al. Diagnosis of HP infection with new non-invasive antigen-based assay. Lancet 1999, 354:30-33
  4. Trevisiani L et al. Detection of HP in faeces by a new EIA method: preliminary results. Scand. J. Gastroenterol. 1998, 33:893-4
  5. Plebani M et al. Letter to Lancet. 1999, 354:9185

Written by:                     Dr Glenn Reeves, Immunology HAPS
Written:                          January 2000

Last Reviewed:             10.5.2001

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