Abstrait

World Gastro 2019: ENDOSCOPIC DIAGNOSIS OF SUSPECTED H. PYLORI INFECTION IN SULAIMANI PEDIATRIC TEACHING HOSPITAL - Heersh HMH Raof Saeed - University of Sulaimani, Iraq

Heersh HMH Raof Saeed

Background

Helicobacter pylori is a common cause for chronic gastritis, gastric atrophy, peptic ulcer disease in pediatric age group. Infection is more common in developing countries; Transmission is fecal-oral, or oral-oral from human-to-human contact. Serology, stool antigen, urea breath test and endoscopy are used for diagnosis.

Objectives

To evaluate endoscopic finding and biopsy results of those children underwent upper gastrointestinal endoscopy

Patients and Methods

We conducted this study on 49 children, all suspected of H. pylori infection, different methods were used for diagnosis serology, stool antigen and urea breath test. Every child checked by anesthesiologist before endoscopy, in all children endoscopy done after giving anesthesia, biopsy taken from every child and sent to histopathology.

Results

In our study, sensitivity of serology was 60%, while sensitivity of stool antigen test for H. pylori was 80% and sensitivity of Urea breath test was 92%. Ninety percent of children with endoscopic finding of nodular gastritis were H. pylori positive on biopsy result while 62% of children with gastritis were positive for H. pylori on biopsy result.

Conclusions

Urea breath test is most accurate test for diagnosis of H. pylori infection, next test is stool for H. pylori antigen while serology is not accurate for diagnosis.

Keywords: H. pylori, Urea breath test, Stool antigen, Gastritis.

INTRODUCTION

In 1983, Robin Warren, a pathologist in Perth, reported the presence of “curved bacterium” in the mucosal layer of the gastric biopsy specimen. Together with Barry Marshall, they subsequently isolated the organism from the gastric biopsy specimens and named it Campylobacter pyloridis (C. pylori) (1). Later reclassified as Helicobacter pylori (H. pylori) (2).

Prevalence of H. pylori, a worldwide infection, varies greatly among countries and among population groups within the same country (3). The pattern of infection is an early childhood acquisition of H. pylori (30%-50%) that reaches over 90% during adulthood in developing countries. This has been attributed to the poor socioeconomic status and overcrowded conditions (4).

Helicobacter pylori infection of stomach induces chronic   inflammation.   Production    of    ammonia by this urease-producing bacteria and release of biochemicals such as proteases, vacuolating cytotoxin A and phospholipases contribute significantly to its inflammatory (gastritis) and carcinogenic potential (5). Furthermore, H. pylori has been linked to a variety of extra-gastric disorders (6).

Acute  phase  of  colonization  with  H.  pylori  may  be associated with transient nonspecific dyspeptic symptoms, such as fullness, nausea, and vomiting, and with considerable inflammation of either the proximal and distal stomach mucosa, or pangastritis.  This  phase is often associated with hypochlorhydria, which can last for months. It is unclear whether this initial colonization can be followed by spontaneous clearance and resolution of gastritis and, if so, how often this occurs (7).

Chronic gastritis the other stomach disorder is characterized by multistep, progressive, and life-long inflammation disease. One may estimate that more than half of the world population have this disease in some degree and extent, indicating that even many hundreds of millions of people worldwide may have chronic gastritis in a form or other (8).

Historically, serology approach was the first suggestion in order to diagnose H. pylori infection. Although the Stool Antigen test is an accurate and precise method this accuracy is influenced by several limiting factors: upper gastrointestinal bleeding, antibiotic consumption, bowel movement, and also proton pump inhibitors (PPIs) uptake (9).

Urea breath test (UBT) is a very attractive method to measure the H. pylori active infection by microbiologists and clinicians, the UBT is a gold standard method (10).Serological diagnosis another way of diagnosis. Due  to the different backgrounds in host genetics, it can be expected that various H. pylori strains induce different levels of antibodies and it may be a considerable item in explaining the reported findings (11).Gastritis updated Sydney grading is used to categorized gastritis according to histopathological change in biopsy sample (12).

PATIENTS AND METHODS

This is a retrospective study conducted in gastro- enterology unit in Pediatric Teaching Hospital in Sulaimani. We collected 49 children suspected of H. pylori infection who underwent upper gastrointestinal endoscopy from April 2017 to August 2018 . Serology, stool test for H. pylori antigen and urea breath test were the methods of investigation used for diagnosis of H. pylori infection in our city. Serology test done by using immunochromatographic strip test for H. pylori IgG, IgM, IgA, all labs uses immunochromatographic monoclonal test for detection of H. pylori antigen in stool.

Selected children with positive test for  H.  pylori  were admitted to hospital on day prior to endoscopy. Patient information were registered on database and information about name, age, sex, date, referred physician and clinical data. Investigation done before admission and procedure were recorded. File maker pro software used for data entry and SPSS  17  used  for data analysis and finding correlation. In our study we used sensitivity (Sensitivity=true positive / true positive + false negative) and specificity (true negative/ true negative + false positive) for comparison.

Endoscopy was done under general anesthesia and biopsy was taken from pyloric region, incisura and body. Biopsy samples were stained by hematoxylin and eosin stain and examined under electron microscopy for H. pylori infection and updated Sydney system grading used for detection of gastritis (13). Children underwent upper endoscopy without documented investigation for diagnosis was excluded from this study.

RESULTS

Forty nine children were enrolled in our study, 23 (46.9%) were male and 26 (53.1%) were female, Table 1.Twenty two children had positive serology for H. pylori: 9 of them proved H. pylori infection by biopsy result, sensitivity of serology test for H. pylori was 60%, and specificity was 7% as shown in Table 2.

Nineteen of children had positive stool antigen test: 16(84%) of  them proved to have H. pylori infection  by biopsy result. Sensitivity of stool test for H. pylori infection was 80%, while specificity was 75%, Table 3.

Twenty eight of children have positive urea breath test: 26 (93%) of them proved H. pylori infection by biopsy result,  sensitivity  of  urea  breath  test  was  92%  and specificity was 50%, Table 4.Thirteen children had normal endoscopic finding, four of them were positive for H. pylori infection on biopsy, another thirteen children had gastritis on endoscopy, eight of them were positive for H. pylori infection on biopsy. Twenty one children had nodular gastritis on endoscopy, nineteen of them were positive for H. pylori infection on biopsy, Table 5.

Table 1. Sex distribution.

 

Gender

 

Frequency

 

Percent

Male

23

46.9

Female

26

53.1

Total

49

100

Table 2. H. pylori results according to serological tests.

 

H. pylori biopsy result

 

Serology for H. pylori

 

 

total

 

Positive

Negative

 

Positive serology

9

13

22

Negative serology

6

1

7

total

15

14

29

Sensitivity

60%

 

 

Specificity

7%

 

 

Predictive value of positive test

40%

 

 

Predictive value of negative test

14%

 

 

Table 3. H. pylori results according to Stool test for H. pylori Ag.

 

H. pylori biopsy result

 

Stool test for H. pylori Ag

 

 

Total

 

Positive

Negative

 

Positive Stool test

16

3

19

Negative Stool test

4

9

13

total

20

12

32

Sensitivity

80%

 

 

Specificity

75%

 

 

Predictive value of positive test

84%

 

 

Predictive value of negative test

69%

 

 

Table 4. H. pylori results according to Urea Breath Test (UBT).

H. pylori biopsy result

Urea Breath Test

 

Positive

 

Negative

Total

Positive UBT

26

2

28

Negative UBT

2

2

4

Total

28

4

32

Sensitivity

92%

 

 

Specificity

50%

 

 

Predictive value of positive test

92%

 

 

Predictive value of negative test

50%

 

 

Table 5. H .pylori infection according to endoscopic finding.

 

H.pylori biopsy result

 

Endoscopic finding

 

 

Total

 

Positive

Negative

 

Normal

4(31%)

9(69%)

13

Gastritis

8(62%)

5(38%)

13

Nodular gastritis

19(90%)

2(10%)

21

Ulceration

2(100%)

0

2

Total

33

16

49

        DISCUSSION

Helicobacter pylori infection is very common infection in community reaching 50% of population according to many recent epidemiological studies,  different  type of investigation including invasive and non- invasive methods are present for detection of H. pylori infection. Except serology test, other tests revealed good correlation with biopsy results.

In our study, from 49 cases: 23 (46.9%) were male and 26 (53.1) were female. This result is similar to another study done in Saudi Arabia were children under 13 years: 48% were male and 52 % were female (14).

In our study sensitivity of H. pylori serology test was 60% and specificity was 7%. According to this finding, this test cannot be used on its own for diagnosis of H. pylori infection because of low sensitivity and very low specificity. Similar results also reported elsewhere, Akbar and Eltahawy who found sensitivity of 90% and specificity of 47% in Saudian population (15), another study done in Iran by Pourakbari et al showed very low sensitivity 29% and high specificity 91% in Iranian children (16), this difference comes from the method used for serology, in our test direct strip test for H. pylori antibody used while in Iran and Saudi Arabia ELISA based technique used.

Regarding stool antigen test: in our study this test showed sensitivity of 80% and specificity of 75% , this result is similar to another study done in Iran by Iranikhah et al who found sensitivity of 85% and specificity of 93% in Iranian children(17) . Our study showed less sensitivity probably because of better exclusion criteria in Iranian study where any child receiving management within one month excluded.

Urea breath test is another modality for H. pylori diagnosis. Our study showed sensitivity 92% and specificity 50% , another study done in Iran by Shadi Kazemi showed sensitivity of 89% and specificity of 73% for urea breath test (18). Another study done in Saudi by Al-fadda showed high sensitivity 85% and specificity 70% (19). We can explain low specificity in our test by excessive use of antibiotic specially macrolide in our region and using of Proton Pump Inhibitors within one month prior to the endoscopy which affect bacterial load and cause high false negative results.

In our study 31% of the children with normal endoscopic confirmed H. pylori infection while 90% of children with nodular gastritis confirmed H. pylori infection.

Another study done in Saudi Arabia showed that nodular gastritis was most common (40% ) endoscopic finding in children with H. pylori (20). M. Najafi Sani,et al. observed that nodular gastritis is commonest finding and 80% will have H. pylori infection on biopsy result

REFERENCES

  1. Warren JR, Marshall BJ. Unidentified curved bacilli on gastric epithelium in active chronic gastritis. Lancet. 1983; 1:1273–5.
  2. Marshall BJ, Warren JR. Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration. Lancet 1984; 1:1311.
  3. Suerbaum S, Michetti P. Helicobacter pylori infection N Engl J Med. 2002 Oct 10;347(15):1175-86
  4. Cheng  H,  HuF,  Zhang  L,  Yang  G,  Ma  J,  Hu  J,  et  al. Prevalence of Helicobacter pylori infection and identification of risk factors in rural and urban Beijing, China. Helicobacter. 2009; 14:128–33.
  5. Hatakeyama M, Higashi H. Helicobacter  pylori  cag A: A new paradigm for bacterial carcinogenesis. Cancer Sci. 2005;96:835–43.
  6. Kuo CH, Chen YH, Goh KL, Chang LL. Helicobacter pylori and Systemic Disease. Gastroenterol Res Pract. 2014;2014:358494..
  7. Kusters JG, van Vliet AH, Kuipers EJ. Pathogenesis of Helicobacter pylori infection. Clin Microbiol Rev. 2006;19(3):449-90.
  8. Sipponen P, Maaroos H-I. Chronic gastritis. Scand J Gastroenterol. 2015;50:657–67
  9. T. Shimoyama, “Stool antigen tests for the management of Helicobacter pylori infection,” World Journal of Gastroenterology, vol. 19, no. 45, pp. 8188– 8191, 2013
  10. H. A. Metanat, S.  M.  Valizadeh,  H.  Fakheri  et  al., “Comparison Between 10- and 14-Day Hybrid Regimens for Helicobacter pylori Eradication: A Randomized Clinical Trial,” Helicobacter, vol. 20, no. 4, pp. 299–304, 2015
  11. D. Vaira and N. Vakil, “Blood, urine, stool, breath, money, and Helicobacter pylori,” Gut, vol. 48, no. 3, pp. 287–289, 2001
  1. Hassan TMM, Al-Najjar SI, Al-Zahrani IH, Alanazi FIB, Alotibi MG. Helicobacter pylori chronic gastritis updated Sydney grading in relation to endoscopic findings and H. pyloriIgG antibody: diagnostic methods. J Microsc Ultrastruct. 2016;4(4):167-174.
  2. Dixon, Michael F.; Genta, Robert; Yardley, John; Correa . Classification and Grading of Gastritis: The Updated Sydney System. The American Journal of Surgical Pathology. 20(10):1161-1181, OCT 1996.
  3. Akeel M, Elmakki E, Shehata A, et al. Prevalence and factors for H. pyloriinfection in Saudi patients with dyspepsia. Electron Physician. 2018;10(9):7279- 7286. Published 2018 Sep 9. doi:10.19082/7279
  4. Daad Akbar and Ahmed Tarif Eltahaway. Helicobacter pylori infection at a university Hospital in Saudi Arabia : prevalence, comparison of diagnostic modalities and endoscopic findings. Indian pathol. microbial 2005;48(2):181-185
  5. Babak Pourakbari, Mona Ghazi, Shima Mahmoudi

. Diagnosis of Helicobacter pylori infection by invasive and noninvasive tests. Brazilian Journal of Microbiology 44, 3, 795-798 (2013) 1678-4405.

  1. Abolfazl Iranikhah, MD; Mohammad-Reza Ghadir, MD; Saeed Sarkeshikian. Stool Antigen Tests for the Detection of Helicobacter Pylori in Children. Iran J pediatr,April (2013):vol 23(no.2),138-142

 

Avertissement: Ce résumé a été traduit à l'aide d'outils d'intelligence artificielle et n'a pas encore été examiné ni vérifié