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Videosurgery and Other Miniinvasive Techniques
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4/2022
vol. 17
 
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Bariatric surgery
Original paper

Is Helicobacter pylori eradication required after laparoscopic sleeve gastrectomy?

Sezer Akbulut
1
,
Hakan Seyit
1
,
Kivanc Derya Peker
1
,
Mehmet Karabulut
1
,
Halil Alis
2

1.
Department of General Surgery, University of Health Sciences, Bakirkoy Dr. Sadi Konuk Health Practice and Research Center, Istanbul, Turkey
2.
Department of General Surgery, University of Istanbul Aydin, Istanbul, Turkey
Videosurgery Miniinv 2022; 17 (4): 705–709
Online publish date: 2022/05/26
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Introduction

Obesity is a multifaceted disease caused by a combination of genetic, environmental, and metabolic factors that has been a growing problem for public health [1]. Bariatric surgery was found to be highly effective in the treatment of obesity over time [2]. The European Association for Endoscopic Surgery (EAES) and the Society of American Gastrointestinal and Endoscopic Surgeons (SAGES) published guidelines in 2004 and 2008, respectively, following the introduction of laparoscopic bariatric surgery [3, 4]. Laparoscopic surgery became the gold standard for bariatric surgery as a result of these guidelines. Laparoscopic sleeve gastrectomy (LSG) which was first proposed as the first step of multi-step surgical treatment in superobese patients, was considered the primary treatment method in morbidly obese patients after its efficacy was reported [5, 6].

H. pylori infection is one of the most common in humans: it has been estimated that more than half the global population will be infected with H. pylori in their lifetime [7]. This bacterium was classified in 1994 as a definitive human carcinogen by the International Agency for Research on Cancer Group of the World Health Organization. Given these considerations, H. pylori infection is a serious public health problem that warrants increased research and treatment efforts.

The frequency of H. pylori infection in morbidly obese patients is controversial. The prevalence of H. pylori in the preoperative period in bariatric surgery candidates was 8.7% in a German cohort study, whereas this rate was 85.5% in a Saudi Arabia cohort study [8, 9]. The reason for the high variability in H. pylori prevalence rates may be the diversity in H. pylori diagnostic tests and the low sample size used in these studies. Histological examinations among diagnostic tests have excellent sensitivity and specificity for H. pylori detection [10].

The sensitivity and specificity of histopathology have been found to be 66–100% and 94–100%, respectively [11].

Many epidemiological studies aiming to elucidate the relationship between H. pylori and body mass index (BMI) have failed to find any statistically significant relationship. BMI was found to be slightly higher in H. pylori-positive patients in a meta-analysis of 18 observational studies involving 10,000 cases [12].

Aim

Our study aims to investigate the effect of LSG – which is increasingly preferred in the treatment of morbid obesity – on H. pylori infection.

Material and methods

Patients who underwent biopsy with upper gastrointestinal endoscopy in the preoperative and postoperative period of LSG between 2014 and 2019 were included in the study. In our clinic, a total of 1368 LSG operations were performed during the study period, yielding a study sample of 162 (11.8%) patients who underwent preoperative and postoperative endoscopy.

Patients over the age of 18 years who underwent surgery were included in the study. These patients were evaluated by the endocrinology, psychiatry, chest diseases, cardiology, and anesthesia teams in the preoperative period. All abdominal ultrasonographies and upper gastrointestinal tract endoscopies were routinely performed in the preoperative period. According to the updated Sydney system recommendations, five biopsy samples should be obtained: two from the corpus, two from the antrum, and one from the incisura angularis [13]. The same number of biopsies were performed in the postoperative endoscopy. Biopsy samples were sent to the Department of Pathology for histological examination and evaluation of H. pylori density in accordance with the Sydney Classification. Their evaluation generated the following classifications: Absence of lesion: 0, mild: 1+, moderate: 2+, severe: 3+

Patients who had a gastric operation history and received H. pylori eradication treatment were excluded from the study. Additionally, patients using antibiotics for any indication in the preoperative and postoperative periods were excluded from the study. In the postoperative period, 40 mg of pantoprazole was prescribed for daily use over a 1-month period to expedite wound healing.

LSG was performed by three obesity surgeons, who operated using a bougie ranging from 32F to 38F. The stomach was resected up to 2 cm away from the angle of His, using staplers with various thicknesses, starting from a distance of 2 cm from the pylorus. Anastomosis leak testing was performed with intraoperative methylene blue. Drainage extending from the left upper quadrant to the esophagogastric junction was placed in all patients. The Enhanced Recovery After Surgery (ERAS) protocol was applied in the postoperative period. All operations were completed laparoscopically.

Patients who underwent LSG in our clinic were followed regularly in the first month, third month, sixth month, and thereafter annually in the postoperative period. Upper gastrointestinal endoscopy is performed in cases of complaints during follow-up that include nausea, vomiting, epigastric burning, and difficulty swallowing. Biopsies are again taken during upper gastrointestinal system endoscopy, and these samples underwent histological examination and evaluation of H. pylori density.

Statistical analysis

The software NCSS (Number Cruncher Statistical System) 2007 (Kaysville, Utah, USA) was used for statistical analyses. Descriptive statistical methods (mean, standard deviation, median, frequency, ratio, minimum, maximum) were used to evaluate the study data, while Pearson’s χ2 test was used to compare qualitative data. The independent samples t-test was used to compare two groups whose data were normally distributed. McNemar’s test was used to compare qualitative data and two-group parameters during follow-up. Statistical significance was set at p < 0.01 and p < 0.05.

Results

Of the 162 patients included in our study, 39 were male and 123 were female, and the mean age of the patients was 41.69 ±10.96 years. BMI was calculated as 47.64 ±6.69, and the time of perform upper gastrointestinal system endoscopy in the postoperative period was calculated as 17.69 ±9.17 months, on average.

Our study has got two experimental groups H. pylori (+) and H. pylori (–) in the preoperative period. No statistically significant differences were found between these two groups in gender distribution, diabetes and hypertension incidence rates, age, weight, and BMI (p > 0.05). Furthermore, no statistically significant differences were found in the time to perform postoperative upper gastrointestinal system endoscopy and time of the follow-up (p > 0.05) (Table I).

Table I

H. pylori demographic data of negative and positive groups in the preoperative period

ParameterTotalH.P.(–)H.P.(+)P-value
Gender:
 Male39 (24.1%)11 (17.5%)28 (28.3%)a0.116
 Female123 (75.9%)52 (82.5%)71 (71.7%)
Age [years] (range)41.69 ±10.96 (18-63)41.7 ±11.33 (18-63)41.69 ±10.78 (18–59)b0.995
Weight [kg]126.28 ±18.94 (95–176)124.25 ±17.02 (95–160)127.58 ±20.04 (96–176)b0.278
BMI [kg/m2]47.64 ±6.69 (39–70)47.13 ±6.67 (39–67)47.96 ±6.71 (40–70)b0.442
Diabetes63 (38.9%)19 (30.2%)44 (44.4%)a0.069
Hypertension45 (27.8%)18 (28.6%)27 (27.3%)a0.857
Postoperative upper gastrointestinal endoscopy time [months] (range)17.69 ±9.17 (3–52)18.6 ±10.13 (6–52)17.1 ±8.51 (3–46)b0.311
Time of follow-up [months] (range)27.33 ±11.77 (4–65)28.9 ±10.69 (11–61)26.33 ±12.35 (4–65)a0.176

a Pearson’s χ2,

b independent samples t-test.

The presence of H. pylori was found to be positive in 99 patients in the preoperative period; of these patients, H. pylori was negative in 62 patients in the biopsy results following LSG. H. pylori was negative in 63 patients in the preoperative period; of these, 51 patients were found to be negative in the biopsy results after LSG. The changes were found to be statistically significant between the preoperative and postoperative pathology results evaluated (p < 0.01). No comparisons were made between other pathology results (Table II).

Table II

Evaluation of postoperative pathology results according to preoperative pathology results

Preoperative pathologyPostoperative pathologyP-valuea
H.P.(–)H.P.(+)H.P.(–)H.P.(+)
63 (38.9%)99 (61.1%)113 (69.8%)49 (30.2%)0.001**

a McNemar test,

** p < 0.01.

Discussion

LSG is increasingly preferred among the methods currently used in the treatment of obesity. Therefore, future research will benefit from access to a large pool of patients who have undergone extensive LSG operations. Treatment regimens to eradicate H. pylori will become even more complex in the future. The effect of H. pylori’s relationship with gastritis and malignancy on patients undergoing bariatric surgery remains unclear [14].

In the extant literature, the relationship between LSG and H. pylori has been broadly examined in terms of postoperative complications. The relationship between LSG and H. pylori has not been associated with complications other than atrophic and chronic gastritis [15].

In the literature, there are very few studies investigating the H. pylori density in patients with LSG. A 2009 study was the first to report that LSG could contribute to H. pylori eradication [16]. The results of 480 patients who underwent LSG were examined in a retrospective study published in 2015, finding that H. pylori eradication would be spontaneous secondary to LSG and, therefore, that eradication treatment would not be required [17].

In our opinion, there may be a decrease in H. pylori density in patients who have undergone extensive gastric resection. It is known that H. pylori tends to colonize and is limited to the antrum due to tissue tropism [18]. Some publications report the proportion of H. pylori-positive patients in the surgical specimen to be 59.5%, while the positivity rate decreases to 28% in the average 3-year postoperative follow-up period in studies on H. pylori remission after partial gastrectomy [19]. It seems unlikely that a tropism based on antrum-specific and appropriate acidic conditions will remain unaffected after LSG. Presence of H. pylori colonization may also change dramatically, due to changes in the stomach environment after bariatric surgery [20].

Our study supports the observation that there is a decrease in H. pylori density after LSG. Our study has limitations. The study design is retrospective and observational. Additionally, our study is limited by its small number of cases and by the fact that it is a single-center study. On the other hand, when compared with other studies in the literature, the strength of our study is the pathological examination of H. pylori.

The effect of LSG on H. pylori infection can be better understood with multicenter, prospective studies with large case series.

Conclusions

The treatment of H. pylori after LSG is an uncertain issue. However, our study showed that LSG can contribute to the eradication of H. pylori.

Conflict of interest

The authors declare no conflict of interest.

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20 

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Copyright: © 2022 Fundacja Videochirurgii This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
 
  
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