JCDR - Register at Journal of Clinical and Diagnostic Research
Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X
Internal Medicine Section DOI : 10.7860/JCDR/2020/46170.14209
Year : 2020 | Month : Nov | Volume : 14 | Issue : 11 Full Version Page : OD03 - OD05

Failure of three Recommended Regimens to Treat a Case of Gastritis Caused by Helicobacter pylori

Musa Basheer Mansour1, Sara Elsheikh Ahmedana1

1 Consultant Physician, Department of Family Medicine, Primary Health Care Corporation, Doha, Qatar.
2 Consultant Physician, Department of Family Medicine, Primary Health Care Corporation, Doha, Qatar.


NAME, ADDRESS, E-MAIL ID OF THE CORRESPONDING AUTHOR: Dr. Musa Basheer Mansour, Qatar Doha PHCC, Ummghwillina H.C. Ain Khalid Str. 220, Zone 56, Building 24, Villa 77, Doha, Qatar.
E-mail: musabasheer97@yahoo.com
Abstract

Helicobacter pylori (H. pylori) is a gram-negative pathogen that leads to chronic bacterial infection. Approximately, 50% of the world’s population is affecting even though the precise route of transmission is not known. Up to 90% of people infected with H. pylori never experience symptoms or complications and the majority remains asymptomatic. Treatment failure can occur and physician must deal with case as recommended by guidelines. This report describes the management of a man with gastritis caused by H. pylori that was failed to the three recommended regimens. The patient was initially (first visit) diagnosed as a case of stomach pain (irritation) due to spicy/chilly food. Then the patient was followed regularly up to six visits approximately for 25 weeks with clinical and laboratory assessment provided by medical prescription of recommended regimens. This paper has been reported to describe an unexpected beneficial response to treatment, report unlabeled or unapproved uses of medication and show a positive personal impact despite, the lack of advanced medical facility.

Keywords

Case Report

A 42-year-old man, in Sudan; Gezira state; came with chief complaint of upper abdominal discomfort, bloating, nausea and feeling of gastric heaviness after eating spicy food since 13 days. The pain was mainly epigastric, dull, and not radiated, relieved by eating small amounts of non-spicy food and aggravated by eating chilly/spicy food. Previous history, social habits, and drug history were insignificant. No history of hospitalisation or surgical operation. A body mass index 24 kg/m2, temperature 37°C, blood pressure of 131/78 mmHg, heart rate of 88 beats/minute, respiratory rate of 18 breath per minute, general and systemic examination revealed nothing significant. The laboratory investigation was not requested. The patient was initially diagnosed as a case of stomach pain (irritation) due to spicy/chilly food. He was reassured and advised to avoid spicy/chilly food and given Mebeverine 200 mg twice a day for five days but the patient again visited the clinic after eight days with the same complaint. On the first visit, no investigations were requested. Eight days later the stool analysis and Widal Test for typhoid fever were requested which were normal and stool analysis tested positive for H. pylori. Seven weeks later, the test of eradication was positive. At the fourth visit stool analysis tested positive for H. pylori. Also, complete blood picture and renal function tests and electrolytes are normal. Seven weeks later stool analysis tested positive for H. pylori. On the sixth visit, stool analysis tested negative for H. pylori. Also, Urea Breath Test (UBT) was performed and it was negative [Table/Fig-1]. The patient was managed by using different regimens for six months under a regular follow-up.

Treatment and outcomes of the patient.

Visit1st Visit2nd Visit3rd Visit4th Visit5th Visit6th Visit
Day24.07.1901.08.1913.09.1916.10.1925.11.1904.01.2020
Symptoms/SignsUpper abdominal discomfort, bloating, nausea and feeling of gastric heaviness after eating. No abnormal physical findings.Same as the first visit. Symptoms might be differing from one patient to another. Other symptoms loss of appetite, anorexia, unexplained weight loss, heart burnAbdominal discomfortNo abnormal physical findings. H. pylori rarely cause abdominal physical findingsSame as the first visitH. pylori rarely cause abdominal physical findingsUpper abdominal discomfort, mild headache Clarithromycin adverse effects {nausea, diarrhea for 4 days}H. pylori rarely cause abdominal physical findingsAsymptomaticThis indicates well response for the regimen
InvestigationsNot requestedNo need for investigations because, it was simple diagnosis (gastric irritation due to spicy food)Stool analysis tested positive for H. pyloriStool analysis tested positive for H. pylori.Stool analysis tested positive for H. pylori.The stool analysis tested positive for H. pylori. Renal function tests and complete blood picture were normal.Stool analysis tested negative for H. pylori. The urea breath test was done in another hospital in different city and it was negative.Urea Breath Test is a good one for irradiation
TreatmentMebeverine capsule 200 mg BID for five days. Decision to give medicine works by relaxing the stomach.(Pantoprazole 40 mg bid + Clarithromycin 500 mg bid + Metronidazole 500 mg tid) for 14 days.(Pantoprazole 40 mg bid + Clarithromycin 500 mg bid + Metronidazole 500 mg bid + Amoxicillin 1 gram bid) for 14 days(Pantoprazole 40 mg bid + Bismuth Subsalicylate 524 mg qid + Metronidazole 375 mg qid +Tetracycline 500 mg qid) for 14 days.(Pantoprazole 40 mg bid + Clarithromycin 500 mg bid + Amoxicillin 1gram bid + doxycycline 100 mg daily) for 14 days.AdvisedEducatedReassuredNo medicine
Follow-up outcomePatient not improved. Eight days later patient came with the same complaint.The patient improved for seven days since starting the treatment in the second visit.The patient improved for 23 days since starting the treatment in the third visitThe patient improved for 19 days since starting the treatment in the fourth visitAsymptomatic,This indicates well response for the regimenGiven an open appointment if needed

Discussion

Helicobacter pylori is a common worldwide infection. Half of the world’s population is affected [1]. The disease is very infectious, and the accurate route of transmission is not clearly understood [2,3]. The majority of infected people around 90% does not have symptoms and complications [4]. The majority remains asymptomatic [5]. The symptoms may include bitter taste, abdominal pain, vomiting and nausea [6,7]. Abdominal pain and nausea are associated with acute gastritis [6]. Chronic gastritis is asymptomatic or bloating, gastric pain, nausea, vomiting, belching and Non-Ulcer Dyspepsia (NUD) can develop [6,8]. Gastritis due to H. pylori is the main cause of peptic ulcer disease by 20-10% [6,9,10]. The faecal-oral or oral-oral are the main routes of transmission [11].

The preferable diagnostic methods include UBT, faecal antigen assay, tissue biopsy [7]. UBT is highly sensitive and specific and the best choice for those who suffer from alarming symptoms in addition to that is the best test for the eradication of H. pylori, then the stool is an alternative for UBT [12,13]. The serological test can be used for the past infection and isn’t useful for monitoring of the effectiveness and can be used without the hold up of Proton Pump Inhibitors (PPIs), antibiotic or bismuth [12,14]. Antibiotic and bismuth should be stopped 30 days and PPIs 14 days before the eradication test for H. pylori to avoid a false negative [12].

Treatment Options

The management of this case depends on different regimens [5,12,14-19].

First line includes many regimens for 14 days as following Clarithromycin 500 mg BID + PPI BID +either amoxicillin 1000 mg BID or metronidazole 500 mg BID; Clarithromycin is well-tolerated and safest; Clarithromycin-resistance and penicillin allergy managed by bismuth quadruple therapy. The Food and Drug Administration (FDA) has approved Pylera that contains 140 mg of bismuth subcitrate potassium+ 125 mg of tetracycline + 125 mg of metronidazole and PPI [5,12,14-19] and second-line levofloxacin 250 mg BID or 500 mg once a day + amoxicillin 1000 mg BID + PPI BID for 14 days. PPI double dose once a day + levofloxacin 250 mg once a day +doxycycline 100 mg once a day + either nitazoxanide 500 mg BID or metronidazole 500 mg BID for 7-10 days. Levofloxacin is a rescue treatment can be used if the first line has failed [16].

The disease can cause complications such as peptic ulcer disease, gastric lymphoma, and gastric cancer [5]. The case demonstrates the failure of three recommended regimens. The report included follow-up of the patient from the first to sixth visit. In all visits history, examination, investigations, advice, and medicine according to the guideline s recommended by the Canadian Association of Gastroenterology (CAG) in the 2016 was taken [14] and United States (US) Pharm in Collaboration [16] with American College of Gastroenterology [15].

Finally, important events such as testing and prescribing as per guidelines, drug adherence, education and follow-up appropriately should be done. In addition to that, the three options of the first-line therapy were failed to treat gastritis except (Pantoprazole 40 mg bid + clarithromycin 500 mg bid + amoxicillin 1gram bid + doxycycline 100 mg daily) for 14 days. The lack of facilities such as endoscopy, biopsy, UBT, and levofloxacin restricted the case management. Doxycycline can be used as a second line with PPI, Levofloxacin and metronidazole [16]. Regimens containing doxycycline are compelling in eradicating H. pylori [20].

We think the gastric pain (irritation) was due to spicy food and chilly taken as a usual habit in our food cooking. Also, the disease (typhoid fever) is widespread in Sudan and usually presents with upper abdominal pain. In addition to that gastritis due to H. pylori occurs because of food and water contamination, lack of health education and inappropriate treatment.

Conclusion(s)

The patient was treated and followed-up approximately for six months without responses and treated with an unexpected beneficial response to treatment, unlabeled or unapproved uses of medication and shows a positive personal impact. The eradication test should be performed at 4 to 8 weeks following therapy. Although failure can take place but, the guidelines should be followed in each case management. Referral to gastroenterology is the main part of management if the patient is not responding to the available regimens or in case of cancer suspicion.

References

[1]Aimasso U, D’Onofrio V, D’Eusebio C, Devecchi A, Pira C, Merlo FD, Helicobacter pylori and nutrition: A bidirectional communication Minerva Gastroenterol Dietol 2019 65(2):116-29.10.23736/S1121-421X.19.02568-630759976  [Google Scholar]  [CrossRef]  [PubMed]

[2]Fürész J, Lakatos S, Németh K, Fritz P, Simon L, Kacserka K, The prevalence and incidence of Helicobacter pylori infections among young recruits during service in the Hungarian Army Helicobacter 2004 9(1):77-80.10.1111/j.1083-4389.2004.00200.x15156907  [Google Scholar]  [CrossRef]  [PubMed]

[3]Piroozmand A, Soltani B, Razavizadeh M, Matini AH, Gilasi HR, Zavareh AN, Comparison of the serum and salivary antibodies to detect gastric Helicobacter pylori infection in Kashan (Iran) Electron Physician 2017 9(12):6129-34.10.19082/612929560169  [Google Scholar]  [CrossRef]  [PubMed]

[4]Bytzer P, Dahlerup JF, Eriksen JR, Jarbøl DE, Rosenstock S, Wildt S, Diagnosis and treatment of Helicobacter pylori infection Dan Med Bull 2011 58(4):C4271  [Google Scholar]

[5]Arslan N, Yılmaz Ö, Demiray-Gürbüz E, Importance of antimicrobial susceptibility testing for the management of eradication in Helicobacter pylori infection World J Gastroenterol 2017 23(16):2854-69.10.3748/wjg.v23.i16.285428522904  [Google Scholar]  [CrossRef]  [PubMed]

[6]Poonyam P, Chotivitayatarakorn P, Vilaichone RK, High Effective of 14-Day high-dose PPI- bismuth-containing quadruple therapy with probiotics supplement for helicobacter pylori eradication: A double blinded-randomized placebo-controlled study Asian Pac J Cancer Prev 2019 20(9):2859-64.10.31557/APJCP.2019.20.9.285931554388  [Google Scholar]  [CrossRef]  [PubMed]

[7]Helicobacter pylori: Chapter 3 Yellow Book Travelers’ Health. CDC” wwwnc.cdc.gov. 9 June 2015. Retrieved 25 April 2017  [Google Scholar]

[8]Ryan, Kenneth. Sherris Medical Microbiology. McGraw-Hill. pp. 573, 576. ISBN 978-0-07-160402-4. 2010  [Google Scholar]

[9]Chang AH, Parsonnet J, Role of bacteria in oncogenesis Clin Microbiol Rev 2010 23(4):837-57.10.1128/CMR.00012-1020930075  [Google Scholar]  [CrossRef]  [PubMed]

[10]Kusters JG, van Vliet AH, Kuipers EJ, Pathogenesis of Helicobacter pylori infection Clin Microbiol Rev 2006 19(3):449-90.10.1128/CMR.00054-0516847081  [Google Scholar]  [CrossRef]  [PubMed]

[11]Monajemzadeh M, Ashtiani MT, Ali AM, Sani MN, Shams S, Kashef N, Helicobacter pylori infection in children: Association with giardiasis Br J Biomed Sci 2010 67(2):86-87.10.1080/09674845.2010.1173029720669765  [Google Scholar]  [CrossRef]  [PubMed]

[12]Malfertheiner P, Megraud F, O’Morain CA, Gisbert JP, Kuipers EJ, Axon AT, Management of Helicobacter pylori infection-the Maastricht V/Florence Consensus Report Gut 2017 66(1):06-30.10.1136/gutjnl-2016-31228827707777  [Google Scholar]  [CrossRef]  [PubMed]

[13]Chey WD, Wong BC, American College of Gastroenterology guideline on the management of Helicobacter pylori infection Am J Gastroenterol 2007 102(8):1808-25.10.1111/j.1572-0241.2007.01393.x17608775  [Google Scholar]  [CrossRef]  [PubMed]

[14]Fallone CA, Chiba N, van Zanten SV, Fischbach L, Gisbert JP, Hunt RH, The Toronto consensus for the treatment of Helicobacter pylori infection in adults Gastroenterology 2016 151(1):51-69.e14.10.1053/j.gastro.2016.04.00627102658  [Google Scholar]  [CrossRef]  [PubMed]

[15]Chey WD, Leontiadis GI, Howden CW, Moss SF, ACG clinical guideline: Treatment of Helicobacter pylori Infection Am J Gastroenterol 2017 112(2):212-39.10.1038/ajg.2016.56328071659  [Google Scholar]  [CrossRef]  [PubMed]

[16]De Francesco V, Bellesia A, Ridola L, Manta R, Zullo A, First-line therapies for Helicobacter pylori eradication: A critical reappraisal of updated guidelines Ann Gastroenterol 2017 30(4):373-79.10.20524/aog.2017.016628655973  [Google Scholar]  [CrossRef]  [PubMed]

[17]Fashner J, Gitu AC, Diagnosis and treatment of peptic ulcer disease and H. pylori Infection Am Fam Physician 2015 91(4):236-42.  [Google Scholar]

[18]Duck WM, Sobel J, Pruckler JM, Song Q, Swerdlow D, Friedman C, Antimicrobial resistance incidence and risk factors among Helicobacter pylori-infected persons, United States Emerg Infect Dis 2004 10(6):1088-94.10.3201/eid1006.03074415207062  [Google Scholar]  [CrossRef]  [PubMed]

[19]McNulty CA, Lasseter G, Shaw I, Nichols T, D’Arcy S, Lawson AJ, Is Helicobacter pylori antibiotic resistance surveillance needed and how can it be delivered? Aliment Pharmacol Ther 2012 35(10):1221-30.10.1111/j.1365-2036.2012.05083.x22469191  [Google Scholar]  [CrossRef]  [PubMed]

[20]Niv Y, Doxycycline in eradication therapy of Helicobacter pylori-A systematic review and meta-analysis Digestion 2016 93:167-73.10.1159/00044368326849820  [Google Scholar]  [CrossRef]  [PubMed]