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. 2021 Nov 28;27(44):7661–7668. doi: 10.3748/wjg.v27.i44.7661

Treatment of Helicobacter pylori infection in the presence of penicillin allergy

Amit Kumar Dutta 1,2, Perminder Singh Phull 3
PMCID: PMC8641050  PMID: 34908805

Abstract

Therapy of Helicobacter pylori (H.pylori) requires a combination of antibiotics together with an acid suppressing agent; most treatment regimens include Amoxicillin as one of the antibiotics, which is an important constituent as resistance to it is low. However, allergies to the penicillin group of antibiotics are not uncommon, and treating H.pylori infection in such individuals can be challenging due to the restricted choice of regimens. The aim of this review is to summarise the evidence for therapeutic options in patients with H.pylori infection and penicillin allergy. A literature search was conducted in PubMed for English language publications using the key words ‘Helicobacter’ and ‘treatment’ or ‘therapy‘ and ‘penicillin’ or ‘beta-lactam’ and ‘allergy’ or ‘anaphylaxis’. Eighteen studies were identified that specifically evaluated H.pylori treatment success in penicillin allergic patients. The number of subjects in most of them was low and many were retrospective, uncontrolled, single cohort studies. The most effective option for first-line treatment appears to be Bismuth-based quadruple therapy for 10-14 d. The evidence supports second-line treatment with Levoflaxacin-based triple therapy for 10 d. Patients with persistent H.pylori infection after 2 treatment courses should be considered for testing to confirm penicillin allergy. Further treatment should be guided by the results of H.pylori culture and sensitivity testing.

Keywords: Helicobacter pylori, Infection, Treatment, Penicillin-allergy, Stomach, Duodenum

Core Tip: Penicillin allergy is a not uncommon occurrence and treating Helicobacter pylori infection in such individuals can be challenging. This review highlights the lack of high-quality studies to help guide management strategies. Recommendations have been made based on the limited data, but it would be important to monitor the success of treatment regimens and use what can be demonstrated to be effective locally.

INTRODUCTION

Infection with Helicobacter pylori (H.pylori) is prevalent worldwide with about half of world’s population estimated to be affected by this gram negative spiral bacterium[1]. The organism is causally implicated in the pathogenesis of peptic ulcer disease[2] and gastric adenocarcinoma[3]. Guidelines for the management of H.pylori infection have been published by a number of national societies and organisations[4-7].

Therapy of H.pylori requires a combination of antibiotics together with an acid suppressing agent (proton-pump inhibitor, PPI); most treatment regimens include Amoxicillin as one of the antibiotics, which is a particularly important constituent as resistance to it is low[8]. However, allergies to the penicillin group of antibiotics are reported in 5% to 15% of patients in developed countries[9] and, consequently, the treatment options in individuals allergic to penicillin are significantly restricted.

In this review we summarise the available evidence for therapeutic options in patients with H.pylori infection and penicillin allergy.

LITERATURE SEARCH

A literature search was conducted in PubMed using the key words ‘Helicobacter’ and ‘treatment’ or ‘therapy‘ and ‘penicillin’ or ‘beta-lactam’ and ‘allergy’ or ‘anaphylaxis’ for English language publications from database commencement until January 31, 2021. Of the 77 publications identified, 18 studies were included in the review (48 were excluded as not relevant, and 11 were review articles)[10-27].

EVIDENCE FOR TREATMENT OF H.PYLORI INFECTION IN THE PRESENCE OF PENICILLIN ALLERGY

Data from studies specifically targeting penicillin allergic patients (Table 1). Considering the large volume of publications on H.pylori therapy, there is relatively little data on treatment of this bacterium in penicillin allergic individuals. A summary of data available from the 18 identified studies is shown in the Table. It should be noted that the number of subjects included in most of them is quite low and many are retrospective, uncontrolled, single cohort studies. All results discussed below are presented on an intention-to-treat basis.

Table 1.

Published studies of Helicobacter pylori eradication therapy in patients allergic to penicillin

Ref.
Yr
Country
Study type
Treatment details
n
Success rate (PP, %)
Success rate (ITT, %)
Prach et al[10] 1998 United Kingdom Prospective,single cohort 1st line O 20 mg b.d., C 500 mg t.d.s, 14 ds 3 100; 100;
Gisbert et al[11] 2005 Spain Prospective, single cohort 1st line O 20 mg b.d., C 500 mg b.d., M 400 mg b.d., 7 d; 2nd line RBC 400 mg b.d., T 500 mg q.d.s., M 250 mg q.d.s., 7 d; 3rd line O 20 mg b.d., C 500 mg b.d., RIF 150 mg b.d., 10 d; 4th line O 20 mg b.d., C 500 mg b.d., LF 500 mg b.d.,10 ds 12; 17; 9; 2 64; 53; 17; 100 58; 47; 11; 100
Rodriguez-Torres et al[12] 2005 Puerto Rico Prospective, single cohort 1st line E 40 mg q.d.s., T 500 mg q.d.s., M 500 mg q.d.s.,10 d; 2nd line E 40 mg q.d.s., T 500 mg q.d.s., M 500 mg q.d.s.,10 d 17; 3 NA; NA 85; 100
Matsushima et al[13] 2006 Japan Retrospective, single cohort 1st line PPI o.d., T 500 mg b.d., M 250 mg b.d., 7-14 d 5 100 80
Gisbert et al[14] 2010 Spain Prospective, single cohort 1st line O 20 mg b.d., C 500 mg b.d., M 400 mg b.d., 7 d; 2nd line O 20 mg b.d., C 500 mg b.d., LF 500 mg b.d.,10 d 50; 15 55; 73 54; 73
Tay et al[15] 2012 Australia Prospective, single cohort 2nd line R 20 mg t.d.s., B 240 mg q.d.s., RIF 150 mg b.d., CF 500 mg b.d., 10 d 69 94.2 94.2
Liang et al[16] 2013 China Prospective, randomised 2nd line 109 pen allergic overall but results reported for whole group including non-allergic; L 30 mg b.d., B 220 mg b.d., T 500 mg t.d.s., F 100 mg t.d.s., 14 d; L 30 mg b.d., B 220 mg b.d., T 500 mg q.d.s., M 400 mg q.d.s., 14 d 108; 107 96.1; 93.1 91.7; 87.9
Furuta et al[17] 2014 Japan Retrospective, single cohort 1st line PPI b.d., SF 100 mg b.d., M 250 mg b.d., 7 d; 1st line PPI b.d., SF 100 mg b.d., M 250 mg b.d., 14 d; 2nd Line PPI b.d., SF 100 mg b.d., M 250 mg b.d., 7 d; 2nd Line PPI b.d., SF 100 mg b.d., M 250 mg b.d., 14 d; 3rd Line PPI b.d., SF 100 mg b.d., M 250 mg b.d., 7 d; 3rd Line PPI b.d., SF 100 mg b.d., M 250 mg b.d., 14 d 7; 4; 9; 3; 3; 2 100; 100; 100; 100; 100; 100 100; 100; 100; 100; 100; 100
Gisbert et al[18] 2015 Spain Prospective, single cohort 1st line O 20 mg b.d., C 500 mg b.d., M 400 mg b.d., 7 d; 2nd line O 20 mg b.d., B 120 mg q.d.s., T 500 mg q.d.s., M 500 mg t.d.s., 10 d; 3rd line O 20 mg b.d., C 500 mg b.d., LF 500 mg b.d.,10 d; 4th line O 20 mg b.d., C 500 mg b.d., RIF 150 mg b.d., 10 d; 3rd line O 20 mg b.d., C 500 mg b.d., RIF 150 mg b.d., 10 d; 4th line O 20 mg b.d., C 500 mg b.d., LF 500 mg b.d.,10 d; 2nd line O 20 mg b.d., C 500 mg b.d., LF 500 mg b.d.,10 d; 3rd line O 20 mg b.d., B 120 mg q.d.s., T 500 mg q.d.s., M 500 mg t.d.s., 10 d; 1st line O 20 mg b.d., B 120 mg q.d.s., T 500 mg q.d.s., M 500 mg t.d.s., 10 d; 2nd line O 20 mg b.d., C 500 mg b.d., LF 500 mg b.d.,10 d 112; 24; 3; 2; 7; 2; 50; 3; 50; 14 59; 38; 50; 0; 20; 100; 73; 100; 75; 64; 57; 37; 33; 50; 14; 100; 64; 100; 74; 64;
Mori et al[19] 2017 Japan Prospective, single cohort 1st line E 20 mg b.d., SF 100 mg b.d., M 250 mg b.d.,10 d; 2nd line E 20 mg b.d., SF 100 mg b.d., M 250 mg b.d.,10 d; 3rd line E 20 mg b.d., SF 100 mg b.d., M 250 mg b.d.,10 d 33; 19; 5 100; 84.2; 40 100; 84.2; 40
Ono et al[20] 2017 Japan Retrospective,single cohort 1st line PPI b.d., C 200 mg b.d., M 250 mg b.d., 7 d; 1st line V 20 mg b.d., C 200 mg b.d., M 250 mg b.d., 7 d; 1st line PPI b.d., SF 100 mg b.d., M 250 mg b.d., 7 d; 1st line V 20 mg b.d., SF 100 mg b.d., M 250 mg b.d., 7 d; 2nd line PPI b.d., C 200 mg b.d., M 250 mg b.d., 7 d; 2nd line V 20 mg b.d., C 200 mg b.d., M 250 mg b.d., 7 d; 2nd line PPI b.d., SF 100 mg b.d., M 250 mg b.d., 7 d; 2nd line V 20 mg b.d., SF 100 mg b.d., M 250 mg b.d., 7 d 10; 13; 20; 14; 3; 1; 24; 3 55.6; 92.3; 100; 100; 33.3; 100; 100; 66.7 50; 92.3; 100; 92.9; 33.3; 100; 100; 66.7
Sue et al[21] 2017 Japan Prospective& retrospective, single cohort 1st line V 20 mg b.d., C 200 or 400 mg b.d., M 250 mg b.d., 7 d; 1st line PPI b.d, C 200 or 400 mg b.d, M 750 mg b.d., 7 d 20; 30 100; 86.2 100; 83.3
Osumi et al[22] 2017 Japan Prospective, single cohort 1st line R 20 mg b.d, Mi 100 mg b.d, M 250 mg b.d., 7 d 5 100 100
Long et al[23] 2018 China Prospective, randomised 1st line E 20 mg b.d., C 500 mg b.d., M 400 mg b.d., 14 d; 1st line E 20 mg b.d., B 600 mg b.d., C 500 mg b.d., M 400 mg b.d., 14 d 33; 33 70; 96 63.6; 84.8
Song et al[24] 2019 China Prospective, single cohort 1st line E 20 mg b.d, B 220 mg b.d., LF 500 mg o.d., Cef 500 mg b.d., 14 d 152 90.1 85.5
Nyssen et al[25] 2020 Europe Retrospective,multi-centre registry 1st line PPI, C, M; 1st line PPI, C, LF; 1st line PPI, B, T, M; 2nd line PPI, C, LF; 2nd line PPI, M, LF; 2nd line PPI, B, T, M; 3rd line PPI, B, T, M; 3rd line PPI, B, C, LF; 3rd line PPI, C, LF (NB drug dose, frequency and duration not specified) 285; 54; 250; 20; 13; 70; 18; 1; 2 69; 82; 92; 73.7; 76.5; 81.8; 77.8; 100; 50 69; 80; 91; 75; 76.5; 78.3; 77.8; 100; 50
Luo et al[26] 2020 China Prospective, single cohort 1st & 2nd line E 20 mg b.d., C 500 mg b.d., M 400 mg b.d., 14 d; 1st & 2nd line E20 mg b.d., B 220 mg b.d., C 500 mg b.d., M 400 mg q.d.s., 14 d; 1st & 2nd line E 20 mg b.d., LF 500 mg o.d., M 400 mg b.d., 14 d; 1st & 2nd line E 20 mg b.d., B 220 mg b.d, LF 500 mg o.d., M 400 mg q.d.s., 14 d; 1st & 2nd line E 20 mg b.d., T 500 mg q.d.s., M 400 mg b.d., 14 d; 1st & 2nd line E 20 mg b.d., B 220 mg b.d, T 500 mg q.d.s., M 400 mg q.d.s., 14 d 5; 22; 1; 10; 2; 72 100; 94.1; 100; 100; 100; 100 100; 81.8; 100; 80; 100; 97.2
Sue et al[27] 2021 Japan Prospective, single cohort 2nd line V 20 mg b.d,, SF 100 mg b.d., M 250 mg b.d., 7 d 17 88.2 88.2
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PP: Per protocol analysis; ITT: Intention to treat analysis; B: Bismuth compound; C: Clarithromycin; Cef: Cefuroxime; CF: Ciprofloxacin; E: Esomeprazole F: Furazolidone; LF: Levofloxacin; M: Metronidazole; Mi: minocycline O: Omeprazole; PPI: proton pump inhibitor; R: Rabeprazole; RBC: ranitidine bismuth subcitrate; RIF: Rifabutin; SF: Sitafloxacin; T: Tetracycline; V: Vonoprazan.

First line therapy

Dual therapy: Prach et al[10] reported 100% treatment success with a 14 d combination of Omeprazole and Clarithromycin; however, this was only in 3 patients.

Triple therapy: The success rate with the 7 d PPI-Clarithromycin-Metronidazole regimen, has been reported as 50%-83.3% in retrospective studies[20,21] and 54-58% in prospective studies[11,14,18]. A longer 14 d regimen also resulted in a low success rate at 63.6%[23]. The European Registry on H.pylori management (Hp-EuReg) has provided the largest experience of treatment in penicillin allergic patients[25]. Although drug dose, frequency and duration details were not provided, the PPI-Clarithromycin-Metronidazole regimen achieved 69% success rate. Two studies from Japan, have shown higher success rates (92.3%-100%) for this 7 d triple therapy when combined with Vonoprazan (a potassium-competitive blocker that inhibits gastric H+K+-ATPase) instead of a PPI[20,21].

In a prospective study, Rodriguez-Torres et al reported a success rate of 85% with a 10 d triple therapy combining Esomeprazole, Tetracycline and Metronidazole[12]. A small retrospective study from Japan also reported a similar success rate of 80% when this regimen was used for 7-14 ds[13]. Osumi et al achieved a 100% success rate using a modified 7 d regimen, substituting Minocycline for Tetracycline in a small study of 5 patients[22].

Levofloxacin in combination with Clarithromycin and PPI has been reported to achieve an 80% success rate[25]. Recent studies from Japan have evaluated treatment regimens utilising the fluoroquinolone, Sitafloxacin, which has a lower minimum inhibitory concentration for H.pylori than Levofloxacin and is effective in strains with the gyrA mutation, which denotes resistance to Levofloxacin[19]. Remarkably high success rates of 100% were reported for 7-14 d treatment regimens combining Sitafloxacin with Metronidazole and PPI, in two retrospective[17,20] and one prospective study[19].

Quadruple therapy: Retrospective data has demonstrated a 91% success rate for the PPI-Bismuth-Tetracycline-Metronidazole quadruple therapy[25]. Three prospective studies have reported success rates of 74% with a 10 d PPI-Bismuth-Tetracycline-Metronidazole combination[18], 84.8% with a 14 d PPI-Bismuth-Clarithromycin-Metronidazole regimen[23] and 85.5% with a 14 d PPI-Bismuth-Levofloxacin-Cefuroxime treatment[24].

Second line therapy

In view of the attrition of successfully treated patients with each course of treatment, patient numbers for studies evaluating second line therapies tend to be low, often in single digits[12,17,20].

Triple therapy: Gisbert et al[14,18] have treated a relatively large number of patients with a 10 d combination of PPI-Clarithromycin-Levofloxacin, demonstrating success rates of 64%-73%. Levofloxacin based triple therapy using Clarithromycin or Metronidazole appears to achieve similar success rates, of 75% and 76.5%, respectively[25]. Sitafloxacin-based triple therapy has shown success rates of 100% in 2 small retrospective studies evaluating a 7 d regimen[17,20], whilst a prospective study investigating a 10 d treatment course reported a lower success rate of 84.2%[19]. Sue et al[27] demonstrated a success rate of 88.2% in a prospective study of a 7 d Sitafloxacin regimen using Vonoprazan instead of a PPI.

Quadruple therapy: An early study from Spain reported a low success rate of 47% using a 7 d regimen of Ranitidine Bismuth citrate-Tetracycline-Metronidazole, which has been considered as quadruple therapy due to an acid-suppressing agent and bismuth being combined into one tablet[11]. The same group of investigators also reported a low success rate of 37% for 10 d PPI-Bismuth-Tetracycline-Metronidazole quadruple therapy[18]. However, the European Registry has demonstrated a success rate of 78.3% for this regimen[25]. In a large prospective study, Liang et al[16] included 109 penicillin allergic patients randomised to 2 wk quadruple therapy with either PPI-Bismuth-Tetracycline-Metronidazole or PPI-Bismuth-Tetracycline-Furazolidine; success rates were 87.9% and 91.7%, with no difference between penicillin allergic and non-allergic patients[16].

A relatively large study from Australia reported on 69 patients with penicillin allergy, who had all failed prior therapy with PPI-Clarithromycin-Metronidazole. Treatment with a 10 d regimen of PPI-Bismuth subcitrate-Rifabutin-Ciprofloxacin achieved a success rate of 94.2%[15].

Luo et al[26] prospectively evaluated an antibiotic susceptibility approach using a variety of 14 d quadruple therapies, and demonstrated high success rates of 80%-100%. However, the results were not presented separately for first-line and rescue treatments[26].

Salvage (third-line) therapy

The published data for salvage therapy after failure of second-line treatment is very limited with 4 studies reporting on patient numbers in single figures[11,17-19]. Details are provided in the Table but it is difficult to draw any meaningful conclusions from the results.

Evidence from non-penicillin combination regimes in unselected groups of patients: Meta-analyses of trials on the efficacy of non-penicillin regimes in treating H.pylori infection are an alternate source of useful information when making treatment decisions about penicillin allergic individuals. These trials generally included unselected group of individuals without considering penicillin allergy status.

The meta-analysis by Gisbert et al[28] demonstrated a success rate of 81% with 7 d triple therapy regimen of PPI-Clarithromycin -Nitroimidazole, similar to the success rate with the regimen containing amoxicillin instead of nitroimidazole.

Two meta-analyses of randomised controlled trials on first line therapy of H.pylori with quadruple therapy of PPI-Bismuth-Tetracycline-Metronidazole have shown success rates of 77%[29,30]. A longer duration (10-14 d) of quadruple therapy was more effective than the 7 d triple therapy of PPI-Clarithromycin-Amoxicillin[30].

SUMMARY AND RECOMMENDATIONS

The triple therapy regimen of PPI-Clarithromycin-Metronidazole is still frequently used as first line therapy for penicillin allergic subjects[25]. However, whilst it demonstrates an acceptable success rate of approximately 80% in unselected patients[28], it does not perform well in penicillin allergic patients[11,14,18,20,21,23,25]. The reasons for this discrepancy are unclear, but it is possible is that the studies of unselected patients may only have had small numbers of penicillin allergic individuals, or the study design may have excluded individuals with antibiotic allergy. Whilst there is a paucity of recent data for this specific regimen, the efficacy of Clarithromycin-based triple therapy has been shown to be significantly impaired in the presence of Clarithromycin resistance, which is an increasingly encountered issue[29]. Whilst increasing the duration of PPI-Amoxicillin-Clarithromycin triple therapy has been shown to improve success rates, this has not been demonstrated convincingly for the PPI-Clarithromycin-Metronidazole regimen[31]. If available, Vonoprazan could be considered as a substitute for PPI in clarithromycin-based triple therapy to improve its efficacy[20,21]. Sitafloxacin-based triple therapy is an alternative option, although this antibiotic is not widely available[17,19,20]. Bismuth-based quadruple therapy, lasting 10-14 d, is the most attractive option for first-line treatment of H.pylori, with a high success rate in patients with penicillin allergy[18,23,24,25], matching that in unselected patients[29,30]. In order to optimise the success of first line treatment, a detailed history of prior antibiotic use could aid the choice of regimen prescribed.

In the event of treatment failure, the published evidence suggests that second-line therapy should be instituted with the 10 d PPI-Levofloxacin-Clarithromycin regimen[14,18]; a Sitafloxacin-based triple therapy is an alternative option[17,19,20,27] . If Bismuth-based quadruple therapy has not been used as first-line treatment, then this regime could be considered for subsequent treatment, although there is variable evidence for the efficacy of PPI-Bismuth-Tetracycline-Metronidazole quadruple therapy[16,18,25]. Alternative antibiotic combinations may be more successful such as PPI-Bismuth-Tetracycline-Furazolidine[16] or PPI-Bismuth-Rifabutin-Ciprofloxacin[15], although there are concerns about the potential for side-effects with rifabutin, especially myelotoxicity[32].

It is not possible to provide any evidence-based recommendations for salvage therapy after failure of two treatment courses. It is generally recommended that in this situation, further treatment should be guided by the results of H.pylori culture and sensitivity testing[5,6,26]. Another approach is to confirm penicillin allergy at this stage, as many patients with this label turn out not to be truly allergic[5,6,9]. A negative penicillin skin test allows the safe use of amoxicillin-containing salvage regimens, as recommended for non-allergic patients.

CONCLUSION

This review of the evidence for treating H.pylori in penicillin-allergic individuals has highlighted the lack of high-quality studies to help guide management strategies. Whilst recommendations have been made based on the limited data, it would be important to monitor the success of treatment regimens and use what can be demonstrated to be effective locally[33]. Regional differences in drug availability will influence the choice of regimen, and patterns of antibiotic resistance rates will influence treatment success.

Footnotes

Conflict-of-interest statement: The authors have no conflicts of interest to declare

Provenance and peer review: Invited article; Externally peer reviewed.

Corresponding Author's Membership in Professional Societies: British Society of Gastroenterology, BSG63939; American Gastroenterological Association, 982600.

Peer-review started: April 12, 2021

First decision: June 3, 2021

Article in press: November 10, 2021

Specialty type: Gastroenterology and hepatology

Country/Territory of origin: United Kingdom

Peer-review report’s scientific quality classification

Grade A (Excellent): 0

Grade B (Very good): B

Grade C (Good): C, C

Grade D (Fair): 0

Grade E (Poor): 0

P-Reviewer: Cheng H, El-Bendary M, Ma H S-Editor: Wang LL L-Editor: A P-Editor: Wang LL

Contributor Information

Amit Kumar Dutta, Department of Gastroenterology, Christian Medical College, Vellore 632004, India; Department of Digestive Disorders, Aberdeen Royal Infirmary, Aberdeen AB25 2ZN, United Kingdom.

Perminder Singh Phull, Department of Digestive Disorders, Aberdeen Royal Infirmary, Aberdeen AB25 2ZN, United Kingdom. perminder.phull@nhs.scot.

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