InTechOpen uses cookies to offer you the best online experience. By continuing to use our site, you agree to our Privacy Policy.

Medicine » Urology and Nephrology » "Hemodialysis", book edited by Hiromichi Suzuki, ISBN 978-953-51-0988-4, Published: February 27, 2013 under CC BY 3.0 license. © The Author(s).

Chapter 12

Helicobacterpylori Infection for Hemodialysis Patients

By Yoshiaki Kawaguchi and Tetsuya Mine
DOI: 10.5772/52270

Article top

Helicobacterpylori Infection for Hemodialysis Patients

Yoshiaki Kawaguchi1 and Tetsuya Mine1

1. Introduction

Helicobacter pylori (HP) infection is reported to be closely associated with upper gastrointestinal disorders, such as gastroduodenal ulcers, chronic gastritis, and gastric cancer. Furthermore, patients with chronic renal failure receiving hemodialysis often complain of digestive symptoms. There are many possible factors causing these symptoms, including reduced gastrointestinal motility attributable to diabetes mellitus, uremia, intestinal ischemia associated with circulatory failure, and adverse reactions to many oral medications including non-steroidal anti-inflammatory drugs. Although HP infection is amongthe factors that may cause upper gastrointestinal disorders in patients with chronic renal failure, the association withHP infection has not as yet been elucidated. According to recent reports, the prevalence of HP infection is significantly lower in patients with chronic renal failure than in controls with normal renal function, and the prevalence is even reported to decrease with longer duration of hemodialysis. However, there are also previous reports presenting contrary findings. This chapter describes HP infection and eradication therapy in hemodialysis patients.

2. Is the prevalence of HP infection low in hemodialysis patients?

It is often reported that the prevalence of HP infection tends to be lower in patients with chronic renal failure receiving hemodialysis than in control groups with normal renal function [1-19]. In a study conducted in 539 hemodialysis patients, the prevalence of HP infection was 48.6%, whereas health check-up examinees with normal renal function showed a significantly higher prevalence of 69.4% (P < 0.001) [15]. Another report also showed that, compared to a 27.5% prevalence of HP infection in hemodialysis patients, the prevalence in patients with chronic renal failure not receiving hemodialysis was significantly higher at 56.0% [4]. Although there is a report showing the prevalence of HP infection to also be low in patients undergoing renal transplantation, it seems that most had received hemodialysis before transplantation [3]. Based on the above observations, the prevalence of HP infection would appear to be low in hemodialysis patients, suggesting that the hemodialysis procedure itself may be involved in the low prevalence of HP infection.

3. Are duration of hemodialysis and prevalence of HP infection inversely correlated?

How are duration of hemodialysis and prevalence of HP infection associated? There are reports that the prevalence of HP infection tends to be lower with longer duration of hemodialysis [9, 15, 20, 21]. Nakajima et al. report that the prevalence of HP infection gradually decreases with a 2-year or longer duration of hemodialysis, and Sugimoto et al reported that the prevalence gradually decreases within 4 years of hemodialysis [15]. Moriyama et al. report that such a tendency is revealed in patients receiving hemodialysis for 8 years or longer [20]. There is also a report that the prevalence of HP infection in health check-up examinees with normal renal function was similar to that in patients with chronic renal failure who had received hemodialysis for less than 1 year [15]. Meanwhile, other studies have shown that there is no such association [22, 23]. However, Sugimoto et al. conducted a 4-year follow-up study in hemodialysis patients with HP infection and found that the prevalence gradually decreased from 51.6% at the start to 38.3% at the end [15]. Given that the spontaneous elimination rate of HP infection is generally reported to be 0.6% annually [24], it must be assumed from these results that the hemodialysis procedure itself contributes to the observed decrease in the prevalence of HP infection.

4. Is there variation in HP infection rates among different countries?

The gastricmucosa of approximately 50% of the world’s populationis infected with HP, and the infectionlevels exceed 70% in some developing areas [25, 26].

There is variation in HP infection ratesamong different countries. It may, therefore, be important to evaluate the infection rate in various countries. In East Asian countries, the prevalence of HPinfection in patients receiving chronic hemodialysis is44.5% (95% confidence interval (CI): 41.5–47.6%], 474/1065), which is significantly lower than in all patients with nor malrenal function [54.0% [95% CI: 50.9–57.1%], 560/1038,P <0.001] [27]. On the other hand, because the prevalenceof HPin other areas, such as Europe, Middle East, and South Asia has a wide variation, it isdifficult to evaluate the prevalence of HPinfectionin those areas.

5. Why does the hemodialysis procedure reduce the prevalence of HP infection?

One reason is eradication of HPby antibiotics that are administeredas therapy for other infections experienced by hemodialysis patients. Antibiotics are the most typically prescribed drugs in general. In hemodialysis patients, antibiotics may be used for the treatment of bacterial infections as often as or even more frequently than in the general population. It is assumed that patients with renal failure are often prescribed reduced doses of antibiotics. However, compared to the general population with normal renal function, blood levels of antibiotics are likely to be higher after administration in patients with renal failure, and the elimination time is expected to be longer. Thus, in hemodialysis patients with a long duration of renal failure, the spontaneous elimination rate of HP infection might be increased by repeated administration of antibiotics. Because blood urea levels are increased in hemodialysis patients, urea levels in gastric juice are also high. The increased urea levels are considered to suppress the growth of HP in the stomach [28]. Another possible explanation is that up-regulation of pro-inflammatory cytokines in hemodialysis patients triggers the infiltration of inflammatory cells activated by the gastric mucosa, resulting in progression of gastric mucosal atrophy, an increase in pH, and ultimately HP elimination [29, 30]. While there are as yet no data clearly supporting this explanation, the prevalence of HP infection may be decreased by a combination of various factors.

6. What are the harmful effects of a decreased prevalence of HP infection on hemodialysis patients?

In general, HP infection is considered to be a cause of gastroduodenal ulcers, and a decrease in the prevalence of HP infection is favorable in this regard. It is widely known that HP eradication suppresses gastric acid secretion, which causes gastric erosion [31]. The frequency of endoscopically detected gastric erosion is reported to be high in hemodialysis patients [20, 32, 33], which may be associated with a decrease in HP infection. Because gastric erosion may cause gastrointestinal bleeding, caution is required especially in hemodialysis patients [20]. They are often receiving anticoagulant or antiplatelet drugs, and gastrointestinal bleeding can thus be fatal.

Prophylactic administration of anti-acid secretory drugs, such as proton pump inhibitors (PPI), is recommended. While long-term hemodialysis is reported to carry a high risk for reflux esophagitis [32-34], this may also be attributable to suppressedgastric acid secretion due to a decrease in HP infection. In patients receiving long-term hemodialysis, administration of anti-acid secretory drugs is recommended to prevent reflux esophagitis.

7. Is HP eradication necessary for hemodialysis patients?

While the previous section described the harmful effects of a reduced prevalence of HP infection on hemodialysis patients, the harmful effects of HP infection include the aforementioned association with gastroduodenal ulcers, chronic gastritis and gastric cancer, as well as gastric mucosa associated-lymphoid tissue lymphoma, etc. Especially in hemodialysis patients, the frequency of gastroduodenal ulcers and gastric cancer is reported to be higher than in healthy people [3, 35]. Because hemodialysis patients are often receiving anticoagulant or antiplatelet drugs, bleeding from gastroduodenal ulcers may be fatal. Thus, HP eradication is considered to be an important treatment for hemodialysis patients in order to prevent gastroduodenal ulcers and gastric cancer. Although spontaneous elimination of HP infection can be expected in hemodialysis patients, the earliest possible HP eradication is recommended especially in those with a history of gastroduodenal ulcer and confirmed current HP infection.

8. How is HP eradication best achieved in hemodialysis patients?

According to recent reports, the major regimen is a combination of a PPI selected from among omeprazole, lansoprazole, and esomeprazole and 2 antibiotics selected from among clarithromycin, amoxicillin, and metronidazole, which are administered for 1 or 2 weeks [1, 6, 36-40]. Although the eradication rate fluctuates slightly from 72.7 to 96.0%, it averages around 90%. There seems to be no substantial difference in comparison with the eradication rate of HP infection in the general population. The factors contributing to eradication failure include a history of previous eradication therapy, suggesting that the presence or absence of resistant strains to antibiotics iskey to the success of eradication therapy [6].

9. What are the precautions for HP eradication therapy in hemodialysis patients?

Caution should be considered in performing eradication therapy for hemodialysis patients to avoidexcessive doses of drugs. Administration of low doses results in high blood levels. However, hemodialysis removes both PPI and antibiotics, lowering their blood levels. In consideration of this fact, without adjustment of the therapy by administering the drugs after the hemodialysis session on the day of hemodialysis, the eradication rate of HP infection may be decreased. Safe and effective optimal dosages and administration procedures should be established. In patients with chronic renal failure before the initiation of hemodialysis, attention should be paid to the nephrotoxicity of amoxicillin, and the eradication therapy needs to be adjusted by substituting amoxicillin with metronidazole [39, 41, 42].

Moreover, hemodialysis patients often receive oral antibiotics, and the duration of circulation of these antibiotics in the body is prolonged due to delayed metabolism. Thus, it seems that HP often acquires resistance to antibiotics. According to a report on resistance to clarithromycin, resistant HP strains were detected in 36.4% of patients with renal failure and 15.2% of healthy volunteers, showing the prevalence of resistant HP strains to be significantly lower in the latter [43].

10. Conclusion

This chapter has described HP infection in hemodialysis patients. Because the prevalence of HP infection is lower in these patients than in healthy people, attention should be paid to symptoms due to gastric hyperacidity. For those with HP infection, eradication therapy is recommended in order to prevent gastrointestinal ulcers and gastric cancer. Even after HP eradication, prophylaxis against gastric erosion and reflux esophagitis should be performed with anti-acid secretory drugs.


1 - Sezer S, Ibis A, Ozdemir BH et al. Association of Helicobacterpylori infection with nutritional status in hemodialysispatients. Transplant Proc 2004;36:47–9.
2 - Sotoudehmanesh R, Ali Asgari A, Ansari R, Nouraie M.Endoscopic findings in end-stage renal disease. Endoscopy2003;35:502–5.
3 - Khedmat H, Ahmadzad-Asl M, Amini M et al. Gastroduodenallesions and Helicobacter pylori infection in uremicpatients and renal transplant recipients. Transplant Proc2007;39:1003–7.
4 - Nakajima F, Sakaguchi M, Amemoto K et al. Helicobacterpylori in patients receiving long-term dialysis. Am J Nephrol2002;22:468–72.
5 - Fabbian F, Catalano C, Bordin V, Balbi T, Di Landro D.Esophagogastroduodenoscopy in chronic hemodialysispatients: 2-year clinical experience in a renal unit. ClinNephrol2002;58:54–9.
6 - Tsukada K, Miyazaki T, Katoh H et al. Seven-day tripletherapy with omeprazole, amoxycillin and clarithromycin forHelicobacter pylori infection in haemodialysis patients. ScandJ Gastroenterol2002;37:1265–8.
7 - Marsenic O, Peco-Antic A, Perisic V, Virijevic V, Kruscic D,Kostic M. Upper gastrointestinal lesions in children on chronichaemodialysis. Nephrol Dial Transplant 2003;18:2687–8.
8 - Lopez T, Quesada M, Almirall J, Sanfeliu I, Segura F, CalvetX. Usefulness of non-invasive tests for diagnosing Helicobacterpylori infection in patients undergoing dialysis forchronic renal failure. Helicobacter 2004;9:674–80.
9 - Nakajima F, Sakaguchi M, Oka H et al. Prevalence of Helicobacterpylori antibodies in long-term dialysis patients. Nephrology2004;9:73–6.
10 - Al-Mueilo SH. Gastroduodenal lesions and Helicobacterpylori infection in hemodialysis patients. Saudi Med J 2004;25:1010–14.
11 - Trimarchi H, Forrester M, Schropp J, Pereyra H, Freixas EA.Low initial vitamin B12 levels in Helicobacter pylori—positivepatients on chronic hemodialysis. Nephron ClinPract2004;96:c28–32.
12 - Blusiewicz K, Rydzewska G, Rydzewski A. Gastric juiceammonia and urea concentrations and their relation to gastricmucosa injury in patients maintained on chronic hemodialysis.RoczAkad Med Bialymst2005;50:188–92.
13 - Lentine KL, Parsonnet J, Taylor I,Wrone EM, Lafayette RA.Associations of serologic markers of infection and inflammationwith vascular disease events and mortality in Americandialysis patients. Clin ExpNephrol2006;10:55–62.
14 - Gioe FP, Cudia B, Romano G et al. Role and clinical importanceof Helicobacter pylori infection in hemodialysis patients.G Chir2008;29:81–4.
15 - Sugimoto M, Sakai K, Kita M, Imanishi J, Yamaoka Y. Prevalenceof Helicobacter pylori infection in long-term hemodialysispatients. Kidney Int2009;75:96–103.
16 - LuiSL,Wong WM, Ng SY, Chan TM, Lai KN, Lo WK. Seroprevalenceof Helicobacter pylori in Chinese patients on continuousambulatory peritoneal dialysis. Nephrology 2005;10:21–4.
17 - Altay M,Turgut F, Akay H et al. Dyspepsia inTurkish patientson continuous ambulatory peritoneal dialysis. IntUrolNephrol2008;40:211–17.
18 - Schoonjans R, Van VB, Vandamme W et al. Dyspepsia andgastroparesis in chronic renal failure: the role of Helicobacterpylori. ClinNephrol2002;57:201–7.
19 - Strid H, Simren M, StotzerPO, Abrahamsson H, BjornssonES. Delay in gastric emptying in patients with chronic renalfailure. Scand J Gastroenterol2004;39:516–20.
20 - Moriyama T, Matsumoto T, Hirakawa K, et al. Helicobacter pylori status and esophagogastroduodenal mucosallesions in patients with end-stage renal failure on maintenancehemodialysis. J Gastroenterol2010;45:515–522.
21 - Munoz de Bustillo E, Sanchez Tomero JA, Sanz JC, Moreno JA,Jimenez I, Lopez-Brea M, et al. Eradication and follow-up ofHelicobacter pylori infection in hemodialysis patients. Nephron.1998;79:55–60.
22 - O° zgur O, Boyacioglu S, Ozdogan M, Gur G, Telatar H, HaberalM. Helicobacter pylori infection in haemodialysis patients andreal transplant recipients. Nephrol Dial Transplant. 1997;12:289–91.
23 - Huang JJ, Huang CJ, Ruaan MK, Chen KW, Yen TS, Sheu BS.Diagnostic efficacy of (13) C-urea breath test for Helicobacterpylori infection in hemodialysis patients. Am J Kidney Dis.2000;36:124–9.
24 - Valle J, Kekki M, Sipponen P, Ihamaki T, Siurala M. Long-termcourse and consequence of Helicobacter pylori gastritis. Resultsof a 32-year follow-up study. Scand J Gastroenterol. 1996;31:546–50.
25 - Rocha GA, Queiroz DM, Mendes EN et al. Indirect immunofluorescencedetermination of the frequency of anti-H. pyloriantibodies in Brazilian blood donors. Braz J Med BiolRes1992;25:683–9.
26 - Perez-Perez GI, Taylor DN, Bodhidatta L et al. Seroprevalenceof Helicobacter pylori infections in Thailand. J Infect Dis1990; 161:1237–41.
27 - Sugimoto M, Yamaoka Y. Review of Helicobacter pylori infection and chronicalfailure. Therapeutic Apheresis and Dialysis 2011; 15:1–9.
28 - Gladziwa U, Haase G, Handt S et al. Prevalence of Helicobacterpylori in patients with chronic renal failure. NephrolDial Transplant 1993; 8:301–6.
29 - Hwang IR, Kodama T, Kikuchi S et al. Effect of interleukin 1polymorphisms on gastric mucosal interleukin 1beta productionin Helicobacter pylori infection. Gastroenterology 2002;123:1793–803.
30 - Wesdorp RI, Falcao HA, Banks PB, Martino J, Fischer JE.Gastrin and gastric acid secretion in renal failure. Am J Surg1981;141:334–8.
31 - Miyake K, Tsukui T, Futagami S, Tatsuguchi A, Shinoki A,Hiratsuka T, et al. Effect of acid suppression therapy on developmentof gastric erosions after cure of Helicobacter pyloriinfection. Aliment PhamacolTher. 2002;16[Suppl 2]:210–6.
32 - Kawaguchi Y, Mine T, Kawana I, et al. Gastroesophageal Reflux Disease in Hemodialysis Patients. Tokai J ExpClin Med. 2009; 34: 48-52.
33 - Kawaguchi Y, Mine T, Kawana I, et al. Gastroesophageal Reflux Disease in Chronic Renal Failure Patients: evaluation by endoscopic examination. Tokai J ExpClin Med. 2009; 34: 80-83.
34 - Doherty CC. Gastrointestinal bleeding in dialysis patients.Nephron. 1993;63:132–6.
35 - Ota K,Yamashita N, Suzuki T, AgishiT.Malignanttumours indialysis patients: a nationwidesurvey. Proc Eur Dial TransplantAssoc1981;18:724–30.
36 - Itatsu T, Miwa H, Nagahara A et al. Eradication of Helicobacterpylori in hemodialysis patients. Ren Fail 2007;29:97–102.
37 - Mak SK, Loo CK,Wong AM et al. Efficacy of a 1-week courseof proton-pump inhibitor-based triple therapy for eradicatingHelicobacter pylori in patients with and without chronic renalfailure. Am J Kidney Dis 2002;40:576–81.
38 - Mak SK, Loo CK, Wong PN et al. A retrospective study onefficacy of proton-pump inhibitor-based triple therapy foreradication of Helicobacter pylori in patients with chronicrenal failure. Singapore Med J 2003;44:74–8.
39 - Sheu BS, Huang JJ,YangHB,HuangAH,WuJJ.The selectionof triple therapy for Helicobacter pylori eradication in chronicrenal insufficiency. Aliment PharmacolTher2003;17:1283–90.
40 - Tseng GY,LinHJ,Fang CT et al. Recurrence of peptic ulcer inuraemic and non-uraemic patients after Helicobacter pylorieradication: a 2-year study. Aliment PharmacolTher2007;26:925–33.
41 - Arancibia A, Drouguett MT, Fuentes G et al. Pharmacokineticsof amoxicillin in subjects with normal and impaired renalfunction. Int J ClinPharmacolTherToxicol1982;20:447–53.
42 - Jones DP, Gaber L, Nilsson GR, Brewer ED, Stapleton FB.Acute renal failure following amoxicillin overdose. ClinPediatr1993;32:735–9.
43 - Aydemir S, Boyacioglu S, Gur G et al. Helicobacter pyloriinfection in hemodialysis patients: susceptibility to amoxicillinand clarithromycin. World J Gastroenterol2005;11:842–5.