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Are proton pump inhibitors the first choice for acute treatment of gastric ulcers? A meta analysis of randomized clinical trials
BMC Gastroenterologyvolume 2, Article number: 17 (2002)
Gastric ulcers are a frequent problem in the United States. Proton pump inhibitors have been shown to increase healing rates and improve clinical symptoms. The objective of this study is to compare gastric ulcer healing rates for patients treated with a proton pump inhibitor (PPI) (omeprazole, rabeprazole, pantoprazole, or lansoprazole), an histamine 2- receptor antagonist (ranitidine) or placebo.
A literature search was conducted to identify randomized, controlled clinical trials that included a PPI in at least one treatment arm and assessed the gastric ulcer healing rates endoscopically. The healing rates were estimated for each treatment at specific time points, and Rate Ratios (RR) and 95% confidence intervals (CI) were estimated for each trial.
Sixteen trials met the inclusion criteria: four compared a PPI versus placebo, nine compared a PPI versus ranitidine (no trials of rabeprazole versus ranitidine met the inclusion criteria), and three compared a newer PPI (lansoprazole, pantoprazole or rabeprazole) versus omeprazole. In relation to ranitidine, the pooled RR of PPIs (lansoprazole, omeprazole and pantoprazole) was 1.33 (95% CI 1.24 to 1.42) at four weeks. In each trial, greater improvement in the studied clinical symptoms was found with the newer PPIs (rabeprazole, pantoprazole and lansoprazole) when compared to omeprazole.
In this study treatment with PPIs resulted in higher healing rates than ranitidine or placebo. This evidence suggests that the first choice for gastric ulcer treatment for the greater relief of symptoms is one of the newer PPIs.
In the United States about four million people have active peptic ulcers and about 350,000 new cases are diagnosed each year, and approximately 3000 deaths per year in the U.S. are due to gastric ulcer . The primary therapeutic approach to gastric ulcer remains the inhibition of gastric acid secretion to produce symptom relief, acceleration of crater healing and the prevention of relapse or recurrence [2, 3], since gastric ulcer can lead to hemorrhage, perforation, obstruction and death [4, 5].
It is established that the H+, K+-ATPase, or proton pump, participates in the final step of acid secretion [6, 7] and all the peripheral parietal cell stimuli converge to activate it . Therefore, blocking the final process in hydrogen ion secretion reduces acid secretion and this is the mechanism of action of the substituted benzimidazole agents known as proton pump inhibitors (PPI). Currently, five PPIs are marketed: rabeprazole, omeprazole, esomeprazole, lansoprazole and pantoprazole, each with a different pharmacokinetic profile, tissue selectivity, binding specificity and potential to interact with the cytochrome P450 enzyme system [8–10]. For example, rabeprazole and esomeprazole achieve more rapid and profound inhibition of acid secretion than do older agents . It is unclear, however, if these pharmacologic differences lead to distinctions in the clinical efficacy of healing gastric ulcers and controlling ulcer symptoms. To address this question we undertook a meta-analysis of all randomized clinical trials that compared at least one of the newer PPI with either ranitidine or placebo.
To identify studies for inclusion in this meta-analysis, two researchers independently conducted searches of MEDLINE®, Cochrane Library documents. The keywords used for these searches were: proton pump inhibitors, PPI, rabeprazole, omeprazole, esomeprazole, lansoprazole, pantoprazole, ranitidine; healing rates, gastric ulcer, stomach ulcer, gastric ulcer disease, peptic ulcer, peptic related disorders; and clinical trials, randomized clinical trials and multicenter studies. Hand searching of medical journals was carried out as well as review of reference lists of other meta-analyses, monographs, pharmacoeconomic studies and reviews.
The search included papers published between January 1990 to July 2001, with no language limitations.
The two researchers independently reviewed the papers and selected all those described as randomized controlled clinical trials, double blind, short-term treatment (less than six months) in patients with endoscopically confirmed diagnosis of gastric ulcer that also included at least one group treated with a PPI. If a paper did not report healing rates, but reported improvement in clinical symptoms, this could be included for the analyses of symptoms.
The decision regarding whether to include a paper was not related to trial results. Papers related to chemical properties of PPI, pharmacokinetic, pharmacodynamic, acidity studies, concomitant duodenal ulcers or gastric ulcers complicated with hemorrhage or perforation, PPI combined with antibiotics or with treatment of Helicobacter pylori were excluded. Papers or abstracts with insufficient data, preliminary results, duplicate reports of the same trials or with more complete reporting in another paper were also excluded. The two researchers reviewed the studies independently and any differences in the data retrieved from the papers were resolved by consensus. The information entered into a database included: study design, population characteristics, diagnosis, severity, PPI and comparator treatment regimens, healing rates and clinical symptoms as well as alcohol consumption, smoking and caffeine use.
Ulcer diagnosis and healing had to be assessed by endoscopy; we accepted the primary study authors' definition for gastric ulcer diagnosis and healing.
Results were retrieved for both intention to treat and per protocol analysis, if the paper provided such data. If the authors reported per protocol results only and mentioned the initial number of subjects in the study, we estimated the healing rates for the intention to treat analysis.
The healing rate ratio (RR) was calculated for each trial by dividing the healing rate of the PPI by the rate with the comparator at the specified time point. Chi-squares and 95% confidence intervals (CI) were calculated using the exact method described by Miettinen .
The appropriateness of combining results from individual studies was examined using the Wald χ2 for statistical homogeneity. We considered a p value less than 0.05 to be significant for all statistical tests. There were no adjustments for multiple comparisons.
As there was no statistically significant evidence of heterogeneity, the healing rates for each treatment were pooled across trials by time point. Overall healing rates of PPIs at four and eight weeks were estimated by pooling the rates for the recommended daily doses: 30 mg/d for lansoprazole, 20 mg/d for omeprazole, 40 mg/d for pantoprazole. Rabeprazole was pooled using dose of 20 mg/d at three and six weeks. Individual trial results were weighted using the inverse of the variance of the RR estimated for each trial. The overall RR was then estimated by dividing the weighted average healing rates for each treatment with the estimates for placebo, ranitidine or omeprazole. These overall RR were assessed using the Mantel-Haenszel χ2 test and 95% CI were calculated using the exact method .
To assess the possibility of publication bias, the RR point estimates were plotted against year of publication and sample size. To identify any studies that exerted a disproportionate influence on the summary treatment effect, we deleted individual studies one at a time. To investigate the possible consequences of including abstracts for which we could not obtain full reports, we excluded these data in secondary analyses.
There were more than one thousand papers on PPI, of which 153 focused on PPI use for the treatment of gastric ulcers. Sixteen trials met all the criteria for inclusion (Table 1) [12–27]. Four trials compared a PPI versus placebo nine compared PPI versus ranitidine (no trials of rabeprazole versus ranitidine met the inclusion criteria), and three compared a newer PPI (lansoprazole, pantoprazole or rabeprazole) versus omeprazole. Omeprazole was studied most often (6), followed by lansoprazole (4), rabeprazole (3) and pantoprazole (3). No study on esomeprazole for the treatment of gastric ulcer met the inclusion criteria.
The criteria for diagnosis of gastric ulcer varied: 57% of the studies required the ulcer size to be 5 to 20 mm and 43% required 3 to 25 mm. The majority (95%) defined healing as the complete re-epithelialization of ulcer crater. The other researchers defined healing, as the endoscopic disappearance of ulcer crater with no visible mucosa breaks. Efficacy results were reported at various time points, ranging from 2 to 8 weeks.
The mean age of the patients in these trials was 56 ± 1.5 years. Approximately half the patients smoked but few studies analyzed the healing rates by smoking status. About half the studies reported on alcohol consumption, and 46% of patients reported alcohol consumption at the baseline visit. Caffeine use was infrequently reported.
It was not possible to pool these results because different symptoms were reported in each study, at different time points, and also the method used to collect data varied (Table 2). However, individual trials showed more improvement or resolution of pain, day pain and night pain was found with the new PPIs rabeprazole, pantoprazole and lansoprazole compared to omeprazole. For example, 82% of patients with pain improved with rabeprazole compared to 65% with omeprazole at 6 weeks  (Table 2).
Healing data are presented for the intention-to-treat analyses as similar results were obtained with the per protocol analysis. For lansoprazole, pantoprazole and omeprazole the results were reported at four and eight weeks and the rabeprazole studies did so at three and six weeks. Therefore, the overall healing rate was obtained at three, four, six and eight weeks.
Healing rates varied between the studies, but were consistently lower with placebo treatment. For the majority of patients receiving placebo treatment the ulcer did not heal during the course of the trial and the maximum recorded as healed was just over a third of the patients (39%) in any of the trials. Whilst higher healing rates were observed after treatment with ranitidine by the end of the trials the ulcers remained for at least half the patients (52%). In contrast, by the end of the trial the ulcers were healed in at least two-thirds of the patients receiving proton pump inhibitors (67%).
As would be expected, when compared with placebo treatment, the PPIs (lansoprazole and omeprazole) improved the pooled healing RR at each time point. In relation to ranitidine, the pooled healing RR of PPIs (lansoprazole, omeprazole and pantoprazole) was also increased at both four and eight weeks. There were no studies versus rabeprazole. The healing RR in each trial of the newer PPIs was found to be comparable or better than omeprazole at each time point (Figure 1).
The healing RR was plotted against sample size but there was no trend with increasing size: small studies had healing RR similar to large studies with the same comparator (Figure 2). There was one abstract  with data obtained at 3 and 6 weeks, which is not included.
In the absence of active treatment, the majority of patients continued to have a gastric ulcer at the end of the trial. A much higher healing rate was observed when patients received treatment with a PPI when compared to either a placebo or ranitidine. This is consistent with the results obtained for treatment with PPIs when compared to ranitidine for both duodenal ulcers and gastro esophageal reflux disease [2, 28]. We also found that, there is some evidence of an advantage to prescribing two of the newer PPIs (lansoprazole or pantoprazole) compared to omeprazole for gastric ulcer, since there was a 15% increase in healing rates at 4 weeks. In addition, the newer PPIs (rabeprazole, lansoprazole and pantoprazole) have all been show to produce superior improvement in clinical symptoms compared to omeprazole at both 2 and 4 weeks [24–26].
Relatively few randomized controlled clinical trials have been published on the efficacy of PPI for treating gastric ulcers when compared with gastro esophageal reflux disease or with duodenal ulcers [29, 30]. This could be due to gastric ulcers being less frequently diagnosed than duodenal ulcer , or the importance of clinicians confirming a differential diagnosis between gastric ulcer and gastric cancer. Some authors have also argued that the classification of gastric and duodenal ulcers is artificial, since ulcers could be driven distally or drawn proximally across the arbitrary boundary of the pylorus . Furthermore, some clinical assessments may be complicated as 10–20% of patients with gastric ulcers also have duodenal ulcers. However, given the severity of the symptoms generally associated with a gastric ulcer, there no longer appears to be a clear justification for continuing to conduct placebo-controlled trials in these patients.
Recent observations have suggested that the duration of treatment with acid secretory inhibitors is more important than the degree of acid inhibition per 24-hours . We could not test the long-term effect of PPIs on ulcer relapse rates, since there was not enough information published. More research into maintenance therapy is clearly required, because the relative long-term efficacy of different treatments, particularly the combination of PPIs with antibiotics, and the effect of dose variation on the relapse and complications from gastric ulcers is not well studied. Other factors known to have an impact on gastric ulcer healing are smoking; alcohol and ulcer size, but the papers did not report the healing results for these subgroups of patients or by those variables. Unfortunately, the researchers reported different clinical symptoms and methods to collect the data and so we could not pool these results.
This study suggests that the first-line drug therapy for patients diagnosed with gastric ulcer should be a PPI, in preference to an H2 antagonist. This study indicated that compared with ranitidine the PPIs provide faster onset of action, greater relief of symptoms and increased healing rates. However, there is also clearly a need for additional studies to determine the appropriate maintenance doses and understand the factors influencing healing and relapse rates.
Proton pump inhibitor
Histamine2 receptor antagonist
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The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/2/17/prepub
This research was supported in part by an unrestricted grant from Janssen Ortho Canada.
All authors participated in the design, analyses, editing and final approval of the manuscript.
Maribel Salas, Alexandra Ward and Jaime Caro contributed equally to this work.