Characteristics of peptic ulcer in military officers/soldiers: a preliminary analysis
Peptic ulcer disease consists of gastric and duodenal ulcers. Gastrointestinal symptoms such as epigastric pain, fullness, bloating, and early satiety, are the main clinical manifestations. Chronic ulcers can also be asymptomatic. Marshall and Warren for the first time found that peptic ulcer was the only endoscopic finding associated with histological gastritis and Helicobacter pylori (1). Current evidence supported the association of Helicobacter pylori with peptic ulcers (2). Additionally, in patients with pylori-negative ulcer disease, non-steroidal anti-inflammatory drugs and aspirin are considered to be another important cause of this disease (3). Hemorrhage is the most frequent complication of peptic ulcers, followed by perforation with the highest mortality (4). In patients with peptic ulcer, it was reported that there were 19.4–57.0 per 100,000 individuals complicated with hemorrhage (5), of which the risk was the highest among people over 60 years of age (6). The incidence of perforation was 3.8–14 per 100,000 individuals (5). Mortality among 30 days associated with peptic ulcer hemorrhage was 1.7% in Scotland (7) and 10.7% in Denmark (8). Mortality among 30 days associated with peptic ulcer perforation was 10.7% in Singapore (9) and 27.0% in Sweden (10), respectively. Until now, few study has explored the characteristics of peptic ulcers in military officers/soldiers, who are a special population always at a stress state.
Herein, we conducted a preliminary retrospective observational study to compare the differences of clinical characteristics and treatment between officers/soldiers and general civilians with peptic ulcer. We enrolled the patients who were diagnosed with peptic ulcer at the Department of Gastroenterology of the Shenyang General Hospital of Military Area and treated by an attending physician, Dr. Xingshun Qi, between January 2016 and October 2017. Data included sex, age, past disease history, clinical presentations, laboratory tests, medication, and in-hospital outcome. Patients were classified as military officers/soldiers and general civilians. Continuous variables were expressed as mean ± standard deviation (SD), and categorical variables were expressed as frequency (%). Continuous variables were tested by the independent sample t-test and categorical variables were analyzed by the chi-square test. P<0.05 was considered as significant statistical difference. Statistical analyses were performed by using by SPSS version 20.0.0 software (SPSS Inc., Chicago, IL, USA).
A total of 53 patients were included in the study, including 7 military officers/soldiers and 46 general civilians (Table 1). Compared with general civilians with peptic ulcers, military officers/soldiers with peptic ulcers were significantly younger (P=0.003) and had a shorter duration of smoking history (P=0.002), a higher albumin level (P=0.012), and a smaller amount of blood transfused (P=0.010). In addition, military officers/soldiers with peptic ulcers had a higher prevalence of Helicobacter pylori infection and a lower prevalence of liver cirrhosis and malignant tumors, but the difference was not statistically different.
Table 1
Variables | Military officers/soldiers | General civilians | P value by t-test or X2 test | |||
---|---|---|---|---|---|---|
No. Pts | Mean ± SD or frequency (%) | No. Pts | Mean ± SD or frequency (%) | |||
Age (years) | 7 | 38.57±21.33 | 46 | 57.62±13.81 | 0.003 | |
Sex (male/female) | 7 | 6 (85.7)/1 (14.3) | 46 | 32 (69.6)/14 (30.4) | 0.377 | |
Duodenal ulcer | 7 | 6 (85.7) | 46 | 26 (56.5) | 0.141 | |
Gastric ulcer | 7 | 1 (14.3) | 46 | 22 (47.8) | 0.095 | |
Helicobacter pylori infection | 7 | 4 (57.1) | 46 | 9 (19.6) | 0.064 | |
Malignant tumor | 7 | 0 (0) | 46 | 9 (19.6) | 0.199 | |
Liver cirrhosis | 7 | 0 (0) | 46 | 6 (13.0) | 0.31 | |
Gastrointestinal bleeding | 7 | 3 (42.9) | 46 | 19 (41.3) | 0.938 | |
Gastroesophageal varices | 7 | 0 (0) | 46 | 7 (15.2) | 0.268 | |
History of peptic ulcer | 7 | 1 (14.3) | 46 | 15 (32.6) | 0.325 | |
History of surgery for peptic ulcer | 7 | 0 (0) | 46 | 3 (6.5) | 0.487 | |
Prior use of NSAIDs | 7 | 1 (14.3) | 46 | 15 (32.6) | 0.325 | |
History of smoking | 7 | 2 (28.6) | 46 | 19 (41.3) | 0.521 | |
Duration of smoking (years) | 7 | 2.14±5.24 | 46 | 12.70±16.80 | 0.002 | |
Number of cigarettes per day | 7 | 2.86±4.88 | 42 | 6.31±10.77 | 0.395 | |
White blood cell (109/L) | 7 | 6.54±0.95 | 46 | 7.51±3.58 | 0.344 | |
Neutrophil (%) | 7 | 59.33±10.63 | 46 | 66.89±10.96 | 0.094 | |
Neutrophils (109/L) | 7 | 3.93±1.08 | 46 | 4.96±2.97 | 0.098 | |
Lymphocyte (%) | 7 | 30.76±12.22 | 46 | 23.70±10.18 | 0.102 | |
Lymphocytes (109/L) | 7 | 1.97±0.75 | 46 | 1.58±0.86 | 0.265 | |
Red blood cell (109/L) | 7 | 4.2514±0.68 | 46 | 3.75±1.02 | 0.217 | |
Hemoglobin (g/L) | 7 | 125.57±31.99 | 46 | 111.78±30.92 | 0.279 | |
Hematocrit (%) | 7 | 37.81±9.19 | 46 | 33.87±9.26 | 0.299 | |
Platelet (109/L) | 7 | 263.14±72.53 | 46 | 219.83±131.50 | 0.401 | |
Mean platelet volume (fL) | 7 | 7.96±0.44 | 46 | 8.44±3.32 | 0.703 | |
Total bilirubin (umol/L) | 7 | 15.89±9.57 | 46 | 17.83±16.04 | 0.757 | |
Direct bilirubin (umol/L) | 7 | 5.47±3.08 | 46 | 7.56±10.55 | 0.608 | |
Alanine aminotransferase (U/L) | 7 | 15.89±5.68 | 46 | 35.16±70.70 | 0.478 | |
Aspartate aminotransferase (U/L) | 7 | 17.13±4.65 | 46 | 32.29±37.64 | 0.296 | |
Alkaline phosphatase (U/L) | 7 | 68.46±24.16 | 46 | 91.34±45.39 | 0.2 | |
Glutamyl transpeptidase (U/L) | 7 | 19.33±11.11 | 46 | 53.69±101.75 | 0.38 | |
Total bile acid (umol/L) | 7 | 4.97±2.69 | 46 | 11.03±14.18 | 0.268 | |
Pre-albumin (mg/L) | 7 | 225.81±57.81 | 46 | 193.08±82.84 | 0.32 | |
Total protein (g/L) | 7 | 66.77±7.47 | 46 | 62.52±9.23 | 0.251 | |
Albumin (g/L) | 7 | 42.30±4.87 | 46 | 35.12±7.00 | 0.012 | |
Blood urea nitrogen (mmol/L) | 7 | 7.28±2.89 | 46 | 7.33±4.12 | 0.976 | |
Serum creatinine (umol/L) | 7 | 75.91±17.37 | 46 | 72.03±24.68 | 0.691 | |
Cystatin C (mg/L) | 7 | 0.69±0.20 | 46 | 0.92±0.43 | 0.176 | |
Blood transfusion | 7 | 0 (0) | 46 | 9 (19.6) | 0.199 | |
Amount of red blood cells transfused (unit) | 7 | 0±0 | 45 | 0.45±1.11 | 0.010 | |
Type of proton pump inhibitors | ||||||
Use of esomeprazole | 7 | 6 (85.7) | 46 | 33 (71.7) | 0.435 | |
Use of pantoprazole | 7 | 2 (28.6) | 46 | 14 (30.4) | 0.92 | |
Use of omeprazole | 7 | 0 (0) | 46 | 1 (2.2) | 0.694 | |
Use of somatostatin or octreotide | 7 | 1 (14.3) | 46 | 16 (34.8) | 0.279 | |
Death during hospitalization | 7 | 0 (0) | 46 | 0 (0) | NA |
On the basis of such a preliminary study, we could identify the characteristics of military officers/soldiers with peptic ulcers. Military officers/soldiers are diagnosed with peptic ulcers when they are younger. In spite of better outcomes, we would like to indicate that the recurrence of peptic ulcer might be more common due to a higher prevalence of Helicobacter pylori infection and stress exposure. In future, the sample size should be expanded to further confirm the present findings.
Acknowledgements
Funding: None.
Footnote
Provenance and Peer Review: This article was commissioned by the editorial office, AME Medical Journal. The article did not undergo external peer review.
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/amj.2018.07.05). Xingshun Qi serves as an Editor-in-Chief of AME Medical Journal. The other authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
References
- Marshall BJ, Warren JR. Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration. Lancet 1984;1:1311-5. [Crossref] [PubMed]
- Gisbert JP, Pajares JM. Helicobacter pylori infection and perforated peptic ulcer prevalence of the infection and role of antimicrobial treatment. Helicobacter 2003;8:159-67. [Crossref] [PubMed]
- Garcia Rodriguez LA, Barreales Tolosa L. Risk of upper gastrointestinal complications among users of traditional NSAIDs and COXIBs in the general population. Gastroenterology 2007;132:498-506. [Crossref] [PubMed]
- Wang YR, Richter JE, Dempsey DT. Trends and outcomes of hospitalizations for peptic ulcer disease in the United States, 1993 to 2006. Ann Surg 2010;251:51-8. [Crossref] [PubMed]
- Lau JY, Sung J, Hill C, et al. Systematic review of the epidemiology of complicated peptic ulcer disease: incidence, recurrence, risk factors and mortality. Digestion 2011;84:102-13. [Crossref] [PubMed]
- Blatchford O, Davidson LA, Murray WR, et al. Acute upper gastrointestinal haemorrhage in west of Scotland: case ascertainment study. BMJ 1997;315:510-4. [Crossref] [PubMed]
- Kubba AK, Choudari C, Rajgopal C, et al. Reduced long-term survival following major peptic ulcer haemorrhage. Br J Surg 1997;84:265-8. [Crossref] [PubMed]
- Mose H, Larsen M, Riis A, et al. Thirty-day mortality after peptic ulcer bleeding in hospitalized patients receiving low-dose aspirin at time of admission. Am J Geriatr Pharmacother 2006;4:244-50. [Crossref] [PubMed]
- Chan WH, Wong WK, Khin LW, et al. Adverse operative risk factors for perforated peptic ulcer. Ann Acad Med Singapore 2000;29:164-7. [PubMed]
- Blomgren LG. Perforated peptic ulcer: long-term results after simple closure in the elderly. World J Surg 1997;21:412-4; discussion 414-5. [Crossref] [PubMed]
Cite this article as: Song T, Sun R, Guo X, Qi X. Characteristics of peptic ulcer in military officers/soldiers: a preliminary analysis. AME Med J 2018;3:78.