Skip to main content

CASE REPORT article

Front. Surg., 31 August 2022
Sec. Visceral Surgery

Spontaneous perforation of a primary duodenal diverticulum stepped treatment model: A 10-patient case report

\r\nBin Zhong,&#x;Bin Zhong1,†Zhonghu Li,&#x;Zhonghu Li2,†Zhenyu LinZhenyu Lin1Yanbing ShenYanbing Shen2Jianxin Zhang
Jianxin Zhang2*Weidong Jin
\r\nWeidong Jin2*
  • 1The First School of Clinical Medicine, Southern Medical University, Guangzhou, China
  • 2Department of General Surgery, Central Theater Command General Hospital of the Chinese People’s Liberation Army, Wuhan, China

After colonic diverticula, a duodenal diverticulum (DD) is the second most common type of gastrointestinal diverticulum. DD is mainly caused by poor congenital development, resulting in a limited outward protrusion of the duodenal wall in a sac (primary diverticula). Perforation is one of the infrequent but most severe complications of DD, most commonly in the second segment of the duodenum (D2, 58%), followed by the third segment (D3, 30%). In the current case reports on the treatment of DD perforation, preoperative diagnosis is rare, with most patients being diagnosed and treated by laparotomy; the surgical approach is complex and varied, with artificial choices; and there is a high rate of complications and mortality (6%–34%) after surgical treatment. This study aimed to review our experience treating spontaneous perforation of the primary duodenal diverticulum, focusing on the surgical treatment model. A retrospective review of all spontaneous perforations of primary DD was conducted at one center between January 2010 and January 2022. We identified 10 patients with spontaneous perforation of primary DD (6 women and 4 men; median age: 51.5 years; range: 24–87 years). The patients had a median American Society of Anesthesiologists (ASA) score of 2. All patients underwent surgical treatment, of which six had percutaneous retroperitoneal drainage, two had diverticulectomy, one had distal gastrectomy + gastrojejunostomy + diverticuloplasty, and one had diverticulum repair. No patients died. The median length of stay was 12 days (range: 3–21 days). There were no long-term complications during the follow-up period (median follow-up of 12 months). A stepwise treatment model for spontaneous perforation of primary DD appears to have more advantages, and transabdominal exploratory surgery should probably not be the preferred treatment modality.

Introduction

The diverticulum is round, oval, or tubular pouches that protrude from the gastrointestinal wall and can occur anywhere in the gastrointestinal tract. Duodenal diverticulum (DD) is the second most common type of gastrointestinal diverticulum after colonic diverticulum. The prevalence of duodenal diverticula in autopsies has been reported to be approximately 22% (1).

Perforation is a rare but severe complication of duodenal diverticula (2). Clinically, most DD perforations occur in the retroperitoneal position, resulting in a lack of characteristic presentation and abdominal signs, and the diagnosis is often delayed (1). At the same time, leakage of digestive fluid and the formation of retroperitoneal abscesses make it difficult for the infection to resolve on its own, often requiring surgical treatment. Laparotomy is still considered necessary in hemodynamic instability patients and patients with sepsis, especially if the diagnosis is unclear (3, 4). Despite the duodenum having gastric juice, bile, pancreatic juice, intestinal juice, and other digestive solutions, the lack of surrounding tissues to aid closure of the perforation and the edema of the intestinal wall around the perforation results in a low success rate of perforation repair.

In contrast, relatively radical procedures (e.g., gastrectomy, diverticulectomy, pancreaticoduodenectomy, etc.) are more invasive and highly risky in emergencies. At the same time, the surgical approach has a considerable impact on the patient's physiological function. Laparotomy disrupts the retroperitoneum, a vital defense barrier of the organism, which may result in postoperative abdominal infection and drainage that cannot be easily completed. This study aimed to review our 12-year experience treating spontaneous perforation of primary DD in a single center, focusing on surgical treatment, to explore an appropriate treatment modality for DD perforation.

Case report

Between January 2010 and January 2022, all perforated DD cases were retrospectively reviewed at the Department of General Surgery, Central Theater Command General Hospital of the Chinese People's Liberation Army. Perforations due to trauma and Iatrogenic perforations (e.g., during endoscopy) were excluded from the study. We identified 10 patients with spontaneous perforation of primary DD (6 women and 4 men; median age: 51.5 years; range: 24–87 years). The patients had a median American Society of Anesthesiologists (ASA) score of 2 (range: 2–3). All patients underwent surgical treatment, of which six had percutaneous retroperitoneal drainage, two had diverticulectomy + drainage, one had distal gastrectomy + gastrojejunostomy + diverticuloplasty, and one had diverticulum repair + retroperitoneal drainage (Table 1). All patients underwent CT scans preoperatively.

TABLE 1
www.frontiersin.org

Table 1. Patient characteristics, treatment modalities, and prognosis.

We here report 10 cases of spontaneous DD perforation (Table 1). The clinical presentation was abdominal pain without fever in five cases, abdominal pain with fever in three cases, right-sided lumbar pain in one case, and vomiting in one case. Seven patients had elevated white blood cell count and C-reactive protein, two patients had white blood cell count and C-reactive protein in the normal range, and one patient had a decreased white blood cell count. None of the patients had a severe infectious shock on admission. Of note, one patient was admitted with a high fever (maximum temperature 40.8°C) without signs of peritoneal irritation, two patients had localized peritoneal irritation signs, and one patient presented with the peritoneal irritation sign throughout the abdomen. In total, 20% (2/10) of the cases could be diagnosed as duodenal diverticulum perforation by CT (Figures 1A,B). DD perforation can be diagnosed by gastrointestinal imaging in 20% (2/10) of the cases (Figure 1C). The rest of the cases were confirmed by intraoperative diagnosis. Eight of these cases had an ASA score of 2, and two had an ASA score of 3. The perforated DD was located in the D2 level in eight cases (80%) and the D3 level in two cases (20%). All patients received postoperative intravenous antibiotic therapy (cefoperazone/sulbactam) for 5 d.

FIGURE 1
www.frontiersin.org

Figure 1. (A,B) Computed tomography scans of cases 5 and 1 and (C) gastrointestinal barium study of case 4, both suggestive of a perforated duodenal diverticulum.

In 2 of the 10 patients, no double driving pipes were placed intraoperatively for continuous postoperative flushing and drainage. In all patients, a nasogastric or nasojejunal tube (1:1) was placed to reduce postoperative bowel tension and facilitate enteral nutrition support. Four of the ten patients had a history of previous abdominal surgery. One patient had a previous diagnosis of adhesive intestinal obstruction and underwent intestinal adhesion lysis, after which he continued to have recurrent abdominal pain for a long time. This admission CT revealed thickening of the gastric wall at the gastric sinus and a diverticulum of the descending duodenum and surrounding exudate. In combination with the patient's previous history of mild vomiting, the patient was considered to have pyloric stenosis. Therefore, a distal gastrectomy + Roux-n-Y anastomosis + duodenal exploratory was planned using the previous median incision. Intraoperative exploration revealed a diverticulum located in the posterior wall of the descending duodenum with a 0.1 cm diverticular rupture, so additional duodenal diverticuloplasty was performed. No double driving pipes were placed.

We considered that with the retroperitoneal barrier intact, the inflammatory exudate due to infection, although showing a gradual increase, was generally limited and did not affect the systemic situation as much as expected. In all six patients, we made a small vertical incision of approximately 5 cm in the right mid-axillary line at the level of the umbilicus for debridement and drainage of the retroperitoneal abscess under ultrasound guidance, which protected the peritoneum, a critical defense barrier of the body, and was less likely to lead to postoperative infection of the peritoneal cavity.

A typical case is described in detail here. The patient was an 87-year-old woman admitted to the hospital with a sudden onset of epigastric pain for 8 h. On admission, her vital signs were stable. On examination, she was found to have mid-upper abdominal pressure and suspicious rebound pain, and the rest of her abdomen was free from peritoneal Irritation signs. Laboratory investigations revealed the following: WBC 5.8*109/L, NP 73.2%, PLT 87*109/L; AMY 1,450U/L, TB 34.90 µmol/L, CB 19.00 µmol/L, ALT 492U/L, and AST 515U/L. The CECT scan suggested (Figure 2A) suspected duodenal diverticulum perforation. Given the patient's stable vital signs and the absence of significant peritoneal irritation, but with advanced age and hepatic insufficiency, there was no better surgical access on the CT scan. We decided to treat the patient with nonoperative management for one week (anti-infective, fasting, gastrointestinal decompression, and maintaining acid–base balance). The patient's blood count and liver and kidney function were dynamically reviewed during conservative treatment. During this period, the patient's white blood cells gradually increased, and she developed intermittent fever with a maximum temperature of 38.5°C. One week later, a repeat CECT revealed a significant increase in fluid accumulation around the lateral descending duodenum, posterior ascending colon, and perirenal fat sac (Figure 2B). Gastrointestinal imaging showed that the diverticulum was located at the beginning of the horizontal segment of the duodenum, and contrast leakage was seen, leading to a definite diagnosis of retroperitoneal perforation of the duodenal diverticulum (Figure 2D). We then performed percutaneous retroperitoneal drainage through a small incision in the right lumbar region under basis anesthesia and local anesthesia with ultrasound localization (Figure 3). The patient's temperature and inflammatory indicators (white blood cell count, C-reactive protein, etc.) gradually returned to normal levels after the operation. A review of CT scans on postoperative day 7 showed a significant reduction in retroperitoneal fluid (Figure 2C), and the patient was discharged 9 days after surgery.

FIGURE 2
www.frontiersin.org

Figure 2. (A,B) Enhanced CT scans of the patient on admission and 7 days after conservative treatment (red arrows point to free abdominal gas, black arrows point to peri-duodenal and retroperitoneal exudate). (C) CT scan 7 days after percutaneous retroperitoneal tube placement for drainage (red arrows point to the placed retroperitoneal double cannula, black arrows point to periduodenal and retroperitoneal exudate). (D) shows a gastrointestinal barium study of the patient.

FIGURE 3
www.frontiersin.org

Figure 3. Hand drawing of retroperitoneal abscess drainage through a small incision in the right lumbar region. The red arrow points to the location of the incision, approximately 3–5 cm. the dotted line is the mid-axillary line.

Only one patient developed a postoperative complication of incisional infection after surgery. The remaining patient had no long-term complications during the postoperative period and postdischarge follow-up (median follow-up of 12 months). The median length of stay was 12 days (range: 3–21 days). One patient considered himself to be recovering well on the third postoperative day and strongly requested to be discharged. There were no long-term complications during the follow-up period (median follow-up of 12 months). The case characteristics, treatment modalities, and prognosis of the 10 patients are placed in Table 1.

Discussion

DD was first described by Chomel in 1710 (5). Since then, scientists have continued to publish reports related to DD (6, 7). DD perforation is rare in the acute abdomen and is often difficult to distinguish from duodenal perforation, which is usually associated with diverticulitis or ischemia due to distention of food within the diverticulum (8). Basically, the causes of perforation are multiple and include diverticulitis, enterolithiasis, ulceration, iatrogenic perforation during ERCP sphincterotomy, trauma, foreign body, and so on (9). Farné et al. (10) recently reviewed the available literature and now reported 210 cases of DD perforation. The preoperative diagnosis and treatment choice are the two issues that currently need to be addressed for DD perforation. The symptoms of DD perforation are often ill-defined from the available case reports. The most common clinical presentation appears to be right upper abdominal pain, as reported in this article. Although DD perforation may have the same presentation on CT as duodenal perforation, there is no denying that the number of cases of preoperative diagnosis of DD perforation has improved since physicians have commonly used CT. We believe that CT/enhanced CT will be the primary diagnostic method for DD perforation in the future. In our clinical work, we do not routinely use oral contrast. Very rarely, we use it when we do not clearly see free intraperitoneal air on the CT scan and there is a persistent suspicion of perforation, but it does not seem to impact our treatment. This is somewhat consistent with the WSES guidelines (11). This test may improve the diagnostic accuracy of duodenal diverticulum perforation, which still needs to be validated in higher quality and multicenter studies. Of course, whether such tests can lead to disease changes and inconvenience to treatment needs further explored.

Due to the small number of cases, there are no relevant guidelines for managing perforated duodenal diverticula. Although there are reports of surgical treatment, conservative treatment, and intermediate treatment, a review of these reports shows that there is still no treatment model available to physicians in clinical practice for these patients. The choice of treatment is a function of the surgeon's experience and control of the condition (7). It has been suggested in the literature that the looseness of the retroperitoneal tissue space and the large size of the retroperitoneal space make it extremely dangerous for infection to spread (12). However, a review of our cases shows that most infections are not very dangerous when duodenal diverticula leads to perforation of the posterior wall; with the posterior peritoneal barrier intact, the infected exudate, although progressively increasing, is generally limited and does not have as significant an impact on the general condition as expected. If the patient is in poor general condition, hemodynamically unstable, or septic, surgical treatment is associated with a high risk. Especially when faced with emergency surgery, even a simple diverticulectomy can be difficult for the surgeon (13). Exploratory laparotomy should probably not be the first choice of treatment. We have developed a step-up treatment model for this purpose for reference (Figure 4). In suspected retroperitoneal perforation of the duodenal diverticulum, nonoperative management (anti-infection, fasting, nutritional support, decompression, etc.) is indicated. In the application of antibiotics, we commonly use drugs that cover Gram-negative bacterium and/or anaerobic organisms (e.g., cefoperazone/sulbactam + metronidazole). We do not usually use antifungals routinely, except when antibiotic therapy is not effective and fungal infection is highly suspected and when a fungal culture of the peritoneal fluid is performed, and based on the culture results, the relevant departments (Infection and Pharmacology) are consulted. The need for antifungal treatment is discussed. This is because fungal cultures (+) often have the potential for false positives [due to improper sampling or specimen contamination) and the effectiveness of antifungal therapy in patients with fungal cultures (+) is currently unclear and controversial (14].

FIGURE 4
www.frontiersin.org

Figure 4. Flow diagram of step-up treatment model for reference.

When conservative treatment is not well controlled, percutaneous retroperitoneal drainage is selected at the right time, and when the patient shows clear signs of peritonitis, open surgery is performed. Diverticulectomy is the major and most common surgical method; it is suggested when conservative treatment fails or indicates a massive hemorrhage or failure of endoscopic hemostasis. However, simple suture closure of the duodenal wall after diverticulectomy is reported to be associated with a risk of duodenal fistula, which carries a mortality of 20%–30% (15). Sometimes diverticulectomy is associated with a biliodigestive bypass to reduce the risk of duodenal leak or fistula and to reduce morbidity. Therefore, we prefer conservative treatment and percutaneous retroperitoneal drainage after repeated revaluation. For percutaneous drainage timing, we can determine the extent of the infection by CT scan. The better time to operate is when the abscess extends posteriorly to the level of the right margin of the ascending colon. At this point, there are several advantages to placing a small incision in the lateral lumbar region for drainage by ultrasound. First, the abscess is closest to the body surface at this time, which has little impact on the patient, and the operation can be completed under basis anesthesia plus local anesthesia. Second, access to the retroperitoneal space is convenient and straightforward at this time, making the operation relatively simple and less likely to injure other organs. Third, the integrity of the retroperitoneal barrier is maintained so that infection and digestive fluid exudation are confined to the retroperitoneal space without contaminating the abdominal cavity, and drainage is complete. We did not study the relationship between the size of perforation and the selection of treatment. However, we believe that the location (the portion or wall of the duodenum) of the perforation also plays a vital role in this question.

This article presents one of the most series of cases published to date (10 patients). The overall results were satisfactory, and no patient died. Recent reviews have reported a mortality rate of approximately 16.7% (13). Our results compare favorably with this. However, as the number of cases is still small, our treatment model needs to be validated with many cases. With the rapid development of endoscopic techniques in recent years, many previously required surgical treatment problems can now be addressed endoscopically. There are reports in the literature that endoscopic drainage of the perforation by endoscopy may be a minimally invasive alternative to percutaneous drainage or exploratory laparotomy when CT scans suggest that the effusion is confined in clinically stable patients to the retroperitoneal space (16, 17). Shirobe et al. (17) and Fan et al. (16) have endoscopically placed drains through the diverticulum to place a drainage tube, while Sasaki et al. (18) used polyglycolic acid sheets and fibrin glue to treat the perforation with endoscopic tissue shielding, and they both achieved good results. Future treatment trends will undoubtedly be toward more accessible application, less invasive, and better prognosis. We need to continue exploring and validating new treatment modalities in clinical practice to advance the cause of medicine.

Conclusion

Surgical treatment by exploratory laparotomy has long been the method of choice for most surgeons when the diagnosis is unknown. However, with advances in medical technology and imaging techniques, less invasive methods are available, and laparotomy surgical treatment may not be the first option. We aim to explore a more rational surgical treatment model by retrospectively reviewing 10 previous cases of spontaneous perforation of primary DD . We suggest a step-up treatment strategy. The clinician may choose the appropriate treatment, either conservative or surgical, depending on the different clinical conditions and thus on the outcomes.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material; further inquiries can be directed to the corresponding author.

Ethics statement

Ethical review and approval were not required for the study on human participants in accordance with the local legislation and institutional requirements. The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author contributions

BZ and Z-HL helped with writing the abstract and figure collection, writing, and formatting. Z-YL helped with writing and formatting. Y-BS helped with writing and editing. J-XZ and W-DJ helped with the review and final editing. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Costa Simões V, Santos B, Magalhães S, Faria G, Sousa Silva D, Davide J. Perforated duodenal diverticulum: surgical treatment and literature review. Int J Surg Case Rep. (2014) 5(8):547–50. doi: 10.1016/j.ijscr.2014.06.008

CrossRef Full Text | Google Scholar

2. Kim KH, Park SH. Conservative treatment of duodenal diverticulitis perforation: a case report and literature review. Open Access Emerg Med. (2018) 10:101–4. doi: 10.2147/oaem.S168487

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Miller G, Mueller C, Yim D, Macari M, Liang H, Marcus S, et al. Perforated duodenal diverticulitis: a report of three cases. Dig Surg. (2005) 22(3):198–202. doi: 10.1159/000087974

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Oddo F, Chevallier P, Souci J, Baque J, Buckley MJ, Fabiani P, et al. [Radiologic aspects of the complications of duodenal diverticula]. J Radiol. (1999) 80(2):134–40. PMID: 10209709

PubMed Abstract | Google Scholar

5. Chomel JB. Report of a case of duodenal diverticulum containing gallstones.

6. Thorson CM, Paz Ruiz PS, Roeder RA, Sleeman D, Casillas VJ. The perforated duodenal diverticulum. Arch Surg. (2012) 147(1):81–8. doi: 10.1001/archsurg.2011.821

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Yeh TC. Laparoscopic resection of perforated duodenal diverticulum–a case report and literature review. Int J Surg Case Rep. (2016) 28:204–10. doi: 10.1016/j.ijscr.2016.10.001

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Duarte B, Nagy KK, Cintron J. Perforated duodenal diverticulum. Br J Surg. (1992) 79(9):877–81. doi: 10.1002/bjs.1800790907

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Chung KT, Shelat VG. Perforated peptic ulcer—an update. World J Gastrointest Surg. (2017) 9(1):1–12. doi: 10.4240/wjgs.v9.i1.1

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Farné GM, Lauro A, Vaccari S, Marino IR, Khouzam S, D’Andrea V, et al. Spontaneous perforated duodenal diverticulum: wait or cut first? Dig Dis Sci. (2021) 66(9):2876–80. doi: 10.1007/s10620-021-07092-1

CrossRef Full Text | Google Scholar

11. Tarasconi A, Coccolini F, Biffl WL, Tomasoni M, Ansaloni L, Picetti E, et al. Perforated and bleeding peptic ulcer: WSES guidelines. World J Emerg Surg. (2020) 15(3):4–24. doi: 10.1186/s13017-019-0283-9

CrossRef Full Text | Google Scholar

12. Zuluaga Gómez A, Jiménez Verdejo A. Retroperitoneal pathology. Actas Urol Esp. (2002) 26(7):445–66. doi: 10.1016/s0210-4806(02)72814-3

CrossRef Full Text | Google Scholar

13. Rossetti A, Christian BN, Pascal B, Stephane D, Philippe M. Perforated duodenal diverticulum, a rare complication of a common pathology: a seven-patient case series. World J Gastrointest Surg. (2013) 5(3):47–50. doi: 10.4240/wjgs.v5.i3.47

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Kwan JR, Lim M, Ng F, Shelat V. Fungal isolates in peritoneal fluid culture do not impact peri-operative outcomes of peptic ulcer perforation. Surg Infect (Larchmt). (2019) 20(8):619–24. doi: 10.1089/sur.2019.024

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Oukachbi N, Brouzes S. Management of complicated duodenal diverticula. J Visc Surg. (2013) 150(3):173–9. doi: 10.1016/j.jviscsurg.2013.04.006

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Fan HS, Talbot ML. Successful management of perforated duodenal diverticulum by use of endoscopic drainage. VideoGIE. (2017) 2(2):29–31. doi: 10.1016/j.vgie.2016.11.006

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Shirobe T, Kawakami H, Abe S, Yokochi T. Retroperitoneal perforation arising from duodenal diverticulum treated by endoscopic drainage: a case report. Clin Case Rep. (2017) 5(5):654–7. doi: 10.1002/ccr3.921

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Sasaki F, Kanmura S, Nasu Y, Hashimoto S, Taguchi H, Numata M, et al. Double-balloon enteroscopy-assisted closure of perforated duodenal diverticulum using polyglycolic acid sheets. Endoscopy. (2015) 47(Suppl 1 UCTN):E204–5:1–2. doi: 10.1055/s-0034-1391651

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: perforation, duodenum diverticulum, duodenum, stepped treatment, surgery

Citation: Zhong B, Li Z, Lin Z, Shen Y, Zhang J and Jin W (2022) Spontaneous perforation of a primary duodenal diverticulum stepped treatment model: A 10-patient case report. Front. Surg. 9:936492. doi: 10.3389/fsurg.2022.936492

Received: 5 May 2022; Accepted: 28 July 2022;
Published: 31 August 2022.

Edited by:

Orestis Ioannidis, Aristotle University of Thessaloniki, Greece

Reviewed by:

Ioannis Dimitrios Passos, 424 General Military Hospital, Greece
Vishal G. Shelat, Tan Tock Seng Hospital, Singapore

© 2022 Zhong, Li, Lin, Shen, Zhang and Jin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Wei-Dong Jin jinwd1972@163.com Jian-Xin Zhang mai_andy0@126.com

These authors have contributed equally to this work

Specialty Section: This article was submitted to Visceral Surgery, a section of the journal Frontiers in Surgery

Abbreviations DD, duodenal diverticulum(a); CT, computed tomography; ASA, American Society of Anesthesiologists; WBC, white blood cell; NP, neutrophil percentage; PLT, platelet; AMY, amylase; TB, total bilirubin; CB, conjugated bilirubin; ALT, alanine transaminase; AST, aspartate transaminase; SOFA, sequential organ failure assessment; CECT, contrast-enhanced computed tomography.

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.