Nicolas Michot1
Pablo Ortega-Deballon
Mehdi Ouaissi- 1Department of Digestive, Oncological, Endocrine, Hepato-Biliary, Pancreatic Surgery and Liver Transplantation, Trousseau Hospital, Tours University Hospital, Chambray-Lès-Tours, France
- 2Department of Digestive Surgery, François Mitterand Hospital, Dijon University Hospital, Dijon, France
- 3Fliedner Fachhochschule, University of Applied Sciences Düsseldorf, Düsseldorf, Germany
Background: The incidence of incisional hernia following laparotomy varies between 2% and 30%. It is well-established that the need to control several risk factors prior to surgery exists (weight loss before surgery, diabetes control). Postoperative abdominal binder (AB) is often recommended by surgeons, yet evidence on this topic is lacking. The aim of this review was to present current evidence on the use of abdominal binders after abdominal surgery.
Material and Methods: A comprehensive literature review between January and May 2024 was conducted using a range of search engines, including PubMed, Science Direct, EMBASE, Google Scholar, and Google. The following keywords were used: “abdominal binder,” “abdominal support,” “hernia,” “girdle and hernia,” “compression belt and hernia,” and “abdominal support and hernia.”
Results: Sixteen articles were selected for further analysis (7 RCTs, 6 non-RCTs and 3 meta-analyses). None of the studies reported a reduction in the incidence of abdominal dehiscence or incisional hernia. Postoperative use of the AB has been shown to reduce postoperative discomfort and pain for a limited period of up to 48–72 h. There was no discernible difference in the incidence of surgical site complications.
Conclusion: The current evidence indicates that the use of AB following abdominal surgery is safe, although no benefit has been established (except 48 h after surgery). AB may enhance comfort in select patients; however, further studies are necessary to justify their routine use, with a particular focus on the medical and economic implications.
Introduction
The incidence of incisional hernia following laparotomy has been reported to range from 2% to 30% in various studies [1–6]. The risk of recurrence after incisional hernia repair in large series is between 25% and 63% [2, 5, 7, 8]. This complication is most frequently observed between 18 and 24 months following the initial surgery [4, 5]. The risk of postoperative hernia is significantly increased by age, diabetes, obesity, smoking, length of the laparotomy size and the onset of surgical site infection significantly increase the risk of postoperative hernia [5, 6]. In France, the French Surgical Association (AFC) reports that 45,242 incisional hernia treatments were performed in 2017. The estimated annual national cost, inclusive of both public and private treatment, is 172 million euros. In light of the significant health burden associated with incisional hernia, prevention and treatment remain a crucial public health concern [9].
A number of preventive measures have been demonstrated to be effective in clinical studies, including weight loss prior to surgery and the management of diabetes [10]. However, the efficacy of other proposed preventive measures remains a topic of debate. Amongst these, the use of abdominal binders (AB) after surgery appears to be an intuitive method of preventing excess abdominal tension in the postoperative period. In 2014, a questionnaire was distributed to a number of French centres specializing in digestive surgery (50 responding centres). A total of 94% of the surgical teams prescribed an AB with the expectation that it would reduce the risk of incisional hernia by 83% [11]. There are few prospective randomized trials that have examined the possible effect of AB on the incidence of postoperative pain, wound complications, or incisional hernias. These trials have relatively small numbers of participants overall, and the procedures performed in the trials vary widely from general surgery to laparoscopic inguinal hernia repair to caesarean section [12–18]. In addition, none of the trials evaluated a possible preventive effect of wearing an AB on the incidence of postoperative incisional hernias after laparotomy as a primary endpoint. Despite the lack of scientific evidence supporting the preventive postoperative use of an AB, many general surgeons prescribe an AB as part of their clinical routine practice. The objective of this review was to ascertain the current evidence regarding the potential clinical benefits of AB after surgery.
Material and Methods
Selection of Articles
A comprehensive literature review was conducted using a range of search engines, including PubMed, Science Direct, EMBASE, Google Scholar, and Google. The following keywords were used: The following search terms were used: “abdominal binder,” “abdominal support,” “hernia,” “girdle and hernia,” “compression belts and hernia,” and “abdominal support and hernia.” All the results were then subjected to a second round of review by two senior surgeons (MO, NM) at our centre, who selected the articles that were deemed to be consistent with the review that we were undertaking. The updated PRISMA guidelines for the reporting of systematic reviews was applied [19]. Only literature from the year 2000 onwards was considered, because at that time the technique of abdominal wall closure was optimized by the use of slow absorbable continuous sutures [20]. Inclusion criteria for our systematic review include publications published between 2000 and 2023 that provide detailed information on the use of postoperative abdominal wall dressings after various abdominal procedures (digestive tract, gynecology, urology). The procedures for wearing an AB had to be detailed, including the duration of wear, the period of time it was to be worn during the day (all day, night, day, during exercise), and the effects of wearing the AB, including the occurrence of postoperative complications and recurrence. Exclusion criteria: cases not involving humans, case reports, articles that only specify the wearing of an AB without defining the stipulations for wearing the AB or explaining the consequences of the procedure (postoperative complications and/or recurrence), articles about wearing the AB in exceptional situations (post-accident abdominal trauma) where surgery had not been performed.
Risk of Bias and Quality Assessment
Two experienced surgeons (MO, NM) independently assessed all articles using the ROBINS-I tool [21] for non-randomized controlled trials and the GRADE score [22].
Results
A total of 52 articles were identified between January and May 2024. After excluding irrelevant articles, sixteen articles were selected for further analysis [11–18, 23–30]. These included a total of seven randomized controlled trials (RCTs), 6 no RCT and 3 meta-analyses (Figure 1 flow charts) (Figure 2). Details of the RCTs selection are shown in Table 1. We therefore identified the articles that primarily investigate the use of AB through questionnaires. In the literature, only two articles are reported (Table 2), which consisted of sending questionnaires to German and French surgical teams asking about the prescription guidance for AB postoperatively. The French study, the only one to analyse the guidance for post-operative prescription with a preventive objective after a first laparotomy, and the second study, which related to the prescription for wearing an AB after surgery for an incisional hernia, were the only ones to address this topic. A first French study from 2014 by Bouvier et al. [11] obtained responses from 50 centres. Among the respondents, 31.9% indicated that they prescribed the AB with the objective of reducing post-operative complications, such as evisceration or incisional hernia. 14.9% of respondents stated that they prescribed the AB for the patient’s comfort, while the remaining respondents indicated that they prescribed it for both reasons. In this study, 40.4% of respondents indicated that they would prescribe the AB following incisional hernia treatment, 25.5% indicated that they would prescribe the AB for all laparotomies, and 17% indicated that they would prescribe it according to the size of the laparotomies. With regard to the duration of prescription, the AB was prescribed for a period of 1 week in 2% of centers, for a period of 1 month in 48.9% of cases, and for a period of 2 to 3 months in 31.9% of cases. The study by Paasch et al. [24] evaluated the various postoperative prescriptions following incisional hernia. Of the 44 centers that responded, 4.45% of teams prescribed the AB for 1 week, 15.9% for 15 days, 2.27% for 40 weeks, and 29.5% did not prescribe one. The AB was to be worn continuously throughout the day, including during exercise. These studies demonstrate that the durations and prescription guidance vary considerably depending on the surgeons and the different centres surveyed. Moreover, the prescriptions appear to be more influenced by the centre’s own common practice than by scientific evidence.
Figure 1. PRISMA 2020 flow diagram. RCT = Randomised controlled trial.
Figure 2. ROBINS-I tool for risk of bias assessment.
Table 1. GRADE evidence profile for randomized controlled trial.
Table 2. Guidance for wearing the abdominal binder (AB).
The analysis of the literature focused on the results relating to pain and the occurrence of seroma in the postoperative period, depending on the use or non-use of an AB.
Post-Operative Pain (Table 3)
Most studies showed no difference in postoperative pain between patients who wore an AB and those who did not. Only 2 randomized articles with 37 and 48 patients, respectively, showed an improvement in pain relief at postoperative day (POD) 2 and POD 5 [15, 25]. In these two studies, pain was assessed using the patient’s visual analog scale (VAS). The first study including 48 patients found that AB had no effect on pulmonary function, but that pain was significantly less in the AB group on POD 5. The second smaller study by Paash et al. reported significantly less postoperative pain in the AB group after hernia repair at POD 2 [14]. This is supported by a meta-analysis by Ossola et al. [28] in 281 patients who found a highly significant reduction in pain in patients with AB compared to patients without AB on POD 1 and 5 (p = 0.001 and <0.001, respectively).
Table 3. Effect of wearing an abdominal binder (AB) on postoperative pain.
Surgical-Site Occurrences (SSO) (Table 4)
Studies focusing on the effect of abdominal support on SSO have often been performed after hernia surgery. A study describing the technique of laparoscopic intraperitoneal mesh placement in 2000 [23] reported that the rate of postoperative seroma was lower after the prescription of an AB (32% vs. 18%).
Table 4. Effect of abdominal binders (AB) on the occurrence of postoperative seroma.
There was no significant difference between the two groups in terms of pain at rest and impaired mobility. Patients in the AB group had a higher rate and larger seroma at day 14 (66.6% vs. 50%). However, the AB group had a significantly lower rate of surgical site infection at day 14 (4.8% vs. 27.8%, p = 0.004) [13]. The studies did not find any side effects attributed to the AB. No difference in respiratory function [15, 28] or abdominal pressure [26].
Other Issues of Abdominal Support
Regarding return to activity, the only randomized trial [18] that found a significant result highlights a better walking distance in patients wearing an AB on postoperative day 5 (60 patients: 30 with and 30 without harness). In addition, 2 studies asked patients about their emotional state using a patient questionnaire. One of these studies [25] conducted on 163 patients, showed that 50 patients felt that the AB reduced their mobility and 115 felt that the AB reduced their pain. The other study [27] of 67 patients found that 64% experienced a subjective improvement in their symptoms (combining pain, heaviness, embarrassment, difficulty dressing, difficulty moving, difficulty breathing) and 97% experienced discomfort (including heat, friction, pain, itching).
Regarding postoperative discomfort, several studies of patients undergoing caesarean section show reduced discomfort in patients in the immediate postpartum period. 3 gynaecologic studies (Table 5) showed an improvement in the SDS (Symptom Distress Scale, calculated by collecting elements of nausea, vomiting, pain, anorexia, sleep disturbance, fatigue, difficulty breathing, cough, crying, restlessness, difficulty concentrating, body temperature, transit, and physical appearance). The first, by Karaca et al. [16] in a prospective randomized trial of 89 patients (45 with and 44 without a support belt), reported a better SDS score in the AB group at 8 h (p = 0.024), 24 h (p < 0.001), and 48 h (p < 0.001) after surgery. Another study by Ghana et al. [17] after randomizing 178 patients (89 with belt and 89 without) reported a significant difference in SDS in favour of the AB at 24 and 48 h with p < 0.001. Finally, a meta-analysis by Abd-ElGawad et al. [29] also found an improvement in SDS with the AB at 24 h (p < 0.001) and 48 h (p = 0.002). However, there are no data on symptoms at 48 h.
Table 5. Effect of wearing a abdominal binder (AB) on patient discomfort.
Discussion
Current evidence on the effects of AB does not support its use after any abdominal surgery: gastrointestinal, gynaecologic, urologic, or plastic. There is little or no evidence of the benefit of an AB in reducing complications and/or recurrence. Prescribing guidelines for these supports do not include specific recommendations on how the support should be worn: daytime, day and nighttime, during exercise, or for how long the belt should be worn [11, 24]. Some data from small randomized trials suggest a reduction in pain during the first postoperative days [13, 15]. The most recent meta-analysis by Ossola et al. [28] also shows that there was significantly less pain in the AB group at the first and fifth PODs and that there was also an increase in physical activity from the fourth POD. Finally, in their meta-analysis, the authors did not find any side effects of wearing the AB. However, due to the small number of RCTs, they also concluded that the evidence for wearing an AB postoperatively is weak and that routine wearing of an AB should not be recommended. Therefore, it does not appear necessary to recommend wearing an AB for more than 1 week.
Regarding the intuitive belief that reduced tension at the time of laparotomy leads to a lower incidence of incisional after laparotomy or fewer recurrences after incisional hernia repair, there is no evidence to support such a practice. Furthermore, the natural history of incisional hernia and incisional hernia recurrence suggests that these events most commonly occur within 18–24 months [4, 5] after abdominal surgery, well beyond the time limit for wearing the support belt.
One of the benefits would be the subjective reassurance of the patient postoperatively, which is difficult to determine as it is so subjective [25, 27]. However, given the paucity of objective evidence and the cost of an AB, it seems difficult to justify a recommendation to wear an AB after any abdominal surgery or even after any laparotomy. This is reaffirmed by the American and European guidelines in 2022 [31] which state: “No recommendation can be made for or against the use of postoperative binders owing to the lack of data on their effect on incisional hernia or burst abdomen.”
However, no harmful effect of this support belt in the postoperative period has been demonstrated [15, 26, 28]. It could lead to a faster return to activity [18], which in turn could have an economic impact due to reduced hospitalization time and a faster return to work.
Conclusion
Based on this literature review, it seems reasonable to conduct a large, multi-centre, prospective, randomized trial to assess the medical and socio-economic effects of wearing an AB postoperatively.
Author Contributions
NM and PO-D: Data acquisition, data analysis, data interpretation and drafting and critical revision of the manuscript. MO, EK, and UP-G data analysis, data interpretation, drafting and critical revision of the manuscript. All authors contributed to the article and approved the submitted version.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The study was funded by the Tourangelle Association for Research in Oncology in the Loire Valley (AT-ROVL), Tours, France.
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.
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Keywords: abdominal binders, laparotomy, abdominal surgery, postoperative complications, postoperative pain
Citation: Michot N, Ortega-Deballon P, Karam E, Pabst-Giger U and Ouaissi M (2024) Is There a Clinical Benefit of Abdominal Binders After Abdominal Surgery: A Systematic Literature Review. J. Abdom. Wall Surg. 3:13506. doi: 10.3389/jaws.2024.13506
Received: 09 July 2024; Accepted: 04 October 2024;
Published: 17 October 2024.
Copyright © 2024 Michot, Ortega-Deballon, Karam, Pabst-Giger and Ouaissi. 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: Mehdi Ouaissi, m.ouaissi@chu-tours.fr