Introduction
Ventral hernias (VH) pose separate and unique challenges for both patient and surgeons alike, with an estimated 25,000 to 350,000 repaired annually in the UK and USA, respectively [
1]. They develop either as primary hernias or secondary to previous surgery (incisional hernia (IH)). Incisional ventral hernias (IVHs) most commonly occur following laparotomies with an incidence of 40% [
2].
In the UK, laparotomies performed in the emergency setting vary between an estimated 25,000 and 30,000 cases per annum, translating into a proportion of patients at risk of developing future IVHs [
3]. Patients with these types of hernias are often categorised into groups based on associated comorbidities. These include patients with malignant conditions presenting with complications such as bowel obstruction or perforation requiring laparotomies and resection, subsequently being complicated by IHs at sites of tumour extraction. A second group are trauma presentations or benign pathologies leading to gastrointestinal obstruction and perforation. In both sets of patients, prolonged and protracted recovery periods may lead to delays in IH repair. The interim increase in size of the abdominal wall defect can make any repair more difficult.
The component separation technique (CST) developed and popularised in the early 1990 s allows large abdominal wall defects to be repaired without the need for bridging mesh [
4]. It achieves this through the medial advancement of abdominal wall muscles via the release of surrounding tissue planes, favouring fascial closure [
5]. In anterior component separation (ACS), dissection is performed in the subcutaneous plane, and the external oblique aponeurosis incised lateral to the rectus sheath facilitating closure of the hernial defect [
6]. In posterior component separation with transversus abdominis release (PCSTAR) a more recent modification - the retro-rectus space is developed and the transversus abdominis muscle released at its insertion. This creates a large, well-vascularised space for mesh placement, often avoiding the need for subcutaneous dissection. The technique allows closure of large midline defects with reduced risk of wound morbidity compared with ACS, especially in obese and multi-morbid patients [
7].
A previously published meta-analysis compared ACS and PCSTAR in terms of wound complications and recurrence rates; however, considerable debate remains within the surgical community regarding the optimal technique [
8]. We performed an updated meta-analysis, incorporating the latest published literature, to compare outcomes between ACS and PCSTAR.
Methods
Study design
The systematic review and meta-analysis were designed and conducted in accordance with the Cochrane Handbook for Systematic Reviews of Interventions and followed the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines for reporting [
9,
10].
Data sources and search strategy
A comprehensive search was conducted using various electronic databases and clinical trial registries, including PubMed, Scopus, Cochrane Central Register of Controlled Trials (CENTRAL), Google Scholar, ClinicalTrials.gov, ScienceDirect, and the Virtual Health Library (VHL). The search was performed by two independent reviewers. It used the following terms: ‘component separation’ AND (‘anterior component separation’ OR ‘posterior component separation’ OR ‘TAR release’) AND ‘transversus abdominis’ OR ‘TAR’ AND ‘ventral incisional hernia’ AND ‘midline hernia’. Additionally, the reference list of relevant studies was manually reviewed and interrogated to identify further published studies.
Study selection
Titles, abstracts, and full texts of the selected studies from the search were independently screened and scrutinised by two reviewers to assess their eligibility against our inclusion criteria. Studies comparing ACS with PCSTAR and published between January 1990 - June 2025 were included. Single-arm trials, case series, case reports, posters, letters to the editor, and review articles were excluded.
Studies reporting outcomes of the surgical techniques of interest (ACS with PCSTAR) were considered eligible for inclusion even if they included a mixed patient population (e.g., primary and recurrent hernias, or ventral and flank hernias). In such instances, inclusion was justified by the relevance of the comparative data reported, and potential heterogeneity was addressed through sensitivity analyses, where possible. Discrepancies between the reviewers regarding the inclusion of studies were resolved through consultation with the wider authorship team. Although the study was not prospectively registered on a systematic review registry such as PROSPERO [
11], it was conducted in accordance with PRISMA guidelines and adhered to Cochrane methodology to ensure transparency and quality.
Data extraction and collection
Two reviewers independently performed data extraction and collected the following information: name and details of the first author, year of study publication, country of origin, study design, total number of participants, patient characteristics/demographics, and study outcomes. Where disagreements arose during this process, a third author from the research team was consulted to reach a consensus.
Study outcomes
Our primary outcomes were postoperative complications (overall wound morbidity, surgical site infection (SSI), seroma and hematoma formation). SSIs were defined according to the National Healthcare Safety Network (NHSN, CDC 2022) criteria, which categorises SSIs into superficial incisional, deep incisional, and organ/space infections occurring within 30 days of the procedure (or within 90 days if prosthetic material is implanted), and meeting specific clinical, laboratory, or radiological findings [
12]. The overall wound morbidity equated to the sum of all wound complications, including SSI, hematoma, and seroma formation.
Our analysed secondary outcomes were: total operative time (minutes), length of hospital stay (LOS), and hernia recurrence rate. Recurrence was measured after complete wound healing and hospital discharge following the index procedure, and diagnosed clinically and/or radiologically.
Risk of bias assessment
The Cochrane risk of bias tool and the Newcastle-Ottawa Scale (NOS) assessed bias risk in the included RCTs and observational studies [
13]. Using the NOS scoring system, studies were categorised as low (score of 9), moderate (scores of 7 or 8), or high risk (scores less than 6). Any disagreements between assessors during this process were resolved by consulting an independent author.
For non-randomised studies, methodological quality was assessed using the Methodological Index for Non-Randomised Studies (MINORS) tool [
14]. This validated scoring system includes 12 items, each scored from 0 to 2, with a maximum possible score of 24 for comparative studies. Two reviewers independently scored each study, and any disagreements were resolved through discussion and reaching a consensus.
Discussion
We aimed to compare two surgical approaches (ACS & PCSTAR) in the management of large VHs. To our knowledge, this is the largest dataset (2,293 patients) available that provides a direct comparison with the exclusion of single-arm studies (done to prevent discrepancies in results due to mismatched patient characteristics).
The repair of large VHs remains challenging, and several prevention techniques, such as prophylactic mesh closure, have been described [
24,
25]. This study included patients with an abdominal wall defect >10 cm (width and/or length). To repair such sizeable defects, CST was introduced and subsequently modified [
26]. The principles of CST enable tissue dissection and approximation of fascial layers, and combined with the release of the transversus abdominis muscle, help create a space for mesh placement, providing further support and augmentation in VH repair. Several approaches to CS have been described in the literature [
27], including ACS and PCSTAR. However, there is ongoing debate and controversy surrounding the outcomes of these repairs, including the impact on quality-of-life metrics.
CST is associated with a high risk of developing post-operative wound issues [
28,
29]. In the present study, overall wound morbidity was 31.3% in the ACS group and 24.7% in the PCSTAR group. This difference was statistically significant, favouring the PCSTAR technique and in agreement with the findings of Oprea et al. [
8]. They reported lower overall wound morbidity in patients undergoing PCSTAR compared with ACS repair (28.5%). This was also reported in a retrospective study [
30], which identified 35 events of wound complications in 30 ACS patients. Lower wound complication rates utilising the PCSTAR technique have also been highlighted by Maloney et al. [
31].
This study found no significant difference in hematoma and seroma formation between the two groups. Seroma formation occurs in approximately 5% to 20% of patients undergoing hernia repair (dependent on surgical approach) [
32]. The placement of mesh and extensive tissue dissection have been suggested as possible causes for this phenomenon. The use of surgical drains may prevent fluid accumulation in the early postoperative period; however, the longer-term benefits are unclear [
33]. For secondary outcomes, both groups showed comparable results regarding total operative time, LOS, and hernia recurrence rates.
However, lower rates of SSI and overall wound complications were observed with the PCSTAR technique, contributing to more favourable patient outcomes. This is important as patients with VHs often have other co-morbidities (obesity, cardio-respiratory conditions). Therefore, surgical technique and its sequela can have detrimental and considerable effects on quality of life.
Cadaveric studies are available showing the length of fascial advancement achieved by these surgical approaches [
34‐
36]. For instance, Loh et al. [
34] compared cadaveric ACS vs. PCSTAR in ten cadavers with various ventral hernia defect sizes. They showed that ACS, on average, provided more medial advancement (35 mm) than PCSTAR (24 mm). This difference is thought to be related to the insertion of the external oblique muscle, providing a tethering effect compared to TAR, which inserts into the rectus sheath. Moreover, the dissecting plane between the external and internal oblique muscles allows more medial advancement of the rectus block compared with TAR.
However, data from a second cadaveric study [
35] showed conflicting results with an average advancement with ACS of 3.38 cm (+/- 0.69), PCS alone of 3.98 cm (+/- 0.94), increasing to 4.31 cm (+/- 0.89) with the addition of TAR (PCSTAR). A further study [
34] supported the addition of TAR release with the CS technique, increasing the advancement of the anterior rectus sheath by 102% and the posterior rectus sheath by 129% from baseline. These results may not necessarily translate into ‘live’ patient scenarios due to factors such as tissue elasticity, size, location of the abdominal wall defect, and abdominal wall compliance. Consequently, the absence of such data on the degree of fascial length achieved by the various surgical techniques makes it difficult to make robust recommendations and draw conclusions. Future, well-designed RCTs are necessary to compare these techniques directly, incorporating intra-operative measurements of tissue advancement as a key parameter. Furthermore, they can address the heterogeneity originating from differences in patient selection and provide clearer guidance on technique selection based on the size of the hernial defect.
Another challenge for patients presenting with large VHs is often the presence of co-morbidities that can prolong post-operative recovery and complicate preoperative assessment. These include cardio-respiratory conditions, diabetes, morbid obesity, or malnutrition (Table
2).
Delays in surgical repair may lead to further enlargement of the abdominal viscera, increasing the size of the hernial defect and causing loss of domain [
36]. This added complexity can make the surgical procedure even more challenging and the post-operative recovery more difficult. Preoperative measures, such as Botox injection and pneumoperitoneum, have been proposed to expand the abdominal cavity, allowing for more medial advancement of the fascial layers [
37,
38].
In the present study, the recurrence rates were 4.2% in the ACS group and 5.3% in the PCSTAR group (
P = 0.31). Although these rates are encouraging, they should be interpreted with caution due to the short follow-up period in some included studies [
22].
The use of mesh augmentation in abdominal wall reconstruction (AWR) helps to reduce recurrence [
39]. However, there is debate over the type of mesh, mesh size, and area of coverage. Different mesh sizes were used in our included studies (Table
2), and the mesh-to-defect ratio remains an important consideration when selecting mesh type. Mesh positioning and fixation sites are other challenges encountered during these repairs [
40].
This study is not without its limitations. Firstly, the nature of the included studies introduces considerable bias and may contribute to increased heterogeneity. Another drawback is the limited data available on the length of fascial advancement achieved through retro-fascial dissection or TAR release, which could help towards a more consistent approach based on defect size. Additionally, short follow-up periods in some studies may impact the validity and generalisability of outcomes, such as recurrence rates.
Moreover, only three RCTs were included in our analysis, all of which carried a moderate risk of attrition bias. The lack of standardised surgical techniques and differences in surgical approaches between centres likely introduces heterogeneity and influences outcomes, further emphasising the need for future well-designed RCTs.
Two included studies had specific design features that could introduce between-study heterogeneity. Toma et al. [
22] included both primary and recurrent ventral hernias and had a relatively short follow-up period (3 months). This may underestimate the actual recurrence rate, and has to be considered when interpreting our findings. Additionally, Maloney et al. [
20] included a proportion of patients with both flank and ventral hernias. Although sensitivity analyses (conducted through excluding these studies) showed no meaningful change in the direction of pooled outcomes, these design elements may well influence effect estimates and again need to be considered when interpreting study results.
Lastly, this study did not address patient quality of life parameters and metrics, necessitating the need for long-term follow-up and patient-led surveys to understand post-operative issues and challenges.
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