Efficacy of intraperitoneal positive pressure gas expulsion in laparoscopic transabdominal preperitoneal hernioplasty: a retrospective cohort study
Wanpeng He, Bo Chen

TL;DR
A new technique for hernia surgery may improve recovery and reduce complications by removing gas from the surgical area.
Contribution
The study introduces a positive-pressure gas expulsion technique to improve mesh fixation and postoperative outcomes in hernia repair.
Findings
The exhaust group had a significantly shorter hospital stay compared to the direct suture group.
The exhaust group showed a 0% recurrence rate at 1-year follow-up, compared to 1.32% in the direct suture group.
The technique reduced the incidence of seroma and mesh infection, though not statistically significant.
Abstract
To investigate the effects of the pneumoperitoneum positive-pressure exhaust technique on mesh fixation and postoperative recovery in laparoscopic transabdominal preperitoneal prosthetic (TAPP) hernia repair. A retrospective cohort analysis was conducted on 655 patients who underwent TAPP between January 2019 and December 2023. Patients were divided into a direct suture group (n=304) and a positive-pressure exhaust group (n=351) on the basis of preperitoneal space management. In the exhaust group, a 20G needle or drainage tube was placed percutaneously before peritoneal closure. After suturing, 12 mmHg pneumoperitoneum pressure was maintained to evacuate residual gas from the preperitoneal space through the externalized needle/tube. The primary outcomes included postoperative complications (bleeding, mesh infection, seroma, reoperation) and hospitalization duration. Baseline…
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Taxonomy
TopicsHernia repair and management · Pelvic and Acetabular Injuries · Abdominal Surgery and Complications
Introduction
Laparoscopic transabdominal preperitoneal prosthetic (TAPP) repair has become the predominant approach for inguinal hernias because of its minimally invasive nature and rapid recovery benefits. However, postoperative recurrence rates remain at 0.4%−8.5% [1]. Studies indicate that mesh displacement and folding are key contributors to surgical failure [2, 3]. Conventional fixation methods—including tacks, sutures, and biological adhesives—present significant limitations: mechanical fixation may lead to chronic pain or intestinal perforation [4, 5]; suturing prolongs the operative time and carries risks of neural injury [6–8]; and, despite their safety profile, biological adhesives incur high costs [6].
Although mesh fixation-free techniques are well established for totally extraperitoneal (TEP) repair [9–11], their application in TAPP remains controversial. This stems primarily from the dual-cavity structure formed by the abdominal and preperitoneal spaces, which predisposes patients to gas retention, compromising mesh-wall apposition and increasing displacement risk [12].
To address this challenge, we propose a novel technique: intraoperative maintenance of 12 mmHg pneumoperitoneum pressure to actively expel residual gas from the preperitoneal space, achieving three-dimensional fixation through friction among the peritoneum, mesh, and abdominal wall. This approach potentially offers three advantages:
- Real-time visualization of mesh positioning to prevent folding/displacement
- Elimination of additional consumables, reducing costs
- Avoidance of foreign body-related complications
As long-term outcomes of comparable techniques remain unreported, we conducted this large-scale retrospective study (n=655) to evaluate the efficacy of positive-pressure gas expulsion on mesh fixation and postoperative recovery, providing new evidence for preperitoneal space management in TAPP procedures.
Materials and methods
Data collection
The clinical records of patients who underwent laparoscopic transabdominal preperitoneal prosthetic (TAPP) repair from January 2019 to December 2023 were retrospectively reviewed.
Inclusion criteria
- Unilateral/bilateral inguinal hernia confirmed by physical examination, ultrasonography, or other imaging, scheduled for elective TAPP
- Age >18 years
- Complete medical documentation
Exclusion criteria
- Concurrent groin pathologies requiring treatment during TAPP (e.g., varicocele, hydrocele, cryptorchidism)
- Recurrent hernias undergoing TAPP repair
- Patients converted to open surgery
- Patients initially scheduled for TEP repair but switched to TAPP
- Combined procedures involving other anatomical sites or organs
Surgical protocol
Preoperative evaluation
All patients underwent diagnostic imaging and physical examination. Those with comorbidities (diabetes, COPD, chronic hepatitis, etc.) received specialist evaluations. Patients with uncontrolled baseline conditions or acute exacerbations underwent optimization prior to final anaesthetic assessment.
Surgical technique
Standard laparoscopic dissection of the myopectineal orifice was performed. Mesh size selection followed the EHS classification:
- Type I-II defects: 8.5×13.7 cm
- Type III defects: 15×10 cm(Bard 3DMax Mesh, Davol Inc.; NMPA registration no. 20173461504)
Key steps
- For internal ring defects ≥2 cm: Continuous 2-0 barbed suture (Stratafix, Ethicon) closure; if tension was excessive, the ring was reduced to <3 cm in diameter.
- Direct suture group: Peritoneal closure with 3-0 barbed suture, CO₂ evacuation after fascial closure.
- Positive-pressure exhaust group:
- Presuture: A 20G needle was inserted at the lateral 1/3 of the line between the ASIS and the umbilicus (avoiding inferior epigastric vessels) without penetrating the mesh.
- Postsuture: A 12 mmHg pneumoperitoneum was maintained to evacuate residual preperitoneal gas through the needle.
- The mesh position was verified laparoscopically before needle removal, with final aspiration.
- Drain placement (F12 tube):
- ◦ Positioned in the dependent preperitoneal space
- ◦ Opened postperitoneal closure under laparoscopic visualization to confirm mesh apposition
- ◦ Connected to suction for 48–72 hours
Drain Indications:
- Difficult peritoneal dissection with significant bleeding/exudate
- Bilateral TAPP or large operative field
- Coagulopathy (e.g., cirrhosis, dialysis) or ascites
- High infection risk (diabetes, HIV, COPD)
Follow-up protocol
- In-person visits: 1 week, 1 month, and 2 months postop
- Telephone follow-up at 1 year
- Evaluations included physical examination, pain assessment, and functional recovery
- Ultrasound/CT for symptomatic patients (pain, palpable masses)
Statistical analysis
The data were analysed using SPSS 22.0.
- Continuous variables: median (IQR) [M(P25, P75)]; Mann‒Whitney U test
- Categorical variables: frequency [n(%)]; χ^2^ test or Fisher’s exact test
- Significance threshold: P<0.05
Results
General data
No significant differences were observed in age, sex, or preoperative comorbidities between the two groups (p>0.05), as shown in Table 1. Table 1. Comparison of baseline characteristics between groupsCharacteristics****Direct suture group (n=304)****Positive pressure group (n=351)****Statistical valueP** value**Sex [n (%)]**χ^2^=0.2540.614 Male298 (98.03)342 (97.44) Female6 (1.97)9 (2.56)Age [years, median (IQR)]63 (61–68)66 (60–69)Z=−1.5150.130Comorbidities [n (%)] Diabetes mellitus21 (6.91)30 (8.55)χ^2^=0.6100.435 COPD23 (7.57)27 (7.69)χ^2^=0.0040.952 Liver cirrhosis9 (2.96)17 (4.84)χ^2^=1.5150.218 Coronary heart disease23 (7.57)20 (5.70)χ^2^=0.9270.336 Autoimmune disease7 (2.30)11 (3.13)χ^2^=0.4210.516 Chronic kidney disease16 (5.26)15 (4.27)χ^2^=0.3540.552Data are presented as “n (%)” for categorical variables; continuous data are presented as medians (IQRs) because of their nonnormal distribution (Shapiro‒Wilk test, P<0.05). Group comparisons were performed using χ^2^ tests for categorical data and the Mann‒Whitney U test (reported as Z values) for nonnormally distributed continuous variablesCOPD Chronic obstructive pulmonary disease
Intraoperative data
This table compares the intraoperative variables between the direct suture group and the positive pressure gas expulsion group. The positive pressure group presented significantly higher internal ring closure rates (64.10% vs. 53.29%, P=0.005), whereas other parameters, including operative time, blood loss, and drain placement, were comparable between the groups (all P>0.05), as shown in Table 2. Table 2. Intraoperative outcomes comparison between groupsVariables****Direct suture group (n=304)****Positive pressure group (n=351)****Statistical valueP** value****Surgical side [n (%)]**χ^2^=0.2370.626 Unilateral268 (88.16)305 (86.89) Bilateral36 (11.84)46 (13.11)**Internal ring closure [n (%)]**χ^2^=7.8970.005 Yes162 (53.29)225 (64.10) No142 (46.71)126 (35.90)**Drain placement [n (%)]**χ^2^=0.0050.946 Yes116 (38.16)133 (37.89) No188 (61.84)218 (62.11)**Operative time [min, median (IQR)]70 (62–78)70 (66–78)Z=−0.6810.496Blood loss [ml, median (IQR)]**5 (5–15)5 (5–15)Z=−0.4950.620Data are presented as “n (%)” for categorical variables; continuous data are presented as medians (IQRs) because of their nonnormal distribution (Shapiro‒Wilk P<.05). Group comparisons were performed using χ^2^ tests for proportions and Mann‒Whitney U tests (reported as Z values) for nonnormally distributed continuous variables (operative time and blood loss)
Postoperative data
The positive pressure group had no patients who required reoperation. In the direct suture group, 8 patients experienced postoperative bleeding (4 with preperitoneal haemorrhage, 2 with umbilical port site bleeding, and 2 with lateral abdominal wall port bleeding). Among these patients, 2 developed preperitoneal haematomas requiring laparoscopic evacuation (1 from spermatic vessel bleeding and 1 from diffuse oozing without an identifiable source), with 1 patient developing recurrent hernia at 7 months postoperatively.
The positive pressure group included 5 cases of bleeding (1 preperitoneal, 2 umbilical ports, and 1 lateral port), all of which were managed successfully with drainage and haemostatic therapy. In the direct suture group, 4 patients developed mesh infection; 2 patients required mesh removal due to failed antibiotic/drainage therapy, and both of them experienced hernia recurrence at 3 and 5 months postoperatively. The positive pressure group had only 1 mesh infection case that resolved with conservative treatment.
Recurrence within 1 year occurred in 4 direct suture cases (1.32%) but not in the positive pressure group (P=0.054, Fisher’s exact test). Type III-IV seromas developed in 51 direct suture cases (16.78%), with 14 requiring percutaneous drainage, compared with 42 cases (11.97%) in the positive pressure group (P=0.079). No significant differences were observed in overall complication rates or reintervention needs (P>0.05), but the positive pressure group had significantly shorter hospitalizations (median 7 [IQR 6–9] vs. 7 [5–10] days, P=0.013), as shown in Table 3. Table 3. Comparison of postoperative recovery outcomes between groupsOutcomes****Direct suture group (n=304)****Positive pressure group (n=351)****Statistical valueP** value****Postoperative complications [n (%)]** Bleeding8 (2.63)5 (1.42)χ^2^=1.2200.269 Mesh infection4 (1.32)1 (0.28)Fisher’s exact0.189 Seroma (type III-IV)51 (16.78)42 (11.97)χ^2^=3.0940.079 Hernia recurrence4 (1.32)0 (0)Fisher’s exact0.054 Reoperation4 (1.32)0 (0)Fisher’s exact0.054**Postoperative drainage [n (%)]14 (5.92)15 (4.27)χ^2^=0.9240.336Hospital stay [days, median (IQR)]**7 (5–10)7 (6–9)Z=−2.4920.013Data are presented as “n (%)” for categorical variables; continuous data are presented as medians (IQRs) because of their nonnormal distribution (Shapiro‒Wilk P<.05). Group comparisons were performed using χ^2^ tests or Fisher’s exact test (for outcomes with expected cell counts <5) for categorical data and the Mann‒Whitney U test (reported as the Z value) for continuous variables. A type III-IV seroma is a clinically significant seroma requiring intervention
Discussion
Key determinants of TAPP surgical outcomes
The success of TAPP primarily hinges on two critical factors: (1) complete anatomical coverage of the myopectineal orifice by the mesh and (2) rapid adhesion formation at the mesh‒tissue interface. In the present study, we identified preperitoneal space stability as the pivotal element governing these outcomes. Given the limited mechanical strength of peritoneal tissue (average thickness: 0.1–0.3 mm), postoperative bleeding or fluid accumulation may increase intracavitary pressure, causing peritoneal tenting and subsequent mesh deformation/migration. More significantly, residual CO₂-induced “gas pocket effects” substantially delay tissue adhesion, creating a window for early mesh displacement [13–15].
Evolution of fixation-free techniques
Although some studies suggest that nonfixation mesh placement in TAPP does not increase recurrence or complications [9, 16, 17], most studies lack detailed technical descriptions regarding the management of the dead space between the mesh, peritoneum, and abdominal wall. This knowledge gap has hindered widespread adoption. Claus et al. [18] demonstrated through radiographically marked meshes that early post-TEP mobilization (including leg raising) does not cause mesh displacement, thereby reducing postoperative pain and bleeding risks—a conclusion corroborated by Yilmaz [19]. This stability likely stems from the inherent negative-pressure environment of TEP, which eliminates dead space and generates bidirectional frictional forces. Soeta’s technique [20] of preperitoneal negative-pressure aspiration, which provides real-time visual confirmation of mesh apposition, inspired our methodology.
Mechanistic advantages of positive-pressure exhaust technique
Our innovation creates two isolated compartments (mesh space vs. the abdominal cavity) and utilizes 12 mmHg pneumoperitoneum to actively evacuate preperitoneal gas via needles/drains, resulting in the following:
- Triple fixation mechanism(under laparoscopic visualization):
- ◦ Negative-pressure adhesion at the peritoneum‒mesh interface (via drainage)
- ◦ Frictional forces between the mesh and the abdominal wall [21]
- ◦ Elimination of potential displacement spaces
- Higher internal ring closure rate (64.10% vs. 53.29%, P= 0.005), reducing dead space and enhancing mesh support.
Clinical outcomes and comparative analysis
In our series of 655 TAPP cases, the positive-pressure group showed clinically meaningful (albeit statistically nonsignificant) improvements:
- Seroma (11.97% vs. 16.78%, P= 0.079)
- Mesh infection (0.28% vs. 1.32%, P = 0.189)
Notably, the zero recurrence rate at the 1-year follow-up (vs. 1.32% in controls) outperformed Mayer’s reported rate of 1.1% [17]. The incidence of seroma in the control group (16.78%) slightly exceeded that reported by Saini (14.1%) [22], whereas the study group (11.97%) demonstrated marked improvement. A statistically significant reduction in hospitalization duration (median 7 vs. 7 days, P=0.013) reflected technical refinements.
Re-evaluation of the drainage strategy
Contrary to the literature neglect, our 35% drainage utilization proved critical:
- Managed 2 preperitoneal haemorrhages and 2 mesh infections in controls
- Resolved 1 haemorrhage and 1 infection in the study group
- Undrained cases exhibited delayed complication recognition
Supporting evidence
Fang/Luo [23, 24] reported reduced seroma rates and enhanced scrotal hernia recovery, whereas Fan/Prassas [25, 26] confirmed no increased infection risk with short-term drainage (<48 h). Negative-pressure systems may further promote early mesh incorporation.
Technical comparisons and safety
Traditional transabdominal suction methods carry risks:
- Peritoneal laceration
- Mesh exposure
- Internal herniation through peritoneal defects [5, 15–17]
- Uncontrolled suction-induced microvascular injury
Our pressure-regulated exhaust technique avoids these pitfalls while matching Soeta’s aspiration [20] in space reduction. The higher internal ring closure rate—a previously underappreciated factor—minimizes residual sac pressure effects on the preperitoneal space.
Conclusions and limitations
This technique offers three advantages:
- Real-time mesh positioning assessment
- Multimodal fixation without additional devices
- Simplified dead space management
The study limitations include the following:
- Potential selection bias inherent to retrospective design
- Intermediate-term (1-year) recurrence follow-up
- Exclusive use of Bard 3DMax heavyweight mesh—lightweight mesh applicability requires further study
- Potential bias from high internal ring suture rates and frequent drain use in this cohort
