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Non-penetrating mesh fixation may reduce pain and hematoma risk in laparoscopic groin hernia repairThe Hernia Fix That Skips the Staples — Does It Actually Work?

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Key Takeaway
Consider non-penetrating fixation may reduce pain and hematoma, but evidence is very uncertain.

This systematic review analyzed 35 randomized controlled trials involving 4329 participants, predominantly men (94%) with a mean or median age ranging from 37 to 66 years, undergoing laparoscopic groin hernia repair for generally primary unilateral inguinal hernias. It compared non-penetrating mesh fixation (using fibrin sealant, cyanoacrylate glue, or self-adhesive mesh) to penetrating mesh fixation (with permanent staples, permanent tacks, absorbable tacks, or sutures), assessing outcomes such as chronic pain at ≥6 months and recurrence at ≥12 months postoperatively.

Main results showed little to no difference in risk for chronic pain (dichotomous: RR 0.62, 95% CI 0.35 to 1.07) and recurrence (RR 0.75, 95% CI 0.33 to 1.67). However, non-penetrating fixation may reduce the level of chronic pain (continuous: MD -0.34, 95% CI -0.56 to -0.11) and acute pain (continuous: MD -0.90, 95% CI -1.31 to -0.49), and may lower hematoma risk (RR 0.43, 95% CI 0.24 to 0.78) and convalescence (dichotomous: RR 1.49, 95% CI 1.10 to 2.01; continuous: MD -0.81, 95% CI -1.38 to -0.23). Other outcomes, including mesh infection, operative time, and serious vascular intraoperative events, showed little to no effect, with wide confidence intervals indicating uncertainty.

Safety and tolerability data were not reported. Key limitations include some concerns or high risk of bias in most outcomes due to missing randomization information or insufficient reporting of missing data, and imprecision from few events, wide confidence intervals, or small populations. The evidence has very low certainty for most outcomes and low certainty for serious vascular intraoperative events, with no dedicated funding reported. In practice, this suggests little to no difference in clinically important outcomes between fixation methods, but associations are uncertain and cannot establish superiority.

Why this question kept coming up

Laparoscopic (keyhole) hernia repair is now the gold standard. During surgery, doctors place a small mesh patch over the weak spot to reinforce it. Most surgeons then attach that mesh using tacks or staples — tiny fasteners that grip the tissue.

The problem? Those tacks and staples can press on nearby nerves. And that pressure is thought to be one reason some patients still feel groin pain months after surgery.

Non-penetrating fixation — using surgical glue or a self-adhesive mesh — doesn't pierce the tissue at all. In theory, no piercing means less nerve irritation and less long-term pain.

The old approach — and why it's being questioned

For years, surgeons assumed that if you didn't firmly anchor the mesh, it might shift. And a shifted mesh could mean the hernia comes back.

But here's the twist: glue holds things together too. It just works differently — like two puzzle pieces held by adhesive instead of screws. The patch bonds to the tissue without any sharp points pressing into nerves.

Researchers wanted to know: does glue work as well as staples at keeping hernia repairs intact? And does it actually reduce pain?

How these two methods stack up

Think of it like two ways to hang a picture. Staples punch into the wall and grip hard. Glue bonds the surfaces without any holes. Both can hold the picture — but one is a lot less invasive to the wall.

In hernia repair, "the wall" is living tissue threaded with nerves. Anything that pierces it has the potential to cause lasting sensitivity. Glue sidesteps that problem entirely.

What the review covered

Researchers pooled data from 35 randomized controlled trials — the gold standard of medical research — involving 4,329 adults, mostly men, who had laparoscopic groin hernia surgery. They compared penetrating methods (tacks, staples, sutures) against non-penetrating methods (fibrin glue, cyanoacrylate glue, self-adhesive mesh). The review was published in the Cochrane Database of Systematic Reviews in April 2026.

For the two most important outcomes — chronic pain (pain lasting six months or more after surgery) and hernia coming back — neither method came out clearly on top. The risk of long-term pain was similar between groups, and so was the rate of recurrence (the hernia returning).

When it came to pain scores on a scale — rather than just yes or no — glue showed a small advantage. Patients in the glue group reported slightly lower pain levels both right after surgery and months later. Glue was also linked to fewer bruising events (hematomas) and a slightly shorter recovery time. These results are promising, but all were rated as very low-certainty evidence.

That means the findings could change significantly as better studies are done.

The honest picture on evidence quality

This is where things get interesting — and important. The researchers rated the certainty of evidence as "very low" for almost every outcome. That's not because the results were bad. It's because many of the 35 trials had gaps in their methods, incomplete data reporting, or were too small to draw firm conclusions.

In medical research, "very low certainty" is a flag that says: this is the best data we have right now, but it may not reflect the full truth.

If you're scheduled for laparoscopic hernia repair, this review is worth knowing about — but it doesn't give you a clear directive yet. Both glue and staples remain accepted options. There is no strong evidence that one is dramatically better than the other for preventing hernia recurrence.

What's worth asking your surgeon: what fixation method they typically use, and whether glue might be appropriate for you — especially if you're worried about long-term nerve pain.

Limitations worth knowing

Most participants in these trials were men with primary, uncomplicated hernias. Women and people with more complex cases were underrepresented. The studies were also conducted across many different countries using slightly different techniques, which makes direct comparisons tricky.

More well-designed trials with clearer methods and longer follow-up are needed before surgeons can confidently recommend one method over the other. The good news is that both approaches appear to be safe. As more high-quality data accumulates, future guidelines may be able to give patients and surgeons a clearer, more personalized answer.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Rationale Groin hernia is a common condition, and the only curative treatment is an operation where laparoscopic groin hernia repair is the recommended choice. During laparoscopic repair, a mesh is placed in the groin, which many surgeons choose to fixate, but the best fixation method regarding chronic pain and recurrence has not been established. Theoretically, non‐penetrating mesh fixation (glue or self‐adhesive mesh) could result in a lower risk of chronic pain, while penetrating mesh fixation (tacks, staples, and sutures) could give a reduced risk of recurrence. Objectives To assess the benefits and harms of penetrating versus non‐penetrating mesh fixation in adults undergoing laparoscopic groin hernia repair. Search methods We searched CENTRAL, MEDLINE Ovid, Embase Ovid, ClinicalTrials.gov, and the WHO International Clinical Trial Registry Platform. Additionally, we performed reference checking, forward and backward citation searching, and contacted study authors to identify eligible studies. The latest search date was 14 November 2024. Eligibility criteria We included randomised controlled trials (RCTs) that compared non‐penetrating (glue or self‐adhesive mesh) with penetrating (tacks, staples, and sutures) mesh fixation in laparoscopic groin hernia repair in adults. Outcomes The critical outcomes were chronic pain measured ≥ 6 months postoperatively and recurrence assessed ≥ 12 months postoperatively. Other important outcomes were acute pain, haematoma, mesh infection, serious vascular intraoperative events, operative time, and convalescence. Risk of bias We used the RoB 2 tool to assess the risk of bias for chronic pain (dichotomous and continuous), recurrence, acute pain (dichotomous and continuous), haematoma, mesh infection, serious vascular intraoperative events, operative time, and convalescence (both dichotomous and continuous). Synthesis methods We synthesised results for each outcome using meta‐analysis where possible by applying a random‐effects model, calculating the risk ratio (RR) using the Mantel‐Haenszel method for dichotomous data and calculating the mean difference (MD) using the inverse‐variance method for continuous data, along with 95% confidence intervals (CIs). Where this was not possible due to the nature of the data, we synthesised the results narratively. We used GRADE to assess the certainty of evidence for each outcome. Included studies We included 35 RCTs with 4329 participants. The studies randomised 2028 participants to non‐penetrating mesh fixation and 2301 participants to penetrating mesh fixation, with a median sample size of 82 (range 30 to 600 participants). The mean or median age ranged from 37 to 66 years, and the majority (94%) were men. In general, the operated hernias were primary unilateral inguinal hernias. Most of the non‐penetrating mesh fixation was fibrin sealant and cyanoacrylate glue, and most of the penetrating mesh fixation was permanent staples, permanent tacks, or absorbable tacks. Synthesis of results RoB 2 assessment Regarding the overall risk of bias, most of the outcomes had some concerns or a high risk of bias. This was mostly due to missing information regarding the randomisation process, insufficient reporting of missing outcome data, or both. GRADE We assessed the certainty of evidence to be very low for most outcomes. This was mainly due to high or unclear risk of bias or due to imprecision because of few events, a wide confidence interval, or a small population. Critical outcomes Non‐penetrating mesh fixation may result in little to no difference in the risk of chronic pain (RR 0.62, 95% CI 0.35 to 1.07; I² = 9%; 7 studies, 553 participants; very low‐certainty evidence) and recurrence (RR 0.75, 95% CI 0.33 to 1.67; I² = 0%; 15 studies, 2165 participants; very low‐certainty evidence), but the evidence is very uncertain. Non‐penetrating mesh fixation may reduce the level of chronic pain (continuous), but the evidence is very uncertain (MD −0.34, 95% CI −0.56 to −0.11; I² = 98%; 7 studies, 639 participants; very low‐certainty evidence). Important outcomes Non‐penetrating mesh fixation may have little to no effect on the risk of acute pain (dichotomous) (RR 0.93, 95% CI 0.50 to 1.73; I² = 56%; 2 studies, 218 participants; very low‐certainty evidence). Non‐penetrating mesh fixation may reduce the level of acute pain (continuous) (MD −0.90, 95% CI −1.31 to −0.49; I² = 98%; 16 studies, 1611 participants; very low‐certainty evidence), the risk of haematoma (RR 0.43, 95% CI 0.24 to 0.78; I² = 0%; 19 studies, 2560 participants; very low‐certainty evidence), convalescence (RR 1.49, 95% CI 1.10 to 2.01; I² = 94%; 9 studies, 1116 participants; very low‐certainty evidence), and the length of convalescence (MD −0.81, 95% CI −1.38 to −0.23; I² = 80%; 7 studies, 589 participants; very low‐certainty evidence), but the evidence is very uncertain. Non‐penetrating mesh fixation may have little to no effect on the risk of mesh infection (RR 0.34, 95% CI 0.01 to 8.23; I² not applicable; 5 studies, 1128 participants; very low‐certainty evidence) and operative time (MD −0.26, 95% CI −3.11 to 2.59; I² = 94%; 20 studies, 1800 participants; very low‐certainty evidence), but the evidence is very uncertain. Lastly, non‐penetrating mesh fixation may result in little to no difference in serious vascular intraoperative events (RR 0.18, 95% CI 0.02 to 1.57; I² = 0%; 9 studies, 1289 participants; low‐certainty evidence). Authors' conclusions There may be little to no difference between non‐penetrating and penetrating mesh fixation regarding the risk of chronic pain (dichotomous), recurrence, acute pain (dichotomous), mesh infections, and operative time, but the evidence is very uncertain. Non‐penetrating mesh fixation may result in little to no difference in serious vascular intraoperative events. While the evidence is very uncertain, non‐penetrating mesh fixation may slightly reduce the level of chronic pain (continuous), the level of acute pain (continuous), and the risk of haematoma, and shorten convalescence (dichotomous and continuous). Overall, this review demonstrated little to no difference in clinically important outcomes between penetrating and non‐penetrating mesh fixation in laparoscopic groin hernia repair in adults, based on low‐ to very low‐certainty evidence. Funding This Cochrane review had no dedicated funding. Registration Protocol available via DOI: 10.1002/14651858.CD016122. PICOs PICOs Population Intervention Comparison Outcome
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