Discussion
We present a meta-analysis comparing Veress needle entry with direct trocar entry in gynecologic surgery. Our results demonstrate that the use of Veress needle entry is associated with a significantly higher incidence of extraperitoneal insufflation compared with direct trocar entry. Veress needle has significantly higher incidences of complications, including failed entry, omental injury, and insertion site infection. These results demonstrate that there is no difference between both groups regarding visceral injury.
The small diameter of the Veress needle contributed to the hypothesis that the Veress needle could have a less significant injury to intra-abdominal structures, such as blood vessels and bowel.25 However, this meta-analysis revealed that the Veress needle actually may have an association with higher risk of omental and vessel injury in addition to a higher incidence of failed entry. Ultimately, injuries to major vessels at the time of laparoscopy are still a leading cause of death in laparoscopic surgeries.
In our assessment, incorrect placement of the needle seemed to be the major cause of these injuries.26 In many discussions regarding the tests to determine the correct needle insertion, there seemed to be agreement that the ‘drop’ test (intra-abdominal pressure vs saline within the Veress needle) seemed to be the most reliable. Also, one author discussed how preoperative insufflation was associated with subsequent difficulty in primary trocar insertion as well as failed entry, which indicates that these two outcomes were likely related.27
One of the largest meta-analyses related to this topic was recently performed including 51 studies, with 134 917 patients in the Veress needle group and 16 739 patients in the direct trocar group. The study identified a total of 10 deaths. Although outnumbering the direct trocar group by about eight to one, the study still found that all entry-related deaths were in the Veress needle group. The other deaths were attributed to non-specified causes such as gas embolism.26 Another study in 2021 performed an analysis of seven randomized trials, showing that the Veress needle carries a significant risk of minor complications and is associated with a high incidence of failed entry, which is consistent with our results.28
A Cochrane review was performed to compare the different laparoscopic entry techniques. This review included 57 randomized controlled trials with a total of 9865 patients undergoing laparoscopy. The study revealed that the DTI was associated with a significant reduction in failed entry compared with Veress needle. There was no significant difference between the two groups regarding the other minor complications.29 The review also compared direct visualization entry versus Veress needle, but the evidence was insufficient to show a difference between the groups. Another meta-analysis by Merlin et al demonstrated that there is a reduced risk of minor complications in open entry compared with the Veress needle entry. This may be a reason why many authors have reported an increase in open laparoscopy technique in recent years.30
When observing the incidence of extraperitoneal insufflation, the 2013 trial by Angioli19 et al demonstrated that this complication was reported more often following Veress needle entry. These conclusions match earlier findings by Günenç et al and Zakherah.12 22 It was also found that both open entry and direct access entry were associated with fewer incidences of minor complications than Veress needle entry.19 These findings were later corroborated by another study in an obese only population from Kassir et al.31
Strengths
This study represents the most recent and conclusive evidence about the safety of direct access entry vrsus Veress needle entry for laparoscopy. We performed a large-scale analysis of all the recent published literature, including 3420 patients undergoing laparoscopic surgery. In addition, we have included only controlled trials to ensure the most precise evidence according to Cochrane guidelines. Another strength of this analysis was the homogeneity between the measured outcomes, which eliminated the need to solve for heterogeneity in all outcomes.
Limitations
Four of the included studies reported inadequate data about allocation concealment. Unclear allocation concealment in controlled trials may bias the results of subjectively determined outcomes in favor of a beneficial effect. Another limitation is that one study was blinded to the participants and personnel, while six studies did not report adequate data to determine blinding. Finally, our study did not consider surgeon experience or the learning curve involved in these techniques. As a result, our conclusions apply across the field generally and may not be applicable for individual experience groups, such as beginners or high-volume experts, for whom different complication rates may apply.