DGE is a common and frustrating complication that may occur after pancreaticoduodenectomy, although it is typically not life threatening. In most cases, DGE resolves spontaneously either with or without prokinetics, but it often requires several weeks or more of conservative management through NGT drainage [20]. However, DGE has a significant impact on the patient’s quality of life, prolongs the hospital stay, and increases hospital costs [11]. The incidence of DGE following pancreaticoduodenectomy is quite high, ranging from 4.5–56.1% [5–8], leading the ISGPS to propose a consensual definition of DGE in 2007 that is composed of a three-grade classification [16]. The exact pathogenesis of DGE is poorly understood and believed to involve multiple factors [7, 8, 14, 21–23]. Avoidance of stomach distention, postoperative nausea, vomiting, aspiration pneumonia, and wound dehiscence are some of the rationales behind the practice of routine placement of NGT following pancreaticoduodenectomy. Therefore, foregoing a NGT following pancreaticoduodenectomy has not been widely accepted by most pancreatic surgeons [11]. This reluctance could stem from the limited data available on this specific indication, the type of pancreatic anastomosis performed, and, notably, the high incidence of DGE associated with pancreaticoduodenectomy [5–8]. Nevertheless, the 2013 Enhanced Recovery After Surgery (ERAS®) guidelines strongly advised against preemptive use of nasogastric tubes postoperatively, as they did not improve outcomes and might impede recovery [24].
Given the high incidence of DGE after OPD, with rates ranging from 12–16%, as evidenced in our previous studies [4, 5, 15], NGT placement had been part of our routine practice following pancreaticoduodenectomy, including cases of both RPD and OPD, until March 2023. However, considering our observation of a low incidence of DGE in RPD, ranging from 3.4–4.4% according to our previous studies [4, 5], we decided to discontinue routine placement of NGT following RPD from March 2022 onwards. It is important to note that the NGT is now consistently removed in the operating room immediately after intratracheal extubation following RPD. In our previous study [5], we proposed three hypotheses to explain the lower incidence of DGE in patients who have undergone RPD. First, “food flow by gravity,” a relatively “vertical and straight” stomach position after extracorporeal hand-sewn gastrojejunostomy via a small umbilical wound might facilitate food passage downward. Second, “separation of inflammation,” “inframesocolic, antecolic, and antiperistaltic (left-sided)” gastrojejunal anastomosis could keep the stomach away from the inflamed area above the mesocolon and transverse colon. Third, “less inflammation/adhesion” with a “smaller wound and less trauma” could result in less inflammation/adhesion.
In this PSM comparative study, we observed a significantly lower incidence of DGE in the RPD group, regardless of whether the patients had a NGT. The DGE rates were 3% in the RPD(-)NGT and 4% in RPD(+)NGT groups, whereas the OPD(+)NGT group had a higher DGE rate of 18%. We found that the LOS was also shorter in the RPD(-)NGT group, with a median duration of 17 days, compared to that in the other two groups: RPD(+) NGT (22 days) and OPD(+)NGT (26 days). After conducting a multivariate analysis, we identified that only the operation type, specifically OPD, remained an independent risk factor for predicting the occurrence of DGE. The findings of this study are consistent with the conclusions of Kunstman et al. [10] who compared routine and selective NGT gastric decompression. Their study demonstrated that patients in the selective group had a decreased incidence of DGE, LOS, and time to dietary tolerance. They concluded that routine postoperative nasogastric decompression in patients undergoing pancreaticoduodenectomy was unnecessary in many cases and could adversely affect the postoperative course. Another retrospective study by Gaignard, et al. [11] also supported these findings, suggesting that absence of systematic nasogastric decompression after pancreaticoduodenectomy might reduce postoperative complications, DGE, and LOS [11]. Based on the results of our current study, we propose that foregoing the placement of a NGT is a feasible approach in RPD cases.
Surgical outcomes, including mortality, Clavien–Dindo complication grades, and POPF, were comparable between the RPD(-)NGT, RPD(+)NGT, and RPD(+)NGT groups in this study. A retrospective study by Choi et al. [1] concluded that the routine insertion of a NGT in patients undergoing pancreaticoduodenectomy provided no advantages in terms of postoperative complications and could potentially increase the occurrence of postoperative pulmonary complications. Additionally, NGT insertion could cause discomfort to patients after surgery. Miyazawa et al. [3] suggested that no NGT management after pancreaticoduodenectomy could actually enhance the quality of life by reducing discomfort and allowing advancement to a fast-track program. In a randomized clinical trial by Bergeat et al. [25] studying nasogastric decompression vs. no decompression after pancreaticoduodenectomy, no significant difference was observed in the occurrence of postoperative complications classified as Clavien-Dindo classification grade II or higher between systematic NGT decompression and no decompression, indicating that avoiding systematic nasogastric decompression is safe. Kleive et al. [12] conducted a prospective observational study and concluded that routine use of NGT after pancreaticoduodenectomy was not justified within an ERAS setting. They demonstrated that immediate removal of the NGT after the procedure could be performed safely, and reinsertion on demand was rarely necessary during uncomplicated courses. Based on these findings, this study further supports the notion that foregoing a NGT has no negative impact on the safety of RPD cases.
This study was limited by the retrospective identification of the variables. Therefore, selection bias is inevitable despite attempts to mitigate this by using propensity score matching to mimic some characteristics of a randomized controlled trial.