|Ahead of print publication
EUS-guided pelvic drainage: A systematic review and meta-analysis
Banreet Singh Dhindsa1, Yassin Naga2, Syed Mohsin Saghir2, Amaninder Dhaliwal3, Daryl Ramai4, Chad Cross5, Shailender Singh1, Ishfaq Bhat1, Douglas G Adler6
1 Division of Gastroenterology and Hepatology, University of Nebraska Medical Center, 982000 Nebraska Medical Center, Omaha, NE, USA
2 Department of Internal Medicine, University of Nevada, Las Vegas School of Medicine, Las Vegas, NV, USA
3 Division of Gastroenterology and Hepatology, Moffitt Cancer Center, Tampa, FL, USA
4 Department of Internal Medicine, The Brooklyn Hospital Center, Brooklyn, New York, USA
5 Department of Biostatistics and Epidemiology, University of Nevada Las Vegas, Las Vegas, NV, USA
6 Department of Gastroenterology and Hepatology, University of Utah, School of Medicine, Huntsman Cancer Center, Salt Lake City, Utah, USA
|Date of Submission||29-May-2020|
|Date of Acceptance||28-Sep-2020|
|Date of Web Publication||12-Jan-2021|
Douglas G Adler,
University of Utah School of Medicine, Huntsman Cancer Center, 30 N 1900 E, Room 4R118, Salt Lake City, Utah 84132
Source of Support: None, Conflict of Interest: None
Background and Objectives: EUS-guided pelvic abscess drainage (EUS-PAD) is a procedure that utilizes an echoendoscope to visualize an area of interest for needle insertion and placement of a stent, catheter, or both for drainage of the target abscess. The aim of this study was to perform a systematic review and meta-analysis for the safety and efficacy of EUS-PAD. Materials and Methods: We conducted a comprehensive search of several databases and conference proceedings including PubMed, EMBASE, Google Scholar, MEDLINE, SCOPUS, and Web of Science databases (earliest inception to February 2020). The primary outcomes for this study were the technical and clinical success of EUS-PAD. The secondary outcomes assessed for this study were adverse events of the procedure and subgroup analysis of individual adverse events. Results: Eight studies with a total of 135 patients combined were included in our analysis. The rate of technical success was 100% and the calculated pooled rate of clinical success was 92% (95% confidence interval [CI]: 87%, 98%; P = 0.31; I2 = 15%). The calculated pooled rate of adverse events was 9.4% (±17.9%), with stent migration (5.5 ± 18.06%) being the most common adverse event. Conclusion: EUS-PAD offers a viable alternative that can minimize the need for surgical intervention in the drainage of pelvic abscesses. EUS-PAD has also demonstrated long-term clinical success with an acceptable rate of complications.
Keywords: abscess, drainage, EUS, meta-analysis, pelvic
|How to cite this URL:|
Dhindsa BS, Naga Y, Saghir SM, Dhaliwal A, Ramai D, Cross C, Singh S, Bhat I, Adler DG. EUS-guided pelvic drainage: A systematic review and meta-analysis. Endosc Ultrasound [Epub ahead of print] [cited 2021 Apr 21]. Available from: http://www.eusjournal.com/preprintarticle.asp?id=306749
| Introduction|| |
Pelvic abscesses may arise from several etiologies including surgery (e.g., low anterior resection), perforation of pelvic viscera, diverticulitis, appendicitis, ischemic colitis, inflammatory bowel disease, or from pelvic inflammatory disease, among other causes., Pelvic abscesses are associated with significant morbidity and mortality. Management, per the Infectious Diseases Society of America and Surgical Infection Society, includes a combination of medical and surgical therapies, of which drainage of the abscess is of utmost importance to obtain source control., Currently, computed tomography (CT)-guided percutaneous drainage (PCD) is the preferred method for drainage of pelvic abscesses. Other modalities include ultrasound (US)-guided transrectal drainage and surgical drainage.
Limitations of PCD and US procedures include, but are not limited to, catheter dislodgment, patient discomfort, and limited access points of fluid drainage secondary to the complexity of pelvic anatomy., EUS-guided pelvic abscess drainage (EUS-PAD) is an alternative minimally invasive procedure which can be used for drainage of pelvic abscesses. With EUS, one can usually target a pelvic abscess since most fluid collections are located close to the rectum and left colon.
EUS-PAD was first described by Giovannini et al. in 2003. The procedure utilizes an echoendoscope to visualize an area of interest for needle insertion and placement of a stent, catheter, or both for drainage of the target abscess. With utilization of this procedure, patients can achieve shorter durations of hospital stay leading to lower costs and a bedside procedure can be performed in critically ill patients if necessary.
The aim of this study was to perform a systematic review and meta-analysis for the safety and efficacy of EUS-PAD.
| Methods|| |
We performed a search of multiple databases including MEDLINE, EMBASE, Google Scholar, Cochrane, and Web of Science databases (earliest inception to February 2020). The literature search utilized a combination of keywords “EUS,” “endoscopic” and “ultrasound,” “pelvic,” “abscess,” and “drainage.” This search was carried out by two authors (BD and YN) who reviewed the titles and abstracts individually and excluded studies that did not meet the inclusion criteria. We conducted the search and narrowed down the final studies as per the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, as well as the Meta-Analysis of Observational Studies in Epidemiology guidelines to identify studies reporting on EUS-guided drainage of pelvic abscesses [Supplementary Figure 1 [Additional file 1]]. The bibliographic section of the selected articles, as well as the systematic and narrative articles on the topic, was manually searched for additional relevant articles.
We included studies that evaluated the clinical efficacy and adverse events of EUS-PAD. Studies were included as long as they provided data needed for the analysis. Exclusion criteria were as follows: (1) studies using other techniques of PAD other than EUS, (2) studies performed in the pediatric population (patient age <18 years) or among prisoners, (3) studies with <5 patients, and (4) studies not published in the English language.
We excluded multiple studies that reported on the same cohort. In case of overlapping cohorts, we included the most appropriate study.
Data abstraction and quality assessment
Two authors independently assessed (BD and SS) and performed quality assessment independently, and any differences were resolved with the help of the third author (YN).
Data collection was recorded as number of reported events (n) out of the total number of patients (N) from each study. The collected data were treated akin to single group cohort studies, and therefore, we used the Newcastle–Ottawa scale (NOS) to assess the quality of studies. This quality score is comprised of 3 categories and 8 questions, the details of which are provided in [Supplementary Table 1 [Additional file 2]].
The primary outcomes for this study were the technical and clinical success of EUS-PAD. The secondary outcomes assessed for this study include adverse events of the procedure and subgroup analysis of individual adverse events.
Technical success was defined as the successful access and drainage of the abscess via EUS. Clinical success was defined as symptom resolution with complete resolution of abscess on subsequent imaging performed 1–4 weeks after the procedure.
We used meta-analysis techniques to calculate the pooled estimates for each outcome of interest following the methods suggested by DerSimonian and Laird using the random-effects model where appropriate. In several instances in the adverse event data, values of 0 occurred. In these instances, we avoided inadvertently adding positive bias to the outcomes by writing syntax to calculate weighted summary statistics. In this way, we preserved the integrity of the actual data values and avoided possible biases in reporting the outcomes. We assessed heterogeneity between study-specific estimates using Cochran's Q statistical test for heterogeneity and the I2 statistics., In this, values of <30%, 30%–60%, 61%–75%, and >75% were suggestive of low, moderate, substantial, and considerable heterogeneity, respectively. Publication bias was ascertained qualitatively by visual inspection of funnel plot and quantitatively by the Luis Furuya-Kanamori (LFK) test; further, the extent of potential bias was ascertained utilizing the Doi plot. Sensitivity analysis was conducted in instances of potential bias by recalculating all statistics after removal of studies leading to LFK asymmetry; if removal of the study impacted estimates, the study was removed from the final analysis. All meta-analyses were performed using MetaXL software (v. 5.3; EpiGear International, Sunrise Beach, Queensland, Australia). The weighted correlation was calculated using the <wtd.cor> script in the “weight” package, with bootstrapped P values calculated with n = 10,000 iterations, using R (v 3.6.1; Vienna, Austria). Finally, we estimated lower and upper confidence limits for clinical success using the Clopper–Pearson exact method implemented in the <PropCI> package, also using R.
| Results|| |
Search results and population characteristics
From an initial group of 173 studies, 8 studies reported data regarding the use of EUS-PAD. Multiple studies with overlapping cohorts were found, and the most appropriate ones were included in the final analysis. The majority of the patient population were male (55.9% reported in 7 studies), and the mean age mentioned in 7/8 studies was 54.22 years. Seventy percent of the abscesses were postsurgical and 30% of the abscesses were related to medical conditions, primarily diverticulitis. The mean abscess size was 63.32 mm, with abscesses being perirectal in 83.7% of the cases and pericolonic in the remainder of the cases.
Drainage was performed with double-pigtail plastic stents in 100 patients (74%) and lumen-apposing metal stent (LAMS) in 23 patients (17%). Twelve patients (9%) underwent needle aspiration only. [Table 1] describes the characteristics of the included studies. The schematic diagram of study selection is illustrated in [Supplementary Figure 1].
Characteristics and quality of included studies
The analysis included 8 independent cohort studies, with a total of 135 patients. There were 2 multicenter studies, no population-based studies, and 6 single-center studies included in our final analysis. Two studies had more than 30 patients, 4 studies had more than 10 patients, and 2 studies had less than 10 patients. Seven studies were published in manuscript form, and one study was published in abstract form. All of the included studies had clear information reported on the technical and clinical success of EUS-PAD. [Table 1] describes the characteristics of the included studies.
Quality assessment was performed with the help of the NOS scale. Seven studies were of good quality, and one study was of poor quality. The details of quality assessment are shown in [Supplementary Table 1].
The rate of technical success was 100% and the calculated pooled rate of clinical success was 92% (95% confidence interval [CI]: 87%, 98%; P = 0.31; I2 = 15%). [Figure 1] shows the forest plot for clinical success of EUS-PAD.
The calculated pooled rate of adverse events was 9.4% (±17.9%), with stent migration (5.5 ± 18.06%) being the most common adverse event. [Table 2] describes the adverse events in different studies.
Validation of meta-analysis results
To assess whether any one study had a dominant effect on the meta-analysis, we excluded one study at a time and analyzed its effect on the main summary estimate. Based on this analysis, no single study significantly affected the outcome or the heterogeneity.
Based on Q statistics and I2 analysis for heterogeneity, low heterogeneity was noted in the analysis of clinical success of EUS-PAD.
Based on visual inspection of the funnel plot and the Doi plot, as well as quantitative measurement based on the LFK test, there was evidence of asymmetry and hence potential publication bias. Sensitivity analysis by removal of asymmetric studies revealed the impact of the possible publication bias, but this did not lead to a statistical change in the calculated estimate or the conclusion of this meta-analysis. However, it should be noted that the ability to detect potential publication bias is limited.
| Discussion|| |
Our study demonstrates that EUS-PAD is an effective and minimally invasive treatment option for the management of pelvic abscesses. This meta-analysis shows that EUS-PAD has high technical and clinical success rates with low rates of adverse events.
The rate of technical success in our meta-analysis was 100%. The straightforward nature of the procedure allows it to be an effective alternative to more invasive approaches, such as image-guided PCD or surgery. The clinical success rate of EUS-PAD, according to our analysis, was also high. Clinical success was related to technical success, indicating the importance of technically successful procedure. The etiology of the abscess also appeared to be a major determinant in treatment success. In a study by Ramesh et al., diverticular abscesses had significantly lower treatment success rates than abscesses of other etiologies. It is hypothesized that the often multiloculated and highly viscous nature of diverticular abscesses resulted in higher rates of treatment failure.
Our study found an adverse event rate of 9.4%. This is comparable to outcomes of US/CT-guided PAD in which the adverse event rate ranges from 5.6% to 10%.,, EUS provides accurate representations of the fluid collections, organs, and vessels, which allows for accurate transmural drainage while minimizing major complications, such as bleeding and perforation. In our meta-analysis, only one perforation was noted, and there were no cases of major bleeding. Perforation occurred, according to the study by Poincloux et al., in a patient with a diverticular abscess. This is consistent with the overall worse outcomes among patients with diverticular abscesses as noted by Ramesh et al. Several minor complications, such as stent migration, abdominal pain, or rectal discomfort, also occurred. There were no procedure-related deaths.
EUS-PAD is performed by various and nonstandardized methods, such as needle aspiration, aspiration with or without tract dilation, and placement of plastic and/or LAMS. Stents are utilized to maintain tract patency and to reduce the risk of premature tract closure. Stent placement is limited by the distance of the abscess to the rectal wall. If the distance is >20 mm, stent placement is often not technically feasible with currently available stents., In the studies using double-pigtail plastic stents, one or two stents were placed. In the studies using LAMS, a single LAMS was placed. The decision to place one or two stents is determined by the operator and individualized to the patient's needs and clinical situation., Historically, plastic stents were utilized. However, LAMS has been used in more recent studies.,, Of the four patients treated with LAMS in the study by Poincloux et al., one developed a recurrence; another with a diverticular abscess had a perforation. Transrectal drainage catheters can also be utilized in conjunction with stenting to prevent obstruction for patients with larger abscesses (>8 cm)., However, these have been associated with rectal discomfort and are not clearly crucial for abscess resolution.,,
Recurrence occurred in 6 patients (4%). Giovannini et al. and Puri et al. reported higher rates of recurrence in patients who only underwent aspiration without dilation or stenting. Three out of six patients who had recurrence underwent aspiration only. These authors hypothesized that further interventions, such as stenting and dilatation, could have reduced the likelihood of recurrence., Overall, careful consideration should be taken with regard to the size, etiology, and maturity of the abscess when considering stent placement. Smaller abscesses appear to be amenable to simple aspiration, whereas larger abscesses benefit from stent placement.
There were several limitations to this meta-analysis. The majority of the studies were retrospective in nature. Most of the studies were also undertaken in single centers with experienced advanced endoscopists, and the results may not be generalizable to the broader endoscopic community. Techniques utilized were individualized between different providers including the size, number, and methods in which stents were placed. Finally, no direct comparison was made to the other techniques used to drain pelvic abscesses (PCD or a surgical approach).
| Conclusion|| |
EUS-PAD offers a viable alternative that can minimize the need for surgical intervention in the drainage of pelvic abscesses. It is best suited for unilocular abscesses with a mature wall that allows for the creation of a fistula to permit drainage., Smaller abscesses < 4 cm can be usually treated without endoscopic intervention. Considerations should be taken for abscesses of diverticular etiology as higher rates of complications were seen. Finally, EUS-PAD should be strictly avoided in patients with ascites or if the abscess is >20 mm from the bowel lumen. EUS-PAD has also demonstrated long-term clinical success with an acceptable rate of complications. However, more well-conducted randomized controlled trials are needed to establish its role as an alternative to imaging-guided abscess drainage.
Supplementary information is linked to the online version of the paper on the Endoscopic Ultrasound website.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Table 1], [Table 2]