Covered versus uncovered self-expandable metallic stents for palliation of malignant gastric outlet obstruction: a systematic review and meta-analysis
© Pan et al.; licensee BioMed Central Ltd. 2014
- Received: 28 April 2014
- Accepted: 24 September 2014
- Published: 30 September 2014
Self-expandable metallic stents (SEMSs) are widely used for palliation of malignant gastric outlet obstruction (GOO). There are two types of SEMS, covered and uncovered, each with its own advantages and disadvantages. We aimed to compare the efficacy and safety between uncovered and covered SEMSs in the palliation of malignant gastric outlet obstruction.
Databases including PubMed, EMBASE, the Cochrane Library, the Science Citation Index and momentous meeting abstracts were searched and evaluated by two reviewers independently.
Nine trials involving 849 patients were analyzed. Meta-analysis showed there was no significant difference in technical success rate (RR 1.0, 95% CI [0.98, 1.01]), clinical success rate (RR 1.04, 95% CI [0.98, 1.11]), post-stenting dysphagia score (WMD −0.01, 95% CI [−0.52, 0.50]), stent patency (WMD −0.31, 95% CI [−1.73, 1.11]), overall complications (RR 1.07, 95% CI [0.87, 1.32]) and reintervention rate (RR 1.30, 95% CI [0.92, 1.83]) between covered and uncovered SEMSs group. However, covered SEMSs were associated with higher migration rate (RR 3.48, 95% CI [2.16, 5.62], P < 0.00001) and lower obstruction rate (RR 0.42, 95% CI [0.24, 0.73], P = 0.002).
In the palliative treatment of malignant gastric outlet obstruction, both covered and uncovered SEMSs are safely and effective. Covered stents can reduce the risk of restenosis, whereas uncovered stents are effective in decreasing stent migration.
- Covered SEMSs
- Uncovered SEMSs
- Gastric outlet obstruction
Malignant gastric outlet obstruction (GOO) is recognized as a complication of advanced malignant disease in the upper gastrointestinal tract, which usually include distal gastric cancer, periampullary carcinoma, lymphoma and metastases to the duodenum [1, 2]. GOO always leads to intractable vomiting, nausea, abdominal discomfort and poor oral food intake, which diminish quality of life. Compared with palliative gastrojejunostomy or other surgical procedures, self-expandable metallic stents (SEMSs) can rapidly relieve obstructive symptoms with fewer complications and mortality [3, 4]. There are two types of SEMSs, covered and uncovered type; both of them are widely used for palliation of GOO [5–7], each with its own advantages and disadvantages.
To the best of our knowledge, a systematic review  on this topic has been published. More recently, additional studies have been published and some conflicting results have emerged. Therefore, we believe an updated systemic review and meta-analysis is required to evaluate the efficacy and safety between uncovered and covered SEMSs for palliation of malignant gastric outlet obstruction.
Study identification and eligibility criteria
This study has been approved by ethics committee of Shu-guang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine. A comprehensive literature search was done to identify all relevant studies that compared covered stents with uncovered stents in the palliation of malignant gastric outlet obstruction. The PubMed, EMBASE, the Cochrane Library and the Science Citation Index were searched systematically for all articles published up to Dec.2013, without language restriction, which included the following terms in their titles, abstracts, or keywords lists: “gastroduodenal obstruction”, “covered stent”, “uncovered stent”, “malignant gastric outlet obstruction”. The references in retrieved articles were also screened manually. The abstracts of United European Gastroenterology week (UEGW) and Digestive Disease Week (DDW) were also searched systematically.
The inclusion criteria were as follows: (1) RCTs and nonrandomized prospective and retrospective studies; (2) analyses of both uncovered stents and covered stents; (3) patients were diagnosed malignant gastric outlet obstruction; (4) outcome measures included technical and clinical success, overall complications, stent patency and reintervention rate; (5) when multiple articles published by the same team from the same institute within the same study interval were identified, only the latest or the most detailed and informative article, or the one with the best quality in methodology, was included. Commentaries, case reports, reviews, or guidelines were excluded.
Two reviewers (YM.P and J.P) abstracted data independently and reached consensus on all items. Data were extracted on: first author; year of publication; study interval; number of patients; age and sex; study design, stent characteristics; technical success rate; clinical success rate; stent obstruction; stent migration; overall complications; reintervention rate; stent patency and GOO scoring system (GOOSS).
Assessment of methodological quality
The quality of all studies was assessed by using the Newcastle-Ottawa Scale with some modifications to match the needs for this meta-analysis . The quality of the studies was evaluated by examining three items: patient selection, comparability of study groups, and assessment of outcome. Studies achieving five or more stars were considered high quality. Methodological quality assessment was independently carried out by two of the authors. Any disagreement was resolved by consensus.
Statistical manipulation was performed with Review Manager Software (Version 5.1, Windows, Nordic Cochrane Center, Copenhagen, Denmark). Values for analysis were extracted from published reports or calculated from crude data. For summary statistics in meta-analyses, the Relative Risk (RR) is recommended for dichotomous data, and the Weighted Mean Difference (WMD) is recommended for continuous data. Pooled estimates were presented with a 95% confidence interval. P < 0.05 was considered significant. A sensitivity analysis  determined how the results would be influenced if one study was removed from the analysis for each outcome; this indicates the extent to which the results are (or are not) robust to assumptions and decisions that were made when carrying out the synthesis. Because of the anticipated clinical heterogeneity across the included studies, we decided to use only the random effect model before pooling data. This adjusts for variability of results among studies and provides a more conservative estimate of an effect by using a wider confidence interval .
Identification of eligible studies
Characteristics of the included studies
Study interval (y)
Patients (n) covered/uncovered
Age (M, y) covered/uncovered
Female (n, %)
Disease diagnosis (n)
Quality score (*)
Yu Kyung Cho 
Jong Pil Im 
Seungmin Bang 
Iruru Maetani 
Kee Myung Lee 
Chan Gyoo Kim 
Chan Ik Park 
Iruru Maetani 
Sang Myung Woo 
Stent characteristics of the included studies
Stent diameter (mm)
Stent length (cm)
Yu Kyung Cho
Jong Pil Im
Kee Myung Lee
Chan Gyoo Kim
Chan Ik Park
Sang Myung Woo
Technical and clinical success rate
The stent patency was reported in 6 studies [6, 13–17]. The median patency duration was 9 to 23 weeks with covered stents and 10 to 22 weeks with uncovered stents respectively. Meta-analysis showed there was no significant difference between covered and uncovered stents group (WMD −0.31, 95% CI [−1.73, 1.11]) (Figure 3b). Chemotherapy after endoscopic stenting was reported in 6 studies, totally 42.7% (270/632) patients underwent chemotherapy. All studies reported that palliative chemotherapy was not associated with stent patency.
Complications and reintervention
Rate (%) (Covered⁄Uncovered)
RR⁄WMD (95% CI)
High quality studies(Star ≥ 5)
Technical success rate
0.99 [0.98, 1.01]
Clinical success rate
1.04 [0.98, 1.11]
−0.01 [−0.52, 0.50]*
−0.05 [−1.50, 1.39]*
3.49 [1.92, 6.32]
0.39 [0.18, 0.84]
1.11 [0.86, 1.44]
1.30 [0.92, 1.83]
Studies containing ≥ 70 patients
Technical success rate
1.00 [0.98, 1.01]
Clinical success rate
1.08 [0.99, 1.18]
0.26 [−0.05, 0.48]*
0.62 [−0.06, 1.18]*
4.00 [2.05, 7.80]
0.35 [0.17, 0.74]
1.22 [0.99, 1.51]
1.25 [0.88, 1.78]
Malignant gastric outlet obstruction without effective intervention would result in progressive deterioration and death . Surgical bypass has been the standard treatment, but it is associated with significantly high morbidity and mortality. Endoscopic stenting is an alternative treatment, which palliates malignant obstruction with lower morbidity and mortality . There are two types SEMSs widely used in clinical, covered and uncovered. Which is better? Maetani et al.  reported covered stents were associated with more frequent need for reintervention than uncovered stents. Kim et al.  reported both covered and uncovered SEMSs were effective and safe in treatment of patients. Recently, a systematic review  on this topic has been published. However, only two RCTs related to GOO were included for analysis in this systematic review, the number of included patients may be too small to make effective statistic analysis. More recently, additional studies have been published and some conflicting results have emerged. Therefore, we believe an updated systemic review and meta-analysis is required to evaluate the efficacy and safety between uncovered and covered SEMSs.
In this meta-analysis, there was no significantly difference between uncovered and covered stents in technical and clinical success rates. Endoscopic stenting was deployed through a guide wire, when the guide wire could not pass the stricture, and then the stent could not be deployed successfully. So the success of stenting is affected by the degree of narrowing and tortuosity of the stricture rather than the difference between the types of stent used.
The GOOSS was used to evaluate the severity of obstructive symptom, the GOOSS assigns a point score depending on the patient’s level of oral intake (no oral intake, 0; liquids only, 1; soft solids, 2; low-residue or full diet, 3) . Most of patients could not intake any fluid before stenting, though most included studies were retrospective, the patients’ characteristics were similar in baseline. There was significant difference in GOOSS pre-stenting and post-stenting, but there was no difference between covered and uncovered stents after stenting. These mean that both stents have similar effect in palliation of malignant obstruction.
Stent patency is an important factor in QOL of patients. Meta-analysis showed there was no significant difference in stent patency between two groups. The main cause influencing patency was stent migration in covered stent group and stent obstruction in uncovered stent group respectively. The covered stent was associated with advantage of preventing tumor ingrowth, but this advantage was offsetted by high migration. Chemotherapy after stent placement could be independently associated with prolonged stent patency, because chemotherapy may stabilize or decrease tumor burden and thereby decrease malignant ingrowth or overgrowth. Some studies [19, 20] reported chemotherapy after stent placement contributed to longer durations of stent patency in gastric cancer patients. However, we could not find any association of stent patency with palliative chemotherapy after stent placement in included studies. Further prospective randomized trials are needed to determine the role of chemotherapy.
Complications included stent obstruction, stent migration, bleeding, stent fracture, perforation and others, the most complications were stent obstruction and migration. There was no difference in overall complications between the covered stent group and uncovered stent group. One study  has shown that covered stents placed in the biliary tract prevent tumor ingrowth without increasing migration frequency. However, in subgroup analysis, our meta-analysis showed that stent migration was more frequent in the covered stent group, which is maybe the expansion force of the covered stent is transferred to the intestinal wall through the covering membrane rather than through the wire mesh, and the friction between stent and tumor might not be enough to keep the stent stationary. The cause of stent obstruction included tumor ingrowth and overgrowth. Meta-analysis showed uncovered stents were associated with higher stent obstruction compared to covered stents, because uncovered stents are often associated with tumor ingrowth through the stent mesh. 3 trials reported the tumor overgrowth rate; there was no significant difference between two groups. When stent migration or stent obstruction occurred, endoscopic or surgical interventions should be taken. Though 3 trials reported uncovered stent was associated with lower re-intervention rate, meta-analysis showed there was no significant difference between covered and uncovered stents.
Several limitations of the present study need to be considered. First, there was significant heterogeneity for main outcomes. The source of heterogeneity may include the different publishing time of studies, the study design (6 none-RCT studies), the selection criteria, the characteristic of patients and stents. Though the data was treated with random effect models, there was still some influence to final results. Second, included studies were associated with small sample sizes, different levels of the intervention, different follow-up duration; those could also influence the results. Third, there were many different causes of GOO, which including gastric cancer, pancreatic cancer and others. The different characteristic of diseases might lead to different stent patency and complications. Fourth, the selective reporting of studies with positive results may result in overestimation of technical, clinical success rate and stent patency, and cause some bias to our meta-analysis.
Both covered and uncovered SEMSs are technically feasible and effective in the palliative treatment of malignant gastric outlet obstruction. Meta-analysis showed there was no significant difference in stent patency, overall complications and reintervention; whereas in subgroup analysis, stent obstruction was more frequent with covered stents, and stent migration occurred more frequently with uncovered stents. The retrospective nature of these reports and their small sample sizes suggest that prospective controlled trials with large sample sizes are required to confirm the results of the current meta-analysis.
Written informed consent was obtained from the patient for the publication of this report and any accompanying images.
We thank Dr Jun Wu for his statistical support in meta-analysis.
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