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Clinics of Surgery
Clinical Paper ISSN: 2638-1451 Volume 7
Surgery or Endovascular Treatment, which is the Better Way to Treat Acute and Chronic
Mesenteric Ischemia: Systematic Review and Meta-Analysis
Liu-Jiang Li1, 2
, Lin-Juan Du2
, Guo-Jian Li2
, Zhen-Huan Ma2
and Yong Yang2*
1
Departments of Vascular Surgery, The Fourth Affiliated Hospital of Kunming Medical University
2
Departments of Vascular Surgery, The Affiliated Hospital of Yunnan University
*
Corresponding author:
Yong Yang,
Departments of Vascular Surgery, Affiliated
Hospital of Yunnan University, 176 Qingnian
Road, Kunming, 650021, Yunnan, P.R. China,
E-mail: llj378096090@outlook.com
Received: 09 Apr 2022
Accepted: 02 May 2022
Published: 06 May 2022
J Short Name: COS
Copyright:
©2022 Yong Yang, This is an open access article distrib-
uted under the terms of the Creative Commons Attribution
License, which permits unrestricted use, distribution, and
build upon your work non-commercially.
Citation:
Yong Yang, A Multi-Disciplinary Team Approach Opti-
mizes Therapy Selections and Improves Survival Out-
comes in Patients with Hepatocellular Carcinoma and Por-
tal Vein Tumor Thrombus. Clin Surg. V7(9): 1-10
clinicsofsurgery.com 1
Keywords:
Mesenteric ischemia; Endovascular intervention;
Open revascularization; Meta-analysis
1. Abstract
1.1. Objective: To investigate the influence of surgical and en-
dovascular treatment on the prognosis of acute and chronic mes-
enteric ischemia and to further evaluate whether endovascular
treatment can reduce postoperative complications by performing
a meta-analysis.
1.2. Methods: We carried out a systematic literature search in
three databases (PubMed, Embase, and Web of Science). All stud-
ies examining outcomes for patients undergoing endovascular in-
tervention and open revascularization interventions for mesenteric
ischemia were included.
1.3. Results: We summarized the available evidence from 25 stud-
ies with a total of 30,775 cases. The pooled results indicated that
surgical intervention increases 30-day mortality (OR 1.45; 95% CI
1.08–1.95) and the incidence of postoperative pulmonary compli-
cations (OR: 1.61; 95% CI 1.28–2.04). However, this result seems
to fit only in the subgroup with a large number of patients included.
1.4. Conclusion: The present study demonstrates that open sur-
gery methods may increase the 30-day mortality in acute and
chronic mesenteric ischemia and the incidence of postoperative
pulmonary complications.
2. Introduction
Mesenteric ischemia (MI) occurs from insufficient blood flow to
the gastrointestinal tract mucosa. MI is not a common cause of ab-
dominal pain,and perhaps for this reason, delayed diagnosis and
untimely treatment will lead to a grim prognosis. Chronic MI is
the most common type of mesenteric vascular disorder, and it is
often underdiagnosed in clinical practice [1]. For acute MI, the
mortality is often as high as 50% to 70 % [2,4]. The treatment goal
of MI is to restore vascular perfusion and minimize trauma [5].
Surgical intervention includes embolectomy and bypass graft, and
endovascular revascularization is used to re-establish blood flow
to the ischemic bowel [6], but the most appropriate treatment still
remains unknown [7]. More importantly, there are no studies that
have simultaneously evaluated appropriate treatment for acute and
chronic MI. The present meta-analysis of current literature aimed
to compare the perioperative outcomes among open surgery and
endovascular approaches in patients with MI and identify the ap-
propriate intervention.
3. Methods
3.1. Search Strategy
A comprehensive search from PubMed, EMBASE, and Web of
Science databases was performed for articles published before
November 2021. The terms (“mesenteric ischaemia” or “MI”)
and (“revascularization” or “surgery” or “endovascular”) were
searched. No language restrictions were imposed. References cit-
ed in the retrieved articles were also reviewed for relevant studies.
Two reviewers (Liu-Jiang Li, Yong Yang) independently screened
all candidate studies and discrepancies were resolved by consen-
sus.
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Volume 7 Issue 9 -2022 Clinical Paper
3.2. Selection and Exclusion Criteria
The inclusion criteria for each study were as follows: patients with
a confirmed diagnosis of MI by duplex ultrasound or other imag-
ing; patients with MI who had undergone endovascular or open
surgical revascularization intervention; reported at least one of the
outcomes of 30-day mortality, in-hospital complications. Studies
were excluded in the current study: (1) The outcome of 30-day
mortality or in-hospital complications in both treatments was zero;
(2) animal studies, reviews, abstracts, letters, case reports and
meetings reports, or full text not available; (3) duplicate articles;
(4) studies including mesenteric venous thrombosis.Atwo-step se-
lection process was used to identify eligible studies. Two indepen-
dent reviewers (Lin-Juan Du, Zhen-Huan Ma) initially screened
all titles and abstracts and then independent pairs of investigators
screened full-text articles.
3.3. Data Extraction
Data were extracted independently by two investigators (Liu-Jiang
Li, Guo-Jian Li), and disagreement was resolved by joint discus-
sion. The data variables on first author, publication year, country,
sample size, age of patients, comorbidities, type of intervention,
and in-hospital outcomes were collected. The study quality was
assessed with the Newcastle–Ottawa quality assessment scale
(NOS). NOS scores of greater than or equal to 6 were regarded as
high-quality studies.
3.4. Data Analysis
Outcomes were reported as risk ratio (RR) with 95% confidence
interval (CI). Meta-analysis was conducted using STATA soft-
ware. Statistical heterogeneity was assessed by the chi-squared
and I-squared tests. if I2
≥ 50% or/and P < 0.10, indicating sub-
stantial heterogeneity, random-effects model was used to calculate
the pooled RR and 95% CI. Otherwise, a fixed-effect model was
used. All statistical tests were two-sided, with P <0.05 indicating
statistical significance.
4. Results
4.1. Characteristics of Included Studies
We identified 208 articles from PubMed, EMBASE, and Web of
Science. After exclusion of 3833 duplicates and 909 articles be-
cause they were not relevant to our research or did not meet our
inclusion criteria by filtering titles or abstracts. We obtained 1916
full articles of potentially relevant studies. After full-text reviews,
we excluded 1819 papers due to insufficient information. A de-
tailed study selection flow chart is provided in Figure 1. We in-
cluded 25 studies [8-33] with a total of 30,775 patients enrolled
in this meta-analysis. These studies were mainly from the United
States (19). The number of people included in each study spans
a wide range, from 13 to 10,381. The basic characteristics of the
included studies and detailed description of each study are summa-
rized and presented in Table 1.
Table 1: Characteristics of the included studies.
Author Year Number Area Age Females (%) Risk factors
Zientara 2021 26 Switzerland 75(64–99) 12 (46.1)
Arterial Hypertension Peripheral arterial disease Coronary arterial
disease Diabetes COPD Dyslipidemia
Menges 2020 63 Germany 71(60–76) 42 (66.7) Diabetes mellitus COPD Smoke Chronic kidney disease
Erben 2018 10381 USA 69(18-98) 6548(63.1) Coronary artery disease Diabetes mellitus Chronic kidney disease
Zhang 2017 30 China 61.9 10 (33.3)
Hypertension Peripheral arterial disease Diabetes Chronic kidney
disease Smoke
Lima 2017 1760 USA 66.2 1248(71)
Arterial Hypertension Peripheral arterial disease Coronary arterial
disease Diabetes Dyslipidemia COPD
Arya 2016 34 USA 64 25(73.5)
Coronary artery disease Diabetes mellitus Chronic kidney disease
Smoke
Eslami 2016 1563 USA 68.7 1016(65)
Peripheral arterial disease Diabetes mellitus Chronic kidney disease
COPD
Arya 2016 81 USA 64 65 (80.2)
Arterial Hypertension Peripheral arterial disease Coronary arterial
disease Diabetes Dyslipidemia COPD
Zacharias 2016 161 USA 69 116 (72) Hypertension Coronary artery disease Diabetes mellitus COPD Smoke
Branco 2015 439 USA 172(39.2) Diabetes mellitus Chronic kidney disease COPD Smoke
Barret 2015 54 France 66.3 33 (61.1) Hypertension Coronary artery disease Diabetes mellitus COPD Smoke
Beaulieu 2014 4665 USA 70.5 2664(57.1)
Arterial Hypertension Peripheral arterial disease Diabetes
Dyslipidemia COPD
Jia 2014 21 China 71 6 (28.6) NA
Kanamori 2014 47 USA 58 42 (89.4) Hypertension Diabetes mellitus Chronic kidney disease COPD Smoke
Ryer 2012 93 USA 68 58 (62.4) NA
Arthurs 2011 70 USA 64 20 (28.6)
Arterial Hypertension Peripheral arterial disease Coronary arterial
disease Diabetes Dyslipidemia COPD Smoke
Block 2010 161 Sweden 76(65-82) 90 (55.9) Ischemic heart disease Cerebrovascular disease Diabetes Smoke
Rawat 2010 76 USA 65(40-86) 54 (71.1)
Ischemic heart disease Transient ischemic attack Diabetes mellitus
Smoke
Schermerhorn 2009 5237 USA NA 3531 (67.4)
Arterial Hypertension Peripheral arterial disease Coronary arterial
disease Diabetes Dyslipidemia COPD
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Davies 2009 32 USA 70 19 (59.4)
Hypertension Peripheral vascular disease Diabetes mellitus Smoke
COPD
Schermerhorn 2009 5583 USA NA 3857 (69.1) Hypertension Coronary artery disease Diabetes mellitus COPD Smoke
Zerbib 2008 29 France NA 12 (41.2) Hypertension Coronary artery disease Diabetes mellitus Smoke
Wyers 2007 13 Lebanon NA NA NA
Atkins 2007 80 USA 65 33 (41.3) NA
Sivamurthy 2006 60 USA 66 44 (73.3)
Hypertension Transient ischemic attack Myocardial infarction
Congestive heart failure Diabetes mellitus Smoke
Brown 2005 47 USA 73 37 (78.7) Hypertension Diabetes mellitus Chronic kidney disease COPD Smoke
Kasirajan 2001 113 Canada NA 81 (71.7) Hypertension Diabetes mellitus Chronic kidney disease COPD smoke
Rose 1995 17 USA NA NA NA
4.2. Quality Assessment
All the available studies were retrospective. Most of the studies
showed low risk of bias in terms of selection of study participants,
ascertainment of exposure, control for confounding, and ascertain-
ment of outcome. Overall judgment of the risk of bias was mostly
low risk. The risk of bias assessment of each included study is
shown in detail in Supplementary Table 2.
4.3. Outcomes of Interest
4.3.1. Thirty-Day Mortality: All of the studies reported the 30-
day mortality. Random-effects model was used to pool all the
included studies and demonstrated that surgical intervention in-
creased the risk of 30-day mortality (OR 1.45; 95% CI 1.08–1.95;
Figure 2) with inter-study heterogeneity (I2
= 96.7%, P < 0.001).
Because of the high I2
and P values in the pooled analysis, sub-
group analyses were also performed. In the subgroup with less
than 100 patients included in the study, the 30-day mortality rate
for open surgery and endovascular intervention was similar to that
in studies with larger populations. We analyzed several possible
sources of heterogeneity and the results are summarized in Table
2. After the introduction of the regression model with the four fac-
tors, the number of people included in the study may be a source
of heterogeneity following meta-regression.
4.3.2. Pulmonary Complications: There were 13 studies report-
ing pulmonary complications. Open surgery was associated with
an increased risk of pulmonary complications (OR: 1.61; 95% CI
1.28–2.04; Figure 3) with a random-effects model. In the subgroup
of acute MI and the subgroup with more than 100 patients enrolled
in the study, open surgery increased postoperative pulmonary com-
plications. After the introduction of the regression model with the
four factors, we determined that the number of patients included in
the study and whether MI was acute or chronic may be sources of
heterogeneity following meta-regression (Table 3).
author Year Selection of studies
Ascertainment of
exposure
control of
confounding
Assessment of
outcome
Was Follow-Up Long
Enough for Outcomes to Occur
Overall
Zientara 2021 1 1 1 1 1 High quality
Menges 2020 1 1 1 1 1 High quality
Erben 2018 1 1 1 1 1 High quality
Zhang 2017 1 1 1 1 1 High quality
Lima 2017 1 1 1 1 1 High quality
Arya 2016 1 1 1 1 1 High quality
Zacharias 2016 1 1 1 1 1 High quality
Arya 2016 1 1 1 1 1 High quality
Eslami 2016 1 1 1 1 1 High quality
Branco 2015 1 1 1 1 1 High quality
Barret 2015 1 1 1 1 1 High quality
Beaulieu 2014 1 1 1 1 1 High quality
Jia 2014 1 1 0 1 1 Low quality
Kanamori 2014 1 1 1 1 1 High quality
Ryer 2012 1 1 0 1 1 Low quality
Arthurs 2011 1 1 1 1 1 High quality
Block 2010 1 1 1 1 1 High quality
Supplementary Table: Studies Quality Evaluation Form
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Volume 7 Issue 9 -2022 Clinical Paper
Rawat 2010 1 1 1 1 1 High quality
Davies 2009 1 1 1 0 1 Low quality
Schermerhorn 2009 1 1 1 1 1 High quality
Schermerhorn 2009 1 1 1 1 1 High quality
Zerbib 2008 1 1 1 1 1 High quality
Wyers 2007 1 1 0 1 1 Low quality
Atkins 2007 1 1 0 1 1 Low quality
Sivamurthy 2006 1 1 1 1 1 High quality
Brown 2005 1 1 1 1 1 High quality
Kasirajan 2001 1 1 1 1 1 High quality
Rose 1995 1 1 0 0 1 Low quality
Covariates Subgroup No. of studies
OR (95% CI) Heterogeneity Meta-regression P
Random-effects model Fixed-effects model P I2
Overall 25 1.45(1.08,1.95) <0.001 96.7%
Area
others 7 1.75(0.87,3.53) 2.27(2.1,2.47) <0.001 97.8%
0.407
USA 18 1.30(1.06,1.58) 1.00(0.95,1.05) <0.001 86.1%
Year
Last 5 years 7 1.74(1.11,2.73) 1.06(0.98,1.14) <0.001 97.8%
0.365
others 18 1.32(0.89,1.95) 1.51(1.30,1.76) <0.001 86.1%
numbers
<100 16 0.94(0.90,0.99) 0.94(0.90,0.99) 0.44 1.1%
<0.001
>100 9 2.46(1.62,3.74) 3.31(3.03,3.61) <0.001 92.2%
Type of MI
Acute 13 1.68(1.01,2.82) 2.41(2.23,2.61) <0.001 96.2%
0.202
Chronic 12 1.05(0.92,1.20) 0.96(0.92,1.01) <0.001 69.4%
Table 2: Subgroup analysis and meta-regression analysis for the studies assess the influence of treatment in 30-day mortality of MI.
Covariates Subgroup
No. of
studies
OR (95% CI) Heterogeneity Meta-regression P
Random-effects model Fixed-effects model P I2
Overall 13 1.61(1.28,2.04) <0.001 95.7%
Area
others 7 1.57 (0.58,4.26) 0.96(0.87,1.05) 0.148 47.7%
0.896
USA 18 1.76(1.33,2.33) 0.99(0.96,1.02) <0.001 95.7%
Year
Last 5 years 3 0.92(0.86,0.99) 0.92(0.86,0.98) 0.326 10. 8%
0.29
others 10 2.11(1.49,3.00) 1.00(0.97,1.04) <0.001 95.7%
numbers
<100 9 0.93(0.86,1.02) 0.96(0.93,0.99) 0.001 69.2%
<0.001
>100 4 5.02(2.48,10.17) 6.78(5.30,8.66) 0.001 80.7%
Type of MI
Acute 5 4.85(2.60,9.05) 2.41(2.23,2.61) 0.02 76.2%
<0.001
Chronic 8 6.64(5.22,8.45) 0.96(0.93,0.98) <0.001 95.7%
Table 3: Subgroup analysis and meta-regression analysis for the studies assess the influence of treatment in pulmonary complications of MI.
clinicsofsurgery.com 5
Volume 7 Issue 9 -2022 Clinical Paper
Figure 1: Flow chart of literature search and study selection.
Figure 2: Forest plots depicting 30-day mortality rate of different treatments. OR was shown with 95% CI. CI: confidence interval.
clinicsofsurgery.com 6
Volume 7 Issue 9 -2022 Clinical Paper
Figure 3: Forest plots depicting pulmonary complications of different treatments.
4.3.3. Renal Complications: There was no statistically signifi-
cant difference in renal complications between the open surgical
intervention and the endovascular approach (OR: 1.08; 95% CI
0.93–1.26; Figure 4). Although we performed subgroup analysis
and regression, no source of heterogeneity was found (Table 4).
Figure 4: Forest plots depicting risk of renal complications of different treatments.
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Volume 7 Issue 9 -2022 Clinical Paper
Covariates Subgroup
No. of
studies
OR (95% CI) Heterogeneity Meta-regression P
Random-effects model Fixed-effects model P I2
Overall 12 1.08(0.93,1.26) <0.001 93.1%
Area
others 3 0.93 (0.88,0.98) 0.93 (0.88,0.98) 0.474 0
0.539
USA 9 1.15(0.92,1.45) 0.97(0.94,1.01) <0.001 94.9%
Year
Last 5 years 3 0.82(0.59,1.15) 0.81(0.76,0.86) <0.001 92.8%
0.168
others 9 1.18(1.00,1.39) 1.00(0.97,1.04) <0.001 91.9%
numbers
<100 7 0.98(0.90,1.05) 0.97(0.94,1.01) <0.001 97.3%
0.718
>100 5 1.18(0.81,1.72) 0.93(0.89,0.98) 0.061 50.2%
Type of MI
Acute 5 1.38(0.66,2.86) 0.86(0.79,0.93) <0.001 96%
0.639
Chronic 7 1.04(0.93,1.17) 0.98(0.94,1.01) <0.001 88.5%
Table 4: Subgroup analysis and meta-regression analysis for the studies assess the influence of treatment in renal complications of MI.
4.3.4. Sensitivity Analysis and Publication Bias: Influence anal-
ysis was performed and demonstrated that no one study could over-
ly affect the summary of the outcomes estimate (Supplementary
Figure 1). Publication bias was assessed by funnel plot analysis
and the plots showed basic symmetry (Supplementary Figure 2).
No significant publication bias was further determined by Begg’s
test (Supplementary Figure 3).
Supplementary Figure. 1: Influence analysis for the studies.
Supplementary Figure 2: Funnel plot of comparison of the included trials.
clinicsofsurgery.com 8
Volume 7 Issue 9 -2022 Clinical Paper
Supplementary Figure 3: Begg’s test result of publication bias.
5. Discussion
MI has no distinguishing clinical manifestations and is often mis-
diagnosed [34]. With the advancements in diagnosis and treatment
technology, MI has become a multidisciplinary disease and is
currently treated mainly through open surgery and interventional
management. However, the optimal management of MI remains
controversial [13,35,36]. The best treatments for MI, acute MI,
and chronic MI have only been meta-analyzed separately. For
the first time, we have comprehensively evaluated the treatment
of two types of MI. Our meta-analysis included 28 articles, in-
cluding 30775 patients with MI, and showed that patients treated
with open surgery have an increased rate of 30-day mortality (OR
1.45; 95% CI 1.08–1.95) and incidence of pulmonary complica-
tions (OR: 1.61; 95% CI 1.28–2.04), especially in studies involv-
ing more than 100 patients. When more than 100 patients were
enrolled, open surgery also significantly increased the incidence
of postoperative pulmonary complications. The open surgery ap-
proach is a traditional treatment method for MI. In recent years,
endovascular treatment has been more popular because it avoids
laparotomy [37]. With regard to 30-day mortality, although the
short-term mortality in patients with chronic MI and acute MI is
very different, open surgery may have a worse prognosis. This is
consistent with previous research results [38,39], although exact
reasons for this remain unclear. This may be caused by bias in
the selection of interventions. Patients with mild symptoms or po-
tential intestinal ischemia but not intestinal necrosis are usually
selected for endovascular interventional therapy. Open surgery in-
terferes greatly with abdominal organs, and abdominal incisions
are also not conducive to patient recovery. However, this conclu-
sion is applicable only to studies with a large number of patients
(more than 100), as we found in this study. Research with a large
sample size is needed to explore this finding further. Open sur-
gery increased the rate of lung complications compared with en-
dovascular therapy. This may be because open surgery needs to be
performed under general anesthesia and endotracheal intubation
with general anesthesia may interfere with the respiratory system,
while the intravascular intervention requires only local anesthesia.
In the subgroup analysis, the increase in pulmonary complications
by open surgery seems to apply only to acute MI and studies in-
cluding more than 100 patients. MI reperfusion injury may induce
remote organ injuries [40,41]; the lung appears to be the first organ
affected by this pathogenic process [42]. In patients with chronic
MI, the body may adapt to the ischemic state because of long-
term circulatory blockage, and the damage during reperfusion is
relatively light. Of course, the influence of large sample size and
high-quality research on the conclusion is obvious.
The rate of bowel resection was not statistically different in dif-
ferent treatment methods of our study. This is inconsistent with
the conclusions of previous studies [43]. This may be related to
requiring laparotomy to remove the necrotic bowel after endovas-
cular treatment [44]. There was no significant difference in renal
complications in the different treatment studies in our study. There
were also no significant differences in the different subgroups with
respect to number of patients included, different regions, and acute
and chronic MI. This is inconsistent with the study of Davenport
et al [45]. Although intravascular interventional therapy produces
mild hemodynamic changes, contrast-induced acute kidney injury
cannot be ignored.
6. Limitations
There are several limitations in our meta-analysis. First, there is
obvious heterogeneity in our meta-analysis. Although sensitivity
analysis, subgroup analysis, and meta-regression were used, high
clinicsofsurgery.com 9
Volume 7 Issue 9 -2022 Clinical Paper
heterogeneity existed among studies. Second, all the included
studies were retrospective studies, so the representativeness of
our study may be limited. Third, most of the studies we included
were from the United States, and the conclusions reached may be
geographically restricted. Fourth, most of the studies analyzed in-
cluded a small number of patients, and this may not represent the
actual efficacy.
7. Conclusions
Endovascular approach for AMI may be associated with decreased
30-day mortality and avoidance of the incidence of postoperative
pulmonary complications. However, more high-quality studies
with larger sample sizes are warranted.
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Surgery or Endovascular Treatment, which is the Better Way to Treat Acute and Chronic Mesenteric Ischemia: Systematic Review and Meta-Analysis

  • 1. Clinics of Surgery Clinical Paper ISSN: 2638-1451 Volume 7 Surgery or Endovascular Treatment, which is the Better Way to Treat Acute and Chronic Mesenteric Ischemia: Systematic Review and Meta-Analysis Liu-Jiang Li1, 2 , Lin-Juan Du2 , Guo-Jian Li2 , Zhen-Huan Ma2 and Yong Yang2* 1 Departments of Vascular Surgery, The Fourth Affiliated Hospital of Kunming Medical University 2 Departments of Vascular Surgery, The Affiliated Hospital of Yunnan University * Corresponding author: Yong Yang, Departments of Vascular Surgery, Affiliated Hospital of Yunnan University, 176 Qingnian Road, Kunming, 650021, Yunnan, P.R. China, E-mail: llj378096090@outlook.com Received: 09 Apr 2022 Accepted: 02 May 2022 Published: 06 May 2022 J Short Name: COS Copyright: ©2022 Yong Yang, This is an open access article distrib- uted under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and build upon your work non-commercially. Citation: Yong Yang, A Multi-Disciplinary Team Approach Opti- mizes Therapy Selections and Improves Survival Out- comes in Patients with Hepatocellular Carcinoma and Por- tal Vein Tumor Thrombus. Clin Surg. V7(9): 1-10 clinicsofsurgery.com 1 Keywords: Mesenteric ischemia; Endovascular intervention; Open revascularization; Meta-analysis 1. Abstract 1.1. Objective: To investigate the influence of surgical and en- dovascular treatment on the prognosis of acute and chronic mes- enteric ischemia and to further evaluate whether endovascular treatment can reduce postoperative complications by performing a meta-analysis. 1.2. Methods: We carried out a systematic literature search in three databases (PubMed, Embase, and Web of Science). All stud- ies examining outcomes for patients undergoing endovascular in- tervention and open revascularization interventions for mesenteric ischemia were included. 1.3. Results: We summarized the available evidence from 25 stud- ies with a total of 30,775 cases. The pooled results indicated that surgical intervention increases 30-day mortality (OR 1.45; 95% CI 1.08–1.95) and the incidence of postoperative pulmonary compli- cations (OR: 1.61; 95% CI 1.28–2.04). However, this result seems to fit only in the subgroup with a large number of patients included. 1.4. Conclusion: The present study demonstrates that open sur- gery methods may increase the 30-day mortality in acute and chronic mesenteric ischemia and the incidence of postoperative pulmonary complications. 2. Introduction Mesenteric ischemia (MI) occurs from insufficient blood flow to the gastrointestinal tract mucosa. MI is not a common cause of ab- dominal pain,and perhaps for this reason, delayed diagnosis and untimely treatment will lead to a grim prognosis. Chronic MI is the most common type of mesenteric vascular disorder, and it is often underdiagnosed in clinical practice [1]. For acute MI, the mortality is often as high as 50% to 70 % [2,4]. The treatment goal of MI is to restore vascular perfusion and minimize trauma [5]. Surgical intervention includes embolectomy and bypass graft, and endovascular revascularization is used to re-establish blood flow to the ischemic bowel [6], but the most appropriate treatment still remains unknown [7]. More importantly, there are no studies that have simultaneously evaluated appropriate treatment for acute and chronic MI. The present meta-analysis of current literature aimed to compare the perioperative outcomes among open surgery and endovascular approaches in patients with MI and identify the ap- propriate intervention. 3. Methods 3.1. Search Strategy A comprehensive search from PubMed, EMBASE, and Web of Science databases was performed for articles published before November 2021. The terms (“mesenteric ischaemia” or “MI”) and (“revascularization” or “surgery” or “endovascular”) were searched. No language restrictions were imposed. References cit- ed in the retrieved articles were also reviewed for relevant studies. Two reviewers (Liu-Jiang Li, Yong Yang) independently screened all candidate studies and discrepancies were resolved by consen- sus.
  • 2. clinicsofsurgery.com 2 Volume 7 Issue 9 -2022 Clinical Paper 3.2. Selection and Exclusion Criteria The inclusion criteria for each study were as follows: patients with a confirmed diagnosis of MI by duplex ultrasound or other imag- ing; patients with MI who had undergone endovascular or open surgical revascularization intervention; reported at least one of the outcomes of 30-day mortality, in-hospital complications. Studies were excluded in the current study: (1) The outcome of 30-day mortality or in-hospital complications in both treatments was zero; (2) animal studies, reviews, abstracts, letters, case reports and meetings reports, or full text not available; (3) duplicate articles; (4) studies including mesenteric venous thrombosis.Atwo-step se- lection process was used to identify eligible studies. Two indepen- dent reviewers (Lin-Juan Du, Zhen-Huan Ma) initially screened all titles and abstracts and then independent pairs of investigators screened full-text articles. 3.3. Data Extraction Data were extracted independently by two investigators (Liu-Jiang Li, Guo-Jian Li), and disagreement was resolved by joint discus- sion. The data variables on first author, publication year, country, sample size, age of patients, comorbidities, type of intervention, and in-hospital outcomes were collected. The study quality was assessed with the Newcastle–Ottawa quality assessment scale (NOS). NOS scores of greater than or equal to 6 were regarded as high-quality studies. 3.4. Data Analysis Outcomes were reported as risk ratio (RR) with 95% confidence interval (CI). Meta-analysis was conducted using STATA soft- ware. Statistical heterogeneity was assessed by the chi-squared and I-squared tests. if I2 ≥ 50% or/and P < 0.10, indicating sub- stantial heterogeneity, random-effects model was used to calculate the pooled RR and 95% CI. Otherwise, a fixed-effect model was used. All statistical tests were two-sided, with P <0.05 indicating statistical significance. 4. Results 4.1. Characteristics of Included Studies We identified 208 articles from PubMed, EMBASE, and Web of Science. After exclusion of 3833 duplicates and 909 articles be- cause they were not relevant to our research or did not meet our inclusion criteria by filtering titles or abstracts. We obtained 1916 full articles of potentially relevant studies. After full-text reviews, we excluded 1819 papers due to insufficient information. A de- tailed study selection flow chart is provided in Figure 1. We in- cluded 25 studies [8-33] with a total of 30,775 patients enrolled in this meta-analysis. These studies were mainly from the United States (19). The number of people included in each study spans a wide range, from 13 to 10,381. The basic characteristics of the included studies and detailed description of each study are summa- rized and presented in Table 1. Table 1: Characteristics of the included studies. Author Year Number Area Age Females (%) Risk factors Zientara 2021 26 Switzerland 75(64–99) 12 (46.1) Arterial Hypertension Peripheral arterial disease Coronary arterial disease Diabetes COPD Dyslipidemia Menges 2020 63 Germany 71(60–76) 42 (66.7) Diabetes mellitus COPD Smoke Chronic kidney disease Erben 2018 10381 USA 69(18-98) 6548(63.1) Coronary artery disease Diabetes mellitus Chronic kidney disease Zhang 2017 30 China 61.9 10 (33.3) Hypertension Peripheral arterial disease Diabetes Chronic kidney disease Smoke Lima 2017 1760 USA 66.2 1248(71) Arterial Hypertension Peripheral arterial disease Coronary arterial disease Diabetes Dyslipidemia COPD Arya 2016 34 USA 64 25(73.5) Coronary artery disease Diabetes mellitus Chronic kidney disease Smoke Eslami 2016 1563 USA 68.7 1016(65) Peripheral arterial disease Diabetes mellitus Chronic kidney disease COPD Arya 2016 81 USA 64 65 (80.2) Arterial Hypertension Peripheral arterial disease Coronary arterial disease Diabetes Dyslipidemia COPD Zacharias 2016 161 USA 69 116 (72) Hypertension Coronary artery disease Diabetes mellitus COPD Smoke Branco 2015 439 USA 172(39.2) Diabetes mellitus Chronic kidney disease COPD Smoke Barret 2015 54 France 66.3 33 (61.1) Hypertension Coronary artery disease Diabetes mellitus COPD Smoke Beaulieu 2014 4665 USA 70.5 2664(57.1) Arterial Hypertension Peripheral arterial disease Diabetes Dyslipidemia COPD Jia 2014 21 China 71 6 (28.6) NA Kanamori 2014 47 USA 58 42 (89.4) Hypertension Diabetes mellitus Chronic kidney disease COPD Smoke Ryer 2012 93 USA 68 58 (62.4) NA Arthurs 2011 70 USA 64 20 (28.6) Arterial Hypertension Peripheral arterial disease Coronary arterial disease Diabetes Dyslipidemia COPD Smoke Block 2010 161 Sweden 76(65-82) 90 (55.9) Ischemic heart disease Cerebrovascular disease Diabetes Smoke Rawat 2010 76 USA 65(40-86) 54 (71.1) Ischemic heart disease Transient ischemic attack Diabetes mellitus Smoke Schermerhorn 2009 5237 USA NA 3531 (67.4) Arterial Hypertension Peripheral arterial disease Coronary arterial disease Diabetes Dyslipidemia COPD
  • 3. clinicsofsurgery.com 3 Volume 7 Issue 9 -2022 Clinical Paper Davies 2009 32 USA 70 19 (59.4) Hypertension Peripheral vascular disease Diabetes mellitus Smoke COPD Schermerhorn 2009 5583 USA NA 3857 (69.1) Hypertension Coronary artery disease Diabetes mellitus COPD Smoke Zerbib 2008 29 France NA 12 (41.2) Hypertension Coronary artery disease Diabetes mellitus Smoke Wyers 2007 13 Lebanon NA NA NA Atkins 2007 80 USA 65 33 (41.3) NA Sivamurthy 2006 60 USA 66 44 (73.3) Hypertension Transient ischemic attack Myocardial infarction Congestive heart failure Diabetes mellitus Smoke Brown 2005 47 USA 73 37 (78.7) Hypertension Diabetes mellitus Chronic kidney disease COPD Smoke Kasirajan 2001 113 Canada NA 81 (71.7) Hypertension Diabetes mellitus Chronic kidney disease COPD smoke Rose 1995 17 USA NA NA NA 4.2. Quality Assessment All the available studies were retrospective. Most of the studies showed low risk of bias in terms of selection of study participants, ascertainment of exposure, control for confounding, and ascertain- ment of outcome. Overall judgment of the risk of bias was mostly low risk. The risk of bias assessment of each included study is shown in detail in Supplementary Table 2. 4.3. Outcomes of Interest 4.3.1. Thirty-Day Mortality: All of the studies reported the 30- day mortality. Random-effects model was used to pool all the included studies and demonstrated that surgical intervention in- creased the risk of 30-day mortality (OR 1.45; 95% CI 1.08–1.95; Figure 2) with inter-study heterogeneity (I2 = 96.7%, P < 0.001). Because of the high I2 and P values in the pooled analysis, sub- group analyses were also performed. In the subgroup with less than 100 patients included in the study, the 30-day mortality rate for open surgery and endovascular intervention was similar to that in studies with larger populations. We analyzed several possible sources of heterogeneity and the results are summarized in Table 2. After the introduction of the regression model with the four fac- tors, the number of people included in the study may be a source of heterogeneity following meta-regression. 4.3.2. Pulmonary Complications: There were 13 studies report- ing pulmonary complications. Open surgery was associated with an increased risk of pulmonary complications (OR: 1.61; 95% CI 1.28–2.04; Figure 3) with a random-effects model. In the subgroup of acute MI and the subgroup with more than 100 patients enrolled in the study, open surgery increased postoperative pulmonary com- plications. After the introduction of the regression model with the four factors, we determined that the number of patients included in the study and whether MI was acute or chronic may be sources of heterogeneity following meta-regression (Table 3). author Year Selection of studies Ascertainment of exposure control of confounding Assessment of outcome Was Follow-Up Long Enough for Outcomes to Occur Overall Zientara 2021 1 1 1 1 1 High quality Menges 2020 1 1 1 1 1 High quality Erben 2018 1 1 1 1 1 High quality Zhang 2017 1 1 1 1 1 High quality Lima 2017 1 1 1 1 1 High quality Arya 2016 1 1 1 1 1 High quality Zacharias 2016 1 1 1 1 1 High quality Arya 2016 1 1 1 1 1 High quality Eslami 2016 1 1 1 1 1 High quality Branco 2015 1 1 1 1 1 High quality Barret 2015 1 1 1 1 1 High quality Beaulieu 2014 1 1 1 1 1 High quality Jia 2014 1 1 0 1 1 Low quality Kanamori 2014 1 1 1 1 1 High quality Ryer 2012 1 1 0 1 1 Low quality Arthurs 2011 1 1 1 1 1 High quality Block 2010 1 1 1 1 1 High quality Supplementary Table: Studies Quality Evaluation Form
  • 4. clinicsofsurgery.com 4 Volume 7 Issue 9 -2022 Clinical Paper Rawat 2010 1 1 1 1 1 High quality Davies 2009 1 1 1 0 1 Low quality Schermerhorn 2009 1 1 1 1 1 High quality Schermerhorn 2009 1 1 1 1 1 High quality Zerbib 2008 1 1 1 1 1 High quality Wyers 2007 1 1 0 1 1 Low quality Atkins 2007 1 1 0 1 1 Low quality Sivamurthy 2006 1 1 1 1 1 High quality Brown 2005 1 1 1 1 1 High quality Kasirajan 2001 1 1 1 1 1 High quality Rose 1995 1 1 0 0 1 Low quality Covariates Subgroup No. of studies OR (95% CI) Heterogeneity Meta-regression P Random-effects model Fixed-effects model P I2 Overall 25 1.45(1.08,1.95) <0.001 96.7% Area others 7 1.75(0.87,3.53) 2.27(2.1,2.47) <0.001 97.8% 0.407 USA 18 1.30(1.06,1.58) 1.00(0.95,1.05) <0.001 86.1% Year Last 5 years 7 1.74(1.11,2.73) 1.06(0.98,1.14) <0.001 97.8% 0.365 others 18 1.32(0.89,1.95) 1.51(1.30,1.76) <0.001 86.1% numbers <100 16 0.94(0.90,0.99) 0.94(0.90,0.99) 0.44 1.1% <0.001 >100 9 2.46(1.62,3.74) 3.31(3.03,3.61) <0.001 92.2% Type of MI Acute 13 1.68(1.01,2.82) 2.41(2.23,2.61) <0.001 96.2% 0.202 Chronic 12 1.05(0.92,1.20) 0.96(0.92,1.01) <0.001 69.4% Table 2: Subgroup analysis and meta-regression analysis for the studies assess the influence of treatment in 30-day mortality of MI. Covariates Subgroup No. of studies OR (95% CI) Heterogeneity Meta-regression P Random-effects model Fixed-effects model P I2 Overall 13 1.61(1.28,2.04) <0.001 95.7% Area others 7 1.57 (0.58,4.26) 0.96(0.87,1.05) 0.148 47.7% 0.896 USA 18 1.76(1.33,2.33) 0.99(0.96,1.02) <0.001 95.7% Year Last 5 years 3 0.92(0.86,0.99) 0.92(0.86,0.98) 0.326 10. 8% 0.29 others 10 2.11(1.49,3.00) 1.00(0.97,1.04) <0.001 95.7% numbers <100 9 0.93(0.86,1.02) 0.96(0.93,0.99) 0.001 69.2% <0.001 >100 4 5.02(2.48,10.17) 6.78(5.30,8.66) 0.001 80.7% Type of MI Acute 5 4.85(2.60,9.05) 2.41(2.23,2.61) 0.02 76.2% <0.001 Chronic 8 6.64(5.22,8.45) 0.96(0.93,0.98) <0.001 95.7% Table 3: Subgroup analysis and meta-regression analysis for the studies assess the influence of treatment in pulmonary complications of MI.
  • 5. clinicsofsurgery.com 5 Volume 7 Issue 9 -2022 Clinical Paper Figure 1: Flow chart of literature search and study selection. Figure 2: Forest plots depicting 30-day mortality rate of different treatments. OR was shown with 95% CI. CI: confidence interval.
  • 6. clinicsofsurgery.com 6 Volume 7 Issue 9 -2022 Clinical Paper Figure 3: Forest plots depicting pulmonary complications of different treatments. 4.3.3. Renal Complications: There was no statistically signifi- cant difference in renal complications between the open surgical intervention and the endovascular approach (OR: 1.08; 95% CI 0.93–1.26; Figure 4). Although we performed subgroup analysis and regression, no source of heterogeneity was found (Table 4). Figure 4: Forest plots depicting risk of renal complications of different treatments.
  • 7. clinicsofsurgery.com 7 Volume 7 Issue 9 -2022 Clinical Paper Covariates Subgroup No. of studies OR (95% CI) Heterogeneity Meta-regression P Random-effects model Fixed-effects model P I2 Overall 12 1.08(0.93,1.26) <0.001 93.1% Area others 3 0.93 (0.88,0.98) 0.93 (0.88,0.98) 0.474 0 0.539 USA 9 1.15(0.92,1.45) 0.97(0.94,1.01) <0.001 94.9% Year Last 5 years 3 0.82(0.59,1.15) 0.81(0.76,0.86) <0.001 92.8% 0.168 others 9 1.18(1.00,1.39) 1.00(0.97,1.04) <0.001 91.9% numbers <100 7 0.98(0.90,1.05) 0.97(0.94,1.01) <0.001 97.3% 0.718 >100 5 1.18(0.81,1.72) 0.93(0.89,0.98) 0.061 50.2% Type of MI Acute 5 1.38(0.66,2.86) 0.86(0.79,0.93) <0.001 96% 0.639 Chronic 7 1.04(0.93,1.17) 0.98(0.94,1.01) <0.001 88.5% Table 4: Subgroup analysis and meta-regression analysis for the studies assess the influence of treatment in renal complications of MI. 4.3.4. Sensitivity Analysis and Publication Bias: Influence anal- ysis was performed and demonstrated that no one study could over- ly affect the summary of the outcomes estimate (Supplementary Figure 1). Publication bias was assessed by funnel plot analysis and the plots showed basic symmetry (Supplementary Figure 2). No significant publication bias was further determined by Begg’s test (Supplementary Figure 3). Supplementary Figure. 1: Influence analysis for the studies. Supplementary Figure 2: Funnel plot of comparison of the included trials.
  • 8. clinicsofsurgery.com 8 Volume 7 Issue 9 -2022 Clinical Paper Supplementary Figure 3: Begg’s test result of publication bias. 5. Discussion MI has no distinguishing clinical manifestations and is often mis- diagnosed [34]. With the advancements in diagnosis and treatment technology, MI has become a multidisciplinary disease and is currently treated mainly through open surgery and interventional management. However, the optimal management of MI remains controversial [13,35,36]. The best treatments for MI, acute MI, and chronic MI have only been meta-analyzed separately. For the first time, we have comprehensively evaluated the treatment of two types of MI. Our meta-analysis included 28 articles, in- cluding 30775 patients with MI, and showed that patients treated with open surgery have an increased rate of 30-day mortality (OR 1.45; 95% CI 1.08–1.95) and incidence of pulmonary complica- tions (OR: 1.61; 95% CI 1.28–2.04), especially in studies involv- ing more than 100 patients. When more than 100 patients were enrolled, open surgery also significantly increased the incidence of postoperative pulmonary complications. The open surgery ap- proach is a traditional treatment method for MI. In recent years, endovascular treatment has been more popular because it avoids laparotomy [37]. With regard to 30-day mortality, although the short-term mortality in patients with chronic MI and acute MI is very different, open surgery may have a worse prognosis. This is consistent with previous research results [38,39], although exact reasons for this remain unclear. This may be caused by bias in the selection of interventions. Patients with mild symptoms or po- tential intestinal ischemia but not intestinal necrosis are usually selected for endovascular interventional therapy. Open surgery in- terferes greatly with abdominal organs, and abdominal incisions are also not conducive to patient recovery. However, this conclu- sion is applicable only to studies with a large number of patients (more than 100), as we found in this study. Research with a large sample size is needed to explore this finding further. Open sur- gery increased the rate of lung complications compared with en- dovascular therapy. This may be because open surgery needs to be performed under general anesthesia and endotracheal intubation with general anesthesia may interfere with the respiratory system, while the intravascular intervention requires only local anesthesia. In the subgroup analysis, the increase in pulmonary complications by open surgery seems to apply only to acute MI and studies in- cluding more than 100 patients. MI reperfusion injury may induce remote organ injuries [40,41]; the lung appears to be the first organ affected by this pathogenic process [42]. In patients with chronic MI, the body may adapt to the ischemic state because of long- term circulatory blockage, and the damage during reperfusion is relatively light. Of course, the influence of large sample size and high-quality research on the conclusion is obvious. The rate of bowel resection was not statistically different in dif- ferent treatment methods of our study. This is inconsistent with the conclusions of previous studies [43]. This may be related to requiring laparotomy to remove the necrotic bowel after endovas- cular treatment [44]. There was no significant difference in renal complications in the different treatment studies in our study. There were also no significant differences in the different subgroups with respect to number of patients included, different regions, and acute and chronic MI. This is inconsistent with the study of Davenport et al [45]. Although intravascular interventional therapy produces mild hemodynamic changes, contrast-induced acute kidney injury cannot be ignored. 6. Limitations There are several limitations in our meta-analysis. First, there is obvious heterogeneity in our meta-analysis. Although sensitivity analysis, subgroup analysis, and meta-regression were used, high
  • 9. clinicsofsurgery.com 9 Volume 7 Issue 9 -2022 Clinical Paper heterogeneity existed among studies. Second, all the included studies were retrospective studies, so the representativeness of our study may be limited. Third, most of the studies we included were from the United States, and the conclusions reached may be geographically restricted. Fourth, most of the studies analyzed in- cluded a small number of patients, and this may not represent the actual efficacy. 7. Conclusions Endovascular approach for AMI may be associated with decreased 30-day mortality and avoidance of the incidence of postoperative pulmonary complications. However, more high-quality studies with larger sample sizes are warranted. References 1. P Sardar, CJ White. Chronic mesenteric ischemia: Diagnosis and management, Prog Cardiovasc Dis. 2021; 65: 71-75. 2. E Klar, PB Rahmanian, A Bucker. Acute mesenteric ischemia: a vas- cular emergency, Dtsch Arztebl Int. 2012; 109: 249-256. 3. B Luther, A Mamopoulos, C Lehmann. The Ongoing Challenge of Acute Mesenteric Ischemia, Visc Med. 2018; 34: 217-223. 4. M Bala, J Kashuk, EE Moore. Acute mesenteric ischemia: guide- lines of the World Society of Emergency Surgery, World J Emerg Surg. 2017; 12: 38. 5. JV Tilsed, A Casamassima, H Kurihara. ESTES guidelines: acute mesenteric ischaemia, Eur J Trauma Emerg Surg. 2016; 42: 253-270. 6. K Gnanapandithan, P Feuerstadt. Review Article: Mesenteric Isch- emia, Curr Gastroenterol Rep. 2020; 22: 17. 7. NT Orr, ED Endean. Part Two: Against the Motion. An Endovas- cular First Strategy is not the Optimal Approach for Treating Acute Mesenteric Ischemia, Eur J Vasc Endovasc Surg. 2015; 50: 276-279. 8. A Zientara, AR Domenghino, I Schwegler. Interdisciplinary ap- proach in emergency revascularization and treatment for acute mes- enteric ischemia, BMC Surg. 2021; 21: 89. 9. AL Menges, B Reutersberg, A Busch. Early and Midterm Outcomes of Open and Endovascular Revascularization of Chronic Mesenteric Ischemia, World J Surg. 2020; 44: 2804-2812. 10. Y Erben, CD Protack, RA Jean. Endovascular interventions decrease length of hospitalization and are cost-effective in acute mesenteric ischemia. J Vasc Surg. 2018; 68: 459-469. 11. Z Zhang, D Wang, G Li. Endovascular Treatment for Acute Throm- boembolic Occlusion of the Superior Mesenteric Artery and the Out- come Comparison between Endovascular and Open Surgical Treat- ments: A Retrospective Study, Biomed Res Int. 2017; 1964765. 12. MD Atkins, CJ Kwolek, GM LaMuraglia. Surgical revasculariza- tion versus endovascular therapy for chronic mesenteric ischemia: a comparative experience, J Vasc Surg. 2007; 45: 1162-1171. 13. S Arya, S Kingman, JP Knepper. Open Mesenteric Interventions Are Equally Safe as Endovascular Interventions and Offer Better Midterm Patency for Chronic Mesenteric Ischemia, Ann Vasc Surg. 2016; 30: 219-226. 14. 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