EXPEDITED PUBLICATION
Endovascular Aortic Repair Versus Open Surgical Repair for Descending Thoracic Aortic DiseaseA Systematic Review and Meta-Analysis of Comparative Studies
Davy Cheng, MD*,*,
Janet Martin, PharmD, MSc (HTA&M)*,
Hani Shennib, MBBS ,
Joel Dunning, PhD ,
Claudio Muneretto, MD ,
Stephan Schueler, PhD, MD||,
Ludwig Von Segesser, MD¶,
Paul Sergeant, MD, PhD# and
Marko Turina, MD*
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* Department of Anesthesia & Perioperative Medicine, Evidence-Based Perioperative Clinical Outcomes Research Group London Health Sciences Centre, The University of Western Ontario, London, Ontario, Canada
Vascular, Heart & Lung Associates, Phoenix, Arizona
Department Cardiothoracic Surgery, James Cook University Hospital, Middlesbrough, United Kingdom
Department of Cardiac Surgery, University of Brescia Medical School, Brescia, Italy
|| Department for Cardiothoracic Surgery, Freeman Hospital, Newcastle upon Tyne, United Kingdom
¶ Cardiovascular Surgery, University Hospital CHUV, Lausanne, Switzerland
# Cardiac Surgery Department, Gasthuisberg University Hospital, Leuven, Belgium
** Cardiac Surgery, University Hospital Zurich, Zurich, Switzerland. Support for the meta-analysis was provided by an unrestricted research grant from the European Association of Cardiothoracic Surgery (EACTS) and the Evidence-Based Perioperative Clinical Outcomes Research Group, University of Western Ontario. Dr. Shennib receives consulting fees from W. L. Gore. Part of this study was presented at the the 2009 ACC i2 Late-Breaking Clinical Trials Summit on March 30, 2009, in Orlando, Florida
Manuscript received September 28, 2009;
revised manuscript received November 12, 2009,
accepted November 19, 2009.
* Reprint requests and correspondence: Dr. Davy Cheng, LHSC-University Hospital, 339 Windermere Road, C3-172, London, Ontario N6A 5A5, Canada. (Email: davy.cheng{at}lhsc.on.ca).
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Abstract
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Objectives: The purpose of this study was to determine whether thoracic endovascular aortic repair (TEVAR) reduces death and morbidity compared with open surgical repair for descending thoracic aortic disease.
Background: The role of TEVAR versus open surgery remains unclear. Metaregression can be used to maximally inform adoption of new technologies by utilizing evidence from existing trials.
Methods: Data from comparative studies of TEVAR versus open repair of the descending aorta were combined through meta-analysis. Metaregression was performed to account for baseline risk factor imbalances, study design, and thoracic pathology. Due to significant heterogeneity, registry data were analyzed separately from comparative studies.
Results: Forty-two nonrandomized studies involving 5,888 patients were included (38 comparative studies, 4 registries). Patient characteristics were balanced except for age, as TEVAR patients were usually older than open surgery patients (p = 0.001). Registry data suggested overall perioperative complications were reduced. In comparative studies, all-cause mortality at 30 days (odds ratio [OR]: 0.44, 95% confidence interval [CI]: 0.33 to 0.59) and paraplegia (OR: 0.42, 95% CI: 0.28 to 0.63) were reduced for TEVAR versus open surgery. In addition, cardiac complications, transfusions, reoperation for bleeding, renal dysfunction, pneumonia, and length of stay were reduced. There was no significant difference in stroke, myocardial infarction, aortic reintervention, and mortality beyond 1 year. Metaregression to adjust for age imbalance, study design, and pathology did not materially change the results.
Conclusions: Current data from nonrandomized studies suggest that TEVAR may reduce early death, paraplegia, renal insufficiency, transfusions, reoperation for bleeding, cardiac complications, pneumonia, and length of stay compared with open surgery. Sustained benefits on survival have not been proven.
Key Words: endovascular • descending aorta • TEVAR • meta-analysis • metaregression • survival
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Abbreviations and Acronyms
| | CI = confidence interval | | OR = odds ratio | | TEVAR = thoracic endovascular aortic repair | | WMD = weighted mean difference |
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Since the introduction of thoracic endovascular aortic repair (TEVAR) using stent grafts for complicated diseases of the descending thoracic aorta, there has been debate regarding the safety, efficacy, and durability of this approach. Until recently, options for the management of thoracic aortic disease were limited to open surgical repair or conservative medical management. After the first formal publication of a case series describing the outcome of 13 patients undergoing TEVAR for descending thoracic aneurysm in the early 1990s (1), the subsequent pace of uptake of TEVAR has outstripped adequate evaluation of the evidence for its benefits and risks. To date, no randomized trials of TEVAR versus open surgical repair for descending thoracic aortic disease have been performed. Most published reports describing TEVAR consist of uncontrolled retrospective cohorts or case series. Recently, a number of nonrandomized phase II studies have compared endovascular repair with a concurrent or historical open surgical group. In the absence of definitive randomized controlled trials, the value of TEVAR relative to conventional open surgical approaches will continue to be debated (2–4).
When randomized trials are unavailable, metaregression can be performed to maximize the knowledge gained from existing comparative studies in order to optimally direct future patient care decisions and need for further research. A methodologically rigorous meta-analysis with metaregression to account for baseline demographics is urgently needed to clarify the overall benefit-to-risk ratio of TEVAR versus open surgical repair for complicated diseases of the descending thoracic aorta, and to better inform further research in this area. Metaregression may also shed light on the balance of outcomes across various patient subgroups with differing pathologies of the aorta. Disease of the descending thoracic aorta requiring surgical or endovascular intervention may include degenerative aneurysm, dissection, traumatic rupture, intramural hematoma, and penetrating aortic ulcer. Previous meta-analyses of TEVAR assessed only noncomparative studies (5), did not include more recent studies (5–7), focused only on 1 pathology such as blunt injury (6–10), or selectively reported only 1 outcome such as death (10). This study was commissioned by the European Association of Cardiothoracic Surgery to address the current evidence for adoption of TEVAR. The objective was to perform a comprehensive meta-analysis with metaregression of available comparative studies to determine whether TEVAR improves morbidity, mortality, and resource-related outcomes compared with open surgery for adults presenting with thoracic aortic disease.
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Methods
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This analysis was planned in accordance with current guidelines for performing comprehensive systematic reviews and meta-analyses with regression, including the PRISMA (Preferred Reporting Items for Systematic reviews Meta-Analyses) (11) and MOOSE (Meta-analysis Of Observational Studies in Epidemiology) (12) guidelines for randomized and nonrandomized studies, respectively. A protocol pre-specified outcomes, search strategies, inclusion criteria, and statistical analyses.
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Search strategy
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A search was performed by bibliographic experts to identify all studies in MEDLINE, Cochrane Central Register of Controlled Trials on The Cochrane Library, International Association of Health Technology Assessment (INAHTA), and EMBASE from 1990 to March 2009, as well as surgical meeting abstracts from 2006 to 2009. The Federal Drug Administration devices database was also accessed for additional unpublished data. Search terms included combinations and derivatives of the following as textwords and MESH terms: (thorac* AND aort*) OR aneurys* OR dissect* OR "penetrating atherosclerotic ulcer" OR "intramural hemorrhage" OR trauma* OR rupture*) AND (endovasc* OR endostent* OR surg* OR operat* OR TEVAR OR EVAR OR stent*). After the initial searches were completed and potentially relevant studies identified, additional tangential searches were conducted using related article links within MEDLINE. In addition, individual searches for specific names of commercial stents were performed to identify further TEVAR studies, including Gore TAG (Gore, Flagstaff, Arizona), Excluder (Gore), AneuRx (Medtronic, Sunnyvale, California), Talent (World Medical Manufacturing, Sunrise, Florida), Vanguard (Boston Scientific, Natick, Massachusetts), Zenith (Cook, Indianapolis, Indiana), Stentor (MinTec, La Ciotat, France), Relay (Bolton Medical, Barcelona, Spain), Endofit (Endomed, Inc., Phoenix, Arizona), E-Vita (Jotec, Heitchingen, Germany), and TX1 or TX2 (Cook). Reference lists of relevant studies and recent overviews were also reviewed for additional studies. Studies in any language, whether published or unpublished, were eligible for inclusion. Selected authors of clinical studies and experts were contacted to further identify unpublished studies of TEVAR versus open surgery management.
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Study retrieval and selection criteria
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Trials identified as potentially relevant on the basis of title or abstract were selected for full review. Two reviewers independently assessed these trials for eligibility based on prespecified inclusion criteria. Disagreement was resolved by consensus with third party adjudication.
For the primary analysis, all studies comparing TEVAR with open surgery were eligible if they enrolled at least 10 adults with descending thoracic aneurysm disease and reported at least 1 clinically relevant or resource-related outcome. Eligible aortic pathologies included thoracic aortic aneurysm, dissection, rupture, trauma, penetrating aortic ulcer, or intramural hemorrhage, whether chronic or acute, emergent or elective. Studies of coarctation or Marfan syndrome, hybrid procedures, Type A aneurysm, and combined thoracic and abdominal aortic disease were excluded. If studies provided outcomes across a number of thoracic aorta pathologies, only the relevant subgroups were included.
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Data extraction and outcomes definitions
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Two reviewers independently assessed studies for inclusion criteria, and data were extracted independently by the lead reviewer and at least 1 additional reviewer. Discrepancies were resolved by consensus with international authors at designated consensus meetings. Data were extracted onto standard forms, and included baseline demographics, aortic pathology, duration of follow-up study sites, study design, years of enrollment, whether patients were consecutively enrolled, and loss to follow-up. Studies from centers that included the same set of patients over different time frames were carefully evaluated to include only updated follow-up data.
For clinical outcomes, definitions provided by authors of the studies were generally used as provided. Death was defined as cumulative incidence of all-cause mortality. Incidence of paraplegia or paraparesis, whether permanent or temporary, was reported as an aggregate outcome, and only post-operative incidence of new paraplegia or paraparesis was considered (i.e., preprocedural paraplegia due to trauma was not considered relevant). Permanent paraplegia was defined as paraplegia persisting at the time of last study follow-up. Renal dysfunction was defined as per the authors' definition (increases in serum creatinine over baseline by more than 50% or need for renal replacement therapy). Incidence of transfusions was defined as the cumulative number of patients transfused blood products post-operatively. The composite outcome of any cardiac complications was recorded only when the study authors provided the number of patients experiencing any complication related to cardiovascular system post-operatively, typically defined as 1 or more episodes of ischemia, infarction, hemodynamic instability, low cardiac output syndrome, or arrhythmia. Endoleaks were classified according to the usual nomenclature (13). Early endoleak was defined as occurring within 30 days, and late endoleak as occurring or persisting at follow-up beyond 30 days.
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Statistical analysis
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Planned subanalyses included analysis by study design (single-center series, multicenter studies, and registries; unfortunately, randomized studies were unavailable), aortic pathology (degenerative aneurysm, dissection, trauma, rupture, and intramural hemorrhage/penetrating aortic ulcer), and by type of stent (commercial and noncommercial or homemade).
Potential confounding due to selection bias or differential intensity of follow-up in the observational studies was evaluated by measuring whether there were important differences between TEVAR and open surgical groups in baseline patient characteristics or study design characteristics including age, sex, aortic pathology, urgency of intervention, and comorbidities including smoking history, chronic obstructive pulmonary disease, diabetes, hypertension, coronary artery disease, and length of follow-up. Metaregression was performed to measure the impact of baseline characteristics and pathologies on the effect size for death, stroke, or paraplegia. To determine the impact of time and the learning curve, metaregression was also performed by year of patient enrollment defined for each study as the median year within the range of years during which patient data were collected. When date ranges for patient enrollment were not provided, the year was assumed to be 3 years prior to the date of publication. Sensitivity analysis was planned for the following indicators of study quality: prospective versus retrospective data collection, consecutive patient recruitment versus nonconsecutive patient inclusion, and historic versus concomitant control groups.
In evaluating multiple publications of overlapping patient populations, we classified all studies by the center(s) and dates of patient enrollment, and selected the most recent and/or most complete series from each center to extract as many relevant outcomes as possible. When the more recent series failed to report all outcomes of interest, we referred to the next most current series from the same center, and extracted the remaining outcomes as far as possible. When it became apparent that a number of single-center experiences were published with overlapping patient datasets as those included in multicenter phase II trials or registries, we decided to present the data aggregated by each study type (consecutive series, multicenter trial, and registries), and to combine the results across multicenter and single-center studies only when the degree of overlap was likely to be low, if any. Registry data were not aggregated together with multicenter and single-center studies, since the degree of overlap was likely to be large, and since significant heterogeneity was detected between the registry aggregate data compared with nonregistry data.
Patient characteristics and outcomes were entered into a database, and analysed using Comprehensive Meta-Analysis Software version 2 (Biostat, Littlewood, New Jersey). For dichotomous variables, individual and pooled statistics were calculated as weighted odds ratios (ORs) with 95% confidence intervals (CIs). For continuous outcomes, individual and pooled statistics were calculated as weighted mean differences (WMD) and 95% CIs. Since heterogeneity was anticipated across the trials, the random effects model was used for all calculations to provide an overall conservative analysis (14). For the primary analysis, data were combined within each category of study type (single-center series, multicenter trials, registries), and presented by study subtype and in aggregate (for single-center and multicenter data only). For subanalyses by pathology, by study design, and by type of stent used, data were combined across subgroups using the mixed effects analysis. The test for interaction was employed to determine whether effect sizes differed significantly across subgroups. We preferentially captured intention-to-treat data whenever available (15).
Heterogeneity across trials was explored for each outcome by calculating I2, which indicates the percent of heterogeneity across trials that cannot be explained by chance variation alone (16,17). I2 >50% was considered to indicate high heterogeneity. Publication bias was assessed through funnel plots, and Egger's regression test was applied (18).
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Results
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In total, 2,894 abstracts were identified for screening, and a total of 42 studies reported in 59 papers involving 5,888 patients met the inclusion criteria for this analysis (19–77). Fifteen papers described 4 multicenter observational trials (23–30,35,42,43,51–54), 3 papers described 3 registries (73–75), and the remainder of papers described cohorts or series of patients undergoing TEVAR versus concurrent or historical control groups, from single centers. Figure 1
outlines the results of the search strategy, and Table 1
describes the included studies.
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Figure 1 Results of Literature Search
The flow chart outlines the total number of potentially relevant citations reviewed and collected for full-text screening. Reasons for inclusion and exclusion are outlined. CoA = coarctation; nRCT = nonrandomized controlled trial.
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Weighted analysis across all studies showed that baseline characteristics were similar between TEVAR and open groups for the following: sex, hypertension, coronary artery disease, chronic obstructive pulmonary disease, and smoking status (Table 2). However, patients included in the TEVAR group were older on average by nearly 3 years than patients included in the open surgery group, and this difference was statistically significant (age 54 ± 13 years for TEVAR versus 51 ± 13 years for open surgery; p = 0.001), underscoring the need for metaregression analysis to assess the impact of age differences at baseline on outcomes estimates for TEVAR versus open surgery.
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Clinical outcomes
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Clinical outcomes are summarized in Table 3, subanalyzed by study category.
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Operative death and all-cause mortality
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Cumulative 30-day all-cause mortality was reduced for TEVAR versus open surgery (OR: 0.44, 95% CI: 0.33 to 0.59). Cumulative all-cause mortality at 1 year (OR: 0.73, 95% CI: 0.53 to 1.02; I2 = 0%) and at 2 to 3 years did not differ significantly between TEVAR and open surgery groups (OR: 0.92, 95% CI: 0.63 to 1.34; I2 = 0%).
The reduction in all-cause mortality at 30 days was greater in multicenter trials (OR: 0.24, 95% CI: 0.13 to 0.44) than for single-center series (OR: 0.53, 95% CI: 0.38 to 0.74), and the p value for interaction across study type was significant (p = 0.020). Mortality at 1 year and beyond was similar in multicenter and single-center studies. Figures 2 through 4
 summarize the results for all-cause mortality at each period of follow-up. Funnel plots (not shown) did not indicate a significant risk of publication bias for the outcome of mortality.
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Figure 2 Death at 30 Days for TEVAR Versus Open Surgery
Meta-analysis comparing death at 30 days for thoracic endovascular aortic repair (TEVAR) versus open surgery. The odds ratio (OR) for death from each included study is plotted. A pooled estimate of overall OR (diamonds) and 95% confidence intervals (width of diamonds) summarizes the effect size using the random effects model. Effects to the left of 1.0 favor TEVAR; effects to the right favor open surgery. When the horizontal bars of an individual study, or the pooled diamond width, cross 1.0, the effect is not significantly different. The I2 for heterogeneity was not significant, suggesting homogeneity in effect size across each study.
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Figure 3 Death at 1 Year for TEVAR Versus Open Surgery
Meta-analysis comparing death at 1 year for thoracic endovascular aortic repair (TEVAR) versus open surgery. The odds ratio (OR) for death from each included study is plotted. A pooled estimate of overall OR (diamonds) and 95% confidence intervals (width of diamonds) summarizes the effect size using the random effects model. Effects to the left of 1.0 favor TEVAR; effects to the right favor open surgery. When the horizontal bars of an individual study, or the pooled diamond width, cross 1.0, the effect is not significantly different. The I2 for heterogeneity was not significant, suggesting homogeneity in effect size across each study.
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Figure 4 Death at 2 to 3 Years for TEVAR Versus Open Surgery
Meta-analysis comparing death at 2 to 3 years for thoracic endovascular aortic repair (TEVAR) versus open surgery. The odds ratio (OR) for death from each included study is plotted. A pooled estimate of overall OR (diamonds) and 95% confidence intervals (width of diamonds) summarizes the effect size using the random effects model. Effects to the left of 1.0 favor TEVAR; effects to the right favor open surgery. When the horizontal bars of an individual study, or the pooled diamond width, cross 1.0, the effect is not significantly different. The I2 for heterogeneity was not significant, suggesting homogeneity in effect size across each study.
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Stroke
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The overall risk of stroke was similar for TEVAR (single-center and multicenter studies combined) versus open surgery (OR: 0.75, 95% CI: 0.50 to 1.13; I2 = 23%). In subgroup analysis, stroke was significantly reduced in multicenter trials of TEVAR versus open surgery (OR: 0.46, 95% CI: 0.25 to 0.85). Subanalysis of single-center series alone did not show significant reduction in stroke for TEVAR versus open surgery (OR: 1.12, 95% CI: 0.64 to 1.94). There was significant interaction across multicenter versus single-center subgroups (p = 0.021) (Fig. 5).
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Figure 5 Stroke for TEVAR Versus Open Surgery
Meta-analysis comparing stroke for thoracic endovascular aortic repair (TEVAR) versus open surgery. The odds ratio (OR) for stroke from each included study is plotted. A pooled estimate of overall OR (diamonds) and 95% confidence intervals (width of diamonds) summarizes the effect size using the random effects model. Effects to the left of 1.0 favor TEVAR; effects to the right favor open surgery. When the horizontal bars of an individual study, or the pooled diamond width, cross 1.0, the effect is not significantly different. The I2 for heterogeneity was not significant, suggesting homogeneity in effect size across each study.
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Paraplegia and paraparesis
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Paraplegia or paraparesis (permanent or temporary) was significantly reduced for TEVAR versus open surgery (OR: 0.42, 95% CI: 0.28 to 0.63) (Fig. 6). Permanent paraplegia was also significantly reduced (OR: 0.30, 95% CI: 0.14 to 0.62; I2 = 0%). The magnitude of reduction in risk of paraplegia or paraparesis and permanent paraplegia was similar in multicenter and single-center studies (p values for interaction across studies were 0.83 and 0.92, respectively).
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Figure 6 Paraplegia or Pareparesis for TEVAR Versus Open Surgery
Meta-analysis comparing paraplegia/pareparesis for thoracic endovascular aortic repair (TEVAR) versus open surgery. The odds ratio (OR) for paraplegia/pareparesis from each included study is plotted. A pooled estimate of overall OR (diamonds) and 95% confidence intervals (width of diamonds) summarizes the effect size using the random effects model. Effects to the left of 1.0 favor TEVAR; effects to the right favor open surgery. When the horizontal bars of an individual study, or the pooled diamond width, cross 1.0, the effect is not significantly different. The I2 for heterogeneity was not significant, suggesting homogeneity in effect size across each study.
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Other clinical outcomes
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Compared with open surgery, TEVAR significantly reduced risk of renal dysfunction (OR: 0.40, 95% CI: 0.25 to 0.63), reoperation for bleeding (OR: 0.26, 95% CI: 0.11 to 0.62), and incidence of transfusion (OR: 0.01, 95% CI: 0.002 to 0.04). Other outcomes that were significantly improved with TEVAR included cardiac, pneumonia, and respiratory complications. TEVAR significantly reduced the composite outcome of any complication compared with open surgery (OR: 0.23, 95% CI: 0.12 to 0.44).
Hospital length of stay was significantly reduced (WMD: –7 days, 95% CI: –10 to –5 days). Similarly, total intensive care unit length of stay was significantly reduced by 4 days (–4 days, 95% CI: –5 to –3 days). Procedure time was significantly reduced by a mean of 140 min for TEVAR versus open surgery (WMD: –142 min, 95% CI: –200 to –87 min; I2 = 90%). The higher heterogeneity in length of stay and procedure time was due to difference in magnitude of effect across studies rather than due to differences in direction of effect or study design.
Clinical outcomes that did not differ between TEVAR and open surgery included myocardial infarction, ischemic complications (gut or limb), vascular complications, wound infections, aortoesophageal fistula, laryngeal nerve injury, phrenic nerve injury, post-operative dissection or rupture, and need for reintervention. These outcomes were less commonly reported in the trials, and power was inadequate to rule out the potential for clinically and statistically significant differences in future studies. Patient-reported outcomes such as pain, functionality, quality of life, and patient satisfaction were not reported in the trials.
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Endoleaks
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The reported incidence of endoleak was 12.1% (95% CI: 13.0 to 17.4%) when limited to studies in which endoleaks were definitively reported. However, this may be an overestimate, since many studies did not expressly report endoleaks, and we did not presume that the incidence was zero when endoleaks were not mentioned. Since most of the studies failed to provide sufficient details about the endoleaks, it was not possible to analyze the aggregate incidence of early versus late endoleak and the different subtypes of endoleaks. Stent fractures and migration were reported rarely.
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Metaregression and other subanalyses
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Metaregression by baseline age did not impact the relative reduction in risk of death, stroke, and paraplegia for TEVAR versus open surgery (i.e., the results were consistent across age groups) (Fig. 7). Similarly, when the results for death, stroke, and paraplegia were analyzed by different aortic pathologies, the relative reductions for TEVAR versus open surgery were similar across subgroups (data not shown). Many comparative studies failed to report outcomes by specific type of pathology, and of those that did, only degenerative aneurysm and trauma were adequately represented in most subanalyses. In addition, ORs for death, stroke, and paraplegia did not differ by prospective versus retrospective design, historic versus concurrent control, consecutive versus nonconsecutive patient recruitment. Metaregression by year of patient recruitment showed that the results were similar over time since the slope of effect size over time was nonsignificant (Figs. 8 to 10).
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Figure 7 Metaregression for Death by Age Differences at Baseline
Metaregression of the effect of baseline age differences on the log odds ratio for the risk of death for thoracic endovascular aortic repair (TEVAR) versus open surgery. Each circle represents a study, telescoped by its weight in the analysis. The relationship was nonsignificant, suggesting that the impact of TEVAR on risk of death was consistent over the years (p = 0.13).
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Figure 8 Metaregression for Death at 30 Days by Enrollment Year
Metaregression of the effect of enrollment year on the log odds ratio for the risk of death at 30 days for thoracic endovascular aortic repair (TEVAR) versus open surgery. Each circle represents a study, telescoped by its weight in the analysis. The relationship was nonsignificant, suggesting that the impact of TEVAR on risk of death was consistent over the years (p = 0.45).
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Figure 9 Metaregression for Stroke by Enrollment Year
Metaregression of the effect of enrollment year on the log odds ratio for the risk of stroke for thoracic endovascular aortic repair (TEVAR) versus open surgery. Each circle represents a study, telescoped by its weight in the analysis. The relationship was nonsignificant, suggesting that the impact of TEVAR on risk of stroke was consistent over the years (p = 0.29).
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Figure 10 Metaregression for Paraplegia by Enrollment Year
Metaregression of the effect of enrollment year on the log odds ratio for the risk of paraplegia/pareparesis for thoracic endovascular aortic repair (TEVAR) versus open surgery. Each circle represents a study, telescoped by its weight in the analysis. The relationship did not reach significance, suggesting that the impact of TEVAR on risk of paraplegia/paraparesis was consistent over the years (p = 0.12).
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Subanalysis by commercial and homemade stent was not possible due to very few patients receiving homemade stents in this analysis. Analysis of outcomes by different types of commercial stents was not possible since most studies used a variety of commercial stents, and few reported outcomes individually by type of stent used.
Examination of publication bias and funnel plots did not reveal a statistically significant risk of publication bias for any of the clinical outcomes, including death, paraplegia, stroke, cardiac complications, and renal dysfunction. For some outcomes, the paucity of data precluded adequate power for robust analysis of publication bias.
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Registry data
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Registry data showed significant reduction in overall complications with TEVAR versus open repair. In contrast to comparative studies, meta-analysis of data from published registries that compared TEVAR with open surgery failed to show significant reduction in all-cause mortality, stroke, myocardial infarction, and renal dysfunction with TEVAR. Paraplegia was not reported in these registries (Table 4). The apparent differences between registry results and clinical studies are not surprising since the registries reported on a small number of patients undergoing TEVAR, and generally included only traumatic aortic injury patients with short-term follow-up and nonconsecutive patient inclusion. In addition, few registries reported on clinical outcomes other than short-term survival. As a result, registry data are likely less reliable than the cumulative evidence from clinical studies of TEVAR versus open surgery.
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Discussion
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This meta-analysis of studies comparing TEVAR with open surgery for the management of descending thoracic aortic disease provides a comprehensive aggregate analysis of the available evidence to date. Given that there are no randomized trials of TEVAR versus open surgery for descending thoracic aortic intervention, the appropriate use of meta-analysis with metaregression represents an important method to extract the best possible information from existing data to examine the relative benefits and risks of TEVAR versus open surgery while accounting for differences in patient characteristics inherent in the observational trials.
Overall, existing evidence suggests that TEVAR reduces the risk of all-cause mortality at 30 days. Survival at 1 year and beyond did not show a definitive benefit for TEVAR compared with open surgery; however, survival data after discharge were less commonly reported in the trials, and the trend was consistently in favor of TEVAR for the studies reporting 1-year cumulative all-cause mortality (p = 0.07), with no significant heterogeneity across the trials for this outcome. At minimum, the existing evidence shows that survival for TEVAR is not worse than for open surgery at midterm. Further studies, preferably randomized, with adequate power and complete follow-up will be needed to better define whether there are important long-term survival benefits for TEVAR over open surgery (78).
This analysis also shows that the risk of paraplegia/paraparesis is reduced for TEVAR versus open surgery. This has important implications for the long-term functionality and quality of life for patients undergoing thoracic aortic repair. Even when the definition was limited to permanent paraplegia, TEVAR provided significant benefit over open surgery. It is important to note that some trials employed protective techniques such as routine cerebrospinal fluid drainage, whereas others did not. Despite these practice differences, there was no detectable statistical heterogeneity across the trials for this outcome, and confidence in this result is heightened.
Other important benefits of TEVAR include reduction of renal dysfunction, transfusions, reoperation for bleeding, cardiac complications, neurologic complications, pneumonia, respiratory complications, reduced incidence of any complication, and shorter procedure time, and length of stay in intensive care unit or hospital.
Since there was generally low heterogeneity across trials, this lends credence to the robustness of the results across studies. Metaregressions and subanalyses of the results by various characteristics, including baseline characteristic differences and study design features, failed to show material changes in the results, again lending credence to the stability of the results across the studies.
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Endoleaks and aortic graft reinterventions
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There was a paucity of information on the true incidence of endoleaks and most studies limited their reporting, if any, to type I and II endoleaks since many had insufficient longitudinal follow-up to adequately ascertain type III and IV endoleaks. The incidence of endoleak was 12% overall; however, this value should be interpreted with caution since a number of trials did not report on endoleaks, and hence did not contribute to the summary estimate of incidence.
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Study strengths and limitations
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This study represents a comprehensive and rigorous systematic review with meta-analysis of existing evidence for TEVAR versus open surgery in the management of descending thoracic aortic disease. Adherence to current guidelines for performing meta-analyses of observational studies was undertaken to ensure highest possible objectivity in analyses (11,12). Unlike previous systematic reviews in this area, this meta-analysis synthesizes all clinically relevant outcomes rather than a few selected outcomes, performs metaregression, and also included all major aortic pathologies rather than focusing on a single pathology only. This allows for comparisons of the balance of clinical outcomes across all pathologies. Where possible, methods to incorporate time-to-event data in the survival analyses were used to ensure best possible estimates of survival at each time point (79,80).
Despite the quality methodology used in this meta-analysis, this analysis should be interpreted in light of the shortcomings of the available data. The most important limitation is the absence of randomized trials comparing TEVAR versus open surgery, and the risks of systematic bias inherent to observational studies. In some studies, TEVAR was compared with a historical control. The historicity of the control group increases the risk of bias favoring TEVAR since outcomes of patients with descending thoracic aortic disease may be improving over time due to better contemporary detection and overall management of aortic disease. Nonetheless, in our regression analysis by historicity of control group, the ORs did not materially change for historical versus contemporaneous controls. In addition, analysis by various features of study design (consecutiveness of patient inclusion, retrospective vs. prospective) also failed to show material changes in the results.
In some studies, the duration of follow-up was longer for the open surgery group than the TEVAR group. This may bias the results against open surgery, since increased passage of time may reveal more adverse events than during shorter follow-up. In a post-hoc sensitivity analysis limited to studies with similar duration of follow-up between TEVAR and open surgery groups, the results for death at 1 year and 2 to 3 years were similar as in the original analysis.
There was inconsistency across studies in the description of criteria used to select patients for TEVAR versus alternative procedures. In some studies, TEVAR was reserved for patients unfit for open surgery, or with comorbidities that would place them at greater risk for complications with open surgery. In some studies, younger and fitter patients were selected for the newer procedure early in the surgeon's experience. Also, in the retrospective studies, it was generally unknown how many of the patients intended to undergo TEVAR were crossed over to open surgery due to difficult morphology or other reasons. If these cross-over patients were reported in the open surgical group, there may be slight overestimation of TEVAR benefit relative to open surgery since cross-over patients are likely to have worse outcomes and more complications than patients who were originally scheduled to undergo open surgery. Nonetheless, the total contribution of crossovers to the open group is likely small, and we used the more conservative random effects analysis to avoid overestimation of benefits.
Despite extensive efforts to systematically address the risk of including overlapping patient populations in this analysis, the authors acknowledge that there may be some remaining undetected overlap within the analysis since duplication and overlapping datasets are difficult to identify, particularly when authors' and centers' names do not exactly match from 1 patient series to the next overlapping series.
In order to maximally address the limitations inherent in nonrandomized studies, we performed metaregression analyses and subgroup analyses to determine whether key patient or study characteristics measurably affected outcomes estimates. Although patient-level data would have substantially improved the ability to evaluate confounders, using study-level data for metaregression allowed for maximal information to be derived from existing evidence in the absence of available patient-level data. It is encouraging that baseline characteristics such as age and aortic pathology were not found to significantly affect the overall estimate of relative benefit of TEVAR over open surgery for all-cause mortality, stroke, or paraplegia/paraparesis. Interestingly, since the relative benefit of TEVAR over open surgery did not differ significantly by year of enrollment, there was no statistically detectable learning-curve effect for earlier trials versus later trials, although, the analyses may be limited in power to detect small differences over time. Importantly, we should not discount the importance of interpreting these results in light of the fact that results of TEVAR and open surgery are inextricably dependent on the skills of the surgeons and their teams, and it is more likely for experienced centers to publish their results than those who are early in the learning curve. The results of this analysis also need to be interpreted with the knowledge that the patient selection for TEVAR versus open surgery was at the surgeon's discretion, and the criteria for determining patient suitability for TEVAR versus open surgery were not explicitly declared in many studies. This analysis does not enable the determination of optimal patient characteristics for selecting TEVAR versus open surgery.
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Conclusions
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In patients requiring intervention for descending thoracic aortic disease, nonrandomized evidence shows that TEVAR may reduce early mortality and paraplegia compared with conventional open surgical management. TEVAR may also reduce length of hospital stay and overall complications including neurologic, cardiac, respiratory, renal, and bleeding complications, without a significant increase in the need for reintervention during mid-term follow-up. Although it remains an important caveat that these conclusions are based on observational comparative studies, the consistency of results across aortic pathologies, baseline age groups, and time periods of patient recruitment increases confidence that the findings are robust. Nonetheless, randomized trials are required to confirm the results of this metaregression. Any future randomized trials should be encouraged to adhere to the guidelines for reporting studies of TEVAR (81) and will need to address clinically important gaps in the existing evidence base, including whether longer-term survival, stroke risk, need for reintervention, quality of life, and patient functionality are improved, and whether the cost-effectiveness warrants broader uptake of TEVAR in place of open surgery.78–80
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Acknowledgments
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The authors acknowledge Kathrin Barben and Kathy McGree for their professional assistance in organizing the consensus conference; Drs. Guyan Wang, Kathy Fang, Myoung Kim, and Ling Pei for their expert data extraction; and Ms. Jennifer Podeszwa-deOliviera for her service in facilitating the literature searches and retrieval.
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References
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Abstract
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