Abstract
Objectives
To compare the safety and efficacy of minimally invasive surgery (MIS) with traditional open surgical approach for congenital diaphragmatic hernia (CDH).
Methods
A literature search was performed using the PubMed database, Embase, and the Cochrane central register of controlled trials using a defined set of criteria. The outcomes, which include post-operative mortality, incidence of hernia recurrence, rates of patch use and complications, were analyzed.
Results
We investigated nine studies, which included 507 patients. All studies were non-randomized historical control trials. The MIS group had a significantly lower rate of post-operative death with a risk ratio of 0.26 [95 % confidence interval (CI) 0.10–0.68; p = 0.006] but a greater incidence of hernia recurrence with a risk ratio of 3.42 (95 % CI 1.98–5.88; p < 0.00001). Rates of prosthetic patch use were similar between the two groups. Fewer cases of surgical complications were found in the MIS group with a risk ratio of 0.66 (95 % CI 0.47–0.94; p = 0.02).
Conclusions
MIS for CDH repair is associated with lower post-operative mortality and morbidity compared with traditional open repair. Although rate of patch use appears to be comparable, the increased risk of CDH recurrence should not be ignored. The lack of well-controlled prospective trials still limits strong evaluations of the two surgical techniques.
Keywords: Congenital diaphragmatic hernia, Minimally invasive surgery, Meta-analysis, Hernia recurrence
Introduction
Congenital diaphragmatic hernia (CDH) is a congenital defect in diaphragm development, which occurs in approximately 1 in 2500–4000 live births [1]. Surgical repair via laparotomy or thoracotomy is the traditional treatment for patients with CDH. Since the first report by Silen et al. on thoracoscopic CDH repair in an adolescent in 1995 [2], minimally invasive surgery (MIS) techniques, both laparoscopic and thoracoscopic, have been considered as alternative approaches for CDH repair. However, this new technique has not gained widespread acceptance among surgeons mainly because of the controversy involving its safety and efficacy, such as mortality, recurrence rate and complication rate.
To compare the safety and efficacy of MIS with traditional surgical approach for CDH, we performed an appropriate meta-analysis of the related studies.
Methods
Studies that met all the following criteria were included in the meta-analysis: (1) the trial was a randomized or non-randomized clinical trial; (2) the study was designed to compare surgical outcomes of neonates with CDH between MIS intervention and open procedures; and (3) data on incidence of mortality, recurrence, patch use, and surgical complication rate were fully or partially reported.
We performed a literature search of the PubMed database (National Library of Medicine, Bethesda, MD, USA) that covered the period from 1966 to December 2013. The search conducted for Embase and the Cochrane Central Register of Controlled Trials was restricted to English-language literature. We applied the following subject heading or keywords: “congenital diaphragmatic hernia (CDH)”, “thoracoscopy”, “endosurgery”, “mortality”, “recurrence”, “patch”, and “complications”. Two authors (Zhu and Wu) independently performed an electronic database search to identify studies that met the eligibility criteria. Reference lists of relevant textbooks, review articles, and abstracts of scientific meetings were also included in the search.
We extracted data from each eligible study, including general information, post-operative mortality, incidence of hernia recurrence, rates of patch use, and complications.
Review Manager 5.0, which was created by the Cochrane Collaboration for meta-analysis (http://www.cochrane.org), was used for statistical analysis. Heterogeneity among studies was assessed using Cochran’s Q statistic to determine whether a fixed (p > 0.1) or random (p < 0.1) effect model should be used. Dichotomous outcomes were expressed in relative risk (RR) with their 95 % confidence interval (CI) values. Statistical significance was assessed using Z test, and the pooled data were considered to be statistically significant at p < 0.05.
Results
Our (Zhu and Wu) preliminary search revealed 70 relevant studies, and 61 of them were eventually excluded because they were merely narrative studies or case reports or did not evaluate the surgical outcomes that were the focus of this review. Figure 1 shows details of study identification, inclusion and exclusion. A total of nine articles were involved in our meta-analysis.
Characteristics of studies
All nine clinical trials [3–11] compared thoracoscopic or laparoscopic (only four laparoscopic cases) repair of CHD with open techniques. All the studies were non-randomized historical control trials. Table 1 shows the detail information of all the trials.
Table 1.
Trial | Study design | Patient number | Sex (male/female) | Age at operation (range) day | Weight (range) kg | Left side (left/total) | Follow-up time (month) | Note |
---|---|---|---|---|---|---|---|---|
1. Cho et al. [3] | Non-randomized historical control trials | TS: 29 OS: 28 |
15/14 16/12 |
NR | 3.2 3.1 |
21/29 23/28 |
11.2 ± 1.9 8.1 ± 1.8 |
Possible bias caused by the simultaneous introduction of a change in critical care and the thoracoscopic approach |
2. Gourlay et al. [4] | Non-randomized historical control trials | TS: 20 OS: 18 |
NR | 5.5 3.8 |
3.2 (2.0–4.5) 3.1(1.6–3.8) |
NR | 14.5 37 |
Possible bias caused by the different time periods when both groups were treated |
3. Lao et al. [5] | Non-randomized historical control trials | TS: 14 OS: 17 |
12/2 10/7 |
3 (2–150) 3 (2–24) |
3.2 (2.1–4.7) 3.2 (2.1–4.0) |
13/14 16/17 |
8.7 13.9 |
The sample size is small |
4. Keijzer et al. [6] | Non-randomized historical control trials | TS: 23 OS: 23 |
13/10 14/9 |
3 (1–6) 4 (2–10) |
3.1(1.6–4.1) 3.3(2.0–5.1) |
21/23 18/23 |
NR | Possible bias as the open treatment cohort contained significantly more patients on ECMO treatment compared to the thoracoscopic approach |
5. McHoney et al. [7] | Non-randomized historical control trials | TS: 13 OS: 35 |
NR | 12.5 (2–45) 11.7 (1–75) |
4.2 (3.0–8.0) 3.6 (2.0–6.0) |
NR | 15 31 |
Possible selection bias as the thoracoscopic treatment cohort is too small |
6. Gander et al. [8] | Non-randomized historical control trials | TS: 26 OS: 19 |
14/12 8/11 |
3 (2–22) 4 (1–10) |
3.2 (1.3–4.2) 3.2 (1.7–3.9) |
23/26 16/19 |
14 14 |
Possible bias caused by difference in surgeons and the number of allocated cases |
7. Szavay et al. [9] | Non-randomized historical control trials | TS/LS: 17/4 OS: 12 |
11/10 9/3 |
4 (0–1017) | 4.3 3.5 |
15/21 10/12 |
NR | It has bias of data collection. The thoracoscopic group has less complicated cases |
8. Jancelewicz et al. [10] | Non-randomized historical control trials | TS: 23 OS: 136 |
15/8 NR |
2 (0–21) 4 (0–4152) |
3.1(1.6–4.9) 3.2(1.2–4.7) |
22/23 NR |
43.2 NR |
The sample size of the TS group is too small |
9. Nam et al. [11] | Non-randomized historical control trials | TS: 16 OS: 34 |
12/4 21/13 |
4.6 4.3 |
3.0 3.0 |
15/16 28/34 |
35.6 ± 24.1 | There were more laparotomy than thoracoscopic cases. The laparotomy group included a larger number of high risk patients, which may cause selection bias |
TS thoracoscopic surgery, OS open surgery, LS laparoscopic surgery, NR not report
Surgical outcomes
Our meta-analysis revealed a significantly lower rate of post-operative death in the MIS group than in the open techniques group with an RR of 0.26 (95 % CI 0.10–0.68; p = 0.006) (Fig. 2). The incidence of hernia recurrence was greater in the MIS group with an RR of 3.42 (95 % CI 1.98–5.88; p < 0.00001) (Fig. 3). The previous two sets of pooled data both showed good homogeneity among the involved trials. Thus, fixed models were applied for analysis. No significant difference was found for the rates of prosthetic patch use between the two groups (Fig. 4). Fewer cases of surgical complications were found for neonates who underwent thoracoscopic or laparoscopic procedures with an RR of 0.66 (95 % CI 0.47–0.94; p = 0.02) (Fig. 5).
Discussion
The use of minimally invasive techniques in pediatric surgery has been increasing in the last decade [12]. MIS offers several advantages over open surgery, such as quicker recovery and improved cosmetic effect. Although several studies have reported success in thoracoscopic repair of CDH [2, 13–15], similarities in outcomes of MIS and standard open operation remains unverified.
Surgical technique
Almost all of the studies we reviewed showed that thoracoscopy is the most common approach of MIS for CDH [3–8, 10, 11]. However, some studies used the laparoscopic approach [9]. Szavay et al. reported that the selection criteria for either thoracoscopic or laparoscopic approach depend on the anatomical site of the hernia. They found that the laparoscopic approach is more appropriate for the accessible left-sided ventral hernias (Morgagni’s hernia) and proved to be better and easier for abdominal cavity operations [9]. All thoracoscopic repairs were performed on patients in the lateral decubitus position with the affected side elevated, utilizing three to four 3 or 5 mm ports for access to the thoracic cavity. Insufflation with carbon dioxide was used in most cases, which could also easily facilitate reduction of herniated viscera. Non-absorbable interrupted suture is recommended to close the defect and resection of the hernia sac. Lao et al., Keijzer et al., and Gander et al. reported that patch repair, extracorporeal membrane oxygenation (ECMO) treatment, and inability to reduce the herniated intrathoracic abdominal organs are considered as the relative contraindications for thoracoscopic approach [5, 6, 8]. Yang et al. also reported herniation of the stomach into the thorax as indicated by nasogastric tube position in the thorax on a chest film as contraindication for the thoracoscopic repair of CDH [13]. However, we considered that given the eventual increase in experience with the thoracoscopic approach over time, indications for the thoracoscopic approach should be broadened. According to our result, which showed no significant difference for the rates of prosthetic patch use between the two groups, patch repair could be accomplished by thoracoscopic approach. In some institutions, prior need for ECMO support, mild persistent pulmonary hypertension, prematurity, low birth weight, and even diaphragmatic agenesis are not considered as contraindications [3]. Currently, the standard care applied is to close large defects using prosthetic patch [16]. Although six of the nine trials revealed longer operative time for the MIS group than the open surgical group, we considered that duration is not related with intraoperative differences in blood loss, transfusion, or patch use. Duration of the operation is reflective of the learning curve on new endoscopic techniques. In most of the articles we reviewed, the operative times gradually decrease with increased experience and refinements in the technique, which had been described by Cho et al. [3].
Rate of prosthetic patch use varied among the trials involved in this analysis for both the MIS and open surgical groups. The meta-analysis revealed no significant difference between the two groups, and high heterogeneity was found among the groups. Different surgical habits might contribute to this disparity. As previously discussed, learning curves of MIS procedures also affect patient selection for patch use. The use of prosthetic patches became controversial because it was associated with a higher rate of recurrence [3, 9]. Conclusion could only be drawn if patch use predisposes the patient to a higher rate of recurrence and when the same criteria are applied for patients who underwent MIS.
Complication
Theoretically, death and recurrence are both post-operative complications. Although the last meta-analysis fails to show a significant difference in survival between endosurgical and open CDH repair [17], our result show a significantly lower rate of post-operative death in the MIS group than in the open techniques group. But we still agree with the previous comments, because this result may be caused by vulnerability to selection and performance bias. For example, surgeons may have favored open surgery for higher risk, more unstable cases. Eight of the nine trials revealed a significantly higher recurrence rate in the MIS group than in the open surgical group. Our pooled data showed an overall recurrence of 18.9 % (35 of 185) for patients who underwent MIS compared with 6.5 % (21 of 322) for patients who underwent open procedures. Our results were consistent with that of a previous meta-analysis [17]. Several factors might contribute to this clinical outcome. As a newly introduced surgical technique, learning curves could not be avoided during the clinical practice of surgeons with limited experience. Jancelewicz et al. reported that for primary thoracoscopic repair, a trend toward decreased recurrence rate is observed from 50 % prior to the year 2008 to 25 % thereafter [10]. Different rates of prosthetic patch use influenced surgical outcomes, including the recurrence rates. However, these explanations are not firmly supported in the patient series. One author performed a comparative analysis on the potential factors involved in post-operative recurrence, such as perinatal conditions, blood gas parameters, and patch use, but none of the clinical data seemed to be predictive of recurrence [8].
All the trials included are susceptible to the limitations of any retrospective review. They all have selection bias, and the numbers of patients are all small to draw a definitive conclusion. Therefore, our meta-analysis also has limitations which are caused by the bias of the included trials. The data we extracted from different retrospective trials, for example, the different follow-up time may raise the possibility of measurement error.
Conclusion
MIS for CDH repair is associated with lower post-operative mortality and morbidity compared with traditional open surgery. Although the rate of patch use appears to be comparable, the increased risk of recurrence of CDH should not be ignored. The lack of well-controlled prospective clinical trials might also be a reason for the inability to find significant predictive factors. High-quality prospective clinical trials are needed to evaluate these two surgical techniques.
Compliance with ethical standards
Conflict of interest
YZ declares no conflict of interest.
YW declares no conflict of interest.
QP declares no conflict of interest.
LM declares no conflict of interest.
HL declares no conflict of interest.
LL declares no conflict of interest.
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