Laparoscopic inguinal hernia repair in children is increasingly performed as it allows contralateral inspection and potentially results in shorter operation time and less complications. Evidence from meta-analyses of randomized controlled trials (RCTs) regarding the superiority of laparoscopic versus open hernia repair is lacking.
Methods
A systematic literature search was performed querying PubMed, Embase, MEDLINE, and the Cochrane Library databases. RCTs comparing laparoscopic with open hernia repair in children were considered eligible, without year and language restrictions. Cochrane Risk of Bias tool was used for quality assessment. Data were pooled using a random-effects model. Subgroup analyses were performed according to the laparoscopic suturing technique (i.e., intracorporeal or extracorporeal).
Results
Eight RCTs (n = 733 patients; age range 4 months–16 years) were included in this meta-analysis. Laparoscopic (LH) and open (OH) hernia repair was performed in 375 and 358 patients, respectively. Complications (seven RCTs, n = 693; pooled OR 0.50, 95% CI 0.14 to 1.79), recurrences (seven RCTs, n = 693; pooled OR 0.88, 95% CI 0.20 to 3.88), and MCIH rates (four RCTs, n = 343; pooled OR 0.28, 95% CI 0.04 to 1.86) were not different between the groups. LH resulted in shorter bilateral operation time (Five RCTs, n = 194; weighted mean difference (WMD) − 7.19, 95% CI − 10.04 to − 4.34). Unilateral operation time, length of hospital stay, and time to recovery were similar. There was insufficient evidence to assess postoperative pain and wound cosmesis, and evidence of substantial heterogeneity between the included studies. Subgroup analyses demonstrated less complications and shorter unilateral operation time for extracorporeal suturing and shorter length of hospital stay for intracorporeal suturing.
Conclusions and relevance
No definite conclusions to decide on the superiority of one of either treatment strategies can yet be drawn from the available literature. There was evidence of substantial heterogeneity and the clinical relevance of most estimated effects is very limited.
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The incidence of pediatric inguinal hernia ranges from 0.8 to 5% and increases to more than 30% in preterm born infants [1, 2]. Treatment is necessary because of the risk of incarceration of bowel, testis, or ovary, which occurs in approximately 3–16% of children with inguinal hernia [2, 3]. Open inguinal hernia repair is the most performed treatment strategy in children; however, the laparoscopic approach is increasingly used in current practice [4]. Although inguinal hernia repair is the most commonly performed operation by pediatric surgeons, there still is no clear consensus which technique is superior in children who need to undergo inguinal hernia repair: the open or laparoscopic.
Laparoscopic hernia repair allows better visualization of the inguinal region thereby enabling detection of a contralateral patent processus vaginalis (CPPV), which can be simultaneously closed since the presence of a CPPV might result in development of a metachronous contralateral inguinal hernia (MCIH). Open repair offers the possibility for loco regional (caudal) anesthesia, which might be beneficial as repeated or prolonged general anesthesia carries risks for near critical incidents and the U.S. Food and Drug Administration (FDA) recently released a warning that repeated or prolonged general anesthesia potentially harms the child’s developmental brain [5, 6]. In 2016, the International Pediatric Endosurgery Group (IPEG) reviewed all existing evidence on minimal access approaches in the treatment of pediatric inguinal hernia and concluded that laparoscopic hernia repair resulted in shorter operation time for bilateral hernia repair and less postoperative complications compared to the open technique [7]. Conversely, there was also a trend towards higher recurrence rates in laparoscopic hernia repair [8].
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Several systematic reviews comparing laparoscopic with open pediatric hernia repair have previously been published [8‐11], although the number of studies providing level 1a evidence is very limited. Moreover, many outcome parameters have not been addressed [11]. Consequently, there still is an ongoing debate about the best treatment strategy and decisive evidence on the superiority of one of either treatment strategies is lacking. The aim of this systematic review and meta-analysis is to provide an extensive state-of-the-art comparison and overview on high-level evidence for most relevant outcome measures including operative and postoperative complications, duration of surgery and hospital admission, postoperative pain, time to full recovery, recurrence rate, MCIH rate, cosmetic appearance, and health care costs.
Materials and methods
Literature search
A systematic review and meta-analysis was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. The protocol was registered in PROSPERO (CRD42018116953). An extensive literature search was performed in November 2017 and updated in August 2018 using PubMed, EMBASE, MEDLINE, and the Cochrane Library databases (see Search strategy, Supplementary Material 1). All studies that compared open versus laparoscopic hernia repair in children with inguinal hernia were considered eligible for inclusion, and no year or language restrictions were applied. Reference lists of eligible articles were also queried. The following subject headings (MeSH) and text words were used: inguinal hernia, children/child, p(a)ediatric, laparoscopic/laparoscopy. Institutional Review Board (IRB) approval and written consent were not required for conducting this meta-analysis.
Eligibility criteria
In this review, all available randomized controlled trials (RCTs) that compared open with laparoscopic hernia repair in children (younger than 18 years old) with inguinal hernia were considered eligible. Only RCTs were included to achieve the highest level of evidence; all other study designs were excluded. Primary outcome measures included operative (i.e., injury of spermatic vessels or spermatic cord, tuba lesions, bleeding, and apnea) and postoperative complications (i.e., hematoma/scrotal edema, hydrocele, wound infection, iatrogenic ascent of the testis, and testicular atrophy). Secondary outcome measures were duration of surgery, length of hospital stay, postoperative pain (pain scores and pain-medication requirement), return to full recovery, recurrence, MCIH, and cosmetic results.
Study selection and methodological quality assessment
The screening and selection of studies based on title and abstract (level 1), full-text screening (level 2), and quality assessment were independently performed by two review authors (SM and KD). Risk of bias was assessed by the two review authors using the Cochrane Risk of Bias tool for Randomized Controlled Trials. Inconsistencies were solved by second joint review of the literature or by consulting a third independent review author (JD).
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Data extraction
Supplementary Material 2 comprises systematically extracted data regarding important study details and patient characteristics from the included studies. Missing data were retrieved by contacting the study author(s) and/or calculated if possible. In case of any disagreement by the two reviewers, a third reviewer (JD) was consulted after joint review, literature review, and discussion.
Different techniques are currently used for laparoscopic repair of pediatric inguinal hernia. Therefore, we categorized the laparoscopic techniques according to the method that was used to close the internal ring: intracorporeal suturing (intracorporeal) or by placing the suture through the abdominal wall (extracorporeal).
Statistical analysis
Statistical analysis was performed using Review Manager (Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014). Heterogeneity was assessed using the I2 statistic. Meta-analyses were performed using a random-effects model. Weighted (WMD) or standardized (SMD) mean differences and odds ratios (OR) with their corresponding 95% confidence intervals (CI’s) were used for the analysis of continuous and dichotomous variables, respectively. Subgroup analyses were performed to address whether the summary effects vary between different laparoscopic techniques, as differences in laparoscopic suturing technique (i.e., intracorporeal suturing and extracorporeal suturing) may modify the effect of the intervention. Sensitivity analyses were conducted to examine the treatment effects caused by studies with high risk of bias regarding the selection of patients (i.e., inclusion of exclusively boys). Regarding the development of MCIH, sensitivity analysis was performed by excluding studies that did not simultaneously close a laparoscopically detected CPPV during unilateral hernia repair.
Results
Literature search
The search strategy yielded 674 potentially eligible articles after removal of duplicates. After the initial screening by title and abstract, 32 full-text articles were assessed for eligibility (see PRISMA flow chart, Supplementary Material 3). Twenty-four studies were excluded as they did not meet the inclusion criteria. After translation of one Turkish and one Chinese article, eight randomized controlled trials (n = 733) were included in this review and meta-analysis [12‐19].
Study characteristics
The eight randomized controlled trials were published between 2005 and 2016 (Table 1). The total study population consisted of 733 children with inguinal hernia: 375 children underwent laparoscopic hernia repair (LH) and 358 children underwent open hernia repair (OH). Laparoscopic hernia repair with intracorporeal suturing was performed in 171 patients, laparoscopic repair with extracorporeal suturing in 204 patients. All children received general anesthesia. Unilateral hernia repair was performed in 434 children, bilateral hernia repair in 194 children, and laterality of the inguinal hernia was not further specified in 27 patients with recurrent inguinal hernia, 40 patients with inguinal hernia and umbilical hernia, and 38 patients with inguinal hernia and questionable other side [18]. Except from two studies [12, 15], the study population consisted of both male and female pediatric patients. Age and mean follow-up time ranged from 4 months to 16 years and 24 h to 2 years, respectively.
Table 1
Summarized study details of the studies included in this meta-analysis
Author
Year
Country
Study design
Patients no. (LH, OH)
Unilateral no. (%)
Bilateral no. (%)
Male no. (%)
Female no. (%)
Age range
Follow-up
Mean (SD)/(range)
Celebi et al.
2014
Turkey
RCT
59 (28, 31)
0 (0)
59 (100)
59 (100)
0 (0)
> 6 yr
3–24 mo
Chan et al.
2005
Hong Kong
RCT
83 (41,42)
80 (96.4)
3 (3.6)
67 (80.7)
16 (19.3)
3 mo–18 yr
LH: 12.2 (2.8) mo
OH: 11.8 (2.5) mo
Gause et al.
2016
USA
RCT
41 (26, 15)
27 (65.9)
14 (34.1)
31 (75.6)
10 (24.4)
< 3 yr
2 yr
Inal et al.
2013
Turkey
RCT
40 (20, 20)
40 (100)
0 (0)
40 (100)
0 (0)
7–14 yr
24 h
Koivusalo et al.
2008
Finland
RCT
89 (47, 42)
89 (100)
0 (0)
66 (74.2)
23 (25.8)
4 mo–16 yr
24 mo
Saranga et al.
2008
India
RCT
69 (35, 34)a
69 (100)
0 (0)
62 (89.9)
7 (10.1)
< 14 yr
3.5 mo
Shalaby et al.
2012
Egypt
RCT
250 (125, 125)b
53 (21.2)
92 (36.8)
179 (71.6)
71 (28.4)
14–96 mo
24 (16–30) mo
Zhu et al.
2015
China
RCT
102 (53, 49)
76 (74.5)
26 (25.5)
71 (69.6)
31 (30.4)
7–63 mo
6 mo
RCT randomized controlled trial, LH laparoscopic hernia repair, OH open hernia repair, SD standard deviation, mo months, yr year, h hours
aIn the laparoscopic group (n = 51), six had bilateral hernias and ten contralateral patency’s of the processus vaginalis (CPPV) were detected intra-operatively and repaired simultaneously. These 16 bilateral hernia repairs were excluded from comparative analysis and are not included in this table
bIn addition to patients who presented with (i) unilateral inguinal hernia in obese children (n = 53) and (ii) bilateral inguinal hernia (n = 92), Shalaby et al. also included patients with (iii) recurrent inguinal hernia (n = 27), (iv) inguinal hernia with umbilical hernia and (n = 40), (v) inguinal hernia with questionable other side (n = 38)
Methodological quality
Quality assessment using the Cochrane Risk of Bias tool for Randomized Controlled Trials showed that all trials were at low risk of bias for incomplete outcome data (see risk of bias graph and risk of bias summary, Supplementary Material 4). 75% of the trials were at low risk of bias for random sequence generation and allocation concealment. Saranga et al. introduced risk of bias by enrolling patients based on the day they visited the outpatient clinic [17]. Only 50% of the trials were at low risk of bias for blinding of participants and personnel and blinding of outcome assessment. Other risk of bias, e.g., selection bias as only boys were included [12, 15], was considered high in 25%, and risk of bias concerning selective reporting could not be assessed.
Primary outcome: operative and postoperative complications
Seven RCTs (n = 693) assessed operative and/or postoperative complications and were included in this part of the meta-analysis. There is a large variety in the kind of complications that were analyzed and no study assessed the risk for near critical incidents, i.e., apneas. Operative complications (i.e., injury of spermatic vessels or spermatic cord, tuba lesions, and bleeding) were only reported in the LH group (Table 2). Overall, the complication rate did not differ between laparoscopic and open hernia repair (OR 0.50, 95% CI 0.14 to 1.79; p = 0.29; I2 = 61%; Fig. 1A). A sensitivity analysis including only studies with low risk of bias due to the selection of patients (no restrictions for gender) did not alter the results (n = 634; OR 0.33, 95% CI 0.10 to 1.06; p = 0.06; I2 = 51%; Table 3). We found improved heterogeneity, but no difference in complications was observed (OR 1.59, 95% CI 0.37 to 6.88; p = 0.53; I2 = 19%; Fig. 1A) when we included only studies that used intracorporeal suturing as closing method for the laparoscopic technique. If only studies were included that used extracorporeal suturing, heterogeneity was improved and lower complication rates were found for laparoscopic repair (OR 0.16, 95% CI 0.05 to 0.48; p = 0.001; I2 = 22%; Fig. 1A). Two studies reported that three (10.7%) and eight (17%) patients in the LH group postoperatively experienced shoulder pain [12, 16].
Table 2
Perioperative and postoperative complications, recurrence, metachronous contralateral inguinal hernia (MCIH) rate, and presence of a contralateral patent processus vaginalis (CPPV)
Author year
Procedure no.
Perioperative complications
Postoperative complications
Recurrence no. (%)
MCIH rate no. (%)
Presence of CPPV no. (%)
Injury spermatic vessels/vas deferens no. (%)
Ovarian lesion no. (%)
Bleeding no. (%)
Hematoma/edema no. (%)
Hydrocele no. (%)
Wound infection no. (%)
Iatrogenic testicular ascent no. (%)
Testicular atrophy no. (%)
Celebi 2014
LH: 28
0 (0)
NA
–
0 (0)
3 (10.7)
–
0 (0)
0 (0)
0 (0)
–
–
OH: 31
0 (0)
NA
–
0 (0)
0 (0)
–
0 (0)
0 (0)
0 (0)
–
NA
Chan 2005
LH: 41
–
–
–
–
1 (2.4)
–
0 (0)
0 (0)
0 (0)
0 (0)
12 (29.3)
OH: 42
–
–
–
–
0 (0)
–
0 (0)
0 (0)
0 (0)
5 (11.9)
NA
Gause 2016
LH: 26
0 (0)
0 (0)
1 (3.8)b
0 (0)
0 (0)
0 (0)
–
0 (0)
1 (3.8)
–
–
OH: 15
0 (0)
0 (0)
0 (0)
0 (0)
0 (0)
1 (6.7)
–
0 (0)
0 (0)
–
NA
Inal 2013
LH: 20
–
NA
–
–
–
–
–
–
–
–
–
OH: 20
–
NA
–
–
–
–
–
–
–
–
NA
Koivusalo 2008
LH: 47
–
–
–
–
–
–
0 (0)
0 (0)
2 (4.3)
3 (6.4)
12 (26)
OH: 42
–
–
–
–
–
–
0 (0)
0 (0)
1 (2.4)
2 (4.8)
NA
Saranga 2008
LH: 35
–
–
2 (5.7)c
0 (0)
2 (5.7)
0 (0)
–
–
0 (0)
0 (0)
10 (22.2)
OH: 34
–
–
0 (0)
2 (5.9)
1 (2.9)
2 (5.9)
–
–
0 (0)
0 (0)
NA
Shalabya 2012
LH: 125
0 (0)
0 (0)
0 (0)
–
3/87 (3.4)
–
0 (0)
0 (0)
1 (0.8)
–
–
OH: 125
0 (0)
0 (0)
0 (0)
–
5/92 (5.4)
–
4/92 (4.4)
3/92 (3.3)
3 (2.4)
–
NA
Zhu 2015
LH: 53
–
–
–
2 (3.8)
–
–
–
–
0 (0)
1 (1.9)
Uncleard
OH: 49
–
–
–
19 (38.8)
–
–
–
–
0 (0)
7 (14.3)
NA
NA not applicable, MCIH metachronous contralateral inguinal hernia, CPPV contralateral patent processus vaginalis
aShalaby assessed the occurrence of hydroceles, iatrogenic ascent, and testicular atrophy in the males of both groups
bPeritoneal bleeding due to needle injury
cMinor bleeding at incision site
dZhu et al. stated that a contralateral processus vaginalis was simultaneously closed when it was found to be patent
Fig. 1
Meta-analysis of operative and postoperative complications, recurrence rate and metachronous contralateral inguinal hernia (MCIH) rate, and cosmetic problems between laparoscopic (LH) and open (OH) inguinal hernia repair. A Operative and postoperative complications; B recurrence; C MCIH; D problems with wound cosmesis. Proportionally sized boxes represent the weight of each study; diamond shows the pooled odds ratio; LH laparoscopic hernia repair, OH open hernia repair, M–H, Mantel–Haenszel, CI confidence interval
Table 3
Meta-analysis and sensitivity analyses of laparoscopic versus open inguinal hernia repair in children
LH laparoscopic hernia repair, OH open hernia repair, CI confidence interval
×
Ipsilateral recurrence rate and MCIH
The recurrence rate (assessed by seven RCTs, n = 693) (OR 0.88, 95% CI 0.20 to 3.88; p = 0.87; I2 = 0%; Fig. 1B) and MCIH rate (assessed by four RCTs, n = 343) (OR 0.28, 95% CI 0.04 to 1.86; p = 0.19; I2 = 52%; Fig. 1C) were not different between both groups (Table 2). Subgroup analysis for recurrence rate including only studies that performed intracorporeal suturing (OR 1.82, 95% CI 0.16 to 20.85; p = 0.63; Fig. 1B) and extracorporeal suturing (OR 0.58, 95% CI 0.09 to 3.72; p = 0.56; I2 = 0%; Fig. 1B) did not change the results. Sensitivity analysis for MCIH rate including only studies that closed a laparoscopically detected CPPV (n = 254) resulted in a lower MCIH rate in the LH group compared to the OH group (OR 0.10, 95% CI 0.02 to 0.58; p = 0.01; I2 = 0%, Table 3).
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Operation time
Seven RCTs (n = 434) reported mean operation times for unilateral hernia repair and five (n = 194) for bilateral hernia repair (Table 4). Overall unilateral operation time (min) was not different between LH and OH (WMD 0.62, 95% CI − 5.70 to 6.95; p = 0.85; Fig. 2A) with evidence of considerable heterogeneity (I2= 97%). Similar results were found when we included only studies that performed intracorporeal suturing (WMD 6.30, 95% CI − 1.63 to 14.24; p = 0.12; I2 = 94%; Fig. 2A). Heterogeneity improved and shorter unilateral operation time was found when only studies that performed extracorporeal suturing were included (WMD − 5.37, 95% CI − 7.50 to − 3.23; p < 0.001; I2 = 48%; Fig. 2A). Sensitivity analysis including only studies without gender restrictions (n = 394) did not change the outcome (WMD − 0.72, 95% CI − 7.50 to − 3.23; p = 0.84; I2 = 97%; Table 3).
Table 4
Intervention characteristics of the included studies
Author year
Closing technique
Trocars
Unilateral operation time, mean (SD), min
Bilateral operation time, mean (SD), min
Length of hospital stay, mean (SD), h
Return to full recovery, mean (SD), h
LH
OH
LH
OH
LH
OH
LH
OH
Celebi 2014
Intracorporeal purse-string suture
Two 3 mm
One 5 mm
NA
NA
32.7 (3.2)
38.6 (3)
< 24
< 24
58.8 (18)
45.6 (12)
Chan 2005
Intracorporeal purse-string suture
Two 3 mm
One 5 mm
23.3 (6.3)
18.4 (5.7)
34 (6.3)
39.1 (13.4)
10.7 (5.3)
10.3 (4.9)
48.2 (28.7)
57.7 (27.5)
Gause 2016
Extracorporeal ligation (SEAL)
Unclear
27.9 (15)
53.2 (30.4)
38 (19.9)
50.4 (19)
Uni: 7 (11.3)
Bil: 24 (31.7)
Uni: 7.2 (11.5)
Bil: 19.2 (10.8)
Uni: 61 (33.4)
Bil: 122.4 (36)
Uni: 78 (78.7)
Bil: 103.9 (27.6)
Inal 2013
Intracorporeal purse-string suture
Two 3 mm
One 5 mm
28.9 (8.1)
20.5 (7.4)
NA
NA
–
–
7.5 (0.4)
5 (1.4)
Koivusalo 2008
Intracorporeal “N”-shaped suture
Three 5 mm
35 (11)
18.3 (6.8)
NA
NA
5.9 (1.9)
4.3 (1.2)
57.6 (33.6)
60 (43.2)
Saranga 2008
Intracorporeal “Z” suture
Three 5 mm
25.3 (13)
30.7 (10.3)
–
–
< 10 (88.6%)
24 (11.4%)
< 10 (97.1%)
24 (2.9%)
–
–
Shalaby 2012
Extracorporeal suturing with Reverdin needle
One 3 mm
7.6 (3.5)a
12.8 (4.5)
11.4 (2.7)
21.9 (7.2)
5 (3.2)
5 (3.2)
<6
<10
Zhu 2015
Extracorporeal suturing with epidural needle
One 3 mm
Two 5 mm
15.4 (2.1)b
20.5 (3.7)
15.4 (2.1)
20.5 (3.7)
48
84
–
–
SD standard deviation, min minutes, mm millimeter, LH laparoscopic hernia repair, OH open hernia repair, uni unilateral, bil bilateral, SEAL subcutaneous endoscopically assisted ligation, NA not applicable
aOnly applicable to patients with unilateral and recurrent unilateral hernia; mean (SD) operation time of obese children with inguinal hernia was 9.2 (4.6) min in the LH group and 14.3 (3.6) min in the OH group
bZhu et al. reported the operation time for unilateral and bilateral hernia repair together
Fig. 2
Meta-analysis of continuous outcomes between laparoscopic versus open inguinal hernia repair. A Operation time (min) unilateral hernia repair; B operation time (min) bilateral hernia repair; C length of hospital stay (h); D time to full recovery (h); E doses of pain medication administered; F cosmetic appearance; proportionally sized boxes represent the weight of each study; diamond shows the pooled weighted mean difference; LH laparoscopic hernia repair, OH open hernia repair, IV inverse variance, CI confidence interval
×
Overall duration of laparoscopic bilateral hernia repair (min) was shorter compared to open bilateral hernia repair (WMD − 7.19, 95% CI − 10.04 to − 4.34; p < 0.001; Fig. 2B), though again there was evidence of substantial heterogeneity (I2 = 73%). This effect was still present when we assessed only studies that used the intracorporeal closing technique (WMD − 5.89, 95% CI − 7.48 to − 4.29; p < 0.001; I2 = 0%; Fig. 2B) or the extracorporeal closing technique (WMD − 8.04, 95% CI − 12.97 to − 3.11; p < 0.001; I2 = 83%; Fig. 2B). In sensitivity analysis including only studies without gender restrictions (n = 135), these findings proved robust (WMD − 7.90, 95% CI − 12.49 to − 3.31; p < 0.001; I2 = 74%; Table 3).
Length of hospital stay
Seven RCTs compared the length of hospital stay, i.e., mean time to discharge (h), between LH and OH (Table 4). However, only five studies (n = 565) were included in this part of the meta-analysis since mean values could not be retrieved or calculated in two studies which only stated that patients were discharged within a specific time frame after surgery [12, 17]. The length of hospital stay (h) in the LH group was not different from the OH group (WMD 0.74, 95% CI − 0.38 to 1.87; p = 0.20; Fig. 2C), with moderate to substantial heterogeneity (I2 = 59%). Assessing only studies that performed intracorporeal suturing, heterogeneity improved and shorter length of hospital stay was observed in the LH group (WMD 1.50, 95% CI 0.87 to 2.12; p < 0.001; I2 = 0%; Fig. 2C).
Time to full recovery
Four RCTs assessed the time to full recovery, i.e., time to resume full activity [12‐14] or time to normal daily activities [16]. Two studies were excluded from this part of the meta-analysis, as Inal et al. assessed the time to first walking [15] and Shalaby et al. only stated that the time to full recovery was < 6 h (LH group) and < 10 h (OH group) [18]. Analysis of pooled data in four RCTs (n = 272) showed that the overall time to return to full recovery (h) was not different between the groups (WMD 2.05, 95% CI − 11.13 to 15.23; p = 0.76; I2= 67%; Fig. 2D) (Table 4). Subgroup analysis on intracorporeal and extracorporeal suturing did not change the outcome (Fig. 2D).
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Postoperative pain and pain-medication requirement
Six studies (n = 381 patients) assessed postoperative pain and the need for administering pain medication. Different strategies were used to measure the amount of pain [e.g., Visual Analogue Scale (VAS); children and infants postoperative pain score (CHIPPS); calculation of medication doses administered] and numerous pain medications were prescribed [e.g., patient controlled analgesia (PCA) with bolus morphine; acetaminophen] (Table 5). Since various pain management protocols were used (conceptual heterogeneity), the standardized mean difference was calculated using a random-effects model including four RCTs (n = 264). Equal doses of pain medication were administered to patients in both groups (SMD − 0.34, 95% CI − 0.65 to − 0.03; p = 0.15; I2= 29%; Fig. 2E). Including only laparoscopic studies that used intracorporeal suturing, improved heterogeneity and less administration of pain medication were observed (SMD − 0.57, 95% CI − 0.87 to − 0.27; p < 0.001; I2= 0%; Fig. 2E).
Table 5
Postoperative pain management, including pain scores and requirement of pain-medication
Author
Pain assessment
Determine severity of pain
Administration
Timing of pain medication
Pain medication
Patients requiring medication
Doses administered/requestedd
LH
OH
LH
OH
Celebi et al.
VAS
VAS (0–10)
Self-administration
During admission
PCA with bolus morphine 10 µg/kg, median (SD)
–
–
A: 8.4 (6.6)
R: 8.8 (6.6)
A: 11.9 (5.6)
R: 12.5 (10.2)
After discharge
Ibuprofen 20 mg/kg, median (SD)
–
–
0.8 (0.8)
1.3 (1.2)
Chan et al.
- CHIPPS
- CHEOPS
CHIPPS/CHEOPS
CHIPPS ≥ 4
CHEOPS ≥ 5
During admission
Acetaminophen (dose/patient), mean (SD)
–
–
0.5 (0.8)
1.1 (1.2)
Gause et al.
FLACC
–
FLACC > 4
During admission
Acetaminophen 15 mg/kg, mean (SD)
–
–
Uni: 5.3 (5.9)
Bil: 9.6 (7.3)
Uni: 9 (9.7)
Bil: 4.8 (1.7)
During admission
Fentanyl 0.5 µg/kgc
% patients
Uni: 50%
Bil: 75%
Uni: 57.1%
Bil: 50%
Uni: 0.8 (0.9)
Bil: 0.8 (0.5)
Uni: 0.9 (1.1)
Bil: 0.5 (0.6)
Inal et al.
VAS
VAS (0–10)
Self-administration
During admission
PCA with bolus morphine 10 µg/kg, mean (SD)
–
–
A: 5.4 (6.1)
R: 10.7 (7.3)
A: 8.8 (5.8)
R: 33.2 (6.2)
Koivusalo et al.
- Modified OPS
- Pain scalea
OPS (0–9)
Pain Scale (0–3)
Judged by attending nurseb
During admission
Fentanyl 1.0 µg, No. (%) patients
37 (79)
20 (48)
37 (79)
20 (48)
After discharge
Ibuprofen 20 mg/kg, median (range)
–
–
1 (0–3)
1 (0–5)
Saranga et al.
- CHIPPS
- CHEOPS
- VRS
- Nil
- Mild
- Moderate
Unclear
During admission
Acetaminophen 15 mg/kg, No. (%) patients
- Nil pain
- Mild pain
- Moderate pain
2 (6)
30 (86)
3 (8)
0 (0)
32 (94)
2 (6)
–
–
Shalaby et al.
–
–
–
–
–
–
–
–
–
Zhu et al.
–
–
–
–
–
–
–
–
–
VAS visual analogue scale, CHIPPS children and infants postoperative pain score (< 3 years), CHEOPS Children’s Hospital of Eastern Ontario Pain Scale (> 3 years), FLACC face, legs, activity, cry, consolability scale, OPS objective pain scale, VRS verbal response score, PCA patient controlled analgesia, PCM paracetamol, iv intravenous, Uni unilateral, Bil bilateral
aNo pain = 0, mild pain = 1, moderate pain = 2, severe pain = 3
bThe attending nurse who judged whether the patient need pain medication was blinded to the operative approach
cAdministered if there was persistent or breakthrough pain
dA means the number of doses which is administered to the patients, R means the number of doses requested by the patients (as the maximum dosage of PCA was 4 mg morphine in 4 h and 10 mg in 24 h and the boluses were administered with a lockout interval of 10 min)
eIf VAS > 4 despite morphine bolus
Cosmetic results
Cosmetic appearance of the wound was assessed in 591 patients (Table 6). Standardized mean difference was calculated using a random-effects model since different scoring systems were used and wound cosmesis was assessed at varying moments. Overall better cosmetic results (three RCTs, n = 183) were reported after open hernia repair (SMD 1.21, 95% CI 0.50 to 1.92; p < 0.001; I2= 75%; Fig. 2F). Assessing only laparoscopic intracorporeal or extracorporeal suturing studies, these results persisted (Fig. 2F). No difference was found in cosmetic problems of the wound (i.e., hypertrophic scar, ugly scar, or stitch granuloma) between laparoscopic and open hernia repair (two RCTs, n = 333; OR 0.20, 95% CI 0.03 to 1.19; p = 0.08; I2= 0%; Fig. 1D).
Table 6
Cosmetic results
Author
Measurement
Measured by
Scoring system
Type of score
Timing of score
Wound score, mean (SD)/median (range)
Cosmesis problems, no. (%)
LH
OH
LH
OH
Celebi et al.
Recovery and wound appearance
Parents
70: fair
80: good
90: very good
100: excellent
Score 70–100
3 mo
89 (4.2)
78 (6.7)*
–
–
Chan et al.
Recovery and wound appearance
Parents
70: fair
80: good
90: very good
100: excellent
Score 70–100
7 d
95.4 (6)
90.2 (6)*
Hypertrophic scar: 1 (2.4)
Hypertrophic scar: 2 (4.8)
Stitch granuloma: 1 (2.4)
Gause et al.
Wound appearance
Parents
1 (not satisfied)
2
3 (adequate)
4
5 (very satisfied)
Score 1–5
7 d
Uni: 4.9 (0.4)
Bil: 4.9 (0.3)
Uni: 4.4 (0.8)
Bil: 5 (0)
–
–
Inal et al.
–
–
–
–
–
–
–
–
–
Koivusalo et al.
Cosmetic result
Patients/parents, attending nurse and surgeon
0: unsatisfactory
1: satisfactory
2: good
3: excellent
Score 0–9
a) 6 mo
b) 2 yr
a) 7 (3–9)
b) 7 (5–9)
7 (3–9)
9 (5–9)
–
–
Saranga et al.
Scar cosmetics
Not clear
Good
Excellent
Excellent/good
Patients, no. (%)
Average 3.5 mo
Good: 0 (0)
Excellent: 35 (100)
34 (100)
0 (0)
–
–
Shalaby et al.
Scar cosmetics
Parents
Ugly scar
Ugly scar
Patients, no. (%)
> 6 mo
–
–
Ugly scar: 0 (0)
Ugly scar: 5 (4)*
Zhu et al.
–
–
–
–
–
–
–
–
–
LH laparoscopic hernia repair, OH open hernia repair, SD standard deviation, d days, mo months, yr year, uni unilateral, bil bilateral
*Significant difference between LH and OH group
Discussion
In this systematic review and meta-analysis including evidence from eight RCTs representing 733 patients, we detected no differences in complication, recurrence, and MCIH rates between laparoscopic and open hernia repair. Unilateral operation time, length of hospital stay, and time to full recovery were also comparable. Laparoscopic hernia repair resulted in a mean reduction in operation time of 7.19 min; however, the clinical relevance of this difference is highly questionable. There is also evidence of substantial heterogeneity, which can only partially be explained by subgroup analysis.
Laparoscopic approaches can be subdivided into two subgroups according to the laparoscopic suturing technique (i.e., intracorporeal suturing and extracorporeal suturing) that was used. Compared to the open technique, less complications and shorter unilateral operation time (− 5.37 min) were noted after laparoscopic repair with extracorporeal suturing. Laparoscopic hernia repair with intracorporeal suturing resulted in shorter length of hospital stay (− 1.5 h). However, the clinical relevance of the latter two results is negligible.
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The included studies had heterogeneous study populations, as two studies only included male children and study outcomes were assessed in different, partially overlapping age groups. However, in sensitivity analyses for complication rate, recurrence rate, and operation time, including only studies with low risk of bias regarding the selection of patients did not substantially change the effect estimates.
In this analysis, the total complication rate was not different between the LH and OH group. These results are supported by Yang et al., who also reported no significant differences in the incidence of hydrocele, wound infection, scrotal edema, erythema, and testicular atrophy [9]. However, the results of this meta-analysis should be interpreted with caution: as reflected in the degree of heterogeneity, the complications that were analyzed largely varied among the included studies. Thereby, selective reporting bias could not be assessed. In 2014, Esposito et al. reviewed 22 studies and concluded that there were less complications in the LH group (0.9% vs. 2.7%; p = 0.001) [10]. More recently, Feng et al. also found less postoperative complications (15 vs. 31 complications) and less major complications (i.e., scrotal edema, iatrogenic ascent of the testis, and testicular atrophy) in boys (4 vs. 14 complications) after laparoscopic hernia repair [11].
One of the benefits of laparoscopic hernia repair is the opportunity for intraoperative inspection of the contralateral groin. Approximately 40% of all children still have a CPPV after 2 years of age [20] and the estimated childhood risk of developing an inguinal hernia following the presence of a CPPV is 25–50% [21]. It can be assumed that contralateral exploration and closure of a CPPV, if present, can prevent development of an MCIH. In this meta-analysis, MCIH rate was not different between the two groups, although the included studies only assessed the presence of a CPPV during laparoscopy and performed subsequent closure of the PPV during the same session. None of the studies performed contralateral exploration and subsequent closure in the OH group. Koivusalo et al. did not close a laparoscopically detected asymptomatic CPPV in 12 patients (26%), but awaited subsequent development of MCIH. During 2 years of follow-up, MCIH developed in 3/12 (25%) patients, which resulted in a slightly higher overall MCIH rate following laparoscopic hernia repair (6.4%) compared to open hernia repair (4.8%) [16]. The latter results emphasize the controversy with respect to contralateral exploration as not every PPV necessarily develops into a clinically relevant hernia. Sensitivity analysis by excluding the study of Koivusalo et al. resulted in lower MCIH rates following laparoscopic repair. Still, these results should be interpreted with caution as the interval estimate of the odds ratio for metachronous contralateral hernia is very wide.
Previous studies repeatedly found a trend towards higher recurrence rates following laparoscopic hernia repair [8, 14, 16], especially in infants weighing three kg or less [22]. However, our meta-analysis shows that recurrence rates between LH and OH do not differ significantly. There was an inconsistent follow-up time that ranged from 24 h to 2 years, and again selective reporting bias could not be assessed. Additionally, as different laparoscopic techniques and advanced methods of minimally invasive closure of the inguinal hernia might affect the risk for recurrence, future analyses remain necessary.
There is insufficient evidence to draw definite conclusions regarding postoperative pain and wound cosmesis. Our results show that less administration of pain medication might be necessary after laparoscopic hernia repair with intracorporeal suturing and that open hernia repair results in better cosmesis. However, there is large conceptual heterogeneity among the included RCTs, since different protocols and scoring systems were used to assess postoperative pain and wound cosmesis. Again, selective reporting bias could not be assessed. Core outcome sets with unequivocal criteria and scoring systems are crucial to draw definitive conclusions about differences in postoperative pain and cosmetic appearance or problems. In this systematic review, we included all currently available RCTs (no language restrictions) in order to estimate treatment effects more precisely, and performed meta-analyses using a random-effects model. This study has several limitations. The quality of the included RCTs varied and there is a certain degree of clinical diversity in patient population (regarding gender and age) and intervention characteristics (e.g., a different number of trocars, varying suture materials, and different knotting techniques were used). Furthermore, reported outcomes and outcome definitions are not the same across studies. This is also reflected by the degree of heterogeneity and imprecision in the confidence intervals of the effect estimates. The certainty of the evidence according to GRADE is predominantly moderate for most outcome variables. Data to assess the risk of apneas and treatment-related healthcare costs were completely lacking.
In conclusion, no definite conclusions to decide on the superiority of one of either treatment strategies can yet be drawn from the available literature. Surgeons facile in both open and laparoscopic approaches can exploit relative advantages for each individual patient. For instance, it is clear that laparoscopic hernia repair offers more peroperative information on both groin areas compared to open surgery. Laparoscopic surgery might therefore be advantageous in cases of high diagnostic uncertainty, in children with high risk of MCIH development (especially infants as the risk increases with declining age) and in children with recurrent hernia repair; however, this treatment strategy does not simply fit all surgeons, and more importantly, all patients. We should take into account what exploitable advantages (or risks) we wish to invoke for a given patient in a given context, rather than simply choose one approach based on personal preference, ability, or clinically irrelevant superiority. Execution of large, prospective randomized trials that take into account all relevant outcome measures, the use of different laparoscopic and anesthetic techniques, and costs are inevitable to obtain homogenous results to decide on the superiority of one of either treatment strategy.
Acknowledgements
The authors would like to thank Mw. Drs. J.W.M. Plevier for her contributions regarding the execution and update of the literature search.
Compliance with ethical standards
Disclosures
Drs. Kelly Dreuning, Sanne Maat, Jos Twisk, Ernest van Heurn, and Joep Derikx have no conflicts of interest or financial ties to disclose.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
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