- Research article
- Open access
- Published:
Long-term outcomes and quality of life of patients with Hirschsprung disease: a systematic review and meta-analysis
BMC Gastroenterology volume 20, Article number: 67 (2020)
Abstract
Background
Advances in surgical techniques and perioperative care have improved the short- and mid-term postoperative outcomes of patients with Hirschsprung disease (HD). However, the long-term outcomes of these patients (older than 10 years) have not been fully investigated. The aim of this systematic review is to clarify the prevalence of long-term outcomes and the quality of life of these patients.
Methods
PubMed, AMED, Cochrane Library, CINAHL and PsycINFO databases were searched from inception to October 2018, following the Meta-analysis of Observational Studies in Epidemiology (MOOSE) guideline. Original studies reporting the outcomes of patients older than ten years with HD were selected and reviewed. The overall prevalence of fecal incontinence, constipation, bowel function score, bladder dysfunction symptoms, and patients’ quality of life were extracted from the included studies and pooled through the random-effects meta-analysis model. The heterogeneity and variation in the pooled estimations were evaluated by Cochrane’s Q test and the I2 test. The sensitivity analysis was conducted by the sequential omission of individual studies. Publication bias was evaluated by Egger’s linear regression test. The whole procedure was conducted with Stata (version 14).
Results
In total, 3406 articles were identified from the literature search, among which twelve studies, including 625 patients, were included for analysis. The pooled prevalences of fecal incontinence, constipation, and bladder dysfunction symptoms and good to excellent bowel function scores were 0.20 (95% CI 0.13–0.28), 0.14 (95% CI 0.06–0.25), 0.07 (95% CI 0.04–0.12), and 0.95 (95% CI: 0.91–0.97), respectively; the pooled mean score of gastrointestinal-related quality of life was 118 (95% CI: 112.56–123.44).
Conclusions
HD patients older than ten years old have an overall high prevalence of fecal incontinence and a low quality of life. Targeted and evidence-based follow-up procedures and transitional care are essential to meet these patients’ long-term care needs. Prospective and multicenter research that focuses on the attributes and predictors of the long-term prognosis of patients with HD are necessary.
Background
New surgery techniques and enhanced recovery after surgery (ERAS) practice have improved the results after surgery for children with Hirschsprung disease (HD) by reducing the length of operation time, blood loss, use of analgesia and length of hospital stay [1,2,3]. Follow-up within the first three years after surgery shows that children who receive new surgical approaches have a lower onset of postoperative complications [4, 5]. Despite the encouraging short-term outcomes of these definitive surgeries, complications including constipation, fecal incontinence, and enterocolitis, among others, continue to burden some HD patients and jeopardize their quality of life (QoL) [6, 7]. To provide targeted interventions for these patients, identifying the prevalence of the prolonged postoperative complications and the characteristics of these patients is necessary.
Several meta-analysis have been conducted to compare the short- and mid-term postoperative outcomes among patients with HD who underwent different surgical approaches [8,9,10,11,12]; however, conclusions regarding the optimal surgical approach to obtain the best postoperative outcomes are conflicting, and the rates of complications are highly variable. To the best of our knowledge, no systematic review has been conducted on the prevalence of the long-term outcomes in children with HD surgical history who lived beyond their childhood.
The purpose of this study is to estimate the prevalences of fecal incontinence, constipation, bowel function, bladder dysfunction symptoms and QoL of patients with HD surgical history who reached ten years old or older. These findings can contribute to knowledge on the prognosis of patients with HD and facilitate the design of evidenced-based follow-up and better transitional care for these patients.
Methods
We conducted a meta-analysis according to the review protocol (see Additional file 1) and Meta-analysis of Observational Studies in Epidemiology (MOOSE) guideline [13]. PubMed, AMED, Cochrane Library, CINAHL and PsycINFO databases were searched from inception to October 2018. To allow for a comprehensive literature search of all studies containing the long-term outcomes of patients with HD surgical history, no language or study design filters were used in our initial search. The search strategy used in PubMed was as follows: (“Hirschsprung Disease”[Mesh]) OR Mega colon) OR aganglionosis)) AND ((((((“Follow-Up Studies”[Mesh]) OR follow-up) OR (“Outcome and Process Assessment (Health Care)”[Mesh])) OR bowel function) OR “Quality of Life”[Mesh]) OR QoL), which was then adapted in line with the indexing systems of other databases. The reference lists of the included studies and existing systematic reviews were reviewed for additional relevant studies. Two key authors were contacted for further potential data relevant to this study.
Selection criteria
Two reviewers independently scanned the titles and abstracts of the acquired articles for the initial screening. Original articles that reported the outcome or quality of life of patients older than ten years old with HD surgical history were included. The exclusion criteria were as follows: 1) non-English language papers, reviews, conference proceedings, and case reports or case series (fewer than 15 participants); 2) studies conducted on animal models or focused on analyzing the molecular biological or pathological mechanisms of HD; 3) studies focusing on parental stress and anxiety; and 4) studies including patients with a wider age range but without reporting the specific number of children older than ten years old. After the initial screening, the full text of 311 included articles was retrieved and read by two reviewers to determine their eligibility for inclusion in the analysis. The full screening process is listed in the PRISMA flowchart (see Fig. 1). Articles that were identified as potentially relevant in the initial screening and of which the full text was read are listed in Additional file 2.
Data extraction
A standardized spreadsheet that included key characteristics, such as the study design, year of publication, geographical region, patients’ age range, category of HD (i.e., recto-sigmoid, long-segment, and total aganglionosis), fecal incontinence, constipation, bowel function score, bladder dysfunction symptoms and quality of life of patients with an HD surgical history, was developed for data collection. Two reviewers independently extracted information from the included articles. Discrepancies in the screening and data extraction process were discussed and resolved by consensus of the two reviewers.
Definitions of related concepts
To differentiate similar soiling symptoms caused by functional constipation, we defined fecal incontinence based on the diagnostic criteria for non-retentive functional fecal incontinence as “uncontrolled loss of feces into places inappropriate to the social context, with no evidence of fecal retention” [14]. We used the definition of constipation that Diseth and colleagues defined in their study, namely, “having fewer than three defecations per week, or the need for regular laxatives, or both” [15]. Bladder dysfunction symptoms were defined by the International Children’s Continence Society (ICCS), including urinary incontinence (involuntary leakage of urine), sudden or unexpected urgent need to void, night enuresis (awakening to void at night), frequent urination (voiding eight or more times during waking hours), the need to apply abdominal pressure to initiate and maintain voiding, and burning or discomfort during voiding [16].
Quality assessment
The quality of the included cohort and case-control studies was evaluated by the Newcastle-Ottawa Scale (NOS) [17], which contains three evaluation criteria: selection, comparability, and exposure. The total score of the NOS is 9, with a higher score indicating higher quality. A NOS score of 0–5, 5–6, and 7–9 was considered as low, medium and high quality respectively [18]. The Agency for Healthcare Research and Quality (AHRQ) checklist [19] was used to assess the quality of the included cross-sectional studies. The AHRQ checklist contains 11 items, with each item individually addresses a certain domain of the quality of the study and is answered with “yes”, “no”, or “unclear”, and does not incorporate an overall score (see Additional file 3).
Statistical analysis
The “metaprop” command was employed to pool the prevalence of binary long-term outcomes (i.e., fecal incontinence, constipation, bladder dysfunction symptoms) [17]. The exact method was used to compute the specific confidence interval of each study. For continuous variables, including bowel function score and QoL score, the “metan” command was used to pool the mean differences. The heterogeneity and variation in the pooled estimations was computed by Cochrane’s Q test and the I2 test, respectively, with the p value < 0.05 considered statistically significant [18]. The pooled prevalence was calculated by the random effects model if the heterogeneity was higher than 25%; otherwise, the fixed effect model was employed. The sensitivity analysis was conducted by the sequential omission of individual studies with the “metaninf” command. A study was considered influential if the pooled mean estimate without it was not within the 95% CI bounds of the overall mean. Publication bias was evaluated by Egger’s linear regression test with the “metabias6” command, with the p value < 0.05 considered statistically significant [19, 20]. When the heterogeneity test showed I2 > 50%, the subgroup analysis was implemented [20]; this analysis was conducted for the geographical area, year of publication, patients’ age range, and age at surgery. Since most of the included studies did not report the specific number of complication events according to different categories of HD (i.e., the level of aganglionosis) or surgical technique, we were unable to perform subgroup analysis on these two factors. The whole procedure was conducted with Stata (version 14; Stata Corporation, College Station, TX).
Results
Study characteristics
The literature search identified 3406 potentially relevant articles (Fig. 1). After scanning the titles and abstracts, 311 articles were included for full-text screening to assess eligibility for inclusion. After full-text review, 12 articles with 625 patients older than ten years with an HD surgical history were included for analysis, among which four were case-control studies, six were cross-sectional studies, and the remaining two were cohort studies. These studies were implemented at various pediatric healthcare institutions in various countries, including Finland [21,22,23,24], Sweden [25, 26], Australia [27, 28], the UK [29], Canada [30], Japan [31], Norway [15] and Thailand [32]. Surgical approaches including the Duhamel and Soave methods were the most frequently reported approaches that were applied to these patients. Ten of the twelve studies included patients with congenital diseases or syndromes, with Down Syndrome being the most frequently reported. Most of the included cohort and case-control studies were evaluated as high or medium quality based on the NOS checklist, whereas most cross-sectional studies failed to mention whether the evaluators of subjective components of the study were masked to other aspects of participants’ status, nor do they describe any assessments undertaken for quality assurance (see Table 1 and Additional file 3).
Fecal incontinence
A total of 508 patients were evaluated for long-term fecal incontinence. The pooled estimation of the prevalence of fecal incontinence is 0.20 (95% CI, 0.13–0.28, Cochran Q test, P < 0.001, I2 = 73.82%, see Fig. 2a), with the largest study (n = 111) reporting a fecal incontinence prevalence of 0.15 (95% CI: 0.09, 0.23) [32].
Constipation
A total of 508 patients underwent a constipation evaluation. The overall pooled prevalence of constipation is 0.14 (95% CI: 0.06–0.25, Cochran Q test, P < 0.001, I2 = 88.52%, see Fig. 2b).
Bowel function score
Six studies reported bowel function scores in a total of 411 participants, with four studies [21, 22, 29, 33] using the Bowel Function Score (BFS) [34] and the remaining two studies [23, 32] using the Holschneider scale [35]. The BFS contains seven items, with each item scored from 0 to 3, except for one item scored from 1 to 2 (see Table 2). The whole score of BFS is 20, and a score ≥ 17 is defined as the lower limit of a normal bowel function [36]. Since one study [33] only reported participants’ mean BFS score from each domain without reporting the overall score, this study was not included in the analysis of bowel function. The pooled overall mean BFS score is 16.78 (95% CI: 16.34–17.17, Cochran Q test, P = 0.27, I2 = 23.1%, see Fig. 2c), and the prevalence of patients with excellent to good Holschneider scores (i.e., score > 10) is 0.95 (95% CI: 0.91–0.97, I2 = 0, see Fig. 2d).
Bladder dysfunction symptoms
Urinary system function was assessed in 172 patients. The overall prevalence of bladder dysfunction symptoms is 0.07 (95% CI: 0.04–0.12, Cochran Q test, P = 0.40, I2 = 1.89%, see Fig. 2e), with the largest study (n = 43) reporting a prevalence rate of 0.12 (95% CI: 0.04, 0.25) [31]. Compared to studies that only included adult patients (> 18 years old), Mills et al. included younger patients aged between 13 and 18 years and reported no bladder dysfunction symptoms among these patients [30].
Gastrointestinal quality of life
Three studies [21, 22, 26] reported HD patients’ gastrointestinal quality of life index (GIQLI) with the mean and standard deviation. The GIQLI is a validated scale that evaluates the quality of life of patients with gastrointestinal issues from 36 items, with the total score of 144, and a score of 125.8 (95% CI 121.5–127.5) as the average score of the general population [21, 37]. The pooled estimation of the mean GIQLI is 120.19 (95% CI: 117.85–122.53, Cochran Q test, P = 0.65, I2 = 0, see Fig. 2f). The mean GIQLI score for the study with the largest sample (n = 89) is 121 (95% CI 117.82–124.18) [21]. The lowest mean GIQLI score is 118 (95% CI: 112.56–123.44) [26], which is higher than the cutoff score (i.e., score of 105) for constant gastrointestinal symptoms [37].
Subgroup analysis
Subgroup analysis of the prevalence of fecal incontinence, constipation and bladder dysfunction were conducted for the following categories: year of publication (before or after 2008), geographic region (Europe, North America, Oceania, or Asia), study design (case control, cohort, or cross-sectional), patient age at follow-up (younger or older than 19 years), and age at surgery (younger or older than 0.5 years). Because of the lack of sufficient data, we were unable to conduct subgroup analysis for three categories that could potentially influence heterogeneity: type of surgery, patients’ length of aganglionic colonic segment, and patients with associated congenital diseases or symptoms.
Although no clinical heterogeneity was found to be caused by the above categories, participants from the Oceania area [27] have the highest prevalence of fecal incontinence, constipation and bladder dysfunction, with pooled prevalences of 0.33, 0.42, and 0.13, respectively. Regarding study design, cross-sectional and case-control studies have the highest prevalence of fecal incontinence and constipation, respectively. Patients who received surgery later than five months of age and patients who had lived to 19 years or older when they received follow-up have higher prevalences of fecal incontinence, constipation and bladder dysfunction (see Table 3).
Sensitivity and publication bias
The sensitivity analysis from sequential omission of the long-term fecal incontinence, constipation, and bladder dysfunction symptom was listed in Fig. 3a, b, and c, respectively, suggesting that the combined relative frequency was not altered after omission. Egger’s regression test showed that the p values of publication bias for the prevalences of fecal incontinence, constipation, bladder dysfunction symptoms, BFS score, Holschneider score, and GIGLI score are 0.23, 0.61, 0.37, 0.95, 0.32, and 0.19, respectively, suggesting that no publication bias is found. Egger’s publication bias graphs are listed in Additional file 4.
Discussion
In this study we estimate that for patients older than ten years with an HD surgical history, the prevalences of fecal incontinence, constipation and bladder dysfunction symptoms are 20, 14 and 7%, respectively; and these patients generally have lower gastrointestinal quality of life index compared to healthy population.
Comparison with other literature
The pooled prevalence of fecal incontinence in patients with HD who were older than ten years is 20% (95% CI 0.13–0.28), which is much higher than that of the general population (1.6% in teenagers and 7.7% in adults) [14, 38]. In other studies that focus on patients with HD, the reported prevalence of fecal incontinence ranges from 9.8 to 37.8% [39,40,41,42]. Discrepancies among these studies may be due to the heterogeneity in geographical regions, sample size, participants’ characteristics, definition of fecal incontinence, and follow-up period of the patients.
Regarding the epidemiology of constipation, we estimated that 14% (95% CI: 0.06–0.25) of patients with HD experience constipation onset when they reach ten years old, which is comparable to the estimate of the prevalence of constipation in the general population (16% in teenagers and 12 to 19% in adults) [43, 44], but slightly lower than that of another study [45] in which 25% of patients with HD were reported to have constipation. Chung et al. reported a constipation prevalence of 17.5% in patients with short-segment HD after 52 months of definitive surgery [46]. Another study employed the Krickenbeck criteria to diagnose constipation and reported a constipation prevalence of 25% [47]. Reasons for the heterogeneity in the prevalence of constipation among different studies may be similar to those for fecal incontinence heterogeneity.
Only a small number of participants (n = 127) were included in the bladder dysfunction symptoms analysis. The overall prevalence of bladder dysfunction symptoms is 0.07 (95% CI: 0.04–0.12), which is slightly higher than the prevalences of urinary urgency, daytime incontinence, emptying difficulties or enuresis in children aged 17 [16]. Xiong et al. reported no occurrence of urinary retention in their cohort of Chinese patients with HD [33], suggesting that patients generally have satisfactory urinary function.
Previous studies have been inconsistent in concluding whether the long-term outcomes for HD patients improve over time. In this study, teenagers have slightly lower prevalences of constipation, fecal incontinence and bladder dysfunction, although this variance is not statistically significant. Meinds et al. reported significant improvements in fecal incontinence in the adult group compared to the children’s group (16.8 versus 37.6%, p < 0.001), but constipation remained constant (22.0% in both groups) [42]. Granström and colleagues reported that the occurrence of constipation decreased from 41 to 14% during a three-year follow-up period, but the prevalence of fecal incontinence remained high among the same patient group (ranged from 56 to 67%) [48]. Another study founded that fecal incontinence improved over time – particularly when children reach late adolescence [49]. Since some of these original studies are limited in their small sample size, moderate rate of loss to follow-up [50], and potential bias in that the person who evaluated the patients’ outcomes was not blinded to the patients’ disease and surgery information, it is difficult to draw conclusions regarding changes in the long-term outcomes of patients with HD. Prospective multicenter studies of these patients’ health-related outcomes that involve longer and more standardized follow-up and thorough research designs are necessary.
All the included original studies in this meta-analysis employed either the Bowel Function Score (BFS) or the Holschneider score to evaluate patients’ bowel function. The pooled overall mean BFS score is 16.78 (95% CI: 16.34–17.17); this score marginally reaches the cutoff value of good/normal bowel function (BFS > 17), while the pooled prevalence of patients with excellent to good Holschneider scores (i.e., score > 10) was 0.95 (95% CI: 0.91–0.97). A study of the long-term outcomes of a cohort of 200 Nordic patients with HD also reported BFS scores for children aged 13–17 years and children older than 18 years of 18 (8–20) and 19 (13–20), respectively [45]; these values are slightly higher than the results of this study. The pooled mean bowel function scores in this meta-analysis and in the results from other literature suggest that most patients older than ten years with an HD surgical history tend to have good to excellent bowel function, despite different tools being used to evaluate the bowel function of these patients.
The pooled mean GIQLI is 120.19 (95% CI: 117.85–122.53), which is higher than the cutoff score (i.e., 105) of constant gastrointestinal symptoms [22]; however, it was lower than the average score of the general population (125.8, 95% CI 121.5–127.5) [37], suggesting that although most patients do not have consistent gastrointestinal symptoms, their health-related quality of life is not as good as their healthy peers. Hartman and colleagues found in their literature review that HD patients could have a good quality of life while experiencing worse disease-specific functioning [51]. The inconsistency between bowel function and quality of life may be due to the psychological symptoms and feelings, such as anxiety and unhappiness caused by HD, which can have a substantial negative influence on these patients’ quality of life. Another possible reason is that parental stress and parental self-efficacy are associated with children’s health outcomes [52, 53], and may even play a mediating role between children’s health-related behavior and quality of life [54]. Two of the included studies [22, 30] employed the PedQoL 4.0 inventory to evaluate children’s quality of life; however, since only one study reported the results of children older than twelve, we were unable to pool the mean scores for quality of life for adolescent patients and to explore how quality of life changes from adolescence to adulthood.
Strengths and limitations
This study is limited in its small number of participants in the included original studies, and the quality of most of the included cross-sectional studies was marginal to fair; thus, the conclusions of this study should be interpreted with caution. Only two studies employed a prospective cohort design, with heterogeneous contents of long-term outcomes and duration and interval of follow-up periods, which makes comparisons between the outcomes of these two patient cohorts difficult. Additionally, most of the included studies failed to report the long-term outcomes from the stratification of the length of aganglionosis colonic bowel segment, type of surgical procedure, and associated congenital diseases, which may influence the prognosis of patients with HD. Another limitation is that only English papers were included in this study; thus, the results may be subject to a language bias. Despite these limitations, this meta-analysis conducted a comprehensive literature search, included the latest evidence, and employed a rigorous statistical method to integrate the pooled prevalence of the long-term prognosis of patients with HD with greater statistical power (by enlarging the whole sample size) [55, 56].
Implications for future research
Providing accurate estimations of the long-term prognosis of patients with HD, recognizing those at a high risk of poor outcomes, and providing these patients with targeted transitional care is of great importance for better recovery and quality of life for the whole group of patients with HD. Future research should involve multicenter studies with standardized outcome indicators, follow-up durations and intervals and should help design evidence-based transitional care for these patients. A more in-depth analysis of the prognosis of patients with HD from the stratification of the length of aganglionosis bowel segment, patients’ age and gender, and surgical procedure is also necessary.
Conclusions
Compared to the general population, adolescent and adult patients with HD surgical history tend to have a higher prevalence of fecal incontinence and lower gastrointestinal-related quality of life, although these patients generally have satisfactory bowel and urinary function. Healthcare professionals should pay closer attention to the long-term prognosis of patients with HD and provide those at a high risk of poor outcomes with more proactive transitional care.
Availability of data and materials
All data generated or analyzed during this study are included in this article.
Abbreviations
- AHRQ:
-
The Agency for Healthcare Research and Quality
- GIQLI:
-
Gastrointestinal Quality of Life Index
- HD:
-
Hirschsprung disease
- ICCS:
-
The International Children’s Continence Society
- MOOSE:
-
Meta-analysis of Observational Studies in Epidemiology
- NOS:
-
The Newcastle-Ottawa Scale
- PedQoL:
-
Pediatric Quality of Life Inventory
- QoL:
-
Quality of Life
References
Deng X, Wu Y, Zeng L, Zhang J, Zhou J, Qiu R. Comparative analysis of modified laparoscopic Swenson and laparoscopic soave procedure for short-segment Hirschsprung disease in children. Eur J Pediatr Surg. 2015;25(5):430–4..
Xia X, Li N, Wei J, Zhang W, Yu D, Zhu T, Feng J. Laparoscopy-assisted versus transabdominal reoperation in Hirschprung's disease for residual aganglionosis and transition zone pathology after transanal pull-through. J Pediatr Surg. 2016;51(4):577–81.
Ademuyiwa AO, Bode CO, Idiodi-Thomas HO, Elebute OA. Early outcome of open primary pull through versus staged pull through in Hirschsprung's disease: a single Centre experience from Nigeria. Nig Q J Hosp Med. 2012;22(3):164–7.
Gunnarsdottir A, Larsson LT, Arnbjornsson E. Transanal endorectal vs. Duhamel pull-through for Hirschsprung's disease. Eur J Pediatr Surg. 2010;20(4):242–6.
Lukac M, Antunovic SS, Vujovic D, Petronic I, Nikolic D, Radlovic V, Krstajic T, Krstic Z. Effectiveness of various surgical methods in treatment of Hirschsprung's disease in children. Vojnosanit Pregl. 2016;73(3):246–50.
Collins L, Collis B, Trajanovska M, Khanal R, Hutson JM, Teague WJ, King SK. Quality of life outcomes in children with Hirschsprung disease. J Pediatr Surg. 2017;52(12):2006–10.
Engum SA, Grosfeld JL. Long-term results of treatment of Hirschsprung's disease. Semin Pediatr Surg. 2004;13(4):273–85.
Zimmer J, Tomuschat C, Puri P. Long-term results of transanal pull-through for Hirschsprung's disease: a meta-analysis. Pediatr Surg Int. 2016;32(8):743–9.
Zhang S, Li J, Wu Y, et al. Comparison of Laparoscopic-Assisted Operations and Laparotomy Operations for the Treatment of Hirschsprung Disease: Evidence From a Meta-Analysis. Medicine. 2015;94:e1632.
Seo S, Miyake H, Hock A, et al. Duhamel and Transanal Endorectal Pull-throughs for Hirschsprung' Disease: A Systematic Review and Meta-analysis. Eur J Pediatr Surg. 2018;28:081–8.
Thomson D, Allin B, Long AM, Bradnock T, Walker G, Knight M. Laparoscopic assistance for primary transanal pull-through in Hirschsprung's disease: a systematic review and meta-analysis. BMJ Open. 2015;5(3):e006063.
Guerra J, Wayne C, Musambe T, Nasr A. Laparoscopic-assisted transanal pull-through (LATP) versus complete transanal pull-through (CTP) in the surgical management of Hirschsprung's disease. J Pediatr Surg. 2016;51(5):770–4.
Stroup DF, Berlin JA, Morton SC, et al. Meta-analysis of Observational Studies in Epidemiology: A Proposal for Reporting. JAMA. 2000;283:2008–12.
Functional fecal incontinence in infants and children: Definition, clinical manifestations and evaluation [https://www-uptodate-com.rpa.skh.org.tw/contents/functional-fecal-incontinence-in-infants-and-children-definition-clinical-manifestations-and-evaluation?search=fecal%20incontinence&source=search_result&selectedTitle=3~150&usage_type=default&display_rank=3]. Accessed 10 Dec 2018.
Diseth TH, Bjornland K, Novik TS, Emblem R. Bowel function, mental health, and psychosocial function in adolescents with Hirschsprung's disease. Arch Dis Child. 1997;76(2):100–6.
Nepple KG, Cooper CSS, SBL, Mattoo TK, SKM. Etiology and clinical features of bladder dysfunction in children. In: UpToDate® UpToDate, Inc.; 2018.
Wells G, Shea B, O’connell D, Peterson J, Welch V, Losos M, Tugwell P. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. In: Ottawa Hospital Research Institute, 2014. Oxford: ASp; 2015.
Springford LR, Kapetanakis VV, Connor MJ, Stefano G. Prevalence of active Long-term problems in patients with Anorectal malformations: a systematic review. Dis Colon Rectum. 2016;59:570–80.
Rostom A, Dubé C, Cranney A, Saloojee N, Sy R, Garritty C, Sampson M, Zhang L, Yazdi F, Mamaladze V, et al. Celiac disease. Evidence report/technology assessment no. 104. (prepared by the University of Ottawa Evidence-based Practice Center, under contract no. 290–02-0021.). In: AHRQ Publication No. 04-E029–2. Rockville: Agency for Healthcare Research and Quality; 2004.
Zhang T, Dong S, Zhou Z. Advanced meta-analysis in Stata [高级Meta分析方法-基于Stata实现]. Fudan University Press. 2015. http://www.fudanpress.com/news/showdetail.asp?bookid=10636. ISBN: 978-7-309-11590-1/C.302.
Jarvi K, Laitakari EM, Koivusalo A, Rintala RJ, Pakarinen MP. Bowel function and gastrointestinal quality of life among adults operated for Hirschsprung disease during childhood: a population-based study. Ann Surg. 2010;252(6):977–81.
Neuvonen MI, Kyrklund K, Rintala RJ, Pakarinen MP. Bowel Function and Quality of Life After Transanal Endorectal Pull-through for Hirschsprung Disease: Controlled Outcomes up to Adulthood. Ann Surg. 2017;265(3):622–9.
Heikkinen M, Rintala RJ, Louhimo I. Bowel function and quality of life in adult patients with operated Hirschsprung's disease. Pediatr Surg Int. 1995;10:342–4.
Heikkinen M, Rintala R, Luukkonen P. Long-term anal sphincter performance after surgery for Hirschsprung's disease. J Pediatr Surg. 1997;32(10):1443–6.
Granström AL, Danielson J, Husberg B, Nordenskjold A, Wester T. Adult outcomes after surgery for Hirschsprung's disease: evaluation of bowel function and quality of life. J Pediatr Surg. 2015;50(11):1865–9.
Gunnarsdottir A, Sandblom G, Arnbjornsson E, Larsson LT. Quality of life in adults operated on for Hirschsprung disease in childhood. J Pediatr Gastroenterol Nutr. 2010;51(2):160–6.
Athanasakos E, Starling J, Ross F, Nunn K, Cass D. An example of psychological adjustment in chronic illness: Hirschsprung's disease. Pediatr Surg Int. 2006;22(4):319–25.
Catto-Smith AG, Trajanovska M, Taylor RG. Long-term continence after surgery for Hirschsprung's disease. J Gastroenterol Hepatol. 2007;22(12):2273–82.
Conway SJ, Craigie RJ, Cooper LH, Turner K, Turnock RR, Lamont GL, Newton S, Baillie CT, Kenny SE. Early adult outcome of the Duhamel procedure for left-sided Hirschsprung disease--a prospective serial assessment study. J Pediatr Surg. 2007;42(8):1429–32.
Mills JL, Konkin DE, Milner R, Penner JG, Langer M, Webber EM. Long-term bowel function and quality of life in children with Hirschsprung's disease. J Pediatr Surg. 2008;43(5):899–905.
Ieiri S, Nakatsuji T, Akiyoshi J, Higashi M, Hashizume M, Suita S, Taguchi T. Long-term outcomes and the quality of life of Hirschsprung disease in adolescents who have reached 18 years or older--a 47-year single-institute experience. J Pediatr Surg. 2010;45(12):2398–402.
Niramis R, Watanatittan S, Anuntkosol M, Buranakijcharoen V, Rattanasuwan T, Tongsin A, Petlek W, Mahatharadol V. Quality of Life of Patients with Hirschsprung’s Disease at 5–20 Years Post Pull-Through Operations. Eur J Pediatr Surg. 2008;18:38–43.
Xiong X, Chen X, Wang G, Feng J. Long term quality of life in patients with Hirschsprung's disease who underwent heart-shaped anastomosis during childhood: a twenty-year follow-up in China. J Pediatr Surg. 2015;50(12):2044–7.
Rintala RJ, Lindahl H. Is normal bowel function possible after repair of intermediate and high anorectal malformations? J Pediatr Surg. 1995;30(3):491–4.
Holschneider A. Elektromanometrie des Enddarms. 2 ed. Munchen: Urban Schwarzenberg; 1982.
Rintala RJ, Lindahl HG, Rasanen M. Do children with repaired low anorectal malformations have normal bowel function? J Pediatr Surg. 1997;32(6):823–6.
Eypasch E, Eypasch E, Williams JI, Williams JI, Wood-Dauphinee S, Wood-Dauphinee S, Ure BM, Ure BM, Schmulling C, Schmulling C, et al. Gastrointestinal quality of life index: development, validation and application of a new instrument. Br J Surg. 1995;82(2):216–22.
Fecal incontinence in adults: Etiology and evaluation [https://www.uptodate.com/contents/fecal-incontinence-in-adults-etiology-and-evaluation/print?search=fecal%20incontinence&source=search_result&selectedTitle=1~150&usage_type=default&display_rank=1]. Accessed 10 Dec 2018.
Bai Y, Chen H, Hao J, Huang Y, Wang W. Long-term outcome and quality of life after the Swenson procedure for Hirschsprung's disease. J Pediatr Surg. 2002;37(4):639–42.
Chumpitazi BP, Nurko S. Defecation disorders in children after surgery for Hirschsprung disease. J Pediatr Gastroenterol Nutr. 2011;53(1):75–9.
Tannuri AC, Ferreira MA, Mathias AL, Tannuri U. Long-term results of the Duhamel technique are superior to those of the transanal pullthrough: a study of fecal continence and quality of life. J Pediatr Surg. 2017;52(3):449–53.
Meinds RJ, van der Steeg AFW, Sloots CEJ, Witvliet MJ, de Blaauw I, van Gemert WG, Trzpis M, Broens PMA. Long-term functional outcomes and quality of life in patients with Hirschsprung's disease. BJS. 2019;106(4):499–507.
Etiology and evaluation of chronic constipation in adults [https://www-uptodate-com.rpa.skh.org.tw/contents/etiology-and-evaluation-of-chronic-constipation-in-adults/print?topicRef=2636&source=see_link]. Accessed 10 Dec 2018.
Mugie SM, Benninga MA, Di Lorenzo C. Epidemiology of constipation in children and adults: a systematic review. Best Pract Res Clin Gastroenterol. 2011;25(1):3–18.
Bjornland K, Pakarinen MP, Stenstrom P, Stensrud KJ, Neuvonen M, Granstrom AL, Graneli C, Pripp AH, Arnbjornsson E, Emblem R, et al. A Nordic multicenter survey of long-term bowel function after transanal endorectal pull-through in 200 patients with rectosigmoid Hirschsprung disease. J Pediatr Surg. 2017;52(9):1458–64.
Chung PHY, Wong KKY, Tam PKH, Leung MWY, Chao NSY, Liu KKW, Chan EKW, Tam YH, Lee KH. Are all patients with short segment Hirschsprung's disease equal? A retrospective multicenter study. Pediatr Surg Int. 2018;34(1):47–53.
Stensrud KJ, Emblem R, Bjornland K. Anal endosonography and bowel function in patients undergoing different types of endorectal pull-through procedures for Hirschsprung disease. J Pediatr Surg. 2015;50(8):1341–6.
Granström AL, Husberg B, Nordenskjold A, Svensson PJ, Wester T. Laparoscopic-assisted pull-through for Hirschsprung's disease, a prospective repeated evaluation of functional outcome. J Pediatr Surg. 2013;48(12):2536–9.
Yanchar NL, Soucy P. Long-term outcome after Hirschsprung's disease: patients' perspectives. J Pediatr Surg. 1999;34(7):1152–60.
Aworanti OM, McDowell DT, Martin IM, Quinn F. Does functional outcome improve with time Postsurgery for Hirschsprung disease? Eur J Pediatr Surg. 2016;26(2):192–9.
Hartman EE, Oort FJ, Aronson DC, Sprangers MAG. Quality of life and disease-specifi c functioning of patients with anorectal malformations or Hirschsprung’s disease: a review; 2010.
Nieuwesteeg AM, Hartman EE, Aanstoot H-J, van Bakel HJA, Emons WHM, van Mil E, Pouwer F. The relationship between parenting stress and parent-child interaction with health outcomes in the youngest patients with type 1 diabetes (0-7 years). Eur J Pediatr. 2016;175(3):329–38.
Dai Y, Ouyang R, Li L, Deng Y, Lin Y. Parental self-efficacy in managing the home care of children with Hirschsprung's disease or anorectal malformation: development and validation of a new measure. J Psychosom Res. 2019;123:109726.
Lohan A, Morawska A, Mitchell A. Associations between parental factors and child diabetes-management-related behaviors. J Dev Behav Pediatr. 2017;38(5):330–8.
Glass GV. Primary, secondary, and meta-analysis of research. Educ Res. 1976;5(10):3–8.
Bo Z, Xin C, Jing-pu S, Ling-yu F, Hai-long W, Xiao-mei W. Meta-Analysis of Rates and Software Implementation [率的Meta分析及软件实现]. Chinese J Evid Based Med. 2014;14(8):1009–16.
Acknowledgements
Not applicable.
Funding
The authors declare that they did not receive funding for this research from any source.
Author information
Authors and Affiliations
Contributions
YD: Designed the study and drafted the manuscript. YFD, RO, and YL screened and evaluated quality of studies, LL and YD extracted data and interpret result and review the manuscript. All authors read and approved the manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Additional file 2.
Reference list of potentially relevant articles that were read in full-text form.
Additional file 3.
Quality appraisal of cross-sectional studies.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Dai, Y., Deng, Y., Lin, Y. et al. Long-term outcomes and quality of life of patients with Hirschsprung disease: a systematic review and meta-analysis. BMC Gastroenterol 20, 67 (2020). https://doi.org/10.1186/s12876-020-01208-z
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12876-020-01208-z