Rectal atresia and rectal stenosis: the ARM-Net Consortium experience

Rectal atresia (RA) and rectal stenosis (RS) are both rare/regional variants of anorectal malformation (ARM), occurring in 1–2% of neonates with ARM [1, 2]. RA/RS are often diagnosed late, potentially due to the normal appearing anus that is located appropriately in the midline, and within the sphincter mechanism [3]. As depicted by Sharma and Gupta, RA/RS can be subdivided into 5 types: type I: RS: (A) intramural, (B) web with a hole; type II: RA with a septal defect; type III: RA with a fibrous cord between two atretic ends; type IV: RA with a gap; type V: multiple: (A) RA with stenosis, (B) multiple RA, and (C) thickened Houston’s valves and/or multiple RS [4]. However, this classification is not yet universally accepted since rectal stenosis is often present in patients with specific features such as pre-sacral mass and/or Currarino syndrome (as is anal stenosis). However, patients with RS should be assessed and approached differently compared to anal stenosis, since they are considered to be different entities. As with other types of ARM, additional anomalies might be present in patients with RA/RS. Therefore, screening for these subsequent anomalies might be also of importance in patients with RA/RS [5].

Due to the rare nature of the subtypes of RA/RS, little is known about this patient population and the optimal technique for reconstructive treatment. Because RA and RS being two distinct congenital ARM, differences might be present in terms of surgical repair. Moreover, in nearly all patients with RA, initially a diverting colostomy is performed, followed by reconstructive surgery, but in some patients with RS, only dilatations are performed. Different techniques have been described for the definitive surgical correction of RA/RS such as pull-through procedures, transanal excision, posterior sagittal anorectoplasty (PSARP), and magnamosis [6‐8]. The chosen approach might differ between types of RA/RS due to distinct disease morphology, clinical presentation, and the surgeon’s preference. Many of the described treatment strategies are invasive surgical procedures (e.g., PSARP, pull-through), and little is known about their mid- and long-term postoperative outcomes in this specific patient group [9]. As all patients with ARM, also patients with RA/RS might be prone to continence problems such as soiling or constipation in the long-term [10]. However, given the normal position of the atretic or stenotic rectum within the sphincter complex, patients with RA/RS might be candidate for good bowel control unless negative prognostic factors are present (e.g., sacral anomaly, spinal dysraphism, poor sacral ratio, and presence of syndromic anomalies) and any surgical procedure should optimize the prognosis for bowel control in the long-term [11].

Given the rarity of RA/RS, literature is scarce and mainly monocentric case reports and case series on specific aspects of the most appropriated treatment strategy are available. Therefore, the aim of this ARM-Net Consortium study is to assess the number and characteristics of patients with RA/RS, and their functional short- (1 year), and mid-term outcomes (5 years) reported in the ARM-Net registry.

This study provides an overview on the patient characteristics of, and treatment strategies performed in, a relative large number of patients with the rare ARM types, RA (n = 18) and RS (n = 18). More than two third of the patients had additional anomalies (n = 23, RA n = 13, RS n = 10). Various treatment strategies were performed, with ostomy in 73% (RA n = 16, RS n = 6) of the patients, and surgical reconstructive treatment in 87% of the patients with RA/RS. PSARP was the most often performed reconstructive surgery for both patients with RA as well as with RS (RA n = 9, RS n = 6). Postoperative complications occurred in 36% of the patients after ostomy surgery and 12% after reconstructive surgery. At 1-year follow-up, 11 of 24 patients (RA n = 5, RS n = 6) were constipated, of whom 9 required therapy. At 5-year follow-up, 8 of 9 patients (RA n = 4, RS n = 4) were constipated, all requiring therapy, but 5-year follow-up data was scarcely available.

The presence of additional anomalies are described for all patients with ARM, regardless of the type of ARM. Also in this study, additional anomalies were identified in 64% of the patients (RA 72.2%, RS 55.6%), which is slightly higher compared to the cohorts including patients with any type of ARM (range 32–62%) [5, 14‐16]. Syndromic, cardiac, and skeletal anomalies were the most frequently identified anomalies in our patient population with RA/RS. With multivariable regression analysis, only the presence of syndromes was independently associated with the presence of additional anomalies. Due to the high prevalence of additional anomalies, it is our opinion that screening for these subsequent anomalies is of great importance for patients with RA/RS.

This study showed a wide variety in applied surgical treatment for patients with RA/RS. As described in previous studies, different types of RA/RS have different disease morphology and therefore might require different treatment approaches [3, 8, 17]. Due to the rarity of the disease, and relative low number of patients available, no recommendations can be made on optimal treatment strategy for the different types of RA/RS based on the results of this study. Postoperative complications were only described for 12% of the patients (n = 3) undergoing surgery. Again, due to the heterogeneity in the results, no differentiation could be made on the surgical intervention carrying the least postoperative complications, and, therefore being the safest. However, assessing PSARP and pull-through procedures as the reconstructive interventions most often performed, functional outcomes might differ due to the nature of these interventions. For instance, with PSARP an incision is made in the sphincter complex, resulting in the formation of scar tissue and subsequent potential damage to the surrounding nerve tissue. In contrast, with pull-through procedures, the sphincter mechanism might undergo potential overstretching, resulting in an inadequate closure mechanism. In addition, previous studies often report on short-term postoperative outcomes after (non-)surgical reconstructive intervention for RA/RS (e.g., on different types of complications), whereas literature on mid- and long-term functional outcomes of patients with RA/RS is lacking [8, 11, 18]. In line with this scarcity in available literature, this study showed that follow-up data was not available for 27% of the patients at 1-year, and 59% at 5-years follow-up. At present, in the ARM-Net registry, only 1-year follow-up data is registered and surgeons were contacted additionally to retrieve 5-year follow-up data. Unfortunately, only few surgeons (n = 8) responded to this request. However, it might be of great importance to evaluate these mid- and long-term outcomes, since at 5-year follow-up, 8/9 patients in whom data was available, were constipated and required subsequent bowel management. Additionally, soiling was reported for 5 patients that might eventually negatively influence their quality of life.

In total, 14 patients (38.9%) were born after 2017. However, in this study, despite the proposed classification by Sharma and Gupta in 2017, the type of RA/RS was specified for none of the patients in the ARM-Net registry. Since RA and RS are very rare conditions, uniform reporting and registration is of great importance to enhance generalizability of data reported in different studies. Therefore, future studies should adopt and implement this proposed classification by Sharma and Gupta, taking into account RA/RS as different entities and not to be mistaken by anal stenosis, to improve uniformity, and decrease heterogeneity in the different types of RA/RS. Because of these different types, uniform data representation is also important for improving data repeatability. In order to make this possible, future research should be conducted among international centers or networks to gain a larger cohort of RA/RS patients.

This study should be interpreted in light of some strengths and limitations. First, to our knowledge this study reports the largest number of patients with RA/RS, very rare types of ARM, in current available literature. Second, we were able to show characteristics on these rare patient groups, with the presence of additional anomalies in 72% and 56% of the included patients with RA and RS respectively. Additionally, a large variety in treatment strategies was performed. However, due to the retrospective nature of this study, some limitations occurred. First, information bias is likely to be present. Subsequently, part of the data from the ARM-Net registry are collected prospectively, but the additional questions concerning 5-year follow-up were collected retrospectively. Therefore, some degree of bias, i.e. incorrect classification or exclusion of data, might have occurred. Second, despite n = 18 for both conditions being a relatively large number for RA/RS, objectively few patients could be included, potentially resulting in a wide variety in reconstructive treatment strategies performed. Third, classification as proposed by Sharma and Gupta (2017) was not applied for the majority of patients, and therefore no clear estimation on the distribution of the different RA/RS types could be provided [4]. Finally, 5-year follow-up data was only available for a small number of patients, and therefore no accurate evaluation of long-term functional outcomes could be done.

Even though numbers are small, it is important to report these data, to open a discussion on what optimal treatment is for patients with different types of RA/RS. In order to do so, future research could evaluate different treatment strategies currently performed for the different types of RA/RS, to eventually create a best practice treatment strategy. In addition, it should be investigated whether the identification of additional anomalies prior to primary intervention were of influence in choice of treatment strategy, and if treatment strategies were subsequently altered after identification of these additional anomalies.

In conclusion, RA and RS are very rare types of ARM, representing 1.3% of all patients included in the ARM-Net registry. The majority of patients with RA/RS had additional anomalies, and various treatment strategies were performed in patients with RA/RS. Most patients had an ostomy followed by reconstructive surgical treatment, of which PSARP was most often performed for both conditions. Follow-up data was scarcely available, especially data on 5-year follow-up was lacking for the majority of patients. Therefore, accurate evaluation of long-term functional outcomes remains challenging.