|Issues in the management of simple and complex meconium ileus.|
|Jump to Full Text|
|PMID: 21512809 Owner: NLM Status: MEDLINE|
|INTRODUCTION: Various surgical methods are used to treat meconium ileus (MI), including resection with enterostomy (RES), primary anastomosis (RPA), and purse-string enterotomy with intra-operative lavage (PSI). The aim of this study is to discuss the surgical treatment of MI, based on our experience.
PATIENTS AND METHODS: Of the 41 MI patients treated at our institution between 1984 and 2007, 18 had simple MI and 23 had complex MI. These groups were analyzed according to treatment modality, concentrating on length of hospital stay, complications [peritonitis, septicemia, adhesive small bowel obstruction (ASBO), and malabsorption/diarrhea], need for additional surgical procedures, mortality.
RESULTS: Of the 18 patients with simple MI, 7 (39%) were successfully treated with diluted Gastrografin® enema. The remaining 11 patients were treated surgically: two underwent RPA, of whom one died; five had RES, of whom one developed ASBO; four underwent PSI, of whom two developed peritonitis. In the complex MI group, 14 patients underwent RPA, with peritonitis occurring in three (one died); nine underwent RES, of whom two developed ASBO.
CONCLUSION: In patients with simple MI, conservative treatment with diluted Gastrografin® enema is an effective initial treatment in our hands. In case of failure, RES is advisable. Patients with complex MI are candidates for RES. RPA and PSI seem to have higher complication rates.
|A Karimi; R R Gorter; Chr Sleeboom; C M F Kneepkens; H A Heij|
Related Documents :
|23153759 - Count sir luigi preziosi and his glaucoma operation: the development of early glaucoma ...
17160499 - The omentum-polypropylene sandwich technique: an attractive method to repair large abdo...
3343679 - Reoperative surgery for early complications following abdominal and abdominothoracic op...
21087799 - A new kaolin-based hemostatic bandage use after coronary diagnostic and interventional ...
18055329 - Pseudomyxoma peritonei secondary to epithelial appendicular neoplasms. experience in a ...
20229519 - Accuracy of peritoneal fluid measurements by transvaginal ultrasonography.
15906139 - Small bowel obstruction: conservative vs. surgical management.
23258099 - Novel non-trocar technique for laparoscopic radiofrequency ablation.
7919649 - Ceramic vertebral body replacement for metastatic spine tumors.
|Type: Comparative Study; Journal Article Date: 2011-04-22|
|Title: Pediatric surgery international Volume: 27 ISSN: 1437-9813 ISO Abbreviation: Pediatr. Surg. Int. Publication Date: 2011 Sep|
|Created Date: 2011-08-17 Completed Date: 2011-12-30 Revised Date: 2013-06-30|
Medline Journal Info:
|Nlm Unique ID: 8609169 Medline TA: Pediatr Surg Int Country: Germany|
|Languages: eng Pagination: 963-8 Citation Subset: IM|
|Pediatric Surgical Center of Amsterdam, Emma Children's Hospital AMC and VU University Medical Center, Amsterdam, The Netherlands.|
|APA/MLA Format Download EndNote Download BibTex|
Ileal Diseases / etiology, surgery*
Ileus / etiology*, surgery*
Severity of Illness Index
Journal ID (nlm-ta): Pediatr Surg Int
Publisher: Springer-Verlag, Berlin/Heidelberg
© The Author(s) 2011
Accepted Day: 4 Month: 4 Year: 2011
Electronic publication date: Day: 22 Month: 4 Year: 2011
pmc-release publication date: Day: 22 Month: 4 Year: 2011
Print publication date: Month: 9 Year: 2011
Volume: 27 Issue: 9
First Page: 963 Last Page: 968
PubMed Id: 21512809
Publisher Id: 2906
|Issues in the management of simple and complex meconium ileus|
|R. R. Gorter1|
|C. M. F. Kneepkens2|
|H. A. Heij1||
Address: +31-20-4442424 +31-20-4442135 firstname.lastname@example.org
1Pediatric Surgical Center of Amsterdam, Emma Children’s Hospital AMC and VU University Medical Center, P. O. Box 22660, 1100 DD Amsterdam, The Netherlands
2Department of Pediatric Gastroenterology, VU University Medical Center, Amsterdam, The Netherlands
Meconium ileus (MI) is defined as an obstruction caused by inspissated meconium at the level of the terminal ileum [1, 2]. In the past, MI was considered to be closely associated with cystic fibrosis (CF).However, recent studies demonstrate that MI occurs frequently in the absence of CF as well [3, 4]. Though the exact pathogenesis of MI in the absence of CF is not known, a spectrum of genetic and pathological abnormalities seem to play a role [3, 4]. Two forms of MI can be discriminated: simple and complex MI [1, 2]. In complex MI, the condition is complicated by associated gastrointestinal pathologies, such as bowel atresia, necrosis, and perforation. When perforation occurs antenatally, meconium can spill into the abdominal cavity, causing (sterile) meconium peritonitis (MP), which may present after birth, with calcifications visible on plain abdominal X-ray [1, 5–7]. In general, the main presenting symptom of MI in newborns is the failure to pass meconium after birth. Complex MI represents a surgical emergency. Differentiating simple and complex MI could be difficult, in spite of the demonstration of marked air-fluid levels and intra-abdominal calcifications on abdominal X-ray, which may be helpful [1, 7–9].
Several options are available for the treatment of MI, but there is a relative lack of literature in examining the treatment outcomes and guidelines are lacking. A vast majority of authors consider enema reductions, such as saline, N-acetyl cysteine and Gastrografin®, as the initial treatment of choice for simple MI [10–13]. The use of enemas is, however, not without risk and the reported success rates vary [11–15]. In case of failure, complication, or complex MI, a surgical procedure is required. Enterotomy and bowel irrigation; T-tube ileostomy; resection of atretic segments, compromised bowel, or strongly dilated bowel followed by primary anastomosis (RPA); Bishop–Koop ileostomy; Santulli procedure and Mikulicz procedure are common procedures for MI [1, 5–7, 16–26]. Although every author seems to have a preferred technique, only few comparative studies have been performed [16–26].
The aim of this retrospective case series study is to compare and discuss various treatment options for neonates with both simple and complex MI.
A total of 44 neonates, treated at the Pediatric Surgical Center Amsterdam between January 1984 and December 2007, met the diagnostic criteria for either simple or complex MI. Newborns with meconium obstruction in other parts of the intestine, neonates with meconium plug syndrome, and newborns with other mechanical or functional causes of bowel obstruction were excluded. Three patients were excluded because of incomplete data concerning the surgical procedure. The remaining 41 neonates were divided into two groups, depending on the type of MI: 18 with simple MI and 23 with complex MI.
Both the groups were subdivided based on the initial treatment. All simple MI patients were initially treated with contrast enema under fluoroscopy. In our center, diluted Gastrografin® is used in the ratio 1 part Gastrografin® (100 + 660 mg/ml, somol = 2,015 mmol/kgH2O) in 1 part 0.9% sodiumchloride (hyperosmolar) in case of meconium ileus. All patients underwent one attempt. During the administration general precautions were taken. In case of failure or complication, one of the following surgical procedures was used: resection with primary anastomosis (RPA), resection with temporary double-barreled enterostomy (RES), or purse-string ileotomy with irrigation (PSI). All newborns with complex MI underwent surgery, either RPA or RES. The procedures were performed by one of the 15 pediatric surgeons, supervised by a senior consultant. The choice of the procedure depended partly on perioperative findings, such as bowel viability, and partly upon the preference of the operating surgeon. Protocols concerning the technical procedure as well as perioperative care were used in order to standardize all treatments.
From the patients record data were extracted for gestational age (in weeks), birth weight (in grams), sex, comorbidity, type of MI, length of hospital stay, time to complete enteral feeding, length of bowel resection, mortality rate, need for additional surgery, and complications. All children were tested for cystic fibrosis (CF) by means of sweat tests after the first week of life (sodium chloride concentrations >60 mmol/L being indicative of CF) and/or DNA analysis of the CFTR gene. Mutations tested included ΔF508, F508C, G542X, R553X, N1303K, R1162X, and E60X. Complications were registered after the initial surgical procedure and divided into four main categories:
1. complications related to the surgical procedure, e.g., peritonitis due to leakage of anastomosis, stoma prolapse;
2. general surgical complications, e.g., adhesive small bowel obstruction (ASBO);
3. illness related complications, e.g., high-output diarrhea;
4. general (non-surgical) complications, e.g., septicemia, urinary tract infection, pneumonia.
Septicemia was defined as either a positive blood culture or a cluster of clinical signs, including tachycardia (>160 beats/min), tachypnea (>50 breathes/min), pyrexia (>38°C), shivering and hypotension (<54/28 mmHg). High-output diarrhea was defined as diarrhea accompanied by malabsorption and failure to thrive. ASBO was defined as small bowel obstruction caused by intra-abdominal adhesions as a result of laparotomy, requiring reoperation. Complications were registered up to 1 year after surgery.
We registered the length of performed resections, and the time to complete enteral feeding. Unfortunately no accurate data could be retrieved concerning growth.
After discharge, patients with CF were monitored by either the Emma Children’s Hospital or the VU University Medical Center cystic fibrosis team. Children without CF were discharged from the 3-monthly follow-up after 1 year. Because of the small number of cases, statistical analysis was limited to comparison of complication rates.
All patients of the simple MI group (n = 18) were initially given a contrast enema under fluoroscopy. All four patients without CF and 3/14 CF patients (21%) were successfully treated with 1:1 diluted Gastrografin® enemas. In 10 patients, Gastrografin® enemas were unsuccessful, as was iohexol in another patient. None of the patients suffered from complications after the enema administration.
The 11 patients (all with CF) in whom contrast enema had failed underwent surgical intervention Table 3. RPA was performed in two patients, both had several complications as outlined in Table 3. Both required additional surgery because of ASBO: enterostomy in one patient and adhesiolysis in the other. The former suffered from 14 episodes of septicemia and died after 380 days of admission. RES was performed in five patients, one of them requiring RPA because of ASBO. Four patients were treated with PSI and irrigation with 1:1 Gastrografin® enema, two of whom required enterostomy and additional adhesiolysis because of peritonitis following perforation. No differences existed between the treatment groups with regard to complications, time to complete enteral feeding, length of resection, initial hospital stay, or mortality rate.
Fifteen patients of the complex MI group, all without signs of perforation or calcifications, were initially given 1:1 Gastrografin® enemas for diagnostic purposes. In one patient extravasation of the enema fluid was seen as an indication of perforation. All 23 patients underwent surgery; complications after surgery are outlined in Table 4. RPA was performed in 14 patients, three of whom required additional surgery: suture of perforation and enterostomy in two patients and adhesiolysis because of ASBO in one. Additionally, one patient suffered from a total of 11 episodes of septicemia and died after 431 days of admission. RES was performed in nine patients, two of whom required additional surgery: adhesiolysis for ASBO in one and exploratory laparatomy persisting signs of intestinal obstruction in the other. All patients of this group survived.
Patients with simple MI were initially treated with contrast enema. In our study, 1:1 diluted Gastrografin® was safe and effective in resolving the obstruction in 39% of the patients with simple MI, which is in line with the published success rates ranging 5–83% [10–17]. The fact that all four patients without CF in this group were successfully treated may well reflect the fact that meconium in these patients is less viscous. Though a recent report suggests that repeated enemas might increase the success rate of the conservative treatment , we chose to reduce the risk of complications by not repeating an unsuccessful attempt.
In mice, Gastrografin® was shown to be more efficacious for the relief of constipation than agents such as saline, Tween-80, Dnase and N-acetyl cysteine . Apart from saline, all agents reduced the viscosity of human meconium immediately after administration; of these, N-acetylcysteine reduced viscosity with more than 99%, but only after an incubation period of 6 h. The use of hyperosmolar agents such as Gastrografin® is, however, not without risk. Perforation, hypovolemia, electrolyte loss, and hepatotoxicity have been reported [14, 18–20] the risk of complications can be diminished by taking care of precautions such as diluting the solution with equal amounts of water, limitation of administration pressure, and the provision of intravenous access to maintain optimal fluid administration. Furthermore, contraindications including signs indicative of perforation should be identified with the help of X-ray studies. None of our simple MI patients suffered from complications, whereas in one complex MI patient leakage of contrast into the abdominal cavity occurred, apparently due to the pre-existing perforation sealed by the intestinal loops. Overall, the minimal invasive nature, the relatively high success rates and the low complication rates make Gastrografin® enema the first choice in simple MI.
In case of failed contrast enema or complications in simple MI, resection with temporary double-barreled enterostomy seems to be the preferable approach. Severe complications related to the surgical procedure itself, such as peritonitis due to anastomotic leakage and perforation due to frequent manipulation, were more often seen in RPA and PSI. Decreased viability of severely dilated bowel in combination with the previous injection of hypertonic solution and manipulation during surgery aimed at advancing the meconium might underlie the greater complication rate following surgery without enterostomy. Moreover, the enterostomy in RES has the advantage that enemas can be applied after surgery in order to evacuate any remaining meconium, so that manual manipulation during surgery can be kept at minimum. The disadvantages of enterostomy, such as enterostomy care, the need for an extra surgical procedure, prolonged hospital stay, and the risk of high-output diarrhea do not outweigh the obvious reduced risk of anastomotic leakage and perforation.
Recent literature does not provide clear guidelines concerning the surgical treatment of simple MI. The Bishop–Koop enterostomy, introduced in 1957 consisting of an end-to-side anastomosis combined with a chimney- like enterostomy, has been widely used [13, 21, 22]. It has the advantage of easy extraperitoneal, bed-side closure of the enterostomy. However, anastomosis is made, in the intraperitoneal cavity, leading to a higher risk of anastomotic leakage. For this reason, we prefer the double-barreled enterostomy. Although PSI is reported to result in reduced admission duration and a relatively low complication rate [13, 16, 20], our data suggest that PSI is not without risk. The injection of hypertonic solution combined with squeezing and milking of the neonatal gut increases the risk of perforation, as is the case with suturing the ileotomy in tissue with impaired vascularisation. RPA, finally, has fallen out of grace for simple MI , as the primary anastomosis of compromised intestine might be hazardous. Recent techniques include variants of enterotomy with irrigation and T-tube ileostomy [24, 25], but information on these techniques is limited.
In the complex MI group, surgical intervention is mandatory. In this group as well, resection with enterostomy in our hands was the safest treatment. None of the patients developed peritonitis, as compared to 21% of the RPA group. The reoperation rates, apart from closure of enterostomy, in RES and RPA were similar. Although RES creates the need of additional surgery to close the enterostomy, this is a safe, elective procedure. Complication rates between patients with and without CF were similar.
Conclusive evidence for the superiority of one or another procedure in complex MI has not been published. RPA has been used infrequently, mostly with atresia. Rescorla and Grosfeld  did not mention the complications while reporting on RPA in 13 out of 27 complex MI patients with atresia, volvulus or perforation. Escobar et al.  suggest that RPA should only be used in case of atresia, RES being preferable in complex MI patients. However, most studies report no significant differences between RPA and RES apart from duration of hospital stay, or focus only on one surgical procedure [13, 24, 25]. Jawaheer et al.  report complications requiring additional surgery in 4 out of 13 patients (31%) after RPA, which is in line with our experience (complications in 21%). They consider RPA as a safe option for all complex MI patients apart from those with unstable condition and impaired perfusion of intestinal margins, the advantages being reduced hospital stay, avoidance of stoma-related morbidity and second laparotomy for stoma closure . However, impaired intestinal perfusion, is often present in complex MI patients, while the manipulation of neonatal intestine for the evacuation of viscous meconium might further impair blood supply and intestinal integrity. As it is hard to objectively assess the viability and condition of the intestine, we consider intra-abdominal anastomosis in these circumstances as hazardous. Fashioning of a double-barreled enterostomy requires less manipulation of the neonatal intestine and enables the application of enemas after surgery, while elective enterostomy closure is a safe procedure.
As this is a retrospective study with a limited number of patients, collected over a period of 23 years, the results should be interpreted with care. Yet, our results suggest that RPA should be used with caution, both in patients with simple and with complex MI. RES seems to be the safer procedure, which might be explained by the fact that intestinal viability is hard to determine during surgery. Enterostomy prevents peritonitis due to anastomotic leakage and enables postoperative retrograde enema use, the necessity of a second operation for the restoration of intestinal continuity being a relative disadvantage. As the present evidence precludes the composition of solid guidelines, prospective multicenter studies seem to be warranted.
This study has been approved by the ethics board of the VU University medical center.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
|1..||Wyllie R,et al. Kliegmann RM,Behrman RE,Jenson HB,Stanton BF,et al.Intestinal atresia, stenosis and malrotationNelson textbook of pediatricsYear: 200718PhiladelphiaSaunders Elsevier15591562|
|2..||Ziegler MM. Meconium ileusCurr Probl SurgYear: 19943173177710.1016/0011-3840(94)90040-X8062591|
|3..||Gorter RR,Karimi A,Sleeboom Chr,et al. Clinical and genetic characteristics of meconium ileus in newborns with and without cystic fibrosisJ Pediatr GastroenterolYear: 2010505569572|
|4..||Fakhoury K,Durie PR,Levinson H,et al. Meconium ileus in the absence of cystic fibrosisArch Dis ChildYear: 1992671204120610.1136/adc.67.10_Spec_No.12041444561|
|5..||Ein SH,et al. Freeman NV,Burge DM,Griffiths DM,et al.Meconium ileusSurgery of the newbornYear: 1994LondonChurchill Livingstone139157|
|6..||Rescorla FJ,et al. O’Neill jr JA,Rowe MI,Grosfeld JL,et al.Meconium IleusPediatric surgeryYear: 19985MissouriMosby Yearbook11591171|
|7..||Kieley E. Puri PMeconium ileusNewborn surgeryYear: 20032LondonArnold465471|
|8..||White H. Meconium ileus: a new roentgen signRadiologyYear: 19566656757113323298|
|9..||Neuhauser EBD. Roentgen changes associated with pancreatic insufficiency in the early lifeRadiologyYear: 19464631932821027364|
|10..||Noblett HR. Treatment of uncomplicated meconium ileus by Gastrografin® enema: a preliminary reportJ Pediatr SurgYear: 1969419019710.1016/0022-3468(69)90390-X5778338|
|11..||Burke MS,Ragi JM,Karamanoukian HL,et al. New strategies in non-operative management of meconium ileusJ Pediatr SurgYear: 2002576076410.1053/jpsu.2002.3227211987095|
|12..||Boyd A,Carachi R,Azmy AF,et al. Gastrografin® enema in meconium ileus: the persistent approachPediatr Surg IntYear: 1988313914010.1007/BF00182769|
|13..||Rescorla FJ,Grosfeld JL. Contemporary management of meconium ileusWorld J SurgYear: 19931731832510.1007/BF016586988337877|
|14..||Ein SH,Shandling B,Reily BJ,et al. Bowel perforation with non operative treatment of meconium ileusJ Pediatr SurgYear: 1987214614710.1016/S0022-3468(87)80434-73820012|
|15..||Copeland DR,St Peter SD,Sharp SW,et al. Diminishing role of contrast enema in simple meconium ileusJ Pediatr SurgYear: 2009442130213210.1016/j.jpedsurg.2009.06.00519944221|
|16..||Nguyen LT,Youssef S,Guttman FM,et al. Meconium ileus: is a stoma necessary?J Pediatr SurgYear: 19862176676810.1016/S0022-3468(86)80362-13772700|
|17..||D’Agostino S,Musi L,Fabbro MA,et al. Uncomplicated meconium ileus: efficacy of enterotomy and bowel irrigationPediatr Surg IntYear: 199510329331|
|18..||Escobar MA,Grosfeld JL,Burdick JJ,et al. Surgical considerations in cystic fibrosis: a 32-year evaluation of outcomesSurgeryYear: 200513856057210.1016/j.surg.2005.06.04916269283|
|19..||Manesksha FR,Betta J,Zawin M,et al. Intraoperative hypoxia and hypotension caused by gastrografin-induced hypovolemiaAnesthesiologyYear: 19846145445610.1097/00000542-198410000-000156486506|
|20..||Venugopal S,Shandling B. Meconium ileus: laparotomy without resection, anastomosis, or enterostomyJ Pediatr SurgYear: 19791471571810.1016/S0022-3468(79)80252-3551149|
|21..||Bishop HC,Koop CE. Management of meconium ileus; resection, Roux-en-Y anastomosis and ileostomy irrigation with pancreatic enzymesAnn SurgYear: 195714541041410.1097/00000658-195703000-0001713403593|
|22..||Del Pin CA,Czyrko C,Ziegler MM,Scanlin TF,Bishop HC. Management and survival of meconium ileus a 30 year reviewAnn SurgYear: 1992217918510.1097/00000658-199202000-000141546905|
|23..||Nagar H. Meconium ileus: Is a single procedure adequate?Asian J SurgYear: 20062916116410.1016/S1015-9584(09)60078-616877216|
|24..||Mak GZ,Harberg FJ,Hiatt P,et al. T-tube ileostomy for meconium ileus: four decades of experiencesJ Pediatr SurgYear: 20003534935210.1016/S0022-3468(00)90038-110693694|
|25..||Steiner Z,Mogilner J,Siplovich L,et al. T-tubes in the management of meconium ileusPediatr Surg IntYear: 19971214014110.1007/BF01349982|
|26..||Jawaheer J,Khalil B,Plummer T,et al. Primary resection and anastomosis for complicated meconium ileus: a safe procedure?Pediatr Surg IntYear: 2007231091109310.1007/s00383-007-2020-917882440|
|ASBO||Adhesive secondary bowel obstruction|
|RPA||Resection with primary anastomosis|
|RES||Resection with enterostomy|
Characteristics of the simple MI group (n = 18)
|Diatrizoate enema (n = 7)||Resection with primary anastomosis (n = 2)||Resection with temporary enterostomy (n = 5)||Purse-string ileotomy (n = 4)|
|Gestational age (weeks)||Mean ± SD||37 ± 2||38 ± 0||39 ± 3||39 ± 3|
|Birth weight (g)||Mean ± SD||2,278 ± 636||2,938 ± 265||3,117 ± 829||3,195 ± 889|
Characteristics of the complex MI group (n = 23)
|Resection with primary anastomsis (n = 14)||Resection with temporary enterostomy (n = 9)|
|Gestational age (weeks)||Mean ± SD||38 ± 3||37 ± 3|
|Birth weight (g)||Mean ± SD||2,760 ± 840||3,035 ± 963|
Complications in surgically treated simple MI patients (n = 11)
|Category||Complication||Resection with primary anastomosis (n = 2)||Resection with enterostomy (n = 5)||Purse-string ileotomy (n = 4)|
|Specific surgical complications||Peritonitis due to leakage of anastomosis||1||0||2|
|General surgical complications||ASBO||2||1||0|
|Resection length (cm) (mean ± SD)||15.0 ± 7.07||3.33 ± 5.77||0.00 ± 0.00|
|Time to complete enteral feeding (days) (mean ± SD)||10 ± 0||32.8 ± 37.6||21.7 ± 9.87|
|Illness related complications||Malabsorption diarrhea||0||0||1|
|General (non-surgical) complications||Pneumonia||0||0||0|
|Hospital stay (mean ± SD)||202 ± 252||23 ± 6||38 ± 23|
|Additional surgery needed||2||1||2|
Complications in the complex MI group (n = 23)
|Category||Complications||Resection with primary anastomosis (n = 14)||Resection with enterostomy (n = 9)|
|Specific surgical complications||Peritonitis due to leakage of anastomosis||2 (14%)||0|
|General surgical complications||ASBO||1 (7%)||0|
|Wound infection||0||2 (22%)|
|Length of resection (cm) (mean ± SD)||18.7 ± 9.40||20.8 ± 20.6|
|Time to complete enteral feeding (days) (mean ± SD)||19.5 ± 8.45||37.8 ± 43.7|
|Illness related complications||Malabsorption diarrhea||0||3 (33%)|
|General (non-surgical) complications||Pneumonia||0||0|
|Septicemia||1 (7%)||1 (11%)|
|Urinary tract infection||0||2 (22%)|
|Hospital stay (mean ± SD)||57 ± 108||60 ± 39|
|Additional surgery needed||3 (21%)||2 (22%)|
|Mortality rate||1 (7%)||0|
Keywords: Keywords Meconium ileus, Meconium peritonitis, Intestinal atresia, Cystic fibrosis, Diatrizoate, Gastrografin®.
Previous Document: Emerging ethical issues in pediatric surgery.
Next Document: Placement of prophylactic drains after laparotomy may increase infectious complications in neonates.