Diagnostic Accuracy of Radiologic Scoring System for Evaluation of Suspicious Hirschsprung Disease in Children

authors:

avatar Mehdi Alehossein 1 , 2 , avatar Ahad Roohi 3 , avatar Masoud Pourgholami 2 , avatar Mansour Mollaeian 4 , avatar Payman Salamati 1 , *

Advanced Diagnostic and Interventional Radiology Research Center (ADIR), Tehran University of Medical Sciences, Tehran, Iran
Department of Radiology, Bahrami Children Hospital, Tehran University of Medical Sciences, Tehran, Iran
Department of Radiology, Tehran University of Medical Sciences, Tehran, Iran
Department of Pediatric Surgery, Bahrami Children Hospital, Tehran University of Medical Sciences, Tehran, Iran

how to cite: Alehossein M, Roohi A, Pourgholami M, Mollaeian M, Salamati P. Diagnostic Accuracy of Radiologic Scoring System for Evaluation of Suspicious Hirschsprung Disease in Children. I J Radiol. 2015;12(2):e12451. https://doi.org/10.5812/iranjradiol.12451.

Abstract

Background:

In 1996, Donovan and colleagues represented a scoring system for better prediction of Hirschsprung disease (HD).

Objectives:

Our objective was to devise another scoring system that uses a checklist of radiologic and clinical signs to determine the probability of HD in suspicious patients.

Patients and Methods:

In a diagnostic accuracy study, 55 children with clinical manifestations of HD that referred to a training hospital from 1998 to 2011 were assessed. A checklist was used to evaluate the items proposed by contrast enema (CE), based on six subscales, including transitional zone, rectosigmoid index (RSI), irregular contractions in aganglionic region, cobblestone appearance, filling defect due to fecaloid materials and lack of meconium defecation during the first 48 hours after birth. The patients were classified as high score and low score. Sensitivity, specificity, positive predictive value and negative predictive value of our scoring system were calculated for identifying HD, in comparison with pathologically proved or ruled out HD.

Results:

Of the 55 patients, 36 (65.4%) cases had HD and 19 (34.6%) cases were without HD. In the HD group, 32 patients showed high scores and four patients had low scores. The sensitivity and specificity of our diagnostic scoring system were 88.9% (95% CI: 78.6% - 99.1%) and 84.2% (95% CI: 68.7 - 100%), respectively. Moreover, positive predictive value (PPV) and negative predictive value (NPV) were 91.4% (95% CI: 82.1% - 100%) and 80% (95% CI: 62.5% - 97.5%), respectively.

Conclusions:

Our new scoring system of CE is a useful diagnostic method in HD. If a patient’s score is high, that patient is highly suspicious to HD and reversely, when one’s score is low, the patient presents a reduced probability to be diagnosed with HD.

1. Background

Hirschsprung disease (HD) or congenital aganglionic megacolon is an intestinal motor disorder with an incidence of 1:5000 live births, ranging from 1:14000 to 1:4000 live births (1). It results in delayed meconium defecation, abdominal distension, lack of appetite, vomiting, and entrocolitis (2). In several cases, the patients may be asymptomatic until adolescence and puberty years and 15% of cases remain undiagnosed until the age of 5 (2, 3).

The gold standard of diagnosis is the pathological evaluation, revealing the absence of ganglion cells in the submucosal and myentric plexus, resulting in aperistaltism in the affected enteric regions and functional intestinal obstruction. Although the initial diagnosis is mainly based on clinical history and examination, followed only afterwards by pathological assessment (4), radiographic contrast assessment may be useful in diagnosis (5, 6). The risks associated with rectal biopsy, such as perforation, scar, stricture, bleeding and also anesthesia-related adverse effects, results in seeking several non-invasive techniques, such as imaging methods (7, 8). A plain radiography may demonstrate a transition zone between a gas-filled colon and a non-dilated proximal colon, as a funnel-shaped region. Contrast enema (CE) with barium may be the first imaging procedure performed in the majority of centers, showing a transition zone, irregular colonic contractions, irregular mucosa suggesting enterocolitis, and an abnormal rectosigmoid index (RSI) (9). These methods may have different sensitivity and specificity, based on age and length of involved region (10-16). Regarding the availability and feasibility of CE in most centers, and considering the role of prompt diagnosis and treatment of disease for the prevention of misdiagnoses and complications, the use of a non-invasive method, such as CE, would help the physicians to achieve a better management of the disease.

2. Objectives

In this study, a scoring system that was using a checklist of radiologic and clinical signs was developed and used for a more accurate diagnosis of HD, and the sensitivity and specificity were determined in comparison with biopsy, as a gold standard method.

3. Patients and Methods

In this cross-sectional study for determining the diagnostic accuracy of a radiologic checklist, the understudy population included 55 children with suspicious HD attending to a training referral hospital since 1998 to 2011, which undergone CE and HD diagnosis was ruled out or confirmed by full thickness bowel biopsy. Therefore, inclusion criteria were having clinical presentation highly suspicious for HD, performing a CE exam and full thickness biopsy. The study was approved by Ethical Committee of Tehran University of Medical Sciences, Tehran, Iran, and the Helsinki Declaration was respected entirely throughout the study.

Patients were divided into three age groups, as follows: < 1 month, 1 - 12 months, > 12 months. A checklist was used to evaluate the items proposed by CE as radiologic signs, including six subscales: 1) transitional zone (TZ), defined as significant change in intestinal diameter from non-dilated to dilated section during CE; 2) RSI, ratio of largest rectal diameter to largest sigmoid diameter (among proximal, distal, and loop sections), is considered abnormal if it is < 1; 3) bizarre large irregular contractions in aganglionic region, with saw teeth appearance, due to dysrhythmia; 4) cobblestone appearance or mucosal irregularity or proximal colon spasm; 5) filling defect due to fecaloid materials; 6) lack of meconium defecation during the first 48 hours after birth. An example of cobble stone appearance and TZ is shown in Figure 1, while an example of bizarre irregular contraction is depicted by Figure 2. Figure 3 shows TZ and reversed RSI in a 3-month-old HD patient. For subscales 1 and 2, if they were positive, we would consider scoring = 2, and, if they were negative, we would consider scoring = 0. For the other subscales, the positive results had scoring = 1 and negative results had score = 0. Furthermore, the patients were evaluated based on scoring system, as follows: high (5-8), and low (0‒4).

All the radiographies were interpreted by a radiologist without knowledge of the pathology results. Data analysis was performed with the SPSS version 20.0 software (IBM, USA). Chi-Square and independent t tests were used for analysis and were considered statistically significant at P < 0.05.

Barium enema in neonate with Hirschsprung disease shows transitional zone and cobblestone appearance
Barium enema in neonate with Hirschsprung disease shows transitional zone and cobblestone appearance
Barium enema in a 1-month-old male with Hirschsprung disease depicts bizarre irregular contraction
Barium enema in a 1-month-old male with Hirschsprung disease depicts bizarre irregular contraction
Barium enema shows transitional zone and reversed rectosigmoid index in a 3-month-old Hirschsprung disease patient
Barium enema shows transitional zone and reversed rectosigmoid index in a 3-month-old Hirschsprung disease patient

4. Results

The mean age was 0.98 ± 1.74 months, ranging from 3 days to 8 years. Males represented 71% of patients while 29% were female. According to pathological results, 36 children (65.4%) had HD and 19 subjects (34.6%) had other diseases.

In HD group, 32 subjects showed high score (5-8) and four subjects low score (0-4). In the non-HD group, 16 subjects showed low score (0-4) and three subjects showed high score (5-8). The sensitivity and specificity of our diagnostic scoring system were 88.9% (95% CI: 78.6-99.1%) and 84.2% (95% CI: 68.7% - 100%), respectively. Moreover, positive predictive value (PPV) and negative predictive value (NPV) were 91.4% (95% CI: 82.1-100%) and 80% (95% CI: 62.5-97.5%), respectively.

Abdominal distension, lack of meconium defecation, and constipation were the most common clinical symptoms with frequencies of 77.7%, 72.2%, and 53%, respectively. The most common findings in CE were TZ and RSI, respectively (Table 1). The sensitivity, specificity, PPV, NPV and accuracy for TZ in CE are shown in Table 2. These items are also demonstrated for each subscale by Table 3.

Table 1.

Contrast Enema Findings in Those with and Without Hirschsprung a, b

CE FindingsWith HirschsprungWithout HirschsprungP Value
Transitional zone34 (94)6 (31.5)0.001
Rectosigmoid index31 (86)6 (31.5)0.001
Irregular contraction15 (43)
Mucosal irregularity7 (21)
Cobblestone appearance3 (10.5)1 (3.5)> 0.05
Delay in passing meconium within 48 hours after birth26 (72.2)5 (26.3)0.001
Table 2.

Diagnostic Indices of Transitional Zone a

Diagnostic IndexTime
< 1 Month1‒12 Months> 12 monthsTotal
Sensitivity1001006094.4
Specificity42.88085.768.4
Positive predictive value8193.37585
Negative predictive value1001007586.7
Accuracy89907585.4
Table 3.

Diagnostic Indices of Each Contrast Enema Findings a, b

TZRSIIrregular ContractionCobblestoneDelay in Passing MeconiumFilling Defect
Sensitivity94.48641.618.372.261.1
Specificity68.468.410094.773.763.1
Positive predictive value8583.710076.583.976
Negative predictive value 86.772.247.536.558.346.1
Accuracy85.48061.839.572.761.8

5. Discussion

Hirschsprung is an uncommon disease seen in all races and may result in decreased quality of life due to chronic constipation and periodic obstructions. It may also be fatal in severe cases with enterocolitis, functional obstruction, and intestinal perforation. Nowadays, the mortality has been decreased from 80% to 13%, mainly owing to prompt diagnosis and subsequent conservative treatments (17), a trend that demonstrates the important role of definite correct diagnosis of HD.

Although the intestinal biopsy is the diagnostic gold standard, the first diagnostic method is CE (12, 18-20). The challenging issues of intestinal biopsy are higher cost, more invasiveness, longer hospital stay and need to follow-up (18, 21). Therefore, in this study, we compared our diagnostic scoring system with full thickness intestinal biopsy, as the gold standard diagnostic method.

In a similar study, Donovan et al. introduced a scoring system with eight items in CE, with scores 0 and 1 for negative and positive results, respectively and the patients were divided into three groups: high (scores 6-8), moderate (scores 4-5), and low (scores 1-3) probability (22). However, this method of scoring was not very effective in our study and we decided to consider two points for positive results in RSI and TZ and one point for positive results related to lack of meconium defecation, cobblestone appearance, irregular contraction, and level of filling defect. We did not use delayed graphy and serration and also sex differences in our scoring system. In the current study, if one’s score is high (5-8), the patient is highly suspicious to HD and if one’s score is low (0-4), the patient presents a reduced probability to have HD, with high sensitivity and specificity. This demonstrates the helper role of scoring system in the diagnosis of HD. However, there are only limited other similar studies for the comparison of scoring systems.

Previous studies have shown the TZ and RSI as the most common signs in CE (23-25). The sensitivity and specificity of CE in the diagnosis of HD has shown a wide range, between 60% to 100% (24-26). This may be due to different techniques and also types of patient selections and different skill levels of the radiologists. Proctor et al. demonstrated that sensitivity and specificity of CE for short segment HD were 92% and 75%, respectively, and they were 63% and 100% for long segment disease, respectively (15). Other factors such as age, sex, and disease duration may also be important in the prediction of sensitivity and specificity of CE in patients with older ages (23).

Reid et al. in their study, demonstrated that the NPV of CE in the post-neonatal period was higher than in the neonatal age and, oppositely, the PPV was high in each group. This shows the higher value of abnormal CE for HD confirmation compared with normal CE for rejection of HD diagnosis (27).

Similar to previous studies, the most common signs in CE were TZ and RSI. Among these, the TZ is pathognomonic for HD. CE would have both diagnostic and therapeutic efficacy in neonates. However, in absence of TZ, the HD may not be ruled out. In older children, the first differential diagnosis of HD is functional megacolon. In several review studies, the frequency of HD in those with TZ was reported at 72%, while in the presence of other signs, it reduced to half (28).

Totally, according to obtained results, our diagnostic scoring system would have high validity for the diagnosis of HD and the scoring can be used as a useful diagnostic tool. However, further multi-centric studies, with larger sample sizes, are suggested for comparison of all diagnostic methods.

References

  • 1.

    Rosai J. Rosai and Ackerman's Surgical Pathology. 2. 9th ed. New York: Mosby; 2004. p. 777-9.

  • 2.

    Kliegman RM, Behrman RE, Jenson HB, Stanton BF. Nelson Textbook of Pediatrics. 18th ed. Philadelphia: Saunders Company; 2007. p. 1565-7.

  • 3.

    Martucciello G. Hirschsprung's disease, one of the most difficult diagnoses in pediatric surgery: a review of the problems from clinical practice to the bench. Eur J Pediatr Surg. 2008;18(3):140-9. [PubMed ID: 18493886]. https://doi.org/10.1055/s-2008-1038625.

  • 4.

    Constipation Guideline Committee of the North American Society for Pediatric Gastroenterology H. Evaluation and treatment of constipation in infants and children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr. 2006;43(3):e1-13. [PubMed ID: 16954945]. https://doi.org/10.1097/01.mpg.0000233159.97667.c3.

  • 5.

    Swenson O. Hirschsprung's disease: a review. Pediatrics. 2002;109(5):914-8. [PubMed ID: 11986456].

  • 6.

    Kapur RP. Practical pathology and genetics of Hirschsprung's disease. Semin Pediatr Surg. 2009;18(4):212-23. [PubMed ID: 19782303]. https://doi.org/10.1053/j.sempedsurg.2009.07.003.

  • 7.

    Boman F, Corsois L, Paraf F. [Hirschsprung's disease: practical considerations]. Ann Pathol. 2004;24(6):486-98. [PubMed ID: 15785397].

  • 8.

    Wester T, Olsson Y, Olsen L. Expression of bcl-2 in enteric neurons in normal human bowel and Hirschsprung disease. Arch Pathol Lab Med. 1999;123(12):1264-8. [PubMed ID: 10583933].

  • 9.

    de Lorijn F, Kremer LC, Reitsma JB, Benninga MA. Diagnostic tests in Hirschsprung disease: a systematic review. J Pediatr Gastroenterol Nutr. 2006;42(5):496-505. [PubMed ID: 16707970]. https://doi.org/10.1097/01.mpg.0000214164.90939.92.

  • 10.

    De Lorijn F, Reitsma JB, Voskuijl WP, Aronson DC, Ten Kate FJ, Smets AM, et al. Diagnosis of Hirschsprung's disease: a prospective, comparative accuracy study of common tests. J Pediatr. 2005;146(6):787-92. [PubMed ID: 15973319]. https://doi.org/10.1016/j.jpeds.2005.01.044.

  • 11.

    Kim HJ, Kim AY, Lee CW, Yu CS, Kim JS, Kim PN, et al. Hirschsprung disease and hypoganglionosis in adults: radiologic findings and differentiation. Radiology. 2008;247(2):428-34. [PubMed ID: 18430875]. https://doi.org/10.1148/radiol.2472070182.

  • 12.

    Diamond IR, Casadiego G, Traubici J, Langer JC, Wales PW. The contrast enema for Hirschsprung disease: predictors of a false-positive result. J Pediatr Surg. 2007;42(5):792-5. [PubMed ID: 17502185]. https://doi.org/10.1016/j.jpedsurg.2006.12.031.

  • 13.

    Garcia R, Arcement C, Hormaza L, Haymon ML, Ward K, Velasco C, et al. Use of the recto-sigmoid index to diagnose Hirschsprung's disease. Clin Pediatr (Phila). 2007;46(1):59-63. [PubMed ID: 17164511]. https://doi.org/10.1177/0009922806289328.

  • 14.

    Jamieson DH, Dundas SE, Belushi SA, Cooper M, Blair GK. Does the transition zone reliably delineate aganglionic bowel in Hirschsprung's disease? Pediatr Radiol. 2004;34(10):811-5. [PubMed ID: 15278325]. https://doi.org/10.1007/s00247-004-1292-7.

  • 15.

    Proctor ML, Traubici J, Langer JC, Gibbs DL, Ein SH, Daneman A, et al. Correlation between radiographic transition zone and level of aganglionosis in Hirschsprung's disease: Implications for surgical approach. J Pediatr Surg. 2003;38(5):775-8. [PubMed ID: 12720192]. https://doi.org/10.1016/jpsu.2003.50165.

  • 16.

    Pratap A, Gupta DK, Tiwari A, Sinha AK, Bhatta N, Singh SN, et al. Application of a plain abdominal radiograph transition zone (PARTZ) in Hirschsprung's disease. BMC Pediatr. 2007;7:5. [PubMed ID: 17257439]. https://doi.org/10.1186/1471-2431-7-5.

  • 17.

    Khan AR, Vujanic GM, Huddart S. The constipated child: how likely is Hirschsprung's disease? Pediatr Surg Int. 2003;19(6):439-42. [PubMed ID: 12698267]. https://doi.org/10.1007/s00383-002-0934-9.

  • 18.

    Kessmann J. Hirschsprung's disease: diagnosis and management. Am Fam Physician. 2006;74(8):1319-22. [PubMed ID: 17087425].

  • 19.

    Stranzinger E, DiPietro MA, Teitelbaum DH, Strouse PJ. Imaging of total colonic Hirschsprung disease. Pediatr Radiol. 2008;38(11):1162-70. [PubMed ID: 18679610]. https://doi.org/10.1007/s00247-008-0952-4.

  • 20.

    Lewis NA, Levitt MA, Zallen GS, Zafar MS, Iacono KL, Rossman JE, et al. Diagnosing Hirschsprung's disease: increasing the odds of a positive rectal biopsy result. J Pediatr Surg. 2003;38(3):412-6. discussion 412-6. [PubMed ID: 12632358]. https://doi.org/10.1053/jpsu.2003.50070.

  • 21.

    Ramanth N. Gastrointestinal Imaging. In: Blickman H, editor. Pediatr Radiol. 2nd ed. Elsevier; 2004.

  • 22.

    O'Donovan AN, Habra G, Somers S, Malone DE, Rees A, Winthrop AL. Diagnosis of Hirschsprung's disease. AJR Am J Roentgenol. 1996;167(2):517-20. [PubMed ID: 8686640]. https://doi.org/10.2214/ajr.167.2.8686640.

  • 23.

    Skaba R. Historic milestones of Hirschsprung's disease (commemorating the 90th anniversary of Professor Harald Hirschsprung's death). J Pediatr Surg. 2007;42(1):249-51. [PubMed ID: 17208575]. https://doi.org/10.1016/j.jpedsurg.2006.09.024.

  • 24.

    Hebra A, Smith VA, Lesher AP. Robotic Swenson pull-through for Hirschsprung's disease in infants. Am Surg. 2011;77(7):937-41. [PubMed ID: 21944363].

  • 25.

    De la Torre-Mondragon L, Ortega-Salgado JA. Transanal endorectal pull-through for Hirschsprung's disease. J Pediatr Surg. 1998;33(8):1283-6. [PubMed ID: 9722005].

  • 26.

    Shankar KR, Losty PD, Lamont GL, Turnock RR, Jones MO, Lloyd DA, et al. Transanal endorectal coloanal surgery for Hirschsprung's disease: experience in two centers. J Pediatr Surg. 2000;35(8):1209-13. [PubMed ID: 10945695]. https://doi.org/10.1053/jpsu.2000.8728.

  • 27.

    Reid JR, Buonomo C, Moreira C, Kozakevich H, Nurko SJ. The barium enema in constipation: comparison with rectal manometry and biopsy to exclude Hirschsprung's disease after the neonatal period. Pediatr Radiol. 2000;30(10):681-4. [PubMed ID: 11075600]. https://doi.org/10.1007/s002470000298.

  • 28.

    Nasir AA, Adeniran JO, Abdur- Rahman LO. Hirschsprung's disease: 8 years experience in a Nigerian teaching hospital. J Indian Assoc Pediatr Surg. 2007;12(6):66-9.