Skip to main content

ORIGINAL RESEARCH article

Front. Pediatr., 31 March 2021
Sec. General Pediatrics and Pediatric Emergency Care

Clinical Characteristics According to Age and Duration of Symptoms to Be Considered for Rapid Diagnosis of Pediatric Intussusception

\nIn Kyu ParkIn Kyu ParkMin Jeng Cho
Min Jeng Cho*
  • Department of Surgery, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, South Korea

Purpose: The purpose of this study was to evaluate whether clinical findings in children with ileocolic intussusception differ based on age and duration of symptoms and to assess the clinical characteristics of diagnosed and undiagnosed patients to determine which symptoms make diagnosis more difficult.

Methods: We reviewed 536 medical records of <15-year-old children diagnosed with ileocolic intussusception between 2008 and 2019. We divided the children into three categories according to age (<1 year, 1–2 years, and ≥2 years). The children were also divided into two groups based on whether symptoms lasted for more or <6 h. Diagnosed and undiagnosed children were assessed separately during for the initial evaluation.

Results: Following analysis of the three age groups, bloody stool, post-enema bloody stool, diarrhea, vomiting, poor oral intake, and lethargy were more frequent in children aged <1 year. In children aged ≥2 years, non-specific abdominal pain was more frequent and the undiagnosed rate was higher. Following analysis of the duration of symptoms, paroxysmal pain was significantly more frequent in the early group (<6 h), and bloody stool and fever were significantly more frequent in the late group (≥6 h). Nonspecific abdominal pain was more frequent and the door-to-diagnosis time was significantly longer in the undiagnosed group than in the diagnosed group.

Conclusions: Clinical findings of ileocolic intussusception vary depending on the age and duration of symptoms. Younger children with paroxysmal pain, vomiting, bloody stool, poor oral intake, or lethargy should be suspected of having intussusception. In older children, non-specific abdominal pain without bloody stool may be a symptom of intussusception. Glycerin enema is helpful in diagnosing intussusception in children with no typical symptoms.

Introduction

Intussusception is the most common cause of acute intestinal obstruction in infants and young children and is a potentially life-threatening condition that is commonly seen in the emergency room (ER) (1, 2). The incidence of intussusception in the pediatric population was reported to be 30–60 cases per 100,000 child-years in North America, Europe, and Australasia (3), while a higher incidence was reported in Asian countries, including South Korea, Vietnam, China, and Singapore (4, 5). In a recent nationwide study in South Korea, the incidences of intussusception in children under 1 and 2 year(s) of age were reported to be 193.2 and 196.7 per 100,000, respectively (6).

Untreated intussusception may lead to bowel necrosis and perforation, and even death (3, 7, 8). Early detection and intervention can significantly reduce the rates of mortality and morbidity. Screening suspected cases of intussusception in the ER is important, but the diagnosis can be difficult in children because of a non-specific presentation and physical examination. Traditional teaching states that intussusception presents with a classic triad of symptoms: paroxysmal abdominal pain, bloody stool, and vomiting (9, 10). However, this classic triad appears only in 10–20% of intussusception cases (2). Many patients present with only irritability or other non-specific complaints. Vomiting, a common presenting symptom, is also a common symptom in other gastrointestinal diseases. The isolated neurological symptomatology, including lethargy, convulsions, and sudden altered mental state, can appear as the initial presentation (11, 12). A major challenge in the diagnosis of intussusception is early determination of which patients are at low risk of intussusception based on clinical signs.

The primary objective of this study was to evaluate whether clinical findings in children with ileocolic intussusception differ based on age and duration of symptoms. The secondary objective was to evaluate the clinical characteristics of diagnosed and undiagnosed patients to determine which symptoms make diagnosis more difficult.

Materials and Methods

Study Design and Participants

We retrospectively reviewed the medical records of children aged 0 to 15 years with discharge diagnoses of intussusception (10th revision of the International Statistical Classification of Diseases, K56.1) between January 2008 and December 2019 (Figure 1). All cases either presented directly to our ER or were transferred to the ER from referring peripheral hospitals for definitive care. Only patients with ileocolic intussusception were included in the study; patients with ileo-ileal and colic-colic intussusceptions were excluded. Patients with a history of intussusception were also excluded. This study was conducted in accordance with the principles embodied in the Declaration of Helsinki, and ethical approval was granted by our hospital's Human Research Ethics Committee (2020-09-008).

FIGURE 1
www.frontiersin.org

Figure 1. Flow chart of study population.

Data Collection and Variable Definition

The following factors were extracted: demographic details and clinical features (abdominal pain, irritability, lethargy, vomiting, grossly bloody stools, diarrhea, altered consciousness, poor oral intake, abdominal mass, and duration of symptoms). The evaluation of patients and recording of data in the pediatric ER of our hospital were performed by pediatric residents, pediatric faculty members, emergency medicine residents, and emergency medicine faculty members. They used a standardized form, which consisted of historical and physical examination variables. Initial assessments were completed before any advanced diagnostic imaging [ultrasound (US), air enema fluoroscopy, or computed tomography (CT)] was conducted. When the clinical signs and symptoms signaled the presence of intussusception, an US was performed. The diagnosis of intussusception was confirmed when a target sign or doughnut sign was noted on the US; ileocolic intussusception was confirmed using air contrast enema. All diagnostic imaging findings were validated by a pediatric radiologist. The final diagnosis was based on the diagnosis of the hospitalized patient at discharge.

We defined fever as a temperature ≥38°C measured at home or in the ER. Paroxysmal pain was defined as severe, cyclic, and cramping abdominal pain, or episodic irritability. Non-specific abdominal pain was defined as non-severe and non-periodic abdominal pain that was not the typical paroxysmal pain. We defined bloody stool as grossly bloody spontaneously passed stool visualized by parents at home. Post-enema bloody stool was defined as the absence of stool until the ER visit with grossly bloody stool after glycerin enema in the ER. The classic triad included typical paroxysmal pain, bloody stool, and vomiting, but does not include post-enema bloody stool. The duration of symptoms was defined as the time from the onset of symptoms as determined by the parents to the ER visit. Door-to-diagnosis time was defined as the time from the ER visit to diagnosis by US/air contrast enema.

Statistical Analysis

We performed an analysis by dividing all children into three categories according to age: <1 year, 1–2 years, and >2 years. The duration of symptoms was analyzed by dividing it into early and late groups, <6 h and ≥6 h, respectively. Based on initial assessment by the initial attending physician, the children were assigned to either the diagnosed or undiagnosed group. The undiagnosed group included patients who were discharged from the ER, admitted on the suspicion of other diseases, and patients who were diagnosed with intussusception based on the US or CT scanning after suspecting other diseases (for example, appendicitis) in the ER.

Continuous variables are presented as medians with ranges or means ± standard deviations. An independent Student's t-test or one-way analysis of variance was applied for continuous variables. Categorical variables were reported using frequencies and proportions and were compared using the Pearson χ2 or Fisher's exact test, as appropriate, or by linear association. The data were analyzed by using the Statistical Program for the Social Sciences (IBM SPSS Statistic Version 24, IBM Inc., Chicago, IL). A P-value of <0.05 was considered to be statistically significant.

Results

A total of 536 patients were included in this study. The median age was 19 months (range, 2–132 months) and 345 (64.4%) patients were male. The classic triad of paroxysmal pain, vomiting, and bloody stool was encountered in 50/536 cases (9.3%). The median duration of symptoms was 11 h (range, 30 min−144 h) and the median door-to-diagnosis time was 2 h (range, 30 min-84 h).

Comparisons by Age Group

Table 1 shows the clinical findings in each age group. Analyzing the three age groups, bloody stool, post-enema bloody stool, diarrhea, vomiting, poor oral intake, and lethargy were significantly more frequent in children <1 year (P < 0.05). In children ≥2 years, non-specific abdominal pain was significantly more frequent (P < 0.001), and the rate of undiagnosed intussusception was higher (P = 0.012). The duration of symptoms and door-to-diagnosis time were significantly longer in the group ≥2 years old than the groups <1 year and 1–2 years (P = 0.009 and P < 0.001, respectively).

TABLE 1
www.frontiersin.org

Table 1. Clinical findings of enrolled patients in different age groups.

Comparisons by the Duration of Symptoms: Early vs. Late Group

In a large proportion of patients (33.8%), the duration of symptoms was <6 h; in only 16.8% of patients, it exceeded 24 h (Figure 2). Table 2 shows the clinical findings of the early (<6 h) and late (≥6 h) groups. In the early group, paroxysmal pain was significant (P < 0.001). Bloody stool and fever were significantly more frequent in the late group than in the early group (P = 0.023 and P < 0.001, respectively).

FIGURE 2
www.frontiersin.org

Figure 2. The duration of symptoms in patients enrolled in the study. Bars are colored according to the number of patients from each age group (<1 year, 1–2 years, and ≥2 years).

TABLE 2
www.frontiersin.org

Table 2. Clinical findings of enrolled patients in the early (<6 h) and late groups (≥6 h) classified based on the duration of symptoms.

Comparisons by Diagnosis Status: Diagnosed vs. Undiagnosed Group

Of the patients included in this study, 108 were transferred from another hospital with a confirmed diagnosis of intussusception. A total of 428 patients were divided into diagnosed and undiagnosed groups according to the initial assessment and were compared. Of these, 367 were suspected of intussusception and 61 were not diagnosed with intussusception. In the diagnosed group, paroxysmal pain, bloody stool, post-enema bloody stool, and abdominal mass were significantly more frequent than in the undiagnosed group (P < 0.05) (Table 3). In the undiagnosed group, non-specific abdominal pain was significantly more frequent than in the diagnosed group (P < 0.001). There was no difference in the duration of symptoms in the two groups, but the door-to-diagnosis time was significantly longer in the undiagnosed than in the diagnosed group (P < 0.001). Table 4 shows the results of the initial assessment of the undiagnosed group. Twenty patients were hospitalized with other suspected diseases, and 41 returned to the ER with persistent or aggravated symptoms after discharge.

TABLE 3
www.frontiersin.org

Table 3. Clinical findings of enrolled patients in the diagnosed and undiagnosed groups.

TABLE 4
www.frontiersin.org

Table 4. Initial assessment of patients in the undiagnosed group.

Discussion

Intussusception is notoriously difficult to diagnose because of the lack of sensitive or specific clinical indicators. However, it is a potentially dangerous disease that can lead to death if left untreated, and it is therefore imperative to prevent underdiagnoses of patients with suspected intussusceptions. This study showed differences in clinical features of ileocolic intussusception with the duration of symptoms and age of the children. In addition, this study analyzed the diagnosed and undiagnosed patients, as determined by the initial attending physician. We also identified cases in which it was difficult to diagnose intussusception and noted various symptoms that are important in preventing underdiagnoses.

In our study, the most common symptom of intussusception was paroxysmal pain, which was observed in 77.4% of patients, regardless of age. Previous studies have reported abdominal pain in 13–22% of patients (13, 14). Our results showed a higher percentage compared to previous studies because our definition of paroxysmal pain included both typical abdominal pain and episodic irritability. In younger children, especially those under 1 year, typical abdominal pain may be mistaken for episodic irritability because they are unable to express themselves verbally. Typical paroxysmal pain is described as severe, cyclic, cramping, abdominal pain, or irritability. Episodes may persist for 4 to 5 min interspersing with a relief period of 10 to 20 min. This paroxysmal pain is an important early indicator that suggests parents to take their child to the ER; therefore, paroxysmal pain is significantly higher in the early (<6 h) than in the late group (≥6 h) in the current study (P < 0.001).

The second most common symptom was vomiting (46.1%, n = 247). Vomiting was significantly more common in younger children (P < 0.001), similar to previous studies (3, 15). Vomiting is caused by a vagal reflex and ileus condition. Older children may have better control of the vomiting reflex, which could be why vomiting was less common in older children.

Bloody stool, though a key feature of intussusception, was less common than other symptoms. Its frequency varied considerably between studies, with reported rates ranging from 9 to 36% (1618). In our study, only 23.1% (n = 124) of all patients had bloody stool, and it was more common in younger children (44.8, 18.2, and 6.9% in the <1, 1–2, and ≥2 year age groups, respectively, P < 0.001). This result was comparable with that of previous studies (19, 20). Yamatomo et al. reported that spontaneously passed grossly bloody stool was more common in the younger age groups (72, 53, 18, and 18% in the <8 month, 8–15 month, 16–35 month, and >3 year age groups, respectively, P = 0.0001) (20). Newman et al. reported a bloody stool rate of 96% in their studies in children younger than 4 months with intussusception (21). In our study, post-enema bloody stool was also more common in younger children (P < 0.001), and children older than 2 years tended to have a normal stool (no blood in the stool) even after glycerin enema (77.1%). Bloody stool may occur as a result of the compression of the mesenteric vessels, mucosal edema, hemorrhage, and ischemia of the bowel, and may not be detected in early cases (15, 19). Bloody stool was significantly more common in the late than in the early group (P = 0.023). This indicates that bloody stool is highly specific for intussusception, but an absence of bloody stool cannot exclude the probability of the presence of intussusception.

The triad of symptoms, including paroxysmal pain, vomiting, and bloody stool, is described in textbooks as the classic triad of intussusception, but several previous studies have reported these symptoms in only 10 to 20% of cases (2, 16, 19). In the current study, 9.3% (50/536) of children showed the classic triad of symptoms, and only two (1.1%) of them were over 2 years. Harrington et al. reported that the combination of the classic triad symptoms showed a positive predictive value of 93% (P < 0.001) (22), but in many children, especially in early cases and older children, the classic triad cannot be the sole diagnostic criteria for intussusception (3, 15, 16).

In this study, poor oral intake and lethargy were significantly higher in younger children than in older children. Vomiting and decreased oral intake can lead to severe dehydration and shock, as well as neurological symptoms such as altered mentality, lethargy, and seizures that may appear as the initial presentation. In our study, two children were misdiagnosed with meningitis due to mental changes without gastrointestinal symptoms and were later diagnosed with intussusception. Dominguez-Carral et al. reported that fewer than 3% of children with intussusception initially presented with isolated neurological symptomatology (lethargy being the most common symptom) out of 351 cases (23). Maldonado et al. recommend checking the stool for occult blood and performing an abdominal US in undiagnosed patients with altered mental status, particularly in those younger than 12 months (12).

In the current study, children older than 2 years had a longer duration of symptoms and door-to-diagnosis time than the other two groups, and were more likely to be undiagnosed. Turner et al. and Kim et al. also reported that children older than 2 years were prone to receiving a delayed diagnosis (24, 25). Older children were more likely to have non-specific abdominal pain than in younger children, and the diagnosis was often difficult. Whereas, bloody stool or vomiting were relatively common in younger children, resulting in parents visiting the ER early, with intussusception quickly being suspected.

When comparing the diagnosed group with the undiagnosed group, the decision to perform an additional image study was easy when there was paroxysmal pain, bloody stool, and abdominal mass, indicative of intussusception. Conversely, in the case of non-specific abdominal pain, other diseases were considered first. When 146 children who did not spontaneously pass bloody stool underwent glycerin enema in the ER, 64 in the undiagnosed group and more in the diagnosed group had bloody stool (P < 0.001). This finding suggests that glycerin enema also helps diagnose intussusception in children without the typical triad of symptoms. A negative post-enema bloody stool cannot exclude intussusception but shows that it as a significant positive predictor. Door-to-diagnosis time in the undiagnosed group was significantly longer than that in the diagnosed group (P < 0.001), showing how important it is to suspect intussusception for timely diagnosis treatment.

For early detection of intussusception, a few recent studies have suggested that bedside US by radiologists and emergency physicians can be an effective diagnostic modality (26, 27). However, it is not routinely available in all clinical settings and is highly operator-dependent. Several studies have included the findings of abdominal X-rays as diagnostic criteria for intussusception (7, 28). However, their diagnostic value remains unclear, with a sensitivity of only 29–50% and the disadvantage of radiation exposure. Definitions and criteria for radiological findings differ for each institution. In our ER, the interpretation of abdominal X-rays by pediatric radiologists was not always available, and attending physicians were forced to discern the possibility of intussusception based on clinical symptoms rather than abdominal X-rays. Therefore, we did not include abdominal X-rays in the analysis.

This study had some limitations. First, this was a retrospective study, and the quality of data collected was dependent on medical records. A standardized form consisting of historical and physical examination variables was used, but data might not be complete or accurate. Second, we divided the diagnosed and undiagnosed groups, based on the clinical suspicion of the attending physician in the ER. Clinical suspicion and assessment can be subjective, as there are multiple attending physicians and clinical experience varies from person to person. This may have affected the analysis of the diagnosed and undiagnosed groups. Finally, this study had no control group, so our data are presented only as absolute numbers and percentages. We cannot comment on the sensitivity, specificity, or positive and negative predictive values of our findings.

In conclusion, the clinical findings of ileocolic intussusception may vary depending on the duration of symptoms and age of the children. If children, especially those under 1 year, have paroxysmal pain, vomiting, bloody stool, poor oral intake, or lethargy, intussusception should be suspected. It is important to keep in mind that in older children, non-specific abdominal pain without bloody stool may be a symptom of intussusception. Glycerin enema also helps in diagnosing intussusception in children with no typical symptoms. Diagnosis of intussusception is still difficult, but carefully identifying and considering all symptoms is essential for timely diagnostic treatment in children. We hope that this study will aid in the timely and appropriate treatment of children of various ages with varying symptoms.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. Requests to access these datasets should be directed to mjtolord@hanmail.net.

Ethics Statement

The studies involving human records were reviewed and approved by Ulsan University Hospital Human Research Ethics Committee.

Author Contributions

MC: study conception and design, critical revision, drafting of the manuscript. IP and MC: analysis, data interpretation, and data acquisition. All authors: contributed to the article and approved the submitted version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Abbreviations

ER, emergency room; US, ultrasound; CT, computed tomography.

References

1. Parashar UD, Holman RC, Cummings KC, Staggs NW, Curns AT, Zimmerman CM, et al. Trends in intussusceptions-associated hospitalizations and deaths among US infants. J Pediatr. (2000) 106:1413–21. doi: 10.1542/peds.106.6.1413

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Buettcher M, Baer G, Bonhoeffer J, Schaad UB, Heininger U. Three-year surveillance of intussusception in children in Switzerland. J Pediatr. (2007) 120:473–80. doi: 10.1542/peds.2007-0035

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Bines JE, Ivanoff B, Justice F, Mulholland K. Clinical case definition for the diagnosis of acute intussusception. J Pediatr Gastroenterol Nutr. (2004) 39:511–8. doi: 10.1097/00005176-200411000-00012

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Van Trang N, Le Nguyen NT, Dao HT, Ho VL, Tran DT, Loewen J, et al. Incidence and epidemiology of intussusception among infants in Ho Chi Minh City, Vietnam. J Pediatr. (2014) 164:366–71. doi: 10.1016/j.jpeds.2013.10.006

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Boudville IC, Phua KB, Quak SH, Lee BW, Han HH, Verstraeten T, et al. The epidemiology of paediatric intussusception in Singapore: 1997 to 2004. Ann Acad Med Singapore. (2006) 35:674–9.

PubMed Abstract | Google Scholar

6. Jo S, Lim IS, Chae SA, Yun SW, Lee NM, Kim SY. Characteristics of intussusception among children in Korea: a nationwide epidemiological study. BMC Pediatr. (2019) 19:211. doi: 10.1186/s12887-019-1592-6

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Kuppermann N, O'Dea T, Pinckney L, Hoecker C. Predictors of intussusception in young children. Arch Pediatr Adolesc Med. (2000) 154:250–5. doi: 10.1001/archpedi.154.3.250

CrossRef Full Text | Google Scholar

8. Bruce J, Huh YS, Cooney DR, Karp MP, Allen JE, Jewett TC Jr. Intussusception: evolution of current management. J Pediatr Gastroenterol Nutr. (1987) 6:663–4. doi: 10.1097/00005176-198709000-00003

CrossRef Full Text | Google Scholar

9. Fisher TK, Bihrmann K, Perch M, Koch A, Wohlfahrt J, Kåre M, et al. Intussusception in early childhood: a cohort study of 1.7 million children. Pediatrics. (2004) 114:782–5. doi: 10.1542/peds.2004-0390

PubMed Abstract | CrossRef Full Text | Google Scholar

10. DiFiore JW. Intussusception. Semin Pediatr Surg. (1999) 8:214–20. doi: 10.1016/S1055-8586(99)70029-6

CrossRef Full Text | Google Scholar

11. Singer J. Altered consciousness as an early manifestation of intussusception. Pediatrics. (1979) 64:93–5.

PubMed Abstract | Google Scholar

12. Maldonado L, Takagishi J. Four-month-old infant with intussusception presenting as altered mental status. SAGE Open Med Case Rep. (2014). doi: 10.1177/2050313X14558903. [Epub ahead of print].

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Sparnon AL, Little KE, Morris LL. Intussusception in childhood: a review of 139 cases. Aust NZ J Surg. (1984) 54:353–6. doi: 10.1111/j.1445-2197.1984.tb05332.x

CrossRef Full Text | Google Scholar

14. Klein EJ, Kapoor D, Shugerman RP. The diagnosis of intussusception. Clin Pediatr. (2004) 43:343–7. doi: 10.1177/000992280404300405

CrossRef Full Text | Google Scholar

15. Aoki Y, Iguchi A, Kitazawa K, Kobayashi H, Senda M, Honda A. Differences in clinical findings based on the duration of symptoms and age of children with ileocolic intussusception: a single-institution survey in rural Japan. Pediatr Emerg Care. (2019). doi: 10.1097/PEC.0000000000001750. [Epub ahead of print].

CrossRef Full Text | Google Scholar

16. Yap Shiyi E, Ganapathy S. Intussusception in children presenting to the emergency department: an Asian perspective. Pediatr Emerg Care. (2017) 33:409–13. doi: 10.1097/PEC.0000000000000548

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Kimia AA, Williams S, Hadar PN, Landschaft A, Porter J, Bachur RG. Positive guaiac and bloody stool are poor predictors of intussusception. Am J Emerg Med. (2018) 36:931–4. doi: 10.1016/j.ajem.2017.10.051

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Ondhia MN, Al-Mutawa Y, Harave S, Losty PD. Intussusception: a 14-year experience at a UK tertiary referral centre. J Pediatr Surg. (2020) 55:1570–3. doi: 10.1016/j.jpedsurg.2019.07.022

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Gierup J, Jorulf H, Livaditis A. Management of intussusception in infants and children: a survey based on 288 consecutive cases. Pediatrics. (1972) 50:535–46.

PubMed Abstract | Google Scholar

20. Yamamoto LG, Morita SY, Boychuk RB, Inaba AS, Rosen LM, Yee LL, et al. Stool appearance in intussusception: assessing the value of the term currant jelly. Am J Emerg Med. (1997) 15:293–8.

PubMed Abstract | Google Scholar

21. Newman J, Schuh S. Intussusception in babies under 4 months of age. CMAJ. (1987) 136:266–9.

PubMed Abstract | Google Scholar

22. Harrington L, Connolly B, Hu X, Wesson DE, Babyn P, Schuh S. Ultrasonographic and clinical predictors of intussusception. J Pediatr. (1998) 132:836–9.

PubMed Abstract | Google Scholar

23. Domínguez-Carral J, Puertas-Martín V, Carreras-Sáez I, Maraña-Pérez AI, Escobar-Delgado T, García-Peñas JJ. Neurological symptoms in children with intussusception. A Pediatr. (2014) 80:293–8. doi: 10.1016/j.anpedi.2013.06.034

CrossRef Full Text | Google Scholar

24. Turner D, Rickwood AM, Brereton RJ. Intussusception in older children. Arch Dis Child. (1980) 55:544–6.

Google Scholar

25. Kim JH, Lee JS, Ryu JM, Lim KS, Kim WY. Risk factors for recurrent intussusception after fluoroscopy-guided air enema. Pediatr Emerg Care. (2018) 34:484–7. doi: 10.1097/PEC.0000000000001071

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Riera A, Hsiao AL, Langhan ML, Goodman TR, Chen L. Diagnosis of intussusception by physician novice sonographers in the emergency department. Ann Emerg Med. (2012) 60:264–8. doi: 10.1016/j.annemergmed.2012.02.007

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Lee JY, Kim JH, Choi SJ, Lee JS, Ryu JM. Point-o f-care ultrasound may be useful for detecting pediatric intussusception at an early stage. BMC Pediatr. (2020) 20:155. doi: 10.1186/s12887-020-02060-6

CrossRef Full Text | Google Scholar

28. Yang ST, Tsai CH, Chen JA, Chiang HJ. Differential diagnosis between intussusception and gastroenteritis by plain film. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. (1995) 36:170–5.

PubMed Abstract | Google Scholar

Keywords: child, clinical characteristics, intussusception, bloody stool, abdominal pain (MeSH)

Citation: Park IK and Cho MJ (2021) Clinical Characteristics According to Age and Duration of Symptoms to Be Considered for Rapid Diagnosis of Pediatric Intussusception. Front. Pediatr. 9:651297. doi: 10.3389/fped.2021.651297

Received: 09 January 2021; Accepted: 05 March 2021;
Published: 31 March 2021.

Edited by:

Rianne Oostenbrink, Erasmus Medical Center, Netherlands

Reviewed by:

Adriana Yock-Corrales, Dr. Carlos Sáenz Herrera National Children's Hospital, Costa Rica
Alain Martinot, Université de Lille, France

Copyright © 2021 Park and Cho. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Min Jeng Cho, mjtolord@hanmail.net

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.