Figures
Abstract
Objective
Subdural hematoma in infants or toddlers has often been linked to abuse, but it is not clear how many cases actually occur and how many are suspected of abuse. The purpose of this study was to investigate subdural hematoma in infants and toddlers in Japan.
Methods
This multicenter, retrospective study reviewed the clinical records of children younger than 4 years with head trauma who were diagnosed with any finding on head computed tomography (CT) and/or magnetic resonance imaging (MRI), such as skull fracture and/or intracranial injury. A total of 452 children were included. The group suspected to have been abused was classified as nonaccidental, and the group considered to have been caused by an accident was classified as accidental. Subdural hematoma and other factors were examined on multivariate analysis to identify which factors increase the risk of nonaccidental injuries.
Results
Of the 452 patients, 158 were diagnosed with subdural hematoma. Subdural hematoma was the most common finding intracranial finding in head trauma in infants and toddlers. A total of 51 patients were classified into the nonaccidental group, and 107 patients were classified into the accidental group. The age of patients with subdural hematoma showed a bimodal pattern. The mean age of the accidental group with subdural hematoma was significantly older than that in the nonaccidental group (10.2 months vs 5.9 months, respectively. p < 0.001). Multivariate analysis showed that patients under 5 months old, retinal hemorrhage, and seizure were significant risk factors for nonaccidental injury (odds ratio (OR) 3.86, p = 0.0011; OR 7.63, p < 0.001; OR 2.49, p = 0.03; respectively). On the other hand, the odds ratio for subdural hematoma was 1.96, and no significant difference was observed (p = 0.34).
Conclusions
At least in Japanese children, infantile subdural hematoma was frequently observed not only in nonaccidental but also in accidental injuries. In infants with head trauma, age, the presence of retinal hemorrhage, and the presence of seizures should be considered when determining whether they were abused. Subdural hematoma is also a powerful finding to detect abuse, but care should be taken because, in some ethnic groups, such as the Japanese, there are many accidental cases.
Citation: Akutsu N, Nonaka M, Narisawa A, Kato M, Harada A, Park Y-S (2022) Infantile subdural hematoma in Japan: A multicenter, retrospective study by the J-HITs (Japanese head injury of infants and toddlers study) group. PLoS ONE 17(2): e0264396. https://doi.org/10.1371/journal.pone.0264396
Editor: Alfio Spina, I.R.C.C.S. San Raffaele Scientific Institute, Vita-Salute San Raffaele University, ITALY
Received: November 4, 2021; Accepted: February 8, 2022; Published: February 25, 2022
Copyright: © 2022 Akutsu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Data cannot be shared publicly because there is still a possibility of identifying specific individuals, even though the information is anonymized, since the current study examined the mechanism of injury and multiple clinical findings. Japan's Act on Protection of Personal Information prohibits the release of information containing personal information to the public, including those whose purpose of use is not clear. Data are available from the Department of Neurosurgery, Kansai Medical University at kansaiidainougeka@gmail.com for researchers who meet the criteria for access to confidential data.
Funding: The author(s) received no specific funding for this work.
Competing interests: Masahiro Nonaka and Young-Soo Park have written statements and appeared in court in child abuse cases both at the request of the prosecutor and the defense. Atsuko Harada has written statements and appeared in court in child abuse cases at the request of the prosecutor. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
Introduction
Head trauma is one of the leading causes of pediatric emergency department visits, and the diagnosis of abusive head trauma (AHT) by neurological imaging is difficult in practice. Many studies have suggested that subdural hematoma is considered characteristic of AHT [1–5]. In Japan, the Ministry of Health, Labor and Welfare publishes the "Guide to Responding to Child Abuse" as a standard for child guidance centers to take temporary custody; the 2014 revision states that the case of the infant with subdural hematoma is highly likely to have been abused and should be treated with suspicion. However, the true incidence of subdural hematoma due to head trauma in infants and toddlers, regardless of abuse or accident, is unknown. In this study, the extent of subdural hematoma in cases where imaging studies were performed after head trauma was examined, and the findings and the extent to which abuse was suspected and not suspected are presented.
Methods
This multicenter, retrospective study reviewed clinical records of children younger than 4 years with head trauma who visited our institutions between January 2014 and August 2020. Patients with some imaging findings such as fracture or intracranial injury were included in the study. Patients without imaging or with only extracranial findings or no obvious findings on imaging were excluded. Two university hospitals, two children’s hospitals, and two general hospitals participated in this study, making it possible to obtain data closer to the real world in Japan. A total of 452 children were included in this study. From the medical charts, the sex and age of the child, mechanism of injury, physical and neurological findings, radiological findings, retinal hemorrhage, surgical intervention, notification to child guidance centers, temporary protection by child guidance centers, and criminal cases were extracted. The imaging studies examined in this study included not only computed tomography (CT), but also magnetic resonance imaging (MRI). Imaging findings were confirmed and recorded by a board-certified pediatric neurosurgeon at each institution. The information about the mechanism of injury was primarily determined from the medical history provided by the caregiver to a physician. If necessary, medical evaluation reports by child protection teams at each facility and adequate investigation reports by police and/or child guidance centers were requested. Because many head injuries in infancy are suspected to be caused by abuse, institutions with a child protection team to assess whether the head injury was caused by abuse were included. Patients were classified into the nonaccidental or accidental groups by our definition (Table 1).
Our definition includes cases that have been taken into temporary custody by the Child Guidance Center, as well as cases that have been determined to be accidents and have not been notified to the Child Guidance Center. We cannot deny the possibility that some of these cases may be accidents or cases of abuse. For this reason, we also have studied cases of obvious abuse (those who confessed and those who were criminally prosecuted) with cases of traffic accidents, and the results were compared with the results from our classification.
IRB/ethics committee approval and a statement regarding patient consent
The protocol for this study was approved by the Ethics Committee of Kansai Medical University (No. 2019232). Need for written patient consent was waived by the ethics committee because data were deidentified. Institutional review board approval was obtained from all participants’ institutions prior to submitting cases for this study.
Statistical analysis
Statistical analysis was performed with JMP 14.2.0. Continuous variables were analyzed using the Wilcoxon rank-sum test. Univariate and multivariate analyses were performed to examine the relationship between nonaccidental injury and prognostic factors. Univariate logistic model was used to compare each prognostic factors. Variables were included in a multivariate logistic regression model if their p value in the univariate analysis was statistically significant. The odds ratios (ORs) and 95% confidence intervals (CIs) were calculated.
Results
Of the 452 patients, 58 were included in the nonaccidental group, and 394 patients were included in the accidental group. The demographics and age distribution of the patients are shown in Table 2 and Fig 1, respectively. The mean age of the nonaccidental group was 5.8 months, and the mean age of the accidental group was 12.1 months (p < 0.001). The number of patients in the nonaccidental group was highest at 2 months and 4 months, and in the accidental group at 4 months (Fig 1). Of the 452 patients, 158 were diagnosed with subdural hematoma. Subdural hematoma was the second most common finding on CT from head trauma in infants after skull fracture, and it was more common than epidural hematoma (Table 2). The causes of injury in the accidental group are summarized and described in Table 3.
A: Total, B: Nonaccidental, C: Accidental.
The mean age was 8.8 months, and the number of patients showed a bimodal peak at 4 months and at 8 months (Fig 2A). Of the patients with subdural hematoma, 51 were classified as the nonaccidental group and 107 as the accidental group. The mean age of patients in the nonaccidental group was 5.9 months, and the mean age of patients in the accidental group was 10.2 months (p < 0.001). The number of patients was highest at 2 months and 4 months in the nonaccidental group (Fig 2B) and at 8 months and 10 months in the accidental group (Fig 2C). Retinal hemorrhage was present in 45 of 58 patients in the nonaccidental group and 40 of 394 patients in the accidental group.
A: Total, B: Nonaccidental, C: Accidental. There is a peak at 2 to 4 of months of age in the nonaccidental group and another peak at 8 to 10 of months of age in the accidental group.
On univariate analysis, age under 5 months (OR 2.83, p < 0.001), subdural hematoma (OR 19.54, p < 0.001), retinal hemorrhage (OR 13.31, p < 0.001), brain edema (OR 6.52, p < 0.001), seizure (OR 12.10, p < 0.001), and surgical case (OR 7.22, p < 0.001) were significantly associated with increased odds of nonaccidental group (Table 4). On the other hand, the odds ratio of the nonaccidental group was significantly lower in cases with skull fracture (OR 0.17, p < 0.001) and epidural hematoma (OR 0.23, p = 0.006). A univariate analysis was conducted on 22 cases in the apparent abuse group, which included both confessed and criminally prosecuted cases, and 39 cases of traffic trauma, for a total of 61 cases. The results showed that there were significant differences in age under 5 months (OR 8.65, p = 0.0005), subdural hematoma (OR 45.71, p < 0.001), retinal hemorrhage (OR 15.30, p = 0.0034), brain edema (OR 4.71, p < 0.017), seizure (OR 18.75, p < 0.001), and surgical case (OR 40.8, p < 0.001) (Table 5). Similarly, the odds ratio of the apparent abuse group was significantly lower in cases with skull fracture (OR 0.10, p = 0.0002). Epidural hematoma (OR 0.12, p = 0.051) was just barely significant, but the OR was similarly low. These results were similar to the results of our analysis of cases classified as accidental and nonaccidental.
Of the 158 cases of subdural hematoma, 127 (80.4%) underwent fundus examination and were included in the multivariate analysis. On multivariate analysis, age under 5 months, retinal hemorrhage, and seizure were significantly associated with increased odds of nonaccidental injury (OR 3.86, p = 0.0011; OR 7.63, p < 0.001; OR 2.49, p = 0.03; respectively). On the other hand, subdural hematoma was not found to be significant (OR 1.96, p = 0.34) (Table 6). Multivariate analysis between the apparent abuse group and the accident group was not performed due to the small number of cases.
Sensitivity, specificity, positive predictive value, and negative predictive value for subdural hematoma, retinal hemorrhage, and brain edema are summarized in Table 7. The sensitivity, specificity, and positive predictive value of subdural hematoma for the diagnosis of nonaccidental injury were 87.9%, 72.8%, and 32.0%, respectively.
Discussion
Based on the literature, AHT should be part of the differential diagnosis in infants and toddlers with subdural hematoma. In a systematic review, subdural hematoma and retinal hemorrhage were strongly associated with AHT (OR 8.92, 95% CI 6.77–11.74; and OR 27.12, 95% CI 15.70–46.84, respectively) [2]. Therefore, infants and toddlers with subdural hematoma and/or retinal hemorrhage due to short falls should be thoroughly investigated for possible AHT. In the present study, the results of univariate analysis showed an odds ratio of 19.5, with a 95% CI of 8.6–44.4, which is similar to previous reports. However, on multivariate analysis, the odds ratio dropped to 1.96, with a 95% CI of 0.5–7.73, which was not significant. The reason for this difference was thought to be the confounding of subdural hematoma with factors such as age, presence of retinal hemorrhage, and presence of seizures. Furthermore, in the present study, subdural hematoma was found in 87.9% of cases in the nonaccidental group, and child abuse represented 32.2% of all traumatic subdural hematomas. Unlike reports from other countries, we therefore consider that subdural hematoma is frequently associated with, but is not characteristic of AHT in Japan.
In Japan, subdural hematoma has long been known to occur due to minor head trauma in infants who are old enough to pull themselves up. This was known as Nakamura’s type 1, and many Japanese neurosurgeons were aware of its existence [6, 7]. However, all of these reports have been criticized for not being fully investigated for child abuse [8]. More recently, Amagasa et al. reported that subdural hematoma, retinal hemorrhage, and neurological sequelae due to short falls were not seen after witnessed falls in children younger than 2 years in Japan [5]. However, in their paper, only 14 cases of subdural hemorrhage were found, and it is difficult to assume that most subdural hematomas in Japan are caused by abuse. In recent years, there have been similar reports of infantile acute subdural hematoma due to accidental minor head trauma from other countries [9–12]. Hogberg et al. reported that 104 of 306 (34.0%) infants with subdural hematoma younger than 1 year in Sweden were caused by accidental falls [13].
The peak incidence of AHT was reported to be 2 to 4 months of age in studies from North America [14–16]. Nuno et al. explained that the cause of the peak was that frustrated parents often use shaking as a means of quieting an infant, and reports of excessive crying at approximately 2 months of age coincide with documented cases of AHT [15]. The present study also shows that cases of head trauma less than 5 months old are more likely to have been abused, which is consistent with previous reports. On the other hand, Fujiwara et al. reported that patients with AHT younger than 2 years in Japan had 2 peaks of age, at 2 to 4 months and at 7 to 9 months [3]. Similarly, there are some reports from Japan that the age distribution of the AHT group had two peaks of age [4, 17]. Ganesh et al. also questioned why the Japanese reports of subdural hematoma with retinal hemorrhage after minor trauma were so very different from the bulk of the world’s literature [18]. However, it was unclear why the data from Japan showed such a bimodal pattern. Fujiwara et al. suggested that the first peak was due to the association between shaken infant syndrome and the peak of crying, and the cause of the second peak, which was not found in Western countries, was the easy availability and taking of head CT in Japan [3]. Amagasa et al. suggested that intense crying, such as sleep-related night-time crying, which peaks at 6 to 8 months in Japanese infants, and sleep sharing could be possible factors for abuse in older infants in Japan [4]. However, there is no evidence to support their suggestions in these papers. In the present study, 158 cases of subdural hematoma were carefully reviewed by the child protection team of each hospital, and cases suspected of abuse were reported to the child guidance center for full consideration of possible abuse. As a result, 107 cases were determined to be accidental, whereas 51 cases were determined to be nonaccidental. Furthermore, the peak age of the nonaccidental cases was 4 months, which is similar to the peak age of abused children in other countries, whereas the peak age of the accidental cases was 8 to 10 months. The second peak in the incidence of subdural hematoma in this study indicates that a large number of accidental head injuries may be included. Furthermore, the previous reports from Japan may have misclassified patients as non-accidental in the older age peak.
Retinal hemorrhage that is bilateral, severe, and includes the posterior pole and peripheral hemorrhage has been reported as characteristic of AHT [19, 20]. In the present study, retinal hemorrhage was also significantly associated with increased odds of AHT. However, an eye examination was not always done within 48 hours of admission in the present study, and subtle retinal hemorrhage might disappear [21]. On the other hand, Scheller reported ten cases of retinal hemorrhage with no evidence of brain injury and suggested that clinicians should reassess the importance of retinal hemorrhage in the setting of suspected AHT [22]. Mechanisms that cause retinal hemorrhage other than vitreoretinal traction, such as abrupt increases in intracranial pressure, have also been suggested [23]. Needless to say, the presence of retinal hemorrhage does not prove AHT, but it is one of the important factors suggesting AHT.
Seizure has also been reported to be associated with AHT. (2) Ichord et al. confirmed that the higher rate of hypoxic-ischemic injury on diffusion-weighted MRI in AHT than in accidental head trauma is likely multifactorial, involving respiratory insufficiency, seizure, and intracranial space occupying lesions requiring neurosurgical intervention [24]. The higher incidence of seizure in AHT compared to accidental head trauma may also be related to the frequency and the pattern of hypoxic-ischemic injury lesions. Seizure in the acutely injured brain may exacerbate injury directly through excitotoxic mechanisms or indirectly by exacerbating respiratory insufficiency [25]. These studies suggest that management of infants and toddlers with head injury, and particularly from AHT, should include meticulous attention to optimizing ventilation, oxygenation, perfusion, and the diagnosis and treatment of seizure.
The current study has several limitations. First, it had a retrospective design, which can result in misclassification because missing values occur frequently. Although children with intracranial injury were included in the sample, the threshold to suspect intracranial injury and order head CT and/or MRI was not clearly defined a priori. In addition, fundoscopy and skeletal surveys were not completed in some cases. Second, the classification of a child as nonaccidental or accidental depends on the judgment of the child guidance center and the CPT of each hospital, which is often based on medical findings. However, there may be a problem with the accuracy of the past reports on which the judgment is based, and as a result, there is a possibility that the judgment may be affected. Third, the nonaccidental group is overrepresented because it includes all cases taken into temporary custody by the child guidance center. Further research should be conducted regarding the differences in the mechanisms of accidental and nonaccidental head injuries in infants and toddlers.
Conclusions
In the present study in Japan, unlike in other countries, more than half of the infantile subdural hematomas were determined to be accidental. This suggests that the likelihood of accidental subdural hematoma in infants may vary by ethnicity. On the other hand, cases younger than 5 months, cases with retinal hemorrhage, and cases with seizure were found to more likely have been abused, as in other countries. The diagnosis of abuse should not be simply judged by applying the standards of one particular region to other regions, but it is necessary to consider the possibility that there are cultural and racial differences in each region.
References
- 1. Kemp AM, Jaspan T, Griffiths J, Stoodley N, Mann MK, Tempest V, et al. Neuroimaging: what neuroradiological features distinguish abusive from non-abusive head trauma? A systematic review. Arch Dis Child. 2011;96(12):1103–12. pmid:21965812
- 2. Piteau SJ, Ward MG, Barrowman NJ, Plint AC. Clinical and radiographic characteristics associated with abusive and nonabusive head trauma: a systematic review. Pediatrics. 2012;130(2):315–23. pmid:22778309
- 3. Fujiwara T, Okuyama M, Miyasaka M. Characteristics that distinguish abusive from nonabusive head trauma among young children who underwent head computed tomography in Japan. Pediatrics. 2008;122(4):e841–7. pmid:18762487
- 4. Amagasa S, Matsui H, Tsuji S, Uematsu S, Moriya T, Kinoshita K. Characteristics distinguishing abusive head trauma from accidental head trauma in infants with traumatic intracranial hemorrhage in Japan. Acute Med Surg. 2018;5(3):265–71. pmid:29988617
- 5. Amagasa S, Uematsu S, Tsuji S. Occurrence of traumatic brain injury due to short falls with or without a witness by a nonrelative in children younger than 2 years. J Neurosurg Pediatr. 2020:1–5. pmid:32916651
- 6. Aoki N, Masuzawa H. Infantile acute subdural hematoma. Clinical analysis of 26 cases. J Neurosurg. 1984;61(2):273–80. pmid:6737052
- 7. Nakamura N, Kobayashi S, Hirakawa K, Yamada H, JImbo M. [Characteristics of head injuries and intracranial hematoms in infants and children. II. Acute and subacute intracranial hematoma]. No To Shinkei (Jpn). 1965;17(8):785–94. pmid:5899337
- 8. Rekate HL. Subdural hematomas in infants. J Neurosurg. 1985;62(2):316–7. pmid:3968573
- 9. Atkinson N, van Rijn RR, Starling SP. Childhood Falls With Occipital Impacts. Pediatr Emerg Care. 2018;34(12):837–41. pmid:28590993
- 10. Fung EL, Sung RY, Nelson EA, Poon WS. Unexplained subdural hematoma in young children: is it always child abuse? Pediatr Int. 2002;44(1):37–42. pmid:11982869
- 11. Denton S, Mileusnic D. Delayed sudden death in an infant following an accidental fall: a case report with review of the literature. Am J Forensic Med Pathol. 2003;24(4):371–6. pmid:14634479
- 12. Gardner HB. A witnessed short fall mimicking presumed shaken baby syndrome (inflicted childhood neurotrauma). Pediatr Neurosurg. 2007;43(5):433–5. pmid:17786015
- 13. Hogberg U, Andersson J, Squier W, Hogberg G, Fellman V, Thiblin I, et al. Epidemiology of subdural haemorrhage during infancy: A population-based register study. PLoS One. 2018;13(10):e0206340. pmid:30379890
- 14. Bass DI, Lee A, Browd SR, Ellenbogen RG, Hauptman JS. Medicolegal issues in abusive head trauma for the pediatric neurosurgeon. Neurosurg Focus. 2020;49(5):E23. pmid:33130608
- 15. Nuno M, Pelissier L, Varshneya K, Adamo MA, Drazin D. Outcomes and factors associated with infant abusive head trauma in the US. J Neurosurg Pediatr. 2015;16(5):515–22. pmid:26230462
- 16. Thompson LW, Bass KD, Agyei JO, Naseem HU, Borngraber E, Wang J, et al. Incidence of nonaccidental head trauma in infants: a call to revisit prevention strategies. J Neurosurg Pediatr. 2019:1–8.
- 17. Yamaoka Y, Fujiwara T, Fujino Y, Matsuda S, Fushimi K. Incidence and Age Distribution of Hospitalized Presumptive and Possible Abusive Head Trauma of Children Under 12 Months Old in Japan. J Epidemiol. 2020;30(2):91–7. pmid:30713261
- 18. Ganesh A, Stephens D, Kivlin JD, Levin AV. Retinal and subdural haemorrhages from minor falls? Br J Ophthalmol. 2007;91(3):396–7. pmid:17322469
- 19. Binenbaum G, Mirza-George N, Christian CW, Forbes BJ. Odds of abuse associated with retinal hemorrhages in children suspected of child abuse. J AAPOS. 2009;13(3):268–72. pmid:19541267
- 20. Maguire SA, Watts PO, Shaw AD, Holden S, Taylor RH, Watkins WJ, et al. Retinal haemorrhages and related findings in abusive and non-abusive head trauma: a systematic review. Eye (Lond). 2013;27(1):28–36. pmid:23079748
- 21. Burge LR, Van Horne BS, Bachim A, Bhatt AR, Donaruma M. Timely recognition of retinal hemorrhage in pediatric abusive head trauma evaluation. J AAPOS. 2021;25(2):89 e1– e7. pmid:33865998
- 22. Scheller J. Infantile retinal haemorrhages in the absence of brain and bodily injury. Acta Paediatr. 2017;106(12):1902–4. pmid:28833451
- 23. Minns RA, Jones PA, Tandon A, Fleck BW, Mulvihill AO, Minns FC. Raised intracranial pressure and retinal haemorrhages in childhood encephalopathies. Dev Med Child Neurol. 2017;59(6):597–604. pmid:28369828
- 24. Ichord RN, Naim M, Pollock AN, Nance ML, Margulies SS, Christian CW. Hypoxic-ischemic injury complicates inflicted and accidental traumatic brain injury in young children: the role of diffusion-weighted imaging. J Neurotrauma. 2007;24(1):106–18. pmid:17263674
- 25. Kochanek PM, Clark RS, Ruppel RA, Adelson PD, Bell MJ, Whalen MJ, et al. Biochemical, cellular, and molecular mechanisms in the evolution of secondary damage after severe traumatic brain injury in infants and children: Lessons learned from the bedside. Pediatr Crit Care Med. 2000;1(1):4–19. pmid:12813280