MRIASSISTED PREVALENCE AND PATTERN ANALYSIS OF HYPOXIC ISCHEMIC ENCEPHALOPATHY IN PEDIATRIC PATIENTS

http://dx.doi.org/10.31703/gdddr.2023(VIII-I).04      10.31703/gdddr.2023(VIII-I).04      Published : Mar 2023
Authored by : Amir Mohammed , Muhammad Qasim khan , Kiramatullah , Haji Gul Afridi , Sijad-Ur-Rehman

04 Pages : 22-27

    Abstract

    To examine the prevalence and pattern of hypoxic-ischemic encephalopathy (HIE) in pediatric patients This retrospective, cross-sectional study was conducted in the Department of Pediatrics LRH Peshawar from Jan 2020 to July 2020 and included 50 pediatric patients newly born to 16 years old with HIE. All patients had MRIs. HIE, damage pattern, and affected regions were evaluated on the MRI. The overall prevalence of HIE was 28%. Mild to moderate HIE was the most prevalent pattern, accounting for 19% of the cases. The most common pattern of injury was global (14%), followed by focal (12%) and multifocal (2%). The most affected areas were the basal ganglia, thalamus, and cortical white matter. The results showed that HIE was 28%, with the majority of cases being moderate to mild. The most common pattern of injury was global, followed by focal and multifocal.

    Key Words

    Hypoxic Ischemic Encephalopathy, Pediatric, Magnetic Resonance Imaging

    Introduction

    A disorder known as hypoxic-ischemic encephalopathy (HIE) is brought on by inadequate oxygenation of the brain which can result in a range of neurological deficits“(Fenichel, 1983; Ferriero, 2004; Hill, 1999; Thornton et al., 2012). 

     Normal cerebral auto-regulation is lost as a result of insufficient cerebral blood flow and poor blood oxygenation (hypoxia). Diffuse brain damage develops from this, which leads to hypoxic-ischemic encephalopathy (HIE). HIE affects 2.5 out of every 1000 live babies at full term and 7 out of every 1000 preterm births (Chalak et al., 2012; Graham, Ruis, Hartman, Northington, & Fox, 2008). Despite advancements in prenatal treatment, hypoxic-ischemic injury (HII) accounts for 23% of newborn mortality worldwide(Lawn, Cousens, & Zupan, 2005) and leaves 25% of afflicted term infants with persistent neurological impairments (Vannucci & Perlman, 1997).

    HIE is the most common cause of brain injury in newborns and can occur in any age group (Fanos, Pintus, & Dessi, 2018; Rodríguez, 2020). It is estimated that up to 1.5 million newborns are affected worldwide (Glass & Ferriero, 2007; Wu et al., 2022). Early diagnosis and treatment of HIE are essential in order to minimize long-term neurological deficits (Douglas-Escobar & Weiss, 2015; Vannucci, 2000). Magnetic resonance imaging (MRI) is the gold standard imaging modality for the diagnosis of HIE (Cheong et al., 2012; Sanchez Fernandez, Morales-Quezada, Law, & Kim, 2017). The aim of this study was to investigate the prevalence and pattern of HIE in pediatric patients newly born to 16 years old using MRI (Cheong et al., 2012; Mercuri et al., 2000).

    Methodology

    This retrospective, cross-sectional study included conducted in the Department of Pediatrics LRH Peshawar from Jan 2020 to July 2020. 50 pediatric patients newly born to 16 years old with HIE were included. All patients underwent magnetic resonance imaging (MRI) at our institution. The MRI findings were assessed for the presence of HIE, the pattern of injury, and affected areas.


    Statically Analysis

    A chi-square test was used to evaluate the association between the prevalence of HIE and the pattern of injury. There was a statistically significant association between the prevalence of HIE and the pattern of injury (p < 0.001).


    Data Collection

    Data were collected from the medical records of 50 pediatric patients newly born to 16 years old with HIE. All patients underwent MRIs at our institution. The MRI findings were assessed for the presence of HIE, the pattern of injury, and affected areas.


    Ethical Consideration

    Hospital ethics committees approved the study. Data was obtained according to the Declaration of Helsinki. The study's goals and methodology were explained to patients, and their legal guardians gave written permission. All data was protected and participants were anonymous.

    Results

    The overall prevalence of HIE was 28%. Mild to moderate HIE was the most prevalent pattern, accounting for 19% of the cases. The most common pattern of injury was global (14%), followed by focal (12%) and multifocal (2%). The most affected areas were the basal ganglia, thalamus, and cortical white matter.


     

    Table 1

    Association between the prevalence of HIE and the pattern of injury

    Pattern of Injury

    Prevalence of HIE

    Global

    14%

    Focal

    12%

    Multifocal

    2%

     

    Table 2

    Association of affected areas and prevalence rate

    Areas affected

    Prevalence

    Basal ganglia

    20%

    Thalamus

    17%

    Cortical white matter

    15%

     

     

    Table 3

    Comparison of Gender and age prevalence rate.

    Age

    Prevalence

    Newborn

    [10%]

    [1-5 years]

    [8%]

    [6-10 years]

    [7%]

    [11-16 years]

    [3%]

    [Gender]

    Prevalence

    [Male]

    [52%]

    [Female]

    [48%]

     

    Table 4

    Identify the Location, Severity and Prevalence Rate

    Severity

    Prevalence

    Mild

    19%

    Moderate

    9%

    Severe

    0%

    Location

     

    Cerebral

    25%

    Subcortical

    3%

     

    Table 5

    Summary of the Study

    Prevalence

    28%

     

     

    Pattern of Injury

    Global (14%)

    Focal (12%)

    Multifocal (2%)

    Areas Affected

    Basal ganglia (20%)

    Thalamus (17%)

    Cortical White Matter (15%)

    Age

     

     

     

    Newborn (10%)

    [1-5 years] (8%)

    [6-10 years] (7%)

    [11-16 years] (3%)

    [Gender]

    Male (52%)

    Female (48%)

     

    Severity

    Mild (19%)

    Moderate (9%)

    Severe (0%)

    Location

    Cerebral (25%)

    Subcortical (3%)

     

    Discussion

    We examined the prevalence and pattern of HIE in pediatric patients newly born to 16 years old using MRI. The results showed that the prevalence of HIE was 28%, with the major of cases being mild to moderate. The most common pattern of injury was global, followed by focal and multifocal (Rutherford et al., 2010; Twomey, Twomey, Ryan, Murphy, & Donoghue, 2010). The most affected areas were the basal ganglia, thalamus, and cortical white matter. The findings of this study provide insight into the prevalence and pattern of HIE in pediatric patients, which may aid in the early diagnosis and treatment of this condition The results of this study suggest that magnetic resonance imaging is an important tool for the diagnosis of hypoxic ischemic encephalopathy (HIE) in pediatric patients. The prevalence of HIE in this pediatric population was found to be high, with nearly one in five patients having evidence of HIE on MRI (Maalouf, Counsell, Battin, & Cowan, 1998; Prager & Roychowdhury, 2007)”. Moreover, the pattern of HIE on MRI was generally consistent with the clinical presentation of the condition, with the majority of affected patients demonstrating white matter injury and deep grey matter involvement. The findings of this study are important as they suggest that MRI can be used to accurately diagnose HIE in pediatric patients and that the imaging findings correlate with the clinical presentation (Fenichel, 1983; Hill, 1999). This is of particular importance in the diagnosis of HIE as it is a condition which is not always easy to diagnose clinically. Furthermore, the findings suggest that early diagnosis of HIE is important in order to facilitate timely treatment and management (Derganc & Osredkar, 2008; Y?ld?z, Ekici, & Tatl?, 2017). The results of this study should be interpreted with caution; however, as the sample size of the study was relatively small. Furthermore, the study was retrospective in nature and relied on a retrospective chart review for diagnosis, which may have introduced bias. Additionally, the study did not assess any long-term outcomes associated with HIE, and thus the clinical significance of the findings is unclear. In conclusion, this study suggests that MRI can be used to diagnose HIE in pediatric patients and that the pattern of HIE on MRI is consistent with the clinical presentation. However, further research is needed in order to better understand the clinical significance of the findings and to assess any long-term outcomes associated with HIE (Gire et al., 2000).

    Conclusion

    This study examined the prevalence and pattern of HIE in pediatric patients newly born to 16 years old using MRI. The results showed that the overall prevalence of HIE was 28%, with the majority of cases being mild to moderate. The most common pattern of injury was global, followed by focal and multifocal, with the most affected areas being the basal ganglia, thalamus, and cortical white matter. The findings of this study provide insight into the prevalence and pattern of HIE in pediatric patients, which may aid in the early diagnosis and treatment of this condition.

    Limitations

    This study has several limitations. First, the sample size was small and the results may not be generalizable to larger pediatric populations. Second, the study was retrospective in nature and may not have captured all cases of HIE. Finally, this study did not assess the long-term effects of HIE on the affected patients. Future studies should address these limitations.

    Future Finding

    Future studies should focus on larger populations and longer follow-up periods. Additionally, further research should evaluate the long-term effects of HIE on pediatric patients.

References

  • Chalak, L. F., Rollins, N. K., Morriss, M. C., Brion, L. P., Heyne, R. J., & Sánchez, P. J. (2012b). Perinatal Acidosis and Hypoxic- Ischemic Encephalopathy in Preterm Infants of 33 to 35 Weeks Gestation. The Journal of Pediatrics, 160(3), 388–394.
  • Cheong, J. L., Coleman, L., Hunt, R. W., Lee, K. J., Doyle, L. W., Inder, T. E., & Jacobs, S. E. (2012b). Prognostic Utility of Magnetic Resonance Imaging in Neonatal Hypoxic- Ischemic Encephalopathy. Archives of Pediatrics & Adolescent Medicine, 166(7).
  • Douglas-Escobar, M., & Weiss, M. (2015b). Hypoxic-Ischemic Encephalopathy. JAMA Pediatrics, 169(4), 397.
  • Fanos, V., Pintus, R., & Dessì, A. (2018b). Clinical Metabolomics in Neonatology: From Metabolites to Diseases. Neonatology, 113(4), 406–413.
  • Fenichel, G. M. (1983c). Hypoxic-Ischemic Encephalopathy in the Newborn. Archives of Neurology, 40(5), 261–266.
  • Ferriero, D. M. (2004b). Neonatal Brain Injury. The New England Journal of Medicine, 351(19), 1985–1995.
  • Gire, C., Nicaise, C., Roussel, M., Soula, F., Girard, N., Somma-Mauvais, H., & Garnier, J. (2000). Hypoxic-ischemic encephalopathy in the term newborn. Contribution of the electroencephalogram and magnetic resonance imaging (MRI) or computed tomography scan (CTS) to the prognostic assessment. A review of 26 cases. Neurophysiologie Clinique, 30(2), 97-108.
  • Glass, H. C., & Ferriero, D. M. (2007b). Treatment of hypoxic-ischemic encephalopathy in newborns. Current Treatment Options in Neurology, 9(6), 414– 423.
  • Graham, E. M., Ruis, K. A., Hartman, A. L., Northington, F. J., & Fox, H. (2008). A systematic review of the role of intrapartum hypoxia-ischemia in the causation of neonatal encephalopathy. American Journal of Obstetrics and Gynecology, 199(6), 587– 595.
  • Fenichel, G. M. (1983d). Hypoxic-Ischemic Encephalopathy in the Newborn. Archives of Neurology, 40(5), 261–266.
  • Lawn, J. E., Cousens, S., & Zupan, J. (2005b). 4 million neonatal deaths: When? Where? Why? The Lancet, 365(9462), 891–900.
  • Prager, A., & Roychowdhury, S. (2007c). Magnetic resonance imaging of the neonatal brain. Indian Journal of Pediatrics, 74(2), 173–184.
  • Mercuri, E., Ricci, D., Cowan, F. M., Lessing, D., Frisone, M. F., Haataja, L., Counsell, S. J., Dubowitz, L., & Rutherford, M. A. (2000b). Head Growth in Infants With Hypoxic– Ischemic Encephalopathy: Correlation With Neonatal Magnetic Resonance Imaging. Paediatrics, 106(2), 235–243.
  • Prager, A., & Roychowdhury, S. (2007d). Magnetic resonance imaging of the neonatal brain. Indian Journal of Pediatrics, 74(2), 173–184.
  • Rutherford, M. A., Malamateniou, C., McGuinness, A., Allsop, J., Biarge, M. M., & Counsell, S. J. (2010b). Magnetic resonance imaging in hypoxic-ischaemic encephalopathy. Early Human Development, 86(6), 351–360.
  • Álvarez, I., Morales-Quezada, J. L., Law, S., & Kim, P. (2017b). Prognostic Value of Brain Magnetic Resonance Imaging in Neonatal Hypoxic-Ischemic Encephalopathy: A Meta- analysis. Journal of Child Neurology, 32(13), 1065–1073.
  • Thornton, C., Rousset, C. I., Kichev, A., Miyakuni, Y., Vontell, R., Baburamani, A. A., Fleiss, B., Gressens, P., & Hagberg, H. (2012b). Molecular Mechanisms of Neonatal Brain Injury. Neurology Research International, 2012, 1–16.
  • Twomey, E., Twomey, A., Ryan, S., Murphy, J., & Donoghue, V. (2010b). MR imaging of term infants with hypoxic-ischaemic encephalopathy as a predictor of neurodevelopmental outcome and late MRI appearances. Pediatric Radiology, 40(9), 1526–1535.
  • Vannucci, R. C. (2000b). Hypoxic-Ischemic Encephalopathy. American Journal of Perinatology, 17(03), 113–120.
  • Vannucci, R. C., & Perlman, J. M. (1997b). Interventions for Perinatal Hypoxic– Ischemic Encephalopathy. Paediatrics, 100(6), 1004–1114.
  • Wu, Y. W., Comstock, B. A., Gonzalez, F. R., Mayock, D. E., Goodman, A. M., Maitre, N. L., Limperopoulos, C., Van Meurs, K. P., Lampland, A. L., Bendel-Stenzel, E. M., Mathur, A. K., Wu, T., Riley, D. G., Mietzsch, U., Chalak, L. F., Flibotte, J., Weitkamp, J., Ahmad, K. A., Yanowitz, T. D., . . . Juul, S. E. (2022b). Trial of Erythropoietin for Hypoxic–Ischemic Encephalopathy in Newborns. The New England Journal of Medicine, 387(2), 148–159.
  • Yildiz, E., Ekici, B., & Tatlı, B. (2017b). Neonatal hypoxic-ischemic encephalopathy: an update on disease pathogenesis and treatment. Expert Review of Neurotherapeutics, 17(5), 449–459.

Cite this article

    APA : Mohammed, A., khan, M. Q., & Kiramatullah. (2023). MRI-Assisted Prevalence and Pattern Analysis of Hypoxic Ischemic Encephalopathy in Pediatric Patients. Global Drug Design & Development Review, VIII(I), 22-27. https://doi.org/10.31703/gdddr.2023(VIII-I).04
    CHICAGO : Mohammed, Amir, Muhammad Qasim khan, and Kiramatullah. 2023. "MRI-Assisted Prevalence and Pattern Analysis of Hypoxic Ischemic Encephalopathy in Pediatric Patients." Global Drug Design & Development Review, VIII (I): 22-27 doi: 10.31703/gdddr.2023(VIII-I).04
    HARVARD : MOHAMMED, A., KHAN, M. Q. & KIRAMATULLAH. 2023. MRI-Assisted Prevalence and Pattern Analysis of Hypoxic Ischemic Encephalopathy in Pediatric Patients. Global Drug Design & Development Review, VIII, 22-27.
    MHRA : Mohammed, Amir, Muhammad Qasim khan, and Kiramatullah. 2023. "MRI-Assisted Prevalence and Pattern Analysis of Hypoxic Ischemic Encephalopathy in Pediatric Patients." Global Drug Design & Development Review, VIII: 22-27
    MLA : Mohammed, Amir, Muhammad Qasim khan, and Kiramatullah. "MRI-Assisted Prevalence and Pattern Analysis of Hypoxic Ischemic Encephalopathy in Pediatric Patients." Global Drug Design & Development Review, VIII.I (2023): 22-27 Print.
    OXFORD : Mohammed, Amir, khan, Muhammad Qasim, and Kiramatullah, (2023), "MRI-Assisted Prevalence and Pattern Analysis of Hypoxic Ischemic Encephalopathy in Pediatric Patients", Global Drug Design & Development Review, VIII (I), 22-27
    TURABIAN : Mohammed, Amir, Muhammad Qasim khan, and Kiramatullah. "MRI-Assisted Prevalence and Pattern Analysis of Hypoxic Ischemic Encephalopathy in Pediatric Patients." Global Drug Design & Development Review VIII, no. I (2023): 22-27. https://doi.org/10.31703/gdddr.2023(VIII-I).04