To Study the Clinical Profile and Short-Term Outcomes of Whole-Body Therapeutic Hypothermia in Patients of Hypoxic Ischemic Encephalopathy
Abstract
Background: Neonatal encephalopathy (NE) is the clinical syndrome of disordered neurological function, and hypoxic ischemic encephalopathy (HIE) is NE that follows a perinatal hypoxic ischemic event. Strict criteria for making this diagnosis are constantly being developed but the essential components are the development of encephalopathy in a term/near term neonate soon after birth following an intrapartum event likely to cause hypoxia-ischemia. Aim: To study the clinical profile and short-term outcomes of whole-body therapeutic hypothermia in patients of hypoxic ischemic encephalopathy. Method: It was a prospective observational study conducted in a level IIIA NICU in Shri Shishu Bhawan Hospital, Bilaspur which is a tertiary care hospital from April – 2022 to March – 2023. It included all the newborn patients admitted with birth asphyxia with convulsions. Epidemiological data was collected, and patients were monitored for other complications. APGAR scores were recorded and Modified Sarnat and Sarnat staging was used to categorize HIE. Data was analyzed through SPSSv30. Results: Out of 12 neonates with birth weight <2.5 kg, 10 (83.33%) neonates were discharged and 2 (16.67%) neonates died while out of 51 neonates with birth weight >2.5 kg, 34 (66.67%) neonates were discharged and 17 (33.33%) neonates died. Results also show mortality in low birth is less than birth weight >2.5 kg. Our study shows outcome is better and low death occur when therapeutic hypothermia starts before 6hrs as compared to initiated after 6hrs. This may be due to early start of therapy leads to early reversal of pathology, early resuscitations and supportive treatment. Conclusion: Therapeutic hypothermia initiated before 6hrs had lesser complication like seizures, persistent acidosis, cardiac arrhythmia, hypotension, hypoglycemia and oliguria compared to initiate after 6hrs this may be due to early reversal of pathology during the first stage which is primary neuronal death and taking benefits of the latent period between primary and delayed neuronal death which is approximately 6 hours. Also, outcomes better if initiation of cooling is within 6hrs compared to after 6hrs mostly due to taking benefits of the latent period between primary and delayed neuronal death which is approximately 6 hours.Keywords:
Encephalopathy, Hypoxic Ischemic Encephalopathy, Therapeutic Hypothermia, NeonatalReferences
1. Liu L, Oza S, Hogan D, et al. Global, regional, and national causes of child mortality in 2000-13, with projections to inform post-2015 priori-ties: an updated systematic analysis. Lancet. 2015; 385:430-40.
2. Peliowski-Davidovich A., Canadian Paediatric Society, Fetus and Newborn Committee. Hypo-thermia for newborns with hypoxic ischemic encephalopathy. Paediatr Child Health. 2012 Jan;17(1):41-6.
3. Thoresen M, Tooley J, Liu X, et al. Time is brain: Starting therapeutic hypothermia within three hours after birth improves motor outcome in asphyxiated newborns. Neonatology 2013; 104:228-33. 10.1159/000353948
4. Wang CH, Chen NC, Tsai MS, et al. Therapeu-tic Hypothermia and the Risk of Hemorrhage: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Medicine (Bal-timore). 2015 Nov;94(47):e2152.
5. Liu W, Yang Q, Wei H, et al. Prognostic value of clinical tests in neonates with hypoxic-is-chemic encephalopathy treated with therapeutic hypothermia: A systematic review and metaa-nalysis. Front Neurol. 2020; 11:133.
6. Goenka A, Yozawitz E, Gomes WA, Nafday SM. Selective Head versus Whole Body Cooling Treatment of Hypoxic-Ischemic En-cephalopathy: Comparison of Electroencepha-logram and Magnetic Resonance Imaging Find-ings. Am J Perinatol. 2020 Oct;37(12):1264-1270.
7. Shankaran S. Therapeutic hypothermia for neo-natal encephalopathy. Curr Treat Options Neu-rol. 2012 Dec;14(6):608-19. doi: 0.1007/s11940-012-0200-y. PMID: 23007949; PMCID: PMC3519960.
8. Burnsed J, Quigg M, Zanelli S, Goodkin H. Clinical severity, rather than body temperature, during the rewarming phase of therapeutic hy-pothermia affect quantitative EEG in neonates with hypoxic ischemic encephalopathy. J Clin Neurophysiol. 2011;28(1)
9. Damoi JK, Sebunya R, Kirabira VN et al. short term outcomes of newborn infants with Hy-poxic Ischaemic Encephalopathy treated with therapeutic hypothermia in a low resource set-ting: A retrospective cohort study, 04 June 2020,
10. Wyatt JS, Gluckman PD, Liu PY, et al. Deter-minants of outcomes after head cooling for ne-onatal encephalopathy. Pediatrics
11. Jia, W., Lei, X., Dong, W. et al. Benefits of starting hypothermia treatment within 6 h vs. 6–12 h in newborns with moderate neonatal hy-poxic-ischemic encephalopathy. BMC Pediatr 18, 50 (2018).
12. Sabir H, Scull-Brown E, Liu X, et al. Immediate hypothermia is not neuroprotective after severe hypoxia-ischemia and is deleterious when de-layed by 12 hours in neonatal rats. Stroke 2012; 43:3364-70.
13. Guillot M, Philippe M, Davila J, et al. Influence of timing of initiation of therapeutic hypother-mia on brain MRI and neurodevelopment at 18 months in infants with HIE: a retrospective co-hort study. BMJ Paediatrics Open 2019.
14. Arca G, Garcia-Alix A, Arnaez J, Blanco D. Se-dation in term or near-term newborns with hy-poxic-ischemic encephalopathy who require therapeutic hypothermia. An Pediatr (Barc). 2015; 82:52-3.
15. Arnaez J, Vega C, Garcia-Alix A, Gutierrez EP, Caserio S, Jimenez MP, Castanon L, Esteban I, Hortelano M, Hernandez N, et al. Multicenter program for the integrated care of newborns with perinatal hypoxic-ischemic insult (ARAHIP). An Pediatr (Barc). 2015; 82:172–82.
Published
Abstract Display: 0
PDF Downloads: 0