Core temperature after birth in babies with neonatal encephalopathy in a sub‐Saharan African hospital setting

Key points Therapeutic hypothermia (HT) to 33.0–34.0°C for 72 h provides optimal therapy for infants with neonatal encephalopathy (NE) in high‐resource settings. HT is not universally implemented in low‐ and middle‐income countries as a result of both limited resources and evidence. Facilitated pass...

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Veröffentlicht in:The Journal of physiology 2019-08, Vol.597 (15), p.4013-4024
Hauptverfasser: Enweronu‐Laryea, Christabel, Martinello, Kathryn A, Rose, Maggie, Manu, Sally, Tann, Cally J, Meek, Judith, Ahor‐Essel, Kojo, Boylan, Geraldine B, Robertson, Nicola J
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container_end_page 4024
container_issue 15
container_start_page 4013
container_title The Journal of physiology
container_volume 597
creator Enweronu‐Laryea, Christabel
Martinello, Kathryn A
Rose, Maggie
Manu, Sally
Tann, Cally J
Meek, Judith
Ahor‐Essel, Kojo
Boylan, Geraldine B
Robertson, Nicola J
description Key points Therapeutic hypothermia (HT) to 33.0–34.0°C for 72 h provides optimal therapy for infants with neonatal encephalopathy (NE) in high‐resource settings. HT is not universally implemented in low‐ and middle‐income countries as a result of both limited resources and evidence. Facilitated passive cooling, comprising infants being allowed to passively lower their body temperature in the days after birth, is an emerging practice in some West African neonatal units. In this observational study, we demonstrate that infants undergoing facilitated passive cooling in a neonatal unit in Accra, Ghana, achieve temperatures within the HT target range ∼20% of the 72 h. Depth of HT fluctuates and can be excessive, as well as not maintained, especially after 24 h. Sustained and deeper passive cooling was evident for severe NE and for those that died. It is important to prevent excessive cooling, to understand that severe NE babies cool more and to be aware of facilitated passive cooling with respect to the design of clinical trials in low‐ and mid‐resource settings. Neonatal encephalopathy (NE) is a significant worldwide problem with the greatest burden in sub‐Saharan Africa. Therapeutic hypothermia (HT), comprising the standard of care for infants with moderate‐to‐severe NE in settings with sophisticated intensive care, is not available to infants in many sub‐Saharan African countries, including Ghana. We prospectively assessed the temperature response in relation to outcome in the 80 h after birth in a cohort of babies with NE undergoing ‘facilitated passive cooling’ at Korle Bu Teaching Hospital, Accra, Ghana. We hypothesized that NE infants demonstrate passive cooling. Thirteen infants (69% male) ≥36 weeks with moderate‐to‐severe NE were enrolled. Ambient mean ± SD temperature was 28.3 ± 0.7°C. Infant core temperature was 34.2 ± 1.2°C over the first 24 h and 35.0 ± 1.0°C over 80 h. Nadir mean temperature occurred at 15 h. Temperatures were within target range for HT with respect to 18 ± 14% of measurements within the first 72 h. Axillary temperature was 0.5 ± 0.2°C below core. Three infants died before discharge. Core temperature over 80 h for surviving infants was 35.3 ± 0.9°C and 33.96 ± 0.7°C for those that died (P = 0.043). Temperature profile negatively correlated with Thompson NE score on day 4 (r2 = 0.66): infants with a Thompson score of 0–6 had higher temperatures than those with a score of 7–15 (P = 0.021) and a score of 16+/deceased (P = 0.007). Mor
doi_str_mv 10.1113/JP277820
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HT is not universally implemented in low‐ and middle‐income countries as a result of both limited resources and evidence. Facilitated passive cooling, comprising infants being allowed to passively lower their body temperature in the days after birth, is an emerging practice in some West African neonatal units. In this observational study, we demonstrate that infants undergoing facilitated passive cooling in a neonatal unit in Accra, Ghana, achieve temperatures within the HT target range ∼20% of the 72 h. Depth of HT fluctuates and can be excessive, as well as not maintained, especially after 24 h. Sustained and deeper passive cooling was evident for severe NE and for those that died. It is important to prevent excessive cooling, to understand that severe NE babies cool more and to be aware of facilitated passive cooling with respect to the design of clinical trials in low‐ and mid‐resource settings. Neonatal encephalopathy (NE) is a significant worldwide problem with the greatest burden in sub‐Saharan Africa. Therapeutic hypothermia (HT), comprising the standard of care for infants with moderate‐to‐severe NE in settings with sophisticated intensive care, is not available to infants in many sub‐Saharan African countries, including Ghana. We prospectively assessed the temperature response in relation to outcome in the 80 h after birth in a cohort of babies with NE undergoing ‘facilitated passive cooling’ at Korle Bu Teaching Hospital, Accra, Ghana. We hypothesized that NE infants demonstrate passive cooling. Thirteen infants (69% male) ≥36 weeks with moderate‐to‐severe NE were enrolled. Ambient mean ± SD temperature was 28.3 ± 0.7°C. Infant core temperature was 34.2 ± 1.2°C over the first 24 h and 35.0 ± 1.0°C over 80 h. Nadir mean temperature occurred at 15 h. Temperatures were within target range for HT with respect to 18 ± 14% of measurements within the first 72 h. Axillary temperature was 0.5 ± 0.2°C below core. Three infants died before discharge. Core temperature over 80 h for surviving infants was 35.3 ± 0.9°C and 33.96 ± 0.7°C for those that died (P = 0.043). Temperature profile negatively correlated with Thompson NE score on day 4 (r2 = 0.66): infants with a Thompson score of 0–6 had higher temperatures than those with a score of 7–15 (P = 0.021) and a score of 16+/deceased (P = 0.007). More severe NE was associated with lower core temperatures. Passive cooling is a physiological response after hypoxia–ischaemia; however, the potential neuroprotective effect of facilitated passive cooling is unknown. An awareness of facilitated passive cooling in babies with NE is important for the design of clinical trials of neuroprotection in low and mid resource settings. Key points Therapeutic hypothermia (HT) to 33.0–34.0°C for 72 h provides optimal therapy for infants with neonatal encephalopathy (NE) in high‐resource settings. HT is not universally implemented in low‐ and middle‐income countries as a result of both limited resources and evidence. Facilitated passive cooling, comprising infants being allowed to passively lower their body temperature in the days after birth, is an emerging practice in some West African neonatal units. In this observational study, we demonstrate that infants undergoing facilitated passive cooling in a neonatal unit in Accra, Ghana, achieve temperatures within the HT target range ∼20% of the 72 h. Depth of HT fluctuates and can be excessive, as well as not maintained, especially after 24 h. Sustained and deeper passive cooling was evident for severe NE and for those that died. It is important to prevent excessive cooling, to understand that severe NE babies cool more and to be aware of facilitated passive cooling with respect to the design of clinical trials in low‐ and mid‐resource settings.</description><identifier>ISSN: 0022-3751</identifier><identifier>ISSN: 1469-7793</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/JP277820</identifier><identifier>PMID: 31168907</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Africa South of the Sahara ; Babies ; Body Temperature ; Brain Diseases - epidemiology ; Brain Diseases - therapy ; Clinical trials ; Encephalopathy ; facilitated passive cooling ; Female ; Global health ; Hospitals - statistics &amp; numerical data ; Humans ; Hypothermia ; Hypothermia, Induced - methods ; Hypoxia ; hypoxic ischaemic encephalopathy ; Infant, Newborn ; Infant, Newborn, Diseases - epidemiology ; Infant, Newborn, Diseases - therapy ; Infants ; Ischemia ; Male ; neonatal encephalopathy ; Neonates ; Neuroprotection ; Neuroscience ; Research Paper ; Temperature ; Temperature effects ; therapeutic hypothermia</subject><ispartof>The Journal of physiology, 2019-08, Vol.597 (15), p.4013-4024</ispartof><rights>2019 The Authors. published by John Wiley &amp; Sons Ltd on behalf of The Physiological Society</rights><rights>2019 The Authors. 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HT is not universally implemented in low‐ and middle‐income countries as a result of both limited resources and evidence. Facilitated passive cooling, comprising infants being allowed to passively lower their body temperature in the days after birth, is an emerging practice in some West African neonatal units. In this observational study, we demonstrate that infants undergoing facilitated passive cooling in a neonatal unit in Accra, Ghana, achieve temperatures within the HT target range ∼20% of the 72 h. Depth of HT fluctuates and can be excessive, as well as not maintained, especially after 24 h. Sustained and deeper passive cooling was evident for severe NE and for those that died. It is important to prevent excessive cooling, to understand that severe NE babies cool more and to be aware of facilitated passive cooling with respect to the design of clinical trials in low‐ and mid‐resource settings. Neonatal encephalopathy (NE) is a significant worldwide problem with the greatest burden in sub‐Saharan Africa. Therapeutic hypothermia (HT), comprising the standard of care for infants with moderate‐to‐severe NE in settings with sophisticated intensive care, is not available to infants in many sub‐Saharan African countries, including Ghana. We prospectively assessed the temperature response in relation to outcome in the 80 h after birth in a cohort of babies with NE undergoing ‘facilitated passive cooling’ at Korle Bu Teaching Hospital, Accra, Ghana. We hypothesized that NE infants demonstrate passive cooling. Thirteen infants (69% male) ≥36 weeks with moderate‐to‐severe NE were enrolled. Ambient mean ± SD temperature was 28.3 ± 0.7°C. Infant core temperature was 34.2 ± 1.2°C over the first 24 h and 35.0 ± 1.0°C over 80 h. Nadir mean temperature occurred at 15 h. Temperatures were within target range for HT with respect to 18 ± 14% of measurements within the first 72 h. Axillary temperature was 0.5 ± 0.2°C below core. Three infants died before discharge. Core temperature over 80 h for surviving infants was 35.3 ± 0.9°C and 33.96 ± 0.7°C for those that died (P = 0.043). Temperature profile negatively correlated with Thompson NE score on day 4 (r2 = 0.66): infants with a Thompson score of 0–6 had higher temperatures than those with a score of 7–15 (P = 0.021) and a score of 16+/deceased (P = 0.007). More severe NE was associated with lower core temperatures. Passive cooling is a physiological response after hypoxia–ischaemia; however, the potential neuroprotective effect of facilitated passive cooling is unknown. An awareness of facilitated passive cooling in babies with NE is important for the design of clinical trials of neuroprotection in low and mid resource settings. Key points Therapeutic hypothermia (HT) to 33.0–34.0°C for 72 h provides optimal therapy for infants with neonatal encephalopathy (NE) in high‐resource settings. HT is not universally implemented in low‐ and middle‐income countries as a result of both limited resources and evidence. Facilitated passive cooling, comprising infants being allowed to passively lower their body temperature in the days after birth, is an emerging practice in some West African neonatal units. In this observational study, we demonstrate that infants undergoing facilitated passive cooling in a neonatal unit in Accra, Ghana, achieve temperatures within the HT target range ∼20% of the 72 h. Depth of HT fluctuates and can be excessive, as well as not maintained, especially after 24 h. Sustained and deeper passive cooling was evident for severe NE and for those that died. It is important to prevent excessive cooling, to understand that severe NE babies cool more and to be aware of facilitated passive cooling with respect to the design of clinical trials in low‐ and mid‐resource settings.</description><subject>Africa South of the Sahara</subject><subject>Babies</subject><subject>Body Temperature</subject><subject>Brain Diseases - epidemiology</subject><subject>Brain Diseases - therapy</subject><subject>Clinical trials</subject><subject>Encephalopathy</subject><subject>facilitated passive cooling</subject><subject>Female</subject><subject>Global health</subject><subject>Hospitals - statistics &amp; numerical data</subject><subject>Humans</subject><subject>Hypothermia</subject><subject>Hypothermia, Induced - methods</subject><subject>Hypoxia</subject><subject>hypoxic ischaemic encephalopathy</subject><subject>Infant, Newborn</subject><subject>Infant, Newborn, Diseases - epidemiology</subject><subject>Infant, Newborn, Diseases - therapy</subject><subject>Infants</subject><subject>Ischemia</subject><subject>Male</subject><subject>neonatal encephalopathy</subject><subject>Neonates</subject><subject>Neuroprotection</subject><subject>Neuroscience</subject><subject>Research Paper</subject><subject>Temperature</subject><subject>Temperature effects</subject><subject>therapeutic hypothermia</subject><issn>0022-3751</issn><issn>1469-7793</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp1kctq3TAQhkVpaE7TQp-gGLrJxqkuti6bQjj0FgIJNF2LsT2OFXwsV5Ibzi6P0Gfsk1SnSQ5toWgxGuabn5n5CXnF6AljTLw9u-RKaU6fkBWrpCmVMuIpWVHKeSlUzQ7J8xhvKGWCGvOMHArGpDZUrYhf-4BFws2MAdKS_9AnDEXjQhoKNxUNNA5jcetyOqGfIMFY4NTiPMDoZ0jDdodBEZfm592PLzBAgKk47YNrcxx8nN2uJWJKbrp-QQ56GCO-fIhH5OuH91frT-X5xcfP69Pzsq2EMaVpueSArKeImimUdcvAaFopw6ToK9Z0ddd3SoEQnOZVesk7hbrljdaqZ-KIvLvXnZdmg12LUwow2jm4DYSt9eDs35XJDfbaf7dS5ad1Fjh-EAj-24Ix2Y2LLY4j5Css0XIulZIinz2jb_5Bb_wSprzeb4qrqs5-7AXb4GMM2O-HYdTuXLSPLmb09Z_D78FH2zJwcg_cuhG3_xWyV2eXTNSVEb8A7CunWA</recordid><startdate>20190801</startdate><enddate>20190801</enddate><creator>Enweronu‐Laryea, Christabel</creator><creator>Martinello, Kathryn A</creator><creator>Rose, Maggie</creator><creator>Manu, Sally</creator><creator>Tann, Cally J</creator><creator>Meek, Judith</creator><creator>Ahor‐Essel, Kojo</creator><creator>Boylan, Geraldine B</creator><creator>Robertson, Nicola J</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9346-5365</orcidid><orcidid>https://orcid.org/0000-0002-9816-4577</orcidid><orcidid>https://orcid.org/0000-0002-5783-0828</orcidid><orcidid>https://orcid.org/0000-0002-7490-7313</orcidid><orcidid>https://orcid.org/0000-0003-0131-4952</orcidid></search><sort><creationdate>20190801</creationdate><title>Core temperature after birth in babies with neonatal encephalopathy in a sub‐Saharan African hospital setting</title><author>Enweronu‐Laryea, Christabel ; Martinello, Kathryn A ; Rose, Maggie ; Manu, Sally ; Tann, Cally J ; Meek, Judith ; Ahor‐Essel, Kojo ; Boylan, Geraldine B ; Robertson, Nicola J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4399-9c262ae1f0ee817e65c1a980479163f41bd5dfd77a3320890f62d7e8c2b887f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Africa South of the Sahara</topic><topic>Babies</topic><topic>Body Temperature</topic><topic>Brain Diseases - epidemiology</topic><topic>Brain Diseases - therapy</topic><topic>Clinical trials</topic><topic>Encephalopathy</topic><topic>facilitated passive cooling</topic><topic>Female</topic><topic>Global health</topic><topic>Hospitals - statistics &amp; numerical data</topic><topic>Humans</topic><topic>Hypothermia</topic><topic>Hypothermia, Induced - methods</topic><topic>Hypoxia</topic><topic>hypoxic ischaemic encephalopathy</topic><topic>Infant, Newborn</topic><topic>Infant, Newborn, Diseases - epidemiology</topic><topic>Infant, Newborn, Diseases - therapy</topic><topic>Infants</topic><topic>Ischemia</topic><topic>Male</topic><topic>neonatal encephalopathy</topic><topic>Neonates</topic><topic>Neuroprotection</topic><topic>Neuroscience</topic><topic>Research Paper</topic><topic>Temperature</topic><topic>Temperature effects</topic><topic>therapeutic hypothermia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Enweronu‐Laryea, Christabel</creatorcontrib><creatorcontrib>Martinello, Kathryn A</creatorcontrib><creatorcontrib>Rose, Maggie</creatorcontrib><creatorcontrib>Manu, Sally</creatorcontrib><creatorcontrib>Tann, Cally J</creatorcontrib><creatorcontrib>Meek, Judith</creatorcontrib><creatorcontrib>Ahor‐Essel, Kojo</creatorcontrib><creatorcontrib>Boylan, Geraldine B</creatorcontrib><creatorcontrib>Robertson, Nicola J</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; 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HT is not universally implemented in low‐ and middle‐income countries as a result of both limited resources and evidence. Facilitated passive cooling, comprising infants being allowed to passively lower their body temperature in the days after birth, is an emerging practice in some West African neonatal units. In this observational study, we demonstrate that infants undergoing facilitated passive cooling in a neonatal unit in Accra, Ghana, achieve temperatures within the HT target range ∼20% of the 72 h. Depth of HT fluctuates and can be excessive, as well as not maintained, especially after 24 h. Sustained and deeper passive cooling was evident for severe NE and for those that died. It is important to prevent excessive cooling, to understand that severe NE babies cool more and to be aware of facilitated passive cooling with respect to the design of clinical trials in low‐ and mid‐resource settings. Neonatal encephalopathy (NE) is a significant worldwide problem with the greatest burden in sub‐Saharan Africa. Therapeutic hypothermia (HT), comprising the standard of care for infants with moderate‐to‐severe NE in settings with sophisticated intensive care, is not available to infants in many sub‐Saharan African countries, including Ghana. We prospectively assessed the temperature response in relation to outcome in the 80 h after birth in a cohort of babies with NE undergoing ‘facilitated passive cooling’ at Korle Bu Teaching Hospital, Accra, Ghana. We hypothesized that NE infants demonstrate passive cooling. Thirteen infants (69% male) ≥36 weeks with moderate‐to‐severe NE were enrolled. Ambient mean ± SD temperature was 28.3 ± 0.7°C. Infant core temperature was 34.2 ± 1.2°C over the first 24 h and 35.0 ± 1.0°C over 80 h. Nadir mean temperature occurred at 15 h. Temperatures were within target range for HT with respect to 18 ± 14% of measurements within the first 72 h. Axillary temperature was 0.5 ± 0.2°C below core. Three infants died before discharge. Core temperature over 80 h for surviving infants was 35.3 ± 0.9°C and 33.96 ± 0.7°C for those that died (P = 0.043). Temperature profile negatively correlated with Thompson NE score on day 4 (r2 = 0.66): infants with a Thompson score of 0–6 had higher temperatures than those with a score of 7–15 (P = 0.021) and a score of 16+/deceased (P = 0.007). More severe NE was associated with lower core temperatures. Passive cooling is a physiological response after hypoxia–ischaemia; however, the potential neuroprotective effect of facilitated passive cooling is unknown. An awareness of facilitated passive cooling in babies with NE is important for the design of clinical trials of neuroprotection in low and mid resource settings. Key points Therapeutic hypothermia (HT) to 33.0–34.0°C for 72 h provides optimal therapy for infants with neonatal encephalopathy (NE) in high‐resource settings. HT is not universally implemented in low‐ and middle‐income countries as a result of both limited resources and evidence. Facilitated passive cooling, comprising infants being allowed to passively lower their body temperature in the days after birth, is an emerging practice in some West African neonatal units. In this observational study, we demonstrate that infants undergoing facilitated passive cooling in a neonatal unit in Accra, Ghana, achieve temperatures within the HT target range ∼20% of the 72 h. Depth of HT fluctuates and can be excessive, as well as not maintained, especially after 24 h. Sustained and deeper passive cooling was evident for severe NE and for those that died. It is important to prevent excessive cooling, to understand that severe NE babies cool more and to be aware of facilitated passive cooling with respect to the design of clinical trials in low‐ and mid‐resource settings.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31168907</pmid><doi>10.1113/JP277820</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9346-5365</orcidid><orcidid>https://orcid.org/0000-0002-9816-4577</orcidid><orcidid>https://orcid.org/0000-0002-5783-0828</orcidid><orcidid>https://orcid.org/0000-0002-7490-7313</orcidid><orcidid>https://orcid.org/0000-0003-0131-4952</orcidid><oa>free_for_read</oa></addata></record>
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source Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Africa South of the Sahara
Babies
Body Temperature
Brain Diseases - epidemiology
Brain Diseases - therapy
Clinical trials
Encephalopathy
facilitated passive cooling
Female
Global health
Hospitals - statistics & numerical data
Humans
Hypothermia
Hypothermia, Induced - methods
Hypoxia
hypoxic ischaemic encephalopathy
Infant, Newborn
Infant, Newborn, Diseases - epidemiology
Infant, Newborn, Diseases - therapy
Infants
Ischemia
Male
neonatal encephalopathy
Neonates
Neuroprotection
Neuroscience
Research Paper
Temperature
Temperature effects
therapeutic hypothermia
title Core temperature after birth in babies with neonatal encephalopathy in a sub‐Saharan African hospital setting
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