Cargando…
Protocolized Brain Oxygen Optimization in Subarachnoid Hemorrhage
BACKGROUND: Brain tissue hypoxia (P(bt)O(2) < 20 mmHg) is common after subarachnoid hemorrhage (SAH) and associated with poor outcome. Recent data suggest that brain oxygen optimization is feasible and reduces the time spent with P(bt)O(2) < 20 mmHg from 45 to 16% in patients with severe traum...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757026/ https://www.ncbi.nlm.nih.gov/pubmed/31218640 http://dx.doi.org/10.1007/s12028-019-00753-0 |
_version_ | 1783453499185430528 |
---|---|
author | Rass, Verena Solari, Daria Ianosi, Bogdan Gaasch, Max Kofler, Mario Schiefecker, Alois J. Miroz, John-Paul Morelli, Paola Thomé, Claudius Beer, Ronny Pfausler, Bettina Oddo, Mauro Helbok, Raimund |
author_facet | Rass, Verena Solari, Daria Ianosi, Bogdan Gaasch, Max Kofler, Mario Schiefecker, Alois J. Miroz, John-Paul Morelli, Paola Thomé, Claudius Beer, Ronny Pfausler, Bettina Oddo, Mauro Helbok, Raimund |
author_sort | Rass, Verena |
collection | PubMed |
description | BACKGROUND: Brain tissue hypoxia (P(bt)O(2) < 20 mmHg) is common after subarachnoid hemorrhage (SAH) and associated with poor outcome. Recent data suggest that brain oxygen optimization is feasible and reduces the time spent with P(bt)O(2) < 20 mmHg from 45 to 16% in patients with severe traumatic brain injury. Here, we intended to quantify the brain tissue hypoxia burden despite implementation of a protocolized treatment approach in poor-grade SAH patients and to identify the simultaneous occurrence of pathologic values potentially amenable to treatment. METHODS: We present a bi-centric observational cohort study including 100 poor-grade SAH patients admitted to two tertiary care centers who underwent multimodal brain monitoring and were managed with a P(bt)O(2)-targeted protocolized approach. P(bt)O(2) optimization (≥ 20 mmHg) included a stepwise neuro-intensive care approach, aiming to prevent low cerebral perfusion pressure (CPP), and blood hemoglobin, and to keep normocapnia, normoxemia, and normothermia. Based on routine blood gas analysis, hemoglobin, PaCO(2,) and PaO(2) data were matched to 2-h averaged data of continuous CPP, P(bt)O(2), core temperature, and to hourly cerebral microdialysis (CMD) samples over the first 11 days. RESULTS: Patients had a Glasgow Coma Scale of 3 (IQR 3–4) and were 58 years old (IQR 48–66). Overall incidence of brain tissue hypoxia was 25%, which was not different between both sites despite differences in the treatment approach. During brain tissue hypoxia, episodes of CPP < 70 mmHg (27%), PaCO(2) < 35 mmHg (19%), PaO(2) < 80 mmHg (14%), Hb < 9 g/dL (11%), metabolic crisis (CMD-lactate/pyruvate ratio > 40, and CMD-glucose < 0.7 mmol/L; 7%), and temperature > 38.3 °C (4%) were common. CONCLUSIONS: Our results demonstrate that brain tissue hypoxia remains common despite implementation of a P(bt)O(2)-targeted therapy in poor-grade SAH patients, suggesting room for further optimization. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12028-019-00753-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6757026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-67570262019-10-07 Protocolized Brain Oxygen Optimization in Subarachnoid Hemorrhage Rass, Verena Solari, Daria Ianosi, Bogdan Gaasch, Max Kofler, Mario Schiefecker, Alois J. Miroz, John-Paul Morelli, Paola Thomé, Claudius Beer, Ronny Pfausler, Bettina Oddo, Mauro Helbok, Raimund Neurocrit Care Original Work BACKGROUND: Brain tissue hypoxia (P(bt)O(2) < 20 mmHg) is common after subarachnoid hemorrhage (SAH) and associated with poor outcome. Recent data suggest that brain oxygen optimization is feasible and reduces the time spent with P(bt)O(2) < 20 mmHg from 45 to 16% in patients with severe traumatic brain injury. Here, we intended to quantify the brain tissue hypoxia burden despite implementation of a protocolized treatment approach in poor-grade SAH patients and to identify the simultaneous occurrence of pathologic values potentially amenable to treatment. METHODS: We present a bi-centric observational cohort study including 100 poor-grade SAH patients admitted to two tertiary care centers who underwent multimodal brain monitoring and were managed with a P(bt)O(2)-targeted protocolized approach. P(bt)O(2) optimization (≥ 20 mmHg) included a stepwise neuro-intensive care approach, aiming to prevent low cerebral perfusion pressure (CPP), and blood hemoglobin, and to keep normocapnia, normoxemia, and normothermia. Based on routine blood gas analysis, hemoglobin, PaCO(2,) and PaO(2) data were matched to 2-h averaged data of continuous CPP, P(bt)O(2), core temperature, and to hourly cerebral microdialysis (CMD) samples over the first 11 days. RESULTS: Patients had a Glasgow Coma Scale of 3 (IQR 3–4) and were 58 years old (IQR 48–66). Overall incidence of brain tissue hypoxia was 25%, which was not different between both sites despite differences in the treatment approach. During brain tissue hypoxia, episodes of CPP < 70 mmHg (27%), PaCO(2) < 35 mmHg (19%), PaO(2) < 80 mmHg (14%), Hb < 9 g/dL (11%), metabolic crisis (CMD-lactate/pyruvate ratio > 40, and CMD-glucose < 0.7 mmol/L; 7%), and temperature > 38.3 °C (4%) were common. CONCLUSIONS: Our results demonstrate that brain tissue hypoxia remains common despite implementation of a P(bt)O(2)-targeted therapy in poor-grade SAH patients, suggesting room for further optimization. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12028-019-00753-0) contains supplementary material, which is available to authorized users. Springer US 2019-06-19 2019 /pmc/articles/PMC6757026/ /pubmed/31218640 http://dx.doi.org/10.1007/s12028-019-00753-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Work Rass, Verena Solari, Daria Ianosi, Bogdan Gaasch, Max Kofler, Mario Schiefecker, Alois J. Miroz, John-Paul Morelli, Paola Thomé, Claudius Beer, Ronny Pfausler, Bettina Oddo, Mauro Helbok, Raimund Protocolized Brain Oxygen Optimization in Subarachnoid Hemorrhage |
title | Protocolized Brain Oxygen Optimization in Subarachnoid Hemorrhage |
title_full | Protocolized Brain Oxygen Optimization in Subarachnoid Hemorrhage |
title_fullStr | Protocolized Brain Oxygen Optimization in Subarachnoid Hemorrhage |
title_full_unstemmed | Protocolized Brain Oxygen Optimization in Subarachnoid Hemorrhage |
title_short | Protocolized Brain Oxygen Optimization in Subarachnoid Hemorrhage |
title_sort | protocolized brain oxygen optimization in subarachnoid hemorrhage |
topic | Original Work |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757026/ https://www.ncbi.nlm.nih.gov/pubmed/31218640 http://dx.doi.org/10.1007/s12028-019-00753-0 |
work_keys_str_mv | AT rassverena protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT solaridaria protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT ianosibogdan protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT gaaschmax protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT koflermario protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT schiefeckeraloisj protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT mirozjohnpaul protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT morellipaola protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT thomeclaudius protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT beerronny protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT pfauslerbettina protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT oddomauro protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage AT helbokraimund protocolizedbrainoxygenoptimizationinsubarachnoidhemorrhage |