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The Importance of P(bt)O(2) Probe Location for Data Interpretation in Patients with Intracerebral Hemorrhage

BACKGROUND/OBJECTIVE: Monitoring of brain tissue oxygen tension (P(bt)O(2)) provides insight into brain pathophysiology after intracerebral hemorrhage (ICH). Integration of probe location is recommended to optimize data interpretation. So far, little is known about the importance of P(bt)O(2) cathet...

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Detalles Bibliográficos
Autores principales: Lindner, Anna, Rass, Verena, Ianosi, Bogdan-Andrei, Schiefecker, Alois J., Kofler, Mario, Rhomberg, Paul, Pfausler, Bettina, Beer, Ronny, Schmutzhard, Erich, Thomé, Claudius, Helbok, Raimund
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179893/
https://www.ncbi.nlm.nih.gov/pubmed/32918157
http://dx.doi.org/10.1007/s12028-020-01089-w
Descripción
Sumario:BACKGROUND/OBJECTIVE: Monitoring of brain tissue oxygen tension (P(bt)O(2)) provides insight into brain pathophysiology after intracerebral hemorrhage (ICH). Integration of probe location is recommended to optimize data interpretation. So far, little is known about the importance of P(bt)O(2) catheter location in ICH patients. METHODS: We prospectively included 40 ICH patients after hematoma evacuation (HE) who required P(bt)O(2)-monitoring. P(bt)O(2)-probe location was evaluated in all head computed tomography (CT) scans within the first 6 days after HE and defined as location in the healthy brain tissue or perilesional when the catheter tip was located within 1 cm of a focal lesion (hypodense or hyperdense). Generalized estimating equations were used to investigate levels of P(bt)O(2) in relation to different probe locations. RESULTS: Patients were 60 [51–66] years old and had a median ICH-volume of 47 [29–60] mL. Neuromonitoring probes remained for a median of 6 [2–11] days. P(bt)O(2)-probes were located in healthy brain tissue in 18/40 (45%) patients and in perilesional brain tissue in 22/40 (55%) patients. In the acute phase after HE (0–72 h), P(bt)O(2) levels were significantly lower (21 ± 12 mmHg vs. 29 ± 10 mmHg, p = 0.010) and brain tissue hypoxia (BTH) was more common in the perilesional area as compared to healthy brain tissue (46% vs. 19%, adjOR 4.0, 95% CI 1.54–10.58, p = 0.005). Episodes of BTH significantly decreased over time in patients with probes in perilesional location (p = 0.001) but remained stable in normal appearing area (p = 0.485). A significant association between BTH and poor functional outcome was only found when probes were located in the perilesional brain tissue (adjOR 6.6, 95% CI 1.3–33.8, p = 0.023). CONCLUSIONS: In the acute phase, BTH was more common in the perilesional area compared to healthy brain tissue. The improvement of BTH in the perilesional area over time may be the result of targeted treatment interventions and tissue regeneration. Due to the localized measurement of invasive neuromonitoring devices, integration of probe location in the clinical management of ICH patients and in research protocols seems mandatory.