Abstract
Inflammation is an important part of the normal physiologic response to acute brain injury (ABI). How inflammation is manifest determines if it augments or hinders the resolution of ABI. Monitoring body temperature, the cellular arm of the inflammatory cascade, and inflammatory proteins may help guide therapy. This summary will address the utility of inflammation monitoring in brain-injured adults. An electronic literature search was conducted for English language articles describing the testing, utility, and optimal methods to measure inflammation in ABI. Ninety-four articles were included in this review. Current evidence suggests that control of inflammation after ABI may hold promise for advances in good outcomes. However, our understanding of how much inflammation is good and how much is deleterious is not yet clear. Several important concepts emerge form our review. First, while continuous temperature monitoring of core body temperature is recommended, temperature pattern alone is not useful in distinguishing infectious from noninfectious fever. Second, when targeted temperature management is used, shivering should be monitored at least hourly. Finally, white blood cell levels and protein markers of inflammation may have a limited role in distinguishing infectious from noninfectious fever. Our understanding of optimal use of inflammation monitoring after ABI is limited currently but is an area of active investigation.
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Abbreviations
- SAH:
-
Subarachnoid hemorrhage
- DCI:
-
Delayed cerebral injury associated with vasospasm
- IL-6:
-
Intraleukin 6
- CRP:
-
C-reactive protein
- TTM:
-
Therapeutic temperature modulation
- WBC:
-
White blood cell count
- TNFα:
-
Tumor necrosis factor
- SIRS:
-
Systemic inflammatory response syndrome
- BSAS:
-
Bedside Shivering Assessment Scale
- IDC:
-
Indirect calorimetry
References
Tracy RP. The five cardinal signs of inflammation: calor, dolor, rubor, tumor… and penuria (apologies to Aulus Cornelius Celsus, De medicina, c. A.D. 25). J Gerontol A. 2006;61(10):1051–2.
Poungvarin N, et al. Effects of dexamethasone in primary supratentorial intracerebral hemorrhage. N Engl J Med. 1987;316(20):1229–33.
Moher D, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J Clin Epidemiol. 2009;62(10):1006–12.
Childs C, et al. Brain temperature and outcome after severe traumatic brain injury. Neurocrit Care. 2006;5(1):10–4.
Fernandez A, et al. Fever after subarachnoid hemorrhage: risk factors and impact on outcome. Neurology. 2007;68(13):1013–9.
Muehlschlegel S, et al. Frequency and impact of intensive care unit complications on moderate-severe traumatic brain injury: early results of the Outcome Prognostication in Traumatic Brain Injury (OPTIMISM) Study. Neurocrit Care. 2013;18(3):318–31.
Oliveira-Filho J, et al. Fever in subarachnoid hemorrhage: relationship to vasospasm and outcome. Neurology. 2001;56(10):1299–304.
Zhang G, Zhang JH, Qin X. Fever increased in-hospital mortality after subarachnoid hemorrhage. Acta Neurochir Suppl. 2011;110(Pt 1):239–43.
Badjatia N, et al. Impact of induced normothermia on outcome after subarachnoid hemorrhage: a case–control study. Neurosurgery. 2010;66(4):696–700; discussion 700–1.
Oddo M, et al. Induced normothermia attenuates cerebral metabolic distress in patients with aneurysmal subarachnoid hemorrhage and refractory Fever. Stroke. 2009;40(5):1913–6.
Puccio AM, et al. Induced normothermia attenuates intracranial hypertension and reduces fever burden after severe traumatic brain injury. Neurocrit Care. 2009;11(1):82–7.
Thompson HJ, Pinto-Martin J, Bullock MR. Neurogenic fever after traumatic brain injury: an epidemiological study. J Neurol Neurosurg Psychiatry. 2003;74(5):614–9.
Albrecht RF 2nd, Wass CT, Lanier WL. Occurrence of potentially detrimental temperature alterations in hospitalized patients at risk for brain injury. Mayo Clin Proc. 1998;73(7):629–35.
Childers MK, Rupright J, Smith DW. Post-traumatic hyperthermia in acute brain injury rehabilitation. Brain Inj. 1994;8(4):335–43.
Meythaler JM, Stinson AM 3rd. Fever of central origin in traumatic brain injury controlled with propranolol. Arch Phys Med Rehabil. 1994;75(7):816–8.
Shapiro NI, et al. Who needs a blood culture? A prospectively derived and validated prediction rule. J Emerg Med. 2008;35(3):255–64.
Darm RM, Hecker RB, Rubal BJ. A comparison of noninvasive body temperature monitoring devices in the PACU. J Post Anesth Nurs. 1994;9(3):144–9.
Erickson RS, Kirklin SK. Comparison of ear-based, bladder, oral, and axillary methods for core temperature measurement. Crit Care Med. 1993;21(10):1528–34.
Henker R, Coyne C. Comparison of peripheral temperature measurements with core temperature. AACN. 1995;6(1):21–30.
Jensen BN, et al. Accuracy of digital tympanic, oral, axillary, and rectal thermometers compared with standard rectal mercury thermometers. Eur J Surg. 2000;166(11):848–51.
Konopad E, et al. A comparison of oral, axillary, rectal and tympanic-membrane temperatures of intensive care patients with and without an oral endotracheal tube. J Adv Nurs. 1994;20(1):77–84.
Lattavo K, Britt J, Dobal M. Agreement between measures of pulmonary artery and tympanic temperatures. Res Nurs Health. 1995;18(4):365–70.
Schmitz T, et al. A comparison of five methods of temperature measurement in febrile intensive care patients. Am J Crit Care. 1995;4(4):286–92.
Singh V, et al. Variation of axillary temperature and its correlation with oral temperature. J Assoc Physicians India. 2000;48(9):898–900.
Smith LS. Temperature measurement in critical care adults: a comparison of thermometry and measurement routes. Biol Res Nurs. 2004;6(2):117–25.
Badjatia N, et al. Metabolic benefits of surface counter warming during therapeutic temperature modulation. Crit Care Med. 2009;37(6):1893–7.
Badjatia N, et al. Metabolic impact of shivering during therapeutic temperature modulation: the Bedside Shivering Assessment Scale. Stroke. 2008;39(12):3242–7.
Hata JS, et al. A prospective, observational clinical trial of fever reduction to reduce systemic oxygen consumption in the setting of acute brain injury. Neurocrit Care. 2008;9(1):37–44.
Sessler DI. Defeating normal thermoregulatory defenses: induction of therapeutic hypothermia. Stroke. 2009;40(11):e614–21.
Olson DM, et al. Interrater reliability of the bedside shivering assessment scale. Am J Crit Care. 2013;22(1):70–4.
Choi HA, et al. Prevention of shivering during therapeutic temperature modulation: the Columbia anti-shivering protocol. Neurocrit Care. 2011;14(3):389–94.
May T, et al. Association of the Bedside Shivering Assessment Scale and derived EMG power during therapeutic hypothermia in survivors of cardiac arrest. Resuscitation. 2011;82(8):1100–3.
Yoshimoto Y, Tanaka Y, Hoya K. Acute systemic inflammatory response syndrome in subarachnoid hemorrhage. Stroke. 2001;32(9):1989–93.
Tam AK, et al. Impact of systemic inflammatory response syndrome on vasospasm, cerebral infarction, and outcome after subarachnoid hemorrhage: exploratory analysis of CONSCIOUS-1 database. Neurocrit Care. 2010;13(2):182–9.
Suzuki S, et al. Acute leukocyte and temperature response in hypertensive intracerebral hemorrhage. Stroke. 1995;26(6):1020–3.
Sturgeon JD, et al. Hemostatic and inflammatory risk factors for intracerebral hemorrhage in a pooled cohort. Stroke. 2008;39(8):2268–73.
Stambrook M, et al. Early metabolic and neurologic predictors of long-term quality of life after closed head injury. Can J Surg. 1990;33(2):115–8.
Sadamasa N, et al. Prediction of mortality by hematological parameters on admission in patients with subarachnoid hemorrhage. Neurol Med Chir. 2011;51(11):745–8.
Nuytinck HK, et al. Whole-body inflammation in trauma patients. An autopsy study. Arch Surg. 1988;123(12):1519–24.
Muroi C, et al. Systemic interleukin-6 levels reflect illness course and prognosis of patients with spontaneous nonaneurysmal subarachnoid hemorrhage. Acta Neurochir Suppl. 2013;115:77–80.
Mrakovcic-Sutic I, et al. Early changes in frequency of peripheral blood lymphocyte subpopulations in severe traumatic brain-injured patients. Scand J Immunol. 2010;72(1):57–65.
Mathiesen T, Lefvert AK. Cerebrospinal fluid and blood lymphocyte subpopulations following subarachnoid haemorrhage. Br J Neurosurg. 1996;10(1):89–92.
Holling M, et al. Prognostic value of histopathological findings in aneurysmal subarachnoid hemorrhage. J Neurosurg. 2009;110(3):487–91.
Forster K, et al. Elevated inflammatory laboratory parameters in spontaneous cervical artery dissection as compared to traumatic dissection: a retrospective case–control study. J Neurol. 2006;253(6):741–5.
Di Piero V, Bastianello S. Prognostic value of peripheral white blood cell count in intracerebral hemorrhage. Stroke. 1987;18(5):957.
Chou SH, et al. Elevated peripheral neutrophils and matrix metalloproteinase 9 as biomarkers of functional outcome following subarachnoid hemorrhage. Transl Stroke Res. 2011;2(4):600–7.
Agnihotri S, et al. Peripheral leukocyte counts and outcomes after intracerebral hemorrhage. J Neuroinflammation. 2011;8:160.
Grau AJ, et al. Increased cytokine release by leucocytes in survivors of stroke at young age. Eur J Clin Invest. 2001;31(11):999–1006.
Maiuri F, et al. The blood leukocyte count and its prognostic significance in subarachnoid hemorrhage. J Neurosurg Sci. 1987;31(2):45–8.
Spallone A, et al. Relationship between leukocytosis and ischemic complications following aneurysmal subarachnoid hemorrhage. Surg Neurol. 1987;27(3):253–8.
Rothoerl RD, et al. Possible role of the C-reactive protein and white blood cell count in the pathogenesis of cerebral vasospasm following aneurysmal subarachnoid hemorrhage. J Neurosurg Anesthesiol. 2006;18(1):68–72.
Provencio JJ, et al. CSF neutrophils are implicated in the development of vasospasm in subarachnoid hemorrhage. Neurocrit Care. 2010;12(2):244–51.
Niikawa S, et al. Correlation between blood parameters and symptomatic vasospasm in subarachnoid hemorrhage patients. Neurol Med Chir. 1997;37(12):881–4; discussion 884–5.
McGirt MJ, et al. Leukocytosis as an independent risk factor for cerebral vasospasm following aneurysmal subarachnoid hemorrhage. J Neurosurg. 2003;98(6):1222–6.
Kasius KM, et al. Association of platelet and leukocyte counts with delayed cerebral ischemia in aneurysmal subarachnoid hemorrhage. Cerebrovasc Dis. 2010;29(6):576–83.
Sun W, et al. Correlation of leukocytosis with early neurological deterioration following supratentorial intracerebral hemorrhage. J Clin Neurosci. 2012;19(8):1096–100.
Cortina MG, et al. Monocyte count is an underlying marker of lacunar subtype of hypertensive small vessel disease. Eur J Neurol. 2008;15(7):671–6.
Kitchen WJ, et al. External ventricular drain infection: improved technique can reduce infection rates. Br J Neurosurg. 2011;25(5):632–5.
Aucoin PJ, et al. Intracranial pressure monitors. Epidemiologic study of risk factors and infections. Am J Med. 1986;80(3):369–76.
Mayhall CG, et al. Ventriculostomy-related infections. A prospective epidemiologic study. N Engl J Med. 1984;310(9):553–9.
Sundbarg G, Nordstrom CH, Soderstrom S. Complications due to prolonged ventricular fluid pressure recording. Br J Neurosurg. 1988;2(4):485–95.
Beeftink MM, et al. Relation of serum TNF-alpha and TNF-alpha genotype with delayed cerebral ischemia and outcome in subarachnoid hemorrhage. Neurocrit Care. 2011;15(3):405–9.
Chou SH, et al. Early elevation of serum tumor necrosis factor-alpha is associated with poor outcome in subarachnoid hemorrhage. J Investig Med. 2012;60(7):1054–8.
Csuka E, et al. IL-10 levels in cerebrospinal fluid and serum of patients with severe traumatic brain injury: relationship to IL-6, TNF-alpha, TGF-beta1 and blood-brain barrier function. J Neuroimmunol. 1999;101(2):211–21.
Dalla Libera AL, et al. IL-6 polymorphism associated with fatal outcome in patients with severe traumatic brain injury. Brain Inj. 2011;25(4):365–9.
Helmy A, et al. The cytokine response to human traumatic brain injury: temporal profiles and evidence for cerebral parenchymal production. J Cereb Blood Flow Metab. 2011;31(2):658–70.
Hergenroeder GW, et al. Serum IL-6: a candidate biomarker for intracranial pressure elevation following isolated traumatic brain injury. J Neuroinflamm. 2010;7:19.
Kirchhoff C, et al. Cerebrospinal IL-10 concentration is elevated in non-survivors as compared to survivors after severe traumatic brain injury. Eur J Med Res. 2008;13(10):464–8.
Li W, et al. Elevated cerebral cortical CD24 levels in patients and mice with traumatic brain injury: a potential negative role in nuclear factor kappa B/inflammatory factor pathway. Mol Neurobiol. 2013;49:187–98.
Maier B, et al. Physiological levels of pro- and anti-inflammatory mediators in cerebrospinal fluid and plasma: a normative study. J Neurotrauma. 2005;22(7):822–35.
Maier B, et al. Delayed elevation of soluble tumor necrosis factor receptors p75 and p55 in cerebrospinal fluid and plasma after traumatic brain injury. Shock. 2006;26(2):122–7.
Polin RS, et al. Detection of soluble E-selectin, ICAM-1, VCAM-1, and L-selectin in the cerebrospinal fluid of patients after subarachnoid hemorrhage. J Neurosurg. 1998;89(4):559–67.
Roberts DJ, et al. Association between the cerebral inflammatory and matrix metalloproteinase responses after severe traumatic brain injury in humans. J Neurotrauma. 2013;30:1727–36.
Semple BD, et al. Role of CCL2 (MCP-1) in traumatic brain injury (TBI): evidence from severe TBI patients and CCL2−/− mice. J Cereb Blood Flow Metab. 2010;30(4):769–82.
Singhal A, et al. Association between cerebrospinal fluid interleukin-6 concentrations and outcome after severe human traumatic brain injury. J Neurotrauma. 2002;19(8):929–37.
Suehiro E, et al. Increased matrix metalloproteinase-9 in blood in association with activation of interleukin-6 after traumatic brain injury: influence of hypothermic therapy. J Neurotrauma. 2004;21(12):1706–11.
Waters RJ, et al. Cytokine gene polymorphisms and outcome after traumatic brain injury. J Neurotrauma. 2013;30:1710–6.
Sarrafzadeh A, et al. Relevance of cerebral interleukin-6 after aneurysmal subarachnoid hemorrhage. Neurocrit Care. 2010;13(3):339–46.
Sattar N, et al. Are markers of inflammation more strongly associated with risk for fatal than for nonfatal vascular events? PLoS Med. 2009;6(6):e1000099.
Peltola HO. C-reactive protein for rapid monitoring of infections of the central nervous system. Lancet. 1982;1(8279):980–2.
Tanner AR, Collins AL, Bull FG. The clinical value of rapid C-reactive protein measurement in cerebro-spinal fluid. Clin Chim Acta. 1985;147(3):267–72.
Rajeshwar K, et al. C-reactive protein and nitric oxide levels in ischemic stroke and its subtypes: correlation with clinical outcome. Inflammation. 2012;35(3):978–84.
Seo WK, et al. C-reactive protein is a predictor of early neurologic deterioration in acute ischemic stroke. J Stroke Cerebrovasc Dis. 2012;21(3):181–6.
Hamidon BB, et al. The prognostic value of C-reactive protein (CRP) levels in patients with acute ischaemic stroke. Med J Malays. 2004;59(5):631–7.
Corso G, et al. Blood C-reactive protein concentration with ABCD(2) is a better prognostic tool than ABCD(2) alone. Cerebrovasc Dis. 2011;32(2):97–105.
Di Napoli M, et al. C-reactive protein level measurement improves mortality prediction when added to the spontaneous intracerebral hemorrhage score. Stroke. 2011;42(5):1230–6.
Roudbary SA, et al. Serum C-reactive protein level as a biomarker for differentiation of ischemic from hemorrhagic stroke. Acta Med Iran. 2011;49(3):149–52.
Jeon YT, et al. The postoperative C-reactive protein level can be a useful prognostic factor for poor outcome and symptomatic vasospasm in patients with aneurysmal subarachnoid hemorrhage. J Neurosurg Anesthesiol. 2012;24(4):317–24.
Juvela S, Kuhmonen J, Siironen J. C-reactive protein as predictor for poor outcome after aneurysmal subarachnoid haemorrhage. Acta Neurochir (Wien). 2012;154(3):397–404.
Berger C, et al. Serum procalcitonin in cerebral ventriculitis. Crit Care Med. 2002;30(8):1778–81.
Tomio R, et al. Procalcitonin as an early diagnostic marker for ventriculoperitoneal shunt infections. Surg Infect. 2013;14:433–6.
Muroi C, et al. Early systemic procalcitonin levels in patients with aneurysmal subarachnoid hemorrhage. Neurocrit Care. 2013;21:73–7.
Hug A, et al. Usefulness of serum procalcitonin levels for the early diagnosis of stroke-associated respiratory tract infections. Neurocrit Care. 2011;14(3):416–22.
Oconnor E, et al. Serum procalcitonin and C-reactive protein as markers of sepsis and outcome in patients with neurotrauma and subarachnoid haemorrhage. Anaesth Intensive Care. 2004;32(4):465–70.
Conflict of interest
Neeraj Badjatia receives consulting fees form Bard and Medivance and is a Scientific Advisor to Cumberland Pharmaceuticals. J. Javier Provencio receives research funding from NIH, Bard Medivance, and Advanced Circulatory Systems, and is on the scientific advisory board of Edge Therapeutics and Minnetronix.
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The Participants in the International Multi-disciplinary Consensus Conference on Multimodality Monitoring are listed in “Appendix”.
Appendix: Participants in the International Multi-Disciplinary Consensus Conference on Multimodality Monitoring
Appendix: Participants in the International Multi-Disciplinary Consensus Conference on Multimodality Monitoring
Peter Le Roux, MD, FACS
Brain and Spine Center
Suite 370, Medical Science Building
Lankenau Medical Center
100 East Lancaster Avenue
Wynnewood, PA 19096, USA
lerouxp@mlhs.org
David K Menon, MD, PhD, FRCP, FRCA, FFICM, FMedSci
Head, Division of Anaesthesia, University of Cambridge
Consultant, Neurosciences Critical Care Unit
Box 93, Addenbrooke’s Hospital
Cambridge CB2 2QQ, UK
dkm13@wbic.cam.ac.uk
Paul Vespa, MD, FCCM, FAAN, FNCS
Professor of Neurology and Neurosurgery
Director of Neurocritical Care
David Geffen School of Medicine at UCLA
Los Angeles, CA 90095, USA
PVespa@mednet.ucla.edu
Giuseppe Citerio
Director NeuroIntensive Care Unit
Department of Anesthesia and Critical Care
Ospedale San Gerardo, Monza
Via Pergolesi 33, Monza 20900, Italy
g.citerio@hsgerardo.org
Mary Kay Bader RN, MSN, CCNS, FAHA, FNCS
Neuro/Critical Care CNS
Mission Hospital
Mission Viejo, CA 92691, USA
Marykay.Bader@stjoe.org
Gretchen M. Brophy, PharmD, BCPS, FCCP, FCCM
Professor of Pharmacotherapy & Outcomes Science and Neurosurgery
Virginia Commonwealth University
Medical College of Virginia Campus
410 N. 12th Street
Richmond, VA 23298-0533, USA
gbrophy@vcu.edu
Michael N. Diringer, MD
Professor of Neurology, Neurosurgery & Anesthesiology
Chief, Neurocritical Care Section
Washington University
Dept. of Neurology, Campus Box 8111
660 S Euclid Ave
St Louis, MO 63110, USA
diringerm@neuro.wustl.edu
Nino Stocchetti, MD
Professor of Anesthesia and Intensive Care
Department of physiopathology and transplant
Milan University
Director Neuro ICU
Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico
Via F Sforza, 35, 20122 Milan, Italy
stocchet@policlinico.mi.it
Walter Videtta, MD
ICU Neurocritical Care
Hospital Nacional ‘Prof. a. Posadas’
El Palomar - Pcia. de Buenos Aires
Argentina
wvidetta@ar.inter.net
Rocco Armonda, MD
Department of Neurosurgery
MedStar Georgetown University Hospital
Medstar Health, 3800 Reservoir Road NW
Washington, DC 20007, USA
Rocco.Armonda@gmail.com
Neeraj Badjatia, MD
Department of Neurology
University of Maryland Medical Center
22 S Greene St
Baltimore, MD 21201, USA
nbadjatia@umm.edu
Julian Bösel, MD
Department of Neurology
Ruprect-Karls University
Hospital Heidelberg, Im Neuenheimer Feld 400
D-69120 Heidelberg, Germany
Julian.Boesel@med.uni-heidelberg.de
Randal Chesnut, MD, FCCM, FACS
Harborview Medical Center
University of Washington Mailstop 359766
325 Ninth Ave
Seattle, WA 98104-2499, USA
chesnutr@u.washington.edu
Sherry Chou, MD, MMSc
Department of Neurology
Brigham and Women’s Hospital
75 Francis Street
Boston, MA 02115 USA
schou1@partners.org
Jan Claassen, MD, PhD, FNCS
Assistant Professor of Neurology and Neurosurgery
Head of Neurocritical Care and Medical Director of the Neurological Intensive Care Unit
Columbia University College of Physicians & Surgeons
177 Fort Washington Avenue, Milstein 8 Center room 300
New York, NY 10032, USA
jc1439@cumc.columbia.edu
Marek Czosnyka, PhD
Department of Neurosurgery
University of Cambridge
Addenbrooke’s Hospital, Box 167
Cambridge CB20QQ, United Kingdom
mc141@medschl.cam.ac.uk
Michael De Georgia, MD
Professor of Neurology
Director, Neurocritical Care Center
Co-Director, Cerebrovascular Center
University Hospital Case Medical Center
Case Western Reserve University School of Medicine
11100 Euclid Avenue
Cleveland, OH 44106, USA
michael.degeorgia@uhhospitals.org
Anthony Figaji, MD, PhD
Head of Pediatric Neurosurgery
University of Cape Town
617 Institute for Child Health
Red Cross Children’s Hospital
Rondebosch, 7700 Cape Town, South Africa
anthony.figaji@uct.ac.za
Jennifer Fugate, DO
Department of Neurology
Mayo Clinic
200 First Street SW
Rochester, MN 55905, USA
Fugate.Jennifer@mayo.edu
Raimund Helbok, MD
Department of Neurology, Neurocritical Care Unit
Innsbruck Medical University
Anichstr. 35, 6020 Innsbruck, Austria
raimund.helbok@uki.at
David Horowitz, MD
Associate Chief Medical Officer
University of Pennsylvania Health System
3701 Market Street
Philadelphia, PA 19104, USA
david.horowitz@uphs.upenn.edu
Peter Hutchinson, MD
Professor of Neurosurgery
NIHR Research Professor
Department of Clinical Neurosciences
University of Cambridge
Box 167 Addenbrooke’s Hospital
Cambridge CB2 2QQ, United Kingdom
pjah2@cam.ac.uk
Monisha Kumar, MD
Department of Neurology
Perelman School of Medicine, University of Pennsylvania
3 West Gates, 3400 Spruce Street
Philadelphia, PA 19104, USA
monisha.kumar@uphs.upenn.edu
Molly McNett, RN, PhD
Director, Nursing Research
The MetroHealth System
2500 MetroHealth Drive
Cleveland, OH 44109, USA
mmcnett@metrohealth.org
Chad Miller, MD
Division of Cerebrovascular Diseases and Neurocritical Care
The Ohio State University
395 W. 12th Ave, 7th Floor
Columbus, OH 43210, USA
ChadM.Miller@osumc.edu
Andrew Naidech, MD, MSPH
Department of Neurology
Northwestern University Feinberg SOM 710
N Lake Shore Drive, 11th floor
Chicago, IL 60611, USA
ANaidech@nmff.org
Mauro Oddo, MD
Department of Intensive Care Medicine
CHUV University Hospital, BH 08-623
Faculty of Biology and Medicine, University of Lausanne
1011 Lausanne, Switzerland
Mauro.Oddo@chuv.ch
DaiWai Olson, RN, PhD
Associate Professor of Neurology, Neurotherapeutics and Neurosurgery
University of Texas Southwestern
5323 Harry Hines Blvd.
Dallas, TX 75390-8897, USA
daiwai.olson@utsouthwestern.edu
Kristine O’Phelan, MD
Director of Neurocritical Care
Associate Professor, Department of Neurology
University of Miami, Miller School of Medicine
JMH, 1611 NW 12th Ave, Suite 405
Miami, FL 33136, USA
USA
kophelan@med.miami.edu
J. Javier Provencio, MD
Associate Professor of Medicine
Cerebrovascular Center and Neuroinflammation Research Center
Lerner College of Medicine
Cleveland Clinic
9500 Euclid Ave, NC30
Cleveland, OH 44195, USA
provenj@ccf.org
Corina Puppo, MD
Assistant Professor, Intensive Care Unit
Hospital de Clinicas, Universidad de la República
Montevideo, Uruguay
coripuppo@gmail.com
Richard Riker, MD
Critical Care Medicine
Maine Medical Center
22 Bramhall Street
Portland, ME 04102-3175, USA
RRiker@cmamaine.com
Claudia Robertson, MD
Department of Neurosurgery
Medical Director of Center for Neurosurgical Intensive Care
Ben Taub Hospital
Baylor College of Medicine
1504 Taub Loop
Houston, TX 77030, USA
claudiar@bcm.tmc.edu
J. Michael Schmidt, PhD, MSc
Director of Neuro-ICU Monitoring and Informatics
Columbia University College of Physicians and Surgeons
Milstein Hospital 8 Garden South, Suite 331
177 Fort Washington Avenue
New York, NY 10032 ,USA
mjs2134@columbia.edu
Fabio Taccone, MD
Department of Intensive Care, Laboratoire de Recherche Experimentale
Erasme Hospital
Route de Lennik, 808
1070 Brussels, Belgium
ftaccone@ulb.ac.be
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Provencio, J.J., Badjatia, N. & And the Participants in the International Multi-disciplinary Consensus Conference on Multimodality Monitoring. Monitoring Inflammation (Including Fever) in Acute Brain Injury. Neurocrit Care 21 (Suppl 2), 177–186 (2014). https://doi.org/10.1007/s12028-014-0038-0
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DOI: https://doi.org/10.1007/s12028-014-0038-0