search
for
 About Bioline  All Journals  Testimonials  Membership  News


Neurology India
Medknow Publications on behalf of the Neurological Society of India
ISSN: 0028-3886 EISSN: 1998-4022
Vol. 53, Num. 2, 2005, pp. 206-207

Neurology India, Vol. 53, No. 2, April-June, 2005, pp. 206-207

Invited Comments

Invited Comment

Department of Neurology, The Institute of Neurological Sciences, CARE Hospital, Hyderabad
Correspondence Address: Department of Neurology, The Institute of Neurological Sciences, CARE Hospital, Hyderabad, jmkmurthy@satyam.net.in

Code Number: ni05062

Related article: ni05060

Fever is frequent in patients with acute neurolgic insult admitted to neurological intensive care units (ICU).[1],[2],[3] There is growing evidence that elevated body temperature may be deleterious in this population. Fever was independently associated with a longer ICU and hospital length of stay (LOS) in a dose-dependent manner, and also with higher mortality rate, and worse outcome. The relationship between elevated body temperature and hospital LOS was significant in all diagnosis groups except spine disease, brain tumors, and subdural hematomas.[3]

The incidence of fever after supratentorial intracerebral hemorrhage (ICH) is high, especially in patients with intraventricular hemorrhage (IVH).[4] Both ICH and subarchnoid hemorrhage (SAH) increase the risk of developing of unexplained, ′central′ fever.[2],[4] The study by Diogaonkar et al .[5] in this issue of the journal confirms the same. Refractory high fever (>42°C) in the immediate aftermath of massive supratentorial or brainstem ICH is well described, and is the basic observation supporting ′central fever′ as a clinical entity.[6],[7],[8] What factors increase the risk for developing ′central fever′ in patients with ICH is not clear. In the Columbia study intraventricular catheter (IVC) placement in patients with SAH and ICH was independently associated with ′central fever.′[2] Fever is generally has been associated with IVH in ICH patients.[4] Both these observations suggest that IVH can cause ′central fever.′ The study by Diogaonkar et al .[5] demonstrates the relationship between elevated body temperature and third ventricular shift. How IVH and third ventricular shift affect hypothalamic function and cause ′central fever′ is speculative.[9] One of the possible mechanisms as suggest by Diogaonkar et al .[5] is by hypothalamic compression resulting in hypothalamic dendrites to buckle and thereby disruption temperature homeostasis. In patients with IVH it may be related to direct hemotoxic damage to thermoregulatory centers.[5]

The risk of developing fever with these risk factors, IVH and third ventricular shift, in patients with ICH is sufficiently high to warrant early active intervention to maintain normothermia and prevent fever. The impact of elevated body temperature control on outcome in patients with acute brain insult, however, has not yet been tested. There has been no prospective study of an attempt to maintain euthermia in patients with acute brain insults. Thus it remains unproven as to whether control of elevated body temperature could improve outcome or decrease hospital LOS. Conventional means of treating fever are not very effective. Acetaminophen and air-cooling blankets effectively treat elevated body temperature in less than half of the patients.[10] Recently studies showed catheter-based heat exchange system significantly improves fever reduction in NICU patients.[11] As we now have an effective tool, catheter-based heat exchange system, for treating fever in this population of patients, an outcome study is possible and should be performed.

REFERENCES

1.Kilpatrick MM, Lowery DW, Firlik AD, Yonas H, Marion DW. Hyperthermia in the neurosurgical intensive care unit. Neurosurgery 2000; 47:850-856.  Back to cited text no. 1    
2.Commichau C, Scarmeas N, Mayer SA. Risk factors for fever in the neurologic intensive care unit. Neurology 2003; 60: 837-41.  Back to cited text no. 2  [PUBMED]  [FULLTEXT]
3.Diringer M, Reaven NL, Funk SE, Uman GC. Elevated body temperature independently contributes to increased length of stay in neurolgic intensive care unit patient. Crit Care Med 2004; 32; 1489-1405.   Back to cited text no. 3    
4.Schwarz S, Hafner K, Aschoff A, Schwab S. Incidence and prognostic significance of fever following intracerebral hemorrhage. Neurology 2000; 54: 354-361.   Back to cited text no. 4  [PUBMED]  [FULLTEXT]
5.Diogaonkar A, De Georgia M, Bae C, Abou-Chebl A, Andrefsky J. Fever is associated with third ventricular shift after intracerebral hemorrhage: pathophysiological implications. Neurol India 2005; 53: 202-6.   Back to cited text no. 5    
6.Chin RL. High temperature with cerebral hemorrhage. Ann Emerg Med 1999; 34: 411. Letter  Back to cited text no. 6    
7.Kitanaka C, Inoh Y, Toyoda T, Sasaki T, Eguchi T. Malignant brain stem hyperthermia caused by brain stem hemorrhage. Stroke 1994; 25: 518-520.  Back to cited text no. 7  [PUBMED]  
8.Erickson TC. Neurogenic hyperthermia (a clinical syndrome and its treatment). Brain 1939; 62: 172-190.  Back to cited text no. 8    
9.Shibata M. Hyperthermia in brain hemorrhage. Med Hypoth 1998; 50: 185-190.   Back to cited text no. 9  [PUBMED]  
10.Mayer SA, Commichau C, Scarmeas N, et al . Clinical trial of an air-circulating cooling blanket for fever control in neuro-ICU patients. Neurology 2001; 56: 292-298.   Back to cited text no. 10    
11.Diringer M for the Neurocritical Care Fever Reduction Trial Group. Treatment of fever in the neurologic intensive care unit with a catheter-based heat exchange system. Crit Care Med 2004; 32: 559-564.   Back to cited text no. 11    

Copyright 2005 - Neurology India

Home Faq Resources Email Bioline
© Bioline International, 1989 - 2024, Site last up-dated on 01-Sep-2022.
Site created and maintained by the Reference Center on Environmental Information, CRIA, Brazil
System hosted by the Google Cloud Platform, GCP, Brazil