BACKGROUND
Mannitol is sometimes dramatically effective in reversing acute brain swelling, but its effectiveness in the on-going management of severe head injury remains open to question. There is evidence that in prolonged dosage mannitol may pass from the blood into the brain, where it might cause reverse osmotic shifts that increase intracranial pressure.
OBJECTIVES
To assess the effects of different mannitol therapy regimens, of mannitol compared to other intracranial pressure (ICP) lowering agents, and to quantify the effectiveness of mannitol administration given at other stages following acute traumatic brain injury.
SEARCH STRATEGY
The review drew on the search strategy for the Injuries Group as a whole. We checked reference lists of trials and review articles, and contacted authors of trials.
SELECTION CRITERIA
Randomised trials of mannitol, in patients with acute traumatic brain injury of any severity. The comparison group could be placebo-controlled, no drug, different dose, or different drug. Trials where the intervention was started more than eight weeks after injury, and cross-over trials were excluded.
DATA COLLECTION AND ANALYSIS
The reviewers independently rated quality of allocation concealment and extracted the data. Relative risks (RR) and 95% confidence intervals (CI) were calculated for each trial on an intention to treat basis.
MAIN RESULTS
Overall there were few eligible trials. There were no trials comparing different doses, or type of administration. One trial compared ICP-directed therapy to 'standard care' (RR for death= 0.83; 95% CI 0.47;1.46). One trial compared mannitol to pentobarbital (RR for death = 0.85; 95% CI 0. 52;1.38). No trials compared mannitol to other ICP lowering agents. One trial tested the effectiveness of pre-hospital administration of mannitol against placebo (RR for death=1.59; 95% CI 0.44;5.79).
REVIEWER'S CONCLUSIONS
There are insufficient data to recommend one form of mannitol infusion over another. Mannitol therapy for raised ICP may have a beneficial effect on mortality when compared to pentobarbital treatment. ICP-directed treatment shows a small beneficial effect compared to treatment directed by neurological signs and physiological indicators. There are insufficient data on the effectiveness of pre-hospital administration of mannitol to preclude either a harmful or a beneficial effect on mortality.
[1]
A. Murdoch.
Irish psychiatric workers criticised
,
1996,
BMJ.
[2]
M. Gaab,et al.
A Comparison Study Between Mannitol and Glycerol Therapy in Reducing Intracranial Pressure
,
1993
.
[3]
CPP and SJO2 with ICP Reduction Therapy After Severe Head Injury
,
1993
.
[4]
D K Menon,et al.
Survey of intensive care of severely head injured patients in the United Kingdom
,
1996,
BMJ.
[5]
Charles Tator,et al.
The University of Toronto Head Injury Treatment Study: A Prospective, Randomized Comparison of Pentobarbital and Mannitol
,
1984,
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[6]
D. Armstrong,et al.
Comparison of mannitol regimens in patients with severe head injury undergoing intracranial monitoring.
,
1986,
Journal of neurosurgery.
[7]
B Matta,et al.
Severe head injury in the United Kingdom and Ireland: a survey of practice and implications for management.
,
1996,
Critical care medicine.
[8]
J. Ghajar,et al.
Survey of critical care management of comatose, head-injured patients in the United States.
,
1995,
Critical care medicine.
[9]
M. Sayre,et al.
Out-of-hospital administration of mannitol to head-injured patients does not change systolic blood pressure.
,
1996,
Academic emergency medicine : official journal of the Society for Academic Emergency Medicine.
[10]
Effect of Hyperventilation, Mannitol, and Ventriculostomy Drainage on Cerebral Blood Flow after Head Injury
,
1994
.
[11]
A. Levin,et al.
Treatment of increased intracranial pressure: a comparison of different hyperosmotic agents and the use of thiopental.
,
1979,
Neurosurgery.
[12]
M. Gaab,et al.
THAM (Tromethamine, “Tris-Buffer”): Effective Therapy of Traumatic Brain Swelling?
,
1989
.
[13]
J. Cruz,et al.
Major Clinical and Physiological Benefits of Early High Doses of Mannitol for Intraparenchymal Temporal Lobe Hemorrhages with Abnormal Pupillary Widening: A Randomized Trial
,
2002,
Neurosurgery.
[14]
J. Cruz,et al.
Improving Clinical Outcomes from Acute Subdural Hematomas with the Emergency Preoperative Administration of High Doses of Mannitol: A Randomized Trial
,
2001,
Neurosurgery.