Detection and monitoring of intracranial pressure dysregulation in liver failure by ultrasound

Citation
K. Helmke et al., Detection and monitoring of intracranial pressure dysregulation in liver failure by ultrasound, TRANSPLANT, 70(2), 2000, pp. 392-395
Citations number
10
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
TRANSPLANTATION
ISSN journal
00411337 → ACNP
Volume
70
Issue
2
Year of publication
2000
Pages
392 - 395
Database
ISI
SICI code
0041-1337(20000727)70:2<392:DAMOIP>2.0.ZU;2-1
Abstract
Background Development of elevated intracranial pressure (ICP) in hepatic f ailure indicates poor prognosis. Its detection by invasive methods poses me thodological problems. We applied ultrasound studies of the optic nerves to noninvasively estimated ICP status, Methods. A total of 22 pediatric patients with hepatic failure mere examine d by serial B scan ultrasound and followed up clically. Outcome was scored as survival or death due to multiorgan failure (MOF) or raised ICP, In 18 p atients, transplantations were performed, Resulsts. Four patients died before transplantation was possible (raised IC P: n=3, MOF: n=1). After OLT there mere 10 survivors and 8 patients died (M OF: n=3, raised ICP: n=5). In 10 patients we found optic nerve sheath diame ter (ONSD) above normal limits. Eight patients died, mostly because of rais ed ICP (n=7). Only 2 of the 10 survivors experienced a transient ONSD incre ase, steadily normalized after transplantation. Preoperatively, normal ONSD was detected in four of seven patients. The outcome of these four eases wa s clearly superior (three survivors and one MOF) compared with abnormal pre -OLT ultrasound findings (raised ICP: n=3), Conclusion. Patients with poor prognosis related to raised ICP in pediatric liver failure can be identified by ultrasound measurement of ONSD without the disadvantages of invasive procedures. Although the exact intracranial p ressure level cannot be deduced from single examinations, ONSD trends can r eflect the evolution of ICP in hepatic encephalopathy.