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Titolo:
THE FIBEROPTIC INTRAPARENCHYMAL CEREBRAL PRESSURE MONITOR IN 244 PATIENTS
Autore:
SHAPIRO S; BOWMAN R; CALLAHAN J; WOLFLA C;
Indirizzi:
WISHARD MEM HOSP,ROOM 323,E OUTPATIENT BLDG,1001 W 10TH ST INDIANAPOLIS IN 46202 INDIANA UNIV,MED CTR,DEPT NEUROSURG INDIANAPOLIS IN 00000
Titolo Testata:
Surgical neurology
fascicolo: 3, volume: 45, anno: 1996,
pagine: 278 - 281
SICI:
0090-3019(1996)45:3<278:TFICPM>2.0.ZU;2-6
Fonte:
ISI
Lingua:
ENG
Soggetto:
FULMINANT HEPATIC-FAILURE; INTRACRANIAL-PRESSURE; DEVICE;
Keywords:
ICP; ICP MONITOR; FIBEROPTIC; INTRACRANIAL PRESSURE MONITOR;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Science Citation Index Expanded
Citazioni:
13
Recensione:
Indirizzi per estratti:
Citazione:
S. Shapiro et al., "THE FIBEROPTIC INTRAPARENCHYMAL CEREBRAL PRESSURE MONITOR IN 244 PATIENTS", Surgical neurology, 45(3), 1996, pp. 278-281

Abstract

BACKGROUND The fiberoptic intraparenchymal pressure monitor has been shown to provide reliable data in patients monitored for a short period of time, An analysis of a large population, including patients monitored for a prolonged period such as weeks, has never been performed. METHODS We conducted a retrospective study in which we evaluated the fiberoptic intraparenchymal cerebral pressure monitor for complications and accuracy. RESULTS The fiberoptic intraparenchymal cerebral pressure (ICP) monitor was used in 244 patients since 1988. Pathology included trauma in 180, intracerebral hemorrhage (ICK) in 19, aneurysmal subarachnoid hemorrhage in 16, arteriovenous malformations in 10, cerebraledema in 12, and tumor in 7. The mean length of monitoring was 7 dayswith 49 patients (20%) monitored 1-2 days, 105 (43%) monitored 3-6 days, 48 monitored for 7-10 days (20%), and 42 (17%) monitored from 10-24 days. Seventy-four 0patients also had ventriculostomies and there was strong correlation with the TCP monitor (p < 0.001). Complications from insertion were 2 patients (0.8%) with ICH, both with hepatic dysfunction. In the group monitored greater than 6 days, 34 patients (38%) required at least one catheter change due to upward drift of the ICP. Fiberoptic breakage requiring replacement was documented in 41 patients (16%). An insertion-site infection occurred in one case monitored for 23 days. Two infected bone flaps occurred that had a monitor placed in the flap. There were no cases of bacterial meningitis or cerebral abscess. CONCLUSIONS The monitor is easy, safe, and reliable to use with a very low rate of infection, Coagulopathic patients may best be monitored by an alternative method.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/09/20 alle ore 22:41:51