Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Neurocrit Care ; 8(3): 360-5, 2008.
Article in English | MEDLINE | ID: mdl-18320144

ABSTRACT

INTRODUCTION: Catheter-associated infection of cerebrospinal fluid (CSF) is a potentially life-threatening complication of external ventricular drainage (EVD). The purpose of this pilot study was to address the efficacy of silver-impregnated EVD catheters in neurological and neurosurgical patients requiring external CSF drainage due to acute occlusive hydrocephalus. METHODS: Nineteen consecutive patients were enrolled in the treatment arm of the study and data were prospectively recorded for these patients. The control group consisted of 20 patients for whom data were retrospectively assessed. CSF samples were drawn at least three times a week and routine bacterial cultures and CSF analyses were done according to standard protocols. The primary endpoint of the study was the occurrence of catheter-associated ventriculitis (CAV) proven by positive CSF culture. Secondary endpoints were bacterial colonization of the catheter tip and CSF pleocytosis. RESULTS: In 20 control patients, 5 CAVs were microbiologically diagnosed. In contrast, no positive CSF cultures were found in the treatment group. This difference was statistically significant (P < 0.05). All CAVs occurred later than day 10 after catheter placement. Colonization of the catheter tip was found in 6 patients in the control group and in 5 patients in the treatment group (not significant). CONCLUSIONS: This pilot study indicates that EVD catheters impregnated with silver nanoparticles might be a new option for preventing CAV in neurocritical care patients, and therefore evaluation in a large prospective randomized study is warranted.


Subject(s)
Hydrocephalus/surgery , Metal Nanoparticles , Prosthesis-Related Infections/diagnosis , Silver , Ventriculostomy/adverse effects , Acute Disease , Aged , Catheters, Indwelling/adverse effects , Catheters, Indwelling/microbiology , Critical Care , Encephalitis/cerebrospinal fluid , Encephalitis/diagnosis , Female , Humans , Hydrocephalus/cerebrospinal fluid , Male , Middle Aged , Pilot Projects , Prospective Studies , Prosthesis-Related Infections/cerebrospinal fluid , Ventriculostomy/instrumentation
2.
Orthopedics ; 31(8): 756, 2008 Aug.
Article in English | MEDLINE | ID: mdl-19292419

ABSTRACT

The aim of this study was to investigate to what extent patients could resume physical activity following surgery for herniated lumbar disks. We analyzed a cohort of 1003 patients who underwent lumbar spine surgery within 1 year. Out of this cohort, 93 patients were selected according to our inclusion criteria (age 20-35 years, mediolateral single level disk herniation, no comorbidity at the lumbar spine, and treatment with conventional subtotal diskectomy). This group was evaluated after a minimum follow-up of 28 months in a telephone questionnaire; participants were questioned about pre- and postoperative physical activities. The questionnaire was answered by 67 patients. Twenty-six patients were lost to follow-up because they had relocated. The follow-up group had a mean age of 30 years. Five patients underwent a second procedure due to recurrent disk herniation. All patients showed a pain reduction. At follow-up, no patient needed constant pain medication. Eighty-two percent of the patients were pain free during practicing sports. Sixty-two patients performed some type of sport after surgery. Concerning the type and frequency of physical activities, no significant change between pre- and postoperative behavior occurred. The 5 patients with recurrent disk herniation did not behave differently. Single-level lumbar disk surgery does not limit or compromise sportive activity in young people.


Subject(s)
Diskectomy/statistics & numerical data , Intervertebral Disc Displacement/epidemiology , Intervertebral Disc Displacement/surgery , Lumbar Vertebrae/surgery , Motor Activity , Sports/statistics & numerical data , Adult , Austria/epidemiology , Female , Humans , Male , Recovery of Function , Treatment Outcome , Young Adult
3.
Pain ; 62(3): 357-361, 1995 Sep.
Article in English | MEDLINE | ID: mdl-8657436

ABSTRACT

This double-blind, placebo-controlled prospective study investigated whether corticosteroids (beta-methasone) influence residual radicular pain after lumbar disc surgery. The study population consisted of 26 patients undergoing surgery for a herniated lumbar disc at our University Neurosurgical Department. Thirteen patients received beta-methasone intrathecally prior to wound closure, and 13 patients received normal saline. Main outcome measures were pain intensity graded on a 100-mm visual analogue pain scale (VAS) and consumption of non-steroidal anti-inflammatory agents (NSAIDs). Both patient groups had comparable presurgical findings and pain intensity level (55 mm and 54 mm, respectively, on a 100-mm VAS). After surgery, residual pain declined gradually in the placebo group (mean 39, 29, 24, 20 mm on days 1-4; 10 mm on day 8) and abruptly in the corticosteroid group (mean 15, 15, 11, 8, mm on days 1-4; 5 mm on day 8). Analysis of variance (ANOVA) showed a highly significant influence of time (P < 0.001), a significant influence of steroid application (P = 0.014) and interaction between time and application of steroids (P = 0.042). Mean daily consumption of NSAIDs did not differ significantly in either group: 124 mg in the treatment vs. 150 mg in the placebo group (P > 0.25). At follow-up after 6 months, residual radicular pain was rated equally by both groups (4 mm in the treatment vs. 5 mm in the placebo group, P > 0.5). Intrathecal application of steroids provides short-lasting, significant pain reduction after lumbar disc surgery. Benefits of intrathecal steroids are probably outweighed by the risks associated with violation of the dural barrier.


Subject(s)
Intervertebral Disc/surgery , Pain, Postoperative/drug therapy , Palliative Care , Steroids/administration & dosage , Adult , Double-Blind Method , Female , Humans , Injections, Spinal , Lumbosacral Region , Male , Pain Measurement , Placebos , Prospective Studies
SELECTION OF CITATIONS
SEARCH DETAIL
...