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1.
Mil Med Res ; 7(1): 23, 2020 05 10.
Article in English | MEDLINE | ID: mdl-32389124

ABSTRACT

BACKGROUND: Intracranial infection after craniotomy is one of the most serious postoperative complications, especially multidrug-resistant (MDR) or extensively drug-resistant (XDR) bacterial meningitis, and strongly affects the prognosis of patients. Current treatment experience regarding these infections is scarce. CASE PRESENTATION: We report a case of severe intracranial infection of XDR Acinetobacter baumannii (A. baumannii) that was treated by intravenous (IV) injection, sequential intraventricular (IVT) injection of tigecycline and polymyxin B, and other anti-infective drugs. Good results were obtained, and the patient was eventually discharged from the hospital. This case is characterized by intracranial infection. CONCLUSIONS: The polymyxin B IV + IVT pathway is an ideal treatment strategy for XDR A. baumannii. The tigecycline IVT pathway is also a safe treatment option.


Subject(s)
Acinetobacter Infections/drug therapy , Polymyxin B/pharmacology , Tigecycline/pharmacology , Acinetobacter Infections/physiopathology , Acinetobacter baumannii/drug effects , Acinetobacter baumannii/pathogenicity , Adult , Humans , Injections, Intraventricular/methods , Injections, Intraventricular/standards , Injections, Intraventricular/statistics & numerical data , Male , Meningitis, Bacterial/drug therapy , Meningitis, Bacterial/physiopathology , Polymyxin B/therapeutic use , Tigecycline/therapeutic use , Tomography, X-Ray Computed/methods
2.
Neurosci Lett ; 322(2): 107-10, 2002 Apr 05.
Article in English | MEDLINE | ID: mdl-11958855

ABSTRACT

Antisense oligodeoxynucleotides (ODNs) can inhibit gene expression in a specific manner. However, several studies described problems with cerebral ODN application. Here, we investigated the immune effects (interleukin-6 (IL-6) release, cell invasion into cerebrospinal fluid (CSF) and brain parenchyma) of 'non-sense' randomized ODNs with different counterions (NH(4)(+), Na(+)) and modifications (with or without thioat-backbone) which were administered intracerebroventricularly for 48 h using osmotic mini-pumps in a rat model. All animals receiving ODNs showed increased IL-6 levels in the CSF as well as cell invasion into the CSF and brain parenchyma (P<0.05). However, the use of thioat-backbone and ammonium as the counterion induced the highest IL-6 levels (7210+/-1696 pg/ml, P<0.05) and the highest cell numbers in the CSF (31.6+/-15.5x10(5)/ml, P<0.05) as well as brain parenchyma (268.1+/-143.2 HIS-48+ cells/mm(2), P<0.01; and 31.3+/-10.7 OX-6+cells/mm(2), P<0.05) compared with the other groups.


Subject(s)
Brain/drug effects , Brain/pathology , Oligodeoxyribonucleotides, Antisense/administration & dosage , Animals , Brain/immunology , Encephalitis/cerebrospinal fluid , Encephalitis/chemically induced , Encephalitis/immunology , Infusion Pumps/statistics & numerical data , Injections, Intraventricular/methods , Injections, Intraventricular/statistics & numerical data , Interleukin-6/cerebrospinal fluid , Male , Rats , Rats, Sprague-Dawley
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