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1.
Tijdschr Psychiatr ; 61(9): 649-653, 2019.
Article in Dutch | MEDLINE | ID: mdl-31560785

ABSTRACT

A 19-year-old female was seen at the emergency department following an auto-intoxication. An oculogyric crisis (ogc) was observed, in the absence of other extrapyramidal symptoms (eps). In a second anamnesis, patient indicated that she had taken risperidone 3 mg (an atypical antipsychotic). This particular case description of an isolated ogc shows that care providers should be attentive to the occurrence of ogc, even if the most frequent eps are absent. This case also emphasizes the importance of a complete history in order to efficiently and timely guide the care provider to the correct diagnosis.


Subject(s)
Antipsychotic Agents/adverse effects , Dystonia/chemically induced , Ocular Motility Disorders/chemically induced , Risperidone/adverse effects , Diagnosis, Differential , Dystonia/diagnosis , Female , Humans , Ocular Motility Disorders/diagnosis , Psychotic Disorders/drug therapy , Young Adult
2.
Tijdschr Psychiatr ; 59(6): 360-365, 2017.
Article in Dutch | MEDLINE | ID: mdl-28613368

ABSTRACT

BACKGROUND: Because psychostimulant intoxication can lead to serious health risks for the patient, it is often necessary to ensure that the patient receives both adequate medical surveillance and rapid tranquillisation.
AIM: To find out whether there is scientific evidence that psychopharmacological intervention helps patients with psychostimulant intoxication to manage aggression and agitation.
METHOD: We searched the literature systematically.
RESULTS: Our study showed that intravenous droperidol worked faster and was more effective than intravenous lorazepam in inducing sedation in patients intoxicated with psychostimulants. In other studies the number of patients intoxicated with psychostimulants was too small or the patient population was not described in sufficient detail for any meaningful conclusions to be drawn.
CONCLUSION: So far, research has been so limited that it has not yet provided convincing evidence about the best medication to use in the treatment of aggressive patients intoxicated with psychostimulants.


Subject(s)
Antipsychotic Agents/therapeutic use , Psychomotor Agitation/drug therapy , Psychotic Disorders/drug therapy , Aggression/drug effects , Droperidol/therapeutic use , Humans
4.
Acta Neurol Belg ; 109(2): 63-80, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19681438

ABSTRACT

Since the development of Deep Brain Stimulation (DBS) for Parkinson's Disease, DBS has been suggested as a treatment option for various other neurological disorders. Stimulation of deep brain structures for refractory epilepsy appears to be a safe treatment option with promising results. As research on the evaluation and optimization of DBS for refractory epilepsy may be difficult and unethical in patients, studies on animal models of epilepsy are indispensable. Various brain structures and specific nuclei such as the basal ganglia, the cerebellum, the locus coeruleus and temporal lobe structures have been investigated as target areas for DBS. Additionally, a wide variety of stimulation parameters are available, with a range of stimulation frequencies, pulse widths and stimulation intensities. This review provides an overview of the relevant literature on experimental animal studies of DBS for epilepsy. Knowledge gained from animal studies can be used to answer questions regarding the optimal brain targets and stimulation parameters in human applications.


Subject(s)
Deep Brain Stimulation/methods , Disease Models, Animal , Epilepsy/therapy , Animals , Humans
5.
Int J Med Inform ; 77(3): 199-207, 2008 Mar.
Article in English | MEDLINE | ID: mdl-17631412

ABSTRACT

OBJECTIVE: To evaluate the feasibility and acceptability of a computer reminder system (CRS) to improve prescribing behaviour in general practice and to explore the strengths and weaknesses of a reminder system. One group of GPs received reminders on cholesterol lowering drugs, the other group on antibiotics, asthma and COPD drugs. METHODS: Process evaluation of the computer reminder system being used by 53 GPs in 20 practices, by means of an analysis of the research database of the CRS. In addition, a questionnaire and semi-structured face-to-face interview were conducted with all GP practices, two project leaders, and one technical consultant. RESULTS: The strategy was largely carried out as planned, although the development period for the CRS had to be extended. Nine percent of the GPs dropped out. We found a significant learning curve without extinguishing effect (p=0.03) for the antibiotics reminders. The questionnaire showed that, in general, GPs were satisfied with the user-friendliness and the content of the different types of reminders, but less satisfied with certain specific technical performance issues of the system. The GPs reported mixed feelings towards the CRS in the interviews. They were generally positive about the guidelines themselves, but negative regarding to the organisational context and the method of implementing the CRS. GPs stated that they sometimes manipulated the system to bypass reminders. Interviews with the project leaders and technical consultant revealed barriers to cooperation and miscommunication between the different parties, and technical problems with multiple updates of the GP information system and the operating system. CONCLUSIONS: This process evaluation demonstrated that the implementation of the CRS was mainly carried out as planned, but the subjective experience of working with the CRS was not only positive. Participating GPs had mixed feelings, and quite a number of barriers need to be addressed to facilitate large-scale implementation of the CRS. Costs cannot be neglected, so it is important to analyse the balance between costs and effects.


Subject(s)
Attitude of Health Personnel , Drug Prescriptions , Practice Patterns, Physicians'/standards , Primary Health Care , Reminder Systems , Anti-Bacterial Agents/therapeutic use , Anticholesteremic Agents/therapeutic use , Asthma/drug therapy , Feasibility Studies , Humans , Interviews as Topic , Netherlands , Pulmonary Disease, Chronic Obstructive/drug therapy , Surveys and Questionnaires
6.
Acta Clin Belg ; 60(6): 329-37, 2005.
Article in English | MEDLINE | ID: mdl-16502593

ABSTRACT

A multidisciplinary expert panel, appointed by the High Council for Public Health, evaluated the scientific evidence on which the recommendations for the appropriate use of the pneumococcal vaccine was based and reviewed the studies that became available since previous reports. The conclusions of the working group, presented in this manuscript, resulted in an update of the Belgian recommendations for pneumococcal vaccination.


Subject(s)
Pneumococcal Infections/prevention & control , Pneumococcal Vaccines/administration & dosage , Adult , Aged , Belgium , Cost-Benefit Analysis , Humans , Pneumococcal Infections/complications , Pneumococcal Vaccines/economics , Practice Guidelines as Topic , Treatment Outcome
7.
J Vet Med Sci ; 57(5): 917-20, 1995 Oct.
Article in English | MEDLINE | ID: mdl-8593302

ABSTRACT

In 3 farrow-to-finish farms with enzootic classical swine fever (CSF) all sick pigs were culled and an intensive vaccination program was introduced. Boars and cows were vaccinated every 6 months and piglets at the age of 6 and 8 weeks. The infection was monitored on clinical grounds and by means of serological examination of the farms. Serological results reflected well the clinical situation in the farms. High titers and high percentage of animals with positive titers were observed in infected farms, compared to lower titers in a clinically "free" farm, which were interpreted as titers due to vaccination. Although clinical improvement was noticed, the rigid vaccination regime was not able to control CSF in none of the farms. In all cases, a small percentage of pigs in the finishing stage was still affected. Since these pigs seemed not to have responded to vaccination at 6 and 8 weeks of age, the programme was questioned. Additionally, very high titers were recorded in sows from infected farms, which would automatically extend the period of passive protection in offspring and postpone the age at which piglets could be vaccinated. More intensive programmes, which include also vaccination beyond the age of 8 weeks, were suggested to bring enzootic infections under control.


Subject(s)
Antibodies, Viral/blood , Classical Swine Fever Virus/immunology , Classical Swine Fever/immunology , Vaccination/veterinary , Viral Vaccines , Aging/immunology , Animals , Classical Swine Fever/epidemiology , Classical Swine Fever/prevention & control , Female , Follow-Up Studies , Longitudinal Studies , Male , Philippines/epidemiology , Swine
9.
Eur J Anaesthesiol Suppl ; 1: 17-24, 1987.
Article in English | MEDLINE | ID: mdl-3126050

ABSTRACT

Owing to the rapid blood:brain equilibration and the short duration of action, alfentanil is well suited for use in infusion techniques. A pharmacokinetic basis is given for alfentanil infusion schemes in patients undergoing routine surgery. Practical schemes can be worked out according to the general principle of a loading dose followed by a maintenance infusion. The loading dose of 100 micrograms kg-1 may be given as a short infusion, as two incremental doses, or as a combination of a single dose and short infusion. The maintenance infusion rate of approximately 1 microgram kg-1 min-1 results in steady-state plasma levels in the therapeutic range in most patients. Application of small extra doses, in addition to the maintenance infusion and modification of the infusion rate, might result in an appropriate and safe anaesthetic technique in most patients and surgical situations.


Subject(s)
Analgesics/pharmacokinetics , Fentanyl/analogs & derivatives , Alfentanil , Analgesics/administration & dosage , Analgesics/blood , Fentanyl/administration & dosage , Fentanyl/blood , Fentanyl/pharmacokinetics , Humans , Infusions, Intravenous/methods
10.
Article in English | MEDLINE | ID: mdl-3126051

ABSTRACT

The administration of alfentanil by infusion appears to present advantages for the induction and maintenance of anaesthesia during general surgery lasting over 1 h. The following dosage scheme is proposed: a loading dose of 100 micrograms kg-1, given either in one or two doses, or as a fast infusion administered over 10 min, followed by a maintenance infusion at a rate of 1 microgram kg-1 min-1. During maintenance anaesthesia, the infusion rate should be the lowest possible compatible with adequate analgesic effect, and should be further decreased 15-20 min before the projected end of surgery. Fine control of the opioid effect can be achieved with small increments of 7-15 micrograms kg-1 or by alterations of the alfentanil infusion rate. Breathing should be carefully monitored during the post-operative phase. Dedicated syringe pumps have been designed to avoid laborious calculations of the infusion rates and allow simple, rapid changes of the infusion rate.


Subject(s)
Anesthetics/administration & dosage , Fentanyl/analogs & derivatives , Alfentanil , Fentanyl/administration & dosage , Humans , Infusions, Intravenous/instrumentation , Infusions, Intravenous/methods
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